Computer-aided auscultation (CAA), or computerized assisted auscultation, is a digital form of auscultation. It includes the recording, visualization, storage, analysis and sharing of digital recordings of heart or lung sounds. The recordings are obtained using an electronic stethoscope or similarly suitable recording device. Computer-aided auscultation is designed to assist health care professionals who perform auscultation as part of their diagnostic process. Commercial CAA products are usually classified as clinical decision support systems that support medical professionals in making a diagnosis. As such they are medical devices and require certification or approval from a competent authority (e.g. FDA approval, CE conformity issued by notified body).
Computer-aided auscultation | |
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Synonyms | Computerized assisted auscultation |
Test of | auscultation via computer assistance |
Benefits of CAA
editCompared to traditional auscultation, computer-aided auscultation (CAA) offers a range of improvements beneficial to multiple stakeholders:
- CAA can yield more accurate and objective results and is likely to outperform the auscultation skills and subjective interpretation of humans.[1]
- With the use of CAA, auscultation is no longer a method reserved for specialists and physicians. For instance, nurses and paramedics can easily be instructed to use CAA systems correctly on their patients.
- CAA opens up new opportunities for telemedicine. Real-time tele-auscultation can help specialists located anywhere in the world to diagnose rare conditions observed in patients in developing countries or remote areas.[2][3][4]
- CAA opens up new opportunities for health monitoring and health management.
- CAA allows analysis findings to be documented electronically. The results can be stored and retrieved as needed and possibly included in electronic patient records.[5][6]
- Standardized auscultation data derived from CAA can help national payers and providers implement more efficient and cost-effective screening programs.
- CAA can be used for teaching and training purposes with medical and nursing students.
Functional principle
editIn a CAA system, sounds are recorded through an electronic stethoscope. The audio data is transferred to an electronic device via Bluetooth or an audio cable connection. Special software on that device visualizes, stores and analyzes the data. With some of the more sophisticated CAA systems, the CAA analysis yields results that can be used to objectify diagnoses (decision support system).[citation needed]
Components in a CAA system
editThe components of a CAA system depend on its complexity. Whereas some of the simpler systems provide only visualization or storage options, other systems combine visualization, storage, analysis and the ability to electronically manage said data.
Electronic stethoscope
editElectronic stethoscopes (also digital stethoscopes) convert acoustic sound waves into digital electrical signals. These signals are then amplified by means of transducers and currently reach levels up to 100 times higher than traditional acoustic stethoscopes. Additionally, electronic stethoscopes can be used to filter out background noise, a feature that can be safety-relevant and facilitate more accurate diagnoses. Whereas sound amplification and filtering are the main functions of an electronic stethoscope, the ability to access the sounds through external means via Bluetooth or audio cables makes them an ideal sound-capturing device for CAA systems.[citation needed]
Device running Graphical User Interface
editDevices that can be used to connect to an electronic stethoscope and record the audio signal (e.g. heart or lung sounds) include PC, laptop and mobile devices like smartphones or tablets. Generally, CAA systems include software that can visualize the incoming audio signal. More sophisticated CAA systems include live noise detection algorithms, designed to help the user achieve the best possible recording quality.
Analysis software
editA key feature of CAA systems is the automated analysis of the recorded audio signals by signal processing algorithms. Such algorithms can run directly on the device used for making the recording, or be hosted in a cloud connected to the device. The degree of autonomy of currently available analysis algorithms varies greatly. While some systems operate fully autonomously,[7] early PC-based systems required significant user interaction and interpretation of results,[8] and other analysis systems require some degree of assistance by the user like manual confirmation/correction of estimated heart rates.[9]
Storage of auscultation based data
editRecorded sounds and associated analytical and patient data can be electronically stored, managed or archived. Patient identifying information might be handled or stored in the process. If the stored data classifies as PHI (protected health information), a system hosting such data must be compliant with country-specific data protection laws like HIPAA for the US or the Data Protection Directive for the EU. Storage options for current CAA systems range from the basic ability to retrieve a downloadable PDF report to a comprehensive cloud-based interface for electronic management of all auscultation-based data.[citation needed]
Cloud-based user interface
editThe user can review all their patient records (including replaying the audio files) via a user interface, e.g. via a web-portal in the browser or stand-alone software on the electronic device. Other functionalities include sharing records with other users, exporting patient records and integration into EHR systems.
CAA of the heart
editComputer-aided auscultation aimed at detecting and characterizing heart murmurs is called computer-aided heart auscultation (also known as automatic heart sound analysis).
