Please use this identifier to cite or link to this item: https://doi.org/10.1007/s11255-020-02542-7
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dc.titleMyocardial ischemia by radionuclide imaging and long-term outcomes after kidney transplantation
dc.contributor.authorLow, Sanmay
dc.contributor.authorChua, Horng-Ruey
dc.contributor.authorWong, Raymond
dc.contributor.authorGoh, Angeline
dc.contributor.authorNg, Yue-Harn
dc.contributor.authorTeo, Boon-Wee
dc.contributor.authorVathsala, Anantharaman
dc.date.accessioned2022-07-25T02:33:56Z
dc.date.available2022-07-25T02:33:56Z
dc.date.issued2020-07-13
dc.identifier.citationLow, Sanmay, Chua, Horng-Ruey, Wong, Raymond, Goh, Angeline, Ng, Yue-Harn, Teo, Boon-Wee, Vathsala, Anantharaman (2020-07-13). Myocardial ischemia by radionuclide imaging and long-term outcomes after kidney transplantation. INTERNATIONAL UROLOGY AND NEPHROLOGY 52 (10) : 1995-2003. ScholarBank@NUS Repository. https://doi.org/10.1007/s11255-020-02542-7
dc.identifier.issn03011623
dc.identifier.issn15732584
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/229102
dc.description.abstractPurpose: We examined the incidence of myocardial ischemia (MI) in kidney transplant recipients (KTR) using myocardial perfusion imaging (MPI), and its association with long-term outcomes after transplantation. Methods: A retrospective observational study was conducted of asymptomatic KTRs who underwent post-transplant MPI screening for MI, as defined by moderate to severe myocardial perfusion defects, post-stress myocardial stunning or balanced ischemia. A composite outcome of all-cause mortality, graft loss, and major adverse cardiovascular events (MACE) was examined over minimum 5 years. Results: We studied 135 KTRs who underwent 226 MPIs, with follow-up duration of 10 (7–13) years. 110 (81%) patients had normal MPIs, 11 (8%) had mild perfusion defects, and 14 (10%) had MI. Correspondingly, composite outcome developed in 6%, 27%, and 43% (p = 0.04), and MACE occurred in 7%, 0%, and 21% (p = 0.11), of the respective subgroups. Twenty-six patients developed the composite outcome after 5 (3–7) years post-transplantation, including 11 patients with MACE. On multivariate analysis, MI, higher low-density lipoprotein levels, and proteinuria ' 0.3 g/day independently predicted the composite outcome; only MI predicted MACE (all p ' 0.05). Ninety-one patients had two serial MPIs, which increased the positive predictive value for MACE from 17 to 25%. Absence of MI had negative predictive value of 83% for MACE and 93% for the composite outcome. Conclusion: MI that is detected early post-kidney transplantation predicts long-term mortality, graft loss, and MACE in KTRs, with excellent negative but poor positive predictive values.
dc.language.isoen
dc.publisherSPRINGER
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectUrology & Nephrology
dc.subjectKidney transplantation
dc.subjectMyocardial ischemia
dc.subjectMyocardial perfusion imaging
dc.subjectHeart
dc.subjectRisk assessment
dc.subjectFollow-up studies
dc.subjectCORONARY-ARTERY-DISEASE
dc.subjectHEART-DISEASE
dc.subjectRENAL-TRANSPLANTATION
dc.subjectCARDIOVASCULAR EVENTS
dc.subjectRISK-FACTORS
dc.subjectPROGNOSTIC VALUE
dc.subjectCARDIAC EVENTS
dc.subjectSCINTIGRAPHY
dc.subjectEXPERIENCE
dc.typeArticle
dc.date.updated2022-07-22T10:05:07Z
dc.contributor.departmentMEDICINE
dc.description.doi10.1007/s11255-020-02542-7
dc.description.sourcetitleINTERNATIONAL UROLOGY AND NEPHROLOGY
dc.description.volume52
dc.description.issue10
dc.description.page1995-2003
dc.published.statePublished
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