[Home ] [Archive]   [ فارسی ]  
:: Main :: About us :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Articles archive::
For Authors::
For Reviewers::
Subscription::
News& Events::
Contact us::
Site Facilities::
Ethics & Permissions::
::
Search in website

Advanced Search
..
Receive site information
Enter your Email in the following box to receive the site news and information.
..
Indexing
                        
..
:: Volume 10, Issue 1 (Spring 2013) ::
Sci J Iran Blood Transfus Organ 2013, 10(1): 86-92 Back to browse issues page
Evaluation of cardiac function in patients with major beta thalassemia in Birjand
T. Chahkandi , T. Kazemi , A. Jalili , F. Ghaderi
Keywords: Key words: beta-Thalassemia, Electrocardiography, Radiography, Echocardiography
Full-Text [PDF 271 kb]   (2181 Downloads)     |   Abstract (HTML)  (14274 Views)
Type of Study: Research | Subject: Hematology
Published: 2013/08/14
Full-Text:   (2354 Views)
References:
  1. Galanello R, Origa R. Beta-thalassemia. Orphanet J Rare Dis 2010; 5: 11.
  2. Flint J, Harding RM, Boyce AJ, Clegg JB. The population genetics of the haemoglobinopathies. Baillieres Clin Haematol 1998; 11(1): 1-51.
  3. Hershko C. Iron loading and its clinical implications. Am J Hematol 2007; 82(12 Suppl): 1147-8.
  4. Chahkandi T, Mofatteh MR, Sharifzadeh GhR, Azarkar Z. Hearing impairment in patients with major thalassemia in Southern Khorasan Province, 2007. Journal of Birjand University of Medical Sciences 2011; 18(2): 102-8. [Article in Farsi]
  5. Kashanchi Langarodi M, Abdolrahim Poorheravi H. Prevalence of HCV among thalassemia patients in Shahid Bahonar Hospital, Karaj. Sci J Blood Transfus Organ  2011; 8(2) 137-42. [Article in Farsi]
  6. Azarkar Z, Sharifzadeh GhR, Chahkandi T, Mahmoudi Rad A, Sandoughi M, Rezaiee N. Survey of HBV and HCV markers in haemodialysis and thalassemia, South Khorasan, Birjand 2007. Sci J Blood Transfus Organ 2009; 6(3): 233-7. [Article in Farsi]
  7. Chahkandi T. Thyroid and Parathyroid function in patients with major thalassemia. Journal of Birjand University of Medical Sciences 2004; 11(2): 9-15. [Article in Farsi]
  8. Borgna-Pignatti C, Cappellini MD, De Stefano P, Del Vecchio GC, Forni GL, Gamberini MR, et al. Survival and complications in thalassemia. Ann N Y Acad Sci 2005; 1054: 40-7.
  9. Taksande A, Prabhu S, Venkatesh S. Cardiovascular aspect of Beta-thalassaemia. Cardiovasc Hematol Agents Med Chem 2012; 10(1): 25-30.
  10. Hahalis G, Alexopoulos D, Kremastinos DT, Zoumbos NC. Heart failure in beta-thalassemia syndromes: a decade of progress. Am J Med 2005; 118(9): 957-67.
  11. Li CG, Liu SX, Mai HR, Wang Y, Wen FQ, Liu RY, et al. Evaluation of heart and liver iron deposition status in patients with β- thalassemia intermedia and major with MRI T2* technique. Zhongguo Dang Dai Er Ke Za Zhi 2012; 14(2): 110-3. [Article in Chinese]
  12. Detterich J, Noetzli L, Dorey F, Bar-Cohen Y, Harmatz P, Coates T, et al. Electrocardiographic consequences of cardiac iron overload in thalassemia major. Am J Hematol 2011. [Epub ahead of print]
  13. Magrì D, Sciomer S, Fedele F, Gualdi G, Casciani E, Pugliese P, et al. Increased QT variability in young asymptomatic patients with beta-thalassemia major. Eur J Haematol 2007; 79(4): 322-9.
  14. Aggeli C, Felekos I, Poulidakis E, Aggelis A, Tousoulis D, Stefanadis C. Quantitative analysis of left
atrial function in asymptomatic patients with b-thalassemia major using real-time three-dimensional echocardiography. Cardiovasc Ultrasound 2011; 9: 38.
  1. Vogel M, Anderson LJ, Holden S, Deanfield JE, Pennell DJ, Walker JM. Tissue Doppler echocardiography in patients with thalassaemia detects early myocardial dysfunction related to myocardial iron overload. Eur Heart J 2003; 24(1): 113-9.
  2. Barzin M, Kowsarian M, Akhlaghpoor S, Jalalian R, Taremi M. Correlation of cardiac MRI T2* with echocardiography in thalassemia major. Eur Rev Med Pharmacol Sci 2012; 16(2): 254-60.
  3. Oztarhan K, Delibas Y, Salcioglu Z, Kaya G, Bakari S, Bornaun H, et al. Assessment of cardiac parameters in evaluation of cardiac functions in patients with thalassemia major. Pediatr Hematol Oncol 2012; 29(3): 220-34.
  4. Malakan Rad E,  Momtazmanesh N. Study of Cardiac complications in patients with major Thalasemai in Kashan during 1999-2000. Razi Journal of Medical Sciences 2002; 8(27): 623-31. [Article in Farsi]
  5. Farhangi H, Zandian Kh, Pedram M, Emamimoghaddam A, Ahmadi F. Evaluation of acquired cardiac complications in major b-thalassemic patients referred to Ahvaz thalassemia center. Scientific Medical Journal of Ahwaz University of Medical Sciences 2010; 8(4): 391-405. [Article in Farsi]
  6. Rahimibashar F, Jafroudi M, Zaridoust A. Survey of Cardiac Complications in beta Thalassemia major patients in 10-20 years old. Journal of Guilan University of Medical Sciences 2008; 16(64): 16-23. [Article in Farsi]
  7. Wood JC. Cardiac iron across different transfusion-dependent diseases. Blood Rev 2008; 22 Suppl 2: S14-21.
  8. Oudit GY, Sun H, Trivieri MG, Koch SE, Dawood F, Ackerley C, et al. L-type Ca2+ channels provide a major pathway for iron entry into cardiomyocytes in iron-overload cardiomyopathy. Nat Med 2003; 9(9): 1187-94.
  9. Bartfay WJ, Bartfay E. Iron-overload cardiomyopathy: evidence for a free radical--mediated mechanism of injury and dysfunction in a murine model. Biol Res Nurs 2000; 2(1): 49-59.
  10. Bazrgar M, Peiravian F, Abedpour F, Karimi M. Causes for hospitalization and death in Iranian patients with β-thalassemia major. Pediatr Hematol Oncol 2011; 28(2): 134-9.
 
