162 results on '"Huart, Caroline"'
Search Results
152. The use of adalimumab for cricoarytenoid arthritis in ankylosing spondylitis—an effective therapy
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Desuter, Gauthier, primary, Duprez, Thierry, additional, Huart, Caroline, additional, Gardiner, Quentin, additional, and Verbruggen, Gust, additional
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- 2011
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153. Increased olfactory bulb volume and olfactory function in early blind subjects
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Rombaux, Philippe, primary, Huart, Caroline, additional, De Volder, Anne G., additional, Cuevas, Isabel, additional, Renier, Laurent, additional, Duprez, Thierry, additional, and Grandin, Cecile, additional
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- 2010
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154. Presence of olfactory event‐related potentials predicts recovery in patients with olfactory loss following upper respiratory tract infection
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Rombaux, Philippe, primary, Huart, Caroline, additional, Collet, Stéphanie, additional, Eloy, Philippe, additional, Negoias, Simona, additional, and Hummel, Thomas, additional
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- 2010
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155. Effect of three-drug delivery modalities on olfactory function in chronic sinusitis.
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Reychler, Gregory, Colbrant, Coralie, Huart, Caroline, Le Guellec, Sandrine, Vecellio, Laurent, Liistro, Giuseppe, and Rombaux, Philippe
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Background Olfactory dysfunction is deemed to be a significant contributor to poor quality of life in chronic rhinosinusitis (CRS). Objective To assess and to compare the effectiveness of three modalities of corticosteroids administration in patients with CRS. Study Design A prospective randomized controlled study Methods Thirty patients with CRS were randomized in three groups depending on the route of corticosteroids administration: 16 days by oral route (Medrol (Pfizer, Belgique), 32 mg/8 days −16 mg/4 days-8 mg/4 days); nasal spray (Rhinocort (AstraZeneca, Belgique), 2 × 2 × 64 µg/nostril); or sonic nebulization (Pulmicort (AstraZeneca, Belgique), 2 × 1 mg/4 mL) (Sonic nebulizer, AOHBOX-NL11SN, DTF, France). Olfactory function was assessed using orthonasal threshold discrimination identification and retronasal psychophysical olfactory tests (RNT) before and after the treatment. Same intranasal modalities were previously tested for in vitro airways scintigraphic deposition. Results In vitro differences in drug deposition pattern between both intranasal modalities were demonstrated. Threshold discrimination identification and RNT were similar between three groups at baseline. Threshold discrimination identification improved by 5.5, 5.8, and −1.1 for sonic nebulization, oral, and nasal spray groups, respectively ( P = 0.010). This improvement was clinically relevant for oral and nebulized administration. It was similar between oral and nebulized administration but significantly higher than nasal spray administration. Retronasal psychophysical olfactory tests improved similarly for the three groups ( P = 0.231) Conclusion Effectiveness of sonic nebulized and oral administration is demonstrated on orthonasal olfactory. The clinical benefit is better than with nasal spray. Level of Evidence 1b. Laryngoscope, 125:549-555, 2015 [ABSTRACT FROM AUTHOR]
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- 2015
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156. COMPARISON BETWEEN DIFFERENT QUESTIONNAIRES FOR THE DIAGNOSIS OF BODY DYSMORPHIC DISORDER IN RHINOSEPTOPLASTY POPULATION.
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Rombaux, Philippe, de Toeuf, Caroline, Hox, Valérie, and Huart, Caroline
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- 2018
157. ASSESSMENT OF A NEW, CHEAP AND TRANSPORTABLE OLFACTOMETER FOR THE RECORDING OF CHEMOSENSORY EVENT-RELATED POTENTIALS.
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Huart, Caroline, Mouraux, André, and Rombaux, Philippe
