Literature DB >> 17880607

Clinical and economic burden of infused iron chelation therapy in the United States.

Krista A Payne1, Marie-Pierre Desrosiers, J Jaime Caro, Jean-François Baladi, Noreen Lordan, Irina Proskorovsky, Khajak Ishak, Diana Rofail.   

Abstract

BACKGROUND: Patients requiring chronic blood transfusions are at risk for iron overload, which, if not treated by iron chelation therapy (ICT), can create serious organ damage and reduce life expectancy. Current ICT requires burdensome 8- to 12-hour infusions five to seven times per week. STUDY DESIGN AND METHODS: A naturalistic study of the burden of infused ICT was conducted in four US centers. Data from the initial and most recent years of ICT were collected from medical charts of consenting thalassemia (n = 40) and sickle cell disease (n = 9) patients. Quality of life (QoL), treatment satisfaction, and ICT-related resource utilization data were also collected from a patient interview.
RESULTS: Mean serum ferritin levels during the initial (2519 +/- 1382 ng/mL) and most recent (2741 +/- 2532 ng/mL) years remained unacceptably high and increased over time (306 +/- 2200 ng/mL; mean of 20+/- years of therapy). Within 30 days before interview, 55 percent of patients suffered at least one ICT-related adverse event; 76 percent missed at least one dose. QoL, measured by the SF-36, and treatment satisfaction appear compromised in this cohort. Although total annual costs of ICT were estimated at USD $30,000 to $35,000, drug accounted for only 50 to 60 percent of this amount.
CONCLUSIONS: Infused ICT may not provide adequate effectiveness in the real world. High ferritin levels seem to be associated with ICT noncompliance, likely in relation to the bothersome mode of administration and side effects. The total cost of ICT appears to well exceed that of drug alone.

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Year:  2007        PMID: 17880607     DOI: 10.1111/j.1537-2995.2007.01398.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  14 in total

1.  Relationship among chelator adherence, change in chelators, and quality of life in thalassemia.

Authors:  Felicia L Trachtenberg; Eric Gerstenberger; Yan Xu; Lauren Mednick; Amy Sobota; Hannah Ware; Alexis A Thompson; Ellis J Neufeld; Robert Yamashita
Journal:  Qual Life Res       Date:  2014-03-30       Impact factor: 4.147

2.  Pain as an emergent issue in thalassemia.

Authors:  Felicia Trachtenberg; Dru Foote; Marie Martin; Susan Carson; Thomas Coates; Owen Beams; Olivia Vega; Manuela Merelles-Pulcini; Patricia J Giardina; Dorothy A Kleinert; Janet Kwiatkowski; Alexis A Thompson; Ellis J Neufeld; Leann Schilling; Vivek Thayalasuthan; Zahra Pakbaz; Robert Yamashita
Journal:  Am J Hematol       Date:  2010-05       Impact factor: 10.047

Review 3.  Pharmacoeconomic considerations in treating iron overload in patients with β-thalassaemia, sickle cell disease and myelodysplastic syndromes in the US: a literature review.

Authors:  Bin Zhang; Prina Z Donga; Mitra Corral; Medha Sasane; Jeffrey D Miller; Chris L Pashos
Journal:  Pharmacoeconomics       Date:  2011-06       Impact factor: 4.981

4.  Quality of life in thalassemia: a comparison of SF-36 results from the thalassemia longitudinal cohort to reported literature and the US norms.

Authors:  A Sobota; R Yamashita; Y Xu; F Trachtenberg; P Kohlbry; D A Kleinert; P J Giardina; J L Kwiatkowski; D Foote; V Thayalasuthan; J B Porter; A A Thompson; L Schilling; C T Quinn; E J Neufeld
Journal:  Am J Hematol       Date:  2011-01       Impact factor: 10.047

5.  Guidelines for the Standard Monitoring of Patients With Thalassemia: Report of the Thalassemia Longitudinal Cohort.

Authors:  Venée N Tubman; Ellen B Fung; Maria Vogiatzi; Alexis A Thompson; Zora R Rogers; Ellis J Neufeld; Janet L Kwiatkowski
Journal:  J Pediatr Hematol Oncol       Date:  2015-04       Impact factor: 1.289

6.  Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.

Authors:  Ellen B Fung; Paul R Harmatz; Meredith Milet; Vinod Balasa; Samir K Ballas; James F Casella; Lee Hilliard; Abdullah Kutlar; Kenneth L McClain; Nancy F Olivieri; John B Porter; Elliott P Vichinsky
Journal:  Transfusion       Date:  2008-05-29       Impact factor: 3.157

7.  Qualitative modification and development of patient- and caregiver-reported outcome measures for iron chelation therapy.

Authors:  Erica G Horodniceanu; Vasudha Bal; Harman Dhatt; John A Carter; Vicky Huang; Kathryn Lasch
Journal:  Health Qual Life Outcomes       Date:  2017-06-23       Impact factor: 3.186

8.  Advances in iron chelation therapy: transitioning to a new oral formulation.

Authors:  Nirmish R Shah
Journal:  Drugs Context       Date:  2017-06-16

Review 9.  Genetic, laboratory and clinical risk factors in the development of overt ischemic stroke in children with sickle cell disease.

Authors:  André Rolim Belisário; Célia Maria Silva; Cibele Velloso-Rodrigues; Marcos Borato Viana
Journal:  Hematol Transfus Cell Ther       Date:  2017-11-26

10.  Health-Related Quality of Life, Treatment Satisfaction, Adherence and Persistence in β-Thalassemia and Myelodysplastic Syndrome Patients with Iron Overload Receiving Deferasirox: Results from the EPIC Clinical Trial.

Authors:  John Porter; Donald K Bowden; Marina Economou; Jacques Troncy; Arnold Ganser; Dany Habr; Nicolas Martin; Adam Gater; Diana Rofail; Linda Abetz-Webb; Helen Lau; Maria Domenica Cappellini
Journal:  Anemia       Date:  2012-08-12
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