A smartphone-based algorithm comprising cough analysis and patient-reported symptoms identifies acute exacerbations of asthma: a prospective, double blind, diagnostic accuracy study.

Objective: Early and accurate recognition of asthma exacerbations reduces the duration and risk of hospitalization. Current diagnostic methods depend upon patient recognition of symptoms, expert clinical examination, or measures of lung function. Here, we aimed to develop and test the accuracy of a smartphone-based diagnostic algorithm that analyses five cough events and five patient-reported features (age, fever, acute or productive cough and wheeze) to detect asthma exacerbations.Methods: We conducted a double-blind, prospective, diagnostic accuracy study comparing the algorithm with expert clinical opinion and formal lung function testing. Results: One hundred nineteen participants >12 years with a physician-diagnosed history of asthma were recruited from a hospital in Perth, Western Australia: 46 with clinically confirmed asthma exacerbations, 73 with controlled asthma. The groups were similar in median age (54yr versus 60yr, p=0.72) and sex (female 76% versus 70%, p=0.5). The algorithm's positive percent agreement (PPA) with the expert clinical diagnosis of asthma exacerbations was 89% [95% CI: 76%, 96%]. The negative percent agreement (NPA) was 84% [95% CI: 73%, 91%]. The algorithm's performance for asthma exacerbations diagnosis exceeded its performance as a detector of patient-reported wheeze (sensitivity, 63.7%). Patient-reported wheeze in isolation was an insensitive marker of asthma exacerbations (PPA=53.8%, NPA=49%). Conclusions: Our diagnostic algorithm accurately detected the presence of an asthma exacerbation as a point-of-care test without requiring clinical examination or lung function testing. This method could improve the accuracy of telehealth consultations and might be helpful in Asthma Action Plans and patient-initiated therapy.

Association between early stage N2 sleep spindle burst characteristics and vigilance groups: an observational study on patients from a tertiary sleep centre.

Objective.Obstructive sleep apnoea (OSA) is associated with impaired vigilance. This paper examines the hypothesis that sleep spindle (Sp) characteristics during nocturnal sleep can be mapped to vigilance deficits measured by the psychomotor vigilance task (PVT) in patients with OSA.Approach.The PVT was performed prior to In-laboratory Polysomnography for 250 patients. PVT outcomes were clustered into three vigilance groups (VGs). Spindles were scored manually for a Training Cohort of 55 patients, (9491 Sps) across different blocks of NREM sleep (SBs) and validated in a Test Cohort (25 patients, 4867 Sps). We proposed a novel set of Sp features including a spindle burst index (SBI), which quantifies the burst characteristics of spindles and constructed models mapping them to VGs. We also explored the performance of conventional Sp features (such as Sp number and density) in our modelling approach.Main results.In the Training Cohort, we observed statistically significant differences in the SBI across VGs and SBs independent of OSA severity (1st stage N2 SBI;p= <0.001 across VGs). In the Test Cohort, a Model based on the proposed SBI predicted VG membership with 88% accuracy. A model based on conventional Sp features mapped to VGs with 80% accuracy, and a model using mixed burst and conventional features reached an accuracy of 88%.Significance.Spindle features measured during diagnostic In-laboratory polysomnography measurements can be mapped to PVT outcomes. The novel SBI proved useful for exploring the relationship between PVT outcomes and sleep. Further studies in larger populations are needed to verify these conclusions.

Diagnostic Errors Are Common in Acute Pediatric Respiratory Disease: A Prospective, Single-Blinded Multicenter Diagnostic Accuracy Study in Australian Emergency Departments.

