Evidence map›Paper›PMID 29363356›Full record

Trial reportThe Annals of pharmacotherapy2018

Sedative Plasma Concentrations and Delirium Risk in Critical Illness.

Joanna L Stollings, Jennifer L Thompson, Benjamin A Ferrell, Mika Scheinin, Grant R Wilkinson, Christopher G Hughes, Ayumi K Shintani, E Wesley Ely, Timothy D Girard, Pratik P Pandharipande and 1 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Annals of pharmacotherapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Observational
  5. Article
  6. 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

11 authors at 5 institutions in 3 countries.

Joanna L Stollings1 Vanderbilt University Medical Center, Nashville, TN, USA.
Jennifer L Thompson2 Vanderbilt University School of Medicine, Nashville, TN, USA.
Benjamin A Ferrell1 Vanderbilt University Medical Center, Nashville, TN, USA.
Mika Scheinin4 University of Turku, Turku, Finland.ORCID 0000-0001-7579-9126
Grant R Wilkinson1 Vanderbilt University Medical Center, Nashville, TN, USA.
Christopher G Hughes1 Vanderbilt University Medical Center, Nashville, TN, USA.
Ayumi K Shintani2 Vanderbilt University School of Medicine, Nashville, TN, USA.
E Wesley Ely1 Vanderbilt University Medical Center, Nashville, TN, USA.
Timothy D Girard8 University of Pittsburgh School of Medicine, PA, USA.
Pratik P Pandharipande1 Vanderbilt University Medical Center, Nashville, TN, USA.
Mayur B Patel1 Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0001-5230-0871
Vanderbilt University · USUniversity of Pittsburgh · USUniversity of Tennessee at Knoxville · USUniversity of Turku · FIVanderbilt University Medical Center · US

Funding

The MIND USA StudyR01AG035117 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ELY, E WESLEY · 2011 to 2016
$7.3M
Altering Sedation Paradigms to Improve Brain Injury and Survival in Severe SepsisR01HL111111 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PANDHARIPANDE, PRATIK · 2012 to 2017
$3.7M
The MIND ICU StudyR01AG027472 · NIA · VANDERBILT UNIVERSITY · PI ELY, E WESLEY · 2006 to 2010
$3.0M
The INSIGHT-ICU Study: Illuminating Neuropsychological dysfunction and Systemic Inflammatory mechanisms Gleaned after Hospitalization in Trauma-ICU StudyR01GM120484 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PATEL, MAYUR B · 2017 to 2021
$3.0M
Mitochondrial Determinants of Cognitive Outcomes in ARDS and Sepsis - SupplementR01HL135144 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GIRARD, TIMOTHY D · 2017 to 2021
$2.2M
Predictors of Cognitive Impairment in Survivors of Critical IllnessK23AG034257 · NIA · VANDERBILT UNIVERSITY · PI GIRARD, TIMOTHY D · 2009 to 2013
$684k
Role of Endothelial and Brain Injury in Acute and Long-term Brain DysfunctionR03AG045085 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HUGHES, CHRISTOPHER · 2014 to 2015
$232k
NHLBI NIH HHS R01 HL111111NHLBI NIH HHS R01 HL135144NIA NIH HHS K23 AG034257NIA NIH HHS R01 AG027472NIA NIH HHS R01 AG035117NIA NIH HHS R03 AG045085NIGMS NIH HHS R01 GM120484
6 · The paper itself

Abstract

backgroundThe relationship between plasma concentration of sedatives and delirium is unknown.

objectiveWe hypothesized that higher plasma concentrations of lorazepam are associated with increased delirium risk, whereas higher plasma concentrations of dexmedetomidine are associated with reduced delirium risk.

methodsThis prospective cohort study was embedded in a double-blind randomized clinical trial, where ventilated patients received infusions of lorazepam and dexmedetomidine. Plasma concentrations of these drugs and delirium assessments were measured at least daily. A multivariable logistic regression model accounting for repeated measures was used to analyze associations between same-day plasma concentrations of lorazepam and dexmedetomidine (exposures) and the likelihood of next-day delirium (outcome), adjusting for same-day mental status (delirium, coma, or normal) and same-day fentanyl doses.

resultsThis critically ill cohort (n = 103) had a median age of 60 years (IQR: 48-66) with APACHE II score of 28 (interquartile range [IQR] = 24-32), where randomization resulted in assignment to lorazepam (n = 51) or dexmedetomidine (n = 52). After adjusting for same-day fentanyl dose and mental status, higher plasma concentrations of lorazepam were associated with increased probability of next-day delirium (comparing 500 vs 0 ng/mL; odds ratio [OR] = 13.2; 95% CI = 1.4-120.1; P = 0.02). Plasma concentrations of dexmedetomidine were not associated with next-day delirium (comparing 1 vs 0 ng/mL; OR = 1.1; 95% CI = 0.9-1.3; P = 0.45).

conclusionsIn critically ill patients, higher lorazepam plasma concentrations were associated with delirium, whereas dexmedetomidine plasma concentrations were not. This implies that the reduced delirium risk seen in patients sedated with dexmedetomidine may be a result of avoidance of benzodiazepines, rather than a dose-dependent protective effect of dexmedetomidine.

Indexed as

AgedCritical IllnessDeliriumDexmedetomidineFemaleHumansHypnotics and SedativesIntensive Care UnitsLogistic ModelsLorazepamMaleMiddle AgedRespiration, ArtificialDexmedetomidineHypnotics and SedativesLorazepamanalgesicsassayscritical caredrug safetydrug trialspharmacodynamicssedativestoxicity

Identifiers

PMID29363356
PMCPMC5930024
OpenAlexW2785035757

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.