Peroral versus intravenous post-operative antibiotics after surgery for complicated appendicitis: protocol for a cluster- randomised cluster-crossover non- inferiority study

被引:0
|
作者
Mohamud, Ahmed Abdirahman [1 ]
Kleif, Jakob [2 ]
Gogenur, Ismail [3 ]
机构
[1] Slagelse Hosp, Dept Surg, Slagelse, Denmark
[2] Copenhagen Univ Hosp, Dept Surg, North Zealand Hosp, Copenhagen, Denmark
[3] Zealand Univ Hosp, Ctr Surg Sci, Dept Surg, Roskilde, Denmark
来源
DANISH MEDICAL JOURNAL | 2021年 / 68卷 / 06期
关键词
APPENDECTOMY; DURATION; DESIGN;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
INTRODUCTION: Complicated appendicitis increases the risk of post-operative intra-abdominal abscess. Treatment of complicated appendicitis is usually a post-operative course of intravenous antibiotics. A study is needed to confirm the results of retrospective studies showing that a post-operative course of oral antibiotics is not inferior to intravenous antibiotics after laparoscopic surgery for complicated appendicitis. METHODS: The Per oral versus Intravenous Postoperative Antibiotics after surgery for complicated appendicitis (PIPA) trial will be a prospective, multicentre, cluster-randomised cluster-crossover non-inferiority study designed to test whether a three-day post-operative course of oral antibiotics is non-inferior to a three-day post-operative course of intravenous antibiotics as standard care after laparoscopic surgery for complicated appendicitis in regards to the risk of post-operative intra-abdominal abscess formation within 30 days. Participating hospitals will either be randomised to a six-month period with an oral antibiotic regime followed by a six-month period with an intravenous antibiotic regime for the post-operative treatment after laparoscopic surgery for complicated appendicitis, or to a six-month period with an intravenous antibiotic regime followed by a six-month period with an oral antibiotic regime for post-operative treatment after laparoscopic surgery for complicated appendicitis. CONCLUSIONS: The primary outcome will be the incidence of intra-abdominal abscess by post-operative day 30. FUNDING: none. TRIAL REGISTRATION: The study was approved by the Danish Data Protection Agency and by the National/Regional Committee on Health Research Ethics.
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