Elke De Wachter

ORCID: 0000-0003-4070-1023
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About
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Research Areas
  • Cystic Fibrosis Research Advances
  • Tracheal and airway disorders
  • Neonatal Respiratory Health Research
  • Respiratory viral infections research
  • Esophageal and GI Pathology
  • Inhalation and Respiratory Drug Delivery
  • Child Nutrition and Feeding Issues
  • Dysphagia Assessment and Management
  • Pediatric health and respiratory diseases
  • Congenital Diaphragmatic Hernia Studies
  • Gastroesophageal reflux and treatments
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Medical Imaging and Pathology Studies
  • Tuberculosis Research and Epidemiology
  • Antifungal resistance and susceptibility
  • Respiratory and Cough-Related Research
  • Diagnosis and treatment of tuberculosis
  • Antimicrobial Resistance in Staphylococcus
  • Pleural and Pulmonary Diseases
  • Congenital Ear and Nasal Anomalies
  • Pneumonia and Respiratory Infections
  • Asthma and respiratory diseases
  • Congenital Heart Disease Studies
  • Mycobacterium research and diagnosis
  • Airway Management and Intubation Techniques

Universitair Ziekenhuis Brussel
2016-2025

Vrije Universiteit Brussel
2014-2024

Antwerp University Hospital
2024

Imperial College London
2020

Medical University Pleven
2020

Centre Hospitalier Universitaire de Besançon
2020

Royal Brompton Hospital
2020

Case Western Reserve University
2012

University School
2012

Derriford Hospital
2012

<h3>Importance</h3> Delirium significantly worsens elective surgery outcomes and costs. risk is highest in elderly populations, whose surgical health care resource consumption (50%) exceeds their demographic proportion (15% to 18%) high-resource countries. Effective nonpharmacologic delirium prevention could safely improve these vulnerable patients, but data from procedure-specific studies are insufficiently compelling drive changes practice. approaches applicable different settings remain...

10.1001/jamasurg.2021.6370 article EN cc-by JAMA Surgery 2021-12-15
Elliot McClenaghan Rebecca Cosgriff K. Brownlee Susannah Ahern Pierre‐Régis Burgel and 95 more Catherine A. Byrnes Carla Colombo Harriet Corvol Stephanie Y. Cheng Géraldine Daneau Alexander Elbert Albert Faro Christopher H. Goss Vincent Gulmans Hector Gutierrez Isabelle de Monestrol Andreas Jung Lutz Nährlich Justus N. Kashirskaya Bruce C. Marshall Edward F. McKone Peter G. Middleton Pedro Mondéjar-López María Dolores Pastor‐Vivero Rita Padoan Samar Rizvi Rasa Ruseckaite Marco Salvatore Anne L. Stephenson Luiz Vicente R. da Silva Filho Joel Melo Marco Zampoli S.B. Carr Scott C. Bell David W. Reid Peter Wark Eva Van Braeckel Sophie Gohy Christiane Knoop Jessica Pirson Elke De Wachter Lieven Dupont L. Hanssens Vicky Nowé Monique Lequesne Rodrigo Abensur Athanazio Daniela Góis Meneses V. Boussaud Graziella Brinchault Emmanuelle Coirier-Duet J.‐C. Dubus Dominique Grenet Sandra de Miranda L. Beaumont Reem Kanaan Muriel Lauraens C. Martín Marie Mittaine Martin Anne Prévötat Martine Reynaud‐Gaubert Isabelle Sermet‐Gaudelus Aurélie Tatopoulos R. Chiron Marie‐Laure Dalphin M. Gérardin Laurence Weiss Nathalie Wizla Sophie Ramel Barry J. Plant Cedric Gunaratnam A. Jackson Rosaria Casciaro Francesca Lucca Valeria Daccò Anna Folino Antonio Manca Barbara Messore Letizia Corinna Morlacchi Giovanna Pisi Piercarlo Poli Annalisa Amato Gianluca Ferrari Karin de Winter- de Groot Bart Luijk Geertjan Wesseling E. Kondratyeva E. Zhekayte E. Amelina M. A. Mukhina О. И. Симонова Antonio Álvarez-Fernández Amparó Solé Isidoro Cortell‐Aznar Rosa Girón A. López Neyra Isabel Ramos-Cancelo Maite Lzaro-Carrasco Marta Ruiz de Valbuena C. Prados-Sánchez J. Colomer

