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Aina Frau-Pascual

Publications and source records attributed to Aina Frau-Pascual.

4 recordsLinked to original sources

Artificial Intelligence for early detection of circulatory shock in ICU patients

Circulatory shock is one of the leading causes of mortality in intensive care units (ICUs), and its early detection is critical to enable timely treatment and improve clinical outcomes. This study aimed to develop and evaluate a two-stage cascade machine learning framework for the early detection and etiological classification of circulatory shock in critically ill patients. Using data from the Medical Information Mart for Intensive Care (MIMIC)-IV database, four patient groups were defined: septic shock, cardiogenic shock, hypovolemic shock, and a non?shock control group, comprising a total of 32,907 patients. Vital signs and laboratory data were collected during the first six hours after ICU admission. After data cleaning and missing-value imputation, the mean value of each variable was used for model development. Several machine learning algorithms were compared, including logistic regression, Random Forest, XGBoost, and multilayer perceptron (MLP) networks. Random Forest and XGBoost achieved the highest overall performance, with an AUROC of approximately 0.82-0.83 for shock detection, and a macro-averaged sensitivity of approximately 0.61 and precision of approximately 0.58 across all four classes. Classification performance was highest for the non?shock group, followed by septic and cardiogenic shock, while hypovolemic shock showed the lowest performance. These results indicate that machine learning models can identify early signs of hemodynamic deterioration associated with circulatory shock and may support clinical decision-making in the ICU. However, further improvements are needed for the classification of specific shock subtypes, particularly hypovolemic and cardiogenic shock, as well as for real-time clinical implementation.

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Gaussian Processes for HRF estimation for BOLD fMRI

We present a non-parametric joint estimation method for fMRI task activation values and the hemodynamic response function (HRF). The HRF is modeled as a Gaussian process, making continuous evaluation possible for jittered paradigms and providing a variance estimate at each point.

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Physiologically Informed Bayesian Analysis of ASL fMRI Data

Arterial Spin Labelling (ASL) functional Magnetic Resonance Imaging (fMRI) data provides a quantitative measure of blood perfusion, that can be correlated to neuronal activation. In contrast to BOLD measure, it is a direct measure of cerebral blood flow. However, ASL data has a lower SNR and resolution so that the recovery of the perfusion response of interest suffers from the contamination by a stronger hemodynamic component in the ASL signal. In this work we consider a model of both hemodynamic and perfusion components within the ASL signal. A physiological link between these two components is analyzed and used for a more accurate estimation of the perfusion response function in particular in the usual ASL low SNR conditions.

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Hemodynamically informed parcellation of cerebral FMRI data

Standard detection of evoked brain activity in functional MRI (fMRI) relies on a fixed and known shape of the impulse response of the neurovascular coupling, namely the hemodynamic response function (HRF). To cope with this issue, the joint detection-estimation (JDE) framework has been proposed. This formalism enables to estimate a HRF per region but for doing so, it assumes a prior brain partition (or parcellation) regarding hemodynamic territories. This partition has to be accurate enough to recover accurate HRF shapes but has also to overcome the detection-estimation issue: the lack of hemodynamics information in the non-active positions. An hemodynamically-based parcellation method is proposed, consisting first of a feature extraction step, followed by a Gaussian Mixture-based parcellation, which considers the injection of the activation levels in the parcellation process, in order to overcome the detection-estimation issue and find the underlying hemodynamics.

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