Motivation
editAuscultation of the heart using a stethoscope is the standard examination method worldwide to screen for heart defects by identifying murmurs. It requires that an examining physician have acute hearing and extensive experience. An accurate diagnosis remains challenging for various reasons including noise, high heart rates, and the ability to distinguish innocent from pathological murmurs. Properly performed, the auscultatory examination of the heart is commonly regarded as an inexpensive, widely available tool in the detection and management of heart disease.[10] The auscultation skills of physicians, however, have been reported to be declining.[11][12][13][14][15][16][17] This leads to missed disease diagnoses and/or excessive costs for unnecessary and expensive diagnostic testing. A study suggests that more than one third of previously undiagnosed congenital heart defects in newborns are missed by their 6-week examination.[18] More than 60% of referrals to medical specialists for costly echocardiography are due to a misdiagnosis of an innocent murmur.[14] CAA of the heart thus has the potential to become a cost-effective screening and diagnostic tool, provided that its underlying algorithms have been clinical tested in stringent, blinded fashions for their ability to detect the difference between normal and abnormal heart sounds.
Heart murmurs and CAA
editHeart murmurs (or cardiac murmurs) are audible noises through a stethoscope, generated by a turbulent flow of blood. Heart murmurs need to be distinguished from heart sounds which are primarily generated by the beating heart and the heart valves snapping open and shut. Generally, heart murmurs are classified as innocent (also called physiological or functional) or pathological (abnormal). Innocent murmurs are usually harmless, often caused by physiological conditions outside the heart, and the result of certain benign structural defects. Pathological murmurs are most often associated with heart valve problems but may also be caused by a wide array of structural heart defects. Various characteristics constitute a qualitative description of heart murmurs, including timing (systolic murmur and diastolic murmur), shape, location, radiation, intensity, pitch and quality. CAA systems typically categorize heart sounds and murmurs as Class I and Class III according to the American Heart Association:[19]
- Class I: pathological murmur
- Class III: innocent murmur or no murmur
More sophisticated CAA systems provide additional descriptive murmur information like murmur timing, grading, or the ability to identify the positions of the S1/S2 heart sounds.
Heart sound analysis
editThe detection of heart murmurs in CAA systems is based on the analysis of digitally recorded heart sounds. Most approaches use the following four stages:
- Heart rate detection: In the first stage, the heart rate is determined based on the audio signal of the heart. It is a crucial step for the following stages and high accuracy is required. Automated heart rate determination based on acoustic recordings is challenging because the heart rate can range from 40-200bpm, noise and murmurs can camouflage the peaks of the heart sounds (S1 and S2), and irregular heartbeats can disturb the quasi-periodic nature of the heartbeat.
- Heart sound segmentation: After the heart rate has been detected, the two main phases of the heartbeat (systole and diastole) are identified. This differentiation is important since most murmurs occur in specific phases during the heartbeat. External noise from the environment or internal noise from the patient (e.g. breathing) make heart sound segmentation challenging.
- Feature extraction: Having identified the phases of the heartbeat, information (features) from the heart sound is extracted that enters a further classification stage. Features can range from simple energy-based approaches to higher-order multi-dimensional quantities.
- Feature classification: During classification, the features extracted in the previous stage are used to classify the signal and assess the presence and type of a murmur. The main challenge is to differentiate no-murmur recordings from low-grade innocent murmurs, and innocent murmurs from pathological murmurs. Usually machine-learning approaches are applied to construct a classifier based on training data.
Clinical evidence of CAA systems
editThe most common types of performance measures for CAA systems are based on two approaches: retrospective (non-blinded) studies using existing data and prospective blinded clinical studies on new patients. In retrospective CAA studies, a classifier is trained with machine learning algorithms using existing data. The performance of the classifier is then assessed using the same data. Different approaches are used to do this (e.g., k-Fold cross-validation, leave-one-out cross-validation). The main shortcoming of judging the quality (sensitivity, specificity) of a CAA system based on retrospective performance data alone comes from the risk that the approaches used can overestimate the true performance of a given system. Using the same data for training and validation can itself lead to significant overfitting of the validation set, because most classifiers can be designed to analyse known data very well, but might not be general enough to correctly classify unknown data; i.e. the results look much better than they would if tested on new, unseen patients. “The true performance of a selected network (CAA system) should be confirmed by measuring its performance on a third independent set of data called a test set”.[20] In summary, the reliability of retrospective, non-blinded studies are usually considered to be much lower than that of prospective clinical studies because they are prone to selection bias and retrospective bias. Published examples include Pretorius et al.[21] Prospective clinical studies, on the other hand, are better suited to assess the true performance of a CAA system (provided that the study is blinded and well controlled). In a prospective clinical study to evaluate the performance of a CAA system, the output of the CAA system is compared to the gold standard diagnoses. In the case of heart murmurs, a suitable gold standard diagnosis would be auscultation-based expert physician diagnosis, stratified by an echocardiogram-based diagnosis. Published examples include Lai et al.[1]
See also
editReferences
edit- ^ a b Lai, Lillian; Andrew N. Redington; Andreas J. Reinisch; Michael J. Unterberger; Andreas J. Schriefl (2016). "Computerized Automatic Diagnosis of Innocent and Pathologic Murmurs in Pediatrics: A Pilot Study". Congenital Heart Disease. 11 (5): 386–395. doi:10.1111/chd.12328. PMID 26990211. S2CID 20921069.
