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先天性巨细胞病毒的治疗及双胎早产儿更昔洛韦治疗药物监测

Treatment of Congenital Cytomegalovirus and Ganciclovir Therapeutic Drug Monitoring in Twin Preterm Infants.

作者信息

Piché-Renaud Pierre-Philippe, Chiasson Charles-Olivier, Autmizguine Julie, Ovetchkine Philippe, Lachance Christian, Théorêt Yves, Martin Brigitte

机构信息

Department of Pediatrics (PPPR), CHU Sainte-Justine, Montréal, Québec.

Department of Pharmacy (COC, BM), CHU Sainte-Justine, Montréal, Québec.

出版信息

J Pediatr Pharmacol Ther. 2023;28(1):93-101. doi: 10.5863/1551-6776-28.1.93. Epub 2023 Feb 3.

Abstract

Congenitally acquired cytomegalovirus (CMV) infection is the most prevalent congenital infection worldwide and the most frequent cause of acquired sensorineural hearing loss. The burden of the disease is even more important in premature and very low birth weight infants. However, few data exist on the treatment with intravenous ganciclovir and oral valganciclovir in this vulnerable population. We report the case of twins congenitally infected with CMV and born prematurely at 27 weeks' gestation. Treatment regimens were initially individualized for their prematurity and renal function, and then adjusted with therapeutic drug monitoring (TDM) to adapt to their continuously evolving physiologic maturation. As infants were aging, the plasmatic half-life of ganciclovir slowly decreased to term infant values around 10 weeks of chronological age, or 37 weeks of postmenstrual age. Results for blood polymerase chain reaction tests became negative and long-term follow-ups were satisfactory in both twins. The limited data for infants born before 32 weeks of gestation or at less than 1200 g and evolution of ganciclovir pharmacokinetic parameters justify the use of TDM in these settings.

摘要

先天性获得性巨细胞病毒(CMV)感染是全球最普遍的先天性感染,也是后天性感音神经性听力损失的最常见原因。在早产儿和极低出生体重儿中,该病的负担更为严重。然而,关于在这一脆弱人群中使用静脉注射更昔洛韦和口服缬更昔洛韦进行治疗的数据很少。我们报告了一对双胞胎的病例,他们在妊娠27周时早产,先天性感染了CMV。治疗方案最初根据他们的早产情况和肾功能进行个体化调整,然后通过治疗药物监测(TDM)进行调整,以适应他们不断发展的生理成熟过程。随着婴儿年龄的增长,更昔洛韦的血浆半衰期在实际年龄约10周或月经后年龄37周时缓慢降至足月儿水平。双胞胎的血液聚合酶链反应检测结果均转为阴性,长期随访情况良好。对于妊娠32周前出生或体重小于1200克的婴儿,以及更昔洛韦药代动力学参数的变化,有限的数据证明在这些情况下使用TDM是合理的。

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