45 results on '"A.-S. Ducloy-Bouthors"'
Search Results
2. Obésité morbide : grossesse et accouchement
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S. Roger-Christoph, B. Julliac, L. Bouvet, P. Diemunsch, D. Chassard, H. Keita, S. Nebout, G. Aya, A. Fournet-Fayard, B. Storme, F. Vial, M. Ruivard, E. Moreau, F. Mercier, C. Fischer, M. Bruyère, A.-S. Ducloy-Bouthors, A. Castel, V. Fuzier, M.-P. Bonnet, P.-Y. Dewandre, M. Bonnin, E. Lopard, and D. Benhamou
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business.industry ,Medicine ,business - Published
- 2021
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3. Analgésie périnéale en post-partum de l’accouchement voie basse
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M.-P. Bonnet, A. Castel, E. Moreau, L. Bouvet, C. Fischer, G. Aya, P.-Y. Dewandre, S. Roger-Christoph, M. Bruyère, H. Keita, A. Fournet-Fayard, E. Lopard, A.-S. Ducloy-Bouthors, F. Mercier, D. Benhamou, M. Ruivard, B. Julliac, D. Chassard, B. Storme, V. Fuzier, M. Bonnin, P. Diemunsch, F. Vial, and S. Nebout
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business.industry ,Medicine ,business - Published
- 2021
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4. Traces pilot pharmacokinetic study dataset
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Gilles Lebuffe, F Loingeville, Sixtine Gilliot, Pascal Odou, B Hennart, A S Ducloy-Bouthors, M Jeanne, CHU Lille, Institut Pasteur de Lille, Université de Lille, Groupe de Recherche sur les formes Injectables et les Technologies Associées - ULR 7365 [GRITA], IMPact de l'Environnement Chimique sur la Santé humaine (IMPECS) - ULR 4483, METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694, Groupe de Recherche sur les formes Injectables et les Technologies Associées (GRITA) - ULR 7365, Groupe de Recherche sur les formes Injectables et les Technologies Associées - ULR 7365 (GRITA), Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Hôpital Jeanne de Flandre [Lille], Evaluation des technologies de santé et des pratiques médicales - ULR 2694 (METRICS), and Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Université de Lille
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Tranexamic acid ,[SDV]Life Sciences [q-bio] ,Body weight ,lcsh:Computer applications to medicine. Medical informatics ,Postpartum haemorrhage ,03 medical and health sciences ,0302 clinical medicine ,Blood loss ,Pharmacokinetics ,Medicine ,Caesarean section ,lcsh:Science (General) ,Data Article ,030304 developmental biology ,Volume of distribution ,0303 health sciences ,Multidisciplinary ,business.industry ,Patient data ,lcsh:R858-859.7 ,business ,Nuclear medicine ,Intravenous ,030217 neurology & neurosurgery ,medicine.drug ,lcsh:Q1-390 - Abstract
The dataset displays the pharmacokinetics data obtained from the TRACES pilot study. The nine patients included were undergoing haemorrhagic caesarean section (blood loss > 800 mL) and receiving a single i.v dose of tranexamic acid (0.5, 1 or 2 g over 1 min). The dataset gathers the tranexamic acid blood and urinary concentrations. With these first elements, a pharmacokinetic compartment model was built as described in Gilliot et al. and the individual pharmacokinetic parameters were estimated. In parallel, the patients anthropometric, biological, and clinical characteristics were collected. The correlation between the patient data and the estimated individual pharmacokinetic parameters were tested. The correlation tests revealed that the dose, the height, the body weight, and the ideal bodyweight had and impact on the volume of distribution of tranexamic acid. According to these results, these latter covariates were explored using a multi-regression analysis in Gilliot et al.
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- 2020
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5. Hypothesis for a partially non urinary elimination of tranexamic acid in haemorrhagic caesarean section: Traces pilot pharmacokinetic study: Pharmacokinetics of tranexamic acid in obstetrics
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F Loingeville, Sixtine Gilliot, B Hennart, Gilles Lebuffe, A S Ducloy-Bouthors, Pascal Odou, and M Jeanne
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medicine.medical_specialty ,medicine.medical_treatment ,Urinary system ,Population ,Urology ,Pharmaceutical Science ,02 engineering and technology ,030226 pharmacology & pharmacy ,03 medical and health sciences ,0302 clinical medicine ,Pharmacokinetics ,Pregnancy ,medicine ,Humans ,Caesarean section ,Compartment (pharmacokinetics) ,education ,Volume of distribution ,education.field_of_study ,business.industry ,Cesarean Section ,021001 nanoscience & nanotechnology ,Urinary elimination ,Obstetrics ,Tranexamic Acid ,Injections, Intravenous ,Female ,0210 nano-technology ,business ,Tranexamic acid ,medicine.drug - Abstract
Background : In previous studies, the choice of doses of tranexamic acid was empirically defined as no pharmacokinetic study had been conducted in haemorrhagic caesarean section. Objective : The objective was to build a pharmacokinetic model in patients receiving a single 0.5, 1 or 2 g intravenous bolus. Method : A preliminary monocentric open study was performed in the Lille centre. Blood samples and one urinary sample were collected in the 6 hours following the injection. Nine patients were included. Tranexamic acid concentration was measured using liquid chromatography system coupled with tandem mass spectrometry. We used Monolix 2019R1 for population pharmacokinetic modelling. A structural model was constructed followed by the investigation of potential covariates. Results : Data were best described with a two-compartment model with a double first-order elimination from the central compartment. The model was improved when the variable ideal weight per dose was affected as a covariate for the apparent volume of distribution. Assuming a dose of 1 g and a height of 160 cm, the pharmacokinetic parameters were estimated at 10.26 L.h−1 for total clearance, 11.5 L for the volume of the central compartment, 15.8 L for the volume of the second compartment, a diffusional clearance of 30.36 L.h−1 , and a urinary excretion fraction of 25.8%. Conclusions : The population pharmacokinetic model of tranexamic acid in haemorrhagic caesarean section was successfully established in our tiny sample of patients. The results of this preliminary TRACES pharmacokinetic study suggested that elimination of tranexamic acid is partially non urinary in contrast with healthy patients.
