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一项针对影像学确诊的单纯性急性阑尾炎的随机、对照、多中心可行性先导试验:小儿患者的阑尾切除术与症状治疗的对比(APPSYPP 试验)研究方案。

A randomized, controlled multicenter feasibility pilot trial on imaging confirmed uncomplicated acute appendicitis: Appendectomy vs. symptomatic treatment in pediatric patients (the APPSYPP) trial study protocol.

机构信息

Department of Pediatric Surgery, Helsinki University Central Hospital, Helsinki, Finland.

Department of Pediatric Surgery, Tampere University Hospital, Tampere, Finland.

出版信息

Contemp Clin Trials. 2022 Dec;123:106970. doi: 10.1016/j.cct.2022.106970. Epub 2022 Oct 22.

DOI:10.1016/j.cct.2022.106970
PMID:36280033
Abstract

INTRODUCTION

Imaging-confirmed uncomplicated acute appendicitis can be effectively and safely treated with antibiotics in most adults and children. Symptomatic treatment may have similar efficacy and safety.

METHODS AND ANALYSIS

The APPSYPP trial is a randomized national multicenter feasibility superiority pilot study comparing appendectomy with symptomatic treatment in children with imaging-confirmed uncomplicated acute appendicitis.

INCLUSION CRITERIA

  1. age ≥ 7 and < 16 years, 2) imaging-confirmed uncomplicated acute appendicitis and 3) CRP ≤ 65 mg/l. Patients are randomized to receive emergency laparoscopic appendectomy or symptomatic treatment. To ensure patient safety, symptomatically treated patients are hospitalized for at least 24 h receiving standard practice intravenous fluids and analgesics according to standard clinical practice. Primary outcome is 30-day treatment success defined by the absence of any treatment failure criteria. In appendectomy, treatment failure is defined as normal appendiceal histopathology or any postintervention complication requiring general anesthesia. In symptomatic treatment, treatment failure is defined as 1) inability for hospital discharge without appendectomy within 48 h after randomization with a finding of histopathologically inflamed appendix, 2) appendectomy during the initial hospital stay due to clinical progression of appendicitis with complicated acute appendicitis both histopathologically and surgically, 3) appendectomy with a histopathological finding of acute appendicitis after hospital discharge, or 4) any complication of appendicitis requiring general anesthesia. Detailed predefined secondary outcomes will be analyzed.

ETHICS AND DISSEMINATION

Study was approved by Ethics Committee of Helsinki University Hospital (ID:HUS/1993/2021), conducted in compliance with the declaration of Helsinki with results disseminated in peer-reviewed scientific journals.

TRIAL REGISTRATION

ClinicalTrials.gov (NCT05289713).

摘要

简介

在大多数成年人和儿童中,影像学确诊的单纯性急性阑尾炎可以通过抗生素进行有效且安全的治疗。对症治疗可能具有相似的疗效和安全性。

方法和分析

APPSYPP 试验是一项比较影像学确诊的单纯性急性阑尾炎患儿接受阑尾切除术与对症治疗的全国多中心可行性优效性先导研究。

纳入标准

1)年龄≥7 岁且<16 岁,2)影像学确诊的单纯性急性阑尾炎,3)CRP≤65mg/L。患者随机分为接受紧急腹腔镜阑尾切除术或对症治疗。为确保患者安全,接受对症治疗的患者至少住院 24 小时,根据标准临床实践接受标准静脉补液和镇痛治疗。主要结局为 30 天治疗成功,定义为无任何治疗失败标准。在阑尾切除术中,治疗失败定义为正常阑尾组织病理学或任何需要全身麻醉的术后并发症。在对症治疗中,治疗失败定义为 1)随机分组后 48 小时内无法出院且阑尾组织病理学显示炎症,2)因阑尾炎临床进展而在初始住院期间行阑尾切除术,且组织病理学和手术均显示为复杂性急性阑尾炎,3)出院后阑尾切除术且组织病理学显示急性阑尾炎,或 4)任何需要全身麻醉的阑尾炎并发症。将详细分析预先定义的次要结局。

伦理和传播

该研究已获得赫尔辛基大学医院伦理委员会的批准(ID:HUS/1993/2021),符合赫尔辛基宣言进行,研究结果将在同行评议的科学期刊上发表。

试验注册

ClinicalTrials.gov(NCT05289713)。

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