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Dive into the research topics where Monique Oswald-Mammosser is active.

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Featured researches published by Monique Oswald-Mammosser.


Chest | 2005

Does thoracic bioimpedance accurately determine cardiac output in COPD patients during maximal or intermittent exercise

Valérie Bougault; Evelyne Lonsdorfer-Wolf; Anne Charloux; Ruddy Richard; Bernard Geny; Monique Oswald-Mammosser

STUDY OBJECTIVES The monitoring of cardiac output (CO) during exercise rehabilitation in patients with COPD, often including strenuous exercise, is advisable. Invasive methods (thermodilution, Fick method) are accurate, but for clinical routine use noninvasive CO estimation is required. We have shown that impedance cardiography (Physio Flow; Manatec Biomedical; Macheren, France) is reliable in COPD patients at rest and during a recumbent, light-intensity exercise. The aim of our study was to evaluate the validity of this noninvasive device in COPD patients during a maximal incremental exercise test (IET) and also during a strenuous intermittent work exercise test (IWET). DESIGN Prospective comparative study of the impedance cardiograph vs the direct Fick method applied to oxygen. PATIENTS Eight patients with moderate-to-severe COPD (59 +/- 6 years old; FEV(1), 38 +/- 15% predicted; residual volume, 194 +/- 64% predicted) [mean +/- SD]. MEASUREMENTS AND MAIN RESULTS Forty-nine simultaneous measurements of CO by means of the direct Fick method (COfick) and CO measured by the impedance cardiograph (COpf) were obtained during the IET, and 108 measurements were made during the IWET. The correlation coefficients between the two measurements were r = 0.85 and r = 0.71 for the IET and the IWET, respectively. COpf was higher than COfick. The difference between the two methods was 3.2 +/- 2.9 L/min during the IET and 2.5 +/- 2.1 L/min during the IWET. Expressed as a percentage of the mean of the two measurements, this corresponded to 31 +/- 21% and 25 +/- 20%, respectively. CONCLUSIONS The relatively high number of values differing by > 20% precludes the use of impedance cardiography in clinical routine in such a difficult setting (hyperinflated patients and intense exercise).


PLOS ONE | 2014

Probiotics (VSL#3) Prevent Endothelial Dysfunction in Rats with Portal Hypertension: Role of the Angiotensin System

Sherzad Rashid; Noureddine Idris Khodja; Cyril Auger; Mahmoud Alhosin; Nelly Boehm; Monique Oswald-Mammosser; Valérie B. Schini-Kerth

Aims Portal hypertension characterized by generalized vasodilatation with endothelial dysfunction affecting nitric oxide (NO) and endothelium-dependent hyperpolarization (EDH) has been suggested to involve bacterial translocation and/or the angiotensin system. The possibility that ingestion of probiotics prevents endothelial dysfunction in rats following common bile duct ligation (CBDL) was evaluated. Methods Rats received either control drinking water or the probiotic VSL#3 solution (50 billion bacteria.kg body wt−1.day−1) for 7 weeks. After 3 weeks, rats underwent surgery with either resection of the common bile duct or sham surgery. The reactivity of mesenteric artery rings was assessed in organ chambers, expression of proteins by immunofluorescence and Western blot analysis, oxidative stress using dihydroethidium, and plasma pro-inflammatory cytokine levels by flow cytometry. Results Both NO- and EDH-mediated relaxations to acetylcholine were reduced in the CBDL group compared to the sham group, and associated with a reduced expression of Cx37, Cx40, Cx43, IKCa and SKCa and an increased expression of endothelial NO synthase (eNOS). In aortic sections, increased expression of NADPH oxidase subunits, angiotensin converting enzyme, AT1 receptors and angiotensin II, and formation of ROS and peroxynitrite were observed. VSL#3 prevented the deleterious effect of CBDL on EDH-mediated relaxations, vascular expression of connexins, IKCa, SKCa and eNOS, oxidative stress, and the angiotensin system. VSL#3 prevented the CBDL-induced increased plasma TNF-α, IL-1α and MCP-1 levels. Conclusions These findings indicate that VSL#3 ingestion prevents endothelial dysfunction in the mesenteric artery of CBDL rats, and this effect is associated with an improved vascular oxidative stress most likely by reducing bacterial translocation and the local angiotensin system.


