Thermistors have been routinely used for the. Effects of Nasal Prongs on Nasal Airflow Resistance*

Similar documents
The diagnosis of obstructive sleep apnea syndrome. Combined Effects of a Nasal Dilator and Nasal Prongs on Nasal Airflow Resistance*

The main sites of nasal airflow resistance (NR) are

Snoring detection during auto-nasal continuous positive airway pressure

Comparison of Nasal Prong Pressure and Thermistor Measurements for Detecting Respiratory Events during Sleep

Nasal pressure recording in the diagnosis of sleep apnoea hypopnoea syndrome

F. Lofaso*, L. Heyer*, A. Leroy**, H. Lorino*, A. Harf*, D. Isabey*

CLINICIAN INFORMATION

CPAP titration by an auto-cpap device based on snoring detection: a clinical trial and economic considerations

Nasal obstruction as a risk factor for sleep apnoea syndrome

Articles. Obstructive Sleep Apnea and Oral Breathing in Patients Free of Nasal Obstruction

Physiological consequences of prolonged periods of flow limitation in patients with sleep apnea hypopnea syndrome

always been clearly established or compared with that of topical vasoconstrictors. Consequently, it nasal dilators.

Philip L. Smith, MD; Christopher P. O Donnell, PhD; Lawrence Allan, BS; and Alan R. Schwartz, MD

(To be filled by the treating physician)

Effect of two types of mandibular advancement splints on snoring and obstructive sleep apnoea

Patient Interface Fitting. Dave Henry RRT Respiratory Clinical Specialist

Heated Humidification or Face Mask To Prevent Upper Airway Dryness During Continuous Positive Airway Pressure Therapy*

ACCURACY OF NASAL CANNULA PRESSURE RECORDINGS FOR ASSESSMENT OF VENTILATION DURING SLEEP

A functional tool to differentiate nasal valve collapse from other causes of nasal obstruction: the FRIED test

Snoring, obstructive sleep apnea (OSA), and upper. impact of basic research on tomorrow. Snoring Imaging* Could Bernoulli Explain It All?

Noninvasive assessment of respiratory resistance in severe chronic respiratory patients with nasal CPAP

Alexandria Workshop on

Pharyngeal Critical Pressure in Patients with Obstructive Sleep Apnea Syndrome Clinical Implications

Detection of Increased Upper Airway Resistance During Overnight Polysomnography

Nasal airflow dynamics: mechanisms and responses associated with an external nasal dilator strip

Sniff nasal inspiratory pressure in patients with chronic obstructive pulmonary disease

Chronic NIV in heart failure patients: ASV, NIV and CPAP

Intelligent CPAP systems: clinical experience

Positive Pressure Therapy

Test Bench for Pressure Calibration of Continuous Positive Airway Pressure (CPAP) Device for Sleep Apnea Applications

NON INVASIVE LIFE SAVERS. Non Invasive Ventilation (NIV)

ROLE OF PRESSURE IN HIGH FLOW THERAPY

Role of different nocturnal monitorings in the evaluation of CPAP titration by autocpap devices

Tongue Protrusion Strength in Arousal State Is Predictive of the Airway Patency in Obstructive Sleep Apnea

NASAL CONTINUOUS POSITIVE AIRWAY PRESSURE FOR OBSTRUCTIVE SLEEP APNEA IN CHILDREN. Dr. Nguyễn Quỳnh Anh Department of Respiration 1

A Sleep Laboratory Evaluation of an Automatic Positive Airway Pressure System for Treatment of Obstructive Sleep Apnea

Patients commonly arouse from sleep and experience awake states.

Comparison of two in-laboratory titration methods to determine evective pressure levels in patients with obstructive sleep apnoea

Monitoring: gas exchange, poly(somno)graphy or device in-built software?

Hypoventilation? Obstructive Sleep Apnea? Different Tests, Different Treatment

PEDIATRIC OBSTRUCTIVE SLEEP APNEA (OSA)

Sleep-disordered breathing is a widespread disease 1. Breath-to-Breath Variability Correlates With Apnea-Hypopnea Index in Obstructive Sleep Apnea*

Let s explore and find what works!

