You are leaving Medscape Education
Cancel Continue
Log in to save activities Your saved activities will show here so that you can easily access them whenever you're ready. Log in here CME & Education Log in to keep track of your credits.
 

CME/CE

Antibiotics for Pediatric Skin Infections Vary in Effectiveness

  • Authors: News Author: Laurie Barclay, MD
    CME Author: Charles P. Vega, MD
  • CME/CE Released: 8/16/2011
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 8/16/2012
Start Activity


Target Audience and Goal Statement

This article is intended for primary care clinicians, emergency medicine specialists, and other specialists who care for children with skin and soft tissue infections.

The goal of this activity is to provide medical news to primary care clinicians and other healthcare professionals in order to enhance patient care.

Upon completion of this activity, participants will be able to:

  1. Describe epidemiologic trends in skin and soft tissue infections in the United States.
  2. Compare 3 types of antibiotics in the management of skin and soft tissue infections among children.


Disclosures

As an organization accredited by the ACCME, Medscape, LLC, requires everyone who is in a position to control the content of an education activity to disclose all relevant financial relationships with any commercial interest. The ACCME defines "relevant financial relationships" as financial relationships in any amount, occurring within the past 12 months, including financial relationships of a spouse or life partner, that could create a conflict of interest.

Medscape, LLC, encourages Authors to identify investigational products or off-label uses of products regulated by the US Food and Drug Administration, at first mention and where appropriate in the content.


Author(s)

  • Laurie Barclay, MD

    Freelance writer and reviewer, Medscape, LLC

    Disclosures

    Disclosure: Laurie Barclay, MD, has disclosed no relevant financial relationships.

Editor(s)

  • Brande Nicole Martin

    CME Clinical Editor, Medscape, LLC

    Disclosures

    Disclosure: Brande Nicole Martin has disclosed no relevant financial relationships.

CME Author(s)

  • Charles P. Vega, MD

    Associate Clinical Professor, Residency Program Director, Prime-LC, University of California-Irvine, Orange, California; Department of Family Medicine, University of California-Irvine, Orange, California

    Disclosures

    Disclosure: Charles P. Vega, MD, has disclosed no relevant financial relationships.

CME Reviewer(s)

  • Sarah Fleischman

    CME Program Manager, Medscape, LLC

    Disclosures

    Disclosure: Sarah Fleischman has disclosed no relevant financial relationships.

Nurse Planner

  • Laurie E. Scudder, DNP, NP

    Nurse Planner, Continuing Professional Education Department, Medscape, LLC; Clinical Assistant Professor, School of Nursing and Allied Health, George Washington University, Washington, DC

    Disclosures

    Disclosure: Laurie E. Scudder, DNP, NP, has disclosed no relevant financial relationships.


Accreditation Statements

    For Physicians

  • Medscape, LLC is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.

    Medscape, LLC designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credit(s)™ . Physicians should claim only credit commensurate with the extent of their participation in the activity.

    This activity, Medscape Education Clinical Briefs has been reviewed and is acceptable for up to 300 Prescribed credits by the American Academy of Family Physicians. AAFP accreditation begins September 1, 2010. Term of approval is for 1 year from this date. Each issue is approved for .25 Prescribed credits. Credit may be claimed for 1 year from the date of this issue.

    Note: Total credit is subject to change based on topic selection and article length.

    Medscape, LLC staff have disclosed that they have no relevant financial relationships.

    AAFP Accreditation Questions

    Contact This Provider

    For Nurses

  • Medscape, LLC is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center's Commission on Accreditation.

    Awarded 0.5 contact hour(s) of continuing nursing education for RNs and APNs; 0.5 contact hours are in the area of pharmacology.

    Accreditation of this program does not imply endorsement by either Medscape, LLC or ANCC.

    Contact This Provider

    For Pharmacists

  • Medscape, LLC is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.

    Medscape designates this continuing education activity for 0.25 contact hour(s) (0.025 CEUs) (Universal Activity Number 0461-0000-11-179-H04-P).

    Contact this provider

For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]


Instructions for Participation and Credit

There are no fees for participating in or receiving credit for this online educational activity. For information on applicability and acceptance of continuing education credit for this activity, please consult your professional licensing board.

