Boscarino Giovanni, Romano Rossana, Tegoni Francesca, Iotti Carlotta, Perrone Serafina, Esposito Susanna, Buonsenso Danilo
Pediatric Clinic, University Hospital, Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
Neonatology Unit, University Hospital, Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
J Clin Med. 2024 Oct 8;13(19):5997. doi: 10.3390/jcm13195997.
Congenital cytomegalovirus (cCMV) is the most common cause of congenital infection and the leading cause of non-genetic sensorineural hearing loss in childhood. While treatment trials have been conducted in symptomatic children, defining asymptomatic infection can be complex. We performed a scoping review to understand how infection severity is defined and treated globally, as well as the various indications for initiating treatment. We conducted an electronic search of MEDLINE, EMBASE, Scopus, and the Cochrane Library, using combinations of the following terms: "newborn", "baby", "child", "ganciclovir", "valganciclovir", and "cytomegalovirus" or "CMV". We included eligible prospective and retrospective studies, case series, and randomized clinical trials (RCTs) published up to May 2024. A total of 26 studies were included, of which only 5 were RCTs. There was significant heterogeneity between studies. The most commonly considered criteria for symptomatic infection were microcephaly (23/24 studies), abnormal neuroimaging (22/24 studies), chorioretinitis/ocular impairment (21/24 studies), and hearing impairment (20/24 studies). Two studies also included asymptomatic newborns in their treatment protocols. Outcome measures varied widely, focusing either on different hearing assessments or neurocognitive issues. Our literature analysis revealed significant variability and heterogeneity in the definition of symptomatic cCMV infection and, consequently, in treatment approaches. A consensus on core outcomes and well-conducted RCTs are needed to establish treatment protocols for specific groups of newborns with varying manifestations of cCMV.
先天性巨细胞病毒(cCMV)感染是先天性感染最常见的病因,也是儿童非遗传性感音神经性听力损失的主要原因。虽然已对有症状的儿童进行了治疗试验,但确定无症状感染可能很复杂。我们进行了一项范围综述,以了解全球如何定义和治疗感染严重程度,以及启动治疗的各种指征。我们使用以下术语组合对MEDLINE、EMBASE、Scopus和Cochrane图书馆进行了电子检索:“新生儿”、“婴儿”、“儿童”、“更昔洛韦”、“缬更昔洛韦”以及“巨细胞病毒”或“CMV”。我们纳入了截至2024年5月发表的符合条件的前瞻性和回顾性研究、病例系列以及随机临床试验(RCT)。总共纳入了26项研究,其中只有5项是RCT。各研究之间存在显著异质性。最常被认为的有症状感染标准是小头畸形(24项研究中的23项)、神经影像学异常(24项研究中的22项)、脉络膜视网膜炎/眼部损害(24项研究中的21项)以及听力损害(24项研究中的20项)。两项研究在其治疗方案中也纳入了无症状新生儿。结局指标差异很大,要么侧重于不同的听力评估,要么侧重于神经认知问题。我们的文献分析显示,有症状的cCMV感染定义以及因此治疗方法存在显著变异性和异质性。需要就核心结局达成共识并开展良好的RCT,以建立针对具有不同cCMV表现的特定新生儿群体的治疗方案。