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Pilot Study of Model-Based Dosage Individualization of Ganciclovir in Neonates and Young Infants with Congenital Cytomegalovirus Infection.基于模型的更昔洛韦剂量个体化在先天性巨细胞病毒感染的新生儿和婴儿中的初步研究。
Antimicrob Agents Chemother. 2018 Apr 26;62(5). doi: 10.1128/AAC.00075-18. Print 2018 May.
2
Diagnosis and management of infants with congenital cytomegalovirus infection.先天性巨细胞病毒感染婴儿的诊断与管理
Paediatr Child Health. 2017 May;22(2):72-74. doi: 10.1093/pch/pxx002. Epub 2017 Apr 4.
3
Congenital cytomegalovirus infection in pregnancy and the neonate: consensus recommendations for prevention, diagnosis, and therapy.先天性巨细胞病毒感染的孕妇和新生儿:预防、诊断和治疗的共识建议。
Lancet Infect Dis. 2017 Jun;17(6):e177-e188. doi: 10.1016/S1473-3099(17)30143-3. Epub 2017 Mar 11.
4
Cytomegalovirus DNA Detection by Polymerase Chain Reaction in Cerebrospinal Fluid of Infants With Congenital Infection: Associations With Clinical Evaluation at Birth and Implications for Follow-up.应用聚合酶链反应检测先天性巨细胞病毒感染婴儿脑脊液中的病毒 DNA:与出生时临床评估的相关性及其随访意义。
Clin Infect Dis. 2017 May 15;64(10):1335-1342. doi: 10.1093/cid/cix105.
5
Therapeutic drug monitoring of ganciclovir for postnatal cytomegalovirus infection in an extremely low birth weight infant: a case report.极低出生体重儿产后巨细胞病毒感染的更昔洛韦治疗药物监测:一例报告
BMC Pediatr. 2016 Aug 22;16(1):141. doi: 10.1186/s12887-016-0683-x.
6
Therapeutic drug monitoring in neonates.新生儿治疗药物监测
Arch Dis Child. 2016 Apr;101(4):377-81. doi: 10.1136/archdischild-2013-305309. Epub 2016 Jan 22.
7
Disseminated Congenital Cytomegalovirus Infection Presenting as Severe Sepsis in a Preterm Neonate.
J Pediatr. 2016 Mar;170:339-e1. doi: 10.1016/j.jpeds.2015.11.069. Epub 2015 Dec 29.
8
Cytomegalovirus Enterocolitis Mimicking Necrotizing Enterocolitis: Case Reports and Review of the Literature.酷似坏死性小肠结肠炎的巨细胞病毒性小肠结肠炎:病例报告及文献复习
J Pediatric Infect Dis Soc. 2013 Mar;2(1):71-5. doi: 10.1093/jpids/pis060. Epub 2012 Jun 22.
9
Determining the prevalence of cytomegalovirus infection in a cohort of preterm infants.确定一组早产儿中巨细胞病毒感染的患病率。
J Neonatal Perinatal Med. 2015;8(2):137-41. doi: 10.3233/NPM-15814057.
10
Anti-viral therapy for congenital cytomegalovirus infection: pharmacokinetics, efficacy and side effects.先天性巨细胞病毒感染的抗病毒治疗:药代动力学、疗效及副作用
J Matern Fetal Neonatal Med. 2016;29(10):1657-64. doi: 10.3109/14767058.2015.1058774. Epub 2015 Jul 27.

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.

DOI:10.5863/1551-6776-28.1.93
PMID:36777981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9901313/
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。