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Volumn 15, Issue 3, 2014, Pages 325-336

The case for and against initiating either hydroxyurea therapy, blood transfusion therapy or hematopoietic stem cell transplant in asymptomatic children with sickle cell disease

Author keywords

Hematopoietic stem cell transplantation; Hydroxyurea; Regular blood transfusion; Sickle cell disease

Indexed keywords

HAEMOPHILUS INFLUENZAE TYPE B VACCINE; HYDROXYUREA; PENICILLIN DERIVATIVE; PNEUMOCOCCUS VACCINE;

EID: 84892692040     PISSN: 14656566     EISSN: 17447666     Source Type: Journal    
DOI: 10.1517/14656566.2014.868435     Document Type: Review
Times cited : (19)

References (72)
  • 1
    • 0034235705 scopus 로고    scopus 로고
    • Reperfusion injury pathophysiology in sickle transgenic mice
    • Osarogiagbon UR, Choong S, Belcher JD, et al. Reperfusion injury pathophysiology in sickle transgenic mice. Blood 2000;96:314-20
    • (2000) Blood , vol.96 , pp. 314-320
    • Osarogiagbon, U.R.1    Choong, S.2    Belcher, J.D.3
  • 2
    • 72049092388 scopus 로고    scopus 로고
    • BABY HUG Investigators. Renal function in infants with sickle cell anemia: Baseline data from the BABY HUG trial
    • Ware RE, Rees RC, Sarnaik SA, et al.; BABY HUG Investigators. Renal function in infants with sickle cell anemia: baseline data from the BABY HUG trial. J Pediatr 2010;156(1):66-70
    • (2010) J Pediatr , vol.156 , Issue.1 , pp. 66-70
    • Ware, R.E.1    Rees, R.C.2    Sarnaik, S.A.3
  • 3
    • 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;146:300-5
    • (2009) Br J Haematol , vol.146 , pp. 300-305
    • Kwiatkowski, J.L.1    Zimmerman, R.A.2    Pollock, A.N.3
  • 4
    • 27944496081 scopus 로고    scopus 로고
    • Outcome of sickle cell anemia: A 4-decade observational study of 1056 patients
    • Powars DR, Chan LS, Hiti A, et al. Outcome of sickle cell anemia: a 4-decade observational study of 1056 patients. Medicine (Baltimore) 2005;84:363-76
    • (2005) Medicine (Baltimore) , vol.84 , pp. 363-376
    • Powars, D.R.1    Chan, L.S.2    Hiti, A.3
  • 5
    • 0142215534 scopus 로고    scopus 로고
    • Causes of death in sickle cell disease: An autopsy study
    • Manci EA, Culberson DE, Yang YM, et al. Causes of death in sickle cell disease: an autopsy study. Br J Haematol 2003;123:359-65
    • (2003) Br J Haematol , vol.123 , pp. 359-365
    • Manci, E.A.1    Culberson, D.E.2    Yang, Y.M.3
  • 6
    • 0022628893 scopus 로고
    • Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial
    • Gaston MH, Verter JI, Woods G, et al. Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. N Engl J Med 1986;314:1593-9
    • (1986) N Engl J Med , vol.314 , pp. 1593-1599
    • Gaston, M.H.1    Verter, J.I.2    Woods, G.3
  • 7
    • 0021930572 scopus 로고
    • Acute splenic sequestration in homozygous sickle cell disease: Natural history and management
    • Emond AM, Collis R, Darvill D, et al. Acute splenic sequestration in homozygous sickle cell disease: natural history and management. J Pediatr 1985;107(2):201-6
