22 results on '"Enaud, Raphael"'
Search Results
2. Classification of PRSS1 variants responsible for chronic pancreatitis: An expert perspective from the Franco-Chinese GREPAN Study Group
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Abrantes, Amandine, Aguilera Munoz, Lina, Albouys, Jérémie, Alric, Laurent, Amiot, Xavier, Archambeaud, Isabelle, Audiau, Solène, Bastide, Laetitia, Baudon, Julien, Bellaiche, Guy, Bellon, Serge, Bertrand, Valérie, Bideau, Karine, Billiemaz, Kareen, Billioud, Claire, Bonnefoy, Sabine, Borderon, Corinne, Bournet, Barbara, Breton, Estelle, Brugel, Mathias, Buscail, Louis, Cadiot, Guillaume, Camus, Marine, Causse, Xavier, Chamouard, Patrick, Chaput, Ulriikka, Cholet, Franck, Ciocan, Dragos Marius, Clavel, Christine, Coffin, Benoit, Coimet-Berger, Laura, Creveaux, Isabelle, Culetto, Adrian, Daboussi, Oussama, De Mestier, Louis, Degand, Thibault, D'Engremont, Christelle, Denis, Bernard, Dermine, Solène, Desgrippes, Romain, Drouet D'Aubigny, Augustin, Enaud, Raphaël, Fabre, Alexandre, Gargot, Dany, Gelsi, Eve, Gentilcore, Elena, Gincul, Rodica, Ginglinger-Favre, Emmanuelle, Giovannini, Marc, Gomercic, Cécile, Gondran, Hannah, Grainville, Thomas, Grandval, Philippe, Grasset, Denis, Grimaldi, Stéphane, Grimbert, Sylvie, Hagege, Hervé, Heissat, Sophie, Hentic, Olivia, Herber-Mayne, Anne, Hervouet, Marc, Hoibian, Solene, Jacques, Jérémie, Jais, Bénédicte, Kaassis, Mehdi, Koch, Stéphane, Lacaze, Elodie, Lacroute, Joël, Lamireau, Thierry, Laurent, Lucie, Le Guillou, Xavier, Le Rhun, Marc, Leblanc, Sarah, Levy, Philippe, Lievre, Astrid, Lorenzo, Diane, Maire, Frédérique, Marcel, Kévin, Matias, Clément, Mauillon, Jacques, Morgant, Stéphanie, Moussata, Driffa, Muller, Nelly, Nambot, Sophie, Napoleon, Bertrand, Olivier, Anne, Pagenault, Maël, Pelletier, Anne-laure, Pennec, Olivier, Pinard, Fabien, Pioche, Mathieu, Prost, Bénédicte, Queneherve, Lucille, Rebours, Vinciane, Reboux, Noemi, Rekik, Samia, Riachi, Ghassan, Rohmer, Barbara, Roquelaure, Bertrand, Rosa Hezode, Isabelle, Rostain, Florian, Saurin, Jean-Christophe, Servais, Laure, Stan-Iuga, Roxana, Subtil, Clément, Texier, Charles, Thomassin, Lucie, Tougeron, David, Tsakiris, Laurent, Valats, Jean-Christophe, Vuitton, Lucine, Wallenhorst, Timothée, Wangerme, Marc, Zanaldi, Hélène, Zerbib, Frank, Bai, Chen-Guang, Bian, Yun, Cai, Zhen-Zhai, Chang, Xiao-Yan, Chen, Guo-Dong, Cheng, Li, Chen, Yu, Guo, Jin-Tao, Guo, Tao, Han, Jun-Ling, He, Chao-Hui, Hu, Liang-Hao, Huang, Hao-Jie, Huang, Li, Huang, Li-Ya, Huang, Si-Lin, Huang, Wei, Jiang, Fei, Jiang, Hui, Lu, Feng-Chun, Lu, Guo-Tao, Lu, Zi-Peng, Li, Hui-Ping, Li, Jing, Li, Le, Li, Qiang, Li, Xiao-Yu, Lin, Qing, Lin, Yu-Li, Liu, Gai-Fang, Liu, Jie-Min, Liu, Li-Xin, Liu, Pi, Liu, Yi-Pin, Lu, Dong, Shao, Xiao-Dong, Shao, Zhuo, Song, Xu-Rui, Wang, Lei, Wang, Li-Juan, Wang, Li-Sheng, Wang, Lin, Wang, Wei, Wang, Zheng, Wen, Li, Wu, Xi, Xin, Lei, Xue, Jing, Yang, Hong, Yang, Jian-Feng, Yin, Tao, Zhang, Bei-Ping, Zhang, Guo-Wei, Zhang, Hong, Zhang, Rong-Chun, Zhao, Yi-Jun, Zhou, Si-Si, Zhu, Ke-Xiang, Masson, Emmanuelle, Zou, Wen-Bin, Pu, Na, Génin, Emmanuelle, Wu, Hao, Lin, Jin-Huan, Wang, Yuan-Chen, Li, Zhao-Shen, Cooper, David N., Férec, Claude, Liao, Zhuan, and Chen, Jian-Min
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- 2023
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3. Cystic fibrosis and noninvasive liver fibrosis assessment methods in children
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Enaud, Raphael, Frison, Eric, Missonnier, Sophie, Fischer, Aude, de Ledinghen, Victor, Perez, Paul, Bui, Stéphanie, Fayon, Michael, Chateil, Jean-François, and Lamireau, Thierry
