메뉴 건너뛰기




Volumn 27, Issue 6, 2013, Pages 279-287

Management of sickle cell disease from childhood through adulthood

Author keywords

Adult; Haematology; Paediatric; Sickle cell disease

Indexed keywords

DEFERASIROX; DEFERIPRONE; DEFEROXAMINE; HEMOGLOBIN S; HYDROMORPHONE; HYDROXYUREA; IBUPROFEN; KETOROLAC; MORPHINE; PLACEBO;

EID: 84887608596     PISSN: 0268960X     EISSN: 15321681     Source Type: Journal    
DOI: 10.1016/j.blre.2013.09.001     Document Type: Article
Times cited : (111)

References (77)
  • 2
    • 0242552237 scopus 로고    scopus 로고
    • Managing sickle cell disease
    • Claster S., Vichinsky E.P. Managing sickle cell disease. BMJ 2003, 327:1151-1155.
    • (2003) BMJ , vol.327 , pp. 1151-1155
    • Claster, S.1    Vichinsky, E.P.2
  • 3
    • 44949128064 scopus 로고    scopus 로고
    • Global epidemiology of haemoglobin disorders and derived service indicators
    • Modell B., Darlison M. Global epidemiology of haemoglobin disorders and derived service indicators. Bull World Health Organ 2008, 86:480-487.
    • (2008) Bull World Health Organ , vol.86 , pp. 480-487
    • Modell, B.1    Darlison, M.2
  • 4
    • 77953952024 scopus 로고    scopus 로고
    • The inherited diseases of hemoglobin are an emerging global health burden
    • Weatherall D.J. The inherited diseases of hemoglobin are an emerging global health burden. Blood 2010, 115:4331-4336.
    • (2010) Blood , vol.115 , pp. 4331-4336
    • Weatherall, D.J.1
  • 6
    • 33846005515 scopus 로고    scopus 로고
    • National evaluation of US newborn screening system components
    • Therrell B.L., Hannon W.H. National evaluation of US newborn screening system components. Ment Retard Dev Disabil Res Rev 2006, 12:236-245.
    • (2006) Ment Retard Dev Disabil Res Rev , vol.12 , pp. 236-245
    • Therrell, B.L.1    Hannon, W.H.2
  • 7
    • 74049150729 scopus 로고    scopus 로고
    • The number of people with sickle-cell disease in the United States: national and state estimates
    • Brousseau D.C., Panepinto J.A., Nimmer M., Hoffmann R.G. The number of people with sickle-cell disease in the United States: national and state estimates. Am J Hematol 2010, 85:77-78.
    • (2010) Am J Hematol , vol.85 , pp. 77-78
    • Brousseau, D.C.1    Panepinto, J.A.2    Nimmer, M.3    Hoffmann, R.G.4
  • 8
    • 77949482609 scopus 로고    scopus 로고
    • Population estimates of sickle cell disease in the U.S
    • Hassell K.L. Population estimates of sickle cell disease in the U.S. Am J Prev Med 2010, 38:S512-S521.
    • (2010) Am J Prev Med , vol.38
    • Hassell, K.L.1
  • 9
    • 77951712618 scopus 로고    scopus 로고
    • Improved survival of children and adolescents with sickle cell disease
    • Quinn C.T., Rogers Z.R., McCavit T.L., Buchanan G.R. Improved survival of children and adolescents with sickle cell disease. Blood 2010, 115:3447-3452.
    • (2010) Blood , vol.115 , pp. 3447-3452
    • Quinn, C.T.1    Rogers, Z.R.2    McCavit, T.L.3    Buchanan, G.R.4
  • 10
    • 0022628893 scopus 로고
    • Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial
    • Gaston M.H., Verter J.I., Woods G., Pegelow C., Kelleher J., Presbury G., et al. Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. N Engl J Med 1986, 314:1593-1599.
    • (1986) N Engl J Med , vol.314 , pp. 1593-1599
    • Gaston, M.H.1    Verter, J.I.2    Woods, G.3    Pegelow, C.4    Kelleher, J.5    Presbury, G.6
  • 11
    • 58349102500 scopus 로고    scopus 로고
    • Implementation of universal newborn bloodspot screening for sickle cell disease and other clinically significant haemoglobinopathies in England: screening results for 2005-7
    • Streetly A., Latinovic R., Hall K., Henthorn J. Implementation of universal newborn bloodspot screening for sickle cell disease and other clinically significant haemoglobinopathies in England: screening results for 2005-7. J Clin Pathol 2009, 62:26-30.
