Szczuka Ireneusz
Przegl Epidemiol. 2002;56(2):205-16.
In Poland, since 1955 BCG mass vaccinations have been compulsory. During the last two decades the vaccination program has been developed and includes: 1) primary vaccination of the newborn, 2) vaccination of children aged 7 and 12, and 3) revaccination of 18 year old adolescents. More than 95% of newborns and about 80% of older children of this population have been vaccinated. BCG vaccine being in use in Poland bases on the Brazilian/Moreau sub strain and has been producing by the Polish Laboratory. Since 1994 the central register of adverse events of BCG has been introduced by National Tuberculosis and Lung Diseases Institute (NTLDRI).
The aim of this study was to evaluate the frequency, trends and clinical type of adverse events after BCG vaccination. In addition, correctness of case-finding and treatment of BCG complications was evaluated.
From January 1, 1994 to December 31, 2000 individual data on adverse events, on special card was reported to NTLDRI. Categories of BCG complications was based on classifications proposed by A. Lotte.
Data of 7,354,780 BCG vaccinated persons was analyzed. Of them 1,559 cases reported AEFI. From the further analysis 98 cases with insufficient data were excluded. The frequency of these cases has been estimated to be 0.2@1000 (2 per 100,000 vaccinated) and was stabile. Among AEFI cases, 773 reported local complication (ulcer, abscess, K.F.) and 647 (44.3%) lymphadenitis including 353 cases with enlargement of lymph nodes and 287 cases of suppurative lymphadenitis (4 per 100,000 vaccinated). Majority of AEFI cases were infants (76%). Only 1 case (infant) with disseminated BCG disease, probably due to the partial interferon gamma receptor deficiency, was reported. Main errors in the diagnosis of complications and the management of adverse events after BCG vaccination were lack of data on the diameter of local changes and size of lymph nodes, as well as attempts to remove the lymph nodes.
The results of the study indicate that BCG vaccinations in Poland rarely produce adverse reactions and therefore may be considered as safe method of tuberculosis prevention. Adverse reactions to BCG appears to be underreported. Surveillance of adverse reactions to vaccines should be included in the national immunization program.
在波兰,自1955年起卡介苗大规模接种成为强制性措施。在过去二十年中,疫苗接种计划不断发展,包括:1)新生儿的初次接种;2)7岁和12岁儿童的接种;3)18岁青少年的复种。该人群中超过95%的新生儿和约80%的大龄儿童已接种疫苗。波兰使用的卡介苗基于巴西/莫罗亚菌株,由波兰实验室生产。自1994年起,国家结核病和肺部疾病研究所(NTLDRI)引入了卡介苗不良事件中央登记系统。
本研究旨在评估卡介苗接种后不良事件的发生频率、趋势和临床类型。此外,还评估了卡介苗并发症的病例发现和治疗的正确性。
1994年1月1日至2000年12月31日期间,关于不良事件的个人数据通过特殊卡片上报给NTLDRI。卡介苗并发症的分类基于A.洛特提出的分类方法。
分析了7354780名接种卡介苗者的数据。其中1559例报告了疑似预防接种异常反应(AEFI)。进一步分析后排除了98例数据不充分的病例。这些病例的发生率估计为0.2‰(每10万接种者中有2例),且较为稳定。在AEFI病例中,773例报告了局部并发症(溃疡、脓肿、瘢痕疙瘩),647例(44.3%)为淋巴结炎,包括353例淋巴结肿大和287例化脓性淋巴结炎(每10万接种者中有4例)。大多数AEFI病例为婴儿(76%)。仅报告了1例(婴儿)播散性卡介苗病病例,可能是由于部分干扰素γ受体缺陷所致。卡介苗接种后并发症诊断和不良事件管理中的主要错误是缺乏局部变化直径和淋巴结大小的数据,以及试图切除淋巴结。
研究结果表明,波兰的卡介苗接种很少产生不良反应,因此可被视为预防结核病的安全方法。卡介苗的不良反应似乎报告不足。疫苗不良反应监测应纳入国家免疫规划。