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

医学 队列 逻辑回归 肺移植 前瞻性队列研究 风险评估 体质指数 内科学 移植 外科 重症监护医学 计算机科学 计算机安全
作者
Joshua M. Diamond,Michaela R. Anderson,Edward Cantu,Emily Clausen,M.G.S. Shashaty,L. Kalman,Michelle Oyster,M. Crespo,Christian Bermudez,Luke Benvenuto,Scott M. Palmer,L.D. Snyder,Matthew G. Hartwig,Keith Wille,Chadi A. Hage,John F. McDyer,Christian A. Merlo,Pali D. Shah,Jonathan B. Orens,Ghundeep S. Dhillon,Vibha N. Lama,Mehul S. Patel,Jonathan P. Singer,Ramsey R. Hachem,Andrew P. Michelson,Jesse Y. Hsu,A. Russell Localio,Jason D. Christie
出处
期刊:Journal of Heart and Lung Transplantation [Elsevier]
卷期号:43 (4): 633-641
标识
DOI:10.1016/j.healun.2023.11.019
摘要

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.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.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.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.
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