Publication | Open Access
Detecting pathogen exposure during the non-symptomatic incubation period using physiological data
11
Citations
52
References
2017
Year
Unknown Venue
Machine LearningPathogen DetectionNipah VirusesNon-symptomatic Incubation PeriodExposure DetectionPathogen ExposureDiagnosisDisease DetectionPathogen TransmissionHealthcare-associated InfectionBiostatisticsInfection ControlAlgorithm TrainingPublic HealthSyndromic SurveillanceDisease SurveillanceEpidemiologyEpidemic IntelligencePhysiological DataPathogenesisDisease TransmissionMedicineHealth Informatics
Abstract Early pathogen exposure detection allows better patient care and faster implementation of public health measures (patient isolation, contact tracing). Existing exposure detection most frequently relies on overt clinical symptoms, namely fever, during the infectious prodromal period. We have developed a robust machine learning based method to better detect asymptomatic states during the incubation period using subtle, sub-clinical physiological markers. Starting with high-resolution physiological waveform data from non-human primate studies of viral (Ebola, Marburg, Lassa, and Nipah viruses) and bacterial ( Y. pestis ) exposure, we processed the data to reduce short-term variability and normalize diurnal variations, then provided these to a supervised random forest classification algorithm and post-classifier declaration logic step to reduce false alarms. In most subjects detection is achieved well before the onset of fever; subject cross-validation across exposure studies (varying viruses, exposure routes, animal species, and target dose) lead to 51h mean early detection (at 0.93 area under the receiver-operating characteristic curve [AUCROC]). Evaluating the algorithm against entirely independent datasets for Lassa, Nipah, and Y. pestis exposures un-used in algorithm training and development yields a mean 51h early warning time (at AUCROC=0.95). We discuss which physiological indicators are most informative for early detection and options for extending this capability to limited datasets such as those available from wearable, non-invasive, ECG-based sensors.
| Year | Citations | |
|---|---|---|
2001 | 119.3K | |
1967 | 15.4K | |
1910 | 4.3K | |
2006 | 2.7K | |
2001 | 2.5K | |
2009 | 2.2K | |
1993 | 1.7K | |
2004 | 1.2K | |
2017 | 939 | |
1997 | 796 |
Page 1
Page 1