{"title":"基线肺同种异体移植功能障碍:现实世界数据的新兴早期移植后临床表型。","authors":"René Hage, Carolin Steinack, Macé M Schuurmans","doi":"10.6002/ect.2025.0097","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Baseline lung allograft dysfunction reflects suboptimal graft recovery and development after lung transplant and is characterized by a persistent low lung function in the first year. Despite its potential prognostic value, baseline lung allograft dysfunction remains insufficiently characterized or defined and thus underreported.</p><p><strong>Materials and methods: </strong>In this retrospective cohort study, we analyzed 80 adult double-lung transplant recipients for the period January 2021 to December 2023. Baseline lung allograft dysfunction was defined as failure to reach a peak forced expiratory volume in 1 second and/or forced vital capacity ≥80% predicted on ≥2 pulmonary function tests at least 3 months apart within the first year. Patients with and without baseline lung allograft dysfunction were compared using demog-raphic, serial functional, and postopera-tive variables.</p><p><strong>Results: </strong>Baseline lung allograft dysfunction occurred in 58.8% of patients. These individuals were younger (P = .044) and had significantly worse lung function at 12 months in absolute values for forced expiratory volume in 1 second (2.12 ± 0.65 vs 3.11 ± 0.82 L; P < .001) and predicted values (67.3 ± 16.2% vs 103.8 ± 23.8%; P < .001). Durations of intensive care unit stays and total hospital stays were longer in the group with baseline lung allograft dysfunction (P = .006), reflecting more complex early postoperative recovery. No significant differences were found in body mass index, sex, underlying diagnosis, acute rejection, or donor-specific antigen presence.</p><p><strong>Conclusions: </strong>Baseline lung allograft dysfunction is a highly prevalent yet underrecognized early allograft dysfunction phenotype that is associated with impaired clinical recovery and prolonged intensive care unit stay and hospital stay. Systemic identification of baseline lung allograft dysfunction phenotype using serial pulmonary function testing enables early risk stratification and may inform future intervention strategies aimed to optimize graft recovery and long-term survival.</p>","PeriodicalId":50467,"journal":{"name":"Experimental and Clinical Transplantation","volume":"23 6","pages":"409-414"},"PeriodicalIF":0.7000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Baseline Lung Allograft Dysfunction: Real-World Data for an Emerging Early Posttransplant Clinical Phenotype.\",\"authors\":\"René Hage, Carolin Steinack, Macé M Schuurmans\",\"doi\":\"10.6002/ect.2025.0097\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Baseline lung allograft dysfunction reflects suboptimal graft recovery and development after lung transplant and is characterized by a persistent low lung function in the first year. Despite its potential prognostic value, baseline lung allograft dysfunction remains insufficiently characterized or defined and thus underreported.</p><p><strong>Materials and methods: </strong>In this retrospective cohort study, we analyzed 80 adult double-lung transplant recipients for the period January 2021 to December 2023. Baseline lung allograft dysfunction was defined as failure to reach a peak forced expiratory volume in 1 second and/or forced vital capacity ≥80% predicted on ≥2 pulmonary function tests at least 3 months apart within the first year. Patients with and without baseline lung allograft dysfunction were compared using demog-raphic, serial functional, and postopera-tive variables.</p><p><strong>Results: </strong>Baseline lung allograft dysfunction occurred in 58.8% of patients. These individuals were younger (P = .044) and had significantly worse lung function at 12 months in absolute values for forced expiratory volume in 1 second (2.12 ± 0.65 vs 3.11 ± 0.82 L; P < .001) and predicted values (67.3 ± 16.2% vs 103.8 ± 23.8%; P < .001). Durations of intensive care unit stays and total hospital stays were longer in the group with baseline lung allograft dysfunction (P = .006), reflecting more complex early postoperative recovery. No significant differences were found in body mass index, sex, underlying diagnosis, acute rejection, or donor-specific antigen presence.