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An Integrated Soft Computing Approach to Hughes Syndrome Risk Assessment
The AntiPhospholipid Syndrome ( APS ) is an acquired autoimmune disorder induced by high levels of antiphospholipid antibodies that cause arterial and veins thrombosis, as well as pregnancy-related complications and morbidity, as clinical manifestations. This autoimmune hypercoagulable state, usuall...
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Published in: | Journal of medical systems 2017-03, Vol.41 (3), p.40-40, Article 40 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The
AntiPhospholipid Syndrome
(
APS
) is an acquired autoimmune disorder induced by high levels of antiphospholipid antibodies that cause arterial and veins thrombosis, as well as pregnancy-related complications and morbidity, as clinical manifestations. This autoimmune hypercoagulable state, usually known as
Hughes
syndrome, has severe consequences for the patients, being one of the main causes of thrombotic disorders and death. Therefore, it is required to be preventive; being aware of how probable is to have that kind of syndrome. Despite the updated of antiphospholipid syndrome classification, the diagnosis remains difficult to establish. Additional research on clinically relevant antibodies and standardization of their quantification are required in order to improve the antiphospholipid syndrome risk assessment. Thus, this work will focus on the development of a diagnosis decision support system in terms of a formal agenda built on a
Logic Programming
approach to knowledge representation and reasoning, complemented with a computational framework based on
Artificial Neural Networks
. The proposed model allows for improving the diagnosis, classifying properly the patients that really presented this pathology (sensitivity higher than 85%), as well as classifying the absence of
APS
(specificity close to 95%). |
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ISSN: | 0148-5598 1573-689X |
DOI: | 10.1007/s10916-017-0688-5 |