Background: Diagnostic errors are a global health priority and a common cause of preventable harm. There is limited data available for the prevalence of misdiagnosis in pediatric acute-care settings. Respiratory illnesses, which are particularly challenging to diagnose, are the most frequent reason for presentation to pediatric emergency departments. Objective: To evaluate the diagnostic accuracy of emergency department clinicians in diagnosing acute childhood respiratory diseases, as compared with expert panel consensus (reference standard). Methods: Prospective, multicenter, single-blinded, diagnostic accuracy study in two well-resourced pediatric emergency departments in a large Australian city. Between September 2016 and August 2018, a convenience sample of children aged 29 days to 12 years who presented with respiratory symptoms was enrolled. The emergency department discharge diagnoses were reported by clinicians based upon standard clinical diagnostic definitions. These diagnoses were compared against consensus diagnoses given by an expert panel of pediatric specialists using standardized disease definitions after they reviewed all medical records. Results: For 620 participants, the sensitivity and specificity (%, [95% CI]) of the emergency department compared with the expert panel diagnoses were generally poor: isolated upper respiratory tract disease (64.9 [54.6, 74.4], 91.0 [88.2, 93.3]), croup (76.8 [66.2, 85.4], 97.9 [96.2, 98.9]), lower respiratory tract disease (86.6 [83.1, 89.6], 92.9 [87.6, 96.4]), bronchiolitis (66.9 [58.6, 74.5], 94.3 [80.8, 99.3]), asthma/reactive airway disease (91.0 [85.8, 94.8], 93.0 [90.1, 95.3]), clinical pneumonia (63·9 [50.6, 75·8], 95·0 [92·8, 96·7]), focal (consolidative) pneumonia (54·8 [38·7, 70·2], 86.2 [79.3, 91.5]). Only 59% of chest x-rays with consolidation were correctly identified. Between 6.9 and 14.5% of children were inappropriately prescribed based on their eventual diagnosis. Conclusion: In well-resourced emergency departments, we have identified a previously unrecognized high diagnostic error rate for acute childhood respiratory disorders, particularly in pneumonia and bronchiolitis. These errors lead to the potential of avoidable harm and the administration of inappropriate treatment.

Identifying acute exacerbations of chronic obstructive pulmonary disease using patient-reported symptoms and cough feature analysis.

Acute exacerbations of chronic obstructive pulmonary disease (AECOPD) are commonly encountered in the primary care setting, though the accurate and timely diagnosis is problematic. Using technology like that employed in speech recognition technology, we developed a smartphone-based algorithm for rapid and accurate diagnosis of AECOPD. The algorithm incorporates patient-reported features (age, fever, and new cough), audio data from five coughs and can be deployed by novice users. We compared the accuracy of the algorithm to expert clinical assessment. In patients with known COPD, the algorithm correctly identified the presence of AECOPD in 82.6% (95% CI: 72.9-89.9%) of subjects (n = 86). The absence of AECOPD was correctly identified in 91.0% (95% CI: 82.4-96.3%) of individuals (n = 78). The diagnostic agreement was maintained in milder cases of AECOPD (PPA: 79.2%, 95% CI: 68.0-87.8%), who typically comprise the cohort presenting to primary care. The algorithm may aid early identification of AECOPD and be incorporated in patient self-management plans.

Diagnosing community-acquired pneumonia via a smartphone-based algorithm: a prospective cohort study in primary and acute-care consultations.

BACKGROUND: Community-acquired pneumonia (CAP) is an essential consideration in patients presenting to primary care with respiratory symptoms; however, accurate diagnosis is difficult when clinical and radiological examinations are not possible, such as during telehealth consultations. AIM: To develop and test a smartphone-based algorithm for diagnosing CAP without need for clinical examination or radiological inputs. DESIGN AND SETTING: A prospective cohort study using data from participants aged >12 years presenting with acute respiratory symptoms to a hospital in Western Australia. METHOD: Five cough audio-segments were recorded and four patient-reported symptoms (fever, acute cough, productive cough, and age) were analysed by the smartphone-based algorithm to generate an immediate diagnostic output for CAP. Independent cohorts were recruited to train and test the accuracy of the algorithm. Diagnostic agreement was calculated against the confirmed discharge diagnosis of CAP by specialist physicians. Specialist radiologists reported medical imaging. RESULTS: The smartphone-based algorithm had high percentage agreement (PA) with the clinical diagnosis of CAP in the total cohort (n = 322, positive PA [PPA] = 86.2%, negative PA [NPA] = 86.5%, area under the receiver operating characteristic curve [AUC] = 0.95); in participants 22-<65 years (n = 192, PPA = 85.7%, NPA = 87.0%, AUC = 0.94), and in participants aged ≥65 years (n = 86, PPA = 85.7%, NPA = 87.5%, AUC = 0.94). Agreement was preserved across CAP severity: 85.1% (n = 80/94) of participants with CRB-65 scores 1 or 2, and 87.7% (n = 57/65) with a score of 0, were correctly diagnosed by the algorithm. CONCLUSION: The algorithm provides rapid and accurate diagnosis of CAP. It offers improved accuracy over current protocols when clinical evaluation is difficult. It provides increased capabilities for primary and acute care, including telehealth services, required during the COVID-19 pandemic.

