Sickle cell disease pain in children and adolescents: Change in pain frequency and coping strategies over time

Journal of Pediatric Psychology

Volumn 18, Issue 5, 1993, Pages 621-637

  Gil, Karen M ^a   Thompson, Robert J ^a   Keith, Barbara R ^a   Tota faucette, Mary ^a   Noll, Stephanie ^a   Kinney, Thomas R ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Childhood pain; Coping strategies; Health care utilization; Longitudinal follow up; Sickle cell disease

Indexed keywords

ADOLESCENT; AGE; ARTICLE; CHILD; CHILD HEALTH CARE; COPING BEHAVIOR; FEMALE; HUMAN; MAJOR CLINICAL STUDY; MALE; PAIN; PAIN ASSESSMENT; REGRESSION ANALYSIS; SICKLE CELL ANEMIA; TIME;

ADAPTATION, PSYCHOLOGICAL; ADOLESCENT; ANEMIA, SICKLE CELL; CHILD; FEMALE; FOLLOW-UP STUDIES; HUMAN; MALE; PAIN MEASUREMENT; PERSONALITY ASSESSMENT; PERSONALITY DEVELOPMENT; SICK ROLE; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027379303     PISSN: 01468693     EISSN: None     Source Type: Journal    
DOI: 10.1093/jpepsy/18.5.621     Document Type: Article

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