Evidence map›Paper›PMID 35524672›Full record

SynthesisCurrent neuropharmacology2022

Melatonin Receptor Agonists for the Prevention of Delirium: An Updated Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Benchalak Maneeton, Subsai Kongsaengdao, Narong Maneeton, Surinporn Likhitsathian, Pakapan Woottiluk, Suttipong Kawilapat, Manit Srisurapanont

Open access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Current neuropharmacology, 2022. 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
1.1field-weighted citation impact, top 25% 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. Trial
  2. Review
  3. Article
  4. Preventing and treating delirium in clinical settings for older adults.Therapeutic advances in psychopharmacology · 2023
    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

7 authors at 2 institutions in 1 country.

Benchalak ManeetonDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Subsai KongsaengdaoDivision of Neurology, Department of Medicine, Rajavithi Hospital, Department of Medical Services, Ministry of Public Health, Bangkok, Thailand.
Narong ManeetonDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Surinporn LikhitsathianDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Pakapan WoottilukPsychiatric Nursing Division, Faculty of Nursing, Chiang Mai University, Chiang Mai, Thailand.
Suttipong KawilapatDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Manit SrisurapanontDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Chiang Mai University · THMinistry of Public Health · TH

Funding

Chiang Mai University in Chiang Mai, Thailand 15/2565
6 · The paper itself

Abstract

backgroundAlthough a previous review illustrated the efficacy of melatonin receptor agonists (MRAs) in preventing delirium, some recent randomized controlled trials (RCTs) did not confirm these effects.

objectivesThis study systematically reviewed the efficacy, acceptability, and tolerability of MRAs for delirium prevention. MATERIALS AND

methodsWe searched electronic databases, including Scopus, PubMed, CINAHL, and Controlled Trials Register, from their inception to February 20, 2022. The primary efficacy outcome was delirium incidence rate after MRA administration; relative risks (RRs), overall discontinuation, and discontinuation due to adverse events are also presented.

resultsThe overall pooled incidence rates of delirium in MRA-treated and placebo-treated groups were significantly different with RR (95% CI)=0.66(0.52, 0.84, ), I2=59%. Similarly, the incidence rate was significantly lower in the melatonin-treated group than in the placebo-treated group [RR (95% CI) =0.65 (0.49, 0.88), I2=65%]. Unfortunately, incidence rates were not significantly different between ramelteon-treated and placebo-treated groups [RR (95% CI) =0.67 (0.42, 1.08), I2=50%]. The pooled incidence rate of delirium in either melatonin or ramelteon-treated groups was not significantly different from the placebo-treated group in elderly patients. The pooled incidence rate of delirium was significantly lower in the melatonin-treated group than in the benzodiazepinetreated group.

conclusionBased on this review, melatonin could prevent delirium with a small effect size. However, ramelteon did not show efficacy in preventing delirium. Additionally, neither melatonin nor ramelteon individually showed effectiveness in preventing delirium in elderly patients. Therefore, using MRAs to prevent delirium in clinical practice should be cautious. However, future welldefined and large sample size studies could verify these findings.

Indexed as

DeliriumReceptors, MelatoninAgedHumansIndenesMelatoninRandomized Controlled Trials as TopicIndenesMelatoninramelteonReceptors, MelatonindeliriumincidencemelatoninMelatonin receptor agonistpreventionramelteon

Identifiers

PMID35524672
PMCPMC9886800
OpenAlexW4229081325

What OpenQuestion holds

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LicenceCC BY-NC
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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.