[HTML][HTML] Prevalence of Transfusion Transmissible Infections in Beta-Thalassemia Major Patients of Pakistan: A Systematic Review

H Ehsan, A Wahab, MA Shafqat, MS Faisal, A Muneeb… - Blood, 2020 - Elsevier
Introduction: β-thalassemia major (TM) is one of the most prevalent inherited
hemoglobinopathies in Pakistan. It has one of the highest prevalence of transfusion …

Problems and approaches for blood transfusion in the developing countries

DJ Roberts, S Field, M Delaney… - Hematology/Oncology …, 2016 - hemonc.theclinics.com
Problems and Approaches for Blood Transfusion in the Developing Countries - Hematology/Oncology
Clinics Skip to Main Content Advertisement Hematology/Oncology Clinics Log in Register Log …

[HTML][HTML] Red blood cell alloimmunisation in transfusion-dependent thalassaemia: a systematic review

M Franchini, GL Forni, G Marano, M Cruciani… - Blood …, 2019 - ncbi.nlm.nih.gov
Background Chronic red blood cell transfusion is the first-line treatment for severe forms of
thalassaemia. This therapy is, however, hampered by a number of adverse effects, including …

Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience

A Belsito, D Costa, S Signoriello, C Fiorito… - … and apheresis science, 2019 - Elsevier
Background The development of alloantibodies may complicate the management of patients
with β-thalassemia. An extended antigenic matching may reduce the risk of …

Red cell alloimmunization in transfusion-dependent and transfusion-independent beta thalassemia: A review from the Eastern Mediterranean Region (EMRO)

AZ Al-Riyami, S Daar - Transfusion and Apheresis Science, 2019 - Elsevier
Background β-Thalassemia is considered one of the common hemoglobin disorders in the
Arabian Peninsula. Red blood cell (RBC) transfusion is a crucial component of the …

Red blood cell alloimmunization in blood transfusion-dependent β thalassemia major patients in Sana'a City-Yemen

MAW Almorish, B Al-Absi, AME Elkhalifa… - Scientific Reports, 2024 - nature.com
The development of erythrocyte alloantibodies complicates transfusion therapy in β
thalassemia major patients. These antibodies increase the need for blood and intensify …

Acute blood transfusion reactions in a tertiary care hospital in Pakistan‐an initiative towards haemovigilance

M Borhany, N Anwar, H Tariq, N Fatima… - Transfusion …, 2019 - Wiley Online Library
Objective In this study, we report acute blood transfusion reactions at our hospital, compare
our analysis with the reported data and identify areas for improvement. Background …

Переливание крови при талассемии у детей

ХС Танкаева, ЕБ Жибурт - Вестник Дагестанской государственной …, 2018 - elibrary.ru
Изучили данные о переливании крови у детей с талассемией. Установлена уникальная
цель трансфузионной терапии-гарантировать баланс между угнетением эритропоэза …

Red Blood Cell Alloimmunization Rates and Related Factors of Patients with Thalassemia in Shiraz, Iran

L Kasraian, E Khodadi, A Talei, MR Morvarid… - Laboratory …, 2022 - academic.oup.com
Objective The development of antibodies against red blood cell (RBC) antigens is one of the
most significant adverse effects of chronic blood transfusions. This study aimed to estimate …

Study of frequency and characteristics of red blood cell alloimmunization in thalassemic patients: multicenter study from Palestine

A Abu Taha, A Yaseen, S Suleiman… - Advances in …, 2019 - Wiley Online Library
Background. β‐Thalassemia is a common inherited hemolytic disorder in Palestine. Red
blood cell (RBC) transfusion is the principal treatment but it may cause RBC …