A negative expiratory pressure test during wakefulness for evaluating the risk of obstructive sleep apnea in patients referred for sleep studies

CLINICAL SCIENCE

A negative expiratory pressure test during wakefulness for evaluating the risk of obstructive sleep apnea in patients referred for sleep studies

Salvatore Romano; Adriana Salvaggio; Anna Lo Bue; Oreste Marrone; Giuseppe Insalaco

National Research Council of Italy-Institute of Biomedicine and Molecular Immunology "A. Monroy", Palermo/Italy

ABSTRACT

OBJECTIVE: Obstructive sleep apnea is characterized by increased upper airway collapsibility during sleep. The present study investigated the use of the negative expiratory pressure test as a method to rule out obstructive sleep apnea.

METHODS: Flow limitation was evaluated in 155 subjects. All subjects underwent a diurnal negative expiratory pressure test and a nocturnal sleep study. The severity of sleep apnea was determined based on the apneahypopnea index. Flow limitation was assessed by computing the exhaled volume at 0.2, 0.5, and 1.0 s (V0.2, V0.5, and V1.0, respectively) during the application of a negative expiratory pressure and expressed as a percentage of the previous exhaled volume. Receiver-operating characteristic curves were constructed to identify the optimal threshold volume at 0.2, 0.5, and 1.0 s for obstructive sleep apnea detection.

RESULTS: Mean expiratory volumes at 0.2 and 0.5 s were statistically higher (p <0.01) in healthy subjects than in all obstructive sleep apneic groups. Increasing disease severity was associated with lower expiratory volumes. The V0.2 (%) predictive parameters for the detection of sleep apnea were sensitivity (81.1%), specificity (93.1%), PPV (98.1%), and NPV (52.9%). Sensitivity and NPV were 96.9% and 93.2%, respectively, for moderate-to-severe obstructive sleep apnea, and both were 100% for severe obstructive sleep apnea.

CONCLUSION: Flow limitation measurement by V _0.2 (%) during wakefulness may be a very reliable method to identify obstructive sleep apnea when the test is positive and could reliably exclude moderate and severe obstructive sleep apnea when the test is negative. The negative expiratory pressure test appears to be a useful screening test for suspected obstructive sleep apnea.

Keywords: Sleep; Upper Airways; Respiratory Measurement; Screening Test.

INTRODUCTION

Obstructive sleep apnea (OSA) is a risk factor for serious health problems, such as cardiovascular disease¹ and postoperative complications,² and could have consequences for the safety of subjects because of decreased physical abilities. ^3-5 The under-recognition of OSA may result in important health and social costs⁶ and reduce the quality of life of affected individuals. ⁷ Obstructive sleep apnea is a disorder characterized by repetitive episodes of upper airway closure during sleep, and increased upper airway collapsibility is one of its main determinants.⁸

Studies have estimated that OSA, which is defined basedo nanapnea-hypopneaindex of 5and excessive daytime somnolence, may affect at least 2-4% of the middle-aged general population.⁹ Intere stingly, preva lence estimates are much higher when individual s are divi ded based on demographic variables, such as age, sex, and body mass index (BMI).¹⁰ In certain subgroups of the pop ulation, such as obese subjects^10-11 and profes sional drivers,¹² theprevalence ofOSA maybehigher than in the general population. OSA diagnostic proce dures are expensive and time consuming, and studies have estimated that nearly 80% of men and 93% of women with moderate-to-severe sleep apnea are undiagnosed.¹³

Although effective screening procedures could help in evaluating OSA risk, current screening criteria remain unsatisfactory. The identification of simple, noninvasive, predictive, and reliable tools to detect OSA would be useful in several fields.

Negative expiratory pressure (NEP) is a noninvasive tool that was initially designed to evaluate flow limitation in patients with obstructive lung disease; however, Koulouris and coworkers have suggested that the flow limitation induced by the NEP application may also reflect upper airway collapsibility. ¹⁴ NEP has been applied in subjects OSA ^15-22 with ob esity and/or to evaluate whether NEP responses could predict OSA, and the results have been variable. Some studies ^15-20 have found that NEP flow- volume curves and quantitative indices during wakefulness are usef ul in the detection of upper airway collapsibility, whereas other studies^21-22 have showed that the NEP techniqu e appears to have limited usefulness as a clinical tool for the routine screening of OSA patients during wakeful ness. The difference between these results could be related to the various flow-limitation measurements that were applied. Effective screening procedures could help to distinguish subjects with different probabilities of being affected by OSA. We have previously demonstrated the effective ness of the NEP test in identifying increased upper airway collapsibility during tidal expiration in severe OSA patients.²³ The aim of the present study was to evaluate whether the flow limitation induced by NEP during wakefulness could be a valuable method to detect subjects with mild or moderate OSA.

