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真实世界环境中应用塞乐西帕治疗肺动脉高压患者的四分层风险评估(EXPOSURE 研究)。

Four-Strata Risk Assessment in Patients with Pulmonary Arterial Hypertension Treated with Selexipag in Real-World Settings (EXPOSURE Study).

机构信息

Department of Pulmonology, Kreisklinik Bad Reichenhall, Riedelstraße 5, 83435, Bad Reichenhall, Germany.

Faculty of Medicine, Department Internal Medicine II, Regensburg University, Regensburg, Germany.

出版信息

Adv Ther. 2024 Sep;41(9):3645-3663. doi: 10.1007/s12325-024-02946-2. Epub 2024 Jul 31.

Abstract

INTRODUCTION

Risk assessment can aid management of pulmonary arterial hypertension (PAH) and clinical decision-making. This analysis describes characteristics, treatment patterns and outcomes of patients with PAH, categorised by risk status at time of treatment escalation with selexipag in clinical settings.

METHODS

Patients initiating selexipag in the ongoing multicentre, prospective EXPOSURE (EUPAS19085) study were grouped as low, intermediate-low, intermediate-high or high risk of 1-year mortality according to the ESC/ERS 4-strata method.

RESULTS

As of November 2022, 77% (535/698) of patients initiating selexipag had data allowing for risk calculation; 14% (N = 76) were low, 31% (N = 168) intermediate-low, 34% (N = 182) intermediate-high and 20% (N = 109) high risk of 1-year mortality. Overall, patients were predominantly female (71%), with idiopathic/heritable PAH (56%) or PAH associated with connective tissue disease (CTD-PAH; 27%), median age of 60 years and prevalent (2 years) disease. From low to high risk, proportion of CTD-PAH and age increased (from 12%-40% and 46-68 years, respectively); time from diagnosis decreased and presence of cardiovascular risk factors increased. Most patients across risk groups (74-81%) initiated selexipag as part of triple oral combination therapy. Overall median (Q1, Q3) selexipag exposure duration was 10.1 (3.5, 24.1) months. Proportions of hospitalised patients increased with increasing risk group (16-42% from low to high, respectively); more hospitalisations were PAH-related for the high risk (71%) versus other risk groups (47-54%). Kaplan-Meier survival estimates were 98%, 98%, 93% and 80% at 1-year and 98%, 92%, 81% and 67% at 2-years, from low to high risk, respectively.

CONCLUSIONS

In clinical settings, selexipag is initiated across all risk groups, predominantly as triple therapy. Only 45% of patients being at low/intermediate-low risk at selexipag initiation suggests an opportunity for more frequent patient monitoring and earlier treatment escalation, given that 4-strata risk assessment was prognostic for hospitalisations and survival in this contemporary PAH cohort. A graphical abstract is available with this article.

摘要

简介

风险评估有助于管理肺动脉高压 (PAH) 和临床决策。本分析描述了在临床环境中,根据开始使用塞立西帕时的风险状况,对接受塞立西帕治疗升级的 PAH 患者进行分类的特征、治疗模式和结局。

方法

正在进行的多中心前瞻性 EXPOSURE (EUPAS19085) 研究中开始使用塞立西帕的患者根据 ESC/ERS 4 分层方法分为 1 年死亡率低、中低、中高或高风险组。

结果

截至 2022 年 11 月,77%(535/698)开始使用塞立西帕的患者有数据可用于风险计算;14%(N=76)为低风险,31%(N=168)为中低风险,34%(N=182)为中高风险,20%(N=109)为 1 年死亡率高风险。总体而言,患者主要为女性(71%),特发性/遗传性 PAH(56%)或与结缔组织疾病相关的 PAH(CTD-PAH;27%),中位年龄为 60 岁,疾病普遍存在(2 年)。从低风险到高风险,CTD-PAH 和年龄的比例增加(分别为 12%-40%和 46-68 岁);从诊断到开始治疗的时间缩短,心血管危险因素的存在增加。大多数风险组(74%-81%)的患者开始使用塞立西帕作为三联口服联合治疗的一部分。总体中位(Q1,Q3)塞立西帕暴露持续时间为 10.1(3.5,24.1)个月。随着风险组的增加,住院患者的比例增加(从低到高分别为 16%-42%);高风险组(71%)的住院与 PAH 相关,而其他风险组(47%-54%)则与 PAH 相关。从低风险到高风险,1 年时的 Kaplan-Meier 生存估计分别为 98%、98%、93%和 80%,2 年时分别为 98%、92%、81%和 67%。

结论

在临床环境中,塞立西帕在所有风险组中均开始使用,主要是作为三联疗法。只有 45%的患者在开始使用塞立西帕时处于低/中低风险,这表明有机会更频繁地监测患者并更早地进行治疗升级,因为 4 分层风险评估对该当代 PAH 队列的住院和生存具有预后意义。本文提供了一个图形摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf8b/11349848/f6080fb96eea/12325_2024_2946_Fig1_HTML.jpg

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