    • (1985) J Pediatr , vol.107 , Issue.2 , pp. 201-206
    • Emond, A.M.1    Collis, R.2    Darvill, D.3
  • 8
    • 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;108:847-52
    • (2006) Blood , vol.108 , pp. 847-852
    • Lee, M.T.1    Piomelli, S.2    Granger, S.3
  • 9
    • 0029587055 scopus 로고
    • Improved survival in homozygous sickle cell disease: Lessons from a cohort study
    • Lee A, Thomas P, Cupidore L, et al. Improved survival in homozygous sickle cell disease: lessons from a cohort study. BMJ 1995;311:1600-2
    • (1995) BMJ , vol.311 , pp. 1600-1602
    • Lee, A.1    Thomas, P.2    Cupidore, L.3
  • 10
    • 0034642592 scopus 로고    scopus 로고
    • Prediction of adverse outcomes in children with sickle cell disease
    • Miller ST, Sleeper LA, Pegelow CH, et al. Prediction of adverse outcomes in children with sickle cell disease. N Engl J Med 2000;342:83-9
    • (2000) N Engl J Med , vol.342 , pp. 83-89
    • Miller, S.T.1    Sleeper, L.A.2    Pegelow, C.H.3
  • 11
    • 0017762582 scopus 로고
    • Polyvalent pneumococcal polysaccharide immunization of patients with sickle cell anemia and patients with splenectomy
    • Ammann AJ, Addiego J, Wara DW, et al. Polyvalent pneumococcal polysaccharide immunization of patients with sickle cell anemia and patients with splenectomy. N Engl J Med 1977;297:897
    • (1977) N Engl J Med , vol.297 , pp. 897
    • Ammann, A.J.1    Addiego, J.2    Wara, D.W.3
  • 12
    • 0029794804 scopus 로고    scopus 로고
    • Antibody responses to Haemophilus influenzae type b conjugate vaccine in sickle cell disease
    • Immunobiology Unit, Institute of Child Health, London
    • Goldblatt D, Johnson M, Evans J. Antibody responses to Haemophilus influenzae type b conjugate vaccine in sickle cell disease. Immunobiology Unit, Institute of Child Health, London. Arch Dis Child 1996;75(2):159-61
    • (1996) Arch Dis Child , vol.75 , Issue.2 , pp. 159-161
    • Goldblatt, D.1    Johnson, M.2    Evans, J.3
  • 13
    • 65349103931 scopus 로고    scopus 로고
    • Utilization of TCD screening for primary stroke prevention in children with sickle cell disease
    • Armstrong-Wells J, Grimes B, Sidney S, et al. Utilization of TCD screening for primary stroke prevention in children with sickle cell disease. Neurology 2009;72:1316-21
    • (2009) Neurology , vol.72 , pp. 1316-1321
    • Armstrong-Wells, J.1    Grimes, B.2    Sidney, S.3
  • 14
    • 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;332:1317-22
    • (1995) N Engl J Med , vol.332 , pp. 1317-1322
    • Charache, S.1    Terrin, M.L.2    Moore, R.D.3
  • 15
    • 84878516824 scopus 로고    scopus 로고
    • The effect of hydroxcarbamide therapy on survival of children with sickle cell disease
    • Lobo CL, Pinto JF, Nascimento EM, et al. The effect of hydroxcarbamide therapy on survival of children with sickle cell disease. Br J Haematol 2013;161:852-60.
