Service de Pneumologie Allergologie
Service de Pneumologie Allergologie
Fillaux J.,Service de Parasitologie Mycologie |
Fillaux J.,University Paul Sabatier |
Bremont F.,Service de Pneumologie Allergologie |
Cassaing S.,Service de Parasitologie Mycologie |
And 4 more authors.
Pediatric Infectious Disease Journal | Year: 2014
BACKGROUND: Aspergillus fumigatus (Af) sensitization and persistent carriage are deleterious to lung function, but no consensus has been reached defining these medical entities. This work aimed to identify possible predictive factors for patients who become sensitized to Af, compared with a control group of non-sensitized Af carriers. METHODS: Between 1995 and 2007, 117 pediatric patients were evaluated. Demographic data, CFTR gene mutations, body mass index and FEV1 were recorded. The presence of Af in sputum, the levels of Af-precipitin, total IgE (t-IgE) and specific IgE to Af (Af-IgE) were determined. Patients were divided into 2 groups: (1) "sensitization": level of Af-IgE > 0.35 IU/mL with t-IgE level < 500 IU/mL and (2) "persistent or transient carriage": Af-IgE level ≤ 0.35 IU/mL with either an Af transient or persistent positive culture. A survival analysis was performed with the appearance of Af-IgE in serum as an outcome variable. RESULTS: Severe mutation (hazard ratio = 3.2), FEV1 baseline over 70% of theoretical value (hazard ratio = 4.9), absence of Pa colonization, catalase activity and previous azithromycin administration (hazard ratio = 9.8, 4.1 and 1.9, respectively) were predictive factors for sensitization. We propose a timeline of the biological events and a tree diagram for risk calculation. CONCLUSIONS: Two profiles of cystic fibrosis patients can be envisaged: (1) patients with nonsevere mutation but low FEV1 baselines are becoming colonized with Af or (2) patients with high FEV1 baselines who present with severe mutation are more susceptible to the Af sensitization and then to the presentation of an allergic bronchopulmonary aspergillosis event. Copyright © 2013 by Lippincott Williams & Wilkins.
Petrovici A.,Service de Pneumologie Allergologie |
Kaiser M.J.,Service de Rhumatologie |
Louis R.,Service de Pneumologie Allergologie |
Nguyen Dang D.,Service de Pneumologie Allergologie
Revue Medicale de Liege | Year: 2016
Over recent years, anti-TNFα have been used to treat rheumatoïd arthritis. The principal secondary effect of anti-TNFα is tuberculosis infections. Another paradoxical effect, previously less well understood, is the development of sarcoid-like granulomatous reactions. We report the case of a 36 year old woman who had been treated for 9 years with anti-TNF alpha. She developed a pulmonary sarcoid-like granulomatosis, complication that is rare but not exceptional in patients treated with TNF-blockers. Discontinuation of anti TNF usually led to recovery. It has been suggested that these reactions mainly occur with etanercept, but this requires further confirmation.
Zysman M.,Nancy University Hospital Center |
Patout M.,UPRES EA 3830 |
Miravitlles M.,CIBER ISCIII |
Van Der Molen T.,University of Groningen |
And 5 more authors.
Revue des Maladies Respiratoires | Year: 2014
Introduction: The organization of care for chronic non-infectious diseases, notably COPD, isa common preoccupation in developed countries in which this disease is among the main causesof mortality and disability. We report a summary of a workshop organized on this theme in April2013 by the Société de pneumologie de langue française. Background: Experts from several European countries presented the organizational practicesfor the management of COPD in their countries, in particular the detection of the disease and the systems of care. The common objectives were to obtain better motivation to stop smoking, earlier detection of the disease and education in the recognition of the signs of exacerbationand their severity. The experts agreed that mass detection is of little benefit and difficult toorganize. Early individual screening is preferable on the basis of precise, easily identified cri-teria. The classification recommended by the GOLD committee since 2011 does not seem to beadopted universally throughout Europe. If there is a real improvement over the previous classi-fication due to taking into account clinical criteria, quality of life and exacerbations, criticismshave arisen concerning the choice of certain pathways and therapeutic recommendations notbased on prospective studies with a high level of evidence. Conclusion: European experiences concerning the management of COPD are varied and com-plementary. One remaining question is who to screen: all subjects at risk (all smokers, alloccupations at risk), only symptomatic subjects, subjects with severe and disabling symptoms? © 2014 SPLF. Published by Elsevier Masson SAS. All rights reserved.
