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See detailPorcine trial validation of model-based cardiovascular monitoring of acute pulmonary embolism
Revie, JA; Stevenson, DJ; Shaw, GM et al

in Proceedings of ANZICS 2011 (2011)

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See detailDiagnosing pulmonary embolism from a model-based cardiac driver function
Stevenson, D; Revie, JA; Chase, JG et al

in Proceedings of ANZICS 2011 (2011)

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See detailProcessing aortic and pulmonary artery waveforms to derive the ventricle time-varying elastance
Stevenson, D; Chase, JG; Hann, CE et al

in Proceedings of the 18th IFAC World Congress, 2011 (2011)

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See detailNeurally Adjusted Ventilatory Assist (NAVA) improves the matching of diaphragmatic electrical activity and tidal volume in comparison to pressure support (PS)
Piquilloud, L; Chiew, YS; Bialais, E et al

in Intensive Care Medicine (2011), 37 (Suppl 1)

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See detailModel-based PEEP optimisation in mechanical ventilation
Chiew, Y. S.; Chase, J. G.; Shaw, G. M. et al

in BioMedical Engineering OnLine (2011), 10

Background: Acute Respiratory Distress Syndrome (ARDS) patients require mechanical ventilation (MV) for breathing support. Patient-specific PEEP is encouraged for treating different patients but there is ... [more ▼]

Background: Acute Respiratory Distress Syndrome (ARDS) patients require mechanical ventilation (MV) for breathing support. Patient-specific PEEP is encouraged for treating different patients but there is no well established method in optimal PEEP selection.Methods: A study of 10 patients diagnosed with ALI/ARDS whom underwent recruitment manoeuvre is carried out. Airway pressure and flow data are used to identify patient-specific constant lung elastance (E <br /> lung) and time-variant dynamic lung elastance (E <br /> drs) at each PEEP level (increments of 5cmH <br /> 2O), for a single compartment linear lung model using integral-based methods. Optimal PEEP is estimated using E <br /> lungversus PEEP, E <br /> drs-Pressure curve and E <br /> drsArea at minimum elastance (maximum compliance) and the inflection of the curves (diminishing return). Results are compared to clinically selected PEEP values. The trials and use of the data were approved by the New Zealand South Island Regional Ethics Committee.Results: Median absolute percentage fitting error to the data when estimating time-variant E <br /> drsis 0.9% (IQR = 0.5-2.4) and 5.6% [IQR: 1.8-11.3] when estimating constant E <br /> lung. Both E <br /> lungand E <br /> drsdecrease with PEEP to a minimum, before rising, and indicating potential over-inflation. Median E <br /> drsover all patients across all PEEP values was 32.2 cmH <br /> 2O/l [IQR: 26.1-46.6], reflecting the heterogeneity of ALI/ARDS patients, and their response to PEEP, that complicates standard approaches to PEEP selection. All E <br /> drs-Pressure curves have a clear inflection point before minimum E <br /> drs, making PEEP selection straightforward. Model-based selected PEEP using the proposed metrics were higher than clinically selected values in 7/10 cases.Conclusion: Continuous monitoring of the patient-specific E <br /> lungand E <br /> drsand minimally invasive PEEP titration provide a unique, patient-specific and physiologically relevant metric to optimize PEEP selection with minimal disruption of MV therapy. © 2011 Chiew et al; licensee BioMed Central Ltd. [less ▲]

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See detailInsulin Sensitivity, Its Variability and Glycemic Outcome: A model-based analysis of the difficulty in achieving tight glycemic control in critical care
Chase, J. Geoffrey; Le Compte, Aaron J.; Preiser, Jean-Charles et al

in 18th World Congress of the International Federation of Automatic Control (IFAC) (2011)

Effective tight glycemic control (TGC) can improve outcomes in intensive care unit (ICU) <br />patients, but is difficult to achieve consistently. Glycemic level and variability, particularly early in a ... [more ▼]

Effective tight glycemic control (TGC) can improve outcomes in intensive care unit (ICU) <br />patients, but is difficult to achieve consistently. Glycemic level and variability, particularly early in a <br />patient’s stay, are a function of variability in insulin sensitivity/resistance resulting from the level and <br />evolution of stress response, and are independently associated with mortality. This study examines the <br />daily evolution of variability of insulin sensitivity in ICU patients using patient data (N = 394 patients, <br />54019 hours) from the SPRINT TGC study. Model-based insulin sensitivity (SI) was identified each hour <br />and hour-to-hour percent changes in SI were assessed for Days 1-3 individually and Day 4 Onward, as <br />well as over all days. Cumulative distribution functions (CDFs), median values, and inter-quartile points <br />(25th and 75th percentiles) are used to assess differences between groups and their evolution over time. <br />Compared to the overall (all days) distributions, ICU patients are more variable on Days 1 and 2 (p < <br />0.0001), and less variable on Days 4 Onward (p < 0.0001). Day 3 is similar to the overall cohort (p = 0.74). <br />Absolute values of SI start lower and rise for Days 1 and 2, compared to the overall cohort (all days), (p < <br />0.0001), are similar on Day 3 (p = .72) and are higher on Days 4 Onward (p < 0.0001). ICU patients have <br />lower insulin sensitivity (greater insulin resistance) and it is more variable on Days 1 and 2, compared to <br />an overall cohort on all days. This is the first such model-based analysis of its kind. Greater variability <br />with lower SI early in a patient’s stay greatly increases the difficulty in achieving and safely maintaining <br />glycemic control, reducing potential positive outcomes. Clinically, the results imply that TGC patients will <br />require greater measurement frequency, reduced reliance on insulin, and more explicit specification of <br />carbohydrate nutrition in Days 1-3 to safely minimise glycemic variability for best outcome. [less ▲]

