Using registry data to improve quality of care
| Autor: | Gilles Rault, Kieran McIntyre, Dominique Pougheon Bertrand |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Pulmonary and Respiratory Medicine
medicine.medical_specialty education.field_of_study Quality management Cystic Fibrosis business.industry Population Health outcomes Quality Improvement 03 medical and health sciences 0302 clinical medicine 030228 respiratory system Family medicine Pediatrics Perinatology and Child Health medicine Humans Registry data Registries 030212 general & internal medicine Quality of care business education |
| Zdroj: | Journal of Cystic Fibrosis. 17:566-572 |
| ISSN: | 1569-1993 |
| DOI: | 10.1016/j.jcf.2018.06.006 |
| Popis: | Patient registries provide clinicians, patients and families with the ability to track important health outcomes at a population, cystic fibrosis (CF) center, and patient level. International quality improvement (QI) work driven by registries has been effective at improving the health and the care delivered to the individual patient. In this review, we examine the role CF registries have played in the QI process over the years and discuss the inherent strengths and limitations that exist when using registry data for this purpose. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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