Spinal muscular atrophy (SMA) is associated with significant burden of illness to both patients and caregivers, including increased financial costs, higher healthcare utilisation and decreased quality of life (QoL). Despite this burden, there is little understanding of how both patients and caregivers evaluate the benefit–risk profile of potential treatments, particularly at regional levels. This poster explores which treatment attributes drive treatment choices in adult patients and caregivers of patients with SMA across Latin America.
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