This activity is designed to be completed within the time designated on the title page; physicians should claim only those credits that reflect the time actually spent in the activity. To successfully earn credit, participants must complete the activity online during the valid credit period that is noted on the title page. To receive AMA PRA Category 1 Credit™, you must receive a minimum score of 70% on the post-test.

Follow these steps to earn CME/CE credit*:

  1. Read the target audience, learning objectives, and author disclosures.
  2. Study the educational content online or printed out.
  3. Online, choose the best answer to each test question. To receive a certificate, you must receive a passing score as designated at the top of the test. MedscapeCME encourages you to complete the Activity Evaluation to provide feedback for future programming.

You may now view or print the certificate from your CME/CE Tracker. You may print the certificate but you cannot alter it. Credits will be tallied in your CME/CE Tracker and archived for 6 years; at any point within this time period you can print out the tally as well as the certificates by accessing "Edit Your Profile" at the top of your Medscape homepage.

*The credit that you receive is based on your user profile.

CME/CE

Antibiotics for Pediatric Skin Infections Vary in Effectiveness

Authors: News Author: Laurie Barclay, MD CME Author: Charles P. Vega, MDFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME/CE Released: 8/16/2011

Valid for credit through: 8/16/2012

processing....

Clinical Context

The emergence of methicillin-resistant Staphylococcus aureus (MRSA) has changed the way clinicians care for patients in the United States as well as epidemiologic trends in skin and soft-tissue infections (SSTIs) itself. Hersh and colleagues evaluated these issues in a study published in the July 28, 2008, issue of the Archives of Internal Medicine. They found that the overall number of healthcare visits for SSTIs increased by 50% between 1997 and 2005, and this increase was most profound among black patients, patients younger than 18 years, and in the South. The use of medications used to treat MRSA increased from 7% at baseline to 28% in 2005, and this change was most pronounced in prescriptions from emergency departments.

When MRSA might account for more than 70% of all staphylococcal infections in some areas of the United States, what types of antibiotics provide superior results? The current analysis of antibiotics for the treatment of SSTIs among children seeks answers to this question.

Study Synopsis and Perspective

Antibiotics vary in efficacy for pediatric SSTIs, according to the results of a retrospective cohort study reported online August 15 in Pediatrics.

"The burden of pediatric ...SSTIs is increasing, largely as a result of the widespread community emergence of methicillin-resistant ...MRSA," write Derek J. Williams, MD, MPH, from the Department of Pediatrics, School of Medicine and Monroe Carell Jr Children's Hospital at Vanderbilt University in Nashville, Tennessee, and colleagues. "Optimal antimicrobial management strategies for SSTIs in the era of community-associated MRSA remain unclear."

The goal of the study was to compare the efficacy of clindamycin (used as the reference standard), trimethoprim-sulfamethoxazole, and β-lactams for the treatment of pediatric SSTIs among children from birth to age 17 years who were enrolled in Tennessee Medicaid and had an incident SSTI between 2004 and 2007. The main study endpoints were treatment failure, defined as an SSTI within 14 days after the incident SSTI, and recurrence, defined as an SSTI occurring between 15 and 365 days. The risk for treatment failure and time to recurrence were estimated from adjusted models stratified on the basis of drainage status.

Treatment failures occurred in 568 (8.9%) of the 6407 children who underwent drainage, and recurrences in 994 (22.8%). For trimethoprim-sulfamethoxazole, the adjusted odds ratio (OR) for treatment failure was 1.92 (95% confidence interval [CI], 1.49 - 2.47); for recurrence, it was 1.26 (95% CI, 1.06 - 1.49). For β-lactams, the adjusted ORs were 2.23 (95% CI, 1.71 - 2.90) and 1.42 (95% CI, 1.19 - 1.69), respectively.

There were 2435 treatment failures (5.9%) and 5436 recurrences (18.2%) among the 41,094 children who did not undergo a drainage procedure. For treatment failure, the adjusted ORs were 1.67 (95% CI, 1.44 - 1.95) for trimethoprim-sulfamethoxazole and 1.22 (95% CI, 1.06 - 1.41) for β-lactams. For recurrence, the adjusted hazard ratios were 1.30 (95% CI, 1.18 - 1.44) for trimethoprim-sulfamethoxazole and 1.08 (95% CI, 0.99 - 1.18) for β-lactams.

