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Volumn 88, Issue 11, 2013, Pages

Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN F; HYDROXYUREA;

EID: 84886285493     PISSN: 03618609     EISSN: 10968652     Source Type: Journal    
DOI: 10.1002/ajh.23531     Document Type: Article
Times cited : (21)

References (36)
  • 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
    • 0034834753 scopus 로고    scopus 로고
    • Cooperative Study of Sickle Cell Disease. Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: A report from the Cooperative Study of Sickle Cell Disease
    • Miller ST, Macklin EA, Pegelow CH, et al. Cooperative Study of Sickle Cell Disease. Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: A report from the Cooperative Study of Sickle Cell Disease. J Pediatr 2001;139:385-390.
    • (2001) J Pediatr , vol.139 , pp. 385-390
    • Miller, S.T.1    Macklin, E.A.2    Pegelow, C.H.3
  • 3
    • 0031965089 scopus 로고    scopus 로고
    • Cerebrovascular accidents in sickle cell disease: Rates and risk factors
    • Ohene-Frempong K, Weiner SJ, Sleeper LA, et al. Cerebrovascular accidents in sickle cell disease: Rates and risk factors. Blood 1998;91:288-294.
    • (1998) Blood , vol.91 , pp. 288-294
    • Ohene-Frempong, K.1    Weiner, S.J.2    Sleeper, L.A.3
  • 4
    • 77749243156 scopus 로고    scopus 로고
    • Design of the silent cerebral infarct transfusion (SIT) trial
    • Casella JF, King AA, Barton B, et al. Design of the silent cerebral infarct transfusion (SIT) trial. Pediatr Hematol Oncol 2010;27:69-89.
    • (2010) Pediatr Hematol Oncol , vol.27 , pp. 69-89
    • Casella, J.F.1    King, A.A.2    Barton, B.3
  • 5
    • 84860328824 scopus 로고    scopus 로고
    • Associated risk factors for silent cerebral infarcts in sickle cell anemia: Low baseline hemoglobin, gender and relative high systolic blood pressure
    • DeBaun MR, Sarnaik SA, Rodeghier MJ, et al. Associated risk factors for silent cerebral infarcts in sickle cell anemia: Low baseline hemoglobin, gender and relative high systolic blood pressure. Blood 2011;119:3684-3690.
    • (2011) Blood , vol.119 , pp. 3684-3690
    • DeBaun, M.R.1    Sarnaik, S.A.2    Rodeghier, M.J.3
  • 6
    • 0037089224 scopus 로고    scopus 로고
    • Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell disease
    • Pegelow CH, Macklin EA, Moser FG, et al. Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell disease. Blood 2002;99:3014-3018.
    • (2002) Blood , vol.99 , pp. 3014-3018
    • Pegelow, C.H.1    Macklin, E.A.2    Moser, F.G.3
  • 7
    • 84861211196 scopus 로고    scopus 로고
    • Silent cerebral infarcts: A review on a prevalent and progressive cause of neurologic injury in sickle cell anemia
    • DeBaun MR, Armstrong FD, McKinstry RC, et al. Silent cerebral infarcts: A review on a prevalent and progressive cause of neurologic injury in sickle cell anemia. Blood 2012;119:4587-4596.
    • (2012) Blood , vol.119 , pp. 4587-4596
    • DeBaun, M.R.1    Armstrong, F.D.2    McKinstry, R.C.3
  • 8
    • 0036220398 scopus 로고    scopus 로고
    • Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke
    • Scothorn DJ, Price C, Schwartz D, et al. Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke. J Pediatr 2002;140:48-54.
    • (2002) J Pediatr , vol.140 , pp. 48-54
    • Scothorn, D.J.1    Price, C.2    Schwartz, D.3
  • 9
    • 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
  • 10
    • 0030696806 scopus 로고    scopus 로고
    • for the French Study Group on Sickle Cell Disease. Three years follow-up of hydroxyurea treatment in severely ill children with sickle cell disease
    • De Montalembert M, Belloy M, Bernaudin F, et al. for the French Study Group on Sickle Cell Disease. Three years follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. J Pediatr Hematol/Oncol 1997;19:313-318.
    • (1997) J Pediatr Hematol/Oncol , vol.19 , pp. 313-318
    • De Montalembert, M.1    Belloy, M.2    Bernaudin, F.3
  • 11
    • 0035096303 scopus 로고    scopus 로고
    • Clinical and hematological responses to hydroxyurea in sicilian patients with HbS/beta-thalassemia
    • Rigano P, Rodgers GP, Renda D, et al. Clinical and hematological responses to hydroxyurea in sicilian patients with HbS/beta-thalassemia. Hemoglobin 2001;25:9-17.
    • (2001) Hemoglobin , vol.25 , pp. 9-17
    • Rigano, P.1    Rodgers, G.P.2    Renda, D.3
  • 12
    • 0037414164 scopus 로고    scopus 로고
    • Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Risks and benefits up to 9 years of treatment
    • Steinberg MH, Barton F, Castro O, et al. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Risks and benefits up to 9 years of treatment. JAMA 2003;289:1645-1651.
