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The impact of nursing delirium preventive interventions in the ICU a multicenter cluster-randomized controlled clinical trial

dc.contributor.authorRood, Paul J T
dc.contributor.authorZegers, Marieke
dc.contributor.authorRamnarain, Dharmanand
dc.contributor.authorKoopmans, Matty
dc.contributor.authorKlarenbeek, Toine
dc.contributor.authorEwalds, Esther
dc.contributor.authorvan der Steen, Marike S
dc.contributor.authorOldenbeuving, Annemarie V
dc.contributor.authorKuiper, Michael A
dc.contributor.authorTeerenstra, Steven
dc.contributor.authorAdang, Eddy
dc.contributor.authorvan Loon, Lex
dc.contributor.authorWassenaar, Annelies
dc.contributor.authorVermeulen, Hester
dc.contributor.authorPickkers, Peter
dc.contributor.authorVan Den Boogaard, Mark H W A
dc.date.accessioned2024-02-21T01:39:58Z
dc.date.issued2021
dc.date.updated2022-10-09T07:17:48Z
dc.description.abstractRationale: Delirium is common in critically ill patients and is associated with deleterious outcomes. Nonpharmacological interventions are recommended in current delirium guidelines, but their effects have not been unequivocally established. Objectives: To determine the effects of a multicomponent nursing intervention program on delirium in the ICU. Methods: A stepped-wedge cluster-randomized controlled trial was conducted in ICUs of 10 centers. Adult critically ill surgical, medical, or trauma patients at high risk of developing delirium were included. A multicomponent nursing intervention program focusing on modifiable risk factors was implemented as standard of care. The primary outcome was the number of delirium-free and coma-free days alive in 28 days after ICU admission. Measurements and Main Results: A total of 1,749 patients were included. Time spent on interventions per 8-hour shift was median (interquartile range) 38 (14-116) minutes in the intervention period and median 32 (13-73) minutes in the control period (P = 0.44). Patients in the intervention period had a median of 23 (4-27) delirium-free and coma-free days alive compared with a median of 23 (5-27) days for patients in the control group (mean difference, 21.21 days; 95% confidence interval, 22.84 to 0.42 d; P = 0.15). In addition, the number of delirium days was similar: median 2 (1-4) days (ratio of medians, 0.90; 95% confidence interval, 0.75 to 1.09; P = 0.27). Conclusions: In this large randomized controlled trial in adult ICU patients, a limited increase in the use of nursing interventions was achieved, and no change in the number of delirium-free and coma-free days alive in 28 days could be determined.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1073-449Xen_AU
dc.identifier.urihttp://hdl.handle.net/1885/313792
dc.language.isoen_AUen_AU
dc.publisherAmerican Thoracic Societyen_AU
dc.rights© 2021 The authorsen_AU
dc.sourceAmerican Journal of Respiratory and Critical Care Medicineen_AU
dc.subjectcritical careen_AU
dc.subjectdeliriumen_AU
dc.subjectnursingen_AU
dc.subjectnonpharmacologicalen_AU
dc.subjectintervention programen_AU
dc.titleThe impact of nursing delirium preventive interventions in the ICU a multicenter cluster-randomized controlled clinical trialen_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue6en_AU
local.bibliographicCitation.lastpage691en_AU
local.bibliographicCitation.startpage682en_AU
local.contributor.affiliationRood, Paul J T, Dept of Intensive Care Medicine, Radboud Institute for Health Sciencesen_AU
local.contributor.affiliationZegers, Marieke, Department of Intensive Care Medicine, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlandsen_AU
local.contributor.affiliationRamnarain, Dharmanand, Department of Intensive Care Medicine, Elisabeth Tweesteden Hospital, Tilburg, the Netherlandsen_AU
local.contributor.affiliationKoopmans, Matty, Medical Center Leeuwardenen_AU
local.contributor.affiliationKlarenbeek, Toine, Department of Intensive Care Medicine, Maxima Medical Center, Veldhoven, the Netherlandsen_AU
local.contributor.affiliationEwalds, Esther, Department of Intensive Care Medicine, Bernhoven, Nistelrodeseweg, Uden, the Netherlandsen_AU
local.contributor.affiliationvan der Steen, Marike S, Department of Intensive Care Medicine, Hospital Gelderse Vallei, Ede, the Netherlandsen_AU
local.contributor.affiliationOldenbeuving, Annemarie V, Department of Intensive Care Medicine, Elisabeth Tweesteden Hospital, Tilburg, the Netherlandsen_AU
local.contributor.affiliationKuiper, Michael A, Department of Intensive Care Medicine, Medical Center Leeuwardenen_AU
local.contributor.affiliationTeerenstra, Steven, Department for Health Evidence, Section Biostatisticsen_AU
local.contributor.affiliationAdang, Eddy, Department for Health Evidenceen_AU
local.contributor.affiliationvan Loon, Lex Maxim, College of Health and Medicine, ANUen_AU
local.contributor.affiliationWassenaar, Annelies, Radboud Institute for Health Sciencesen_AU
local.contributor.affiliationVermeulen, Hester, Radboud Institute for Health Sciencesen_AU
local.contributor.affiliationPickkers, Peter, Radboud University Nijmegenen_AU
local.contributor.affiliationVan Den Boogaard, Mark H W A, Radbound University Medical Centeren_AU
local.contributor.authoruidvan Loon, Lex Maxim, u1099389en_AU
local.description.embargo2099-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor320212 - Intensive careen_AU
local.identifier.ariespublicationa383154xPUB31473en_AU
local.identifier.citationvolume204en_AU
local.identifier.doi10.1164/rccm.202101-0082OCen_AU
local.identifier.scopusID2-s2.0-85115635577
local.publisher.urlhttps://www.atsjournals.org/en_AU
local.type.statusPublished Versionen_AU

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