Drug-related hypophosphatemia: Descriptive study and case/non-case analysis of the French national pharmacovigilance database

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY Therapie Pub Date : 2024-05-01 DOI:10.1016/j.therap.2023.07.007
Eve-Marie Thillard , Paula Sade , Joelle Michot , Virginie Bres , Annie-Pierre Jonville-Bera
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Abstract

Phosphorus is an essential element for all living organisms and is involved in various biological pathways. A severe hypophosphatemia can lead to serious complications (acute heart or respiratory failure, rhabdomyolysis, hemolysis…) and increases mortality in patients at risk. Various drugs are known to induce hypophosphatemia through various mechanisms. The aim of this study was to highlight the main drugs associated with hypophosphatemia and to deduce the underlying mechanisms based on a descriptive analysis and a case/non-case analysis using the cases of drug-induced hypophosphatemia reported to the French Pharmacovigilance Network. A total of 368 cases of hypophosphatemia were included in the study. Patients’ mean age was 52 ± 18 years. One hundred and ninety-one cases (52%) were serious including 131 (36%) hospitalizations. The median value of serum phosphorus level was 0.54 mmol/L [0.40–0.66] (n = 309). Those 368 cases corresponded to 185 different suspected substances among which the most frequent drugs were tenofovir disoproxil (n = 175; 48%), ferric carboxymaltose (n = 29; 8%), denosumab (n = 16; 4%), zoledronic acid (n = 14; 4%) and hydrochlorothiazide (n = 10; 3%). For these five drugs, a significant disproportionality was found. Tenofovir-disoproxil related hypophosphatemia occurred more than one year after its introduction, and a renal tubulopathy (Fanconi's syndrome) was reported in 44 cases (25%). Hypophosphatemia related to iron carboxymaltose occurred within a median of 20 days after injection and was mostly severe. Mechanism included the fibroblast growth factor 23 which can be measured to confirm drug origin. Concerning anti-osteoporosis treatments, hypophosphatemia could be explained by their mechanism of action (abrupt increase of parathormone induced by hypocalcemia) but the patient history (malignancy condition) was a major bias. For hydrochlorothiazide, hyphosphatemia was often moderate, associated with other electrolytic disturbances and occurred during a long-term treatment. Awareness of healthcare professionals is essential to detect as soon as possible hypophosphatemia and its complications related to these drugs.

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与药物有关的低磷血症:法国国家药物警戒数据库的描述性研究和病例/非病例分析。
磷是所有生物体的必需元素,参与各种生物途径。严重的低磷血症可导致严重的并发症(急性心脏或呼吸衰竭、横纹肌溶解、溶血......),并增加高危患者的死亡率。众所周知,各种药物可通过不同机制诱发低磷血症。本研究的目的是通过描述性分析和病例/非病例分析,利用向法国药物警戒网络报告的药物诱发低磷血症病例,重点分析与低磷血症相关的主要药物,并推断其基本机制。研究共纳入了 368 例低磷血症病例。患者的平均年龄为 52±18 岁。191例(52%)病情严重,其中131例(36%)住院治疗。血清磷水平的中位值为 0.54mmol/L [0.40-0.66](n=309)。这 368 个病例涉及 185 种不同的可疑物质,其中最常见的药物是替诺福韦酯(175 人;48%)、羧甲基铁(29 人;8%)、地诺舒单抗(16 人;4%)、唑来膦酸(14 人;4%)和氢氯噻嗪(10 人;3%)。在这五种药物中,发现了明显的比例失调。与替诺福韦-地索前列醇相关的低磷血症发生在该药上市一年多之后,有 44 例(25%)报告了肾小管病变(范可尼综合征)。与羧甲基亚铁有关的低磷血症发生在注射后的中位数 20 天内,大多数情况都很严重。其机制包括成纤维细胞生长因子 23,可通过测定该因子来确认药物来源。关于抗骨质疏松症治疗,低磷酸盐血症可以用其作用机制(低钙血症引起的副磷脂激素突然增加)来解释,但患者病史(恶性肿瘤情况)是一个主要偏差。就氢氯噻嗪而言,低磷血症通常为中度,伴有其他电解紊乱,且发生在长期治疗期间。医护人员必须提高认识,以便尽快发现低磷血症及其与这些药物有关的并发症。
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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来源期刊
Therapie
Therapie 医学-药学
CiteScore
3.50
自引率
7.70%
发文量
132
审稿时长
57 days
期刊介绍: Thérapie is a peer-reviewed journal devoted to Clinical Pharmacology, Therapeutics, Pharmacokinetics, Pharmacovigilance, Addictovigilance, Social Pharmacology, Pharmacoepidemiology, Pharmacoeconomics and Evidence-Based-Medicine. Thérapie publishes in French or in English original articles, general reviews, letters to the editor reporting original findings, correspondence relating to articles or letters published in the Journal, short articles, editorials on up-to-date topics, Pharmacovigilance or Addictovigilance reports that follow the French "guidelines" concerning good practice in pharmacovigilance publications. The journal also publishes thematic issues on topical subject. The journal is indexed in the main international data bases and notably in: Biosis Previews/Biological Abstracts, Embase/Excerpta Medica, Medline/Index Medicus, Science Citation Index.
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