Cellulitis and Abscess Pathway
Cellulitis and Abscess Pathway
Cellulitis and Abscess Pathway
1
Executive Summary
PHASE I (E.D.)
Test Your Knowledge
Exclusion Criteria
Hospital-acquired, surgical site &
device-associated infections
Presumed necrotizing fasciitis
Orbital/periorbital cellulitis
Immunodeficiency
Pressure ulcers
Solitary dental abscess
!
Labs
if systemic illness
or necrotizing
fasciitis suspected
!
Consider tetanus
immunization status
as necessary
Provider Assessment
Determine if special
situation present.
Concern for:
Deep extremity infection (e.g., tenosynovitis, septic
arthritis, osteomyelitis)
Deep puncture wound of hand/fingers/feet
Yes
Yes
Involve General
Surgery
Yes
Involve ENT
No
Concern for:
Peri-anal abscess (within 1cm of anal verge)
Breast abscess
Perineal abscess
Pilonidal cyst
Large or complex abscess
No
Concern for:
Neck abscess
No
Concern for:
Yes
No
Yes
No
Off
Pathway
PHASE I (E.D.)
Test Your Knowledge
Inclusion Criteria
Suspected skin/soft tissue
infection in children > 44 weeks CGA
Exclusion Criteria
Labs
if systemic illness
or necrotizing
fasciitis suspected
Alter antibiotic
selection if >48h
of prior antibiotics given
Non-purulent
Purulent
Fluctuant or
abscess 1cm on ultrasound:
Sedation / pain control
I&D and culture wound
No routine labs
Determine Disposition
Systemic illness
Not tolerating PO
Treatment failure on >48h of
appropriate antibiotics
Rapidly progressive lesion
Pain control / wound care
All < 2 mo; consider if <6 mo
Inadequate F/U
Discharged
patients
Purulent Definition
Actively draining pus
History of drainage
Abscess present
Admitted patients
!
Non-purulent
Medical Treatment
Oral cephalexin
Clindamycin if failed
outpatient treatment,
cephalosporin allergic or if
MRSA risks
Purulent
Antibiotic
selection by
condition
Medical Treatment
Non-purulent
Medical Treatment
No systemic antibiotics
after I&D if low risk
Oral clinda if not low risk
TMP/SMX (or doxycycline
if >8 years) if presumed
clindamycin-resistant
MRSA
IV cefazolin
Clindamycin if failed
outpatient treatment,
cephalosporin allergic or if
MRSA risks
Consider vancomycin if
systemic toxicity
Purulent
Medical Treatment
IV clindamycin
Vancomycin if presumed
clindamycin-resistant
MRSA
Consider vancomycin if
systemic toxicity, failed
outpatient clindamycin
Discharge
Instructions
7-10 days total
treatment
PMD f/u within
24-48 hours
Go to Inpatient Phase
PHASE II (INPATIENT)
Test Your Knowledge
!
Labs
if systemic illness
or necrotizing
fasciitis suspected
Daily re-evaluation
Clinical exam
Culture data
Improving
!
Antibiotic
selection by condition
Not Improving
Discharge Criteria
(Meets all)
Lesion(s) show signs of
improvement
Tolerating PO
Pain controlled
Afebrile >24 hours
F/U assured within 48 hours
Discharge
Instructions
7-10 days total
treatment
PMD f/u within
48 hours
Cefazolin
IV choice
IV Alternatives
Clindamycin
Vancomycin if presumed
clindamycin resistant MRSA;
rapidly progressive lesion;
Clindamycin if cephalosporin
hemodynamic instability; illallergic
appearing; failed oral
clindamycin as outpatient;
Consider vancomycin if
abscess in an area difficult to
rapidly progressive lesion;
drain completely such as
hemodynamic instability; illface/hand/genitals
appearing
Bite wounds
Ampicillin/sulbactam
Facial cellulitis of
dental origin
Penicillin OR
Ampicillin/sulbactam
Cefoxitin (transition to
clindamycin AND
Clindamycin if penicillin allergic
ciprofloxacin at discharge)
if penicillin allergic
Cephalexin
PO choice
Amoxicillin/clavulanate
Penicillin OR
Amoxicillin/clavulanate
Clindamycin otherwise
TMP/SMX if presumed
clindamycin resistant MRSA
PO Alternatives
*Low risk criteria: Age 1 year; no fever; well-appearing; adequate I&D; no significant comorbidities
Return to ED Simple
Cellulitis / Abscess Phase
Initial ED phase
ED simple cellulitis/
abscess
Inpatient Phase
Bibliography
Literature SearchSearch Methods, Soft Tissue Infections Cellulitis, Clinical
Standard Work
Studies were identified by searching electronic databases using search strategies developed and
executed by a medical librarian, Susan Klawansky. Searches were performed in November 2012
in the following databases on the Ovid platform: Medline and Cochrane Database of Systematic
Reviews; elsewhere: Embase, Clinical Evidence, National Guideline Clearinghouse and TRIP.
