Impact of achieving euthyroidism on pulmonary artery systolic pressures in hyperthyroidism-associated pulmonary hypertension - a systematic review.

IF 1.3
American journal of cardiovascular disease Pub Date : 2022-08-15 eCollection Date: 2022-01-01
Shireen R Chacko, Pradhum Ram, Tamaryn Fox, Naveen Sooknanan, Kevin Bryan Lo, Ritesh G Menezes, Savita Lasrado, Glenn Eiger, Anjali Vaidya
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Abstract

In this systematic review, we seek to clarify the impact of treatment of hyperthyroidism on pulmonary hypertension in patients with both these conditions. We included 39 of 709 articles retrieved, that studied patients with hyperthyroidism and pulmonary hypertension (PH). From these, those with a documented pre-treatment Pulmonary Artery Systolic Pressure (PASP) > 35 mmHg and complete follow up were analyzed, yielding 3 case series and 22 case reports with a total of 81 cases. A significant improvement in PASP was noted with achieving euthyroidism in the 3 case series. The case reports showed a significant reduction in mean PASP from 60.5 ± 13.2 mmHg to 37.5 ± 10.1 mmHg (p < 0.001) in patients with Grave's disease with achieving euthyroidism. No deaths were reported during the follow up period. Achievement of a euthyroid state in patients with hyperthyroidism is associated with statistically significant reductions in PASP.

实现甲状腺功能亢进对甲亢相关性肺动脉高压患者肺动脉收缩压的影响——一项系统综述。
在这篇系统综述中,我们试图阐明甲状腺机能亢进治疗对合并这两种疾病的肺动脉高压患者的影响。我们在检索到的709篇研究甲状腺功能亢进和肺动脉高压(PH)患者的文章中纳入了39篇。从这些病例中,分析了治疗前记录的肺动脉收缩压(PASP) > 35 mmHg并完成随访的患者,得到3个病例系列和22个病例报告,共81例。在3例患者中,PASP显著改善,甲状腺功能恢复正常。病例报告显示,graves病患者的平均PASP从60.5±13.2 mmHg显著降低到37.5±10.1 mmHg (p < 0.001)。随访期间无死亡报告。甲亢患者达到甲状腺功能正常状态与PASP显著降低相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of cardiovascular disease
American journal of cardiovascular disease CARDIAC & CARDIOVASCULAR SYSTEMS-
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