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婴幼儿接种七价结合肺炎球菌疫苗的有效性和成本效益

Effectiveness and cost-effectiveness of general immunisation of infants and young children with the heptavalent conjugated pneumococcal vaccine.

作者信息

Antony Katja, Pichlbauer Ernest, Stürzlinger Heidi

机构信息

ÖBIG - Österreichisches Bundesinstitut für Gesundheitswesen, Wien, Österreich.

出版信息

GMS Health Technol Assess. 2005 Nov 2;1:Doc05.

Abstract

BACKGROUND

The European Agency for the Evaluation of Medicinal Products (EMEA) granted market authorisation to the heptavalent pneumococcal vaccine Prevenar (Wyeth) in the year 2001. The indication of Prevenar is the active immunisation of infants and young children under the age of two against invasive disease caused by Streptococcus pneumonia serotypes 4, 6B, 9V, 14, 18C, 19F and 23F. At the time of this study the German vaccination scheme advises the immunisation with Prevenar only for children at high risk.

OBJECTIVES

The objective of the study is first to determine the efficacy and effectiveness of the immunisation of all children with the heptavalent conjugated pneumococcal vaccine in Germany and second, whether a general recommendation for vaccination of all children would be cost-effective.

METHODS

A systematic literature search was performed in 29 relevant databases for the period of January 1999 to June 2004. Thus 1,884 articles were identified which were then assessed according to predefined selection criteria.

RESULTS

There is evidence for the medical effectiveness of Prevenar against invasive pneumococcal disease caused by the covered serotypes from a major double-blinded RCT undertaken in California. The vaccine shows lower values of effectiveness against otitis media and pneumonia. The values for effectiveness of the vaccine in Germany are below the data for California because of the different incidence of Serotypes. The cost-effectiveness rates for an immunisation of all children with Prevenar vary across different countries. One reason - besides different Health Systems - can be seen in the uncertainty about the duration of protection, another in the assumption on regional serotype coverage of the vaccine. From the healthcare payers' perspective a general vaccination of all children in Germany is not cost-effective, from a societal perspective the benefits from vaccination could prevail the cost. The actual price of the vaccine (if financed by the Healthcare Payer, 2004) has dropped and is lower than the assumed price in the German cost-effectiveness study. This fact could raise the cost-effectiveness-ratio of a general immunisation.

DISCUSSION

The low evidence of information on the herd immunity effect of pneumococcal immunisation, the occurrence on serotype-replacement phenomenon and the effects on the prevalence of antibiotic-resistant strains shall be considered when deciding whether the pneumococcal vaccination for all infants and young children should be added to the German vaccination scheme. There is also little information on the duration of vaccine effectiveness and regional effectiveness because of different serotype incidence. The economic models thus incorporate some uncertainties.

CONCLUSION

At present, relatively few pneumococcal strains in Germany show antibiotic resistance. This situation shall further be observed while improving the data evidence for future decisions (epidemiologic data of incidence of pneumococcal diseases and serotyping of pneumococcal bacteria). From the economic perspective no distinct recommendation to add the conjugated vaccination for all children to the German vaccination scheme can be given. This situation may change if the price for the vaccine further decreases. Furthermore a future cost-effectiveness analysis for Germany should incorporate the effects of the replacement phenomenon, the herd immunisation effects and the effects of the vaccination on the antibiotic-resistant pneumococcal strains.

摘要

背景

欧洲药品评估局(EMEA)于2001年批准七价肺炎球菌疫苗沛儿(惠氏公司生产)上市。沛儿的适应症是对两岁以下婴幼儿进行主动免疫,预防由4、6B、9V、14、18C、19F和23F型肺炎链球菌引起的侵袭性疾病。在本研究开展时,德国的疫苗接种计划建议仅对高危儿童接种沛儿。

目的

本研究的目的一是确定在德国对所有儿童接种七价结合肺炎球菌疫苗的有效性和实际效果,二是确定对所有儿童进行普遍接种建议是否具有成本效益。

方法

在1999年1月至2004年6月期间,对29个相关数据库进行了系统的文献检索。共识别出1884篇文章,然后根据预先确定的选择标准进行评估。

结果

在加利福尼亚州进行的一项大型双盲随机对照试验提供了证据,证明沛儿对其所覆盖血清型引起的侵袭性肺炎球菌疾病具有医学有效性。该疫苗对中耳炎和肺炎的有效性较低。由于血清型发病率不同,德国该疫苗的有效性数值低于加利福尼亚州的数据。对所有儿童接种沛儿的成本效益率在不同国家有所不同。除了卫生系统不同之外,一个原因是保护期的不确定性,另一个原因是对疫苗区域血清型覆盖率的假设。从医疗保健支付方的角度来看,对德国所有儿童进行普遍接种不具有成本效益,从社会角度来看,接种疫苗的益处可能超过成本。该疫苗的实际价格(如果由医疗保健支付方出资,2004年)已经下降,低于德国成本效益研究中假设的价格。这一事实可能会提高普遍接种的成本效益比。

讨论

在决定是否应将对所有婴幼儿进行肺炎球菌疫苗接种纳入德国疫苗接种计划时,应考虑肺炎球菌免疫接种的群体免疫效应信息证据不足、血清型替代现象的发生以及对抗生素耐药菌株流行率的影响。由于血清型发病率不同,关于疫苗有效性持续时间和区域有效性的信息也很少。因此,经济模型存在一些不确定性。

结论

目前德国肺炎球菌菌株中显示抗生素耐药的相对较少。在为未来决策改进数据证据(肺炎球菌疾病发病率的流行病学数据和肺炎球菌细菌血清分型)时,应继续观察这种情况。从经济角度来看,无法明确建议将对所有儿童进行结合疫苗接种纳入德国疫苗接种计划。如果疫苗价格进一步下降,这种情况可能会改变。此外,未来针对德国的成本效益分析应纳入替代现象的影响、群体免疫效应以及疫苗接种对抗生素耐药肺炎球菌菌株的影响。

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