    • (2013) Br J Haematol , vol.161 , pp. 852-860
    • Lobo, C.L.1    Pinto, J.F.2    Nascimento, E.M.3
  • 16
    • 38349193738 scopus 로고    scopus 로고
    • Prediction of adverse outcomes in children with sickle cell anemia: A study of the Dallas Newborn Cohort
    • Quinn CT, Lee NJ, Shull EP, et al. Prediction of adverse outcomes in children with sickle cell anemia: a study of the Dallas Newborn Cohort. Blood 2008;111:544-8
    • (2008) Blood , vol.111 , pp. 544-548
    • Quinn, C.T.1    Lee, N.J.2    Shull, E.P.3
  • 17
    • 33846006850 scopus 로고    scopus 로고
    • Prognostic significance of early vasoocclusive complications in children with sickle cell anemia
    • Quinn CT, Shull EP, Ahmad N, et al. Prognostic significance of early vasoocclusive complications in children with sickle cell anemia. Blood 2007;109:40-5
    • (2007) Blood , vol.109 , pp. 40-45
    • Quinn, C.T.1    Shull, E.P.2    Ahmad, N.3
  • 18
    • 34948867270 scopus 로고    scopus 로고
    • A network model to predict the risk of death in sickle cell disease
    • Sebastiani P, Nolan VG, Baldwin CT, et al. A network model to predict the risk of death in sickle cell disease. Blood 2007;110:2727-35
    • (2007) Blood , vol.110 , pp. 2727-2735
    • Sebastiani, P.1    Nolan, V.G.2    Baldwin, C.T.3
  • 19
    • 0035659821 scopus 로고    scopus 로고
    • 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. 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;139:785-9
    • (2001) J Pediatr , vol.139 , pp. 785-789
    • Miller, S.T.1    Wright, E.2    Abboud, M.3
  • 20
    • 0034654139 scopus 로고    scopus 로고
    • Impact of bone marrow transplantation for symptomatic sickle cell disease: An interim report. Multicenter investigation of bone marrow transplantation for sickle cell disease
    • Walters MC, Storb R, Patience M, et al. Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Multicenter investigation of bone marrow transplantation for sickle cell disease. Blood 2000;95:1918-24
    • (2000) Blood , vol.95 , pp. 1918-1924
    • Walters, M.C.1    Storb, R.2    Patience, M.3
  • 21
    • 74249110516 scopus 로고    scopus 로고
    • Decision analysis of treatment strategies in children with severe sickle cell disease
    • O'Brien SH, Hankins JS. Decision analysis of treatment strategies in children with severe sickle cell disease. J Pediatr Hematol Oncol 2009;31:873-8
    • (2009) J Pediatr Hematol Oncol , vol.31 , pp. 873-878
    • O'Brien, S.H.1    Hankins, J.S.2
  • 22
    • 34248198838 scopus 로고    scopus 로고
    • Therapy preference and decision-making among patients with severe sickle cell anemia and their families
    • Hankins J, Hinds P, Day S, et al. Therapy preference and decision-making among patients with severe sickle cell anemia and their families. Pediatr Blood Cancer 2007;48:705-10
    • (2007) Pediatr Blood Cancer , vol.48 , pp. 705-710
    • Hankins, J.1    Hinds, P.2    Day, S.3
  • 23
    • 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;289:1645-51
    • (2003) JAMA , vol.289 , pp. 1645-1651
    • Steinberg, M.H.1    Barton, F.2    Castro, O.3
  • 24
    • 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;115:2354-63
    • (2010) Blood , vol.115 , pp. 2354-2363
    • Voskaridou, E.1    Christoulas, D.2    Bilalis, A.3
  • 26
    • 84869803950 scopus 로고    scopus 로고
    • Impact of hydroxyurea on clinical events in the BABY HUG trial
    • quiz 4448
    • Thornburg CD, Files BA, Luo Z, et al. Impact of hydroxyurea on clinical events in the BABY HUG trial. Blood 2012;120:4304-10; quiz 4448
    • (2012) Blood , vol.120 , pp. 4304-4310
    • Thornburg, C.D.1    Files, B.A.2    Luo, Z.3
  • 27
    • 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;85:403-8.
    • (2010) Am J Hematol , vol.85 , pp. 403-408
    • Steinberg, M.H.1    McCarthy, W.F.2    Castro, O.3
  • 28
    • 0028291736 scopus 로고
    • Mortality in sickle cell disease. Life expectancy and risk factors for early death
    • Platt OS, Brambilla DJ, Rosse WF, et al. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med 1994;330(23):1639-44
    • (1994) N Engl J Med , vol.330 , Issue.23 , pp. 1639-1644
    • Platt, O.S.1    Brambilla, D.J.2    Rosse, W.F.3
  • 29
    • 69549107429 scopus 로고    scopus 로고
    • Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions
    • Kato GJ, Hebbel RP, Steinberg MH, et al. Vasculopathy in sickle cell disease: biology, pathophysiology, genetics, translational medicine, and new research directions. Am J Hematol 2009;84:618-25
    • (2009) Am J Hematol , vol.84 , pp. 618-625
    • Kato, G.J.1    Hebbel, R.P.2    Steinberg, M.H.3
  • 30
    • 84886292309 scopus 로고    scopus 로고
    • 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
    • Investigators of the Stroke With Transfusions Changing to Hydroxyurea Clinical Trial (SWiTCH)
    • Alvarez O, Yovetich NA, Scott JP, et al.; Investigators of the Stroke With Transfusions Changing to Hydroxyurea Clinical Trial (SWiTCH). 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. Am J Hematol 2013;88(11):932-8.
