{"title":"1985-1990年爱沙尼亚永久性儿童听力障碍的流行病学研究。","authors":"K Uus, A C Davis","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>This paper describes a retrospective study of permanent childhood hearing impairment (PCHI) > or = 40 dB HL in the better ear in children born between 1985 and 1990 and resident in Estonia. The prevalence rate of all permanent hearing impairment for the birth cohort 1985-1990 was 172 (95 per cent (CI 151-194) per 100,000 live births and that of congenital impairment was 152 (CI 134-170) per 100,000. For the congenitally-impaired children, 11 per cent had stayed in a neonatal intensive care unit for 48 hours or more, 2 per cent had a craniofacial abnormality, and 31 per cent had a family history of PCHI. As for aetiology, hereditary causes were stated most frequently in 36 per cent of all of the cases of PCHI. The aetiology remained unknown in 34 per cent of cases. Additional disabilities were found in 23 per cent of all cases. Specific syndromes were recognized in 2 per cent of hereditary cases. The mean age at the confirmation of hearing impairment was 46.4 months and at hearing aid fitting 57.0 months. The results were compared with other European studies, particularly the Trent study.</p>","PeriodicalId":75571,"journal":{"name":"Audiology : official organ of the International Society of Audiology","volume":"39 4","pages":"192-7"},"PeriodicalIF":0.0000,"publicationDate":"2000-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Epidemiology of permanent childhood hearing impairment in Estonia, 1985-1990.\",\"authors\":\"K Uus, A C Davis\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This paper describes a retrospective study of permanent childhood hearing impairment (PCHI) > or = 40 dB HL in the better ear in children born between 1985 and 1990 and resident in Estonia. The prevalence rate of all permanent hearing impairment for the birth cohort 1985-1990 was 172 (95 per cent (CI 151-194) per 100,000 live births and that of congenital impairment was 152 (CI 134-170) per 100,000. For the congenitally-impaired children, 11 per cent had stayed in a neonatal intensive care unit for 48 hours or more, 2 per cent had a craniofacial abnormality, and 31 per cent had a family history of PCHI. As for aetiology, hereditary causes were stated most frequently in 36 per cent of all of the cases of PCHI. The aetiology remained unknown in 34 per cent of cases. Additional disabilities were found in 23 per cent of all cases. Specific syndromes were recognized in 2 per cent of hereditary cases. The mean age at the confirmation of hearing impairment was 46.4 months and at hearing aid fitting 57.0 months. The results were compared with other European studies, particularly the Trent study.</p>\",\"PeriodicalId\":75571,\"journal\":{\"name\":\"Audiology : official organ of the International Society of Audiology\",\"volume\":\"39 4\",\"pages\":\"192-7\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Audiology : official organ of the International Society of Audiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Audiology : official organ of the International Society of Audiology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
本文描述了1985年至1990年出生的爱沙尼亚居民的永久性儿童听力障碍(PCHI) >或= 40 dB HL的较好耳的回顾性研究。1985-1990年出生队列中所有永久性听力障碍的患病率为每10万活产172例(95% (CI 151-194)),先天性听力障碍患病率为每10万活产152例(CI 134-170)。对于先天受损的儿童,11%在新生儿重症监护病房待了48小时或更长时间,2%有颅面异常,31%有PCHI家族史。至于病因,遗传原因在所有PCHI病例中最常见,占36%。34%的病例病因不明。在所有病例中,有23%发现有其他残疾。在2%的遗传病例中发现了特定综合征。确诊听力障碍时的平均年龄为46.4个月,助听器验配时的平均年龄为57.0个月。研究结果与其他欧洲研究,特别是特伦特研究进行了比较。
Epidemiology of permanent childhood hearing impairment in Estonia, 1985-1990.
This paper describes a retrospective study of permanent childhood hearing impairment (PCHI) > or = 40 dB HL in the better ear in children born between 1985 and 1990 and resident in Estonia. The prevalence rate of all permanent hearing impairment for the birth cohort 1985-1990 was 172 (95 per cent (CI 151-194) per 100,000 live births and that of congenital impairment was 152 (CI 134-170) per 100,000. For the congenitally-impaired children, 11 per cent had stayed in a neonatal intensive care unit for 48 hours or more, 2 per cent had a craniofacial abnormality, and 31 per cent had a family history of PCHI. As for aetiology, hereditary causes were stated most frequently in 36 per cent of all of the cases of PCHI. The aetiology remained unknown in 34 per cent of cases. Additional disabilities were found in 23 per cent of all cases. Specific syndromes were recognized in 2 per cent of hereditary cases. The mean age at the confirmation of hearing impairment was 46.4 months and at hearing aid fitting 57.0 months. The results were compared with other European studies, particularly the Trent study.