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1.
Soft Matter ; 19(9): 1739-1748, 2023 Mar 01.
Article in English | MEDLINE | ID: mdl-36779239

ABSTRACT

Methyl cellulose (MC) is a widely used material in various microfluidic applications in biology. Due to its biocompatibility, it has become a popular crowding agent for microfluidic cell deformability measurements, which usually operate at high shear rates (>10 000 s-1). However, a full rheological characterization of methyl cellulose solutions under these conditions has not yet been reported. With this study, we provide a full shear-rheological description for solutions of up to 1% MC dissolved in phosphate-buffered saline (PBS) that are commonly used in real-time deformability cytometry (RT-DC). We characterized three different MC-PBS solutions used for cell mechanical measurements in RT-DC with three different shear rheometer setups to cover a range of shear rates from 0.1-150 000 s-1. We report viscosities and normal stress differences in this regime. Viscosity functions can be well described using a Carreau-Yasuda model. Furthermore, we present the temperature dependency of shear viscosity and first normal stress difference of these solutions. Our results show that methyl cellulose solutions behave like power-law liquids in viscosity and exhibit first normal stress difference at shear rates between 5000-150 000 s-1. We construct a general viscosity equation for each MC solution at a certain shear rate and temperature. Furthermore, we investigated how MC concentration influences the rheology of the solutions and found the entanglement concentration at around 0.64 w/w%. Our results help to better understand the viscoelastic behavior of MC solutions, which can now be considered when modelling stresses in microfluidic channels.

2.
Can J Anaesth ; 67(6): 664-673, 2020 06.
Article in English | MEDLINE | ID: mdl-32128723

ABSTRACT

PURPOSE: To compare the clinical judgement of electroencephalogram (EEG)-naïve anesthesiologists with an EEG-based measurement of anesthetic depth (AD) using the Narcotrend® monitor. METHODS: In this prospective cohort study including 600 patients, AD during stable anesthesia was assessed by clinical judgement of the attending, EEG-blinded anesthesiologist (using a scale staging the AD as mid-adequate, adequate but fairly deep, or adequate but fairly light) and by simultaneously recorded Narcotrend measurements. RESULTS: In 42% of patients (n = 250), the anesthesiologist's clinical judgement was in agreement with anesthetic levels as measured by the Narcotrend monitor. In 46% of patients (n = 274), the anesthesiologist's judgement and the Narcotrend monitor differed by one AD level (minor discordance). Major discordance was observed in 76 (13%) measurements (judged deeper than measured, n = 29 [5%]; judged lighter than measured, n = 47 [8%]). In 7% of patients (n = 44), the Narcotrend index was outside the limits of adequate AD (too deep, n = 28 [5%]; too superficial, n = 16 [3%]). The overall level of agreement between the anesthesiologist's judgement and the Narcotrend monitor was not statistically significant (Cohen's kappa, -0.039; P = 0.17). Using a random forests algorithm, age, mean blood pressure, the American Society of Anesthesiologists classification, body mass index, and frailty were the variables with the highest relative feature importance to predict the level of agreement. CONCLUSION: These results suggest that clinical judgement of AD during stable anesthesia was not in agreement with EEG-based assessment of anesthetic depth in 58% of cases. Nevertheless, this finding could be influenced by the lack of validated scales to clinically judge AD. TRIAL REGISTRATION: www.clinicaltrials.gov (NCT02766894); registered 10 May, 2016.


RéSUMé: OBJECTIF: Notre objectif était de comparer le jugement clinique d'anesthésiologistes n'ayant pas accès à un électroencéphalogramme (EEG) à une mesure de la profondeur anesthésique (PA) fondée sur l'EEG utilisant le moniteur Narcotrend®. MéTHODE: Dans cette étude de cohorte prospective de 600 patients, la PA a été évaluée pendant la phase de maintien stable de l'anesthésie selon le jugement clinique de l'anesthésiologiste traitant, qui n'avait pas accès à l'EEG (sur une échelle évaluant la PA comme étant adéquate, adéquate mais relativement profonde ou adéquate mais relativement légère) et par des mesures simultanément enregistrées par le Narcotrend. RéSULTATS: Chez 42 % des patients (n = 250), le jugement clinique de l'anesthésiologiste concordait aux niveaux anesthésiques tels que mesurés par le moniteur Narcotrend. Chez 46 % des patients (n = 274), le jugement de l'anesthésiologiste et le moniteur Narcotrend différaient d'un niveau de PA (discordance mineure). Une discordance majeure a été observée dans 76 (13 %) mesures (jugées plus profondes que mesurées, n = 29 [5 %], jugées plus légères que mesurées, n = 47 [8 %]). Chez 7 % des patients (n = 44), l'indice Narcotrend était situé au-delà des limites d'une PA adéquate (trop profond, n = 28 [5 %]; trop superficiel, n = 16 [3 %]). Le niveau global de concordance entre le jugement de l'anesthésiologiste et le moniteur Narcotrend n'était pas significatif d'un point de vue statistique (kappa de Cohen, -0,039; P = 0,17). En se fondant sur un algorithme de forêt d'arbres décisionnels (random forests algorithm), l'âge, la tension artérielle moyenne, la classification selon l'American Society of Anesthesiologists, l'indice de masse corporelle et l'index de fragilité ont été identifiés comme les variables ayant la plus grande importance relative pour prédire le niveau de concordance. CONCLUSION: Ces résultats suggèrent que, dans 58 % des cas, le jugement clinique de la PA ne concordait pas à l'évaluation par EEG de la profondeur anesthésique pendant une phase de maintien stable de l'anesthésie. Toutefois, ces résultats pourraient être influencés par l'absence d'échelles validées pour juger la PA d'un point de vue clinique. ENREGISTREMENT DE L'éTUDE: www.clinicaltrials.gov (NCT02766894); enregistrée le 10 mai 2016.


