EVALUATION OF PULMONARY IRON OVER LOAD IN PATIENTS WITH Β-THALASSEMIA MAJOR USING SPIROMETRY

Authors

  • ghazizadeh, farid Assistant professor of pediatrics department, pediatric hematologist and oncologist, Urmia University of Medical Sciences (Corresponding author)
Abstract:

Background & Aims: Spirometry changes in thalassemic patients can be obstructive or restrictive and pulmonary dysfunction depends on age and body iron overload. In this study the effectiveness of lung spirometry in detecting iron overload in patients with β-thalassemia was investigated. Materials & Methods: This cross-sectional (descriptive-analytic) study investigated the spirometry test results and their association with iron stores in patients with thalassemia major. Complete physical examination, CBC, MRI T2*of heart, and serum ferritin were performed. A two-stage spirometry was also taken 2 weeks after blood transfusion in the sitting position. Results: This clinical trial study was carried out on 31 patients. The spirometry test results in 10 (32.3%) patients were normal, while the spirometry test results were abnormal in 21 (67.8%) patients. Of the 17 patients with abnormal heart MRI T2*, spirometry results were abnormal in 15 patients and 2 patients had normal spirometry. Conclusion: Ferritin stores have no significant relationship with spirometry changes in patients with β-thalassemia major. But there was a significant correlation between MRI T2*of the heart and spirometry changes.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Evaluation of tissue doppler echocardiography and T2* magnetic resonance imaging in iron load of patients with thalassemia major

Background: Iron-mediated cardiomyopathy is the main complication of thalassemia major (TM) patients. Therefore, there is an important clinical need in the early diagnosis and risk stratification of patients. The aim of this study was to evaluate the efficacy of tissue doppler imaging (TDI) to study cardiac iron overload in patients with TM using T2* magnetic resonance (MR) as the gold-standard...

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

Evaluation of relationship between biochemical parameters and osteoporosis in patients with β-thalassemia major

Background: Osteoporosis is one of the late complications of β-Thalassemia major. The pathogenesis of osteoporosis depends on different factors. Ineffectiveness of hematopoiesis is the major factor, and the other factors are defected by hormonal functions or biochemical parameters. Osteoclasts hyperactivity in thalassemia increases the serum receptor activator of nuclear factor Kappa B ligand (...

full text

Effective iron chelation practice for patients with β-thalassemia major.

Chronic blood transfusion is the only treatment for severe anemia in patients with β-thalassemia major. However, red blood cell transfusions lead to iron overload and subsequent organ damage because of the toxic effects of iron. The heart is particularly vulnerable to iron toxicity, and heart failure is the leading cause of death among these patients. Iron chelation therapy prevents or reverses...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 30  issue 2

pages  155- 162

publication date 2019-05

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

No Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023