The psychosocial impact of leg ulcers in patients with sickle cell disease: I don’t want them to know my little secret

Keyphrases

• Sickle Cell Disease 100%
• Leg Ulcer 100%
• Psychosocial Impact 100%
• Social Isolation 42%
• Physical Function 42%
• Psychosocial Factors 28%
• Disease-associated 28%
• Quality of Life 28%
• Ulcer 28%
• Living with 28%
• Social Relationships 28%
• United States 14%
• Clinical Manifestations 14%
• Cutaneous Manifestations 14%
• Health Status 14%
• Clinical Approach 14%
• Structured Interview 14%
• Pain Intensity 14%
• Embarrassment 14%
• Social Networks 14%
• Disease Impact 14%
• Relationship Support 14%
• Pain Acute 14%
• Pain Duration 14%
• Religious Support 14%
• Family Social 14%
• Qualitative Phase 14%
• Religion/spirituality 14%
• Self-induced 14%
• Pain Chronicity 14%
• Chronic Leg Ulcer 14%
• Family Support Network 14%

Nursing and Health Professions

• Patient with Sickle Cell Disease 100%
• Leg Ulcer 100%
• Sickle Cell Anemia 50%
• Social Isolation 37%
• Physical Function 37%
• Ulcer 25%
• Patient Social Context 25%
• Quality of Life 25%
• Pain 12%
• Health Status 12%
• Medical Decision Making 12%
• Chronic Pain 12%
• Thematic Analysis 12%
• Social Network 12%
• Family Relationship 12%
• Salicylate Sodium 12%

Medicine and Dentistry

• Patient with Sickle Cell Disease 100%
• Leg Ulcer 100%
• Sickle-Cell Disease 50%
• Social Isolation 37%
• Quality of Life 25%
• Ulcer 25%
• Patient Social Context 25%
• Social Interaction 25%
• Chronic Pain 12%
• Pain 12%
• Health Status 12%
• Medical Decision Making 12%
• Social Network 12%
• Salicylate Sodium 12%
• Family Relationship 12%