Respirology | 2010

The opening interrupter technique for respiratory resistance measurements in children

Monique Oswald-Mammosser; Anne Charloux; Irina Enache; Evelyne Lonsdorfer-Wolf

Background and objective:  The interrupter resistance (Rint) can be calculated from various estimates of alveolar pressure based on mouth pressure during occlusion. We compared Rint, as measured by the opening interrupter technique (Rint1), and the linear back‐extrapolation method (Rint2), with the ‘gold standard’ airway resistance measured by plethysmography (Raw).


Respiratory Medicine | 2009

A comparison of four algorithms for the measurement of interrupter respiratory resistance in adults

Monique Oswald-Mammosser; Anne Charloux; Irina Enache; E. Lonsdorfer-Wolf; B. Geny

The aim of our study was to compare four algorithms for the measurement of respiratory resistance in adults using the interrupter technique. Four methods to estimate alveolar pressure from the mouth pressure during occlusion were assessed in 122 normal adults (57 males, 65 females, aged 18-79 yr, mean 41.2 +/- 15.6): taking the mean oscillation pressure (Rint), performing a linear back extrapolation (RintL) or a linear regression for the whole curve (RintRL), taking the end-occlusion pressure (RintE). Mean values for Rint, RintL and RintRL in males were respectively 0.23 +/- 0.04, 0.22 +/- 0.04 and 0.22 +/- 0.04 kPa s L(-1), not statistically different. In females values were respectively 0.27 +/- 0.05, 0.26 +/- 0.05 and 0.26 +/- 0.05 kPa s L(-1), not statistically different. RintE was higher than the remainder and was the only measure correlating weakly with morphometric variables: RintE = 1.152 - (0.00152 x age (yr)) - (0.00382 x height (cm)), r = 0.31 (p < 0.05) in females; RintE = 0.227 - (0.00122 x age (yr)) + (0.00830 x body mass index (kg m(-2))) with r = 0.34 (p < 0.05) in males. We conclude that it is equivalent to estimate alveolar pressure from or extrapolating it to the beginning of occlusion in healthy adults but when taking the end-occlusion pressure, resistance is higher and depends in part on morphometric parameters.


Respiration | 2013

Impact of 3D Conformal Radiotherapy on Lung Function of Patients with Lung Cancer: A Prospective Study

Irina Enache; Georges Noel; Mi Young Jeung; Nicolas Meyer; Monique Oswald-Mammosser; Cristina Pistea; Guy-Michel Jung; Bertrand Mennecier; Elisabeth Quoix; Anne Charloux

Background: The development of three-dimensional conformal radiotherapy (3D-RT) has enabled the restriction of the dose to normal lung, limiting radiation-induced lung injury. Objectives: This study was designed to describe the time course of lung function until 7.5 months after 3D-RT in patients with lung cancer, and assess the relationship between lung function changes and dose-volume histogram (DVH) analysis or computed tomography scan changes. Radiation doses were optimized according to recent guidelines. Methods: Sixty-five lung cancer patients treated with 3D-RT agreed to participate in this prospective, hospital-based study. Lung volumes, forced expiratory volume in 1 s (FEV1) and diffusing capacity of the lung for carbon monoxide (DLCO) were measured before radiotherapy (RT), 10 weeks, 4 and 7.5 months after the beginning of 3D-RT. Results: Eleven lung cancer patients (17%) developed grade 2-3 respiratory symptoms after RT. At 7.5 months, vital capacity (VC) was 96 ± 2%, total lung capacity (TLC) 95 ± 2%, FEV1 93 ± 2% and DLCO 90 ± 2% of the initial value. Only 15% of patients showed pulmonary function reduction >20%. Patients with FEV1 or DLCO <60% before RT did not show significant changes after RT. There were weak correlations between reduction of VC, TLC, FEV1 or DLCO and radiation dosimetric parameters and between reduction of VC or FEV1 and radiation-induced pneumonitis images. Conclusions: In lung cancer, the reduction of lung function within 7.5 months after 3D-RT was small and correlated, albeit weakly, with DVH parameters. Patients with initially impaired lung function showed tiny changes in spirometry and DLCO values.


Radiation Oncology | 2012

Can exhaled NO fraction predict radiotherapy-induced lung toxicity in lung cancer patients?