MATERIALS AND METHODS

The present study included 155 subjects (130 males and 25 females) who were referred to our sleep laboratory (we evaluated spirometry to exclude subjects with bronchial obstruction from the study). Patients with major craniofacial or upper airway abnormalities and/or acute or known chronic pulmonary or neuromuscular disease were excluded from the study. The mean age of the subjects was 51±11 years, and the mean BMI was 32.6±7.1 kg/m² (the BMI was >30 for 58.7% of the subjects). Pulmonary function tests were performed during the day using a MEDGRAPHICS Elite plethysmograph (MEDGRAPHICS Corporation; St. Paul, Minnesota, USA). Each patient gave informed consent, and the study protocol was approved by the local ethical committee. All subjects underwent a diurnal NEP test and nocturnal monitoring using a portable cardio-respiratory system.²⁴

Nocturnal monitoring was performed using a portable computerized system (Somte' Compumedics Inc.; Abbotsford, VIC, Australia). The recorded signals were airflow, snoring, thoracic effort, abdominal effort, limb movement, body position, electrocardiogram, arterial oxygen saturation, pulse rate, and pulse waveform. All were recorded for at least 6 h.

Polygraphic recordings were analyzed manually by scorers who were blinded to the results of the NEP test. Apneas were defined based on the lack of airflow or a >90% reduction in the airflow signal for at least 10 s. Hypopneas were defined based on a discernible drop in flow by >30% of the baseline value for a period lasting at least 10 s, followed by a >4% drop in SaO ₂ .²⁵ The apnea-hypopnea index (AHI) was calculated as the total number of apneas and hypopneas per hour of estimated total sleep time. Subjects with an AHI >5 were classified as having OSA, and subjects with an AHI, 5 were classified as healthy. OSA severity was determined based on the AHI as mild (5<8804; AHI ,15), moderate (15< AHI <30), or severe (AHI >30).

NEP test

NEP tests were performed in awake subjects at -10 cm H ₂ O during the morning before the portable home monitor testing session. The NEP tests were performed while patients were in the sitting position with the neck in a neut ral position and quietly breathing. All subjects were wearing a nose clip. The NEP test was performed as previously described.²³ A Super Air Amplifier (Exair model 1200 21 Cincinnati, Ohio, USA) was able to generate a range of n egative pressures as compressed air was delivered through the device. Air was supplied by a tank of compres sed air and controlled using an electrically operated solenoid valve (Norgren Ltd model 95004, Warwickshire, UK). The solenoid was automatically activated during early tidal expiration and kept open for 2 s by software control.

The Super Air Amplifier device was placed at the distal end of a pneumotachograph (Hans Rudolph model 3830; Kansas City, MO, USA), and mouth pressure was measured using a pressure transducer (PCLA0050, Sensortechnics GmbH, Puchheim, D). The signals recorded by the pneumotachograph and the mouth pressure transducer were filtered and digitized at 200 Hz. The volume was obtained by numerically integrating the airflow signal. Airflow and mouth pressure were displayed in real time on the computer screen and recorded for subsequent analysis. Signal analysis and solenoid valve control were performed using software developed in our laboratory using LabVIEW 8.2 (National Instruments; Austin, TX, USA).

The NEP of -10 cm H ₂ O was set by occluding the pneumotachograph with a stopper and adjusting the flow of the compressed air to the air amplifier. NEP application during tidal expiration could produce a sudden and variable flow reduction that was dependent on upper airway narro wing. Flow limitation was evaluated by measuri ng the expired volume at 0.2, 0.5, and 1.0 s (V _0.2, V _0.5 , and V _1.0 , respectively) immediately after NEP applica tion (Figure 1). We waited for at least four regular breaths (as observed by visual inspection of the flow signal on the computer screen) between consecutive NEP applications.

