259 results on '"Maitre, Bernard"'
Search Results
2. International survey among hepatologists and pulmonologists on the hepatic hydrothorax: plea for recommendations
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Cadranel, Jean-François David, Ollivier-Hourmand, Isabelle, Cadranel, Jacques, Thevenot, Thierry, Zougmore, Honoré, Nguyen-Khac, Eric, Bureau, Christophe, Allaire, Manon, Nousbaum, Jean-Baptiste, Loustaud-Ratti, Véronique, Causse, Xavier, Sogni, Philippe, Hanslik, Bertrand, Bourliere, Marc, Peron, Jean-Marie, Ganne-Carrie, Nathalie, Dao, Thong, Thabut, Dominique, Maitre, Bernard., Debzi, Nabil, Smadhi, Ryad, Sombie, Roger, Kpossou, Raimi, Nouel, Olivier, Bissonnette, Julien, Ruiz, Isaac, Medmoun, Mourad, Dastis, Sergio Negrin, Deltenre, Pierre, Artru, Florent, Raherison, Chantal, Elkrief, Laure, and Lemagoarou, Tristan
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- 2023
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3. Beyond lung cancer screening, an opportunity for early detection of chronic obstructive pulmonary disease and cardiovascular diseases.
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Gendarme, Sébastien, Maitre, Bernard, Hanash, Sam, Pairon, Jean-Claude, Canoui-Poitrine, Florence, and Chouaïd, Christos
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Background Lung cancer screening programs concern smokers at risk for cardiovascular diseases (CVDs) and chronic obstructive pulmonary disease (COPD). The LUMASCAN (LUng Cancer Screening, MArkers and low-dose computed tomography SCANner) study aimed to evaluate the acceptability and feasibility of screening for these 3 diseases in a community population with centralized organization and to determine low-dose computed tomography (CT) markers associated with each disease. Methods This cohort enrolled participants meeting National Comprehensive Cancer Network criteria (v1.2014) in an organized lung cancer–screening program including low-dose CT scans; spirometry; evaluations of coronary artery calcifications (CACs); and a smoking cessation plan at inclusion, 1, and 2 years; then telephone follow-up. Outcomes were the participation rate and the proportion of participants affected by lung cancer, obstructive lung disease, or CVD events. Logistic-regression models were used to identify radiological factors associated with each disease. Results Between 2016 and 2019, a total of 302 participants were enrolled: 61% men; median age 58.8 years; 77% active smoker; 11% diabetes; 38% hypertension; and 27% taking lipid-lowering agents. Inclusion, 1-year, and 2-year participation rates were 99%, 81%, 79%, respectively. After a median follow-up of 5.81 years, screenings detected 12 (4%) lung cancer, 9 of 12 via low-dose CT (78% localized) and 3 of 12 during follow-up (all stage IV), 83 (27%) unknown obstructive lung disease, and 131 (43.4%) moderate to severe CACs warranting a cardiology consultation. Preexisting COPD and moderate to severe CACs were associated with major CVD events with odds ratios of 1.98 (95% confident interval [CI] = 1.00 to 3.88) and 3.27 (95% CI = 1.72 to 6.43), respectively. Conclusion The LUMASCAN study demonstrated the feasibility of combined screening for lung cancer, COPD, and CVD in a community population. Its centralized organization enabled high participation and coordination of healthcare practitioners. [ABSTRACT FROM AUTHOR]
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- 2024
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4. Low income and outcome in idiopathic pulmonary fibrosis: An association to uncover
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Bouvry, Diane, Brillet, Pierre Yves, Camus, Philippe, Chabrol, Juliette, Cordier, Jean François, Cracco, Christophe, Delaval, Philippe, Didier, Morgane, Duchemann, Boris, Feuillet, Sevrine, Freynet, Olivia, Gagnadoux, Frédéric, Germaud, Patrick, Gindre, Louise, Guetta, André, Haussman, Patrick, Jouneau, Stephane, Kambouchner, Marianne, Khouatra, Chahera, Lacronique, Jacques, Molard, Anita, Picard, Clément, Planes, Carole, Rosental, Paul Andrés, Sanchez, Olivier, Similowski, Thomas, Thiberville, Luc, Uzuhnan, Yurdagül, Sesé, Lucile, Caliez, Julien, Annesi-Maesano, Isabella, Cottin, Vincent, Pesce, Giancarlo, Carton, Zohra, Israel-Biet, Dominique, Crestani, Bruno, Dudoret, Stéphanie Guillot, Cadranel, Jacques, Wallaert, Benoit, Tazi, Abdellatif, Maître, Bernard, Prévot, Grégoire, Marchand-Adam, Sylvain, Hirschi, Sandrine, Dury, Sandra, Giraud, Violaine, Gondouin, Anne, Bonniaud, Philippe, Traclet, Julie, Juvin, Karine, Borie, Raphael, Bernaudin, Jean François, Valeyre, Dominique, Cavalin, Catherine, and Nunes, Hilario
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- 2021
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5. Infertility and pregnancy outcomes among adults with primary ciliary dyskinesia.
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Schreck, Leonie D, Pedersen, Eva S L, Dexter, Katie, Manion, Michele, Group, Living with PCD Study Advisory, Massin, Nathalie, Maitre, Bernard, Goutaki, Myrofora, and Kuehni, Claudia E
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REPRODUCTIVE technology ,HIGH-risk pregnancy ,CILIARY motility disorders ,PREGNANCY outcomes ,MALE infertility ,ECTOPIC pregnancy - Abstract
STUDY QUESTION What is the prevalence of infertility and ectopic pregnancies among individuals with primary ciliary dyskinesia (PCD)? SUMMARY ANSWER We found that 39 of 50 men (78%) and 72 of 118 women (61%) with PCD were infertile and that women with PCD had an increased risk of ectopic pregnancies (7.6 per 100 pregnancies, 95% CI 4.7–12.2). WHAT IS KNOWN ALREADY PCD is a heterogeneous multiorgan disease caused by mutations in genes required for the function and structure of motile cilia. Previous studies identified a link between PCD and infertility, but original data on prevalence of infertility and risk of ectopic pregnancies, the use and efficacy of medically assisted reproduction (MAR), and the association of fertility with PCD genotype are extremely limited. STUDY DESIGN, SIZE, DURATION We performed a cross-sectional survey about fertility within the Living with PCD study (formerly COVID-PCD). Living with PCD is an international, online, participatory study that collects information directly from people with PCD. People with PCD of any age from anywhere in the world can participate in the study. At the time of the survey, 482 adults with PCD were registered within the Living with PCD study. PARTICIPANTS/MATERIALS, SETTING, METHODS We sent a questionnaire on fertility on 12 July 2022, to all participants older than 18 years enrolled in the Living with PCD study. Responses were collected until 8 March 2023. The fertility questionnaire covered topics related to pregnancy attempts, use of MAR, and pregnancy outcomes. Data were collected via the Research Electronic Data Capture (REDCap) platform. We defined infertility as failure to achieve a clinical pregnancy after 12 months or use of MAR for at least one pregnancy. MAIN RESULTS AND THE ROLE OF CHANCE In total, 265 of 482 adult participants (55%) completed the fertility questionnaire. Among 168 adults who had tried to conceive, 39 of 50 men (78%) and 72 of 118 women (61%) were infertile. Of the infertile men, 28 had tried MAR, and 17 of them (61%) fathered a child with the help of MAR. Among infertile women, 59 had used MAR, and 41 of them (69%) became pregnant with the help of MAR. In our population, women with PCD showed a relatively high risk of ectopic pregnancies: 1 in 10 women who became pregnant had at least one ectopic pregnancy and 7.6% of pregnancies were ectopic (95% CI 4.7–12.2). We evaluated the association between fertility and affected PCD genes in 46 individuals (11 men, 35 women) with available genetic and fertility information, and found differences between genotypes, e.g. all five women with a mutation in CCDC40 were infertile and all five with DNAH11 were fertile. LIMITATIONS, REASONS FOR CAUTION The study has limitations, including potential selection bias as people experiencing problems with fertility might be more likely to fill in the questionnaire, which may have influenced our prevalence estimates. We were unable to validate clinical data obtained from participant self-reports owing to the anonymous study design, which is likely to lead to recall bias. WIDER IMPLICATIONS OF THE FINDINGS The study underlines the need for addressing infertility in routine PCD care, with a focus on informing individuals with PCD about their increased risk. It emphasizes the utility and efficacy of MAR in PCD-related infertility. Additionally, women attempting conception should be made aware of the increased risk of ectopic pregnancies and seek systematic early consultation to confirm an intrauterine pregnancy. Fertility, efficacy of MAR, and risk for adverse pregnancy outcomes differ between people with PCD—depending on genotypes—and close monitoring and support might be needed from fertility specialists to increase chances of successful conception. STUDY FUNDING/COMPETING INTEREST(S) Our research was funded by the Swiss National Science Foundation, Switzerland (SNSF 320030B_192804), the Swiss Lung Association, Switzerland (2021-08_Pedersen), and we also received support from the PCD Foundation, USA; the Verein Kartagener Syndrom und Primäre Ciliäre Dyskinesie, Germany; the PCD Support UK, UK; and PCD Australia, Australia. M. Goutaki received funding from the Swiss National Science Foundation, Switzerland (PZ00P3_185923). B. Maitre participates in the RaDiCo-DCP funded by INSERM France. The study authors participate in the BEAT-PCD Clinical Research Collaboration supported by the European Respiratory Society. All authors declare no conflict of interest. TRIAL REGISTRATION NUMBER ClinicalTrials.gov ID NCT04602481. [ABSTRACT FROM AUTHOR]
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- 2024
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6. Alveolar compartmentalization of inflammatory and immune cell biomarkers in pneumonia-related ARDS
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Bendib, Inès, Beldi-Ferchiou, Asma, Schlemmer, Frédéric, Surenaud, Mathieu, Maitre, Bernard, Plonquet, Anne, Carteaux, Guillaume, Razazi, Keyvan, Godot, Veronique, Hüe, Sophie, Mekontso Dessap, Armand, and de Prost, Nicolas
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- 2021
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7. COPD after "Tabouna" Exposure: A Distinct Phenotype in Tunisian Women?