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- 2019
6. La femme enceinte obèse : le point de vue de l’anesthésiste
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B. Storme, E. Moreau, D. Chassard, M. Bonnin, A.-S. Ducloy-Bouthors, and H. Keita-Meyer
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Gynecology ,medicine.medical_specialty ,business.industry ,medicine ,General Earth and Planetary Sciences ,business ,General Environmental Science - Abstract
La parturiente obese est a haut risque de morbimortalite peripartum par l’association des modifications physiologiques de l’obesite et d’eventuelles comorbidites associees aux modifications physiologiques de la grossesse. La prise en charge anesthesique doit privilegier l’anesthesie locoregionale afin d’eviter le recours a l’anesthesie generale et les risques auxquels elle expose. L’analgesie peridurale obstetricale est une indication medicale pour l’accouchement par voie basse et la rachianesthesie avec peridurale combinee est la technique a recommander pour la cesarienne. L’antibioprophylaxie pour la cesarienne devra utiliser des posologies adaptees a l’IMC, certains recommandant meme une bitherapie. La thromboprophylaxie pourra etre indiquee meme en cas d’accouchement par voie basse et sera dans tous les cas adaptee a l’IMC.
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- 2016
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7. Core outcome sets for prevention and treatment of postpartum haemorrhage: an international Delphi consensus study
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Ahmet Metin Gülmezoglu, G. Gyte, K. Gutteridge, Peter William Collins, A. S. Ducloy-Bouthors, Jennifer Blum, Shuba Mallaiah, Anna Cuthbert, Nasreen Aflaifel, Shireen Meher, Paula R Williamson, Declan Devane, Zulfiqar A Bhutta, Andrew Weeks, J. M. Smith, Jamie J Kirkham, Caroline S.E. Homer, Zarko Alfirevic, A. Bishop, Edgardo Abalos, and Bukola Fawole
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medicine.medical_specialty ,Blood transfusion ,Consensus ,Delphi Technique ,medicine.medical_treatment ,International Cooperation ,Population ,Breastfeeding ,Delphi method ,Outcome Assessment (Health Care) ,03 medical and health sciences ,0302 clinical medicine ,Patient satisfaction ,Pregnancy ,Outcome Assessment, Health Care ,Medicine ,Humans ,Obstetrics & Reproductive Medicine ,Adverse effect ,education ,education.field_of_study ,030219 obstetrics & reproductive medicine ,business.industry ,Postpartum Hemorrhage ,Obstetrics and Gynecology ,medicine.disease ,Systematic review ,Patient Satisfaction ,Family medicine ,Maternal death ,Female ,business - Abstract
© 2018 Royal College of Obstetricians and Gynaecologists Objective: To develop core outcome sets (COS) for studies evaluating interventions for (1) prevention and (2) treatment of postpartum haemorrhage (PPH), and recommendations on how to report the COS. Design: A two-round Delphi survey and face-to-face meeting. Population: Healthcare professionals and women's representatives. Methods: Outcomes were identified from systematic reviews of PPH studies and stakeholder consultation. Participants scored each outcome in the Delphi on a Likert scale between 1 (not important) and 9 (critically important). Results were discussed at the face-to-face meeting to agree the final COS. Consensus at the meeting was defined as ≥ 70% of participants scoring the outcome as critically important (7–9). Lectures, discussion and voting were used to agree how to report COS outcomes. Main outcome measures: Outcomes from systematic reviews and consultations. Results: Both Delphi rounds were completed by 152/205 (74%) participants for prevention and 143/197 (73%) for treatment. For prevention of PPH, nine core outcomes were selected: blood loss, shock, maternal death, use of additional uterotonics, blood transfusion, transfer for higher level of care, women's sense of wellbeing, acceptability and satisfaction with the intervention, breastfeeding, and adverse effects. For treatment of PPH, 12 core outcomes were selected: blood loss, shock, coagulopathy, hysterectomy, organ dysfunction, maternal death, blood transfusion, use of additional haemostatic intervention, transfer for higher level of care, women's sense of wellbeing, acceptability and satisfaction with the intervention, breastfeeding, and adverse effects. Recommendations were developed on how to report these outcomes where possible. Conclusions: These COS will help standardise outcome reporting in PPH trials. Tweetable abstract: Core outcome sets for PPH: nine core outcomes for PPH prevention and 12 core outcomes for PPH treatment.
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- 2018
8. Dissection aortique et grossesse
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Philippe Deruelle, F. Pontana, Damien Subtil, M. Trudel, V. Debarge, C. Coulon, M. Koussa, and A.-S. Ducloy-Bouthors
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Aortic dissection ,Pregnancy ,medicine.medical_specialty ,Diagnostic methods ,business.industry ,General surgery ,Chest ct ,Obstetrics and Gynecology ,General Medicine ,medicine.disease ,Connective tissue disease ,Reproductive Medicine ,medicine ,Surgical emergency ,Risk factor ,Presentation (obstetrics) ,business - Abstract
During pregnancy, the occurrence of aortic dissection is a rare event immediately threatening fetal and maternal prognosis. Its occurrence is more common in cases of connective tissue disease. But the absence risk factor shall not exclude or delay diagnosis. We must learn to think about it, because the prognosis is highly dependent on time management. The clinical presentation of this medical and surgical emergency varies, and pregnancy adds its own symptoms. We have to ask without hesitation that echocardiography or chest CT be performed since these diagnostic methods are both reliable and available.