    • (2009) J Clin Pathol , vol.62 , pp. 26-30
    • Streetly, A.1    Latinovic, R.2    Hall, K.3    Henthorn, J.4
  • 12
    • 62649144053 scopus 로고    scopus 로고
    • Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002
    • Yanni E., Grosse S.D., Yang Q., Olney R.S. Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002. J Pediatr 2009, 154:541-545.
    • (2009) J Pediatr , vol.154 , pp. 541-545
    • Yanni, E.1    Grosse, S.D.2    Yang, Q.3    Olney, R.S.4
  • 13
    • 40949107353 scopus 로고    scopus 로고
    • Effectiveness of the 7-valent pneumococcal conjugate vaccine in children with sickle cell disease in the first decade of life
    • Adamkiewicz T.V., Silk B.J., Howgate J., Baughman W., Strayhorn G., Sullivan K., et al. Effectiveness of the 7-valent pneumococcal conjugate vaccine in children with sickle cell disease in the first decade of life. Pediatrics 2008, 121:562-569.
    • (2008) Pediatrics , vol.121 , pp. 562-569
    • Adamkiewicz, T.V.1    Silk, B.J.2    Howgate, J.3    Baughman, W.4    Strayhorn, G.5    Sullivan, K.6
  • 15
    • 84887611971 scopus 로고    scopus 로고
    • Managing the acutely ill adult with sickle cell disease
    • 90-2
    • Brown M. Managing the acutely ill adult with sickle cell disease. Br J Nurs 2012, 21(90-2):5-6.
    • (2012) Br J Nurs , vol.21 , pp. 5-6
    • Brown, M.1
  • 17
    • 64149099554 scopus 로고    scopus 로고
    • Neutrophil sandwiches injure the microcirculation
    • Looney M.R., Matthay M.A. Neutrophil sandwiches injure the microcirculation. Nat Med 2009, 15:364-366.
    • (2009) Nat Med , vol.15 , pp. 364-366
    • Looney, M.R.1    Matthay, M.A.2
  • 18
    • 84876571521 scopus 로고    scopus 로고
    • Available at, [accessed July 18, 2013] Novartis AG Iron Health Alliance
    • Novartis AG Iron Health Alliance Sickle cell disease Available at, [accessed July 18, 2013]. http://www.ironhealthalliance.com/disease-states/sickle-cell-disease.jsp.
    • Sickle cell disease
  • 19
    • 54349103017 scopus 로고    scopus 로고
    • Growth and nutritional status of children with homozygous sickle cell disease
    • Al-Saqladi A.W., Cipolotti R., Fijnvandraat K., Brabin B.J. Growth and nutritional status of children with homozygous sickle cell disease. Ann Trop Paediatr 2008, 28:165-189.
    • (2008) Ann Trop Paediatr , vol.28 , pp. 165-189
    • Al-Saqladi, A.W.1    Cipolotti, R.2    Fijnvandraat, K.3    Brabin, B.J.4
  • 20
    • 80053374132 scopus 로고    scopus 로고
    • Asthma morbidity and treatment in children with sickle cell disease
    • Anim S.O., Strunk R.C., DeBaun M.R. Asthma morbidity and treatment in children with sickle cell disease. Expert Rev Respir Med 2011, 5:635-645.
    • (2011) Expert Rev Respir Med , vol.5 , pp. 635-645
    • Anim, S.O.1    Strunk, R.C.2    DeBaun, M.R.3
  • 21
    • 36348959032 scopus 로고    scopus 로고
    • Management of vasoocclusive pain events in sickle cell disease
    • quiz 8-41
    • Ellison A.M., Shaw K. Management of vasoocclusive pain events in sickle cell disease. Pediatr Emerg Care 2007, 23:832-838. quiz 8-41.
    • (2007) Pediatr Emerg Care , vol.23 , pp. 832-838
    • Ellison, A.M.1    Shaw, K.2
  • 22
    • 34147223415 scopus 로고    scopus 로고
    • Anxiety and depression in children and adolescents with sickle cell disease
    • Benton T.D., Ifeagwu J.A., Smith-Whitley K. Anxiety and depression in children and adolescents with sickle cell disease. Curr Psychiatry Rep 2007, 9:114-121.
