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柏林病例对照监测研究中的药物诱导免疫性溶血性贫血。

Drug induced immune haemolytic anaemia in the Berlin Case-Control Surveillance Study.

机构信息

Bremen Institute for Prevention Research and Social Medicine, University of Bremen, Bremen, Germany.

出版信息

Br J Haematol. 2011 Sep;154(5):644-53. doi: 10.1111/j.1365-2141.2011.08784.x. Epub 2011 Jul 12.

Abstract

Drug-induced immune haemolytic anaemia is a rare but serious condition. This study investigated the possibility of drug aetiology of immune haemolytic anaemia (IHA) in 134 patients with new onset of IHA who were identified in the Berlin Case-Control Surveillance Study between 2000 and 2009. Single drugs related to IHA in three or more patients and assessed more than once as a certain or probable cause of IHA in a standardized causality assessment included diclofenac, fludarabine, oxaliplatin, ceftriaxone and piperacillin. In a case-control study including all 124 IHA cases developed in outpatient care and 731 controls, significantly increased odds ratios (OR) were observed for beta-lactam antibiotics (OR=8·8; 95% confidence interval [CI] 3·2-25·2), cotrimoxazole (OR=6·5; CI 1·1-37·9), ciprofloxacin (OR=6·9, CI 1·3-38·5), fludarabine (OR=22·2; CI: 2·8-454·5) and lorazepam (OR=5·3; CI: 1·2-21·2). Excluding new onset cases with a chronic IHA disease course, an increased risk became also apparent for diclofenac with an OR of 3·1 (CI 1·3-7·0). This is the first case-control study investigating drugs as risk factors for IHA. It corroborates an increased risk for several drugs that have been implicated as a cause of IHA in the standardized causality assessment of individual cases.

摘要

药物性免疫性溶血性贫血是一种罕见但严重的疾病。本研究调查了在 2000 年至 2009 年期间柏林病例对照监测研究中发现的 134 例新发免疫性溶血性贫血(IHA)患者中药物病因的可能性。在标准化因果关系评估中,有三种或三种以上患者与单一药物相关且被评估为 IHA 的确定或可能原因的药物包括双氯芬酸、氟达拉滨、奥沙利铂、头孢曲松和哌拉西林。在一项包括所有在门诊治疗中发生的 124 例 IHA 病例和 731 例对照的病例对照研究中,β-内酰胺类抗生素(OR=8.8;95%置信区间 [CI] 3.2-25.2)、复方磺胺甲噁唑(OR=6.5;CI 1.1-37.9)、环丙沙星(OR=6.9,CI 1.3-38.5)、氟达拉滨(OR=22.2;CI:2.8-454.5)和劳拉西泮(OR=5.3;CI:1.2-21.2)的比值比(OR)显著升高。排除慢性 IHA 病程的新发病例,双氯芬酸的风险比也明显升高(OR=3.1;CI 1.3-7.0)。这是第一项调查药物作为 IHA 危险因素的病例对照研究。它证实了几种药物的风险增加,这些药物在对个别病例的标准化因果关系评估中被认为是 IHA 的原因。

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