肺动脉高压附加序贯三联疗法的长期影响:现实世界的经验。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-01-01 DOI:10.1177/17534666231199693
Himanshu Deshwal, Tatiana Weinstein, Rachel Salyer, Jesse Thompson, Frank Cefali, Rebecca Fenton, Eric Bondarsky, Roxana Sulica
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引用次数: 0

摘要

背景:建议对肺动脉高压(PAH)患者进行序贯三联治疗,这些患者在双重治疗方面没有达到治疗目标,但关于疗效和安全性的长期数据很少。目的:评估序贯三联疗法对不符合双重联合治疗目标的PAH患者的长期影响。研究设计和方法:我们对一组种族/民族多样的PAH患者进行了回顾性观察性研究,这些患者采用稳定的双重治疗方案,仍属于中高风险类别,随后开始接受连续的三重联合治疗。我们研究了功能、超声心动图和血液动力学参数的间期变化,REVEAL 2.0风险类别和ERS/ESC 2022简化的四层风险类别。进行多变量逻辑回归分析,以确定成功降低风险(达到或维持REVEAL 2.0低风险类别)的独立预测因素。Kaplan-Meier生存曲线用于评估风险降低对生存率的影响。结果:在我们的项目中看到的414名PAH患者中,55名患者接受了附加顺序三联方案,并有随访的血液动力学数据。平均年龄57岁 女性占85%。PAH最常见的病因是特发性/遗传性(41.8%)。大多数患者为世界卫生组织功能III级(76.4%),34.5%的患者为高危型(REVEAL 2.0) 周,世界卫生组织功能分类有显著改善(p 结论:联合序贯三联治疗显著提高了功能、超声心动图和血液动力学参数,改善了风险类别和生存率。
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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Long-term impact of add-on sequential triple combination therapy in pulmonary arterial hypertension: real world experience.

Background: Sequential triple combination therapy is recommended for pulmonary arterial hypertension (PAH) patients who are not at therapeutic goal on dual therapy, but long-term data on efficacy and safety is scarce.

Objective: To assess the long-term impact of sequential triple combination therapy in patients with PAH who are not at goal on dual combination therapy.

Study design and methods: We performed a retrospective observational study in a racially/ethnically diverse cohort of consecutive PAH patients on a stable dual therapy regimen who remained in intermediate- or high-risk category and were subsequently initiated on sequential triple combination therapy. We studied interval change in functional, echocardiographic, and hemodynamic parameters, REVEAL 2.0 risk category and ERS/ESC 2022 simplified four-strata risk category. Multivariate logistic regression analysis was performed to identify independent predictors of successful risk reduction (achievement or maintenance of REVEAL 2.0 low-risk category). Kaplan-Meier survival curves were created to assess the effect of risk reduction on survival.

Results: Out of 414 PAH patients seen in our program, 55 patients received add-on sequential triple combination regimen and had follow-up hemodynamic data. The mean age was 57 years, with 85% women. The most common etiology of PAH was idiopathic/heritable (41.8%). Most patients were WHO functional class III (76.4%), and 34.5% of patients were in high-risk category (REVEAL 2.0). On a median follow-up of 68 weeks, there was a significant improvement in WHO Functional Class (p < 0.001), six-minute walk distance (35 m) with 61.8% of patients achieving low-risk status by REVEAL 2.0, and a 28% of patients' improvement in pulmonary vascular resistance. Female gender was identified as a strong predictor of successful risk reduction, whereas Hispanic ethnicity estimated right atrial pressure on echocardiogram and pericardial effusion predicted lower probability of risk reduction. Patients who achieved or maintained low-risk status had significantly improved survival.

Conclusion: Add-on sequential triple combination therapy significantly increased functional, echocardiographic, and hemodynamic parameters with improvement in risk category and survival.

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