T. Myat, H. M. Thu, Htin Lin, Nang Sarm Hom, Win Lei Kay Khine, M. Kham, T. Shwe, W. Mar, Thida Kyaw, K. S. Aye, H. Thu, Khin Khin Oo, Khaing Moe Aung, M. Htun, Ye Myint Kyaw, K. Thant
{"title":"轮状病毒胃肠炎监测(2015-2017年):缅甸轮状病毒疫苗引入前期轮状病毒流行病学和循环轮状病毒基因型","authors":"T. Myat, H. M. Thu, Htin Lin, Nang Sarm Hom, Win Lei Kay Khine, M. Kham, T. Shwe, W. Mar, Thida Kyaw, K. S. Aye, H. Thu, Khin Khin Oo, Khaing Moe Aung, M. Htun, Ye Myint Kyaw, K. Thant","doi":"10.59096/osir.v12i3.262954","DOIUrl":null,"url":null,"abstract":"A hospital-based prospective active surveillance for rotavirus gastroenteritis (RVGE) was conducted among hospitalised acute gastroenteritis (AGE) patients to identify the infecting rotavirus strains and to provide epidemiological information on RVGE in Myanmar. Stool samples were collected from children less than 5 years old admitted to Yangon Children’s Hospital (YCH) for AGE during January 2015 to September 2017. Collected stool samples were screened for rotavirus antigen by ELISA and genotyped by reverse transcription polymerase chain reaction (RT-PCR). Overall, 48.8% (1,167/2,393) of samples were ELISA positive for rotavirus and the most affected were children aged 6-23 months, 81.9% (956/1,167). RVGE occurred in a seasonal cycle with peak detection in the cold and dry months (November to February). As compared with non-RVGE, RVGE cases had significant higher percentage of vomiting (84.5% versus 73.0%; P<0.05), fever (80.1% versus 71.8%; P<0.05) and severe clinical scoring (79.4% versus 67.5%; P<0.05). Genotyping revealed that G9P[8] was predominant in the year 2015 (53.3%) and 2016 (30.9%), but it was replaced in 2017 by G3P[8] (58.2%). Information from this surveillance not only highlights facts for consideration of rotavirus vaccine introduction plan in pre-vaccination era, but also provides vital baseline data for post-vaccination monitoring of vaccine impact and effectiveness.","PeriodicalId":296285,"journal":{"name":"Outbreak, Surveillance, Investigation & Response (OSIR) Journal","volume":"31 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Surveillance of Rotavirus Gastroenteritis (2015-2017): Epidemiology and Circulating Rotavirus Genotypes in Pre-rotavirus Vaccine Introduction Period in Myanmar\",\"authors\":\"T. Myat, H. M. Thu, Htin Lin, Nang Sarm Hom, Win Lei Kay Khine, M. Kham, T. Shwe, W. Mar, Thida Kyaw, K. S. Aye, H. Thu, Khin Khin Oo, Khaing Moe Aung, M. Htun, Ye Myint Kyaw, K. 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As compared with non-RVGE, RVGE cases had significant higher percentage of vomiting (84.5% versus 73.0%; P<0.05), fever (80.1% versus 71.8%; P<0.05) and severe clinical scoring (79.4% versus 67.5%; P<0.05). Genotyping revealed that G9P[8] was predominant in the year 2015 (53.3%) and 2016 (30.9%), but it was replaced in 2017 by G3P[8] (58.2%). 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引用次数: 2
摘要
对缅甸住院急性胃肠炎(AGE)患者进行了轮状病毒胃肠炎(RVGE)的医院前瞻性主动监测,以确定感染轮状病毒株并提供有关RVGE的流行病学信息。收集了2015年1月至2017年9月期间仰光儿童医院(YCH)因AGE入院的5岁以下儿童的粪便样本。收集粪便标本,采用ELISA法筛选轮状病毒抗原,逆转录聚合酶链反应(RT-PCR)分型。总体而言,48.8%(1167 / 2393)的样本轮状病毒酶联免疫吸附试验呈阳性,其中6-23月龄儿童感染最多,为81.9%(956/ 1167)。RVGE的发生具有季节性,在寒冷和干燥月份(11月至2月)达到高峰。与非RVGE患者相比,RVGE患者的呕吐率显著高于非RVGE患者(84.5% vs 73.0%;P<0.05),发热(80.1%比71.8%;P<0.05)和重度临床评分(79.4% vs 67.5%;P < 0.05)。基因分型显示G9P[8]在2015年(53.3%)和2016年(30.9%)占主导地位,但在2017年被G3P[8](58.2%)取代。来自这一监测的信息不仅突出了在疫苗接种前考虑轮状病毒疫苗引入计划的事实,而且还为疫苗接种后监测疫苗影响和有效性提供了重要的基线数据。
Surveillance of Rotavirus Gastroenteritis (2015-2017): Epidemiology and Circulating Rotavirus Genotypes in Pre-rotavirus Vaccine Introduction Period in Myanmar
A hospital-based prospective active surveillance for rotavirus gastroenteritis (RVGE) was conducted among hospitalised acute gastroenteritis (AGE) patients to identify the infecting rotavirus strains and to provide epidemiological information on RVGE in Myanmar. Stool samples were collected from children less than 5 years old admitted to Yangon Children’s Hospital (YCH) for AGE during January 2015 to September 2017. Collected stool samples were screened for rotavirus antigen by ELISA and genotyped by reverse transcription polymerase chain reaction (RT-PCR). Overall, 48.8% (1,167/2,393) of samples were ELISA positive for rotavirus and the most affected were children aged 6-23 months, 81.9% (956/1,167). RVGE occurred in a seasonal cycle with peak detection in the cold and dry months (November to February). As compared with non-RVGE, RVGE cases had significant higher percentage of vomiting (84.5% versus 73.0%; P<0.05), fever (80.1% versus 71.8%; P<0.05) and severe clinical scoring (79.4% versus 67.5%; P<0.05). Genotyping revealed that G9P[8] was predominant in the year 2015 (53.3%) and 2016 (30.9%), but it was replaced in 2017 by G3P[8] (58.2%). Information from this surveillance not only highlights facts for consideration of rotavirus vaccine introduction plan in pre-vaccination era, but also provides vital baseline data for post-vaccination monitoring of vaccine impact and effectiveness.