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- 2015
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9. 37th International Symposium on Intensive Care and Emergency Medicine (part 2 of 3)
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D. Rob, R. Špunda, J. Lindner, J. Šmalcová, O. Šmíd, T. Kovárník, A. Linhart, J. Bìlohlávek, M. M. Marinoni, G. Cianchi, S. Trapani, M. L. Migliaccio, L. Gucci, M. Bonizzoli, A. Cramaro, M. Cozzolino, S. Valente, A. Peris, E. Grins, E. Kort, M. Weiland, N. Manandhar Shresta, P. Davidson, L. Algotsson, S. Fitch, G. Marco, J. Sturgill, S. Lee, M. Dickinson, T. Boeve, A. Khaghani, P. Wilton, S. Jovinge, A. N. Ahmad, R. Loveridge, S. Vlachos, S. Patel, E. Gelandt, L. Morgan, S. Butt, M. Whitehorne, V. Kakar, C. Park, M. Hayes, C. Willars, T. Hurst, T. Best, A. Vercueil, G. Auzinger, B. Adibelli, N. Akovali, A. Torgay, P. Zeyneloglu, A. Pirat, Z. Kayhan, S. S. Schmidbauer, J. Herlitz, T. Karlsson, H. Friberg, R. Knafelj, P. Radsel, F. Duprez, T. Bonus, G. Cuvelier, S. Mashayekhi, M. Maka, S. Ollieuz, G. Reychler, R. Mosaddegh, S. Abbasi, S. Talaee, V. Z. Zotzmann, D. S. Staudacher, T. W. Wengenmayer, D. D. Dürschmied, C. B. Bode, A. Nelskylä, J. Nurmi, M. Jousi, A. Schramko, E. Mervaala, G. Ristagno, M. Skrifvars, G. Ozsoy, T. Kendirli, E. Azapagasi, O. Perk, U. Gadirova, E. Ozcinar, M. Cakici, C. Baran, S. Durdu, A. Uysalel, M. Dogan, M. Ramoglu, T. Ucar, E. Tutar, S. Atalay, R. Akar, M. Kamps, G. Leeuwerink, J. Hofmeijer, O. Hoiting, J. Van der Hoeven, C. Hoedemaekers, A. Konkayev, V. Kuklin, T. Kondratyev, M. Konkayeva, N. Akhatov, M. Sovershaev, T. Tveita, V. Dahl, L. Wihersaari, M. B. Skrifvars, S. Bendel, K. M. Kaukonen, J. Vaahersalo, J. Romppanen, V. Pettilä, M. Reinikainen, A. Lybeck, T. Cronberg, N. Nielsen, M. Rauber, K. Steblovnik, A. Jazbec, M. Noc, P. Kalasbail, F. Garrett, E. Kulstad, D. J. Bergström, H. R. Olsson, S. Schmidbauer, I. Mandel, S. Mikheev, Y. Podoxenov, I. Suhodolo, A. Podoxenov, J. Svirko, A. Sementsov, L. Maslov, V. Shipulin, L. V. Vammen, S. R. Rahbek, N. S. Secher, J. P. Povlsen, N. J. Jessen, B. L. Løfgren, A. G. Granfeldt, A. Grossestreuer, S. Perman, P. Patel, S. Ganley, J. Portmann, M. Cocchi, M. Donnino, Y. Nassar, S. Fathy, A. Gaber, S. Mokhtar, Y. C. Chia, R. Lewis-Cuthbertson, K. Mustafa, A. Sabra, A. Evans, P. Bennett, W. Eertmans, C. Genbrugge, W. Boer, J. Dens, C. De Deyne, F. Jans, A. Skorko, M. Thomas, M. Casadio, A. Coppo, A. Vargiolu, J. Villa, M. Rota, L. Avalli, G. Citerio, J. B. Moon, J. H. Cho, C. W. Park, T. G. Ohk, M. C. Shin, M. H. Won, P. Papamichalis, V. Zisopoulou, E. Dardiotis, S. Karagiannis, D. Papadopoulos, T. Zafeiridis, D. Babalis, A. Skoura, I. Staikos, A. Komnos, S. Silva Passos, F. Maeda, L. Silva Souza, A. Amato Filho, T. Araújo Guerra Granjeia, M. Schweller, D. Franci, M. De Carvalho Filho, T. Martins Santos, P. De Azevedo, R. Wall, I. Welters, P. Tansuwannarat, P. Sanguanwit, T. Langer, M. Carbonara, A. Caccioppola, C. Ferraris Fusarini, E. Carlesso, E. Paradiso, M. Battistini, E. Cattaneo, F. Zadek, R. Maiavacca, N. Stocchetti, A. Pesenti, A. Ramos, F. Acharta, J. Toledo, M. Perezlindo, L. Lovesio, A. Dogliotti, C. Lovesio, N. Schroten, B. Van der Veen, M. C. De Vries, J. Veenstra, Y. B. Abulhasan, S. Rachel, M. Châtillon-Angle, N. Alabdulraheem, I. Schiller, N. Dendukuri, M. Angle, C. Frenette, S. Lahiri, K. Schlick, S. A. Mayer, P. Lyden, M. Akatsuka, J. Arakawa, M. Yamakage, J. Rubio, J. A. Rubio Mateo-Sidron, R. Sierra, M. Celaya, L. Benitez, S. Alvarez-Ossorio, A. Fernandez, O. Gonzalez, H. Engquist, E. Rostami, P. Enblad, L. Canullo, J. Nallino, M. Perreault, J. Talic, A. J. Frenette, L. Burry, F. Bernard, D. R. Williamson, D. Adukauskiene, J. Cyziute, A. Adukauskaite, L. Malciene, L. Luca, A. Rogobete, O. Bedreag, M. Papurica, M. Sarandan, C. Cradigati, S. Popovici, C. Vernic, D. Sandesc, V. Avakov, I. Shakhova, H. Trimmel, M. Majdan, G. H. Herzer, C. S. Sokoloff, M. Albert, D. Williamson, C. Odier, J. Giguère, E. Charbonney, Z. Husti, T. Kaptás, Z. Fülep, Z. Gaál, M. Tusa, J. Donnelly, M. Aries, M. Czosnyka, C. Robba, M. Liu, A. Ercole, D. Menon, P. Hutchinson, P. Smielewski, R. López, J. Graf, J. M. Montes, M. Kenawi, A. Kandil, K. Husein, A. Samir, J. Heijneman, J. Huijben, F. Abid-Ali, M. Stolk, J. Van Bommel, H. Lingsma, M. Van der