Irina Enache; Georges Noel; M-Young Jeung; Nicolas Meyer; Monique Oswald-Mammosser; Emile Urban-Kraemer; C. Schumacher; Bernard Geny; Elisabeth Quoix; Anne Charloux

BackgroundA large increase in nitric oxide fraction (FeNO) after radiotherapy (RT) for lung cancer may predict RT-induced lung toxicity.MethodsIn this study, we assessed the relationships between FeNO variations and respiratory symptoms, CT scan changes or dose volume histogram (DVH) parameters after RT. We measured FeNO before RT, 4, 5, 6, 10 weeks, 4 and 7.5 months after RT in 65 lung cancer patients.ResultsEleven lung cancer patients (17%) complained of significant respiratory symptoms and 21 (31%) had radiation pneumonitis images in >1/3 of the irradiated lung after RT. Thirteen patients (20%) showed increases in FeNO >10 ppb. The sensitivity and specificity of a >10 ppb FeNO increase for the diagnosis of RT-associated respiratory symptoms were 18% and 83%, respectively. There was no correlation between DVH parameters or CT scan changes after RT and FeNO variations. Three patients (5%) showed intriguingly strong (2 or 3-fold, up to 55 ppb) and sustained increases in FeNO at 4 and 5 weeks, followed by significant respiratory symptoms and/or radiation-pneumonitis images.ConclusionSerial FeNO measurements during RT had a low ability to identify lung cancer patients who developed symptoms or images of radiation pneumonitis. However, three patients presented with a particular pattern which deserves to be investigated.


Respiration | 2011

Impact of altered alveolar volume on the diffusing capacity of the lung for carbon monoxide in obesity.

Irina Enache; Monique Oswald-Mammosser; Stéphanie Scarfone; Chantal Simon; Jean-Louis Schlienger; Bernard Geny; Anne Charloux

Background: Studies on the diffusing capacity of the lung for carbon monoxide (DL<sub>CO</sub>) in obese patients are conflicting, some studies showing increased DL<sub>CO</sub> and others unaltered or reduced values in these subjects. Objectives: To compare obese patients to controls, examine the contribution of alveolar volume (VA) and CO transfer coefficient (K<sub>CO</sub>) to DL<sub>CO</sub>, and calculate DL<sub>CO</sub> values adjusted for VA. Methods: We measured body mass index (BMI), waist circumference (WC), spirometry and DL<sub>CO</sub> in 98 adult obese patients without cardiopulmonary or smoking history and 48 healthy subjects. All tests were performed in the same laboratory. Results: Using conventional reference values, mean DL<sub>CO</sub> and VA were lower (–6%, p < 0.05, and –13%, p < 0.001, respectively), and K<sub>CO</sub> was higher (+9%, p < 0.05) in obese patients than in controls. VA decreased whereas K<sub>CO</sub> increased with increasing BMI and WC in the obese group. Patients with lower DL<sub>CO</sub> had low K<sub>CO</sub> in addition to decreased VA. In contrast, some obese patients maintained normal VA, which, coupled with high K<sub>CO</sub>, resulted in higher DL<sub>CO</sub>. The main result is that diffusion capacity differences between obese patients and controls disappeared using reference equations adjusting DL<sub>CO</sub> for VA. Conclusions: Using conventional reference equations, our obese patients show slightly lower mean DL<sub>CO,</sub> lower mean VA and higher mean K<sub>CO</sub> than controls, but with a large range of DL<sub>CO</sub> values and patterns. Adjusting DL<sub>CO</sub> for VA suggests that low lung volumes are the main cause of low DL<sub>CO</sub> and high K<sub>CO</sub> values in obese patients.


Amyotrophic Lateral Sclerosis | 2017

Ability of pulmonary function decline to predict death in amyotrophic lateral sclerosis patients

Irina Enache; Cristina Pistea; Marie Fleury; Mickaël Schaeffer; Monique Oswald-Mammosser; Andoni Echaniz-Laguna; Christine Tranchant; Nicolas Meyer; Anne Charloux

