CBAHI Hospital Accreditation Guide October 2016
CBAHI Hospital Accreditation Guide October 2016
CBAHI Hospital Accreditation Guide October 2016
October 2016
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Introduction
The Saudi Central Board for Accreditation of Healthcare Institutions (CBAHI) Hospital Accreditation
Process Guide was developed to serve as a reference for hospitals during the preparation for
accreditation surveys as well as maintenance of accreditation. This guide is to be used in conjunction
with the third edition of CBAHI Hospital Accreditation Standards manual. It has been created to help
hospitals learn about the third edition of the national hospital accreditation standards’ survey process.
In addition, the guide has been designed to provide hospitals with an authoritative resource to use in
preparation for an accreditation survey. It addresses the activities required for conduction of a hospital
survey and form the basis for a successful accreditation survey. Additionally, it provides hospitals with
a means of ongoing self-assessment and continuous improvement.
CBAHI employs a dynamic development process to fulfill our mission as a driver for continuous
improvement. Any further modifications will be communicated to the hospitals through later editions
and amendments.
About CBAHI
What is CBAHI?
CBAHI, or the Central Board for Accreditation of Healthcare Institutions is a governmental organization
that promotes the quality, value, and optimal outcomes of health. CBAHI currently accredits in the
following areas:
Hospitals
Primary Healthcare Centers (PHC)
Regional labs and blood banks
Mission
To promote quality and safety by supporting healthcare facilities to continuously comply with
accreditation standards.
Vision
To be the regional leader in improving the healthcare quality and safety.
Values
Commitment to excellence
Team spirit
Integrity
Professionalism
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Registration with CBAHI
All hospitals are required to register with CBAHI. To register, the following steps are followed:
1. Leadership (LD)
2. Human Resources (HR)
3. Management of Information (MOI)
4. Medical Records (MR)
5. Quality Management and Patient Safety (QM)
6. Social Care Services (SC)
7. Patient and Family Rights (PFR)
8. Medical Staff (MS)
9. Radiology Services (RD)
10. Physiotherapy Services (PT)
11. Respiratory Care Services (RS)
12. Dietary Services (DT)
13. Nursing Care (NR)
14. Patient and Family Education (PFE)
15. Provision of Care (PC)
16. Anesthesia Care (AN)
17. Emergency Care (ER)
18. Critical Care (ICU – CCU-PICU)
19. Operating Room (OR)
20. Medication Management (MM)
21. Infection Prevention and Control (IPC)
22. Laboratory (LB)
23. Facility Management and Safety (FMS)
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Goal of Accreditation Surveys
The goal of the survey is to determine if the hospital is in compliance with CBAHI Hospital
Accreditation Standards. Also where appropriate, CBAHI surveyors provide education and consultation
to the hospital’s staff throughout the survey to help them improve their clinical and administrative
processes.
Assessment of Compliance
The CBAHI expects substantial compliance with all applicable standards. The surveyors assess
compliance with standards through a combination of data sources that include at least one of the
following:
1. Interviews with hospital Leadership, clinical and support staff, patient and family. Observation
of patient care and services provided.
2. Building tour and observation of patient care areas, building facilities, equipment management,
and diagnostic testing services.
3. Review of written documents such as policies and procedures, orientation and training plans and
documents, budgets, and quality assurance plans.
4. Review of personnel files.
5. Review of patients’ medical records.
6. Evaluation of the hospital’s achievement of specific outcome measures (e.g., hospital-acquired
infection rates, patient satisfaction) through a review and discussion of monitoring and
improvement activities.
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“2” = Satisfactory compliance when ≥ 80 % compliance with the sub-standard or compliance is for
four months prior to the initial survey or twelve months for the triennial survey.
“NA” = Not Applicable indicates that the standard/sub-standard does not apply to the hospital.
The overall score of the hospital is automatically calculated by the software application using the
average (arithmetic mean) score of all applicable sub-standards, i.e. as the sum of all values divided by
the number of values added.
When one or more chapters, standards, and/or sub-standards of the standards manual are not applicable
in a particular hospital, they are indicated by “N/A”. Non applicable chapters and standards are not
scored and are not included in either the numerator or denominator of the overall score.
Scoring guidelines apply a similar method to sub-standards requiring a sample for assessment of
compliance. For example, if observations are positive in ≥ 80 % of cases, if interviewees provide proper
answers in ≥ 80 % or if the average of positive findings in personnel records or medical records is ≥ 80
%, the score of the sub-standard will be fully met.
The Accreditation Decision Committee shall recommend one of the following accreditation decisions:
Accredited:
Accreditation will be awarded when the surveyed hospital demonstrates an overall acceptable
compliance with all applicable standards at the time of the initial (or reaccreditation) on-site survey, and
there are no issues of concern related to the safety of patients, staff or visitors.
Accreditation will also be recommended when the healthcare facility has successfully addressed all
requirements following a conditional accreditation and does not meet any rules for other accreditation
decisions. The decision to grant accreditation is not always straightforward. In some cases though, the
Accreditation Decision Committee
may consider the need for more clarification and/or a follow up focused survey of specific
standards/areas of concern or noncompliance before a consensus decision to grant accreditation can be
reached. This will also give the hospital a period of time to come into acceptable compliance.
Scoring Guidelines:
Overall score 85% or above and
All essential safety requirements are in satisfactory compliance and
No other issues of concern related to the safety of patients, visitors or staff.
Conditional Accreditation:
Conditional Accreditation is granted when the hospital demonstrates a tangible compliance with all
applicable standards at the time of the on-site survey but still has not met requirements for accredited
status. The hospital is required then to develop a “Standards Compliance Progress Report”, followed by
a “follow up Focused Survey”
if required before changing the accreditation status. The non-compliant standards may include essential
safety requirements and/or other standards/issues of concern related to the safety of patients, staff or
visitors.
Scoring Guidelines:
Overall score 75% or above and less than 85% and/or
Some of the essential safety requirements (but not exceeding 25% of them) are not in satisfactory
compliance.
Denial of Accreditation:
Results when a health care facility shows a significant noncompliance with the accreditation standards
at the time of the on-site survey. It also results if one or more of the other reasons leading to preliminary
denial of accreditation have not been resolved. When the hospital is denied accreditation, it is prohibited
from participating in the accreditation program for a period of six months, unless the Director General
of CBAHI, for good reason, waives all or a portion of the waiting period.
Scoring Guidelines:
Overall score less than 75% and/or
More than 25% of the essential safety requirements are not in satisfactory compliance.
Hospital Responsibilities
Hospital’s survey coordinator
When the hospital completes its survey application, the hospital should select a person to serve as
hospital’s survey coordinator to handle the logistics of the survey visit. The hospital’s survey coordinator
designated by the hospital will serve as the liaison with the Healthcare Accreditation Department (HAD)
and the survey team leader about the survey visit arrangements.
Survey Team
A list of survey team members, with their biographies, will be sent to the hospital prior to the survey
visit. The hospital should contact the Healthcare Accreditation Department (HAD) promptly if any
surveyor is deemed to be inappropriate due to conflict of interest or other valid reasons.
Note: CBAHI cannot honor requests for specific surveyors for the purpose of objectivity.
Travel Arrangements
The hotel and flight reservations will be arranged by CBAHI. All flights are booked to be the night
before the survey. A list of assigned surveyors together with their flights’ details and mobile numbers
will be sent to the hospital’s survey coordinator prior to the survey. The hospital should arrange ground
transportation from the airport to the hotel. The hospital should decide how to transport the team
members each day between their hotel and the hospital and to any remote sites they will visit as part of
the survey. The survey team leader and hospital’s survey coordinator should determine where and when
the team will be picked up or meet at the hotel. Additionally, the hospital should arrange transportation
from the hotel to the airport according to the departure time of surveyors.
Staff Involvement
A well-conducted survey requires important information from a broad range of staff for the deliberations
of the survey team. All survey team members interview different staff categories about a variety of
topics to ensure that the team has access to truly representative information related to implementation
of CBAHI standards from staff.
Conflict of Interest
CBAHI works to ensure the integrity and fairness of all businesses run by the employees working in the
central office as well as the surveyors. In addition, all healthcare facilities engaged in CBAHI
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accreditation process are required to refrain from any actual or potential act or behavior that might create
a conflict of interest including:
Proposing any fee, remuneration, gift, or gratuity of any value to CBAHI employees or surveyors
for performance of their duties or survey-related activities.
Employing or contracting or having any financial relationship with CBAHI employees or
surveyors for the purpose of the provision of consulting or related services in any capacity, either
directly or through another party. This includes services provides in preparation for the survey,
assisting in preparation of the self-assessment, conducting mock surveys, helping in the
interpretation of the standards, and alike. All requests for consulting services utilizing one of
CBAHI associates shall be directed to CBAHI central office.
Not declaring to CBAHI any business (including consulting) or recruiting relationship with one
or more of CBAHI surveyors either directly or through another party with whom he or she is
affiliated, at any time during the preceding three (3) years.
Survey Logistics
Hospitals should provide appropriate logistics that include the following:
A workroom that is large enough for the survey team members to review documents and leave
computers and binders. The workroom needs to be furnished with a desk or table, access to
electrical outlets, and internet access.
A workroom(s) for group meetings and interviews with staff as specified in the survey agenda.
Assigning a counterpart for each surveyor who is a responsible person for the same specialty
during the survey.
Hospital Observers
When the hospital’s team includes an observer, who may represent a consulting firm or staff from other
hospitals, the hospital must inform CBAHI and obtain its official approval at least one week prior to the
survey. Observers must not participate in the survey activities.
CBAHI observers/mentors
One or more observers or mentors may join the CBAHI survey team as part of the surveyors’ training
process. Observers and mentors from CBAHI side will be included in the list of the surveyors sent by
hospital accreditation department prior to the survey.
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CBAHI Survey Process
Overview
This section details the various activities of a hospital survey. For better understanding of the
accreditation survey process, the survey related activities are organized into the following three sections
in this guide:
Pre-Survey Activities
On-Site Survey Activities
Post-Survey Activities
Pre-Survey Activities
Enrollment for Survey
The accreditation process begins with selection of the hospitals to be surveyed. Each year, CBAHI selects the
hospitals to be enrolled in the accreditation program. CBAHI sends a letter of enrollment to the selected hospitals
to start their application process.
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Some hospitals will prefer to go for a Mock Survey but this is subject to the availability of adequate
resources at CBAHI and the requirement of its operational plans. CBAHI therefore is not obliged to
respond to all incoming mock survey requests.
6. Consultative Visit
CBAHI provides consultative visits upon request. These visits are optional and depend on the
availability of CBAHI resources. The consultative visits provide in-depth explanation of one or more
of the functions or areas covered by the standards.
7. Requests for Interpretation of Accreditation Standards and Policies
CBAHI responds to requested interpretation of an existing accreditation standard or policy. Requests
must be made in writing. Information on submitting a written request is available on the CBAHI website.
The requester can fill out a “contact us” form.
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Understand more clearly the issues that are of interest to CBAHI
Export the data for analysis and evaluation by CBAHI
How this self-assessment tool is constructed
The SAT is designed to walk the user through all the CBAHI hospital accreditation standards. The tool
is designed to include all standards arranged per chapters that parallel the CBAHI standards manual.
The tool allows the users to keep track of the specific planning and response considerations their hospital
has addressed. This SAT contains a number of sections under each chapter:
A standard section that contains a standard with its related sub-standards drawn from current
CBAHI standards manual.
An activity section that contains the activity (and related activities, if applicable) that will be
used to assess this sub-standard.
A document description section that contains the name and the description of the document
required in this sub-standard (if applicable).
A scoring section contains scoring points which you consider when reflecting on a sub-standard
statement.
A comments box gives you space to record the assessment findings of your compliance, highlight
strengths and weaknesses and document your improvement plan.
How frequently should the self-assessment be performed?
CBAHI accreditation policies require hospitals to conduct self-assessment during preparation for an
initial survey and at the middle of an accreditation cycle of an accredited hospital, i.e., eighteen months
after awarding accreditation.
During preparation for an initial survey, the SAT facilitates the process of evaluation of the
hospital’s readiness for an accreditation survey in addition to helping the hospital in preparation
for the survey.
o All registered hospitals with CBAHI should do self-assessment and submit to CBAHI
within 3 months of notification of their enrollment in CBAHI visit plan per that year.
o To be eligible for CBAHI visit you should have a SAT score of 70% or more and all
ESRs are in full compliance.
o If SAT score below 70% and/or ESRs are not in full compliance, the hospital will be not
eligible for CBAHI visit temporarily till re-submission of SAT again after more 3 months
to re-evaluate their readiness and hospital visit will be decided thereafter.
Three months before the middle of an accreditation cycle (fifteen months after the accreditation
award), each accredited hospital will be notified regarding its due time for submission of its
SAT. The hospital has three months to conduct and submit its self-assessment. The hospital is
required to send CBAHI its self-assessment together with an action plan for standards that are
not in full compliance. The CBAHI requirements related to the mid-term self-assessment are
detailed in the accreditation policies section of the standard manual.
CBAHI considers that the self-assessment is an important part of the process of hospital improvement,
and is recommended to be an ongoing activity within the hospital. Hospitals are recommended to
perform the self-assessment more frequently (e.g., quarterly) to ensure ongoing compliance, look at
progress overtime, and consequently improve the quality and safety of services provided.
How to use this tool
There are three point rating scales which ask you where the hospital is with respect to the issues
underlying the sub-standards. The hospital staff record which standards the hospital has insufficient
compliance, partial compliance or satisfactory compliance. Each sub-standard is scored from 0–2 where
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0 = insufficient compliance, 1 = partial compliance, and 2 = satisfactory compliance. Some standards
may not be applicable to your hospital. These standards should be marked as “NA” = Not Applicable.
The rating scales are expected to help you determine where to focus your improvement efforts. When
you repeat the self-assessment, the rating scales may also help you to monitor the progress you have
made over time.
The self-assessment results in the compilation of compliance reports. These reports are then used to
identify non-compliance areas as well as other opportunities for improvement. Initiating and maintaining
improvement steps are most effective when they are planned and implemented organization-wide. The
hospital leaders collaborate with relevant staff members to prioritize, plan and implement corrective
action plans that address all identified noncompliant areas. The action plan should identify all non-
compliant standards, the required interventions with defined dates, the responsible staff members, and
as applicable, monitoring measures that ensure sustainability of the implemented interventions. These
plans, when implemented and routinely monitored, contribute to the proper compliance with standards
and consequent provision of quality care.
How the hospitals can access the self-assessment tool
The SAT is freely available on the hospital portal to use. Upon registration, the hospital receives a user
name and password that are used to download the tool. This section is designed for users responsible for
self-assessment administration and completion of the online self-assessment. It provides step-by-step
instructions on how to complete a task.
The self-assessment is an internet based program that provides features for:
• Entering self-assessment findings
• Sending surveys to respondents for completion
Appearance may differ in other environments. If you require further assistance, contact the System
Administrator at had@cbahi.gov.sa
System requirements
The online self-assessment is best viewed in the latest Internet Explorer or Google Chrome. Minimal
system requirements include:
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Off-Site Survey Activities
The hospital scheduled for the onsite survey shall send a list of the off-site required documents, listed
below, for the off-site review by the surveyors at least two (2) weeks prior to the date of the onsite
survey. The list shall be communicated, as a signed and scanned PDF document, with the Healthcare
Accreditation Department (HAD).