 
 
 
 
 


 
 
Original Article
 
 
 
 
Sci J Iran Blood Transfus Organ 2013; 10 (1): 86-92
 
 
 

Evaluation of cardiac function in patients with
major beta thalassemia in Birjand
 
Chahkandi T.1, Kazemi T.1, Jalili A.2, Ghaderi F.3
 
 
1Birjand Atherosclerosis and Coronary Artery Research Center, Birjand University of Medical Sciences, Birjand, Iran
2Birjand Research Committee. Birjand University of Medical Sciences, Birjand, Iran
3Mashhad University of Medical Sciences, Mashhad, Iran
 
 
Abstract
Background and Objectives
The most common leading causes of death in patients with major beta thalassemia are cardiac complications.The purpose of this study is to determine cardiac function in patients with major thalassemia in Birjand.
 
Materials and Methods
This descriptive-analytical study was conducted on all patients with major beta thalassemia having referred to special clinics of Valiasr Hospital in Birjand. Variables such as age, sex, frequency of transfusions, serum ferritin, and hemoglobin were studied. For all patients after a thorough examination of heart, ECG, chest X-ray, and echocardiography were performed. All data were collected and analyzed with SPSS software 15.5 by t-test at α ≤ 0.05.
 
Results
We studied 35 patients with major beta thalassemia. The mean age was 9.06 ± 4.33 years. The mean hemoglobin was 9.2 gr/dl and the mean ferritin 2121.6 ng/ml, respectively. Cardiac examinations showed 62.9% of patients to be normal. ECG and chest X-ray in 71.6% and 57.1% of patients were normal, respectively. Out of the total number of patients, 77.8% had abnormal echocardiography. The most common abnormal findings in echocardiography were restrictive diastolic dysfunction. No significant correlation was found between abnormal findings on echocardiography with both ferritin and the number of blood transfusions. However, left ventricular diastolic dysfunction and hemoglobin were not significantly associated (8.5 ± 0.69 gr/dL in normal diastolic function, 9.6 ± 0.99 gr/dL in diastolic dysfunction p= 0.007).
 
Conclusions 
The most common finding in our study was left ventricular diastolic dysfunction. Therefore, periodic echocardiography to determine the risk of heart involvement is very valuable.
 
Key words: beta-Thalassemia, Electrocardiography, Radiography, Echocardiography
 
 
Received: 19 May 2012
Accepted: 21 Aug 2012
 
 
 

Correspondence: Kazemi T., MD. Associate Professor of Cardiology. Birjand Atherosclerosis and Coronary Artery Research Center of Birjand University of Medical Sciences. Valiasr Hospital, Ghaffari St.
Postal Code: 9717964151, Birjand, Iran. Tel: (+98561) 4443001; Fax: (+98561) 4433004
                E-mail: med_847@yahoo.com
Send email to the article author

Add your comments about this article
Your username or Email:

CAPTCHA


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Chahkandi T, Kazemi T, Jalili A, Ghaderi F. Evaluation of cardiac function in patients with major beta thalassemia in Birjand. Sci J Iran Blood Transfus Organ 2013; 10 (1) :86-92
URL: http://bloodjournal.ir/article-1-742-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 10, Issue 1 (Spring 2013) Back to browse issues page
فصلنامه پژوهشی خون Scientific Journal of Iran Blood Transfus Organ
The Scientific Journal of Iranian Blood Transfusion Organization - Copyright 2006 by IBTO
Persian site map - English site map - Created in 0.07 seconds with 39 queries by YEKTAWEB 4645