Retrieval was limited to 2004 to current, humans, and English language. In Medline and Embase,
appropriate Medical Subject Headings (MeSH) and Emtree headings were used respectively, along
with text words, and the search strategy was adapted for other databases as appropriate.
Concepts searched were soft tissue infections, cellulitis and many other related conditions, some
of which are skin abscess, bites and stings, impetigo, carbuncle, infectious skin diseases and
penetrating wounds. All retrieval was further limited to certain publication types representing
high order evidence.
Susan Klawansky, MLS, AHIP
April 9, 2013
Identification
383 records identified through
database searching
Screening
396 records after duplicates removed
Elgibility
Included
44 studies included in pathway
Flow diagram adapted from Moher D et al. BMJ 2009;339:bmj.b2535
To Bibliography, Pg 1
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Inpatient Phase
Bibliography
1)
Kilburn SA, Featherstone P, Higgins B, Brindle R. Interventions for cellulitis and erysipelas.
Cochrane Database of Systematic Reviews 2010 (6). DOI:10.1002/14651858.CD004299.pub2.
2)
Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ, Kaplan SL, Karchmer AW, Levine DP,
Murray BE, Rybak MJ, Talan DA, Chambers HF. Clinical practice guidelines by the Infectious Diseases
Society of America for the treatment of methicillin-resistant staphylococcus aureus infections in adults and
children. Clin Infect Dis 2011 Feb;52:1-38.
3)
JL Robinson, MI Salvadori; Canadian Paediatric Society Infectious Diseases and Immunization
Committee, Management of community associated methicillin-resistant Staphylococcus aureus skin
abscesses in children. Paediatr Child Health 2011; 16(2):115-6
4)
May A et al. Treatment of complicated skin and soft tissues infections, Surgical Infection Society
Guidelines. Surgical Infections 2009 Vol 10, Number 5, 467-501
5)
Paydar, K Z, Hansen, SL, Charlebois, ED, Harris, HW, Young, DL. Inappropriate antibiotic use in soft
tissue infections. Archives of Surgery 2006; 141(9), 850-856.
6)
Elliott DJ, Zaoutis TE, Troxel AB, Loh A, Keren R. Empiric antimicrobial therapy for pediatric skin and
soft-tissue infections in the era of methicillin-resistant Staphylococcus aureus. Pediatrics 2009; 123(6),
e959-966.
7)
Duong et al, Randomized Controlled Trial of Antibiotics in the Management of CommunityAcquired Skin Abscesses in the Pediatric Patient. Ann Emerg Med 2010;55(5):401-7.
8)
Stevens DL et al. Practice guidelines for the diagnosis and management of skin and soft tissue
infections. Clin Infect Dis 2005;41:1373-406.
9)
Williams DJ et al. Comparative effectiveness of antibiotic treatment strategies for pediatric skin
and soft-tissue infections. Pediatrics 2011;128(3) e1-e9.
10)
Chen AE et al. Randomized Controlled Trial of Cephalexin Versus Clindamycin for Uncomplicated
Pediatric Skin Infections. Pediatrics 2011;127(3);e573.
11)
Squire et al. ABSCESS: Applied Bedside Sonography for Convenient Evaluation of Superficial Soft
Tissue Infections. Acad Emerg Med 2005 Vol. 12, No. 7, 601-606
12)
Tayal, VS, Hasan, N, Norton, HJ et al, The effect of soft-tissue ultrasound on the management of
cellulitis in the emergency department. Acad Emerg Med 2006, 13, 4, 384-388.
