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老年特发性肺动脉高压患者:COMPERA 注册研究结果。

Elderly patients diagnosed with idiopathic pulmonary arterial hypertension: results from the COMPERA registry.

机构信息

Department of Respiratory Medicine and German Center of Lung Research, Hannover Medical School, Hannover, Germany.

出版信息

Int J Cardiol. 2013 Sep 30;168(2):871-80. doi: 10.1016/j.ijcard.2012.10.026. Epub 2012 Nov 17.

Abstract

BACKGROUND

Originally reported to occur predominantly in younger women, idiopathic pulmonary arterial hypertension (IPAH) is increasingly diagnosed in elderly patients. We aimed to describe the characteristics of such patients and their survival under clinical practice conditions.

METHODS

Prospective registry in 28 centers in 6 European countries. Demographics, clinical characteristics, hemodynamics, treatment patterns and outcomes of younger (18-65 years) and elderly (>65 years) patients with newly diagnosed IPAH (incident cases only) were compared.

RESULTS

A total of 587 patients were eligible for analysis. The median (interquartile, [IQR]) age at diagnosis was 71 (16) years. Younger patients (n=209; median age, 54 [16] years) showed a female-to-male ratio of 2.3:1 whereas the gender ratio in elderly patients (n=378; median age, 75 [8] years) was almost even (1.2:1). Combinations of PAH drugs were widely used in both populations, albeit less frequently in older patients. Elderly patients were less likely to reach current treatment targets (6 min walking distance>400 m, functional class I or II). The survival rates 1, 2, and 3 years after the diagnosis of IPAH were lower in elderly patients, even when adjusted for age- and gender-matched survival tables of the general population (p=0.006 by log-rank analysis).

CONCLUSIONS

In countries with an aging population, IPAH is now frequently diagnosed in elderly patients. Compared to younger patients, elderly patients present with a balanced gender ratio and different clinical features, respond less well to medical therapy and have a higher age-adjusted mortality. Further characterization of these patients is required.

CLINICAL TRIALS REGISTRATION

NCT01347216.

摘要

背景

特发性肺动脉高压(IPAH)最初主要发生在年轻女性中,但现在在老年患者中也越来越常见。本研究旨在描述此类患者的特点及其在临床实践条件下的生存情况。

方法

这是在欧洲 6 个国家的 28 个中心进行的前瞻性登记研究。比较了新诊断为 IPAH 的年轻(18-65 岁)和老年(>65 岁)患者(仅包括首发患者)的人口统计学、临床特征、血流动力学、治疗模式和结局。

结果

共有 587 例患者符合分析条件。诊断时的中位(四分位距,[IQR])年龄为 71(16)岁。年轻患者(n=209;中位年龄 54[16]岁)的男女比例为 2.3:1,而老年患者(n=378;中位年龄 75[8]岁)的性别比例几乎相等(1.2:1)。两种人群均广泛使用 PAH 药物联合治疗,但老年患者使用频率较低。老年患者更难以达到目前的治疗目标(6 分钟步行距离>400 m,功能分级 I 或 II)。即使根据一般人群年龄和性别匹配的生存表进行校正,老年患者在 IPAH 诊断后 1、2 和 3 年的生存率也较低(对数秩检验,p=0.006)。

结论

在人口老龄化的国家中,现在 IPAH 经常在老年患者中诊断。与年轻患者相比,老年患者的性别比例更为均衡,临床特征不同,对药物治疗的反应较差,且年龄调整后的死亡率更高。需要进一步对这些患者进行特征描述。

临床试验注册

NCT01347216。

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