PEDIATRIC PAP TITRATION PROTOCOL

DEVELOPMENT OF A CUSTOMIZED CPAP MASK USING REVERSE ENGINEERING AND ADDITIVE MANUFACTURING. Zhichao Ma*, Javier Munguia, Philip Hyde, Michael Drinnan

Effects of continuous positive airway pressure on nasal and pharyngeal symptoms in patients with obstructive sleep apnea*

CONTINUOUS POSITIVE AIRWAY PRESSURE (CPAP) DEFINITION

NON-INVASIVE MEASUREMENT OF DIAPHRAGMATIC CONTRACTION TIMING IN DOGS

BTS sleep Course. Module 10 Therapies I: Mechanical Intervention Devices (Prepared by Debby Nicoll and Debbie Smith)

Index SLEEP MEDICINE CLINICS. Note: Page numbers of article titles are in boldface type.

Comparison of patient spirometry and ventilator spirometry

This pamphlet has been designed as

Sleep Diordered Breathing (Part 1)

Snoring. Forty-five percent of normal adults snore at least occasionally and 25

NASAL OBSTRUCTION. Andy Whyte PERTH RADIOLOGICAL CLINIC UNIVERSITY OF MELBOURNE UNIVERSITY OF WA

During the therapeutic titration of nasal continuous

Precision Sleep Medicine

MND Study Day. Martin Latham CNS Leeds Sleep Service

EVect of breathing circuit resistance on the measurement of ventilatory function

How to write bipap settings

Obstructive Sleep Apnoea

The effect of nasal tramazoline with dexamethasone in obstructive sleep apnoea patients

Titration and monitoring of CPAP in infants

Breathe Easier. Single-Prong Cannula Represents Important Breakthrough in Oxygen Therapy for COPD Patients

NON-INVASIVE VENTILATION MADE RIDICULOUSLY SIMPLE

Small Airways Disease. Respiratory Function In Small Airways And Asthma. Pathophysiologic Changes in the Small Airways of Asthma Patients

Influence of correction of flow limitation on continuous positive airway pressure efficiency in sleep apnoea/hypopnoea syndrome

SLEEP APNOEA AND DYSFUNCTIONAL BREATHING

Nasal Valve Obstruction

A 74-year-old man with severe ischemic cardiomyopathy and atrial fibrillation

TNI 20: Breathe Easier without a Mask

Lumis Tx: the all-in-one hospital ventilation solution

Introducing Infant Flow Advance SIPAP. By Joanne Cookson March 2008

The Ear, Nose and Throat in MPS

Airway and Airflow Characteristics In OSAS

Provent Sleep Apnea Therapy (Ventus Medical, Belmont,

Improving Care & Outcomes

Competency Title: Continuous Positive Airway Pressure

BiPAPS/TVAPSCPAPASV???? Lori Davis, B.Sc., R.C.P.T.(P), RPSGT

Procedures/Risks: pulmonology, sleep, critical care

Expiratory valves used for home devices: experimental and clinical comparison

U ntil recently the restoration of airflow which terminates

RHINO-SYS. Rhinomanometry Rhinoresistometry Acoustic Rhinometry Longtime-Rhinoflowmetry

The Familial Occurrence of Obstructive Sleep Apnoea Syndrome (OSAS)

Development of a portable device for home monitoring of. snoring. Abstract

Ron Hosp, MS-HSA, RRT Regional Respiratory Specialist. This program has been approved for 1 hour of continuing education credit.

Obstructive sleep apnoea How to identify?

Rhino-CFD! CFD-Analysis of Unclear Nasal Breathing Problems! Dr. med. T. Hildebrandt! Dr.-Ing. Leonid Goubergrits! M.Sc. Jan Osman!!!!!!!!

DECLARATION OF CONFLICT OF INTEREST

PARTITIONING OF INHALED VENTILATION BETWEEN THE NASAL AND ORAL ROUTES DURING SLEEP IN NORMAL SUBJECTS. Michael F. Fitzpatrick. Helen S.

