메뉴 건너뛰기




Volumn 88, Issue 11, 2013, Pages 932-938

Pain and other non-neurological adverse events in children with sickle cell anemia and previous stroke who received hydroxyurea and phlebotomy or chronic transfusions and chelation: Results from the SWiTCH clinical trial

Author keywords

[No Author keywords available]

Indexed keywords

DEFERASIROX; DEFEROXAMINE; HEMOGLOBIN F; HYDROXYUREA;

EID: 84886292309     PISSN: 03618609     EISSN: 10968652     Source Type: Journal    
DOI: 10.1002/ajh.23547     Document Type: Article
Times cited : (42)

References (21)
  • 1
    • 0032474692 scopus 로고    scopus 로고
    • Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography
    • Adams RJ, McKie VC, Hsu L, et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N Engl J Med 1998;339:5-11.
    • (1998) N Engl J Med , vol.339 , pp. 5-11
    • Adams, R.J.1    McKie, V.C.2    Hsu, L.3
  • 2
    • 33746594094 scopus 로고    scopus 로고
    • Stroke prevention trial in sickle cell anemia (STOP): Extended follow-up and final results
    • Lee MT, Piomelli S, Granger S, et al. Stroke prevention trial in sickle cell anemia (STOP): Extended follow-up and final results. Blood 2006;108:847-852.
    • (2006) Blood , vol.108 , pp. 847-852
    • Lee, M.T.1    Piomelli, S.2    Granger, S.3
  • 3
    • 34247108061 scopus 로고    scopus 로고
    • The pathophysiology, prevention, and treatment of stroke in sickle cell disease
    • Wang W. The pathophysiology, prevention, and treatment of stroke in sickle cell disease. Curr Opin Hematol 2007;14:191-197.
    • (2007) Curr Opin Hematol , vol.14 , pp. 191-197
    • Wang, W.1
  • 4
    • 0035659821 scopus 로고    scopus 로고
    • STOP Investigators. Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia
    • Miller ST, Wright E, Abboud M, et al; STOP Investigators. Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia. J Pediatr 2001;139:785-789.
    • (2001) J Pediatr , vol.139 , pp. 785-789
    • Miller, S.T.1    Wright, E.2    Abboud, M.3
  • 5
    • 33845893343 scopus 로고    scopus 로고
    • Transfusion prevents acute chest syndrome predicted by elevated secretory phospholipase A2
    • Styles LA, Abboud M, Larkin S, et al. Transfusion prevents acute chest syndrome predicted by elevated secretory phospholipase A2. Br J Haematol 2007;136:343-344.
    • (2007) Br J Haematol , vol.136 , pp. 343-344
    • Styles, L.A.1    Abboud, M.2    Larkin, S.3
  • 6
    • 79952149367 scopus 로고    scopus 로고
    • Approaches to transfusion therapy and iron overload in patients with sickle cell disease: Results of an international survey
    • transfusion committee.
    • Vichinsky EP, Ohene-Frempong K; transfusion committee. Approaches to transfusion therapy and iron overload in patients with sickle cell disease: Results of an international survey. Pediatr Hematol Oncol 2011;28:37-42.
    • (2011) Pediatr Hematol Oncol , vol.28 , pp. 37-42
    • Vichinsky, E.P.1    Ohene-Frempong, K.2
  • 7
    • 77957204379 scopus 로고    scopus 로고
    • Decreased blood red cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylation
    • Bartolucci P, Chaar V, Picot J, et al. Decreased blood red cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylation. Blood 2010;116:2152-2159.
    • (2010) Blood , vol.116 , pp. 2152-2159
    • Bartolucci, P.1    Chaar, V.2    Picot, J.3
  • 8
    • 0029025475 scopus 로고
    • Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia
    • Charache S, Terrin ML, Moore RD, et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med 1995;332:1317-1322.
    • (1995) N Engl J Med , vol.332 , pp. 1317-1322
    • Charache, S.1    Terrin, M.L.2    Moore, R.D.3
  • 9
    • 45549105597 scopus 로고    scopus 로고
    • Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease
    • Lanzkron S, Strouse JJ, Wilson R, et al. Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease. Ann Intern Med 2008;148:939-955.
    • (2008) Ann Intern Med , vol.148 , pp. 939-955
    • Lanzkron, S.1    Strouse, J.J.2    Wilson, R.3
  • 10
    • 0035383785 scopus 로고    scopus 로고
    • Five years of experience with hydroxyurea in children and young adults with sickle cell disease
    • Ferster A, Tahriri P, Vermylen C, et al. Five years of experience with hydroxyurea in children and young adults with sickle cell disease. Blood 2001;97:3628-3632.
    • (2001) Blood , vol.97 , pp. 3628-3632
    • Ferster, A.1    Tahriri, P.2    Vermylen, C.3
  • 11
    • 77953057530 scopus 로고    scopus 로고
    • The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow up
