Evidence map›Paper›PMID 37927051›Full record

ArticleThe Australian and New Zealand journal of psychiatry2024

Alternative metrics for characterizing longer-term clinical outcomes in difficult-to-treat depression: II. Sensitivity to treatment effects.

Scott T Aaronson, Harold A Sackeim, Mei Jiang, Sarah Badejo, Teresa Greco, Mark T Bunker, Charles R Conway, Koen Demyttenaere, Allan H Young, R Hamish McAllister-Williams and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Australian and New Zealand journal of psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Article
  3. Observational
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

11 authors at 10 institutions in 5 countries.

Scott T AaronsonDepartment of Clinical Research, Sheppard Pratt Health System, Baltimore, MD, USA.
Harold A SackeimDepartments of Psychiatry and Radiology, Columbia University, New York, NY, USA.ORCID 0000-0002-1107-4553
Mei JiangLivaNova USA PLC, Minneapolis, MN, USA.
Sarah BadejoLivaNova PLC, Milan, Italy.
Teresa GrecoJazz Pharmaceuticals PLC, Milan, Italy.
Mark T BunkerLivaNova USA PLC, Houston, TX, USA.
Charles R ConwayDepartment of Psychiatry, Washington University in St. Louis, St. Louis, MO, USA.
Koen DemyttenaerePsychiatry, Leuven Brain Institute, University Psychiatric Center KU Leuven, Faculty of Medicine, KU Leuven, Leuven, Belgium.
Allan H YoungDepartment of Psychological Medicine, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
R Hamish McAllister-WilliamsNorthern Centre for Mood Disorders, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0001-9966-1834
A John RushDuke-NUS Medical School, National University of Singapore, Singapore.
LivaNova (United States) · USColumbia University · USCumbria Northumberland Tyne and Wear NHS Foundation Trust · GBJazz Pharmaceuticals (Italy) · ITKing's College London · GBKU Leuven · BELivaNova (Italy) · ITNational University of Singapore · SGSheppard Pratt Health System · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCharacteristics of difficult-to-treat depression (DTD), including infrequent symptom remission and poor durability of benefit, compel reconsideration of the outcome metrics historically used to gauge the effectiveness of antidepressant interventions.

methodsSelf-report and clinician assessments of depression symptom severity were obtained regularly over a 2-year period in a difficult-to-treat depression registry sample receiving treatment as usual (TAU), with or without vagus nerve stimulation (VNS). Alternative outcome metrics for characterizing symptom change were compared in effect size and discriminating power in distinguishing the vagus nerve stimulation + treatment as usual and treatment as usual treatment groups. We expected metrics based on remission status to produce weaker between-group separation than those based on the classifications of partial response or response and metrics that integrate information over time to produce greater separation than those based on single endpoint assessment.

resultsMetrics based on remission status had smaller effect size and poorer discrimination in separating the treatment groups than metrics based on partial response or response classifications. Metrics that integrated information over the 2-year observation period had stronger performance characteristics than those based on symptom scores at single endpoint assessment. For both the clinician-rated and self-report depression ratings, the metrics with the strongest performance characteristics were the median percentage change in symptom scores over the observation period and the proportion of the observation period in partial response or better.

conclusionIn difficult-to-treat depression, integrative symptom severity-based and time-based measures are sensitive and informative outcomes for assessing between-group treatment effects, while metrics based on remission status are not.

Indexed as

DepressionVagus Nerve StimulationAntidepressive AgentsHumansRegistriesTreatment OutcomeAntidepressive AgentsDifficult-to-treat depressionoutcome metricsregistryvagus nerve stimulation

Identifiers

PMID37927051
PMCPMC10903145
OpenAlexW4388416798

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.