Evidence map›Paper›PMID 39471272›Full record

ArticleJournal of managed care & specialty pharmacy2024

Patient-reported disability progression outcomes among patients with multiple sclerosis: Results of an outcomes-based agreement.

Elizabeth C S Swart, Samuel K Peasah, Jacqueline Alderson, RaeAnn Maxwell, Chronis Manolis, Chester B Good

Abstract read
In one paragraph

Article in Journal of managed care & specialty pharmacy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

Elizabeth C S SwartValue-Based Pharmacy Initiatives, UPMC Center for High-Value Health Care, Pittsburgh, PA.
Samuel K PeasahValue-Based Pharmacy Initiatives, UPMC Center for High-Value Health Care, Pittsburgh, PA.
Jacqueline AldersonPharmacy Services, UPMC Insurance Services Division, Pittsburgh, PA.
RaeAnn MaxwellBiogen, Cambridge, MA.
Chronis ManolisPharmacy Services, UPMC Insurance Services Division, Pittsburgh, PA.
Chester B GoodDivision of General Internal Medicine, University of Pittsburgh, Pittsburgh, PA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOutcomes-based agreements (OBAs) are agreements between payers and manufacturers in which payment for medications is tied to patient outcomes. These contracts aim to measure the value of prescription medications on predefined clinical indicators in real-world patient populations. OBAs are gaining traction in the United States as the health care industry shifts from volume-based to value-based care. Multiple sclerosis (MS) is an appealing therapeutic area for OBAs because of its prevalence, high cost of medications, and multiple effective therapeutic options.

objectiveTo describe findings from an OBA that was prospectively conducted in a large regional health system for patients with MS taking interferon β-1a or dimethyl fumarate.

methodsIn this prospective real-world analysis, commercial or health insurance exchange members were included based on the parameters of the OBA. Disability progression was assessed using a patient-reported outcome, patient-determined disease steps (PDDS). In the OBA, members aged 18 years or older with an MS diagnosis were included in the contract. A baseline score was collected for eligible members, with follow-up scores occurring between a 90-day and 180-day postbaseline score. If a follow-up score was greater than the baseline score, a subsequent PDDS score was collected between 90-days and 120-days to determine if the PDDS score remained elevated, indicating that the member had disability progression.

resultsDuring the contract period, 410 patients were eligible for PDDS collection, with 241 and 169 patients in the dimethyl fumarate and interferon β-1a cohorts, respectively. There were 162 patients who were lost to follow-up, and 64 patients who were ineligible per contract parameters. Of the remaining 184 eligible patients (107 on dimethyl fumarate and 77 on interferon β-1a), 21 (11%) patients had confirmed disability progression (6 on dimethyl fumarate [5.6%] and 15 on interferon β-1a [19.5%]).

conclusionsOur findings suggest that meaningful patient-reported outcomes, such as disability progression, can be operationalized in an innovative OBA.

Indexed as

Dimethyl FumarateDisease ProgressionInterferon beta-1aMultiple SclerosisPatient Reported Outcome MeasuresAdultDisability EvaluationFemaleHumansMaleMiddle AgedProspective StudiesUnited StatesDimethyl FumarateInterferon beta-1a

Identifiers

PMID39471272
PMCPMC11522456

What OpenQuestion holds

Textmetadata
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.