IQWiG - Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen
"The evaluation of the benefits and harms of medical procedures following the methods of evidence based medicine is one of the main principles of every health technology assessment."
Prof. Dr. Peter T. Sawicki
Director, IQWiG
History and structure
With the introduction of the healthcare reform in 2003 (Health Care Modernization Act), legislation enabled the establishment of a new institute, independent of the state, within the German healthcare system. In June 2004, the Federal Joint Committee (Gemeinsamer Bundesausschuss) set up the Institute for Quality and Efficiency in Health Care (IQWiG) as a non-profit, non-government, private foundation with legal status. (The Federal Joint Committee is the decision-making body for self-administration of German healthcare services.)
The Institute is an establishment of the foundation and under independent scientific management. The Foundation's governing bodies include the Foundation Board and the Board of Directors. The Institute's advisory committees are the Board of Trustees and the Scientific Advisory Board.
IQWiG is financed by contributions from the statutory health insurance and may also accept funding from the Federal Ministry of Health.
Mission
The Institute's primary goal is to contribute to improvements in health care in Germany. IQWiG undertakes and publishes assessments addressing the effectiveness, quality, and efficiency of health services, and is particularly active in the following areas: evaluating the benefits and harms of drug and non-drug interventions; evaluating evidence-based guidelines for diseases having the greatest epidemiological importance, and providing easily understandable general information to the public on the quality and efficiency of health care.
IQWiG's responsibilities were expanded from April 1, 2007 with the "Act to Promote Competition" of statutory health insurance (GKV Wettbewerbsstärkungsgesetz). For drugs, IQWiG was previously only commissioned to conduct benefit assessments (ie, to evaluate benefits and harms of drug interventions), but now may also consider costs and perform cost-benefit assessments.
How IQWiG works
The Institute produces reports on specific topics requested by the Federal Joint Committee or the Federal Ministry of Health, following the principles of evidence based medicine. IQWiG also undertakes projects and research work on its own initiative. The work of the Institute's staff is supplemented by external contracting of projects, which are advertised publicly. Work on these projects must be conducted according to the current methods of the Institute (the English version is available under www.iqwig.de/download/englische_uebersetzung_methoden_vers2.pdf).
Stakeholders and interested public citizens can also become involved in the work of the Institute. IQWiG publishes all results of its work on the Internet, and interested persons and parties may submit written comments on report plans (protocols) and on the preliminary reports. This written hearing may lead to changes in the final report.
Dissemination activities
IQWiG publishes its methods and the preliminary and final results of its work on the website www.iqwig.de. This information is targeted at a scientific audience.
As part of its legislative mandate to inform the public, IQWiG also publishes a bilingual website for consumers and patients (www.gesundheitsinformation.de; www.informedhealthonline.org). The website includes information based on the Institute's own scientific publications and on topics it chooses. The website will also include items of patient information commissioned by the Federal Joint Committee or Federal Ministry of Health.
Dissemination activities involve communication with the media and organizing and participating in scientific meetings and workshops.
Current projects
The Federal Joint Committee has awarded a series of research commissions, ranging widely in content, to the Institute. Among other projects, the Institute will analyze drug therapies in comparison to each other and in comparison to non-drug therapies for widespread diseases, eg, diabetes mellitus types 1 and 2, hypertension, asthma, and depression. Further responsibilities include evaluation of the following topics: stem cell transplantation for selected indications (eg, acute myeloblastic leukemia); early diagnosis of defective hearing in newborns; positron emission tomography (PET) and PET/computer tomography for 14 indications; and the quality of health care in children with cancer.
IQWiG is also developing methodology to assess clinical practice guidelines.
Future plans
Creating and maintaining reliable and stable cooperation with external partners is essential to IQWiG. Hence, we are forming and financially supporting a worldwide network of research groups to recruit external experts on a long-term basis. We are working to expand our national and international collaboration. IQWiG has established a regular exchange with counterparts in France (HAS) and Britain (NICE). As a first step, we are discussing our respective methods and assessing whether, and to what extent, they are compatible. Our long-term aim is to foster better and broader cooperation, including the exchange of methods and results with several countries.
Information box
Country: Germany
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Contact information
Director: Prof. Dr. Peter T. Sawicki
Contact person: Dr. Peter Kolominsky-Rabas
Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen
Dillenburger Str. 27
DE-51105 Cologne Germany
Tel:
+49 221 35685 6
Fax:
+49 221 35685 804
Internet:
http://www.iqwig.deEmail:
peter.kolominsky-rabas@iqwig.de