메뉴 건너뛰기




Volumn 92, Issue 12, 2017, Pages 1333-1339

A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapy

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN F; HYDROXYUREA; ANTISICKLING AGENT;

EID: 85030630188     PISSN: 03618609     EISSN: 10968652     Source Type: Journal    
DOI: 10.1002/ajh.24906     Document Type: Article
Times cited : (62)

References (45)
  • 1
    • 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):1639–1644.
    • (1994) N Engl J Med. , vol.330 , Issue.23 , pp. 1639-1644
    • Platt, O.S.1    Brambilla, D.J.2    Rosse, W.F.3
  • 2
    • 79960147525 scopus 로고    scopus 로고
    • Fetal hemoglobin in sickle cell anemia
    • Akinsheye I, Alsultan A, Solovieff N, et al. Fetal hemoglobin in sickle cell anemia. Blood. 2011;118(1):19–27.
    • (2011) Blood. , vol.118 , Issue.1 , pp. 19-27
    • Akinsheye, I.1    Alsultan, A.2    Solovieff, N.3
  • 3
    • 0024446352 scopus 로고
    • Mortality in children and adolescents with sickle cell disease. Cooperative Study of Sickle Cell Disease
    • Leikin SL, Gallagher D, Kinney TR, Sloane D, Klug P, Rida W. Mortality in children and adolescents with sickle cell disease. Cooperative Study of Sickle Cell Disease. Pediatrics. 1989;84(3):500–508.
    • (1989) Pediatrics. , vol.84 , Issue.3 , pp. 500-508
    • Leikin, S.L.1    Gallagher, D.2    Kinney, T.R.3    Sloane, D.4    Klug, P.5    Rida, W.6
  • 4
    • 0019365327 scopus 로고
    • Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood
    • Stevens MC, Hayes RJ, Vaidya S, Serjeant GR. Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. J Pediatr. 1981;98(1):37–41.
    • (1981) J Pediatr. , vol.98 , Issue.1 , pp. 37-41
    • Stevens, M.C.1    Hayes, R.J.2    Vaidya, S.3    Serjeant, G.R.4
  • 5
    • 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(1):11–16.
    • (1991) N Engl J Med. , vol.325 , Issue.1 , pp. 11-16
    • Platt, O.S.1    Thorington, B.D.2    Brambilla, D.J.3
  • 6
    • 84907016412 scopus 로고    scopus 로고
    • Management of sickle cell disease: Summary of the 2014 evidence-based report by expert panel members
    • Yawn BP, Buchanan GR, Afenyi-Annan AN, et al. Management of sickle cell disease: Summary of the 2014 evidence-based report by expert panel members. JAMA. 2014;312(10):1033–1048.
    • (2014) JAMA. , vol.312 , Issue.10 , pp. 1033-1048
    • Yawn, B.P.1    Buchanan, G.R.2    Afenyi-Annan, A.N.3
  • 7
    • 27144448031 scopus 로고    scopus 로고
    • Long-term hydroxyurea therapy for infants with sickle cell anemia: The HUSOFT extension study
    • Hankins JS, Ware RE, Rogers ZR, et al. Long-term hydroxyurea therapy for infants with sickle cell anemia: The HUSOFT extension study. Blood. 2005;106(7):2269–2275.
    • (2005) Blood. , vol.106 , Issue.7 , pp. 2269-2275
    • Hankins, J.S.1    Ware, R.E.2    Rogers, Z.R.3
  • 8
    • 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(9778):1663–1672.
    • (2011) Lancet. , vol.377 , Issue.9778 , pp. 1663-1672
    • Wang, W.C.1    Ware, R.E.2    Miller, S.T.3
  • 9
    • 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(6):2039–2045.
    • (2004) Blood. , vol.103 , Issue.6 , pp. 2039-2045
    • Zimmerman, S.A.1    Schultz, W.H.2    Davis, J.S.3
  • 11
    • 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(13):1645–1651.
    • (2003) JAMA. , vol.289 , Issue.13 , pp. 1645-1651
    • Steinberg, M.H.1    Barton, F.2    Castro, O.3
  • 12
    • 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(12):2354–2363.
    • (2010) Blood. , vol.115 , Issue.12 , pp. 2354-2363
    • Voskaridou, E.1    Christoulas, D.2    Bilalis, A.3
  • 13
    • 84905510021 scopus 로고    scopus 로고
    • Population pharmacokinetics of hydroxyurea for children and adolescents with sickle cell disease
    • Wiczling P, Liem RI, Panepinto JA, et al. Population pharmacokinetics of hydroxyurea for children and adolescents with sickle cell disease. J Clin Pharmacol. 2014;54(9):1016–1022.
