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澳大利亚人乳头瘤病毒疫苗的安全性:目前的经验及监测问题

Human papillomavirus vaccine safety in Australia: experience to date and issues for surveillance.

作者信息

Gold Michael S, McIntyre Peter

机构信息

Discipline of Paediatrics, School of Paediatrics and Reproductive Health, University of Adelaide, SA 5001, Australia.

出版信息

Sex Health. 2010 Sep;7(3):320-4. doi: 10.1071/SH09153.

Abstract

Australia was one of the first countries to licence a quadrivalent human papillomavirus (HPV) vaccine, rapidly followed by a federally funded program of universal vaccination of a broad age group of females through schools (12 to 18 years) and primary care (19 to 26 years). As of August 2009, more than 5.8 million doses of Gardasil((R)) (quadrivalent; Merck, New Jersey, USA) have been distributed in Australia and a total of 1394 suspected adverse events following immunisation (AEFI) have been reported to the passive surveillance system. Most reports are of common and expected reactions. Case series of more uncommon and serious AEFI, both known to be potentially vaccine related (anaphylaxis, conversion disorders and lipoatrophy) and otherwise (multiple sclerosis and pancreatitis) have been published.

摘要

澳大利亚是最早批准四价人乳头瘤病毒(HPV)疫苗上市的国家之一,随后迅速开展了一项由联邦政府资助的项目,通过学校(12至18岁)和初级保健机构(19至26岁)对广大年龄组的女性进行普遍接种。截至2009年8月,澳大利亚已分发了超过580万剂加德西(Gardasil)(四价;美国新泽西州默克公司),被动监测系统共收到1394例免疫接种后疑似不良事件(AEFI)报告。大多数报告为常见和预期反应。已发表了关于更罕见和严重AEFI的病例系列,包括已知可能与疫苗相关的(过敏反应、转换障碍和脂肪萎缩)以及其他情况(多发性硬化症和胰腺炎)。

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