Initial ED phase
ED simple cellulitis/
abscess
Inpatient Phase
Executive Summary
Objective
To improve the quality and safety of care for uncomplicated community acquired soft tissue infections in children
older than 30 days of life, specifically:
Reduce use of broader spectrum, inappropriate, or more toxic antibiotics for cellulitis and abscess
Reduce the use of systemic antibiotics for children with simple abscess who meet low risk criteria
Decrease unnecessary laboratory testing
Increase the use of laboratory testing that will allow for targeted antimicrobial therapy
Decrease unnecessary hospital days
Recommendations
1.
Use bedside ultrasound where available to improve the accuracy in diagnosis of subcutaneous abscesses.
2.
Obtain wound cultures when possible.
3.
Do NOT obtain routine blood testing (CBC, CRP, blood culture) for most children with cellulitis or abscess.
4.
No incision and drainage is needed for abscesses <1 cm on bedside ultrasound; these patients may be
discharged home on antibiotics alone.
5.
Do NOT prescribe oral antibiotics for simple abscesses that have been incised and drained completely, if
the patient is >1 year of age, afebrile, well-appearing, with no significant comorbidities and adequate follow up
assured.
6.
Prescribe oral clindamycin for outpatient treatment of abscesses that could not have an adequate I&D, or
do not meet low-risk criteria.
7.
Prescribe cephalexin for outpatient treatment of simple cellulitis without an abscess, drainage, history of
drainage, or failure of outpatient antibiotic course (>48 h on appropriate antibiotics).
8.
Prescribe oral clindamycin for outpatient treatment of purulent cellulitis or cellulitis that has not responded
to anti-MSSA therapy (beta lactam, >48 hours).
9.
Prescribe cefazolin for inpatient treatment of simple cellulitis without an abscess, drainage, history of
drainage, or failure of outpatient antibiotic course (>48 h on appropriate antibiotic).
10.
Prescribe IV clindamycin for inpatient treatment of purulent cellulitis or cellulitis that has not responded to
anti-MSSA therapy (beta lactam, >48 hours) .
11.
Prescribe IV vancomycin for inpatient treatment of cellulitis in patients who are systemically ill (fever >38,
tachycardia, vomiting) or have failed antibiotic therapy that covers MRSA .
12.
Obtain general surgery, orthopedics, ENT, or dental consultation for the appropriate special clinical
scenarios.
Implementation Items
Created three care algorithms (two for the Emergency Department, and one for inpatients) as well as an
antibiotic table to address common clinical scenarios
Developed a Learning Center training module for the management of community acquired cellulitis and
abscess
ED Antibiotics for Home Rate AIM: reduce antibiotic prescription rate to 15% among patients undergoing I&D
for abscess who are discharged from the ED
PDCA Plan
Quarterly Review of Metrics, Literature Review, E-Feedback, and Audit Reports will inform Improvement efforts
Revision History
Date Approved:
August, 2013
ED simple cellulitis/
Initial ED phase
Inpatient Phase
Next Review Date:
August, 2016
abscess
Executive Summary
Initial ED phase
ED simple cellulitis/
abscess
Inpatient Phase
Self-Assessment
Completion qualifies you for 1 hour of Category II CME credit. If you are taking this self-assessment as a
part of required departmental training at Seattle Childrens Hospital, you MUST logon to Learning Center.
b)
c)
d)
b)
Well appearing
c)
d)
Initial ED phase
ED simple cellulitis/
abscess
Inpatient Phase
Self-Assessment
Completion qualifies you for 1 hour of Category II CME credit. If you are taking this self-assessment as a
part of required departmental training at Seattle Childrens Hospital, you MUST logon to Learning Center.
Cephalexin
b)
Trimethoprim-Sulfamethoxazole
c)
Clindamycin
d)
No antibiotics.
Plastic surgery
b)
General surgery
c)
Orthopedic surgery
d)
Initial ED phase
ED simple cellulitis/
abscess
Inpatient Phase
Self-Assessment
Completion qualifies you for 1 hour of Category II CME credit. If you are taking this self-assessment as a
part of required departmental training at Seattle Childrens Hospital, you MUST logon to Learning Center.
