David J Taber1, Arun P Palanisamy, Titte R Srinivas, Mulugeta Gebregziabher, John Odeghe, Kenneth D Chavin, Leonard E Egede, Prabhakar K Baliga. 1. 1 Medical University of South Carolina, Division of Transplant Surgery, Charleston, SC. 2 Ralph H Johnson VAMC, Department of Pharmacy, Charleston, SC. 3 Medical University of South Carolina, Division of Transplant Nephrology, Charleston, SC. 4 Medical University of South Carolina, Department of Public Health Sciences, Charleston, SC. 5 Medical University of South Carolina, College of Medicine. 6 Medical University of South Carolina, Center for Health Disparities Research, Charleston, SC. 7 Ralph H Johnson VAMC, Center of Innovation (COIN), Charleston, SC.
Abstract
BACKGROUND: Thirty-day readmissions (30DRA) are a highly scrutinized measure of healthcare quality and relatively frequent among kidney transplants (KTX). Development of predictive risk models is critical to reducing 30DRA and improving outcomes. Current approaches rely on fixed variables derived from administrative data. These models may not capture clinical evolution that is critical to predicting outcomes. METHODS: We directed a retrospective analysis toward: (1) developing parsimonious risk models for 30DRA and (2) comparing efficiency of models based on the use of immutable versus dynamic data. Baseline and in-hospital clinical and outcomes data were collected from adult KTX recipients between 2005 and 2012. Risk models were developed using backward logistic regression and compared for predictive efficacy using receiver operating characteristic curves. RESULTS: Of 1147 KTX patients, 123 had 30DRA. Risk factors for 30DRA included recipient comorbidities, transplant factors, and index hospitalization patient level clinical data. The initial fixed variable model included 9 risk factors and was modestly predictive (area under the curve, 0.64; 95% confidence interval [95% CI], 0.58-0.69). The model was parsimoniously reduced to 6 risks, which remained modestly predictive (area under the curve, 0.63; 95% CI, 0.58-0.69). The initial predictive model using 13 fixed and dynamic variables was significantly predictive (AUC, 0.73; 95% CI, 0.67-0.80), with parsimonious reduction to 9 variables maintaining predictive efficacy (AUC, 0.73; 95% CI, 0.67-0.79). The final model using dynamically evolving clinical data outperformed the model using static variables (P=0.009). Internal validation demonstrated that the final model was stable with minimal bias. CONCLUSIONS: We demonstrate that modeling dynamic clinical data outperformed models using immutable data in predicting 30DRA.
BACKGROUND: Thirty-day readmissions (30DRA) are a highly scrutinized measure of healthcare quality and relatively frequent among kidney transplants (KTX). Development of predictive risk models is critical to reducing 30DRA and improving outcomes. Current approaches rely on fixed variables derived from administrative data. These models may not capture clinical evolution that is critical to predicting outcomes. METHODS: We directed a retrospective analysis toward: (1) developing parsimonious risk models for 30DRA and (2) comparing efficiency of models based on the use of immutable versus dynamic data. Baseline and in-hospital clinical and outcomes data were collected from adult KTX recipients between 2005 and 2012. Risk models were developed using backward logistic regression and compared for predictive efficacy using receiver operating characteristic curves. RESULTS: Of 1147 KTXpatients, 123 had 30DRA. Risk factors for 30DRA included recipient comorbidities, transplant factors, and index hospitalization patient level clinical data. The initial fixed variable model included 9 risk factors and was modestly predictive (area under the curve, 0.64; 95% confidence interval [95% CI], 0.58-0.69). The model was parsimoniously reduced to 6 risks, which remained modestly predictive (area under the curve, 0.63; 95% CI, 0.58-0.69). The initial predictive model using 13 fixed and dynamic variables was significantly predictive (AUC, 0.73; 95% CI, 0.67-0.80), with parsimonious reduction to 9 variables maintaining predictive efficacy (AUC, 0.73; 95% CI, 0.67-0.79). The final model using dynamically evolving clinical data outperformed the model using static variables (P=0.009). Internal validation demonstrated that the final model was stable with minimal bias. CONCLUSIONS: We demonstrate that modeling dynamic clinical data outperformed models using immutable data in predicting 30DRA.
Authors: Ruben Amarasingham; Billy J Moore; Ying P Tabak; Mark H Drazner; Christopher A Clark; Song Zhang; W Gary Reed; Timothy S Swanson; Ying Ma; Ethan A Halm Journal: Med Care Date: 2010-11 Impact factor: 2.983
Authors: Ashish K Jha; Timothy G Ferris; Karen Donelan; Catherine DesRoches; Alexandra Shields; Sara Rosenbaum; David Blumenthal Journal: Health Aff (Millwood) Date: 2006-10-11 Impact factor: 6.301
Authors: Mara A McAdams-DeMarco; Israel O Olorundare; Hao Ying; Fatima Warsame; Christine E Haugen; Rasheeda Hall; Jacqueline M Garonzik-Wang; Niraj M Desai; Jeremy D Walston; Silas P Norman; Dorry L Segev Journal: Transplantation Date: 2018-02 Impact factor: 4.939
Authors: Julien Hogan; Michael D Arenson; Sandesh M Adhikary; Kevin Li; Xingyu Zhang; Rebecca Zhang; Jeffrey N Valdez; Raymond J Lynch; Jimeng Sun; Andrew B Adams; Rachel E Patzer Journal: Transplant Direct Date: 2019-07-29
Authors: Kyla L Naylor; Gregory A Knoll; Justin Slater; Eric McArthur; Amit X Garg; Ngan N Lam; Britney Le; Alvin H Li; Megan K McCallum; Marlee Vinegar; S Joseph Kim Journal: Can J Kidney Health Dis Date: 2021-11-29
Authors: Alejandro Schuler; Liam O'Súilleabháin; Gina Rinetti-Vargas; Patricia Kipnis; Fernando Barreda; Vincent X Liu; Oleg Sofrygin; Gabriel J Escobar Journal: JAMA Netw Open Date: 2020-10-01