Literature DB >> 12401311

Monitoring chelation therapy to achieve optimal outcome in the treatment of thalassaemia.

John B Porter1, Bernard A Davis.   

Abstract

Effective management of iron overload in thalassaemia requires monitoring both for iron toxicity and the effects of excessive chelation. Careful monitoring together with adherence to established regimens using desferrioxamine (DFO) results in a 78% survival rate at 40 years of age at UCLH, with steadily improving survival as progressive cohorts receive chelation earlier in life. By contrast, survival is considerably below this in non-specialist centres. The prognostic significance of the measures being used in monitoring should be known so that decisions about chelation management are evidence-based. Serum ferritin measurement, although easy to perform frequently, is subject to variability and falsely high or falsely low values in relation to body iron are frequently obtained. However, there is evidence that persistently high ferritin values above 2500 microg/l have poor prognostic significance in patients treated with DFO. Liver iron predicts total body iron in a more predictable way than serum ferritin in thalassaemia. Liver iron concentrations of 15 mg/g dry weight appear to predict those patients who develop heart failure in subjects treated with DFO. The prognostic significance of this measurement or indeed other measurements of iron overload in patients treated with other chelation regimens is not known. Recent advances with MRI imaging have aroused interest in its use for monitoring patients with thalassaemia. A recent publication suggests a relationship between left ventricular ejection fraction and cardiac T2*, the value of which shortens with increasing iron concentrations in the liver and hence by inference in the heart. The prognostic value of this technique has not yet been demonstrated in prospective studies and hence changes in therapy based on this measurement alone should be considered with caution at this time. The value of monitoring to decrease morbidity from iron overload is also discussed, particularly with reference to the estimation of iron deposition in the pituitary.

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Year:  2002        PMID: 12401311

Source DB:  PubMed          Journal:  Best Pract Res Clin Haematol        ISSN: 1521-6926            Impact factor:   3.020


  21 in total

1.  Liver iron concentration quantification by MRI: are recommended protocols accurate enough for clinical practice?

Authors:  Agustin Castiella; Jose M Alústiza; Jose I Emparanza; Eva Ma Zapata; Belen Costero; Maria I Díez
Journal:  Eur Radiol       Date:  2010-08-06       Impact factor: 5.315

2.  Liver, bone marrow, pancreas and pituitary gland iron overload in young and adult thalassemic patients: a T2 relaxometry study.

Authors:  Maria I Argyropoulou; Dimitrios N Kiortsis; Loukas Astrakas; Zafiria Metafratzi; Nikolaos Chalissos; Stavros C Efremidis
Journal:  Eur Radiol       Date:  2007-06-05       Impact factor: 5.315

3.  Providers' Perspectives on Treating Patients With Thalassemia.

Authors:  Taylor Radke; Susan Paulukonis; Mary M Hulihan; Lisa Feuchtbaum
Journal:  J Pediatr Hematol Oncol       Date:  2019-10       Impact factor: 1.289

4.  Factors affecting health-related quality of life in Thai children with thalassemia.

Authors:  Montarat Thavorncharoensap; Kitti Torcharus; Issarang Nuchprayoon; Arthorn Riewpaiboon; Kaemthong Indaratna; Bang-On Ubol
Journal:  BMC Blood Disord       Date:  2010-01-21

5.  Ophthalmic Evaluation in Beta-Thalassemia.

Authors:  Rashid H Merchant; Hrishikesh Punde; Neepa Thacker; Deepak Bhatt
Journal:  Indian J Pediatr       Date:  2017-04-03       Impact factor: 1.967

6.  Iron overload in Beta thalassaemia major and intermedia patients.

Authors:  Amit Kumar Mishra; Archana Tiwari
Journal:  Maedica (Buchar)       Date:  2013-09

7.  Bone loss caused by iron overload in a murine model: importance of oxidative stress.

Authors:  Jaime Tsay; Zheiwei Yang; F Patrick Ross; Susanna Cunningham-Rundles; Hong Lin; Rhima Coleman; Philipp Mayer-Kuckuk; Stephen B Doty; Robert W Grady; Patricia J Giardina; Adele L Boskey; Maria G Vogiatzi
Journal:  Blood       Date:  2010-06-16       Impact factor: 22.113

8.  Antiproliferative and apoptotic effects in rat and human hepatoma cell cultures of the orally active iron chelator ICL670 compared to CP20: a possible relationship with polyamine metabolism.

Authors:  G Lescoat; K Chantrel-Groussard; N Pasdeloup; H Nick; P Brissot; F Gaboriau
Journal:  Cell Prolif       Date:  2007-10       Impact factor: 6.831

9.  Psychometric properties of the Specific Thalassemia Quality of Life Instrument for adults.

Authors:  Georgios N Lyrakos; Demetra Vini; Helen Aslani; Marouso Drosou-Servou
Journal:  Patient Prefer Adherence       Date:  2012-07-02       Impact factor: 2.711

Review 10.  Management of the thalassemias.

Authors:  Nancy F Olivieri; Gary M Brittenham
Journal:  Cold Spring Harb Perspect Med       Date:  2013-06-01       Impact factor: 6.915

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