Vancomycin
b)
Clindamycin
c)
Cefazolin
d)
Trimethoprim-sulfamethoxazole
e)
Cephalexin
Initial ED phase
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abscess
Inpatient Phase
Answer Key
1. d
2. d
3. a
4. b
5. b
Initial ED phase
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Inpatient Phase
Evidence Ratings
We used the GRADE method of rating evidence quality. Evidence is first assessed as to
whether it is from randomized trial, or observational studies. The rating is then adjusted in
the following manner:
Quality ratings are downgraded if studies:
Have serious limitations
Have inconsistent results
If evidence does not directly address clinical questions
If estimates are imprecise OR
If it is felt that there is substantial publication bias
Quality ratings can be upgraded if it is felt that:
The effect size is large
If studies are designed in a way that confounding would likely underreport the magnitude
of the effect OR
If a dose-response gradient is evident
Quality of Evidence:
High quality
Moderate quality
Low quality
Very low quality
Expert Opinion (E)
Reference: Guyatt G et al. J Clin Epi 2011: 383-394
To Bibliography
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Medical Disclaimer
Medicine is an ever-changing science. As new research and clinical experience
broaden our knowledge, changes in treatment and drug therapy are required.
The authors have checked with sources believed to be reliable in their efforts to
provide information that is complete and generally in accord with the standards
accepted at the time of publication.
However, in view of the possibility of human error or changes in medical sciences,
neither the authors nor Seattle Childrens Healthcare System nor any other party
who has been involved in the preparation or publication of this work warrants that
the information contained herein is in every respect accurate or complete, and
they are not responsible for any errors or omissions or for the results obtained
from the use of such information.
Readers should confirm the information contained herein with other sources and
are encouraged to consult with their health care provider before making any
health care decision.
Initial ED phase
Background
Many patients present to their health care providers, urgent care clinics,
or the emergency department for evaluation and treatment of soft
tissue infections. Some have a simple cellulitis that is often easily
treated with antibiotics, while others have more complicated infections
that require extensive incision and drainage or hospitalization. In
addition to Streptococcus pyogenes and methicillin-sensitive
Staphylococcus aureus (MSSA), methicillin-resistant Staphylococcus
aureus (MRSA) has also become a real consideration in these types of
infections.
This pathways intent is to standardize to the extent possible the
diagnosis and management of such soft tissue infections at Seattle
Childrens.
Initial ED phase
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Inpatient Phase
Pressure ulcers
Orbital/periorbital cellulitis
Immunodeficiency
Initial ED phase
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abscess
Inpatient Phase
Initial ED phase
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abscess
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Microbiology
Nonpurulent cellulitis is usually due to group A
streptococci (although studies are limited due to the
difficulty culturing from these infections)
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Diagnostic testing
Routine blood testing (CBC, CRP, blood culture) is not necessary for
most children with SSTI (Stevens , LC)
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Inpatient Phase
Surgical consultation
Specific locations of cellulitis/abscess warrant subspecialist
consultation to evaluate for deeper and more serious/complicated
extension of infection.
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(LC)
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All patients who have had an I&D procedure should have reliable
follow-up for re-evaluation with their PCP in 24 - 48 hours
Return to Home
Initial ED phase
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Inpatient Phase
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IV choice
Cefazolin
Facial cellulitis of
dental origin
Bite wounds
Ampicillin/sulbactam
Penicillin OR
Ampicillin/sulbactam
IV Alternatives
PO choice
Cephalexin
Amoxicillin/clavulanate
Penicillin OR
Amoxicillin/clavulanate
Clindamycin otherwise
TMP/SMX if presumed clindamycin
resistant MRSA
PO Alternatives
Clindamycin if cephalosporin
allergic
Initial ED phase
ED simple cellulitis/
abscess
Clindamycin if penicillin
allergic
Inpatient Phase
Admission criteria
Patients who should be admitted:
Initial ED phase
ED simple cellulitis/
abscess
Inpatient Phase
Initial ED phase
ED simple cellulitis/
abscess
Reevaluate lesion
daily or with
significant changes
Follow microbiology
cultures, and change
to the narrowest
spectrum antibiotic
once sensitivities are
available
Consult general
surgery if an abscess
develops that
necessitates
drainage
Inpatient Phase
Treatment failure
Initial ED phase
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abscess
Inpatient Phase
Initial ED phase
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abscess
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Discharge criteria
A patient is ready for discharge when:
Tolerating PO
Initial ED phase
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abscess
Inpatient Phase