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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/28264
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dc.contributor.advisorDoyle, Thomas E.-
dc.contributor.authorKhan, Md Asif-
dc.date.accessioned2023-01-27T19:41:05Z-
dc.date.available2023-01-27T19:41:05Z-
dc.date.issued2022-
dc.identifier.urihttp://hdl.handle.net/11375/28264-
dc.description.abstractChronic pain (CP) is a personal and economic burden that affects more than 30% of the world's population. While being the leading cause of disability, it is complicated to diagnose and manage. The optimal way to treat CP is to identify the pain mechanism or the underlying cause. The substantial overlap of the pain mechanisms (i.e., Nociceptive, Neuropathic, and Nociplastic) usually makes identification unreachable in a clinical setting where finding the dominant mechanism is complicated. Additionally, many specialists regard CP classification as a spectrum or continuum. Despite the importance, a data-driven way to identify co-existing CP mechanisms and quantification is still absent. This work successfully identified the co-existing CP mechanisms within a patient using Unsupervised Learning while quantifying them without the help of diagnosis established by the clinicians. Two different datasets from different cohorts comprised of patient-reported history and questionnaires were used in this work. Unsupervised Learning (k-prototypes) revealed notable overlaps in the data. It was further emphasized by the outcomes of the Semi-supervised Learning algorithms when the same trend was observed with some diagnosis or class information. It became evident that the CP mechanisms overlap and cannot be classified as distinct conditions. Additionally, mixed pain mechanisms do not make an individual cluster or class, and CP should be considered as a continuum. To reduce data dimension and extract hidden features, Autoencoder was used. Using an overlapping clustering technique, the pain mechanisms were identified. The pain mechanisms were also quantified while elucidating overlaps, and the dominant CP mechanism was successfully pointed out with explainable element. The hamming loss of 0.43 and average precision of 0.5 were achieved when considered as a multi-label classification problem. This work is a data-driven validation that there are significant overlaps in CP conditions, and CP should be considered a continuum where all CP mechanisms may co-exist.en_US
dc.language.isoenen_US
dc.subjectUnsupervised Learningen_US
dc.subjectChronic Painen_US
dc.subjectSemi-supervised Learningen_US
dc.subjectCo-existing Chronic Pain Mechanismen_US
dc.subjectOverlapping Clusteringen_US
dc.subjectAutoencoderen_US
dc.subjectChronic Pain as a Continuumen_US
dc.subjectChronic Pain Quantificationen_US
dc.subjectMachine Learningen_US
dc.subjectArtificial Intelligenceen_US
dc.titleChronic Pain as a Continuum: Autoencoder and Unsupervised Learning Methods for Archetype Clustering and Identifying Co-existing Chronic Pain Mechanismsen_US
dc.title.alternativeChronic Pain as a Continuum: Unsupervised Learning for Identification of Co-existing Chronic Pain Mechanismsen_US
dc.typeThesisen_US
dc.contributor.departmentElectrical and Computer Engineeringen_US
dc.description.degreetypeThesisen_US
dc.description.degreeMaster of Applied Science (MASc)en_US
dc.description.layabstractChronic pain (CP) is a global burden and the primary cause for patients to seek medical attention. Despite continuous efforts in this area, CP remains clinically challenging to manage. The most effective method of treating CP is identifying the underlying cause or mechanism, which is often unattainable. This thesis attempted to identify the CP mechanisms existing in a patient while quantifying them from patient-reported history and questionnaire data. Unsupervised Learning was used to identify clinically meaningful clusters that revealed the three main CP mechanisms, i.e., Nociceptive, Neuropathic, and Nociplastic, achieving acceptable hamming loss (0.43) and average precision (0.5). The results exhibited that the CP mechanisms co-exist and CP should be regarded as a continuum rather than distinct entities. The algorithm successfully indicated the dominant CP mechanism, a goal for optimal CP management and treatment. The results were also validated by a comparative analysis with data from another cohort that demonstrated a similar trend.en_US
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