肺动脉高压对高原肺纤维化患者移植后生存的影响:一项前瞻性队列研究。

IF 2.1 4区 医学 Q3 RESPIRATORY SYSTEM
Canadian respiratory journal Pub Date : 2025-02-24 eCollection Date: 2025-01-01 DOI:10.1155/carj/1861990
Fabio Varón-Vega, Luis J Telléz, Eduardo Tuta-Quintero, Adriana Rincón, Diana Casas, Camilo Rodriguez, David Mendoza, Luis Fernando Giraldo-Cadavid
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引用次数: 0

摘要

背景:肺纤维化接受肺移植(LT)患者的肺动脉高压(PH)可损害肺功能,减少身体活动,降低生存率。然而,关于1年和5年随访结果的数据仍然有限。方法:在这项前瞻性队列研究中,对移植前、出院时、移植后3、6和12个月的肺功能、6分钟步行测试(6MWT)和圣乔治呼吸问卷(SGRQ)进行评估。此外,还评估了有和没有PH的患者之间的最小临床重要差异(MCIDs)。生存率采用Kaplan-Meier法计算,log-rank检验分析。结果:本研究纳入39例因肺纤维化而行肝移植的患者。其中,82%(32/39)患有PH,中位年龄为52.6岁(SD: 10.2)。在PH组和非PH组中,肺功能、6MWD和SGRQ总分从移植前到移植后1年都有进行性改善。没有PH的患者从lt前到6个月和12个月的随访中,在6MWT和SGRQ总分中表现出MCID。总1年生存率为84.6%,平均生存10.51个月(95% CI: 9.29-11.73)。5年总生存率为61.5%,平均生存期44.89个月(95% CI: 37.62 ~ 52.16)。1岁和5岁时,性别(p=0.322和0.206)、平均肺动脉压(mPAP) (p=0.232和0.486)、年龄(p=0.375和0.959)或体重指数(BMI) (p=0.884和0.594)的生存率无统计学差异。结论:ph患者的1年和5年生存率较低。然而,基于性别、mPAP、年龄或BMI,生存率没有显著差异。在LT前后观察到FVC、FEV1、6MWT和SGRQ总分的统计学显著改善,持续随访1年。在PH和非PH患者中,6MWT和SGRQ均在手术前和随访6个月和12个月时显示MCID。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Pulmonary Hypertension on Posttransplant Survival of Patients With Pulmonary Fibrosis at High Altitude: A Prospective Cohort Study.

Background: Pulmonary hypertension (PH) in patients undergoing lung transplantation (LT) for pulmonary fibrosis can impair lung function, reduce physical activity, and decrease survival. However, data on outcomes at 1 and 5 years of follow-up remain limited. Methods: In this prospective cohort study, pulmonary function, the 6-min walk test (6MWT), and the St. George's Respiratory Questionnaire (SGRQ) were assessed pretransplant, at hospital discharge, and at 3, 6, and 12 months posttransplant. Additionally, minimal clinically important differences (MCIDs) between patients with and without PH were evaluated. Survival rates were calculated using the Kaplan-Meier method and analyzed using the log-rank test. Results: The study included 39 patients undergoing LT for pulmonary fibrosis. Of these, 82% (32/39) had PH, with a median age of 52.6 years (SD: 10.2). In both the PH and non-PH groups, lung function, 6MWD, and SGRQ total scores showed progressive improvement from pre-LT to 1 year posttransplant. Patients without PH demonstrated MCID in 6MWT and SGRQ total scores from pre-LT through the 6- and 12-month follow-up. The overall 1-year survival rate was 84.6%, with an average survival of 10.51 months (95% CI: 9.29-11.73). The 5-year overall survival rate was 61.5%, with an average survival of 44.89 months (95% CI: 37.62-52.16). No statistically significant differences in survival were found based on sex (p=0.322 and 0.206), mean pulmonary artery pressure (mPAP) (p=0.232 and 0.486), age (p=0.375 and 0.959), or body mass index (BMI) (p=0.884 and 0.594) at 1 and 5 years. Conclusion: Survival at 1 and 5 years was lower in patients with PH. However, no significant differences in survival were observed based on sex, mPAP, age, or BMI. Statistically significant improvements in FVC, FEV1, 6MWT, and SGRQ total scores were observed both before and after LT, continuing through 1 year of follow-up. The 6MWT and SGRQ showed MCID both prior to surgery and during follow-up at 6 and 12 months, in both PH and non-PH patients.

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来源期刊
Canadian respiratory journal
Canadian respiratory journal 医学-呼吸系统
CiteScore
4.20
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: Canadian Respiratory Journal is a peer-reviewed, Open Access journal that aims to provide a multidisciplinary forum for research in all areas of respiratory medicine. The journal publishes original research articles, review articles, and clinical studies related to asthma, allergy, COPD, non-invasive ventilation, therapeutic intervention, lung cancer, airway and lung infections, as well as any other respiratory diseases.
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