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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Intensive care medicine 22 (1996), S. 752-759 
    ISSN: 1432-1238
    Keywords: Weaning ; Extubation ; Indices ; Subjective ; Critically ill ; Mechanical ventilation ; CPAP ; Pressure support
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective To assess the outcome of a clinical judgementbased approach to weaning and extubation and to adduce the predictive accuracy of various mechanical respiratory indices measured in parallel. Design Prospective study. Setting Multidisciplinary intensive care unit at a university teaching hospital. Patients 163 consecutive mechanically ventilated patients, excluding tracheotomy, for weaning trial and extubation. Interventions Using bedside clinical assessment, aided by arterial gas analysis, patients were weaned from mechanical ventilation to spontaneous ventilation via the continuous positive airway pressure (CPAP) circuit (with pressure support) of a microprocessor-controlled ventilator. Extubation occurred from the CPAP circuit at 7 cmH2O pressure support, fractional inspired oxygen (FIO2)≤0.5 and CPAP level of ≤5 cmH2O, such that the partial pressure of oxygen in arterial blood (PaO2) was ≥65 mmHg. Before extubation, observation for a 1-h (T0 and T60) trial period allowed measurement of vital capacity (VC), expired minute volume (VE), respiratory rate/tidal volume (f/VT) and maximal inspiratory pressure (MIP) using a one-way valve technique over 25 s. Measurements and main results Over 7 months, 163 patients (62 females and 101 males; mean(SD) age 64(15) years) were considered. There were 91 surgical (18 with chronic obstructive pulmonary disease; COPD) and 72 medical (28 with COPD) patients. Ventilation was for ≥1 day (median 5 days, range 1–31) in 115 [group I; APACHE II score 23(8)] and ≤1 day in 48 [Group II; APACHE II score 17(6)]. Three patients (all Group I: 2 surgical, 1 medical) were reintubated within 24 h, an overall extubation failure rate of 1.8%. In group I, at T0, PaO2/FIO2 was 238(65), f/VT 50(26), MIP 44(21) cmH2O, VE 10.6(3.7) l/min, VC 13(5) ml/kg. Cardiorespiratory variables did not change significantly in either group, T0 to T60. For prediction of reintubation (n=163), only VE (threshold 〉10 l/min) and f/VT (threshold 〉100) demonstrated moderate sensitivity and specificity at T60∶67 and 52% and 33 and 94%, respectively. Conclusions Bedside clinicla judgement of weaning and extubation produces satisfactory outcomes. As a routine, mechanical predictive indices have limited utility.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Intensive care medicine 22 (1996), S. 752-759 
    ISSN: 1432-1238
    Keywords: Key words Weaning ; Extubation ; Indices ; Subjective ; Critically ill ; Mechanical ventilation ; CPAP ; Pressure support
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective: To assess the outcome of a clinical judgement-based approach to weaning and extubation and to adduce the predictive accuracy of various mechanical respiratory indices measured in parallel. Design: Prospective study. Setting: Multidisciplinary intensive care unit at a university teaching hospital. Patients: 163 consecutive mechanically ventilated patients, excluding tracheotomy, for weaning trial and extubation. Interventions: Using bedside clinical assessment, aided by arterial gas analysis, patients were weaned from mechanical ventilation to spontaneous ventilation via the continuous positive airway pressure (CPAP) circuit (with pressure support) of a microprocessor-controlled ventilator. Extubation occurred from the CPAP circuit at 7 cmH2O pressure support, fractional inspired oxygen (FIO2) ≤0.5 and CPAP level of ≤5 cmH2O, such that the partial pressure of oxygen in arterial blood (PaO2) was ≥65 mmHg. Before extubation, observation for a 1-h (T0 and T60) trial period allowed measurement of vital capacity (VC), expired minute volume (VE), respiratory rate/tidal volume (f/VT) and maximal inspiratory pressure (MIP) using a one-way valve technique over 25 s. Measurements and main results: Over 7 months, 163 patients (62 females and 101 males; mean(SD) age 64(15) years) were considered. There were 91 surgical (18 with chronic obstructive pulmonary disease; COPD) and 72 medical (28 with COPD) patients. Ventilation was for ≥1 day (median 5 days, range 1–31) in 115 [group I; APACHE II score 23(8)] and ≤1 day in 48 [Group II; APACHE II score 17(6)]. Three patients (all Group I: 2 surgical, 1 medical) were reintubated within 24 h, an overall extubation failure rate of 1.8%. In group I, at T0, PaO2/FIO2 was 238(65), f/VT 50(26), MIP 44(21) cmH2O, VE 10.6(3.7) l/min, VC 13(5) ml/kg. Cardiorespiratory variables did not change significantly in either group, T0 to T60. For prediction of reintubation (n=163), only VE (threshold 〉10 l/min) and f/VT (threshold 〉 100) demonstrated moderate sensitivity and specificity at T60: 67 and 52% and 33 and 94%, respectively. Conclusions: Bedside clinical judgement of weaning and extubation produces satisfactory outcomes. As a routine, mechanical predictive indices have limited utility.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    ISSN: 1432-1238
    Keywords: Procainamide ; Amiodarone ; Antiarrhythmics ; Atrial tachyarrhythmias ; Critically ill
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective To compare the efficacy and safety of intravenous (IV) amiodarone and procainamide for the treatment of atrial tachyarrhythmias (AT) in the critically ill. Design In this prospective study, patients were allocated to drug treatment on the basis of hospital identification number, even for procainamide and odd for amiodarone. Setting Patients were recruited from a teaching hospital ICU and did not include postoperative cardiac patients. Patients and participants 26 patients with AT sustained for at least 1 h and failure to respond to correction of possible precipitating factors were entered in the study. Exclusion criteria were systolic blood pressure (SBP)〈80 mmHg, and known hypersensitivity to either drug. Two patients with chronic atrial fibrillation (who received amiodarone) were later excluded from the analysis. In the final analysis, 14 patients received procainamide and 10 amiodarone. Interventions IV amiodarone (3 mg/kg followed by 10 mg/kg/24h, with repeat dose of 3 mg/kg at 1 h if no response) or IV procainamide (10 mg/kg at 1 mg/kg/min followed by infusion of 2–4 mg/min for 24 h, with repeat dose of 5 mg/kg at 1 h if no response). Measurements and results In the procainamide group 10/14 (71%) and in the amiodarone group 7/10 (70%) had converted to sinus rhythm by 12 h. There was no significant difference in response between the groups. SBP was not significantly different from baseline after administration of either drug. Conclusions Procainamide and amiodarone appear to be safe and equally effective in the treatment of AT in the critically ill.
    Type of Medium: Electronic Resource
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