Literature DB >> 29228163

Ethical Challenges Confronted When Providing Nusinersen Treatment for Spinal Muscular Atrophy.

Alyssa M Burgart1, David Magnus1, Holly K Tabor1, Erin Daksha-Talati Paquette2, Joel Frader2, Jaqueline J Glover3, Brian M Jackson3, Charlotte H Harrison4,5, David K Urion5,6, Robert J Graham7, John F Brandsema8, Chris Feudtner9.   

Abstract

The US Food and Drug Administration's December 2016 approval of nusinersen for the treatment of patients with all subtypes of spinal muscular atrophy ushered in a new era for patients with spinal muscular atrophy, their families, and all those involved in their care. The extreme cost of the medication and the complicated logistical requirements for administering nusinersen via lumbar puncture have created practical challenges that raise important ethical considerations. We discuss 6 challenges faced at the institutional level in the United States: cost, limited evidence, informed consent, treatment allocation, fair distribution of responsibilities, and transparency with stakeholders. These challenges must be understood to ensure that patients with spinal muscular atrophy benefit from treatment, are protected from harm, and are treated fairly.

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Year:  2018        PMID: 29228163     DOI: 10.1001/jamapediatrics.2017.4409

Source DB:  PubMed          Journal:  JAMA Pediatr        ISSN: 2168-6203            Impact factor:   16.193


  15 in total

Review 1.  Nusinersen: A Review in 5q Spinal Muscular Atrophy.

Authors:  Sheridan M Hoy
Journal:  CNS Drugs       Date:  2018-07       Impact factor: 5.749

Review 2.  RNA therapy: Are we using the right molecules?

Authors:  Ai-Ming Yu; Chao Jian; Allan H Yu; Mei-Juan Tu
Journal:  Pharmacol Ther       Date:  2018-12-04       Impact factor: 12.310

Review 3.  Artificial Intelligence in Medical Imaging and its Impact on the Rare Disease Community: Threats, Challenges and Opportunities.

Authors:  Navid Hasani; Faraz Farhadi; Michael A Morris; Moozhan Nikpanah; Arman Rhamim; Yanji Xu; Anne Pariser; Michael T Collins; Ronald M Summers; Elizabeth Jones; Eliot Siegel; Babak Saboury
Journal:  PET Clin       Date:  2022-01

Review 4.  Restoring Protein Expression in Neuromuscular Conditions: A Review Assessing the Current State of Exon Skipping/Inclusion and Gene Therapies for Duchenne Muscular Dystrophy and Spinal Muscular Atrophy.

Authors:  Omar Sheikh; Toshifumi Yokota
Journal:  BioDrugs       Date:  2021-06-07       Impact factor: 5.807

5.  RNA Drugs and RNA Targets for Small Molecules: Principles, Progress, and Challenges.

Authors:  Ai-Ming Yu; Young Hee Choi; Mei-Juan Tu
Journal:  Pharmacol Rev       Date:  2020-10       Impact factor: 25.468

6.  Cost-Effectiveness of Nusinersen and Universal Newborn Screening for Spinal Muscular Atrophy.

Authors:  Ali Jalali; Erin Rothwell; Jeffrey R Botkin; Rebecca A Anderson; Russell J Butterfield; Richard E Nelson
Journal:  J Pediatr       Date:  2020-07-11       Impact factor: 4.406

7.  Patient and family social media use surrounding a novel treatment for a rare genetic disease: a qualitative interview study.

Authors:  Alexander A Iyer; Julie R Barzilay; Holly K Tabor
Journal:  Genet Med       Date:  2020-06-30       Impact factor: 8.822

8.  Obligations of the "Gift": Reciprocity and Responsibility in Precision Medicine.

Authors:  Sandra Soo-Jin Lee
Journal:  Am J Bioeth       Date:  2020-12-16       Impact factor: 11.229

9.  Experiences of caregivers of children with spinal muscular atrophy participating in the expanded access program for nusinersen: a longitudinal qualitative study.

Authors:  Petra Kiefer; Janbernd Kirschner; Astrid Pechmann; Thorsten Langer
Journal:  Orphanet J Rare Dis       Date:  2020-07-29       Impact factor: 4.123

10.  A multidisciplinary approach to dosing nusinersen for spinal muscular atrophy.

Authors:  Carla D Zingariello; John Brandsema; Elizabeth Drum; Alicia A Henderson; Scott Dubow; Allan M Glanzman; Oscar Mayer; Sabrina W Yum; Elizabeth A Kichula
Journal:  Neurol Clin Pract       Date:  2019-10
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