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Biomedical subjects

M G Morris

Publications and source records attributed to M G Morris.

9 recordsLinked to original sources

The bias flow nitrogen washout technique for measuring the functional residual capacity in infants. ERS/ATS Task Force on Standards for Infant Respiratory Function Testing.

The functional residual capacity (FRC) is the most commonly measured static lung volume in infants. It is important for interpreting volume-dependent pulmonary mechanics, e.g. airway resistance, and defining normal lung growth. The bias flow nitrogen washout technique is widely used for measuring FRC because the dead space and circuit resistance are low, making it suitable for small or sick infants. Moreover, data acquisition and calculation are easily programmed for a personal computer. The aim of this paper is to provide recommendations pertaining to equipment requirements, study procedures and reporting of data for functional residual capacity measurements. While measuring the functional residual capacity is regarded as physiologically and clinically important, the accuracy of the measurement is undoubtedly equally important. Hence, the paper also emphasizes factors influencing the accuracy of functional residual capacity measurements independent of equipment requirements. These recommendations represent the "State of the Art" in 2000.

Clinical Protocols↗

High fever after flexible bronchoscopy and bronchoalveolar lavage in noncritically ill immunocompetent children.

Flexible bronchoscopy (FB) and bronchoalveolar lavage (BAL) have been applied increasingly to the evaluation of pulmonary disease in children. Although several complications have been reported following FB and BAL, high fever after BAL in immunocompetent children has not previously been reported. To determine the frequency, clinical characteristics, and outcome of these complications in children who developed high fever post-BAL, we retrospectively reviewed all bronchoscopic procedures done on an outpatient basis between August 1995 and July 1997. We identified 78 immunocompetent noncritically ill children who had undergone FB and BAL as an outpatient procedure for evaluation of underlying pulmonary disease, of whom 13 (17%) developed temperature (T) higher than or equal to 39 degrees C (fever group). The 13 patients in the fever group had a median age of 10 (range, 4-48) months and a reported T of 39.4 degrees C (39.1-40.6 degrees C) occurring 7.5 (4-12) hr after BAL. To determine if there were differences in clinical or BAL fluid (BALF) characteristics, we compared each child in the fever group to two children in the nonfever group, based upon primary indications and age. There were no differences in demographic or clinical characteristics between the two groups. Lymphocyte concentrations in BALF were significantly reduced in the fever group (P = 0.03). An abnormal BALF cell differential (defined as one or more of the following: neutrophils >10%, lymphocytes >30%, or eosinophils >1%) was significantly more common in the fever group (P = 0.008, odds ratio 3.6). We conclude that high fever is a frequent adverse event following BAL in noncritically ill immunocompetent children with underlying pulmonary disease. Pre-BAL clinical characteristics are not associated with development of high fever. However, the finding of an abnormal BALF cell differential is strongly associated with development of high fever post-BAL.

Bronchoalveolar Lavage↗

A novel non-invasive technique for measuring the residual lung volume by nitrogen washout with rapid thoracoabdominal compression in infants.

BACKGROUND: The functional residual capacity (FRC), the only lung volume to be routinely measured in infants, is an unreliable volume landmark. In addition to FRC, the residual volume (RV) was measured by nitrogen washout using rapid thoracoabdominal compression (RTC) in nine infants with cystic fibrosis aged 5-31 months. METHODS: A commercial system for nitrogen washout to measure lung volumes and a custom made system to perform RTC were used. Lung volume was raised to an airway opening pressure of 30 cm H(2)O (V(30)). RTC was performed from V(30). The jacket pressure (Pj; 65-92 cm H(2)O) which generated the highest forced expiratory volume (mean 40.2 ml/kg; 95% confidence interval (CI) 33.03 to 47.33) was used during the RV manoeuvre. The infants were manually hyperventilated to inhibit the respiratory drive briefly. RTC was initiated during the last passive expiration. RV was estimated by measuring the volume of nitrogen expired after end forced expiratory switching of the inspired gas from room air to 100% oxygen while jacket inflation was maintained at the time of switching into oxygen during the post-expiratory pause. RESULTS: In each infant RV and FRC measurements were reproducible and did not overlap; the difference between mean values, which is the expiratory reserve volume, was statistically significant (p<0.05). Mean RV was 21.3 (95% CI 18.7 to 24.0), FRC was 25.5 (95% CI 22.8 to 28.1), and TLC(30) (total lung capacity at V(30)) was 61.5 (95% CI 54.4 to 68.7) ml/kg. These values were dependent on body length, weight and age. When measuring RV the period between switching to oxygen and the end of the Pj plateau was 0.301 (95% CI 0.211 to 0.391) s. The washout duration was longer for RV than for FRC measurement (80.9 s (95% CI 71.3 to 90.4) versus 72. 4 s (95% CI 64.9 to 79.8)) (p<0.001). CONCLUSIONS: A new non-invasive and reliable technique for routine measurement of RV in infants is presented.

