Cellulitis Oral Case Pres
Cellulitis Oral Case Pres
Cellulitis Oral Case Pres
CHIEF COMPLAINT:
HEENT: (-) headache, (-) blurring of vision, (-) ptosis, (-) loss of hearing, (-) tinnitus, (-)
aural discharge, (-) dysphagia, (-) hoarseness of voice, (-) neck rigidity, (-) lymph gland
enlargement
Gastrointestinal: (-) vomiting, (-) abdominal pain, (-) constipation, (-) diarrhea
I. CASE VIGNETTE
REVIEW OF SYSTEMS
Musculoskeletal: (+) joint pain, (-) muscle cramps, (-) muscle weakness
Neurologic: (-) aphasia, (-) numbness, (-) loss of sensation, (-) tremors, (-) dizziness
● I: no anosmia
● II: pupils 2-3 mm equally reactive to light , normal direct and consensual pupillary reflex,
good accommodation and convergence in near reaction
● III, IV, VI: extraocular muscles intact
● V: no facial sensory deficit, good bite strength
● VII: able to wrinkle forehead, raise eyebrow, puff cheeks, whistle and show teeth, normal
taste perception
● VIII: normal hearing acuity
● IX X : with gag reflex, soft palate rises on phonation, uvula midline on phonation
● XI: able to shrug shoulder against resistance, can turn face against resistance
● XII: tongue midline
PHYSICAL EXAMINATION
A: Trachea is at midline.
B: No active lung infiltrates seen. Pulmonary
vascular markings are within normal limits.
Pleura is not visible.
C: Heart is not enlarged. Aorta is partially
calcified.
D: Diaphragm is intact. Right diaphragm is
higher than the left. Costophrenic angles are
clearly visible.
E: Note of sternotomy wires. Visualized osseous
structures are unremarkable.
● No demonstrable fracture or ● Cortical erosions are seen in the head of first and
dislocation in the radiographs taken. 2nd metatarsal heads and bases of 1st and 2nd
● Soft tissue swelling is noted in the proximal phalanges.
distal leg. ● Subtle soft tissue hyperdensity is noted along
● Included joint spaces appear intact. metacarpophalangeal joint of 1st digit. Consider
gouty arthritis.
● Included joint spaces and soft tissue outlines
appear intact.
Admitting orders (10/16/22):
● IVF: PNSS 1L x 80 cc/hr
● Low salt low fat diet
● Diagnostics:
○ Awaiting RT PCR
○ For blood CS x 2 sites
○ For procalcitonin
○ For AV duplex scan of lower extremities
○ For FBS, LP
● Medications:
○ Clindamycin 600 mg IV q6
○ Omeprazole 40 mg/tab OD
○ Paracetamol 500 mg/tab q4 PRN for T>/= 37.8
○ Tramadol 50 mg IV q8 PRN for pain
○ Valsartan 160 mg/tab OD
○ Amlodipine 10 mg/tab OD
○ Clopidogrel 75 mg/tab OD
○ ISMN 60 mg/tab OD
● WOF: fever, DOB, chest pain
● VS q4
● Monitor I & O q shift
V. COURSE IN THE WARD
1ST HOSPITAL DAY
S:
A:
(-) fever
Cellulitis, left leg and foot,
(-) DOB
non-purulent skin and soft tissue
(-) chest pain
infection, moderate; Transaminitis;
(-) abdominal pain
HASCVD CAD s/p CABG (PHC, 2004)
(-) changes in
urination/bowel movement
P:
O: IVF: PNSS 1L X 80 cc/hr
BP: 110/80 mmHg HR: 89 bpm Diet: Low salt, low fat diet
RR: 18 cpm Temp: 36.6 Dx: For FBS, lipid profile, AV duplex scan, blood CS
1. Clindamycin 600 mg IV Q6 (D1)
Awake, conscious, not in cardiorespiratory distress
2. Omeprazole 40 mg/tab OD
Anicteric sclerae, pink palpebral conjunctiva, no 3. Paracetamol 500 mg/tab q4 PRN for T>/= 37.8
cervical lymphadenopathies 4. Tramadol 50 mg IV q8 PRN for pain
