Agrawal Anurag, Durrani Shireen, Leiper Keith, Ellis Anthony, Morris Anthony I, Rhodes Jonathan M
Department of Gastroenterology, Royal Liverpool University Hospital, Liverpool, United Kingdom.
Clin Gastroenterol Hepatol. 2005 Dec;3(12):1215-20. doi: 10.1016/s1542-3565(05)00759-7.
BACKGROUND & AIMS: Systemic corticosteroid therapy increases risk of postoperative sepsis in Crohn's disease. This study investigates its effect on risk for sepsis in non-operated patients.
A retrospective case-control study was performed in 432 patients with Crohn's disease (the 94% of our database for whom adequate documentation could be retrieved). Two analyses were performed. The first tested the hypothesis that patients with perforating Crohn's disease (n = 86) were more likely to develop intra-abdominal or pelvic abscess (n = 29) if they had received systemic corticosteroids during the previous 3 months. The second analysis, confined to interventions since 1998, tested the hypothesis that corticosteroid therapy was more common during the 3 months before presentation with intra-abdominal or pelvic abscess (n = 12) than during the 3 months after presentation with a relapse of nonperforating disease (n = 24 consecutive patients). In both analyses adjustment was made for any other significant variable.
Systemic corticosteroid therapy was associated with an adjusted odds ratio (OR) for intra-abdominal or pelvic abscess of 9.03 (95% confidence interval [CI], 2.40-33.98) in patients with perforating Crohn's disease. Patients receiving prednisolone > or = 20 mg per day had an OR of 2.81 (95% CI, 0.99-7.99) for abscess compared with those receiving a lower dose. In patients with relapsed active disease, corticosteroid therapy was associated with an unadjusted OR of 9.31 (95% CI, 1.03-83.91) for intra-abdominal or pelvic abscess. Neither smoking nor azathioprine usage was associated with increased risk for abscess.
Systemic corticosteroid therapy for Crohn's disease is associated with increased risk for intra-abdominal or pelvic abscess.
全身用糖皮质激素治疗会增加克罗恩病患者术后发生败血症的风险。本研究调查其对未接受手术患者发生败血症风险的影响。
对432例克罗恩病患者进行了一项回顾性病例对照研究(占我们数据库中可检索到充分记录患者的94%)。进行了两项分析。第一项分析检验了以下假设:患有穿孔性克罗恩病的患者(n = 86),如果在过去3个月内接受过全身用糖皮质激素治疗,则更有可能发生腹腔或盆腔脓肿(n = 29)。第二项分析仅限于1998年以来的干预措施,检验了以下假设:与出现非穿孔性疾病复发(n = 24例连续患者)后的3个月相比,在出现腹腔或盆腔脓肿前的3个月内,糖皮质激素治疗更为常见(n = 12)。在两项分析中均对任何其他显著变量进行了校正。
在患有穿孔性克罗恩病的患者中,全身用糖皮质激素治疗与腹腔或盆腔脓肿的校正比值比(OR)为9.03(95%置信区间[CI],2.40 - 33.98)相关。与接受较低剂量泼尼松龙的患者相比,接受泼尼松龙≥20 mg/天的患者发生脓肿的OR为2.81(95%CI,0.99 - 7.99)。在复发的活动性疾病患者中,糖皮质激素治疗与腹腔或盆腔脓肿的未校正OR为9.31(95%CI,1.03 - 83.91)相关。吸烟和使用硫唑嘌呤均与脓肿风险增加无关。
克罗恩病的全身用糖皮质激素治疗与腹腔或盆腔脓肿风险增加相关。