10.1016/j.jcf.2020.10.003 article EN publisher-specific-oa Journal of Cystic Fibrosis 2020-11-01

Background. Precise etiologic diagnosis in pediatric community-acquired pneumonia (CAP) remains challenging. Methods. We conducted a retrospective study of CAP etiology 2 groups patients who underwent flexible bronchoscopy (FOB) with bronchoalveolar lavage (BAL); children acute nonresponsive (NR-CAP; n = 127) or recurrent (Rec-CAP; 123). Procedural measures were taken to limit contamination risk and quantitative bacterial culture BAL fluid (significance cutoff point, ≥104 colony-forming...

10.1093/cid/cir235 article EN Clinical Infectious Diseases 2011-05-31

Increased gastroesophageal reflux (GER) is common in children with cystic fibrosis (CF). We studied the occurrence of acid, weakly acidic (WA), and alkaline (WALK) CF evaluated a possible surrogate marker for risk gastric content aspiration.Twenty-four underwent impedance-pH monitoring detection acid (pH < 4), WA 4-7), WALK-GER > or = 7). In 11 children, cough was objectively recorded esophageal manometry symptom association probability calculated to determine reflux-cough relation. Presence...

10.1097/mpg.0b013e3181acae98 article EN Journal of Pediatric Gastroenterology and Nutrition 2010-01-16

10.1016/j.jcf.2022.09.012 article EN Journal of Cystic Fibrosis 2022-11-10

Abstract Introduction Assessment of the reflux–cough association in children is challenging. Esophageal (impedance) pH recording sensitive to recognize reflux. However, cough recorded by an event marker, possibly lacks accuracy. We aim ed study exact time relationship between reflux and with chronic cough. Methods Twenty‐six (12 boys; 1–10.5 years) unexplained underwent ambulatory impedance–pH–manometry recordings. Manometry was used for precise recognition. Reflux assessed impedance‐pH...

10.1002/ppul.21365 article EN Pediatric Pulmonology 2010-10-22

Pharmacological rescue of mutant cystic fibrosis transmembrane conductance regulator (CFTR) in (CF) depends on the specific defect caused by different mutation classes. We asked whether a patient with rare p.Gly970Asp (c.2909G>A) could benefit from CFTR pharmacotherapy since similar missense p.Gly970Arg (c.2908G>C) was previously found to be sensitive potentiators vitro but not vivo. By complementary DNA transfection, we that both mutations are associated defective function amenable...

10.1002/humu.23741 article EN Human Mutation 2019-03-09

We tested the in vitro susceptibility of ceftazidime-avibactam and ceftolozane-tazobactam 13 other antibiotics against 91 Burkholderia cepacia complex (BCC) strains isolated from cystic fibrosis patients since 2012. The highest (82%) was found for trimethoprim-sulfamethoxazole.