Abstract Objectives: Objectives were to evaluate the relative risk of death associated with lung function decline in patients with amyotrophic lateral sclerosis (ALS), and to examine the ability of ALS patients to perform volitional pulmonary function tests (PFTs). Methods: The PFTs of 256 consecutive patients referred to the Strasbourg University Hospital ALS Centre over an eight-year period were reviewed. Slow vital capacity (VC), maximal inspiratory and expiratory pressures (MIP, MEP), sniff nasal inspiratory pressure (SNIP), and peak cough flow (PCF) were performed at diagnosis and then every four months. The instantaneous risk of death associated with PFTs deterioration was calculated using time-dependent covariate Cox models. The changes of each PFT over time were examined and compared. Results: A total of 985 acceptable PFT sessions were recorded. The risk of death was significantly associated with the decline in pulmonary function, regardless of the PFT parameter and its expression. When VC, MIP/SNIP and MEP (% of predicted) decreased by 10%, or PCF decreased by 50 L/min, the risk of death was multiplied by 1.31 (95% CI 1.21–1.41), 1.48 (1.32–1.66), 1.54 (1.32–1.79), and 1.32 (1.19–1.75), respectively. MIP, SNIP and MEP were decreased earlier in the course of disease and plunged deeper than VC within months before death, but were more affected by learning effect. Conclusions: This study provides tools to calculate the increase in risk of death from a PFT decline. At an individual level, since each test showed some flaws, the use of a combination of PFTs for ALS respiratory monitoring is recommended.


Fundamental & Clinical Pharmacology | 2015

Effect of the oestrogen receptor antagonist fulvestrant on the cirrhotic rat lung

Monique Oswald-Mammosser; Sherzad Rashid; Nelly Boehm; Arnaud Agin; Bernard Geny; Valérie B. Schini-Kerth; Anne Charloux

It has been postulated that cirrhosis‐related lung vasodilatation and the subsequent hepatopulmonary syndrome are partly explained by an increased estradiol level through an enhanced endothelial formation of nitric oxide (NO). In this study, we assessed whether the oestrogen receptor antagonist fulvestrant (F) improves cirrhosis‐related lung abnormalities. Cirrhosis was induced in rats by chronic bile duct ligation (CBDL). Four groups were studied: CBDL, CBDL+F, sham, and sham+F. Histological, immunohistochemical, and Western blot analyses were performed on lung samples. In the lung, the endothelial NO synthase and the nitrotyrosine protein expressions were increased in CBDL as compared to sham rats. Both parameters were significantly reduced by fulvestrant in the CBDL rats. Surprisingly, the level of pVASP (an indirect marker of NO formation and action) was decreased in CBDL rats, and fulvestrant had no effect on this parameter. The level of the vascular endothelial growth factor, the diameter of small lung vessels, and the number of macrophages were increased in CBDL lungs in comparison with sham lungs, and these parameters were unaffected by fulvestrant treatment. In conclusion, fulvestrant may not be relevant to improve lung abnormalities in cirrhosis because NO may not be biologically active and because key events contributing to the lung abnormalities are not affected by fulvestrant.


European Neurology | 2012

Asthma as a cause of persistent dyspnea in treated myasthenia gravis patients.

Andoni Echaniz-Laguna; Cristina Pistea; Nathalie Philippi; Irina Enache; Monique Oswald-Mammosser; Jérôme De Seze; Anne Charloux

Aims: The aim of this study was to evaluate the proportion of patients with treated myasthenia gravis (MG) who present with dyspnea not related to MG. Methods: We analyzed the files of 63 consecutive adult patients with treated MG and persistent dyspnea who had been referred to our Pulmonary Function Test (PFT) Department between 2000 and 2010. Results: We observed that asthma was the first cause of MG-unrelated dyspnea in MG patients, with 9 patients (14%) presenting with asthma-related PFT abnormalities. Six patients had asthma for several years before developing MG, and 3 patients (4%) developed asthma a few months after MG was diagnosed, suggesting a non-coincidental association between the two conditions. In all 3 cases, asthma appeared in elderly patients with severe late-onset AchR-Ab- positive MG, treated with pyridostigmine and corticosteroids and/or intravenous immunoglobulins. In all 3 patients, β2-adrenergic agonist treatment allowed only partial control of dyspnea. In one case, respiratory symptoms were alleviated when pyridostigmine dosage was reduced. Conclusions: Patients with treated MG and persistent dyspnea should be investigated for asthma using PFT before being diagnosed with refractory MG. If asthma is diagnosed, a bronchodilator treatment should be instituted and a reduction in pyridostigmine dosage should be proposed.

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Anne Charloux

University of Strasbourg

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Irina Enache

University of Strasbourg

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Bernard Geny

University of Strasbourg

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Ruddy Richard

Louis Pasteur University

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Nelly Boehm

University of Strasbourg

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Sherzad Rashid

University of Strasbourg

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Bernard Geny

University of Strasbourg

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