Puig-Junoy Jaume, Moreno-Torres Iván
Research Centre for Economics and Health (CRES), Department of Economics and Business, Universitat Pompeu Fabra, Barcelona, Spain.
Pharmacoeconomics. 2007;25(8):637-48. doi: 10.2165/00019053-200725080-00002.
Policies consisting of or including prior authorisation (PA) of pharmaceutical prescriptions have been increasingly implemented by public and private insurers in the last decade, especially in the US, in order to control drug spending. We conducted a systematic review of published articles determining the effects of these policies on drug use, healthcare utilisation, healthcare expenditures and health outcomes.A literature search was carried out in the electronic databases PubMed (which includes MEDLINE), EconLit, Web of Science and online sources including Google Scholar, from 1 January 1985 to 12 September 2006. Reference lists of retrieved articles were also searched. Peer-reviewed studies that provided empirical results about the impact of pharmaceutical PA policies, including randomised and non-randomised controlled trials, repeated measures studies, interrupted time series analyses and before-and-after studies were included. Use of, and expenditure on, directly affected drugs per patient, and overall drug expenditure, significantly decreased after PA implementation, or increased after PA removal. Health outcome changes attributed to PA policies were not directly evaluated. In most cases, except for cimetidine, PA implementation was not associated with significant changes in the utilisation of other medical services. Although the literature indicates a reduction in drug expenditure and a non-negative impact on use of other health services, policy recommendations still require improved study designs, and evidence cannot be easily transferred from one setting to another. The evidence still remains mainly limited to US Medicaid settings and to a small number of drug classes. There is a lack of consideration of implications of PA policies as heterogeneous interventions, outcome measurements require improvement, and there is a notable lack of evidence of medium- and long-term policy effects.
在过去十年中,公共和私人保险公司越来越多地实施了包含或包括药品处方预先授权(PA)的政策,尤其是在美国,目的是控制药品支出。我们对已发表的文章进行了系统综述,以确定这些政策对药物使用、医疗保健利用、医疗保健支出和健康结果的影响。我们在电子数据库PubMed(包括MEDLINE)、EconLit、Web of Science以及包括谷歌学术在内的在线资源中进行了文献检索,检索时间范围为1985年1月1日至2006年9月12日。我们还检索了所检索文章的参考文献列表。纳入了提供有关药品PA政策影响的实证结果的同行评审研究,包括随机和非随机对照试验、重复测量研究、中断时间序列分析和前后研究。PA实施后,每位患者直接受影响药物的使用和支出以及总体药物支出显著下降,或在PA取消后增加。未直接评估归因于PA政策的健康结果变化。在大多数情况下,除了西咪替丁外,PA的实施与其他医疗服务利用的显著变化无关。尽管文献表明药品支出有所减少,且对其他医疗服务的使用没有负面影响,但政策建议仍需要改进研究设计,而且证据不易从一种情况转移到另一种情况。证据仍然主要局限于美国医疗补助计划的情况以及少数药物类别。缺乏对PA政策作为异质性干预措施影响的考虑,结果测量需要改进,而且明显缺乏中长期政策效果的证据。