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Hamdi, Besma, Louhaichi, Sabrine, Jebali, Mohamed Aymen, Schlemmer, Frédéric, Maitre, Bernard, and Hamzaoui, Agnes
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CHRONIC obstructive pulmonary disease ,SMOKING ,TOBACCO smoke ,RESPIRATORY insufficiency ,OLDER patients - Abstract
Background: COPD due to exposure to combustible biomass is an increasingly recognized phenotype, particularly among women who use traditional ovens, known as 'Tabouna', for baking bread. This paper aims to investigate the clinical and functional characteristics of COPD in Tunisian female patients attributed to the use of 'Tabouna'. Methods: A retrospective single-center cohort study was conducted on patients recruited from the Department of Respiratory Disease at A. Mami Hospital, who were diagnosed with COPD between January 2014 and December 2022. The diagnosis of COPD adhered to the standards defined in GOLD 2022. Results: Out of the 95 women included in the study, 48 (50.5%) were exposed to tobacco smoke, while 47 (49.5%) were exposed to the 'Tabouna'. The median age was 70.4 ± 11.5 years, ranging from 40 to 95 years. Patients exposed to biomass were notably older, with a median age of 75.4 compared to 64.6 (p = 0.04). A significant association was observed between COPD and biomass smoke exposure, both in women residing in rural and urban areas (p = 0.006). The frequency of patients exposed to biomass with comorbidities was higher than in the group exposed to tobacco, but only hypertension showed statistically significant results (p = 0.01). Tobacco smoke induced more impairment in lung function than biomass in the group with FEV1 ≤ 30% (p = 0.04). Long-acting muscarinic antagonists were more commonly prescribed to smokers (p = 0.04). Serious complications such as chronic respiratory failure and intensive care admissions were similar in both groups (p = 0.8 and 0.4). Conclusions: COPD in women after exposure to the 'Tabouna' was observed in older patients and characterized by delayed diagnosis. Despite these clinical differences, poor COPD outcomes were similar in both groups. [ABSTRACT FROM AUTHOR]
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- 2023
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8. Lung function after matched‐related donor allogeneic hematopoietic stem cell transplantation in children with sickle cell disease
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Gros, Marion, primary, Pondarre, Corinne, additional, Arnaud, Cécile, additional, Kamdem, Annie, additional, Bernaudin, Françoise, additional, Maitre, Bernard, additional, Epaud, Ralph, additional, and Delestrain, Céline, additional
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- 2023
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9. Neutrophil Extracellular Traps Are Elevated in Patients with Pneumonia-related Acute Respiratory Distress Syndrome
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Bendib, Inès, de Chaisemartin, Luc, Granger, Vanessa, Schlemmer, Frédéric, Maitre, Bernard, Hüe, Sophie, Surenaud, Mathieu, Beldi-Ferchiou, Asma, Carteaux, Guillaume, Razazi, Keyvan, Chollet-Martin, Sylvie, Mekontso Dessap, Armand, and de Prost, Nicolas
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- 2019
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10. Prevalence and course of disease after lung resection in primary ciliary dyskinesia: a cohort & nested case-control study
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Kouis, Panayiotis, Goutaki, Myrofora, Halbeisen, Florian S., Gioti, Ifigeneia, Middleton, Nicos, Amirav, Israel, on behalf of the Israeli PCD Consortium, Barbato, Angelo, on behalf of the Italian PCD Consortium, Behan, Laura, Boon, Mieke, Emiralioglu, Nagehan, Haarman, Eric G., Karadag, Bulent, Koerner-Rettberg, Cordula, Lazor, Romain, on behalf of the Swiss PCD Group, Loebinger, Michael R., Maitre, Bernard, on behalf of the French Reference Centre for Rare Lung Diseases, Mazurek, Henryk, Morgan, Lucy, Nielsen, Kim Gjerum, Omran, Heymut, Özçelik, Ugur, Price, Mareike, Pogorzelski, Andrzej, Snijders, Deborah, on behalf of the PCD Italian Consortium, Thouvenin, Guillaume, on behalf of the French Reference Centre for Rare Lung Diseases, Werner, Claudius, Zivkovic, Zorica, Kuehni, Claudia E., and Yiallouros, Panayiotis K.