Background: Bedside ultrasound is emerging as a useful tool in the assessment of

Auto Servo Ventilation Indications, Basics of Algorithm, and Titration

Equivalence of Nasal and Oronasal Masks during Initial CPAP Titration for Obstructive Sleep Apnea Syndrome

Treatment of Snoring. Useful Telephone Numbers. Information for Patients on. North Hampshire ENT Partnership Hampshire Clinic

Using an Inhaler and Nebulizer

Prediction of sleep-disordered breathing by unattended overnight oximetry

Comfort and pressure profiles of two autoadjustable positive airway pressure devices: a technical report

Disclosures. Michael Gunnuscio RPSGT, Bob Chase RRT, Umakanth Khatwa MD

Upper airway resistance syndrome: evaluation of patients with excessive day time sleepiness non-invasively

AIRWAY MANAGEMENT SUZANNE BROWN, CRNA

Transcription:

Effects of Nasal Prongs on Nasal Airflow Resistance* Anne-Marie Lorino, PhD; Hubert Lorino, PhD; Estelle Dahan; Marie Pia d Ortho, MD; André Coste, MD; Alain Harf, MD; and Frédéric Lofaso, MD Study objectives: The aim of this study was to investigate whether nasal prongs, which have been proposed to assess nasal flow during sleep, affect nasal airflow resistance (NR). Design: NR was estimated by posterior rhinomanometry at a 0.5 L/s flow, under eight conditions: in the basal state, and with seven different nasal prongs. Participants: The study was performed in 17 healthy supine subjects, 8 of whom had basal NR values within the normal range (< 2cmH 2 O L 1 s, group 1), and 9 had increased basal NR values (> 2.5 cm H 2 O L 1 s, group 2), because of nare narrowness and/or deviated nasal septum. Measurements and results: NR increased significantly while breathing with nasal prongs (p < 0.0001 in both groups). The changes in NR ( NR) induced by the different nasal prongs were characterized by large intersubject and intrasubject variability, with a maximum NR of 24.2 cm H 2 O L 1 s. Significant differences were found between the NR induced by the different nasal prongs (p < 0.001 in group 1, and p < 0.0003 in group 2), and for six of them, NR was significantly higher in group 1 than in group 2 (p < 0.02). Conclusions: This study demonstrates that nasal prongs can markedly increase NR in subjects presenting with nare narrowness and/or deviated nasal septum. Further investigations that would include nocturnal polysomnography are still required to evaluate the possible influence of nasal prongs on the diagnosis of obstructive sleep apnea syndrome and its severity. (CHEST 2000; 118:366 371) Key words: posterior rhinomanometry; nasal airflow resistance; nasal prongs Abbreviations: NR nasal airflow resistance; OSAS obstructive sleep apnea syndrome; Ptn transnasal pressure; UAR upper airway resistance; V nasal flow Thermistors have been routinely used for the diagnosis of obstructive sleep apnea syndrome (OSAS). However, they have poor accuracy and do not allow the detection of inspiratory flow limitation, which is a predictive index for upper airway narrowing. 1,2 Presently, the reference method recommended for nasal airflow measurement is a pneumotachograph attached to a tight-fitting face mask. 3 An alternative to nasal airflow is nasal pressure, which is measured by nasal prongs originally designed for O 2 therapy (O 2 nasal prongs) or for measurements of expired CO 2 concentration (CO 2 nasal prongs) connected to a pressure transducer. 3 Nasal pressure *From Service de Physiologie (Drs. A. Lorino, d Ortho, Harf, and Ms. Dahan), and INSERM U 492 (Drs. H. Lorino and Coste), Hôpital Henri Mondor, AP-HP, et Service de Physiologie (Dr. Lofaso), Hôpital Raymond Poincaré, AP-HP, Garches, France. Manuscript received July 8, 1999; revision accepted March 7, 2000. Correspondence to: Anne-Marie Lorino, PhD, Service de Physiologie - Explorations Fonctionnelles, Hôpital Henri Mondor, 94010 Créteil, France; e-mail: anne-marie.lorino@hmn.ap-hopparis.fr is used for the visual detection of respiratory events during sleep, 4,5 as well as in computer-controlled devices designed for automatic diagnosis of OSAS and nasal continuous positive airway pressure titration. 6,7 Lastly, it has been demonstrated that, when appropriately corrected, nasal pressure was comparable to the signal of a conventional pneumotachograph. 8 However, although it has been suggested that nasal prongs might increase nasal airflow resistance (NR) in individuals with small nares, 4 the effect of occluded nasal prongs on NR has never been quantified. Therefore, the aim of the present study was to evaluate the potential effects of nasal prongs on NR assessed by posterior rhinomanometry. Subjects Materials and Methods The study was performed in a group of 17 asymptomatic healthy volunteers (5 men and 12 women), aged 22 to 54 years, with no upper or lower respiratory complaints. Eight subjects had 366 Clinical Investigations

Figure 1. Scanned pictures of the different nasal prongs. All nasal prongs were made of nonrigid material, except the Taema device. normal nasal morphology and basal NR values within the normal range, ie, 2cmH 2 O L 1 s (group 1); nine subjects had nasal anatomic abnormalities, such as nare narrowness and/or deviated nasal septum, and NR basal values 2.5 cm H 2 O L 1 s (group 2). NR Measurement NR was measured by posterior rhinomanometry. The subjects breathed quietly through a nasal mask, with the mouth occluded by a closed mouth piece in which a 3-mm inner-diameter catheter was inserted to measure pharyngeal pressure. Transnasal pressure (Ptn) was measured by a differential pressure transducer (Validyne DP45, 14 cm H 2 O; Validyne; Northridge, CA), with one port connected to the nasal mask and the other to the catheter. Nasal flow (V ) was sensed by a screen pneumotachograph (Fleisch n 1; Fleisch; Lausanne, Switzerland) connected to a differential pressure transducer (Validyne DP45, 2.25 cm H 2 O; Validyne). Pressure and flow signals were sampled at 32 Hz by an analog-to-digital converter. To determine nasal inspiratory airflow resistance, Ptn and V inspiratory data were analyzed by linear regression analysis of Ptn over V V, according to the following equation: Ptn KV V NR was then calculated at the 0.5 L/s airflow, as NR 0.5 K, where K is the slope of the regression line. Three to four consecutive measurements were performed within a 1-min period, and NR was taken as the average of the NR estimates corresponding to an r 2 value 99%. Experimental Protocol Six O 2 nasal prong devices (Allegiance Healthcare, McGaw Park, IL; Invacare, Elyria, OH; Kendal, Neustadt, Germany; CHEST / 118 / 2/ AUGUST, 2000 367

Figure 2. Illustrative Ptn-V curves obtained in a subject presenting with a deviated nasal septum (basal NR value 3.3 cm H 2 O L 1 s [l.s -1 ]), in the basal state, and with the Uno, Kendal, and Allegiance devices. The Ptn-V curves obtained with the other devices have been omitted for clarity. Sims, Ft. Myers, FL; Taema, Antony, France; and Uno, Maersk Medical, Lynge, Denmark), and one CO 2 device (Pro-Tech, Woodinville, WA) were successively tested in a randomly selected order in each subject (Fig 1). For each of the devices, NR was measured in the basal state, while breathing with nasal prongs, and in the basal state once again. Great care was taken to avoid air leaks at the mask and to position the nasal prongs correctly. For this purpose, the lateral prong tubing was shortened to allow its subsequent nasal positioning inside the nasal mask, a thin strip was introduced into the tubing, and the tubing ends were occluded and made airtight by silicone gel. The tips of the nasal prongs were then inserted into the nostrils, and the two extremities of the strip were passed over both ears and tied together under the chin to simulate the usual placement of the nasal prongs. Finally, the nasal mask was positioned, and its airtightness was checked. All NR measurements were performed in the supine position. In order to avoid nasal congestion that may progressively occur in this position, the subjects were asked to sit up for 5 min before each set of NR measurements. The absence of nasal congestion was checked by comparing the NR basal values obtained before and after the measurements with nasal prongs. The effect of each type of nasal prongs on NR was assessed by the corresponding change in NR. Statistical Analysis Statistical analysis was performed using parametric and nonparametric tests, depending on whether the data distribution could be assumed to be gaussian or not. Basal NR values were compared by one-way analysis of variance for repeated measures. NR values with nasal prongs and NR values were compared by the Friedman test (nonparametric analysis of variance), and the Wilcoxon and the Mann-Whitney rank sum tests. A p value 0.05 was considered significant. Values are means SEM, except when otherwise indicated. Results In the initial basal state, NR ranged from 1.2 to 1.8 cm H 2 O L 1 s in group 1, with a mean value of Figure 3. Mean values of NR observed in the basal state (Base) and with the different nasal prongs (Allegiance [Alle], Invacare [Inva], Kendal [Kend], Sims, Taema [Taem], Uno, and Pro-Tech [Pro-T]) in subjects with normal nasal morphology (group 1, n 8) and with nasal anatomic abnormalities (group 2, n 9). Bars indicate SE., *, and **: significantly higher than NR basal values (p 0.03, 0.02, and 0.008, respectively). Note the different scales for NR in both groups. cmh 2 0.l -1.s cm H 2 O L 1 s. 2.4 0.1 cm H 2 O L 1 s, and from 2.5 to 4.5 cm H 2 O L 1 s in group 2, with a mean value of 3.0 0.2 cm H 2 O L 1 s. No significant difference was observed between the NR basal values obtained before and after each measurement with nasal prongs (p 0.6). When breathing with nasal prongs, the Ptn V relationship became more curved (Fig 2), and NR significantly increased in both groups (p 0.0001 in both groups) for all the nasal prongs (Fig 3). NR greatly varied from one subject to another and from one type of nasal prongs to another, reaching a value of 24.2 cm H 2 O L 1 s with the Uno device in a subject of group 2 who had an NR basal value of 2.9 cm H 2 O L 1 s (Fig 4). It should be noted that relatively small changes in NR were observed in group 1 subjects, whereas clear increases were observed in group 2 subjects (Fig 4, 5). Despite the large interindividual variability in the NR response to a given type of nasal prongs, significant differences were found between the NR 368 Clinical Investigations

Figure 5. Mean increases in NR ( NR) observed in subjects with normal nasal morphology (group 1, n 8) and nasal anatomic abnormalities (group 2, n 9) with the different nasal prongs (Allegiance, Invacare, Kendal, Sims, Taema, Uno, and Pro-Tech). Bars indicate SE., *,, and **: significantly higher than in group 1 (p 0.02, 0.005, 0.002, and 0.001, respectively). See Figure 3 legend for abbreviations. Figure 4. Intraindividual changes in NR ( NR) observed in both groups with the different nasal prongs. Note that the scales for NR are different in both groups, and that subjects with normal nasal morphology (group 1) exhibited relatively small changes in NR, whereas those with nasal anatomic abnormalities (group 2) exhibited large increases. The largest increases in the subjects of group 2 were observed with different nasal prongs, indicating an interaction between the nose morphology and the nasal prong design. See Figure 3 legend for abbreviations. induced by the different types (p 0.001 in group 1, and p 0.0003 in group 2), and the Taema and Pro-Tech devices were found to result in the lowest NRs (Fig 5 and Table 1). Discussion Nasal prongs were demonstrated to be convenient for ventilation monitoring during sleep, even if their sensitivity and specificity for assessing the severity of flow limitation are lower than those found using a pneumotachograph. 9 As easily usable as thermistors, they provide a semiquantitative evaluation of airflow, and thereby are more sensitive for the detection of sleep respiratory events, including inspiratory flow limitation. 4,5 However, the main requirement for nasal prongs to be routinely used during sleep is that they do not partly occlude the nasal passage, which might cause sleep breathing disorders associated with brief arousals. 10 The present study was therefore initiated to evaluate the potential effects of nasal prongs on nasal resistance. As NR is flow dependent, a choice has to be made with regard to the flow or pressure level at which it is calculated. The NR index retained in the present study has proved suitable for assessing the effects of Table 1 Significance Observed Between the Increases in NR Induced by the Different Nasal Prongs in Subjects With Normal Nasal Morphology (Group 1) and With Nasal Anatomic Abnormalities (Group 2)* Devices Allegiance Invacare Kendal Sims Taema Uno Group 1 (n 8) Invacare NS Kendal NS NS Sims NS NS NS Taema p 0.04 NS p 0.02 NS Uno p 0.05 p 0.05 p 0.04 NS NS Pro-Tech p 0.02 p 0.05 NS NS NS NS Group 2 (n 9) Invacare p 0.03 Kendal p 0.02 NS Sims NS p 0.05 NS Taema p 0.03 p 0.03 p 0.04 p 0.01 Uno NS NS NS NS NS Pro-Tech p 0.02 NS NS p 0.01 NS p 0.01 *The p values are derived from the Wilcoxon rank sum test; NS not significant. CHEST / 118 / 2/ AUGUST, 2000 369

topical decongestants and nasal mechanical dilators on NR. 11,12 To avoid any influence of diurnal variation on NR, 13 all of our subjects were studied at the same time of day. The nasal prongs were occluded to reproduce the conditions in which they are used to measure nasal pressure, ie, with their tubing connected to a pressure transducer. The effect of nasal prongs on NR was evaluated in the supine position, the one used for subjects undergoing polysomnographic studies, because increases in NR have been reported when shifting from the sitting to the supine position. 14 This postural influence on NR is partly attributable to an increase in mucosal thickness due to vascular dilation, 14 which makes NR values unstable (unpublished results). It therefore appeared important to prevent the development of nasal congestion by shortening the period spent in the supine position. In that way, the changes we observed in NR were exclusively attributable to the nasal prongs. Nasal prongs resulted in a significant increase in NR in both groups (Fig 3), which can be attributed to the fact that they reduce the nasal cross-sectional area available for airflow. Moreover, in certain subjects, some nasal prongs increased NR to a resistance level comparable to the normal uninasal resistance level, ie, NR became roughly equivalent to NR during complete obstruction of one nostril, a situation known to induce a significant increase in the apnea and arousal indexes. 10 One of the most interesting results of this study concerns the wide intersubject and intrasubject variability of NR (Fig 4), which proves that the different types of nasal prongs cannot be used indiscriminately. For example, the same devices could result in the lowest or the highest NR, depending on the subject (Fig 4). Both intersubject and intrasubject variabilities are explained by the combination of the following: (1) the great diversity of the nasal prong tips used in the present study as regards their section profile, their maximal external diameter, their length, their curvature, and their stiffness (Fig 1); and (2) the great diversity of nose morphology, especially of the nare geometry in the region located downstream of the nasal valve, which determines the depth of nasal prong penetration and the nasal cross-sectional area remaining available for airflow. For example, nasal prongs made of nonrigid material and with a large maximal diameter result in a NR all the more high, as their tips occlude the nasal passage, ie, as the nares are narrow and/or the nasal septum is deviated. Similarly, the increase in NR will be all the more marked, as the nonrigid tips are long and the nares short, because the tips will then reach the valve region. The highest NR was indeed observed with the Uno device, which had the longest nonrigid tips (Fig 1), in a group 2 subject who had both deviated nasal septum and short narrow nares (Fig 4). Such a high NR value was probably due to the fact that the Uno device resulted at the same time in the total occlusion of one nare, and a marked reduction of the cross-sectional area of the other. By contrast, the Taema nasal prongs, which are the only ones made of rigid material that were tested in this study, tend to dilate the nares and thereby limit their occlusive effect. Another interesting result is that, when compared to the other devices, the Taema and Pro-Tech nasal prongs resulted in the lowest NRs in both groups (Fig 4, 5 and Table 1). This finding may be easily explained by the respective designs of these two devices (Fig 1). Due to the length and stiffness of their tips, the Taema nasal prongs have an expanding effect on nasal valves, comparable to the one of a mechanical internal nasal dilator. Indeed when breathing with this device, most subjects reported the sensation of nasal dilation, sometimes associated with the feeling of discomfort resulting from the hardness of the tip material. This expanding effect may have partly, and sometimes even completely counterbalanced the increase in NR induced by the reduction of the nasal cross-sectional area available for airflow (Fig 4). Conversely, the Pro-Tech nasal prongs, which were originally designed to measure the CO 2 concentration in the expired gas, are characterized by very short and narrow soft tips, which considerably limit the reduction of the nasal crosssectional area available for airflow and induces no sensation of discomfort. Besides, although their tips are a little longer, they are narrower than those of the conventional pediatric O 2 nasal prongs, and their inter-tips space allows them to better fit an adult nose. Our results also demonstrate that whereas nasal prongs have relatively little effect on NR in subjects with normal nasal anatomy, they can dramatically increase NR in subjects with nasal anatomic abnormalities (Figs 3 5). In patients presenting with a deviated nasal septum, certain types of nasal prongs might even result in the total occlusion of one nare. Consequently, the choice of a type of nasal prongs for a polysomnographic study in a patient consulting for suspected OSAS is all the more tricky, as the patient has a high NR basal value. Moreover, the NR values observed in the present study do not allow prediction of the total increase in upper airway resistance (UAR) resulting from the use of nasal prongs. It has indeed been shown that external resistive loads result in significant increases in UAR during nonrapid eye movement sleep in healthy men, which closely correlated with the basal UAR values. 15 Consequently, in certain patients presenting with highly resistive nares, 370 Clinical Investigations

the use of nasal prongs for airflow monitoring during sleep might induce dramatic increases in total UAR and thereby promote the occurrence of sleep respiratory events. In conclusion, our results demonstrate that nasal prongs may dramatically increase NR in subjects presenting with nare narrowness and/or deviated nasal septum. Further studies that would include nocturnal polysomnography are still required to accurately evaluate the possible influence of nasal prongs on the diagnosis of OSAS and its severity. References 1 Condos R, Norman RG, Krishnasamy I, et al. Flow limitation as a noninvasive assessment of residual upper-airway resistance during continuous positive airway pressure therapy of obstructive sleep apnea. Am J Respir Crit Care Med 1994; 150:470 480 2 Montserrat JM, Ballester E, Olivi H, et al. Time-course of stepwise CPAP titration. Am J Respir Crit Care Med 1995; 152:1854 1859 3 Sleep-related. breathing disorders in adults: recommendations for syndrome definition and measurement techniques in clinical research. Sleep 1999; 22:667 689 4 Norman RG, Ahmed MM, Walsleben JA, et al. Detection of respiratory events during NPSG: nasal cannula/pressure sensor versus thermistor. Sleep 1997; 20:1175 1184 5 Hosselet JJ, Norman RG, Ayappa I, et al. Detection of flow limitation with a nasal cannula/pressure transducer system. Am J Respir Crit Care Med 1998; 157:1461 1467 6 Gugger M, Mathis J, Bassetti C. Accuracy of an intelligent CPAP machine with in-built diagnostic abilities in detecting apnoeas: a comparison with polysomnography. Thorax 1995; 50:1199 1201 7 Bradley PA, Mortimore IL, Douglas NJ. Comparison of polysomnography with ResCare Autoset in the diagnosis of the sleep apnoea/hypopnea syndrome. Thorax 1995; 50:1201 1203 8 Montserrat JM, Farré R, Ballester E, et al. Evaluation of nasal prongs for estimating nasal flow. Am J Respir Crit Care Med 1997; 155:211 215 9 Clark SA, Wilson CR, Satoh M, et al. Assessment of inspiratory flow limitation invasively and noninvasively during sleep. Am J Respir Crit Care Med 1998; 158:713 722 10 Lavie P, Fischel N, Zomer J, et al. The effects of partial and complete mechanical occlusion of the nasal passages on sleep structure and breathing in sleep. Acta Otolaryngol 1983; 95:161 166 11 Lorino AM, Lofaso F, Drogou I, et al. Effects of different mechanical treatments on nasal resistance assessed by rhinometry. Chest 1998; 114:166 170 12 Lorino AM, Lofaso F, Dahan E, et al. Combined effects of a mechanical nasal dilator and a topical decongestant on nasal airflow resistance. Chest 1999; 115:1515 1518 13 Eccles R. The central rhythm of the nasal cycle. Acta Otolaryngol Stockh 1978; 86:464 868 14 Desfonds P, Planès C, Fuhrman C, et al. Nasal resistance in snorers with and without sleep apnea: effect of posture and nasal ventilation with continuous positive airway pressure. Sleep 1998; 21:622 629 15 Wiegand L, Zwilling CW, White DP. Collapsibility of the human upper airway during normal sleep. J Appl Physiol 1989; 66:1800 1808 CHEST / 118 / 2/ AUGUST, 2000 371