2022
DOI: 10.1186/s12913-022-07663-6
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Healthcare resource utilization and direct costs of transfusion-dependent thalassemia patients in Dubai, United Arab Emirates: a retrospective cost-of-illness study

Abstract: Background Patients with transfusion-dependent thalassemia (TDT) require lifelong blood transfusions and iron chelation therapy. Thus, patients afflicted with TDT often have to undergo blood transfusion and iron chelation therapy, which causes a major economic burden on them. However, this topic has not been reported in Dubai, United Arab Emirates (UAE). Hence, this study aimed to evaluate healthcare resource utilization and associated direct costs related to patients with TDT in Dubai, UAE. … Show more

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Cited by 17 publications
(21 citation statements)
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References 62 publications
(92 reference statements)
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“…In contrast, the prevalence of thalassemia is widespread across the nation and all ethnic groups [ 4 ]. Thalassemia is associated with significant consumption of healthcare resources [ 5 ]. In Nepal, the financial burdens associated with thalassemia diagnosis and treatment have not been studied.…”
Section: Tablementioning
confidence: 99%
“…In contrast, the prevalence of thalassemia is widespread across the nation and all ethnic groups [ 4 ]. Thalassemia is associated with significant consumption of healthcare resources [ 5 ]. In Nepal, the financial burdens associated with thalassemia diagnosis and treatment have not been studied.…”
Section: Tablementioning
confidence: 99%
“…The main driver of the medical costs for the participants is iron chelation therapy, which accounts for AED 78,372 (59.8%) of the total direct medical costs. 5 However, it is important to note that the financial cost of thalassemia may vary depending on the healthcare system, country, and individual patient factors. The considerable economic burden poses challenges for ensuring sustained access to optimal therapy for patients in Europe.…”
Section: Evidence On Generic Medications In Thalassemiamentioning
confidence: 99%
“…Thalassemias are a group of inherited hematologic disorders caused by defects in the synthesis of one or more of the hemoglobin chains [ 1 ], α thalassemia and β thalassemia are most common clinically. There were about 399 million thalassemia carriers in 2019 worldwide [ 2 ], mainly in sub-Saharan Africa, the Mediterranean region, and East and South-East Asia, and thalassemia is becoming more common in Europe and North America due to migration factors [ 3 , 4 ]. The increased morbidity of thalassemia has resulted in serious health threats and heavy economic burdens to the patients [ 5 ], especially in low and middle-income countries [ 4 ].…”
Section: Introductionmentioning
confidence: 99%
“…The increased morbidity of thalassemia has resulted in serious health threats and heavy economic burdens to the patients [ 5 ], especially in low and middle-income countries [ 4 ]. It was estimated that the global cost of treatment for thalassemia was approximately USD842 million in 2017 and is expected to increase by 7.9% from 2018 to 2026 [ 2 ]. In the 2017 Global Burden of Disease report, thalassemia has resulted in 582,000 disability-adjusted life-years (DALYs) [ 6 ].…”
Section: Introductionmentioning
confidence: 99%