Incidence of Pulmonary Hypertension in the Echocardiography Referral Population.

Jonah D Garry, Suman Kundu, Jeffrey Annis, Chuck Alcorn, Svetlana Eden, Emily Smith, Robert Greevy, Bradley A Maron, Matthew Freiberg, Evan L Brittain
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Abstract

Rationale: Incidence rates for pulmonary hypertension using diagnostic data in patients with cardiopulmonary disease are not known.

Objectives: To determine incidence rates of, risk factors for, and mortality hazard associated with pulmonary hypertension among patients referred for transthoracic echocardiography.

Methods: Retrospective cohort study using data from the Veterans Health Administration (1999-2020) and Vanderbilt University Medical Center (1994-2020). Pulmonary hypertension was defined as pulmonary artery systolic pressure >35mmHg with prevalent cases excluded. Heart failure and chronic obstructive pulmonary disease were the primary exposures of interest. The primary outcome was incident pulmonary hypertension. Secondarily, we examined mortality rate following incident diagnosis.

Measurements and main results: We identified 245,067 VA patients (94% male, 20% Black) and 117,526 Vanderbilt patients (46% male, 11% Black) without pulmonary hypertension, of whom 38,882 VA patients and 8,061 Vanderbilt patients developed pulmonary hypertension. Only 18-19% of patients with echo-based pulmonary hypertension also had a diagnostic code. Hazard of pulmonary hypertension was 4-fold higher in patients with heart failure and chronic obstructive pulmonary disease compared to patients without either. Mortality rates increased from pulmonary artery systolic pressure of 35mmHg to 45mmHg then plateaued. Independent risk factors for incident pulmonary hypertension included older age, male sex, black race, and cardiometabolic comorbidities.

Conclusions: Pulmonary hypertension incidence rates estimated by diagnostic data are higher than code-based rates. Heart failure and chronic obstructive pulmonary disease strongly associate with incident pulmonary hypertension. Pulmonary artery systolic pressure >45mmHg at diagnosis is associated with high mortality. New pulmonary hypertension on echocardiography is an important prognostic sign.

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理由:利用心肺疾病患者的诊断数据得出的肺动脉高压发病率尚不清楚:确定转诊接受经胸超声心动图检查的患者中肺动脉高压的发病率、风险因素和死亡率:方法:使用退伍军人健康管理局(1999-2020 年)和范德堡大学医学中心(1994-2020 年)的数据进行回顾性队列研究。肺动脉收缩压大于 35mmHg 即为肺动脉高压,不包括流行性病例。心力衰竭和慢性阻塞性肺病是主要的研究对象。主要结果是肺动脉高压的发病率。其次,我们还研究了事件诊断后的死亡率:我们发现 245,067 名退伍军人患者(94% 为男性,20% 为黑人)和 117,526 名范德比尔特患者(46% 为男性,11% 为黑人)没有肺动脉高压,其中 38,882 名退伍军人患者和 8,061 名范德比尔特患者出现肺动脉高压。只有 18-19% 的回波肺动脉高压患者有诊断代码。与没有心力衰竭和慢性阻塞性肺病的患者相比,有心力衰竭和慢性阻塞性肺病的患者患肺动脉高压的危险性高出4倍。死亡率从肺动脉收缩压为35毫米汞柱上升到45毫米汞柱,然后趋于平稳。肺动脉高压发病的独立风险因素包括年龄偏大、男性、黑人和心脏代谢合并症:结论:根据诊断数据估算的肺动脉高压发病率高于根据编码估算的发病率。心力衰竭和慢性阻塞性肺病与肺动脉高压发病率密切相关。诊断时肺动脉收缩压>45mmHg与高死亡率有关。超声心动图显示的新肺动脉高压是一个重要的预后信号。
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