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- 2019
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11. Respiratory recovery trajectories after severe-to-critical COVID-19: a 1-year prospective multicentre study
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Schlemmer, Frédéric, primary, Valentin, Simon, additional, Boyer, Laurent, additional, Guillaumot, Anne, additional, Chabot, François, additional, Dupin, Clairelyne, additional, Le Guen, Pierre, additional, Lorillon, Gwenael, additional, Bergeron, Anne, additional, Basille, Damien, additional, Delomez, Julia, additional, Andrejak, Claire, additional, Bonnefoy, Valentine, additional, Goussault, Hélène, additional, Assié, Jean-Baptiste, additional, Choinier, Pascaline, additional, Ruppert, Anne-Marie, additional, Cadranel, Jacques, additional, Mennitti, Maria Chiara, additional, Roumila, Mehdi, additional, Colin, Charlotte, additional, Günther, Sven, additional, Sanchez, Olivier, additional, Gille, Thomas, additional, Sésé, Lucile, additional, Uzunhan, Yurdagul, additional, Faure, Morgane, additional, Patout, Maxime, additional, Morelot-Panzini, Capucine, additional, Laveneziana, Pierantonio, additional, Zysman, Maeva, additional, Blanchard, Elodie, additional, Raherison-Semjen, Chantal, additional, Giraud, Violaine, additional, Giroux-Leprieur, Etienne, additional, Habib, Stéfanie, additional, Roche, Nicolas, additional, Dinh-Xuan, Anh Tuan, additional, Sifaoui, Islem, additional, Brillet, Pierre-Yves, additional, Jung, Camille, additional, Boutin, Emmanuelle, additional, Layese, Richard, additional, Canoui-Poitrine, Florence, additional, and Maitre, Bernard, additional
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- 2023
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12. Automated computed tomographic scoring of lung disease in adults with primary ciliary dyskinesia
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Hoang-Thi, Trieu-Nghi, Revel, Marie-Pierre, Burgel, Pierre-Régis, Bassinet, Laurence, Honoré, Isabelle, Hua-Huy, Thong, Martin, Charlotte, Maitre, Bernard, and Chassagnon, Guillaume
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- 2018
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13. Impact of the COVID-19 pandemic and associated lockdown measures on the management, health, and behavior of the cystic fibrosis population in France during 2020 (MUCONFIN)
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Oubaya, Nadia, primary, Pombet, Thibaud, additional, Delestrain, Celine, additional, Remus, Natascha, additional, Douvry, Benoit, additional, Grenet, Dominique, additional, Corvol, Harriet, additional, Thouvenin, Guillaume, additional, Prulière-Escabasse, Virginie, additional, Mounir, Hakima, additional, Argoud, Dominique, additional, Fretigne, Cédric, additional, Costes, Laurence, additional, Mackiewicz, Marie-Pierre, additional, Jung, Camille, additional, Ahamada, Laitissia, additional, Lanone, Sophie, additional, Maitre, Bernard, additional, Bégot, Anne-Cécile, additional, and Epaud, Ralph, additional
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- 2022
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14. Are Systemic Manifestations Ascribable to COPD in Smokers? A Structural Equation Modeling Approach
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Boyer, Laurent, Bastuji-Garin, Sylvie, Chouaid, Christos, Housset, Bruno, Le Corvoisier, Philippe, Derumeaux, Geneviève, Boczkowski, Jorge, Maitre, Bernard, Adnot, Serge, and Audureau, Etienne
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- 2018
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15. Beclin1 circulating levels and accelerated aging markers in COPD
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Schlemmer, Frédéric, Boyer, Laurent, Soumagne, Thibaud, Ridoux, Audrey, Chouaid, Christos, Maitre, Bernard, Lanone, Sophie, Adnot, Serge, Audureau, Etienne, and Boczkowski, Jorge
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- 2018
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16. Otological Manifestations in Adults with Primary Ciliary Dyskinesia: A Controlled Radio-Clinical Study
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Alexandru, Mihaela, primary, de Boissieu, Paul, additional, Benoudiba, Farida, additional, Moustarhfir, Malik, additional, Kim, Sookyung, additional, Bequignon, Émilie, additional, Honoré, Isabelle, additional, Garcia, Gilles, additional, Mitri-Frangieh, Rana, additional, Legendre, Marie, additional, Crestani, Bruno, additional, Taillé, Camille, additional, Escudier, Estelle, additional, Maitre, Bernard, additional, Papon, Jean-François, additional, and Nevoux, Jérôme, additional
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- 2022
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17. Air pollution as an early determinant of COPD
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Lu, Zhuyi, primary, Coll, Patrice, additional, Maitre, Bernard, additional, Epaud, Ralph, additional, and Lanone, Sophie, additional
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- 2022
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18. The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTN
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Raidt, Johanna, primary, Maitre, Bernard, additional, Pennekamp, Petra, additional, Altenburg, Josje, additional, Anagnostopoulou, Pinelopi, additional, Armengot, Miguel, additional, Bloemsma, Lizan D., additional, Boon, Mieke, additional, Borrelli, Melissa, additional, Brinkmann, Folke, additional, Carr, Siobhan B., additional, Carroll, Mary P., additional, Castillo-Corullón, Silvia, additional, Coste, André, additional, Cutrera, Renato, additional, Dehlink, Eleonora, additional, Destouches, Damien M.S., additional, Di Cicco, Maria E., additional, Dixon, Lucy, additional, Emiralioglu, Nagehan, additional, Erdem Eralp, Ela, additional, Haarman, Eric G., additional, Hogg, Claire, additional, Karadag, Bulent, additional, Kobbernagel, Helene E., additional, Lorent, Natalie, additional, Mall, Marcus A., additional, Marthin, June K., additional, Martinu, Vendula, additional, Narayanan, Manjith, additional, Ozcelik, Ugur, additional, Peckham, Daniel, additional, Pifferi, Massimo, additional, Pohunek, Petr, additional, Polverino, Eva, additional, Range, Simon, additional, Ringshausen, Felix C., additional, Robson, Evie, additional, Roehmel, Jobst, additional, Rovira-Amigo, Sandra, additional, Santamaria, Francesca, additional, Schlegtendal, Anne, additional, Szépfalusi, Zsolt, additional, Tempels, Petra, additional, Thouvenin, Guillaume, additional, Ullmann, Nicola, additional, Walker, Woolf T., additional, Wetzke, Martin, additional, Yiallouros, Panayiotis, additional, Omran, Heymut, additional, and Nielsen, Kim G., additional
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- 2022
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19. The disease-specific clinical trial network for primary ciliary dyskinesia:PCD-CTN
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Raidt, Johanna, Maitre, Bernard, Pennekamp, Petra, Altenburg, Josje, Anagnostopoulou, Pinelopi, Armengot, Miguel, Bloemsma, Lizan D., Boon, Mieke, Borrelli, Melissa, Brinkmann, Folke, Carr, Siobhan B., Carroll, Mary P., Castillo-Corullón, Silvia, Coste, André, Cutrera, Renato, Dehlink, Eleonora, Destouches, Damien M.S., Di Cicco, Maria E., Dixon, Lucy, Emiralioglu, Nagehan, Eralp, Ela Erdem, Haarman, Eric G., Hogg, Claire, Karadag, Bulent, Kobbernagel, Helene E., Lorent, Natalie, Mall, Marcus A., Marthin, June K., Martinu, Vendula, Narayanan, Manjith, Ozcelik, Ugur, Peckham, Daniel, Pifferi, Massimo, Pohunek, Petr, Polverino, Eva, Range, Simon, Ringshausen, Felix C., Robson, Evie, Roehmel, Jobst, Rovira-Amigo, Sandra, Santamaria, Francesca, Schlegtendal, Anne, Szépfalusi, Zsolt, Tempels, Petra, Thouvenin, Guillaume, Ullmann, Nicola, Walker, Woolf T., Wetzke, Martin, Yiallouros, Panayiotis, Omran, Heymut, Nielsen, Kim G., Raidt, Johanna, Maitre, Bernard, Pennekamp, Petra, Altenburg, Josje, Anagnostopoulou, Pinelopi, Armengot, Miguel, Bloemsma, Lizan D., Boon, Mieke, Borrelli, Melissa, Brinkmann, Folke, Carr, Siobhan B., Carroll, Mary P., Castillo-Corullón, Silvia, Coste, André, Cutrera, Renato, Dehlink, Eleonora, Destouches, Damien M.S., Di Cicco, Maria E., Dixon, Lucy, Emiralioglu, Nagehan, Eralp, Ela Erdem, Haarman, Eric G., Hogg, Claire, Karadag, Bulent, Kobbernagel, Helene E., Lorent, Natalie, Mall, Marcus A., Marthin, June K., Martinu, Vendula, Narayanan, Manjith, Ozcelik, Ugur, Peckham, Daniel, Pifferi, Massimo, Pohunek, Petr, Polverino, Eva, Range, Simon, Ringshausen, Felix C., Robson, Evie, Roehmel, Jobst, Rovira-Amigo, Sandra, Santamaria, Francesca, Schlegtendal, Anne, Szépfalusi, Zsolt, Tempels, Petra, Thouvenin, Guillaume, Ullmann, Nicola, Walker, Woolf T., Wetzke, Martin, Yiallouros, Panayiotis, Omran, Heymut, and Nielsen, Kim G.
- Abstract
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by impaired mucociliary clearance leading to irreversible lung damage. In contrast to other rare lung diseases like cystic fibrosis (CF), there are only few clinical trials and limited evidence-based treatments. Management is mainly based on expert opinions and treatment is challenging due to a wide range of clinical manifestations and disease severity. To improve clinical and translational research and facilitate development of new treatments, the clinical trial network for PCD (PCD-CTN) was founded in 2020 under the framework of the European Reference Network (ERN)-LUNG PCD Core. Applications from European PCD sites interested in participating in the PCD-CTN were requested. Inclusion criteria consisted of patient numbers, membership of ERN-LUNG PCD Core, use of associated standards of care, experience in PCD and/or CF clinical research, resources to run clinical trials, good clinical practice (GCP) certifications and institutional support. So far, applications from 22 trial sites in 18 European countries have been approved, including >1400 adult and >1600 paediatric individuals with PCD. The PCD-CTN is headed by a coordinating centre and consists of a steering and executive committee, a data safety monitoring board and committees for protocol review, training and standardisation. A strong association with patient organisations and industrial companies are further cornerstones. All participating trial sites agreed on a code of conduct. As CTNs from other diseases have demonstrated successfully, this newly formed PCD-CTN operates to establish evidence-based treatments for this orphan disease and to bring new personalised treatment approaches to patients.