</p><p><strong>Conclusions: </strong>Baseline lung allograft dysfunction is a highly prevalent yet underrecognized early allograft dysfunction phenotype that is associated with impaired clinical recovery and prolonged intensive care unit stay and hospital stay. Systemic identification of baseline lung allograft dysfunction phenotype using serial pulmonary function testing enables early risk stratification and may inform future intervention strategies aimed to optimize graft recovery and long-term survival.</p>\",\"PeriodicalId\":50467,\"journal\":{\"name\":\"Experimental and Clinical Transplantation\",\"volume\":\"23 6\",\"pages\":\"409-414\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Experimental and Clinical Transplantation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.6002/ect.2025.0097\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"TRANSPLANTATION\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental and Clinical Transplantation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.6002/ect.2025.0097","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"TRANSPLANTATION","Score":null,"Total":0}
引用次数: 0
摘要
目的:肺同种异体移植物的基线功能障碍反映了肺移植后移植物恢复和发育不理想,其特征是在第一年持续低肺功能。尽管具有潜在的预后价值,但基线的同种异体肺移植功能障碍仍然没有充分的特征或定义,因此报告不足。材料和方法:在这项回顾性队列研究中,我们分析了2021年1月至2023年12月期间80名成人双肺移植受者。基线同种异体肺移植功能障碍被定义为在1秒内未达到峰值用力呼气量和/或用力肺活量≥80%,≥2次肺功能试验预测在第一年内至少间隔3个月。使用人口统计学、系列功能和术后变量对有和无基线肺移植功能障碍的患者进行比较。结果:58.8%的患者出现同种异体肺移植基线功能障碍。这些个体更年轻(P = 0.044),并且在12个月时肺功能明显差于1秒用力呼气量的绝对值(2.12±0.65 vs 3.11±0.82 L;P < 0.001)和预测值(67.3±16.2% vs 103.8±23.8%;P < 0.001)。同种异体肺移植基线功能障碍组的重症监护病房住院时间和总住院时间更长(P = 0.006),反映出更复杂的术后早期恢复。在体重指数、性别、基础诊断、急性排斥反应或供体特异性抗原存在方面没有发现显著差异。结论:基线肺同种异体移植物功能障碍是一种高度普遍但未被充分认识的早期同种异体移植物功能障碍表型,与临床恢复受损、重症监护病房和住院时间延长有关。通过一系列肺功能测试系统识别基线同种异体肺移植功能障碍表型可以实现早期风险分层,并可能为未来旨在优化移植物恢复和长期生存的干预策略提供信息。
Baseline Lung Allograft Dysfunction: Real-World Data for an Emerging Early Posttransplant Clinical Phenotype.
Objectives: Baseline lung allograft dysfunction reflects suboptimal graft recovery and development after lung transplant and is characterized by a persistent low lung function in the first year. Despite its potential prognostic value, baseline lung allograft dysfunction remains insufficiently characterized or defined and thus underreported.
Materials and methods: In this retrospective cohort study, we analyzed 80 adult double-lung transplant recipients for the period January 2021 to December 2023. Baseline lung allograft dysfunction was defined as failure to reach a peak forced expiratory volume in 1 second and/or forced vital capacity ≥80% predicted on ≥2 pulmonary function tests at least 3 months apart within the first year. Patients with and without baseline lung allograft dysfunction were compared using demog-raphic, serial functional, and postopera-tive variables.
Results: Baseline lung allograft dysfunction occurred in 58.8% of patients. These individuals were younger (P = .044) and had significantly worse lung function at 12 months in absolute values for forced expiratory volume in 1 second (2.12 ± 0.65 vs 3.11 ± 0.82 L; P < .001) and predicted values (67.3 ± 16.2% vs 103.8 ± 23.8%; P < .001). Durations of intensive care unit stays and total hospital stays were longer in the group with baseline lung allograft dysfunction (P = .006), reflecting more complex early postoperative recovery. No significant differences were found in body mass index, sex, underlying diagnosis, acute rejection, or donor-specific antigen presence.
Conclusions: Baseline lung allograft dysfunction is a highly prevalent yet underrecognized early allograft dysfunction phenotype that is associated with impaired clinical recovery and prolonged intensive care unit stay and hospital stay. Systemic identification of baseline lung allograft dysfunction phenotype using serial pulmonary function testing enables early risk stratification and may inform future intervention strategies aimed to optimize graft recovery and long-term survival.
期刊介绍:
The scope of the journal includes the following:
Surgical techniques, innovations, and novelties;
Immunobiology and immunosuppression;
Clinical results;
Complications;
Infection;
Malignancies;
Organ donation;
Organ and tissue procurement and preservation;
Sociological and ethical issues;
Xenotransplantation.