Literature DB >> 21728720

Complications of β-thalassemia intermedia in Iran during 1996-2010 (single-center study).

Khadijeh Arjmandi Rafsanjani1, Negar Mafi, R Isa Tafreshi.   

Abstract

Patients with thalassemia intermedia (TI) experience many complications, of which the incidence varies greatly among cases. Considering the high prevalence of thalassemia in Iran, the study was carried out to determine the frequency of TI complications in Iranian patients and to find possible risk factors for each of them. Using the sampling method of "census," the authors included 153 patients who were seen in their tertiary hematology clinic with the diagnosis of TI during 1996-2010; an analytical cross-sectional study was performed and the data was analyzed by SPSS software using univariate and regression analyses. Mean age of the patients at the time of the study was 17.4 years and 36.5% were receiving transfusions (regularly or occasionally). Mean hemoglobin was 9.2 g/dL and mean serum ferritin was 858 ng/mL. Splenectomy was performed in 46.9% and it was correlated with age and the age at diagnosis in regression analysis. Cholelithiasis was found in 25.5% and was correlated with age and history of splenectomy. Pulmonary hypertension, detected in 23.5%, was correlated with thrombocytosis and mitral valve regurgitation in univariate analysis. Endocrine disease (hypogonadism, hypothyroidism, and adrenal insufficiency) was detected in 8% of the patients. In univariate analysis, endocrine disease was correlated with age of the patients. Regarding bone density of the spine, 53% of cases had osteoporosis. Thrombocytosis was present in 42% of patients and was correlated with their age. Since the severity of thalassemia intermedia vary greatly among patients, a careful evaluation of clinical, laboratory, and genetic aspects is necessary to differentiate TI in a patient at presentation. Moreover, TI patients should be carefully followed up for early detection and management of newly developed complications. The authors also suggest confirmatory controlled studies with larger sample sizes to assist in developing guidelines for surveillance and treatment of TI.

Entities:  

Mesh:

Year:  2011        PMID: 21728720     DOI: 10.3109/08880018.2011.572144

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  6 in total

1.  Subclinical Left Ventricular Dysfunction in Children and Adolescence With Thalassemia Intermedia.

Authors:  Roya Isa Tafreshi; Mohammad Radgoodarzi; Kadijeh Arjmandi Rafsanjani; Fahimeh Soheilipour
Journal:  Front Pediatr       Date:  2022-06-17       Impact factor: 3.569

2.  Cholelithiasis in Thalassemia Major Patients: A Report from the South-East of Iran.

Authors:  Iraj Shahramian; Razieh Behzadmehr; Mahdi Afshari; Atefeh Allahdadi; Mojtaba Delaramnasab; Ali Bazi
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2018-04-01

3.  Molecular Characterization and Disease-Related Morbidities of β-Thalassemia Patients from the Northeastern Part of Iraq.

Authors:  Shaema Amin; Sana Jalal; Kosar Ali; Luqman Rasool; Tara Osman; Omed Ali; Abdalhamid M-Saeed
Journal:  Int J Gen Med       Date:  2020-12-09

4.  Prevalence of Pulmonary Hypertension in Patients with Thalassemia Intermedia in 2009: a single center's experience.

Authors:  Hassan Mottaghi Moghaddam; Zahra Badiei; Kambiz Eftekhari; Reza Shakeri; Hamid Farhangi
Journal:  Electron Physician       Date:  2015-07-20

5.  The survival rate of patients with beta-thalassemia major and intermedia and its trends in recent years in Iran.

Authors:  Alireza Ansari-Moghaddam; Hossein Ali Adineh; Iraj Zareban; Mehdi Mohammadi; Mahtab Maghsoodlu
Journal:  Epidemiol Health       Date:  2018-10-03

6.  Beta-Thalassemia Intermedia: A Single Thalassemia Center Experience from Northeastern Iraq.

Authors:  Shaema Salih Amin; Sana Dlawar Jalal; Kosar Muhammed Ali; Ali Ibrahim Mohammed; Luqman Khalid Rasool; Tara Jamel Osman
Journal:  Biomed Res Int       Date:  2020-02-28       Impact factor: 3.411

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.