10.1128/aac.00590-18 article EN Antimicrobial Agents and Chemotherapy 2018-06-19
S.B. Carr Elliot McClenaghan Alexander Elbert Albert Faro Rebecca Cosgriff and 95 more Olzhas Abdrakhmanov K. Brownlee Pierre‐Régis Burgel Catherine A. Byrnes Stephanie Y. Cheng Carla Colombo Harriet Corvol Géraldine Daneau Christopher H. Goss Vincent Gulmans Hector Gutierrez Satenik Harutyunyan Meagan Helmick Andreas Jung N. Kashirskaya Edward F. McKone Joel Melo Peter G. Middleton Pedro Mondéjar-López Isabelle de Monestrol Lutz Nährlich Rita Padoan Megan Parker María Dolores Pastor‐Vivero Samar Rizvi Rasa Ruseckaite Marco Salvatore Luiz Vicente R. F. da Silva-Filho Nick Versmessen Marco Zampoli Bruce C. Marshall Anne L. Stephenson Scott C. Bell David W. Reid Peter Wark Eva Van Braeckel Sophie Gohy Christiane Knoop Jessica Pirson Elke De Wachter Lieven Dupont L. Hanssens Vicky Nowé Monique Lequesne Rodrigo Abensur Athanazio Daniela Góis Meneses V. Boussaud Graziella Brinchault Emmanuelle Coirier-Duet J.‐C. Dubus Dominique Grenet Sandra de Miranda L. Beaumont Reem Kanaan Muriel Lauraens C. Martín M. Mittaine Anne Prévötat Martine Reynaud‐Gaubert Isabelle Sermet‐Gaudelus Aurélie Tatopoulos R. Chiron Marie‐Laure Dalphin M. Gérardin Laurence Weiss Nathalie Wizla Sophie Ramel Barry J. Plant Cedric Gunaratnam A. Jackson Karin de Winter- de Groot Bart Luijk Geertjan Wesseling E. Kondratyeva E. Zhekayte E. Amelina M. A. Mukhina О. И. Симонова Antonio Álvarez-Fernández Amparó Solé Isidoro Cortell‐Aznar Rosa Girón A. López Neyra Isabel Ramos-Cancelo Maite Lázaro-Carrasco Dolores Pastor Vivero Marta Ruiz de Valbuena Concepción Prados‐Sánchez J. Colomer Silvia Gärtner Layla Diab-Cáceres M. Gilljam Ulrika Lindberg S. Diemer Mark I. Allenby

10.1016/j.jcf.2022.06.006 article EN publisher-specific-oa Journal of Cystic Fibrosis 2022-06-13

Although different chronic arthritic diseases are defined by clinical factors like gender, psoriasis and auto-antibodies, the biology of inflamed joints while comparing remains neglected. Here, after curating an joint derived T-cell receptor (TCR) database, our new TRIASSIC tool identified 66303 significantly convergent TCR clonotypes. Clustering clonotypes showed that synovial fluid convergence clusters (SFCCs) characterized HLA-B27+ mediated (spondyloarthritis, SpA, enthesitis-related...

10.1101/2025.01.10.632345 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2025-01-14

In children with persistent respiratory symptoms despite regular anti-asthma inhalation treatment, diagnostic investigations to exclude underlying disease are warranted. 124 were prospectively enrolled, and 24-h oesophageal pH measurement fibreoptic bronchoscopy bronchoalveolar lavage (BAL) performed. BAL fluid (BALF) was processed for neutrophil counting bacterial culture. Inflammation of the mucosa assessed. A structural abnormality central airways found in 47% subjects (40% females). 19%...

10.1183/09031936.00035111 article EN European Respiratory Journal 2011-07-20

To investigate a computed tomographic (CT) protocol with iterative reconstruction at conventional radiography dose levels for the assessment of structural lung abnormalities in patients cystic fibrosis ( CF ).In this institutional review board-approved study, 38 (age range, 6-58 years; 21 <18 years and 17 >18 years) underwent investigative CT (at minimal exposure settings combined reconstruction) as replacement yearly follow-up posteroanterior chest radiography. Verbal informed consent was...

10.1148/radiol.14132201 article EN Radiology 2014-07-24

Purpose Different respiratory sampling methods exist to identify lower airway pathogens in patients with cystic fibrosis (CF), of which bronchoalveolar lavage (BAL) and expectorated sputum are considered the ‘gold standard’. Because BAL cannot be repeated limitless, diagnosis tract infections non-expectorating is challenging. Other techniques nasal swab, cough swab induced sputum. The purpose this study (NCT02363764) was compare concordance between microbiological yield expectorating...

10.3389/fped.2018.00403 article EN cc-by Frontiers in Pediatrics 2018-12-18

Pseudomonas aeruginosa is the major respiratory pathogen causing severe lung infections among CF patients, leading to high morbidity and mortality. Once infection established, early antibiotic treatment able postpone transition chronic infection. In order optimize detection, we compared sensitivity of microbiological culture quantitative PCR (qPCR) for detection P. in samples not chronically infected patients. this national study, followed patients during periods between 1 15 months. For a...

10.1186/1471-2180-10-245 article EN cc-by BMC Microbiology 2010-01-01
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