Evidence map›Paper›PMID 25867095›Full record

Observational studyPloS one2015

Long-term persistence with injectable therapy in relapsing-remitting multiple sclerosis: an 18-year observational cohort study.

Simon Zhornitsky, Jamie Greenfield, Marcus W Koch, Scott B Patten, Colleen Harris, Winona Wall, Katayoun Alikhani, Jodie Burton, Kevin Busche, Fiona Costello and 7 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

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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

17 authors at 1 institution in 1 country.

Simon ZhornitskyDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Jamie GreenfieldDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Marcus W KochDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Scott B PattenDepartment of Psychiatry, Faculty of Medicine, University of Calgary, Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Colleen HarrisDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Winona WallDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Katayoun AlikhaniDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Jodie BurtonDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Kevin BuscheDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Fiona CostelloDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Jeptha W DavenportDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Scott E JarvisDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Dina LavaratoDepartment of Psychiatry, Faculty of Medicine, University of Calgary, Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Helene ParpalDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
David G PatryDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Michael YeungDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
Luanne M MetzDepartment of Clinical Neurosciences, Faculty of Medicine, University of Calgary; Calgary, Canada; Hotchkiss Brain Institute, Faculty of Medicine, University of Calgary, Calgary, Canada.
University of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease modifying therapies (DMTs) reduce the frequency of relapses and accumulation of disability in multiple sclerosis (MS). Long-term persistence with treatment is important to optimize treatment benefit. This long-term, cohort study was conducted at the Calgary MS Clinic. All consenting adults with relapsing-remitting MS who started either glatiramer acetate (GA) or interferon-β 1a/1b (IFN-β) between January 1st, 1996 and July 1st, 2011 were included. Follow-up continued to February 1st, 2014. Time-to-discontinuation of the initial and subsequently-prescribed DMTs (switches) was analysed using Kaplan-Meier survival analyses. Group differences were compared using log-rank tests and multivariable Cox regression models. Analysis included 1471 participants; 906 were initially prescribed GA and 565 were initially prescribed IFN-β. Follow-up information was available for 87%; 29 (2%) were lost to follow-up and 160 (11%) moved from Southern Alberta while still using DMT. Median time-to-discontinuation of all injectable DMTs was 11.1 years. Participants with greater disability at treatment initiation, those who started treatment before age 30, and those who started between 2006 and 2011 were more likely to discontinue use of all injectable DMTs. Median time-to-discontinuation of the initial DMT was 8.6 years. Those initially prescribed GA remained on treatment longer. Of 610 participants who discontinued injectable DMT, 331 (54%) started an oral DMT, or a second-line DMT, or resumed injectable DMT after 90 days. Persistence with injectable DMTs was high in this long-term population-based study. Most participants who discontinued injectable DMT did not remain untreated. Further research is required to understand treatment outcomes and outcomes after stopping DMT.

Indexed as

AdultCohort StudiesFemaleGlatiramer AcetateHumansInjections, SubcutaneousInterferon beta-1aInterferon beta-1bMaleMiddle AgedMultiple Sclerosis, Relapsing-RemittingGlatiramer AcetateInterferon beta-1aInterferon beta-1b

Identifiers

PMID25867095
PMCPMC4395027
OpenAlexW2034710262

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.