    • (2007) Curr Psychiatry Rep , vol.9 , pp. 114-121
    • Benton, T.D.1    Ifeagwu, J.A.2    Smith-Whitley, K.3
  • 23
    • 2542455639 scopus 로고    scopus 로고
    • Survival of children with sickle cell disease
    • Quinn C.T., Rogers Z.R., Buchanan G.R. Survival of children with sickle cell disease. Blood 2004, 103:4023-4027.
    • (2004) Blood , vol.103 , pp. 4023-4027
    • Quinn, C.T.1    Rogers, Z.R.2    Buchanan, G.R.3
  • 24
    • 34548753905 scopus 로고    scopus 로고
    • Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London
    • Telfer P., Coen P., Chakravorty S., Wilkey O., Evans J., Newell H., et al. Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London. Haematologica 2007, 92:905-912.
    • (2007) Haematologica , vol.92 , pp. 905-912
    • Telfer, P.1    Coen, P.2    Chakravorty, S.3    Wilkey, O.4    Evans, J.5    Newell, H.6
  • 25
    • 69649101810 scopus 로고    scopus 로고
    • The excess burden of stroke in hospitalized adults with sickle cell disease
    • Strouse J.J., Jordan L.C., Lanzkron S., Casella J.F. The excess burden of stroke in hospitalized adults with sickle cell disease. Am J Hematol 2009, 84:548-552.
    • (2009) Am J Hematol , vol.84 , pp. 548-552
    • Strouse, J.J.1    Jordan, L.C.2    Lanzkron, S.3    Casella, J.F.4
  • 26
    • 34247108061 scopus 로고    scopus 로고
    • The pathophysiology, prevention, and treatment of stroke in sickle cell disease
    • Wang W.C. 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.C.1
  • 27
    • 84860328824 scopus 로고    scopus 로고
    • Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure
    • DeBaun M.R., Sarnaik S.A., Rodeghier M.J., Minniti C.P., Howard T.H., Iyer R.V., et al. Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure. Blood 2012, 119:3684-3690.
    • (2012) Blood , vol.119 , pp. 3684-3690
    • DeBaun, M.R.1    Sarnaik, S.A.2    Rodeghier, M.J.3    Minniti, C.P.4    Howard, T.H.5    Iyer, R.V.6
  • 28
    • 0031775847 scopus 로고    scopus 로고
    • Cognitive screening examinations for silent cerebral infarcts in sickle cell disease
    • DeBaun M.R., Schatz J., Siegel M.J., Koby M., Craft S., Resar L., et al. Cognitive screening examinations for silent cerebral infarcts in sickle cell disease. Neurology 1998, 50:1678-1682.
    • (1998) Neurology , vol.50 , pp. 1678-1682
    • DeBaun, M.R.1    Schatz, J.2    Siegel, M.J.3    Koby, M.4    Craft, S.5    Resar, L.6
  • 29
    • 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 R.J., McKie V.C., Hsu L., Files B., Vichinsky E., Pegelow C., 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    Files, B.4    Vichinsky, E.5    Pegelow, C.6
  • 30
    • 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., Kronish D., Shiboski S.C., Adams R.J., et al. Utilization of TCD screening for primary stroke prevention in children with sickle cell disease. Neurology 2009, 72:1316-1321.
    • (2009) Neurology , vol.72 , pp. 1316-1321
    • Armstrong-Wells, J.1    Grimes, B.2    Sidney, S.3    Kronish, D.4    Shiboski, S.C.5    Adams, R.J.6
  • 31
    • 85044805921 scopus 로고    scopus 로고
    • Healthcare provision for sickle cell disease: challenges for the African context
    • Dennis-Antwi J.A., Dyson S.M., Ohene-Frempong K. Healthcare provision for sickle cell disease: challenges for the African context. Divers. Health Soc. Care 2008, 5:241-254.
    • (2008) Divers. Health Soc. Care , vol.5 , pp. 241-254
    • Dennis-Antwi, J.A.1    Dyson, S.M.2    Ohene-Frempong, K.3
  • 32
    • 64549106465 scopus 로고    scopus 로고
    • Asthma management: reinventing the wheel in sickle cell disease
    • Morris C.R. Asthma management: reinventing the wheel in sickle cell disease. Am J Hematol 2009, 84:234-241.