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- 2022
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4. Functional abdominal pain disorders and patient- and parent-reported outcomes in children with inflammatory bowel disease in remission
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Tran, Léa Chantal, Bridoux-Henno, Laure, Gastineau, Swellen, Dabadie, Alain, Carré, Emilie, Hugot, Jean-Pierre, Martinez-Vinson, Christine, Mosca, Alexis, Coopman, Stéphanie, Lamireau, Thierry, Enaud, Raphaël, Clouzeau, Haude, Bertrand, Valérie, Pigneur, Bénédicte, Ruemmele, Frank, Degas, Vanessa, Breton, Anne, Mas, Emmanuel, Lacotte, Édouard, Chaillou-Legault, Emilie, Caron, Nicolas, Languepin, Jane, Willot, Stéphanie, Bouazza, Ahlem, Spyckerelle, Claire, Dimitrov, Georges, Thomassin, Nadège, Djeddi, Djamal, Vanrenterghem, Audrey, Grandjean, Camille, Viala, Jérôme, and Dupont-Lucas, Claire
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- 2021
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5. Risk factors for surgery in stricturing small bowel Crohn's disease: A retrospective cohort study from the GETAID pédiatrique.
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Lacotte, Edouard, Boujonnier, Louis, Martinez‐Vinson, Christine, Viala, Jérôme, Ley, Delphine, Coopman, Stéphanie, Lerisson, Héloïse, Dabadie, Alain, Dumant‐Forrest, Clémentine, Pigneur, Bénédicte, Ruemmele, Frank, Enaud, Raphael, Comte, Aurélie, Rebeuh, Julie, Bertrand, Valérie, Caron, Nicolas, Breton, Anne, Duclaux‐Loras, Rémi, Vasies, Ioana, and Dupont‐Lucas, Claire
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- 2024
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6. A European Survey on Digestive Perianastomotic Ulcerations, a Rare Crohn-like Disorder Occurring in Children and Young Adults
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Madre, Chrystele, Mašić, Mario, Prlenda-Touilleux, Daniela, Brueckner, Annecarin, Koletzko, Sibylle, Fabre, Alexandre, Viala, Jérome, Lima, Rosa, Enaud, Raphael, Lemale, Julie, Kolho, Kaija-Leena, Bergoin, Charlotte, Martinez-Vinson, Christine, Dugelay, Emmanuelle, Alvisi, Patrizia, Aloi, Marina, Miele, Erasmo, Duclaux-Loras, Remi, Nachury, Maria, Languepin, Jane, Willot, Stephanie, Dupont-Lucas, Claire, Mosca, Alexis, Tzivinikos, Christos, Shamasneh, Ibrahim, Kolaček, Sanja, and Hugot, Jean-Pierre
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- 2021
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7. Clinical and bronchial parameters associated with the exacerbation frequency of severe preschool wheezers
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Siao-Him-Fa, Valerie, Auriol, Françoise, Blanchon, Sylvain, Carles, Dominique, Boisserie-Lacroix, Vincent, Brémont, François, Bui, Stéphanie, Simon, Guillaume, Choukroun, Marie-Luce, Debelleix, Stéphane, Feghali, Hala, Labouret, Géraldine, Martin Blondel, Audrey, Marais, Sébastien, Mittaine, Marie, Nacka, Fabienne, Ousova, Olga, Rouquette, Isabelle, Semjen, François, Sgoifo, Frédérique, Beaufils, Fabien, Esteves, Pauline, Enaud, Raphael, Prevel, Renaud, Henrot, Pauline, Campagnac, Marilyne, Maurat, Elise, Michelet, Marine, Lavrand, Frederic, Begueret, Hugues, Trian, Thomas, Fayon, Michael, and Berger, Patrick
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- 2024
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8. Pre-hospital triage of children at risk of oesophageal button battery impaction: the button battery impaction score.
