Smith Stephen R, Pockney Peter, Holmes Ryan, Doig Fiona, Attia John, Holliday Elizabeth, Carroll Rosemary, Draganic Brian
Department of Colorectal Surgery, John Hunter Hospital, The University of Newcastle, Newcastle, New South Wales, Australia.
The University of Newcastle, Newcastle, New South Wales, Australia.
ANZ J Surg. 2018 May;88(5):440-444. doi: 10.1111/ans.13937. Epub 2017 Mar 17.
Anastomotic leakage is a feared complication following colorectal surgery. Early prediction results in improved clinical outcome, but accurate predictive factors remain elusive. Many biomarkers have been studied with respect to diagnosis of anastomotic leakage but the concept of trajectory testing, using biomarkers, has not been assessed with regards to early diagnosis of anastomotic leak.
C-reactive protein (CRP), procalcitonin (PCT), white cell count (WCC) and gamma-glutamyl transferase were assessed for predictive utility in diagnosing anastomotic leakage with emphasis on identifying an association with change in their levels or trajectory. Levels were collected preoperatively and daily for the first 5 post-operative days on patients undergoing elective colorectal surgery, involving an anastomosis. Anastomotic leakage was defined clinically by operative or radiological intervention. Comparison was made between biomarkers and clinical anastomotic leakage, using receiver operator characteristic curves for logistic models, based on trajectory of the four biomarkers.
A total of 197 consecutive patients were analysed. Eleven patients developed clinical anastomotic leakage. An association of biomarker trajectory with anastomotic leakage was observed for WCC, PCT and CRP, but not for gamma-glutamyl transferase. CRP was the superior biomarker based on trajectory, with area under the receiver operator curve of 0.961.
This study identifies change in CRP, WCC and PCT as potential markers of anastomotic leakage following colorectal surgery and in particular highlights CRP trajectory as extremely accurate in diagnosing anastomotic leakage requiring intervention. External validation should be sought before incorporating this into routine clinical practice, given the numbers in this study.
吻合口漏是结直肠手术后令人担忧的并发症。早期预测可改善临床结局,但准确的预测因素仍不明确。关于吻合口漏的诊断,已经对许多生物标志物进行了研究,但使用生物标志物的轨迹测试概念尚未针对吻合口漏的早期诊断进行评估。
评估了C反应蛋白(CRP)、降钙素原(PCT)、白细胞计数(WCC)和γ-谷氨酰转移酶在诊断吻合口漏方面的预测效用,重点是确定其水平或轨迹变化之间的关联。对接受择期结直肠手术且涉及吻合术的患者,在术前及术后第1至5天每天收集这些指标的水平。吻合口漏通过手术或放射学干预进行临床定义。基于四种生物标志物的轨迹,使用逻辑模型的受试者工作特征曲线,对生物标志物与临床吻合口漏进行比较。
共分析了197例连续患者。11例患者发生临床吻合口漏。观察到WCC、PCT和CRP的生物标志物轨迹与吻合口漏有关,但γ-谷氨酰转移酶无关。基于轨迹,CRP是 superior生物标志物,受试者工作曲线下面积为0.961。
本研究确定CRP、WCC和PCT的变化为结直肠手术后吻合口漏的潜在标志物,尤其突出了CRP轨迹在诊断需要干预的吻合口漏方面极为准确。鉴于本研究中的样本量,在将其纳入常规临床实践之前应寻求外部验证。