Literature DB >> 16956817

Survival of medically treated thalassemia patients in Cyprus. Trends and risk factors over the period 1980-2004.

Paul Telfer1, Pietro G Coen, Soteroula Christou, Michael Hadjigavriel, Anita Kolnakou, Evangelia Pangalou, Nicos Pavlides, Michael Psiloines, Krikor Simamonian, Georghios Skordos, Maria Sitarou, Michael Angastiniotis.   

Abstract

BACKGROUND AND OBJECTIVES: A large number of patients with thalassemia major have been born and treated exclusively in Cyprus. They have been managed according to standard international practice, but few have been transplanted. In 1999, a combination chelation regime with desferrioxamine and deferiprone was introduced. We analyzed survival trends in Cypriots and tried to identify factors associated with prolonged survival. DESIGN AND METHODS: We had incomplete information on births pre-1974 and complete information from 1974 onwards. Clinical data were incomplete pre-1980 and complete thereafter. We analyzed data on 539 patients born after 1960 and followed over the period 1980 to the end of 2004.
RESULTS: There were 58 deaths, 31 (53.4%) of which where due to cardiac causes. In the complete birth cohort of 284 patients born after 1974, survival (95% CI) at 10, 20 and 30 years was 100% (0); 98.5% (96.1-99.4) and 92.7% (86.7-96.1) respectively. There was a significant trend of increasing cardiac deaths between 1980 and 2000 (p<0.001) and a decline after 2000 (p=0.06). In multivariate survival analysis, protective effects were found for female sex (hazard ratio, 0.37, 95% CI 0.21-0.66; p<0.001), and post-2000 follow-up (hazard ratio, 0.44, 95% CI 0.20-0.99; p<0.05), but not for genotype, treatment center or birth cohort. INTERPRETATION AND
CONCLUSIONS: Most patients born after 1974 survive to at least the age of 30. There has been a marked improvement in survival for patients of all ages since 2000, which may be due to the introduction of combination chelation therapy.

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Year:  2006        PMID: 16956817

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  53 in total

1.  Umbilical cord blood transplantation for children with thalassemia and sickle cell disease.

Authors:  Annalisa Ruggeri; Mary Eapen; Andromachi Scaravadou; Mitchell S Cairo; Monica Bhatia; Joanne Kurtzberg; John R Wingard; Anders Fasth; Luca Lo Nigro; Mouhab Ayas; Duncan Purtill; Karim Boudjedir; Wagnara Chaves; Mark C Walters; John Wagner; Eliane Gluckman; Vanderson Rocha
Journal:  Biol Blood Marrow Transplant       Date:  2011-01-28       Impact factor: 5.742

2.  In search of the optimal iron chelation therapy for patients with thalassemia major.

Authors:  Vasilios Berdoukas; John Wood
Journal:  Haematologica       Date:  2011-01       Impact factor: 9.941

3.  Chelation use and iron burden in North American and British thalassemia patients: a report from the Thalassemia Longitudinal Cohort.

Authors:  Janet L Kwiatkowski; Hae-Young Kim; Alexis A Thompson; Charles T Quinn; Brigitta U Mueller; Isaac Odame; Patricia J Giardina; Elliott P Vichinsky; Jeanne M Boudreaux; Alan R Cohen; John B Porter; Thomas Coates; Nancy F Olivieri; Ellis J Neufeld
Journal:  Blood       Date:  2012-01-25       Impact factor: 22.113

4.  Improved survival in thalassemia major patients on switching from desferrioxamine to combined chelation therapy with desferrioxamine and deferiprone.

Authors:  Paul T Telfer; Fiona Warburton; Soteroula Christou; Michael Hadjigavriel; Maria Sitarou; Anita Kolnagou; Michael Angastiniotis
Journal:  Haematologica       Date:  2009-10-08       Impact factor: 9.941

5.  Complications and treatment of patients with β-thalassemia in France: results of the National Registry.

Authors:  Isabelle Thuret; Corinne Pondarré; Anderson Loundou; Dominique Steschenko; Robert Girot; Dora Bachir; Christian Rose; Vincent Barlogis; Jean Donadieu; Mariane de Montalembert; Isabelle Hagege; Brigitte Pegourie; Claire Berger; Marguerite Micheau; Françoise Bernaudin; Thierry Leblanc; Laurence Lutz; Frédéric Galactéros; Marie-Claude Siméoni; Catherine Badens
Journal:  Haematologica       Date:  2009-12-08       Impact factor: 9.941

6.  Global epidemiology of haemoglobin disorders and derived service indicators.

Authors:  Bernadette Modell; Matthew Darlison
Journal:  Bull World Health Organ       Date:  2008-06       Impact factor: 9.408

7.  Pregnancy and beta-thalassemia: an Italian multicenter experience.

Authors:  Raffaella Origa; Antonio Piga; Giovanni Quarta; Gian Luca Forni; Filomena Longo; Angela Melpignano; Renzo Galanello
Journal:  Haematologica       Date:  2009-11-10       Impact factor: 9.941

8.  Pregnancy Outcomes in Women with Homozygous Beta Thalassaemia: A single-centre experience from Oman.

Authors:  Nihal Al-Riyami; Maha Al-Khaduri; Shahina Daar
Journal:  Sultan Qaboos Univ Med J       Date:  2014-07-24

Review 9.  Beta-thalassemia.

Authors:  Renzo Galanello; Raffaella Origa
Journal:  Orphanet J Rare Dis       Date:  2010-05-21       Impact factor: 4.123

10.  Screening for beta thalassaemia.

Authors:  Mary Petrou
Journal:  Indian J Hum Genet       Date:  2010-01
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