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- 2018
158. UNIRHINAL OLFACTORY TESTING FOR THE DIAGNOSTIC WORKUP OF MILD COGNITIVE IMPAIRMENT - 4 YEARS FOLLOW-UP STUDY.
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Huart, Caroline, Hanseeuw, Bernard, Quenon, Lisa, Ivanoiu, Adrian, Mouraux, André, and Rombaux, Philippe
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- 2018
159. Programming cochlear implants with artificial intelligence
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Wathour, Justine, UCL - SSS/IONS - Institute of NeuroScience, UCL - Faculté de pharmacie et des sciences biomédicales, Deggouj, Naima, Govaerts, Paul, Huart, Caroline, Szmalec, Arnaud, Rombaux, Philippe, Avan, Paul, Thai-Van, Hung, and Missal, Marcus
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Artificial intelligence ,Programmation ,Programming ,Implant cochléaire ,Cochlear implant ,Intelligence artificielle - Abstract
Cochlear implant (CI) is the most effective solution for the restoration of hearing function in severe to profound sensorineural hearing loss. The main objective of this PhD thesis is to answer the question: « Does AI-assisted programming of a cochlear implant provide similar or better results than manual programming, with less time investment for the patient and the clinician? ». A first study that was conducted in 4 French-speaking centers in Belgium and in France showed a large variability of CI programming within and between centers. This context supports the use of a tool using artificial intelligence, such as the Fitting to Outcome eXpert® (FOX®). A pilot study on 2 subjects who had limited results with their manually programmed CI showed encouraging benefits. Secondly, FOX® was used on a larger scale in 2 prospective interventional studies. The first study evaluated the benefits of using FOX® in former patients who had been implanted and formerly manually programmed for several years. 89% of the subjects showed better auditory performances (psychoacoustic battery A§E®) with the FOX® map than with the manual map. This significant but not systematic gain is discussed, considering the impact of FOX® as a novelty among other factors. The second study compared the manual and FOX® types of programming in a randomised longitudinal study with a crossover design in newly implanted "naïve" subjects. The crossover design involved each group changing programming type at one year post-activation. The FOX® group achieved better speech test results more rapidly than the manual group and maintained these results at one year post-activation. Due to the crossover, FOX® improved the results of 81% of the patients initially programmed manually. In terms of time gain, the number of programming sessions decreased by 55% over one year in patients initially programmed with FOX® compared to those initially programmed manually. A general discussion and a conclusion nuance the results. AI-assisted programming provides support to clinicians and shows positive results in terms of hearing performance and time gain. Current clinical practice is heading in the direction of developing advanced technological solutions up to remote treatment, which FOX® will enable. L’implant cochléaire (IC) est la solution la plus efficace, en termes de restauration de la fonction auditive, dans le cadre d’une surdité neurosensorielle sévère à profonde. L’objectif principal de cette thèse de doctorat est de répondre à la question : « La programmation d’un implant cochléaire assistée par l’intelligence artificielle donne-t-elle des résultats semblables voire meilleurs que ceux obtenus par la programmation manuelle, avec moins d’investissement en temps pour le patient et le clinicien ? ». Une première étude réalisée auprès de 4 centres francophones en Belgique et en France rend compte de la grande variabilité des programmations d’ICs intra et inter-centres. Ce contexte justifie l’apport d’un outil utilisant l’intelligence artificielle, comme le Fitting to Outcome eXpert® (FOX®). Une étude pilote sur 2 sujets présentant des résultats limités avec leur IC programmé manuellement relève des bénéfices encourageants. Ensuite, FOX® est utilisé à plus grande échelle dans 2 études prospectives interventionnelles. La première évalue son apport chez d’anciens patients implantés et programmés manuellement depuis des années. 89% des sujets présentent de meilleures performances auditives (batterie psychoacoustique A§E®) avec la map FOX® qu’avec la map manuelle. Ce gain significatif mais non systématique se discute, en tenant compte, entre autres, de l’impact du FOX® en tant que nouveauté. La deuxième compare chez de nouveaux sujets implantés « naïfs » les types de programmation, manuelle et FOX®, dans une étude longitudinale randomisée avec un cross-over. Le design cross-over implique que chaque groupe change de type de programmation à un an post-activation. Le groupe FOX® obtient plus rapidement de meilleurs résultats aux tests vocaux que le groupe manuel, résultats qu’il maintient à un an post-activation. Suite au cross-over, FOX® améliore les résultats de 81% patients initialement programmés manuellement. Au niveau du gain de temps, le nombre de sessions de programmation diminue de 55% sur un an chez les patients initialement programmés avec FOX® par rapport à ceux initialement programmés manuellement. Une discussion générale et une conclusion nuancent les résultats. La programmation assistée par l’intelligence artificielle fournit une aide aux cliniciens et montre des résultats positifs en termes de performance auditive et de gain de temps. La pratique clinique actuelle va dans le sens du développement de solutions technologiques de pointe allant jusqu’au traitement à distance, ce que permettra FOX®. (BIFA - Sciences biomédicales et pharmaceutiques) -- UCL, 2022