"Compared with clindamycin, use of trimethoprim-sulfamethoxazole or β-lactams was associated with increased risks of treatment failure and recurrence," the study authors write. "Associations were stronger for those with a drainage procedure."

Limitations of this study include residual confounding, the lack of microbiologic data, and potential misclassification of antibiotic exposure and outcomes.

"These findings, from a cohort of nearly 50 000 children with incident SSTIs, bring into question the use of trimethoprim-sulfamethoxazole for treatment of purulent SSTIs in community-associated MRSA–prevalent regions in which clindamycin resistance remains low," the study authors conclude. "β-lactams, however, may still be effective for nonpurulent SSTIs."

The Agency for Healthcare Research and Quality supported this study in part. The study authors have disclosed no relevant financial relationships.

Pediatrics. Published online August 15, 2011.

Related Link
The Clinical Practice Guidelines by the Infectious Diseases Society of America for the Treatment of Methicillin-Resistant Staphylococcus Aureus Infections in Adults and Children are available in full text online.

Study Highlights

  • Researchers used diagnosis and procedure code data from a database of Medicaid patients in Tennessee to conduct their analysis.
  • Children included in the study were between the ages of 0 and 17 years and were enrolled in TennCare between 2004 and 2007. All children had an outpatient claim for SSTI with no similar claim during the past year. Children in the current study also had a prescription claim for clindamycin, trimethoprim-sulfamethoxazole, or a β-lactam filled within 2 days of the SSTI claim.
  • Children with burns, postsurgical infection, or foreign body injuries were excluded from study analysis.
  • The main study outcome was another SSTI claim within 14 days (treatment failure) or 1 year (recurrence) of the original SSTI claim. Researchers accounted for study year; visit diagnosis; and the age, sex, and race/ethnicity of the children in their analysis.
  • 47,501 children had data related to the SSTIs. Most SSTIs did not require surgical drainage. The study cohort was fairly evenly divided among infants, young children, and adolescents.
  • 15.7% of children receive clindamycin, which was used as the referent standard. 22.3% received trimethoprim-sulfamethoxazole, and 61.9% received a β-lactam. The treatment course for all 3 types of antibiotics was an average between 9 and 10 days.
  • Trimethoprim-sulfamethoxazole use increased during the study period, whereas the proportion of β-lactam prescriptions declined.
  • Children who underwent a drainage procedure were more likely to receive clindamycin or trimethoprim-sulfamethoxazole.
  • 6407 children underwent drainage procedures, of whom 568 (8.9%) experienced treatment failure. The adjusted ORs for treatment failure in comparing treatment with trimethoprim-sulfamethoxazole and β-lactams vs clindamycin were 1.92 (95% CI, 1.49 - 2.47) and 2.23 (95% CI, 1.71 - 2.90), respectively.
  • There were also 994 recurrences (22.8%) among children receiving drainage. The ORs for recurrences for trimethoprim-sulfamethoxazole and β-lactams were 1.26 (95% CI, 1.06 - 1.49) and 1.42 (95% CI, 1.19 - 1.69), respectively, vs clindamycin.
  • 41,094 children did not have a drainage procedure, and 2435 (5.9%) of these children experienced treatment failure. The OR for treatment failure in comparing treatment with trimethoprim-sulfamethoxazole and β-lactams vs clindamycin were 1.67 (95% CI, 1.44 - 1.95) and 1.22 (95% CI, 1.06 - 1.41), respectively.
  • There were also 5436 recurrences (18.2%) among children not receiving drainage. The OR for recurrence for trimethoprim-sulfamethoxazole vs clindamycin was 1.30 (95% CI, 1.18 - 1.44). However, clindamycin was not superior to β-lactams in this outcome.

Clinical Implications

  • A previous study found that the overall number of healthcare visits for SSTIs in the United States increased by 50% between 1997 and 2005, and this increase was most profound among black patients, patients younger than 18 years, and in the South. The use of medications used to treat MRSA increased from 7% at baseline to 28% in 2005, and this change was most pronounced in prescriptions from emergency departments.
  • The current study suggests that clindamycin is generally superior to trimethoprim-sulfamethoxazole and β-lactams in the treatment of SSTIs among children.

CME Test

  • Print