Symmetric chest expansion, clear breath sounds, no 5. Valsartan 160 mg/tab OD
chest retractions 6. Amlodipine 10 mg/tab OD
Adynamic precordium, no murmur 7. Clopidogrel 75 mg/tab OD
Soft, nontender abdomen 8. ISMN 60 mg/tab OD
(+) Swelling of left leg and foot, warm to touch, Monitor VS Q4
Monitor I & O q shift
erythematous, minimal pain on movement
WOF: DOB, desaturation, fever, hypotension
(+) Tophi on both feet
BLOOD CHEM (10/17/22)
2ND HOSPITAL DAY
S:
A:
(-) fever
Cellulitis, left leg and foot,
(-) DOB
non-purulent, moderate;
(-) chest pain
Transaminitis; HASCVD CAD s/p CABG
(-) abdominal pain
(PHC, 2004)
(-) changes in
urination/bowel movement
P:
IVF: PNSS 1L x 80 cc/hr
O: Diet: Law salt, low fat diet
BP: 100/80 mmHg HR: 90 bpm Dx: For CBC PC, BUN, Crea, SGOT, SGPT, Na, K Cl, still for
RR: 18 cpm Temp: 36.0 AV Duplex Scan, Awaiting blood CS
Awake, conscious, not in cardiorespiratory distress 1. Clindamycin 600 mg IV Q6 (D2)
Anicteric sclerae, pink palpebral conjunctiva, no cervical 2. Omeprazole 40 mg/tab OD
lymphadenopathies 3. Paracetamol 500 mg/tab q4 PRN for T>/= 37.8
Symmetric chest expansion, clear breath sounds, no chest 4. Tramadol 50 mg IV q8 PRN for pain
retractions 5. Valsartan 160 mg/tab OD
Adynamic precordium, no murmur 6. Amlodipine 10 mg/tab OD
Soft, nontender abdomen 7. Clopidogrel 75 mg/tab OD
(+) Decreased swelling of left leg and foot, warm to 8. ISMN 60 mg/tab OD
touch, erythematous, minimal pain on movement Monitor VS Q4
(+) Tophi on both feet Monitor I & O q shift
WOF: DOB, desaturation, fever, hypotension
3RD HOSPITAL DAY IM IDS NOTES:
● No objection for
discharge
S:
A: ● Shift to oral
(-) fever antibiotics for 2
Cellulitis, left leg and foot,
(-) DOB weeks
non-purulent, moderate;
(-) chest pain ● For AV Duplex
Transaminitis; HASCVD CAD s/p CABG scan as OPD
(-) abdominal pain
(PHC, 2004) ● Refer
(-) changes in
urination/bowel movement
P:
IVF: PNSS 1L x 80 cc/hr
O: Diet: Law salt, low fat diet
BP: 120/80 mmHg HR: 74 bpm Dx: Still for CBC PC, Bun, Crea, SGOT, SGPT, Na, K, CL, For
RR: 20 cpm Temp: 36.2 AV Duplex Scan as OPD, Awaiting blood CS
Awake, conscious, not in cardiorespiratory distress 1. Clindamycin 600 mg IV Q6 (D3)
Anicteric sclerae, pink palpebral conjunctiva, no 2. Omeprazole 40 mg/tab OD
cervical lymphadenopathies 3. Paracetamol 500 mg/tab q4 PRN for T>/= 37.8
Symmetric chest expansion, clear breath sounds, no 4. Tramadol 50 mg IV q8 PRN for pain
5. Valsartan 160 mg/tab OD
chest retractions
6. Amlodipine 10 mg/tab OD
Adynamic precordium, no murmur 7. Clopidogrel 75 mg/tab OD
Soft, nontender abdomen 8. ISMN 60 mg/tab OD
(+) Decreased swelling and tenderness of left leg Monitor VS Q4
and foot, warm to touch, erythematous, Monitor I & O q shift
(+) Tophi on both feet WOF: DOB, desaturation, fever, hypotension
BLOOD CHEM (10/20/22)
V. DISCUSSION
Cellulitis
● Definition:
○ Acute bacterial infection causing inflammation
of the deep dermis and surrounding
subcutaneous tissue.
● Characterized by:
○ Localized pain
○ Erythema
○ Swelling
○ Heat
● Usually without an abscess or purulent discharge
● Etiology:
○ Beta-hemolytic streptococci typically cause
cellulitis, generally group A streptococcus (i.e.,
Streptococcus pyogenes), followed by
methicillin-sensitive Staphylococcus aureus.
