Bronchodilation in infants with malacia or recurrent wheeze.

BACKGROUND: Controversy remains regarding the effectiveness of bronchodilators in wheezy infants. AIMS: To assess the effect of inhaled beta(2) agonists on lung function in infants with malacia or recurrent wheeze, and to determine whether a negative effect of beta(2) agonists on forced expiratory flow (V'(maxFRC)) is more pronounced in infants with airway malacia, compared to infants with wheeze. METHODS: We retrospectively analysed lung function data of 27 infants: eight with malacia, 19 with recurrent wheeze. Mean (SD) age was 51 (18) weeks. Mean V'(maxFRC) (in Z score) was assessed before and after inhalation of beta(2) agonists. RESULTS: Baseline V'(maxFRC) was below reference values for both groups. Following inhalation of beta(2) agonists the mean (95% CI) change in mean V'(maxFRC) in Z scores was -0.10 (-0.26 to 0.05) and -0.33 (-0.55 to -0.11) for the malacia and wheeze group, respectively. CONCLUSIONS: In infants with wheeze, inhaled beta(2) agonists caused a significant reduction in mean V'(maxFRC). Infants with malacia were not more likely to worsen after beta(2) agonists than were infants with recurrent wheeze.

Exhaled nitric oxide measurements with dynamic flow restriction in children aged 4-8 yrs.

Fractional exhaled nitric oxide concentration (FENO) depends on exhalation flow; however, children often are unable to perform controlled flow procedures. Therefore, a device was developed for off-line FENO sampling, with dynamic flow restriction (DFR). The authors compared off-line with on-line FENO, assessed feasibility, and obtained normal values for FENO in children aged 4-8 yrs. Subjects inhaled nitric oxide (NO)-free air and exhaled into the device, where DFR kept exhalation flow constant at 50 mL x s(-1). Dead space air was discarded. Exhaled air was collected in a 150 mL mylar balloon. On-line measurements were performed and values compared with off-line FENO in 19 adult volunteers. Seventy-nine children performed off-line sampling. All samples were analysed with a chemiluminescence NO-analyser. Normal values were obtained in 34 healthy children. There was an excellent correlation between on- and off-line values. Bland and Altman plots showed good agreement between on- and off-line FENO. Seventy-four out of 79 children were able to perform a correct off-line procedure. Geometric mean+/-SEM FENO in healthy children was 4.9+/-1.2 parts per billion (ppb) for male children and 7.6+/-1.1 ppb for female children. It can be concluded that off-line fraction of exhaled nitric oxide measurements with dynamic flow restriction are feasible in young children and correspond to on-line values.

Noninvasive monitoring of nonshunted pulmonary capillary blood flow in the acute respiratory distress syndrome.

OBJECTIVE: Noninvasive monitoring of nonshunted pulmonary capillary blood flow, using the alveolar amplitude response technique (AART) in a porcine model of the acute respiratory distress syndrome. DESIGN: Experimental animal study. SETTING: University center for animal experiments. INTERVENTIONS: In 12 mechanically ventilated pigs, the nonshunted pulmonary capillary blood flow was varied by means of lung lavages and the application of positive end-expiratory pressure. MEASUREMENTS AND MAIN RESULTS: Nonshunted pulmonary capillary blood flow was determined by AART. Cardiac output (determined by the thermodilution method) corrected for venous admixture was used for comparison (r2 varied between .58 and .94; p < .01). The trend in the development of nonshunted pulmonary capillary blood flow as measured with AART was in agreement with the trend detected by cardiac output corrected for venous admixture in 92% of all events. CONCLUSIONS: We conclude that AART can be used to monitor changes in nonshunted pulmonary capillary blood flow in cases of acute respiratory distress syndrome noninvasively and continuously.

Aerosol delivery from spacers in wheezy infants: a daily life study.

The aims of this study were to assess and compare dose delivery and dose variability of pressurized metered dose inhalers (pMDI)/spacers in wheezy infants in daily life and to investigate factors influencing aerosol delivery. In an open randomized crossover study in 25 wheezy infants aged 5-26 months, a metal spacer (Nebuchamber), a detergent coated (DC) and a non-detergent coated (nonDC) plastic spacer (Babyhaler) were tested at home for 7 days each. Budesonide (200 microg b.i.d) was administered via a Nebuchamber or fluticasone (125 microg b.i.d) via a Babyhaler. Aerosol was trapped in filters, positioned between the spacer and face mask. Cooperation was scored on diary cards. Electrostatic charge (ESC) of the spacers was measured. Evaluations of the administration technique were made from video recordings. Median (range) dose delivery of the filters expressed as per cent (%) of nominal dose, was 34% (3-59), 23% (1-49), and 41% (12-55) for the Nebuchamber, nonDC-Babyhaler, and DC-Babyhaler respectively. Considerable dose variability was found, median (range) within-subject dose variability, expressed as coefficient of variation, for the Nebuchamber (49% (15-249)) was significantly higher when compared with both nonDC- (36% (12-325)) and DC-Babyhalers (27% (10-122)), for which dose variabilities were similar. Detergent coating was effective to reduce electrostatic charge, and to increase dose delivery, but had no effect on dose variability. Bad cooperation was an important cause for high dose variability for all spacers (r=0.5-0.6, p<0.02). Many mistakes were made during the administration procedure.

