Evidence map›Paper›PMID 40921193›Full record

ArticleNeuropsychopharmacology reports2025

Effect of Lemborexant-Based Sleep Medication Formulary on Benzodiazepine Reduction and Clinical Outcomes: A Single-Center Retrospective Study.

Shunya Aoki, Katsutoshi Takada, Tatsuru Sugama, Mitsugi Kimiwada, Tatsuya Hoshino, Kaori Koike, Hirokazu Akada, Takahisa Saiga, Shigeki Sato, Ryosuke Shinkai and 2 more

Abstract read
In one paragraph

Article in Neuropsychopharmacology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

12 authors.

Shunya AokiPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.ORCID https://orcid.org/0009-0005-6539-1932
Katsutoshi TakadaPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Tatsuru SugamaPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Mitsugi KimiwadaPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Tatsuya HoshinoNursing Department, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Kaori KoikeDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Hirokazu AkadaDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Takahisa SaigaDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Shigeki SatoDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita, Chiba, Japan.
Ryosuke ShinkaiDepartment of Pharmaceutical Sciences, School of Pharmacy at Narita International University of Health and Welfare, Narita, Chiba, Japan.
Yukihiro ShibataDepartment of Pharmaceutical Sciences, School of Pharmacy at Narita International University of Health and Welfare, Narita, Chiba, Japan.ORCID https://orcid.org/0000-0002-0797-468X
Takashi TomitaDepartment of Pharmaceutical Sciences, School of Pharmacy at Narita International University of Health and Welfare, Narita, Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Benzodiazepine and non-benzodiazepine hypnotics (Z-drugs) are known risk factors for adverse events, including delirium and falls. Although formularies are intended to promote appropriate prescribing, few comprehensive studies have assessed their clinical impact in the context of sleep medications. This study aimed to evaluate changes in hypnotic prescribing patterns and associated clinical outcomes following the implementation of a sleep medication formulary. A psychiatric liaison team developed and implemented a formulary in April 2024, recommending lemborexant as the first-line treatment and eszopiclone as the second-line option. This single-center, retrospective study compared patients admitted and discharged during the 12 months before (April 2023 to March 2024; n = 12 633) and after (April 2024 to March 2025; n = 12 931) implementation. Outcome measures included monthly prescription volumes, diazepam equivalents, use in clinical pathways and prescription sets, delirium incidence, nighttime falls, and length of hospital stay. Statistical analyses were performed using the Mann-Whitney U-test and Fisher's exact test. Following implementation, prescription volumes of lemborexant and eszopiclone increased significantly, whereas diazepam equivalents decreased from 10 682 mg to 4117 mg. All 104 clinical pathways and prescription sets previously using benzodiazepine hypnotics or Z-drugs were converted to lemborexant. Monthly delirium cases declined from 12.5 to 8.0, and the proportion of nighttime falls among patients receiving benzodiazepine hypnotics or Z-drugs decreased from 24.0% to 11.5%. The median hospital stay also decreased from 8 to 7 days. These findings suggest that formulary implementation effectively optimized hypnotic prescribing and contributed to improved clinical outcomes and patient safety in an acute care setting.

Indexed as

BenzodiazepinesHypnotics and SedativesPractice Patterns, Physicians'PyridinesPyrimidinesAccidental FallsAdultAgedAged, 80 and overDeliriumEszopicloneFemaleHumansLength of StayMaleMiddle AgedBenzodiazepinesEszopicloneHypnotics and SedativeslemborexantPyridinesPyrimidinesaccidental fallsdeliriumformularyhypnotics and sedativeslemborexant

Identifiers

PMID40921193
PMCPMC12416910

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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.