    • (2013) Am J Hematol , vol.88 , Issue.11 , pp. 932-938
    • Alvarez, O.1    Yovetich, N.A.2    Scott, J.P.3
  • 31
    • 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;377:1663-72.
    • (2011) Lancet , vol.377 , pp. 1663-1672
    • Wang, W.C.1    Ware, R.E.2    Miller, S.T.3
  • 32
    • 84862907017 scopus 로고    scopus 로고
    • Low fixed-dose hydroxyurea in severely affected Indian children with sickle cell disease
    • Jain DL, Sarathi V, Desai S, et al. Low fixed-dose hydroxyurea in severely affected Indian children with sickle cell disease. Hemoglobin 2012;36(4):323-32
    • (2012) Hemoglobin , vol.36 , Issue.4 , pp. 323-332
    • Jain, D.L.1    Sarathi, V.2    Desai, S.3
  • 33
    • 84878154737 scopus 로고    scopus 로고
    • Optimizing Hydroxyurea use in children with sickle cell disease: Low dose regimen is effective
    • Sharef SW, Al-Hajri M, Beshlawi I, et al. Optimizing Hydroxyurea use in children with sickle cell disease: low dose regimen is effective. Eur J Haematol 2013;90(6):519-24
    • (2013) Eur J Haematol , vol.90 , Issue.6 , pp. 519-524
    • Sharef, S.W.1    Al-Hajri, M.2    Beshlawi, I.3
  • 34
    • 41349090417 scopus 로고    scopus 로고
    • Hydroxyurea for children with sickle cell disease
    • x
    • Heeney MM, Ware RE. Hydroxyurea for children with sickle cell disease. Pediatr Clin North Am 2008;55:483-501, x
    • (2008) Pediatr Clin North Am , vol.55 , pp. 483-501
    • Heeney, M.M.1    Ware, R.E.2
  • 35
    • 80051815757 scopus 로고    scopus 로고
    • Monitoring toxicity, impact, and adherence of hydroxyurea in children with sickle cell disease
    • Brandow AM, Panepinto JA. Monitoring toxicity, impact, and adherence of hydroxyurea in children with sickle cell disease. Am J Hematol 2011;86(9):804-6
    • (2011) Am J Hematol , vol.86 , Issue.9 , pp. 804-806
    • Brandow, A.M.1    Panepinto, J.A.2
  • 36
    • 36549089997 scopus 로고    scopus 로고
    • Fetal hemoglobin in sickle cell anemia: Genetic determinants of response to hydroxyurea
    • Ma Q, Wyszynski DF, Farrell JJ, et al. Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Pharmacogenomics J 2007;7:386-94
    • (2007) Pharmacogenomics J , vol.7 , pp. 386-394
    • Ma, Q.1    Wyszynski, D.F.2    Farrell, J.J.3
  • 37
    • 46849120215 scopus 로고    scopus 로고
    • Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males
    • Berthaut I, Guignedoux G, Kirsch-Noir F, et al. Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males. Haematologica 2008;93:988-93
    • (2008) Haematologica , vol.93 , pp. 988-993
    • Berthaut, I.1    Guignedoux, G.2    Kirsch-Noir, F.3
  • 38
    • 50049110309 scopus 로고    scopus 로고
    • Provider barriers to hydroxyurea use in adults with sickle cell disease: A survey of the Sickle Cell Disease Adult Provider Network
    • Lanzkron S, Haywood C Jr, Hassell KL, et al. Provider barriers to hydroxyurea use in adults with sickle cell disease: a survey of the Sickle Cell Disease Adult Provider Network. J Natl Med Assoc 2008;100:968-73
    • (2008) J Natl Med Assoc , vol.100 , pp. 968-973
    • Lanzkron, S.1    Haywood Jr., C.2    Hassell, K.L.3