Jagt, R. C. Cihlar, G. Mancino, P. Bertini, F. Forfori, F. Guarracino, D. Pavelescu, I. Grintescu, L. Mirea, S. Alamri, M. Tharwat, N. Kono, H. Okamoto, H. Uchino, T. Ikegami, T. Fukuoka, M. Simoes, E. Trigo, P. Coutinho, J. Pimentel, A. Franci, D. Basagni, M. Boddi, V. Anichini, A. Cecchi, D. Markopoulou, K. Venetsanou, I. Papanikolaou, T. Barkouri, D. Chroni, I. Alamanos, E. Cingolani, M. G. Bocci, L. Pisapia, A. Tersali, S. L. Cutuli, V. Fiore, A. Palma, G. Nardi, M. Antonelli, R. Coke, A. Kwong, D. J. Dwivedi, M. Xu, E. McDonald, J. C. Marshall, A. E. Fox-Robichaud, P. C. Liaw, I. Kuchynska, I. R. Malysh, L. V. Zgrzheblovska, L. Mestdagh, E. F. Verhoeven, I. Hubloue, J. Ruel-laliberte, R. Zarychanski, F. Lauzier, P. Lessard Bonaventure, R. Green, D. Griesdale, R. Fowler, A. Kramer, D. Zygun, T. Walsh, S. Stanworth, C. Léger, A. F. Turgeon, D. M. Baron, J. Baron-Stefaniak, G. C. Leitner, R. Ullrich, O. Tarabrin, A. Mazurenko, Y. Potapchuk, D. Sazhyn, P. Tarabrin, A. González Pérez, J. Silva, V. Artemenko, A. Bugaev, I. Tokar, S. Konashevskaya, I. M. Kolesnikova, E. V. Roitman, T. Rengeiné Kiss, Z. Máthé, L. Piros, E. Dinya, E. Tihanyi, A. Smudla, J. Fazakas, R. Ubbink, P. Boekhorst te, E. Mik, L. Caneva, G. Ticozzelli, S. Pirrelli, D. Passador, F. Riccardi, F. Ferrari, E. M. Roldi, M. Di Matteo, I. Bianchi, G. A. Iotti, G. Zurauskaite, A. Voegeli, M. Meier, D. Koch, S. Haubitz, A. Kutz, M. Bargetzi, B. Mueller, P. Schuetz, G. Von Meijenfeldt, M. Van der Laan, C. Zeebregts, K. B. Christopher, P. Vernikos, T. Melissopoulou, G. Kanellopoulou, M. Panoutsopoulou, D. Xanthis, K. Kolovou, T. Kypraiou, J. Floros, H. Broady, C. Pritchett, M. Marshman, N. Jannaway, C. Ralph, C. L. Lehane, C. K. Keyl, E. Z. Zimmer, D. T. Trenk, A. S. Ducloy-Bouthors, M. J. Jonard, F. Fourrier, F. Piza, T. Correa, A. Marra, J. Guerra, R. Rodrigues, A. Vilarinho, V. Aranda, S. Shiramizo, M. R. Lima, E. Kallas, A. B. Cavalcanti, M. Donoso, P. Vargas, J. McCartney, S. Ramsay, K. McDowall, I. Novitzky-Basso, C. Wright, M Grgic Medic, L Bielen, V Radonic, O Zlopasa, N Gubarev Vrdoljak, V Gasparovic, R Radonic, G. Narváez, D. Cabestrero, L. Rey, M. Aroca, S. Gallego, J. Higuera, R. De Pablo, L. Rey González, G. Narváez Chávez, J. Higuera Lucas, D. Cabestrero Alonso, M. Aroca Ruiz, L. Jaramillo Valarezo, R. De Pablo Sánchez, A. Quinza Real, T. W. Wigmore, I. Bendavid, J. Cohen, I. Avisar, I. Serov, I. Kagan, P. Singer, J Hanison, U Mirza, D Conway, A. Takasu, H. Tanaka, N. Otani, S. Ohde, S. Ishimatsu, F Coffey, P Dissmann, K Mirza, M Lomax, P. Dissmann, F. Coffey, K. Mirza, M. Lomax, JR Miner, R Leto, AM Markota, PG Gradišek, VA Aleksejev, AS Sinkovič, S. Romagnoli, C. Chelazzi, G. Zagli, F. Benvenuti, P. Mancinelli, P. Boninsegni, L. Paparella, A. T. Bos, O. Thomas, T. Goslar, A. Martone, P. R. Sandu, V. A. Rosu, A. Capilnean, P. Murgoi, A. Lecavalier, D. Jayaraman, P. Rico, P. Bellemare, C. Gelinas, T. Nishida, T. Kinoshita, N. Iwata, K. Yamakawa, S. Fujimi, L. Maggi, F. Sposato, G. Citterio, C. Bonarrigo, M. Rocco, V. Zani, R. A. De Blasi, D Alcorn, L Barry, M. A. Riedijk, D. M. Milstein, J. Caldas, R. Panerai, L. Camara, G. Ferreira, E. Bor-Seng-Shu, M. Lima, F. Galas, N. Mian, R. Nogueira, G. Queiroz de Oliveira, J. Almeida, J. Jardim, T. G. Robinson, F. Gaioto, L. A. Hajjar, I. Zabolotskikh, T. Musaeva, W. Saasouh, J. Freeman, A. Turan, S. Saseedharan, E. Pathrose, S. Poojary, J. Messika, Y. Martin, N. Maquigneau, M. Henry-Lagarrigue, C. Puechberty, A. Stoclin, L. Martin-Lefevre, F. Blot, D. Dreyfuss, A. Dechanet, D. Hajage, J. Ricard, E. Almeida, G. Landoni, J. Fukushima, E. Fominskiy, C. De Brito, L. Cavichio, L. Almeida, U. Ribeiro, E. Osawa, R. Boltes, L. Battistella, L. Hajjar, P. Fontela, T. Lisboa, L. Forgiarini Junior, G. F. Friedman, F. Abruzzi, J. Azevedo Peixoto Primo, P. Marques Filho, J. Stormorvski de Andrade, K. Matos Brenner, M. Scorsato boeira, C. Leães, C. Rodrigues, A. Vessozi, A. SantAnna Machado, M. Weiler, H. Bryce, A. Hudson, T. Law, R. Reece-Anthony, A. Molokhia, F. Abtahinezhadmoghaddam, E. Cumber, L. Channon, A. Wong, R. Groome, D. Gearon, J. Varley, A. Wilson, J. Reading, F. G. Zampieri, F. A. Bozza, M. Ferez, H. Fernandes, A. Japiassú, J. Verdeal, A. C. Carvalho, M. Knibel, J. I. Salluh, M. Soares, J. Gao, E. Ahmadnia, B. Patel, A. MacKay, S. Binning, R. J. Pugh, C. Battle, C. Hancock, W. Harrison, T. Szakmany, F. Mulders, J. Vandenbrande, J. Dubois, B. Stessel, K. Siborgs, D. Ramaekers, U. V. Silva, W. S. Homena, G. C. Fernandes, A. P. Moraes, L. Brauer, M. F. Lima, F. De Marco, N. Maric, M. Mackovic, N. Udiljak, CE Bosso, RD Caetano, AP Cardoso, OA Souza, R Pena, MM Mescolotte, IA Souza, GM Mescolotte, H. Bangalore, E. Borrows, D. Barnes, V. Ferreira, L. Azevedo, G. Alencar, A. Andrade, A. Bierrenbach, L. Tadini Buoninsegni, L. Cecci, J. Lindskog, K. Rowland, P. Sturgess, A. Ankuli, R Rosa, T Tonietto, A Ascoli, L Madeira, W Rutzen, M