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- 2022
20. Functional Ex Vivo Testing of Alveolar Monocytes in Patients with Pneumonia-Related ARDS
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Bendib, Inès, primary, Beldi-Ferchiou, Asma, additional, Schlemmer, Frédéric, additional, Maitre, Bernard, additional, Surenaud, Mathieu, additional, Hüe, Sophie, additional, Carteaux, Guillaume, additional, Razazi, Keyvan, additional, Lelièvre, Jean-Daniel, additional, Lévy, Yves, additional, Mekontso Dessap, Armand, additional, Godot, Véronique, additional, and de Prost, Nicolas, additional
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- 2021
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21. Impact of a rare respiratory diseases reference centre set-up on primary ciliary dyskinesia care pathway
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Epaud, Salome, primary, Epaud, Ralph, additional, Salaün-Penquer, Noemie, additional, Belozertseva, Ekatarina, additional, Remus, Natascha, additional, Douvry, Benoit, additional, Bequignon, Emilie, additional, Coste, Andre, additional, Prulière-Escabasse, Virginie, additional, Schlemmer, Frédéric, additional, Jung, Camille, additional, Ortala, Matthieu, additional, Maitre, Bernard, additional, and Delestrain, Céline, additional
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- 2021
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22. Air pollution as an early determinant of COPD.
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Zhuyi Lu, Coll, Patrice, Maitre, Bernard, Epaud, Ralph, and Lanone, Sophie
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AIR pollution ,OBSTRUCTIVE lung diseases ,RESPIRATORY diseases ,AIR pollutants ,BRONCHITIS - Abstract
COPD is a progressive and debilitating disease often diagnosed after 50 years of age, but more recent evidence suggests that its onset could originate very early on in life. In this context, exposure to air pollution appears to be a potential contributor. Although the potential role of air pollution as an early determinant of COPD is emerging, knowledge gaps still remain, including an accurate qualification of air pollutants (number of pollutants quantified and exact composition) or the "one exposure-one disease" concept, which might limit the current understanding. To fill these gaps, improvements in the field are needed, such as the use of atmosphere simulation chambers able to realistically reproduce the complexity of air pollution, consideration of the exposome, as well as improving exchanges between paediatricians and adult lung specialists to take advantage of reciprocal expertise. This review should lead to a better understanding of the current knowledge on air pollution as an early determinant of COPD, as well as identify the existing knowledge gaps and opportunities to fill them. Hopefully, this will lead to better prevention strategies to scale down the development of COPD in future generations. [ABSTRACT FROM AUTHOR]
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- 2022
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23. Etiological Work-Up for Adults with Bronchiectasis: A Predictive Diagnostic Score for Primary Ciliary Dyskinesia and Cystic Fibrosis
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Schlemmer, Frederic, primary, Hamzaoui, Agnes, additional, Zebachi, Sonia, additional, Le Thuaut, Aurelie, additional, Mangiapan, Gilles, additional, Monnet, Isabelle, additional, Boudjema, Amel, additional, Jabot, Laurence, additional, Housset, Bruno, additional, Bastuji-Garin, Sylvie, additional, Bassinet, Laurence, additional, and Maitre, Bernard, additional
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- 2021
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24. Cardiovascular phenotypes predict clinical outcomes in sickle cell disease: An echocardiography‐based cluster analysis
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d'Humières, Thomas, primary, Savale, Laurent, additional, Inamo, Jocelyn, additional, Deux, Jean‐François, additional, Deswarte, Simon, additional, Lionnet, Francois, additional, Loko, Gylna, additional, Chantalat, Christelle, additional, Damy, Thibaud, additional, Guillet, Henri, additional, Pham Hung d'Alexandry d'Orengiani, Anne Laure, additional, Galactéros, Frédéric, additional, Audureau, Etienne, additional, Maitre, Bernard, additional, Humbert, Marc, additional, Derumeaux, Geneviève, additional, and Bartolucci, Pablo, additional
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- 2021
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25. International BEAT-PCD Consensus Statement for Infection Prevention and Control for Primary Ciliary Dyskinesia in collaboration with ERN-LUNG PCD Core NETWORK and patient representatives
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Marthin, June K., primary, Lucas, Jane S., additional, Boon, Mieke, additional, Casaulta, Carmen, additional, Crowley, Suzanne, additional, Destouches, Damien M.S., additional, Eber, Ernst, additional, Escribano, Amparo, additional, Haarman, Eric, additional, Hogg, Claire, additional, Maitre, Bernard, additional, Marsh, Gemma, additional, Martinu, Vendula, additional, Moreno-Galdó, Antonio, additional, Mussaffi, Huda, additional, Omran, Heymut, additional, Pohunek, Petr, additional, Rindlisbacher, Bernhard, additional, Robinson, Phil, additional, Snijders, Deborah, additional, Walker, Woolf T., additional, Yiallouros, Panayiotis, additional, Johansen, Helle Krogh, additional, and Nielsen, Kim G., additional
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- 2021
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26. Additional file 1 of Alveolar compartmentalization of inflammatory and immune cell biomarkers in pneumonia-related ARDS
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Bendib, Inès, Beldi-Ferchiou, Asma, Schlemmer, Frédéric, Surenaud, Mathieu, Maitre, Bernard, Plonquet, Anne, Carteaux, Guillaume, Razazi, Keyvan, Godot, Veronique, Hüe, Sophie, Dessap, Armand Mekontso, and Prost, Nicolas De
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Additional file 1. Tables S1 to S5, Figures S1 to S4.
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- 2021
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27. International BEAT-PCD consensus statement for infection prevention and control for primary ciliary dyskinesia in collaboration with ERN-LUNG PCD Core Network and patient representatives
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Marthin, June K, Lucas, Jane S, Boon, Mieke, Casaulta, Carmen, Crowley, Suzanne, Destouches, Damien M S, Eber, Ernst, Escribano, Amparo, Haarman, Eric, Hogg, Claire, Maitre, Bernard, Marsh, Gemma, Martinu, Vendula, Moreno-Galdó, Antonio, Mussaffi, Huda, Omran, Heymut, Pohunek, Petr, Rindlisbacher, Bernhard, Robinson, Phil, Snijders, Deborah, Walker, Woolf T, Yiallouros, Panayiotis, Johansen, Helle Krogh, Nielsen, Kim G., Marthin, June K, Lucas, Jane S, Boon, Mieke, Casaulta, Carmen, Crowley, Suzanne, Destouches, Damien M S, Eber, Ernst, Escribano, Amparo, Haarman, Eric, Hogg, Claire, Maitre, Bernard, Marsh, Gemma, Martinu, Vendula, Moreno-Galdó, Antonio, Mussaffi, Huda, Omran, Heymut, Pohunek, Petr, Rindlisbacher, Bernhard, Robinson, Phil, Snijders, Deborah, Walker, Woolf T, Yiallouros, Panayiotis, Johansen, Helle Krogh, and Nielsen, Kim G.
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Introduction In primary ciliary dyskinesia (PCD) impaired mucociliary clearance leads to recurrent airway infections and progressive lung destruction, and concern over chronic airway infection and patient-to-patient transmission is considerable. So far, there has been no defined consensus on how to control infection across centres caring for patients with PCD. Within the BEAT-PCD network, COST Action and ERS CRC together with the ERN-Lung PCD core a first initiative has now been taken towards creating such a consensus statement.Methods A multidisciplinary international PCD expert panel was set up to create a consensus statement for infection prevention and control (IP&C) for PCD, covering diagnostic microbiology, infection prevention for specific pathogens considered indicated for treatment and segregation aspects. Using a modified Delphi process, consensus to a statement demanded at least 80% agreement within the PCD expert panel group. Patient organisation representatives were involved throughout the process.Results We present a consensus statement on 20 IP&C statements for PCD including suggested actions for microbiological identification, indications for treatment of Pseudomonas aeruginosa, Burkholderia cepacia and nontuberculous mycobacteria and suggested segregation aspects aimed to minimise patient-to-patient transmission of infections whether in-hospital, in PCD clinics or wards, or out of hospital at meetings between people with PCD. The statement also includes segregation aspects adapted to the current coronavirus disease 2019 (COVID-19) pandemic.Conclusion The first ever international consensus statement on IP&C intended specifically for PCD is presented and is targeted at clinicians managing paediatric and adult patients with PCD, microbiologists, patient organisations and not least the patients and their families.
