Global Economic Burden of Spinal Muscular Atrophy: A Systematic Literature Review
Rawda Elshahawy, Baher Elezbawy, Rasha Ashmawy, Rowan Elshahawy, Yosra S Mahmoud, Nada Korra, Sherif Abaza, Amal Alnajjar, Hana A Al-Abdulkarim, Hussain A Al-Omar, Sahar Fahmy, Sara Al Dallal, Ahmad N Fasseeh

TL;DR
This study reviews the global economic impact of spinal muscular atrophy, highlighting high costs and the need for standardized evaluation methods.
Contribution
The study provides a systematic analysis of the economic burden across SMA subtypes, emphasizing the need for standardized evaluation approaches.
Findings
The weighted average annual cost for an SMA patient is US$109,906, with type 1 patients having the highest direct medical costs.
Non-medical costs and caregiver productivity losses are significant, with 2,947 hours of caregiving required annually.
The study highlights the heterogeneity of economic data and the need for standardized approaches to evaluate SMA's financial impact.
Abstract
Spinal muscular atrophy (SMA) is a rare inherited neuromuscular disease classified into four main subtypes and characterized by severe muscle weakness and loss of motor function. Its high mortality rates, high treatment costs, and lengthy care requirements place a heavy burden on patients, caregivers, and the healthcare system. This study aims to explore the economic burden of SMA subtypes by analyzing costs, healthcare resource use, and loss of productivity for patients and their caregivers. We conducted a systematic literature review, searching for studies published since 2010 via Medline, Embase, Google Scholar, and gray literature databases. We extracted data concerning costs, healthcare resources, and productivity losses among SMA subtypes. The quality of the included studies was assessed using the Newcastle-Ottawa Scale and the Quality of Health Economic Studies tools. We…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1
Figure 2
Figure 3Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsNeurogenetic and Muscular Disorders Research · Muscle Physiology and Disorders · Mechanical Circulatory Support Devices