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Vaucel, Jules-Antoine, Gil-Jardine, Cédric, Paradis, Camille, Enaud, Raphael, Labadie, Magali, Deguigne, Marie, Le Roux, Gaël, Descatha, Alexis, Azzouz, Ramy, Nisse, Patrick, Patat, Anne-Marie, Paret, Nathalie, Blanc-Brisset, Ingrid, Nardon, Audrey, Courtois, Arnaud, de Haro, Luc, Simon, Nicolas, Delcourt, Nicolas, Pelissier, Fanny, and Tournoud, Christine
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BATTERY storage plants ,ESOPHAGEAL perforation ,MEDICAL triage ,RAPID tooling ,JOB descriptions ,HEALTH facilities - Abstract
Button battery ingestion in children can be fatal if oesophageal perforation occurs. Such children require chest radiography in the emergency department to determine the button battery position and number. Current guidelines recommend that a button battery impacted in the oesophagus should be removed within two hours. We developed a clinical tool (the button battery impaction score) to estimate the risk of oesophageal impaction and help determine the most appropriate healthcare facility for initial assessment, either a local medical centre or a medical centre with the infrastructure for endoscopic retrieval. A multi-centre retrospective study was conducted over seven years in eight French poison centres. We included patients aged less than 12 years with radiography showing the button battery position and a symptom description before radiography. Button battery impaction scores were calculated using backward stepwise selection. A total of 1,430 patients were included, of whom 86, 461, and 375 had a button battery in their oesophagus, stomach, and post-pyloric position, respectively. No button batteries were identified by radiography in 508 patients. Sixteen of thirty-five factors independently predicted oesophageal impaction before chest radiography (P < 0.05). After the backward stepwise selection, the following seven factors contributed to the button battery impaction score: cough, drooling, dysphagia/food refusal, fever, pain (unspecified location), vomiting, and button battery ≥ 15 mm. The button battery impaction score showed an area under the curve value of 0.87, a negative predictive value of 0.98, and a sensitivity of 0.86. No cases of death, stricture, or haemorrhage were observed in patients with negative scores, including those with oesophageal impaction. A button battery impaction score used readily available data to predict the risk of oesophageal impaction after button battery ingestion and before chest radiography. When further validated, this rapid tool may be widely applicable in determining an appropriate facility for patient transfer to either a local medical centre or a medical centre with the infrastructure for endoscopic retrieval. [ABSTRACT FROM AUTHOR]
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- 2023
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9. Identification of protease-sensitive but not misfolding PNLIP variants in familial and hereditary pancreatitis
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Abrantes, Amandine, Aguilera Munoz, Lina, Albouys, Jérémie, Alric, Laurent, Amiot, Xavier, Archambeaud, Isabelle, Audiau, Solène, Bastide, Laetitia, Baudon, Julien, Bellaiche, Guy, Bellon, Serge, Bertrand, Valérie, Bideau, Karine, Billiemaz, Kareen, Billioud, Claire, Bonnefoy, Sabine, Borderon, Corinne, Bournet, Barbara, Breton, Estelle, Brugel, Mathias, Buscail, Louis, Cadiot, Guillaume, Camus, Marine, Causse, Xavier, Chamouard, Patrick, Chaput, Ulriikka, Cholet, Franck, Ciocan, Dragos Marius, Clavel, Christine, Coffin, Benoit, Coimet-Berger, Laura, Creveaux, Isabelle, Culetto, Adrian, Daboussi, Oussama, Dalstein, Véronique, De Mestier, Louis, Degand, Thibault, d'Engremont, Christelle, Denis, Bernard, Dermine, Solène, Desgrippes, Romain, Drouet d'Aubigny, Augustin, Enaud, Raphaël, Fabre, Alexandre, Gargot, Dany, Gelsi, Eve, Gentilcore, Elena, Gincul, Rodica, Ginglinger-Favre, Emmanuelle, Giovannini, Marc, Gomercic, Cécile, Gondran, Hannah, Grainville, Thomas, Grandval, Philippe, Grasset, Denis, Grimaldi, Stéphane, Grimbert, Sylvie, Hagege, Hervé, Heissat, Sophie, Hentic, Olivia, Herber-Mayne, Anne, Hervouet, Marc, Hoibian, Solene, Jacques, Jérémie, Jais, Bénédicte, Kaassis, Mehdi, Koch, Stéphane, Lacaze, Elodie, Lacroute, Joël, Lamireau, Thierry, Laurent, Lucie, Le Guillou, Xavier, Leblanc, Sarah, Levy, Philippe, Lievre, Astrid, Lorenzo, Diane, Maire, Frédérique, Marcel, Kévin, Matias, Clément, Mauillon, Jacques, Morgant, Stéphanie, Moussata, Driffa, Muller, Nelly, Nambot, Sophie, Napoleon, Bertrand, Olivier, Anne, Pagenault, Maël, Pelletier, Anne-laure, Pennec, Olivier, Pinard, Fabien, Pioche, Mathieu, Prost, Bénédicte, Queneherve, Lucille, Rebours, Vinciane, Reboux, Noemi, Rekik, Samia, Riachi, Ghassan, Rohmer, Barbara, Roquelaure, Bertrand, Rosa Hezode, Isabelle, Rostain, Florian, Saurin, Jean-Christophe, Servais, Laure, Stan-Iuga, Roxana, Subtil, Clément, Texier, Charles, Thomassin, Lucie, Tougeron, David, Tsakiris, Laurent, Valats, Jean-Christophe, Vuitton, Lucine, Wallenhorst, Timothée, Wangerme, Marc, Zanaldi, Hélène, Zerbib, Frank, Masson, Emmanuelle, Berthet, Stéphanie, Le Gac, Gerald, Le Rhun, Marc, Ka, Chandran, Autret, Sandrine, Gourlaouen, Isabelle, Cooper, David N., Férec, Claude, and Chen, Jian-Min
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- 2023
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10. Assessment of Liver Disease Progression in Cystic Fibrosis Using Transient Elastography
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Gominon, Anne-Laure, Frison, Eric, Hiriart, Jean-Baptiste, Vergniol, Julien, Clouzeau, Haude, Enaud, Raphael, Bui, Stephanie, Fayon, Michael, de Ledinghen, Victor, and Lamireau, Thierry
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- 2018
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11. Ustekinumab Use in Pediatric Inflammatory Bowel Disease: A French Multicenter Study From the Pediatric GETAID.
