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CP-145 Quality of life in multiple sclerosis patients: experience in a university hospital outpatient pharmacy
  1. AM Horta Hernández1,
  2. M Blanco Crespo1,
  3. AL Alvarez Nonay1,
  4. P De Juan-García Torres1,
  5. A Yusta Izquierdo2,
  6. B Escalera Izquierdo3
  1. 1University Hospital of Guadalajara, Pharmacy Department, Guadalajara, Spain
  2. 2University Hospital of Guadalajara, Neurology Department, Guadalajara, Spain
  3. 3Faculty of Pharmacy-Alcalá University, Pharmaceutical Technology Department, Alcalá de Henares, Spain


Background Multiple Sclerosis (MS) is a chronic demyelinating CNS disease that negatively affects patient quality of life (QoL). The hospital pharmacist dispenses MS disease modifying therapies (DMT) at the outpatient pharmacy.

Purpose To analyse QoL in MS patients who collect firstline DMT at the outpatient pharmacy.

Material and methods A prospective study was performed from March to September 2016. QoL was assessed according to an internal questionnaire. It was designed by a pharmacist and included: demographic characteristics, employment status, home adaptations, mobility, need for support with everyday activities, vacation and leisure habits, and MS medical history during the last year. An Excel database was designed to analyse the results. All MS patients were asked to complete a questionnaire at the outpatient pharmacy when collecting DMT. Firstline DMT included: parenteral drugs (interferon beta-1A and 1B, glatiramer acetate) and oral drugs (dimethyl fumarate, teryflunomide).

Results 100 of 107 MS patients with the following characteristics completed the questionnaire: mean age 44.83 years (±11.08), 73% women and 91% lived with relatives. 16% were treated with firstline oral DMT. Nearly half of MS patients (45%) were occupationally active. Home adaptations were reported by 13% of patients. 55% did not require support for everyday activities and 79% could move normally. 36% of patients had changed their holiday habits and 58% their leisure activities because of MS. During the last year, 7% of MS patients had suffered a relapse and were admitted to hospital, and 51% reported daily activity disturbances because of MS (mean lost days per year 57). The average number of visits per patient to the neurologist during the last year was 2.

Conclusion Most patients included in this study were young active women living with relatives. A high percentage of patients reported an acceptable QoL related to mobility, home adaptations and independence with routine activities, which could be explained by early DMT treatment according to clinical guidelines. Assessing QoL in MS patients is not common in everyday clinical practice. As part of clinical practice, it has the potential to improve communication between the patient and pharmacist, identify frequently overlooked problems and detect those patients most in need of pharmaceutical care.

No conflict of interest

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