Falavigna, C Robinson, J Salluh, A Cavalcanti, L Azevedo, R Cremonese, D Da Silva, A Dornelles, Y Skrobik, J Teles, T Ribeiro, C Eugênio, C Teixeira, M. Zarei, H. Hashemizadeh, M. Eriksson, G. Strandberg, M. Lipcsey, A. Larsson, M. Lignos, E. Crissanthopoulou, K. Flevari, P. Dimopoulos, A. Armaganidis, JG Golub, AS Stožer, H. Rüddel, C. Ehrlich, C. M. Burghold, C. Hohenstein, J. Winning, W. Sellami, Z. Hajjej, M. Bousselmi, H. Gharsallah, I. Labbene, M. Ferjani, J. Sattler, D. Steinbrunner, H. Poppert, G. Schneider, M. Blobner, K. G. Kanz, S. J. Schaller, K. Apap, G. Xuereb, L. Massa, N. Delvau, A Penaloza, G Liistro, F Thys, I. K. Delattre, P. Hantson, P. M. Roy, P. Gianello, L Hadîrcă, A Ghidirimschi, N Catanoi, N Scurtov, M Bagrinovschi, Y. S. Sohn, Y. C. Cho, B. Golovin, O. Creciun, A. Ghidirimschi, M. Bagrinovschi, R. Tabbara, J. Z. Whitgift, A. Ishimaru, A. Yaguchi, N. Akiduki, M. Namiki, M. Takeda, J. N. Tamminen, A. Uusaro, C. G. Taylor, E. D. Mills, A. D. Mackay, C. Ponzoni, R. Rabello, A. Serpa, M. Assunção, A. Pardini, G. Shettino, T. Corrêa, P. V. Vidal-Cortés, L. Álvarez-Rocha, P. Fernández-Ugidos, A. Virgós-Pedreira, M. A. Pérez-Veloso, I. M. Suárez-Paul, L. Del Río-Carbajo, S. Pita Fernández, A. Castro-Iglesias, A. Butt, A. A. Alghabban, S. K. Khurshid, Z. A. Ali, I. N. Nizami, N. S. Salahuddin, M. Alshahrani, A. W. Alsubaie, A. S. Alshamsy, B. A. Alkhiliwi, H. K. Alshammari, M. B. Alshammari, N. K. Telmesani, R. B. Alshammari, L. P. Asonto, L. P. Damiani, F Bozza, A. El Khattate, M. Bizrane, N. Madani, J. Belayachi, R. Abouqal, D. Ramnarain, B. Gouw-Donders, C. Benstoem, A. Moza, P. Meybohm, C. Stoppe, R. Autschbach, D. Devane, A. Goetzenich, L. U. Taniguchi, L. Araujo, G. Salgado, J. M. Vieira, J. Viana, N. Ziviani, I. Pessach, A. Lipsky, A. Nimrod, M. O´Connor, I. Matot, E. Segal, A. Kluzik, A. Gradys, P. Smuszkiewicz, I. Trojanowska, M. Cybulski, A. De Jong, M. Sebbane, G. Chanques, S. Jaber, R. Rosa, C. Robinson, M. Bessel, L. Cavalheiro, L. Madeira, W. Rutzen, R. Oliveira, J. Maccari, M. Falavigna, E. Sanchez, F. Dutra, C. Dietrich, P. Balzano, J. Rezende, C. Teixeira, S. Sinha, K. Majhi, J. G. Gorlicki, F. P. Pousset, J. Kelly, J. Aron, A. Crerar Gilbert, N. Prevec Urankar, M. Irazabal, M. Bosque, J. Manciño, A. Kotsopoulos, N. Jansen, W. Abdo, Ú. M. Casey, B. O’Brien, R. Plant, and B. Doyle
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Fatal outcome ,business.industry ,Traumatic brain injury ,030208 emergency & critical care medicine ,030204 cardiovascular system & hematology ,Critical Care and Intensive Care Medicine ,medicine.disease ,Outcome (game theory) ,03 medical and health sciences ,0302 clinical medicine ,Anesthesia ,Medicine ,business ,Acute subdural hematoma - Published
- 2017
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10. Réhabilitation après césarienne. Pas seulement une réhabilitation postopératoire
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A.-S. Ducloy-Bouthors and H. Keïta
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Gynecology ,medicine.medical_specialty ,Anesthesiology and Pain Medicine ,Rehabilitation ,Enhanced recovery ,business.industry ,medicine.medical_treatment ,Caesarean delivery ,Medicine ,General Medicine ,business ,Post partum - Published
- 2013
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11. Hypnose en anesthésie et analgésie en obstétrique et en gynécologie
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P. Richart, A. S. Ducloy-Bouthors, F. Bernard, O. Cottencin, J.-C. Ducloy, and A. Hamdani
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Gynecology ,medicine.medical_specialty ,business.industry ,General Earth and Planetary Sciences ,Medicine ,business ,General Environmental Science - Abstract
L’hypnose est un etat modifie de conscience, spontane ou induit, different du sommeil et de l’etat de veille. Elle augmente les seuils de reaction a la douleur en diminuant sa composante cognitive, ainsi que ses composantes emotionnelles et comportementales. L’hypnose conversationnelle, fondee sur le langage positif, est utilisee couramment par les soignants. L’hypnose formelle est la base de l’hypnosedation et de l’hypnoanalgesie. Les applications de cette technique en anesthesie et analgesie gyneco-obstetricale completent les outils therapeutiques dans les indications suivantes: analgesie de l’accouchement ou des gestes de diagnostic antenatal, accompagnement de l’anesthesie pour cesarienne, pour les urgences obstetricales et les pathologies de la grossesse, anesthesie en gynecologie et pathologies de la reproduction ainsi qu’en oncologie et senologie.