    • (2014) J Clin Pharmacol. , vol.54 , Issue.9 , pp. 1016-1022
    • Wiczling, P.1    Liem, R.I.2    Panepinto, J.A.3
  • 14
    • 84958113265 scopus 로고    scopus 로고
    • Best pharmaceuticals for children act-pediatric trials network administrative core committee
    • Estepp JH, Melloni C, Thornburg CD, et al. Best pharmaceuticals for children act-pediatric trials network administrative core committee. J Clin Pharmacol. 2016;56(3):298–306.
    • (2016) J Clin Pharmacol. , vol.56 , Issue.3 , pp. 298-306
    • Estepp, J.H.1    Melloni, C.2    Thornburg, C.D.3
  • 15
    • 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(20):1317–1322.
    • (1995) N Engl J Med. , vol.332 , Issue.20 , pp. 1317-1322
    • Charache, S.1    Terrin, M.L.2    Moore, R.D.3
  • 16
    • 84957891583 scopus 로고    scopus 로고
    • Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to Hydroxyurea (TWiTCH): A multicentre, open-label, phase 3, non-inferiority trial
    • Ware RE, Davis BR, Schultz WH, et al. Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to Hydroxyurea (TWiTCH): A multicentre, open-label, phase 3, non-inferiority trial. Lancet. 2016;387(10019):661–670.
    • (2016) Lancet. , vol.387 , Issue.10019 , pp. 661-670
    • Ware, R.E.1    Davis, B.R.2    Schultz, W.H.3
  • 17
    • 77956840802 scopus 로고    scopus 로고
    • Hydroxyurea therapy requires HbF induction for clinical benefit in a sickle cell mouse model
    • Lebensburger JD, Pestina TI, Ware RE, Boyd KL, Persons DA. Hydroxyurea therapy requires HbF induction for clinical benefit in a sickle cell mouse model. Haematologica. 2010;95(9):1599–1603.
    • (2010) Haematologica. , vol.95 , Issue.9 , pp. 1599-1603
    • Lebensburger, J.D.1    Pestina, T.I.2    Ware, R.E.3    Boyd, K.L.4    Persons, D.A.5
  • 18
    • 13044277572 scopus 로고    scopus 로고
    • Safety of hydroxyurea in children with sickle cell anemia: Results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group
    • Kinney TR, Helms RW, O'branski EE, et al. Safety of hydroxyurea in children with sickle cell anemia: Results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group. Blood. 1999;94(5):1550–1554.
    • (1999) Blood. , vol.94 , Issue.5 , pp. 1550-1554
    • Kinney, T.R.1    Helms, R.W.2    O'branski, E.E.3
  • 19
    • 84961657081 scopus 로고    scopus 로고
    • Amelioration of murine sickle cell disease by nonablative conditioning and gamma-globin gene-corrected bone marrow cells
    • Pestina TI, Hargrove PW, Zhao H, et al. Amelioration of murine sickle cell disease by nonablative conditioning and gamma-globin gene-corrected bone marrow cells. Mol Ther Methods Clin Dev. 2015;2:15045.
    • (2015) Mol Ther Methods Clin Dev. , vol.2 , pp. 15045
    • Pestina, T.I.1    Hargrove, P.W.2    Zhao, H.3
  • 21
    • 0021343093 scopus 로고
    • Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?
    • Powars DR, Weiss JN, Chan LS, Schroeder WA. Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia? Blood. 1984;63(4):921–926.
    • (1984) Blood. , vol.63 , Issue.4 , pp. 921-926
    • Powars, D.R.1    Weiss, J.N.2    Chan, L.S.3    Schroeder, W.A.4
  • 22
    • 84881491135 scopus 로고    scopus 로고
    • Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia
    • Bhatnagar P, Keefer JR, Casella JF, et al. Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia. Pediatr Blood Cancer. 2013;60(10):E125–E127.
    • (2013) Pediatr Blood Cancer. , vol.60 , Issue.10 , pp. E125-E127
    • Bhatnagar, P.1    Keefer, J.R.2    Casella, J.F.3
  • 23
    • 74749106742 scopus 로고    scopus 로고
    • Hydroxyurea for children with sickle cell disease
    • Heeney MM, Ware RE. Hydroxyurea for children with sickle cell disease. Hematol Oncol Clin North Am. 2010;24(1):199–214.
    • (2010) Hematol Oncol Clin North Am. , vol.24 , Issue.1 , pp. 199-214
    • Heeney, M.M.1    Ware, R.E.2
  • 24
    • 74049123836 scopus 로고    scopus 로고
    • Definitions of the phenotypic manifestations of sickle cell disease
    • Ballas SK, Lieff S, Benjamin LJ, et al. Definitions of the phenotypic manifestations of sickle cell disease. Am J Hematol. 2010;85(1):6–13.