The diagnosis of respiratory disease in children using a phone-based cough and symptom analysis algorithm: The smartphone recordings of cough sounds 2 (SMARTCOUGH-C 2) trial design.

The diagnosis of acute respiratory diseases in children can be challenging, and no single objective diagnostic test exists for common pediatric respiratory diseases. Previous research has demonstrated that ResAppDx, a cough sound and symptom-based analysis algorithm, can identify common respiratory diseases at the point of care. We present the study protocol for SMARTCOUGH-C 2, a prospective diagnostic accuracy trial of a cough and symptom-based algorithm in a cohort of children presenting with acute respiratory diseases. The objective of the study is to assess the performance characteristics of the ResAppDx algorithm in the diagnosis of common pediatric acute respiratory diseases.

Stratifying asthma severity in children using cough sound analytic technology.

Introduction: Asthma is a common childhood respiratory disorder characterized by wheeze, cough and respiratory distress responsive to bronchodilator therapy. Asthma severity can be determined by subjective, manual scoring systems such as the Pulmonary Score (PS). These systems require significant medical training and expertise to rate clinical findings such as wheeze characteristics, and work of breathing. In this study, we report the development of an objective method of assessing acute asthma severity based on the automated analysis of cough sounds.Methods: We collected a cough sound dataset from 224 children; 103 without acute asthma and 121 with acute asthma. Using this database coupled with clinical diagnoses and PS determined by a clinical panel, we developed a machine classifier algorithm to characterize the severity of airway constriction. The performance of our algorithm was then evaluated against the PS from a separate set of patients, independent of the training set.Results: The cough-only model discriminated no/mild disease (PS 0-1) from severe disease (PS 5,6) but required a modified respiratory rate calculation to separate very severe disease (PS > 6). Asymptomatic children (PS 0) were separated from moderate asthma (PS 2-4) by the cough-only model without the need for clinical inputs.Conclusions: The PS provides information in managing childhood asthma but is not readily usable by non-medical personnel. Our method offers an objective measurement of asthma severity which does not rely on clinician-dependent inputs. It holds potential for use in clinical settings including improving the performance of existing asthma-rating scales and in community-management programs.AbbreviationsAMaccessory muscleBIbreathing indexCIconfidence intervalFEV1forced expiratory volume in one secondLRlogistic regressionPEFRpeak expiratory flow ratePSpulmonary scoreRRrespiratory rateSDstandard deviationSEstandard errorWAWestern Australia.

Polysomnographic risk factors for vigilance-related cognitive decline and obstructive sleep apnea.

