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克罗恩病治疗相关的严重感染与死亡率:TREAT注册研究

Serious infections and mortality in association with therapies for Crohn's disease: TREAT registry.

作者信息

Lichtenstein Gary R, Feagan Brian G, Cohen Russell D, Salzberg Bruce A, Diamond Robert H, Chen Donny M, Pritchard Michelle L, Sandborn William J

机构信息

Department of Medicine, Division of Gastroenterology, Hospital of the University of Pennsylvania, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-4283, USA.

出版信息

Clin Gastroenterol Hepatol. 2006 May;4(5):621-30. doi: 10.1016/j.cgh.2006.03.002.

Abstract

BACKGROUND & AIMS: Long-term safety data for infliximab and other therapies in Crohn's disease (CD) are needed.

METHODS

We prospectively evaluated patients for prespecified safety-related outcomes.

RESULTS

As of August 2004, 6290 patients were enrolled; 3179 received infliximab (5519 patient-years), 87% of whom received at least 2 infusions, and 3111 received other therapies (6123 patient-years). The mean length of follow-up evaluation was 1.9 years. More infliximab-treated patients had moderate-to-severe (30.8% vs 10.3%) or severe-fulminant (2.5% vs .6%) CD, and had surgical (17.5% vs 13.8%) or medical (14.4% vs 9.1%) hospitalizations in the previous year. More patients were taking prednisone (27.4% vs 16.1%), immunomodulators (49.4% vs 32.2%), or narcotic analgesics (9.8% vs 5.4%) when compared with those receiving other therapies (P<.001, all comparisons). The mortality rates were similar for infliximab- and non-infliximab-treated patients (.53 per 100 patient-years vs .43; relative risk, 1.24; 95% confidence interval [CI], .73-2.10). In multivariate logistic regression analysis, only prednisone was associated with an increased mortality risk (odds ratio [OR], 2.10; 95% CI, 1.15-3.83; P=.016). Although the unadjusted analysis showed an increased risk for infection with infliximab use, multivariate logistic regression analysis suggested that infliximab was not an independent predictor of serious infections (OR, .99; 95% CI, .64-1.54). Factors independently associated with serious infections included prednisone use (OR, 2.21; 95% CI, 1.46-3.34; P<.001), narcotic analgesic use (OR, 2.38; 95% CI, 1.56-3.63; P<.001), and moderate-to-severe disease activity (OR, 2.11; 95% CI, 1.10-4.05; P=.024).

CONCLUSIONS

Mortality rates were similar between infliximab- and non-infliximab-treated patients. The increased risk for serious infection observed with infliximab likely was owing to disease severity and prednisone use.

摘要

背景与目的

需要获得英夫利昔单抗及其他疗法用于克罗恩病(CD)的长期安全性数据。

方法

我们对患者进行前瞻性评估以观察预先设定的与安全性相关的结果。

结果

截至2004年8月,共纳入6290例患者;3179例接受英夫利昔单抗治疗(5519患者年),其中87%接受了至少2次输注,3111例接受其他疗法(6123患者年)。随访评估的平均时长为1.9年。接受英夫利昔单抗治疗的患者中,中度至重度(30.8%对10.3%)或重度暴发性(2.5%对0.6%)克罗恩病患者更多,且上一年接受手术治疗(17.5%对13.8%)或住院治疗(14.4%对9.1%)的患者更多。与接受其他疗法的患者相比,更多患者正在服用泼尼松(27.4%对16.1%)、免疫调节剂(49.4%对32.2%)或麻醉性镇痛药(9.8%对5.4%)(所有比较P<0.001)。接受英夫利昔单抗治疗和未接受英夫利昔单抗治疗患者的死亡率相似(每100患者年0.53对0.43;相对风险,1.24;95%置信区间[CI],0.73 - 2.10)。在多因素逻辑回归分析中,仅泼尼松与死亡风险增加相关(比值比[OR],2.10;95% CI,1.15 - 3.83;P = 0.016)。尽管未校正分析显示使用英夫利昔单抗会增加感染风险,但多因素逻辑回归分析表明英夫利昔单抗并非严重感染的独立预测因素(OR,0.99;95% CI,0.64 - 1.54)。与严重感染独立相关的因素包括使用泼尼松(OR,2.21;95% CI,1.46 - 3.34;P<0.001)、使用麻醉性镇痛药(OR,2.38;95% CI,1.56 - 3.63;P<0.001)以及中度至重度疾病活动(OR,2.11;95% CI,1.10 - 4.05;P = 0.024)。

结论

接受英夫利昔单抗治疗和未接受英夫利昔单抗治疗患者的死亡率相似。观察到的英夫利昔单抗导致严重感染风险增加可能归因于疾病严重程度和泼尼松的使用。

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