Literature DB >> 21848963

Erythrocytapheresis versus phlebotomy in the initial treatment of HFE hemochromatosis patients: results from a randomized trial.

Eva Rombout-Sestrienkova1, Fred H M Nieman, Brigitte A B Essers, Paulus A H van Noord, Mirian C H Janssen, Cees Th B M van Deursen, Laurens P Bos, Ferdinand Rombout, Rogier van den Braak, Peter W de Leeuw, Ger H Koek.   

Abstract

BACKGROUND: Standard treatment of newly diagnosed HFE hemochromatosis patients is phlebotomy. Erythrocytapheresis provides a new therapeutic modality that can remove up to three times more red blood cells per single procedure and could thus have a clinical and economic benefit. STUDY DESIGN AND METHODS: To compare the number of treatment procedures between erythrocytapheresis and phlebotomy needed to reach the serum ferritin (SF) target level of 50 µg/L, a two-treatment-arms, randomized trial was conducted in which 38 newly diagnosed patients homozygous for C282Y were randomly assigned in a 1:1 ratio to undergo either erythrocytapheresis or phlebotomy. A 50% decrease in the number of treatment procedures for erythrocytapheresis compared to phlebotomy was chosen as the relevant difference to detect.
RESULTS: Univariate analysis showed a significantly lower mean number of treatment procedures in the erythrocytapheresis group (9 vs. 27; ratio, 0.33; 95% confidence interval [CI], 0.25-0.45; Mann-Whitney p < 0.001). After adjustments for the two important influential factors initial SF level and body weight, the reduction ratio was still significant (0.43; 95% CI, 0.35-0.52; p < 0.001). Cost analysis showed no significant difference in treatment costs between both procedures. The costs resulting from productivity loss were significantly lower for the erythrocytapheresis group.
CONCLUSION: Erythrocytapheresis is highly effective treatment to reduce iron overload and from a societal perspective might potentially also be a cost-saving therapy.
© 2011 American Association of Blood Banks.

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Year:  2011        PMID: 21848963     DOI: 10.1111/j.1537-2995.2011.03292.x

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


  9 in total

Review 1.  Current applications of therapeutic phlebotomy.

Authors:  Tarek Bou Assi; Elizabeth Baz
Journal:  Blood Transfus       Date:  2013-10-03       Impact factor: 3.443

2.  Erythrocytapheresis compared with whole blood phlebotomy for the treatment of hereditary haemochromatosis.

Authors:  Tatjana Sundic; Tor Hervig; Signe Hannisdal; Jörg Assmus; Rune J Ulvik; Richard W Olaussen; Sigbjørn Berentsen
Journal:  Blood Transfus       Date:  2013-10-23       Impact factor: 3.443

Review 3.  The clinical management of hereditary haemochromatosis.

Authors:  Marinos Pericleous; Claire Kelly
Journal:  Frontline Gastroenterol       Date:  2017-09-23

4.  Telomere length and elevated iron: the influence of phenotype and HFE genotype.

Authors:  Arch G Mainous; Robert U Wright; Mary M Hulihan; Waleed O Twal; Christine E McLaren; Vanessa A Diaz; Gordon D McLaren; W Scott Argraves; Althea M Grant
Journal:  Am J Hematol       Date:  2013-05-13       Impact factor: 10.047

Review 5.  Interventions for hereditary haemochromatosis: an attempted network meta-analysis.

Authors:  Elena Buzzetti; Maria Kalafateli; Douglas Thorburn; Brian R Davidson; Emmanuel Tsochatzis; Kurinchi Selvan Gurusamy
Journal:  Cochrane Database Syst Rev       Date:  2017-03-08

6.  Patients with hereditary hemochromatosis reach safe range of transferrin saturation sooner with erythrocytaphereses than with phlebotomies.

Authors:  Eva Rombout-Sestrienkova; Lloyd Brandts; Ger H Koek; Cees Th B M van Deursen
Journal:  J Clin Apher       Date:  2021-12-13       Impact factor: 2.605

7.  Indications and use of therapeutic phlebotomy in polycythemia vera: which role for erythrocytapheresis?

Authors:  Luciana Teofili; Caterina Giovanna Valentini; Elena Rossi; Valerio De Stefano
Journal:  Leukemia       Date:  2018-12-05       Impact factor: 11.528

8.  Iron chelators reverse organ damage in type 4B hereditary hemochromatosis: Case reports.

Authors:  Ling-Yan Wu; Zhen-Ya Song; Qing-Hai Li; Li-Jun Mou; Ying-Ying Yu; Si-Si Shen; Xiao-Xiao Song
Journal:  Medicine (Baltimore)       Date:  2021-04-02       Impact factor: 1.817

9.  A predictive model for estimating the number of erythrocytapheresis or phlebotomy treatments for patients with naïve hereditary hemochromatosis.

Authors:  Eva Rombout-Sestrienkova; Bjorn Winkens; Marian van Kraaij; Cees Th B M van Deursen; Mirian C H Janssen; Alexander M J Rennings; Dorothea Evers; Jean-Louis Kerkhoffs; Ad Masclee; Ger H Koek
Journal:  J Clin Apher       Date:  2020-12-24       Impact factor: 2.821

  9 in total

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