Evaluation of mental health and quality of life among β-thalassemia major patients

Authors

  • Alireza yahyaei Non-Communicable Pediatric Diseases Research Center, Amirkola Children’s Hospital, Health Research Institute
  • Elmira Khodabakhsh Babol University of Medical Science
  • Farzan Khairkhah Department of Psychology
  • Hassan Mahmoodi Nesheli Non-Communicable Pediatric Diseases Research Center, Amirkola Children’s Hospital, Health Research Institute
  • Seyed Reza Hosseini Social Determinants of Health (SDH) Research Center
Abstract:

Background: Since the reduction of mental health in patients with Thalassemia may affect the quality of life and cause dysfunction in various dimensions, so the assessment of this disorder is necessary to choose the appropriate treatment. Therefore, the aim of this study was to investigate the mental health and quality of life in patients with Thalassemia major. Methods: In this cross-sectional descriptive study, all Thalassemia major patients with 15 or more than 15 years old, referred to Amirkola Institute, were recruited. Mental health status and quality of life were measured via GHQ28 and SF-36 standard questionnaires, respectively. Results: A total of 80 women and 70 men with the mean &acirc;g&eacute; of 24.17&plusmn;7.34 were included in the study. The results indicated that in case of quality of life, the physical activity part was singnifantly correlated with stress, social dysfunction, physical symptoms and depression (P<0.001).&nbsp; Social activity, mental health and general health (except depression) were significantly correlated (P<0.001). Social dysfunction was more prevalent in men (P=0.016) but there was no significant difference between men and women in quality of life. Conclusions: There is an association between some of the areas of mental health and areas of quality of life, therefore a reduction in mental health status in thalassemia major patients may affect their quality of life. &nbsp;The incidence of mental disorders in this study was twofold more than previous studies and since none of patients met any psychologist during their treatment period, it is suggested that the screening test should be considered for mental disorders in Thalassemia major patients.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

evaluation of mental health and quality of life among β-thalassemia major patients

background: since the reduction of mental health in patients with thalassemia may affect the quality of life and cause dysfunction in various dimensions, so the assessment of this disorder is necessary to choose the appropriate treatment. therefore, the aim of this study was to investigate the mental health and quality of life in patients with thalassemia major. methods: in this cross-sectional...

full text

Assessment of oral health and quality of life in hemophilia and thalassemia major patients

Background and Aims: The chronic blood disorders could have negative effects on various fields of patient’s quality of life. The aim of this study was to evaluate the relationship between the quality of life and oral health in major thalassemia and hemophilia patients. Materials and Methods: This cross- sectional study was performed in 1398 on 56 hemophilia patients and 35 thalassemia major pa...

full text

Health-Related Quality of Life in β Thalassemia Major Children in North of Iran

Background: Advances in treatment of thalassemia major have improved the life expectancy of the patients and therefore their quality of life as other chronic diseases. This study was conducted to assess health- related quality of life in these patients in Guilan province. Methods: In a cross-sectional study, thirty-one children, aged 8-12 years, with &beta;-thalassemia major were interviewed i...

full text

Quality of life in patients with thalassemia major

Background With modern medical management, thalassemia major is now extending into adulthood and it is expected to have a negative impact on the quality of life (QOL) of the patients. The aim of this study was to evaluate quality of life in patients with thalassemia major. Materials and Methods This is an analytic case control study. Two hundred and fifty patients and 51 participants a...

full text

Quality of life among patients with beta-thalassemia major in Shahrekord city, Iran

Background and aims: Nowadays introduction of regular blood transfusion therapy has obviously improved the life expectancy of patients with thalassemia. However, these patients face with newer challenges which influence their quality of life (QoL). In this study, the aim of this study was to measure QoL among patients with β-thalassemia major (β-TM). Methods:</str...

full text

associates of poor physical and mental health-related quality of life in beta thalassemia-major/intermedia

background : using two logistic regression models, we determined the associates of poor physical and mental health related quality of life (hrqol) among beta thalassemia patients. methods : in this cross-sectional study which was conducted during 2006 and 2007 in outpatient adult thalassemia clinic, blood transfusion organization, tehran, iran, short form 36 (sf-36) was used for measuring hrqol...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 1  issue None

pages  54- 59

publication date 2015-09

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

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023