Patient-reported experience measure in sickle cell disease.

Keyphrases

• Patient-reported Experience Measures 100%
• Sickle Cell Disease 100%
• Experience of Care 42%
• Cognitive Testing 42%
• Focus Group Discussion 28%
• Carers 28%
• Patient Demographics 14%
• Online Questionnaire 14%
• Health Care Services 14%
• Young People 14%
• Lived Experience 14%
• Healthcare Professionals 14%
• Questionnaire Development 14%
• Construct Validity 14%
• Quality of Care 14%
• In Care 14%
• Service Delivery 14%
• Patient Experience 14%
• Service Improvement 14%
• Emergency Setting 14%
• Hospital Setting 14%
• Validated Questionnaire 14%
• Service Development 14%
• Community Events 14%
• Pain Relief 14%
• Stakeholder Consultation 14%
• Construct Validation 14%
• Non-hospital 14%
• Validity Evidence 14%
• Planned Care 14%
• Picker 14%
• Face Completion 14%

Nursing and Health Professions

• Sickle Cell Anemia 100%
• Patient with Sickle Cell Disease 66%
• Health Service 33%
• Lived Experience 33%
• Health Care Personnel 33%
• Hospital 33%
• Prevalence 33%
• Patient Population 33%
• Health Care Delivery 33%
• Service Development 33%
• Adolescent 33%
• Analgesia 33%
• Hospital Setting 33%
• Construct Validity 33%

Medicine and Dentistry

• Sickle-Cell Disease 100%
• Sickle Cell 66%
• Patient with Sickle Cell Disease 66%
• Personal Experience 33%
• Consultation 33%
• Prevalence 33%
• Analgesia 33%
• Patient Experience 33%
• Patient Population 33%
• Adolescence 33%