  • 39
    • 84879232521 scopus 로고    scopus 로고
    • Exploring barriers and facilitators to clinical trial enrollment in the context of sickle cell anemia and hydroxyurea
    • Lebensburger JD, Sidonio RF, Debaun MR, et al. Exploring barriers and facilitators to clinical trial enrollment in the context of sickle cell anemia and hydroxyurea. Pediatr Blood Cancer 2013;60:1333-7
    • (2013) Pediatr Blood Cancer , vol.60 , pp. 1333-1337
    • Lebensburger, J.D.1    Sidonio, R.F.2    Debaun, M.R.3
  • 40
    • 78650177166 scopus 로고    scopus 로고
    • Hydroxyurea (therapeutics and mechanism): Metabolism, carbamoyl nitroso, nitroxyl, radicals, cell signaling and clinical applications
    • Kovacic P. Hydroxyurea (therapeutics and mechanism): metabolism, carbamoyl nitroso, nitroxyl, radicals, cell signaling and clinical applications. Med Hypotheses 2011;76:24-31
    • (2011) Med Hypotheses , vol.76 , pp. 24-31
    • Kovacic, P.1
  • 41
    • 84869104356 scopus 로고    scopus 로고
    • DNA damage in leukocytes of sickle cell anemia patients is associated with hydroxyurea therapy and with HBBS haplotype
    • da Silva RLB, Dias EDB, Barbosa MC, et al. DNA damage in leukocytes of sickle cell anemia patients is associated with hydroxyurea therapy and with HBBS haplotype. Mutat Res 2012;749:48-52
    • (2012) Mutat Res , vol.749 , pp. 48-52
    • Da Silva, R.L.B.1    Dias, E.D.B.2    Barbosa, M.C.3
  • 42
    • 77954934323 scopus 로고    scopus 로고
    • Assessment of genotoxicity associated with hydroxyurea therapy in children with sickle cell anemia
    • Flanagan JM, Howard TA, Mortier N, et al. Assessment of genotoxicity associated with hydroxyurea therapy in children with sickle cell anemia. Mutat Res 2010;698:38-42
    • (2010) Mutat Res , vol.698 , pp. 38-42
    • Flanagan, J.M.1    Howard, T.A.2    Mortier, N.3
  • 43
    • 1542373662 scopus 로고    scopus 로고
    • Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease
    • Zimmerman SA, Schultz WH, Davis JS, et al. Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. Blood 2004;103:2039-45
    • (2004) Blood , vol.103 , pp. 2039-2045
    • Zimmerman, S.A.1    Schultz, W.H.2    Davis, J.S.3
  • 44
    • 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(1):5-11
    • (1998) N Engl J Med , vol.339 , Issue.1 , pp. 5-11
    • Adams, R.J.1    McKie, V.C.2    Hsu, L.3
  • 45
    • 0035133221 scopus 로고    scopus 로고
    • Indications for red cell transfusion in sickle cell disease
    • Ohene-Frempong K. Indications for red cell transfusion in sickle cell disease. Semin Hematol 2001;38:5-13
    • (2001) Semin Hematol , vol.38 , pp. 5-13
    • Ohene-Frempong, K.1
  • 46
    • 0034778419 scopus 로고    scopus 로고
    • Principles and problems of transfusion in sickle cell disease
    • Telen MJ. Principles and problems of transfusion in sickle cell disease. Semin Hematol 2001;38:315-23
    • (2001) Semin Hematol , vol.38 , pp. 315-323
    • Telen, M.J.1
  • 47
    • 0031007362 scopus 로고    scopus 로고
    • Chronic transfusion programmes in sickle cell disease: Problem or panacea?
