Survival and early outcomes following lung transplantation for interstitial lung disease associated with non-scleroderma connective tissue disease: a national cohort study.

IF 3.4 4区 医学 Q2 RHEUMATOLOGY Clinical and experimental rheumatology Pub Date : 2025-01-14 DOI:10.55563/clinexprheumatol/tjnyz5
Caikang Luo, Jiang Shi, Jiaqin Zhang, Yanwei Lin, Yining Pan, Jie Zhang, Chao Yang, Guilin Peng, Jianxing He, Xin Xu
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Abstract

Objectives: The progressive decline in interstitial lung disease associated with non-scleroderma connective tissue disease (ILD-NSCTD) is linked to poor prognosis and frequently results in respiratory failure. Lung transplantation (LTx) offers a viable treatment option, yet its outcomes in ILD-NSCTD remain contentious, particularly across different subtypes.

Methods: This retrospective cohort study included patients with idiopathic pulmonary fibrosis (IPF) (n=11,610) and ILD-NSCTD (n=610) listed in the United Network for Organ Sharing (UNOS) database who underwent lung transplantation between May 5, 2005, and December 31, 2022. We used the Kaplan-Meier method to evaluate cumulative survival rates and logistic regression to assess the risk of post-operative complications.

Results: Compared to IPF patients, those with ILD-NSCTD are generally younger, with a lower proportion of male and white patients. After propensity matching, overall survival rates remained similar between the groups (log-rank, p=0.953). However, ILD-NSCTD was associated with a significantly higher risk of post-operative stroke (adjusted OR 1.75, 95% CI 1.12-2.74, p=0.015) and longer post-operative hospital stays (p<0.001). Subgroup analyses yielded consistent results. Finally, infection was identified as the leading cause of death.

Conclusions: Compared to IPF, patients with ILD-NSCTD have a significantly higher risk of post-operative stroke and extended hospital stays, potentially due to complications inherent to ILD-NSCTD. However, the underlying causes of these outcomes remain unclear. Despite these differences, short-term and long-term survival rates are comparable between the two groups, with consistent findings across various ILD-NSCTD subgroups. Therefore, ILD-NSCTD should not be regarded as a relative contraindication for lung transplantation. Nonetheless, the influence of extra-pulmonary complications in ILD-NSCTD patients requires further investigation.

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肺移植治疗与非硬皮病结缔组织病相关的间质性肺疾病后的生存和早期结果:一项国家队列研究
目的:与非硬皮病结缔组织病(ILD-NSCTD)相关的间质性肺疾病的进行性下降与预后不良有关,并经常导致呼吸衰竭。肺移植(LTx)提供了一种可行的治疗选择,但其治疗ILD-NSCTD的结果仍然存在争议,特别是在不同亚型之间。方法:本回顾性队列研究纳入了联合器官共享网络(UNOS)数据库中2005年5月5日至2022年12月31日期间接受肺移植的特发性肺纤维化(IPF) (n=11,610)和ILD-NSCTD (n=610)患者。我们采用Kaplan-Meier法评估累积生存率,logistic回归评估术后并发症的风险。结果:与IPF患者相比,ILD-NSCTD患者普遍年轻化,男性和白人患者比例较低。倾向匹配后,两组间的总生存率保持相似(log-rank, p=0.953)。然而,ILD-NSCTD与术后卒中风险显著升高(调整OR为1.75,95% CI为1.12-2.74,p=0.015)和术后住院时间延长相关。结论:与IPF相比,ILD-NSCTD患者术后卒中风险显著升高,住院时间延长,这可能是由于ILD-NSCTD固有的并发症。然而,这些结果的根本原因尚不清楚。尽管存在这些差异,但两组之间的短期和长期生存率是相当的,在各种ILD-NSCTD亚组中也有一致的发现。因此,不应将ILD-NSCTD视为肺移植的相对禁忌症。尽管如此,肺外并发症对ILD-NSCTD患者的影响仍需进一步研究。
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来源期刊
CiteScore
6.10
自引率
18.90%
发文量
377
审稿时长
3-6 weeks
期刊介绍: Clinical and Experimental Rheumatology is a bi-monthly international peer-reviewed journal which has been covering all clinical, experimental and translational aspects of musculoskeletal, arthritic and connective tissue diseases since 1983.
期刊最新文献
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