    • (2009) Am J Hematol , vol.84 , pp. 234-241
    • Morris, C.R.1
  • 33
    • 35748980612 scopus 로고    scopus 로고
    • Asthma is associated with increased mortality in individuals with sickle cell anemia
    • Boyd J.H., Macklin E.A., Strunk R.C., DeBaun M.R. Asthma is associated with increased mortality in individuals with sickle cell anemia. Haematologica 2007, 92:1115-1118.
    • (2007) Haematologica , vol.92 , pp. 1115-1118
    • Boyd, J.H.1    Macklin, E.A.2    Strunk, R.C.3    DeBaun, M.R.4
  • 34
    • 18044397307 scopus 로고    scopus 로고
    • Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significance
    • Ballas S.K., Lusardi M. Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significance. Am J Hematol 2005, 79:17-25.
    • (2005) Am J Hematol , vol.79 , pp. 17-25
    • Ballas, S.K.1    Lusardi, M.2
  • 36
    • 0031035337 scopus 로고    scopus 로고
    • Acute chest syndrome in sickle cell disease: clinical presentation and course. Cooperative Study of Sickle Cell Disease
    • Vichinsky E.P., Styles L.A., Colangelo L.H., Wright E.C., Castro O., Nickerson B. Acute chest syndrome in sickle cell disease: clinical presentation and course. Cooperative Study of Sickle Cell Disease. Blood 1997, 89:1787-1792.
    • (1997) Blood , vol.89 , pp. 1787-1792
    • Vichinsky, E.P.1    Styles, L.A.2    Colangelo, L.H.3    Wright, E.C.4    Castro, O.5    Nickerson, B.6
  • 39
    • 81255210779 scopus 로고    scopus 로고
    • The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease
    • Strouse J.J., Lanzkron S., Urrutia V. The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease. Expert Rev Hematol 2011, 4:597-606.
    • (2011) Expert Rev Hematol , vol.4 , pp. 597-606
    • Strouse, J.J.1    Lanzkron, S.2    Urrutia, V.3
  • 40
    • 84856155504 scopus 로고    scopus 로고
    • Evidence-based management of sickle cell disease in the emergency department
    • [quiz]
    • Glassberg J. Evidence-based management of sickle cell disease in the emergency department. Emerg Med Pract 2011, 13:1-20. [quiz].
    • (2011) Emerg Med Pract , vol.13 , pp. 1-20
    • Glassberg, J.1
  • 41
    • 51949116346 scopus 로고    scopus 로고
    • Management of sickle cell disease
    • de Montalembert M. Management of sickle cell disease. BMJ 2008, 337:a1397.
    • (2008) BMJ , vol.337
    • de Montalembert, M.1
  • 42
    • 0029005136 scopus 로고
    • Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions
    • Pegelow C.H., Adams R.J., McKie V., Abboud M., Berman B., Miller S.T., et al. Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions. J Pediatr 1995, 126:896-899.
    • (1995) J Pediatr , vol.126 , pp. 896-899
    • Pegelow, C.H.1    Adams, R.J.2    McKie, V.3    Abboud, M.4    Berman, B.5    Miller, S.T.6
  • 43
    • 0037167227 scopus 로고    scopus 로고
    • New therapies in sickle cell disease
    • Vichinsky E. New therapies in sickle cell disease. Lancet 2002, 360:629-631.
    • (2002) Lancet , vol.360 , pp. 629-631
    • Vichinsky, E.1
  • 44
    • 84862254136 scopus 로고    scopus 로고
    • Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children
    • Strouse J.J., Heeney M.M. Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children. Pediatr Blood Cancer 2012, 59:365-371.
    • (2012) Pediatr Blood Cancer , vol.59 , pp. 365-371
    • Strouse, J.J.1    Heeney, M.M.2
  • 45
    • 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 M.L., Moore R.D., Dover G.J., Barton F.B., Eckert S.V., 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    Dover, G.J.4    Barton, F.B.5    Eckert, S.V.6
  • 46
    • 0029845949 scopus 로고    scopus 로고
    • Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial
    • Ferster A., Vermylen C., Cornu G., Buyse M., Corazza F., Devalck C., et al. Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial. Blood 1996, 88:1960-1964.