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Koudsi, Mounzer, Martinez‐Vinson, Christine, Pigneur, Bénédicte, Willot, Stéphanie, Djamal, Djeddi, Enaud, Raphael, Rebeuh, Julie, Dupont, Claire, Dabadie, Alain, Bertrand, Valérie, Hugot, Jean‐Pierre, Lachaux, Alain, Ruemmele, Franck, Viala, Jérôme, Duclaux‐Loras, Rémi, and Pédiatrique, GETAID
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- 2023
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12. The respiratory microbiota alpha-diversity in chronic lung diseases: a systematic review and meta-analysis
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Avalos, Marta, Alin, Thibaud, Métayer, Clémence, Thiébaut, Rodolphe, Enaud, Raphael, Delhaes, Laurence, Statistics In System biology and Translational Medicine (SISTM), Inria Bordeaux - Sud-Ouest, Institut National de Recherche en Informatique et en Automatique (Inria)-Institut National de Recherche en Informatique et en Automatique (Inria)- Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut National de Recherche en Informatique et en Automatique (Inria), Université de Bordeaux (UB), CHU Bordeaux [Bordeaux], CHU de Bordeaux Pellegrin [Bordeaux], Centre de recherche Cardio-Thoracique de Bordeaux [Bordeaux] (CRCTB), and Université Bordeaux Segalen - Bordeaux 2-CHU Bordeaux [Bordeaux]-Institut National de la Santé et de la Recherche Médicale (INSERM)
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[STAT.AP]Statistics [stat]/Applications [stat.AP] ,[STAT.ML]Statistics [stat]/Machine Learning [stat.ML] ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,[STAT.ME]Statistics [stat]/Methodology [stat.ME] - Abstract
International audience; Imbalance in microbial composition (i.e. dysbiosis) in the gut microbiome is consensually considered an indicator of deteriorated health and has been associated to different chronic health conditions. However, there is no clear evidence how this generalizes to the other human microbiomes. Especially, researches on the relationship between respiratory microbiota imbalance and chronic lung diseases are recent whereas microbial colonization of the airways respiratory tract have characterized chronic lung diseases. Imbalance is mainly measured through the relative abundance of microbial species in space and time within a given community (i.e. alpha-diversity). Identifying a range of values in alpha-diversity when comparing exacerbated, stable patients and healthy subjects may lead to identify new biomarker in chronic respiratory diseases. In the present work, we propose a systematic review of studies investigating the lung microbiota alpha-diversity in patients with chronic respiratory diseases in which a control group based on disease status or healthy subjects is provided for comparison. We focused on the most common measures of alpha-diversity (Chao1, Shannon, and Simpson) indexes and the most common chronic diseases (asthma, chronic obstructive pulmonary disease –COPD-, cystic fibrosis –CF-, bronchiectasis, and pulmonary hypertension). Subsequently, we conducted a meta-analysis based on random-effects models using the R package metafor to characterize the difference in alpha-diversity indexes when comparing cases to controls. We also explored heterogeneity of sources and risk of bias though Factor Analysis of Mixed Data (FAMD) using the FactoMineR R package.After removing duplicate records, we screened 351 articles on title and abstract, of which 27 met our inclusion criteria for the systematic review. Finally, data from 25 studies were used in the meta-analysis. Eight studies deal with CF, 8 with COPD, 10 with asthma and 1 with bronchiectasis. All of the studies dedicated to the respiratory tract microbiota, mainly based on sputum samples analysis and, the majority of the studies used metataxonomy approaches. As highlighted by the meta-analysis, these metataxonomy methods exhibited numerous heterogeneities. Differences in alpha-diversity indexes between healthy and diseased people were observed only in some of the diseases studied. However, prudence is required in its interpretation because of substantial heterogeneity.
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- 2022
13. Intraperitoneal Fetus in Fetu: A Rare Cause of Abdominal Mass
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Enaud, Raphael, Lavrand, Frederic, Le Manh, Carole, Rullier, Anne, and Lamireau, Thierry
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- 2017
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14. Respiratory mycobiome and suggestion of inter-kingdom network during acute pulmonary exacerbation in cystic fibrosis.
