Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Department of Biology, McMaster University, Hamilton, Ontario, Canada.
Inflamm Bowel Dis. 2020 Nov 19;26(12):1796-1807. doi: 10.1093/ibd/izaa020.
To assess the impact of inflammatory bowel disease (IBD) medications on postoperative infection risk within 30 days of surgery.
We searched multiple electronic databases and reference lists of articles dating up to August 2018 for prospective and retrospective studies comparing postoperative infection risk in patients treated with an IBD medication perioperatively with the risk in patients who were not taking that medication. Outcomes were overall infectious complications and intra-abdominal infections within 30 days of surgery.
Sixty-three studies were included. Overall infectious complications were increased in patients who received anti-tumor necrosis factor (TNF) agents (odds ratio [OR] 1.26; 95% confidence interval [CI], 1.07-1.50) and corticosteroids (OR 1.34; 95% CI, 1.25-1.44) and decreased in those who received 5-aminosalicylic acid (OR 0.63; 95% CI, 0.46-0.87). No difference was observed in those treated with immunomodulators (OR 1.08; 95% CI, 0.94-1.25) or anti-integrin agents (OR 1.06; 95% CI, 0.67-1.69). Both corticosteroids and anti-TNF agents were associated with increased intra-abdominal infection risk (OR 1.63; 95% CI, 1.33-2.00 and OR 1.46; 95% CI, 1.08-1.97, respectively), whereas no impact was observed with 5-aminosalicylates, immunomodulators, or anti-integrin therapy. Twenty-two studies had low risk of bias while the remaining studies had very high risk.
Corticosteroids and anti-TNF agents were associated with increased overall postoperative infection risk as well as intra-abdominal infection in IBD patients, whereas no increased risk was observed for immunomodulators or anti-integrin therapy. Although these results may result from residual confounding rather than from a true biological effect, prospective studies that control for potential confounding factors are required to generate higher-quality evidence.
评估炎症性肠病(IBD)药物对术后 30 天内手术感染风险的影响。
我们检索了多个电子数据库和文献的参考文献列表,以寻找比较围手术期接受 IBD 药物治疗的患者与未接受该药物治疗的患者术后感染风险的前瞻性和回顾性研究。结果为术后 30 天内的总体感染并发症和腹腔内感染。
共纳入 63 项研究。接受抗肿瘤坏死因子(TNF)药物(比值比[OR] 1.26;95%置信区间[CI],1.07-1.50)和皮质类固醇(OR 1.34;95%CI,1.25-1.44)治疗的患者总体感染并发症增加,而接受 5-氨基水杨酸(OR 0.63;95%CI,0.46-0.87)治疗的患者感染并发症减少。免疫调节剂(OR 1.08;95%CI,0.94-1.25)或抗整合素药物(OR 1.06;95%CI,0.67-1.69)治疗的患者无差异。皮质类固醇和抗 TNF 药物均与腹腔内感染风险增加相关(OR 1.63;95%CI,1.33-2.00 和 OR 1.46;95%CI,1.08-1.97),而 5-氨基水杨酸、免疫调节剂或抗整合素治疗则无影响。22 项研究的偏倚风险较低,其余研究的偏倚风险很高。
皮质类固醇和抗 TNF 药物与 IBD 患者的总体术后感染风险以及腹腔内感染相关,而免疫调节剂或抗整合素治疗则没有增加风险。尽管这些结果可能是由于残余混杂因素而不是真正的生物学效应所致,但需要进行前瞻性研究来控制潜在的混杂因素,以产生更高质量的证据。