Clinical relevance and outcome of routine endomyocardial biopsy to detect rejection after heart transplantation

Leendert C. Kieviet BsC , Steven A. Muller MD , Mariusz K. Szymanski MD PhD , Manon G. van der Meer MD PhD , M. Louis Handoko MD PhD , Saskia Z.H. Rittersma MD PhD , Saskia C.A. de Jager , Egidius E. van Aarnhem MD PhD , Annelotte Vos MD , Pim van der Harst MD PhD , Linda W. van Laake MD PhD , Marish I.F.J. Oerlemans MD PHD
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Abstract

Background

Endomyocardial biopsy has been the cornerstone of monitoring rejection after heart transplantation for decades. Although recommendations advise routine biopsies during the first 3-12 months, this timeframe is broad, and intercenter variability persists in its application. Here, we report the yield and complication rate of routine endomyocardial biopsies during the past 36 years of post-transplantation care to monitor acute cellular rejection.

Methods

In this retrospective, single-center study, we collected all routine biopsy data after transplantation between 1986 and 2022. The total number of biopsies, type of rejection, complications, and survival were analyzed in the total population as well as per different endomyocardial biopsy protocol over time period (Period 1: 1986-1994; Period 2: 1994-2009; Period 3: 2009-2022).

Results

In 474 patients (71.1% male, age at transplant 47.7 ± 12.6 years), 8185 routine biopsy procedures were performed: 29.9 ± 11.1 per patient for Period 1 (n = 83), 16.9 ± 3.8 for Period 2 (n = 220) and 11.6 ± 2.4 for Period 3 (n = 171). Complication rate was low (1.7%; n = 139/8185) and 19.8% (n = 94/474) patients experienced clinically-relevant rejection (≥2R) which mainly occurred <6 months post-transplantation (89.4%; n = 84/94). The incidence of rejection decreased over time, leading to an improved rejection-free survival (p < 0.001) with a subsequent increase in Number-Needed-to-Diagnose. Importantly, severe acute cellular rejection did not occur in Period 3 in the first year post-transplantation.

Conclusion

Acute cellular rejection, including clinically-relevant rejection, has declined significantly over time and is rare beyond 6 months post-transplantation. A low-frequency approach seems feasible and safe, which is relevant for the transition towards less-invasive protocols to detect rejection, especially early post-transplantation.

Abstract Image

心脏移植术后常规心内膜活检检测排斥反应的临床意义和结果
几十年来,心内膜肌活检一直是监测心脏移植后排斥反应的基础。虽然建议在头3-12个月进行常规活检,但这个时间范围很广,而且在应用时中心间的差异仍然存在。在这里,我们报告了在过去36年的移植后护理中常规心内膜活检的产量和并发症发生率,以监测急性细胞排斥反应。方法在这项回顾性的单中心研究中,我们收集了1986年至2022年间移植后的所有常规活检数据。分析了总活检次数、排斥反应类型、并发症和生存率,以及不同时期的不同心内膜活检方案(第一阶段:1986-1994;第二期:1994-2009;第三期:2009-2022)。结果474例患者(71.1%为男性,移植时年龄47.7±12.6岁)共行8185例常规活检:第一阶段(83例)29.9±11.1例,第二阶段(220例)16.9±3.8例,第三阶段(171例)11.6±2.4例。并发症发生率低(1.7%;n = 139/8185)和19.8% (n = 94/474)的患者出现临床相关排斥反应(≥2R),主要发生在移植后6个月(89.4%;n = 84/94)。随着时间的推移,排斥反应的发生率降低,导致无排斥生存的改善(p <;0.001),随后需要诊断的人数增加。重要的是,移植后第一年的第3期没有发生严重的急性细胞排斥反应。结论急性细胞排斥反应,包括临床相关的排斥反应,随着时间的推移显著下降,移植后6个月后罕见。低频方法似乎可行且安全,这与向低侵入性方案过渡以检测排斥反应有关,特别是移植后早期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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