    • Serjeant GR. Chronic transfusion programmes in sickle cell disease: problem or panacea? Br J Haematol 1997;97:253-5
    • (1997) Br J Haematol , vol.97 , pp. 253-255
    • Serjeant, G.R.1
  • 48
    • 0035135628 scopus 로고    scopus 로고
    • Transfusion-related iron overload in sickle cell anemia
    • Vichinsky E. Transfusion-related iron overload in sickle cell anemia. Semin Hematol 2001;38:1-84
    • (2001) Semin Hematol , vol.38 , pp. 1-84
    • Vichinsky, E.1
  • 49
    • 70449499193 scopus 로고    scopus 로고
    • Absence of cardiac siderosis by MRI T2 despite transfusion burden, hepatic and serum iron overload in Lebanese patients with sickle cell disease
    • Inati A, Musallam KM, Wood JC, et al. Absence of cardiac siderosis by MRI T2 despite transfusion burden, hepatic and serum iron overload in Lebanese patients with sickle cell disease. Eur J Haematol 2009;83:565-71
    • (2009) Eur J Haematol , vol.83 , pp. 565-571
    • Inati, A.1    Musallam, K.M.2    Wood, J.C.3
  • 50
    • 84886874276 scopus 로고    scopus 로고
    • High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors
    • Chou ST, Jackson T, Vege S, et al. High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors. Blood 2013;122:1062-71
    • (2013) Blood , vol.122 , pp. 1062-1071
    • Chou, S.T.1    Jackson, T.2    Vege, S.3
  • 51
    • 0029942003 scopus 로고    scopus 로고
    • The risk of transfusiontransmitted viral infections. The retrovirus epidemiology donor study
    • Schreiber GB, Busch MP, Kleinman SH, Korelitz JJ. The risk of transfusiontransmitted viral infections. The Retrovirus Epidemiology Donor Study. N Engl J Med 1996;334(26):1685-90
    • (1996) N Engl J Med , vol.334 , Issue.26 , pp. 1685-1690
    • Schreiber, G.B.1    Busch, M.P.2    Kleinman, S.H.3    Korelitz, J.J.4
  • 52
    • 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;117:772-9.
    • (2011) Blood , vol.117 , pp. 772-779
    • Hulbert, M.L.1    McKinstry, R.C.2    Lacey, J.L.3
  • 53
    • 0034307369 scopus 로고    scopus 로고
    • Financial analysis of chronic transfusion for stroke prevention in sickle cell disease
    • Wayne AS, Schoenike SE, Pegelow CH. Financial analysis of chronic transfusion for stroke prevention in sickle cell disease. Blood 2000;96:2369-72
    • (2000) Blood , vol.96 , pp. 2369-2372
    • Wayne, A.S.1    Schoenike, S.E.2    Pegelow, C.H.3
  • 54
    • 84892759639 scopus 로고    scopus 로고
    • Allogeneic transplantation strategies including haploidentical transplantation in sickle cell disease
    • Gluckman E. Allogeneic transplantation strategies including haploidentical transplantation in sickle cell disease. Hematology Am Soc Hematol Educ Program 2013;2013:370-6
    • (2013) Hematology Am Soc Hematol Educ Program , vol.2013 , pp. 370-376
    • Gluckman, E.1
  • 55
    • 34247858963 scopus 로고    scopus 로고
    • Matched-related donor transplantation for sickle cell disease: Report from the Center for International Blood and Transplant Research
    • Panepinto JA, Walters MC, Carreras J, et al. Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research. Br J Haematol 2007;137:479-85
    • (2007) Br J Haematol , vol.137 , pp. 479-485
    • Panepinto, J.A.1    Walters, M.C.2    Carreras, J.3
  • 56
    • 0028147445 scopus 로고
    • Availability of related donors for bone marrow transplantation in sickle cell anemia
    • Mentzer WC, Heller S, Pearle PR, et al. Availability of related donors for bone marrow transplantation in sickle cell anemia. Am J Pediatr Hematol Oncol 1994;16:27-9
    • (1994) Am J Pediatr Hematol Oncol , vol.16 , pp. 27-29
    • Mentzer, W.C.1    Heller, S.2    Pearle, P.R.3
  • 58
    • 75149170038 scopus 로고    scopus 로고
