-
1
-
-
70350630223
-
A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease
-
Haywood C Jr, Beach MC, Lanzkron S, et al. A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease. J Natl Med Assoc. 2009;101(10):1022-1033.
-
(2009)
J Natl Med Assoc
, vol.101
, Issue.10
, pp. 1022-1033
-
-
Haywood, C.1
Beach, M.C.2
Lanzkron, S.3
-
2
-
-
38749109710
-
Daily assessment of pain in adults with sickle cell disease
-
Smith WR, Penberthy LT, Bovbjerg VE, et al. Daily assessment of pain in adults with sickle cell disease. Ann Intern Med. 2008;148(2):94-101.
-
(2008)
Ann Intern Med
, vol.148
, Issue.2
, pp. 94-101
-
-
Smith, W.R.1
Penberthy, L.T.2
Bovbjerg, V.E.3
-
3
-
-
78851469729
-
Health-related quality of life in adults with sickle cell disease (SCD): A report from the comprehensive sickle cell centers clinical trial consortium
-
Dampier C, LeBeau P, Rhee S, et al. Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium. Am J Hematol. 2011;86(2): 203-205.
-
(2011)
Am J Hematol
, vol.86
, Issue.2
, pp. 203-205
-
-
Dampier, C.1
LeBeau, P.2
Rhee, S.3
-
4
-
-
0036905062
-
Characteristics of pain managed at home in children and adolescents with sickle cell disease by using diary self-reports
-
Dampier C, Ely B, Brodecki D, O'Neal P. Characteristics of pain managed at home in children and adolescents with sickle cell disease by using diary self-reports. J Pain. 2002;3(6):461-470.
-
(2002)
J Pain
, vol.3
, Issue.6
, pp. 461-470
-
-
Dampier, C.1
Ely, B.2
Brodecki, D.3
O'Neal, P.4
-
5
-
-
38349113187
-
Pain and stress in a systems perspective: Reciprocal neural, endocrine, and immune interactions
-
Chapman CR, Tuckett RP, Song CW. Pain and stress in a systems perspective: reciprocal neural, endocrine, and immune interactions. J Pain. 2008;9(2):122-145.
-
(2008)
J Pain
, vol.9
, Issue.2
, pp. 122-145
-
-
Chapman, C.R.1
Tuckett, R.P.2
Song, C.W.3
-
6
-
-
0032212220
-
Serum levels of substance P are elevated in patients with sickle cell disease and increase further during vaso-occlusive crisis
-
Michaels LA, Ohene-Frempong K, Zhao H, Douglas SD. Serum levels of substance P are elevated in patients with sickle cell disease and increase further during vaso-occlusive crisis. Blood. 1998;92(9):3148-3151.
-
(1998)
Blood
, vol.92
, Issue.9
, pp. 3148-3151
-
-
Michaels, L.A.1
Ohene-Frempong, K.2
Zhao, H.3
Douglas, S.D.4
-
7
-
-
79951579664
-
Central sensitization: Implications for the diagnosis and treatment of pain
-
Woolf CJ. Central sensitization: implications for the diagnosis and treatment of pain. Pain. 2011;152(3 Suppl):S2-S15.
-
(2011)
Pain
, vol.152
, Issue.3
, pp. S2-S15
-
-
Woolf, C.J.1
-
9
-
-
85020951144
-
Identifying central sensitization in adults with sickle cell disease: Differences in clinical features and psychobehavioral factors
-
Moscou-Jackson G, Campbell C, Finan P, et al. Identifying central sensitization in adults with sickle cell disease: differences in clinical features and psychobehavioral factors. J Pain. 2015;16(4):S31.
-
(2015)
J Pain
, vol.16
, Issue.4
, pp. S31
-
-
Moscou-Jackson, G.1
Campbell, C.2
Finan, P.3
-
11
-
-
33845461527
-
Physical therapy alone compared with core decompression and physical therapy for femoral head osteonecrosis in sickle cell disease:results of a multicenter study at a mean of three years after treatment
-
Neumayr LD, Aguilar C, Earles AN, et al. Physical therapy alone compared with core decompression and physical therapy for femoral head osteonecrosis in sickle cell disease:results of a multicenter study at a mean of three years after treatment. J Bone Joint Surg Am. 2006;88(12):2573-2582.
-
(2006)
J Bone Joint Surg Am
, vol.88
, Issue.12
, pp. 2573-2582
-
-
Neumayr, L.D.1
Aguilar, C.2
Earles, A.N.3
-
12
-
-
70349492889
-
The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization
-
Carroll CP, Haywood C Jr, Fagan P, Lanzkron S. The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization. Am J Hematol. 2009;84(10):666-670.