PURPOSE: Cognitive decline (CD) and obstructive sleep apnea (OSA) are often comorbid. Some modifiable risk factors (RF) for CD are also associated with OSA. Diagnostic polysomnography (PSG) measures these RF and may identify at risk patients prior to the onset of CD. We aim to determine whether there are severe RF associated with established CD and an increasing severity of OSA that could identify patients at risk for CD for medical intervention. METHODS: We gathered information from subjects having type 1 PSG for suspected OSA. The psychomotor vigilance task (PVT) measured established CD (group 0 and group1). We compared levels of severe RF in group 0 and group 1 with a larger group (group 2) without the PVT. We used severe standardized values of excessive daytime sleepiness (Epworth Sleepiness Score [ESS]), overnight change of systolic blood pressure (ΔSBP), change of oxygen desaturation (ΔSpO2), and sleep arousal (ArI) as RF. We compared the severe levels of ESS, ΔSBP, ΔSpO2, and ArI by group and OSA severity. RESULTS: A total of 136 patients underwent diagnostic PSG. PVT parameters were available for 43 subjects. The severity of the RF was consistent with risk for CD (ΔSBP 22.0 ± 5.6, ESS 18.2 ± 2.2, ArI 58.8 ± 18.7, ΔSpO2 61.7 ± 21.9). The levels of RF increased with increasing severity of OSA. There were significant between-group differences for severe ΔSpO2 (p = 0.004) and ΔSpO2 + ArI (p = 0.019). CONCLUSION: The levels of RF increase with increasing OSA severity. Subjects with severe RF ΔSpO2 and ΔSpO2 + ArI are likely to have PVT-determined CD. Risk factor analysis may screen for CD.

Diagnosing Chronic Obstructive Airway Disease on a Smartphone Using Patient-Reported Symptoms and Cough Analysis: Diagnostic Accuracy Study.

BACKGROUND: Rapid and accurate diagnosis of chronic obstructive pulmonary disease (COPD) is problematic in acute care settings, particularly in the presence of infective comorbidities. OBJECTIVE: The aim of this study was to develop a rapid smartphone-based algorithm for the detection of COPD in the presence or absence of acute respiratory infection and evaluate diagnostic accuracy on an independent validation set. METHODS: Participants aged 40 to 75 years with or without symptoms of respiratory disease who had no chronic respiratory condition apart from COPD, chronic bronchitis, or emphysema were recruited into the study. The algorithm analyzed 5 cough sounds and 4 patient-reported clinical symptoms, providing a diagnosis in less than 1 minute. Clinical diagnoses were determined by a specialist physician using all available case notes, including spirometry where available. RESULTS: The algorithm demonstrated high positive percent agreement (PPA) and negative percent agreement (NPA) with clinical diagnosis for COPD in the total cohort (N=252; PPA=93.8%, NPA=77.0%, area under the curve [AUC]=0.95), in participants with pneumonia or infective exacerbations of COPD (n=117; PPA=86.7%, NPA=80.5%, AUC=0.93), and in participants without an infective comorbidity (n=135; PPA=100.0%, NPA=74.0%, AUC=0.97). In those who had their COPD confirmed by spirometry (n=229), PPA was 100.0% and NPA was 77.0%, with an AUC of 0.97. CONCLUSIONS: The algorithm demonstrated high agreement with clinical diagnosis and rapidly detected COPD in participants presenting with or without other infective lung illnesses. The algorithm can be installed on a smartphone to provide bedside diagnosis of COPD in acute care settings, inform treatment regimens, and identify those at increased risk of mortality due to seasonal or other respiratory ailments. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry ACTRN12618001521213; http://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=375939.

Overnight airway obstruction severity prediction centered on acoustic properties of smart phone: validation with esophageal pressure.

