Jennifer Conway MD , Tara Pidborochynski MSc , James K. Kirklin MD , Ryan Cantor PhD , Hong Zhao PhD , Aryaz Sheybani MD , Jacqueline Lamour MD , Lakshmi Gokanapudy Hahn MD , Leslie Collins MD , Jessica Laks MD , Darren H. Freed MD, PhD
{"title":"Severe primary graft failure: Are there lasting impacts? Analysis from the PHTS Database","authors":"Jennifer Conway MD , Tara Pidborochynski MSc , James K. Kirklin MD , Ryan Cantor PhD , Hong Zhao PhD , Aryaz Sheybani MD , Jacqueline Lamour MD , Lakshmi Gokanapudy Hahn MD , Leslie Collins MD , Jessica Laks MD , Darren H. Freed MD, PhD","doi":"10.1016/j.jhlto.2024.100184","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Primary graft failure (PGF) is a leading cause of early morbidity and mortality after heart transplantation (HTx). PGF is secondary to graft ischemia and ischemia-reperfusion injuries to the cardiomyocytes and vasculature of the donor heart after transplantation. Longer-term outcomes after PGF are not well studied.</div></div><div><h3>Methods</h3><div>Patients with an HTx (January 1, 2010 to June 30, 2022) were identified using the Pediatric Heart Transplant Society registry. PGF was defined as death, retransplantation, or need for mechanical circulatory support within 72 hours of HTx. Kaplan-Meier analysis and Cox proportional hazard modeling were utilized.</div></div><div><h3>Results</h3><div>Of the 4,982 patients with a primary HTx, 5.4% (<em>n</em> = 269) met criteria for PGF. Patients with PGF were younger, with higher proportion of congenital heart disease, longer cardiopulmonary bypass and ischemic times (IT), and more likely to be on extracorporeal membrane oxygenation or ventilator at HTx (all <em>p</em> < 0.0001, IT <em>p</em> = 0.0006). PGF resulted in lower overall survival (1 year: 54% vs 94%, <em>p</em> < 0.001). This remained true when conditional survival was examined at 30 and 90 days but not at 1 year (<em>p</em> = 0.1143). Freedom from rejection did not differ between the groups at overall or conditional on 30 days but was slightly higher for those with PGF at 90 and 365 days. There was no difference in freedom from coronary allograft vasculopathy (CAV). PGF was an independent predictor of overall graft loss (hazard ratios [HR] 4.7, <em>p</em> < 0.0001) and conditional survival to 30 days (HR 2.47, <em>p</em> < 0.0001) and 90 days (HR 1.6, <em>p</em> = 0.012) but not beyond 1 year.</div></div><div><h3>Conclusions</h3><div>Severe PGF is an independent predictor of early mortality post-HTx but subsequently does not further impact long-term survival, overall risk of rejection, or CAV. Understanding the impact of milder forms of PGF on survival and long-term outcomes is still needed. Methods to decrease the risk of PGF, such as alternative preservation and storage techniques, may impact early mortality post-HTx.</div></div>","PeriodicalId":100741,"journal":{"name":"JHLT Open","volume":"7 ","pages":"Article 100184"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JHLT Open","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950133424001332","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Primary graft failure (PGF) is a leading cause of early morbidity and mortality after heart transplantation (HTx). PGF is secondary to graft ischemia and ischemia-reperfusion injuries to the cardiomyocytes and vasculature of the donor heart after transplantation. Longer-term outcomes after PGF are not well studied.
Methods
Patients with an HTx (January 1, 2010 to June 30, 2022) were identified using the Pediatric Heart Transplant Society registry. PGF was defined as death, retransplantation, or need for mechanical circulatory support within 72 hours of HTx. Kaplan-Meier analysis and Cox proportional hazard modeling were utilized.
Results
Of the 4,982 patients with a primary HTx, 5.4% (n = 269) met criteria for PGF. Patients with PGF were younger, with higher proportion of congenital heart disease, longer cardiopulmonary bypass and ischemic times (IT), and more likely to be on extracorporeal membrane oxygenation or ventilator at HTx (all p < 0.0001, IT p = 0.0006). PGF resulted in lower overall survival (1 year: 54% vs 94%, p < 0.001). This remained true when conditional survival was examined at 30 and 90 days but not at 1 year (p = 0.1143). Freedom from rejection did not differ between the groups at overall or conditional on 30 days but was slightly higher for those with PGF at 90 and 365 days. There was no difference in freedom from coronary allograft vasculopathy (CAV). PGF was an independent predictor of overall graft loss (hazard ratios [HR] 4.7, p < 0.0001) and conditional survival to 30 days (HR 2.47, p < 0.0001) and 90 days (HR 1.6, p = 0.012) but not beyond 1 year.
Conclusions
Severe PGF is an independent predictor of early mortality post-HTx but subsequently does not further impact long-term survival, overall risk of rejection, or CAV. Understanding the impact of milder forms of PGF on survival and long-term outcomes is still needed. Methods to decrease the risk of PGF, such as alternative preservation and storage techniques, may impact early mortality post-HTx.
背景:原发性移植物衰竭(PGF)是心脏移植术后早期发病和死亡的主要原因。PGF继发于移植后供心心肌细胞和血管的缺血再灌注损伤。PGF后的长期结果尚未得到很好的研究。方法使用儿科心脏移植协会注册表识别HTx患者(2010年1月1日至2022年6月30日)。PGF定义为HTx术后72小时内死亡、再移植或需要机械循环支持。采用Kaplan-Meier分析和Cox比例风险模型。结果4982例原发性HTx患者中,5.4% (n = 269)符合PGF标准。PGF患者更年轻,先天性心脏病比例更高,体外循环和缺血时间(IT)更长,HTx时使用体外膜氧合或呼吸机的可能性更大(均p <;0.0001, IT p = 0.0006)。PGF导致总生存率降低(1年:54% vs 94%, p <;0.001)。在30天和90天检查条件生存时仍然如此,但在1年检查时则不然(p = 0.1143)。总的来说,在30天内,两组之间的排斥自由程度没有差异,但在90天和365天,PGF组的排斥自由程度略高。在冠状动脉移植物血管病变(CAV)的自由度上没有差异。PGF是移植物整体损失的独立预测因子(风险比[HR] 4.7, p <;0.0001)和条件生存至30天(HR 2.47, p <;0.0001)和90天(HR 1.6, p = 0.012),但不超过1年。结论:严重PGF是htx后早期死亡的独立预测因子,但随后不会进一步影响长期生存、总排斥风险或CAV。了解温和形式的PGF对生存和长期预后的影响仍然是必要的。降低PGF风险的方法,如替代保存和储存技术,可能会影响htx后的早期死亡率。