List of policies to be sent prior to the survey
# Document Name Related Standards
1. Policy for Development and Maintenance of Policies LD.20
2. Medical Records Documentation Policy MR.5
3. Information confidentiality, security, and integrity PFR.7, MOI.6
4. Committee Management Policy LD.9
5. Policy for Delegation of Authority LD.17
LD.11.2, LD.11.3, LD.12.1,
LD.12.2, LD.12.3, LD.12.4,
LD.12.5, LD.12.6, LD.12.7,
Strategic Plan
LD.15.1, LD.15.2, LD.15.3,
LD.15.4, LD.15.5, LD.15.6,
6. LD.15.11
7. Policy for Contracted Services LD.21, IPC.1
8. Job Description Policy HR.3
9. Policy for Management of Personnel Files HR.4
10. Probationary Period Evaluation Policy HR.8
11. Regular Performance Evaluation Policy HR.9
12. Safe Disposal of Medical Wastes Policy LD.23, IPC.26
MS.1.1, MS.1.2, MS.1.3,
Medical staff bylaws
13. MS.1.4, MS.1.5, MS.1.6
14. Multidisciplinary Medication Management Plan MM.4.1
15. Hospital Drug Formulary MM.8.1
16. Pharmacy Organization Structure MM.2.1
17. Pharmacy Scope of Services LD.28.2
18. Safety of the Building Management Plan FMS.1.1.1
19. Security Management Plan FMS.1.1.2
20. Life/Fire Safety Management Plan FMS.1.1.6
21. Internal Disaster Management Plan FMS.1.1.5
22. External Disaster Management Plan FMS.1.1.4
23. Hazardous Materials and Waste Management Plan FMS.1.1.3
24. Medical Equipment Management Plan. FMS.1.1.7
25. Utility Management Plan. FMS.1.1.8
Civil Defense License/Assessment Report along with
FMS.4.1, FMS.4.2
26. corrective action plan.
27. Safety Committee Terms of Reference FMS.3.1, FMS.3.2, FMS.3.3
Running construction/Renovation/Demolition works (if
FMS.5.1
28. applicable)
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Role of the Visit Team Leader:
Responsibilities of the team leader include but not limited to:
Review the uploaded hospital profile.
Review hospital website (if any) for any additional information related to the survey.
Ensure all logistical arrangements for survey visit via communication with HAD’s accreditation
coordinator.
Coordinating with hospital visit coordinator to finalize the hospital chapter applicability.
Coordinating with hospital visit coordinator to finalize the survey agenda.
Clarify the purpose of the survey visit for the health care facility leaders.
Ensure abidance by the agenda according to the allocated activities.
Deal with any conflicts arising between surveyors and/or with the hospital.
Communicate with hospital visit coordinator the required medical records and personnel files
prior to review sessions.
Coordinate and arrange a new session “if needed”.
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On-Site Survey Activities
Understanding the organization and assessing compliance is accomplished through a number of
activities specified in the survey agenda. The survey commences with an opening conference followed
by a review of documents’ session. A facility tour and departments/units’ visits are also conducted
during the on-site survey where the surveyors observe compliance with standards, interview staff, and
examine open patient medical records and additional documents. This is followed by reviewing a
selected sample of closed medical records as well as personnel files
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o Treat all information provided by other team members with confidence during the
review.
o Timely data entry.
o Daily team meetings (time & venue).
o Strengths & areas for improvement.
o Required materials for exit conference.
Opening Conference
Objectives
To explain the scope of survey and what is expected from the hospital during the survey.
To orient the surveyors about the hospital’s structure, scope of services, staffing, mission, and
vision.
To officially start the on-site survey.
Participants
From CBAHI: The entire survey team
From Hospital: it may include
o Hospital Director
o Medical Director
o Nursing Director
o Administrative Director
o Operations Director
o Quality Improvement Director
o Surveyors' counterpart
Logistics
A workroom that is large enough to hold all participants with data show facility.
Agenda:
The team leader will introduce survey team members.
The hospital leadership will introduce:
o The hospital scope of services
o Highlight the hospital improvement initiatives.
o The surveyors' counterpart to facilitate the smooth flow of the survey process.
Team leader may:
Discuss any modification in the agenda with the hospital leaders.
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Request a short meeting with hospital director or medical director for further clarification of the
scope of activities that were doubted.
Clarify any confusion regarding certain applicability and scope of services with the hospital
leaders.
Review of Documents
Objectives
To evaluate compliance with standards that should be evidenced in written documents.
Participants
From CBAHI: The entire survey team
From Hospital: Staff who are familiar with the hospital’s documents
Logistics
A workroom that accommodates the surveyors together with staff familiar with the hospital’s
documents.
Procedures
Documents required to be reviewed include, but not limited to, policies and procedures manuals,
plans, meeting minutes, and quality indicators. The required documents for review must be
current and approved by relevant leaders.
To facilitate the review of documents, the documents required for review during the document
review session of the on-site survey must be available at the time of the survey. The hospital is
expected to organize the required documents in binders for easy access. The hospital is required
to organize the documents required for review for each surveyor in a separate binder. The binders
should be arranged according to the list provided in this guide in Annex B. At the discretion of
the survey team, surveyors may request additional documents for review during the survey.
It shall be noted, by the hospital, that whenever a standard or a substandard listed in the CBAHI
Standards Manual requires a policy and procedure, the hospital shall prepare the required policy
and procedure for the document review session of the on-site survey listed below, whether or
not it is specified in the list of required documents.
When the hospital elects to present the required documents in an electronic format, the hospital
should provide a printer to be used in case a surveyor requires a hard copy of any document.
It is very much encouraged that the staff accompanying the surveyor (i.e., the surveyor
counterpart) are oriented to the document arrangement.
o Survey team present their findings with special emphasis to cross-linked items.
o Team members may request colleagues from other chapters to assess/check doubtful
issue/s related to their specialty.
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o Team members to present any major/significant issue encounter during the survey.
o Team members to report encountered difficulties in time management.
o Team members to clarify any activity-overlap issue.
o Team members present their next survey activities.
Surveyors Debriefing
There should be no surprises in the survey report, because the surveyors will have already raised any
issues and the hospital is kept abreast of findings. During the survey, the surveyors maintain ongoing
communication with their counterparts from the hospital. This occurs informally as questions arise. The
surveyors present their findings to their counterparts for discussion and clarification. This allows for
direct face-to-face interaction with the surveyors, allows the hospital to clarify or explain possible
discrepancies or compliance issues, and allows for consultation and education. Additionally, the daily
debriefing and the closing conference, at the end of the survey, allow hospitals to challenge cited
deficiencies. Finally, the hospital will review a draft exit report for feedback or correction of any issues
of fact as a step before making the accreditation decision.
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Surveyors will use both closed and open medical records. While closed records determine the
past practice and the frequency of a deficient practice, open patient records reflect services
provided at the time of the survey. See Annex C for standards requiring documentation in the
medical records.
The selection of closed medical records for review is guided by the services provided by the
hospital and any available source of information during the period prior to the survey such as the
top diagnoses and procedures and patient discharge lists. The open medical records for review
are selected from a list of active records provided by the hospital.
Selection Criteria
Physician Closed Medical Record Review
o A sample of medical records will be requested within the look-back period for the
survey (4 months prior to the 1st cycle of accreditation and 1 year for subsequent
accreditation cycles).and it will include –but not limited to- the following:
1. Two terminally ill patient referred to home care (if applicable) or referred to any
other service
2. Two patient transferred to other organizations
3. Two surgical patient
4. Two Sedation patient discharge directly to home after the procedure
5. Two patient refused treatment
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6. Two ICU patient
7. Two CCU patient
8. Two delivery patient
9. Two patient with nutritional risk
10. Two patient receiving therapeutic diet
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Required Personnel Files
LD & QM Surveyor
Hospital Director
Head of Medical Department
Finance Director
Quality Director
HR Director
Medical Records Director
Medical Records Staff
Clinical Coder
Part Time Department Head
Duty Manager
Head of Social Services
Social Workers
Patient Safety Officer
Randomly selected files:
o Contracted Worker
o New Hire
o Admin Staff
o Medical Staff
o Nursing Staff
MD Surveyor
Medical Director
Head of OB/GYN
Head of Anesthesia
Head of OR
Head of ICU
Head of PICU
Head of NICU
Head of CCU
Head of Hemodialysis
Head of ER
Head of Radiology
Head of Burn Unit
Head of Oncology & Radiotherapy
Head of Respiratory Therapy
Head of Physiotherapy
Head of Dental
Randomly selected files:
o Physician who perform sedation
o Anesthesiologist
o Psychiatrist
o Hemodialysis physician
o Hemodialysis nurse
o ER physician
o ER Nurse
o ICU physician
o PICU physician
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o NICU physician
o CCU physician
o OB/GYN physician
o Burn Unit physician
o Oncology physician
o Respiratory Therapist
o Physiotherapist
o Dentist
o Dental Technician
o New hire
NR Surveyor
Nursing Director
Deputy nursing director
Nurse involved in restraint
Nursing assistant
OR nurse manager
ICU nurse manager
PICU nurse manager
NICU nurse manager
CCU nurse manager
OB/GYN nurse manager
ORT nurse manager
Hemodialysis nurse manager
ER nurse manager
Burn unit nurse manager
Randomly selected files:
o Nurse involved in sedation
o ICU nurse
o PICU nurse
o NICU nurse
o CCU nurse
o OB/GYN nurse
o Midwifes
o Newborn nurse
o Hemodialysis nurse
o ER nurse
o Burn unit nurse
o ORT nurse
o Dietary supervisor
o Dietitian
o New hire
MM Surveyor
Pharmacy Director
Pharmacy Quality coordinator
IV pharmacist
IV technician
TPN pharmacist
TPN technician
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Chemotherapy pharmacist
Chemotherapy technician
Drug Information pharmacist
Randomly selected files:
o Nurse compounding sterile products
o Medication administration nurse
o Selected pharmacy staff
o New hire
IC Surveyor
IC Director
IC Practitioners
CSSD Supervisor
CSSD staff
Randomly selected files:
o Contracted worker
o Sample From Hospital
o New hire
LB Surveyor
Lab director
Lab supervisor
Lab sections heads
Lab technicians
Blood bank technicians
POCT technician
Randomly selected files:
o POCT staff
o Contracted worker
o New hire
FMS Surveyor
FMS Director
Safety Officer
Staff Handling Nuclear Material
Security Staff
House Keeper
Store Keeper
Biomedical Engineer
Electrical Engineer
Maintenance Engineer
SFDA Liaison Officer
HVAC System Maintenance Engineer
Water System Maintenance Engineer/Technician
PMG System Maintenance Engineer/Technician
Randomly selected files:
o Maintenance staff
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o Nursing Staff
o Contracted Worker
o New Hire
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Facility Tour and Unit Visits
Objectives
To interview staff to evaluate their education about the standards.
To observe the implementation of standards and ensure that they are in place, e.g., condition of
the hospital (FMS chapter) and infection control practices (IPC chapter).
To examine open medical records in patient care areas.
To review additional documents in respective departments/services, e.g., pharmacy, laboratory,
infection control, and facility management and safety.
To interview patients.
Participants
From CBAHI: The entire survey team
From Hospital: Staff and management involved in the patient’s care or other services in the area
visited.
Logistics
Hospitals should assign a counterpart for each surveyor to guide the surveyor to the various
survey sites.
Procedures
During this activity, the surveyor moves through the hospital and visits all areas of the hospital
that affect the delivery of care and services. The From Hospital are interviewed, facilities are
observed, and records are checked to ensure compliance with certain standards’ requirements.
This activity also includes a facility tour conducted for review of infection control and facility
management and safety standards.
The surveyors determine the units, departments, and other areas to be visited during the survey
process.
At all times during the unit visits, the surveyors gather information with minimal disruption of
the daily activities of the hospital being surveyed.
Hospitals are expected to have their key personnel present during their respective area visit. In
addition, the surveyors may request a particular staff category, when needed.
Specialty-specific visits and a facility tour are also included in this activity. Surveyors will
interview individuals responsible for managing the following departments / committee(s) in
addition to review of related documents in their respective departments. Areas/departments
visited by surveyors during the specialty-specific visits include:
Laboratory (LB chapter): laboratory department.
Pharmacy (MM chapter): pharmacy, outpatient clinics, and any other area where a
medication may exist.
Facility Management and Safety (FMS chapter): roof, kitchen, laundry, generator, electrical
room, medical gases room, workshops, main store, reverse osmosis plant, biomedical
workshop, procedures room, central sterilization, patient care rooms, bathrooms, waste
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collection rooms, staircases, corridors, main entrances, emergency exits, isolation room,
ambulances, and nurse stations.
Infection Control (IPC chapter): operating rooms, central sterilization, kitchen, infection
control unit, isolation rooms, staff health clinic, laundry, dental clinic, and any other areas
that may be used by patients.
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CBAHI SURVEY / MEETINGS AND COMMITTEES:
No Activity Venue/ Room Set- Day Duration Chairperson
. st up Style
1. 1 Day Surveyor planning Conference 1st Day 30 minutes VTL
session Room
2. Opening Conference Hospital Auditorium 1st Day 30 minutes VTL
4. 1st Day Surveyors End of the Conference Style 1st Day 60 minutes VTL
Day Meeting Room
5. 2nd Day Surveyor planning Conference Style 2nd Day 30 minutes VTL
session Room
6. 2nd Day Surveyors Debriefing Hospital Auditorium 2nd Day 30 minutes VTL
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Executive Leadership Interview Session
Aim:
To clarify and discuss findings encounter during the survey.
The survey team may also explore the leadership’s support for different functions within the
organization by forwarding, to the Executive Interview Session, survey activities related to
patient and family rights, outcomes of hospital committees, and departmental improvement
projects.
Attendees:
CBAHI:
The entire survey team.
Hospital:
1. Governing Body representative
2. Hospital Director
3. Medical Director
4. Operations Director
5. Nursing Director
6. Quality Improvement Director
7. Others may be invited based on need (VTL will ifor the hpspita; QM
Duration: 60 minutes
Schedule: To be held on the 3rd day of the survey, before compiling the Exit Report”.
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2. Discussion; Survey team members who have forwarded survey activity(ies) to the session
will take turns in presenting their questions/inquiries as per the agreed upon sequence.
3. Closing; the VTL shall bring the meeting to closure by identifying the remaining activity in
the survey agenda, convening the projected time for the “Exit Conference”
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Quality and Patient Safety Committee and Data Management Session
Aim: To have an overview on the hospital-wide quality improvement and patient safety program, including how
data and information are managed and communicated to end users to better hospital services.
Attendees: Current members of the committee with a minimum number to meet the quorum as per terms of
reference. According to the available specialties in the hospital, the following are the least number required to
attend:
Duration: 90 minutes (30 minutes for review of related documents + 60 minutes Interactive discussion)
Schedule: To be held on the 2 nd day of the survey. Avoid overlap with any other meetings to augment
membership attendance.
Agenda:
1. Introduction
2. Hospital presentation on the quality improvement and patient safety program to include:
a. QI program structure
b. QI program flow (how it is integrated with other hospital-wide programs)
c. Highlight on an improvement project
d. Performance indicators’ monitoring process
e. Key performance indicators’ reports submitted to the governing body
f. Risk management initiatives and data trends
g. Management of data and information processes
i. Information needs assessment process
ii. Information management structure
iii. Data management education and training
iv. Data and report flow and management
3. Open discussion between surveyor and hospital representative.
4. Other topics may be raised and discussed based on the surveyor findings during the hospital visit.
Required Documents:
The hospital is requested to have documentations related to its quality improvement program, patient safety
initiatives, risk management program and activities, data and information management process, and
improvement projects present during this session. These may include, but not limited to:
1. Terms of reference of the quality improvement committee, patient safety team or equivalent.
2. Committee membership list.
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3. Minutes of meetings for the tracking period.
4. Managerial and clinical performance monitoring indicators
5. Patient safety indicators.
6. Improvement projects or programs (may include list of projects and teams if available)
7. Improvement activities based on information resulting from data analysis
8. Risk management program
9. Patient safety program
10. Key performance indicators’ reports submitted to the governing body
11. Incidents reporting system and data trends
12. Annual review of committee performance
13. Information needs assessment process and report
14. Information management related activities, education and reports
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Infection Prevention and Control Committee Interview
Aim:
To have an overview about the infection prevention and control program and to ensure it is implemented
in the hospital as a multidisciplinary process.
To discuss the role of the committee in monitoring and supporting the IPC program.
Attendees:
Duration: 60 minutes (15 Min. for review of related documents + 45 Min. Interactive discussion)
Schedule: To be held on the late afternoon of the 2nd day of the survey. Avoid overlap with quality and data
session or any other meetings to augment membership attendance.
Agenda:
1. Introduction
2. Discussion about the essential role of the committee and its outcome
3. Review of the required documents
4. Other topics may be raised and discussed based on the surveyor findings during the hospital visit.
Required Documents:
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Pharmacy and Therapeutics Committee Interview
Aim:
To have an overview about the medication management program and to ensure it is implemented in the
hospital as a multidisciplinary process.