PubMed | Aarhus Universitetshospital, General Practice Surgery, Nancy University Hospital Center, University of Groningen and 4 more.
Type: Journal Article | Journal: Revue des maladies respiratoires | Year: 2014
The organization of care for chronic non-infectious diseases, notably COPD, is a common preoccupation in developed countries in which this disease is among the main causes of mortality and disability. We report a summary of a workshop organized on this theme in April 2013 by the Socit de pneumologie de langue franaise.Experts from several European countries presented the organizational practices for the management of COPD in their countries, in particular the detection of the disease and the systems of care. The common objectives were to obtain better motivation to stop smoking, earlier detection of the disease and education in the recognition of the signs of exacerbation and their severity. The experts agreed that mass detection is of little benefit and difficult to organize. Early individual screening is preferable on the basis of precise, easily identified criteria. The classification recommended by the GOLD committee since 2011 does not seem to be adopted universally throughout Europe. If there is a real improvement over the previous classification due to taking into account clinical criteria, quality of life and exacerbations, criticisms have arisen concerning the choice of certain pathways and therapeutic recommendations not based on prospective studies with a high level of evidence.European experiences concerning the management of COPD are varied and complementary. One remaining question is who to screen: all subjects at risk (all smokers, all occupations at risk), only symptomatic subjects, subjects with severe and disabling symptoms?
PubMed | McMaster University, Service des Maladies Respiratoires, Service de Pneumologie allergologie, Takeda Pharmaceuticals International GmbH and University of Cape Town
Type: | Journal: Pulmonary pharmacology & therapeutics | Year: 2016
Roflumilast, a phosphodiesterase-4 inhibitor, has an established place in the treatment of chronic obstructive pulmonary disease. Its potential role as a treatment for asthma is unclear.We report the results from seven double-blind, parallel group, phase II or III studies designed to compare roflumilast with two anti-inflammatory treatments, beclomethasone dipropionate (BDP) and montelukast, in patients with asthma.The studies of 6-12 week duration were conducted at 309 sites in Europe, North America, South Africa and Australia from 1998 to 2005. Data from 3802 patients, aged 12-70 years who received either roflumilast 100g, 250g or 500g once daily, BDP 400g or 500g twice daily, or 10mg montelukast once daily was analyzed. Primary endpoints were mean change and time averaged excess area under the curve in forced expiratory volume in one second (FEV1) over the duration of the study. Secondary endpoints included change in forced vital capacity and peak expiratory flow, asthma symptoms and the concomitant use of rescue medication.Roflumilast was non-inferior to BDP and montelukast and consistently increased FEV1. Use of rescue medication and all asthma symptom scores decreased significantly with all treatments, but no statistically significant between-group differences were observed. Secondary lung function endpoints generally supported the conclusions of the primary outcome measure.Roflumilast improves FEV1 and asthma symptoms in patients with mild to moderate asthma, and is non-inferior compared with both BDP and montelukast. It deserves further study as a potentially effective anti-inflammatory treatment for asthma.
Birnbaum J.,Service de pneumologie allergologie
Revue Francaise d'Allergologie | Year: 2010
While secondary reactions to antituberculosis drugs are frequent, IgE-dependent allergic reactions are rare. The sensitivity and specificity of skin tests for the diagnosis of these reactions have not been evaluated, and positive skin tests reported in some studies were false positives. Here we report four clinical cases who presented with immediate cutaneous reactions after taking Rifater®, the results of their skin tests and management of this allergy through oral desensitization. Rifampycin, a component of Rifater®, was implicated as the cause of the reaction based on positive skin tests with a 1/10,000 dilution (containing 0.006 mg/ml) of that drug. Successful oral desensitization allowed the drug to be continued. © 2009 Elsevier Masson SAS. All rights reserved.
