Assessment of pulmonary function in the early phase of ARDS in pediatric patients.

Scant data are available on lung function in acute respiratory distress syndrome (ARDS) in pediatric patients. We measured respiratory mechanics by single-breath occlusion and maximum expiratory flow-volume curves by forced deflation in ten critically ill infants with clinical ARDS. Ten mechanically ventilated infants without lung disease served as the control group. To assess the severity of the lung injury in the infants with ARDS, we modified an adult scoring system that calculates a score (from 0 to 4; > 2.5 indicates severe lung injury) based on the extent of chest radiographic changes, degree of hypoxemia, amount of positive end-expiratory pressure (PEEP), and total respiratory system compliance. The lung injury scores of our patients were in the range of 2.75 to 3.75. The lung injury scores of the control group were zero. The predominant alteration in lung function was restrictive, as characterized by a significant decrease in total respiratory system compliance (0.41 +/- 0.13 ml/cmH2O/kg versus 1.12 +/- 0.16 ml/cmH2O/kg of controls; P < 0.001) and forced vital capacity (21.5 +/- 6.5 ml/kg versus 59.2 +/- 6.3 ml/kg of controls; P < 0.001). Maximum expiratory flow rates at 10% forced vital capacity were significantly increased (23.6 +/- 20.1 ml/kg/sec versus 8.4 +/- 2.5 ml/kg/sec of controls; P < 0.05), confirming the absence of any significant obstructive abnormalities. The passive expiratory flow-volume curves were curvilinear and convex in shape, indicating inhomogeneous lung pathology. The inhomogeneous distribution of lung injury in ARDS restricts the validity of respiratory mechanics measurements that rely on a single-compartment model. However, the forced deflation technique allows accurate spirometric assessments of the severity of restrictive (and obstructive) lung function changes in intubated infants with severe ARDS. Such measurements can be incorporated into lung injury scoring systems to classify the severity of the disease process for the purpose of outcome evaluation and to evaluate the effect of therapeutic interventions.

Flow limitation in anesthetized rhesus monkeys: a comparison of rapid thoracoabdominal compression and forced deflation techniques.

Rapid thoracoabdominal compression (RTC) and forced deflation (FD) allow the examination of maximal expiratory flow-volume (MEFV) curves in animals and human infants unable to generate a voluntary maximal expiratory maneuver. We compared flows generated by these two techniques and by constructing isovolume pressure-flow (IVPF) curves examined each method's potential to produce flow limitation. RTC and FD were performed in seven intubated rhesus monkeys from +40 cm H2O inspiratory pressure with deflation pressures ranging from -20 to -100 cm H2O and jacket pressures from +20 to +100 cm H2O (arms outside jacket). We also performed RTC maneuvers in all monkeys with the arms inside the jacket at +100 cm H2O jacket pressure. Maximal expiratory flows achieved by FD and RTC were analyzed at isovolume points. Both techniques produced flow limitation conditions over the last 25% of the MEFV curve. Individual IVPF curves generated by the two techniques demonstrated remarkable differences in shape and flow rates. Maximal transpulmonary pressures achieved with FD were higher than those with RTC in this experiment. Negative effort dependence was observed with higher deflation pressures in the majority of the monkeys. Flows achieved by RTC with the arms in were lower than those achieved with the arms out when compared at identical pressure gradients. We conclude that the difference in expiratory flow rates at isovolume-pressure points is most likely related to different effects on the behavior of intrapulmonary airways and choke point characteristics by the two techniques.

Validation of the phase angle technique as an objective measure of upper airway obstruction.

Thoraco-abdominal asynchrony (TAA) during upper airway obstruction (UAO) in small children can be documented by phase angle analysis of the Lissajous figure from the output of a noncalibrated respiratory inductance plethysmograph. Phase angle measurements have not been related to levels of inspiratory resistance, nor to the effect of breathing a 79% helium-21% oxygen mixture (heliox) during inspiratory resistance. We examined the effects of graded inspiratory loading (5-1000 cm H2O/L/sec) on TAA as measured by phase angle in 10 male, anesthetized, and intubated Rhesus monkeys, breathing room air and heliox. Phase angles increased with inspiratory loading from a baseline value of 22 +/- 3 degrees to 165 +/- 8 degrees at 1,000 cm H2O/L/sec resistance and correlated significantly with the level of inspiratory loading (r = 0.82). End-tidal carbon dioxide PETCO2 increased from 39 +/- 1 to 49 +/- 3 mm Hg at the highest load, but correlated only weakly with phase angle measurements (r = 0.60) and the level of inspiratory loading (r = 0.56). By changing to heliox breathing at the highest tolerated resistance, PETCO2 dropped significantly from 49 +/- 3 to 40.5 +/- 4 mmHg (P < 0.001) with no significant change in phase angles: 169 +/- 13 degrees and 165 +/- 8 degrees, respectively (P > 0.05). We conclude that heliox therapy for acute alveolar hypoventilation during UAO improves ventilation, but does not decrease TAA at high inspiratory resistance. Continuous monitoring of the relative changes in phase angles is useful to observe the severity of UAO in the early stages.(ABSTRACT TRUNCATED AT 250 WORDS)

Cuffed endotracheal tubes in pediatric intensive care.