All subjects underwent seven NEP applications, and a minimum of four valid measures of expiratory volumes at 0.2, 0.5, and 1.0 s were averaged for each subject. These values were expressed as the percent of the mean expiratory volumes of the three breaths preceding each NEP application. Measured volumes at 0.2, 0.5, and 1.0 s were only accepted under regular breathing conditions (i.e., the differences between inspiratory and expiratory volumes for each of the three breaths before each NEP application were less than 10%).

Statistical analysis

Data are reported as means±SD. A p-value of <0.05 was considered significant. Differences between healthy and OSA subjects with different severity were evaluated using the Tukey-Kramer test. Logistic regression for the analysis of continuous factors with categorical responses was applied. Receiver-operating characteristic (ROC) curves were constructed to determine the optimalV _0.2 (%), V _0.5 (%), and V _1.0 (%) threshold values for OSA detection. We also calculated sensitivity, specificity, and positive (PPV) and negative predictive values (NPV) at various levels of the measured volumes. A ROC curve was also constructed for BMI. Statistical analysis was performed using the commercial software JMP 8.0.1 (SAS Institute Inc., Cary, NC, USA).

RESULTS

All subjects had normal forced expiratory flow volume loops (FVC 99±16%, FEV1 99±16%, and FEF25-75 88±27% of the predicted values, respectively).

The entire spectrum of OSA severity was represented in the study population. Nocturnal monitoring showed a mean AHI of 32±28 events/h in the study population.

Table 1 shows the anthropometric and respiratory characteristics of the healthy and OSA subjects with different degrees of severity.

The mean NEP test results for V _0.2 (%), V _0.5 (%), and V _1.0 (%) in the study population were 19.4±12.2%, 56.4±29.9% and 100.4±46.0%, respectively. The relationships between AHI an dV _0.2 (%), V _0.5 (% ), and V _1.0 (%) are shown in Figure 2.

Figure 3 shows the mean expiratory volumes at V _0.2 (%), V _0.5 (%) , and V _1.0 (%) for the healthy subjects and the subjects in the three different OSA severity groups. Exhaled V _0.2 (%) and V _0.5 (%) volumes were significantly lower (p <0.01) in all OSA severity groups, than in healthy subjects. The exhaled V _1.0 (%) volume, however, was only significa nt for the healthy subjects compared with the moderat e and severe OSA subjects. The expiratory volumes were associated with disease severity (i.e., the expiratory volume decreased as disease severity increased), and the highest volumes were found in the healthy subjects.

A ROC curve analysis was applied to evaluate the predictive effectiveness ofV _0.2 (%), V _0.5 (%), andV _1.0 (%) for OSA subjects with AHI >5, AHI >15 and AHI .30. The predictive parameters forV _0.2 (%), V _0.5 (%), and V _1.0 (%) are reported in Table 2. Interestingly, V _1.0 (%) was the least effective volume parameter in distinguishing between healthy and OSA subjects.V _0.2 (%) identified subjects with AHI > 15 and .30 (i.e., moderate-to-severe OSA) with very high sensitivity and identified subjects with an AHI ,5 (i.e., healthy subjects) with very high specificity. A negative test result indicated 100% probability of having an AHI not exceeding 30, 93.2% probability of having an AHI not exceeding 15, but an equal probability of being healthy or having mild OSA. A positive test result indicated 98% probabil ity of having an AHI >5, 84.8% probability of having an AHI >15 and 56.1% probability of having an AHI >30. Thus, the measurement of flow limitation usingV _0.2 (%), which was determined using NEP, was an effective predictor of OSA.

The ROC curve analysis applied to the BMI measurements showed that BMI was significantly less reliable (p<0.007) than V _0.2 (%) in discriminating OSA subjects. The areas under the ROC curves for BMI andV _0.2 (%) were 0.79 (95 % CI: 0.72 to 0.85) and 0.91 (95% CI: 0.85 to 0.95), respectively.

Figure 4 illustrates the relationship between AHI and V _0.2 (%) graphically. The optimal cutoff point to discriminate subjects with an AHI >30 was 23%, and only five subjects with values of V _0.2 lower than 23% (p ositive for OSA) were healthy. No subject with aV _0.2 value higher than 23% (negative for OSA) had severe OSA. Only three subjects with aV _0.2 value higher than 23% had moderate OSA, and 15 subjects had mild OSA (1.9 and 9.6%, respectively).

DISCUSSION

The present study verified the efficacy of the flow limitation induced by NEP and evaluated by V _0.2 (%), V _0.5 (%) and V _1.0 (%) as a screening tool to detect OSA risk. Our results indicated that theV _0.2 (%) parameter is more sensitive in detecting patients with moderate and severe OSA.V _0.2 (%) identified subjects with moderate and severe OSA with very high sensitivity and identified healthy subjects with very high specificity. When the NEP test was negative for OSA, there was a high probability that the subject did not have moderate or severe OSA. When the test was positive, most OSA subjects (AHI >5) were identified. For a positive test, the predictive value to identify OSA was very high, but the predictive value for distinguishing severity was lower. Conversely, a negative test was predictive of subjects who did not have moderate and severe OSA. Thus, the measurement of flow limitation byV _0.2 (%) induced by NEP is a valuable predictor for OSA and can reliably distinguish between OSA and healthy subjects.

Obesity and increased upper airway collapsibility are consider ed two of the most important determinants of OSA. Previous studies regarding obese male subjects have shown that at least 40% are affected by OSA. ^26-27 Because obesity is consider ed to be a major cause of OSA, we compared the ROC curve forV _0.2 (%) induced by NEP to the ROC curve for BMI to identify OSA subjects. TheV _0.2 (%) curve had better discriminatory power than BMI, which agreed with the supposition that collapsibility is the main mechanism of upper airway obstruction during sleep.

It is important to heighten public awareness regarding the potential hazards and health risks that surround untreated sleep apnea.^1-7,28-34 In addition, certain groups of indivi dual s, such as commercial drivers, need to realize that OSA is dangerous to them and to others. Physicians and the general population are widely aware of the potentially deleterious effects of OSA on an individual patient's health and wellbeing, and there is even increasing awareness among public administrators of the traffic hazards and acci dents at work that are linked to untreated OSA. Many patients who present for surgical procedures may have undiagn osed OSA, despite an improved awareness and increased frequency of diagnosis. ^29-31 Untreated OSA patients are known to have higher incidences of difficult intu bation, postoperative complications, increased intensive care unit admissions, and longer hospital stays.³² Several case reports have documented an increase in the incidence of postoperative complications and deaths among patients suspected of having OSA.^33-34 In previous studies, 24% of patients with OSA had significant postoperative complications, compared with 9% of the patients in the control group.Identifying patients at risk for OSA is the first step in preventing postoperative complications due to OSA.

Polysomnography is the gold standard for diagnosis of OSA, but increasing awareness of the importance of identifying patients with OSA has increased the waiting lists for diagnosis and proper treatment. Nevertheless, it would take several years to satisfy the current requirement for polysomnography in the general population with existing resources.³⁵ The use of portable monitoring devices for the diagnosis of OSA would probably not be sufficient to overcom e the growing demand for diagnostic testing.³⁶ Althoug h sleep recordings are mandatory for OSA diag nosis, it would be useful to identify simple, reliable and inexpensive screening methods for physicians to detect subjects who are more likely to be at risk for upper airway obstruction.

A highly sensitive and positive predictive screening tool with an acceptable specificity and negative predictive ability is a basic requirement when screening patients for a disease that has an important impact on health. OSA screening tests have demonstrated considerable variability in predictive ability, which depends on the screening tool, the patient populati on, and the OSA severity. An OSA screening question naire that was tested in patients from sleep centers resulted in 70% to 93% sensitivity.^37-41 Ross et al.⁴² publishe d a meta-analysis of screening tests for OSA in 2000 and found that a lack of discriminatory analysis makes it difficult to recommend an evidence-based choice of tests for preo perative screening. In addition, the Berlin ques tionnaire⁴¹ has shown varied results that depend on the patient population studied. For example, the sensitivity was 86% in primary care patients⁴⁰ and 57-68% in sleep laboratory patients.⁴³

