Evidence map›Paper›PMID 38093196›Full record

ArticleBMC psychiatry2023

Real-world clinical outcomes and treatment patterns in patients with MDD treated with vortioxetine: a retrospective study.

Brandon T McDaniel, Victor Cornet, Jeanne Carroll, Lambros Chrones, Joseph Chudzik, Jeanette Cochran, Shion Guha, Debra F Lawrence, Maggie McCue, Sara Sarkey and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

12 authors at 4 institutions in 2 countries.

Brandon T McDanielParkview Mirro Center for Research and Innovation, 10622 Parkview Plaza Drive, Fort Wayne, IN, 46845, US.
Victor CornetParkview Mirro Center for Research and Innovation, 10622 Parkview Plaza Drive, Fort Wayne, IN, 46845, US.
Jeanne CarrollParkview Mirro Center for Research and Innovation, 10622 Parkview Plaza Drive, Fort Wayne, IN, 46845, US.
Lambros ChronesTakeda Pharmaceuticals U.S.A., Inc, Lexington, MA, US.
Joseph ChudzikParkview Mirro Center for Research and Innovation, 10622 Parkview Plaza Drive, Fort Wayne, IN, 46845, US.
Jeanette CochranParkview Physicians Group - Mind-Body Medicine, Fort Wayne, IN, US.
Shion GuhaParkview Mirro Center for Research and Innovation, 10622 Parkview Plaza Drive, Fort Wayne, IN, 46845, US.
Debra F LawrenceTakeda Pharmaceuticals U.S.A., Inc, Lexington, MA, US.
Maggie McCueTakeda Pharmaceuticals U.S.A., Inc, Lexington, MA, US.
Sara SarkeyTakeda Pharmaceuticals U.S.A., Inc, Lexington, MA, US.
Betty LorenzTakeda Pharmaceuticals U.S.A., Inc, Lexington, MA, US.
Jay FawverParkview Physicians Group - Mind-Body Medicine, Fort Wayne, IN, US. Jay.Fawver@parkview.com.
Takeda (United States) · USParkview Health · USParkview Mirro Center for Research and InnovationUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study included evaluation of the effectiveness of vortioxetine, a treatment for adults with major depressive disorder (MDD), using patient-reported outcome measures (PROMs) in a real-world setting.

methodsThis retrospective chart review analyzed the care experiences of adult patients with a diagnosis of MDD from Parkview Physicians Group - Mind-Body Medicine, Midwestern United States. Patients with a prescription for vortioxetine, an initial baseline visit, and ≥ 2 follow-up visits within 16 weeks from September 2014 to December 2018 were included. The primary outcome measure was effectiveness of vortioxetine on depression severity as assessed by change in Patient Health Questionnaire-9 (PHQ-9) scores ~ 12 weeks after initiation of vortioxetine. Secondary outcomes included changes in depression-related symptoms (i.e., sexual dysfunction, sleep disturbance, cognitive function, work/social function), clinical characteristics, response, remission, and medication persistence. Clinical narrative notes were also analyzed to examine sleep disturbance, sexual dysfunction, appetite, absenteeism, and presenteeism. All outcomes were examined at index (start of vortioxetine) and at ~ 12 weeks, and mean differences were analyzed using pairwise t tests.

resultsA total of 1242 patients with MDD met inclusion criteria, and 63.9% of these patients had ≥ 3 psychiatric diagnoses and 65.9% were taking ≥ 3 medications. PHQ-9 mean scores decreased significantly from baseline to week 12 (14.15 ± 5.8 to 9.62 ± 6.03, respectively; p < 0.001). At week 12, the response and remission rates in all patients were 31.0% and 23.1%, respectively, and 67% continued vortioxetine treatment. Overall, results also showed significant improvements by week 12 in anxiety (p < 0.001), sexual dysfunction (p < 0.01), sleep disturbance (p < 0.01), cognitive function (p < 0.001), work/social functioning (p = 0.021), and appetite (p < 0.001). A significant decrease in presenteeism was observed at week 12 (p < 0.001); however, no significant change was observed in absenteeism (p = 0.466).

conclusionsUsing PROMs, our study results suggest that adults with MDD prescribed vortioxetine showed improvement in depressive symptoms in the context of a real-world clinical practice setting. These patients had multiple comorbid psychiatric and physical diagnoses and multiple previous antidepressant treatments had failed.

Indexed as

Major Depressive DisorderSexual Dysfunction, PhysiologicalAdultAntidepressive AgentsDouble-Blind MethodHumansRetrospective StudiesTreatment OutcomeVortioxetineAntidepressive AgentsVortioxetineCognitive functioningComorbid psychiatric diagnosesDepression severityMajor depressive disorderPatient-reported outcome measuresPrevious antidepressant treatmentsReal-world clinical practice settingSexual dysfunctionSocial functioningVortioxetine

Identifiers

PMID38093196
PMCPMC10720213
OpenAlexW4389686039

What OpenQuestion holds

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LicenceCC BY
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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.