Tendon displacement assessment by pulsed Doppler tissue imaging: validation with a reciprocating string test target.

After hand trauma and surgery, assessment of tendon excursion is important in reconstructive surgery and rehabilitation. Aimed as a more reliable alternative to traditional noninvasive methods, a colour Doppler imaging scanner was adapted to measure longitudinal tendon displacement. Displacement was quantified by integrating the velocity estimated from the zero-crossing rate of the Doppler signal. The system was tested by measuring displaced distances of a rubber string that was moved back and forth. At a determined optimal receiver gain, 1.5-cm string displacements were measured with less than +/- 0.05-cm bias throughout an echo-signal dynamic range of 22 dB; standard deviations were around 0.05 cm. Regression analysis between measured and true displacements in the range 0.5-2.5 cm resulted in a best fit straight line with slope 0.927, intercept 0.041 cm and residual standard error of 0.06 cm. A transfer technique was conceived to ensure accuracy when measuring tendons in the body. This CDI-based pulsed Doppler system merits verification for measurement of tendon excursion in patients.

Measurement of sacroiliac joint stiffness in peripartum pelvic pain patients with Doppler imaging of vibrations (DIV).

OBJECTIVES: The research question of the present study was: are sacroiliac joint stiffness levels of peripartum pelvic pain patients different from those of healthy subjects? STUDY DESIGN: A cross-sectional comparative sacroiliac joint stiffness analysis of peripartum pelvic pain patients with healthy subjects. In previous studies we introduced a new technique, Doppler imaging of vibrations (DIV), to assess sacroiliac joint stiffness using colour Doppler imaging and vibrations. The measurements were performed on a group of peripartum pelvic pain patients (n=56) and on a control group (n=52). The differences in sacroiliac joint stiffness between the patient group and the control group were tested statistically by means of the Wilcoxon's two sample test, the chi-square test and Student's t-tests. RESULTS: Both patients and controls displayed stiff as well as unstiff joints with no significant difference. There was a significant difference between the groups with regard to the relative difference of sacroiliac joint stiffness between left and right. CONCLUSIONS: A diagnostic tool which can possibly be developed in the future could demonstrate an objective finding among women with peripartum pelvic pain. DIV is easy to apply and non-invasive. Asymmetric stiffness of the sacroiliac joints seems to be more directly related to low back pain and pelvic pain, not the stiffness level of a single sacroiliac joint.

Tendon excursion measurements with colour Doppler imaging.

We assessed the applicability of tendon excursion measurement by means of Colour Doppler Imaging (CDI) on human specimens, and also assessed the correlation between values measured by Doppler and by displacement meters. Muscles were separately connected to a mass of 1 kg with a steel wire running over a pulley. This weight moved the telescopic end of a digital displacement meter up and down during passive extension and flexion of the fingers. Excursion was measured with a pulsed multi-channel CDI scanner on the same arm. Assessment of finger tendon excursion with CDI correlated well with the mechanical micro displacement meter, the latter being considered the most accurate method in cadaver studies.

A novel method of evaluation of three heat-moisture exchangers in six different ventilator settings.

