Prevention of severe infectious complications after colorectal surgery using preoperative orally administered antibiotic prophylaxis (PreCaution): study protocol for a randomized controlled trial

被引:6
作者
Mulder, Tessa [1 ]
Kluytmans-van den Bergh, Marjolein F. Q. [1 ,2 ,3 ]
de Smet, Anne Marie G. A. [4 ]
van't Veer, Nils E. [5 ]
Roos, Daphne [6 ]
Nikolakopoulos, Stavros [1 ]
Bonten, Marc J. M. [1 ,7 ]
Kluytmans, Jan A. J. W. [1 ]
机构
[1] Univ Utrecht, Univ Med Ctr Utrecht, Ctr Hlth Sci & Primary Care, Div Julius, Utrecht, Netherlands
[2] Amphia Acad Infect Dis Fdn, Amphia Hosp, Breda, Netherlands
[3] Amphia Hosp, Lab Microbiol & Infect Control, Breda, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Crit Care, Groningen, Netherlands
[5] Amphia Hosp, Dept Clin Pharm, Breda, Netherlands
[6] Reinier Graaf Gasthuis, Dept Surg, Delft, Netherlands
[7] Univ Utrecht, Univ Med Ctr Utrecht, Dept Med Microbiol, Utrecht, Netherlands
关键词
Surgical site infection; Colorectal surgery; Preoperative oral antibiotic prophylaxis; Infection control; Randomized controlled trial; Placebo; Drug intervention trial; Mortality; SURGICAL SITE INFECTIONS; MECHANICAL BOWEL PREPARATION; DIGESTIVE-TRACT; SELECTIVE DECONTAMINATION; INTENSIVE-CARE; CLINICAL-TRIAL; COLON; RESISTANCE; OROPHARYNX; BACTERIA;
D O I
10.1186/s13063-018-2439-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Colorectal surgery is frequently complicated by surgical site infections (SSIs). The most important consequences of SSIs are prolonged hospitalization, an increased risk of surgical reintervention and an increase in mortality. Perioperative intravenously administered antibiotic prophylaxis is the standard of care to reduce the risk of SSIs. In the last few decades, preoperative orally administered antibiotics have been suggested as additional prophylaxis to further reduce the risk of infection, but are currently not part of routine practice in most hospitals. The objective of this study is to evaluate the efficacy of a preoperative orally administered antibiotic prophylaxis (Pre-OP) in addition to intravenously administered perioperative antibiotic prophylaxis to reduce the incidence of deep SSIs and/or mortality after elective colorectal surgery. Methods/design: The PreCaution trial is designed as a multicenter, double-blind, randomized, placebo-controlled clinical trial that will be carried out in The Netherlands. Adult patients who are scheduled for elective colorectal surgery are eligible to participate. In total, 966 patients will be randomized to receive the study medication. This will either be Pre-OP, a solution that consists of tobramycin and colistin sulphate, or a placebo solution. The study medication will be administered four times daily during the 3 days prior to surgery. Perioperative intravenously administered antibiotic prophylaxis will be administered to all patients in accordance with national infection control guidelines. The primary endpoint of the study is the cumulative incidence of deep SSIs and/or mortality within 30 days after surgery. Secondary endpoints include both infectious and non-infectious complications of colorectal surgery, and will be evaluated 30 days and/or 6 months after surgery. Discussion: To date, conclusive evidence on the added value of preoperative orally administered antibiotic prophylaxis in colorectal surgery is lacking. The PreCaution trial should determine the effects of orally administered antibiotics in preventing infectious complications in elective colorectal surgery.
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页数:9
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