无尿血液透析患者未被发现的医源性药物引起的并发症:1例报告及文献复习。

IF 0.7 Q4 UROLOGY & NEPHROLOGY Case Reports in Nephrology and Dialysis Pub Date : 2022-10-27 eCollection Date: 2022-09-01 DOI:10.1159/000527197
Edouard Cubilier, Mohamed Tayeb Salaouatchi, Maxime Taghavi, Saleh Kaysi, Joëlle Nortier, Maria do Carmo Filomena Mesquita
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引用次数: 1

摘要

无尿血液透析终末期肾病患者容易出现多种并发症和合并症,因此经常使用各种药物治疗。药物不良反应和导致这些不良反应的危险因素在这类服用多种药物的患者中很难辨别。大多数关于低磷酸盐水平的问题在临床实践中经常被误诊,有时在这些常规高磷血症患者中被忽视。血液透析血管通路经常受到感染,因此需要适当的抗生素治疗。我们报告一例隐匿性严重多因子低磷血症的无尿血液透析患者,有多种合并症,需要两次住院治疗脑病,癫痫发作和心力衰竭。对医疗记录的回顾性分析揭示了低磷血症的几个潜在原因,以及未被发现的与头孢菌素相关的药物不良反应的危险因素。在常规临床实践中对这些问题采取全球方法将提高对这些患者中经常被忽视的低磷血症和药物处方相关问题的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Undetected Iatrogenic Drug-Induced Complications in a Hemodialyzed Anuric Patient: A Case Report and Review of the Literature.

Anuric hemodialyzed end-stage renal disease patients are prone to multiple complications and comorbidities and are therefore often treated with various medications. Adverse drug reactions and risk factors leading to them can be difficult to discern in such polymedicated patients. Most problems regarding low phosphate levels are frequently underdiagnosed in clinical practice and sometimes overlooked in these regularly hyperphosphatemic patients. Hemodialysis vascular accesses are frequently subject to infections and therefore require adapted antibiotic treatments. We report a case of an occult severe multifactorial hypophosphatemia in an anuric hemodialyzed patient with multiple comorbidities who required two hospitalizations for encephalopathy, seizures, and cardiac failure. Retrospective analysis of the medical record revealed several underlying causes of hypophosphatemia, as well as undetected risk factors for adverse drug reactions related to cephalosporins. A global approach to these concerns in routine clinical practice would raise awareness of often disregarded issues related to hypophosphatemia and drug prescription in these patients.

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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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