- ^ Vaidyanathan, B; Sathish G; Mohanan ST; Sundaram KR; Warrier KK; Kumar RK (2011). "Clinical screening for Congenital heart disease at birth: a prospective study in a community hospital in Kerala". Indian Pediatrics. 48 (1): 25–30. doi:10.1007/s13312-011-0021-1. PMID 20972295. S2CID 10788521.
- ^ Zühlke, Z; Myer L; Mayosi BM (2012). "The promise of computer-assisted auscultation in screening for structural heart disease and clinical teaching". Cardiovascular Journal of Africa. 23 (7): 405–408. doi:10.5830/CVJA-2012-007. PMC 3721800. PMID 22358127.
- ^ Mandal, S; Basak K; Mandana KM; Ray AK; Chatterjee J; Mahadevappa M (2011). "Development of cardiac prescreening device for rural population using ultralow-power embedded system". IEEE Transactions on Biomedical Engineering. 58 (3): 745–749. doi:10.1109/TBME.2010.2089457. PMID 21342805. S2CID 7771478.
- ^ Iwamoto, J; Ogawa H; Maki H; Yonezawa Y; Hahn AW; Caldwell WM (2011). "A mobile phone-based ecg and heart sound monitoring system". Biomedical Sciences Instrumentation. 47: 160–164. PMID 21525614.
- ^ Koekemoer, H. L.; Scheffer, C. (2008). "Heart sound and electrocardiogram recording devices for telemedicine environments". 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. Vol. 2008. pp. 4867–4870. doi:10.1109/IEMBS.2008.4650304. ISBN 978-1-4244-1814-5. PMID 19163807. S2CID 32681936.
- ^ a b c "Home". eMURMUR.
- ^ "Zargis Cardioscan".
- ^ a b "Diacoustic Medical Devices".
- ^ Becket Mahnke, C. (2009). "Automated heartsound analysis/Computer-aided auscultation: A cardiologist's perspective and suggestions for future development". 2009 Annual International Conference of the IEEE Engineering in Medicine and Biology Society. Vol. 2009. pp. 3115–3118. doi:10.1109/IEMBS.2009.5332551. PMID 19963568. S2CID 630335.
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- ^ Kumar, Komal; W. Reid Thompson (2012). "Evaluation of Cardiac Auscultation Skills in Pediatric Residents". Clinical Pediatrics. 52 (1): 66–73. doi:10.1177/0009922812466584. PMID 23185081. S2CID 29237618.
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- ^ Germanakis, I; Petridou ET; Varlamis G; Matsoukis IL; Papadopoulou-Legbelou K.; Kalmanti M (2013). "Skills of primary healthcare physicians in paediatric cardiac auscultation". Acta Paediatrica. 102 (2): 74–78. doi:10.1111/apa.12062. PMID 23082851. S2CID 10518559.
- ^ Gaskin, PR; Owens SE; Talner NS; Sanders SP; Li JS (2000). "Clinical auscultation skills in pediatric residents". Pediatrics. 105 (6): 1184–1187. doi:10.1542/peds.105.6.1184. PMID 10835055. S2CID 14993738.
- ^ Caddell, AJ; Wong KK; Barker AP; Warren AE (2015). "Trends in pediatric cardiology referrals, testing, and satisfaction at a Canadian tertiary centre". Canadian Journal of Cardiology. 31 (1): 95–98. doi:10.1016/j.cjca.2014.10.028. PMID 25547558.
- ^ Wren, Christopher; Sam Richmond; Liam Donaldson (1999). "Presentation of congenital heart disease in infancy: implications for routine examination". Arch Dis Child Fetal Neonatal Ed. 80 (1): F49–F53. doi:10.1136/fn.80.1.f49. PMC 1720871. PMID 10325813.
- ^ Bonow, Robert O.; Blase A. Carabello; Kanu Chatterjee; Antonio C. de Leon; David P. Faxon; Michael D. Freed; William H. Gaasch; Bruce Whitney Lytle; Rick A. Nishimura; Patrick T. O’Gara; Robert A. O’Rourke; Catherine M. Otto; Pravin M. Shah; Jack S. Shanewise (2006). "ACC/AHA 2006 Guidelines for the Management of Patients With Valvular Heart Disease". Circulation. 114 (5): 84–231. doi:10.1161/CIRCULATIONAHA.106.176857. PMID 16880336.
- ^ Bishop, Christopher (1995). Neural Networks for Pattern Recognition. Oxford University Press.
- ^ Pretorius, Eugene; Cronje, Matthys L.; Strydom, Otto (2010). "Development of a pediatric cardiac computer aided auscultation decision support system". 2010 Annual International Conference of the IEEE Engineering in Medicine and Biology. Vol. 2010. pp. 6078–6082. doi:10.1109/IEMBS.2010.5627633. ISBN 978-1-4244-4123-5. PMID 21097128. S2CID 27940646.