OBJECTIVE: The purpose of this study was to assess and compare the humidification, heating, and resistance properties of three commercially available heat-moisture exchangers (HMEs). To mimic clinical conditions, a previously validated, new, realistic experimental set-up and measurement protocol was used. DESIGN: Prospective, comparative experimental study. SETTING: Surgical Intensive Care Unit, University Hospital of Rotterdam. MATERIALS: An experimental set-up consisting of a patient model, measurement systems, and ventilator and three different HME types. INTERVENTIONS: The air flow, pressure in the ventilation circuit, pressure difference over the HME, and partial water vapour pressure and temperature at each side of the HMEs were measured. Measurements were repeated every 30 min during the first 2 h and every hour up to 24 h for each HME at six different ventilator settings. The mean inspiratory and maximum expiratory resistance, flow-weighted mean absolute humidity and temperature outputs, and humidification and heating efficiencies of HMEs were calculated. MEASUREMENTS AND RESULTS: The Dar Hygroster had the highest humidity output, temperature output, humidification efficiency, and heating efficiency values throughout the study (32.8 +/- 21. mg/l, 32.2 +/- 0.8 degrees C, 86.3 +/- 2.3%, and 0.9 +/- 0.01%, respectively) in comparison to the Humid-Vent Filter (25.3 +/- 3.2 mg/l, 31.9 +/- 0.8 degrees C, 72.2 +/- 5.3%, 0.9 +/- 0.02%, respectively) and the Pall Ultipor BB100 breathing circuit filter (23.4 +/- 3 mg/l, 28.3 +/- 0.7 degrees C, 68.8 +/- 5.9%, 0.8 +/- 0.02%, respectively). The inspiratory and expiratory resistance of the HMEs remained below clinically acceptable maximum values (2.60 +/- 0.04 and 2.45 +/- 0.05 cmH2O/l per s, respectively). CONCLUSION: The Dar Hygroster filter was found to have the highest humidity and temperature output of all three HMEs, the Humid-Vent filter had a satisfactory humidity output only at low tidal volume flow rate and minute volume settings, whereas the Pall Ultipore BB 100 never achieved a sufficient humidity and temperature output.

The micro-plethysmograph: a new device to measure small volume displacements by isolated human airway segments.

For the study of airway responsiveness in vitro, airway segments have important advances over strip or spiral preparations. The method to study isobaric contraction of segments is not well established. The aim of this work was to develop a model to assess the smooth muscle responses in isolated airway segments under isobaric conditions. We developed a microplethysmograph with a volume measurement range of 10 to 700 microL, a resolution of 0.02-0.4 microL, and a drift of 2.6-0.7% of measurement range min(-1) for its most and least sensitive setting, respectively. The plethysmograph is able to compensate for the pressure changes induced by the volume changes, enabling for true isobaric measurements. We show examples of the isobaric contraction and relaxation of isolated human airway segments after stimulation of an airway segment by methacholine, isoprenaline, or electrical field stimulation. Apart from studying airway responses, the micro-plethysmograph is potentially useful to study the contractile properties of watertight and hollow structures like blood vessels, gut, and ureter. In addition, this device can be used to measure leak or diffusion at any transmural pressure.

Measurement of tendon excursion velocity with colour Doppler imaging: a preliminary study on flexor pollicis longus muscle.

PURPOSE: To study the use of colour Doppler imaging (CDI) for the measurement of maximum and mean tendon velocity. Recent studies showed that CDI, normally used for blood flow examinations, can be used for the imaging of tendons at the hand and wrist region. Although other modalities are available for imaging of the muscle-skeletal system, in vivo measurements of the velocity of tendon excursion are not possible. METHODS: The flexor pollicis longus (FPL) tendon of 16 healthy volunteers was measured bilaterally at two levels (wrist and thenar). A splint from the fingers along the proximal lower arm was applied. The thumb was fixed to the splint from the the first phalanx to allow flexion of the interphalangeal (IP) joint only. Pulsed CDI was used for the measurements. The maximum and mean velocities of the FPL tendon were measured at spectrum display mode during continuous voluntary contractions. At least 10 sequential Doppler peaks (cm/s) were recorded at every trial. The measurements were repeated three times. Paired t-test and correlation coefficients were calculated between levels on the same side and the opposite side. RESULTS: No significant differences were found between two levels of the same hand and of the opposite hand. As expected, the data revealed variations in the inter-individual tendon velocities. CONCLUSIONS: The velocity of the excursion of the FPL tendon can be measured with CDI with good reproducibility. It is expected that velocity measurements can be used in the future for the assessment of other tendons affected by various disorders.

The use of color Doppler imaging for the assessment of sacroiliac joint stiffness: a study on embalmed human pelvises.

PURPOSE: The validity and reproducibility of an instrumented dynamic examination method to measure sacroiliac (SI) joint stiffness was tested in vitro. METHODS: Four embalmed human female pelvises were excitated by a pelvic vibrator. A color Doppler imaging (CDI) scanner was used to image the amplitude of vibrations at different sites of the pelvis. Vibrations were applied to the anterior superior iliac spines unilaterally and were received by CDI all over the ipsilateral SI region. Three different stability conditions were created in the SI joints: no intervention, screwed and ligaments cut. Test results were quantified by taking the minimum threshold levels of the bones. The relative difference of vibration intensity between ipsilateral ilium and sacrum at each stability condition is accepted as the stiffness level for the SI joint. RESULTS: Statistics showed high reproducibility and significant differences between the stability conditions. Dynamic testing based on the use of vibrations provides visible and quantifiable intra- and inter-individual differences between SI joint stiffnesses. CONCLUSIONS: This new method is objective and reproducible. Future in vivo application is promising since there are no technical and safety restrictions.