Subject(s)
Anesthesia , Anesthetics, Intravenous , Clinical Reasoning , Electroencephalography , Humans , Monitoring, Intraoperative , Propofol , Prospective Studies
4.
ASAIO J ; 63(1): 109-111, 2017.
Article in English | MEDLINE | ID: mdl-27748657

ABSTRACT

Peripartum cardiomyopathy (PPCMP) requiring mechanical circulatory support is rare; however, it is a life-threatening disease with recovery rates poorer than expected. Herein, we describe a case of successful recovery of a patient with PPCMP. Implantation of a biventricular ventricular assist device was performed; additionally, the patient's hyperprolactinemia was treated with cabergoline, resulting in a fast complete restoration of ventricular function.


Subject(s)
Cardiomyopathies/therapy , Heart Ventricles/physiopathology , Heart-Assist Devices , Hyperprolactinemia/drug therapy , Puerperal Disorders/therapy , Adult , Cardiomyopathies/physiopathology , Female , Humans , Pregnancy , Puerperal Disorders/physiopathology
5.
Med Phys ; 39(9): 5547-56, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22957621

ABSTRACT

PURPOSE: To determine the effects of imager source and panel positioning uncertainties on the accuracy of dual intensity-based 2D∕3D image registration of cranial images. METHODS: An open source 2D∕3D image registration algorithm has been developed for registration of two orthogonal x-rays to a 3D volumetric image. The initialization files of the algorithm allow for nine degrees of freedom system calibration including x, y, z positions of the source and panel, and three rotational degrees of freedom of the panel about each of the three translational axes. A baseline system calibration was established and a baseline 2D∕3D registration between two orthogonal x-rays and the volumetric image was determined. The calibration file was manipulated to insert errors into each of the nine calibration variables of both imager geometries. Rigid six degrees of freedom registrations were iterated for each panel or source positional error over a range of predetermined calibration errors to determine the resulting error in the registration versus the baseline registration due to the manipulated error of the panel or source calibration. RESULTS: Panel and source translational errors orthogonal to the imager∕panel axis introduced the greatest errors in the registration accuracy (4.0 mm geometric error results in up to 2.7 mm registration error). Panel rotation about the imaging direction also resulted in errors of the registration (2.0° geometric error results in up to 1.7° registration error). Differences in magnification and panel tilt and roll, i.e., source and∕or panel translation along the imaging direction and panel rotations about the orthogonal axes had minimal effects on the registration accuracy (below 0.3 mm and 0.2° registration error). CONCLUSIONS: While five of the nine imaging system variables were found to have a considerable effect on 2D∕3D registration accuracy of cranial images, the other four variables showed minimal effects. Vendors typically provide simplified calibration procedures which aim to remove encountered geometric uncertainties by accounting for two panel translations. This study shows that at least the five relevant positional variables should be separately calibrated, if accurate alignment is required for 2D∕3D registration.


Subject(s)
Imaging, Three-Dimensional/methods , Skull/diagnostic imaging , Tomography, X-Ray Computed/methods , Uncertainty , Algorithms , Humans , Tomography, X-Ray Computed/instrumentation
6.
Neurosurg Rev ; 29(1): 30-5, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16184406

ABSTRACT

Meningiomas of the ventricle system are extremely rare. We report on a series of 16 intraventricular meningiomas (IVMs) treated at our institution between 1980 and 2004, with a special interest on the surgical outcome of using the intra/inter-parietal and parieto-occipital approach and the benefits of neuro-navigation. A retrospective analysis of the medical files for clinicoradiological findings, surgical interventions and surgical outcome was carried out. In 16 IVM patients with a female/male ratio of 11:5, age ranged from 24 years to 84 years (median 44 years). Duration of symptoms ranged from a few days to several years, and the cardinal symptoms were signs of increased intracranial pressure (86%), followed by corticospinal tract signs (43%), visual field defects (36%), cognitive changes (29%) and seizures (7%). The majority of tumours was located in the trigone (88%), and one was found in each the temporal horn and in the fourth ventricle. Tumour size ranged from 2.5 cm to 8 cm (median 5 cm), and the radiological appearance was uniform. The neuropathological workup revealed most IVMs as meningothelial, transitional (mixed) or lymphoplasmacyte-rich meningiomas (81%). Three tumours were classified as atypical (19%) and the MIB-1 proliferation index ranged from 1% to 40%. Complete resection was possible in all but one case. The trigonal IVMs were resected via an intraparietal/inter-parietal or parieto-occipital approach, and neuro-navigation was used in eight tumours. We encountered one perioperative death and one severely disabled patient. All other patients had a Glasgow outcome scale score of 5, and most of the pre-existing symptoms disappeared or improved after surgery. IVMs are a surgically curable tumour entity in most cases. The intraparietal/inter-parietal and parieto-occipital approach is very safe, and neuro-navigation allows early devascularisation of the tumour.


Subject(s)
Meningeal Neoplasms/diagnosis , Meningeal Neoplasms/pathology , Meningioma/diagnosis , Meningioma/pathology , Adult , Aged , Aged, 80 and over , Brain/blood supply , Brain/diagnostic imaging , Brain/pathology , Female , Glasgow Outcome Scale , Humans , Magnetic Resonance Angiography , Male , Meningeal Neoplasms/diagnostic imaging , Meningeal Neoplasms/surgery , Meningioma/diagnostic imaging , Meningioma/surgery , Middle Aged , Neuronavigation , Neurosurgical Procedures/methods , Retrospective Studies , Tomography, X-Ray Computed , Treatment Outcome
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