Evidence map›Paper›PMID 41474732›Full record

ArticlePloS one2025

How much is too much? A medication use evaluation of VA ICU sedation practice during the COVID-19 pandemic.

Ian C Murphy, Kelly Bryan, Muriel Burk, Rong Jiang, Francesca Cunningham, Sarah Providence, Elizabeth Rightnour, Sarah Zavala, Kathleen Morneau, Trisha Exline and 16 more

Abstract read
In one paragraph

Article in PloS one, 2025. 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

26 authors.

Ian C MurphyYale University School of Medicine, New Haven, Connecticut, United States of America.
Kelly BryanVeterans Affairs Center for Medication Safety-Pharmacy Benefits Management ServicesWashington, District of Columbia, United States of America.
Muriel BurkVeterans Affairs Center for Medication Safety-Pharmacy Benefits Management ServicesWashington, District of Columbia, United States of America.ORCID https://orcid.org/0009-0005-0278-5918
Rong JiangVeterans Affairs Center for Medication Safety-Pharmacy Benefits Management ServicesWashington, District of Columbia, United States of America.
Francesca CunninghamVeterans Affairs Center for Medication Safety-Pharmacy Benefits Management ServicesWashington, District of Columbia, United States of America.
Sarah ProvidenceVeterans Affairs Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, United States of America.
Elizabeth RightnourNewton D. Baker VA Medical Center, Martinsburg, West Virginia, United States of America.
Sarah ZavalaJesse Brown Veterans Affairs Medical Center, Chicago, Illinois, United States of America.ORCID https://orcid.org/0009-0007-0139-5760
Kathleen MorneauSouth Texas Veterans Health Care System, San Antonio, Texas, United States of America.
Trisha ExlineNewton D. Baker VA Medical Center, Martinsburg, West Virginia, United States of America.
Stacey RiceUnited States of America Department of Veterans Affairs, Eastern Colorado Health Care System, Aurora, Colorado, United States of America.
Travis SchmittVeterans Healthcare System of the Ozarks, Fayetteville, Arkansas, United States of America.
Kelly DrumrightVeterans Affairs Tennessee Valley Healthcare System, Nashville, Tennessee, United States of America.
Jennifer LeeVeterans Affairs Long Beach Health Care System, Long Beach, California, United States of America.
BreAnna DavidsRalph H. Johnson Veterans Affairs Medical Center, Charleston, South Carolina, United States of America.
Tram GuilbeaultAugusta Veterans Affairs Medical Center, Augusta, GeorgiaUnited States of America.
Brooke KlenoskyCorporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, Pennsylvania, United States of America.
Ann-Marie SutherlandVeterans Affairs Tennessee Valley Healthcare System, Nashville, Tennessee, United States of America.
Abbie RosenMalcom Randall Veterans Affairs Medical Center, North Florida/South Georgia Veterans Health System, Gainesville, Florida, United States of America.
Lauren RatliffVeterans Healthcare System of the Ozarks, Fayetteville, Arkansas, United States of America.
Kenneth BukowskiVeterans Affairs Center for Medication Safety-Pharmacy Benefits Management ServicesWashington, District of Columbia, United States of America.
Margaret A PisaniYale University School of Medicine, New Haven, Connecticut, United States of America.
Andrew FranckMalcom Randall Veterans Affairs Medical Center, North Florida/South Georgia Veterans Health System, Gainesville, Florida, United States of America.
Mark WongSouth Texas Veterans Health Care System, San Antonio, Texas, United States of America.
Preston WitcherUnited States of America Department of Veterans Affairs, Eastern Colorado Health Care System, Aurora, Colorado, United States of America.
Kathleen M AkgünYale University School of Medicine, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0003-2623-7463

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesEarly data suggested higher sedative requirements for ventilated COVID+ patients, deviating from established guidelines. We assessed the relationship between sedative use and outcomes in mechanically ventilated Veterans during the COVID-19 pandemic.

designRetrospective Medication Use Evaluation.

settingNational Sample of 13 Distinct VA Medical Center Intensive Care Units. PATIENTS: Critically ill Veteran patients requiring mechanically ventilation for ≥2 days.

interventionsNone. MEASUREMENTS AND MAIN

resultsThe proportion of patients receiving fentanyl, midazolam and propofol was higher during COVID years. Compared with pre-COVID, median fentanyl dose was higher during Years 1 and 2 (1575mcg [(IQR) 1000-1650] vs. 1900 [1250-3000] vs. 1910 [1150-3500]). Adjuvant antipsychotics use was relatively low but tended to increase over time (pre = 10.5% vs. Year 1 = 12.3% vs. Year 2 = 14.1%). Most patients started on antipsychotics in the ICU were continued on the drug after extubation. Mortality was higher during COVID years (pre = 26.9% vs. 1 = 36.8% and 2 = 35.9%). In stratified analyses by COVID status years 1-2 (n = 79, 27%), a higher proportion of COVID+ patients received fentanyl (96% vs. 84%) and propofol (90% vs. 77%) and at higher doses (fentanyl = 1650mcg vs. 2688mcg median cumulative dose; propofol maximum infusion rate = 30 mc/kg/min (20-50) vs. 40 (25-50)). Sedative doses were similar to pre-COVID among non-COVID patients. Anti-psychotics were more frequently continued post extubation among COVID+ (34.6% vs. non-COVID+=14.9%). COVID+ patients were also less likely to have awakening and breathing trials at 48 hours after intubation (18% vs. 46%).

conclusionsSedative use and dosing increased during the first two years of COVID compared to pre-COVID, especially for COVID+ patients. The sustained elevated levels of fentanyl use in Year 2 suggests possible 'therapeutic creep' away from guideline-concordant practices for COVID+ patients. Antipsychotic prescription during intubation and following extubation was also more common among COVID + . These findings could inform development and implementation of safer sedation practices across VA ICUs during respiratory pandemics.

Indexed as

COVID-19Hypnotics and SedativesIntensive Care UnitsAgedFemaleFentanylHumansMaleMidazolamMiddle AgedPandemicsPropofolRespiration, ArtificialRetrospective StudiesSARS-CoV-2United StatesFentanylHypnotics and SedativesMidazolamPropofol

Identifiers

PMID41474732
PMCPMC12755820

What OpenQuestion holds

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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.