    • (2003) JAMA , vol.289 , pp. 1645-1651
    • Steinberg, M.H.1    Barton, F.2    Castro, O.3
  • 13
    • 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. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia and MSH Patients' 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. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia and MSH Patients' 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
  • 14
    • 77950622293 scopus 로고    scopus 로고
    • The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: Results of a 17-year, single-center trial (LaSHS)
    • Voskaridou E, Christoulas D, Bilalis A, et al. The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: Results of a 17-year, single-center trial (LaSHS). Blood 2010;115:2354-2363.
    • (2010) Blood , vol.115 , pp. 2354-2363
    • Voskaridou, E.1    Christoulas, D.2    Bilalis, A.3
  • 15
    • 20144386780 scopus 로고    scopus 로고
    • Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: The Belgian experience
    • Gulbis B, Haberman D, Dufour D, et al. Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: The Belgian experience. Blood 2005;105:2685-2690.
    • (2005) Blood , vol.105 , pp. 2685-2690
    • Gulbis, B.1    Haberman, D.2    Dufour, D.3
  • 16
    • 38349127617 scopus 로고    scopus 로고
    • Use of hydroxyurea in prevention of stroke in children with sickle cell disease
    • Lefèvre N, Dofour D, Gulbis B, et al. Use of hydroxyurea in prevention of stroke in children with sickle cell disease. Blood 2008;111:963-964.
    • (2008) Blood , vol.111 , pp. 963-964
    • Lefèvre, N.1    Dofour, D.2    Gulbis, B.3
  • 17
    • 34547961356 scopus 로고    scopus 로고
    • Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anemia
    • Zimmerman SA, Schultz WH, Burgett S, et al. Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anemia. Blood 2007;110:1043-1047.
    • (2007) Blood , vol.110 , pp. 1043-1047
    • Zimmerman, S.A.1    Schultz, W.H.2    Burgett, S.3
  • 18
    • 84860348352 scopus 로고    scopus 로고
    • SWiTCH Investigators. Stroke with transfusions changing to hydroxyurea (SWiTCH)
    • Ware RE, Helms RW, 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
  • 19
    • 34948830175 scopus 로고    scopus 로고
    • Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease
    • Bernaudin F, Socie G, Kuentz M, et al. Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease. Blood 2007;110:2749-2756.
    • (2007) Blood , vol.110 , pp. 2749-2756
    • Bernaudin, F.1    Socie, G.2    Kuentz, M.3
  • 20
    • 20044369570 scopus 로고    scopus 로고
    • Brain parenchymal damage after haematopoietic stem cell transplantation for severe sickle cell disease
    • Woodard P, Helton KJ, Khan RB, et al. Brain parenchymal damage after haematopoietic stem cell transplantation for severe sickle cell disease. Br J Haematol 2005;129:550-552.
    • (2005) Br J Haematol , vol.129 , pp. 550-552
    • Woodard, P.1    Helton, K.J.2    Khan, R.B.3
  • 21
    • 2542537653 scopus 로고    scopus 로고
    • Central nervous system abnormalities in asymptomatic young patients with Sbeta-thalassemia
    • Zafeiriou DI, Prengler M, Gombakis N, et al. Central nervous system abnormalities in asymptomatic young patients with Sbeta-thalassemia. Ann Neurol 2004;55:835-839.
    • (2004) Ann Neurol , vol.55 , pp. 835-839
    • Zafeiriou, D.I.1    Prengler, M.2    Gombakis, N.3
  • 22
    • 0042810696 scopus 로고    scopus 로고
    • Silent brain infarcts in adult Kuwaiti sickle cell disease patients
    • Marouf R, Gupta R, Haider MZ, Adekile AD. Silent brain infarcts in adult Kuwaiti sickle cell disease patients. Am J Hematol 2003;73:240-243.
    • (2003) Am J Hematol , vol.73 , pp. 240-243
    • Marouf, R.1    Gupta, R.2    Haider, M.Z.3    Adekile, A.D.4
  • 23
    • 0034120108 scopus 로고    scopus 로고
    • Multicenter prospective study of children with sickle cell disease: Radiographic and psychometric correlation
    • Bernaudin F, Verlhac S, Freard F, et al. Multicenter prospective study of children with sickle cell disease: Radiographic and psychometric correlation. J Child Neurol 2000;15:333-343.
    • (2000) J Child Neurol , vol.15 , pp. 333-343
    • Bernaudin, F.1    Verlhac, S.2    Freard, F.3
  • 24
    • 0032697251 scopus 로고    scopus 로고
    • MR imaging of the brain: Findings in asymptomatic patients with thalassemia intermedia and sickle cell-thalassemia disease
    • Manfre L, Giarratano E, Maggio A, et al. MR imaging of the brain: Findings in asymptomatic patients with thalassemia intermedia and sickle cell-thalassemia disease. AJR Am J Roentgenol 1999;173:1477-1480.
