The Cystic Fibrosis Foundation Patient Registry as a tool for use in quality improvement.
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Longevity of Patients With Cystic Fibrosis in 2000 to 2010 and Beyond: Survival Analysis of the Cystic Fibrosis Foundation Patient RegistryAn overview of international literature from cystic fibrosis registries. Part 5: Update 2012-2015 on lung disease.Background and EpidemiologyOnset of persistent pseudomonas aeruginosa infection in children with cystic fibrosis with interval censored data.A blue fluorescent labeling technique utilizing micro- and nanoparticles for tracking in LIVE/DEAD® stained pathogenic biofilms of Staphylococcus aureus and Burkholderia cepaciaImproving chronic care delivery and outcomes: the impact of the cystic fibrosis Care Center Network.Accelerating implementation of biomedical research advances: critical elements of a successful 10 year Cystic Fibrosis Foundation healthcare delivery improvement initiative.Patient experience in cystic fibrosis care: Development of a disease-specific questionnaire.Implementing quality measures for inflammatory bowel disease.Socioeconomic status and health outcomes: cystic fibrosis as a model.The utility of including pathology reports in improving the computational identification of patients.The Cystic Fibrosis Foundation Patient Registry. Design and Methods of a National Observational Disease Registry.Data that empower: The success and promise of CF patient registries.Impact of clinical registries on quality of patient care and clinical outcomes: A systematic review.Weight gain during acute treatment of an initial pulmonary exacerbation is associated with a longer interval to the next exacerbation in adults with cystic fibrosis.Changing Epidemiology of the Respiratory Bacteriology of Patients With Cystic Fibrosis.Reducing practice variation through clinical pathways-Is it enough?A Person-Centered, Registry-Based Learning Health System for Palliative Care: A Path to Coproducing Better Outcomes, Experience, Value, and Science.Are data from national quality registries used in quality improvement at Swedish hospital clinics?Comparison of Nutrition and Lung Function Outcomes in Patients with Cystic Fibrosis Living in Canada and the United States.Longitudinal development of initial, chronic and mucoid Pseudomonas aeruginosa infection in young children with cystic fibrosis.
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The Cystic Fibrosis Foundation Patient Registry as a tool for use in quality improvement.
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article científic
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The Cystic Fibrosis Foundation Patient Registry as a tool for use in quality improvement.
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The Cystic Fibrosis Foundation Patient Registry as a tool for use in quality improvement.
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The Cystic Fibrosis Foundation Patient Registry as a tool for use in quality improvement.
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P2860
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The Cystic Fibrosis Foundation Patient Registry as a tool for use in quality improvement.
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Aliza K Fink
Karen Homa
Michael S Schechter
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P356
10.1136/BMJQS-2013-002378
P478
23 Suppl 1
P577
2014-01-17T00:00:00Z