    • Steinberg MH, McCarthy WF, Castro O, et al. The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow up. Am J Hematol 2010;85:403-408.
    • (2010) Am J Hematol , vol.85 , pp. 403-408
    • Steinberg, M.H.1    McCarthy, W.F.2    Castro, O.3
  • 12
    • 79955909191 scopus 로고    scopus 로고
    • Hydroxycarbamide in very young children with sickle-cell anaemia: A multicenter, randomised, controlled trial (BABY HUG)
    • Wang WC, Ware RE, Miller ST, et al. Hydroxycarbamide in very young children with sickle-cell anaemia: A multicenter, randomised, controlled trial (BABY HUG). Lancet 2011;377:1663-1672.
    • (2011) Lancet , vol.377 , pp. 1663-1672
    • Wang, W.C.1    Ware, R.E.2    Miller, S.T.3
  • 13
    • 4444309490 scopus 로고    scopus 로고
    • Prevention of secondary stroke and resolution of transfusional iron overload in children with sickle cell anemia using hydroxyurea and phlebotomy
    • Ware RE, Zimmerman SA, Sylvestre PB, et al. Prevention of secondary stroke and resolution of transfusional iron overload in children with sickle cell anemia using hydroxyurea and phlebotomy. J Pediatr 2004;145:346-352.
    • (2004) J Pediatr , vol.145 , pp. 346-352
    • Ware, R.E.1    Zimmerman, S.A.2    Sylvestre, P.B.3
  • 14
    • 84860348352 scopus 로고    scopus 로고
    • Stroke with transfusions changing to hydroxyurea (SWiTCH)
    • for the SWiTCH Investigators
    • Ware RE, Helms RW; for the SWiTCH Investigators. Stroke with transfusions changing to hydroxyurea (SWiTCH). Blood 2012;119:3925-3932.
    • (2012) Blood , vol.119 , pp. 3925-3932
    • Ware, R.E.1    Helms, R.W.2
  • 15
    • 80052684368 scopus 로고    scopus 로고
    • Stroke with transfusions changing to hydroxyurea (SWiTCH): A phase III randomized clinical trial for treatment of children with sickle cell anemia, stroke, and iron overload
    • Ware RE, Schultz WH, Yovetich N, et al. Stroke with transfusions changing to hydroxyurea (SWiTCH): A phase III randomized clinical trial for treatment of children with sickle cell anemia, stroke, and iron overload. Pediatr Blood Cancer 2011;57:1011-1017.
    • (2011) Pediatr Blood Cancer , vol.57 , pp. 1011-1017
    • Ware, R.E.1    Schultz, W.H.2    Yovetich, N.3
  • 16
    • 0025770390 scopus 로고
    • Pain in sickle cell disease. Rates and risk factors
    • Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med 1991;325:11-16.
    • (1991) N Engl J Med , vol.325 , pp. 11-16
    • Platt, O.S.1    Thorington, B.D.2    Brambilla, D.J.3
  • 17
    • 0029017748 scopus 로고
    • Clinical events in the first decade in a cohort of infants with sickle cell disease
    • Gill FM, Sleeper LA, Weiner SJ, et al. Clinical events in the first decade in a cohort of infants with sickle cell disease. Blood 1995;86:778-783.
    • (1995) Blood , vol.86 , pp. 778-783
    • Gill, F.M.1    Sleeper, L.A.2    Weiner, S.J.3
  • 18
    • 10244278094 scopus 로고    scopus 로고
    • Sickle cell vasoocclusion: Heterotypic, multicellular aggregations driven by leukocyte adhesion
    • Frenette PS. Sickle cell vasoocclusion: Heterotypic, multicellular aggregations driven by leukocyte adhesion. Microcirculation 2004;11:167-177.
    • (2004) Microcirculation , vol.11 , pp. 167-177
    • Frenette, P.S.1
  • 19
    • 0034702282 scopus 로고    scopus 로고
    • Causes and outcomes of the acute chest syndrome in sickle cell disease. National Acute Chest Syndrome Study Group
    • Vichinksy EP, Neumayr LD, Earles AN, et al. Causes and outcomes of the acute chest syndrome in sickle cell disease. National Acute Chest Syndrome Study Group. N Engl J Med 2000;342:1855-1865.
    • (2000) N Engl J Med , vol.342 , pp. 1855-1865
    • Vichinksy, E.P.1    Neumayr, L.D.2    Earles, A.N.3
  • 20
    • 0028234283 scopus 로고
    • The acute chest syndrome in sickle cell disease: Incidence and risk factors. The Cooperative Study of Sickle Cell Disease
    • Castro O, Brambilla DJ, Thorington B, et al. The acute chest syndrome in sickle cell disease: Incidence and risk factors. The Cooperative Study of Sickle Cell Disease. Blood 1994;84:643-649.
    • (1994) Blood , vol.84 , pp. 643-649
    • Castro, O.1    Brambilla, D.J.2    Thorington, B.3
  • 21
    • 0023177444 scopus 로고
    • Painful sickle cell crises precipitated by stopping prophylactic exchange transfusions
    • Keidan AJ, Marwah SS, Vaughan GR, et al. Painful sickle cell crises precipitated by stopping prophylactic exchange transfusions. J Clin Pathol 1987;40:505-507.
    • (1987) J Clin Pathol , vol.40 , pp. 505-507
    • Keidan, A.J.1    Marwah, S.S.2    Vaughan, G.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.