    • Pulmonary, gonadal, and central nervous system status after bone marrow transplantation for sickle cell disease
    • Walters MC, Hardy K, Edwards S, et al. Pulmonary, gonadal, and central nervous system status after bone marrow transplantation for sickle cell disease. Biol Blood Marrow Transplant 2010;16:263-72
    • (2010) Biol Blood Marrow Transplant , vol.16 , pp. 263-272
    • Walters, M.C.1    Hardy, K.2    Edwards, S.3
  • 59
    • 4043162728 scopus 로고    scopus 로고
    • Effects of allogeneic bone marrow transplantation on pulmonary function in 80 children in a single paediatric centre
    • Bruno B, Souillet G, Bertrand Y, et al. Effects of allogeneic bone marrow transplantation on pulmonary function in 80 children in a single paediatric centre. Bone Marrow Transplant 2004;34:143-7
    • (2004) Bone Marrow Transplant , vol.34 , pp. 143-147
    • Bruno, B.1    Souillet, G.2    Bertrand, Y.3
  • 60
    • 45749146298 scopus 로고    scopus 로고
    • Longitudinal analysis of pulmonary function in adults with sickle cell disease
    • Field JJ, Glassberg J, Gilmore A, et al. Longitudinal analysis of pulmonary function in adults with sickle cell disease. Am J Hematol 2008;83:574-6
    • (2008) Am J Hematol , vol.83 , pp. 574-576
    • Field, J.J.1    Glassberg, J.2    Gilmore, A.3
  • 61
    • 57349179187 scopus 로고    scopus 로고
    • Growth of lung function in children with sickle cell anemia
    • Field JJ, De Baun MR, Yan Y, et al. Growth of lung function in children with sickle cell anemia. Pediatr Pulmonol 2008;43:1061-6
    • (2008) Pediatr Pulmonol , vol.43 , pp. 1061-1066
    • Field, J.J.1    De Baun, M.R.2    Yan, Y.3
  • 62
    • 43449091559 scopus 로고    scopus 로고
    • HLA-haploidentical bone marrow transplantation for hematologic malignancies using nonmyeloablative conditioning and high-dose, posttransplantation cyclophosphamide
    • Luznik L, O'Donnell PV, Symons HJ, et al. HLA-haploidentical bone marrow transplantation for hematologic malignancies using nonmyeloablative conditioning and high-dose, posttransplantation cyclophosphamide. Biol Blood Marrow Transplant 2008;14:641-50
    • (2008) Biol Blood Marrow Transplant , vol.14 , pp. 641-650
    • Luznik, L.1    O'Donnell, P.V.2    Symons, H.J.3
  • 63
    • 3042753988 scopus 로고    scopus 로고
    • Reduced intensity haemopoietic stem-cell transplantation for treatment of nonmalignant diseases in children
    • Jacobsohn DA, Duerst R, Tse W, et al. Reduced intensity haemopoietic stem-cell transplantation for treatment of nonmalignant diseases in children. Lancet 2004;364:156-62
    • (2004) Lancet , vol.364 , pp. 156-162
    • Jacobsohn, D.A.1    Duerst, R.2    Tse, W.3
  • 64
    • 12144289379 scopus 로고    scopus 로고
    • Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia
    • Iannone R, Casella JF, Fuchs EJ, et al. Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia. Biol Blood Marrow Transplant 2003;9:519-28
    • (2003) Biol Blood Marrow Transplant , vol.9 , pp. 519-528
    • Iannone, R.1    Casella, J.F.2    Fuchs, E.J.3
  • 65
    • 71849118976 scopus 로고    scopus 로고
    • Allogeneic hematopoietic stem-cell transplantation for sickle cell disease
    • Hsieh MM, Kang EM, Fitzhugh CD, et al. Allogeneic hematopoietic stem-cell transplantation for sickle cell disease. N Engl J Med 2009;361:2309-17
    • (2009) N Engl J Med , vol.361 , pp. 2309-2317
    • Hsieh, M.M.1    Kang, E.M.2    Fitzhugh, C.D.3
  • 66
    • 12844273651 scopus 로고    scopus 로고
    • Transplantation of 2 partially HLA-matched umbilical cord blood units to enhance engraftment in adults with hematologic malignancy
