Evidence map›Paper›PMID 41493892›Full record

ArticleDigestion2026

Continuous versus Intermittent Midazolam Sedation in Balloon-Assisted Enteroscopy: A Multicenter Randomized Trial.

Yuko Sakakibara, Tomohiko Mannami, Toshio Kuwai, Takashi Kagaya, Tatsuya Toyokawa, Shinji Katsushima, Toshihiro Kanda, Masaaki Shimada, Mizuki Kuramochi, Shohei Hamada and 15 more

Abstract read
In one paragraph

Article in Digestion, 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

25 authors.

Yuko SakakibaraDepartment of Gastroenterology, NHO Osaka National Hospital, Osaka, Japan, yuko.sb@gmail.com.
Tomohiko MannamiDepartment of Gastroenterology, NHO Okayama Medical Center, Okayama, Japan.
Toshio KuwaiDepartment of Gastroenterology, NHO Kure Medical Center and Chugoku Cancer Center, Kure, Japan.
Takashi KagayaDepartment of Gastroenterology, NHO Kanazawa Medical Center, Kanazawa, Japan.
Tatsuya ToyokawaDepartment of Gastroenterology, NHO Fukuyama Medical Center, Fukuyama, Japan.
Shinji KatsushimaDepartment of Gastroenterology, NHO Kyoto Medical Center, Kyoto, Japan.
Toshihiro KandaDepartment of Gastroenterology, NHO Higashi-ohmi General Medical Center, Higashi-ohmi, Japan.
Masaaki ShimadaDepartment of Gastroenterology, NHO Nagoya Medical Center, Nagoya, Japan.
Mizuki KuramochiDepartment of Gastroenterology, NHO Saitama Hospital, Saitama, Japan.
Shohei HamadaDepartment of Gastroenterology, NHO Kyushu Medical Center, Fukuoka, Japan.
Hiroyuki FujiiDepartment of Gastroenterology, NHO Fukuokahigashi Medical Center, Koga, Japan.
Noriko WatanabeDepartment of Gastroenterology, NHO Mie Chuo Medical Center, Tsu, Japan.
Toshiyuki WakatsukiDepartment of Gastroenterology, NHO Okayama Medical Center, Okayama, Japan.
Yuzuru TamaruDepartment of Gastroenterology, NHO Kure Medical Center and Chugoku Cancer Center, Kure, Japan.
Naoki EsakaDepartment of Gastroenterology, NHO Kyoto Medical Center, Kyoto, Japan.
Yoshihiro SasakiDepartment of Gastroenterology, NHO Disaster Medical Center, Tokyo, Japan.
Kimitoshi KuboDepartment of Gastroenterology, NHO Hakodate National Hospital, Hakodate, Japan.
Katsuhiro MabeDepartment of Gastroenterology, NHO Hakodate National Hospital, Hakodate, Japan.
Takuya YamadaDepartment of Gastroenterology, NHO Osaka National Hospital, Osaka, Japan.
Akio IshiharaDepartment of Gastroenterology, NHO Osaka National Hospital, Osaka, Japan.
Toshio UraokaDepartment of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi, Japan.
Mototsugu KatoDepartment of Gastroenterology, NHO Hakodate National Hospital, Hakodate, Japan.
Akiko KadaClinical Research Center, NHO Nagoya Medical Center, Nagoya, Japan.
Akiko M SaitoClinical Research Center, NHO Nagoya Medical Center, Nagoya, Japan.
Naohiko HaradaDepartment of Gastroenterology, NHO Kyushu Medical Center, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSedation protocols for balloon-assisted enteroscopy (BAE) are not yet standardized. The aim of this study was to compare the efficacy and safety between continuous infusion and intermittent bolus administration of midazolam for sedation during BAE. The study hypothesis was that continuous infusion would provide a greater proportion of time under conscious sedation than would intermittent bolus administration.

methodsWe conducted a multicenter, prospective, double-blind, randomized controlled trial at 15 institutions of the National Hospital Organization in Japan. Patients scheduled for diagnostic or therapeutic BAE were randomly assigned to receive continuous infusion or intermittent bolus administration of intravenous midazolam. The primary endpoint was the proportion of time under conscious sedation, defined as a Ramsay Sedation Scale score of 3-4. Secondary endpoints included body movements causing procedure interruption, endoscopist and patient satisfaction, total drug dosage, adverse events, and termination of the procedure.

resultsOf 76 enrolled patients (39 continuous infusion group, 37 intermittent bolus group), one from each group discontinued before treatment, leaving 74 patients (38 continuous group, 36 intermittent bolus group) for analysis. The proportion of time under conscious sedation was comparable between groups (mean ± SD: 0.637 ± 0.315 vs. 0.609 ± 0.272, p = 0.721). However, the continuous infusion group showed a lower incidence of body movements causing procedure interruption (7.9% vs. 25.0%, p = 0.091). The total midazolam dose was higher in the continuous infusion group, whereas the incidence of adverse events was comparable between the two groups.

conclusionContinuous infusion of midazolam did not demonstrate superiority over intermittent bolus administration with regard to the proportion of time under conscious sedation. However, continuous infusion suppressed body movements during BAE without increasing adverse events; thus, it could be one of the feasible sedation options for BAE in clinical practice.

Indexed as

AnalgesicsAnesthesiaConscious sedationDouble-balloon endoscopySingle-balloon endoscopy

Identifiers

PMID41493892
PMCPMC12956316

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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.