OBJECTIVE: Obstructive sleep apnea is characterized by a number of airway obstructions. Esophageal pressure manometry (EPM) based estimation of consecutive peak to trough differences (ΔPes) is the gold standard method to quantify the severity of airway obstructions. However, the procedure is rarely available in sleep laboratories due to invasive nature. There is a clinical need for a simplified, scalable technology that can quantify the severity of airway obstructions. In this paper, we address this and propose a pioneering technology, centered on sleep related respiratory sound (SRS) to predict overnight ΔPes signal. APPROACH: We recorded streams of SRS using a bedside iPhone 7 smartphone from subjects undergoing diagnostic polysomnography (PSG) studies and EPM was performed concurrently. Overnight data was divided into epochs of 10 s duration with 50% overlap. Altogether, we extracted 42 181 such epochs from 13 subjects. Acoustic features and features from the two PSG signals serve as an input to train a machine learning algorithm to achieve mapping between non-invasive features and ΔPes values. A testing dataset of 14 171 epochs from four new subjects was used for validation. MAIN RESULTS: The SRS based model predicted the ΔPes with a median of absolute error of 6.75 cmH2O (±0.59, r = 0.83(±0.03)). When information from the PSG were combined with the SRS, the model performance became: 6.37cmH2O (±1.02, r = 0.85(±0.04)). SIGNIFICANCE: The smart phone based SRS alone, or in combination with routinely collected PSG signals can provide a non-invasive method to predict overnight ΔPes. The method has the potential to be automated and scaled to provide a low-cost alternative to EPM.

A prospective multicentre study testing the diagnostic accuracy of an automated cough sound centred analytic system for the identification of common respiratory disorders in children.

BACKGROUND: The differential diagnosis of paediatric respiratory conditions is difficult and suboptimal. Existing diagnostic algorithms are associated with significant error rates, resulting in misdiagnoses, inappropriate use of antibiotics and unacceptable morbidity and mortality. Recent advances in acoustic engineering and artificial intelligence have shown promise in the identification of respiratory conditions based on sound analysis, reducing dependence on diagnostic support services and clinical expertise. We present the results of a diagnostic accuracy study for paediatric respiratory disease using an automated cough-sound analyser. METHODS: We recorded cough sounds in typical clinical environments and the first five coughs were used in analyses. Analyses were performed using cough data and up to five-symptom input derived from patient/parent-reported history. Comparison was made between the automated cough analyser diagnoses and consensus clinical diagnoses reached by a panel of paediatricians after review of hospital charts and all available investigations. RESULTS: A total of 585 subjects aged 29 days to 12 years were included for analysis. The Positive Percent and Negative Percent Agreement values between the automated analyser and the clinical reference were as follows: asthma (97, 91%); pneumonia (87, 85%); lower respiratory tract disease (83, 82%); croup (85, 82%); bronchiolitis (84, 81%). CONCLUSION: The results indicate that this technology has a role as a high-level diagnostic aid in the assessment of common childhood respiratory disorders. TRIAL REGISTRATION: Australian and New Zealand Clinical Trial Registry (retrospective) - ACTRN12618001521213 : 11.09.2018.

Correction to: Exhaustive mathematical analysis of simple clinical measurements for childhood pneumonia diagnosis.

In the original publication of the article "Declaration of conflict of interest" were not included. The following text is given below.

Corrections to "Automatic Croup Diagnosis Using Cough Sound Recognition".

Presents corrections to shareholder information from this paper, "Automatic croup diagnosis using cough sound recognition," (Sharan, R.V., et al), IEEE Trans. Biomed. Eng., vol. 66, no. 2, pp. 485-495, Feb. 2019.

Corrigendum: Predicting spirometry readings using cough sound features and regression (2018 Physiol. Meas. 39 095001).

The purpose of this submission is to provide missing information to complete the conflict of interest statement associated with the article. The statements provided here augment the already provided information rather than replace it.

Automatic Croup Diagnosis Using Cough Sound Recognition.

OBJECTIVE: Croup, a respiratory tract infection common in children, causes an inflammation of the upper airway restricting normal breathing and producing cough sounds typically described as seallike "barking cough." Physicians use the existence of barking cough as the defining characteristic of croup. This paper aims to develop automated cough sound analysis methods to objectively diagnose croup. METHODS: In automating croup diagnosis, we propose the use of mathematical features inspired by the human auditory system. In particular, we utilize the cochleagram for feature extraction, a time-frequency representation where the frequency components are based on the frequency selectivity property of the human cochlea. Speech and cough share some similarities in the generation process and physiological wetware used. As such, we also propose the use of mel-frequency cepstral coefficients which has been shown to capture the relevant aspects of the short-term power spectrum of speech signals. Feature combination and backward sequential feature selection are also experimented with. Experimentation is performed on cough sound recordings from patients presenting various clinically diagnosed respiratory tract infections divided into croup and non-croup. The dataset is divided into training and test sets of 364 and 115 patients, respectively, with automatically segmented cough sound segments. RESULTS: Croup and non-croup patient classification on the test dataset with the proposed methods achieve a sensitivity and specificity of 92.31% and 85.29%, respectively. CONCLUSION: Experimental results show the significant improvement in automatic croup diagnosis against earlier methods. SIGNIFICANCE: This paper has the potential to automate croup diagnosis based solely on cough sound analysis.