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- 2022
160. Recent Smell Loss Is the Best Predictor of COVID-19 Among Individuals With Recent Respiratory Symptoms.
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Gerkin RC, Ohla K, Veldhuizen MG, Joseph PV, Kelly CE, Bakke AJ, Steele KE, Farruggia MC, Pellegrino R, Pepino MY, Bouysset C, Soler GM, Pereda-Loth V, Dibattista M, Cooper KW, Croijmans I, Di Pizio A, Ozdener MH, Fjaeldstad AW, Lin C, Sandell MA, Singh PB, Brindha VE, Olsson SB, Saraiva LR, Ahuja G, Alwashahi MK, Bhutani S, D'Errico A, Fornazieri MA, Golebiowski J, Dar Hwang L, Öztürk L, Roura E, Spinelli S, Whitcroft KL, Faraji F, Fischmeister FPS, Heinbockel T, Hsieh JW, Huart C, Konstantinidis I, Menini A, Morini G, Olofsson JK, Philpott CM, Pierron D, Shields VDC, Voznessenskaya VV, Albayay J, Altundag A, Bensafi M, Bock MA, Calcinoni O, Fredborg W, Laudamiel C, Lim J, Lundström JN, Macchi A, Meyer P, Moein ST, Santamaría E, Sengupta D, Rohlfs Dominguez P, Yanik H, Hummel T, Hayes JE, Reed DR, Niv MY, Munger SD, and Parma V
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- Adult, Anosmia etiology, COVID-19 complications, Cross-Sectional Studies, Female, Humans, Male, Middle Aged, Prognosis, SARS-CoV-2 isolation & purification, Self Report, Smell, Anosmia diagnosis, COVID-19 diagnosis
- Abstract
In a preregistered, cross-sectional study, we investigated whether olfactory loss is a reliable predictor of COVID-19 using a crowdsourced questionnaire in 23 languages to assess symptoms in individuals self-reporting recent respiratory illness. We quantified changes in chemosensory abilities during the course of the respiratory illness using 0-100 visual analog scales (VAS) for participants reporting a positive (C19+; n = 4148) or negative (C19-; n = 546) COVID-19 laboratory test outcome. Logistic regression models identified univariate and multivariate predictors of COVID-19 status and post-COVID-19 olfactory recovery. Both C19+ and C19- groups exhibited smell loss, but it was significantly larger in C19+ participants (mean ± SD, C19+: -82.5 ± 27.2 points; C19-: -59.8 ± 37.7). Smell loss during illness was the best predictor of COVID-19 in both univariate and multivariate models (ROC AUC = 0.72). Additional variables provide negligible model improvement. VAS ratings of smell loss were more predictive than binary chemosensory yes/no-questions or other cardinal symptoms (e.g., fever). Olfactory recovery within 40 days of respiratory symptom onset was reported for ~50% of participants and was best predicted by time since respiratory symptom onset. We find that quantified smell loss is the best predictor of COVID-19 amongst those with symptoms of respiratory illness. To aid clinicians and contact tracers in identifying individuals with a high likelihood of having COVID-19, we propose a novel 0-10 scale to screen for recent olfactory loss, the ODoR-19. We find that numeric ratings ≤2 indicate high odds of symptomatic COVID-19 (4 < OR < 10). Once independently validated, this tool could be deployed when viral lab tests are impractical or unavailable., (© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
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- 2021
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161. The best COVID-19 predictor is recent smell loss: a cross-sectional study.
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Gerkin RC, Ohla K, Veldhuizen MG, Joseph PV, Kelly CE, Bakke AJ, Steele KE, Farruggia MC, Pellegrino R, Pepino MY, Bouysset C, Soler GM, Pereda-Loth V, Dibattista M, Cooper KW, Croijmans I, Di Pizio A, Ozdener MH, Fjaeldstad AW, Lin C, Sandell MA, Singh PB, Brindha VE, Olsson SB, Saraiva LR, Ahuja G, Alwashahi MK, Bhutani S, D'Errico A, Fornazieri MA, Golebiowski J, Hwang LD, Öztürk L, Roura E, Spinelli S, Whitcroft KL, Faraji F, Fischmeister FPS, Heinbockel T, Hsieh JW, Huart C, Konstantinidis I, Menini A, Morini G, Olofsson JK, Philpott CM, Pierron D, Shields VDC, Voznessenskaya VV, Albayay J, Altundag A, Bensafi M, Bock MA, Calcinoni O, Fredborg W, Laudamiel C, Lim J, Lundström JN, Macchi A, Meyer P, Moein ST, Santamaría E, Sengupta D, Domínguez PP, Yanık H, Boesveldt S, de Groot JHB, Dinnella C, Freiherr J, Laktionova T, Mariño S, Monteleone E, Nunez-Parra A, Abdulrahman O, Ritchie M, Thomas-Danguin T, Walsh-Messinger J, Al Abri R, Alizadeh R, Bignon E, Cantone E, Cecchini MP, Chen J, Guàrdia MD, Hoover KC, Karni N, Navarro M, Nolden AA, Mazal PP, Rowan NR, Sarabi-Jamab A, Archer NS, Chen B, Di Valerio EA, Feeney EL, Frasnelli J, Hannum M, Hopkins C, Klein H, Mignot C, Mucignat C, Ning Y, Ozturk EE, Peng M, Saatci O, Sell EA, Yan CH, Alfaro R, Cecchetto C, Coureaud G, Herriman RD, Justice JM, Kaushik PK, Koyama S, Overdevest JB, Pirastu N, Ramirez VA, Roberts SC, Smith BC, Cao H, Wang H, Balungwe P, Baguma M, Hummel T, Hayes JE, Reed DR, Niv MY, Munger SD, and Parma V