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Soret, Perrine, Vandenborght, Louise-Eva, Francis, Florence, Coron, Noémie, Enaud, Raphael, Avalos, Marta, Schaeverbeke, Thierry, Berger, Patrick, Fayon, Michael, Thiebaut, Rodolphe, Delhaes, Laurence, The Mucofong Investigation Group, Chabe, Magali, Audebert, Christophe, Durand-Joly, Isabelle, Boldron, Amale, Pin, Isabelle, Cognet, Odile, Pelloux, Herve, and Prevotat, Anne
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LUNG infections ,MYCOBIOME ,DISEASE exacerbation ,CYSTIC fibrosis ,RIBOSOMAL RNA - Abstract
Lung infections play a critical role in cystic fibrosis (CF) pathogenesis. CF respiratory tract is now considered to be a polymicrobial niche and advances in high-throughput sequencing allowed to analyze its microbiota and mycobiota. However, no NGS studies until now have characterized both communities during CF pulmonary exacerbation (CFPE). Thirty-three sputa isolated from patients with and without CFPE were used for metagenomic high-throughput sequencing targeting 16S and ITS2 regions of bacterial and fungal rRNA. We built inter-kingdom network and adapted Phy-Lasso method to highlight correlations in compositional data. The decline in respiratory function was associated with a decrease in bacterial diversity. The inter-kingdom network revealed three main clusters organized around Aspergillus, Candida, and Scedosporium genera. Using Phy-Lasso method, we identified Aspergillus and Malassezia as relevantly associated with CFPE, and Scedosporium plus Pseudomonas with a decline in lung function. We corroborated in vitro the cross-domain interactions between Aspergillus and Streptococcus predicted by the correlation network. For the first time, we included documented mycobiome data into a version of the ecological Climax/Attack model that opens new lines of thoughts about the physiopathology of CF lung disease and future perspectives to improve its therapeutic management. [ABSTRACT FROM AUTHOR]
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- 2020
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15. A European ECMM‐ESCMID survey on goals and practices for mycobiota characterisation using next‐generation sequencing.
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Gangneux, Jean‐Pierre, Guegan, Hélène, Vandenborght, Louise‐Eva, Buffet‐Bataillon, Sylvie, Enaud, Raphael, Delhaes, Laurence, Lackner, Michaela, Freiberger, Tomas, Hare, Rasmus, Leth Mortensen, Klaus, Hedayati, Mohammad T., Moran, Gary, Vehreschild, Maria, Steinmann, Jörg, Botterel, Françoise, Roilides, Emmanuel, Ben‐Ami, Ronen, Lo Cascio, Giuliana, Treviño‐Rangel, Rogelio de Jesús, and Meis, Jacques
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NUCLEOTIDE sequencing ,CYSTIC fibrosis ,FUNGI ,MICROBIAL communities ,ENVIRONMENTAL sciences ,BACTERIAL communities - Abstract
Summary: Although substantial efforts have been made to investigate about the composition of the microbiota, fungi that constitute the mycobiota play a pivotal role in maintaining microbial communities and physiological processes in the body. Here, we conducted an international survey focusing on laboratory's current procedures regarding their goals and practices of mycobiota characterisation using NGS. A questionnaire was proposed to laboratories affiliated to working groups from ECMM (NGS study group) and ESCMID (ESGHAMI and EFISG study groups). Twenty‐six questionnaires from 18 countries were received. The use of NGS to characterise the mycobiota was not in routine for most of the laboratories (N = 23, 82%), and the main reason of using NGS was primary to understand the pathophysiology of a dysbiosis (N = 20), to contribute to a diagnosis (N = 16) or to implement a therapeutic strategy (N = 12). Other reported reasons were to evaluate the exposome (environmental studies) (N = 10) or to investigate epidemics (N = 8). Sputum is the main sample studied, and cystic fibrosis represents a major disease studied via the analysis of pulmonary microbiota. No consensus has emerged for the choice of the targets with 18S, ITS1 and ITS2 used alternatively among the laboratories. Other answers are detailed in the manuscript. We report a photography of mycobiota analysis that may become a major tool in the near future. We can draw some conclusions on the diversity of approaches within the answers of the 27 laboratories and underline the need for standardisation. [ABSTRACT FROM AUTHOR]
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- 2019
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16. Altered pulmonary gas transfer capacity and capillary blood volume in pediatric Crohn's disease.
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Verstraete, Marie, Choukroun, Marie-Luce, Siao-Him Fa, Valerie, Fayon, Michael, Rebouissoux, Laurent, Enaud, Raphael, and Lamireau, Thierry
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- 2017
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17. Frequency and risk factors for malnutrition in children undergoing general anaesthesia in a French university hospital.
