Healthcare resource use and clinical events associated with neutropenia among adult kidney transplant recipients receiving valganciclovir or ganciclovir prophylaxis: a matched case-control cohort study.

IF 2.4 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Current Medical Research and Opinion Pub Date : 2025-04-01 Epub Date: 2025-05-13 DOI:10.1080/03007995.2025.2498674
Weijia Wang, Pamela A Moise, Michael Wong, Wei Gao, Cheryl Xiang, Abigail Zion, Flavio Vincenti, Andrew P Beyer
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引用次数: 0

Abstract

Background: Cytomegalovirus prophylaxis with valganciclovir and ganciclovir is associated with increased neutropenia risk in kidney transplant recipients. This study assessed the association between neutropenia and short-term healthcare resource utilization (HCRU) and clinical events for adults receiving valganciclovir and/or ganciclovir prophylaxis post-kidney transplantation in the United States.

Methods: Adult kidney transplant recipients from 2012 to 2020 who received valganciclovir and/or ganciclovir prophylaxis were identified in the TriNetX database. Patients with a neutropenia event during the 1-year post-kidney transplant were identified as cases and those without were identified as controls. Cases and controls were matched 1:1 on patient characteristics in the 1-year period before the kidney transplant. HCRU and clinical event rates in the year following the first neutropenia event were compared between the cases and controls.

Results: Of 3564 identified case-control pairs, the average age was 52 years and 59.57% were male. Cases had higher HCRU in the first year after neutropenia than controls, characterized by 1.40-, 1.28-, and 1.33-times higher rates of inpatient, outpatient, and emergency department visits (all p < 0.001). Cases also had higher incident rates for cytomegalovirus-related events, use of granulocyte colony stimulating factor, and opportunistic infections (all adjusted incident rate ratios >1 with p < 0.01), and greater risks of death, graft loss, and acute graft rejection (all adjusted hazard ratios >1 with p < 0.001).

Conclusion: Higher HCRU and clinical burden were observed within the first year following post-transplant neutropenia. New options for cytomegalovirus prophylaxis that are less likely to induce neutropenia are needed to improve patient outcomes.

在接受缬更昔洛韦或更昔洛韦预防的成人肾移植受者中,与中性粒细胞减少相关的医疗资源使用和临床事件:一项匹配的病例对照队列研究
背景:用缬更昔洛韦和更昔洛韦预防巨细胞病毒与肾移植受者中性粒细胞减少的风险增加有关。本研究评估了美国肾移植后接受缬更昔洛韦和/或更昔洛韦预防治疗的成人中性粒细胞减少症与短期医疗资源利用(HCRU)和临床事件之间的关系。方法:在TriNetX数据库中识别2012年至2020年接受过缬更昔洛韦和/或更昔洛韦预防治疗的成人肾移植受者。肾移植后1年内发生中性粒细胞减少事件的患者被确定为病例,未发生中性粒细胞减少事件的患者被确定为对照组。在肾移植前1年的患者特征上,病例和对照组按1:1匹配。在病例和对照组之间比较首次中性粒细胞减少事件后一年的HCRU和临床事件发生率。结果:3564对病例对照中,平均年龄52岁,男性占59.57%。病例在中性粒细胞减少后第一年的HCRU高于对照组,住院、门诊和急诊科就诊率分别是对照组的1.40倍、1.28倍和1.33倍(均为p 1与p 1与p)。结论:移植后中性粒细胞减少后第一年的HCRU和临床负担较高。需要新的巨细胞病毒预防方案,不太可能诱导中性粒细胞减少,以改善患者的预后。
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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来源期刊
Current Medical Research and Opinion
Current Medical Research and Opinion 医学-医学:内科
CiteScore
4.40
自引率
4.30%
发文量
247
审稿时长
3-8 weeks
期刊介绍: Current Medical Research and Opinion is a MEDLINE-indexed, peer-reviewed, international journal for the rapid publication of original research on new and existing drugs and therapies, Phase II-IV studies, and post-marketing investigations. Equivalence, safety and efficacy/effectiveness studies are especially encouraged. Preclinical, Phase I, pharmacoeconomic, outcomes and quality of life studies may also be considered if there is clear clinical relevance
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