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血液透析患者肺动脉高压的患病率、决定因素和预后。

Prevalence, determinants and prognosis of pulmonary hypertension among hemodialysis patients.

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Nephrol Dial Transplant. 2012 Oct;27(10):3908-14. doi: 10.1093/ndt/gfr661. Epub 2012 Jan 30.

Abstract

BACKGROUND

The prevalence, determinants and prognosis of pulmonary hypertension among long-term hemodialysis patients in the USA are poorly understood.

METHODS

A cross-sectional survey of prevalence and determinants of pulmonary hypertension was performed, followed by longitudinal follow-up for all-cause mortality. Pulmonary hypertension was defined as an estimated systolic pulmonary artery pressure of >35 mmHg using echocardiograms performed within an hour after the end of dialysis.

RESULTS

Prevalent in 110/288 patients (38%), the independent determinants of pulmonary hypertension were the following: left atrial diameter (odds ratio 10.1 per cm/m(2), P < 0.0001), urea reduction ratio (odds ratio 0.94 per %, P < 0.01) and vitamin D receptor activator use (odds ratio 0.41 for users, P < 0.01). Over a median follow-up of 2.15 years, 97 (34%) patients died yielding a crude mortality rate (CMR) of 114.2 per 1000 patient-years. Of these, 58 deaths occurred among 110 patients with pulmonary hypertension (53%, CMR 168.9/1000 patient-years) and 39 among 178 without pulmonary hypertension (22%, CMR 52.5/1000 patient-years) [unadjusted hazard ratio (HR) for death 2.12 (95% confidence interval 1.41-3.19), P < 0.001]. After multivariate adjustment, pulmonary hypertension remained an independent predictor for all-cause mortality [HR 2.17 (95% confidence interval 1.31-3.61), P < 0.01].

CONCLUSIONS

Among hemodialysis patients, pulmonary hypertension is common and is strongly associated with an enlarged left atrium and poor long-term survival. Reducing left atrial size such as through volume control may be an attractive target to improve pulmonary hypertension. Improving pulmonary hypertension in this group of patients may improve the dismal outcomes.

摘要

背景

美国长期血液透析患者中肺动脉高压的患病率、决定因素和预后尚不清楚。

方法

对肺动脉高压的患病率和决定因素进行了横断面调查,然后对所有原因的死亡率进行了纵向随访。肺动脉高压定义为在透析结束后 1 小时内进行的超声心动图检查中估计的收缩期肺动脉压>35mmHg。

结果

在 288 名患者中有 110 名(38%)患有肺动脉高压,其独立决定因素为:左心房直径(每平方厘米/米 10.1 的比值比,P<0.0001)、尿素降低率(每降低 1%的比值比,P<0.01)和维生素 D 受体激动剂的使用(使用者的比值比为 0.41,P<0.01)。在中位随访 2.15 年期间,97 名(34%)患者死亡,粗死亡率(CMR)为 114.2/1000 患者年。其中,110 名肺动脉高压患者中有 58 例死亡(53%,CMR 168.9/1000 患者年),178 名无肺动脉高压患者中有 39 例死亡(22%,CMR 52.5/1000 患者年)[死亡的未调整危险比(HR)为 2.12(95%置信区间 1.41-3.19),P<0.001]。经过多变量调整后,肺动脉高压仍然是全因死亡的独立预测因素[HR 2.17(95%置信区间 1.31-3.61),P<0.01]。

结论

在血液透析患者中,肺动脉高压很常见,与左心房增大和长期生存率低密切相关。通过容量控制等方法降低左心房大小可能是改善肺动脉高压的一个有吸引力的目标。改善这组患者的肺动脉高压可能会改善其预后。

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