The measurements of sacroiliac joint stiffness with colour Doppler imaging: a study on healthy subjects.

RATIONALE AND OBJECTIVES: Primary peripartum pelvic and low back pain is a common complaint of females. The etiologic relation between pain and pelvic stability has been shown in previous studies, but at present there is no objective clinical testing method to evaluate pelvic stability. METHODS: In this study, a dynamic measurement method using sonoelasticity to assess the sacroiliac joint (SI) stiffness was tested in vivo in 14 healthy female volunteers. With the subjects in supine position vibrations were unilaterally applied to the anterior iliac spine. The vibrations were registered by a Colour Doppler Imaging (CDI) transducer over the ipsilateral SI joint. Since the threshold level of the apparatus has a direct relation with the power of the vibrations, the intensity of the vibrations (sonoelasticity) on the sacrum and ilium was measured indirectly in threshold units. The differences between the threshold values were accepted as the power loss of vibrations through the SI joint. One-way analysis of variance-test and T-test for paired samples were applied on the measurement results (P < 0.05). RESULTS: Statistically, the results showed a satisfactory intraindividual reproducibility and inter-individual variability. There was no significant difference between the data derived from the left SI joint and right SI joint. CONCLUSIONS: Based on the promising results on healthy female volunteers, this method will be specifically used in future studies on patients with peripartum pelvic pain.

An experimental set-up to test heat-moisture exchangers.

OBJECTIVES: The purpose of this study was to build an experimental set-up to assess continuously the humidification, heating and resistance properties of heat-moisture exchangers (HMEs) under clinical conditions. DESIGN: The experimental set-up consists of a patient model, measurement systems and a ventilator. SETTING: Surgical ICU, University Hospital of Rotterdam. MATERIALS: A clinically used HME. MEASUREMENTS AND RESULTS: The air flow, pressure in the ventilation circuit, pressure difference over the HME, and partial water vapour pressure and temperature at each side of the HME were measured. The resistance, absolute humidity, humidification efficiency and temperature difference at the patient side of the HME were calculated. Measurements were performed during 24 h. The temperature output, humidity output and lung mechanics of the patient model were similar to values found in mechanically ventilated patients. The measurement system was in agreement with the ISO draft standard and was capable of measuring dynamic variation of water and heat exchange over the range of a clinically used ventilator setting. CONCLUSION: The experimental set-up described is reliable for evaluating HMEs and can also be used for future clinical evaluation of HMEs. The main advantages of this set-up over those described previously are: (i) measurements of dynamic variations of water and heat exchange; (ii) on-line measurements of expiratory, as well as inspiratory resistance.

A simple handheld push-button device for in situ calibration of pneumotachographs.

A simple and compact flow calibrator has been devised for generating precise predetermined constant flow rates for checking the calibration of laboratory and clinical flow transducers used in respiratory measurements. The standard version delivers preset flows of 0.5 and 1 l/s, whereas a tuned-up version can produce preset flows of 2.5 and 5 l/s, with an accuracy of +/- 2%. The pressure generated is sufficient to cope with most commonly used respiratory flowmeters. The flow calibrator is built from inexpensive components that are readily obtainable: a fan, a turbine flowmeter, and a feedback circuit in a compact housing. The device is easy to connect to other equipment and to operate. Three flow calibrators have been built and are in regular use in a lung function laboratory and on intensive care wards.

A simple device to inject indicator gas for wash-out tests during mechanical ventilation.

OBJECTIVE: To evaluate a simple device which injects a constant fraction of indicator gas to the inspiratory mixture for performing multi-breath wash-out tests during controlled ventilation. DESIGN: the technique in which the indicator gas is injected at the mouth of the patient (post-mix) is compared with the technique where the indicator gas is administered in the bellows of the ventilator (pre-mix). SETTING: Surgical Intensive Care Unit of a University Hospital. PATIENTS: 10 post-operative mechanically ventilated patients. INTERVENTIONS: None. MEASUREMENTS AND RESULTS: 3 wash-out tests with the post-mix and 3 wash-out tests with the pre-mix method were performed within an hour on every patient. The calculated mean end expiratory lung volume (EEV) was 1.91 +/- 0.871 with the post-mix technique and 1.89 +/- 0.881 with the pre-mix technique. There was a good agreement with a mean difference of -1.9 +/- 6.5% in the calculated EEV values by the two different techniques. CONCLUSION: The described injector is an affordable device, is easy to assemble and can be incorporated in most electronically regulated ventilators to perform multi-breath indicator gas wash-out tests for pulmonary monitoring at the bed side of ICU patients.

