Journal of Pharmaceutical Care، جلد ۱۰، شماره ۱، صفحات ۴۰-۴۱
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عنوان انگلیسی Challenges of Blood Transfusions in β-Thalassemia during COVID-19 Pandemic in Low Middle-Income Country
چکیده انگلیسی مقاله In China Hubei province, Wuhan was recognized as the focus of an epidemic of pneumonia of unidentified origin in December 2019. Ultimately, intense focus on the disease was raised worldwide and in China. as a result, on January 7, 2020, Chinese research scientists identified the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in an affected patient in Wuhan. Beta thalassemia is a congenital hereditary disorder of inefficient erythropoiesis that leads to peripheral red cell breakdown due to defective β-globin series. The severity of the disease depends on multiple genetic and environmental factors. Individuals with beta-thalassemia are classified based on their transfusion demands as having transfusion-dependent thalassemia (TDT) or non-transfusion-dependent thalassemia (NTDT). Routine transfusion remains the recommended standard management for beta-thalassemia, as it efficiently controls the thalassemia symptoms. If left untreated, Beta thalassemia major (BTM) can eventually induce spleen enlargement, deformation of bone because of bone marrow growth, and heart failure as a result of severe anemia.3, 4, 5, 6
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نویسندگان مقاله | Kashif Ali
Dow university of health sciences


| Kashif Rizvi
Cardiac Per fusionist, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.


| Saqib Hussain Ansari
Haematology and Bone Marrow Transplant Department, National Institute of Blood Diseases and Bone Marrow Transplantation, Karachi, Pakistan


| Faisal Zahid
Staff Pharmacist, Cleveland Clinical Abu Dhabi, Abu Dhabi, United Arab.
نشانی اینترنتی https://jpc.tums.ac.ir/index.php/jpc/article/view/464
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