Literature DB >> 3329185

Management of iron overload in the pediatric patient.

A Cohen1.   

Abstract

Iron overload is a major complication of long-term transfusion therapy. In the absence of treatment, the excessive iron causes diffuse organ damage, usually culminating in death from heart disease. Deferoxamine, an iron-chelating drug, removes tissue iron, prevents iron-induced organ dysfunction, and prolongs life. Proper administration of deferoxamine requires careful attention to dose, route and duration of administration, and compliance. Better chelators are needed but are unlikely to be available soon. Other methods for preventing or reducing iron accumulation involve alterations in the transfusion program or the blood product. Prevention of iron overload should improve the lives of patients with transfusion-dependent anemias and extend the usefulness of transfusion in chronic hematologic disorders.

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Year:  1987        PMID: 3329185

Source DB:  PubMed          Journal:  Hematol Oncol Clin North Am        ISSN: 0889-8588            Impact factor:   3.722


  10 in total

1.  Serum ferritin levels, socio-demographic factors and desferrioxamine therapy in multi-transfused thalassemia major patients at a government tertiary care hospital of Karachi, Pakistan.

Authors:  Haris Riaz; Talha Riaz; Muhammad Ubaid Khan; Sina Aziz; Faizan Ullah; Anis Rehman; Qandeel Zafar; Abdul Nafey Kazi
Journal:  BMC Res Notes       Date:  2011-08-11

2.  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

3.  Cost effectiveness of once-daily oral chelation therapy with deferasirox versus infusional deferoxamine in transfusion-dependent thalassaemia patients: US healthcare system perspective.

Authors:  Thomas E Delea; Oleg Sofrygin; Simu K Thomas; Jean-Francois Baladi; Pradyumna D Phatak; Thomas D Coates
Journal:  Pharmacoeconomics       Date:  2007       Impact factor: 4.981

4.  Cardiac iron overload in thalassemic patients: an endomyocardial biopsy study.

Authors:  T Lombardo; C Tamburino; G Bartoloni; M L Morrone; V Frontini; F Italia; S Cordaro; A Privitera; V Calvi
Journal:  Ann Hematol       Date:  1995-09       Impact factor: 3.673

5.  Can multi-slice or navigator-gated R2* MRI replace single-slice breath-hold acquisition for hepatic iron quantification?

Authors:  Ralf B Loeffler; M Beth McCarville; Anne W Wagstaff; Matthew P Smeltzer; Axel J Krafft; Ruitian Song; Jane S Hankins; Claudia M Hillenbrand
Journal:  Pediatr Radiol       Date:  2016-10-17

6.  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

7.  Atrial and ventricular function in thalassemic patients with supra-ventricular arrhythmias.

Authors:  Ines Monte; Davide Capodanno; Elisa Nicolosi; Salvatore Licciardi; Enrica Talini; Vitantonio Di Bello
Journal:  Heart Int       Date:  2009-06-30

8.  Psychological Aspects in Children and Adolescents With Major Thalassemia: A Case-Control Study.

Authors:  Fatemeh Behdani; Zahra Badiee; Paria Hebrani; Fatemeh Moharreri; Amir Hossein Badiee; Negin Hajivosugh; Zohreh Rostami; Amir Akhavanrezayat
Journal:  Iran J Pediatr       Date:  2015-06-27       Impact factor: 0.364

Review 9.  MRI evaluation of tissue iron burden in patients with beta-thalassaemia major.

Authors:  Maria I Argyropoulou; Loukas Astrakas
Journal:  Pediatr Radiol       Date:  2007-08-21

10.  Effectiveness of Deferasirox in Pediatric Thalassemia Patients: Experience from a Tertiary Care Hospital of Odisha.

Authors:  Mousumee Panigrahi; Trupti Rekha Swain; Rabindra Kumar Jena; Ashutosh Panigrahi; Nishant Debta
Journal:  Indian J Pharmacol       Date:  2020-08-04       Impact factor: 1.200

  10 in total

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