If Ppih Covid 19 Recommendations

Recommendations for Antimicrobial Management of Adult Hospitalized
Patients with COVID-19
Prepared By: The COVID-19 Antimicrobial Management Working Group, Alberta Health Services
Note: This is interim guidance and this document will be frequently updated as new information
becomes available. As such, the most current web-based version of this document should
preferentially be used.
The COVID-19 Antimicrobial Management Working Group notes that there are no fully
evidence-based effective therapies for the treatment of the novel coronavirus, SARS-CoV-2,
and supportive care remains the mainstay of therapy for infected individuals.
Prophylaxis, preemptive therapy are outside the scope of this document. Updated COVID-
19 therapy guidelines from the Public Health Agency of Canada (PHAC)/Association of
Medical Microbiology and Infectious Diseases (AMMI) Canada, the Infectious Diseases
Society of America (IDSA), the American Thoracic Society (ATS), and the AHS ECC
Scientific Advisory Group review of hydroxychloroquine evidence have been reviewed in
preparing this update.
Recommendations:
1) The use of experimental treatments for patients with COVID-19 should occur
within the context of controlled clinical trials
2) There should be no COVID-19-specific therapies in order sets or standing orders

Rationale: To date, there is no proven specific therapy for COVID-19. Experimental treatments
cannot be routinely recommended given equivocal data on benefit and emerging data on
harm.
3) If, after review of these recommendations and the guidelines mentioned above,
the use of agents for COVID-19 outside of clinical trials is being considered, the
significant potential risks (adverse reactions, including QT interval prolongation (see
QTc-prolonging medications); drug interactions (see http://covid19-
druginteractions.org/ or Lexicomp)) versus unverified benefits must be considered
and discussed with the patient, and consent documented on the chart.
Consultation with other specialties (e.g. Infectious Diseases, Respiratory Medicine) can be
considered to help assess the risks and benefits for an individual patient. As recommended
by AHS Ethics, any off-label use of medication requires the prescriber’s careful consideration
of risk/benefit, consultation between experts and attending physician as needed, and
documenting consent from the patient after discussion of the current state of evidence of
benefit and harms. Adverse events with respect to off-label use of medications for inpatient
treatment should be documented and reported by clinicians through the AHS Reporting and
Learning System for Patient Safety at
https://insite.albertahealthservices.ca/tools/rls/Page1820.aspx.
Page 1 of 6
Recommendations for Antimicrobial Management
Last updated: 04/22/2020 1000hr
ECC Approved: 4/22/2020 1216hr
Considerations for Potential COVID-19 Antiviral Agents
Consult your site administration or Pharmacy department to determine if enrollment

into clinical trials is possible.
• Clinicians may be interested in pursuing any available therapy. A rapid review of
antiviral therapies requested by the Public Health Agency of Canada (February 26,
2020) concluded “The current evidence for the effectiveness of antiviral therapies for
coronavirus is not conclusive and suffers from a lack of well-designed prospective
trials or observational studies. None of the interventions examined in this review can
be recommended for use in patients with coronavirus”. Three major therapy
guidelines (PHAC/AMMI Canada, IDSA, ATS) released in the last week support this
assessment. Please also refer to the Scientific Advisory Group Rapid Review on
hydroxychloroquine for more information about that agent.
• The three agents that are currently felt to offer the best ratio of possible benefit to
harm (and are being assessed for further study in the CATCO trial) are:
i. lopinavir/ritonavir (Kaletra)
ii. hydroxychloroquine (Plaquenil)
iii. remdesivir (pending availability)
Considerations for Antibiotic Therapy (see below)

• Antibiotics will have a limited role in managing COVID-19 patients, but recognizing the
frequency with which antibiotics are used in patients with acute undiagnosed
pneumonia syndromes and Acute Respiratory Distress Syndrome (ARDS), as well as
the role of guidance and stewardship, the recommendations provided here are for:
i. empiric management of patients with severe pneumonia while COVID-19 is
being confirmed and bacterial infection excluded, and
ii. initial management of potential bacterial superinfection.
Please note the listed investigations below are for clinical consideration and not required tests.
Work is underway to standardize the laboratory tests and investigations in standing orders and
care pathways. Please use the Laboratory tests and Investigations incorporated into care
pathways and order sets if there are differences between those and the list below.
Investigations for suspect or confirmed COVID-19 patients under consideration for