    • (1996) Blood , vol.88 , pp. 1960-1964
    • Ferster, A.1    Vermylen, C.2    Cornu, G.3    Buyse, M.4    Corazza, F.5    Devalck, C.6
  • 47
    • 84864917063 scopus 로고    scopus 로고
    • Effect of hydroxyurea treatment on renal function parameters: results from the multi-center placebo-controlled BABY HUG clinical trial for infants with sickle cell anemia
    • Alvarez O., Miller S.T., Wang W.C., Luo Z., McCarville M.B., Schwartz G.J., et al. Effect of hydroxyurea treatment on renal function parameters: results from the multi-center placebo-controlled BABY HUG clinical trial for infants with sickle cell anemia. Pediatr Blood Cancer 2012, 59:668-674.
    • (2012) Pediatr Blood Cancer , vol.59 , pp. 668-674
    • Alvarez, O.1    Miller, S.T.2    Wang, W.C.3    Luo, Z.4    McCarville, M.B.5    Schwartz, G.J.6
  • 48
    • 84861094707 scopus 로고    scopus 로고
    • Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: results from the BABY-HUG phase III clinical trial
    • McGann P.T., Flanagan J.M., Howard T.A., Dertinger S.D., He J., Kulharya A.S., et al. Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: results from the BABY-HUG phase III clinical trial. Pediatr Blood Cancer 2012, 59:254-257.
    • (2012) Pediatr Blood Cancer , vol.59 , pp. 254-257
    • McGann, P.T.1    Flanagan, J.M.2    Howard, T.A.3    Dertinger, S.D.4    He, J.5    Kulharya, A.S.6
  • 49
    • 84869803950 scopus 로고    scopus 로고
    • Impact of hydroxyurea on clinical events in the BABY HUG trial
    • [quiz 448]
    • Thornburg C.D., Files B.A., Luo Z., Miller S.T., Kalpatthi R., Iyer R., et al. Impact of hydroxyurea on clinical events in the BABY HUG trial. Blood 2012, 120:4304-4310. [quiz 448].
    • (2012) Blood , vol.120 , pp. 4304-4310
    • Thornburg, C.D.1    Files, B.A.2    Luo, Z.3    Miller, S.T.4    Kalpatthi, R.5    Iyer, R.6
  • 50
    • 0028046507 scopus 로고
    • Effects of a long-term transfusion regimen on sickle cell-related illnesses
    • Styles L.A., Vichinsky E. Effects of a long-term transfusion regimen on sickle cell-related illnesses. J Pediatr 1994, 125:909-911.
    • (1994) J Pediatr , vol.125 , pp. 909-911
    • Styles, L.A.1    Vichinsky, E.2
  • 51
    • 78651378996 scopus 로고    scopus 로고
    • Iron-chelating therapy for transfusional iron overload
    • Brittenham G.M. Iron-chelating therapy for transfusional iron overload. N Engl J Med 2011, 364:146-156.
    • (2011) N Engl J Med , vol.364 , pp. 146-156
    • Brittenham, G.M.1
  • 53
    • 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 D.J., Price C., Schwartz D., Terrill C., Buchanan G.R., Shurney W., 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, 140:348-354.
    • (2002) J Pediatr , vol.140 , pp. 348-354
    • Scothorn, D.J.1    Price, C.2    Schwartz, D.3    Terrill, C.4    Buchanan, G.R.5    Shurney, W.6
  • 54
    • 78751697297 scopus 로고    scopus 로고
    • Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
    • Hulbert M.L., McKinstry R.C., Lacey J.L., Moran C.J., Panepinto J.A., Thompson A.A., 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    Moran, C.J.4    Panepinto, J.A.5    Thompson, A.A.6
  • 55
    • 84860348352 scopus 로고    scopus 로고
    • Stroke With Transfusions Changing to Hydroxyurea (SWiTCH)
    • Ware R.E., Helms R.W., Investigators S.W. 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    Investigators, S.W.3
  • 56
    • 77953461487 scopus 로고    scopus 로고
    • Current strategies for the management of children with sickle cell disease
    • de Montalembert M. Current strategies for the management of children with sickle cell disease. Expert Rev Hematol 2009, 2:455-463.
    • (2009) Expert Rev Hematol , vol.2 , pp. 455-463
    • de Montalembert, M.1
  • 57
    • 84859412957 scopus 로고    scopus 로고
    • Primary prophylaxis in sickle cell disease: is it feasible? Is it effective?
