Evidence map›Paper›PMID 42457810›Full record

ArticleScientific reports2026

Public thresholds for antidepressant effectiveness and adverse drug reaction rates: a cross-sectional study.

Katharina Apel, Jennifer Scheel-Barteit, Matthias Berking, Thomas Kühlein, Maria Sebastião

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Katharina ApelInstitute of General Practice, Friedrich-Alexander-University Erlangen- Nuremberg, Erlangen (Bavaria), Germany.
Jennifer Scheel-BarteitInstitute of General Practice, Friedrich-Alexander-University Erlangen- Nuremberg, Erlangen (Bavaria), Germany.
Matthias BerkingDepartment of Clinical Psychology and Psychotherapy, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen (Bavaria), Germany.
Thomas KühleinInstitute of General Practice, Friedrich-Alexander-University Erlangen- Nuremberg, Erlangen (Bavaria), Germany.
Maria SebastiãoInstitute of General Practice, Friedrich-Alexander-University Erlangen- Nuremberg, Erlangen (Bavaria), Germany. maria.sebastiao@uk-erlangen.de.ORCID 0000-0002-0838-7989

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effectiveness of antidepressants (ADs) in the treatment of depression is continuously discussed regarding its clinical relevance. The objective of this study was to explore thresholds of members of the public for effectiveness of ADs relative to the frequency of adverse drug reactions (ADRs) deemed acceptable. We conducted a cross-sectional online survey in Germany that included individuals with and without experiences of depression and ADs. Participants were presented a case scenario describing a moderate depressive episode, operationalized with the Montgomery Åsberg Depression Rating Scale (MADRS). Participants were asked to rate the effectiveness of different treatment options, estimate the frequency of 15 ADRs, and indicate the minimal level of treatment effectiveness they would require to accept certain ADRs. The survey was completed by 208 participants (144 female, 64 male), 44 were taking ADs. The effectiveness of ADs was significantly overestimated (t(204) = 8.96, p < 0.001, d = 0.63). For 13 ADRs, participants selected package-insert frequency categories that were significantly lower than the corresponding reference categories. For example, to accept the potential ADR of seizures, participants required a symptom improvement of M = 23.51 (SD = 8.82) points on the MADRS. We propose that patient-physician communication about risks and benefits of AD treatment should explicitly address individual expectations.

Indexed as

Antidepressive AgentsDepressionDrug-Related Side Effects and Adverse ReactionsAdultAgedCross-Sectional StudiesFemaleGermanyHumansMaleMiddle AgedSurveys and QuestionnairesTreatment OutcomeYoung AdultAntidepressive AgentsDepressive disorderDrug-related side effects and adverse reactionsMembers of the publicMinimum acceptable benefitShared decision making

Identifiers

PMID42457810
PMCPMC13373223

What OpenQuestion holds

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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.