Pediatr Crit Care Me
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Pediatr Crit Care Me · Jul 2002
Comparison of end-tidal CO2 and Paco2 in children receiving mechanical ventilation.
To determine whether end-tidal CO(2) (Petco(2)) measurement provides a reliable estimate of ventilation in critically ill children who are mechanically ventilated. DESIGN: Prospective, nonrandomized, consecutive enrollment study. SETTING: A university-affiliated children's hospital pediatric intensive care unit. PATIENTS: All intubated, mechanically ventilated pediatric patients. INTERVENTIONS: All Petco(2)-Paco(2) pairs were from patients ventilated with a Servo 300 Ventilator (Siemens-Elema AB, Stockholm, Sweden). When a blood gas sample was obtained, Petco(2) as measured by a continuous mainstream Petco(2) capnograph was recorded. Measurements: The results of blood gas measurements and corresponding Petco(2) measurements were recorded. Demographic data and primary diagnosis were noted. Petco(2)-Paco(2) pairs obtained from patients with intracardiac shunts or obtained during high-frequency oscillation or extracorporeal membrane oxygenation at the time of measurement were excluded from analysis. Linear regression was used to analyze Petco(2)-Paco(2) pairs. Repeated measure analysis of variance with the mixed-model algorithm in SAS software (SAS Institute, Carey, NC) was used to analyze the trend in the Petco(2) and Paco(2) relationship. Chi-square was used to analyze categorical data. Statistical significance was considered p <.05. ⋯ In most intubated, mechanically ventilated infants and children, Petco(2) reliably estimates ventilation.
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Pediatr Crit Care Me · Jul 2002
Cisatracurium infusion for neuromuscular blockade in the pediatric intensive care unit: A dose-finding study.
To evaluate the safety and efficacy of cisatracurium besylate, a neuromuscular blocking agent in infants zero to 2 yrs of age. DESIGN: An open-label study to evaluate efficacy and safety of cisatracurium as a continuous infusion in infants. SETTING: A tertiary pediatric intensive care unit. PATIENTS: Eleven children, 0-2 yrs of age, requiring prolonged neuromuscular blockade. INTERVENTIONS: Cisatracurium besylate, 0.1 mg/kg, was administered as an intravenous bolus dose and repeated if necessary until a >90% neuromuscular blockade, as determined by train-of-four response, was achieved. Patients were allowed to recover to 90% blockade (I/IV twitch) after the initial bolus and were administered continuous infusion at 2 &mgr;g/kg/min. The continuous infusion rate was adjusted to maintain a train-of-four response of 0-I/IV, with an increase in the rate preceded by a bolus dose of cisatracurium besylate. An electromyographic monitor was used to measure recovery at the end of infusion, when possible. Heart rate and blood pressure were recorded after the initial bolus dose and after changes in infusion rates. Blood samples were drawn at steady-state during cisatracurium infusion at several different times during the study and at the end of infusion for measurement of plasma cisatracurium and laudanosine concentrations. MEASUREMENTS AND MAIN ⋯ A longer period of recovery from neuromuscular blockade was observed compared with reports of older children. Recovery from neuromuscular blockade after long-term use was not associated with any adverse events in the immediate postinfusion period. Cisatracurium besylate is a safe and effective neuromuscular blocking agent for children 0-2 yrs of age.
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Pediatr Crit Care Me · Jul 2002
Outcome of critically ill children before and after the establishment of a pediatric retrieval service as a component of a national strategy for pediatric intensive care.
To compare outcomes of critically ill children transferred for intensive care by specialist and nonspecialist retrieval before and after the establishment of a dedicated pediatric intensive care transfer service. DESIGN: Prospective, observational study. SETTING: All hospitals that admitted children in a defined geographic region of the United Kingdom. PATIENTS: There were a total of 284 critically ill children (<16 yrs old) transferred from a district general hospital to a tertiary pediatric intensive care unit. MEASUREMENTS AND MAIN ⋯ We conclude that the establishment of a regional transfer service coincided with a fall in standardized mortality that reflected more general changes in intensive care performance rather than a specific benefit of a specialist transfer team.
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Pediatr Crit Care Me · Apr 2002
Randomized clinical trials in pediatric critical care: Rarely done but desperately needed.
To review the benefits and challenges of using the randomized, controlled trial (RCT) study design to evaluate preventive and therapeutic interventions in pediatric critical care medicine. ⋯ The RCT design is able to control for many sources of potential bias that other types of study designs cannot. The findings of RCTs often contradict the findings of less rigorous study designs. Before performing an RCT, there must exist a state of clinical equipoise, a sufficient number of eligible patients must be available, and the epidemiology of the disorder in question must be well studied. There are many challenges to performing high-quality RCTs. Studying multiple element support strategies in the critically ill patient population is more complex than studying a single drug therapy. High patient and practice variability and hazy diagnostic definitions can dilute the signal-to-noise ratio. Most interventions in critical care are expected to have a modest or small effect. This markedly increases the requisite sample size. There is a paucity of accepted clinically important measurements of the outcome of critical care, making mortality a common outcome to evaluate with a not-so-common incidence. Developmental issues, the inability to give informed consent, and the failure to perform the appropriate pharmacokinetic and safety studies are additional challenges facing pediatric investigators. Despite these limitations, a good RCT remains the best way to prove that an intervention is working or not. Indeed, RCTs are and will remain the "gold standard" method to estimate the efficacy of a therapeutic or prophylactic intervention.
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Pediatr Crit Care Me · Apr 2002
Failed extubation after cardiac surgery in young children: Prevalence, pathogenesis, and risk factors.
A total of 212 children =36 months of age underwent 230 congenital heart operations. Eleven children (5.2%) died perioperatively. After excluding patients who died, there were 219 surgeries among 202 patients; 25.9% (51 of 197), 51.8% (102 of 197), and 72.6% (143 of 197) of patients were successfully extubated by 12, 24, and 48 hrs, respectively. There were 22 cases in which an initial attempt at extubation failed at a median of 67.8 hrs (range, 2.4-335.5 hrs). Five patients failed a subsequent attempt at extubation at a median of 189.5 hrs (range, 115.8-602.5 hrs). The most common causes of initial FE were cardiac dysfunction (n = 6), lung disease (n = 6), and airway edema (n = 3). Risk factors for FE included pulmonary hypertension (EOR, 38.7; 95% CI, 2.9-25.8; p <.001), Down syndrome (EOR, 4.6; 95% CI, 1.8-11.8; p =.002), and deep hypothermic circulatory arrest (EOR, 4.5; 95% CI, 1.3-17.5; p =.018). All were independent predictors of FE (area under the curve, 0.837). The strongest predictor was pulmonary hypertension, which when used alone to predict FE provided a sensitivity of 0.83 (95% CI, 0.59-0.94) and a specificity of 0.75 (95% CI, 0.68-0.80). ⋯ Extubation fails after approximately 10% of congenital heart surgery in young patients. Causes of FE are diverse. In our population, preoperative pulmonary hypertension, presence of a congenital syndrome, and intraoperative circulatory arrest are risk factors for FE. Prospective validation of our predictive model with larger numbers and at multiple institutions would improve its utility.