An Investigation of Critical Frequency Sub-bands of Snoring Sounds for OSA Diagnosis.

Obstructive Sleep Apnea (OSA) is a result of upper airway narrowing during sleep. The upper airway characteristics are likely to manifest in the acoustic characteristics of snoring sounds as snoring is a result of upper airway structure vibrations. In previous studies, researchers have used different regions of the frequency spectrum to diagnose OSA and determine sites of obstruction as well. However, there is no agreement among researchers about the frequency ranges critical for OSA diagnosis. This paper provides the results of a study of snore sound based OSA diagnosis performance using a multiple acoustic features and multiple classifiers. The results of the study may provide useful insights for researchers to identify frequency sub-bands critical for OSA diagnosis.

Smart Phone based Snoring Sound analysis to Identify Upper Airway Obstructions.

Obstructive sleep apnea (OSA) is characterized by upper airway obstructions known as apnea/hypopnea events. Narrowing of the upper airway during or near the vicinity of apnea/hypopnea causes the spectrum of the snores to shift to higher frequencies. Using an instrumentation quality wideband (WB) microphone (4Hz-100kHz), we previously demonstrated that potentially diagnostically useful frequency shifts could be detected even in regions beyond the human hearing range. WB-microphone based systems are expensive and not available for home use or population screening application. In this paper we explore the feasibility of using smart phones to analyze snoring sounds in the 20Hz-22kHz band to identify events of upper airway obstructions. Modern smart phones have internal microphones with bandwidths up to 22kHz, above the nominal human hearing range, and provide a good platform for sound acquisition and processing. For the work of this paper we used a Samsung Galaxy S3 phone and recorded overnight respiratory sound data from 8 patients undergoing routine Polysomnography (PSG) study in a hospital. Our target was to develop models to classify each standard 30 second epoch of data as non-apnea or apnea. Using 700 epochs we developed logistic regression models with the input as snoring sound features and the outputs as the diagnostic classification of each event (apnea/non-apnea). Models developed within a 20Hz-15kHz band had accuracies of 89-93%, sensitivities 70-78% and kappa index ranging 0.75-0.83 on validation data set. When the same models were developed on the 20Hz-22kHz frequency band the improved performance shows accuracies 94- 97%, sensitivities 93-100%, and kappa ranging 0.86-0.91. The study shows that smart phones based high frequency band (15-22kHz) of snoring sounds carry information about the upper airway obstructions. Our non-contact, smart phone based snoring sound technology has potential to identify upper airway obstructions.

Predicting spirometry readings using cough sound features and regression.

