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二氢吡啶类钙通道阻滞剂导致腹膜透析患者透析液浑浊

Dihydropyridine type calcium channel blocker-induced turbid dialysate in patients undergoing peritoneal dialysis.

作者信息

Yoshimoto K, Saima S, Nakamura Y, Nakayama M, Kubo H, Kawaguchi Y, Nishitani H, Nakamura Y, Yasui A, Yokoyama K, Kuriyama S, Shirai D, Kugiyama A, Hayano K, Fukui H, Horigome I, Amagasaki Y, Tsubakihara Y, Kamekawa T, Ando R, Tomura S, Okamoto R, Miwa S, Koyama T, Echizen H

机构信息

Department of Pharmacotherapy, Meiji College of Pharmacy, Tananshi, Tokyo, Japan.

出版信息

Clin Nephrol. 1998 Aug;50(2):90-3.

PMID:9725779
Abstract

We previously reported that manidipine, a new dihydropyridine type calcium channel blocker, produced chylous peritoneal dialysate being visually indistinguishable from infective peritonitis in 5 patients undergoing continuous ambulatory peritoneal dialysis (CAPD) [Yoshimoto et al. 1993]. To study whether such an adverse drug reaction would also be elicited by other commonly prescribed calcium channel blockers in CAPD patients, we have conducted postal inquiry to 15 collaborating hospitals and an institutional survey in International Medical Center of Japan as to the possible occurrence of calcium channel blocker-associated non-infective, turbid peritoneal dialysate in CAPD patients. Our diagnostic criteria for drug-induced turbidity of dialysate as a) it developed within 48 h after the administration of a newly introduced calcium channel blocker to the therapeutic regimen, b) absence of clinical symptoms of peritoneal inflammation (i.e., pyrexia, abdominal pain, nausea or vomiting), c) the fluid containing normal leukocyte counts and being negative for bacterial and fungal culture of the fluid, and d) it disappeared shortly after the withdrawal of the assumed causative agent. Results showed that 19 out of 251 CAPD patients given one of the calcium channel blockers developed non-infective turbid peritoneal dialysis that fulfilled all the above criteria. Four calcium channel blockers were suspected to be associated with the events: benidipine [2 out of 2 (100%) patients given the drug], manidipine [15 out of 36 (42%) patients], nisoldipine [1 out of 11 (9%) patients] and nifedipine [1 out of 159 (0.6%)] in descending order of frequency. None of the patients who received nicardipine, nilvadipine, nitrendipine, barnidipine and diltiazem (25, 7, 2, 1 and 8 patients, respectively) exhibited turbid dialysate. In conclusion, we consider that certain dihydropyridine type calcium channel blockers would cause turbid peritoneal dialysate being similar to that observed in patients developing infective peritonitis. To avoid unnecessary antibiotic therapy the possibility of this adverse reaction should be ruled out whenever a CAPD patient receiving a dihydropyridine type calcium channel blocker develops turbid dialysate.

摘要

我们之前报道过,新型二氢吡啶类钙通道阻滞剂马尼地平在5例接受持续性非卧床腹膜透析(CAPD)的患者中导致乳糜性腹膜透析液,在视觉上与感染性腹膜炎无法区分[吉本等人,1993年]。为了研究CAPD患者中其他常用的钙通道阻滞剂是否也会引发这种药物不良反应,我们向15家合作医院进行了邮政调查,并在日本国际医疗中心进行了机构调查,以了解CAPD患者中钙通道阻滞剂相关的非感染性浑浊腹膜透析液的可能发生情况。我们将药物引起透析液浑浊的诊断标准定为:a)在将新引入的钙通道阻滞剂用于治疗方案后48小时内出现;b)无腹膜炎症的临床症状(即发热、腹痛、恶心或呕吐);c)液体中白细胞计数正常,且液体的细菌和真菌培养为阴性;d)在停用假定的致病药物后不久消失。结果显示,在251例接受其中一种钙通道阻滞剂治疗的CAPD患者中,有19例出现了符合上述所有标准的非感染性浑浊腹膜透析。有四种钙通道阻滞剂被怀疑与这些事件有关:贝尼地平[2例患者中2例(占100%)使用该药物]、马尼地平[36例患者中15例(占42%)]、尼索地平[11例患者中1例(占9%)]和硝苯地平[159例患者中1例(占0.6%)],按频率从高到低排列。接受尼卡地平、氨氯地平、尼群地平、巴尼地平及地尔硫䓬治疗的患者(分别为25例、7例、2例、1例和8例)均未出现透析液浑浊。总之,我们认为某些二氢吡啶类钙通道阻滞剂会导致浑浊的腹膜透析液,类似于感染性腹膜炎患者中观察到的情况。为避免不必要的抗生素治疗,当接受二氢吡啶类钙通道阻滞剂治疗的CAPD患者出现浑浊透析液时,应排除这种不良反应的可能性。

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