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Cultural preferences and limited public resources influence the spectrum of thalassemia in Egypt.
Adly, Amira A M; Ebeid, Fatma Soliman El Sayed.
Affiliation
  • Adly AA; Thalasemia Centre, Pediatric Hematology/Oncology Department, Ain Shams University, Cairo, Egypt.
J Pediatr Hematol Oncol ; 37(4): 281-4, 2015 May.
Article in En | MEDLINE | ID: mdl-25811748
ABSTRACT

BACKGROUND:

Cultural beliefs of Egyptians with respect to the origin of thalassemia and its prevention, as well as national resources available for care, often differ from those of Western countries.

OBJECTIVES:

To assess the impact of cultural attitudes and the effect of limited medical and financial resources that could affect the management of Egyptian thalassemic patients.

SUBJECTS:

A cross sectional study included 205 Egyptians ß-thalassemia major (ß-TM) patients, with a mean age of 149±87.90 months and a male to female ratio of 94111.

METHODS:

Demographic data stressing on order of birth, consanguineous marriage, and family history of ß-TM, transfusion, and chelation therapy, were reported. HCV-Ab, HBV-Ag, and complete blood count were recorded with calculation of mean pretransfusional hemoglobin.

RESULTS:

The age distribution was relatively nonhomogenous, with 39% of patients between 10 and 20 years of age and 16% were younger than 5. There were high family birth rates and 35% of patients were third or more in order of birth and a marked cultural preference for consanguineous marriage, representing 61% of all the parents' marriages, as well as a high rate (59.5%) of a positive family history of ß-TM. Patients transfused on low pretransfusion hemoglobin levels around 8 g/dL, and those receiving blood transfusion before the establishment of National Blood Transfusion Services showed a statistically significant higher rate of positive hepatitis B and C viral infections. Chelation therapy tended to start at late age, mean age was around 4 years. Before 2000, subcutaneous deferoxamine was the most widely used chelation, and since then a considerable number of patients (50%) had started to use oral iron chelators.

CONCLUSIONS:

The strong cultural preferences for consanguineous marriage and limited preventive programmes and resources have had a negative impact on the management of Egyptians thalassemic patients.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thalassemia / Culture Type of study: Observational_studies Aspects: Determinantes_sociais_saude / Patient_preference Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: J Pediatr Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2015 Document type: Article Affiliation country: Egipto Country of publication: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thalassemia / Culture Type of study: Observational_studies Aspects: Determinantes_sociais_saude / Patient_preference Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: J Pediatr Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2015 Document type: Article Affiliation country: Egipto Country of publication: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA