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SLEEP 2011 Abstract Supplement

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B. Clinical Sleep Science I. Sleep Disorders – Breathing<br />

0329<br />

DETECTION OF HYPOVENTILATION BY CONTINUOUS<br />

MONITORING OF MAIN STREAM END-TIDAL CO2 IN<br />

OBESE PATIENTS WITH SUSPECTED <strong>SLEEP</strong> APNEA<br />

Capozzolo B 1 , Baltzan M 1,2,3 , Verschelden P 1,4,5,6<br />

1<br />

OSR Medical Sleep Disorders Centre, Town of Mount-Royal, QC,<br />

Canada, 2 Mount Sinai Hospital, Montreal, QC, Canada, 3 McGill<br />

University, Montreal, QC, Canada, 4 Institut de Médecine Spécialisé<br />

de Laval, Laval, QC, Canada, 5 Cité de la Santé de Laval, Laval, QC,<br />

Canada, 6 Université de Montréal, Montreal, QC, Canada<br />

Introduction: Hypoventilation is considered both a serious co-morbidity<br />

and consequence of sleep apnea, which increases with prevalence in<br />

obese patients. It is substantially under-diagnosed prior to the advent of<br />

clinical respiratory failure. We evaluated the incidence of a new diagnosis<br />

of hypoventilation using the systematic monitoring of main stream<br />

end-tidal CO2 (ETCO2) the extent of under-diagnosis.<br />

Methods: Three hundred eighty-four community-based obese adults<br />

with a body mass index (BMI) of 30 kg/m2 or more were referred for<br />

clinically suspected sleep apnea. All patients were monitored with nocturnal<br />

polysomnography over a 17-month period. Participants were<br />

evaluated by a sleep medicine specialist, questionnaire and one night of<br />

polysomnography. Main stream ETCO2 was monitored on all patients,<br />

including during the diagnostic portion of split-night polysomnography.<br />

Results: Patients were a mean (SD) age of 50.5 (SD 11.9) years and<br />

71.4% were men. The mean apnea-hypopnea index was 53.0(SD 37.0)<br />

and 85.4% of patients met diagnostic criteria for at least moderate obstructive<br />

sleep apnea. Of the patients with obesity, 233 (60.7% of 384)<br />

had a BMI of 30-35.9 kg/m2, 83 (21.6% of 384) had a BMI of 36-40.9<br />

kg/m2 and 68 (17.7% of 384) had a BMI of 41 kg/m2 or more. Overall,<br />

23 (6.0% of 384) had at least 10% of total sleep time with an ETCO2 of<br />

50mmHg or higher. With increasing obesity, the number with this degree<br />

of hypoventilation was 6 (2.6% of BMI 30-35.9), 5 (6.0% of BMI 36-<br />

40.9), and 12 (17.6 % of BMI 41 or more). None of these patients were<br />

known for hypoventilation prior to polysomnography.<br />

Conclusion: We conclude that hypoventilation is frequent in patients<br />

with obesity, and that continuous monitoring of main stream ETCO2<br />

facilitates diagnoses that were previously undiagnosed.<br />

0330<br />

A PILOT EVALUATION OF A NOVEL SCREENING TOOL<br />

FOR <strong>SLEEP</strong> RELATED BREATHING DISORDERS<br />

suraiya S 1 , Pillar G 1 , Colman J 2 , Shalev I 2 , Ronen M 2 , Weissbrod R 2 ,<br />

Lain D 2<br />

1<br />

Sleep laboratory, Technion Instiute of technology, haifa, Israel, 2 R&D,<br />

Oredion Medical 1987 LTD, Jerusalem, Israel<br />

Introduction: Polysomnography (PSG) is the standard procedure for<br />

the diagnosis of sleep related breathing disorders (SRDB) and patients<br />

are typically referred for overnight studies when they are identified as<br />

being at risk by a clinician. Various tools are in use today to identify<br />

patients at risk for SRDB and refer them subsequently for studies. The<br />

ASA (American Society of Anesthesiologists) and other professional<br />

bodies have published guidelines calling for the recognition of patients<br />

suffering from SRDB during perioperative care. The Capnostream20p<br />

capnograph/pulse oximeter with SSDx algorithm is used in many hospital<br />

type environments whenever patient monitoring is required. The<br />

monitor provides an Apnea Index (AI), based on summation of the nobreath<br />

events per hour recognized by the capnograph, and an Oxygen<br />

Desaturation Index (ODI), using pulse oximetry. The information is presented<br />

in a simple summary report. The purpose of our evaluation was<br />

to assess the level of agreement between the indices generated by the<br />

device and overnight polysomnograph studies.<br />

Methods: During routine overnight sleep studies 39 adult patients were<br />

monitored with the device. The sleep study was interpreted by a trained<br />

clinician who was blinded to the device. The AI and ODI values generated<br />

by the device were compared to the sleep study outcomes.<br />

Results: A statistically significant model using the maximal AI and<br />

ODI values to predict OSA was defined. At a cut-off point of 19 - (ODI<br />

max+AI max) >19., sensitivity equals 0.87 and specificity 0.82. The<br />

PPV with actual prevalence of 0.68 (per the clinical data gathered)<br />

equals 0.91 and NPV = 0.75.<br />

Conclusion: The results indicated that the device showed high sensitivity<br />

and specificity, and hence can be used as a tool for screening and<br />

assisting in the diagnosis of adult patients with medium and severe Obstructive<br />

Sleep Apnea in the hospital environment.<br />

Support (If Any): Oredion Medical 1978 LTD<br />

0331<br />

OBSTRUCTIVE <strong>SLEEP</strong> APNEA PREDICTION BY BREATH<br />

SOUND ANALYSIS DURING WAKEFULNESS<br />

Moussavi Z, Montazeri A<br />

Electrical & computer Engineering, University of Manitoba, Winnipeg,<br />

MB, Canada<br />

Introduction: Obstructive sleep apnea (OSA) is highly prevalent in the<br />

general population. While prompt initiation of treatment is particularly<br />

important for patients with severe OSA, only about 30% of the patients<br />

referred to a sleep lab are found to be in that category. Although there<br />

are clinical algorithms that can predict the likelihood of a patient having<br />

OSA, there are no easy clinical or laboratory predictors for the severity<br />

of OSA other than a sleep study. The goal of this study was to investigate<br />

the feasibility of developing a fast, simple and accurate screening tool<br />

for stratification of severity of OSA during wakefulness.<br />

Methods: We studied 35 OSA patients with various degrees of severity<br />

and 17 age-matched control subjects, who were also tested by full-night<br />

polysomnography (PSG) for validation. The subjects were instructed to<br />

breathe, once through their nose and once through their mouth with a<br />

nose clip in place, at their normal breathing level for at least 5 breaths,<br />

and then breathe at the their maximum flow level for another 5 breaths.<br />

The breath sound signals were picked up by a Sony (ECM-77B) microphone<br />

placed over the neck and digitized at 10240 Hz rate. The recordings<br />

were repeated in two body positions: sitting upright, and supine.<br />

Data were analyzed using spectral and waveform fractal dimension<br />

techniques followed by statistical analysis to extract the most significant<br />

features for stratification of OSA severity.<br />

Results: Several sound features were found to be statistically significant<br />

between the OSA and non-OSA groups. Using Maximum Relevancy<br />

Minimum Redundancy method, we reduced the number of features<br />

to two. Unsupervised clustering of the two most significant features<br />

showed an overall accuracy of over 84% (sensitivity=88%, specificity=80%)<br />

for separating healthy from OSA patients as well as stratification<br />

of the OSA severity among the patients group.<br />

Conclusion: The results hold promise in sound analysis of different<br />

breathing maneuvers for OSA screening during wakefulness. It is known<br />

that OSA patients on average have smaller and more collapsible pharynx.<br />

This is compensated by the increased dilator muscle activity during<br />

wakefulness. They tend to have more negative pharyngeal pressure,<br />

which is detectable by breathing sound through the nose due to higher<br />

resistance. Given that breath sounds are directly related to the pharyngeal<br />

pressure, our proposed method is sensitive to the severity of OSA<br />

even during wakefulness.<br />

Support (If Any): This project was supported financially by the TR-<br />

Labs Winnipeg.<br />

<strong>SLEEP</strong>, Volume 34, <strong>Abstract</strong> <strong>Supplement</strong>, <strong>2011</strong><br />

A116

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