Evidence map›Paper›PMID 36645543›Full record

ArticleAdvances in therapy2023

Examining Real-World Adherence to Nusinersen for the Treatment of Spinal Muscular Atrophy Using Two Large US Data Sources.

Bora Youn, Crystal M Proud, Nasha Wang, Qiang Hou, Emma Viscidi, Susan Eaton, Angela D Paradis, Bridget A Neville, Nicole B Johnson

Open access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Clinical perspectives: Treating spinal muscular atrophy.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Bora YounBiogen, Cambridge, MA, USA.
Crystal M ProudChildren's Hospital of the King's Daughters, Norfolk, VA, USA.
Nasha WangBiogen, Research Triangle Park, NC, USA.
Qiang HouBiogen, Cambridge, MA, USA.
Emma ViscidiBiogen, Cambridge, MA, USA.
Susan EatonBiogen, Research Triangle Park, NC, USA.
Angela D ParadisBiogen, Cambridge, MA, USA.
Bridget A NevilleBiogen, Cambridge, MA, USA.
Nicole B JohnsonBiogen, Cambridge, MA, USA. nicole.johnson@biogen.com.
Biogen (United States) · USChildren's Hospital of The King's Daughters · USTriangle · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSpinal muscular atrophy (SMA) is a rare neuromuscular disease characterized by progressive muscular atrophy and weakness. Nusinersen was the first treatment approved for SMA. Per the US label, the nusinersen administration schedule consists of three loading doses at 14-day intervals, a fourth loading dose 30 days later, and maintenance doses every 4 months thereafter. Using two large US databases, we evaluated real-world adherence to nusinersen with its unique dosing schedule among generalizable populations of patients with SMA.

methodsPatients with SMA treated with nusinersen, likely to have complete information on date of treatment initiation, were identified in the Optum

resultsTotals of 67 and 291 patients were identified in the EHR and claims databases, respectively. Most nusinersen doses were received on time (93.9% EHR, 80.5% claims). Adherence was higher during the maintenance phase (90.6%) than the loading phase (71.1%) in the claims analysis, in contrast with the EHR analysis (95.5% and 92.6%, respectively), suggesting that not all loading doses of nusinersen may be accurately captured in claims. Inter-dose intervals captured in both databases aligned with the expected dosing schedule.

conclusionMost nusinersen doses were received on time, consistent with the recommended schedule. Our findings also highlight the importance of careful methodological approaches when using real-world administrative databases for evaluation of nusinersen treatment patterns.

Indexed as

Information SourcesMuscular Atrophy, SpinalHumansInsurance Claim ReviewOligonucleotidesUnited StatesnusinersenOligonucleotidesCommercial and Medicaid claimsElectronic health recordsNusinersenReal-world adherenceSpinal muscular atrophy

Identifiers

PMID36645543
PMCPMC9841927
OpenAlexW4316661848

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.