Evidence map›Paper›PMID 34550647›Full record

ArticleACR open rheumatology2021

Real-World Treatment Patterns and Healthcare Costs in Patients with Psoriatic Arthritis Treated with Ixekizumab: A Retrospective Study.

Mwangi J Murage, Nicole Princic, Julie Park, William Malatestinic, Baojin Zhu, Bilal Atiya, Scott A Kern, Keri B Stenger, Aubrey Trevelin Sprabery, Alexis Ogdie

Open access · goldAbstract read
In one paragraph

Article in ACR open rheumatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 10 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

10 authors at 3 institutions in 1 country.

Mwangi J MurageEli Lilly and Company, Indianapolis, Indiana.
Nicole PrincicIBM Watson Health, Cambridge, Massachusetts.ORCID https://orcid.org/0000-0003-3127-4365
Julie ParkIBM Watson Health, Cambridge, Massachusetts.
William MalatestinicEli Lilly and Company, Indianapolis, Indiana.
Baojin ZhuEli Lilly and Company, Indianapolis, Indiana.
Bilal AtiyaEli Lilly and Company, Indianapolis, Indiana.
Scott A KernEli Lilly and Company, Indianapolis, Indiana.
Keri B StengerEli Lilly and Company, Indianapolis, Indiana.
Aubrey Trevelin SpraberyEli Lilly and Company, Indianapolis, Indiana.
Alexis OgdieHospital of the University of Pennsylvania, Philadelphia.
Eli Lilly (United States) · USIBM (United States) · USHospital of the University of Pennsylvania · US

Funding

Eli Lilly and Company
6 · The paper itself

Abstract

objectiveTo describe adherence, persistence, discontinuation, restarting, switching, dosing, and health care costs among patients with psoriatic arthritis (PsA) treated with ixekizumab (IXE).

methodsMarketScan administrative claims databases were used to select adults (≥18 years) initiating IXE between January 1, 2016, and June 30, 2019, for this retrospective study (earliest IXE claim = index). Eligible patients had one or more PsA diagnoses during the 12 months preceding the index and had 12 months of follow-up time after the index. Adherence (measured by proportion of days covered [PDC]) persistence (<60-day gap), discontinuation (≥90-day gap), switching, and dosing patterns were reported. Health care costs were reported per patient per month (PPPM) during follow-up and were assessed after adjusting PsA treatment costs for discount rates reported by the Institute for Clinical and Economic Review (ICER).

resultsA total of 496 patients met the selection criteria (mean age, 51.1 years; 50.4% female). Over the 12-month follow-up, 52.8% remained persistent, 38.7% discontinued, 13.5% had no other treatment, 4.6% restarted, and 20.6% switched to a new biologic/traditional synthetic disease-modifying antirheumatic drug. 70.6%of patients were identified as highly adherent (i.e. PDC > 0.80)to IXE prior to discontinuation. Dose values were consistent with prescribing information for patients with and without comorbid psoriasis. Although IXE costs ($5233 [SD = $2497]) accounted for 85.6% of PsA-related health care costs, only 3.5% of IXE costs were patient out-of-pocket expenses. Adjusting for the ICER discounts decreased all-cause and PsA-related costs by $2509 PPPM.

conclusionResults from this real-world analysis suggest that treatment patterns and costs among patients with PsA initiating IXE are consistent with prior literature for other biologics.

Identifiers

PMID34550647
PMCPMC8672175
OpenAlexW3201047607

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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.