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      Patient Preference and Adherence (submit here)

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      Is Open Access

      Proxy-Reported Quality of Life and Access to Nusinersen Among Patients with Spinal Muscular Atrophy in Saudi Arabia

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          Abstract

          Background

          The recent approval of innovative therapies for spinal muscular atrophy (SMA), such as nusinersen, has brought hope to patients and their families.

          Objective

          The aims of this study were to compare the characteristics and HRQoL of SMA patients treated with nusinersen and those treated with the standard of care.

          Methods

          This was a cross-sectional, interviewer-administered telephone questionnaire, which used a purposive sampling of SMA patients through a social support network. EuroQol five-dimensions-3-level (EQ-5D-3L) and the visual analog scale (VAS) have been used to assess the HRQoL. Different descriptive and inferential tests have been performed to compare the characteristics, EQ-5D responses, and mean scores of EQ-VAS between patients on nusinersen and the standard of care.

          Results

          Eleven out of 36 SMA patients (30.55%) have been treated with nusinersen. Patients with type I SMA represented 54% of those treated with nusinersen ( P=0.012). Only 12.5% of SMA patients living in the Mecca region are treated with nusinersen in comparison to 50% of patients living in the Riyadh region ( P=0.029). No difference was noticed in the proxy-responses for the five domains of the EQ-5D or the mean VAS scores for patients on nusinersen and the standard of care despite controlling for the SMA type and the ability to breathe independently (β= 1.39, 95% CI= – 5.15-7.93, P=0.667). However, the mean VAS score for patients who are unable to breathe independently was significantly lower than their counterparts who are able to breathe independently even after controlling for the SMA type and nusinersen treatment (β= –31.61, 95% CI= – 51.59 - –11.63, P=0.003).

          Conclusion

          The results of this study highlight the uncertainty about the impact of nusinersen on SMA patients’ HRQoL. Therefore, the impact of nusinersen on HRQoL should be examined using more robust study designs.

          Most cited references34

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          World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects.

          (2013)
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            Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy

            New England Journal of Medicine, 377(18), 1723-1732
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              Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy

              Nusinersen is an antisense oligonucleotide drug that modulates pre-messenger RNA splicing of the survival motor neuron 2 ( SMN2) gene. It has been developed for the treatment of spinal muscular atrophy (SMA).
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                Author and article information

                Journal
                Patient Prefer Adherence
                Patient Prefer Adherence
                ppa
                ppa
                Patient preference and adherence
                Dove
                1177-889X
                13 April 2021
                2021
                : 15
                : 729-739
                Affiliations
                [1 ]Department of Clinical Pharmacy, College of Pharmacy, King Saud University , Riyadh, Saudi Arabia
                [2 ]Pharmacoeconomics Research Unit, College of Pharmacy, King Saud University , Riyadh, Saudi Arabia
                [3 ]College of Medicine, King Saud University , Riyadh, Saudi Arabia
                [4 ]Pediatric Intensive Care Unit, Pediatric Department, King Saud University Medical City , Riyadh, Saudi Arabia
                [5 ]Division of Neurology, Department of Pediatrics, King Saud University Medical City , Riyadh, Saudi Arabia
                Author notes
                Correspondence: Yazed AlRuthia Department of Clinical Pharmacy, College of Pharmacy, King Saud University , Riyadh, Saudi ArabiaTel +996 114677483Fax +966 114677480 Email yazeed@ksu.edu.sa
                Author information
                http://orcid.org/0000-0002-0029-5924
                http://orcid.org/0000-0002-4389-9322
                http://orcid.org/0000-0002-8279-403X
                http://orcid.org/0000-0003-3707-0582
                http://orcid.org/0000-0003-1436-6727
                Article
                305849
                10.2147/PPA.S305849
                8053517
                33880016
                b8a9af5c-7fba-447b-9dc9-d90a2257253e
                © 2021 AlRuthia et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 08 February 2021
                : 19 March 2021
                Page count
                Figures: 3, Tables: 5, References: 34, Pages: 11
                Categories
                Original Research

                Medicine
                spinal muscular atrophy,health-related quality of life,nusinersen,health services accessibility,saudi arabia

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