供体-血清阳性和受体-血清阴性心脏移植受者接受缬更昔洛韦预防3或6个月后巨细胞病毒感染的风险

The Canadian journal of hospital pharmacy Pub Date : 2025-05-14 eCollection Date: 2025-01-01 DOI:10.4212/cjhp.3701
Vincent Leclerc, Nathalie Châteauvert
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引用次数: 0

摘要

背景:巨细胞病毒(CMV)疾病是心脏移植术后常见的疾病,特别是在供体-血清阳性,受体-血清阴性(D+/R-) CMV状态的患者中。建议使用缬更昔洛韦预防3至6个月,但很少有数据支持对接受心脏移植的患者使用6个月而不是3个月的预防。目的:比较心脏移植后1年内接受3个月或6个月预防治疗的CMV D+/R-患者CMV感染和首次发生CMV疾病的风险。方法:本回顾性分析包括2015年10月至2022年10月期间在研究中心接受D+/R-心脏移植的所有患者。患者至少需要1年的随访才能纳入研究。结果:35例患者符合纳入标准。缬更昔洛韦预防疗程(由医疗小组确定)22例为3个月,13例为6个月。3个月组和6个月组CMV感染率分别为68.2%(15/22)和30.8%(4/13)(风险差异为37.4%,95%可信区间[CI] 1.75 ~ 65.8, p = 0.04)。接受3个月预防的患者中有54.5%(12/22)发生巨细胞病毒疾病,接受6个月预防的患者中有23.1%(3/13)发生巨细胞病毒疾病(风险差异31.4%,95% CI -3.7 ~ 59.4, p = 0.09)。大多数巨细胞病毒感染和疾病发生在预防结束后的3个月内。结论:心脏移植后,与接受6个月预防的患者相比,接受3个月预防的CMV D+/R-患者CMV感染的风险更高,CMV疾病的风险也更高,无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of Cytomegalovirus Infection after 3 or 6 Months of Valganciclovir Prophylaxis among Donor-Seropositive, Recipient-Seronegative Heart Transplant Recipients.

Background: Cytomegalovirus (CMV) disease is frequent following heart transplant, especially among patients with donor-seropositive, recipient-seronegative (D+/R-) CMV status. Valganciclovir prophylaxis for 3 to 6 months is recommended, but few data support the use of 6 rather than 3 months of prophylaxis for patients who have undergone heart transplant.

Objective: To compare the risk of CMV infection and a first occurrence of CMV disease after heart transplant among CMV D+/R- patients who received 3 or 6 months of prophylaxis in the first year after transplant.

Methods: This retrospective analysis included every D+/R- heart transplant recipient at the study centre between October 2015 and October 2022. Patients had to have a minimum of 1 year of follow-up for inclusion.

Results: Thirty-five patients met the inclusion criteria. The duration of valganciclovir prophylaxis (determined by the medical team) was 3 months for 22 patients and 6 months for 13 patients. CMV infection occurred in 68.2% (15/22) and 30.8% (4/13) of the 3-month and 6-month groups, respectively (risk difference 37.4%, 95% confidence interval [CI] 1.75 to 65.8, p = 0.04). CMV disease occurred in 54.5% (12/22) of patients who received 3 months of prophylaxis and 23.1% (3/13) of those who received 6 months of prophylaxis (risk difference 31.4%, 95% CI -3.7 to 59.4, p = 0.09). Most CMV infections and diseases occurred in the 3 months after the end of prophylaxis.

Conclusions: After heart transplant, CMV D+/R- patients who received 3 months of prophylaxis had a higher risk of CMV infection and a non-statistically significant higher risk of CMV disease relative to those who received 6 months of prophylaxis.

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