-
(2009)
Am J Hematol
, vol.84
, Issue.10
, pp. 666-670
-
-
Carroll, C.P.1
Haywood, C.2
Fagan, P.3
Lanzkron, S.4
-
13
-
-
79958701433
-
Prediction of onset and course of high hospital utilization in sickle cell disease
-
Carroll CP, Haywood C Jr, Lanzkron S. Prediction of onset and course of high hospital utilization in sickle cell disease. J Hosp Med. 2011;6(5):248-255.
-
(2011)
J Hosp Med
, vol.6
, Issue.5
, pp. 248-255
-
-
Carroll, C.P.1
Haywood, C.2
Lanzkron, S.3
-
14
-
-
85010967387
-
-
Institute for Clinical Systems Improvement. Assessment and Management of Chronic Pain. Institute for Clinical Systems Improvement, 2013. Accessed July 31
-
Institute for Clinical Systems Improvement. Assessment and Management of Chronic Pain. Institute for Clinical Systems Improvement, 2013. Accessed July 31, 2015. https://www.icsi.org/guidelines-more/catalog-guidelines-and-more/catalog-guidelines/catalog-neurological guidelines/pain/
-
(2015)
-
-
-
15
-
-
77950825015
-
Practice guidelines for chronic pain management: An updated report by the American Society of anesthesiologists task force on chronic pain management and the American society of regional anesthesia and pain medicine
-
American Society of Anesthesiologists Task Force on Chronic Pain Management; American Society of Regional Anesthesia and Pain Medicine
-
American Society of Anesthesiologists Task Force on Chronic Pain Management; American Society of Regional Anesthesia and Pain Medicine. Practice guidelines for chronic pain management: an updated report by the American Society of Anesthesiologists Task Force on Chronic Pain Management and the American Society of Regional Anesthesia and Pain Medicine. Anesthesiology. 2010;112(4):810-833.
-
(2010)
Anesthesiology
, vol.112
, Issue.4
, pp. 810-833
-
-
-
16
-
-
45749124385
-
Detection and assessment of stroke in patients with sickle cell disease: Neuropsychological functioning and magnetic resonance imaging
-
Gold JI, Johnson CB, Treadwell MJ, Hans N, Vichinsky E. Detection and assessment of stroke in patients with sickle cell disease: neuropsychological functioning and magnetic resonance imaging. Pediatr Hematol Oncol. 2008;25(5):409-421.
-
(2008)
Pediatr Hematol Oncol
, vol.25
, Issue.5
, pp. 409-421
-
-
Gold, J.I.1
Johnson, C.B.2
Treadwell, M.J.3
Hans, N.4
Vichinsky, E.5
-
17
-
-
79251628870
-
Impact of early transcranial Doppler screening and intensive therapy on cerebral vasculopathy outcome in a newborn sickle cell anemia cohort
-
Bernaudin F, Verlhac S, Arnaud C, et al. Impact of early transcranial Doppler screening and intensive therapy on cerebral vasculopathy outcome in a newborn sickle cell anemia cohort. Blood. 2011;117(4): 1130-1140.
-
(2011)
Blood
, vol.117
, Issue.4
, pp. 1130-1140
-
-
Bernaudin, F.1
Verlhac, S.2
Arnaud, C.3
-
18
-
-
77952297450
-
Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia
-
Vichinsky EP, Neumayr LD, Gold JI, et al. Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia. JAMA. 2010;303(18):1823-1831.
-
(2010)
JAMA
, vol.303
, Issue.18
, pp. 1823-1831
-
-
Vichinsky, E.P.1
Neumayr, L.D.2
Gold, J.I.3
-
19
-
-
84898752802
-
Neuroimaging abnormalities in adults with sickle cell anemia: Associations with cognition
-
Mackin RS, Insel P, Truran D, et al. Neuroimaging abnormalities in adults with sickle cell anemia: associations with cognition. Neurology. 2014;82(10):835-841.
-
(2014)
Neurology
, vol.82
, Issue.10
, pp. 835-841
-
-
Mackin, R.S.1
Insel, P.2
Truran, D.3
-
20
-
-
18944374033
-
The Montreal Cognitive Assessment, MoCA: A brief screening tool for mild cognitive impairment
-
Nasreddine ZS, Phillips NA, Bedirian V, et al. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005;53(4):695-699.
