PREVALENCE OF CARDIAC COMPLICATIONS IN PATIENTS WITH MAJOR THALASSEMIA IN IRANIAN PATIENTS: A SYSTEMATIC REVIEW AND META-ANALYSIS

Introduction: Thalassemia major is one of the most common blood diseases in Iran. Cardiac complications are one of the leading causes of death in these patients. The aim of this study was evaluated the Prevalence of Cardiac complications in patients with major thalassemia in Iranian patients. Methods: The methods used in this systematic review were based on the Checklist (PRISMA) Guidelines. The searches were conducted by two independent researchers and the aim was to find the relevant studies published from 1/1/2000 to 30/5/2019. Results: A total of 2516 patients and a total of 7 studies from 7 provinces that met the inclusion criteria were evaluated. Of the studies were retrospective. According to the random effect model, the total Prevalence of Cardiac complications in 2516 patients was 11% (10%-12% at a 95% confidence interval, I2 = 93.7%). Conclusion: Early diagnosis of cardiac dysfunction is essential. Since the most important cause of death for patients with thalassemia major is cardiac involvement, regular control of the heart conditions of patients is essential. Also, clinical examinations, electrocardiography, and chest x-ray in the early stages of cardiac involvement of these patients are normal and the most common abnormal finding of patients is left ventricular diastolic failure that can be evaluated via thoracic transthoracic echocardiography. In recent studies, however, ECG and its variations have been of great importance. Therefore, it is recommended that the ECG be monitored regularly for ST-T changes or arrhythmias. Key words: Major thalassemia , complication, Diastolic dysfunction , Echocardiography

[1]  M. Bobrova,et al.  Metabolic syndrome: review , 2021, Journal of Education, Health and Sport.

[2]  Z. Mahmood The association of stress, HTN and DM during pregnancy , 2017 .

[3]  Z. Mahmoodi Myocardial infarction in pregnant women - A review , 2017 .

[4]  V. Positano,et al.  Different patterns of myocardial iron distribution by whole-heart T2* magnetic resonance as risk markers for heart complications in thalassemia major. , 2014, International journal of cardiology.

[5]  T. Kazemi,et al.  Evaluation of cardiac function in patients with major beta thalassemia in Birjand , 2013 .

[6]  R. Mohammadi,et al.  THE FREQUENCY OF β-THALASEMIA MAJOR COMPLICATIONS IN PATIENTS REFERRED TO KERMAN CENTER FOR SPECIAL DISEASES DURING 6 MONTHS , 2011 .

[7]  Ioanna Tzoumari,et al.  Oral chelators in transfusion-dependent thalassemia major patients may prevent or reverse iron overload complications. , 2011, Blood cells, molecules & diseases.

[8]  M. Cappellini,et al.  Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study. , 2010, Blood.

[9]  P. Cianciulli,et al.  Improving survival with deferiprone treatment in patients with thalassemia major: a prospective multicenter randomised clinical trial under the auspices of the Italian Society for Thalassemia and Hemoglobinopathies. , 2009, Blood cells, molecules & diseases.

[10]  D J Pennell,et al.  Cardiac T2* magnetic resonance for prediction of cardiac complications in thalassemia major , 2009, Circulation.

[11]  P. Cianciulli,et al.  Guideline recommendations for heart complications in thalassemia major , 2008, Journal of cardiovascular medicine.

[12]  M. Tsironi,et al.  Thalassemia heart disease: a comparative evaluation of thalassemia major and thalassemia intermedia. , 2005, Chest.

[13]  M. Tsironi,et al.  Reversal of heart failure in thalassemia major by combined chelation therapy: a case report , 2005, European journal of haematology.

[14]  E. Neufeld,et al.  Complications of (cid:1) -thalassemia major in North America , 2004 .