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D. Herzig (1), G. Glaeske (2), W. Schramm (3)
(1) Kompetenzzentrum Arzneimittel, AOK Schleswig-Holstein, Kiel; (2) Zentrum für Sozialpolitik, Universität Bremen; (3) Abt. Transfusionsmedizin und Hämostaseologie, Klinikum der Universität München
Although hospitals primarily provide treatment for in-patients, treatment is also given to a large number of out-patients. The law covering haemophilia patients, who receive their treatment as out-patients, actually has several different bases. This has advantages and disadvantages. The question concerning us: Which, at the moment, is the best legal basis for any care-agreement? Another important factor for any agreement between the two parties, is that there should be a broad consensus, based on shared interests. The common aim should be the future guarantee for the treatment of patients suffering from haemophilia in suitable medical facilities. At the same time care must be taken to provide an efficient and economically viable care-service for these patients, as well as ensuring that the quality and efficiency of the service remain transparent.
Agreement, hospital, Haemophilia, registry, out-patients treatment
| 1. | ||
B. Haschberger (1), J. Hesse (1), M. Heiden (1), R. Seitz (1), W. Schramm (2, 3) Hämostaseologie Supplement 2010 2010 30 1: S62-S64 | ||
| 2. | Update and annual survey 2009 | |
N. von der Weid (1) Hämostaseologie Supplement 2010 2010 30 1: S15-S19 | ||
| 3. | Up-date 2008 | |
S. Reitter (1), R. Sturn (1), W. Streif (2), T. Schabetsberger (3), F. Wozak (3), C. Male (4), W. Muntean (5), I. Pabinger (1) Hämostaseologie Supplement 2009 2009 29: 13-15 | ||