A Case of Clozapine-Associated Pancreatitis

M. Raja, A. Azzoni
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引用次数: 5

Abstract

Acute pancreatitis is a very rare complication of clozapine treatment. We report a new case of symptomatic pancreatitis subsequent to starting of clozapine treatment. In this case, the diagnosis of pancreatitis can be considered de- finitive and the etiological link between clozapine and pancreatitis highly likely. Recovery was not complete. In a 10-year period, we treated 363 cases (196 patients) with clozapine. We diagnosed clozapine-associated pancreatitis only in this pa- tient. However, we did not check amylase and lipase plasma levels in all patients and possibly missed several cases of pancreatitis. We suggest monitoring pancreatic enzymes routinely, at least in the first months of clozapine therapy. Between 2 and 5% of cases of acute pancreatitis are drug related (1). Drugs cause pancreatitis either by a hypersensi- tivity reaction or by the generation of a toxic metabolite. The autodigestion by proteolytic enzymes activated in pancreas rather than in the intestinal lumen is the suspected patho- genic mechanism. Rechallenge tests, consistent case reports, animal experiments, data on the incidence in drug trials pro- vide evidence of a definite association with pancreatitis for didanosine, valproic acid, aminosalicylates, estrogen, cal- cium, anticholinesterases, and sodium stibogluconate. An association with pancreatitis is likely, but not definitely proven, for thiazide diuretics, pentamidine, ACE inhibitors, asparaginase, vinca alkaloids, nonsteroidal anti- inflammatory drugs, and clozapine (2). In a pharmacovigi- lance study of spontaneously reported adverse events (3), 192 patients developed pancreatitis during antipsychotic treatment. Most cases of pancreatitis occurred within 6 months after the start of antipsychotics. Of the reports of pancreatitis associated with antipsychotics, 40%, 33%, 16%, and 12% were in patients receiving clozapine, olanzapine, risperidone, and haloperidol, respectively. In 50% of the patients receiving haloperidol, an atypical antipsychotic was listed as a concomitant drug. Valproate was administered concomitantly in 23% of patients.
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氯氮平相关性胰腺炎1例
急性胰腺炎是氯氮平治疗非常罕见的并发症。我们报告一个新的病例症状性胰腺炎后开始氯氮平治疗。在这种情况下,胰腺炎的诊断可以被认为是决定性的,氯氮平和胰腺炎之间的病因学联系很可能。恢复还没有完成。在10年的时间里,我们用氯氮平治疗了363例(196例患者)。我们只在这个病人身上诊断出氯氮平相关性胰腺炎。然而,我们没有检查所有患者的淀粉酶和脂肪酶血浆水平,可能遗漏了几个胰腺炎病例。我们建议至少在氯氮平治疗的头几个月常规监测胰酶。2 - 5%的急性胰腺炎病例与药物有关(1)。药物引起胰腺炎要么是过敏反应,要么是产生有毒代谢物。胰脏内而非肠腔内活化的蛋白水解酶的自体消化被怀疑是致病机制。再挑战试验、一致的病例报告、动物实验和药物试验中发病率的数据提供了与胰腺炎有明确关联的证据,证明二腺苷、丙戊酸、氨基水杨酸、雌激素、钙、抗胆碱酯酶和抑制葡萄糖酸钠。噻嗪类利尿剂、喷他脒、ACE抑制剂、天冬酰胺酶、长春花生物碱、非甾体抗炎药和氯氮平可能与胰腺炎有关,但尚未得到明确证实(2)。在一项自发报告的不良事件的药理学研究中,192例患者在抗精神病药物治疗期间发生了胰腺炎。大多数胰腺炎病例发生在抗精神病药物开始使用后6个月内。在与抗精神病药物相关的胰腺炎报告中,分别有40%、33%、16%和12%的患者接受氯氮平、奥氮平、利培酮和氟哌啶醇治疗。在50%接受氟哌啶醇治疗的患者中,一种非典型抗精神病药物被列为伴随用药。23%的患者同时服用丙戊酸盐。
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