To discuss the role of the committee in monitoring and supporting the medication management program.
Attendees:
Duration: 60 minutes (15 Min. for Review of related documents + 45 Min. Interactive discussion)
Schedule: To be held on the afternoon of the 2nd day of the survey. Avoid overlap with quality and data session
or any other meetings to augment membership attendance.
Agenda:
1. Introduction
2. Discussion about the essential role of the committee and its outcome
3. Review of the required documents
4. Other topics may be raised and discussed based on the surveyor findings during the hospital visit.
Required Documents:
The hospital is requested to have documentations present at the P&T review session
1. Terms of reference of the P&T committee.
2. Committee membership list.
3. Meeting minutes for the last twelve months.
4. Drug Formulary.
5. Relevant indicators (e.g. drug utilization review reports)
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Environmental Safety Committee Interview
Aim:
To have an overview on how the hospital manages its facilities and ensures safety of its employees,
patients, and visitors at all times.
To discuss the activities of the safety committee and the optimal utilization of its functions in improving
a safe work and care environment at the hospital.
Attendees:
Duration: 60 minutes (15 Min. for Review of related documents + 45 minutes interactive discussion)
Schedule: To be held on the afternoon of the 2 nd day of the survey. Avoid overlap with other meetings to
augment membership attendance.
Agenda:
1. Introduction
2. Discussion on the committee role and its outcome
3. Discussion on the required programs
4. Discussion on risk management process related to hospital and environmental hazards
5. Other topics may be raised and discussed based on the surveyor findings during the hospital visit.
Required Documents:
The hospital is requested to have documentations related to safety committee. These may include, but not
limited to:
1. Terms of reference of the Safety Committee.
2. Committee membership list.
3. Agenda and meeting minutes approved by the hospital director.
4. Attendance sheet.
5. Facility safety tour reports.
6. Corrective and preventive action plans and budgeting of long-term upgrading and replacement
resulted from facility tours.
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7. Occurrence Variance Reports (OVRs) related to the FMS program with proper action plan to
avoid reoccurrences.
Aim:
To have an overview on how outsourced and contracted services are planned, monitored, managed, and
improved in the hospital.
To discuss the role of hospital stakeholders in ensuring the level of safety and quality of outsourced and
contracted services.
Attendees:
CBAHI: Facility Management and Safety (FMS) and Infection Control Surveyors.
Hospital: Hospital entity in charge of establishing and monitoring outsourced and contracted services
leaders, including:
Duration: 60 minutes (15 Min. for Review of related documents + 45 minutes interactive discussion)
Schedule: To be held on the afternoon of the 2 nd day of the survey. Avoid overlap with other meetings to
augment membership attendance.
Agenda:
1. Introduction
2. Hospital presentation to address the following outline within the scope of the related standards
requirements:
h. Number of outsourced services/ contracts
i. List of contracted companies (within the hospital premises and off-site)
j. Company selection processes
k. Outsourced and contracted services performance monitoring tools and process
l. Roles and responsibilities in monitoring contracted services
m. Outsourced/contracted services’ performance monitoring reports and flow processes
n. Sample of outsourced/contracted services performance monitoring reports content
o. Sample of actions taken by hospital leadership based on contract monitoring reports
p. Risk management process related to a company with unsatisfactory compliance
q. New employees screening and immunization process for contracted workers
r. Contract renewal process
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s. Contracts to manage constructions and renovation works
t. Open discussion
3. Other topics may be raised and discussed based on the surveyor findings during the hospital visit.
Required Documents:
The hospital is requested to have documentations related to safety committee. These may include, but not
limited to:
1. Policies and procedures to ensure the quality and safety of all contracted services, including
company/service selection criteria.
2. Policies and procedures indicating how to track and monitor all contracted services
3. Sample contract
4. List of laws and regulations relevant to the scope of contracted services (e.g. medical waste
disposal laws).
5. Number of renewed contracts and contracts that were aborted.
6. New employees screening and immunization process for contracted workers.
7. Laboratory services contract (if outsourced).
8. Contracts to manage constructions and renovation works.
9. Policy to address agent or contractor repairs.
10. Evidence for reporting medical supplies adverse effects.
11. Corrective and preventive action plans and budgeting of long-term upgrading and
replacement resulted from contracted services monitoring outcome.
12. Occurrence Variance Reports (OVRs) related to the contracted services program with proper
action plan to avoid reoccurrence.
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Report Preparation session (before exit conference)
Only surveyors attend this meeting which will include the following activities:
Objectives
To prepare an initial exit report that can be shared with the hospital at the end of the on-site
survey
To provide the hospital with the possible challenges and areas for improvement
Provide the hospital with the list of non-compliant “ESR’s” that need immediate leadership
attention.
Participants
From CBAHI: The entire survey team.
Logistics
A workroom that can accommodate all the surveyors together
Procedures
After each surveyor has completed scoring all the sub-standards under his scope of on-site
assessment, the whole team has to integrate their findings into one report that will be shared with
the hospital at the end of the on-site survey.
The Visit Team Leader (VTL) shall be responsible to ensure integration of the findings and
recommendations for the sub-standards that are scored by more than one surveyor to ensure
accuracy and reliability of the initial report.
Closing Conference
Objectives
To provide the hospital with an initial overview on the outcome of the survey.
To allow the hospital to clarify or explain possible discrepancies or compliance issues.
To provide the leaders with the hospital’s strengths and areas for improvements.
Participants
From CBAHI: The entire survey team
From Hospital: Chief medical and administrative staff of the hospital. It is encouraged that
various From Hospital (especially those at supervisory levels) attend this session.
Logistics
A workroom that is large enough to hold all participants.
Procedures
At the conclusion of the on-site survey, after collection of final data, the surveyors hold a closing
conference at which they present key findings and the hospital’s areas for improvement. Exit
report will be provided to the hospital director including the draft of major findings in ESRs and
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other standards in all specialties. Other information provided may include how the hospital could
have access to the detailed report and possible follow-up decisions or activities.
As the surveyors are “fact finders” for the CBAHI, they do not render the final accreditation
decision, but instead they report findings to the CBAHI. Therefore, during the exit conference,
the surveyors will not state whether the hospital will be awarded an accreditation.
Members of the leadership group are encouraged to take this opportunity to comment and
provide feedback on the findings for which there are issues of interpretation, as well as express
their perceptions of the survey.
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Post Survey Activities
Accreditation Decision and plan for correcting ESR’s
Following completion of the survey, CBAHI renders an accreditation decision and delivers a report.
Types of possible accreditation decisions, follow up activities, required accreditation maintenance
activities are fully explained in part two of the standards manual. The surveyed hospital receives official
documents from CBAHI detailing the accreditation decision and any required follow-up activities within
thirty days after the conclusion of the survey. Hospitals will be able to access the survey report through
the use of their username and password through the hospital portal.
Survey Report
CBAHI provides a survey report to the hospital for on-site visits. The first page of the report contains
items such as the dates of the survey, the names of the surveyors, the services and sites assessed, and
the scope of the survey and the standards used. The main part of the report contains the findings of the
survey team for all sub-standards that had insufficient or partial compliance.
Survey Feedback
In order to evaluate and improve its performance, CBAHI appreciates each surveyed hospital’s
feedback. This feedback is very beneficial in ensuring the continuing growth and improvement of
CBAHI’s accreditation program. An email is sent to the hospital’s survey coordinator after the survey
visit has been completed requesting their feedback about CBAHI standards, survey process and
surveyors’ performance
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Terms of Accreditation
The CBAHI accreditation is granted for a three years period. CBAHI will send a renewal letter to
accredited hospitals describing how to begin the renewal process before the accreditation expires.
Accreditation Maintenance
The maintenance of the accreditation process pertains only to hospitals already accredited. When a
hospital receives accreditation, the hospital is responsible for maintaining compliance with the CBAHI
standards for the full duration of the accreditation term. CBAHI reserves the right to review the
accreditation status where there is substantial evidence to suggest that accreditation standards are not
being met. CBAHI adopted procedures that facilitate maintenance of accreditation. These procedures
are intended to create an ongoing “maintenance of accreditation” signaling that once a hospital has
achieved accreditation, a process of continuous improvement maintains the accreditation status. The
maintenance of accreditation procedures are fully described in the accreditation policies part of the third
edition of the CBAHI standards manual. As part of accreditation maintenance procedures, the mid-term
self-assessment serves as an opportunity for a hospital to engage in a process of rigorous self-review
and improvement against CBAHI standards.
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Annex A
Standard Survey Agenda
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Standard Survey Agenda
Note 1:
For the Medical and Nursing Surveyors’ Units Visit, please select the units from the following list and
specify it in the particular slot in the schedule, taking in consideration that both surveyors shall not be
visiting the same area at the same time. The sequence of units shall be determined based on the physical
layout of the organization that will allow a smooth flow and ideal utilization of the surveyor time. Please
note that this is a standard agenda so according to the hospital scope of services you may add or eliminate
some units.
1. ER;
2. OR;
3. Surgical Ward;
4. Medical Ward;
5. Pediatrics Ward;
6. ICU;
7. PICU;
8. NICU;
9. CCU;
10. OPD;
11. Physiotherapy;
12. Radiology;
13. Oncology;
14. Dental;
15. Hemodialysis;
16. L&D;
17. Burn Unit; and
18. Day Surgery.
1. ER;
2. OR;
3. L&D;
4. Surgical Ward;
5. Medical Ward;
6. Pediatrics Ward;
7. ICU;
8. PICU;
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9. NICU;
10. CCU;
11. OPD;
12. Oncology;
13. Nursery; and
14. Burn Unit.
The information verification session at the third day of the survey is a specially designed session to
allow more flexibility for the surveyor if he/she wants to verify any of the information collected over
the three survey days
Note 2:
For the FMS Surveyors’ Units Visit, please select the units from the following two lists (external and
internal locations) and specify it in the particular slot in the schedule, surveyors shall not be visiting the
same area at the same time. The sequence of units shall be determined based on the physical layout of
the organization that will allow a smooth flow and ideal utilization of the surveyor time. Please note that
this is a standard agenda so according to the hospital scope of services you may add or eliminate some
units.
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Interior locations to be visited by the FMS surveyor:
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TYPE OF SURVEY – FACILITY NAME
Activity Document Review Document Review Document Review Document Review Document Review Document Review Document Review
09:00
To
12:00 Location
Counterpart(s)
12:00 Activity Surveyors' Business Lunch
To
13:00 Location
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DAY 1, Day of the week, DD MMM, YYYY (Afternoon)
Time/Activity LD MD NR IC MM LB FMS
Activity Unit Visit Unit Visit Unit Visit Documents Review Unit Visit Documents Review Documents Review
13:00
To Location(s) (Social Services) (Inpatient
14:00 Pharmacy)
Counterparts
Lab Leadership
Activity Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit
Interview
Facility Tour
14:00
To Location(s) (Patient Affairs) (CSSD / Endoscopy (ER /
15:00 / Laundry) Ambulance)
Counterparts
Activity Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit Facility Tour
15:00
Location(s) (Medical Supply / (Utility Rooms / (OPD /
To Admission Waste Segregation Outpatient
Office/ Duty Areas / Morgue) Pharmacy)
16:00 Manager Office)
Counterparts
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DAY 2, Day of the week, DD MMM, YYYY (Morning)
Time/Activity LD MD NR IC MM LB FMS
08:00 Activity Surveyor Planning Session (list of “Closed Medical Records” should be provided at the end of session)
To
08:30 Location
QM Department
Activity Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit Facility Tour
Visit
Location(s) (NICU / PICU / (Pharmacy
09:00
ICU/CCU) Warehouse
To
10:00
/Narcotics)
Counterparts
QM Committee
Activity Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit Facility Tour
Interview
Location(s) (Burn Unit / Regular (IV Clean Room)
10:00 Ward/Staff Health (TPN /)
To Clinic)
11:00
Counterparts
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12:00 Interview
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DAY 2, Day of the week, DD MMM, YYYY (Afternoon)
Time/Activity LD MD NR IC MM LB FMS
P and T Committee
Activity Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit Facility Tour
Interview
13:00
To Location(s) (Medical Records (OR)
14:00
Counterparts
Closed Medical Records Closed Medical Records Unit Visit Closed Medical Records Environmental Safety
Activity Unit Visit Review Review Unit Visit
Review Committee Interview
14:00 Location(s) (Inpatient Unit/ OPD/ (ER) (ICU / NICU)
To Hospital Tour)
15:00
(Dental / Kitchen)
Counterparts
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DAY 3, Day of the week, DD MMM, YYYY (Morning)
Time/Activity LD MD NR IC MM LB FMS
08:00 Activity Surveyor Planning Session (list of “Personnel Files” should be provided at the end of session)
To
08:30
Location
Activity Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit Unit Visit Facility Tour
Personnel Files
Personnel Files Personnel Files Personnel Files Review and Personnel Files Personnel Files Personnel Files
10:00
Activity
Review Review Review Closed Medical Review Review Review
To Records Review
11:00
Location
Counterparts
Information Verification
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Information Verification
Information Verification
DAY 3, Day of the week, DD MMM, YYYY (Afternoon)
Time/Activity LD MD NR IC MM LB FMS
Counterparts
16:30
Activity Exit Conference (Optional session if the facility opt to have “Pre-Exit Conference”)
To
Location
17:00
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Annex B
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1. Leadership & Quality Management Surveyor (Closed Session)
Required Documents Related Standards
Policy on Policy
1. Policy for Development and Maintenance of Policies LD.20.1
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29. Terms of Reference of Patient Rights/Patient Advocacy PFR.1.1
Committee
30. Terms of Reference of Research Committee PFR.16.3
31. Medical Records/Forms Committee MR.16.2
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31. Evidence on Systematic Approach of New or Modified LD.19.1
Processes
32. List of Identified Customers and their Needs LD.19.2
33. Risk Assessment LD.19.4
34. Pilot Testing Report LD.19.5
35. New Process Indicators LD.19.6
36. Staff Training Records for New Processes LD.19.7
Patient Affairs
37. Patient and Family Rights Statement PFR.1.3, PFR.4.2, PFR.8.1, PFR.8.2,
PFR.8.3
38. Policy for Patient and Family Rights PFR.1.4, PFR.8.1, PFR.8.2, PFR.8.3,
PFR.8.4, PFR.17.5
39. General Hospital Orientation Program / Employee PFR.2.1
Handbook
40. Policy for the Protection of Patient Belongings PFR.4.1, PFR.4.3
41. Policy for Information Confidentiality, Security and PFR.7.1, PFR.7.2
Integrity
42. Terms of Reference of Research Committee PFR.7.2
43. Patient's Booklet/Handbook PFR.8.6
44. Policy for Patient Complaint PFR.14.1
45. Evidence of Patient Complaints Management PFR.14.3
46. Patient Satisfaction Program PFR.15.1, PFR.15.2
Social Services
Policy For Refusal of Treatment PFR.11.1, PFR.11.2, PFR.11.3 PFR.11.4,
47.