OBJECTIVE: Spirometry is a commonly used method of measuring lung function. It is useful in the definitive diagnosis of diseases such as asthma and chronic obstructive pulmonary disease (COPD). However, spirometry requires cooperative patients, experienced staff, and repeated testing to ensure the consistency of measurements. There is discomfort associated with spirometry and some patients are not able to complete the test. In this paper, we investigate the possibility of using cough sound analysis for the prediction of spirometry measurements. APPROACH: Our approach is based on the premise that the mechanism of cough generation and the forced expiratory maneuver of spirometry share sufficient similarities enabling this prediction. Using an iPhone, we collected mostly voluntary cough sounds from 322 adults presenting to a respiratory function laboratory for pulmonary function testing. Subjects had the following diagnoses: obstructive, restrictive, or mixed pattern diseases, or were found to have no lung disease along with normal spirometry. The cough sounds were automatically segmented using the algorithm described in Sharan et al (2018 IEEE Trans. Biomed. Eng.). We then represented cough sounds with various cough sound descriptors and built linear and nonlinear regression models connecting them to spirometry parameters. Augmentation of cough features with subject demographic data is also experimented with. The dataset was divided into 272 training subjects and 50 test subjects for experimentation. MAIN RESULTS: The performance of the auto-segmentation algorithm was evaluated on 49 randomly selected subjects from the overall dataset with a sensitivity and PPV of 84.95% and 98.51%, respectively. Our regression models achieved a root mean square error (and correlation coefficient) for standard spirometry parameters FEV1, FVC, and FEV1/FVC of 0.593L (0.810), 0.725L (0.749), and 0.164 (0.547), respectively, on the test dataset. In addition, we could achieve sensitivity, specificity, and accuracy of 70% or higher by applying the GOLD standard for COPD diagnosis on the estimated spirometry test results. SIGNIFICANCE: The experimental results show high positive correlation in predicting FEV1 and FVC and moderate positive correlation in predicting FEV1/FVC. The results show possibility of predicting spirometry results using cough sound analysis.

Snore Sound Analysis Can Detect the Presence of Obstructive Sleep Apnea Specific to NREM or REM Sleep.

STUDY OBJECTIVES: Severities of obstructive sleep apnea (OSA) estimated both for the overall sleep duration and for the time spent in rapid eye movement (REM) and non-rapid eye movement (NREM) sleep are important in managing the disease. The objective of this study is to investigate a method by which snore sounds can be analyzed to detect the presence of OSA in NREM and REM sleep. METHODS: Using bedside microphones, snoring and breathing-related sounds were acquired from 91 patients with OSA (35 females and 56 males) undergoing routine diagnostic polysomnography studies. A previously developed automated mathematical algorithm was applied to label each snore sound as belonging to either NREM or REM sleep. The snore sounds were then used to compute a set of mathematical features characteristic to OSA and to train a logistic regression model (LRM) to classify patients into an OSA or non-OSA category in each sleep state. The performance of the LRM was estimated using a leave-one-patient-out cross-validation technique within the entire dataset. We used the polysomnography-based diagnosis as our reference method. RESULTS: The models achieved 80% to 86% accuracy for detecting OSA in NREM sleep and 82% to 85% in REM sleep. When separate models were developed for females and males, the accuracy for detecting OSA in NREM sleep was 91% in females and 88% to 89% in males. Accuracy for detecting OSA in REM sleep was 88% to 91% in females and 89% to 91% in males. CONCLUSIONS: Snore sounds carry sufficient information to detect the presence of OSA during NREM and REM sleep. Because the methods used include technology that is fully automated and sensors that do not have a physical connection to the patient, it has potential for OSA screening in the home environment. The accuracy of the method can be improved by developing sex-specific models.

Automatic picking of snore events from overnight breath sound recordings.

Snoring is one of the earliest symptoms of Obstructive Sleep Apnea (OSA). However, the unavailability of an objective snore definition is a major obstacle in developing automated snore analysis system for OSA screening. The objectives of this paper is to develop a method to identify and extract snore sounds from a continuous sound recording following an objective definition of snore that is independent of snore loudness. Nocturnal sounds from 34 subjects were recorded using a non-contact microphone and computerized data-acquisition system. Sound data were divided into non-overlapping training (n = 21) and testing (n = 13) datasets. Using training dataset an Artificial Neural Network (ANN) classifier were trained for snore and non-snore classification. Snore sounds were defined based on the key observation that sounds perceived as `snores' by human are characterized by repetitive packets of energy that are responsible for creating the vibratory sound peculiar to snorers. On the testing dataset, the accuracy of ANN classifier ranged between 86 - 89%. Our results indicate that it is possible to define snoring using loudness independent, objective criteria, and develop automated snore identification and extraction algorithms.