- Published
- 2012
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12. Systematic prophylactic oxytocin injection and the incidence of postpartum hemorrhage: A before-and-after study
- Author
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Damien Subtil, Sophie Gautier, M. Simon, Philippe Deruelle, E. Closset, A.-S. Ducloy-Bouthors, Charles Garabedian, S. Depret, and A. Schaffar
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Adult ,Context (language use) ,Oxytocin ,Chemoprevention ,Injections ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Pregnancy ,medicine ,Humans ,Young adult ,Practice Patterns, Physicians' ,030219 obstetrics & reproductive medicine ,Vaginal delivery ,business.industry ,Incidence (epidemiology) ,Incidence ,Postpartum Hemorrhage ,Obstetrics and Gynecology ,General Medicine ,Anterior shoulder ,medicine.disease ,Delivery, Obstetric ,Reproductive Medicine ,Anesthesia ,Practice Guidelines as Topic ,Oxytocin Injection ,Female ,business ,030217 neurology & neurosurgery ,Labor Stage, Third ,medicine.drug - Abstract
Assess the impact of routine injection of 5 units of oxytocin as soon as the anterior shoulder is delivered on the incidence of postpartum haemorrhage (PPH) in a context of daily practice.Single-centre before-and-after study evaluating the effect of a change in the protocol for PPH prevention as applied in our obstetrical unit. During the first period, oxytocin (5 units) was to be injected only in case of PPH risk factors. During the second period, the injection was systematic.In the "before" study period, there were 1953 patients vaginal deliveries and 843 (43%) oxytocin injections, with a protocol compliance of 85%. In the "after" study period, 2018 women had vaginal deliveries and 1911 (95%) had an oxytocin injection (protocol compliance: 95%). The whole study period was associated with a reduced risk of moderate haemorrhage (13.4% vs. 9.2%, P0.001), but no significant reduced risk of severe haemorrhage was observed (2.1% vs. 2.0%, P=0.79). After logistic regression, the study period remained associated with a significant reduction in the risk of moderate PPH (OR=0.72 [0.58-0.89]).Routine injection of 5 units of oxytocin makes it possible to reduce the risk of moderate PPH, but it does not affect the risk of severe PPH.
- Published
- 2015
13. Postures maternelles pendant le travail : description et interférence avec l'analgésie péridurale
- Author
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B. De Gasquet, A. S. Ducloy-Bouthors, M. Cuisse, and M. Davette
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musculoskeletal diseases ,medicine.medical_specialty ,Supine position ,Ropivacaine ,Local anesthetic ,medicine.drug_class ,business.industry ,medicine.medical_treatment ,Kneeling ,General Medicine ,Sitting ,Surgery ,Sufentanil ,Position (obstetrics) ,Anesthesiology and Pain Medicine ,Anesthesia ,medicine ,Nerve block ,business ,medicine.drug - Abstract
The evolution of birth is of interest for obstetricians and midwives. Postures with asymmetric stretching and balance, kneeling, or sitting have been claimed to be able to help foetal head rotation. Although walking during labour have no influence on the outcome of labour, hip-flexed postures enlarging the pelvic diameter are yet evaluated to improve the obstetric course of labour. In a prospective randomised study including 93 parturients, we compared the supine 30 degrees lateral tilt (control group) to three hip-flexed postures: sitting (S), right hip-flexed left lateral position (L) and left hip-flexed right lateral position (R). Epidural analgesia with 12 ml ropivacaine 0.1% and sufentanil 0.5 microg/ml was administered over a period of six minutes. The total epidural spread was 15+/-0.3 dermatomes and the upper level of thermo-analgesic blockade reached T7-T8 (T5 to T10) in each group. There were no differences between groups for the left and right total spread and upper level of epidural blockade, for the time to maximal block and pain relief. There was no motor block and no maternal or foetal side effects. We conclude that, for the three hip-flexed postures tested, position does not influence local anesthetic spread or symmetry of analgesia after induction of obstetric epidural anaesthesia.
- Published
- 2006
- Full Text
- View/download PDF
14. Thrombocytémie essentielle
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B. Wibaut and A.-S. Ducloy-Bouthors
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business.industry ,Medicine ,business - Published
- 2015
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15. Sclérose en plaques
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A.-F. Dalmas, A.-S. Ducloy-Bouthors, and R. Krivosic-Horber
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business.industry ,Medicine ,business - Published
- 2015
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- View/download PDF
16. Drépanocytoses
- Author
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A.-S. Ducloy-Bouthors and B. Wibaut
- Subjects
medicine.anatomical_structure ,business.industry ,Cell ,Immunology ,Medicine ,Disease ,business - Published
- 2015
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- View/download PDF
17. Transplantation pulmonaire
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L. Wémeau, A.-S. Ducloy-Bouthors, and J. Corouge
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Transplantation ,medicine.medical_specialty ,business.industry ,Medicine ,business ,Surgery - Published
- 2015
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18. Déficit congénital en facteurs vitamine K dépendants
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B. Wibaut and A.-S. Ducloy-Bouthors
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Clotting factor ,medicine.medical_specialty ,Endocrinology ,business.industry ,Internal medicine ,Medicine ,Dependant ,Vitamin k ,business - Published
- 2015
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19. Déficit congénital en facteur XI
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A.-S. Ducloy-Bouthors and B. Wibaut
- Subjects
medicine.medical_specialty ,Endocrinology ,business.industry ,Internal medicine ,medicine ,business ,Factor XI - Published
- 2015
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20. Syndrome de Churg et Strauss
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L. Wémeau, A.-S. Ducloy-Bouthors, and J. Corouge
- Subjects
Strauss churg ,medicine.medical_specialty ,business.industry ,Eosinophilic ,medicine ,Disease ,Granulomatosis with polyangiitis ,medicine.disease ,business ,Dermatology - Published
- 2015
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21. Syndrome hémolytique et urémique de l’adulte
- Author
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F. Provot and A.-S. Ducloy-Bouthors