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- 2021
28. Endothelial-derived FGF2 contributes to the progression of pulmonary hypertension in humans and rodents
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Izikki, Mohamed, Guignabert, Christophe, Fadel, Elie, Humbert, Marc, Tu, Ly, Zadigue, Patricia, Dartevelle, Philippe, Simonneau, Gerald, Adnot, Serge, Maitre, Bernard, Raffestin, Bernadette, and Eddahibi, Saadia
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Fibroblast growth factors -- Physiological aspects ,Fibroblast growth factors -- Genetic aspects ,Fibroblast growth factors -- Research ,Pulmonary hypertension -- Risk factors ,Pulmonary hypertension -- Development and progression ,Pulmonary hypertension -- Genetic aspects ,Pulmonary hypertension -- Research - Abstract
Pulmonary hypertension (PH) is a progressive, lethal lung disease characterized by pulmonary artery SMC (PA-SMC) hyperplasia leading to right-sided heart failure. Molecular events originating in pulmonary ECs (P-ECs) may contribute to the PA-SMC hyperplasia in PH. Thus, we exposed cultured human PA-SMC to medium conditioned by P-EC from patients with idiopathic PH (IPH) or controls and found that IPH P-EC--conditioned medium increased PA-SMC proliferation more than control P-EC medium. Levels of FGF2 were increased in the medium of IPH P-ECs over controls, while there was no detectable difference in TGF-[beta]1, PDGF-BB, or EGF levels. No difference in FGF2-induced proliferation or FGF receptor type 1 (FGFR1) mRNA levels was detected between IPH and control PA-SMCs. Knockdown of FGF2 in P-EC using siRNA reduced the PA-SMC growth-stimulating effects of IPH P-EC medium by 60% and control P-EC medium by 10%. In situ hybridization showed FGF2 overproduction predominantly in the remodeled vascular endothelium of lungs from patients with IPH. Repeated intravenous FGF2-siRNA administration abolished lung FGF2 production, both preventing and nearly reversing a rat model of PH. Similarly, pharmacological FGFR1 inhibition with SU5402 reversed established PH in the same model. Thus, endothelial FGF2 is overproduced in IPH and contributes to SMC hyperplasia in IPH, identifying FGF2 as a promising target for new treatments against PH., Introduction Pulmonary hypertension (PH) develops either as a complication of various disease states or as an idiopathic condition (1). Mutations in the bone morphogenic protein receptor type 2 (BMPR2) have [...]
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- 2009
29. Standardised clinical data from patients with primary ciliary dyskinesia:FOLLOW-PCD
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Goutaki, Myrofora, Papon, Jean-François, Boon, Mieke, Casaulta, Carmen, Eber, Ernst, Escudier, Estelle, Halbeisen, Florian S, Harris, Amanda, Hogg, Claire, Honore, Isabelle, Jung, Andreas, Karadag, Bulent, Koerner-Rettberg, Cordula, Legendre, Marie, Maitre, Bernard, Nielsen, Kim G, Rubbo, Bruna, Rumman, Nisreen, Schofield, Lynne, Shoemark, Amelia, Thouvenin, Guillaume, Willkins, Hannah, Lucas, Jane S, Kuehni, Claudia E, Goutaki, Myrofora, Papon, Jean-François, Boon, Mieke, Casaulta, Carmen, Eber, Ernst, Escudier, Estelle, Halbeisen, Florian S, Harris, Amanda, Hogg, Claire, Honore, Isabelle, Jung, Andreas, Karadag, Bulent, Koerner-Rettberg, Cordula, Legendre, Marie, Maitre, Bernard, Nielsen, Kim G, Rubbo, Bruna, Rumman, Nisreen, Schofield, Lynne, Shoemark, Amelia, Thouvenin, Guillaume, Willkins, Hannah, Lucas, Jane S, and Kuehni, Claudia E
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Clinical data on primary ciliary dyskinesia (PCD) are limited, heterogeneous and mostly derived from retrospective chart reviews, leading to missing data and unreliable symptoms and results of physical examinations. We need standardised prospective data collection to study phenotypes, severity and prognosis and improve standards of care. A large, international and multidisciplinary group of PCD experts developed FOLLOW-PCD, a standardised clinical PCD form and patient questionnaire. We identified existing forms for clinical data collection via the Better Experimental Approaches to Treat PCD (BEAT-PCD) COST Action network and a literature review. We selected and revised the content items with the working group and patient representatives. We then revised several drafts in an adapted Delphi process, refining the content and structure. FOLLOW-PCD has a modular structure, to allow flexible use based on local practice and research focus. It includes patient-completed versions for the modules on symptoms and lifestyle. The form allows a comprehensive standardised clinical assessment at baseline and for annual reviews and a short documentation for routine follow-up. It can either be completed using printable paper forms or using an online REDCap database. Data collected in FOLLOW-PCD version 1.0 is available in real-time for national and international monitoring and research. The form will be adapted in the future after extensive piloting in different settings and we encourage the translation of the patient questionnaires to multiple languages. FOLLOW-PCD will facilitate quality research based on prospective standardised data from routine care, which can be pooled between centres, to provide first-line and real-time evidence for clinical decision-making.
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- 2020
30. Phospholipase A2 receptor 1 promotes lung cell senescence and emphysema in obstructive lung disease
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Beaulieu, Delphine, primary, Attwe, Aya, additional, Breau, Marielle, additional, Lipskaia, Larissa, additional, Marcos, Elisabeth, additional, Born, Emmanuelle, additional, Huang, Jin, additional, Abid, Shariq, additional, Derumeaux, Geneviève, additional, Houssaini, Amal, additional, Maitre, Bernard, additional, Lefevre, Marine, additional, Vienney, Nora, additional, Bertolino, Philippe, additional, Jaber, Sara, additional, Noureddine, Hiba, additional, Goehrig, Delphine, additional, Vindrieux, David, additional, Bernard, David, additional, and Adnot, Serge, additional
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- 2021
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31. Topological data analysis reveals genotype–phenotype relationships in primary ciliary dyskinesia
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Shoemark, Amelia, primary, Rubbo, Bruna, additional, Legendre, Marie, additional, Fassad, Mahmoud R., additional, Haarman, Eric G., additional, Best, Sunayna, additional, Bon, Irma C.M., additional, Brandsma, Joost, additional, Burgel, Pierre-Regis, additional, Carlsson, Gunnar, additional, Carr, Siobhan B., additional, Carroll, Mary, additional, Edwards, Matt, additional, Escudier, Estelle, additional, Honoré, Isabelle, additional, Hunt, David, additional, Jouvion, Gregory, additional, Loebinger, Michel R., additional, Maitre, Bernard, additional, Morris-Rosendahl, Deborah, additional, Papon, Jean-Francois, additional, Parsons, Camille M., additional, Patel, Mitali P., additional, Thomas, N. Simon, additional, Thouvenin, Guillaume, additional, Walker, Woolf T., additional, Wilson, Robert, additional, Hogg, Claire, additional, Mitchison, Hannah M., additional, and Lucas, Jane S., additional
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- 2021
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32. Conflicting Physiological and Genomic Cardiopulmonary Effects of Recruitment Maneuvers in Murine Acute Lung Injury
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Mekontso Dessap, Armand, Voiriot, Guillaume, Zhou, Tong, Marcos, Elisabeth, Dudek, Steven M., Jacobson, Jeff R., Machado, Roberto, Adnot, Serge, Brochard, Laurent, Maitre, Bernard, and Garcia, Joe G. N.