PFR.11.5
48. Policy on "No Code" PFR.12.1
49. Policy for Experimental Research PFR.16.1, PFR.16.2,
Sample of patient's informed consent for participating in
50.
research. PFR.16.4, PFR.16.5
Medical Records
51. Departmental Staffing Plan MR.1.3
52. Policy for Medical Records Documentation MR.5.1, MR.5.6
53. Policy for Medical Records Protection MR.6.3, MR.13.1, MR.13.3
54. Policy for Access to Medical Records MR.9.1
55. Medical Records Management Process MR.11.3, MR.15.1, MR.15.2
56. Policy for Medical Records Retention MR.12.1, MR.12.2
57. Policy for Release of Medical Records MR.14.1, MR.14.2, MR.14.3
58. Medical Records Review Reports MR.17.1, MR.17.2, MR.17.3, MR.17.4,
MR.17.5
IT
59. Policy for Data and Information Retention MOI.2.5, MOI.8.1, MOI.8.2, MOI.8.3
60. Policy for Information Confidentiality, Security and MOI.6.1, MOI.6.2, MOI.6.3, MOI.6.4,
Integrity MOI.6.9
Property Control
61. Evidence for Qualification of Medical Suppliers LD.23.2
62. Documents Reflecting Implementation of Safe LD.23.4, LD.23.9
Management of Medical Supplies and Devices Process
63. Medical Supplies and Devices Inspection Reports LD.23.5
64. Evidence for Reporting Medical Supplies Adverse Effects LD.23.6
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65. Risk Assessment QM.24.6
Hospital-wide
66. Departmental Organization Chart LD.26.1, LD.26.2
67. Departmental Mission Statement LD.27.1, LD.28.2
68. Departmental Scope of Services LD.28. 2
69. Annual Departmental Plan LD.15.9
70. Departmental Staffing Plan LD.30.2, LD.30.3, HR.2.1, HR.2.3, HR.2.4
71. Departmental Meeting Minutes LD.18.2
72. Policy for Development and Maintenance of Policies LD.20.1, LD.20.2
73. Policies and Procedures LD.20.3, LD.20.4
74. Interdepartmental Agreement LD.27.2
75. Departmental Manual LD.29.1
76. Multidisciplinary Policies and Procedures (Sample) LD.29.2
77. Departmental Request for Resources and Staffing LD.30.1
78. Performance Improvement Projects/Reports LD.31.1, LD.31.2, LD.31.4
79. Departmental Indicators Report LD.31.3
80. Evidences of rewarding recognized staff HR.15.1
81. Information System Downtime Procedures and Forms MOI.9.1
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2. Medical Surveyor (Closed Session)
Required Documents Related Standards
Medical Staff Bylaws
1. Medical Staff Bylaws MS.1.1, MS.1.2, MS.1.3, MS.1.4, MS.1.5,
MS.1.6
Medical Committees
2. Medical Executive Committee MS.3.1, MS.3.2, MS.3.3, MS.3.4, MS.10.3
3. Cardiopulmonary Resuscitation Committee PC.32.7, MS.18.1, MS.18.2, MS.18.4,
MS.18.5
4. RRT Committee Meeting Minutes PC.33.4
5. Credentialing and Privileging Committee MS.5.1, MS.5.2
6. Policy for Credentialing and Privileging MS.6.2, MS.6.6, MS.7.3, MS.7.4
7. Hospital Mortality and Morbidity Committee MS.12.1, MS.12.2, MS.12.3, MS.12.4,
MS.12.5, MS.12.6
8. Medical Records/Forms Committee MS.13.1, MS.13.2, MS.13.3, MS.13.4
9. Utilization Review Committee MS.14.1, MS.14.2, MS.14.3
10. Operating Room Committee MS.17.1, MS.17.2, MS.17.3, MS.17.4
11. Oncology and Radiotherapy Committee/Tumor Board ORT.5.1, ORT.5.2, ORT.5.3, ORT.5.4
12. Committee Terms of Reference (Sample) LD.9.3
Medical Staff Performance Evaluation
13. Documented Evidence of Peer Review MS.4.4
14. Policy for Unplanned Review of Medical Staff MS.8.2
Performance
15. Credentialing and Privileging Committee MS.10.2
Policies
a. for Patient Care Hospital-wide
16. Policy for Patient Assessment and Re-assessment PC.6.1
17. Policy for Care of Psychiatric Patient PC.27.3, PC.28.1, PC.28.2
18. Policy for Cardio-pulmonary Resuscitation PC.32.1, PC.32.2
19. Cardio-pulmonary Resuscitation (CPR) Form PC.32.3
20. Policy for Rapid Response Team PC.33.1
21. Policy for Care of Vulnerable Patient PC.34.1, PC.34.2
22. Policy for Patient Transfer PC.38.9, PC.39.1, PC.39.4
23. Policy for Informed Consent PFR.10.1, PFR.10.4
24. Policy for Moderate and Deep Sedation/Analgesia AN.13.1, AN.14.1, AN.14.2
Policies
a. for Organ Donation
25. Policy for Organ Donation ICU.12.5, PC.43.1, PC.43.3, PC.43.4,
PFR.18.1, PFR.18.3, PFR.18.4, ICU.12.1,
ICU.12.2, PICU.13.2, CCU.13.1, CCU.13.2,
CCU.13.5
26. Policy for Organ Transplantation PC.43.2, PC.43.3
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Medical Surveyor (Units Documents)
Required Documents Related Standards
Hospital-wide
1. Departmental Staffing Plan HR.2.1, LD.30.2, HR.2.3, HR.2.4, LD.30.3
2. Departmental Request for Resources and Staffing LD.30.1
3. Departmental Organization Chart LD.26.1, LD.26.2
4. Handover Documentation PC.20.3
5. Evidence of Implementing the Research Outcomes PFR.16.6
6. Departmental Mission Statement LD.28.1
7. Departmental Scope of Services LD.28.2, LD.27.1
8. Interdepartmental Agreement LD.27.2
9. Part-time Department Head Evidence of Visits LD.25.3
10. Departmental Manual LD.29.1
11. Multidisciplinary Policies and Procedures (Sample) LD.29.2
12. List of Essential Medical Supplies and Devices LD.23.1
13. Departmental Meeting Minutes LD.18.2
14. Departmental Mortality and Morbidity Meetings MS.11.1, MS.11.2, MS.11.3, MS.11.4,
MS.11.5
15. Medical Staff Privileging List MS.7.1
16. Medical Staff Bylaws PC.15.3
17. Clinical Practice Guidelines PC.18.2
18. Medical On-call Schedule PC.22.2
19. Safe Operation of Medical Equipment Training Records FMS.27.1, FMS.27.3
Day Surgery
20. Policy for Day Surgery OR.8.1, OR.8.2, OR.8.3
Emergency
21. Criteria for Accepting Patients in the Hospital PC.2.1
22. Emergency Department On-call Schedule ER.2.1
23. Policy for Consultation ER.2.3, ER.13.1, ER.13.5
24. Emergency Department Policies and Procedures ER.9.1, ER.9.2, ER.9.4, ER.10.1
25. Clinical Practice Guidelines ER.9.3
26. Laboratory policy and procedures on reference ER.11.2
laboratory services
27. Departmental Indicators Report ER.14.1
OR
28. Policies for the Provision of Anesthesia AN.3.1, AN.3.2, AN.8.1, AN.11.1
Hemodialysis
29. Medical On-call Schedule HM.3.9
30. Admission and Discharge Criteria HM.4.1, HM.4.2
31. Policy for Patient Care in Hemodialysis HM.5.1
ICU
32. ICU On-call Schedule ICU.3.1
33. Departmental Scope of Services ICU.4.1
34. Admission and Discharge Criteria ICU.4.2, ICU.4.3, ICU.4.4
35. Handover Documentation ICU.5.1
36. Policy for Handover ICU.11.4
37. Policy for Patient Assessment and Re-assessment ICU.11.1
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38. Evidence-Based Criteria for Intubation, Weaning off ICU.11.3
ventilator and Extubation
39. Policy on "No Code" ICU.11.6
40. ICU Policies and Procedures (Sample) ICU.11.7
PICU
41. PICU On-call Schedule PICU.4.1
42. Departmental Scope of Services PICU.5.1
43. Admission and Discharge Criteria PICU.5.3, PICU.5.2, PICU.5.4
44. Handover Documentation PICU.6.1
45. Policy for Handover PICU.12.4
46. Policy for Patient Assessment and Re-assessment PICU.12.1, PICU.12.2
47. Evidence-Based Criteria for Intubation, Weaning off PICU.12.3
ventilator and Extubation
48. Policy for Organ Donation PICU.12.6, PICU.13.1, PICU.13.3,
PICU.13.4, PICU.13.5
49. PICU Policies and Procedures (Sample) PICU.12.7
NICU
50. NICU On-Call Schedule NICU.4.1
51. Handover Documentation NICU.6.1
52. Evidence-Based Criteria for Intubation, Weaning off NICU.12.3
ventilator and Extubation
53. Policy for Handover NICU.12.4
54. Departmental Scope of Services NICU.5.1
55. Admission and Discharge Criteria NICU.5.2, NICU.5.3, NICU.5.4
56. Policy for Patient Assessment and Re-assessment NICU.12.1
57. Policy for Organ Donation NICU.12.7
58. NICU Policies and Procedures (Sample) NICU.12.8
CCU
59. CCU On-call Schedule CCU.4.1
60. Departmental Scope of Services CCU.5.1
61. Evidence-Based Criteria for Intubation, Weaning off CCU.12.3
ventilator and Extubation
62. Handover Documentation CCU.6.1
63. Multidisciplinary Patient Care Team Meeting Minutes CCU.7.1
64. Admission and Discharge Criteria CCU.5.2, CCU.5.3, CCU.5.4
65. Policy for Handover CCU.12.4
66. Policy for Patient Assessment and Re-assessment CCU.12.1
67. CCU Policies and Procedures (Sample) CCU.12.7
Radiology
68. Radiology Department Policies and Procedures RD.1.2, RD.3.1, RD.9.1, RD.9.2
69. Departmental Scope of Services RD.2.1
70. Radiology On-call Schedule RD.2.3
71. Radiology Request Form RD.4.1, RD.4.2
72. Policy for Reporting Critical Radiology Results RD.6.1, RD.6.2, RD.6.3, RD.6.4
Burn
73. Burn Unit On-call Schedule BC.2.1, BC.3.3
74. Admission and Discharge Criteria BC.6.1, BC.6.2
75. Burn Unit Policies and Procedures BC.8.1
L&D
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76. OB/Gyn On-call Schedule L&D.2.1, L&D.2.3, L&D.2.4
77. Admission and Discharge Criteria L&D.5.1, L&D.5.2, L&D.5.3
78. L&D Policies and Procedures L&D.6.1, L&D.6.2
ORT
79. Departmental Organization Chart ORT.3.1
80. Oncology and Radiotherapy Policies and Procedures ORT.6.1
81. Admission and Discharge Criteria ORT.8.1, ORT.8.2
Respiratory
82. Respiratory Care On-call Schedule RS.1.1
83. Respiratory Care Policies and Procedures RS.2.1
Physiotherapy
a.
84. Policies for Physiotherapy PT.2.1, PT.2.2
85. Policy for Patient Assessment and Re-assessment PT.3.2, PT.3.5
Psychiatry
86. Admission and Discharge Criteria PC.27.2
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3. Nursing Surveyor (Closed Session)
Required Documents Related Standards
Nursing Organization
1. Nursing Organization Chart LD.26.1, LD.26.2, NR.1.5
2. Nursing Education Program NR.1.5
3. Nursing Quality Plan NR.1.5
4. Departmental Mission Statement LD.28.1
5. Departmental Scope of Services LD.28.2
Nursing Director
6. Hospital Executive Committee NR.2.1, NR.2.2
7. Pharmacy and Therapeutics Committee Meeting Minutes NR.2.3
8. Infection Control Committee Meeting Minutes NR.2.3
9. Quality Management Committee Meeting Minutes NR.2.3
10. Multidisciplinary Policies and Procedures (Sample) NR.3.1, NR.3.2, NR.3.5
11. Policy for Nursing Care Delivery NR.3.8
Nursing Staffing Plan
12. Departmental Request for Resources and Staffing LD.30.1
13. Departmental Staffing Plan LD.30.2, LD.30.3, HR.2.1, HR.2.3, HR.2.4,
NR.6.1, NR.6.2, NR.6.3, NR.9.1, ICU.8.1,
ICU.8.2, ER.4.1
Nursing Policies
14. Policy for Admission PC.3.1
15. Patient and Family Education Policy PFE.1.1
16. Policy for Handover ICU.11.4, PICU.12.4, NICU.12.4, CCU.12.4
17. Emergency Department Policies and Procedures PC.3.2
18. Policy for Patient Assessment and Re-assessment PC.6.1, ICU.11.1, NICU.12.1, PC.7.2,
PC.13.1, PC.13.2
19. Policy for Management of Suspected Abuse, Neglect, or PC.13.3
Domestic Violence Cases.
20. Policy for Pain Management PC.14.2
21. Policy for Restraints PC.29.1, PC.29.2
22. Policy for Out On-pass PC.35.1, PC.35.2, PC.35.3, PC.35.4
23. Multidisciplinary Policies and Procedures (Sample) NR.3.6, LD.29.2
24. Policy for Nursing Scheduling NR.7.1
25. Par Level Policy NR.12.2
26. Departmental Meeting Minutes PFE.1.7
27. Policy for Care of Vulnerable Patient PFR.5.5
28. Policy for Nutritional Assessment DT.2.2
29. Policy for Psycho-Social Assessment SC.2.2, SC.2.4
Orientation, Training, and Competency
30. Policy for Nursing Competencies Assessment NR.5.2
31. Cross Training Policy NR.8.1
32. Cross-trained Nurses List NR.8.2
Departmental Staffing
33. Departmental Staffing Plan BC.5.1, CCU.9.1, L&D.4.1, PICU.9.1,
PICU.9.2, CCU.9.2, NICU.9.1, NICU.9.2
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Nursing Surveyor (Units Documents)
Required Documents Related Standards
Hospital-wide
1. List of Essential Medical Supplies and Devices LD.23.1
2. Handover Documentation PC.20.3, QM.21.2
3. Safe Operation of Medical Equipment Training Records FMS.27.3, FMS.27.1
4. Performance Improvement Projects/Reports LD.31.4
5. Nursing Schedule NR.7.2
6. Par Level Policy NR.12.2
7. Periodic Preventive Maintenance (PPM) Records QM.19.3
8. Policy for Nutritional Assessment DT.2.6
9. Dietary Manual DT.4.4, DT.4.5
10. Information System Downtime Procedures and Forms MOI.9.1
11. Sample of Hazardous Materials Inventory List FMS.14.2
ORT
12. Oncology and Radiotherapy Policies and Procedures ORT.4.2, ORT.6.1
Emergency
13. Policy for Patients Triage in Emergency Room ER.8.1
14. Patient's Booklet/Handbook PFR.8.6
15. Red Crescent Services Communication Sheet/Log ER.15.1
OR
16. Policies for the Provision of Anesthesia AN.12.1
17. Policies for Patient Care in Operating Room OR.2.2, OR.5.1, OR.5.2, OR.6.1, OR.6.2,
OR.7.1, OR.7.2
ICU
18. ICU Policies and Procedures (Sample) ICU.2.2, ICU.11.7
19. Handover Documentation ICU.5.2
20. Multidisciplinary Patient Care Team Meeting Minutes ICU.6.1
21. Tools and Equipment Availability and Functionality Daily ICU.10.3
Check Sheet/Log
22. Policy for Monitoring Critically-ill Patients ICU.11.2
23. Policy on "No Code" ICU.11.6
PICU
a.