    • Thompson A.A. Primary prophylaxis in sickle cell disease: is it feasible? Is it effective?. Hematology Am Soc Hematol Educ Program 2011, 2011:434-439.
    • (2011) Hematology Am Soc Hematol Educ Program , vol.2011 , pp. 434-439
    • Thompson, A.A.1
  • 58
    • 79959244335 scopus 로고    scopus 로고
    • Stem-cell transplantation in children and adults with sickle cell disease: an update
    • Khoury R., Abboud M.R. Stem-cell transplantation in children and adults with sickle cell disease: an update. Expert Rev Hematol 2011, 4:343-351.
    • (2011) Expert Rev Hematol , vol.4 , pp. 343-351
    • Khoury, R.1    Abboud, M.R.2
  • 59
    • 70249132888 scopus 로고    scopus 로고
    • Hematopoietic stem cell transplantation for children with sickle cell disease
    • Oringanje C., Nemecek E., Oniyangi O. Hematopoietic stem cell transplantation for children with sickle cell disease. Cochrane Database Syst Rev 2009, CD007001.
    • (2009) Cochrane Database Syst Rev
    • Oringanje, C.1    Nemecek, E.2    Oniyangi, O.3
  • 60
    • 38949178118 scopus 로고    scopus 로고
    • Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: an educational void
    • Solomon L.R. Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: an educational void. Blood 2008, 111:997-1003.
    • (2008) Blood , vol.111 , pp. 997-1003
    • Solomon, L.R.1
  • 61
    • 0036360040 scopus 로고    scopus 로고
    • Clinical significance of RBC alloantibodies and autoantibodies in sickle cell patients who received transfusions
    • Aygun B., Padmanabhan S., Paley C., Chandrasekaran V. Clinical significance of RBC alloantibodies and autoantibodies in sickle cell patients who received transfusions. Transfusion 2002, 42:37-43.
    • (2002) Transfusion , vol.42 , pp. 37-43
    • Aygun, B.1    Padmanabhan, S.2    Paley, C.3    Chandrasekaran, V.4
  • 62
    • 77956419792 scopus 로고    scopus 로고
    • A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease
    • Taylor L.E., Stotts N.A., Humphreys J., Treadwell M.J., Miaskowski C. A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease. J Pain Symptom Manage 2010, 40:416-435.
    • (2010) J Pain Symptom Manage , vol.40 , pp. 416-435
    • Taylor, L.E.1    Stotts, N.A.2    Humphreys, J.3    Treadwell, M.J.4    Miaskowski, C.5
  • 63
    • 63449117520 scopus 로고    scopus 로고
    • Barriers to effective pain management in sickle cell disease
    • Wright K., Adeosum O. Barriers to effective pain management in sickle cell disease. Br J Nurs 2009, 18:158-161.
    • (2009) Br J Nurs , vol.18 , pp. 158-161
    • Wright, K.1    Adeosum, O.2
  • 64
    • 0037288007 scopus 로고    scopus 로고
    • Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease
    • Telfair J., Haque A., Etienne M., Tang S., Strasser S. Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease. Public Health Rep 2003, 118:27-36.
    • (2003) Public Health Rep , vol.118 , pp. 27-36
    • Telfair, J.1    Haque, A.2    Etienne, M.3    Tang, S.4    Strasser, S.5
  • 65
    • 0033931159 scopus 로고    scopus 로고
    • Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina
    • Haque A., Telfair J. Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina. J Rural Health 2000, 16:43-55.
    • (2000) J Rural Health , vol.16 , pp. 43-55
    • Haque, A.1    Telfair, J.2
  • 66
    • 0036898681 scopus 로고    scopus 로고
    • Implementing transitions for youth with complex chronic conditions using the medical home model
    • Kelly A.M., Kratz B., Bielski M., Rinehart P.M. Implementing transitions for youth with complex chronic conditions using the medical home model. Pediatrics 2002, 110:1322-1327.
    • (2002) Pediatrics , vol.110 , pp. 1322-1327
    • Kelly, A.M.1    Kratz, B.2    Bielski, M.3    Rinehart, P.M.4
  • 67
    • 77951619147 scopus 로고    scopus 로고
    • Sickle cell disease in the United States: looking back and forward at 100years of progress in management and survival
    • Prabhakar H., Haywood C., Molokie R. Sickle cell disease in the United States: looking back and forward at 100years of progress in management and survival. Am J Hematol 2010, 85:346-353.
