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1.
J Gynecol Obstet Hum Reprod ; 52(7): 102624, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37321400

ABSTRACT

BACKGROUND: class III obese women, are at a higher risk of cesarean section during labor, and cesarean section is responsible for increased maternal and neonatal morbidity in this population. OBJECTIVE: the objective of this project was to develop a method with which to quantify cesarean section risk before labor. METHODS: this is a multicentric retrospective cohort study conducted on 410 nulliparous class III obese pregnant women who attempted vaginal delivery in two French university hospitals. We developed two predictive algorithms (a logistic regression and a random forest models) and assessed performance levels and compared them. RESULTS: the logistic regression model found that only initial weight and labor induction were significant in the prediction of unplanned cesarean section. The probability forest was able to predict cesarean section probability using only two pre-labor characteristics: initial weight and labor induction. Its performances were higher and were calculated for a cut-point of 49.5% risk and the results were (with 95% confidence intervals): area under the curve 0.70 (0.62,0.78), accuracy 0.66 (0.58, 0.73), specificity 0.87 (0.77, 0.93), and sensitivity 0.44 (0.32, 0.55). CONCLUSIONS: this is an innovative and effective approach to predicting unplanned CS risk in this population and could play a role in the choice of a trial of labor versus planned cesarean section. Further studies are needed, especially a prospective clinical trial. FUNDING: French state funds "Plan Investissements d'Avenir" and Agence Nationale de la Recherche.


Subject(s)
Cesarean Section , Obesity , Infant, Newborn , Female , Pregnancy , Humans , Retrospective Studies , Prospective Studies , Obesity/epidemiology , Machine Learning
2.
PLoS One ; 12(8): e0182169, 2017.
Article in English | MEDLINE | ID: mdl-28792506

ABSTRACT

Lymphadenopathy continues to be a common problem to radiologists and treating physicians because of the difficulty in confidently categorizing a node as being benign or malignant using standard diagnostic techniques. The goal of our research was to assess whether magnetic resonance (MR) spectroscopy contains the necessary information to allow differentiation of benign from malignant lymph nodes in an in-vitro approach using a modern pattern recognition method. Tissue samples from a tissue bank were analyzed on a nuclear magnetic resonance (NMR) spectrometer. A total of 69 samples were studied. The samples included a wide variety of malignant and benign etiologies. Using 45 samples, we initially created a model which was able to predict if a certain spectrum originates from benign or malignant lymph nodes using a pattern-recognition technique which takes into account the entire magnetic spectrum rather than single peaks alone. The remaining 24 samples were blindly loaded in the model to assess its performance. We obtained an excellent accuracy in differentiating benign and malignant lymphadenopathy using the model. It correctly differentiated as malignant or benign, in a blinded fashion, all of the malignant samples (13 of 13) and 10 out of the 11 benign samples. We thus showed that magnetic spectroscopy is able to differentiate benign from malignant causes of lymphadenopathy. Additional experiments were performed to verify that the differentiating abilities of our model were not due to differential tissue decay in between benign and malignant tissues. If future experiments demonstrate that a similar approach could be executed with standard MR imaging, this technique could be useful as a problem-solving tool when assessing lymphadenopathy in general. Alternatively, our in-vitro technique could also be useful to pathologists faced with indeterminate pathologies of the lymph nodes after validating our results with a larger sample size.


Subject(s)
Lymph Nodes/diagnostic imaging , Lymphadenopathy/diagnostic imaging , Lymphatic Metastasis/diagnostic imaging , Proton Magnetic Resonance Spectroscopy , Diagnosis, Computer-Assisted , Diagnosis, Differential , Discriminant Analysis , Humans , Lymph Nodes/metabolism , Lymph Nodes/pathology , Lymphadenopathy/etiology , Lymphadenopathy/metabolism , Lymphadenopathy/pathology , Lymphatic Metastasis/pathology , Lymphatic Metastasis/physiopathology , Models, Theoretical , Single-Blind Method , Software
3.
J Biopharm Stat ; 24(2): 378-97, 2014.
Article in English | MEDLINE | ID: mdl-24605975

ABSTRACT

The use of two or more primary correlated endpoints is becoming increasingly common. A mandatory approach when analyzing data from such clinical trials is to control the family-wise error rate (FWER). In this context, we provide formulas for computation of sample size and for data analysis. Two approaches are discussed: an individual method based on a union-intersection procedure and a global procedure, based on a multivariate model that can take into account adjustment variables. These methods are illustrated with simulation studies and applications. An R package known as rPowerSampleSize is also available.


Subject(s)
Clinical Trials as Topic , Computer Simulation , Endpoint Determination/methods , Clinical Trials as Topic/statistics & numerical data , Computer Simulation/statistics & numerical data , Endpoint Determination/statistics & numerical data , Humans , Sample Size
4.
Eur J Neurosci ; 27(6): 1432-40, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18364022

ABSTRACT

A central question in chemical senses is the way that odorant molecules are represented in the brain. To date, many studies, when taken together, suggest that structural features of the molecules are represented through a spatio-temporal pattern of activation in the olfactory bulb (OB), in both glomerular and mitral cell layers. Mitral/tufted cells interact with a large population of inhibitory interneurons resulting in a temporal patterning of bulbar local field potential (LFP) activity. We investigated the possibility that molecular features could determine the temporal pattern of LFP oscillatory activity in the OB. For this purpose, we recorded the LFPs in the OB of urethane-anesthetized, freely breathing rats in response to series of aliphatic odorants varying subtly in carbon-chain length or functional group. In concordance with our previous reports, we found that odors evoked oscillatory activity in the LFP signal in both the beta and gamma frequency bands. Analysis of LFP oscillations revealed that, although molecular features have almost no influence on the intrinsic characteristics of LFP oscillations, they influence the temporal patterning of bulbar oscillations. Alcohol family odors rarely evoke gamma oscillations, whereas ester family odors rather induce oscillatory patterns showing beta/gamma alternation. Moreover, for molecules with the same functional group, the probability of gamma occurrence is correlated to the vapor pressure of the odor. The significance of the relation between odorant features and oscillatory regimes along with their functional relevance are discussed.


Subject(s)
Anesthesia , Biological Clocks/physiology , Odorants , Olfactory Bulb/physiology , Action Potentials/drug effects , Action Potentials/physiology , Alcohols/administration & dosage , Alcohols/standards , Anesthesia/methods , Animals , Biological Clocks/drug effects , Esters/administration & dosage , Esters/standards , Male , Olfactory Bulb/drug effects , Pressure , Rats , Rats, Wistar , Smell/drug effects , Smell/physiology , Volatilization
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