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N/A N=36 Randomized Other

Fast Track Appendectomy for Suppurative Appendicitis

Suppurative Appendicitis

Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Sep 2015
Primary outcome: Primary: Post Operative Length of Stay — 8.2; 23.4 Hours

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Patients discharged home the same day following appendectomy (Other)
Age
Pediatric, Adult · 5+ yrs
Sex
All
Sponsor
Johns Hopkins All Children's Hospital
Primary completion
Dec 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Post Operative Length of Stay
8.2; 23.4
SECONDARY
Thirty Day Complication Rate
2; 1

Summary

The literature has reported that fast track surgery can be safely applied to children undergoing appendectomy for acute appendicitis. There is no current evidence regarding the application of same day discharge protocol in children with intra-operative findings of suppurative appendicitis. The current standard of care for patients who present with intra-operative findings of suppurative appendicitis includes post-operative admission and treatment with intravenous antibiotics. Patients are discharged home once they have met the following discharge criteria: temperature less than 38.5 degrees Celsius, pain control with oral pain medication, and tolerating a liquid diet. Given the evidence in the literature that has shown that same day discharge of patients with acute appendicitis is safe and effective, we propose that fast track surgery protocol can be safely applied to patients with intraoperative findings of suppurative appendicitis. We hypothesize that this will result in a decreased postoperative length of stay, without an increase in 30-day complication rate.

Eligibility Criteria

Inclusion Criteria

  • Pediatric patients aged 5-18
  • Diagnosis of appendicitis and scheduled for appendectomy during the hours of 0600-1800.
  • Intraoperative findings of suppurative appendicitis

Exclusion Criteria

  • Pregnancy
  • Complex medical history not appropriate for same day discharge
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02137603). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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