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肺动脉高压患者的临床特征与治疗:美国、欧洲和日本的一项真实世界研究

Clinical Characteristics and Treatment of Patients Diagnosed with Pulmonary Arterial Hypertension: A Real-World Study in the USA, Europe and Japan.

作者信息

Vizza C D, Klok R, Harley J, Small M, Scott M, Lautsch D, White R J

机构信息

Pulmonary Hypertension Unit, Department of Cardiovascular and Respiratory Disease, La Sapienza University of Rome, Rome, Italy.

Merck & Co., Inc., Rahway, NJ, USA.

出版信息

Adv Ther. 2025 Jan;42(1):193-215. doi: 10.1007/s12325-024-03026-1. Epub 2024 Nov 4.

Abstract

INTRODUCTION

This study aimed to describe the clinical characteristics of patients with pulmonary arterial hypertension, treatment received, and factors predicting initial or earlier combination therapy.

METHODS

The Adelphi Real World Pulmonary Arterial Hypertension (PAH) Disease Specific Programme™ is a cross-sectional survey with retrospective data collection conducted in the USA, Europe (France, Germany, Italy, Spain, and the UK), and Japan from March to August 2022. Physicians reported patient characteristics, treatment history, and reasons for treatment selection. Descriptive statistics were grouped by country and World Health Organization functional classification. A multivariable Cox regression analysis investigated factors predicting initial or earlier combination therapy use.

RESULTS

Data for 1173 patients was provided by 293 physicians. Patients' mean (standard deviation) age was 58.7 (13.8) years and 54.6% were female. Overall, 91.2% of patients were receiving, or had previously received, PAH-specific treatment. About three-quarters of the cohort were still taking the initial treatment strategy: for this group, 54% were prescribed monotherapy and 32% combination therapy; 15% of patients received supportive therapy alone. The proportion of patients receiving PAH-specific treatment was lowest in the USA (82.0%) and highest in France (94.6%). The proportion of patients receiving PAH on combination therapy was lowest in the USA (23.8%) and highest in Germany (36.5%). Treatment was prescribed for PAH in 87.6%, 89.8%, 89.3%, and 75.0% of patients who were functional class I, II, III, and IV, respectively, and combination therapy usage was more likely for those with more advanced functional class. Higher risk status, care by a pulmonologist, Japanese residence, more complete assessments, and hospitalization in the past 12 months were statistically associated with decreased time to combination therapy for PAH. Older age was statistically associated with increased time to combination therapy.

CONCLUSION

In this real-world, geographically diverse sample, monotherapy treatment was common, even among patients with advanced disease.

摘要

引言

本研究旨在描述肺动脉高压患者的临床特征、接受的治疗以及预测初始或早期联合治疗的因素。

方法

阿德尔菲真实世界肺动脉高压(PAH)疾病特定项目™是一项横断面调查,于2022年3月至8月在美国、欧洲(法国、德国、意大利、西班牙和英国)和日本进行回顾性数据收集。医生报告了患者特征、治疗史和治疗选择原因。描述性统计按国家和世界卫生组织功能分级进行分组。多变量Cox回归分析研究了预测初始或早期联合治疗使用的因素。

结果

293名医生提供了1173名患者的数据。患者的平均(标准差)年龄为58.7(13.8)岁,54.6%为女性。总体而言,91.2%的患者正在接受或曾接受过PAH特异性治疗。约四分之三的队列仍采用初始治疗策略:对于该组患者,54%接受单药治疗,32%接受联合治疗;15%的患者仅接受支持性治疗。接受PAH特异性治疗的患者比例在美国最低(82.0%),在法国最高(94.6%)。接受联合治疗的PAH患者比例在美国最低(23.8%),在德国最高(36.5%)。分别有87.6%、89.8%、89.3%和75.0%的功能分级为I、II、III和IV级的患者接受了PAH治疗,功能分级越高级别的患者越有可能使用联合治疗。更高的风险状态、由肺科医生护理、居住在日本、更全面的评估以及过去12个月内住院与PAH联合治疗时间缩短在统计学上相关。年龄较大与联合治疗时间延长在统计学上相关。

结论

在这个来自不同地理区域的真实世界样本中,即使在晚期疾病患者中,单药治疗也很常见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8271/11782444/c11a4b150564/12325_2024_3026_Fig1_HTML.jpg

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