We prospectively studied 282 consecutive tracheal intubations (243 patients) in a pediatric intensive care unit during a 7-month period to compare cuffed and uncuffed endotracheal tube (ETT) utilization and outcome. The incidence of postextubation stridor in each ETT group was the major outcome measure after controlling for various patient risk factors. Patients whose ETTs were inserted in the operating room, who were less than 1 year of age, or who had ETTs in place for less than 72 hours were more likely to have had insertion of an uncuffed ETT. Patients whose ETTs were inserted in the emergency department or who were more than 5 years of age were more likely to have had insertion of a cuffed ETT. Those who had a cuffed ETT were older (mean 8.1 vs 2.5 years) and had ETTs in place longer (mean 6.1 vs 3.7 days) than patients with an uncuffed ETT. Of the 188 patients who subsequently had removal of their ETTs, the overall incidence of postextubation stridor was 14.9%, with no significant difference between the two ETT groups even after controlling for patient age, duration of intubation, trauma, leak around ETT before extubation, and pediatric risk of mortality score. Two patients in the cuffed ETT group and four patients in the uncuffed ETT group required reintubation for severe postextubation stridor. Long-term follow-up identified 33 patients (17%) who required hospital readmission. None of these was admitted with an upper airway problem. Two patients who previously had insertion of a cuffed ETT subsequently received tracheostomies for the primary purpose of long-term mechanical ventilation unrelated to any problem with the upper airway. We conclude that cuffed endotracheal intubation is not associated with an increased risk of postextubation stridor or significant long-term sequelae.

Laryngotracheobronchitis as a complication of measles during an urban epidemic.

OBJECTIVE: To evaluate demographic and clinical correlates of laryngotracheobronchitis (LTB) as a complication of measles during a community-wide epidemic. DESIGN: Retrospective review of medical records. SETTING: Childrens Hospital Los Angeles, a large urban pediatric facility, during a regional epidemic of measles studied January through June 1990. PATIENTS: All patients identified at our hospital who met Centers for Disease Control criteria for measles. MEASUREMENTS AND RESULTS: Of 440 patients with measles, 82 also had LTB (18.6%). Patients in whom LTB developed were significantly younger (mean +/- SD: 14.7 +/- 8.2 months) than the cohort (24.8 +/- 30.1 months) (p less than 0.001) and more likely to require hospitalization (91.5%) than the cohort (44.3%) (p less than 0.001). Thirteen patients (17.3%) required intensive care, including 9 (11%) who required endotracheal intubation for a mean of 8.3 +/- 7.1 days. Pulmonary function testing of five patients with an endotracheal tube in place, including three not clinically assessed as having pneumonia, indicated the presence of concomitant lower respiratory tract disease. CONCLUSION: Laryngotracheobronchitis was a frequent and often severe complication of measles. The likelihood that LTB would develop was inversely related to age, generally required inpatient care, and necessitated endotracheal intubation in severely affected patients.

Dexamethasone in the prevention of postextubation stridor in children.

To assess whether there is any advantage in the use of corticosteroid to prevent postextubation stridor in children, we conducted a prospective, randomized, double-blind trial of dexamethasone versus saline solution. The patients were evaluated and then randomly selected to receive either dexamethasone or saline solution according to a stratification based on risk factors for postextubation stridor: age, duration of intubation, upper airway trauma, circulatory compromise, and tracheitis. Dexamethasone, 0.5 mg/kg, was given every 6 hours for a total of six doses beginning 6 to 12 hours before and continuing after endotracheal extubation in a pediatric intensive care setting. There was no statistical difference in incidence of postextubation stridor in the two groups; 23 of 77 children in the placebo group and 16 of 76 in the dexamethasone group had stridor requiring therapy (p = 0.21). We conclude that the routine use of corticosteroids for the prevention of postextubation stridor during uncomplicated pediatric intensive care airway management is unwarranted.

Effect of positive end-expiratory pressure on respiratory compliance in children with acute respiratory failure.