- Subjects
business.industry ,Medicine ,business - Published
- 2015
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- View/download PDF
22. Déficit congénital en facteur X
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B. Wibaut and A.-S. Ducloy-Bouthors
- Subjects
medicine.medical_specialty ,Endocrinology ,business.industry ,Internal medicine ,medicine ,X factor ,business - Published
- 2015
- Full Text
- View/download PDF
23. Déficit congénital en facteur II
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B. Wibaut and A.-S. Ducloy-Bouthors
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medicine.medical_specialty ,Endocrinology ,Prothrombin deficiency ,business.industry ,Internal medicine ,medicine ,business - Published
- 2015
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24. Mucoviscidose
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A.-S. Ducloy-Bouthors, L. Wémeau, and J. Corouge
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Pathology ,medicine.medical_specialty ,business.industry ,medicine ,medicine.disease ,business ,Cystic fibrosis - Published
- 2015
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25. Dystrophies myotoniques
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A.-S. Ducloy-Bouthors, A.-F. Dalmas-Laurent, and R. Krivosic-Horber
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Pathology ,medicine.medical_specialty ,business.industry ,Medicine ,business ,medicine.disease ,Myotonic dystrophy - Published
- 2015
- Full Text
- View/download PDF
26. Déficit combiné en facteur V et facteur VIII
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B. Wibaut and A.-S. Ducloy-Bouthors
- Subjects
biology ,business.industry ,Factor VIII deficiency ,Factor V ,biology.protein ,Medicine ,business ,Molecular biology - Published
- 2015
- Full Text
- View/download PDF
27. Histiocytose X
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L. Wémeau, A.-S. Ducloy-Bouthors, and J. Corouge
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business.industry ,Histiocytosis X ,Medicine ,business ,Nuclear medicine - Published
- 2015
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28. Hyperthermie maligne
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R. Krivosic-Horber, A.-F. Dalmas, and A.-S. Ducloy-Bouthors
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business.industry ,Cancer research ,Malignant hyperthermia ,Medicine ,business ,medicine.disease - Published
- 2015
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29. Pseudo-xanthome élastique
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A.-S. Ducloy-Bouthors and M. Lambert
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business.industry ,Medicine ,business - Published
- 2015
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30. Hémoglobinurie paroxystique nocturne
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A.-S. Ducloy-Bouthors, G. Socié, and B. Wibaut
- Subjects
medicine.medical_specialty ,business.industry ,Internal medicine ,medicine ,Paroxysmal nocturnal hemoglobinuria ,Cardiology ,medicine.disease ,business - Published
- 2015
- Full Text
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31. Purpura thrombotique thrombocytopénique
- Author
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A.-S. Ducloy-Bouthors and F. Provot
- Subjects
medicine.medical_specialty ,Purpura ,business.industry ,Thrombotic thrombocytopenic purpura ,Medicine ,medicine.symptom ,business ,medicine.disease ,Dermatology - Published
- 2015
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32. Œdème angioneurotique
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P.-Y. Hatron and A.-S. Ducloy-Bouthors
- Subjects
business.industry ,Medicine ,business ,Angio-oedema - Published
- 2015
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33. Microangiopathies thrombotiques
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A.-S. Ducloy-Bouthors and F. Provot
- Subjects
Pathology ,medicine.medical_specialty ,Thrombotic microangiopathy ,business.industry ,medicine ,medicine.disease ,business - Published
- 2015
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34. Polyangéite microscopique
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A.-S. Ducloy-Bouthors, J. Corouge, and L. Wémeau
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Pathology ,medicine.medical_specialty ,business.industry ,medicine ,Microscopic polyangiitis ,medicine.disease ,business - Published
- 2015
- Full Text
- View/download PDF
35. Déficit congénital en fibrinogène
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B. Wibaut and A.-S. Ducloy-Bouthors
- Subjects
Pediatrics ,medicine.medical_specialty ,Afibrinogenemia ,business.industry ,Medicine ,Hypofibrinogenemia ,business - Published
- 2015
- Full Text
- View/download PDF
36. Déficit congénital en facteur XII
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B. Wibaut and A.-S. Ducloy-Bouthors
- Subjects
medicine.medical_specialty ,Endocrinology ,business.industry ,Internal medicine ,Factor XII deficiency ,medicine ,business - Published
- 2015
- Full Text
- View/download PDF
37. Déficit congénital en facteur VII
- Author
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A.-S. Ducloy-Bouthors and B. Wibaut
- Subjects
medicine.medical_specialty ,Endocrinology ,business.industry ,Internal medicine ,medicine ,Factor XIII deficiency ,business ,medicine.disease - Published
- 2015
- Full Text
- View/download PDF
38. Hémophilie B
- Author
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A.-S. Ducloy-Bouthors and P.-Y. Dewandre
- Subjects
medicine.medical_specialty ,business.industry ,Medicine ,Disease ,business ,Dermatology - Published
- 2015
- Full Text
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39. Recombinant human FVIIa for reducing the need for invasive second-line therapies in severe refractory postpartum hemorrhage: a multicenter, randomized, open controlled trial
- Author
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A. Mignon, Géraldine Lavigne-Lissalde, E. Morau, Céline Chauleur, S. Bouvet, A. Bongain, S. Roger-Christoph, P. De Moerloose, A.G. Aya, F.J. Mercier, Jean-Christophe Gris, Pascale Fabbro-Peray, A.-S. Ducloy-Bouthors, M. Raucoules, Françoise Boehlen, Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), Caractéristiques féminines des dysfonctions des interfaces cardio-vasculaires (EA 2992), Université Montpellier 1 (UM1)-Université de Montpellier (UM), Service d'anesthésie [Béclère], Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP - Hôpital Antoine Béclère [Clamart], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Hôpital privé d’Antony, CHU Saint-Etienne, Groupe de recherche sur la thrombose (GRT (EA 3065)), Université Jean Monnet [Saint-Étienne] (UJM), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Unité de Soins Intensifs [CHU Cochin], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Cochin [AP-HP], Centre Hospitalier Universitaire de Nice (CHU Nice), Hôpital Universitaire de Genève, BESPIM, and Aide à la Décision pour une Médecine Personnalisé - Laboratoire de Biostatistique, Epidémiologie et Recherche Clinique - EA 2415 (AIDMP)
