Management of Skin and Soft Tissue Abscesses in Pediatric Patients After Incision and Drainage

Baylor College of Medicine23 enrolled

Overview

The purpose of the study is to compare rates of cure of abscesses with and without antibiotic treatment after incision and drainage. The purpose of this study is to compare successful rates of cure of abscesses less than 5 cm with antibiotic (oral TMP/SMX) versus non-antibiotic treatment after incision and drainage.

This study is a randomized controlled trial of antibiotic treatment versus placebo after incision and drainage of skin and soft tissue abscesses less than 5 cm in pediatric patients. Eligible patients whose parents/guardians consented them to enrollment were randomized to receive one of two interventions: oral trimethoprim/sulfamethoxazole (TMP/SMX) or placebo after incision and drainage. Every attempt was made to make the placebo capsules and suspensions appear in all aspects like the true drug (was done by the investigational pharmacy department at our institution). Equal numbers of subjects were randomized at the outset to both study groups. Randomization, also done by our investigational pharmacy department, was done in blocks of 20. Patients were followed up in our emergency center at 24 to 48 hours to have any packing removed and to have their clinical/wound status assessed. They were not charged for this visit, and their valet parking was validated. If an individual patient, or an individual patient's wound, was felt to be not improving adequately, that patient was started on formal antibiotic therapy at the treating attending physician's discretion. Primary outcome: 1\. Abscess resolution by parental report 7-10 days after incision and drainage Secondary outcomes: 1. Admission to the hospital because of worsening infection 2. Receipt of antibiotics (placebo arm) or change in antibiotics (antibiotic arm)

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Abscess

Interventions

oral trimethoprim/sulfamethoxazoleDRUG

80 mg caps or 8 mg/ml suspension every 12 hours for 10 days

PlaceboDRUG

Placebo caps or suspension every 12 hours for 10 days

Eligibility

Sex: ALLMin age: 90 DaysMax age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1.) Abscess \< 5 cm (\< 5 cm of induration and fluctuance) requiring incision and drainage 2.) Age \> 90 days and \< 18 years 3.) Abscess on the trunk, scalp, extremities, or axillae Exclusion Criteria: 1. Multiple abscesses 2. Abscess located on the hands, face, or perineum 3. Abscess as a result of a bite wound 4. Immunocompromised patient - i.e., diabetes, sickle cell, chronic steroid therapy (\> 10 days), etc. 5. Previously failed 48 hours or greater therapy on any antibiotic regimen 6.) Drug allergy to TMP/SMX 7.) Fever \> or = 102.2 degrees Fahrenheit in the previous 24 hours 8.) Systemic symptoms on presentation - i.e., nausea , vomiting, persistent tachycardia, hypotension, diaphoresis, etc. 9.) Signs /symptoms of another infection or illness - i.e., influenza, croup, etc.

Locations (1)

Texas Children's Hospital

Houston, Texas, United States

Outcomes

Primary Outcomes

Number of Participants With Abscess Resolution

Outcomes will be measured by resolution of size, tenderness, and induration with erythema by parental report 7 - 10 days after initial visit to the Emergency Center

Time frame: 10 days

Secondary Outcomes

Number of Participants Requiring Admission for Failure of Abscess Resolution

Percentage of patients requiring admission to Texas Children's or another hospital within 10 days of incision and drainage

Time frame: 10 days

Number of Participants Requiring New or Modified Antibiotics for Failure of Abscess to Resolve

For the antibiotic arm, we determined if the child was prescribed a different antibiotic. For the placebo arm, we determined if the child received a prescription for an antibiotic at a subsequent visit (e.g., in the emergency department, by their pediatrician, etc) within 10 days of incision and drainage

Time frame: 10 days

Data from ClinicalTrials.gov

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