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- 2012
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33. Telomere Dysfunction Causes Sustained Inflammation in Chronic Obstructive Pulmonary Disease
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Amsellem, Valerie, Gary-Bobo, Guillaume, Marcos, Elisabeth, Maitre, Bernard, Chaar, Vicky, Validire, Pierre, Stern, Jean-Baptiste, Noureddine, Hiba, Sapin, Elise, Rideau, Dominique, Hue, Sophie, Le Corvoisier, Philippe, Le Gouvello, Sabine, Dubois-Randé, Jean-Luc, Boczkowski, Jorge, and Adnot, Serge
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- 2011
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34. Pulmonary Artery Thrombosis during Acute Chest Syndrome in Sickle Cell Disease
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Dessap, Armand Mekontso, Deux, Jean-François, Abidi, Nour, Lavenu-Bombled, Cécile, Melica, Giovanna, Renaud, Bertrand, Godeau, Bertrand, Adnot, Serge, Brochard, Laurent, Brun-Buisson, Christian, Galacteros, Frederic, Rahmouni, Alain, Habibi, Anoosha, and Maitre, Bernard
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- 2011
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35. TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella
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Thomas, Lucie, primary, Bouhouche, Khaled, additional, Whitfield, Marjorie, additional, Thouvenin, Guillaume, additional, Coste, Andre, additional, Louis, Bruno, additional, Szymanski, Claire, additional, Bequignon, Emilie, additional, Papon, Jean-François, additional, Castelli, Manon, additional, Lemullois, Michel, additional, Dhalluin, Xavier, additional, Drouin-Garraud, Valérie, additional, Montantin, Guy, additional, Tissier, Sylvie, additional, Duquesnoy, Philippe, additional, Copin, Bruno, additional, Dastot, Florence, additional, Couvet, Sandrine, additional, Barbotin, Anne-Laure, additional, Faucon, Catherine, additional, Honore, Isabelle, additional, Maitre, Bernard, additional, Beydon, Nicole, additional, Tamalet, Aline, additional, Rives, Nathalie, additional, Koll, France, additional, Escudier, Estelle, additional, Tassin, Anne-Marie, additional, Touré, Aminata, additional, Mitchell, Valérie, additional, Amselem, Serge, additional, and Legendre, Marie, additional
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- 2020
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36. Concomitant Presence of Aspergillus Species and Mycobacterium Species in the Respiratory Tract of Patients: Underestimated Co-occurrence?
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Dellière, Sarah, primary, Angebault, Cécile, additional, Fihman, Vincent, additional, Foulet, Françoise, additional, Lepeule, Raphaël, additional, Maitre, Bernard, additional, Schlemmer, Frédéric, additional, and Botterel, Françoise, additional
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- 2020
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37. Standardised clinical data from patients with primary ciliary dyskinesia: FOLLOW-PCD
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Goutaki, Myrofora, primary, Papon, Jean-François, additional, Boon, Mieke, additional, Casaulta, Carmen, additional, Eber, Ernst, additional, Escudier, Estelle, additional, Halbeisen, Florian S., additional, Harris, Amanda, additional, Hogg, Claire, additional, Honore, Isabelle, additional, Jung, Andreas, additional, Karadag, Bulent, additional, Koerner-Rettberg, Cordula, additional, Legendre, Marie, additional, Maitre, Bernard, additional, Nielsen, Kim G., additional, Rubbo, Bruna, additional, Rumman, Nisreen, additional, Schofield, Lynne, additional, Shoemark, Amelia, additional, Thouvenin, Guillaume, additional, Willkins, Hannah, additional, Lucas, Jane S., additional, and Kuehni, Claudia E., additional
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- 2020
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38. Acute kidney injury in sickle patients with painful crisis or acute chest syndrome and its relation to pulmonary hypertension
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Audard, Vincent, Homs, Sébastien, Habibi, Anoosha, Galacteros, Frederic, Bartolucci, Pablo, Godeau, Bertrand, Renaud, Bertrand, Levy, Yves, Grimbert, Philippe, Lang, Philippe, Brun-Buisson, Christian, Brochard, Laurent, Schortgen, Frederique, Maitre, Bernard, and Mekontso Dessap, Armand
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- 2010
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39. Efficacy of Whole-Lung Lavage in Pulmonary Alveolar Proteinosis: A Multicenter International Study of GELF
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Gay, Pierre, Wallaert, Benoit, Nowak, Stefan, Yserbyt, Jonas, Anevlavis, Stavros, Hermant, Christophe, Lovis, Alban, Menard, Olivier, Maitre, Bernard, Vandemoortele, Thomas, Dutau, Hervé, Briault, Amandine, Bourdin, Arnaud, Vergnon, Jean-Michel, Froudarakis, Marios, Service de Pneumologie [Saint-Etienne], CHU Saint-Etienne, Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Département pneumologie et addictologie [Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Arnaud de Villeneuve, Service de pneumologie [Toulouse], CHU Toulouse [Toulouse]-Hôpital Larrey [Toulouse], CHU Toulouse [Toulouse], Service de Pneumologie [CHRU Nancy], Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Service de Pneumologie [CHI Créteil], CHI Créteil, Assistance Publique - Hôpitaux de Marseille (APHM), CHU Grenoble, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Physiologie & médecine expérimentale du Cœur et des Muscles [U 1046] (PhyMedExp), Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Herrada, Anthony, Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), and Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
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Adult ,Male ,Pulmonary and Respiratory Medicine ,medicine.medical_specialty ,Adolescent ,Pulmonary Alveolar Proteinosis ,030204 cardiovascular system & hematology ,Bronchoalveolar Lavage ,[SDV.MHEP.PSR]Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract ,Pulmonary function testing ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Bronchoscopy ,Humans ,Medicine ,In patient ,Respiratory system ,Flexible bronchoscopy ,Aged ,medicine.diagnostic_test ,business.industry ,Whole lung lavage ,Middle Aged ,medicine.disease ,Respiratory Function Tests ,3. Good health ,Endoscopy ,Surgery ,Treatment Outcome ,030228 respiratory system ,[SDV.MHEP.PSR] Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract ,Female ,Respiratory Insufficiency ,business ,Pulmonary alveolar proteinosis ,Rare disease - Abstract
Background: New therapies have emerged in the treatment of pulmonary alveolar proteinosis (PAP) and, therefore, there is a real need to evaluate the efficacy of whole-lung lavage (WLL) in this rare disease. Objectives: The aim of this study was to assess the efficacy of WLL in patients with PAP. Methods: We included 33 patients from 12 centers, which are members of the French-Speaking Thoracic Endoscopy Group, for analysis. Data collection concerned patients and disease characteristics, pulmonary function tests (PFTs) and technical information on the procedure. Results: The median age of the patients was 44 years (range 13-77). There were 23 (71.9%) patients with respiratory insufficiency at presentation. All patients underwent WLL by general anesthesia and selective lung ventilation, except 1 who underwent awake flexible bronchoscopy. We noted differences in the technique, as 12 (36.36%) patients had percussion during the procedure and only 4 (12.1%) patients underwent 2-lung lavage during 1 anesthesia. A median of 12 L was used to perform WLL (1.0-40 L). Complications occurred in 11 (33.3%) patients, and 18 (56.25%) of them relapsed in a median period of 16.9 months. No significant changes were found in any PFT parameters studied, except for PaO2, which was significantly improved by 6.375 mm Hg (p = 0.0213) after the procedure compared to before. Conclusions: Although the application of the WLL technique was variable, overall, it significantly improved patients' short-term respiratory condition by improving PaO2. However, a long-term effect needs to be confirmed, as many of our patients relapsed.
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- 2017
40. Shortened Telomeres in Circulating Leukocytes of Patients with Chronic Obstructive Pulmonary Disease
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Savale, Laurent, Chaouat, Ari, Bastuji-Garin, Sylvie, Marcos, Elisabeth, Boyer, Laurent, Maitre, Bernard, Sarni, Mourad, Housset, Bruno, Weitzenblum, Emmanuel, Matrat, Mireille, Le Corvoisier, Philippe, Rideau, Dominique, Boczkowski, Jorge, Dubois-Randé, Jean-Luc, Chouaid, Christos, and Adnot, Serge
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- 2009
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41. Pulmonary Hypertension and Cor Pulmonale during Severe Acute Chest Syndrome in Sickle Cell Disease
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Dessap, Armand Mekontso, Leon, Rusel, Habibi, Anoosha, Nzouakou, Ruben, Roudot-Thoraval, Françoise, Adnot, Serge, Godeau, Bertrand, Galacteros, Frederic, Brun-Buisson, Christian, Brochard, Laurent, and Maitre, Bernard
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- 2008
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42. Time trends in diagnostic testing for PCD in Europe
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Halbeisen, Florian S., Shoemark, Amelia, Barbato, Angelo, Boon, Mieke, Carr, Siobhan, Crowley, Suzanne, Hirst, Robert A., Karadag, Bulent, Koerner-Rettberg, Cordula, Loebinger, Michael R., Lucas, Jane, Maitre, Bernard, Mazurek, Henryk, Özçelik, Uğur, Martinu, Vendula, Schwerk, Nicolaus, Thouvenin, Guillaume, Tschanz, Stefan, Yiallouros, Panayiotis, Goutaki, Myrofora, and Kuehni, Claudia E.