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See detailSafety and Performance of Stochastic Targeted (STAR) TGC of Insulin and Nutrition
Shaw, GM; Le Compte, Aaron; Evans, A et al

in Proceedings of SQAO 2011 (2011)

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See detailPilot Trials of STAR Target to Range Glycemic Control
Penning, Sophie ULg; Le Compte, Aaron; Massion, Paul et al

in Intensive Care Medicine (2011), 37 (Suppl 1)

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See detailVariability of insulin sensitivity for diabetics and non-diabetics during the first 3 days of ICU stay
Pretty, Christopher G.; Le Compte, Aaron; Preiser, Jean-Charles et al

in Intensive Care Medicine (2011), 37 (Suppl 1)

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See detailPatient-ventilator synchrony and tidal volume variability using NAVA and pressure support mechanical ventilation modes
Moorhead, K. T.; Piquilloud, L.; LAMBERMONT, Bernard ULg et al

in Proceedings of the 18th IFAC world congress, 2011 (2011)

Neurally Adjusted Ventilatory Assist (NAVA) is a new ventilatory mode in which ventilator settings are adjusted based on the electrical activity detected in the diaphragm (Eadi). This mode offers ... [more ▼]

Neurally Adjusted Ventilatory Assist (NAVA) is a new ventilatory mode in which ventilator settings are adjusted based on the electrical activity detected in the diaphragm (Eadi). This mode offers significant advantages in mechanical ventilation over standard pressure support (PS) modes, since ventilator input is determined directly from patient ventilatory demand. A comparative study of 22 patients undergoing mechanical ventilation in both PS and NAVA modes was conducted, and it was concluded that for a given variability in Eadi, there is greater variability in tidal volume and correlation between the tidal volume and the diaphragmatic electrical activity with NAVA compared to PS. These results are consistent with the improved patient-ventilator synchrony reported in the literature. © 2011 IFAC. [less ▲]

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See detailModel-based diagnosis of acute pulmonary embolism and septic shock in porcine trials
Revie, JA; Stevenson, D; Chase, JG et al

in Proceedings of the Health Research Society of Christchurch Annual Scientific Session 2011 (2011)

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See detailEnteral nutrition-associated incretin effect in the critically ill
Preiser, JC; Jamaludin, U; Docherty, P et al

in Proceedings of the 33rd Congress of Clinical Nutrition and Metabolism (ESPEN 2011) (2011)

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See detailObservation of the Incretin Effect in Critically Ill patients
Jamaludin, U.; Docherty, P; Chase, JG et al

in Proceedings of the 11th Annual Diabetes Technology Meeting (DTM2011) (2011)

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See detailProcessing aortic and pulmonary artery waveforms to derive the ventricle time-varying elastance
Stevenson, D. J.; Hann, C. E.; Chase, G. J. et al

in IFAC Proceedings Volumes (IFAC-PapersOnline) (2011), 18(PART 1), 587-592

Time-varying elastance of the ventricles is an important metric both clinically and as an input for a previously developed cardiovascular model. However, currently time-varying elastance is not normally ... [more ▼]

Time-varying elastance of the ventricles is an important metric both clinically and as an input for a previously developed cardiovascular model. However, currently time-varying elastance is not normally available in an Intensive Care Unit (ICU) setting, as it is an invasive and ethically challenging metric to measure. A previous paper developed a method to map less invasive metrics to the driver function, enabling an estimate to be achieved without invasive measurements. This method requires reliable and accurate processing of the aortic and pulmonary artery pressure waveforms to locate the specific points that are required to estimate the driver function. This paper details the method by which these waveforms are processed, using a data set of five pigs induced with pulmonary embolism, and five pigs induced with septic shock (with haemofiltration), adding up to 88 waveforms (for each of aortic and pulmonary artery pressure), and 616 points in total to locate. 98.2% of all points were located to within 1% of their true value, 0.81% were between 1% and 5%, 0.65% were between 5% and 10%, the remaining 0.32% were below 20%.© 2011 IFAC. [less ▲]