    • (2010) Am J Hematol , vol.85 , pp. 346-353
    • Prabhakar, H.1    Haywood, C.2    Molokie, R.3
  • 68
    • 78650383011 scopus 로고    scopus 로고
    • Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research
    • Treadwell M., Telfair J., Gibson R.W., Johnson S., Osunkwo I. Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research. Am J Hematol 2011, 86:116-120.
    • (2011) Am J Hematol , vol.86 , pp. 116-120
    • Treadwell, M.1    Telfair, J.2    Gibson, R.W.3    Johnson, S.4    Osunkwo, I.5
  • 69
    • 77950478131 scopus 로고    scopus 로고
    • Acute care utilization and rehospitalizations for sickle cell disease
    • Brousseau D.C., Owens P.L., Mosso A.L., Panepinto J.A., Steiner C.A. Acute care utilization and rehospitalizations for sickle cell disease. JAMA 2010, 303:1288-1294.
    • (2010) JAMA , vol.303 , pp. 1288-1294
    • Brousseau, D.C.1    Owens, P.L.2    Mosso, A.L.3    Panepinto, J.A.4    Steiner, C.A.5
  • 70
    • 0036483674 scopus 로고    scopus 로고
    • A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services
    • Wojciechowski E.A., Hurtig A., Dorn L. A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services. J Pediatr Nurs 2002, 17:18-27.
    • (2002) J Pediatr Nurs , vol.17 , pp. 18-27
    • Wojciechowski, E.A.1    Hurtig, A.2    Dorn, L.3
  • 71
    • 77649243106 scopus 로고    scopus 로고
    • From cradle to commencement: transitioning pediatric sickle cell disease patients to adult providers
    • Doulton D.M. From cradle to commencement: transitioning pediatric sickle cell disease patients to adult providers. J Pediatr Oncol Nurs 2010, 27:119-123.
    • (2010) J Pediatr Oncol Nurs , vol.27 , pp. 119-123
    • Doulton, D.M.1
  • 72
  • 73
    • 34147141453 scopus 로고    scopus 로고
    • Sickle cell disease: old discoveries, new concepts, and future promise
    • Frenette P.S., Atweh G.F. Sickle cell disease: old discoveries, new concepts, and future promise. J Clin Invest 2007, 117:850-858.
    • (2007) J Clin Invest , vol.117 , pp. 850-858
    • Frenette, P.S.1    Atweh, G.F.2
  • 74
    • 33646779583 scopus 로고    scopus 로고
    • Recent advances in globin gene transfer for the treatment of beta-thalassemia and sickle cell anemia
    • Sadelain M. Recent advances in globin gene transfer for the treatment of beta-thalassemia and sickle cell anemia. Curr Opin Hematol 2006, 13:142-148.
    • (2006) Curr Opin Hematol , vol.13 , pp. 142-148
    • Sadelain, M.1
  • 75
    • 72449211881 scopus 로고    scopus 로고
    • A systems biology consideration of the vasculopathy of sickle cell anemia: the need for multi-modality chemo-prophylaxsis
    • Hebbel R.P., Vercellotti G., Nath K.A. A systems biology consideration of the vasculopathy of sickle cell anemia: the need for multi-modality chemo-prophylaxsis. Cardiovasc Hematol Disord Drug Targets 2009, 9:271-292.
    • (2009) Cardiovasc Hematol Disord Drug Targets , vol.9 , pp. 271-292
    • Hebbel, R.P.1    Vercellotti, G.2    Nath, K.A.3
  • 76
    • 18844446494 scopus 로고    scopus 로고
    • Platelet-vessel wall interactions in the microcirculation
    • Tailor A., Cooper D., Granger D.N. Platelet-vessel wall interactions in the microcirculation. Microcirculation 2005, 12:275-285.
    • (2005) Microcirculation , vol.12 , pp. 275-285
    • Tailor, A.1    Cooper, D.2    Granger, D.N.3
  • 77
    • 56749163948 scopus 로고    scopus 로고
    • Pulmonary complications of sickle cell disease
    • Gladwin M.T., Vichinsky E. Pulmonary complications of sickle cell disease. N Engl J Med 2008, 359:2254-2265.
    • (2008) N Engl J Med , vol.359 , pp. 2254-2265
    • Gladwin, M.T.1    Vichinsky, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.