Evidence map›Paper›PMID 33203427›Full record

ArticleBMC psychiatry2020

Investigation of early and lifetime clinical features and comorbidities for the risk of developing treatment-resistant depression in a 13-year nationwide cohort study.

Shiau-Shian Huang, Hsi-Han Chen, Jui Wang, Wei J Chen, Hsi-Chung Chen, Po-Hsiu Kuo

Open access · goldAbstract read
In one paragraph

Article in BMC psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.5field-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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Trajectory of response to esketamine nasal spray for treatment resistant depression: Findings from ESCAPE-TRD.European psychiatry : the journal of the Association of European Psychiatrists · 2026
    Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Depression and the Aberrant Intestinal Microbiome.Gastroenterology & hepatology · 2024
    Article
  11. Intravenous ketamine for benzodiazepine deprescription and withdrawal management in treatment-resistant depression: a preliminary report.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  12. Review
  13. Observational
  14. Article
  15. Review
  16. Article
  17. Review
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

6 authors at 4 institutions in 1 country.

Shiau-Shian HuangDepartment of Public Health & Institute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan.
Hsi-Han ChenDepartment of Psychiatry, Yang Ji Mental Hospital, Keelung, Taiwan.
Jui WangDepartment of Public Health & Institute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan.
Wei J ChenDepartment of Public Health & Institute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan.
Hsi-Chung ChenDepartment of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan. hsichungchen@ntu.edu.tw.
Po-Hsiu KuoDepartment of Public Health & Institute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan. phkuo@ntu.edu.tw.ORCID 0000-0003-0365-3587
Jianan Mental Hospital · TWNational Taiwan University · TWNational Health Research Institutes · TWNational Yang Ming Chiao Tung University · TW

Funding

National Science Council NSC101-3114-Y-002-003
6 · The paper itself

Abstract

backgroundTo investigate the risk of treatment-resistant depression (TRD) in patients with depression by examining their clinical features, early prescription patterns, and early and lifetime comorbidities.

methodsIn total, 31,422 depressive inpatients were followed-up from diagnostic onset for more than 10-years. Patients were diagnosed with TRD if their antidepressant treatment regimen was altered ≥two times or if they were admitted after at least two different antidepressant treatments. Multiple Cox regression model were used to determine whether physical and psychiatric comorbidities, psychosis, and prescription patterns increased the risk of TRD by controlling for relevant demographic covariates. Survival analyses were performed for important TRD-associated clinical variables.

resultsFemales with depression (21.24%) were more likely to suffer from TRD than males (14.02%). Early anxiety disorders were more commonly observed in the TRD group than in the non-TRD group (81.48 vs. 58.96%, p < 0.0001). Lifetime anxiety disorders had the highest population attributable fraction (42.87%). Seventy percent of patients with multiple psychiatric comorbidities developed TRD during follow-up. Cox regression analysis further identified that functional gastrointestinal disorders significantly increased TRD risk (aHR = 1.19). Higher doses of antidepressants and benzodiazepines and Z drugs in the early course of major depressive disorder increased TRD risk (p < 0.0001).

conclusionOur findings indicate the need to monitor early comorbidities and polypharmacy patterns in patients with depression associated with elevated TRD risk.

Indexed as

Depressive Disorder, Treatment-ResistantMajor Depressive DisorderAntidepressive AgentsCohort StudiesDepressionFemaleHumansMaleAntidepressive AgentsAntidepressantsEarly and lifetime comorbiditiesHealth-seeking behaviorPrescription patternTreatment-resistant depression

Identifiers

PMID33203427
PMCPMC7672820
OpenAlexW3105022449

What OpenQuestion holds

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LicenceCC BY
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.