Literature DB >> 25843562

Assessing Parental Knowledge About Thalassemia in a Thalassemia Center of Karachi, Pakistan.

Humaira Maheen1, Farrukh Malik1, Barera Siddique1, Asim Qidwai2.   

Abstract

Thalassemia is the leading haemoglobinopathy after sickle cell anemia that accounts for 1.5 % of the global population. In Pakistan, every 1-4 per 1000 infants suffers from Thalassemia. Regardless of being a population "at high risk" for Thalassemia major, evidence suggest that Pakistanis possess poor knowledge of the disease. The present study aimed to assess parents' accurate knowledge about Thalassemia disease at Afzaal Memorial Thalassemia Foundation in Karachi, Pakistan. A total of 172 parents of existing patients who were receiving regular blood transfusion from the center were included in the study. Parents' knowledge was assessed via a pre-tested and validated Thalassemia knowledge questionnaire. Findings show that 40 % of the sample showed lower knowledge scores about Thalassemia. Among different ethnic origins, Urdu speaking respondents showed a higher average score of correct knowledge about Thalassemia major (21.6 ± 4.41) as compared to the Siraiki (17.9 ± 4.48) and the Pathans (17.2 ± 4.34). These latter two ethnic groups also showed poor knowledge about Thalassemia minor. Generally parents provided correct answers about treatment of Thalassemia major. The findings suggest targeted interventions are required for high risk ethnic groups. Thalassemia education programs should be offered to extended family members of existing patients by all Thalassemia centers. High risk ethnic groups (Siraiki and Pathan) need rigorous interventions, and Thalassemia worker program should be introduced nationwide.

Entities:  

Keywords:  Awareness raising program; Ethnicity; Genetic counseling; Pakistan; Parental knowledge; Thalassemia knowledge; Thalassemia major; Thalassemia minor

Mesh:

Year:  2015        PMID: 25843562     DOI: 10.1007/s10897-015-9830-z

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  21 in total

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Authors:  Ashraf Samavat; Bernadette Modell
Journal:  BMJ       Date:  2004-11-13

2.  Attitude of Saudi families affected with hemoglobinopathies towards prenatal screening and abortion and the influence of religious ruling (Fatwa).

Authors:  F S Alkuraya; R A Kilani
Journal:  Prenat Diagn       Date:  2001-06       Impact factor: 3.050

3.  Prenatal diagnosis of beta-thalassaemia in Pakistan: experience in a Muslim country.

Authors:  S Ahmed; M Saleem; N Sultana; Y Raashid; A Waqar; M Anwar; B Modell; K A Karamat; M Petrou
Journal:  Prenat Diagn       Date:  2000-05       Impact factor: 3.050

Review 4.  Changing patterns of thalassemia worldwide.

Authors:  Elliott P Vichinsky
Journal:  Ann N Y Acad Sci       Date:  2005       Impact factor: 5.691

5.  Comparing knowledge of beta-thalassemia in samples of Italians, Italian-Americans, and non-Italian-Americans.

Authors:  Christina Armeli; Steven J Robbins; Deborah Eunpu
Journal:  J Genet Couns       Date:  2005-10       Impact factor: 2.537

6.  Screening extended families for genetic hemoglobin disorders in Pakistan.

Authors:  Suhaib Ahmed; Mohammed Saleem; Bernadette Modell; Mary Petrou
Journal:  N Engl J Med       Date:  2002-10-10       Impact factor: 91.245

7.  'Rakter dosh'--corrupting blood: The challenges of preventing thalassemia in Bengal, India.

Authors:  Sreeparna Chattopadhyay
Journal:  Soc Sci Med       Date:  2006-08-09       Impact factor: 4.634

8.  Awareness among parents of β-thalassemia major patients, regarding prenatal diagnosis and premarital screening.

Authors:  Fouzia Ishaq; Hasnain Abid; Farkhanda Kokab; Adil Akhtar; Shahid Mahmood
Journal:  J Coll Physicians Surg Pak       Date:  2012-04       Impact factor: 0.711

9.  Nutritional deficiencies in patients with thalassemia.

Authors:  Ellen B Fung
Journal:  Ann N Y Acad Sci       Date:  2010-08       Impact factor: 5.691

10.  Molecular genetic diagnosis of beta thalassemia in Pakistan.

Authors:  S N Khan; A U Zafar; S Riazuddin
Journal:  J Pak Med Assoc       Date:  1995-03       Impact factor: 0.781

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  5 in total

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2.  Enabling routine β-thalassemia Prevention and Patient Management by scalable, combined Thalassemia and Hemochromatosis Mutation Analysis.

Authors:  Ghazala Hashmi; Asim Qidwai; Kristopher Fernandez; Michael Seul
Journal:  BMC Med Genet       Date:  2020-05-15       Impact factor: 2.103

3.  Socio-religious Prognosticators of Psychosocial Burden of Beta Thalassemia Major.

Authors:  Muhammad Abo Ul Hassan Rashid; Saif-Ur-Rehman Saif Abbasi; Malik Maliha Manzoor
Journal:  J Relig Health       Date:  2020-12

4.  The Incidence of Minor β-thalassemia Among Individuals Participated in Premarital Screening Program in Ardabil Province: North-west of Iran.

Authors:  Afshin Fathi; Firouz Amani; Nahaleh Mazhari
Journal:  Mater Sociomed       Date:  2019-12

5.  Epidemiology of Thalassemia in Gulf Cooperation Council Countries: A Systematic Review.

Authors:  Amani Abu-Shaheen; Humariya Heena; Abdullah Nofal; Doaa A Abdelmoety; Abdulrahman Almatary; Mohammed Alsheef; Isamme AlFayyad
Journal:  Biomed Res Int       Date:  2020-10-28       Impact factor: 3.411

  5 in total

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