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Contemporary trends in PGD incidence, outcomes, and therapies.当代 PGD 发生率、结局和治疗的趋势。
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2
Expected effect of the lung Composite Allocation Score system on US lung transplantation.肺综合分配评分系统对美国肺移植的预期效果。
Am J Transplant. 2022 Dec;22(12):2971-2980. doi: 10.1111/ajt.17160. Epub 2022 Aug 9.
3
Impact of incorporating long-term survival for calculating transplant benefit in the US lung transplant allocation system.将长期生存纳入美国肺移植分配系统中计算移植获益的影响。
J Heart Lung Transplant. 2022 Jul;41(7):866-873. doi: 10.1016/j.healun.2022.02.012. Epub 2022 Feb 26.
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Risk of primary graft dysfunction following lung transplantation in selected adults with connective tissue disease-associated interstitial lung disease.结缔组织病相关间质性肺疾病患者行肺移植后发生原发性移植物功能障碍的风险。
J Heart Lung Transplant. 2021 May;40(5):351-358. doi: 10.1016/j.healun.2021.01.1391. Epub 2021 Jan 23.
5
Extracorporeal Membrane Oxygenation for Primary Graft Dysfunction After Lung Transplantation.体外膜肺氧合在肺移植后原发性移植物功能障碍中的应用。
ASAIO J. 2021 Sep 1;67(9):1071-1078. doi: 10.1097/MAT.0000000000001350.
6
The impact of HLA-DR mismatch status on retransplant-free survival and bronchiolitis obliterans syndrome‒free survival among sensitized lung transplant recipients.致敏肺移植受者中 HLA-DR 错配状态对无再移植生存和闭塞性细支气管炎综合征无生存的影响。
J Heart Lung Transplant. 2020 Dec;39(12):1455-1462. doi: 10.1016/j.healun.2020.09.016. Epub 2020 Sep 30.
7
Local complement activation is associated with primary graft dysfunction after lung transplantation.局部补体激活与肺移植后原发性移植物功能障碍有关。
JCI Insight. 2020 Sep 3;5(17):138358. doi: 10.1172/jci.insight.138358.
8
The value of high-resolution HLA in the perioperative period of non-sensitized lung transplant recipients.高分辨率HLA在非致敏肺移植受者围手术期的价值
Ann Transl Med. 2020 Feb;8(3):37. doi: 10.21037/atm.2019.10.45.
9
OPTN/SRTR 2018 Annual Data Report: Lung.OPTN/SRTR 2018 年度数据报告:肺。
Am J Transplant. 2020 Jan;20 Suppl s1:427-508. doi: 10.1111/ajt.15677.
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肺移植候选者原发性移植功能障碍预测算法的开发与验证

Development and validation of primary graft dysfunction predictive algorithm for lung transplant candidates.

作者信息

Diamond Joshua M, Anderson Michaela R, Cantu Edward, Clausen Emily S, Shashaty Michael G S, Kalman Laurel, Oyster Michelle, Crespo Maria M, Bermudez Christian A, Benvenuto Luke, Palmer Scott M, Snyder Laurie D, Hartwig Matthew G, Wille Keith, Hage Chadi, McDyer John F, Merlo Christian A, Shah Pali D, Orens Jonathan B, Dhillon Ghundeep S, Lama Vibha N, Patel Mrunal G, Singer Jonathan P, Hachem Ramsey R, Michelson Andrew P, Hsu Jesse, Russell Localio A, Christie Jason D

机构信息

Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

J Heart Lung Transplant. 2024 Apr;43(4):633-641. doi: 10.1016/j.healun.2023.11.019. Epub 2023 Dec 6.

DOI:10.1016/j.healun.2023.11.019
PMID:38065239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10947904/
Abstract

BACKGROUND

Primary graft dysfunction (PGD) is the leading cause of early morbidity and mortality after lung transplantation. Accurate prediction of PGD risk could inform donor approaches and perioperative care planning. We sought to develop a clinically useful, generalizable PGD prediction model to aid in transplant decision-making.

METHODS

We derived a predictive model in a prospective cohort study of subjects from 2012 to 2018, followed by a single-center external validation. We used regularized (lasso) logistic regression to evaluate the predictive ability of clinically available PGD predictors and developed a user interface for clinical application. Using decision curve analysis, we quantified the net benefit of the model across a range of PGD risk thresholds and assessed model calibration and discrimination.

RESULTS

The PGD predictive model included distance from donor hospital to recipient transplant center, recipient age, predicted total lung capacity, lung allocation score (LAS), body mass index, pulmonary artery mean pressure, sex, and indication for transplant; donor age, sex, mechanism of death, and donor smoking status; and interaction terms for LAS and donor distance. The interface allows for real-time assessment of PGD risk for any donor/recipient combination. The model offers decision-making net benefit in the PGD risk range of 10% to 75% in the derivation centers and 2% to 10% in the validation cohort, a range incorporating the incidence in that cohort.

CONCLUSION

We developed a clinically useful PGD predictive algorithm across a range of PGD risk thresholds to support transplant decision-making, posttransplant care, and enrich samples for PGD treatment trials.

摘要

背景

原发性移植肺功能障碍(PGD)是肺移植术后早期发病和死亡的主要原因。准确预测PGD风险可为供体选择方法和围手术期护理计划提供依据。我们试图开发一种临床实用、可推广的PGD预测模型,以辅助移植决策。

方法

我们在一项对2012年至2018年受试者的前瞻性队列研究中推导了一个预测模型,随后进行了单中心外部验证。我们使用正则化(套索)逻辑回归来评估临床可用的PGD预测指标的预测能力,并开发了一个用于临床应用的用户界面。使用决策曲线分析,我们在一系列PGD风险阈值范围内量化了模型的净效益,并评估了模型的校准和区分度。

结果

PGD预测模型包括供体医院到受体移植中心的距离、受体年龄、预测的总肺容量、肺分配评分(LAS)、体重指数、肺动脉平均压、性别和移植指征;供体年龄、性别、死亡机制和供体吸烟状况;以及LAS和供体距离的交互项。该界面允许对任何供体/受体组合实时评估PGD风险。在推导中心,该模型在PGD风险范围为10%至75%时提供决策净效益,在验证队列中为2%至10%,该范围涵盖了该队列中的发病率。

结论

我们开发了一种临床实用的PGD预测算法,适用于一系列PGD风险阈值,以支持移植决策、移植后护理,并为PGD治疗试验富集样本。