-
(2005)
J Am Geriatr Soc
, vol.53
, Issue.4
, pp. 695-699
-
-
Nasreddine, Z.S.1
Phillips, N.A.2
Bedirian, V.3
-
21
-
-
82255179811
-
Normative data for the Montreal Cognitive Assessment (MoCA) in a population-based sample
-
Rossetti HC, Lacritz LH, Cullum CM, Weiner MF. Normative data for the Montreal Cognitive Assessment (MoCA) in a population-based sample. Neurology. 2011;77(13):1272-1275.
-
(2011)
Neurology
, vol.77
, Issue.13
, pp. 1272-1275
-
-
Rossetti, H.C.1
Lacritz, L.H.2
Cullum, C.M.3
Weiner, M.F.4
-
22
-
-
84982783657
-
Screening for Neurocognitive Dysfunction in an Adult Population with Sickle Cell Disease
-
Abstract 2717
-
Cichowitz C, Carroll CP, Strouse JJ, Haywood C Jr, S L. Screening for Neurocognitive Dysfunction in an Adult Population with Sickle Cell Disease. Blood. 2014: Abstract 2717.
-
(2014)
Blood
-
-
Cichowitz, C.1
Carroll, C.P.2
Strouse, J.J.3
Haywood, C.4
-
23
-
-
84920020261
-
Eligibility for and prescription of urate-lowering treatment in patients with incident gout in England
-
Kuo CF, Grainge MJ, Mallen C, Zhang W, Doherty M. Eligibility for and prescription of urate-lowering treatment in patients with incident gout in England. JAMA. 2014;312(24):2684-2686.
-
(2014)
JAMA
, vol.312
, Issue.24
, pp. 2684-2686
-
-
Kuo, C.F.1
Grainge, M.J.2
Mallen, C.3
Zhang, W.4
Doherty, M.5
-
24
-
-
0036222518
-
Impaired creatinine secretion after an intravenous creatinine load is an early characteristic of the nephropathy of sickle cell anaemia
-
Herrera J, Avila E, Marin C, odriguez-Iturbe B. Impaired creatinine secretion after an intravenous creatinine load is an early characteristic of the nephropathy of sickle cell anaemia. Nephrol Dial Transplant. 2002;17(4):602-607.
-
(2002)
Nephrol Dial Transplant
, vol.17
, Issue.4
, pp. 602-607
-
-
Herrera, J.1
Avila, E.2
Marin, C.3
Odriguez-Iturbe, B.4
-
25
-
-
0031001007
-
Natural history of blood pressure in sickle cell disease: Risks for stroke and death associated with relative hypertension in sickle cell anemia
-
Pegelow CH, Colangelo L, Steinberg M, et al. Natural history of blood pressure in sickle cell disease: risks for stroke and death associated with relative hypertension in sickle cell anemia. Am J Med. 1997;102(2):171-177.
-
(1997)
Am J Med
, vol.102
, Issue.2
, pp. 171-177
-
-
Pegelow, C.H.1
Colangelo, L.2
Steinberg, M.3
-
26
-
-
84983165476
-
Gout and sickle cell disease: Not all pain is sickle cell pain
-
Prepublished on April 20
-
Gupta S, Yui JC, Xu D, et al. Gout and sickle cell disease: not all pain is sickle cell pain. Br J Haematol. Prepublished on April 20, 2015, as DOI 10.1111/bjh.13433.
-
(2015)
Br J Haematol
-
-
Gupta, S.1
Yui, J.C.2
Xu, D.3
-
27
-
-
0036903163
-
Accuracy of the urinary albumin to creatinine ratio as a predictor of albuminuria in adults with sickle cell disease
-
Lima CS, Bottini PV, Garlipp CR, Santos AO, Costa FF, Saad ST. Accuracy of the urinary albumin to creatinine ratio as a predictor of albuminuria in adults with sickle cell disease. J Clin Pathol. 2002;55(12): 973-975.
-
(2002)
J Clin Pathol
, vol.55
, Issue.12
, pp. 973-975
-
-
Lima, C.S.1
Bottini, P.V.2
Garlipp, C.R.3
Santos, A.O.4
Costa, F.F.5
Saad, S.T.6
-
28
-
-
0031898063
-
A randomized trial of captopril for microalbuminuria in normotensive adults with sickle cell anemia
-
Foucan L, Bourhis V, Bangou J, Merault L, Etienne-Julan M, Salmi RL. A randomized trial of captopril for microalbuminuria in normotensive adults with sickle cell anemia. Am J Med. 1998;104(4):339-342.