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Gerbaud-Morlaes, Louis, Frison, Eric, Babre, Florence, De Luca, Arnaud, Didier, Anne, Borde, Maryline, Zaghet, Brigitte, Batoz, Hélène, Semjen, François, Nouette-Gaulain, Karine, Enaud, Raphael, Hankard, Régis, and Lamireau, Thierry
- Abstract
Background: Malnutrition is often underdiagnosed in hospitalised children, although it is associated with postoperative complications, longer hospital lengths of stay and increased healthcare-related costs.Objective: We aimed to estimate the frequency of, and identify factors associated with, malnutrition in children undergoing anaesthesia.Design: Cross-sectional observational study.Setting: Paediatric anaesthesia department at the University Children's Hospital, Bordeaux, France.Participants: A total of 985 patients aged less than 18 years.Main Outcome Measures: Anthropometric measurements, American Society of Anesthesiologists physical status classification score and the Pediatric Nutritional Risk Score (PNRS) recorded at the pre-anaesthesia evaluation.Results: When assessed as a Waterlow index less than 80%, malnutrition was present in 7.6% children. This increased to 8.1% of children assessed by clinical signs and to 11% of children when defined by a BMI less than the third percentile. In a univariate analysis, children with a BMI less than the third percentile were more often born prematurely (22.4 vs 10.4%; P = 0.0008), were small for gestational age at birth (18.4 vs 4.5%; P < 0.0001), were admitted from the emergency department (12.0 vs 5.6%; P = 0.02), had a high American Society of Anesthesiologists score (P < 0.0001), or had a high Pediatric Nutritional Risk Score (P < 0.0001). Presence (P = 0.01) and type (P = 0.002) of chronic disease were also associated with malnutrition. In the multivariate analysis, a premature birth, a lower birth weight and a higher Pediatric Nutritional Risk Score were significantly associated with a higher odds of malnutrition when defined by BMI.Conclusion: All children should be screened routinely for malnutrition or the risk of malnutrition at the pre-anaesthesia visit, allowing a programme of preoperative and/or postoperative nutritional support to be initiated. We suggest that as well as weight and height, BMI and a pediatric nutritional risk score such as PNRS should be recorded routinely at the pre-anaesthesia visit. [ABSTRACT FROM AUTHOR]- Published
- 2017
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18. New Insights in Microbial Species Predicting Lung Function Decline in CF: Lessons from the MucoFong Project.
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Francis, Florence, Enaud, Raphael, Soret, Perrine, Lussac-Sorton, Florian, Avalos-Fernandez, Marta, Bui, Stéphanie, Fayon, Michael, Thiébaut, Rodolphe, and Delhaes, Laurence
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BACTERIAL colonies , *FUNGAL colonies , *FORCED expiratory volume , *STENOTROPHOMONAS maltophilia , *ACHROMOBACTER , *SPECIES , *STREPTOCOCCUS , *MUCOCILIARY system - Abstract
Several predictive models have been proposed to understand the microbial risk factors associated with cystic fibrosis (CF) progression. Very few have integrated fungal airways colonisation, which is increasingly recognized as a key player regarding CF progression. To assess the association between the percent predicted forced expiratory volume in 1 s (ppFEV1) change and the fungi or bacteria identified in the sputum, 299 CF patients from the "MucoFong" project were included and followed-up with over two years. The relationship between the microorganisms identified in the sputum and ppFEV1 course of patients was longitudinally analysed. An adjusted linear mixed model analysis was performed to evaluate the effect of a transient or chronic bacterial and/or fungal colonisation at inclusion on the ppFEV1 change over a two-year period. Pseudomonas aeruginosa, Achromobacter xylosoxidans, Stenotrophomonas maltophilia, and Candida albicans were associated with a significant ppFEV1 decrease. No significant association was found with other fungal colonisations. In addition, the ppFEV1 outcome in our model was 11.26% lower in patients presenting with a transient colonisation with non-pneumoniae Streptococcus species compared to other patients. These results confirm recently published data and provide new insights into bacterial and fungal colonisation as key factors for the assessment of lung function decline in CF patients. [ABSTRACT FROM AUTHOR]
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- 2021
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19. A European Survey on Digestive Perianastomotic Ulcerations, a Rare Crohn-like Disorder Occurring in Children and Young Adults
- Author
