Inflammatory Markers After COloRectal Surgery)
- Conditions
- Infectious Complications After Colorectal Surgery
- Registration Number
- NCT01510314
- Lead Sponsor
- Centre Hospitalier Universitaire Dijon
- Brief Summary
The clinical symptoms of septic complications (SC) (responsible for the majority of morbidity in colorectal surgery) become apparent only 5-7 days after the operation, whereas the efficacy of treatment depends on early diagnosis. By detecting such complications early it could be possible to reduce their severity, the length of hospitalisation, repeat colostomy and the number of readmissions. Our team has shown that C-reactive protein (CRP) \> 125 mg/L at postoperative day 4 (D4) was a predictor of SC in this context. Procalcitonin (PCT) is a marker of sepsis currently used in intensive care, but its use in the follow-up of elective surgery, particularly colorectal surgery, has not been fully evaluated.
The aim of this study is to compare the ability of CRP and PCT to detect SC as early as postoperative day 2 (D2) (intra-abdominal or systemic SC, such as those defined by the CDC) after elective colorectal surgery.
Adult patients about to undergo elective colorectal surgery with anastomosis will be included once they have given their written informed consent. Levels of CRP and PCT will be measured the day before the surgery, then at D1, D2, D3 and D4. The clinical data (temperature, recovery of bowel movement, pain, pain on palpation) will be recorded daily. Imaging examinations will be performed at the discretion of the surgeon; the only obligation will be to perform a contrast-enhanced abdominopelvic CT-scan if CRP at D4 \> 125 mg/L with no other clinical anomalies. The discriminating ability (measured by the area under the ROC curve) of CRP at D2 was 0.653 in our previous study. An improvement of at least 0.1 will be necessary to show the superiority of PCT over CRP in clinical terms and with regard to the cost.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 552
- Patients undergoing elective colorectal surgery with anastomosis for benign or malignant disease
- > 18 years old
- Giving written informed consent
- Included in the national health insurance
- Emergent surgery
- Previous infection
- Patients undergoing Hyperthermic Intraperitoneal Chemotherapy
- Pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraabdominal infection
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (3)
CHU Dijon
🇫🇷Dijon, France
CHU Besançon
🇫🇷Besançon, France
CGFL
🇫🇷Dijon, France