Progress and Challenges in the Management of Congenital Cytomegalovirus Infection.

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Clinics and Practice Pub Date : 2024-11-12 DOI:10.3390/clinpract14060191
Weronika Szulc, Natalia Szydłowska, Julia M Smyk, Anna Majewska
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Abstract

Congenital cytomegalovirus (CMV) infection is the most common intrauterine viral infection with a significant impact on the foetus and newborn. Current diagnostic practice includes serological testing for specific antibodies, but there are no global screening protocols. Maternal CMV screening is often performed in conjunction with antenatal ultrasound. While most infections are asymptomatic, severe cases can lead to long-term disability or death. Antiviral therapies, mainly ganciclovir and valganciclovir, are reserved for symptomatic patients, especially those with central nervous system involvement. Although effective, these treatments are associated with significant side effects such as neutropenia and hepatotoxicity. Foscarnet and cidofovir are used as alternatives, but their efficacy and safety require further study in paediatric patient populations. The effectiveness of passive prophylaxis is still uncertain. The lack of universally accepted guidelines for diagnosis, treatment, and prevention and the risk of serious side effects highlight the need for continued research. This review evaluates current therapeutic strategies, discusses their efficacy and associated risks, and highlights the need for innovative approaches to improve outcomes for affected neonates.

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先天性巨细胞病毒感染管理的进展与挑战。
先天性巨细胞病毒(CMV)感染是最常见的宫内病毒感染,对胎儿和新生儿有重大影响。目前的诊断方法包括特异性抗体的血清学检测,但还没有全球性的筛查方案。母体 CMV 筛查通常与产前超声检查同时进行。虽然大多数感染是无症状的,但严重病例可导致长期残疾或死亡。抗病毒疗法,主要是更昔洛韦和缬更昔洛韦,主要用于有症状的患者,尤其是中枢神经系统受累的患者。这些疗法虽然有效,但副作用很大,如中性粒细胞减少和肝毒性。Foscarnet 和 cidofovir 可作为替代药物,但其疗效和安全性还需要在儿科患者中进一步研究。被动预防的有效性仍不确定。由于缺乏普遍接受的诊断、治疗和预防指南,且存在严重副作用的风险,因此需要继续开展研究。本综述对目前的治疗策略进行了评估,讨论了其疗效和相关风险,并强调了采用创新方法改善受影响新生儿预后的必要性。
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来源期刊
Clinics and Practice
Clinics and Practice MEDICINE, GENERAL & INTERNAL-
CiteScore
2.60
自引率
4.30%
发文量
91
审稿时长
10 weeks
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