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评估两种剂量方案在儿科实体器官移植受者中更昔洛韦的中性粒细胞减少症风险。

Evaluation of valganciclovir's neutropenia risk in pediatric solid organ transplant recipients utilizing two dosing regimens.

机构信息

The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.

出版信息

Pediatr Transplant. 2024 Mar;28(2):e14714. doi: 10.1111/petr.14714.

Abstract

BACKGROUND

Valganciclovir is approved for cytomegalovirus prophylaxis in pediatrics using the Pescovitz algorithm. There are reports of valganciclovir overdoses in children with low body surface area and overestimated creatinine clearance utilizing this algorithm. This study compared the incidence of neutropenia and cytomegalovirus infection between the Pescovitz and weight-based dosing algorithms.

METHODS

A single-center retrospective chart review from January 2010 to September 2018 was performed on pediatric heart, liver, and kidney transplant recipients, who received valganciclovir. Data were collected from the initiation of valganciclovir prophylaxis to 30 days after discontinuation. The primary objective was the incidence of neutropenia in patients receiving valganciclovir dosed by the Pescovitz versus weight-based dosing algorithms.

RESULTS

This study included 187 pediatric transplant recipients who received valganciclovir dosed via the Pescovitz (62 recipients) or weight-based dosing algorithms (125 recipients). The incidence of neutropenia was higher in the Pescovitz (69.4%) compared to the weight-based dosing group (53.6%; p = .04) including moderate and severe neutropenia. Cytomegalovirus viremia was not significantly different between the two groups and occurred in 4.8% of the Pescovitz group compared to 2.4% of the weight-based group (p = .4).

CONCLUSIONS

The incidence of neutropenia was greater in recipients receiving valganciclovir dosed via the Pescovitz algorithm compared to the weight-based dosing. There were no significant differences in regard to cytomegalovirus viremia or disease between the two groups.

摘要

背景

缬更昔洛韦(valganciclovir)经 Pescovitz 算法批准用于儿科巨细胞病毒预防。有报道称,在使用该算法时,对于体表面积低和估算肌酐清除率过高的儿童,可能会发生缬更昔洛韦过量。本研究比较了 Pescovitz 算法和基于体重的剂量算法之间中性粒细胞减少症和巨细胞病毒感染的发生率。

方法

对 2010 年 1 月至 2018 年 9 月在单中心接受心脏、肝脏和肾脏移植的儿科患者进行了回顾性图表审查,这些患者接受了缬更昔洛韦治疗。数据收集从开始使用缬更昔洛韦预防到停药后 30 天。主要目的是比较接受 Pescovitz 算法与基于体重的剂量算法的患者使用缬更昔洛韦治疗时中性粒细胞减少症的发生率。

结果

本研究纳入了 187 名接受缬更昔洛韦治疗的儿科移植受者,其中 62 名接受 Pescovitz 算法剂量治疗,125 名接受基于体重的剂量算法治疗。Pescovitz 算法组(69.4%)的中性粒细胞减少症发生率高于基于体重的剂量算法组(53.6%;p=0.04),包括中度和重度中性粒细胞减少症。两组之间巨细胞病毒病毒血症无显著差异,Pescovitz 算法组发生率为 4.8%,基于体重的算法组为 2.4%(p=0.4)。

结论

与基于体重的剂量算法相比,接受 Pescovitz 算法给药的缬更昔洛韦受者中性粒细胞减少症发生率更高。两组间巨细胞病毒病毒血症或疾病无显著差异。

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