Previous studies have used different methods to evaluate the flow limitation induced by NEP during wakefulness and assess upper airway collapsibility in OSA and healthy subjects.^14-22 Some studies have applied methods that were the same as those adopted f or the evaluation of flow limitatio n in patients with bronchial obstruction, ¹⁴ whereas others have introduced new methods to evaluate upper airway obstruction.^15-22 The various methods have demon strat ed that NEP can play a role in the identification of upper a irway flow limitation without reaching entirely satisfacto ry discriminatory levels. Ferretti et al. ²¹ evaluated flow limitation by measuring the expiratory volume at 0.5 and 1.0 s after NEP application and concluded that the NEP test appears to have a limited usefulness as a clinical tool for routine screening. In addition, Van Meerhaeghe et al.¹⁷ expresse d the expiratory flow limitation as the percentage of the expired tidal volume over which the NEP-induced flow did not exceed the spontaneous flow, and they concluded that NEP may be useful in predicting OSA with AHI >15 in a clinic-based population (the sensitivity was 81.9% and the specificity was 69.1%). Tamisier et al.²⁰ used the ratio betw een the areas under the curves of the NEP flow-volume loop and the spontaneous flow-volume loop and reported that the quantitative index was higher in healthy subjects than in patients with any type of breathing-related sleep diso rder (the predictive positive value was 96.6% and the pred ictive negative value was 76.9%). Subjects with breath ing-relat ed sleep disorders and healthy subjects exhibited significa nt differences, there was a trend toward a lower quantitative index in patients with severe OSA who exhibited greater expression of a collapsible upper airway. Subjects with mild OSA, however, were not included in this study. In our study, we measured the expiratory volume (express ed as the percent of the mean expiratory volume of the three breaths preceding NEP application) at the very beginning of expiration (V _0.2 ), at 0.5 s (V _0.5 ), and at 1.0 s (V _1.0 ) in a large sample of subjects and showed thatV _0.2 and V _0.5 wer e predictive of OSA (V _1.0 was less useful). The NEP test may provide an objective assessment to identify patients at high risk for OSA and could be widely applied to reduce socioeconomic impact of this disease.

This investigation was limited by the various anthropometric characteristics of the different groups. In addition, we only enrolled subjects who had attended a sleep laboratory, and these subjects may not represent the general population. Importantly, the present study included subjects who represented the entire spectrum of disease severity, which prevented the exaggeration of diagnostic accuracy that could occur when a diagnostic test is evaluated in a sample with a limited severity spectrum.⁴⁴

In conclusion, the evaluation of flow limitation during wakefulness using the NEP technique was predictive of OSA. The NEP test was able to reliably discriminate among subjects who had an AHI >5 and subjects who had an AHI ,15.The NEPtestcould be adoptedas a screening test for the evaluation of suspected OSA patients because it appears to be a very reliable diurnal test that can objectively predict OSA. The NEP test may be even more useful when combined with anamnestic data, such as the symptoms of snoring and hypersomnolence. Further studies should be performed to evaluate whether OSA can be screened using NEP in the general population. The measurement of flow limitation based onV _0.2 (%) during wakefulness may be a very reliable method to identify healthy subjects when the test is negative and subjects with OSA when the test is positive. Further data are required to determine the operating characteristics of the technique for OSA screening in patients who are awake.

ACKNOWLEDGEMENTS

The authors are indebted to Dr. Pietro Abate and Mr. Giovanni Sciortino for their technical support.

This study was supported by the Italian National Research Council grant number ME.P01.006.

AUTHOR CONTRIBUTIONS

Romano S and Insalaco G were responsible for the design and coordination of the study, statistical analysis, preparation and approval of the final version of the manuscript. Salvaggio A was responsible for the design of the study, recruitment and clinical care of subjects, compilation of database, revision and approval of the final version of the manuscript. Lo Bue A was responsible for the recruitment of subjects, compilation of database, reading and approval of the final version of manuscript. Marrone O was responsible for the recruitment, revision and approval of the final version of the manuscript.

Received for publication on May 9, 2011; First review completed on May 30, 2011; Accepted for publication on July 13, 2011

No potential conflict of interest was reported.

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Publication Dates

• Publication in this collection
  11 Nov 2011
• Date of issue
  2011

History

• Received
  09 May 2011
• Accepted
  13 July 2011
• Reviewed
  30 May 2011