24. PICU Policies and Procedures (Sample) PICU.2.2, PICU.12.7
25. Handover Documentation PICU.6.2
26. Multidisciplinary Patient Care Team Meeting Minutes PICU.7.1
27. Tools and Equipment Availability and Functionality Daily PICU.11.3
Check Sheet/Log
28. Policy for Patient Assessment and Re-assessment PICU.12.1, PICU.12.2
NICU
29. NICU Policies and Procedures (Sample) NICU.2.2, NICU.12.8
30. Handover Documentation NICU.6.2
31. Multidisciplinary Patient Care Team Meeting Minutes NICU.7.1
32. Tools and Equipment Availability and Functionality Daily NICU.11.3
Check Sheet/Log
33. Policy for Monitoring Critically-ill Patients NICU.12.2
CCU
34. CCU Policies and Procedures (Sample) CCU.2.2, CCU.12.5
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35. Handover Documentation CCU.6.2
36. Multidisciplinary Patient Care Team Meeting Minutes CCU.7.1
37. Tools and Equipment Availability and Functionality Daily CCU.11.3
Check Sheet/Log
38. Policy for Patient Assessment and Re-assessment CCU.12.1, CCU.12.2
Conscious sedation areas
39. Policy for Moderate and Deep Sedation/Analgesia AN.19.1
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4. Infection Control Surveyor (Closed Session)
Required Documents Related Standards
IPC Department
1. Hospital Organization Chart IPC.2.2
2. Infection Control Department Organization Chart IPC.3.1, LD.26.1, LD.26.2
3. Lectures Attendance Sheets IPC.8.1
4. Environmental Microbiological Culture Log IPC.24.6
5. Reports of Communicable Diseases to MOH IPC.35.2
6. Anti-biogram Report IPC.37.1
7. Departmental Meeting Minutes LD.18.2
8. Departmental Scope of Services LD.27.1, LD.28.2
9. Interdepartmental Agreement LD.27.2
10. Departmental Mission Statement LD.28.1
11. Departmental Manual LD.29.1
12. Departmental Request for Resources and Staffing LD.30.1
13. Departmental Staffing Plan LD.30.2, LD.30.3
Infection Control Plan / Program
14. Infection Control Plan/Program IPC.5.1, IPC.5.2, IPC.5.3, IPC.5.4, IPC.5.5
15. Infection Control Annual Plan IPC.6.1, IPC.6.2, IPC.6.3, IPC.6.4, IPC.6.6,
IPC.15.2
16. Annual Departmental Plan LD.15.9
Infection Control Manual
17. Infection Control Manual IPC.7.1, IPC.7.2, IPC.7.3
18. Policies and Procedures (Sample) LD.20.3, LD.20.4
19. Care Bundles Elements IPC.40.1
20. Documents Reflecting Implementation of Safe LD.23.8
Management of Medical Supplies and Devices Process
21. Policy for Management of Infection Outbreaks IPC.11.1, IPC.11.2
22. Outbreak Management Report IPC.11.1, IPC.11.2
23. Policy for Handling of Sharps IPC.12.1, IPC.12.2
24. Policy for Standard and Transmission-based Precautions IPC.14.1, IPC.15.6
25. Policy for Personal Protective Equipment IPC.15.8, IPC.32.2
26. Policies and Procedures for Endoscopy Unit IPC.17.1
27. Policy for Reprocessing of Single-Use Items IPC.22.1, IPC.22.2
28. Policy for Housekeeping IPC.23.1, IPC.23.2
29. Pest Control Program IPC.24.5
30. Blood/Body Fluids Spills Management Program IPC.25.1
31. Process for Safe Disposal of Medical Supplies IPC.26.1
32. Policy for Handling Bodies Postmortem IPC.27.1, IPC.27.3
33. Policy for Kitchen Environment and Infection Control IPC.28.10, IPC.29.1
34. Policy for Linen Management IPC.30.1
35. Infection Control Guidelines for Demolition and IPC.31.1
Construction
36. Hand Hygiene Program IPC.33.1
37. Policy for Reporting of Communicable Diseases IPC.35.1
38. Policy for Use of Aseptic Technique Policy IPC.38.1
39. Policy for Ventilator-Associated Pneumonia (VAP) IPC.39.1
40. Policy for Catheter-associated Urinary Tract Infection IPC.41.1
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41. Policy for Catheter-associated Blood Stream Infection IPC.42.1
42. Policy for Prevention of Multi-drug Resistant Organisms IPC.43.1
43. Waste Management Plan FMS.15.1
44. Dental Infection Control Guidelines DN.6.1
45. Burn Unit Infection Control Policies BC.9.1
46. CCU Infection Control Guidelines CCU.12.6
47. NICU Infection Control Guidelines NICU.12.5
48. PICU Infection Control Guidelines PICU.12.5
49. ICU Infection Control Guidelines ICU.11.5
50. Multidisciplinary Policies and Procedures (Sample) LD.29.2
Infection Control Surveillance
51. Policy for Infection Control Surveillance IPC.9.1, IPC.9.2, IPC.9.3, IPC.9.4, IPC.10.2
52. Infection Control Indicators Report IPC.10.1, IPC.39.2, IPC.41.2, IPC.42.2,
IPC.43.2,
53. Infection Control Performance Improvement Projects IPC.10.4, IPC.10.5
54. Departmental Indicators Report LD.31.3
55. Care Bundle Report IPC.40.2
56. Performance Improvement Projects/Reports LD.31.4, LD.31.1, LD.31.2
57. Periodic Departmental Performance Improvement Reports LD.31.6
58. Infection Control Surveillance Report IPC.9.1, IPC.9.2, IPC.9.3, IPC.9.4
59. Hand Hygiene Compliance Reports IPC.33.3
60. Hospital Indicators Reports QM.10.1
Staff Health and Safety
61. Staff Health Clinic Scope of Services IPC.36.1
62. PPD Conversion Rate Documents IPC.36.8
63. Policy for Employee Immunization IPC.36.2, IPC.36.3
64. Occupational Health and Safety Program HR.13.1, HR.13.2, HR.13.3, HR.13.4
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13. Policies and Procedures for CSSD IPC.18.2
14. CSSD Sterilization Records IPC.19.4, IPC.19.5
15. Engineering Control Records IPC.20.3
16. FMS Report on Sterilizers Maintenance IPC.21.5, IPC.21.6
17. Chemical and Biological Indicators Log IPC.21.7
18. Material Safety Data Sheets (MSDS) IPC.21.9
Kitchen
19. Engineering Control Records IPC.28.5, IPC.28.8
20. Kitchen Staff Health Log IPC.29.3, IPC.29.4
21. Dietary Manual DT.6.1, DT.6.2
Mortuary
22. Engineering Control Records IPC.27.2
23. Morgue Housekeeping Log IPC.27.4
24. Endoscopy
25. Engineering Control Records IPC.17.2
ICU
26. Tools and Equipment Cleaning and Disinfection ICU.10.4
Check Sheet/Log
27. Cleaning Schedule ICU.13.1
28. Care Bundles Elements ICU.13.3
PICU
29. Tools and Equipment Cleaning and Disinfection PICU.11.4
Check Sheet/Log
30. Cleaning Schedule PICU.14.1
31. Care Bundles Elements PICU.14.3
NICU
32. Tools and Equipment Cleaning and Disinfection NICU.11.4
Check Sheet/Log
33. Cleaning Schedule NICU.13.1
34. Care Bundles Elements NICU.13.3
35. NICU Policies and Procedures (Sample) NICU.13.3
CCU
36. Tools and Equipment Cleaning and Disinfection CCU.11.4
Check Sheet/Log
37. Cleaning Schedule CCU.14.1
38. Care Bundles Elements CCU.14.3
Burn Care
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48. Evidence that the Leadership Supporting Patient LD.2.7
and Staff Safety
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5. Medication Management Surveyor (Closed Session)
Required Documents Related Standards
Organization and Management
1. Pharmacy Department Organization Chart LD.26.1, LD.26.2
2. Departmental Scope of Services LD.27.1, LD.28.2, MM.4.5
3. Departmental Mission Statement LD.28.1
4. Departmental Request for Resources and Staffing LD.30.1
5. Multidisciplinary Medication Management Plan or Policy MM.4.1
6. Pharmacy On-call Schedule MM.4.6
Policies and Procedures
7. Policies and Procedures LD.20.3, LD.20.4
8. Departmental Manual LD.29.1
9. Multidisciplinary Medication Management Policies and MM.4.2, LD.29.2
Procedures
Patient Specific Information
10. Policy for Accessibility of Patient Specific Information MM.1.1
Staffing Plan and Performance Measurement
11. Pharmacy Staffing Plan and workload statistics MM.3.2
12. Departmental Staffing Plan LD.30.2, LD.30.3
13. Continuing Education Program MM.3.7
14. Performance Improvement Projects/Reports LD.31.1, LD.31.2
High Alert Medications
15. High-alert Medications and Hazardous Chemicals MM.5.1
Multidisciplinary Plan
16. High-Alert Medications and Hazardous Chemicals List MM.5.2
LASA Medications
17. Policy for Handling Look-alike/Sound-alike Medications MM.6.1
18. Hospital List of Confusing Drug Names, MM.6.2
Storage of Pharmaceuticals and Hazardous Chemicals
19. Policy for Non-formulary Medication Management MM.9.1
20. Policy for Proper Storage and Control of Medications MM.11.1, MM.11.2
21. Policy for Storage and Control of Refrigerated and Frozen MM.12.1
Medications
22. Policy for Storage and Handling of Hazardous Medications MM.13.1
and Chemicals
23. Multi-dose Vial Stability Guidelines MM.14.1
24. Crash Cart Medication Management System MM.15.1
25. Policy for Floor Stock Medications Assignment MM.16.1
26. Policy and Procedures on Patient’s Own Medications MM.17.1
Management
27. Policy for Proper Storage of Narcotics and Controlled MM.18.1
Medications
28. Policy for Out-of-stock, Shortage, and during Disaster MM.10.1
Medication Management
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29. Pharmacy Emergency Preparedness Plan MM.10.4
30. Hazardous Materials Management Plan FMS.14.6
Ordering and Prescribing
31. Policy and Procedures for Prescribing Medications MM.20.1
32. Policy and Procedures on Specific Types of Medication MM.21.1
Orders
33. Policy and Procedures on Prescribing Privileges MM.19.1
34. Guidelines on Antibiotics Prescribing MM.22.1
35. Policy for Prescribing Non-formulary Medications MM.24.1
36. Policy and Procedures on Prescribing Formulary MM.24.2
Medications for Off-label Indications.
37. Policy for Telephone and Verbal Orders MM.23.1, MM.23.3, QM.25.1, QM.25.2,
MM.23.4, QM.25.3
38. List of Approved and Prohibited Abbreviations and Symbols MOI.7.1, MOI.7.2, MOI.7.3, MOI.7.4,
MOI.7.5
Preparing and Dispensing
39. Aseptic Technique and IV Admixture Manual MM.26.1
40. Policy on Preparation and Dispensing of TPN. MM.27.1, NICU.12.6
41. Guidelines on Stability and Compatibility of TPN MM.27.8
42. Policy for Preparation and Dispensing of Chemotherapy. MM.28.1
43. Policy for Non-sterile Pharmaceutical Compounding MM.29.1
44. Policy for Obtaining Medications After Working Hours MM.33.1
45. Policy for Handling Recalled, Discontinued and Damaged MM.34.1
Medications
Drug Administration
46. Document that defines nurses and other clinical staff MM.36.1
authorized to administer medications
47. Policy for Medication Verification before Administration MM.37.1
48. Policy for Monitoring Patient Response to Medications MM.39.1
Drug Monitoring
49. Policy for Handling Adverse Drug Reactions (ADRs) Reports MM.40.1, MM.40.2
50. Policy for Handling Medication Errors, Near-misses, and MM.41.1, MM.41.2
Hazardous Situations
51. Medication Errors Reporting System MM.41.5
Contracted Services
52. TPN Outsource Contract and Contract Service Monitoring MM.27.9
53. Chemotherapy Outsource Contract and Contract Service MM.28.16
monitoring
54. Extemporaneous Preparations Outsource Contract and MM.29.6
Contract Service Monitoring
Drug Formulary
55. Hospital Drug Formulary MM.8.1, MM.8.4, MM.8.5, MM.8.6,
MM.8.7, MM.8.8, MM.8.9
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Medication Management Surveyor (Units Documents)
Required Documents Related Standards
Inpatient/Outpatient Pharmacy
1. Patient Medication Profile MM.25.1, MM.31.6
2. Extemporaneous Preparations Manual MM.29.4
(Formulation Book)
3. Extemporaneous Preparations Log Book MM.29.5
4. Outpatient Education Materials MM.35.2
Pharm Admin/QI
5. Pharmacy Department Organization Chart MM.2.1
6. Non-formulary Drug Request Form MM.9.2, MM.24.3, MM.24.5
7. Policy for Floor Stock Medications Assignment MM.11.13
8. Floor Stock Inspection Records MM.11.13
9. Reports of Medication Quality to Saudi FDA MM.11.15
10. Crash Cart Check Sheet MM.15.7
11. Un-approved Indication Request Form MM.24.4, MM.24.5
12. Pharmacy Monthly Inspection of Nursing Units MM.26.13
Performing IV Admixture.
13. Pharmacy Monthly Evaluation of Nursing Staff MM.26.14
Performance of IV Admixture
14. List of Approved Medications to be Accessible to MM.33.3
Non-pharmaceutical Staff
15. Pharmacy On-call Schedule MM.33.4
16. Drug Recall File MM.34.2
17. ADR file and Analysis of ADR Reports MM.40.7
18. Medication Errors Reporting System MM.41.7
19. Root-cause Analysis of Significant Medication MM.41.8
Errors
20. Reports of Serious ADRs to Saudi FDA MM.40.9
21. Reports of Sentinel Events MM.41.12
22. Internal Disaster Plan (pharmacy preparedness FMS.17.2
plan)
23. Departmental Meeting Minutes LD.18.2
24. Departmental Indicators Report LD.31.3
25. Performance Improvement Projects/Reports LD.31.4
26. Periodic Departmental Performance LD.31.6
Improvement Reports
27. Information System Downtime Procedures and MOI.9.1
Forms
IV Clean Room
28. Parenteral Drugs Stability and Compatibility MM.26.11
Guidelines
29. Hospital Guidelines on Safe Recycling of Un-used MM.26.15
Sterile Compounded Preparations
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30. Operational Efficiency and Maintenance MM.30.7
Certificate of LAFH
31. Cleaning Schedule MM.30.8
Chemotherapy
32. Chemotherapy Stability and Compatibility MM.28.10
Guidelines
Hospital-wide
33. Temperature Log Sheets (refrigerators, freezers, MM.11.9, MM.12.4, MM.12.8
etc.)
