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托伐普坦在 90 岁以上急性失代偿性心力衰竭患者中的临床疗效和不良事件。

Clinical effectiveness and adverse events associated with tolvaptan in patients above 90 years of age with acute decompensated heart failure.

机构信息

Division of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.

出版信息

Heart Vessels. 2021 Jun;36(6):836-843. doi: 10.1007/s00380-020-01753-3. Epub 2021 Feb 2.

Abstract

With the aging society, the number of very-elderly (VE) patients with acute decompensated heart failure (ADHF) is increasing. Although tolvaptan is recommended for patients with ADHF in whom conventional diuretic therapy is ineffective, few reports exist on VE patients over 90 years of age. Therefore, we aimed to evaluate the clinical effectiveness and adverse events associated with tolvaptan in VE patients with ADHF. From January 2011 to December 2018, we retrospectively studied 180 patients with ADHF who were first administered tolvaptan during hospitalization. Patients were divided into two groups, namely, VE patients who were ≥ 90 years of age (n = 32) and not-VE patients (NVE) who were < 90 years of age (n = 148). The primary effective endpoints were the total urine volume and change in body weight. The safety endpoints evaluated were the incidence of hypernatremia (≥ 150 mEq/L) and worsening renal function (WRF) at any time during hospitalization. The median [interquartile range] patient age was 93 [91-94] years in the VE group and 80 [69-85] years in the NVE group. The mean dose of tolvaptan for the first week of administration was similar between groups (7.9 ± 5.0 mg, VE group; 7.3 ± 3.7 mg, NVE group; p = 0.52). There were no significant differences between the two groups in the total urine volume at 24 h (1901 ± 666 mL, VE group; 2101 ± 1167 mL, NVE group; p = 0.33) and that at 48 h (3707 ± 1274 mL, VE group; 4195 ± 1990 mL, NVE group; p = 0.19) and in the mean change in body weight (- 2.5 ± 2.0 kg, VE group; -2.7 ± 2.4 kg, NVE group; p = 0.70). The median duration of hospitalization was 24 [20-9] and 31 [20-42] days in the VE and NVE groups, respectively (p = 0.67). The incidence of hypernatremia (6.3% (2/32), VE group; 3.4% (5/148), NVE group; p = 0.61) and WRF (25.0% (8/32) VE group; 19.6% (29/148), NVE group; p = 0.31) was similar between the groups. In conclusion, tolvaptan has similar clinical effectiveness in increasing urine volume and decreasing body weight, without increased adverse events, in VE patients with ADHF who were ≥ 90 years of age compared to NVE patients with ADHF.

摘要

随着社会老龄化,患有急性失代偿性心力衰竭(ADHF)的超高龄(VE)患者数量不断增加。尽管托伐普坦被推荐用于常规利尿剂治疗无效的 ADHF 患者,但对于 90 岁以上的 VE 患者,相关报告却很少。因此,我们旨在评估托伐普坦在 VE 伴有 ADHF 患者中的临床疗效和不良事件。从 2011 年 1 月至 2018 年 12 月,我们回顾性研究了 180 例在住院期间首次接受托伐普坦治疗的 ADHF 患者。患者分为 VE 组(年龄≥90 岁,n=32)和非 VE 组(年龄<90 岁,n=148)。主要的有效终点是总尿量和体重变化。评估的安全性终点是住院期间任何时间高钠血症(≥150 mEq/L)和肾功能恶化(WRF)的发生率。VE 组患者的中位[四分位间距]年龄为 93[91-94]岁,非 VE 组为 80[69-85]岁。第 1 周托伐普坦的平均剂量在两组间相似(VE 组为 7.9±5.0mg;非 VE 组为 7.3±3.7mg;p=0.52)。两组在 24 小时时的总尿量(VE 组 1901±666mL;非 VE 组 2101±1167mL;p=0.33)和 48 小时时的总尿量(VE 组 3707±1274mL;非 VE 组 4195±1990mL;p=0.19)以及平均体重变化(VE 组为-2.5±2.0kg;非 VE 组为-2.7±2.4kg;p=0.70)方面无显著差异。VE 组和非 VE 组的中位住院时间分别为 24[20-9]和 31[20-42]天(p=0.67)。高钠血症的发生率(VE 组为 6.3%(2/32);非 VE 组为 3.4%(5/148);p=0.61)和 WRF 的发生率(VE 组为 25.0%(8/32);非 VE 组为 19.6%(29/148);p=0.31)在两组间相似。总之,与非 VE 伴有 ADHF 患者相比,托伐普坦在增加尿量和降低体重方面具有相似的临床疗效,且不良事件发生率无增加,在年龄≥90 岁的 VE 伴有 ADHF 患者中是安全有效的。

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