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Elevated Cardiac Troponin I in Preservation Solution Is Associated With Primary Graft Dysfunction
Matthew A Schechter1, Michael J Watson1, Bryan J Feger1
1Department of Surgery, Duke University Medical Center, Durham, North Carolina.
Journal of Cardiac Failure
|September 15, 2015
Summary
Primary graft dysfunction (PGD) after heart transplant is linked to higher cardiac troponin I (cTnI) levels in preservation solution. This suggests preservation injury may drive PGD development.
Area of Science:
- Cardiology
- Transplantation Medicine
- Biomarker Research
Background:
- Primary graft dysfunction (PGD) is a major cause of early mortality and morbidity after heart transplantation.
- Mechanisms underlying PGD development remain incompletely understood.
Purpose of the Study:
- To investigate the association between cardiac troponin I (cTnI) concentrations in preservation solutions and the incidence of PGD.
- To explore potential mechanisms of PGD, specifically focusing on preservation injury.
Main Methods:
- Analysis of preservation solutions from 43 heart transplant procedures using the i-STAT System.
- Measurement of normalized cardiac troponin I (cTnI) levels, adjusted for left ventricular mass.
- Review of recipient medical records to diagnose PGD based on 2014 ISHLT criteria.
Main Results:
- Nineteen patients developed PGD post-transplantation.
- Significantly elevated normalized cTnI levels were observed in preservation solutions of patients who developed PGD compared to those who did not (P = .031 for UW, P = .034 for Custodiol).
- cTnI levels correlated with ischemic time in the University of Wisconsin (UW) solution group, but not in the Custodiol group.
Conclusions:
- Elevated cTnI in preservation solution is significantly associated with PGD development.
- These findings suggest that preservation-induced injury may be a key mechanism contributing to PGD after heart transplantation.
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