Remifentanil-propofol analgo-sedation shortens duration of ventilation and length of ICU stay compared to a conventional regimen: A centre randomised, cross-over, open-label study in the Netherlands

Objective: Compare duration of mechanical ventilation (MV), weaning time, ICU-LOS (ICU-LOS), efficacy and safety of remifentanil-based regimen with conventional sedation and analgesia. Design: Centre randomised, open-label, crossover, 'real-life' study. Setting: 15 Dutch hospitals. Patients: Adult medical and post-surgical ICU patients with anticipated short-term (2-3 days) MV. Interventions: Patient cohorts were randomised to remifentanil-based regimen (n = 96) with propofol as required, for a maximum of 10 days, or to conventional regimens (n = 109) of propofol, midazolam or lorazepam combin... Mehr ...

Verfasser: Rozendaal, F.W. (Frans)
Spronk, P.E. (Peter)
Snellen, F.F. (Ferdinand)
Schoen, A. (Adri)
Zanten, A.R.H. (Arthur) van
Foudraine, N.A. (Norbert)
Mulder, P.G.H. (Paul)
Bakker, J. (Jan)
Dokumenttyp: Artikel
Erscheinungsdatum: 2009
Schlagwörter: Analgesia / Intensive care / Mechanical ventilation / Netherlands / Remifentanil / Sedation / Weaning / adult / aged / article / artificial ventilation / clinical trial / cohort analysis / comparative study / controlled clinical trial / controlled study / crossover procedure / drug dose reduction / drug withdrawal / extubation / female / fentanyl / heart rate / hospital discharge / human / hypnotic agent / hypotension / intensive care nursing / intensive care unit / length of stay / lorazepam / major clinical study / male / mean arterial pressure / midazolam / morphine / motor dysfunction / multicenter study / neuritis / nurse / open study / postoperative care / propofol / randomized controlled trial / satisfaction / time / treatment duration
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27607890
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://repub.eur.nl/pub/18523

Objective: Compare duration of mechanical ventilation (MV), weaning time, ICU-LOS (ICU-LOS), efficacy and safety of remifentanil-based regimen with conventional sedation and analgesia. Design: Centre randomised, open-label, crossover, 'real-life' study. Setting: 15 Dutch hospitals. Patients: Adult medical and post-surgical ICU patients with anticipated short-term (2-3 days) MV. Interventions: Patient cohorts were randomised to remifentanil-based regimen (n = 96) with propofol as required, for a maximum of 10 days, or to conventional regimens (n = 109) of propofol, midazolam or lorazepam combined with fentanyl or morphine. Measurements and main results: Outcomes were weaning time, duration of MV, ICU-LOS, sedation- and analgesia levels, intensivist/ICU nurse satisfaction, adverse events, mean arterial pressure, heart rate. Median duration of ventilation (MV) was 5.1 days with conventional treatment versus 3.9 days with remifentanil (NS). The remifentanil-based regimen reduced median weaning time by 18.9 h (P = 0.0001). Median ICU-LOS was 7.9 days versus 5.9 days, respectively (NS). However, the treatment effects on duration of MV and ICU stay were time-dependent: patients were almost twice as likely to be extubated (P = 0.018) and discharged from the ICU (P = 0.05) on day 1-3. Propofol doses were reduced by 20% (P = 0.05). Remifentanil also improved sedation-agitation scores (P < 0.0001) and intensivist/ICU nurse satisfaction (P < 0.0001). All other outcomes were comparable. Conclusions: In patients with an expected short-term duration of MV, remifentanil significantly improves sedation and agitation levels and reduces weaning time. This contributes to a shorter duration of MV and ICU-LOS.