Consequences and costs of noncompliance with iron chelation therapy in patients with transfusion‐dependent thalassemia: a literature review
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T. Delea | T. Coates | P. Phatak | J. Edelsberg | J. Baladi | Simu K. Thomas | O. Sofrygin | Simu K. Thomas
[1] I. Proskorovsky,et al. Total Annual Costs of Infused Iron Chelation Therapy in the United States. , 2006 .
[2] S. Perrotta,et al. A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. , 2006, Blood.
[3] T. Delea,et al. PHM4 COSTS AND CONSEQUENCES OF INADEQUATE COMPLIANCE WITH DEFEROXAMINE THERAPY IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA , 2006 .
[4] Mark A Westwood,et al. Randomized controlled trial of deferiprone or deferoxamine in beta-thalassemia major patients with asymptomatic myocardial siderosis. , 2006, Blood.
[5] R. Osborne,et al. An Oral Iron Chelator and Quality of Life. , 2005 .
[6] E. Neufeld,et al. Relationship of Transfusion and Iron-Related Complications to Cost of Care in Thalassemia. , 2005 .
[7] P. Marks,et al. A Randomized, Controlled Phase II Trial in Sickle Cell Disease Patients with Chronic Iron Overload Demonstrates That the Once-Daily Oral Iron Chelator Deferasirox (Exjade ® , ICL670) Is Well Tolerated and Reduces Iron Burden. , 2005 .
[8] T. Delea,et al. Costs and Consequences of Inadequate Compliance with Deferoxamine Therapy in Patients with Transfusion-Dependent Thalassemia. , 2005 .
[9] E. Neufeld,et al. Complications of beta-thalassemia major in North America. , 2004, Blood.
[10] R. Galanello,et al. Safety and effectiveness of long-term therapy with the oral iron chelator deferiprone. , 2003, Blood.
[11] G. Bosi,et al. Left ventricular remodelling, and systolic and diastolic function in young adults with β thalassaemia major: a Doppler echocardiographic assessment and correlation with haematological data , 2003, Heart.
[12] R. Hider,et al. Monitoring long‐term efficacy of iron chelation therapy by deferiprone and desferrioxamine in patients with β‐thalassaemia major: application of SQUID biomagnetic liver susceptometry , 2003, British journal of haematology.
[13] P. Acklin,et al. Development of tridentate iron chelators: from desferrithiocin to ICL670. , 2003, Current medicinal chemistry.
[14] M. Zago,et al. Urinary iron excretion induced by intravenous infusion of deferoxamine in beta-thalassemia homozygous patients. , 2002, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.
[15] J. Caro,et al. An international survey of patients with thalassemia major and their views about sustaining life-long desferrioxamine use , 2002, BMC clinical pharmacology.
[16] D. Tsiapras,et al. Heart failure in beta thalassemia: a 5-year follow-up study. , 2001, The American journal of medicine.
[17] J D Graham,et al. Modeling for health care and other policy decisions: uses, roles, and validity. , 2001, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.
[18] A. Inati,et al. Comparison between deferoxamine and deferiprone (L1) in iron‐loaded thalassemia patients , 2001, European journal of haematology.
[19] C. Pegelow,et al. Financial analysis of chronic transfusion for stroke prevention in sickle cell disease. , 2000, Blood.
[20] A. Hoffbrand,et al. Hepatic iron concentration combined with long‐term monitoring of serum ferritin to predict complications of iron overload in thalassaemia major , 2000, British journal of haematology.
[21] J. Karnon,et al. Lifetime treatment costs of beta-thalassaemia major. , 1999, Clinical and laboratory haematology.
[22] P. Groncy,et al. Iron chelation with deferoxamine: comparing the results of a critical pathway to a national survey. , 1999, Journal of pediatric hematology/oncology.
[23] G. Koren,et al. An investigation into variability in the therapeutic response to deferiprone in patients with thalassemia major. , 1999, Therapeutic drug monitoring.
[24] K. Bailey,et al. Congestive heart failure in the community: trends in incidence and survival in a 10-year period. , 1999, Archives of internal medicine.
[25] K. Fleming,et al. Long-term safety and effectiveness of iron-chelation therapy with deferiprone for thalassemia major. , 1998, The New England journal of medicine.
[26] G. Koren,et al. Iron-chelation therapy with oral deferiprone in patients with thalassemia major. , 1995, The New England journal of medicine.
[27] G Koren,et al. Critical Comparison of Novel and Existing Methods of Compliance Assessment During a Clinical Trial of an Oral Iron Chelator , 1994, Journal of clinical pharmacology.
[28] C. McLaren,et al. Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major. , 1994, The New England journal of medicine.
[29] A. Hoffbrand,et al. The effect of deferiprone (L1) and desferrioxamine on myelopoiesis using a liquid culture system , 1994, British journal of haematology.
[30] S. Menahem,et al. Prevention of heart disease by subcutaneous desferrioxamine in patients with thalassaemia major. , 1993, Australian and New Zealand journal of medicine.
[31] G Koren,et al. Compliance assessed by the Medication Event Monitoring System. , 1991, Archives of disease in childhood.
[32] K. Ehlers,et al. Prolonged survival in patients with beta-thalassemia major treated with deferoxamine. , 1991, The Journal of pediatrics.
[33] Alan R. Cohen,et al. Management of iron overload in the pediatric patient. , 1987, Hematology/oncology clinics of North America.
[34] S. Colan,et al. Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major. , 1985, The New England journal of medicine.
[35] A. Cnaan,et al. Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine. , 2004, Haematologica.
[36] A. Piga,et al. Comparative effects of deferiprone and deferoxamine on survival and cardiac disease in patients with thalassemia major: a retrospective analysis. , 2003, Haematologica.
[37] Milton C Weinstein,et al. Principles of good practice for decision analytic modeling in health-care evaluation: report of the ISPOR Task Force on Good Research Practices--Modeling Studies. , 2003, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.
[38] F Reed Johnson,et al. Modeling for health care and other policy decisions: uses, roles, and validity. , 2002, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.
[39] G. D’Amico,et al. Deferiprone versus deferoxamine in patients with thalassemia major: a randomized clinical trial. , 2002, Blood cells, molecules & diseases.
[40] A. Piga,et al. Results of long-term iron-chelating therapy. , 1996, Acta haematologica.
[41] S. Beratis. Noncompliance with iron chelation therapy in patients with β thalassaemia , 1989 .
[42] S. Beratis. Noncompliance with iron chelation therapy in patients with beta thalassaemia. , 1989, Journal of psychosomatic research.