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Christos Tzivinikos, Ibrahim Shamasneh, Marina Aloi, Patrizia Alvisi, Erasmo Miele, Rémi Duclaux-Loras, Jérôme Viala, Stéphanie Willot, Rosa Lima, Claire Dupont-Lucas, Mario Mašić, Julie Lemale, Daniela Prlenda-Touilleux, J. Languepin, Sanja Kolaček, Chrystèle Madre, Alexandre Fabre, Kaija-Leena Kolho, Charlotte Bergoin, Sibylle Koletzko, Jean-Pierre Hugot, Raphaël Enaud, Christine Martinez-Vinson, Maria Nachury, Alexis Mosca, Annecarin Brueckner, Emmanuelle Dugelay, Hôpital Robert Debré, University of Zagreb, Centre Hospitalier Universitaire de Saint-Etienne [CHU Saint-Etienne] (CHU ST-E), Dr von Hauner Children's Hospital [Munich, Germany], Ludwig-Maximilians-Universität München (LMU), Service de pédiatrie multidisciplinaire [Hôpital de la Timone Enfants - APHM], Hôpital de la Timone [CHU - APHM] (TIMONE), Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de recherche sur l'Inflammation (CRI (UMR_S_1149 / ERL_8252 / U1149)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Centro Hospitalar do Porto, CHU Bordeaux [Bordeaux], Hôpital Trousseau, Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Geriatrics Unit [Pierre-Bénite], Université de Lyon-Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), Hospices Civils de Lyon (HCL)-Hospices Civils de Lyon (HCL), Ospedale Maggiore Carlo Alberto Pizzardi di Bologna, Nutrition, Inflammation et axe Microbiote-Intestin-Cerveau (ADEN), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institute for Research and Innovation in Biomedicine (IRIB), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), University of Naples Federico II = Università degli studi di Napoli Federico II, Hospices Civils de Lyon (HCL), Institute for Translational Research in Inflammation - U 1286 (INFINITE (Ex-Liric)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), CHU Limoges, Service de Neuropédiatrie et Handicaps, Hôpital Gatien de Clocheville, CHU Tours, Université de Caen Normandie (UNICAEN), Normandie Université (NU), Institute for Research and Innovation in Biomedicine (IRIB), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Service de Pédiatrie Médicale [Caen], Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), Al Jalila Children's Specialty Hospital, Medical Genetics Unit, Shaare Zedek Medical Center, Hevrew University Medical School, Clinicum, Children's Hospital, HUS Children and Adolescents, Madre, Chrystele, Mašić, Mario, Prlenda-Touilleux, Daniela, Brueckner, Annecarin, Koletzko, Sibylle, Fabre, Alexandre, Viala, Jérome, Lima, Rosa, Enaud, Raphael, Lemale, Julie, Kolho, Kaija-Leena, Bergoin, Charlotte, Martinez-Vinson, Christine, Dugelay, Emmanuelle, Alvisi, Patrizia, Aloi, Marina, Miele, Erasmo, Duclaux-Loras, Remi, Nachury, Maria, Languepin, Jane, Willot, Stephanie, Dupont-Lucas, Claire, Mosca, Alexi, Tzivinikos, Christo, Shamasneh, Ibrahim, Kolaček, Sanja, and Hugot, Jean-Pierre
- Subjects
Male ,intestinal resection ,Abdominal pain ,Pediatrics ,Hirschsprung disease ,Inflammatory bowel disease ,0302 clinical medicine ,3123 Gynaecology and paediatrics ,Interquartile range ,030212 general & internal medicine ,Child ,Digestive System Surgical Procedures ,Anastomosis, Surgical ,Gastroenterology ,Crohn disease ,COMPLICATION ,Short bowel syndrome ,3. Good health ,Failure to thrive ,Necrotizing enterocolitis ,Female ,digestive perianastomotic ulcerations ,030211 gastroenterology & hepatology ,gut inflammation ,medicine.symptom ,ileocaecal valve ,medicine.medical_specialty ,RESECTION ,short bowel syndrome ,Anastomosis ,Young Adult ,03 medical and health sciences ,Bloating ,medicine ,Humans ,enteral nutrition ,ANEMIA ,Ulcer ,necrotizing enterocolitis ,business.industry ,Infant, Newborn ,Infant ,ANASTOMOTIC ULCERS ,abdominal surgery ,medicine.disease ,3121 General medicine, internal medicine and other clinical medicine ,Pediatrics, Perinatology and Child Health ,business ,[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology ,INFLAMMATORY-BOWEL-DISEASE - Abstract
International audience; Objectives: Digestive perianastomotic ulcerations (DPAU) resembling Crohn disease lesions are long-term complications of intestinal resections, occurring in children and young adults. They are known to be uncommon, severe and difficult to treat.Methods: In the absence of recommendations, we performed a large European survey among the members of the ESPGHAN working group on inflammatory bowel disease (IBD) in order to collect the experience of expert pediatric gastroenterologists on DPAU.Results: Fifty-one patients (29 boys and 22 girls) were identified from 19 centers in 8 countries. Most patients were followed after necrotizing enterocolitis (n = 20) or Hirschsprung disease (n = 11). The anastomosis was performed at a median age (interquartile range) of 6 [1–23] months, and first symptoms occurred 39 [22–106] months after surgery. Anemia was the most prevalent symptom followed by diarrhea, abdominal pain, bloating, and failure to thrive. Hypoalbuminemia, elevated CRP, and fecal calprotectin were common. Deep ulcerations were found in 59% of patients usually proximally to the anastomosis (68%). During a median follow-up of 40 [19–67] months, treatments reported to be the most effective included exclusive enteral nutrition (31/35, 88%), redo anastomosis (18/22, 82%), and alternate antibiotic treatment (37/64, 58%).Conclusions: Unfortunately, persistence of symptoms, failure to thrive, and abnormal laboratory tests at last follow-up in most of patients show the burden of DPAU lacking optimal therapy and incomplete understanding of the pathophysiology.