    • (1999) AJR Am J Roentgenol , vol.173 , pp. 1477-1480
    • Manfre, L.1    Giarratano, E.2    Maggio, A.3
  • 25
    • 0032989606 scopus 로고    scopus 로고
    • Silent cerebral infarcts in sickle cell anemia: A risk factor analysis. The Cooperative Study of Sickle Cell Disease
    • Kinney TR, Sleeper LA, Wang WC, et al. Silent cerebral infarcts in sickle cell anemia: A risk factor analysis. The Cooperative Study of Sickle Cell Disease. Pediatrics 1999;103:640-645.
    • (1999) Pediatrics , vol.103 , pp. 640-645
    • Kinney, T.R.1    Sleeper, L.A.2    Wang, W.C.3
  • 26
    • 67650484216 scopus 로고    scopus 로고
    • Silent infarcts in young children with sickle cell disease
    • Kwiatkowski JL, Zimmerman RA, Pollock AN, et al. Silent infarcts in young children with sickle cell disease. Br J Haematol 2009;146:300-305.
    • (2009) Br J Haematol , vol.146 , pp. 300-305
    • Kwiatkowski, J.L.1    Zimmerman, R.A.2    Pollock, A.N.3
  • 27
    • 78751697297 scopus 로고    scopus 로고
    • Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
    • Hulbert ML, McKinstry RC, Lacey JL, et al. Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease. Blood 2011;117:772-779.
    • (2011) Blood , vol.117 , pp. 772-779
    • Hulbert, M.L.1    McKinstry, R.C.2    Lacey, J.L.3
  • 28
    • 0035942334 scopus 로고    scopus 로고
    • Poor school and cognitive functioning with silent cerebral infarcts and sickle cell disease
    • Schatz J., Brown RT, Pascual JM, et al. Poor school and cognitive functioning with silent cerebral infarcts and sickle cell disease. Neurology 2001;56:1106-1111.
    • (2001) Neurology , vol.56 , pp. 1106-1111
    • Schatz, J.1    Brown, R.T.2    Pascual, J.M.3
  • 29
    • 0037002828 scopus 로고    scopus 로고
    • Lesion burden and cognitive morbidity in children with sickle cell disease
    • Schatz J, White DA, Moinuddin A, Lesion burden and cognitive morbidity in children with sickle cell disease. J Child Neurol 2002;17:891-895.
    • (2002) J Child Neurol , vol.17 , pp. 891-895
    • Schatz, J.1    White, D.A.2    Moinuddin, A.3
  • 30
    • 77952297450 scopus 로고    scopus 로고
    • Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia
    • Vichinsky EP, Neumayr LD, Gold JI, et al. Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia. JAMA 2010;303:1823-1831.
    • (2010) JAMA , vol.303 , pp. 1823-1831
    • Vichinsky, E.P.1    Neumayr, L.D.2    Gold, J.I.3
  • 31
    • 65949124657 scopus 로고    scopus 로고
    • Mechanisms of vasculopathy in sickle cell disease and thalassemia
    • Morris CR. Mechanisms of vasculopathy in sickle cell disease and thalassemia. Hematology Am Soc Hematol Educ Prog 2008:177-185.
    • (2008) Hematology Am Soc Hematol Educ Prog , pp. 177-185
    • Morris, C.R.1
  • 32
    • 29544447720 scopus 로고    scopus 로고
    • Preventing stroke in sickle cell anemia
    • Platt OS. Preventing stroke in sickle cell anemia. New Engl J Med 2005;353:2743-2745.
    • (2005) New Engl J Med , vol.353 , pp. 2743-2745
    • Platt, O.S.1
  • 33
    • 33846279380 scopus 로고    scopus 로고
    • Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes
    • Kato GJ, Gladwin MT, Steinberg MH. Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Rev 2007;21:37-47.
    • (2007) Blood Rev , vol.21 , pp. 37-47
    • Kato, G.J.1    Gladwin, M.T.2    Steinberg, M.H.3
  • 34
    • 10744233940 scopus 로고    scopus 로고
    • Pulmonary hypertension as a risk factor for death in patients with sickle cell disease
    • Gladwin MT, Sachdev V, Jison ML, et al. Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med 2004;350:886-895.
    • (2004) N Engl J Med , vol.350 , pp. 886-895
    • Gladwin, M.T.1    Sachdev, V.2    Jison, M.L.3
  • 35
    • 84874541582 scopus 로고    scopus 로고
    • The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and Europe
    • Nouraie M, Lee JS, Zhang Y, et al. The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and Europe. Haematologica 2013;98:464-472.
    • (2013) Haematologica , vol.98 , pp. 464-472
    • Nouraie, M.1    Lee, J.S.2    Zhang, Y.3
  • 36
    • 79955909191 scopus 로고    scopus 로고
    • Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG)
    • Wang WC, Ware RE, Miller ST, et al. Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, 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


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