Recém-nascidos com risco de toxoplasmose congênita, revisão de 16 anos

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Joana Verdelho Andrade, Catarina Resende, Joana Campos, Cristina Batista, Cristina Faria, C. Figueiredo, Vitor Bastos, Nuno Andrade, I. Andrade
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引用次数: 1

Abstract

AIMS: To analyze the data on pregnancies with risk of congenital toxoplasmosis and to investigate the newborns' outcome, in a level II hospital in Portugal.METHODS: A cross-sectional retrospective study included newborns at risk for congenital toxoplasmosis and their mothers, whose delivery occurred between January 2000 and December 2015. The inclusion criteria were mother with seroconversion to toxoplasmosis during pregnancy or first serum sample with positive specific IgM and IgG. The diagnosis of congenital toxoplasmosis was defined by positive specific IgM at birth and/or polymerase chain reaction positive in amniotic fluid and/or persistence of specific IgG up to 12 months of life. Congenital toxoplasmosis was defined as symptomatic when clinical findings were attributed to the disease. Chi-square or Fisher's exact tests were used to test associations between variables, assuming statistical significance when p <0.05.RESULTS: There were 39,585 live births in the study period and 98 cases with risk of congenital toxoplasmosis were identified, of which 89 completed the follow-up. The prevalence of anti-T. gondii IgG in the pregnant women was 26% (95% confidence interval [CI] 24-27%). Twenty-two cases of congenital toxoplasmosis (5.6 per 10,000 live births, 95%CI 3.5-8.5 per 10,000) were confirmed. Of the 22 newborns, 18 (82%, 95%CI 61-93%) were symptomatic. The most frequent clinical findings were intracranial calcification (64%), hepatomegaly and / or elevation of transaminases (32%) and retinochoroiditis (14%). Cerebral lesions were more frequent when maternal infection was documented in the first and second trimester compared to the third trimester (p=0.018). In 31 cases (35%), the pregnant women were treated from the time of diagnosis until delivery with spiramycin, and no differences were found regarding the rate of vertical transmission or the appearance of clinical manifestations among the newborns of treated and non-treated mothers treated.CONCLUSIONS: The prevalence of congenital toxoplasmosis was higher than that reported in other European countries. The prevalence of intracranial calcifications was higher than that described in the literature, whereas retinochoroiditis and strabismus occurrence was lower. Brain lesions in newborns were more frequent in first- and second-trimester infections. There was no difference in the rate of vertical transmission and in the occurrence of clinical manifestations among newborns whose mothers received spiramycin during gestation and those whose mothers did not receive treatment.
新生儿先天性弓形虫病风险,回顾16年
目的:分析葡萄牙一家二级医院中有先天性弓形虫病风险的妊娠数据,并调查新生儿的结局。方法:对2000年1月至2015年12月间出生的有先天性弓形虫病风险的新生儿及其母亲进行横断面回顾性研究。纳入标准为妊娠期血清转化为弓形虫病的母亲或首次血清特异性IgM和IgG阳性。先天性弓形虫病的诊断定义为出生时特异性IgM阳性和/或羊水聚合酶链反应阳性和/或特异性IgG持续到12个月。先天性弓形虫病被定义为有症状时,临床表现归因于该疾病。采用卡方检验或Fisher精确检验来检验变量之间的相关性,当p <0.05时假设有统计学意义。结果:研究期间共有39585例活产婴儿,鉴定出有先天性弓形虫病风险的98例,其中89例完成了随访。抗t病毒的流行。孕妇弓形虫IgG阳性率为26%(95%可信区间[CI] 24 ~ 27%)。确诊22例先天性弓形虫病(5.6 / 10,000活产,95%可信区间3.5-8.5 / 10,000)。22例新生儿中,18例(82%,95%CI 61-93%)出现症状。最常见的临床表现是颅内钙化(64%)、肝肿大和/或转氨酶升高(32%)和视网膜脉管炎(14%)。与孕晚期相比,孕早期和孕中期母体感染的大脑病变更频繁(p=0.018)。31例(35%)孕妇从确诊至分娩均给予螺旋霉素治疗,治疗母亲与未治疗母亲的新生儿在垂直传播率和临床表现方面均无差异。结论:先天性弓形虫病的患病率高于其他欧洲国家的报道。颅内钙化的发生率高于文献中所描述的,而视网膜脉络膜炎和斜视的发生率较低。新生儿脑损伤在妊娠早期和中期感染中更为常见。妊娠期间母亲接受螺旋霉素治疗的新生儿与母亲未接受治疗的新生儿在垂直传播率和临床表现方面无差异。
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来源期刊
Scientia Medica
Scientia Medica MEDICINE, GENERAL & INTERNAL-
CiteScore
0.70
自引率
20.00%
发文量
14
审稿时长
10 weeks
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