A pilot study on the effects of the transition of paediatric to adult health care in patients with haemophilia and in their parents: Patient and parent worries, parental illness-related distress and health-related Quality of Life

Haemophilia

Volumn 14, Issue 5, 2008, Pages 1007-1013

  Geerts, Erwin ^a   Van De Wiel, H ^a   Tamminga, R ^b  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^b UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

Haemophilia; Psychosocial effects; Quality of life; Transition

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHILD CARE; CLINICAL ARTICLE; DISTRESS SYNDROME; FEMALE; HEALTH CARE SYSTEM; HEALTH PROGRAM; HEALTH SERVICE; HEMOPHILIA; HUMAN; MALE; PARENTAL BEHAVIOR; PILOT STUDY; PRIORITY JOURNAL; QUALITY OF LIFE; SCORING SYSTEM; SELF CONCEPT; SOCIAL PSYCHOLOGY;

ADOLESCENT; ADOLESCENT HEALTH SERVICES; ADULT; ANXIETY; ATTITUDE TO HEALTH; CONTINUITY OF PATIENT CARE; FAMILY HEALTH; FEMALE; HEALTH STATUS INDICATORS; HEMOPHILIA A; HUMANS; MALE; MIDDLE AGED; NETHERLANDS; PARENTS; PATIENT SATISFACTION; PILOT PROJECTS; PSYCHOMETRICS; QUALITY OF LIFE; SEX FACTORS; STRESS, PSYCHOLOGICAL; YOUNG ADULT;

EID: 51249121541     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2008.01798.x     Document Type: Article

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