- Subjects
Compassionate Use Trials ,Time Factors ,FVIIa activated ,Deep vein ,Factor XIIa ,Severity of Illness Index ,law.invention ,Second line ,treatment efficacy ,Randomized controlled trial ,law ,Pregnancy ,Risk Factors ,Venous Thrombosis/chemically induced ,Treatment Failure ,hysterectomy ,Infusions, Intravenous ,ComputingMilieux_MISCELLANEOUS ,Venous Thrombosis ,ddc:616 ,[SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology ,Hematology ,Delivery mode ,Thrombosis ,Postpartum Hemorrhage/diagnosis/drug therapy/mortality ,3. Good health ,Pulmonary embolism ,medicine.anatomical_structure ,postpartum hemorrhage ,Female ,France ,Switzerland ,Adult ,medicine.medical_specialty ,macromolecular substances ,Hysterectomy ,Coagulants/administration & dosage/adverse effects/therapeutic use ,Dinoprostone ,Drug Administration Schedule ,Factor VIII/administration & dosage/adverse effects/therapeutic use ,Refractory ,medicine ,Humans ,Hemostatic Techniques/adverse effects ,Coagulants ,Hemostatic Techniques ,business.industry ,medicine.disease ,Surgery ,Dinoprostone/analogs & derivatives/therapeutic use ,Relative risk ,treatment outcome ,business - Abstract
SummaryBackground Case reports on recombinant human factor VIIa (rhuFVIIa) use in women with severe postpartum hemorrhage (PPH) showed encouraging results, but no randomized controlled trial (RCT) is available. Patients and methods Eighty-four women with severe PPH unresponsive to uterotonics were randomized to receive one early single rhuFVIIa infusion (n = 42) or standard care (no rhuFVIIa; n = 42). The primary efficacy outcome measure was the reduction of the need for specific second-line therapies, such as interventional hemostatic procedures, for blood loss and transfusions. The primary safety outcome measure was the number of deaths and thrombotic events during the 5 days following rhuFVIIa infusion. Results rhuFVIIa was associated with a reduction in the number of patients who needed second-line therapies compared with controls (standard care). Specifically, 39/42 (93%) patients in the standard care arm received second-line therapies and 22/42 (52%) patients in the rhuFVIIa arm (absolute difference, 41%; range, 18–63%; relative risk RR, 0.56 [0.42–0.76]). The delivery mode (vaginal or Cesarean section) did not affect the primary outcome. No death occurred. Two venous thrombotic events were recorded in the rhuFVIIa arm: one ovarian vein thrombosis and one deep vein thrombosis with a non-severe pulmonary embolism. Conclusion This open RCT in women with severe PPH refractory to uterotonics shows that rhuFVIIa reduces the need for specific second-line therapies in about one in three patients, with the occurrence of non-fatal venous thrombotic events in one in 20 patients.
- Published
- 2015
- Full Text
- View/download PDF
40. Hémophilie A
- Author
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P.-Y. Dewandre and A.-S. Ducloy-Bouthors
- Subjects
business.industry ,Medicine ,business - Published
- 2015
- Full Text
- View/download PDF
41. Maladie et syndrome de Marfan
- Author
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S. Langlois and A.-S. Ducloy-Bouthors
- Subjects
business.industry ,Medicine ,business - Published
- 2015
- Full Text
- View/download PDF
42. Pathologies thrombo-emboliques
- Author
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N. Trillot, A.-S. Ducloy-Bouthors, and F. Bretelle
- Subjects
business.industry ,Medicine ,business - Published
- 2014
- Full Text
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43. Hémostase et prééclampsie
- Author
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A.-S. Ducloy-Bouthors
- Subjects
business.industry ,Medicine ,business - Published
- 2009
- Full Text
- View/download PDF
44. Hip-flexed postures do not affect local anaesthetic spread following induction of epidural analgesia for labour
- Author
-
R Krivosic-Horber, Patrick Devos, M Davette, G Le Fahler, S Depret-Mosser, and A.-S Ducloy-Bouthors
- Subjects
musculoskeletal diseases ,Adult ,medicine.medical_specialty ,Supine position ,Posture ,Sitting ,Sufentanil ,Double-Blind Method ,Pregnancy ,medicine ,Supine Position ,Humans ,Thermosensing ,Prospective Studies ,Anesthetics, Local ,Prospective cohort study ,Pain Measurement ,Local anaesthetic ,Hip ,Ropivacaine ,business.industry ,Obstetrics and Gynecology ,Analgesia, Patient-Controlled ,Surgery ,Blockade ,Analgesia, Epidural ,Position (obstetrics) ,Anesthesiology and Pain Medicine ,Anesthesia ,Analgesia, Obstetrical ,Female ,business ,medicine.drug - Abstract
Hip-flexed postures enlarging the pelvic diameter are used to improve the obstetric course of labour. Although most investigations show that lateral and sitting positions do not affect the spread of epidural analgesia, the effect of recently introduced hip-flexed postures has yet to be confirmed. This prospective randomised study included 93 parturients. Ropivacaine 0.1% 12 mL plus sufentanil 0.5 micrograms/mL was administered epidurally over a period of 6 min in one of four postures: sitting, right hip-flexed left lateral position, left hip-flexed right lateral position and supine 30 degrees lateral tilt as a control group. Left and right cephalad and sacral epidural spread were measured every 2 min over a period of 30 min. Pain relief, motor blockade and maternal and fetal side effects were noted. The total epidural spread was 15+/-0.3 dermatomes and the upper level of thermo-algesic blockade T7-T8 (range T3 to T10) in all groups. There were no differences between groups in left or right total spread or upper level of epidural blockade, time to maximal block or pain relief. There was no motor block nor any maternal or fetal side effects. The power of the study (1 - beta) was 93%. We conclude that, for the three hip-flexed postures tested, position does not influence local anaesthetic spread or symmetry of thermo-algesic blockade after induction of obstetric epidural analgesia.
- Published
- 2003
45. W363 POINT-OF-CARE PROTHROMBIN TIME TESTING AS AN EARLY PREDICTOR OF SEVERE POST PARTUM HEMORRHAGE
- Author
-
A.-S. Ducloy-Bouthors, C. Barre, C. Pilla, S. Susen, A. Bauters, and A. Tournoys
- Subjects
Prothrombin time ,medicine.medical_specialty ,medicine.diagnostic_test ,business.industry ,Obstetrics ,medicine ,Post-partum hemorrhage ,Obstetrics and Gynecology ,General Medicine ,business ,Point of care - Published
- 2012
- Full Text
- View/download PDF
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