-
(1998)
Am J Med
, vol.104
, Issue.4
, pp. 339-342
-
-
Foucan, L.1
Bourhis, V.2
Bangou, J.3
Merault, L.4
Etienne-Julan, M.5
Salmi, R.L.6
-
29
-
-
84875982878
-
Improved survival among sickle cell kidney transplant recipients in the recent era
-
Huang E, Parke C, Mehrnia A, et al. Improved survival among sickle cell kidney transplant recipients in the recent era. Nephrol Dial Transplant. 2013;28(4):1039-1046.
-
(2013)
Nephrol Dial Transplant
, vol.28
, Issue.4
, pp. 1039-1046
-
-
Huang, E.1
Parke, C.2
Mehrnia, A.3
-
30
-
-
57149146076
-
Hypercoagulability in sickle cell disease: New approaches to an old problem
-
Ataga KI, Key NS. Hypercoagulability in sickle cell disease: new approaches to an old problem. Hematology Am Soc Hematol Educ Program. 2007:91-96.
-
(2007)
Hematology Am Soc Hematol Educ Program
, pp. 91-96
-
-
Ataga, K.I.1
Key, N.S.2
-
31
-
-
84858425678
-
Biomarkers of inflammation, growth factor, and coagulation activation in patients with sickle cell disease
-
Qari MH, Dier U, Mousa SA. Biomarkers of inflammation, growth factor, and coagulation activation in patients with sickle cell disease. Clin Appl Thromb Hemost. 2012;18(2):195-200.
-
(2012)
Clin Appl Thromb Hemost
, vol.18
, Issue.2
, pp. 195-200
-
-
Qari, M.H.1
Dier, U.2
Mousa, S.A.3
-
32
-
-
84882260106
-
Endothelial activation and inflammation biomarkers in children and adolescents with sickle cell disease
-
Hatzipantelis ES, Pana ZD, Gombakis N, et al. Endothelial activation and inflammation biomarkers in children and adolescents with sickle cell disease. Int J Hematol. 2013;98(2):158-163.
-
(2013)
Int J Hematol
, vol.98
, Issue.2
, pp. 158-163
-
-
Hatzipantelis, E.S.1
Pana, Z.D.2
Gombakis, N.3
-
33
-
-
38549131853
-
Coagulation activation and inflammation in sickle cell disease-associated pulmonary hypertension
-
Ataga KI, Moore CG, Hillery CA, et al. Coagulation activation and inflammation in sickle cell disease-associated pulmonary hypertension. Haematologica. 2008;93(1):20-26.
-
(2008)
Haematologica
, vol.93
, Issue.1
, pp. 20-26
-
-
Ataga, K.I.1
Moore, C.G.2
Hillery, C.A.3
-
34
-
-
84876268737
-
Venous thromboembolism in adults with sickle cell disease: A serious and under-recognized complication
-
Naik RP, Streiff MB, Haywood C, Jr., Nelson JA, Lanzkron S. Venous thromboembolism in adults with sickle cell disease: a serious and under-recognized complication. Am J Med. 2013;126(5):443-449.
-
(2013)
Am J Med
, vol.126
, Issue.5
, pp. 443-449
-
-
Naik, R.P.1
Streiff, M.B.2
Haywood, C.3
Nelson, J.A.4
Lanzkron, S.5
-
35
-
-
84916613390
-
Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease
-
Naik RP, Streiff MB, Haywood C Jr, Segal JB, Lanzkron S. Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease. J Thromb Haemost. 2014;12(12):2010-2016.
-
(2014)
J Thromb Haemost
, vol.12
, Issue.12
, pp. 2010-2016
-
-
Naik, R.P.1
Streiff, M.B.2
Haywood, C.3
Segal, J.B.4
Lanzkron, S.5
-
36
-
-
84906791796
-
Impact of sickle hemoglobinopathies on pregnancy-related venous thromboembolism
-
Porter B, Key NS, Jauk VC, Adam S, Biggio J, Tita A. Impact of sickle hemoglobinopathies on pregnancy-related venous thromboembolism. Am J Perinatol. 2014;31(9):805-809.
-
(2014)
Am J Perinatol
, vol.31
, Issue.9
, pp. 805-809
-
-
Porter, B.1
Key, N.S.2
Jauk, V.C.3
Adam, S.4
Biggio, J.5
Tita, A.6
-
37
-
-
47949118488
-
Morbidity associated with sickle cell disease in pregnancy
-
Villers MS, Jamison MG, De Castro LM, James AH. Morbidity associated with sickle cell disease in pregnancy. Am J Obstet Gynecol. 2008;199(2):125.e1-5.