    • (2010) Am J Hematol. , vol.85 , Issue.1 , pp. 6-13
    • Ballas, S.K.1    Lieff, S.2    Benjamin, L.J.3
  • 25
    • 33748343357 scopus 로고    scopus 로고
    • Methods for evaluation of medication adherence and persistence using automated databases
    • discussion 575-567
    • Andrade SE, Kahler KH, Frech F, Chan KA. Methods for evaluation of medication adherence and persistence using automated databases. Pharmacoepidem Drug Safe. 2006;15(8):565–574. discussion 575-567.
    • (2006) Pharmacoepidem Drug Safe. , vol.15 , Issue.8 , pp. 565-574
    • Andrade, S.E.1    Kahler, K.H.2    Frech, F.3    Chan, K.A.4
  • 26
    • 30444437059 scopus 로고    scopus 로고
    • Suboptimal medication adherence in Parkinson's disease
    • Grosset KA, Bone I, Grosset DG. Suboptimal medication adherence in Parkinson's disease. Mov Disord. 2005;20(11):1502–1507.
    • (2005) Mov Disord. , vol.20 , Issue.11 , pp. 1502-1507
    • Grosset, K.A.1    Bone, I.2    Grosset, D.G.3
  • 28
  • 30
    • 77949463046 scopus 로고    scopus 로고
    • Advances in the use of hydroxyurea. Hematology American Society of
    • Ware RE, Aygun B. Advances in the use of hydroxyurea. Hematology American Society of. Hematol Educ Program. 2009;62–69.
    • (2009) Hematol Educ Program. , pp. 62-69
    • Ware, R.E.1    Aygun, B.2
  • 31
    • 84993960918 scopus 로고    scopus 로고
    • Hydroxycarbamide treatment and brain MRI/MRA findings in children with sickle cell anaemia
    • Nottage KA, Ware RE, Aygun B, et al. Hydroxycarbamide treatment and brain MRI/MRA findings in children with sickle cell anaemia. Br J Haematol. 2016;175(2):331–338.
    • (2016) Br J Haematol. , vol.175 , Issue.2 , pp. 331-338
    • Nottage, K.A.1    Ware, R.E.2    Aygun, B.3
  • 32
    • 84911973714 scopus 로고    scopus 로고
    • Predictors of splenic function preservation in children with sickle cell anemia treated with hydroxyurea
    • Nottage KA, Ware RE, Winter B, et al. Predictors of splenic function preservation in children with sickle cell anemia treated with hydroxyurea. Eur J Haematol. 2014;93(5):377–383.
    • (2014) Eur J Haematol. , vol.93 , Issue.5 , pp. 377-383
    • Nottage, K.A.1    Ware, R.E.2    Winter, B.3
  • 33
    • 84872972122 scopus 로고    scopus 로고
    • Hydroxyurea treatment decreases glomerular hyperfiltration in children with sickle cell anemia
    • Aygun B, Mortier NA, Smeltzer MP, Shulkin BL, Hankins JS, Ware RE. Hydroxyurea treatment decreases glomerular hyperfiltration in children with sickle cell anemia. Am J Hematol. 2013;88(2):116–119.
    • (2013) Am J Hematol. , vol.88 , Issue.2 , pp. 116-119
    • Aygun, B.1    Mortier, N.A.2    Smeltzer, M.P.3    Shulkin, B.L.4    Hankins, J.S.5    Ware, R.E.6
  • 34
    • 80052460693 scopus 로고    scopus 로고
    • Glomerular hyperfiltration and albuminuria in children with sickle cell anemia
    • Aygun B, Mortier NA, Smeltzer MP, Hankins JS, Ware RE. Glomerular hyperfiltration and albuminuria in children with sickle cell anemia. Pediatr Nephrol. 2011;26(8):1285–1290.
    • (2011) Pediatr Nephrol. , vol.26 , Issue.8 , pp. 1285-1290
    • Aygun, B.1    Mortier, N.A.2    Smeltzer, M.P.3    Hankins, J.S.4    Ware, R.E.5
  • 35
    • 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(11):3628–3632.
    • (2001) Blood. , vol.97 , Issue.11 , pp. 3628-3632
    • Ferster, A.1    Tahriri, P.2    Vermylen, C.3
  • 36
    • 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(7):2685–2690.