admission, or being admitted:
1. Laboratory tests:
Laboratory tests may not be required in otherwise ambulatory patients who are
clinically stable, and not felt to be at elevated risk of decompensation. In the presence
of higher clinical severity and/or comorbidities, the following laboratory tests may be
considered:
• CBC & differential - low lymphocyte count and/or neutrophil/lymphocyte ratio of
>3.13 may be suggestive of COVID-19/more severe disease
• AST, ALT, bilirubin, Cr, CRP
• Blood cultures
• COVID-19 PCR and RVP swabs OR sputum or ET aspirate for COVID-19 PCR
Page 2 of 6
Also consider for select patients:
• HIVAb
• Sputum (or endotracheal (ET) aspirate if intubated) for Gram stain and culture. NB:
Do not do bronchoscopy only to procure specimens.
• MRSA nasal swab (to determine need for empiric MRSA pneumonia coverage
pending cultures)
2. CXR - AP (portable) or PA/LAT depending on site policies for ED based COVID-19
patients
3. Laboratory tests that can be considered in specific patients based on clinical status
and comorbidities (NB: the current literature does not support a specific role for these
parameters in guiding clinical management but they may be useful in evolving
prognostic models):
• ABG
• INR
• D-dimer
• fibrinogen
• ferritin
• troponin
• If immunocompromised and clinically indicated, ET aspirate, bronchoscopy (if
required), or induced sputum for PJP
Other considerations for Patients Hospitalized with COVID-19
Clinical progression to more severe disease usually begins between 5-7 days after symptom
onset. Risk factors for disease progression include older age and presence of underlying
medical conditions (e.g. hypertension, obesity, diabetes, chronic lung diseases, and
immunocompromised state). However, younger, previously healthy individuals can develop
severe illness.
• Avoid nebulized medications and do not do bronchoscopy for obtaining specimens

alone (ET aspirate preferred) to reduce aerosolization risk
• If oxygen demand is increasing, consider early referral for appropriate respiratory
supports depending on access and infrastructure, as patient outcomes may be
superior and planned intubations are at a lower risk for infection transmission than
emergent ones.
• There is no evidence that ACE Inhibitors and Angiotensin Receptor Blockers
need to be stopped. There is a theoretic concern about ACE inhibition and viral
receptors there are no clinical data supporting risk. Major cardiovascular societies
(https://hypertension.ca/wp-content/uploads/2020/03/2020-30-15-Hypertension-
Canada-Statement-on-COVID-19-ACEi-ARB.pdf) recommend that suspect and
confirmed COVID-19 patients on ACE inhibition should be maintained on their therapy
if it is otherwise indicated to avoid decompensation of cardiac disease.
• There is no specific contraindication to NSAIDS: There is current anecdotal
concern about the antecedent use of NSAIDs in patients with severe disease, but no
Page 3 of 6
clinical data are yet available. As other symptomatic therapy can be substituted
(acetaminophen, appropriately dosed) it may be reasonable to prefer acetaminophen
to NSAIDS for COVID-19 symptoms, but patients with inflammatory conditions on
stable doses of NSAIDS should remain on them.
Other investigational therapies that are NOT currently recommended:

• High dose steroid therapy – may cause harm; worse outcomes in SARS and influenza
• IVIG – IS not expected to have neutralizing antibody, and may worsen ARDS
• Ribavirin as an adjunct to lopinavir/ritonavir - high dose has toxicity concerns, and
must be used in combination
• Anti-IL6 inhibitors (tocilizumab) and other immune modulating therapies for CRS
(anakinra, other) – At this time in AHS, immune modulating therapies for COVID-19
can only be pursued in the context of clinical trials. If a clinician would like AHS to
provide immunomodulatory therapy, an application must be made through STEDT,
and it will be considered based on the evidence submitted.
Empiric Antimicrobial Therapy of Pneumonia in Hospitalized Suspect COVID-19

ADULT Patients
For patients who are pending confirmation of COVID-19 infection, with possible bacterial
infection, the following initial therapy can be considered (and may be stopped if COVID-19 is
confirmed as the cause of pneumonia)
For antimicrobial recommendations in other settings (e.g. outpatient, long term care) or
circumstances (bronchiectasis, allergies), refer to other references such as Bugs & Drugs.
**REASSESS at 48-72 hours WITH VIRAL AND BACTERIAL LAB RESULTS**
[Ceftriaxone 1 g (2 g if > 100 kg) IV daily x 3 days

AND one of:
Azithromycin 500 mg PO (IV if NPO) daily x 3 days
OR
Doxycycline 200 mg PO then 100 mg PO BID x 3 days]
Alternative: levofloxacin 750 mg PO (IV if NPO) daily
If history of MRSA colonization or high suspicion for MRSA, add:

Vancomycin 25-30 mg/kg IV load (round to nearest 250mg; max 3 g) followed by 15
mg/kg (round to nearest 250mg; max 2 g) q 8-12h for target trough 15-20 mg/L x 3 days
Alternative if renal dysfunction or known prior MRSA pneumonia: Linezolid 600 mg IV/PO
q 12h x 3 days
Discontinue vancomycin or linezolid if MRSA screening swab negative OR if bacterial

respiratory cultures are negative for MRSA
Page 4 of 6
If symptoms clinically compatible with influenza and influenza RVP pending or positive,
consider:
Oseltamivir 75 mg PO bid (if normal renal function), discontinue if influenza RVP negative.
Management of Possible Secondary Bacterial Infection/Ventilator Associated

