{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,3]],"date-time":"2026-06-03T00:25:02Z","timestamp":1780446302305,"version":"3.54.1"},"reference-count":12,"publisher":"BMJ","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Archives of Disease in Childhood"],"published-print":{"date-parts":[[1996,9,1]]},"DOI":"10.1136\/adc.75.3.199","type":"journal-article","created":{"date-parts":[[2008,12,22]],"date-time":"2008-12-22T23:07:28Z","timestamp":1229987248000},"page":"199-203","source":"Crossref","is-referenced-by-count":125,"title":["Pain, quality of life, and coping in sickle cell disease."],"prefix":"10.1136","volume":"75","author":[{"given":"P","family":"Fuggle","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P A","family":"Shand","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L J","family":"Gill","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S C","family":"Davies","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"500","DOI":"10.1542\/peds.84.3.500","article-title":"Mortality in children and adolescents with sickle cell disease","volume":"84","author":"Leikin, S.L.; Gallagher, D.; Kinney, T.R.","year":"1989","unstructured":"Leikin SL, Gallagher D, Kinney TR, et al. Mortality in children and adolescents with sickle cell disease. Pediatrics 1989; 84: 500-8.","journal-title":"Pediatrics"},{"issue":"2","key":"ref_2","article-title":"Report on the VIth annual meeting of the WHO working group on the feasibility study of hereditary disease community control programmes (hereditary anaemia)","volume":"89","author":"World Health Organisation","year":"1989","unstructured":"World Health Organisation. Report on the VIth annual meeting of the WHO working group on the feasibility study of hereditary disease community control programmes (hereditary anaemia). Geneva: WHO, 1989 (WHO\/HDP\/HA\/89.2)."},{"key":"ref_3","article-title":"Sickle cell","author":"Barnhart, M.I.; Henry, R.L.; Lusher, J.M.","year":"1976","unstructured":"Barnhart MI, Henry RL, Lusher JM. Sickle cell. Kalamazoo, MI: A Scope Publication, The Upjohn Company, 1976."},{"key":"ref_4","article-title":"Psychological adjustment and family functioning in a group of British children with sickle cell disease: preliminary empirical findings, and a meta-analysis. BrJ Clin Psychol","author":"Midence, K.; Fuggle, P.; Davies, S.C.; McManus, C.","unstructured":"Midence K, Fuggle P, Davies SC, McManus C. Psychological adjustment and family functioning in a group of British children with sickle cell disease: preliminary empirical findings, and a meta-analysis. BrJ Clin Psychol (in press)."},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"429","DOI":"10.1093\/jpepsy\/11.3.429","article-title":"Psychological and social concomitants of sickle cell anaemia in adolescents","volume":"11","author":"Morgan, S.A.; Jackson, J.","year":"1986","unstructured":"Morgan SA, Jackson J. Psychological and social concomitants of sickle cell anaemia in adolescents. J Pediatr Psychol 1986; 11: 429-40.","journal-title":"J Pediatr Psychol"},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"859","DOI":"10.1016\/S0022-3476(76)81132-8","article-title":"and personal and social adjustmnent in children with sickle cell anaemia","volume":"88","author":"Kumar, S.; Powars, D.; Allen, J.; Anxiety, Haywood U.; self-concept","year":"1976","unstructured":"Kumar S, Powars D, Allen J, Haywood U. Anxiety, self-concept, and personal and social adjustmnent in children with sickle cell anaemia. J Pediatr 1976; 88: 859-63.","journal-title":"J Pediatr"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"621","DOI":"10.1093\/jpepsy\/18.5.621","article-title":"Sickle cell disease pain in children and adolescents: change in pain frequency and coping strategies over time","volume":"18","author":"Gil, K.M.; Thompson, R.J.; Keith, B.R.; Tota-Faucette, M.; Noll, S.; Kinney, T.R.","year":"1993","unstructured":"Gil KM, Thompson RJ, Keith BR, Tota-Faucette M, Noll S, Kinney TR. Sickle cell disease pain in children and adolescents: change in pain frequency and coping strategies over time. Y Pediatr Psychol 1993; 18: 621-37.","journal-title":"Y Pediatr Psychol"},{"key":"ref_8","first-page":"531","article-title":"The acute painful episode","volume-title":"cel disease: basic principles and clinical practice","author":"Shapiro, B.S.; Ballas, S.K.","year":"1994","unstructured":"Shapiro BS, Ballas SK. The acute painful episode. In: Embury SH, Hebbel RP, Mohabdas N, Steinberg MH, eds. Sickle cel disease: basic principles and clinical practice. New York: Raven Press, 1994:531-43."},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1056\/NEJM199107043250103","article-title":"Pain in sickle cell disease. Rates and risk factors","volume":"325","author":"Platt, O.S.; Thorington, B.D.; Brambilla, D.J.","year":"1991","unstructured":"Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. NEnglJMed 1991; 325: 11-6.","journal-title":"NEnglJMed"},{"key":"ref_10","first-page":"328","article-title":"Multidisciplinary approach to pain management in sickle cell disease","volume":"4","author":"Vichinsky, E.P.; Johnson, R.; Lubin, B.H.","year":"1982","unstructured":"Vichinsky EP, Johnson R, Lubin BH. Multidisciplinary approach to pain management in sickle cell disease. Am J Pediatr Hematol Oncol 1982; 4: 328-33.","journal-title":"Am J Pediatr Hematol Oncol"},{"key":"ref_11","first-page":"313","article-title":"Recording of crisis pain in sickle cell disease","volume":"15","author":"Shapiro, B.S.; Dinges, D.F.; Carota-Orne, E.; Ohene-Frempong, K.; Orne, M.T.","year":"1990","unstructured":"Shapiro BS, Dinges DF, Carota-Orne E, Ohene-Frempong K, Orne MT. Recording of crisis pain in sickle cell disease. Advances in Pain Research Therapy 1990; 15: 313-21.","journal-title":"Advances in Pain Research Therapy"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1093\/jpepsy\/15.5.643","article-title":"Pain in children and adolescents with sickle cell disease: a descriptive study","volume":"15","author":"Walco, G.A.; Dampier, C.D.","year":"1990","unstructured":"Walco GA, Dampier CD. Pain in children and adolescents with sickle cell disease: a descriptive study. J Pediatr Psychol 1990; 15: 643-58.","journal-title":"J Pediatr Psychol"}],"container-title":["Archives of Disease in Childhood"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/adc.75.3.199","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,23]],"date-time":"2023-05-23T03:58:48Z","timestamp":1684814328000},"score":1,"resource":{"primary":{"URL":"https:\/\/adc.bmj.com\/lookup\/doi\/10.1136\/adc.75.3.199"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,9,1]]},"references-count":12,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1996,9,1]]}},"URL":"https:\/\/doi.org\/10.1136\/adc.75.3.199","relation":{},"ISSN":["0003-9888","1468-2044"],"issn-type":[{"value":"0003-9888","type":"print"},{"value":"1468-2044","type":"electronic"}],"subject":[],"published":{"date-parts":[[1996,9,1]]}}}