Prevalence, aetiology, and outcomes of native pulmonary regurgitation in the general adult population.

IF 6.7 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Jwan A Naser, Hossam Ibrahim, Kartik Andi, Christopher G Scott, Patricia A Pellikka, Austin M Kennedy, Heidi M Connolly, Vuyisile T Nkomo, Maurice Enriquez-Sarano, Sorin V Pislaru, Carole A Warnes, Charles C Jain, Barry A Borlaug, Alexander C Egbe
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Abstract

Aims: Pulmonary regurgitation (PR) after reparative intervention for congenital heart disease has been studied extensively. However, the burden, distribution of causes, and outcome of PR in adults is unknown. The study aimed to evaluate the prevalence, types, and outcomes of moderate/severe PR in adults in the community setting.

Methods and results: A total of 398 adult residents of Olmsted County who had clinically indicated echocardiography 2004-2023 at Mayo Clinic, Rochester, and had moderate or severe PR were identified retrospectively. The median age was 77 years, 48% were females, and 61 (51%) had severe PR. The age- and sex-adjusted US prevalence was 0.11% (vs. 0.67% for ≥moderate tricuspid regurgitation). Moderate/severe PR was due to pulmonary hypertension in 77%, congenital/iatrogenic in 11%, primary pulmonary valve disease in 2% (88% due to carcinoid), and idiopathic isolated in 10%. In contrast, severe PR was due to congenital/iatrogenic disease in 52%, pulmonary hypertension in 39%, primary PR in 5%, and isolated idiopathic in 3%. The all-cause mortality rate per 100 person-year was 73 in primary (mostly carcinoid) PR, 16 in pulmonary hypertension-related PR (not different vs. propensity-matched patients without PR), and 6 in isolated idiopathic PR (not different vs. matched patients without PR).

Conclusion: Moderate or severe PR had a lower prevalence vs. TR. The most frequent cause was pulmonary hypertension for ≥moderate PR and congenital/iatrogenic for severe PR. Mortality in patients with acquired ≥moderate PR appeared to be related to the underlying cause, with no excess mortality compared with matched patients without PR. Whether specifically severe PR confers excess mortality requires future investigation.

普通成人先天性肺反流的患病率、病因学和结局。
目的:对先天性心脏病恢复性干预后肺返流(PR)进行了广泛的研究。然而,成人PR的负担、病因分布和结果尚不清楚。该研究旨在评估社区成人中/重度PR的患病率、类型和结局。方法和结果:回顾性分析2004-2023年在罗切斯特梅奥诊所接受临床超声心动图检查并患有中度或重度PR的奥姆斯特德县398名成年居民。中位年龄为77岁,48%为女性,61例(51%)患有严重PR。年龄和性别调整后的美国患病率为0.11%(对≥中度三尖瓣反流的患病率为0.67%)。中度/重度肺动脉高压占77%,先天性/医源性占11%,原发性肺瓣膜疾病占2%(88%由于类癌),特发性孤立性占10%。相比之下,52%的严重PR是由于先天性/医源性疾病,39%是肺动脉高压,5%是原发性PR, 3%是孤立的特发性PR。原发性(主要是类癌)PR的全因死亡率为每100人年73人,肺动脉高压相关PR的全因死亡率为16人(与没有PR的倾向匹配的患者没有差异),孤立的特发性PR的全因死亡率为6人(与没有PR的匹配患者没有差异)。结论:中度或重度PR的患病率低于TR。≥中度PR最常见的原因是肺动脉高压,严重PR最常见的原因是先天性/医源性。获得性≥中度PR患者的死亡率似乎与潜在原因有关,与没有PR的匹配患者相比,没有额外的死亡率。是否特别严重的PR会导致额外的死亡率需要进一步的研究。
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来源期刊
European Heart Journal - Cardiovascular Imaging
European Heart Journal - Cardiovascular Imaging CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
11.60
自引率
9.70%
发文量
708
审稿时长
4-8 weeks
期刊介绍: European Heart Journal – Cardiovascular Imaging is a monthly international peer reviewed journal dealing with Cardiovascular Imaging. It is an official publication of the European Association of Cardiovascular Imaging, a branch of the European Society of Cardiology. The journal aims to publish the highest quality material, both scientific and clinical from all areas of cardiovascular imaging including echocardiography, magnetic resonance, computed tomography, nuclear and invasive imaging. A range of article types will be considered, including original research, reviews, editorials, image focus, letters and recommendation papers from relevant groups of the European Society of Cardiology. In addition it provides a forum for the exchange of information on all aspects of cardiovascular imaging.
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