● Epidemiology:
○ common; most often occurs in middle-aged and
older adults
● Risk factors:
○ Immunocompromised host (DM,
lymphedema, malnourished, older patients,
obese, peripheral arterial disease)
○ General infection risk: History of cellulitis
(highest risk factor)
● Risk factors for MRSA Cellulitis:
○ Increased exposure to MRSA (Contact sports,
crowded living conditions, health care
workers, indigenous descent)
○ Increased susceptibility (Immunodeficiency,
young age)
Pathophysiology
of Cellulitis
Evaluation
● Cellulitis is diagnosed clinically based on the presence of spreading
erythematous inflammation of the deep dermis and subcutaneous tissue.
● Two of the four criteria (warmth, erythema, edema, or tenderness) are
required to make the diagnosis.
● Its most common presentation is on the lower extremities but can affect any area
of the body.
● Most often unilateral and rarely presents bilaterally
● Patient's skin should be thoroughly evaluated to find the potential source for the
cellulitis by looking for microabrasions of the skin secondary to injuries, insect
bites, pressure ulcers, or injection sites.
● Cultures of blood or cutaneous aspirates, biopsies, or swabs: not routinely
recommended
Management
Lifted from Practice Guidelines for
the Diagnosis and Management
of Skin and Soft Tissue Infections:
2014 Update by the Infectious
Diseases Society of America
Management
● According to the IDSA Guidelines, cellulitis can be divided into 3 classifications:
○ Mild: without systemic signs of infection
■ Oral medications
● Penicillin VK or
● Cephalosporin or
● Dicloxacillin or
● Clindamycin
○ Moderate: with systemic signs of infection
■ Intravenous medications
● Penicillin or
● Ceftriaxone or
● Cefazolin or
● Clindamycin
○ Severe: associated with penetrating trauma, evidence of MRSA infection
elsewhere, nasal colonization with MRSA, injection drug use, or SIRS (Systemic
Inflammatory Response Syndrome)
■ Empiric treatment
● Vancomycin PLUS Piperacillin/Tazobactam
Review: Systemic Inflammatory Response Syndrome (SIRS)
Lifted from Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014
Update by the Infectious Diseases Society of America
Management
● The recommended duration of antimicrobial therapy: 5 days
○ should be extended if the infection has not improved within this time
period.
● Elevation of the affected area and treatment of predisposing factors are
recommended .
● In lower-extremity cellulitis, interdigital toe spaces should be carefully examined.
○ treating fissuring, scaling, or maceration may eradicate colonization with
pathogens and reduce the incidence of recurrent infection.
● Outpatient therapy: recommended for patients who do not have SIRS, altered
mental status, or hemodynamic instability (mild nonpurulent).
● Hospitalization: recommended if there is concern for a deeper or necrotizing
infection, for patients with poor adherence to therapy, for infection in a severely
immunocompromised patient, or if outpatient treatment is failing (moderate or
severe nonpurulent infection).
Complications
● If the bacterial infection reaches the bloodstream, it could lead to bacteremia.
Bacteremia can be diagnosed by obtaining blood cultures in patients who exhibit
systemic symptoms. Failure to identify and treat bacteremia from cellulitis can lead to
endocarditis, an infection of the inner lining (endocardium) of the heart.
● Patients who have cellulitis along with two or more SIRS criteria (fever over 100.4
degrees F, tachypnea, tachycardia, or abnormal white cell count) → sepsis.
● If cellulitis moves from the deep dermis and subcutaneous tissue to the bone, it can
lead to osteomyelitis.
● Cellulitis that leads to bacteremia, endocarditis, or osteomyelitis will require a longer
duration of antibiotics and possibly surgery.
Prognosis
● If cellulitis is promptly identified and treated with correct antibiotics
→ improvement in signs and symptoms within 48 hours
● Annual recurrence of cellulitis occurs in about 8-20% of patients
○ Overall recurrence rate as high as 49%
● Prompt treatment of cuts or abrasions, proper hand hygiene, as well as effectively
treating any underlying comorbidities can prevent recurrence.
● Overall, cellulitis has a good prognosis.
Patient Education