- Abstract
Background: COVID-19 has heterogeneous manifestations, though one of the most common symptoms is a sudden loss of smell (anosmia or hyposmia). We investigated whether olfactory loss is a reliable predictor of COVID-19., Methods: This preregistered, cross-sectional study used a crowdsourced questionnaire in 23 languages to assess symptoms in individuals self-reporting recent respiratory illness. We quantified changes in chemosensory abilities during the course of the respiratory illness using 0-100 visual analog scales (VAS) for participants reporting a positive (C19+; n=4148) or negative (C19-; n=546) COVID-19 laboratory test outcome. Logistic regression models identified singular and cumulative predictors of COVID-19 status and post-COVID-19 olfactory recovery., Results: Both C19+ and C19- groups exhibited smell loss, but it was significantly larger in C19+ participants (mean±SD, C19+: -82.5±27.2 points; C19-: -59.8±37.7). Smell loss during illness was the best predictor of COVID-19 in both single and cumulative feature models (ROC AUC=0.72), with additional features providing no significant model improvement. VAS ratings of smell loss were more predictive than binary chemosensory yes/no-questions or other cardinal symptoms, such as fever or cough. Olfactory recovery within 40 days was reported for ~50% of participants and was best predicted by time since illness onset., Conclusions: As smell loss is the best predictor of COVID-19, we developed the ODoR-19 tool, a 0-10 scale to screen for recent olfactory loss. Numeric ratings ≤2 indicate high odds of symptomatic COVID-19 (10
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- 2020
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162. Prognostic value of olfactory bulb volume measurement for recovery in postinfectious and posttraumatic olfactory loss.
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Rombaux P, Huart C, Deggouj N, Duprez T, and Hummel T
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- Adult, Aged, Brain Injuries complications, Female, Humans, Magnetic Resonance Imaging methods, Male, Middle Aged, Olfaction Disorders diagnosis, Olfaction Disorders etiology, Organ Size, Prognosis, Prospective Studies, Psychophysics, Respiratory Tract Infections complications, Young Adult, Olfaction Disorders physiopathology, Olfactory Bulb pathology, Recovery of Function physiology, Smell physiology
- Abstract
Objectives: Several prognostic factors influencing the recovery from olfactory dysfunction have been described. The aim of this study was to investigate whether olfactory bulb volume could be used as a new predictor of olfactory recovery in postinfectious and posttraumatic olfactory loss., Study Design: Cohort study; Level of evidence, 4. Setting Tertiary university clinic, department of otolaryngology., Subjects and Methods: A cohort of 60 patients with postinfectious (n = 28) and posttraumatic olfactory loss (n = 32) was investigated. Assessment of olfactory function was performed using orthonasal (Sniffin' Sticks test) and retronasal psychophysical olfactory tests, at the time of the diagnosis (t1) and 15 months later (t2). All patients were examined on 3 tesla magnetic resonance imaging, and the olfactory bulbs volume was assessed using planimetric contouring at the time of the diagnosis (t1)., Results: Recovery rate was 25% in patients with posttraumatic olfactory loss and 36% in patients with postinfectious olfactory loss. There was a correlation between both orthonasal and retronasal olfactory testing and the initial measurement of the total olfactory bulb volume. In addition, we observed a significant correlation between changes in olfactory functions and initial measurement of the total olfactory bulb volume, with larger volumes relating to higher improvement of olfactory function. Finally, we found that none of the patients with a total olfactory bulb volume of 40 mm(3) or less exhibited recovery of olfactory function., Conclusion: Olfactory bulb volume seems to be a predictor of olfactory recovery in patients with postinfectious and posttraumatic olfactory loss.
- Published
- 2012
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