We studied the effect of positive end-expiratory pressure (PEEP) on the compliance of the respiratory system (Crs) in 25 children (age, 3 weeks to 10 years) requiring mechanical ventilation. Functional residual capacity (FRC) measurements were performed at 2 cm H2O increments, from 0 to 18 cm H2O of PEEP, and the FRC values were regressed versus PEEP. Static Crs, Crs/kg, and specific compliance (Crs/FRC) were calculated for each PEEP level. When FRC normality was reached Crs/kg improved in 15/25 (60%) patients but decreased in 2/25 (8%). Overall, Crs/kg increased from a mean +/- SE of 0.94 +/- 0.09 to 1.35 +/- 0.13 mL/cm H2O/kg (P = 0.003) and Crs/FRC from a mean +/- SE of 0.067 +/- 0.006 to 0.077 +/- 0.007 mL/cm H2O/mL (P = 0.057). The maximum compliance (mean Max Crs/kg, 1.56 +/- 0.12 mL/cm H2O/kg, and mean Max Crs/FRC, 0.089 +/- 0.005 mL/cm H2O/mL) was significantly higher than the compliance at the clinically chosen PEEP level and the compliance at the PEEP that normalized FRC. Maximum compliance was achieved within 4 cm H2O of the PEEP that normalized FRC. In 14/25 (60%) of cases the PEEP at maximum compliance coincided with the PEEP that resulted in FRC normalization. We concluded that static respiratory compliance improves in most (but not all) children with acute respiratory failure when FRC is normalized. Static respiratory compliance reaches maximum levels at PEEP values that are close (but not equal) to those that result in FRC normalization. Thus, assessment of the effect of PEEP on compliance is required in individual patients.

An automated bedside method for measuring functional residual capacity by N2 washout in mechanically ventilated children.

Beside measurement of functional residual capacity (FRC) in ventilated children is impractical. Using a simple technique based on open circuit N2 washout, we measured FRC in ventilated children. The system was evaluated in the laboratory and in patients. Using a mechanical lung, the reproducibility of 200 studies over a range of 100-500 mL at each of four different flow rates (10 determinations at each level) was very high with a mean coefficient of variation of 2.3% (range 0.5-5.1%). Linearity of the integrated N2 signal for volumes of 100-500 mL washed out at different flow rates was excellent (range 7.4-17.9 L/min), r = 0.99. The mean difference between measured and preset mechanical lung volumes was 2.4% (range 0-4.6%). In vivo, reproducibility of six to 10 FRC determinations in each of 30 children gave a mean coefficient of variation of 2.7%. Comparison to the conventional Douglas bag collection method showed a high correlation (r = 0.97). We conclude that this is an easy, highly reproducible, and accurate method for FRC determination suitable to ventilated infants and children.

Functional residual capacity in ventilated infants and children.

Positive end expiratory pressure (PEEP) is an accepted treatment for children with acute respiratory failure secondary to restrictive lung diseases. Using a simple technique based on open circuit nitrogen washout, we determined the functional residual capacity (FRC) in 25 ventilated children (age 3 wk-10 y) with acute respiratory failure secondary to restrictive lung disease (pulmonary edema, bilateral pneumonia). FRC measured at a physiologic level of PEEP (2-4 cm H2O) was 45.0 +/- 3.6% (mean +/- SEM; range 12-80%) lower than normal predicted values. At the PEEP level chosen clinically (4-10 cm H2O, mean = 6.0), the FRC was below normal predicted values for nonintubated children by a mean of 31.8% (range 0-73%) (p = 0.0001) and only seven patients (28%) had FRC within 20% below predicted normal values. FRC normalized at PEEP levels of 6-18 cm H2O (mean = 11.6), which was up to 200% above the clinically chosen PEEP level. In six children without lung disease who were ventilated at a PEEP level of 2-4 cm H2O, the FRC was within normal range in two, but significantly higher (by 45%) in the other four. We conclude that FRC in ventilated children with acute restrictive lung disease is significantly lower than normal and the clinically chosen PEEP fails to normalize the FRC in most of the cases.

Thoracoabdominal asynchrony in acute upper airway obstruction in small children.

The assessment of the severity and response to therapy of acute upper airway obstruction (UAO) in small children relies on subjective parameters. Using a noncalibrated respiratory inductance plethysmograph (RIP), we quantitated the rib cage (RC) to abdominal (AB) asynchrony and the lag phase in chest wall expansion by the phase angle from the RC versus AB signal curve. Phase angles were obtained in 17 children aged 1 to 50 months with acute UAO and 30 normal control subjects. The phase angle in UAO (16 to 165 degrees; mean = 83.6 degrees) was significantly higher than in control subjects (3 to 25 degrees; mean = 11.5 degrees), p less than 0.001. Following 29 episodes of inhalation treatment with 0.03 ml/kg of racemic epinephrine, the phase angle in the UAO group decreased to 7 to 160 degrees (mean = 38.3; p = 0.001) as the shape of the RC versus AB loop became narrower. In response to the treatment, the clinical severity of UAO decreased and the tidal breathing flow-volume loop improved. A high association was observed between the phase angle and the degree of stridor (p less than 0.005 Fisher's exact test), and in 90% (26 of 29) the changes in the phase angle and in the degree of stridor were in agreement. We conclude that the RC-AB asynchrony in acute UAO can be objectively quantitated by phase-angle measurement from a noncalibrated RIP and is thus suitable for use in infants and small children. The phase angle may be used to assess objectively the response of UAO to therapy.