    • Barker JN, Weisdorf DJ, DeFor TE, et al. Transplantation of 2 partially HLA-matched umbilical cord blood units to enhance engraftment in adults with hematologic malignancy. Blood 2005;105:1343-7
    • (2005) Blood , vol.105 , pp. 1343-1347
    • Barker, J.N.1    Weisdorf, D.J.2    Defor, T.E.3
  • 67
    • 34547428427 scopus 로고    scopus 로고
    • Unrelated cord blood transplantation in children with sickle cell disease: Review of four-center experience
    • Adamkiewicz TV, Szabolcs P, Haight A, et al. Unrelated cord blood transplantation in children with sickle cell disease: review of four-center experience. Pediatr Transplant 2007;11(6):641-4
    • (2007) Pediatr Transplant , vol.11 , Issue.6 , pp. 641-644
    • Adamkiewicz, T.V.1    Szabolcs, P.2    Haight, A.3
  • 68
    • 80051666676 scopus 로고    scopus 로고
    • Umbilical cord blood transplantation for children with thalassemia and sickle cell disease
    • Eurocord Registry; Center for International Blood and Marrow Transplant Research; New York Blood Center
    • Ruggeri A, Eapen M, Scaravadou A, et al.; Eurocord Registry; Center for International Blood and Marrow Transplant Research; New York Blood Center. Umbilical cord blood transplantation for children with thalassemia and sickle cell disease. Biol Blood Marrow Transplant 2011;17(9):1375-82
    • (2011) Biol Blood Marrow Transplant , vol.17 , Issue.9 , pp. 1375-1382
    • Ruggeri, A.1    Eapen, M.2    Scaravadou, A.3
  • 69
    • 84864005843 scopus 로고    scopus 로고
    • Unrelated donor cord blood transplantation for children with severe sickle cell disease: Results of one cohort from the phase II study from the Blood and Marrow Transplant Clinical Trials Network (BMT CTN)
    • Kamani NR, Walters MC, Carter S, et al. Unrelated donor cord blood transplantation for children with severe sickle cell disease: results of one cohort from the phase II study from the Blood and Marrow Transplant Clinical Trials Network (BMT CTN). Biol Blood Marrow Transplant 2012;18(8):1265-72
    • (2012) Biol Blood Marrow Transplant , vol.18 , Issue.8 , pp. 1265-1272
    • Kamani, N.R.1    Walters, M.C.2    Carter, S.3
  • 70
    • 84886897873 scopus 로고    scopus 로고
    • Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLA-identical sibling
    • Eurocord and European Blood and Marrow Transplantation (EBMT) group
    • Locatelli F, Kabbara N, Ruggeri A, et al.; Eurocord and European Blood and Marrow Transplantation (EBMT) group. Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLA-identical sibling. Blood 2013;122(6):1072-8
    • (2013) Blood , vol.122 , Issue.6 , pp. 1072-1078
    • Locatelli, F.1    Kabbara, N.2    Et Al., R.A.3
  • 71
    • 84869813639 scopus 로고    scopus 로고
    • HLA-haploidentical bone marrow transplantation with posttransplant cyclophosphamide expands the donor pool for patients with sickle cell disease
    • Bolanos-Meade J, Fuchs EJ, Luznik L, et al. HLA-haploidentical bone marrow transplantation with posttransplant cyclophosphamide expands the donor pool for patients with sickle cell disease. Blood 2012;120:4285-91.
    • (2012) Blood , vol.120 , pp. 4285-4291
    • Bolanos-Meade, J.1    Fuchs, E.J.2    Luznik, L.3
  • 72
    • 0031870487 scopus 로고    scopus 로고
    • Haematopoietic stem cell transplantation for sickle cell anaemia: The first 50 patients transplanted in Belgium
    • Vermylen C, Cornu G, Ferster A, et al. Haematopoietic stem cell transplantation for sickle cell anaemia: the first 50 patients transplanted in Belgium. Bone Marrow Transplant 1998;22(1):1-6
    • (1998) Bone Marrow Transplant , vol.22 , Issue.1 , pp. 1-6
    • Vermylen, C.1    Cornu, G.2    Ferster, A.3


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