Evidence map›Paper›PMID 35962369›Full record

ArticleBMC psychiatry2022

Real-world effectiveness of vortioxetine in outpatients with major depressive disorder: functioning and dose effects.

Eugenia Papalexi, Andreas Galanopoulos, Dimitrios Kontis, Maria Markopoulou, Georgia Balta, Evaggelos Karavelas, Panagiotis Panagiotidis, Themistoklis Vlachos, Anders Ettrup

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
2.4field-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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Article
  5. 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 6 institutions in 2 countries.

Eugenia PapalexiLundbeck Hellas, 109 Kifisias Avenue & Sina, 15124, Maroussi, Athens, Greece. EUGE@Lundbeck.com.
Andreas GalanopoulosLundbeck Hellas, 109 Kifisias Avenue & Sina, 15124, Maroussi, Athens, Greece.
Dimitrios Kontis4th Psychiatric Department, Psychiatric Hospital of Attica, Athens, Greece.
Maria MarkopoulouDepartment of Forensic Psychiatry, Psychiatric Hospital of Thessaloniki, Stavroupolis, Thessaloniki, Greece.
Georgia BaltaDepartment of Pharmacology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Evaggelos KaravelasEnsynaisthisis, Thessaloniki, Greece.
Panagiotis PanagiotidisDepartment of Psychiatry, 424 General Military Hospital of Thessaloniki, Thessaloniki, Greece.
Themistoklis VlachosDepartment of Psychiatry, 251 Airforce Military Hospital, Athens, Greece.
Anders EttrupH. Lundbeck A/S, Valby, Denmark.
424 General Military Hospital · GRGeneral Hospital of Attica · GRHellenic Airforce General Hospital · GRLundbeck (Denmark) · DKNational and Kapodistrian University of Athens · GRSenologic Hellenic Society · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFunctional recovery is an important treatment goal in major depressive disorder (MDD). This study assessed the real-world effectiveness of vortioxetine in patients with MDD, with particular focus on functioning; dose-response was also assessed.

methodsThis was a non-interventional, prospective, multicenter study conducted in Greece. Adult outpatients with MDD (n = 336) initiating vortioxetine (5-20 mg/day flexible dosing) as treatment for a current major depressive episode were followed for 3 months. Analyses were stratified according to vortioxetine dosage at 3 months: 5-10 mg/day versus 15-20 mg/day. Functioning was assessed using the Sheehan Disability Scale (SDS).

resultsMean ± standard error SDS total score decreased (improved) from 18.7 ± 0.3 at baseline to 12.9 ± 0.3 after 1 month of vortioxetine treatment and 7.8 ± 0.4 after 3 months (p < 0.001 vs. baseline for all comparisons). Functional recovery (SDS score ≤ 6) was achieved in 14.6% of patients after 1 month of treatment and 48.4% of patients after 3 months. Improvement from baseline in SDS total and domain scores at 3 months was more pronounced in patients receiving vortioxetine 15-20 mg/day than in those receiving vortioxetine 5-10 mg/day. The mean ± standard error change in SDS total score from baseline was 9.2 ± 0.8 in the 5-10 mg/day group and 12.1 ± 0.4 in the 15-20 mg/day group (p < 0.001). Limitations of this study include its non-interventional study design and lack of a control group or active comparator.

conclusionsStatistically significant and clinically relevant improvements in functioning were seen in patients with MDD treated with vortioxetine in a real-world setting. Higher doses of vortioxetine were associated with significantly greater improvements in functioning.

Indexed as

Major Depressive DisorderAdultDouble-Blind MethodGreeceHumansOutpatientsProspective StudiesTreatment OutcomeVortioxetineVortioxetineDose-responseFunctioningMajor depressive disorder (MDD)Real-world effectivenessVortioxetine

Identifiers

PMID35962369
PMCPMC9373318
OpenAlexW4291634973

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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.