# “Rethinking High‐KDPI Kidneys: A Multidomain Approach to Predicting Success”

**Authors:** Xingyu Zhang, Chethan Puttarajappa, Frank Spitz, Jason Mial‐Anthony, Berkay Demirors, Abiha Abdullah, Vrishketan Sethi, Matthew Yu‐Sheng Lin, Andrew Crane, Winn Cashion, Charbel Elias, Han Shwe, Timothy Fokken, Bradley Phelp, Ryugen Takahashi, Hao Liu, Christof Kaltenmeier, Stalin Dharmayan, Vikraman Gunabushanam, Armando Ganoza, Martin N.Wijkstrom, Amit Tevar, Michele Molinari

PMC · DOI: 10.1111/ctr.70472 · 2026-02-04

## TL;DR

This study explores factors affecting outcomes of high-KDPI kidney transplants, suggesting a more comprehensive approach could improve transplant decisions.

## Contribution

The study identifies new predictors of transplant success beyond KDPI, including recipient and immunologic factors.

## Key findings

- Delayed graft function was linked to factors like donation after circulatory death and cold ischemia time.
- Recipient diabetes and prolonged dialysis were associated with graft loss.
- A multidomain assessment could improve transplant acceptance decisions.

## Abstract

The allocation and acceptance of deceased‐donor kidneys in the United States is influenced by theKidney Donor Profile Index (KDPI). We conducted a national analysis of high‐KDPI kidney transplants performed from 2014 to 2021 to identify key predictors of post‐transplant outcomes beyond those incorporated in KDPI.

This retrospective cohort study used data extracted from the Scientific Registry of Transplant Recipients (SRTR). Adult, first‐time recipients of kidney‐only deceased‐donor transplants with KDPI greater than 85% were included. Regression models were used to identify independent predictors of delayed graft function (DGF), primary graft nonfunction (PGNF), patient survival, overall graft survival, and death‐censored graft survival.

Among 4,911 recipients, DGF occurred in 33.8% and PGNF in 4.0%. DGF was independently associated with donation after circulatory death, terminal donor creatinine > 1.5 mg/dL, recipient obesity, dialysis duration > 3 years, and cold ischemia time (CIT) ≥ 24 h, whereas machine perfusion was protective. PGNF was associated with donation after circulatory death, terminal donor creatinine > 2.0 mg/dL, high‐risk cytomegalovirus (CMV) serostatus, and donor injury patterns within the high‐KDPI range, including younger donor age. Five‐year patient and graft survival were 72% and 62%, respectively. Graft loss was independently associated with DGF, elevated intrarenal resistive index (RI), recipient diabetes, prolonged dialysis exposure, and high‐risk CMV/EBV serostatus.

Outcomes after high‐KDPI kidney transplantation reflect both KDPI‐defined donor risk and additional recipient, immunologic, and perioperative factors. A multidomain, offer‐time assessment may support more individualized acceptance decisions and improve utilization.

## Linked entities

- **Diseases:** diabetes (MONDO:0005015)

## Full-text entities

- **Diseases:** underweight (MESH:D013851), hypertension (MESH:D006973), graft failure (MESH:D051437), sarcopenia (MESH:D055948), cerebrovascular accident (MESH:D020521), frailty (MESH:D000073496), ischemic (MESH:D002545), acute kidney injury (MESH:D058186), obesity (MESH:D009765), CMV (MESH:D003586), brain death (MESH:D001926), proteinuria (MESH:D011507), anoxia (MESH:D000860), injury (MESH:D014947), PGNF (MESH:D055031), death (MESH:D003643), CIT (MESH:D007511), DGF (MESH:D051799), head trauma (MESH:D006259), diabetes (MESH:D003920), Metabolic (MESH:D008659), circulatory death (MESH:D012769), peripheral vascular disease (MESH:D016491), glomerulosclerosis (MESH:D005921), renal injury (MESH:D007674), reperfusion injury (MESH:D015427), ESRD (MESH:D007676), ischemic injury (MESH:D017202)
- **Chemicals:** creatinine (MESH:D003404), sodium (MESH:D012964)
- **Species:** Cytomegalovirus (genus) [taxon 10358], hepatitis C virus [taxon 11103], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12872201/full.md

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Source: https://tomesphere.com/paper/PMC12872201