Does a Clinical Pathway Improve the Quality of Care for Sickle Cell Anemia?
- 1 April 2003
- journal article
- Published by Elsevier in The Joint Commission Journal on Quality and Safety
- Vol. 29 (4) , 181-190
- https://doi.org/10.1016/s1549-3741(03)29022-5
Abstract
No abstract availableKeywords
Funding Information
- Health Resources and Services Administration (HRSA) Award, Division of Medicine, Bureau of Health Professions (5T32PE10004-06)
This publication has 32 references indexed in Scilit:
- Why Don't Physicians Follow Clinical Practice Guidelines?JAMA, 1999
- Revised Guidelines for Prevention of Early-onset Group B Streptococcal (GBS) InfectionPediatrics, 1997
- Clinical Practice Guidelines in Pediatric and Newborn Medicine: Implications for Their Use in PracticePediatrics, 1997
- Pain, quality of life, and coping in sickle cell disease.Archives of Disease in Childhood, 1996
- Extending the Application of Critical Path MethodsQuality Management in Health Care, 1995
- An introduction to critical pathsQuality Management in Health Care, 1992
- White blood cell count as a predictor of mortality: Results over 18 years from the normative aging studyJournal of Clinical Epidemiology, 1990
- The relationship between fetal hemoglobin and disease severity in children with sickle cell anemiaAmerican Journal of Medical Genetics, 1987
- Acute admissions of patients with sickle cell disease who live in Britain.BMJ, 1987
- Causes of death in sickle-cell disease in Jamaica.BMJ, 1982