Quantifying the economic impact of caregiving for Duchenne muscular dystrophy (DMD) in Spain

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Abstract
Aim To establish the potential economic burden in caregivers to patients with DMD and the potential causative factors. Method Caregivers to patients with DMD were recruited through the DMD patients Register and questioned about several economic aspects using “ad-hoc” questionnaires. Results All families, apart from one (97.2% n = 36), incurred in monthly medical costs (44% of the families more than 50 euros/month). 97.2% of the households considered looking after a patient of DMD as financially burdensome, and 80.5% of households declared to have suffered work changes, especially the mothers (job timetable-related mainly). The presence of obsessive–compulsive disorders (OCD) in patients was significantly associated with caregivers’ high financial burden as these were six times more likely to have this perception OR = 6468 IC 95% (1056–39,601), p = 0.043. Also, when patients had learning difficulties, caregivers had up to six times more chances to incur in monthly expenditure for formal care OR = 6089 IC 95% (1112–33,342), p = 0.037. Interpretation Caregivers have relevant financial burden that might be conditioned by the clinical condition of the patient. What this paper adds Quantitative data about financial burden in DMD Spanish families providing informal care. Identification of the patient’s main clinical issues associated with financial burden.
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