Mailhol C.,Service de pneumologie allergologie |
Didier A.,Service de pneumologie allergologie
Revue Francaise d'Allergologie | Year: 2011
Allergic symptoms in physical effort context, should evoke food dependant exercise induced anaphylaxis diagnosis. A 43-year-old woman suffered from anaphylaxis symptoms after a short run following a meal in a pancake restaurant. Skin prick tests were positive for wheat and buckwheat, serum specific IgE determination confirmed sensitization to wheat, buckwheat and ω5-gliadin. Wheat dependant exercise induced anaphylaxis diagnosis was retained and exercise challenge test was not indicated because of typical clinical and biological features. Wheat dependant exercise induced anaphylaxis is a well-characterized type of food dependant exercise induced anaphylaxis. Most often ω5-gliadin is involved and is known as associated with potential severe reactions. Molecular diagnosis may allow the clinician to reject challenge test that might be at risk for the patient. The cost and the constraint of a hospitalisation to realize exercise challenge tests are also avoided. © 2011 Elsevier Masson SAS.
Louzir B.,Service de Pneumologie Allergologie
La Tunisie médicale | Year: 2012
Pulmonary embolism (PE) is a fairly common condition that can be fatal. The variability of presentation sets clinician up for potentially missing the diagnosis. Routine laboratory findings are nonspecific and are not helpful in diagnosis of PE.Diagnosis is based on clinical prediction rule in combination with laboratory tests such as the D-dimers test leading to the realization ofa confirming examination. To precise the confirming examinations of PE and propose analgorithm based on clinical prediction rules in combination with D-Dimers. A Pub Med search was conducted using the following keywords: pulmonary embolism,computed tomogramphy pulmonary angiography, scintigraphy and D Dimer. The study was based on are view of 18 studies including meta analysis, reviews and original articles referring recent strategy diagnosis of pulmonary embolism. Ventilation/perfusion scan is a type of examination that is used less often because it is not a widespread technology. However,it may be useful in patients who have an allergy to iodinated contrast.Ultrasonography of the legs, also known as leg doppler, in search of deep venous thrombosis (DVT) may help the diagnosis approach particularly when other exams are not available or contraindicated.This may be a valid approach in pregnancy. The gold standard for diagnosing PE is pulmonary angiography. It is used less often due to wider acceptance of multi detector CT scans, which are non-invasive.A normal ventilation/perfusion scan rules out the diagnosis of PE with negative predictive value of 97%. There is no consensus in pregnancy. Finally, the MRI has a low and insufficient sensibility to diagnose PE.Conclusion: D Dimers, multidetector CT, ventilation/ perfusion scintigraphy and ultrasonography of the legs are the most useful examinations to diagnose PE. Many algorithms were established depends on medical experience and examination availability
Duysinx B.,Service de pneumologie allergologie
Revue des Maladies Respiratoires Actualites | Year: 2013
The PET scanner has its place in the pleura imaging: it can be used in the diagnose of benign and malignant pleural diseases (threshold SUV. = 2.2). It improves the staging of mesothelioma including good efficiency on mediastinal lymph node. It can also be used in therapeutic response and to guide pleural biopsies.So, far from replacing the pleuroscopy, PET scanner fits into the process of exploration of pleural disease and can avoid invasive diagnostic exams. © 2013 Elsevier Masson SAS.
Mailhol C.,Service de Pneumologie allergologie |
Didier A.,Service de Pneumologie allergologie
Revue des Maladies Respiratoires | Year: 2013
Since its description by Noon in 1911, desensitization or allergen-specific immunotherapy (SIT) has been largely given by sub cutaneous injection in the treatment of allergic diseases. It remains the only treatment for allergic diseases aimed at the etiology. The development of sublingual route as an alternative to sub cutaneous injection, and of new forms of medication, has led to large-scale clinical trials, many of them performed with allergen tablets, particularly in the field of pollen allergy. These studies have confirmed that SIT is efficient in reducing allergic respiratory symptoms. Data on long term benefits and sustained efficacy after stopping treatment have also been published. These show an impact on the natural history of allergic disease and, in particular, a reduction in the risk of asthma in desensitized rhinitic subjects and in the acquisition of new sensitivities. The basic mechanisms of immunotherapy are becoming better understood and allow us to envisage improvements in this technique in the future. The sublingual route improves the risk/benefit ratio of desensitization and reduces the risk of serious side effects. These data suggest that the indications for SIT may be extended in a large number of patients with allergic respiratory diseases. © 2012 SPLF. Published by Elsevier Masson SAS. All rights reserved.