Yong Tuck Yean, Huang Jessica Emily, Lau Su Yin, Li Jordan Yuanzhi
Department of General Medicine, Flinders Medical Centre, Flinders Drive, Bedford Park, SA 5042, Australia.
Curr Drug Saf. 2011 Jul;6(3):134-7. doi: 10.2174/157488611797579249.
The aim of this study is to evaluate patients' demographics, patterns of presentation and outcomes of admissions with severe hyponatremia and other electrolyte disturbances that are related to indapamide.
Patients with severe indapamide-related hyponatremia (defined as serum sodium <125 mmol/L) admitted to the Department of General Medicine of a tertiary teaching hospital between 1 July 2006 and 30 June 2009 were evaluated in this study. Patients' characteristics, clinical features of their presentation and other electrolyte disturbances were analyzed retrospectively.
Eleven patients were admitted with severe hyponatremia and other electrolyte disturbances associated with indapamide use. All patients were female and elderly (age: 81.7 ± 5.8 years). Their mean weight was 59.0 ± 8.8 kg. Indapamide sustained release (SR) 1.5 mg daily was taken by eight of eleven patients and the others took indapamide 2.5 mg in combination with perindopril. The mean serum sodium concentration on presentation was 110.9 ± 5.9 mmol/L and was associated with findings of hypokalemia in ten patients and hypomagnesemia in eight patients. All patients presented predominantly with neurological manifestations, delirium (six patients) being the most common. Electrocardiographic changes were common (nine patients) including prolonged QT interval in six patients. All the patients' electrolyte abnormalities were corrected without any life-threatening complications.
This study highlights that the use of indapamide is associated with severe hyponatremia and other electrolyte disturbances. Therefore clinicians should be aware of severe electrolyte disturbances arising from indapamide. New onset of neurological symptoms such as delirium and unsteady gait in the elderly taking indapamide should prompt evaluation of their electrolyte profile.
本研究旨在评估严重低钠血症及其他与吲达帕胺相关的电解质紊乱患者的人口统计学特征、就诊模式及入院结局。
本研究对2006年7月1日至2009年6月30日期间入住某三级教学医院普通内科的严重吲达帕胺相关性低钠血症(定义为血清钠<125 mmol/L)患者进行评估。对患者的特征、就诊时的临床特征及其他电解质紊乱情况进行回顾性分析。
11例患者因严重低钠血症及其他与吲达帕胺使用相关的电解质紊乱入院。所有患者均为老年女性(年龄:81.7±5.8岁)。平均体重为59.0±8.8 kg。11例患者中有8例每日服用吲达帕胺缓释片(SR)1.5 mg,其余患者服用吲达帕胺2.5 mg联合培哚普利。就诊时平均血清钠浓度为110.9±5.9 mmol/L,10例患者伴有低钾血症,8例患者伴有低镁血症。所有患者主要表现为神经学症状,谵妄(6例患者)最为常见。心电图改变常见(9例患者),其中6例患者QT间期延长。所有患者的电解质异常均得到纠正,未出现任何危及生命的并发症。
本研究强调吲达帕胺的使用与严重低钠血症及其他电解质紊乱有关。因此,临床医生应意识到吲达帕胺可引发严重电解质紊乱。服用吲达帕胺的老年人若出现谵妄和步态不稳等新发神经学症状,应促使医生对其电解质状况进行评估。