» Articles » PMID: 26212506

Analysis of Survival Data in Thalassemia Patients in Shiraz, Iran

Overview
Specialty Public Health
Date 2015 Jul 28
PMID 26212506
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: The survival rate of thalassemia patients has not been conclusively established, and the factors associated with survival remain unclear. This study aimed to determine the survival rate of thalassemia among patients in southern Iran and to identify the factors associated with mortality from thalassemia.

Methods: This retrospective cohort study was conducted based on a retrospective review of the medical records of 911 beta-thalassemia patients in 2014. Data analysis was conducted using the Kaplan-Meier method and Cox regression analysis.

Results: Overall, 212 patients (23.3%) died, and 26.8% had thalassemia intermedia. The 20-year, 40-year, and 60-year survival rates were 85%, 63%, and 54%, respectively. Both crude and adjusted analyses found that education, marital status, ferritin levels, and comorbidities were related to mortality.

Conclusions: Sociodemographic and hematological factors were found to be significantly associated with the survival rate of thalassemia. Addressing these factors may help healthcare providers and physicians to provide the best possible care and to improve the survival rate.

Citing Articles

Mortality and complications in Omani patients with beta-thalassemia major: a long-term follow-up study.

Daar S, Al-Naamani K, De Sanctis V, Al Rahbi S, Al Zadjali S, Khan H Acta Biomed. 2023; 94(4):e2023191.

PMID: 37539594 PMC: 10440768. DOI: 10.23750/abm.v94i5.14856.


Atrial Fibrillation in β-Thalassemia: Overview of Mechanism, Significance and Clinical Management.

Malagu M, Marchini F, Fiorio A, Sirugo P, Clo S, Mari E Biology (Basel). 2022; 11(1).

PMID: 35053146 PMC: 8772694. DOI: 10.3390/biology11010148.


Economic burden in the management of transfusion-dependent thalassaemia patients in Malaysia from a societal perspective.

Shafie A, Wong J, Mohd Ibrahim H, Mohammed N, Chhabra I Orphanet J Rare Dis. 2021; 16(1):157.

PMID: 33827621 PMC: 8028190. DOI: 10.1186/s13023-021-01791-8.


Eradication of hepatitis C virus infection in thalassemia patients in Iran using various treatment strategies.

Moghimbeygi M, Alavian S J Virus Erad. 2020; 6(3):100006.

PMID: 33251024 PMC: 7646675. DOI: 10.1016/j.jve.2020.100006.


Changing patterns in the epidemiology of β-thalassemia.

Kattamis A, Forni G, Aydinok Y, Viprakasit V Eur J Haematol. 2020; 105(6):692-703.

PMID: 32886826 PMC: 7692954. DOI: 10.1111/ejh.13512.


References
1.
Weatherall D, Clegg J . Inherited haemoglobin disorders: an increasing global health problem. Bull World Health Organ. 2001; 79(8):704-12. PMC: 2566499. View

2.
Borgna-Pignatti C, Rugolotto S, De Stefano P, Zhao H, Cappellini M, Del Vecchio G . Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine. Haematologica. 2004; 89(10):1187-93. View

3.
Samavat A, Modell B . Iranian national thalassaemia screening programme. BMJ. 2004; 329(7475):1134-7. PMC: 527686. DOI: 10.1136/bmj.329.7475.1134. View

4.
Borgna-Pignatti C, Cappellini M, De Stefano P, Del Vecchio G, Forni G, Gamberini M . Survival and complications in thalassemia. Ann N Y Acad Sci. 2005; 1054:40-7. DOI: 10.1196/annals.1345.006. View

5.
Telfer P, Coen P, Christou S, Hadjigavriel M, Kolnakou A, Pangalou E . Survival of medically treated thalassemia patients in Cyprus. Trends and risk factors over the period 1980-2004. Haematologica. 2006; 91(9):1187-92. View