Didier Lepelletier

Prof. Dr. Didier Lepelletier

orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 August 2020 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Open access
PDF file
DLDidier Lepelletier
Didier Lepelletier
JMJean Yves Maillard
Jean Yves Maillard
BPBruno Pozzetto
Bruno Pozzetto
ASAnne Simon
Anne Simon
Nasal decolonization is an integral part of the strategies used to control and prevent the spread of methicillin-resistant Staphylococcus aureus (MRSA) infections. The two most commonly used agents for decolonization are intranasal mupirocin 2% ointment and chlorhexidine wash, but the increasing emergence of resistance and treatment failure has underscored the need for alternative therapies. This article discusses povidone iodine (PVP-I) as an alternative decolonization agent and is based on literature reviewed during an expert’s workshop on resistance and MRSA decolonization. Compared to chlorhexidine and mupirocin, respectively, PVP-I 10 and 7.5% solutions demonstrated rapid and superior bactericidal activity against MRSA in in vitro and ex vivo studies. Notably, PVP-I 10 and 5% solutions were also active against both chlorhexidine-resistant and mupirocin-resistant strains, respectively. Unlike chlorhexidine and mupirocin, available reports have not observed a link between PVP-I and the induction of bacterial resistance or cross-resistance to antiseptics and antibiotics. These preclinical findings also translate into clinical decolonization, where intranasal PVP-I significantly improved the efficacy of chlorhexidine wash and was as effective as mupirocin in reducing surgical site infection in orthopedic surgery. Overall, these qualities of PVP-I make it a useful alternative decolonizing agent for the prevention of S. aureus infections, but additional experimental and clinical data are required to further evaluate the use of PVP-I in this setting.

1 May 2005 in Infection Control & Hospital Epidemiology
Verified
Journal Article
Closed access
PDF file
DLDidier Lepelletier
Didier Lepelletier
SPStéphanie Perron
Stéphanie Perron
PBPhilippe Bizouarn
Philippe Bizouarn
JCJocelyne Caillon
Jocelyne Caillon
HDHenri Drugeon
Henri Drugeon
DDDaniel Duveau
Daniel Duveau
Objective: To identify risk factors associated with surgical-site infection according to the depth of infection, the cardiac procedure, and the National Nosocomial Infections Surveillance System risk index.Design: Prospective survey conducted during a 12-month period.Setting: A 48-bed cardiac surgical department in a teaching hospital.Patients: Patients admitted for cardiac surgery between February 2002 and January 2003.Results: Surgical-site infections were diagnosed in 3% of the patients (38 of 1,268). Of the 38 surgical-site infections, 20 were superficial incisional infections and 18 were mediastinitis for incidence rates of 1.6% and 1.4%, respectively. Cultures were positive in 28 cases and the most commonly isolated pathogen wasStaphylococcus. A National Nosocomial Infections Surveillance System risk index score of 2 or greater was associated with a risk of surgical-site infection (relative risk, 2.4;P< .004). Heart transplantation, mechanical circulatory assistance, coronary artery bypass graft with the use of internal mammary artery, and reoperation for cardiac tamponade or pericard effusion were independent risk factors associated with surgical-site infection.Conclusions: Data surveillance using incidence rates stratified by cardiac procedure and type of infection is relevant to improving infection control efforts. Risk factors in patients who developed superficial infection were different from those in patients who developed mediastinitis. Coronary artery bypass graft using internal mammary artery was associated with a high risk of surgical-site infection, and independent factors such as reoperation for cardiac tamponade or pericard effusion increased the risk of infection.

1 July 2020 in Journal of Hospital Infection
Verified
Journal Article
Closed access
DLDidier Lepelletier
Didier Lepelletier
BGB. Grandbastien
B. Grandbastien
SRS. Romano-Bertrand
S. Romano-Bertrand
LALudwig Serge Aho-Glele
Ludwig Serge Aho-Glele
CCC. Chidiac
C. Chidiac
FCF. Chauvin
F. Chauvin

1 October 2013 in Medecine Et Maladies Infectieuses
Verified
Journal Article
Closed access
DLDidier Lepelletier
Didier Lepelletier
CBC. Bourigault
C. Bourigault
JRJ.C. Roussel
J.C. Roussel
CLC. Lasserre
C. Lasserre
BLB. Leclère
B. Leclère
PDP. Despins
P. Despins

1 July 2015 in Journal of Hospital Infection
Verified
Journal Article
Closed access
DLDidier Lepelletier
Didier Lepelletier
PBP Berthelot
P Berthelot
JLJ-C Lucet
J-C Lucet
SFS Fournier
S Fournier
VJV Jarlier
V Jarlier
NGNational Working Group
National Working Group

15 August 2011 in Journal of Travel Medicine
Verified
Journal Article
Open access
PDF file
DLDidier Lepelletier
Didier Lepelletier
AAAntoine Andremont
Antoine Andremont
BGBruno Grandbastien
Bruno Grandbastien
TGthe National Working Group
the National Working Group
The rapid development of transport and communication, environmental exchanges, and migration of populations creates opportunities for the spread of infectious d