Archives of rehabilitation research and clinical translation · 2026
Exploring Treatment Expectations and Clinical Meaningfulness in Spinal Muscular Atrophy Using the Goal Attainment Scale.
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Casiraghi Jacopo, Lizio Andrea, Beretta Maria, Greco Lucia, Coratti Giorgia, Salmin Francesca, Franchino Valentina, De Felice Lisa, Piras Rachele, Cerri Federica, Albamonte Emilio, Mercuri Eugenio, Sansone Valeria Ada
Аннотация
OBJECTIVES: To investigate how Goal Attainment Scale (GAS) in spinal muscular atrophy (SMA) identifies patient-reported clinically meaningful improvement after disease-modifying treatment and to evaluate whether the patient-stated goals identified through GAS are already captured by items in existing motor assessment scales.
DESIGN: Longitudinal retrospective study considering the first available follow-up.
SETTING: The study was conducted in a rehabilitation center dedicated to neuromuscular diseases.
PARTICIPANTS: The GAS was recorded from N=58 SMA patients on treatment with nusinersen or risdiplam regularly followed for clinical follow-up in 2023.
MAIN OUTCOME MEASURES: Clinical and demographic data, SMA type, Hammersmith Functional Motor Scale, Children's Hospital of Philadelphia scale, Revised Upper Limb Module, 6 Minute Walk Test, and GAS questionnaire were collected.
RESULTS: One hundred forty-nine SMART goals were clustered in 15 macrodomains, with the most frequent being mobility, upper limb strength, and activities of daily living. Most smart goals (72%) could be redirected to items of standardized motor and functional scales. Unmet goals primarily involved activities of daily living, endurance, and mobility, with a particular focus on upper limb strength.
CONCLUSIONS: The GAS provides an individualized, reliable, and quantifiable measure of goal attainment, and is useful in setting realistic treatment expectations that could guide patients and physicians to interpret changes over time.
DESIGN: Longitudinal retrospective study considering the first available follow-up.
SETTING: The study was conducted in a rehabilitation center dedicated to neuromuscular diseases.
PARTICIPANTS: The GAS was recorded from N=58 SMA patients on treatment with nusinersen or risdiplam regularly followed for clinical follow-up in 2023.
MAIN OUTCOME MEASURES: Clinical and demographic data, SMA type, Hammersmith Functional Motor Scale, Children's Hospital of Philadelphia scale, Revised Upper Limb Module, 6 Minute Walk Test, and GAS questionnaire were collected.
RESULTS: One hundred forty-nine SMART goals were clustered in 15 macrodomains, with the most frequent being mobility, upper limb strength, and activities of daily living. Most smart goals (72%) could be redirected to items of standardized motor and functional scales. Unmet goals primarily involved activities of daily living, endurance, and mobility, with a particular focus on upper limb strength.
CONCLUSIONS: The GAS provides an individualized, reliable, and quantifiable measure of goal attainment, and is useful in setting realistic treatment expectations that could guide patients and physicians to interpret changes over time.