Caregiving time in sickle cell disease: Psychological effects in maternal caregivers

Pediatric Blood and Cancer

Volumn 48, Issue 1, 2007, Pages 64-71

  Moskowitz, Judith Tedlie ^a   Butensky, Ellen ^b   Harmatz, Paul ^b   Vichinsky, Elliott ^b   Heyman, Melvin B ^a   Acree, Michael ^a   Wrubel, Judith ^a   Wilson, Leslie ^a,c   Folkman, Susan ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CHILDREN S HOSPITAL OAKLAND   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Caregiver; Caregiving burden; Depression; HIV; Informal care; Sickle cell disease

Indexed keywords

ADULT; ARTICLE; CAREGIVER BURDEN; CHILD; CHILD CARE; CHRONIC DISEASE; CLINICAL ARTICLE; CONTROLLED STUDY; CRISIS INTERVENTION; FEMALE; HEALTH CARE MANAGEMENT; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; MALE; MATERNAL BEHAVIOR; PRIORITY JOURNAL; PSYCHOLOGICAL ASPECT; RESOURCE ALLOCATION; SICKLE CELL ANEMIA; STIGMA; TIME; WORK SCHEDULE;

ADAPTATION, PSYCHOLOGICAL; ADOLESCENT; ADULT; ANEMIA, SICKLE CELL; CAREGIVERS; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; FEMALE; HIV INFECTIONS; HOME NURSING; HOSPITALIZATION; HUMANS; INFANT; INTERVIEWS; MALE; MIDDLE AGED; MOTHERS; QUALITY OF LIFE; STRESS, PSYCHOLOGICAL;

EID: 33845330891     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.20792     Document Type: Article

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