Transferring HIS data to population-based cancer registries - concept and first implementations.
作者： Bernhard Breil , Martin Dugas
DOI: 10.3233/978-1-60750-044-5-86
关键词:
摘要: Cancer is the second leading cause of death worldwide and in focus epidemiological research. In Germany cancer registration law stipulates an electronic report to population-based registry (PBCR). this context Comprehensive Centre Munster (CCCM) required a new concept support obligation register diseases. We analysed Hospital Information System (HIS) data structures related documentation PBCR documents. Our main idea was export available items from HIS convert them into import format PBCR. developed XML-based converter reporting procedure. Using can avoid redundant entry supports information workflow within CCCM. provide secondary use beyond clinical routine form reporting, quality assurance
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sci-hub.st 参考文章(10)
D. Max Parkin, Freddie Bray, Evaluation of data quality in the cancer registry: Principles and methods Part II. Completeness. European Journal of Cancer. ,vol. 45, pp. 756- 764 ,(2009) , 10.1016/J.EJCA.2008.11.033
Bernhard Breil, Axel Semjonow, Martin Dugas, HIS-based electronic documentation can significantly reduce the time from biopsy to final report for prostate tumours and supports quality management as well as clinical research BMC Medical Informatics and Decision Making. ,vol. 9, pp. 5- 5 ,(2009) , 10.1186/1472-6947-9-5
Inger Kristin Larsen, Milada Småstuen, Tom Børge Johannesen, Frøydis Langmark, Donald Maxwell Parkin, Freddie Bray, Bjørn Møller, Data quality at the Cancer Registry of Norway: An overview of comparability, completeness, validity and timeliness European Journal of Cancer. ,vol. 45, pp. 1218- 1231 ,(2009) , 10.1016/J.EJCA.2008.10.037
Rebecca Kush, Liora Alschuler, Roberto Ruggeri, Sally Cassells, Nitin Gupta, Landen Bain, Karen Claise, Monica Shah, Meredith Nahm, Implementing Single Source: the STARBRITE proof-of-concept study. Journal of the American Medical Informatics Association. ,vol. 14, pp. 662- 673 ,(2007) , 10.1197/JAMIA.M2157
Freddie Bray, D. Max Parkin, Evaluation of data quality in the cancer registry: Principles and methods. Part I: Comparability, validity and timeliness European Journal of Cancer. ,vol. 45, pp. 747- 755 ,(2009) , 10.1016/J.EJCA.2008.11.032
D Edwards, J Bell, Cancer registries - future development and uses in Britain Journal of Public Health. ,vol. 22, pp. 216- 219 ,(2000) , 10.1093/PUBMED/22.2.216
Donald M. Parkin, The evolution of the population-based cancer registry Nature Reviews Cancer. ,vol. 6, pp. 603- 612 ,(2006) , 10.1038/NRC1948
A Gondos, Freddie Bray, DH Brewster, JWW Coebergh, Timo Hakulinen, MLG Janssen-Heijnen, Juozas Kurtinaitis, Hermann Brenner, EUNICE Survival Working Group, Recent trends in cancer survival across Europe between 2000 and 2004: a model-based period analysis from 12 cancer registries. European Journal of Cancer. ,vol. 44, pp. 1463- 1475 ,(2008) , 10.1016/J.EJCA.2008.03.010
H.-P. Spötl, E. Ammenwerth, The time needed for clinical documentation versus direct patient care. A work-sampling analysis of physicians' activities. Methods of Information in Medicine. ,vol. 48, pp. 84- 91 ,(2009) , 10.3414/ME0569
S. W Pascoe, R. D Neal, P. L Heywood, V. L Allgar, J. N. Miles, J. Stefoski-Mikeljevic, Identifying patients with a cancer diagnosis using general practice medical records and Cancer Registry data. Family Practice. ,vol. 25, pp. 215- 220 ,(2008) , 10.1093/FAMPRA/CMN023