Exercise capacity of children with pediatric lung disease.

BACKGROUND: Pulmonary function of children with cystic fibrosis (CF) and bronchopulmonary dysplasia (BPD) is similar at rest even though the mechanisms of injury differ. We sought to compare the peak exercise responses in children with BPD versus CF while controlling for pulmonary impairment, nutritional status, gender, age, height, and predicted forced expired volume in 1 second (approximately 73% of predicted). METHODS: Nine BPD children and 9 CF children underwent spirometry and a progressive exercise test to maximum on a cycle ergometer. RESULTS: There was no difference between groups in body mass percentile (CF:97 +/- 13%, BPD: 98 +/- 11%), peak power output (Wpeak) (CF:67 +/- 19 W, BPD:73 +/- 28 W), % predicted Wpeak (CF:83 +/- 28%, BPD:88 +/- 15%), peak oxygen uptake (VO2peak, CF: 38 +/- 7 ml/kg/min, BPD: 39 +/-6 ml/kg/min), or % predicted VO2peak (CF:99 +/- 16 %, BPD:96 +/- 27%). CONCLUSIONS: Children with mild pulmonary impairments are able to achieve a near normal peak power output and a normal VO2peak. Neither the aetiology nor the developmental onset of the process appears to be important influences on VO2peak or Wpeak.

Long-term pulmonary sequelae of severe bronchopulmonary dysplasia.

OBJECTIVE: To evaluate the long-term pulmonary sequelae of survivors of bronchopulmonary dysplasia (BPD) of sufficient severity to have required supplemental oxygen for at least 1 month after term. STUDY DESIGN: Fifteen patients with a mean age of 1.1 years were matched to preterm infants of similar gestational age and age at time of study. Pulmonary function testing included spirometry, plethysmographic lung volumes, carbon monoxide diffusion capacity, and in 9 of 15 subjects with BPD, measurement of lung static elastic recoil pressures. RESULTS: The subjects with BPD had a mean expiratory volume in 1 second (FEV1) of 64% +/- 21% predicted (4 had an FEV1 < 50% predicted) compared with 85% +/- 11% (P < .01) for the preterm children in the control group. Subjects with BPD had a significant degree of gas trapping with a residual volume to total lung capacity ratio of 37% +/- 13% compared with 25% +/- 4% for the control group (P < .01). An inverse relationship was seen between the FEV1 and the time on supplemental oxygen (r = -0.84, P < .0001), with 3 of the 4 children whose FEV1 was < 50% requiring oxygen for more than 900 days. Those with the greatest degree of airflow limitation and gas trapping had the greatest abnormalities in both shape and position of the pressure volume curves of the lung. CONCLUSION: Severe BPD may result in moderate to severe long-term abnormalities in pulmonary function tests.

Exercise ability in survivors of severe bronchopulmonary dysplasia.

There is limited information concerning the exercise performance of long-term survivors of bronchopulmonary dysplasia (BPD), and much of what is available pertains to those with relatively mild disease. The present study was undertaken to describe exercise responses in patients with a history of severe BPD, defined as those patients with a clinical and radiographic diagnosis of BPD who required supplemental oxygen at least until they were 44 wk postconceptual age and who were discharged home on oxygen. Fifteen children with a history of severe BPD were matched for gestational age with 15 children who had previously had respiratory distress syndrome but who did not develop BPD (Prem). These Prem control children were subsequently compared with 13 healthy control children born at term (Control) who were of similar postnatal age. Participants underwent pulmonary function testing, progressive exercise testing on a cycle ergometer, and a steady-state exercise test with cardiac output determined by CO2-rebreathing. Despite the patients with BPD having a lower FEV1 than those in the Prem group, who had lower values than the Control group (BPD, 64 +/- 21%; Prem, 85 +/- 11%; Control, 95 +/- 8%), the exercise capacity did not differ between the BPD and the Prem and between the Prem and the Control groups (BPD, 84 +/- 15%; Prem, 81 +/- 17%; Control, 91 +/- 12%). However, the BPD patients used a greater percentage of their ventilatory reserve (VEmax/40 FEV1: BPD, 93 +/- 20%; Prem, 67 +/- 12%; Control, 59 +/- 13%). Of the four patients with BPD who had significant oxygen desaturation with exercise, three had the lowest values for FEV1. Cardiac output was appropriate for oxygen consumption in most patients.

Estimation of mixed venous PCO2 for determination of cardiac output in children.