    • (2005) Blood. , vol.105 , Issue.7 , pp. 2685-2690
    • Gulbis, B.1    Haberman, D.2    Dufour, D.3
  • 37
    • 0030893396 scopus 로고    scopus 로고
    • Fetal hemoglobin in sickle cell anemia: Determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea
    • Steinberg MH, Lu ZH, Barton FB, Terrin ML, Charache S, Dover GJ. Fetal hemoglobin in sickle cell anemia: Determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea. Blood. 1997;89(3):1078–1088.
    • (1997) Blood. , vol.89 , Issue.3 , pp. 1078-1088
    • Steinberg, M.H.1    Lu, Z.H.2    Barton, F.B.3    Terrin, M.L.4    Charache, S.5    Dover, G.J.6
  • 38
    • 0033505007 scopus 로고    scopus 로고
    • Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: Implications for pharmacological intervention
    • Marcus SJ, Ware RE. Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: Implications for pharmacological intervention. J Pediatr Hematol Oncol. 1999;21(5):407–411.
    • (1999) J Pediatr Hematol Oncol. , vol.21 , Issue.5 , pp. 407-411
    • Marcus, S.J.1    Ware, R.E.2
  • 39
    • 0031012328 scopus 로고    scopus 로고
    • Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease
    • Marcus SJ, Kinney TR, Schultz WH, O'branski EE, Ware RE. Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease. Am J Hematol. 1997;54(1):40–46.
    • (1997) Am J Hematol. , vol.54 , Issue.1 , pp. 40-46
    • Marcus, S.J.1    Kinney, T.R.2    Schultz, W.H.3    O'branski, E.E.4    Ware, R.E.5
  • 40
    • 77950478131 scopus 로고    scopus 로고
    • Acute care utilization and rehospitalizations for sickle cell disease
    • Brousseau DC, Owens PL, Mosso AL, Panepinto JA, Steiner CA. Acute care utilization and rehospitalizations for sickle cell disease. JAMA. 2010;303(13):1288–1294.
    • (2010) JAMA. , vol.303 , Issue.13 , pp. 1288-1294
    • Brousseau, D.C.1    Owens, P.L.2    Mosso, A.L.3    Panepinto, J.A.4    Steiner, C.A.5
  • 41
    • 85011901148 scopus 로고    scopus 로고
    • Crizanlizumab for the prevention of pain crises in sickle cell disease
    • Ataga KI, Kutlar A, Kanter J, et al. Crizanlizumab for the prevention of pain crises in sickle cell disease. N Engl J Med. 2017;376(5):429–439.
    • (2017) N Engl J Med. , vol.376 , Issue.5 , pp. 429-439
    • Ataga, K.I.1    Kutlar, A.2    Kanter, J.3
  • 42
    • 85027941976 scopus 로고    scopus 로고
    • New developments in anti-sickling agents: Can drugs directly prevent the polymerization of sickle haemoglobin in vivo?
    • Oder E, Safo MK, Abdulmalik O, Kato GJ. New developments in anti-sickling agents: Can drugs directly prevent the polymerization of sickle haemoglobin in vivo?. Br J Haematol. 2016;175(1):24–30.
    • (2016) Br J Haematol. , vol.175 , Issue.1 , pp. 24-30
    • Oder, E.1    Safo, M.K.2    Abdulmalik, O.3    Kato, G.J.4
  • 43
    • 84940040459 scopus 로고    scopus 로고
    • Acute hemolytic vascular inflammatory process are prevented by nitric oxide replacement or a single dose of hydroxyurea
    • Almeida CB, Souza LE, Leonardo FC, et al. Acute hemolytic vascular inflammatory process are prevented by nitric oxide replacement or a single dose of hydroxyurea. Blood. 2017;126(6):711–720.
    • (2017) Blood. , vol.126 , Issue.6 , pp. 711-720
    • Almeida, C.B.1    Souza, L.E.2    Leonardo, F.C.3
  • 44
    • 77955905049 scopus 로고    scopus 로고
    • How I use hydroxyurea to treat young patients with sickle cell anemia
    • Ware RE. How I use hydroxyurea to treat young patients with sickle cell anemia. Blood. 2010;115(26):5300–5311.
    • (2010) Blood. , vol.115 , Issue.26 , pp. 5300-5311
    • Ware, R.E.1
  • 45
    • 0027981469 scopus 로고
    • Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease
    • Brown AK, Sleeper LA, Miller ST, Pegelow CH, Gill FM, Waclawiw MA. Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease. Arch Pediatr Adolesc Med. 1994;148(8):796–804.
    • (1994) Arch Pediatr Adolesc Med. , vol.148 , Issue.8 , pp. 796-804
    • Brown, A.K.1    Sleeper, L.A.2    Miller, S.T.3    Pegelow, C.H.4    Gill, F.M.5    Waclawiw, M.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.