Child, Preschool↗

The open circuit nitrogen washout technique for measuring the lung volume in infants: methodological aspects.

BACKGROUND: Lung volume measurement by nitrogen washout is widely used in infants, though a lack of accuracy and changes of calibration over time have been reported. The potential sources of error were explored in order to increase the accuracy and reliability of the technique. METHODS: A commercial system for nitrogen washout and a 0.5 litre calibrating syringe as a lung model were used to perform over 2000 in vitro washouts, including simulated rapid breathing, shallow breathing, periodic breathing, sighs, and brief apnoeas. A constant 10 l/min bias flow of oxygen and extended equipment warming times were employed. A collapsible breathing bag was incorporated into the washout circuit. Following a single two point calibration, known air volumes from 42 ml to 492 ml were measured by nitrogen washout over a 14 hour period. The flow waveform in the nitrogen mixing chamber during a washout in vitro, with and without the breathing bag in the circuit, was also studied. RESULTS: The mean coefficient of variation of all volumes was 0.66%. The mean difference between measured and known volumes was 0.30 ml (95% confidence interval (CI) -0.18 to 0.79). This difference was not statistically significant (p = 0.22). The mean percentage error was -0.1% (range -0.47% to 0.46%). Nitrogen calibration remained stable for 14 hours. Without the breathing bag flow transients were frequent in the mixing chamber during in vitro washout. CONCLUSIONS: This technique increases the accuracy in vitro and the precision in vivo of volume measurement by nitrogen washout. Sources of potential errors including baseline drifting and inadequate equipment warming times were identified. The breathing bag acted as a buffer reservoir, preventing large swings in flows within the nitrogen mixing chamber during washouts, and should be an integral component of the nitrogen washout circuit.

Breath Tests↗

A simple new technique to measure the effective dead space of the face mask with a water volumeter in infants.

Measuring the effective dead space (EDS) of a face mask has been difficult in infants and the appropriate volume being deducted from lung volume measurements has varied between laboratories. This study measured EDS in 16 infants (age range, 5-36 months) who have cystic fibrosis, undergoing lung volume measurement by N2 washout. A thin plastic bladder, whose neck resided in the mask port, was shaped to fill a size 1 clear face mask. A water volumeter was made by inserting the body of a 20 mL plastic syringe into the neck of the bladder forming a tight seal with a snug fit against the inner surface of the mask port. The mask was placed on a horizontal surface and water was added until a level appeared in the syringe body (V1). At end-inspiration, the mask was briefly placed on the mouth and nose of the sleeping infant, causing the water level to rise in the syringe body (V2). The actual total dead space (V) of the mask when connected to the mouth port of the slide valve was 23 mL. EDS = V- (V2 - V1). Mean (95% confidence interval (95%CI)) EDS was 12.4 (95% CI 11.2, 13.6) mL. The smallest EDS was 8 mL since the connected ports (dead space, 8 mL) were unlikely to be penetrated by the infant's nose or lips. EDS decreased with increasing body weight and height, but seemed to be influenced by individual facial features too. In conclusion, a reliable noninvasive volumetric technique for the routine measurement of the effective dead space in infants has been developed.

Cystic Fibrosis↗

Hemodynamic characteristics of patients with hypothermia due to occult infection and other causes.

Eighty-five consecutive patients with hypothermia were prospectively evaluated to assess clinical and laboratory data that would differentiate those patients with hypothermia caused by severe infection and bacteremia and those with hypothermia of other causes. Thirty-two patients had hemodynamic monitoring, allowing us to assess hemodynamic differences between the two groups. Clinical characteristics, including admission temperature, leukocyte count, mean arterial pressure, pulse rate, respiratory rate, arterial pH, and pulmonary capillary wedge pressure, did not distinguish between the two groups. However, patients with infection with bacteremia had lower calculated systemic vascular resistances (486.0 +/- 125.0 compared with 1759.9 +/- 331.0 dynes.s.cm-5; p = 0.001) and higher cardiac indices (7.1 +/- 1.9 compared with 2.8 +/- 0.7 L/min X M2; p = 0.006) than patients without severe infections. Thus, our data suggest that hemodynamic characteristics are different in patients with infection-related hypothermia and patients with hypothermia associated with other causes, and appear to depend on the underlying disease.

Adult↗