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See detailA simplified model for mitral valve dynamics.
Moorhead, K. T.; Paeme, Sabine ULg; Chase, J. G. et al

in Computer Methods & Programs in Biomedicine (2011)

Located between the left atrium and the left ventricle, the mitral valve controls flow between these two cardiac chambers. Mitral valve dysfunction is a major cause of cardiac dysfunction and its dynamics ... [more ▼]

Located between the left atrium and the left ventricle, the mitral valve controls flow between these two cardiac chambers. Mitral valve dysfunction is a major cause of cardiac dysfunction and its dynamics are little known. A simple non-linear rotational spring model is developed and implemented to capture the dynamics of the mitral valve. A measured pressure difference curve was used as the input into the model, which represents an applied torque to the anatomical valve chords. A range of mechanical model hysteresis states were investigated to find a model that best matches reported animal data of chord movement during a heartbeat. The study is limited by the use of one dataset found in the literature due to the highly invasive nature of getting this data. However, results clearly highlight fundamental physiological issues, such as the damping and chord stiffness changing within one cardiac cycle, that would be directly represented in any mitral valve model and affect behaviour in dysfunction. Very good correlation was achieved between modeled and experimental valve angle with 1-10% absolute error in the best case, indicating good promise for future simulation of cardiac valvular dysfunction, such as mitral regurgitation or stenosis. In particular, the model provides a pathway to capturing these dysfunctions in terms of modeled stiffness or elastance that can be directly related to anatomical, structural defects and dysfunction. [less ▲]

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See detailClinical detection and monitoring of acute pulmonary embolism: proof of concept of a computer-based method.
Revie, James A; Stevenson, David J; Chase, J Geoffrey et al

in Annals of Intensive Care (2011), 1(1), 33

ABSTRACT: BACKGROUND: The diagnostic ability of computer-based methods for cardiovascular system (CVS) monitoring offers significant clinical potential. This research tests the clinical applicability of a ... [more ▼]

ABSTRACT: BACKGROUND: The diagnostic ability of computer-based methods for cardiovascular system (CVS) monitoring offers significant clinical potential. This research tests the clinical applicability of a newly improved computer-based method for the proof of concept case of tracking changes in important hemodynamic indices due to the influence acute pulmonary embolism (APE). METHODS: Hemodynamic measurements from a porcine model of APE were used to validate the method. Of these measurements, only those that are clinically available or inferable were used in to identify pig-specific computer models of the CVS, including the aortic and pulmonary artery pressure, stroke volume, heart rate, global end diastolic volume, and mitral and tricuspid valve closure times. Changes in the computer-derived parameters were analyzed and compared with experimental metrics and clinical indices to assess the clinical applicability of the technique and its ability to track the disease state. RESULTS: The subject-specific computer models accurately captured the increase in pulmonary resistance (Rpul), the main cardiovascular consequence of APE, in all five pigs trials, which related well (R2 = 0.81) with the experimentally derived pulmonary vascular resistance. An increase in right ventricular contractility was identified, as expected, consistent with known reflex responses to APE. Furthermore, the modeled right ventricular expansion index (the ratio of right to left ventricular end diastolic volumes) closely followed the trends seen in the measured data (R2 = 0.92) used for validation, with sharp increases seen in the metric for the two pigs in a near-death state. These results show that the pig-specific models are capable of tracking disease-dependent changes in pulmonary resistance (afterload), right ventricular contractility (inotropy), and ventricular loading (preload) during induced APE. Continuous, accurate estimation of these fundamental metrics of cardiovascular status can help to assist clinicians with diagnosis, monitoring, and therapy-based decisions in an intensive care environment. Furthermore, because the method only uses measurements already available in the ICU, it can be implemented with no added risk to the patient and little extra cost. CONCLUSIONS: This computer-based monitoring method shows potential for real-time, continuous diagnosis and monitoring of acute CVS dysfunction in critically ill patients. [less ▲]

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See detailVariability of insulin sensitivity for diabetics and non-diabetics during the first 3 days of ICU stay
Pretty, Christopher G.; Le Compte, Aaron; Preiser, Jean-Charles et al

Poster (2011)

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See detailSafety and Performance of Stochastic Targeted (STAR) Glycemic Control of Insulin and Nutrition - First Pilot Results
Shaw, Geoffrey M.; Le Compte, Aaron; Evans, Alicia et al

Poster (2011)

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See detailSafety and Performance of Stochastic Targeted (STAR) Glycemic Control of Insulin and Nutrition – First Pilot Results
Shaw, Geoffrey M.; Le Compte, Aaron; Evans, Alicia et al

in Intensive Care Medicine (2011)

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See detailPilot Trials of STAR Target to Range Glycemic Control
Penning, Sophie ULg; Le Compte, Aaron; Massion, Paul et al

Poster (2011)

Detailed reference viewed: 8 (2 ULg)