Chest
Clinical Investigations in Critical CareUse of Sedatives and Neuromuscular Blockers in a Cohort of Patients Receiving Mechanical Ventilation
Section snippets
Materials and Methods
We analyzed the database of a prospective, multicenter, international cohort of 5,183 adult patients who received mechanical ventilation for > 12 h at 361 ICUs in 20 countries.20 The general physiologic and clinical characteristics of these patients were previously described and reported.20 The institutional review board at each center approved the study protocol. For the purpose of this study, we collected the following information: demographic data (age, gender, simplified acute physiology
Use of Sedatives
Of the 5,183 ICU patients admitted during the study period, 3,540 patients (68%; 95% confidence interval [CI], 67 to 69%) received a sedative at any time while receiving mechanical ventilation. For these patients, the median number of days receiving a sedative was 3 days (IQR, 2 to 6 days).Figure 1 shows the daily percentage of patients who received a sedative according to the duration of ventilatory support. Since we registered information on sedation for 28 days, we were able to monitor
Discussion
The main findings of this prospective, international, multicentric, observational study are as follows: (1) 68% (3,540 of 5183 patients receiving mechanical ventilation) received a sedative at any time while receiving mechanical ventilation; (2) the persistent use of sedatives was associated with more days of mechanical ventilation, more weaning days, and longer length of stay in the ICU; (3) NMBs were used in 13% (686 of 5,183 patients); and (4) patients requiring NMB has a longer duration of
Mechanical Ventilation Study Group
Argentina: Coordinators: C. Apezteguia, F. Palizas. R. Alasino (Hospital Municipal de Urgencias, Córdoba); R. Bastianelli (Hospital Militar, Villa Revol); J. Berón (Hospital Pablo Soria, San Salvador); C. Bevilacqua (Clínica Modelo de Morón, Morón); M. Cafaro (Hospital Regional Río Gallegos, Río Gallegos); E. Capparelli (Hospital Eva Perón, San Martín); G. Cardonatti (Hospital San Isidro, San Isidro); R. Correa (Hospital Central, Mendoza); A. Díez (Hospital Provincial del Centenario, Rosario);
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Cited by (0)
This study was supported by grant 98/0233 from the Fondo de Investigacion Sanitaria, Spain, Red GIRA (G03/063) and Red RESPIRA (C03/11) from Instituto de Salud Carlos III, Spain.
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