-
(2008)
Am J Obstet Gynecol
, vol.199
, Issue.2
, pp. 125e1-1255
-
-
Villers, M.S.1
Jamison, M.G.2
De Castro, L.M.3
James, A.H.4
-
38
-
-
33646117733
-
Venous thromboembolism during pregnancy and the postpartum period: Incidence, risk factors, and mortality
-
James AH, Jamison MG, Brancazio LR, Myers ER. Venous thromboembolism during pregnancy and the postpartum period: incidence, risk factors, and mortality. Am J Obstet Gynecol. 2006;194(5):1311-1315.
-
(2006)
Am J Obstet Gynecol
, vol.194
, Issue.5
, pp. 1311-1315
-
-
James, A.H.1
Jamison, M.G.2
Brancazio, L.R.3
Myers, E.R.4
-
39
-
-
84916242270
-
Venous thromboembolism in pregnant women with sickle cell disease: A retrospective database analysis
-
Seaman CD, Yabes J, Li J, Moore CG, Ragni MV. Venous thromboembolism in pregnant women with sickle cell disease: a retrospective database analysis. Thromb Res. 2014;134(6):1249-1252.
-
(2014)
Thromb Res
, vol.134
, Issue.6
, pp. 1249-1252
-
-
Seaman, C.D.1
Yabes, J.2
Li, J.3
Moore, C.G.4
Ragni, M.V.5
-
40
-
-
84902536593
-
Emerging pathogens-how safe is blood?
-
Schmidt M, Geilenkeuser WJ, Sireis W, Seifried E, Hourfar K. Emerging pathogens-how safe is blood? Transfus Med Hemother. 2014;41(1):10-17.
-
(2014)
Transfus Med Hemother
, vol.41
, Issue.1
, pp. 10-17
-
-
Schmidt, M.1
Geilenkeuser, W.J.2
Sireis, W.3
Seifried, E.4
Hourfar, K.5
-
41
-
-
84891862866
-
Cost-effectiveness of prospective red blood cell antigen matching to prevent alloimmunization among sickle cell patients
-
Kacker S, Ness PM, Savage WJ, et al. Cost-effectiveness of prospective red blood cell antigen matching to prevent alloimmunization among sickle cell patients. Transfusion. 2014;54(1):86-97.
-
(2014)
Transfusion
, vol.54
, Issue.1
, pp. 86-97
-
-
Kacker, S.1
Ness, P.M.2
Savage, W.J.3
-
42
-
-
44849111534
-
Hyperhemolysis syndrome in sickle cell disease: Case report (recurrent episode) and literature review
-
Win N, New H, Lee E, de la Fuente J. Hyperhemolysis syndrome in sickle cell disease: case report (recurrent episode) and literature review. Transfusion. 2008;48(6):1231-1238.
-
(2008)
Transfusion
, vol.48
, Issue.6
, pp. 1231-1238
-
-
Win, N.1
New, H.2
Lee, E.3
De La Fuente, J.4
-
43
-
-
69249169929
-
Delayed hemolytic transfusion reaction in sickle cell disease patients: Evidence of an emerging syndrome with suicidal red blood cell death
-
Chadebech P, Habibi A, Nzouakou R, et al. Delayed hemolytic transfusion reaction in sickle cell disease patients: evidence of an emerging syndrome with suicidal red blood cell death. Transfusion. 2009;49(9):1785-1792.
-
(2009)
Transfusion
, vol.49
, Issue.9
, pp. 1785-1792
-
-
Chadebech, P.1
Habibi, A.2
Nzouakou, R.3
-
44
-
-
84944212801
-
Iron overload in adults with sickle cell disease who have received intermittent red blood cell transfusions
-
Prepublished on February 25, 2015
-
Pack-Mabien A, Brown B, Herbert DE, Haynes J Jr. Iron overload in adults with sickle cell disease who have received intermittent red blood cell transfusions. J Am Assoc Nurse Pract. 2015. Prepublished on February 25, 2015, as DOI 10.1002/2327-6924.12221.
-
(2015)
J Am Assoc Nurse Pract
-
-
Pack-Mabien, A.1
Brown, B.2
Herbert, D.E.3
Haynes, J.4
-
45
-
-
84924619556
-
Multicenter COMPACT study of complications in patients with sickle cell disease and utilization of iron chelation therapy
-
Jordan L, Adams-Graves P, Kanter-Washko J, et al. Multicenter COMPACT study of complications in patients with sickle cell disease and utilization of iron chelation therapy. Curr Med Res Opin. 2015;31(3): 513-523.
-
(2015)
Curr Med Res Opin
, vol.31
, Issue.3
, pp. 513-523
-
-
Jordan, L.1
Adams-Graves, P.2
Kanter-Washko, J.3
|