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- 2019
43. Time trends in diagnostic testing for primary ciliary dyskinesia in Europe
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Yiallouros, Panayiotis, Halbeisen, Florian S., Shoemark, Amelia, Barbato, Angelo, Boon, Mieke, Carr, Siobhan, Crowley, Suzanne, Hirst, Rob, Karadag, Bulent, Koerner-Rettberg, Cordula, Loebinger, Michael R., Lucas, Jane S., Maitre, Bernard, Mazurek, Henryk, Özçelik, Uğur, Martinů, Vendula, Schwerk, Nicolaus, Thouvenin, Guillaume, Tschanz, Stefan A., Goutaki, Myrofora, Kuehni, Claudia E., Yiallouros, Panayiotis [0000-0002-8339-9285], Goutaki, Myrofora [0000-0001-8036-2092], and Kuehni, Claudia E. [0000-0001-8957-2002]
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Pulmonary and Respiratory Medicine ,Male ,medicine.medical_specialty ,Nitric Oxide ,03 medical and health sciences ,0302 clinical medicine ,otorhinolaryngologic diseases ,Medicine ,Humans ,Medical physics ,030212 general & internal medicine ,Child ,Microscopy, Video ,business.industry ,Time trends ,Diagnostic test ,3. Good health ,Europe ,Microscopy, Electron ,030228 respiratory system ,Child, Preschool ,Practice Guidelines as Topic ,Female ,Guideline Adherence ,Nasal Cavity ,business ,Ciliary Motility Disorders - Abstract
Extract Despite recent advances in diagnostic methods, diagnosis of primary ciliary dyskinesia (PCD) remains complex. We need a combination of different diagnostic tests, and all have their limitations [1]. In 2009, the first European Respiratory Society (ERS) Task Force on PCD in children published recommendations [2], suggesting that: 1) nasal nitric oxide (nNO) should be measured to screen for PCD in patients aged ≥5 years [3] and 2) video microscopy (VM) analysis of ciliary beat pattern and frequency [4] plus electron microscopy (EM) [5] should be the key confirmatory diagnostic tests. Genetic testing was not recommended as part of the initial diagnostic testing, but as an additional test for inconclusive cases. The recommended test combination was nNO, VM and EM for patients aged ≥5 years and VM plus EM for younger patients. Tweetable abstract @ERSpublications click to tweetAdherence to the 2009 ERS task force diagnostic recommendations was low. To further improve PCD diagnosis, we must be more diligent and engaging in implementing the new evidence-based guidelines published in 2017. http://bit.ly/2zvjpBh 54 4
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- 2019
44. Pulmonary exacerbations in patients with primary ciliary dyskinesia: an expert consensus definition for use in clinical trials
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Lucas, Jane S., Gahleitner, Florian, Amorim, Adelina, Boon, Mieke, Brown, Philippa, Constant, Carolina, Cook, Simon, Crowley, Suzanne, Destouches, Damien M. S., Eber, Ernst, Mussaffi, Huda, Haarman, Eric, Harris, Amanda, Koerner-Rettberg, Cordula, Kuehni, Claudia E., Latzin, Philipp, Loebinger, Michael R., Lorent, Natalie, Maitre, Bernard, Moreno-Galdó, Antonio, Nielsen, Kim G., Özçelik, Uğur, Philipsen, Lue Katrine Drasbæk, Pohunek, Petr, Polverino, Eva, Rademacher, Jessica, Robinson, Phil, Snijders, Deborah, Yiallouros, Panayiotis, Carr, Siobhán B., Universitat Autònoma de Barcelona, Repositório da Universidade de Lisboa, Institut Català de la Salut, [Lucas JS, Gahleitner F] Primary Ciliary Dyskinesia Centre, NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, UK. [Amorim A] Pulmonology Dept, Centro Hospitalar S. João, Porto, Portugal. Faculty of Medicine, Porto University, Porto, Portugal. [Boon M] Dept of Paediatrics, University Hospital Gasthuisberg, Leuven, Belgium. [Brown P] PCD Family Support Group, UK. [Constant C] Paediatric Pulmonology Unit, Paediatrics Dept, Centro Hospitalar Lisboa Norte, Lisbon Academic Medical Centre, Lisbon, Portugal. [Moreno-Galdó A] Servei d'al•lergologia pediàtrica, Hospital Universitari Vall d'Hebron, Barcelona, Spain. Universitat Autònoma de Barcelona, Barcelona, Spain. [Polverino E] Vall d’Hebron Institut de Recerca, Barcelona, Spain. Servei de pneumologia, Hospital Universitari Vall d'Hebron, Barcelona, Spain., Hospital Universitari Vall d'Hebron, Pediatrics, CCA - Cancer biology and immunology, Amsterdam Reproduction & Development (AR&D), Other Research, Vall d'Hebron Barcelona Hospital Campus, Yiallouros, Panayiotis [0000-0002-8339-9285], Latzin, Philipp [0000-0002-5239-1571], and Kuehni, Claudia E. [0000-0001-8957-2002]
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Pulmonary and Respiratory Medicine ,medicine.medical_specialty ,Sistema Respiratorio::Pulmón [ANATOMÍA] ,Other subheadings::Other subheadings::/physiopathology [Other subheadings] ,Otros calificadores::Otros calificadores::/fisiopatología [Otros calificadores] ,Primary Ciliary Dyskinesia ,lcsh:Medicine ,610 Medicine & health ,Malaise ,Lethargy ,Enfermedades Respiratorias::Enfermedades Respiratorias::Trastornos de la Motilidad Ciliar::Enfermedades Respiratorias::Síndrome de Kartagener [ENFERMEDADES] ,360 Social problems & social services ,otorhinolaryngologic diseases ,medicine ,In patient ,Intensive care medicine ,Primary ciliary dyskinesia ,Lung ,business.industry ,lcsh:R ,Expert consensus ,Original Articles ,medicine.disease ,Respiratory System::Lung [ANATOMY] ,Clinical trial ,Pulmons - Malalties ,medicine.anatomical_structure ,Clinical research ,Respiratory Tract Diseases::Respiratory Tract Diseases::Ciliary Motility Disorders::Respiratory Tract Diseases::Kartagener Syndrome [DISEASES] ,medicine.symptom ,business - Abstract
Pulmonary exacerbations are a cause of significant morbidity in patients with primary ciliary dyskinesia (PCD) and are frequently used as an outcome measure in clinical research into chronic lung diseases. So far, there has been no consensus on the definition of pulmonary exacerbations in PCD. 30 multidisciplinary experts and patients developed a consensus definition for children and adults with PCD. Following a systematic review, the panel used a modified Delphi process with a combination of face-to-face meetings and e-surveys to develop a definition that can be used in research settings for children and adults with PCD. A pulmonary exacerbation was defined by the presence of three or more of the following seven items: 1) increased cough, 2) change in sputum volume and/or colour, 3) increased shortness of breath perceived by the patient or parent, 4) decision to start or change antibiotic treatment because of perceived pulmonary symptoms, 5) malaise, tiredness, fatigue or lethargy, 6) new or increased haemoptysis, and 7) temperature >38°C. The consensus panel proposed that the definition should be used for future clinical trials. The definition should be validated and the usability assessed during these studies., A consensus definition for pulmonary exacerbations in children and adults with PCD for use in clinical trials http://ow.ly/Rcfr30n4Gn4
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- 2019
45. Angiopoietin/Tie2 Pathway Influences Smooth Muscle Hyperplasia in Idiopathic Pulmonary Hypertension
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Dewachter, Laurence, Adnot, Serge, Fadel, Elie, Humbert, Marc, Maitre, Bernard, Barlier-Mur, Anne-Marie, Simonneau, Gerald, Hamon, Michel, Naeije, Robert, and Eddahibi, Saadia
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- 2006
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46. Pulmonary exacerbations in patients with primary ciliary dyskinesia:an expert consensus definition for use in clinical trials
