Achinger Steven G, Ayus Juan Carlos, Kumar Ambuj, Tsalatsanis Athanasios
Department of Nephrology and Hypertension, University of South Florida, Tampa, FL.
Department of Nephrology, Watson Clinic, LLP, Lakeland, FL.
Kidney Med. 2024 Dec 9;7(2):100941. doi: 10.1016/j.xkme.2024.100941. eCollection 2025 Feb.
RATIONALE & OBJECTIVE: There are likely over 42 million patients with hypertension taking thiazides in the United States and many more worldwide. Hyponatremia is a common complication of thiazide therapy. It is not currently known if thiazide-associated hyponatremia is also associated with increased mortality. The objective of this study was to determine if outpatients who start thiazide diuretic treatment and develop early hyponatremia are at increased risk of mortality when compared with those who do not develop hyponatremia after starting a thiazide.
A retrospective cohort study.
SETTING & PARTICIPANTS: This study used data from the TriNetX federated health research network comprising deidentified electronic medical records of ∼93 million patients from 76 health care organizations located primarily in the United States. The study population was adult patients 40-90 years old, with essential hypertension and who started on a thiazide diuretic between January 1, 2010, and December 31, 2021. The patients were then subdivided into a hyponatremia cohort and a control cohort. 22,057 patients met the inclusion criteria for the hyponatremia cohort, and 234,466 patients met the inclusion criteria for the control cohort. After propensity score matching, 22,052 remained in both cohorts. The primary outcome is one-year mortality.
The hyponatremia cohort developed early hyponatremia defined as a serum sodium ≤ 135 mmol/L within 6 months after initiation of thiazide versus a control that had a serum sodium 136-144 mmol/L after initiation of thiazide.
Primary outcome is mortality. Secondary outcomes include development of sepsis, pneumonia, urinary tract infection, cellulitis, myocardial infarction, stroke, congestive heart failure, ataxia, fall, and hip fracture.
The design is a retrospective cohort study, propensity score matched.
Patients in the hyponatremia cohort had a higher hazard of mortality than patients in control, HR 1.96 (95% CI, 1.72-2.28; < 0.001). In addition, patients in the hyponatremia cohort had higher hazard of developing sepsis, pneumonia, urinary tract infection, cellulitis, myocardial infarction, stroke, congestive heart failure, ataxia, and hip fracture.
The study had a retrospective design.
Patients who develop early hyponatremia (serum sodium ≤ 135 mmol/L) following initiation of a thiazide diuretic have a higher risk of mortality when compared with those who do not develop hyponatremia after initiation of a thiazide diuretic.
在美国,可能有超过4200万高血压患者正在服用噻嗪类药物,全球范围内更多。低钠血症是噻嗪类药物治疗的常见并发症。目前尚不清楚噻嗪类药物相关的低钠血症是否也与死亡率增加有关。本研究的目的是确定开始噻嗪类利尿剂治疗并发生早期低钠血症的门诊患者与开始使用噻嗪类药物后未发生低钠血症的患者相比,死亡率是否增加。
一项回顾性队列研究。
本研究使用了TriNetX联合健康研究网络的数据,该网络包含来自主要位于美国的76个医疗机构的约9300万患者的去识别化电子病历。研究人群为40-90岁的成年原发性高血压患者,他们在2010年1月1日至2021年12月31日期间开始使用噻嗪类利尿剂。然后将患者分为低钠血症队列和对照队列。22057名患者符合低钠血症队列的纳入标准,234466名患者符合对照队列的纳入标准。经过倾向评分匹配后,两个队列中各有22052名患者。主要结局是一年死亡率。
低钠血症队列发生早期低钠血症,定义为开始使用噻嗪类药物后6个月内血清钠≤135 mmol/L,而对照组在开始使用噻嗪类药物后血清钠为136-144 mmol/L。
主要结局是死亡率。次要结局包括败血症、肺炎、尿路感染、蜂窝织炎、心肌梗死、中风、充血性心力衰竭、共济失调、跌倒和髋部骨折的发生情况。
该设计为回顾性队列研究,采用倾向评分匹配。
低钠血症队列患者的死亡风险高于对照组,风险比为1.96(95%置信区间,1.72-2.28;P<0.001)。此外,低钠血症队列患者发生败血症、肺炎、尿路感染、蜂窝织炎、心肌梗死、中风、充血性心力衰竭、共济失调和髋部骨折的风险更高。
本研究采用回顾性设计。
与开始使用噻嗪类利尿剂后未发生低钠血症的患者相比,开始使用噻嗪类利尿剂后发生早期低钠血症(血清钠≤135 mmol/L)的患者死亡风险更高。