Login / Signup

Systematic review and evidence gap assessment of the clinical, quality of life, and economic burden of alpha-thalassemia.

Khaled M MusallamVip ViprakasitLouise LombardKeely GilroyAmey RaneLydia VinalsCandice TamMaria RizzoThomas D Coates
Published in: EJHaem (2024)
A recent evidence gaps assessment of the clinical, health-related quality of life, and economic burden associated with α-thalassemia is lacking. We conducted a systematic literature review (SLR) following the methodological and reporting requirements of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses and the Cochrane Handbook for Systematic Reviews, using available literature over the past decade. This SLR identified a considerable evidence gap with regard to understanding the current burden of α-thalassemia as evident from paucity of studies published in the past 10 years. The limited data available still indicate that patients with α-thalassemia experience substantial morbidity and quality of life/economic burden that is generally comparable to patients with β-thalassemia.
Keyphrases
  • meta analyses
  • systematic review
  • sickle cell disease
  • randomized controlled trial
  • adverse drug
  • emergency department
  • electronic health record
  • risk factors
  • artificial intelligence