the correlation between the cardiac and hepatic iron-overload in patients with thalassemia major who received multiple transfusion

Authors

حمید کلانتری

دانشیار، گروه داخلی، دانشکده ی پزشکی، دانشگاه علوم پزشکی اصفهان، اصفهان، ایران ندا راد

دستیار، گروه داخلی، دانشکده ی پزشکی، دانشگاه علوم پزشکی اصفهان، اصفهان، ایران طالب آزرم

. استاد، گروه داخلی، دانشکده ی پزشکی، دانشگاه علوم پزشکی اصفهان، ایران

abstract

background: the aim of this study was to investigate the correlation between the cardiac and hepatic iron-overload as assessed by magnetic resonance imaging t2 star (mrit 2 -star) technique and serum ferritin level in patients with thalassemia major. methods: in this cross-sectional study we evaluated 170 patients in sayed shohada hospital in isfahan in the year of 2009, cardiac and hepatic iron-overloaded values were calculated in patients using magnetic resonance imaging t2 star techniques. serum ferritin level and left ventricular ejection fraction (lvef) were determined for all patients. findings: we studied 170 beta-thalassemic patients, 90 (52.9%) females and 80 (47.1%) males, mean age 20.6 ± 6.2 years. mean cardiac iron-overloaded was 22.7 ± 14.7, mean hepatic iron-overloaded was 3.2 ± 2.4, mean serum ferritin level was 2310 ± 1554 and mean left ventricular ejection fraction was 60.5% ± 7.7 percent. pearson’s tests gave a significant correlation coefficient between cardiac iron-overloaded and hepatic iron-overloaded (r = 0.29, p < 0.001). there were weak inversely associated between serum ferritin level with hepatic iron (r = -0.32, p < 0.001) and cardiac iron (r = -0.21, p = 0.006). conclusion: myocardial iron deposition can be reproducibly quantified using myocardial  and this is the most significant variable for predicting the need for ventricular dysfunction treatment. the finding of this study demonstrated a significant correlation between cardiac and hepatic iron-overloaded level in patients with thalassemia major.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Evaluation of the relationship between hepatic and cardiac iron overload with MRI T2* and carotid intima media thickness with Doppler ultrasound in beta thalassemia major patients

Background: Iron overload is caused early progression of atherosclerosis in beta thalassemia patients due to regular repeated blood transfusion. MRI T2* is a gold standard non-invasive method for detecting hepatic and cardiac iron overload. The aim of this study was the comparison of carotid intima media thickness (CIMT) in the patients and healthy control groups with Doppler ultrasound for ear...

full text

Correlation between QRS Complex Changes and Cardiac Iron Overload in Beta Thalassemia Major Patients Using T2*MRI

Background and purpose: Cardiac magnetic resonance imaging (MRI) is a costly method to assess cardiac iron overload. The presence of fragmented QRS (fQRS) indicates changes due to iron overload in cardiac tissue. The aim of this study was to evaluate the correlation between fQRS and cardiac iron overload using cardiac MRI in patients with β-thalassemia major (β-TM). Materials and methods: This...

full text

Endocrine Dysfunctions in Iron Overload in Patients with Major Thalassemia

Abstract Background The aim of the present study was to determine the endocrine dysfunction in patients with major thalassemia, who receive hyper transfusion. Materials and Methods This cross sectional study was performed during one year, which included 65 major thalassemia patients (31 females and 34 males), aged between 14 month to 27 years old (median 10,3). Growth assessment was measur...

full text

Treating iron overload in patients with non-transfusion-dependent thalassemia

Despite receiving no or only occasional blood transfusions, patients with non-transfusion-dependent thalassemia (NTDT) have increased intestinal iron absorption and can accumulate iron to levels comparable with transfusion-dependent patients. This iron accumulation occurs more slowly in NTDT patients compared to transfusion-dependent thalassemia patients, and complications do not arise until la...

full text

Triple Drug Iron Chelation Therapy in Thalassemia Major; A Case Report

Regular packed cell transfusion in patients with thalassemia major leads to iron overload. Chelation therapy is one of the important aspects of thalassemia care as iron overload causes significant cardiac, hepatic, and endocrine dysfunction. We report a case of thalassemia major with severe iron overload causing cardiac and liver dysfunction who benefitted from triple drug chelation therapy. Tr...

full text

The correlation between zinc and monocyte phagocytosis in patients with major b-thalassemia

Background: Zinc depletion decreases monocyte functions and survival while excessive amount of zinc inhibits monocyte activation. Monocytes shift from conducting intercellular communication to becoming innate immune function as a response. This study aims to examine the influence of zinc status on the monocyte phagocytosis in patients with major beta-thalassemia. Materials and Methods: This st...

full text

My Resources

Save resource for easier access later


Journal title:
مجله دانشکده پزشکی اصفهان

جلد ۲۸، شماره ۱۱۱، صفحات ۰-۰

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023