Non-operative Management of Early Appendicitis in Children

Peter Minneci

Status: Active, not recruiting

Conditions: Appendicitis

Study type: Observational

Funder types: Other

Identifiers

NCT01718275

IRB12-00406

Details and patient eligibility

About

The purpose of this study is to determine the feasibility of non-operative management of early appendicitis in children. We hypothesize that non-operative management of early appendicitis in children with antibiotics alone will be successful in 80% of children at 1 year follow-up.

Full description

Non-operative management of appendicitis with antibiotics alone has recently emerged as a viable treatment alternative to appendectomy. There have been several clinical trials in adults which conclude that antibiotics alone are a safe initial treatment for appendicitis; none of these studies included children.

The primary objective of this study is to determine: conversion to surgery (failure of nonoperative management), 30 day, 6 month and 1 year recurrence rate of appendicitis in children treated with non-operative management. Recurrence is defined as need for appendectomy. The secondary objective is to compare adverse outcomes, length of stay, days to return to school, costs of care and quality of life measures between the study group and those that receive standard of care.We hypothesize that non-operative management of early appendicitis in children with antibiotics alone will be successful in 80% of children at 1 year follow-up.

This is a prospective, non-randomized single-site trial measuring the feasibility of treating children (7-17 years old) with early appendicitis with antibiotics only (non-operative management). There will be two cohorts; those who agree to receive non-operative management (Non-Operative Group) and those that permit us to track their standard treatment course (Surgery Group).

Enrollment: 102 patients

Sex: All

Ages: 7 to 17 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age : 7-17 years
• Ultrasound (US) or CT scan confirmed early appendicitis (US: hyperemia, <1.1 cm in diameter, compressible or non-compressible, no abscess, no fecalith, no phlegmon; CT: hyperemia, fat stranding, <1.1 cm in diameter, no abscess, no fecalith, no phlegmon)
• White blood cell count (WBC) < 15,000
• C reactive protein (CRP) <4 (if obtained)
• Focal abdominal pain </= 36 hours prior to receiving antibiotics

Exclusion criteria

• English is not the primary language of either the child or parent/guardian
• Other significant co-morbidities: cardiovascular disease, malignancy, pulmonary disease, diabetes, obesity (BMI ≥ 95th percentile for age and sex), severe developmental delay
• Positive urine pregnancy test
• Diffuse peritonitis
• Fecalith
• History of chronic intermittent abdominal pain
• WBC >/= 15
• CRP>/= 4 (if obtained)
• Pain > 36 hours prior to first antibiotic dose or any evidence on imaging studies concerning for evolving perforated appendicitis including abscess or phlegmon

Trial design

102 participants in 2 patient groups

Non-operative Group

Description:

Patients and caregivers who agree to receive non-operative management with antibiotics alone

Surgery Group

Description:

Patients and caregivers who decide to undergo appendectomy that permit us to track their standard treatment course