| Literature DB >> 22269341 |
Joachim Szecsenyi1, Bjoern Broge, Joerg Eckhardt, Guenther Heller, Petra Kaufmann-Kolle, Michel Wensing.
Abstract
The hospital benchmarking system in Germany was originally introduced to detect unintended consequences of reimbursement based on diagnosis-related groups. The new nationwide SQG programme aims to provide information on quality and outcomes of health care provided in hospital, ambulatory specialist and primary care settings, including the healthcare delivery across different sectors. In 2010 the topics for indicator development were cataract surgery, cervical conization, colectoral cancer and percutaneous coronary interventions or coronary angiography. A systematic stepwise modified RAND/UCLA procedure is applied to develop quality indicators in each of these domains. A general framework for data collection is implemented. Benchmarking results are fed back to providers on a regular basis.Entities:
Mesh:
Year: 2012 PMID: 22269341 PMCID: PMC3297368 DOI: 10.1093/intqhc/mzr086
Source DB: PubMed Journal: Int J Qual Health Care ISSN: 1353-4505 Impact factor: 2.038
Steps in the development of quality monitoring for a specific topic
The Federal Joint Committee defines a topic for quality monitoring and improvement, after consultation with various stakeholders. The AQUA-institute invites experts and stakeholders for a scoping workshop to discuss key issues for indicator development. The AQUA-institute starts a public procedure to recruit experts for a panel. Additionally, two patient representatives are nominated by patient organizations for the panel. All panel members have to state their conflicts of interest. A structured search for indicators from agencies worldwide and systematic literature searches is performed. Duplicates are deleted from the list of potential indicators. After an introductory workshop where panelists are informed and trained, two panel-rounds each with written ratings and face-to-face discussions are performed. This results in the final set of indicators. Instruments for data collection (such as for the electronic clinical records) for the indicators are developed and data fields are described. A preliminary report which describes the development process, the set of indicators and the instruments in detail is sent out to all relevant stakeholder organizations. These have 6 weeks to send their comments back. A final report with an appraisal of the comments is completed by the AQUA-institute within 6 weeks. The Federal Joint Committee officially approves the final report. The Federal Joint Committee decides whether a feasibility study and field testing is needed. After final positive evaluation, a directive of the Federal Joint Committee makes quality measurement and monitoring, mandatory for all health care providers. A planning is made and communicated for inclusion of indicators in data collection and in the annual reports that are provided by the AQUA-institute. |