Evidence map›Paper›PMID 34664207›Full record

ArticlePharmaceutical research2021

Midazolam Infusion and Disease Severity Affect the Level of Sedation in Children: A Parametric Time-to-Event Analysis.

Parth J Upadhyay, Nienke J Vet, Sebastiaan C Goulooze, Elke H J Krekels, Saskia N de Wildt, Catherijne A J Knibbe

Open access · hybridAbstract read
In one paragraph

Article in Pharmaceutical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 84% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

6 authors at 4 institutions in 1 country.

Parth J UpadhyayGorlaeus Laboratories, Division of Systems Biomedicine and Pharmacology, Leiden Academic Centre for Drug Research (LACDR), Leiden University, PO Box 9502, 2300RA, Leiden, The Netherlands.
Nienke J VetDepartment of Paediatrics, St Antonius Hospital, Nieuwegein, The Netherlands.
Sebastiaan C GouloozeGorlaeus Laboratories, Division of Systems Biomedicine and Pharmacology, Leiden Academic Centre for Drug Research (LACDR), Leiden University, PO Box 9502, 2300RA, Leiden, The Netherlands.
Elke H J KrekelsGorlaeus Laboratories, Division of Systems Biomedicine and Pharmacology, Leiden Academic Centre for Drug Research (LACDR), Leiden University, PO Box 9502, 2300RA, Leiden, The Netherlands.
Saskia N de WildtDepartment of Pharmacology & Toxicology, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Catherijne A J KnibbeGorlaeus Laboratories, Division of Systems Biomedicine and Pharmacology, Leiden Academic Centre for Drug Research (LACDR), Leiden University, PO Box 9502, 2300RA, Leiden, The Netherlands. c.knibbe@antoniusziekenhuis.nl.
Centre for Human Drug Research · NLSt. Antonius Ziekenhuis · NLLeiden University · NLRadboud University Medical Center · NL

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek Knibbe 2013
6 · The paper itself

Abstract

aimIn critically ill mechanically ventilated children, midazolam is used first line for sedation, however its exact sedative effects have been difficult to quantify. In this analysis, we use parametric time-to-event (PTTE) analysis to quantify the effects of midazolam in critically ill children.

methodsIn the PTTE analysis, data was analyzed from a published study in mechanically ventilated children in which blinded midazolam or placebo infusions were administered during a sedation interruption phase until, based on COMFORT-B and NISS scores, patients became undersedated and unblinded midazolam was restarted. Using NONMEM® v.7.4.3., restart of unblinded midazolam was analysed as event. Patients in the trial were divided into internal and external validation cohorts prior to analysis.

resultsData contained 138 events from 79 individuals (37 blinded midazolam; 42 blinded placebo). In the PTTE model, the baseline hazard was best described by a constant function. Midazolam reduced the hazard for restart of unblinded midazolam due to undersedation by 51%. In the blinded midazolam group, time to midazolam restart was 26 h versus 58 h in patients with low versus high disease severity upon admission (PRISM II < 10 versus > 21), respectively. For blinded placebo, these times were 14 h and 33 h, respectively. The model performed well in an external validation with 42 individuals.

conclusionThe PTTE analysis effectively quantified the effect of midazolam in prolonging sedation and also the influence of disease severity on sedation in mechanically ventilated critically ill children, and provides a valuable tool to quantify the effect of sedatives. Clinical trial number and registry URL: Netherlands Trial Register, Trial NL1913 (NTR2030), date registered 28 September 2009 https://www.trialregister.nl/trial/1913 .

Indexed as

AdolescentChildChild, PreschoolCritical IllnessFemaleHumansHypnotics and SedativesInfantInfant, NewbornInfusions, IntravenousMaleMidazolamModels, StatisticalNetherlandsRespiration, ArtificialSeverity of Illness IndexHypnotics and SedativesMidazolamcritical carepaediatricspharmacodynamics

Identifiers

PMID34664207
PMCPMC8523120
OpenAlexW3206994915

What OpenQuestion holds

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LicenceCC BY
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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.