Pneumonia in Adult COVID-19 patients
See other references for HAP/VAP such as Bugs & Drugs.
Culture directed therapy is preferred; the following are empiric therapy recommendations
pending sputum/ET aspirate culture results:
**REASSESS at 48-72 hours WITH BACTERIAL LAB RESULTS**
Piperacillin-tazobactam 4.5 g IV q6h x 3 days

OR
Meropenem 500 mg IV q6h x 3 days
Plus, if not documented MRSA negative, vancomycin or linezolid as listed above
Discontinue vancomycin or linezolid if MRSA screening swab and bacterial respiratory

cultures are negative for MRSA.
Worsening pneumonia may also be due to inflammation so prolonged antibiotic therapy

beyond 3- 5 days in the absence of positive cultures is not recommended.
Page 5 of 6
Selected references:
1. American Thoracic Society COVID‐19: Interim Guidance on Management Pending
Empirical Evidence.
2. Arabi YM, et al. Am J Respir Crit Care Med. 2018;197(6):757-767.
3. Arabi YM, et al. Clin Infect Dis. 2019 Jun 25. pii: ciz544.
4. Chu CM, et al. Thorax. 2004;59(3):252-6.
5. Cortegiani A, et al. J Crit Care 2020.
6. Gilead Sciences. January, 2020 (web link)
7. Infectious Diseases Society of America (IDSA) Guidelines on the Treatment and
Management of Patients with COVID-19
8. Lee N, et al. N Engl J Med. 2003;348(20):1986-94.
9. Lee N, et al. J Clin Virol. 2004;31(4):304- 9.
10. Loutfy MR, et al. JAMA. 2003;290(24):3222-8. Cao B, et al. NEJM Mar 18.
11. Mulangu S, et al. N Engl J Med. 2019;381(24):2293-2303.
12. Park SY, et al. J Hosp Infect. 2019;101(1):42-46.
13. Paton NI, et al. Lancet Infect Dis. 2011;11(9):677-83.
14. Public Health Agency of Canada (PHAC)/Association of Medical Microbiology and
Infectious Diseases (AMMI) Canada Clinical management of patients with moderate to
severe COVID-19 - Interim guidance
15. Sheahan TP, et al. Nat Commun. 2020;11(1):222.
16. Stockman LJ, et al. PLoS Med. 2006;3(9):e343.
17. Sung JJ, et al. Thorax. 2004;59(5):414-20.
18. Yao X, et al. Clin Infect Dis. 2020 Mar 9, ciaa237.
19. Zumla A, et al. Lancet. 2015;386(9997):995-1007.
Additional resource: bibliography and review can be found at

https://pubs.acs.org/doi/10.1021/acscentsci.0c00272
Submitted by Dr. Lynora Saxinger, Dr. Nelson Lee, Dr. John Conly, Dr. John Gill, Susan
Fryters, and Jeremy Slobodan on behalf of the COVID-19 Antimicrobial Management
Working Group and reviewers (Critical Care, Infectious Diseases, Pharmacy, Emergency
Medicine, Immunology).
Page 6 of 6

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Recommendations for Antimicrobial Management of Adult Hospitalized

Patients with COVID-19

2) There should be no COVID-19-specific therapies in order sets or standing orders

Consult your site administration or Pharmacy department to determine if enrollment

Considerations for Antibiotic Therapy (see below)

Investigations for suspect or confirmed COVID-19 patients under consideration for

Other considerations for Patients Hospitalized with COVID-19

• Avoid nebulized medications and do not do bronchoscopy for obtaining specimens

Other investigational therapies that are NOT currently recommended:

Empiric Antimicrobial Therapy of Pneumonia in Hospitalized Suspect COVID-19

**REASSESS at 48-72 hours WITH VIRAL AND BACTERIAL LAB RESULTS**

[Ceftriaxone 1 g (2 g if > 100 kg) IV daily x 3 days

Alternative: levofloxacin 750 mg PO (IV if NPO) daily

If history of MRSA colonization or high suspicion for MRSA, add:

Discontinue vancomycin or linezolid if MRSA screening swab negative OR if bacterial

Management of Possible Secondary Bacterial Infection/Ventilator Associated

See other references for HAP/VAP such as Bugs & Drugs.

**REASSESS at 48-72 hours WITH BACTERIAL LAB RESULTS**

Piperacillin-tazobactam 4.5 g IV q6h x 3 days

Discontinue vancomycin or linezolid if MRSA screening swab and bacterial respiratory

Worsening pneumonia may also be due to inflammation so prolonged antibiotic therapy

Additional resource: bibliography and review can be found at

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REASSESS at 48-72 hours WITH VIRAL AND BACTERIAL LAB RESULTS

REASSESS at 48-72 hours WITH BACTERIAL LAB RESULTS