Clinical Epidemiology (Oct 2016)

The Danish National Database for Obstructive Sleep Apnea

  • Jennum PJ,
  • Larsen P,
  • Cerqueira C,
  • Schmidt T,
  • Tønnesen P

Journal volume & issue
Vol. Volume 8
pp. 573 – 576

Abstract

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Poul Jørgen Jennum,1 Preben Larsen,2 Charlotte Cerqueira,3 Thor Schmidt,4 Philip Tønnesen1 1Department of Clinical Neurophysiology, Faculty of Health Sciences, Danish Center for Sleep Medicine, University of Copenhagen, Rigshospitalet, Copenhagen, 2Section of Respiratory Disease, Medical Department, Fredericia Hospital, Fredericia, 3Registry Support Centre (East) – Epidemiology and Biostatistics, Research Centre for Prevention and Health, 4Registry Support Centre (East) – Clinical Quality Improvement and Health Informatics, Capital Region of Denmark, Copenhagen, Denmark Aim: The aim of the Danish National Database for Obstructive Sleep Apnea (NDOSA) was to evaluate the clinical quality (diagnostic, treatment, and management) for obstructive sleep apnea and obesity hypoventilation syndrome in Denmark using a real-time national database reporting to the Danish National Patient Registry. Study population: All patients diagnosed with obstructive sleep apnea or obesity hypoventilation syndrome at public and private in- and out-hospital departments in Denmark were included. Main variables: The NDOSA contains information about baseline characteristics, comorbidity, diagnostic procedures conducted, treatment (continuous positive airway pressure and similar treatments, surgery, mandibular advancement devices, etc) complications, and treatment status. Descriptive data: Yearly report with indicators for diagnostic procedures, treatment, and follow-up comparing different departments was involved in the management of sleep apnea in Denmark for the purpose of quality improvement. Conclusion: The NDOSA has proven to be a real-time national database using diagnostic and treatment procedures reported to the Danish National Patient Registry. Keywords: obstructive sleep apnea, obesity hypoventilation syndrome, quality of care, clinical registry

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