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Volumn 16, Issue 3, 2009, Pages 173-178

Acute pain in children and adults with sickle cell disease: Management in the absence of evidence-based guidelines

Author keywords

Pain; Sickle cell disease; Vaso occlusion

Indexed keywords

IBUPROFEN; MORPHINE; OPIATE; PARACETAMOL;

EID: 67749118113     PISSN: 10656251     EISSN: 15317048     Source Type: Journal    
DOI: 10.1097/MOH.0b013e328329e167     Document Type: Review
Times cited : (38)

References (27)
  • 1
    • 67749121655 scopus 로고    scopus 로고
    • Sickle cell disease population estimation: Application of available contemporary data to traditional methods
    • Washington, DC
    • Hassell K. Sickle cell disease population estimation: application of available contemporary data to traditional methods. In: 35th Anniversary Convention of the National Sickle Cell Disease Program; 2007; Washington, DC.
    • (2007) 35th Anniversary Convention of the National Sickle Cell Disease Program
    • Hassell, K.1
  • 2
    • 0018679483 scopus 로고
    • Adhesion of normal and sickle erythrocytes to endothelial monolayer cultures
    • Hoover R, Rubin R, Wise G, Warren R. Adhesion of normal and sickle erythrocytes to endothelial monolayer cultures. Blood 1979; 54:872-876.
    • (1979) Blood , vol.54 , pp. 872-876
    • Hoover, R.1    Rubin, R.2    Wise, G.3    Warren, R.4
  • 3
    • 0018885938 scopus 로고
    • Erythrocyte adherence to endothelium in sickle cell anemia: A possible determinant of disease severity
    • Hebbel RP, Boogaerts MA, Eaton JW, et al. Erythrocyte adherence to endothelium in sickle cell anemia: a possible determinant of disease severity. N Engl J Med 1980; 302:992-995.
    • (1980) N Engl J Med , vol.302 , pp. 992-995
    • Hebbel, R.P.1    Boogaerts, M.A.2    Eaton, J.W.3
  • 4
    • 10244278094 scopus 로고    scopus 로고
    • Sickle cell vasoocclusion: Heterotypic, multicellular aggregations driven by leukocyte adhesion
    • Frenette PS. Sickle cell vasoocclusion: heterotypic, multicellular aggregations driven by leukocyte adhesion. Microcirculation 2004; 11:167-177.
    • (2004) Microcirculation , vol.11 , pp. 167-177
    • Frenette, P.S.1
  • 5
    • 0034307274 scopus 로고    scopus 로고
    • Activated monocytes in sickle cell disease: Potential role in the activation of vascular endothelium and vasoocclusion
    • Belcher JD, Marker PH, Weber JP, et al. Activated monocytes in sickle cell disease: potential role in the activation of vascular endothelium and vasoocclusion. Blood 2000; 96:2451-2459.
    • (2000) Blood , vol.96 , pp. 2451-2459
    • Belcher, J.D.1    Marker, P.H.2    Weber, J.P.3
  • 6
    • 0025350965 scopus 로고
    • Enhancement of sickle erythrocyte adherence to endothelium by autologous platelets
    • Antonucci R, Walker R, Herion J, Orringer E. Enhancement of sickle erythrocyte adherence to endothelium by autologous platelets. Am J Hematol 1990; 34:44-48.
    • (1990) Am J Hematol , vol.34 , pp. 44-48
    • Antonucci, R.1    Walker, R.2    Herion, J.3    Orringer, E.4
  • 7
    • 0031147997 scopus 로고    scopus 로고
    • Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia
    • Wun T, Paglieroni T, Tablin F, et al. Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia. J Lab Clin Med 1997; 129:507-516.
    • (1997) J Lab Clin Med , vol.129 , pp. 507-516
    • Wun, T.1    Paglieroni, T.2    Tablin, F.3
  • 8
    • 3242792093 scopus 로고    scopus 로고
    • The endothelial biology of sickle cell disease: Inflammation and a chronic vasculopathy
    • Hebbel RP, Osarogiagbon R, Kaul D. The endothelial biology of sickle cell disease: inflammation and a chronic vasculopathy. Microcirculation 2004; 11:129-151.
    • (2004) Microcirculation , vol.11 , pp. 129-151
    • Hebbel, R.P.1    Osarogiagbon, R.2    Kaul, D.3
  • 9
    • 0025770390 scopus 로고
    • Pain in sickle cell disease. Rates and risk factors
    • Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med 1991; 325:11-16.
    • (1991) N Engl J Med , vol.325 , pp. 11-16
    • Platt, O.S.1    Thorington, B.D.2    Brambilla, D.J.3
  • 10
    • 0016794848 scopus 로고
    • Role of hybrid tetramer formation in gelation of haemoglobin S
    • Bookchin RM, Nagel RL, Balazs T. Role of hybrid tetramer formation in gelation of haemoglobin S. Nature 1975; 256:667-668.
    • (1975) Nature , vol.256 , pp. 667-668
    • Bookchin, R.M.1    Nagel, R.L.2    Balazs, T.3
  • 11
    • 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 Program 2008; 2008: 177-185.
    • (2008) Hematology Am Soc Hematol Educ Program 2008 , pp. 177-185
    • Morris, C.R.1
  • 12
    • 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
  • 13
    • 33644775612 scopus 로고    scopus 로고
    • Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease
    • Kato GJ, McGowan V, Machado RF, et al. Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease. Blood 2006; 107:2279-2285.
    • (2006) Blood , vol.107 , pp. 2279-2285
    • Kato, G.J.1    McGowan, V.2    Machado, R.F.3
  • 14
    • 0025969263 scopus 로고
    • Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells
    • Ballas SK. Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells. Am J Hematol 1991; 36:122-130.
    • (1991) Am J Hematol , vol.36 , pp. 122-130
    • Ballas, S.K.1
  • 15
    • 4143132048 scopus 로고    scopus 로고
    • Are there clinical phenotypes of homozygous sickle cell disease?
    • Alexander N, Higgs D, Dover G, Serjeant GR. Are there clinical phenotypes of homozygous sickle cell disease? Br J Haematol 2004; 126:606-611.
    • (2004) Br J Haematol , vol.126 , pp. 606-611
    • Alexander, N.1    Higgs, D.2    Dover, G.3    Serjeant, G.R.4
  • 16
    • 62449189504 scopus 로고    scopus 로고
    • Risk factors for hospital readmission within 30 days: A new quality measure for children with sickle cell disease
    • This study finds that lack of outpatient follow-up within 30 days after hospital discharge is a risk for readmission
    • Frei-Jones MJ, Field JJ, DeBaun MR. Risk factors for hospital readmission within 30 days: a new quality measure for children with sickle cell disease. Pediatr Blood Cancer 2009; 52:481-485. This study finds that lack of outpatient follow-up within 30 days after hospital discharge is a risk for readmission.
    • (2009) Pediatr Blood Cancer , vol.52 , pp. 481-485
    • Frei-Jones, M.J.1    Field, J.J.2    DeBaun, M.R.3
  • 17
    • 38749109710 scopus 로고    scopus 로고
    • Daily assessment of pain in adults with sickle cell disease
    • This study establishes that adults with sickle cell disease frequently manage acute pain events at home without physician contact
    • Smith WR, Penberthy LT, Bovbjerg VE, et al. Daily assessment of pain in adults with sickle cell disease. Ann Intern Med 2008; 148:94-101. This study establishes that adults with sickle cell disease frequently manage acute pain events at home without physician contact
    • (2008) Ann Intern Med , vol.148 , pp. 94-101
    • Smith, W.R.1    Penberthy, L.T.2    Bovbjerg, V.E.3
  • 18
    • 33747478249 scopus 로고    scopus 로고
    • Painful episodes in children with sickle cell disease and asthma are temporally associated with respiratory symptoms
    • Glassberg J, Spivey JF, Strunk R, et al. Painful episodes in children with sickle cell disease and asthma are temporally associated with respiratory symptoms. J Pediatr Hematol Oncol 2006; 28:481-485.
    • (2006) J Pediatr Hematol Oncol , vol.28 , pp. 481-485
    • Glassberg, J.1    Spivey, J.F.2    Strunk, R.3
  • 19
    • 54049147444 scopus 로고    scopus 로고
    • Association between wind speed and the occurrence of sickle cell acute painful episodes: Results of a case-crossover study
    • Nolan VG, Zhang Y, Lash T, et al. Association between wind speed and the occurrence of sickle cell acute painful episodes: results of a case-crossover study. Br J Haematol 2008; 143:433-438.
