2022
DOI: 10.1177/03946320221096909
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Prevalence of transfusion-transmitted infections in multiple blood transfusion-dependent thalassemic patients in Asia: A systemic review

Abstract: Background Thalassemia is a hereditary hemolytic anemia marked by a defect in synthesizing one or more globin chains in hemoglobin. In Pakistan, approximately 10,000 patients with thalassemia are primarily dependent on blood transfusions. The β-thalassemia patients require blood transfusions and iron chelation therapy. Patients who need blood transfusions are at an increased risk of contracting transfusion-transmitted infections (TTIs) such as hepatitis B and C viruses (HBV and HCV, respectively), as well as t… Show more

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Cited by 10 publications
(6 citation statements)
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References 55 publications
(42 reference statements)
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“…Patients with thalassemia are at increased risk for contracting blood borne microbiological infectious disorders, among other issues stemming from the need for frequent blood transfusions 8 . This has the potential to worsen thalassemia victims' health and quality of life, and perhaps raise their risk of complications and fatality.…”
Section: Introductionmentioning
confidence: 99%
“…Patients with thalassemia are at increased risk for contracting blood borne microbiological infectious disorders, among other issues stemming from the need for frequent blood transfusions 8 . This has the potential to worsen thalassemia victims' health and quality of life, and perhaps raise their risk of complications and fatality.…”
Section: Introductionmentioning
confidence: 99%
“…Thalassemia, being an autosomal recessive disorder exhibits a unique characteristic of severe hemolysis in its victims. It is the most common blood disorder recognized globally with some serious impacts like higher death rates along with economical and emotional stress on the families of affected individuals (Angastiniotis and Lobitz, 2019;Riaz et al, 2022). The root cause of this deadly disease is the different types of mutations that can alter the amino acid sequence of hemoglobin molecules that results in partial or complete absence of globin chains (Shang and Xu, 2017).…”
Section: Introductionmentioning
confidence: 99%
“…The therapies for the treatment of thalassemia patients include iron chelation, folic acid supplements and regular blood transfusion. The cornerstone therapy is one of the best methods for a better lifespan of the thalassemia patients which includes adequate blood transfusion along with iron chelation (Riaz et al, 2022). The major source for the sustainability of the lives of beta thalassemia major patients is the regular blood transfusion, but this practice can put the lives of patients in danger if the blood will not be properly screened before transfusion.…”
Section: Introductionmentioning
confidence: 99%
“…In other to prevent infection, most transfusion centre's apply the Enzyme Linked Immunosorbent Assay (ELISA) test for HBV detection during donor screening, yet cases of post-transfusion Hepatitis infection has been reported indicating that ELISA test is not entirely effective [5]. The highly recommended and more reliable Nucleic Acid tests such as Polymerase Chain Reaction (PCR) tests are costly and currently not a routine test for donor blood in lowincome resource countries such as the Sub-Saharan Africa.…”
Section: Introductionmentioning
confidence: 99%