34. List of Hazardous Medications And Chemicals MM.13.2
35. Hazardous Materials Management Plan FMS.14.2
36. Pharmacy Interventions for Incomplete, Illegible, MM.20.7
or Unclear Orders
Hospital-wide - Crash Cart
37. Crash Cart Medication Management System MM.15.6
38. Crash Cart Check Sheet PC.31.3, PC.31.4, PC.31.5
Hospital-wide - High Alert/LASA
39. Evidence of Implementation of Standard MM.5.4
Concentrations of IV Infusions
40. Staff education material and attendance record MM.6.3
for LASA medications
Hospital-wide - Narcotics
41. Narcotics Documents for Inventory, MM.18.4, MM.18.5, MM.36.5
Endorsement and Accountability
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6. Laboratory Surveyor (Closed Session)
- Laboratory Organization Structure
1. 1 Laboratory scope of services LB.1.1, LB.1.2, LD.28.1, LD.28.2
2. 2 Laboratory organizational chart LB.1.5, LD.26.1, LD.26.2
3. 3 Departmental Meeting Minutes LD.18.2
4. Internal Disaster Plan FMS.17.2
Laboratory Customer Focus
5. Departmental Scope of Services LD.27.1
6. Interdepartmental Agreement LD.27.2
7. Point-of Care-Testing program LB.28.1
8. Assignment POCT coordinator LB.28.2
9. Blood Supply/Exchange Agreements LB.62.1
10. Laboratory policy on Turn Around Time LB.19.1
11. Evidence of establishing TAT in agreement with all LB.19.2
relevant clinical departments
Laboratory Facilities and Safety Program
12. Laboratory safety and infection control manual LB.17.1,FMS.14.6, FMS.15.1
13. Laboratory safety and infection control training LB.17.2
program
14. Laboratory policy and procedures on monitoring LB.17.3
the safety and infection control
Laboratory Personnel
15. Departmental Request for Resources and Staffing LD.30.1
16. Departmental Staffing Plan LD.30.2
17. Laboratory/facility policy on job description and LB.3.1, LD.30.3
samples of job descriptions (lab staff)
18. Policy for Delegation of Authority LD.17.2
19. Laboratory training and competency assessment LB.5.1
program
Laboratory Purchasing and Inventory
20. Laboratory policy and procedure on receipt LB.6.1
inspection and testing of materials/services
21. Laboratory policy and procedure on tracking and LB.6.2
inventory management of supplies and reagents
22. Laboratory policy and procedure on reagents and LB.7.1
solutions labeling
23. Laboratory policy and procedure on supplies and LB.7.2
reagents storage
24. Laboratory policy and procedures on water types LB.7.3
25. Laboratory policy and procedures on reference LB.27.1
laboratory services
Laboratory Equipment
26. List of Essential Medical Supplies and Devices LD.23.1
27. Laboratory/Facility Policy and/or process LB.8.1
description on critical equipment selection
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28. Laboratory policy, process and procedure on LB.9.1
equipment validation
29. Laboratory policy and procedures on the selection LB.58.1, LB.58.2, LB.58.3, LB.58.4,
and monitoring of blood storage devices LB.58.5, LB.58.6
30. Laboratory policy and procedures on standardizing LB.12.1, LB.12.2
of laboratory instruments
31. Laboratory policy and procedure on calibration LB.38.1, LB.38.2
and adjustment of blood shakers
Laboratory Process Management Plan
32. Lab audit trail system LB.4.1
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52. Laboratory policy and procedure on donor LB.37.1, LB.37.2, LB.37.3
notification of significant findings
53. Laboratory policy process and procedure on LB.57.1, LB.57.2, LB.57.3, LB.57.4
therapeutic procedures
54. Laboratory policy and procedure on handling RBC LB.42.1, LB.42.2, LB.42.3, LB.42.4,
components LB.42.5
55. Laboratory policy and procedure on handling PC LB.43.1, LB.43.2, LB.43.3, LB.43.4,
components LB.43.5, LB.46.3
56. Laboratory policy and procedure on handling FFP LB.44.1, LB.44.2, LB.44.3, LB.44.4,
components LB.44.5
57. Laboratory policy and procedures on handling LB.45.1, LB.45.2, LB.45.3, LB.45.4,
Cryoprecipitate LB.45.5
58. Laboratory policy and procedures on handling LB.46.1, LB.46.2
platelet apheresis
59. Laboratory policy and procedures on handling LR- LB.47.1, LB.47.2, LB.47.3
RBC
60. Laboratory policy and procedures on handling LR- LB.48.1, LB.48.2, LB.48.3
PC
61. Laboratory policy and procedures on irradiated LB.49.1, LB.49.2, LB.49.3, LB.49.4
cellular blood products
62. Laboratory policy and procedure on handling LB.59.1, LB.59.2, LB.59.3, LB.59.4,
thawed FFP units LB.59.5
63. Laboratory policy and procedure on handling LB.60.1, LB.60.2, LB.60.3, LB.60.4
thawed CRYO units
64. Laboratory policy and procedure on LB.50.1, LB.50.2
immunohematological testing of donor samples
65. Laboratory policy, process and procedures on LB.51.1
transfusion transmitted disease testing
66. Laboratory policy, process and procedures on LB.51.2
limiting and detecting bacterial contamination in
PC
67. Laboratory policy and procedure on handling LB.52.1, LB.52.2
unsuitable units
68. Laboratory policy and procedure on labeling of LB.53.1, LB.53.2
blood and blood components
69. Laboratory policy and procedure on group/type LB.54.1, LB.54.2
conformation of RBC components
70. Laboratory policy and procedure on the release of LB.55.1, LB.55.2, LB.55.3, LB.55.4
blood and blood components to the available
inventory
71. Laboratory policy and procedure on the release of LB.56.1, PC.25.5, LB.56.2, LB.56.3
incompletely tested blood/blood components
72. Multidisciplinary and/or Blood Utilization PC.25.1, PC.25.2, PC.25.3, PC.25.4,
Committee Approved Policies and Procedures on PC.25.6, PC.25.8, PC.25.9, PC.25.10
Handling, Use and Administration of Blood and
Blood Components
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73. Laboratory policy and procedure on LB.62.2
requesting/sending blood/blood products from/to
outside facilities
74. Laboratory policy and procedure on receipt and LB.62.3
inspection of incoming blood/blood components
75. Laboratory policy and procedure blood bank LB.61.1, LB.61.2, LB.61.3, LB.61.4,
reagents quality control LB.61.5, LB.61.6
76. Laboratory policy and procedures on pre- LB.63.1, LB.63.2, LB.63.3, LB.63.4
transfusion testing of the recipient sample
77. Laboratory policy on the selection of RBC LB.64.1
components for transfusion
78. Laboratory policy on the selection of plasma LB.64.2
components for transfusion
79. Laboratory policy on the selection of blood/blood LB.64.3
components for patients with special
requirements
80. Laboratory policy and procedures on compatibility LB.65.1, LB.65.2, LB.65.3, LB.65.4
testing
81. Laboratory policy and procedures on LB.66.1, LB.66.2, LB.66.3, LB.66.4,
intrauterine/neonatal testing and transfusion LB.66.5
82. Laboratory policy and procedure on issuing blood LB.67.1, LB.67.2, LB.67.3, LB.67.4
and blood products for transfusion
83. Laboratory policy and procedure on emergency LB.68.1, LB.68.2, LB.68.3, LB.68.4,
blood release LB.68.5
84. Blood utilization committee terms of MS.15.1, LD.9.3, MS.15.2, MS.15.3,
reference/formation order and meeting minutes MS.15.4, MS.15.5, MS.15.6
85. Laboratory policy on gross examination of surgical LB.71.1, LB.71.2
pathology specimens
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93. Laboratory policy process and procedure on LB.26.1
amending/correcting reported results
94. Laboratory policy on compiling surgical pathology LB.75.1
reports
95. Laboratory policy and procedures on reference LB.11.1
ranges and cut-off values
Laboratory Documents and Records
96. Master list or table of contents of laboratory policy LB.15.1, LD.29.1, LD.29.2, LD.20.3,
and procedures manual(s) LD.20.4
97. Laboratory policy and procedure on the control of LB.16.1, LB.16.2, LB.16.3
deviations and exceptions
98. Laboratory policy on documents and records LB.29.1, LB.29.2, LB.29.3, LB.29.4,
management LB.29.5
Laboratory Information Management
99. Information System Downtime Procedures and MOI.9.1
Forms
Laboratory Nonconforming Events Management
100. Laboratory policy and procedure on recognizing LB.40.1
and handling adverse donor reaction
101. Hospital or transfusion committee approved policy LB.69.1, LB.69.3
and procedure on recognizing, handling and
reporting adverse transfusion events.
102. Laboratory policy and procedure on investigating LB.69.2
suspected transfusion reaction
103. Hospital or transfusion committee approved policy LB.70.1
on the investigation of post-transfusion infection
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Laboratory Surveyor (Units Documents)
Patient Care Unit
1. POCT QC, training and competency assessment LB.28.1
records
General Lab
2. Laboratory Staff Schedule LB.1.3
3. Records of approving exceptions to policies LB.16.1, LB.16.2, LB.16.3
4. Laboratory safety and infection control audit LB.17.3
reports
5. Sample of Hazardous Materials Inventory List FMS.14.2
6. Computer or paper record of complete audit trail LB.4.1
(who perform the task)
7. Computer or paper records of complete audit trail LB.4.2
(When and where the task performed)
8. Laboratory personnel training and competency LB.5.1
assessment records on newly acquired equipment
or method
9. Safe Operation of Medical Equipment Training FMS.27.1
Records
10. Records of receipt, inspection, and testing of LB.6.1
incoming critical material and service
11. Computer or paper records of tracing materials LB.6.2
12. Reagents and materials storage temperature LB.7.2
monitoring record
13. Water testing records LB.7.3
14. Laboratory equipment selection records LB.8.1
15. laboratory equipment receipt, installation and LB.8.2
identification records
16. Evidence for Qualification of Medical Suppliers LD.23.2
17. Laboratory equipment validation records LB.9.1
18. Laboratory method validation records LB.10.1
19. Laboratory records of establishing/validating LB.11.1
reference ranges and cut off values
20. Laboratory instruments standardization records LB.12.1
21. Laboratory methods/instruments correlation LB.13.1
records
22. Laboratory methods/instruments quality control LB.14.1
records
23. Proficiency Testing Reports LB.32.1
24. Computer or paper lab report LB.24.1
25. Records and report of critical lab results LB.25.1, LB.25.2
26. Records and reports corrected/amended lab LB.26.1
results
27. Reference lab agreement, reports and records of LB.27.1
send-out tests
Sample Collection/Reception
28. Laboratory specimen receipt/reject records LB.21.1
29. Records of accepting sub-optimal specimens LB.23.1
Donor Collection
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30. Whole Blood donation records LB.33.1, LB.34.1, LB.34.2, LB.34.6,
LB.36.1
31. Apheresis donation records LB.35.1, LB.36.1
32. Notification letters for donors with significant LB.37.1, LB.37.2, LB.37.3
findings
33. Records of monitoring, calibration and adjustment LB.38.1, LB.38.2
of blood shakers
34. Confidential unit exclusion records LB.39.4
35. Adverse donation event reports LB.40.1
36. Therapeutic procedures records LB.57.1
Components Production
37. RBC preparation records LB.42.1
38. RBC transportation records LB.42.3
39. RBC QC records LB.42.5
40. PC preparation records LB.43.1
41. PC transportation records LB.43.3
42. PC QC records LB.43.5
43. FFP preparation records LB.44.1
44. FFP transportation records LB.44.3
45. FFP QC records LB.44.5
46. CRYO preparation records LB.45.1
47. CRYO transportation records LB.45.3
48. CRYO QC records LB.45.5
49. Platelet pheresis collection records LB.46.1
50. Platelet apheresis QC records LB.46.2
51. LR-RBC preparation records LB.47.1
52. LP-RBC QC records LB.47.2
53. LR-PC preparation records LB.48.1
54. LP-PC QC records LB.48.2
55. Blood irradiator dosimetry assessment record LB.49.2
56. Records of ABO/Rh testing of donor samples LB.50.1
57. TTDT Records LB.51.1
58. Testing records and validation documents of the LB.51.2
employed bacterial detection method
59. Records of identification and discard of unsuitable LB.52.1
units
60. Records of ABO/Rh-D conformation of RBC LB.54.1
components
61. Records of releasing blood/blood components to LB.55.1, LB.55.2, LB.55.3, LB.55.4
the available inventory
Transfusion Services
62. Records of receiving/sending blood/blood LB.62.1, LB.62.2, LB.62.3
products from/to outside facilities
63. Records of monitoring blood storage devices LB.58.3, LB.58.4, LB.58.5, LB.58.6
64. Blood bank reagents QC records LB.61.1, LB.61.2, LB.61.3, LB.61.4,
LB.61.5, LB.61.6
65. Patient's Pre-transfusion testing records LB.63.4
66. Patient's transfusion records LB.64.1, LB.64.2, LB.64.3, LB.65.3,
LB.68.5
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67. Intra-uterine and neonatal testing and transfusion LB.66.1, LB.66.2, LB.66.3, LB.66.4,
records LB.66.5
68. Blood/blood component issue records LB.67.4
69. Emergency blood release records LB.68.1, LB.68.2, LB.68.4, LB.68.5
70. Records of releasing incompletely tested LB.56.1
blood/blood components
71. Records of investigating and reporting adverse LB.69.2, LB.69.3
transfusion events
72. Records of reporting, investigating and follow-up LB.70.1
post-transfusion infection
73. Records of Look Back investigations LB.70.2
Anatomical Pathology
74. Records of daily review of all technical activities in LB.72.1
anatomical pathology
75. Training and competency assessment records of LB.71.2
non-medical personnel performing gross
examination
76. Records and reports of intra-operative surgical LB.73.1
pathology
77. Intra/inter departmental consultation reports LB.74.1, LB.74.2
78. Records and reports of solving disparities in LB.76.2
anatomical pathology
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7. Facility Management and Safety Surveyor (Closed Session)
Hospital Leadership
1. Evidence that the Leadership Supporting Hospital LD.2.7
Safety
2. Evidence for Reporting Medical Supplies Adverse LD.23.7
Effects
3. Documents Reflecting Implementation of Safe LD.23.8
Management of Medical Supplies and Devices
Process
4. Periodic Departmental Performance LD.31.6
Improvement Reports
5. An evidence of acquiring the necessary FMS.1.2
equipment
6. Hospital Expenditure on Safety Management FMS.1.4
Program
7. Documented Communications from the FMS FMS.2.4
Program Director
Departmental Planning
8. FMS Departmental Organization Chart FMS.2.1
9. Annual Departmental Plan LD.15.9
10. Departmental Organization Chart LD.26.1, LD.26.2
11. Departmental Scope of Services LD.27.1, LD.28.2
12. Departmental Mission Statement LD.28.1
13. Departmental Manual LD.29.1
14. Multidisciplinary Policies and Procedures LD.29.2
(Sample)
15. Departmental Request for Resources and Staffing LD.30.1
16. Departmental Staffing Plan LD.30.3
17. Performance Improvement Projects/Reports LD.31.1, LD.31.2, LD.31.4
18. Departmental Indicators Report LD.31.3
Facility Management and Safety Program
19. Facility Management and Safety Program FMS.1.1, FMS.1.3
20. Radiation Safety Policy FMS.9.1
21. FMS Departmental Organization Chart FMS.2.3
22. Safety Liaison Officers List FMS.2.5
23. Evidence of Liaison Officers Activity FMS.2.5
Fire Safety Plan
24. Procured Furniture Specs Sheet FMS.19.1
25. OR Fire Drill Report OR.13.5
26. Floor layouts showing installed fire rated walls FMS.19.3
27. Fire extinguishers training schedule FMS.19.5
28. Fire Extinguishers Inventory and Distribution FMS.20.1
29. Fire Extinguishers Inspection Reports FMS.20.4
30. Fire Alarm Inspection Schedule and Reports FMS.21.1
31. Fire Alarm Testing Schedule and Reports FMS.21.2
32. Fire Alarm Maintenance Schedule and Reports FMS.21.3
33. Fire Alarm System Distribution FMS.21.4
34. Sprinkler system maintenance and inspection FMS.22.1
schedule and reports
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35. Clean agent system maintenance and inspection FMS.22.2
schedule and reports
36. Wet chemical system maintenance and inspection FMS.22.3
schedule and reports
37. Stand Pipes and Hose System Maintenance and FMS.22.4
Inspection schedule and reports
38. Policy for No Smoking FMS.24.1
Safety of The Building Plan
39. Civil Defense License (for private hospitals) FMS.4.1
40. Civil Defense inspection report (for governmental FMS.4.1
hospitals)
41. Approved hospital action plan for Civil Defense FMS.4.2
findings
42. Policy for safety and security during construction, FMS.5.1
renovation, or demolition
43. Security, safety and infection control inspection FMS.5.1
reports during construction work
44. Evidence of penalties incurred on contractors for FMS.5.1
violating the construction policy
Security Management Plan
45. Policy for Preventing Children and Neonates FMS.11.3
Abduction
46. Policy for Lost and Found Items FMS.11.3
47. Policy for Safe Keeping of Patient Belongings FMS.11.3
48. Policy for Involvement of Police in Certain Cases FMS.11.3
49. Policy for Incidents of Violence FMS.11.3
50. Policy for Women and Child Abuse FMS.11.3
51. Staff Security Training Schedule and Records FMS.11.4
52. Policy on How to Deal with a Bomb Threat FMS.12.1
53. External Disaster Plan FMS.13.4
54. Internal Disaster Plan FMS.13.4
55. Policy for No Smoking FMS.13.4
56. Security Rounds Policy and Reports FMS.13.6
Hazardous Materials and waste Management
Plan
57. KACST License for Radioactive Materials FMS.9.3
58. TLD Monitoring Records FMS.9.7
59. Hazardous Materials Management Plan FMS.14.1
60. Sample of Hazardous Materials Inventory List FMS.14.2
61. Hazardous material exposure Report/OVR FMS.14.6
62. Waste Management Plan FMS.15.1
63. Oncology and Radiotherapy Quality Control ORT.10.1
Records
External Disaster Management Plan
64. External Disaster Plan and Action Cards FMS.16.1
65. External disaster drill report and action plan FMS.16.2
Internal Disaster Management Plan
66. Ambulance Function Log book ER.15.6
67. Internal Disaster Plan and Action Cards FMS.17.1
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68. Internal Disaster Plan including pharmacy FMS.17.2
preparedness plan
69. Sample of Department-Specific Disaster Plan FMS.17.2
70. Fire Drills Schedule FMS.18.1
71. Fire Drills Reports FMS.18.2, FMS.18.3
72. Improvement initiatives related to fire drills FMS.18.4
73. Full fire drill report and action plan FMS.18.5
Biomedical Equipment Management Plan
74. Departmental Staffing Plan FMS.25.1
75. Dialysis Equipment Maintenance Plan and HM.6.2
Records
76. Preventive maintenance records for radiology RD.10.1
department equipment
77. Biomedical Equipment Management Plan FMS.25.2
78. Medical Equipment Inventory List FMS.25.2
79. Sample of Preventive Work Orders FMS.25.2
80. Sample of corrective and preventive work orders FMS.25.6
with action taken
81. Service Reports for Contracted Maintenance FMS.25.7
Services
82. Department Specific Medical Equipment Failure FMS.25.9
Back-up plan
83. Medical Equipment Upgrading/Replacement Plan FMS.25.10
84. Policy for New Equipment Inspection FMS.26.1
85. Sample of inspection records for medical FMS.26.1
equipment received
86. Policy for Proper Tagging of Medical Equipment FMS.26.2
87. Policy for Removal of Equipment from Service FMS.26.3
88. Policy for Agent and Contractors Repairs FMS.26.4
89. Policy for Eliminating the use of Electric Extension FMS.26.5
Cords
90. Policy for Use of Cellular Phones in Critical Areas FMS.26.6
91. Safe Operation of Medical Equipment Training FMS.27.3
Records
92. Infusion pumps and vital signs monitors QM.20.1
preventive maintenance schedule and records
93. License for the Provision of Radiotherapy Services ORT.2.1
from Relevant Authorities
Utilities Management Plan
94. Utility Management Plan Including Utility Failure FMS.28.2, FMS.28.3
95. Annual Testing of Utility Failure Plan with Action FMS.28.4
Plan
96. Utilities' distribution drawings and layouts FMS.28.5
97. Utility systems performance statistical data with FMS.28.5
improvement recommendations
98. Water System Preventive Maintenance Schedule FMS.37.1
and Records
99. Evidence of Implementing Utility Management FMS.37.2
Plan
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100. Utility 52-week Maintenance Schedule and FMS.29.1
Reports
101. Thermal Inspection Reports FMS.30.2
102. Emergency Circuit Diagram FMS.31.1
103. Generators’ testing records FMS.31.2
104. PMG maintenance schedule and records FMS.32.1
105. Compressed medical air system humidity and FMS.32.3
purity testing reports
106. Policy and Procedure on Effective Use of Medical FMS.32.2
Gas System
107. Policy for Handling Various Types of Compressed FMS.33.1
Gases
108. HVAC contract and contractor profile FMS.34.1
109. HVAC System Maintenance Schedule and Records FMS.34.2
110. HVAC filters, ducts and grills cleaning / FMS.34.3
replacement records
111. HEPA filters monthly monitoring and replacement FMS.34.4
records
112. Air Change Per Hour Monitoring Records FMS.34.5
113. Evidence of Air-Flow/Pressure Monitoring FMS.35.1, FMS.35.2, FMS.35.3,
FMS.35.4, FMS.35.5, FMS.35.6,
FMS.35.7, FMS.35.8, FMS.35.9
114. Sewage disposal policy FMS.38.1
115. Laundry Equipment Maintenance Schedule and FMS.39.1
Records
116. Engineering Control Records FMS.39.2
117. Kitchen Equipment Maintenance Schedule and FMS.39.2
Records
118. Kitchen Cold Rooms Temperature Monitoring Log FMS.39.2
119. Periodic Preventive Maintenance (PPM) Records FMS.39.2
120. Cooking filters weekly cleaning records FMS.39.2
121. Pantries’ equipment preventive maintenance FMS.39.2
records
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9. Radiology Equipment Maintenance Folder RD.10.2
10. Shielding Certificate of the X-ray Room FMS.9.5
11. Annual Testing Records of Lead Aprons FMS.9.6
12. Log book for radiation dosimetry. RD.8.6, RD.8.7,
Laser
13. Laser Safety Manual FMS.10.4
ER
14. Ambulance Function Log book ER.15.5
Hospital-wide
15. Safe Operation of Medical Equipment Training Records FMS.27.1
16. Departmental Staffing Plan LD.30.2
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Annex C
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Closed Medical Record Review
MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
AVG
Sub-Std
(10)
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
Sub-Standard
No.
