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with significant disability, a considerable proportion report good or even excellent quality of life despite severe functional impairment.6,10 Clear definitions are essential to this debate."Poor outcome" or disability is commonly quantified using functional scales such as the Glasgow Outcome Scale-Extended (GOSE), which primarily reflects global functional status and independence but provides limited insight into subjective wellbeing, whereas health-related quality of life (HRQoL) captures the patient's own judgment across physical, cognitive, emotional, and social domains.7 Patient-reported outcomes (PROs), which directly capture this perspective, often diverge from clinicianrated function, reflecting adaptation, coping mechanisms, and shifts in internal standards over time.7,11 Across multiple studies, a consistent pattern emerges: HRQoL among survivors of sTBI is highly heterogeneous; functional disability does not reliably predict perceived quality of life; and cognitive, emotional, and psychosocial factors often outweigh injury severity as determinants of well-being.Consequently, two patients with comparable levels of disability may experience profoundly different lives, an observation that lies at the heart of the disability paradox.[10][11][12] These findings do not suggest that disability is benign.Rather, they underscore that "severe disability" and "an unacceptable life" are not equivalent constructs.They further indicate that the range of patient-valued outcomes is broader than clinicians often assume.
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Airton Leonardo de Oliveira Manoel (2026) studied this question.
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