- Published
- 2021
20. Clinical and bronchial parameters associated with the exacerbation frequency of severe preschool wheezers.
- Author
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Beaufils F, Esteves P, Enaud R, Prevel R, Henrot P, Campagnac M, Maurat E, Michelet M, Lavrand F, Begueret H, Trian T, Fayon M, and Berger P
- Subjects
- Humans, Child, Preschool, Educational Status, Respiratory Sounds, Bronchi, Asthma diagnosis, Asthma epidemiology
- Published
- 2024
- Full Text
- View/download PDF
21. Effects of Lumacaftor-Ivacaftor on Airway Microbiota-Mycobiota and Inflammation in Patients with Cystic Fibrosis Appear To Be Linked to Pseudomonas aeruginosa Chronic Colonization.
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Enaud R, Lussac-Sorton F, Charpentier E, Velo-Suárez L, Guiraud J, Bui S, Fayon M, Schaeverbeke T, Nikolski M, Burgel PR, Héry-Arnaud G, and Delhaes L
- Abstract
Lumacaftor-ivacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator combination approved for patients with cystic fibrosis (CF) who are homozygous for the F508del allele. This treatment showed significant clinical improvement; however, few studies have addressed the evolution of the airway microbiota-mycobiota and inflammation in patients receiving lumacaftor-ivacaftor treatment. Seventy-five patients with CF aged 12 years or older were enrolled at the initiation of lumacaftor-ivacaftor therapy. Among them, 41 had spontaneously produced sputa collected before and 6 months after treatment initiation. Airway microbiota and mycobiota analyses were performed via high-throughput sequencing. Airway inflammation was assessed by measuring the calprotectin levels in sputum; the microbial biomass was evaluated via quantitative PCR (qPCR). At baseline ( n = 75), bacterial alpha-diversity was correlated with pulmonary function. After 6 months of lumacaftor-ivacaftor treatment, a significant improvement in the body mass index and a decreased number of intravenous antibiotic courses were noted. No significant changes in bacterial and fungal alpha- and beta-diversities, pathogen abundances, or calprotectin levels were observed. However, for patients not chronically colonized with Pseudomonas aeruginosa at treatment initiation, calprotectin levels were lower, and a significant increase in bacterial alpha-diversity was observed at 6 months. This study shows that the evolution of the airway microbiota-mycobiota in CF patients depends on the patient's characteristics at lumacaftor-ivacaftor treatment initiation, notably chronic colonization with P. aeruginosa. IMPORTANCE The management of cystic fibrosis has been transformed recently by the advent of CFTR modulators, including lumacaftor-ivacaftor. However, the effects of such therapies on the airway ecosystem, particularly on the microbiota-mycobiota and local inflammation, which are involved in the evolution of pulmonary damage, are unclear. This multicenter study of the evolution of the microbiota under protein therapy supports the notion that CFTR modulators should be started as soon as possible, ideally before the patient is chronically colonized with P. aeruginosa. (This study has been registered at ClinicalTrials.gov under identifier NCT03565692).
- Published
- 2023
- Full Text
- View/download PDF
22. Management of Central Venous Catheters in Children and Adults on Home Parenteral Nutrition: A French Survey of Current Practice.
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Gotchac J, Poullenot F, Guimber D, Ecochard-Dugelay E, Schneider S, Peretti N, Billiauws L, Borderon C, Breton A, Chaillou Legault E, Chambrier C, Comte A, Coste ME, Djeddi D, Dubern B, Dupont C, Espeso L, Fayemendy P, Flori N, Fotsing G, Gastineau S, Goulet O, Guiot E, Jirka A, Languepin J, Layec S, Quilliot D, Rebouissoux L, Seguy D, Talon I, Turquet A, Vallee M, Willot S, Lamireau T, and Enaud R
- Subjects
- Adult, Child, Cross-Sectional Studies, Humans, Retrospective Studies, Catheterization, Central Venous adverse effects, Central Venous Catheters adverse effects, Parenteral Nutrition, Home adverse effects
- Abstract
Although central venous catheter (CVC)-related thrombosis (CRT) is a severe complication of home parenteral nutrition (HPN), the amount and quality of data in the diagnosis and management of CRT remain low. We aimed to describe current practices regarding CVC management in French adult and pediatric HPN centers, with a focus on CVC obstruction and CRT. Current practices regarding CVC management in patients on HPN were collected by an online-based cross-sectional survey sent to expert physicians of French HPN centers. We compared these practices to published guidelines and searched for differences between pediatric and adult HPN centers' practices. Finally, we examined the heterogeneity of practices in both pediatric and adult HPN centers. The survey was completed by 34 centers, including 21 pediatric and 13 adult centers. We found a considerable heterogeneity, especially in the responses of pediatric centers. On some points, the centers' responses differed from the current guidelines. We also found significant differences between practices in adult and pediatric centers. We conclude that the management of CVC and CRT in patients on HPN is a serious and complex situation for which there is significant heterogeneity between HPN centers. These findings highlight the need for more well-designed clinical trials in this field.
- Published
- 2022
- Full Text
- View/download PDF
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