The program includes, but is not limited to, the following:
HR.13.4.1 Pre-employment medical evaluation of new employees.
Response to the health problems of the employees through direct treatment (e.g., a staff clinic) or
HR.13.4.2
referral.
HR.13.4.3 Periodic medical evaluation of staff members.
HR.13.4.4 Screening for exposure and/or immunity to infectious diseases.
HR.13.4.5 Staff preventive immunizations.
HR.13.4.6 Management of exposure to blood borne pathogens and other work-related conditions.
HR.13.4 Measures to reduce occupational exposures and hazards, including the use of protective equipment
HR.13.4.7
and clothing, stress management, and ergonomics.
Staff education on the risks within the hospital environment as well as on their specific job-related
HR.13.4.8 hazards (e.g., lifting techniques, safe use of medical devices, and detecting, assessing, and reporting
risks).
Documentation and management of staff incidents (e.g., injuries or illnesses, taking corrective
HR.13.4.9
actions, and setting measures in place to prevent recurrences).
There is appropriate record keeping and management (e.g., employee health records that are filed
HR.13.4.10
separately).
The hospital implements a policy and procedure that defines the assessment process and its scope and content for
PC.6.2
all categories of patients (adults, geriatrics, pediatrics, pregnant women, trauma patients and others).
The hospital implements a policy and procedure that defines the assessment process and its scope and content for
PC.6.3
all disciplines (physicians, nurses, physiotherapists, social service and others).
PC.6.4 The policy defines the staff categories qualified by license, certification, and experience to assess patients.
PC.8.1 The hospital has criteria to identify patients requiring discharge planning before or upon admission
The hospital implements a policy that defines the time frame for completing the medical, nursing, and other
PC.9.1
assessments required for different care settings and services.
Each patient undergoes an initial medical assessment that includes a health history and physical examination,
covering the following:
PC.10.1.1 Main complaint.
PC.10.1
PC.10.1.2 Details of the present illness.
PC.10.1.3 Systems review.
PC.10.1.4 Past history including previous admissions and surgeries.
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MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
AVG
Sub-Std
(10)
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
Sub-Standard
No.
PC.10.1.5 Allergies and prior adverse drug reactions.
PC.10.1.6 Drug history.
PC.10.1.7 Family history.
PC.10.1.8 Psycho-social history.
PC.10.1.9 Economic factors.
PC.10.1.10 Pain (screening followed by assessment if required).
PC.10.1.11 Risk for fall (screening followed by assessment if required).
PC.10.1.12 Physical status and functionality (screening followed by assessment if required).
PC.10.1.13 Complete physical examination.
PC.10.1.14 Diagnostic test(s) as indicated by the patient’s condition.
PC.10.1.15 Need for additional or specialized assessment as indicated by the patient’s
PC.10.1.16 Need for discharge planning as indicated by the patient’s condition.
PC.10.1.17 Provisional diagnosis.
Medical assessment is performed by the most responsible physician or a member of the team who is qualified by
PC.10.3
license, certification, and experience.
PC.10.6 The medical assessment is documented in the patient’s medical record.
All patients are reassessed at appropriate intervals to determine:
PC.17.1.1 Response to treatment.
PC.17.1 PC.17.1.2 Compliance with treatment.
PC.17.1.3 Complications and side effects.
PC.17.1.4 Plan for continued treatment or completion of treatment.
Nursing reassessment must be performed on every shift with a frequency dictated by the patient’s condition,
PC.17.3
response to treatment, and physician’s order.
The hospital defines situations where re-assessments are performed more infrequently (e.g., long stay patients
PC.17.5
mainly requiring a nursing care).
When required, the hospital provides referral and transfer services to other facility that can provide palliative care
PC.24.5
(e.g., bed or resources availability).
When applicable, the hospital provides or arrange for a nursing home care (e.g., inability to refer, or patient/family
PC.24.6
wish).
Only physicians order blood and in accordance with a policy clarifying when blood and blood products may be
PC.25.2
ordered.
The physician obtain informed consent for transfusion of blood and blood products. Elements of patient consent
include:
PC.25.3 PC.25.3.1 Description of the transfusion process.
PC.25.3.2 Identification of the risks and benefits of the transfusion.
PC.25.3.3 Identification of alternatives including the consequences of refusing the treatment.
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MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
MRN
AVG
Sub-Std
(10)
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
Sub-Standard
No.
PC.25.3.4 Giving the opportunity to ask questions.
PC.25.3.5 Giving the right to accept or refuse the transfusion.
Two staff members verify the patient’s identity prior to blood drawing for cross match and prior to the
PC.25.4
administration of blood.
PC.25.6 Blood is transfused according to accepted transfusion practices from recognized professional organizations.
PC.25.8 Patients receiving blood are closely monitored.
PC.25.9 Transfusion reactions are reported and analyzed for preventive and corrective actions.
Side effects or complications are immediately reported to the medical staff and blood bank and the transfused unit
PC.25.10
is sent to the blood bank for further investigations.
PC.33.3 Activities of the rapid response teams are documented.
PC.38.1 The patient and the family are involved in the discharge process with clear follow up instructions.
PC.38.2 Discharge is based on the patient’s condition and relevant policies or criteria.
PC.38.3 Patients' needs after discharge are assessed as early in the care process as possible.
PC.38.4 The discharge process identifies the post-service needs and supports continuity of care after discharge.
PC.38.5 The post-service needs are communicated to relevant staff members.
PC.38.6 Staff members ensure coordination with various departments involved in the discharge process.
Whenever required, staff members ensure coordination with outside organizations and post-service providers as
PC.38.7
appropriate to the patient's needs.
PC.38.8 Staff members ensure that all patients’ needs are met prior to discharge.
Transfer is based on the patient's health needs for continuing care and the resources available for both referring
PC.39.2
and receiving organizations.
The most responsible physician determines the need for transfer, the most suitable time for transfer, resources
PC.39.3 required during transfer, and whether the receiving organization can meet the patient’s health and supportive
needs.
There is a written acceptance for transfer of responsibility for the patient's care by the receiving
PC.39.5
provider/organization.
The hospital communicates with all potential receiving organizations and necessary arrangements are made
PC.39.6
whenever applicable.
PC.40.1 The most responsible physician assesses the transportation needs of the patient according to his condition.
PC.40.2 Transportation needs of the patient are communicated to the relevant staff.
PC.40.4 The most responsible physician ensures that all patient’s health needs during transportation are met.
PC.40.5 Adequate equipment and supplies are available during transportation.
PC.40.6 A qualified staff member accompanies the patient during transportation.
PC.40.7 The patient is monitored as appropriate during transfer.
PC.40.8 Handover is completed to staff at the receiving organization
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A summary of the patient's condition (e.g., a discharge summary) is sent with the patient to the receiving
organization. The summary includes:
PC.41.1.1 Reason for the patient’s admission.
PC.41.1.2 Patient diagnosis.
Brief summary of hospitalization and services provided (therapies, consultations, procedures to
PC.41.1 PC.41.1.3
date).
PC.41.1.4 Medication list and time of last dose(s) given.
PC.41.1.5 Patient condition and physical status at the time of transfer.
PC.41.1.6 Rationale for transfer.
PC.41.1.7 Results of the patient’s diagnostic investigations (e.g., laboratory and radiology).
PC.42.1 Whenever required, follow up appointments are arranged for the patient prior to discharge.
PC.42.3 The hospital provides a discharge summary for all inpatients upon discharge.
PC.42.4 A copy of the discharge summary is kept in the patient’s medical record.
PC.42.5 A copy of the discharge summary is given to the patient.
PC.42.7 The discharge summary is complete and typewritten.
The scope and content of the nursing assessment is defined in hospital policies and may include:
NR.10.2.1 History of the patient’s main complaint.
NR.10.2.2 Drug allergies.
NR.10.2.3 Physical condition.
NR.10.2.4 Psychosocial status.
NR.10.2
NR.10.2.5 Pain assessment.
NR.10.2.6 Nutritional Status.
NR.10.2.7 Discharge planning.
NR.10.2.8 Skin assessment.
NR.10.2.9 Fall risk assessment.
QM.14.5 Patients receive response when involved in significant incidents with documentation in the medical records.
QM.18.2 The process consists of three phases: verification, site marking, and time out.
A pre-procedure verification of the patient information is carried out including the patient’s identity, consent, full
QM.18.3
details of the procedure, laboratory tests and images, and any implant or prosthesis.
The surgical/procedural site is marked before conducting the surgery/procedure.
The site is marked especially in bilateral organs and multiple structures (e.g. fingers, toes, and
QM.18.4.1
spine).
QM.18.4 QM.18.4.2 The site is marked by the individual who will perform the procedure.
QM.18.4.3 The patient is involved in the marking process.
QM.18.4.4 The marking method is consistent throughout the hospital.
QM.18.4.5 The mark is visible after the patient is prepped and draped.
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QM.22.1 All patients are assessed for pressure ulcers on admission using a standard risk assessment tool.
QM.22.2 All patients are re-assessed for pressure ulcers every twenty four hours.
QM.22.3 The hospital implements evidence-based interventions that prevent pressure ulcers.
QM.23.1 Patients are assessed for the risk of fall on admission
Patients are reassessed for the risk of fall after a change in risk factors (e.g., post-operatively, after receiving
QM.23.2
sedating medications) and upon transfer from another unit.
PFR.9.2 The disclosure process is documented in the patient’s medical record.
PFR.11.3 Patients are informed about available care and treatment alternatives.
PFR.12.2 Patient/family decision about the resuscitative order is documented in the patient’s medical record.
AN.2.2 Qualified anesthesiologist is present inside the operating room throughout the operation.
Anesthesia consultant administers and supervises anesthesia for major/specialized operations or high risk patients,
AN.2.3.1 Pediatric operations.
AN.2.3 AN.2.3.2 Cardio-pulmonary operations.
AN.2.3.3 Neurosurgery operations.
AN.2.3.4 Transplant operations.
The pre-anesthesia assessment includes:
Patient interview and physical examination, including airway assessment and limited intra-vascular
AN.6.2.1
access.
AN.6.2.2 Medical history including anesthesia, drug and allergy history
Other additional pre-anesthesia evaluation if applicable and as required in accordance with the
AN.6.2 AN.6.2.3 standard practice prior to administering anesthesia (e.g., stress tests or additional specialist
consultations).
AN.6.2.4 Notation of anesthesia risk according to established standards of practice (ASA classification).
AN.6.2.5 Anesthetic plan and discussion of the risks and benefits.
AN.6.2.6 Documentation of an informed consent.
AN.6.2.7 Appropriate pre-medication and prophylactic antibiotic orders (if indicated).
The anesthesiologist reassesses the patient immediately prior to induction of anesthesia focusing on the
AN.6.3 physiologic stability and readiness of the patient for anesthesia. Findings are documented in the patient’s medical
record.
The planned anesthesia care is documented in anesthesia record for each patient during anesthesia. The following
information must be documented:
AN.7.1.1 Age, sex, weight, height, and pre-operative vital signs.
AN.7.1
AN.7.1.2 The anesthetic agent.
AN.7.1.3 The dosage, time, and route of administration of all medications and anesthetic agents used.
AN.7.1.4 The techniques used to administer the anesthesia.
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AN.7.1.5 If blood is used, the amount of blood, rationale for administration, and the time given.
AN.7.1.6 Investigations carried out e.g. blood glucose, blood gases.
AN.7.1.7 Unusual events or complications.
AN.7.1.8 The patient’s status at the end of the procedure.
AN.7.1.9 Intravenous fluids given.
AN.7.1.10 The anesthesiologist and anesthesia assistant(s).
AN.8.2 The patient’s physiological status is continuously monitored and documented during anesthesia.
The pre-sedation assessment is performed by a qualified physician and includes:
AN.17.1.1 History and physical examination.
History of medication allergy and adverse experience with sedation and analgesia as well as with
AN.17.1.2
anesthesia.
AN.17.1.3 History of systemic illness or major organ impairment.
AN.17.1
AN.17.1.4 Verification of the patient (NPO) status.
AN.17.1.5 American Society of Anesthesiologists (ASA) physical status class.
AN.17.1.6 Vital signs.
AN.17.1.7 Age and weight.
AN.17.1.8 ECG findings.
AN.17.2 The pre-sedation assessment is documented in the patient’s medical record.
When patients are directly discharged home:
AN.19.4.1 The physician writes a discharge order.
AN.19.4 Patients are discharged in the company of a responsible adult who assumes responsibility and is
AN.19.4.2
capable of taking care of the patient.
AN.19.4.3 Patient/family education and follow-up care instructions are provided prior to discharge.
In emergency situations where a complete medical assessment cannot be documented, a brief note is written by
OR.4.2
the most responsible physician.
OR.8.4 The most responsible physician writes a discharge order.
OR.8.6 Patient/family education and follow-up care instructions are provided prior to discharge.
