Report on the Drug Situation 2010 - Bundesministerium für ...
Report on the Drug Situation 2010 - Bundesministerium für ...
Report on the Drug Situation 2010 - Bundesministerium für ...
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nati<strong>on</strong>al quality standards for medical treatment has started later than in o<strong>the</strong>r<br />
countries. The Federal Act <strong>on</strong> <strong>the</strong> Quality of Health-care Services (GQG; BGBl I<br />
2004/179) effective as of 1 January 2005 provides <strong>the</strong> legal framework for <strong>the</strong><br />
advancement of systematic quality research. The Act provides that quality standards<br />
for <strong>the</strong> delivery of health-care services be developed, in cooperati<strong>on</strong> with <strong>the</strong> relevant<br />
stakeholders, in particular <strong>the</strong> health-care professi<strong>on</strong>als involved as well as patients.<br />
Then <strong>the</strong> Federal Minister for Health may ei<strong>the</strong>r issue Federal Quality Guidelines (BQLL)<br />
which recommend <strong>the</strong> use of <strong>the</strong> resulting quality standards or adopt a binding Decree<br />
stipulating <strong>the</strong>ir use as Federal Quality Directives (BQRL). The standards must permit<br />
nati<strong>on</strong>wide implementati<strong>on</strong> across sectors and professi<strong>on</strong>s, and must be in line with<br />
<strong>the</strong> general principles of health promoti<strong>on</strong> and transparency as well as <strong>the</strong> state of <strong>the</strong><br />
art of medicine and experience with regard to effectiveness and efficiency. In order to<br />
perform this task, in 2007 BIQG was established, an institute specialising in healthcare<br />
quality, as a business unit of GÖG, a nati<strong>on</strong>al research and planning institute for<br />
health care in Austria.<br />
Since September 2007, BIQG has focused <strong>on</strong> providing a basis for producing quality<br />
standards. Internati<strong>on</strong>al experience and recommendati<strong>on</strong>s were used as input for<br />
preparing a metaguideline (GÖG under preparati<strong>on</strong>), which defines <strong>the</strong> process of<br />
drawing up guidelines. According to <strong>the</strong> Metaguideline for Methods of Developing and<br />
Implementing Quality Guidelines, organisati<strong>on</strong>s may propose <strong>the</strong>mes for Federal<br />
Quality Guidelines or Directives. These <strong>the</strong>mes are weighted and ranked in a defined<br />
prioritisati<strong>on</strong> process and eventually guidelines are drawn up <strong>on</strong> behalf of <strong>the</strong> Federal<br />
Ministry of Health or <strong>the</strong> Federal Health Agency (BGA). In additi<strong>on</strong>, it is possible to file<br />
applicati<strong>on</strong>s for recogniti<strong>on</strong> of papers as Federal Quality Directives (e.g., if a medical<br />
society or associati<strong>on</strong> has already produced a quality standard): in this case, it is<br />
verified in an accreditati<strong>on</strong> procedure whe<strong>the</strong>r <strong>the</strong> formal criteria for Federal Quality<br />
Directives are met. At present, six <strong>the</strong>mes are being reviewed. In order to draw up a<br />
Federal Quality Guideline or Directive <strong>on</strong> addicti<strong>on</strong> treatment, it would be necessary to<br />
propose this <strong>the</strong>me for fur<strong>the</strong>r examinati<strong>on</strong>.<br />
Both BQLL and BQRL quality standards specify a certain path of acti<strong>on</strong> and decisi<strong>on</strong>making<br />
with regard to treatment and care services and recommend proven, effective<br />
instruments and procedures, departure from which is admissible or may even be<br />
required in well-founded cases. Any deviati<strong>on</strong>s should adequately be documented,<br />
however. Ei<strong>the</strong>r type of standard (BQLL and BQRL) is produced by multidisciplinary<br />
teams in a systematic procedure, with decisi<strong>on</strong>s based <strong>on</strong> c<strong>on</strong>sensus. Different to o<strong>the</strong>r<br />
member states of <strong>the</strong> EU, in Austria <strong>the</strong> focus is not solely placed <strong>on</strong> medical<br />
treatment, but o<strong>the</strong>r services are also included. Any existing medical, care or treatment<br />
standards are taken into c<strong>on</strong>siderati<strong>on</strong> as source standards if <strong>the</strong>ir quality meets <strong>the</strong><br />
defined criteria.<br />
100 © GÖG/ÖBIG, <str<strong>on</strong>g>Report</str<strong>on</strong>g> <strong>on</strong> <strong>the</strong> <strong>Drug</strong> Situati<strong>on</strong> <strong>2010</strong>