Design and validation of an indicator gas injector for multiple gas washout tests in mechanically ventilated patients.

A device to produce a stepwise indicator gas fraction variation to initiate a washout test in mechanically ventilated patients is described. The device, which can be used in conjunction with the commonly used Siemens-Elema series 900 ventilators, is based on simple, off-the-shelf technology. It features the simultaneous use of two indicator gases (so that the influence of diffusion processes in the gas exchange to the patient can be measured) and maintains a nearly constant FIO2 during a washout procedure. With this indicator gas injector, the transition time of the indicator gas fraction at the beginning of a washout proved to be short enough to detect ventilation inhomogeneity by visual inspection of the washout curves. Functional residual capacity measurements using this device are presented on a test lung with known volume, on healthy volunteers, and on critically ill patients.

Effective airway resistance: a reliable variable from body plethysmography.

Since the introduction of whole-body plethysmography in pulmonary function routines, airway resistance measurements by this method have been plagued by a side-effect of the ventilation process. Warming up and humidifying of inspired air and the cooling and condensation of expired air lead to a change in volume of the gas in the system and thus to a change in pressure in the body box which is superimposed on the regular box pressure. One generally applied solution is to compensate electronically for the disturbing pressure change. However, the required adjustment of the size of the compensating signal is difficult or impossible to obtain with patients who have obstructive lung diseases. In this paper we show that if no correction at all is applied the measurement error in the effective airway resistance remains relatively small. Moreover the magnitude of the error appears to depend on certain symmetrical and asymmetrical properties of the mouth flow curve. The maximum error in the effective resistance, as computed from a number of measured flow patterns, was found to be -18% for the normal persons and -9% for patients with obstructive lung diseases. We conclude that the uncorrected effective airway resistance is reasonably accurate. Alternatively, a good accuracy can be obtained with only a coarse adjustment of the correction circuit.

A calorimetric system for metabolic studies of newborn babies.

This paper describes a closed circuit calorimetric system designed to determine the amount of energy required for synthesis of new tissue in a newborn baby. This amount can be estimated from the difference between indirect and direct calorimetric measurements. The system allows the simultaneous measurement of oxygen consumption, carbon dioxide production, evaporative water loss and heat loss through convection and radiation in newborn babies under 2.5 kg bodyweight. The babies are exposed to a well defined climate, they can be observed continuously and are fed via a nasogastric tube during the experiment, which may last 24 h or more. Special features of the system are the compensation methods for O2 and CO2 measurements and the double gradient layer for the measurement of dry heat loss. The overall accuracy of the system is of the order of 0.1 W. The value obtained for the energy cost of growth is in close agreement with Hommes' theoretical estimate.

Design and validation of an automatic metabolic monitor.

A self-calibrating fully automatic instrument for the measurement of oxygen consumption, carbon dioxide production and the respiratory quotient of mechanically ventilated patients has been developed. The instrument is based on commercially available conventional oxygen and carbon dioxide gas analysers and a domestic natural gas volumetric flow meter. The distribution of the different gas flows, i.e. calibration gases, the inspiratory mixture sample and the expiratory mixture sample, are controlled by in inexpensive microprocessor, which also performs the necessary calculations. The accuracy of the instrument has been validated by bench tests. The present prototype has been in use for over 3000 h without major failures.

Indicator dilution theory for convective dispersion in laminar flow through straight tubes.

From an analysis of the dispersion of indicator in steady laminar fluid flow, expressions are derived for the determination of flow in a straight tube in circumstances in which the familiar Stewart-Hamilton relations for indicator dilution do not generally apply, namely when the method of detection of the tagged blood flow depends on the density of the indicator in the system, as with X-ray videodensitometry. The analysis assumes no diffusion of indicator, and is carried out for arbitrary profiles of fluid flow velocity and tube cross-section. Injections of finite width and finite duration are considered, whereby the indicator is distributed over the tube cross-section either uniformly or in proportion to velocity. Spatial resolution of the detector is considered. A new method is proposed to utilise a priori information when the type of flow is known beforehand. The application of the results is illustrated by several examples for cases with laminar flow. The study is theoretical and is intended only as a first step towards the measurement of blood flow in the human circulation.