STUDY OBJECTIVES: Cardiac output (Q) can be estimated noninvasively during exercise by employing CO2-rebreathing techniques (equilibrium and exponential) to estimate the oxygenated mixed venous PCO2 (PvCO2). It has been found in adults and children that the equilibrium method underestimates Q as a result of overestimation of PvCO2, unless PvCO2 is "downstream corrected." In adults, it has been found that the exponential method does not require downstream correction and yields values similar to those obtained by the equilibrium method with downstream correction. The objectives of this study were as follows: to test whether the exponential method gives similar results to the equilibrium method with downstream correction in children; to verify that downstream correction is required in children; and to test whether a single equation could be used in adults and children to predict Q from oxygen consumption (VO2). DESIGN: Descriptive. SETTING: Exercise laboratory of a university hospital. PARTICIPANTS: 23 children (16 boys, 7 girls) with a mean age of 11.0 +/- 1.9 years (7.1 to 13.9 years), and 12 adults (7 men, 5 women) with a mean age of 33.6 +/- 7.2 years (24 to 48 years). INTERVENTIONS: While performing steady-state exercise on an ergometer, PvCO2 was determined in 14 children using both the equilibrium and exponential methods, and in all other subjects using the equilibrium method alone. MEASUREMENTS AND RESULTS: For the 14 children who underwent testing by both the equilibrium and exponential methods, the uncorrected equilibrium PvCO2 was significantly different from both the corrected PvCO2 and the exponential PvCO2. We found a strong relationship between Q (L/min), calculated using the downstream corrected values of PvCO2, and VO2 (L/min) (r2 = 0.95), and this relationship was similar to that obtained by dye dilution in other studies. When weight was included, it was determined that one equation could be used for children and adults: Q (L/min) = 1.42 + 5.80.VO2 (L/min) + 0.06.wt (kg), r2 = 0.97, SEY = 0.67. CONCLUSIONS: CO2-rebreathing techniques can be used to determine Q in children; the exponential method gives values that are similar to the equilibrium method with the downstream correction; and one prediction can be used for Q in adults and children.

Cardiorespiratory sleep studies for children can often be performed in the home.

We developed a portable recording system, suitable for unattended use in a patient's home, that quantitates the essential diagnostic elements of pediatric obstructive sleep apnea syndrome (OSAS): obstructive, mixed and central apneas and hyponeas; hemoglobin saturation, sleep vs. wakefulness; body and head positions; snoring: and sleep disturbance. The present paper reviews validation studies and summarizes two recent studies that demonstrate the unique advantages of performing clinical and research cardiorespiratory sleep studies in the child's home. Development of inexpensive, portable records that integrate audiovisual and physiologic information will make such home recordings more widely available.

Home testing for pediatric obstructive sleep apnea syndrome secondary to adenotonsillar hypertrophy.

The objective of this study was to determine the accuracy and practicality of home testing for pediatric obstructive sleep apnea syndrome (OSAS) secondary to adenotonsillar hypertrophy. Twenty-one children aged 2-12 years and referred for possible OSAS were studied twice, once at home and once in the sleep laboratory. The home test consisted of two parts: 1) a cardiorespiratory recording of saturation (SaO2), pulse rate, pulse waveform, electrocardiogram, and respiratory inductive plethysmography; and 2) an 8-hour videotape recording of the sleeping child. In the laboratory, standard nocturnal polysomnography including electroencephalography was performed. Experiences with another 62 children who underwent home testing alone were also reviewed and are reported. At home, saturation, respiratory, and video data were obtained 96.4 +/- 13.3% (mean +/- SD) 99.4 +/- 1.6%, and 90.0 +/- 78% of the time, respectively. The sleep efficiency was greater at home than in the laboratory, 91.1 +/- 3.9% vs. 86.1 +/- 7.2%, with a mean difference of 5.0% (P < 0.01). The median environmentally induced movement/arousal index was lower in the home than in the laboratory, 0.0 (inter-quartile range, 0.0-0.3 vs. 2.4/hr (inter-quartile range 1.2-4.2), with a median difference of 2.4/h (P < 0.001). Study duration, apnea/hypopnea index, desaturation index, respiratory and spontaneous movement/arousal indices, and oxygen saturation during sleep were similar for home and laboratory studies. Although neither sleep state nor PCO2 (transcutaneous or end-tidal) was measured in the home, this information would have modified patient management in, at most, one case. In the second group of 62 children, exclusively studied at home, all studies were successfully recorded despite a wide range of sleep efficiencies, apnea/hypopnea indices, and desaturation indices. We conclude that home testing, using a simplified cardiorespiratory montage plus video recording, is accurate and of practical use in the routine evaluation of OSAS in patients with adenotonsillar hypertrophy.