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Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals
BACKGROUND: Various international studies have shown that a substantial number of patients suffer from injuries or even die as a result of care delivered in hospitals. The occurrence of injuries among patients caused by health care management in Dutch hospitals has never been studied systematically....
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810530/ https://www.ncbi.nlm.nih.gov/pubmed/17319971 http://dx.doi.org/10.1186/1472-6963-7-27 |
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author | Zegers, Marieke de Bruijne, Martine C Wagner, Cordula Groenewegen, Peter P Waaijman, Roelof van der Wal, Gerrit |
author_facet | Zegers, Marieke de Bruijne, Martine C Wagner, Cordula Groenewegen, Peter P Waaijman, Roelof van der Wal, Gerrit |
author_sort | Zegers, Marieke |
collection | PubMed |
description | BACKGROUND: Various international studies have shown that a substantial number of patients suffer from injuries or even die as a result of care delivered in hospitals. The occurrence of injuries among patients caused by health care management in Dutch hospitals has never been studied systematically. Therefore, an epidemiological study was initiated to determine the incidence, type and impact of adverse events among discharged and deceased patients in Dutch hospitals. METHODS/DESIGN: Three stage retrospective patient record review study in 21 hospitals of 8400 patient records of discharged or deceased patients in 2004. The records were reviewed by trained nurses and physicians between August 2005 and October 2006. In addition to the determination of presence, the degree of preventability, and causes of adverse events, also location, timing, classification, and most responsible specialty of the adverse events were measured. Moreover, patient and admission characteristics and the quality of the patient records were recorded. DISCUSSION: In this paper we report on the design of the retrospective patient record study on the occurrence of adverse events in Dutch hospitals. Attention is paid to the strengths and limitations of the study design. Furthermore, alterations made in the original research protocol in comparison with former international studies are described in detail. |
format | Text |
id | pubmed-1810530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18105302007-03-07 Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals Zegers, Marieke de Bruijne, Martine C Wagner, Cordula Groenewegen, Peter P Waaijman, Roelof van der Wal, Gerrit BMC Health Serv Res Study Protocol BACKGROUND: Various international studies have shown that a substantial number of patients suffer from injuries or even die as a result of care delivered in hospitals. The occurrence of injuries among patients caused by health care management in Dutch hospitals has never been studied systematically. Therefore, an epidemiological study was initiated to determine the incidence, type and impact of adverse events among discharged and deceased patients in Dutch hospitals. METHODS/DESIGN: Three stage retrospective patient record review study in 21 hospitals of 8400 patient records of discharged or deceased patients in 2004. The records were reviewed by trained nurses and physicians between August 2005 and October 2006. In addition to the determination of presence, the degree of preventability, and causes of adverse events, also location, timing, classification, and most responsible specialty of the adverse events were measured. Moreover, patient and admission characteristics and the quality of the patient records were recorded. DISCUSSION: In this paper we report on the design of the retrospective patient record study on the occurrence of adverse events in Dutch hospitals. Attention is paid to the strengths and limitations of the study design. Furthermore, alterations made in the original research protocol in comparison with former international studies are described in detail. BioMed Central 2007-02-25 /pmc/articles/PMC1810530/ /pubmed/17319971 http://dx.doi.org/10.1186/1472-6963-7-27 Text en Copyright © 2007 Zegers et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Study Protocol Zegers, Marieke de Bruijne, Martine C Wagner, Cordula Groenewegen, Peter P Waaijman, Roelof van der Wal, Gerrit Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals |
title | Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals |
title_full | Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals |
title_fullStr | Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals |
title_full_unstemmed | Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals |
title_short | Design of a retrospective patient record study on the occurrence of adverse events among patients in Dutch hospitals |
title_sort | design of a retrospective patient record study on the occurrence of adverse events among patients in dutch hospitals |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810530/ https://www.ncbi.nlm.nih.gov/pubmed/17319971 http://dx.doi.org/10.1186/1472-6963-7-27 |
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