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Publication
Featured researches published by E. Demonchy.
PLOS ONE | 2017
K. Risso; Francine Guillouet-de-Salvador; Laure Valerio; Pascal Pugliese; Alissa Naqvi; Jacques Durant; E. Demonchy; Isabelle Perbost; E. Cua; Charles-Hugo Marquette; P.-M. Roger
Background COPD is a frequent and significant cause of respiratory morbidity in HIV-infected patients despite the control of HIV. We aimed to analyze the factors correlated with COPD in this population to evaluate the existence of specific indicators of vulnerability in this population. Methods and Findings 623 HIV-infected outpatients were enrolled during one year. This population was characterised by a dedicated questionnaire and electronic patient records. COPD screening was performed according to recommended spirometric criteria. The prevalence of COPD was 9.0%. Age and smoking were independently correlated with COPD (OR, 1.61 per 10 years increase, P = 0.007; OR, 1.28 per 10 pack-year increase, P = 0.003, respectively). Body mass index (BMI) and CD4 cell-count were independently and negatively correlated with COPD (OR, 0.78, P < 0.001; 0R, 0.77 per 100 cell/mm3 increase, P < 0.001, respectively). Among COPD patients, 77% did not know their diagnosis. Five COPD-patients never smoked and 44.2% did not have any respiratory symptoms and so were not eligible to perform a spirometry according to the guidelines. Conclusions In addition to known risk factors, immune defect through CD4 cell count was independently and strongly correlated with COPD. COPD is largely underdiagnosed and thus unmanaged. However, early management and urgent smoking cessation are essential to improve prognosis. Clinicians’ awareness on the particular vulnerability for COPD in HIV-infected patients is crucial. Moreover, indications to perform conventional spirometry to diagnose COPD may include more parameters than tobacco-smoking and respiratory complaints with a particular concern toward patients with a profound CD4 cell count defect.
International Journal of Antimicrobial Agents | 2018
E. Demonchy; Johan Courjon; Estelle Ughetto; Matthieu Durand; K. Risso; Rodolphe Garraffo; P.-M. Roger
The emergence of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) infections requires re-assessment of therapeutic choices. Here we report the efficacy of cefoxitin-based antibiotic therapy for ESBL-E prostatitis. A prospective study including patients with ESBL-E prostatitis resistant to trimethoprim/sulfamethoxazole and fluoroquinolones from January 2014 to March 2016 was conducted. Cefoxitin was administered by continuous infusion for 3 weeks in the case of acute bacterial prostatitis or 6 weeks in the case of chronic bacterial prostatitis (CBP), with intravenous fosfomycin for the first 5 days. Urological investigations were performed to diagnose underlying urinary tract pathology. Clinical and microbiological efficacy were evaluated 3 months (M3) and 6 months (M6) after the end of therapy. A total of 23 patients were included in the study. The median patient age was 74 years (range 48-88 years). Of the 23 infections, 14 (61%) were CBP and 12 (52%) were healthcare-associated infections. The bacteria involved were Escherichia coli in 11 cases, Klebsiella pneumoniae in 10 cases and Klebsiella oxytoca in 2 cases. Clinical cure was observed in 19/23 patients (83%) at M3 and in 17/22 patients (77%) at M6. Urocultures were sterile in 13/23 patients (57%) at M3 and in 9/19 patients (47%) and M6. Urinary colonisation was observed in 6/19 patients (32%) with clinical cure at M3 and 5/14 patients (36%) with clinical cure at M6. No resistance to cefoxitin was detected. Surgical treatment was required for 7/23 patients (30%). In conclusion, cefoxitin-based antibiotic therapy is suitable for difficult-to-treat ESBL-E infections such as prostatitis.
Infectious diseases | 2017
Nicolas Weiss; J. Courjon; Christian Pradier; Cécile Caisso; V. Mondain; P.-M. Roger; E. Demonchy
Abstract Purpose: Since 2010, the Infectious Diseases (ID) department of the Nice university hospital (France) has implemented a fast track consultation (FTC): it allows General Practitioners (GP) to directly reach an ID specialist through a dedicated phone number for initial advice. Depending on the first observation, a formal consultation can be planned within 48 h. Our aim was to evaluate in a pilot study, the contribution of the FTC regarding the management of patients 28 days after the first phone contact. Methods: This prospective current care study was conducted between November 2014 and January 2015 in our ID department. The GP indicates the most likely diagnosis, the therapeutic strategy and the patient’s management he would have applied. After the formal consultation, ID specialist provides his diagnosis, therapeutic strategy and patient’s management. An adjudicative committee has evaluated the benefit of the FTC after 28 days of follow-up. Results: Fifty-one patients referred by 49 GP were included. ID specialists modified the diagnosis in 22 (43%) patients, antibiotic treatment in 35 (68%) and treatment plan in 30 patients (59%). FTC provided at least one service for 41/51 patients (94%): antibiotic treatment was reassessed for 11 (22%) patients, averted for 9 (18%) patients, unnecessary hospitalization was avoided for 8 (16%) of them and emergency room visit averted for 5 (10%) patients. Conclusions: FTC can provide significant improvement in the management of the patients in terms of decrease in unnecessary hospitalization, emergency room visit averted and appropriate use of antibiotics.
Journal of Acquired Immune Deficiency Syndromes | 2017
Marine Dutertre; Lise Cuzin; E. Demonchy; Pascal Pugliese; Véronique Joly; Marc-Antoine Valantin; Laurent Cotte; Thomas Huleux; Pierre Delobel; Guillaume Martin-Blondel
Annals of Clinical Microbiology and Antimicrobials | 2017
J. Courjon; E. Demonchy; Nicolas Degand; K. Risso; Raymond Ruimy; P.-M. Roger
European Journal of Clinical Microbiology & Infectious Diseases | 2017
J. Courjon; E. Demonchy; E. Cua; E. Bernard; P.-M. Roger
European Journal of Clinical Microbiology & Infectious Diseases | 2018
D. Chirio; Marion Le Marechal; Pamela Moceri; Arnaud de la Chapelle; Sylvie Chaillou-Optiz; Anaïs Mothes; Cédric Foucault; Laurence Maulin; Chirine Parsaï; P.-M. Roger; E. Demonchy
Medecine Et Maladies Infectieuses | 2017
J. Courjon; E. Demonchy; D. Chirio; K. Risso; R. Ruimy; P.-M. Roger
Medecine Et Maladies Infectieuses | 2017
M. Dutertre; Lise Cuzin; E. Demonchy; Pascal Pugliese; V. Joly; Marc-Antoine Valantin; Laurent Cotte; Thomas Huleux; Pierre Delobel; Guillaume Martin-Blondel
Revue de Médecine Interne | 2016
D. Chirio; E. Demonchy; N. Martis; P. Moceri; A. Mothes; C. Foucault; A. De La Chapelle; S. Chaillou; P. Pietri; F. Tiger; J.G. Fuzibet; P.-M. Roger