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Lucas, Jane S, Gahleitner, Florian, Amorim, Adelina, Boon, Mieke, Brown, Philippa, Constant, Carolina, Cook, Simon, Crowley, Suzanne, Destouches, Damien M S, Eber, Ernst, Mussaffi, Huda, Haarman, Eric, Harris, Amanda, Koerner-Rettberg, Cordula, Kuehni, Claudia E, Latzin, Philipp, Loebinger, Michael R, Lorent, Natalie, Maitre, Bernard, Moreno-Galdó, Antonio, Nielsen, Kim G, Özçelik, Uğur, Philipsen, Lue Katrine Drasbæk, Pohunek, Petr, Polverino, Eva, Rademacher, Jessica, Robinson, Phil, Snijders, Deborah, Yiallouros, Panayiotis, Carr, Siobhán B, Lucas, Jane S, Gahleitner, Florian, Amorim, Adelina, Boon, Mieke, Brown, Philippa, Constant, Carolina, Cook, Simon, Crowley, Suzanne, Destouches, Damien M S, Eber, Ernst, Mussaffi, Huda, Haarman, Eric, Harris, Amanda, Koerner-Rettberg, Cordula, Kuehni, Claudia E, Latzin, Philipp, Loebinger, Michael R, Lorent, Natalie, Maitre, Bernard, Moreno-Galdó, Antonio, Nielsen, Kim G, Özçelik, Uğur, Philipsen, Lue Katrine Drasbæk, Pohunek, Petr, Polverino, Eva, Rademacher, Jessica, Robinson, Phil, Snijders, Deborah, Yiallouros, Panayiotis, and Carr, Siobhán B
- Abstract
Pulmonary exacerbations are a cause of significant morbidity in patients with primary ciliary dyskinesia (PCD) and are frequently used as an outcome measure in clinical research into chronic lung diseases. So far, there has been no consensus on the definition of pulmonary exacerbations in PCD. 30 multidisciplinary experts and patients developed a consensus definition for children and adults with PCD. Following a systematic review, the panel used a modified Delphi process with a combination of face-to-face meetings and e-surveys to develop a definition that can be used in research settings for children and adults with PCD. A pulmonary exacerbation was defined by the presence of three or more of the following seven items: 1) increased cough, 2) change in sputum volume and/or colour, 3) increased shortness of breath perceived by the patient or parent, 4) decision to start or change antibiotic treatment because of perceived pulmonary symptoms, 5) malaise, tiredness, fatigue or lethargy, 6) new or increased haemoptysis, and 7) temperature >38°C. The consensus panel proposed that the definition should be used for future clinical trials. The definition should be validated and the usability assessed during these studies.
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- 2019
47. Prevalence and course of disease after lung resection in primary ciliary dyskinesia:A cohort & nested case-control study
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Kouis, Panayiotis, Goutaki, Myrofora, Halbeisen, Florian S., Gioti, Ifigeneia, Middleton, Nicos, Amirav, Israel, Barbato, Angelo, Behan, Laura, Boon, Mieke, Emiralioglu, Nagehan, Haarman, Eric G., Karadag, Bulent, Koerner-Rettberg, Cordula, Lazor, Romain, Loebinger, Michael R., Maitre, Bernard, Mazurek, Henryk, Morgan, Lucy, Nielsen, Kim Gjerum, Omran, Heymut, Özçelik, Ugur, Price, Mareike, Pogorzelski, Andrzej, Snijders, Deborah, Thouvenin, Guillaume, Werner, Claudius, Zivkovic, Zorica, Kuehni, Claudia E., Yiallouros, Panayiotis K., Kouis, Panayiotis, Goutaki, Myrofora, Halbeisen, Florian S., Gioti, Ifigeneia, Middleton, Nicos, Amirav, Israel, Barbato, Angelo, Behan, Laura, Boon, Mieke, Emiralioglu, Nagehan, Haarman, Eric G., Karadag, Bulent, Koerner-Rettberg, Cordula, Lazor, Romain, Loebinger, Michael R., Maitre, Bernard, Mazurek, Henryk, Morgan, Lucy, Nielsen, Kim Gjerum, Omran, Heymut, Özçelik, Ugur, Price, Mareike, Pogorzelski, Andrzej, Snijders, Deborah, Thouvenin, Guillaume, Werner, Claudius, Zivkovic, Zorica, Kuehni, Claudia E., and Yiallouros, Panayiotis K.
- Abstract
Background: Lung resection is a controversial and understudied therapeutic modality in Primary Ciliary Dyskinesia (PCD). We assessed the prevalence of lung resection in PCD across countries and compared disease course in lobectomised and non-lobectomised patients. Methods: In the international iPCD cohort, we identified lobectomised and non-lobectomised age and sex-matched PCD patients and compared their characteristics, lung function and BMI cross-sectionally and longitudinally. Results: Among 2896 patients in the iPCD cohort, 163 from 20 centers (15 countries) underwent lung resection (5.6%). Among adult patients, prevalence of lung resection was 8.9%, demonstrating wide variation among countries. Compared to the rest of the iPCD cohort, lobectomised patients were more often females, older at diagnosis, and more often had situs solitus. In about half of the cases (45.6%) lung resection was performed before presentation to specialized PCD centers for diagnostic work-up. Compared to controls (n = 197), lobectomised patients had lower FVC z-scores (-2.41 vs-1.35, p = 0.0001) and FEV1 z-scores (-2.79 vs-1.99, p = 0.003) at their first post-lung resection assessment. After surgery, lung function continued to decline at a faster rate in lobectomised patients compared to controls (FVC z-score slope:-0.037/year Vs-0.009/year, p = 0.047 and FEV1 z-score slope:-0.052/year Vs-0.033/year, p = 0.235), although difference did not reach statistical significance for FEV1. Within cases, females and patients with multiple lobe resections had lower lung function. Conclusions: Prevalence of lung resection in PCD varies widely between countries, is often performed before PCD diagnosis and overall is more frequent in patients with delayed diagnosis. After lung resection, compared to controls most lobectomised patients have poorer and continuing decline of lung function despite lung resection. Further studies benefiting from prospective data collection are needed to confirm these fin
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- 2019
48. Induced Sputum versus Bronchoalveolar Lavage during Acute Chest Syndrome in Sickle Cell Disease
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Lechapt, Emmanuelle, Habibi, Anoosha, Bachir, Dora, Galacteros, Frederic, Schaeffer, Annette, Desvaux, Dominique, Brochard, Laurent, Housset, Bruno, Godeau, Bertrand, and Maitre, Bernard
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- 2003
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49. Continuous Positive Airway Pressure during Fiberoptic Bronchoscopy in Hypoxemic Patients: A Randomized Double-Blind Study Using A New Device
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MAITRE, BERNARD, JABER, SAMIR, MAGGIORE, SALVATORE M., BERGOT, EMMANUEL, RICHARD, JEAN CHRISTOPHE, BAKTHIARI, HAMID, HOUSSET, BRUNO, BOUSSIGNAC, GEORGES, and BROCHARD, LAURENT
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- 2000
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50. Clinical phenotypes and outcomes of precapillary pulmonary hypertension of sickle cell disease
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Savale, Laurent, primary, Habibi, Anoosha, additional, Lionnet, François, additional, Maitre, Bernard, additional, Cottin, Vincent, additional, Jais, Xavier, additional, Chaouat, Ari, additional, Artaud-Macari, Elise, additional, Canuet, Matthieu, additional, Prevot, Grégoire, additional, Chantalat-Auger, Christelle, additional, Montani, David, additional, Sitbon, Olivier, additional, Galacteros, Fréderic, additional, Simonneau, Gérald, additional, Parent, Florence, additional, Bartolucci, Pablo, additional, and Humbert, Marc, additional
- Published
- 2019
- Full Text
- View/download PDF
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