Evidence map›Paper›PMID 31727915›Full record

Trial reportScientific reports2019

Safety profile of sedative endoscopy including cognitive performance in liver cirrhosis: A double-blind randomized controlled trial.

Jeong-Ju Yoo, Hyeon Jeong Goong, Ji Eun Moon, Sang Gyune Kim, Young Seok Kim

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 28% 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, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Review
  4. PropofolWorld journal of gastrointestinal endoscopy · 2020
    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

5 authors at 1 institution in 1 country.

Jeong-Ju YooDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Soonchunhyang University school of medicine Bucheon Hospital, Bucheon, Korea.ORCID http://orcid.org/0000-0002-7802-0381
Hyeon Jeong GoongDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Soonchunhyang University school of medicine Bucheon Hospital, Bucheon, Korea.
Ji Eun MoonDepartment of Biostatistics, Clinical Trial Center, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.
Sang Gyune KimDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Soonchunhyang University school of medicine Bucheon Hospital, Bucheon, Korea.ORCID http://orcid.org/0000-0001-8694-777X
Young Seok KimDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Soonchunhyang University school of medicine Bucheon Hospital, Bucheon, Korea. liverkys@schmc.ac.kr.
Soonchunhyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The indiscriminate use of sedative drugs during endoscopy can pose multiple risks including cognitive impairment in advanced liver cirrhosis. However, the data are scarce regarding which sedative drugs are safest in these populations. The aim of this study was to evaluate the safety profiles including cognitive performance among midazolam, propofol, and combination therapy in advanced cirrhotic patients. This double-blind randomized controlled study included 60 consecutive advanced cirrhotic patients who underwent upper gastrointestinal endoscopy. The Stroop application was used to screen for cognitive impairment. Patients were randomly assigned to one of 3 groups, midazolam, propofol, or the combination group, and underwent Stroop test before and two hours after the completion of endoscopy. Hemodynamic safety and the subjective satisfaction score were also evaluated. Patients did not show significant changes in on-time or off-time on the Stroop test before and two hours after sedatives, and there was no significant difference among the 3 treatment groups. Also, there were no significant vital sign changes after sedatives. Time-to-recovery was longest in midazolam group, and patient awakening and patient memory were highest in propofol group. However, all 3 groups showed no difference in patient satisfaction, but the combination group was more preferred in terms of subjective satisfaction by physicians. Factors affecting worsened Stroop speed after sedatives were older age, low education level and high MELD score. All sedative methods using midazolam, propofol, or combination therapy showed similar safety profile in advanced cirrhosis, and were not associated with increased risk of cognitive impairment.

Indexed as

AdultAgedCognitionDouble-Blind MethodEndoscopy, GastrointestinalFemaleHumansHypnotics and SedativesLiver CirrhosisMaleMemoryMidazolamMiddle AgedPatient SatisfactionPropofolRisk FactorsHypnotics and SedativesMidazolamPropofol

Identifiers

PMID31727915
PMCPMC6856546
OpenAlexW2988509994

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.