| Literature DB >> 28834181 |
Babak J Orandi1, Xun Luo2, Elizabeth A King2, Jacqueline M Garonzik-Wang2, Sunjae Bae2, Robert A Montgomery3, Mark D Stegall4, Stanley C Jordan5, Jose Oberholzer6, Ty B Dunn7, Lloyd E Ratner8, Sandip Kapur9, Ronald P Pelletier10, John P Roberts1, Marc L Melcher11, Pooja Singh12, Debra L Sudan13, Marc P Posner14, Jose M El-Amm15, Ron Shapiro16, Matthew Cooper17, George S Lipkowitz18, Michael A Rees19, Christopher L Marsh20, Bashir R Sankari21, David A Gerber22, Paul W Nelson23, Jason Wellen24, Adel Bozorgzadeh25, A Osama Gaber26, Dorry L Segev2.
Abstract
Thirty percent of kidney transplant recipients are readmitted in the first month posttransplantation. Those with donor-specific antibody requiring desensitization and incompatible live donor kidney transplantation (ILDKT) constitute a unique subpopulation that might be at higher readmission risk. Drawing on a 22-center cohort, 379 ILDKTs with Medicare primary insurance were matched to compatible transplant-matched controls and to waitlist-only matched controls on panel reactive antibody, age, blood group, renal replacement time, prior kidney transplantation, race, gender, diabetes, and transplant date/waitlisting date. Readmission risk was determined using multilevel, mixed-effects Poisson regression. In the first month, ILDKTs had a 1.28-fold higher readmission risk than compatible controls (95% confidence interval [CI] 1.13-1.46; P < .001). Risk peaked at 6-12 months (relative risk [RR] 1.67, 95% CI 1.49-1.87; P < .001), attenuating by 24-36 months (RR 1.24, 95% CI 1.10-1.40; P < .001). ILDKTs had a 5.86-fold higher readmission risk (95% CI 4.96-6.92; P < .001) in the first month compared to waitlist-only controls. At 12-24 (RR 0.85, 95% CI 0.77-0.95; P = .002) and 24-36 months (RR 0.74, 95% CI 0.66-0.84; P < .001), ILDKTs had a lower risk than waitlist-only controls. These findings of ILDKTs having a higher readmission risk than compatible controls, but a lower readmission risk after the first year than waitlist-only controls should be considered in regulatory/payment schemas and planning clinical care.Entities:
Keywords: clinical research/practice; desensitization; economics; health services and outcomes research; hospital readmission; kidney transplantation/nephrology; kidney transplantation: living donor; organ transplantation in general; quality of care/care delivery
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Year: 2017 PMID: 28834181 PMCID: PMC5820188 DOI: 10.1111/ajt.14472
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086