OR.10.3 The report of the examination is signed by the pathologist and made part of the medical record.
OR.11.1 A post-operative plan of care is written by the responsible surgeon.
The post-operative plan of care includes:
OR.11.2.1 Post-operative monitoring parameters and its frequency.
OR.11.2.2 Wound care.
OR.11.2 OR.11.2.3 Care of drains and catheters.
OR.11.2.4 Special patient positioning requirements.
OR.11.2.5 Nutritional instructions.
OR.11.2.6 When to start mobilization.
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OR.11.2.7 Special referrals (e.g. physical therapy, respiratory therapy)
OR.11.2.8 A new order for all required medications.
OR.11.2.9 Any other post-operative care needed including required follow up.
ICU.6.4 Care is coordinated amongst the multidisciplinary team members and documented in the patient’s medical record.
A summary of the intensive care stay is written by the ICU physician and made available at the time of discharge
ICU.7.2
from intensive care to a lower acuity level.
The intensive care unit reports all cases of potential deceased Donors after Brain Death (DBD) to SCOT on a
ICU.12.3
timely manner.
The intensive care unit reports all cases of potential deceased Donors after Circulatory Death (DCD) to SCOT on
ICU.12.4
a timely manner.
A summary of the neonatal intensive care stay is written by the NICU physician and made available at the time
NICU.8.1
of discharge from critical care to a lower acuity level.
When the patient is discharged from the unit, the neonatal intensive care unit physician ensures that the receiving
team is well informed about the patient’s status and ongoing patient needs
NICU.8.3 The patient’s plan of care and medications are written in detail by the physician including how to
NICU.8.3.1
continue them on the floor.
NICU.8.3.2 Any special care requirements are documented in the medical record.
CCU.7.4 Care is coordinated amongst the multidisciplinary team members and documented in the patient’s medical record.
A summary of the coronary care stay is written by the physician and made available at the time of discharge from
CCU.8.2
critical care to a lower acuity level.
CCU.13.3 The CCU reports all cases of potential Donation after Circulatory Death (DCD) to SCOT in appropriate time.
CCU.13.4 The CCU reports all cases of potential Donation after Brain Death (DBD) to SCOT in appropriate time.
The following information must be available in patients' records before discharge from the delivery room:
L&D.9.1.1 Completed assessment and reassessment.
L&D.9.1.2 Completed partogram.
L&D.9.1.3 Secured cardio-tocography.
LD.9.1 L&D.9.1.4 Initial neonatal assessment.
Delivery summary including method of delivery, date and time of delivery, name and designation
of the healthcare professional who conducted the delivery and any assistants, type of anesthesia
L&D.9.1.5
or sedation used during delivery, neonatal outcome, status of placenta and membranes, any
postpartum instructions, and postpartum observations and discharge criteria.
HM.3.1 Hemodialysis procedures are ordered by a qualified nephrologist.
HM.3.2 Comprehensive assessment and reassessment is performed for each patient in the hemodialysis unit.
The need for dialysis and choice of modality are based on sound clinical principles and a thorough clinical
HM.3.3
evaluation of the clinical condition and any associated co-morbidities.
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Informed consent is obtained for all dialysis patients after providing adequate information about the different
HM.3.4 modalities and the modality that is most appropriate for the patient’s needs. The consent is updated regularly (e.g.,
yearly) and when the risk level is changing.
Multi-disciplinary plan of care is developed for each patient in coordination with other relevant health
HM.3.5
professionals (e.g., physician, nurse, dietitian, pharmacist, and social worker).
HM.3.6 There is an appropriate multi-disciplinary patient education plan.
HM.3.8 Plan of care is documented in the patient’s medical record
HM.8.5 Staff and employees have checkups for Hepatitis B, Hepatitis C, and HIV upon hiring and annually.
Staff and employees susceptible to Hepatitis B are immunized with Hepatitis B vaccine and tested for antibodies
HM.8.6
to evaluate response, and all non-responders are given a second series of the HBV vaccine.
ER.10.3 The transfer of responsibility is documented at times of shifts, handovers, referral and admission.
ER.11.3 Results of investigations are available to the emergency staff within a defined time frame.
Levels of consultations are identified including Immediate (life, limb, or function threatening) and emergent
ER.13.2
consultations.
ER.13.3 Level of consulted physicians and the ways of communications are included.
ER.13.4 Timelines of phone response and physical presence to different types of consultations are included.
RD.9.3 Findings of patient assessment and monitoring are documented in the patient’s medical record.
DT.1.3 Activities conducted by the dietician as part of the process of care is documented in the patient’s medical record.
Nutritional screening is conducted by qualified From Hospital (e.g., registered nurse) to determine the patient’s
DT.2.1
need for comprehensive nutritional assessment by a licensed dietitian
Comprehensive nutritional assessment is performed by a qualified dietitian for:
DT.2.3.1 All patients identified at nutritional risk during the initial screening or assessment.
DT.2.3
DT.2.3.2 All patients identified at nutritional risk during the course of treatment.
DT.2.3.3 All patients prescribed for a therapeutic diet.
DT.2.4 Patients identified at nutritional risk are referred to a licensed dietitian for comprehensive nutritional assessment.
DT.2.5 Nutritional assessment is preferably completed within twenty four hours of referral.
DT.2.7 The nutritional screening and assessment findings are documented in the patient’s medical record.
The dietitian, in collaboration with other clinical staff, develops an appropriate nutritional plan of care for patients
DT.3.1
with nutritional disorders.
DT.3.2 Patients cultural and food preferences are respected to the extent possible.
The nutritional plan allows for consideration of:
Enteral tube feeding for malnourished or patients at risk of malnutrition and have inadequate oral
DT.3.3.1
DT.3.3 intake and a functioning gastrointestinal tract
DT.3.3.2 Parenteral nutrition for patients with a non-functioning gastrointestinal tract.
DT.3.3.3 Therapeutic diet prescribed for specific health conditions.
DT.3.4 Patients are reassessed for response by the dietitian at regular intervals and adjustments are made accordingly.
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DT.3.5 The nutritional plan is documented in the patient’s medical record.
DT.4.3 The dietary manual is used as the basis for diet orders and for planning therapeutic diets.
DT.5.1 Therapeutic diets are prescribed by the most responsible physician based on the patient’s needs.
The plan for a therapeutic diet must emphasize:
DT.5.3.1 Total calories required.
DT.5.3.2 Any restrictions.
DT.5.3
DT.5.3.3 The route and frequency of feeds.
When required, education about nutritional needs is provided to the patient and family upon
DT.5.3.4
discharge.
DT.5.4 Discharge diets are prescribed by the most responsible physician in collaboration with the supervising dietitian.
DT.5.5 Patients are educated on their nutritional needs upon discharge.
DT.5.6 Education is documented in the patient’s medical record.
Functional screening is conducted by qualified From Hospital (e.g., registered nurse) to determine the patient’s
PT.3.1
need for a comprehensive functional assessment by a licensed therapist.
Comprehensive functional assessment is performed by a qualified therapist for each patient identified at functional
PT.3.3
risk during the initial screening or assessment.
PT.3.4 Functional assessment is completed within twenty four hours of referral.
PT.3.6 Functional screening and assessment findings are documented in the patient’s medical record.
The physiotherapist, in collaboration with other clinical staff, develops a suitable plan of care for patients with
PT.4.1
functional disorders.
PT.4.2 The plan of care meets the medical needs of the patient.
PT.4.3 The plan of care has measurable goals.
PT.4.4 Patients are educated about the plan of care and the procedures and rehabilitative exercises.
Patients are reassessed by a physiotherapist at regular intervals, their response to the plan of care is monitored,
PT.4.5
and adjustments are made accordingly.
The plan of care is documented in the patient’s medical record as part of multidisciplinary team planning,
PT.4.6
whenever applicable.
DN.3.1 Patients are educated and informed about the nature of the problem.
DN.3.2 Patients are educated and informed about treatments and procedures required.
DN.3.3 Patients are educated and informed about time needed to complete the course of treatment.
Comprehensive assessment is performed for each patient to include:
DN.4.1.1 History of allergic reactions.
DN.4.1.2 Chronic illnesses (e.g., congenital heart disease, rheumatic heart and diabetes).
DN.4.1
DN.4.1.3 Infectious diseases.
DN.4.1.4 Hematological diseases (e.g., hemophilia).
DN.4.1.5 Chief complaints.
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DN.4.1.6 The need for antibiotic prophylaxis.
DN.4.1.7 Radiological procedures needed.
DN.4.1.8 Treatment plan including procedure(s) to be performed.
DN.4.1.9 Dose of local anesthesia, the tooth treated and the material used.
DN.4.2 The assessment findings and the treatment plan are documented in the patient’s medical record.
DN.5.1 Informed consent is obtained for all high-risk procedures.
General anesthesia and moderate or deep sedation are performed safely and according to the hospital’s related
DN.5.2
policies and procedures.
Medical record completion is a requirement within thirty days of patient discharge and before any elective vacation
MR.5.5
or period of absence of the staff member entering the notes in the medical record.
MR.5.7 The most responsible physician is responsible for the completion of his own records.
MR.7.1 There is a discharge summary for all discharged patients.
The discharge summary is complete and includes:
MR.7.2.1 The reason for the patient’s admission.
MR.7.2.2 The patient’s diagnosis.
Brief summary of hospitalization (therapies, consultations, interventions and results of any
MR.7.2.3
important diagnostic testing).
MR.7.2
MR.7.2.4 A list of medications used.
MR.7.2.5 Any surgery or procedures performed and their outcome.
MR.7.2.6 The patient’s condition at discharge.
MR.7.2.7 All medications to be taken by the patient after discharge.
MR.7.2.8 Any special care the patient requires after discharge.
The hospital uses the International Statistical Classification of Diseases and Related Health Problems, 10th
MR.8.1
Revision, Australian Modification (ICD-10-AM) for diagnosis coding.
MR.8.2 The hospital uses Australian Classification of Health Interventions (ACHI) for procedure coding.
The different sections of the medical record are organized chronologically (e.g., the physician orders start with
MR.10.3
the initial set written when the patient was admitted to the hospital and end with the discharge order).
During each hospitalization episode, both in-patient and outpatient medical records are separated into different
MR.10.4
sections in the patients’ medical record (e.g., for doctors’ orders, nursing notes, progress notes).
The hospital uses standardized forms in medical records, generated based on hospital needs and the needs of
MR.16.1
healthcare professionals.
IPC.26.10 Labor working in medical disposal are well trained and vaccinated against blood borne pathogens.
IPC.29.3 Personnel with respiratory infections or gastroenteritis are restricted from handling food.
Stool tests and cultures are performed routinely upon hiring, every six months, and after returning back from
IPC.29.4
vacation.
IPC.36.4 All employees have baseline screening for hepatitis B, C, HIV, and tuberculosis.
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The immune status of newly hired staff against hepatitis B, measles, mumps, rubella, and varicella is determined
IPC.36.5
by serological testing. Appropriate vaccine(s) is administered to those who are susceptible.
Response to hepatitis B vaccination is monitored in vaccinated employees four weeks after completing vaccine
IPC.36.6
series. Non-responders to hepatitis B vaccine are offered at least a second series of the vaccine.
Newly hired staff are screened for tuberculosis upon contracting with PPD test, and the test is repeated annually
IPC.36.7
for those who are non-reactive.
IPC.36.12 The screening, immunization, and post exposure management data are kept in staff medical records
LB.57.1 The process ensures all therapeutic procedures are ordered and justified by an authorized physician.
The process ensures the blood bank medical director or designee is responsible for reviewing therapeutic
LB.57.2 procedures orders for appropriateness and evaluating patient clinical and laboratory data before approving the
procedure.
LB.57.3 The process ensures therapeutic procedures are explained to the patient and consented.
Surgical specimens are subjected to gross examination by a qualified pathologist or another qualified individual
LB.71.1
under the supervision of a qualified pathologist.
There is a process for the provision of intra-operative surgical pathology services which addresses:
LB.73.1.1 Scheduling of cases.
LB.73.1 LB.73.1.2 Specimen acceptance, accessioning, processing and testing.
LB.73.1.3 Documentation of direct verbal communication with the surgeon.
LB.73.1.4 Inclusion of the frozen section results with the final surgical pathology report.
There is a process for intra-departmental and extra-departmental consultations that addresses circumstances for
LB.74.1
the inclusion of the consultation in the final pathology report.
LB.74.2 The process addresses circumstances for separate filing of the consultation report.
There are implemented guidelines for compiling surgical pathology reports, addressing the following elements:
LB.75.1 LB.75.1.1 Gross description (type, number, dimensions).
LB.75.1.2 Essential processing information and performed studies.
LB.75.1.3 Other relevant report elements necessary for the management of the patient.
LB.76.1 There is a policy mandating the inclusion of review results with the current patient report.
PC.23.1 There is a nursing pre-operative checklist that is completed by the assigned nurse.
PC.23.2 The checklist uses the "Yes", "No" and "Not Applicable" format.
PC.23.3 Patients are not transferred to the operating room if the checklist is not completed except in dire emergencies.
The assigned nurse endorses all the findings of the pre-operative checklist to the receiving nurse in the operating
PC.23.4
room.
The receiving nurse in the operating room reviews all the findings of the pre-operative checklist with the assigned
PC.23.5
nurse and confirms in writing.
The nursing pre-operative checklist contains the following elements as a minimum:
PC.23.6.1 The nursing pre-operative checklist contains the following elements as a minimum:
PC.23.6.2 Evidence of completed relevant consents.
PC.23.6.3 Evidence of completed history and physical examination by medical and nursing staff.
PC.23.6.4 Evidence of site marking.
PC.23.6
PC.23.6.5 Availability of results of requested investigations.
PC.23.6.6 Availability of requested blood or blood products.
Evidence of removal of dentures and loose objects such as eye lenses, eyeglasses, and removable
PC.23.6.7
nails.
PC.23.6.8 Evidence of removal of jewelry and patient's valuables.
The hospital assesses and responds to the unique needs of end of life patients, including psychological, spiritual,
PC.24.1
social, and cultural assessment.
The hospital provides an effective palliative care for terminally ill patients (e.g., management of pain and
PC.24.2
management of other distressing symptoms).
PC.24.3 Family members are involved in care decisions.
PC.24.4 Family members are educated on how to care for their patient.
PC.26.1 Patients are screened for the risk of developing venous thromboembolism.
PC.26.2 Patients at risk receive prophylaxis according to current evidence-based practice.
LD.25.3.3 Provides guidance as well as continued assessment of the individual in charge of the
department during his absence.
LD.25.3.4 The frequency and duration of the visits must be documented in the contract.
HR.5.2 The hospital gathers, verifies, and evaluates the credentials (license, education, training, certification and
experience) of those medical staff, nursing staff, and other health professionals licensed to provide patient
care.
HR.5.3 Credentials are verified from the original source.
HR.5.4 Job responsibilities and clinical work assignments/ privileges are based on the evaluation of the verified
credentials.
HR.5.5 The hospital ensures the registration of all healthcare professionals with the Saudi Commission for Health
Specialties.
HR.5.6 Staff licensed to provide patient care must always have and maintain a valid license to practice only within
their profession.
MS.5.3 The credentialing and privileging committee ensures that only qualified physicians and dentists are appointed
and granted privileges.
MS.5.4 Applicants for initial appointment submit a complete set of documents required for the credentialing and
privileging process , including:
MS.7.2 Clinical privileges are reviewed and updated every two years and as needed.
MS.7.3 The hospital identifies the circumstances under which temporary or emergency privileges are granted.
MS.7.5 When a new privilege is requested by a medical staff member, the relevant credentials are verified and
evaluated prior to approval.
MS.8.1 The department head together with the medical director evaluate the performance and competency of medical
staff members at least annually and when indicated by the findings of performance improvement activities.
MS.8.2 The hospital identifies the circumstances under which an unplanned review of the performance of a medical
staff member may be initiated.
MS.8.3 The performance evaluation includes, but is not limited to, the following:
MS.8.3.1 Assessment of patients.
MS.8.3.2 Adverse events.
MS.8.3.3 Moderate and deep sedation.
MS.8.3.4 Quality of medical records.
MS.8.3.5 Medication errors.
MS.8.3.6 Sentinel events.
MS.8.3.7 Outcome of high-risk procedures and surgeries.