    • (2008) Br J Haematol , vol.143 , pp. 433-438
    • Nolan, V.G.1    Zhang, Y.2    Lash, T.3
  • 20
    • 33644788545 scopus 로고    scopus 로고
    • Windy weather and low humidity are associated with an increased number of hospital admissions for acute pain and sickle cell disease in an urban environment with a maritime temperate climate
    • Jones S, Duncan ER, Thomas N, et al. Windy weather and low humidity are associated with an increased number of hospital admissions for acute pain and sickle cell disease in an urban environment with a maritime temperate climate. Br J Haematol 2005; 131:530-533.
    • (2005) Br J Haematol , vol.131 , pp. 530-533
    • Jones, S.1    Duncan, E.R.2    Thomas, N.3
  • 21
    • 18044397307 scopus 로고    scopus 로고
    • Hospital readmission for adult acute sickle cell painful episodes: Frequency, etiology, and prognostic significance
    • Ballas SK, 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
  • 22
    • 11144279969 scopus 로고    scopus 로고
    • Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease
    • Panepinto JA, Brousseau DC, Hillery CA, Scott JP. Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease. Pediatr Blood Cancer 2005; 44:182-186.
    • (2005) Pediatr Blood Cancer , vol.44 , pp. 182-186
    • Panepinto, J.A.1    Brousseau, D.C.2    Hillery, C.A.3    Scott, J.P.4
  • 23
    • 62449175675 scopus 로고    scopus 로고
    • A question of quality in sickle cell disease
    • Quinn CT. A question of quality in sickle cell disease. Pediatr Blood Cancer 2009; 52:435-436.
    • (2009) Pediatr Blood Cancer , vol.52 , pp. 435-436
    • Quinn, C.T.1
  • 24
    • 0037265771 scopus 로고    scopus 로고
    • Examining the validity, reliability, and preference of three pediatric pain measurement tools in African-American children
    • Luffy R, Grove SK. Examining the validity, reliability, and preference of three pediatric pain measurement tools in African-American children. Pediatr Nurs 2003; 29:54-59.
    • (2003) Pediatr Nurs , vol.29 , pp. 54-59
    • Luffy, R.1    Grove, S.K.2
  • 25
    • 0347763461 scopus 로고    scopus 로고
    • Patient-controlled analgesia for sickle cell pain crisis in a pediatric emergency department
    • Melzer-Lange MD, Walsh-Kelly CM, Lea G, et al. Patient-controlled analgesia for sickle cell pain crisis in a pediatric emergency department. Pediatr Emerg Care 2004; 20:2-4.
    • (2004) Pediatr Emerg Care , vol.20 , pp. 2-4
    • Melzer-Lange, M.D.1    Walsh-Kelly, C.M.2    Lea, G.3
  • 26
    • 0025768807 scopus 로고
    • Intermittent injection vs patientcontrolled analgesia for sickle cell crisis pain. Comparison in patients in the emergency department
    • Gonzalez ER, Bahal N, Hansen LA, et al. Intermittent injection vs patientcontrolled analgesia for sickle cell crisis pain. Comparison in patients in the emergency department. Arch Intern Med 1991; 151:1373-1378.
    • (1991) Arch Intern Med , vol.151 , pp. 1373-1378
    • Gonzalez, E.R.1    Bahal, N.2    Hansen, L.A.3
  • 27
    • 35549003236 scopus 로고    scopus 로고
    • Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial
    • This study demonstrates that patient-controlled analgesia reduces the consumption of morphine during an acute pain event and is equally effective at controlling pain compared to a continuous infusion
    • van Beers EJ, van Tuijn CF, Nieuwkerk PT, et al. Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial. Am J Hematol 2007; 82:955-960. This study demonstrates that patient-controlled analgesia reduces the consumption of morphine during an acute pain event and is equally effective at controlling pain compared to a continuous infusion.
    • (2007) Am J Hematol , vol.82 , pp. 955-960
    • van Beers, E.J.1    van Tuijn, C.F.2    Nieuwkerk, P.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.