Synopsis:
Clinical evidence research needs to uncover as much relevant literature as possible to be reliable. Medical databases such as Embase and MEDLINE, are highly structured with complex indexing rules; but a key advantage of these databases is that they can be searched electronically both for words in the title or abstract (free text) and by using the standardised indexing terms (controlled vocabulary of subject headings), assigned to each record. However, a certain level of skill and experience is necessary to achieve good (sensitive and precise) results. To systematically retrieve a maximum number of references and extract the evidence, it is necessary to plan the search strategy in advance. Formulating a focussed search question, aids the search strategy design and optimises the process used to identify relevant results.
The review question provides the framework for the search elements and the inter-relationship between these concepts. PICO is a four-part model used to identify the main concepts being examined – PICO is an acronym for patient (or participant or population or problem), intervention, comparison and outcome. PICO plus study design become the architectural elements for the electronic search. The Peer Review of Electronic Search Strategies Guideline for literature searching with its evidence based checklist component provides the basis upon which a search strategy may be assessed. This presentation plans to highlight these initiatives and other factors to consider when translating a review question, developing a search brief or designing search strategies.
Target audience:
All, but especially anyone likely to be responsible for preparing a brief from which searches are conducted.
Learning objectives :
Part 2: Health Technology Assessment in Australia – Who Said What, When: A Literature Review
As the role of health technology assessment (HTA) agencies becomes more influential, decisions to list drugs on national formularies are increasingly subjected to scrutiny across many jurisdictions. Various players within the pharmaceutical market have sought to deepen their understanding of the role of HTA agencies, amidst tightening budgetary controls imposed by payers in response to escalating costs. Parallel to this observation is the increasing number of research publications that examined the role of HTA agencies.
With this in mind, a literature review was conducted focusing on the Pharmaceutical Benefits Advisory Committee (PBAC). Some articles can be traced to the early 1990s, a period which coincided with the compulsory inclusion of an economic assessment in new drug applications seeking public subsidy. Drummond1 and Henry2 separately highlighted Australia as the first country that was using economic evaluation to inform policy decisions on the rational diffusion of health technology. Both authors commented on the PBAC Guidelines of which key aspects remain until today, such as the choice of the comparator drug, the evaluation perspective, the range of costs and the valuation of outcomes.
The growing influence of the PBAC has been matched by the increasing number of publications found in the literature. These included studies which examined the timeliness of patient access3, factors that influence PBAC outcomes4 and the industry methodology in estimating health-related QoL5. Others compared the PBAC with different HTA agencies in their decision-making6,7 and their broader policy implications on social fairness8 and political acceptability9.
Given the diversity of articles with wide ranging subject matter, the aim of the presentation is to provide a framework to look at these publications broadly in order to uncover some general themes and trends that may contribute to a better understanding of what the literature says about the HTA environment in this country.
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