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Therapeutic Methods and Therapies TCIM
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1.
Trends Microbiol ; 30(7): 612-614, 2022 07.
Article in English | MEDLINE | ID: mdl-35599112

ABSTRACT

Despite susceptibility testing, recurrent infections are common and are associated with resistance. Using whole-genome sequencing, Stracy et al. demonstrated that recurrence is often driven by a different strain than the original infection. By machine-learning analysis, they developed an algorithm for patient-specific recommendations to minimize antimicrobial resistance (AMR) at the individual-patient level.


Subject(s)
Anti-Bacterial Agents , Drug Resistance, Bacterial , Anti-Bacterial Agents/pharmacology , Bacteria/genetics , Genome, Bacterial , Humans , Machine Learning , Microbial Sensitivity Tests , Recurrence
2.
Int J Antimicrob Agents ; 54(5): 668-672, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31400471

ABSTRACT

Dalbavancin is a glycopeptide antibiotic with a long half-life, recently marketed in Europe for skin and soft-tissue infections (SSTIs), but its real-life use is not well known. The aim of this study was to describe all first prescriptions in France over an 16-month period. A retrospective study on all adult patients receiving at least one dose of dalbavancin from 1 June 2017 to 31 September 2018 was performed (75 patients from 29 French hospitals). Data were collected via a standard questionnaire. Failure was defined as persistence or reappearance of signs of infection, and/or switch to suppressive antibiotic treatment, and/or death from infection. The main indications were bone and joint infection (BJI) (64.0%), endocarditis (25.3%), and SSTI (17.3%). The main bacteria involved were Staphylococcus aureus (51.4%), including methicillin-resistant S. aureus (MRSA) (19.4%), and coagulase-negative staphylococci (44.4%). Median minimum inhibitory concentrations (MICs) for staphylococci to vancomycin and dalbavancin ranged from 0.875-2.0 mg/L and 0.032-0.064 mg/L, respectively. Dalbavancin was used after a mean of 2.3 ± 1.2 lines of antimicrobial treatment. The main treatment regimens for dalbavancin were a two-dose regimen (1500 mg each) in 38 cases (50.7%) and a single-dose regimen (1500 mg) in 13 cases (17.3%). Overall, at the patient's last visit, clinical cure was observed in 54/68 patients, whilst failure was observed in 14/68 patients. First use of dalbavancin in France was mostly off-label. Most were due to BJI, often as rescue therapy for severe infections. Even in off-label situations, dalbavancin appears safe and effective.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Endocarditis/drug therapy , Methicillin-Resistant Staphylococcus aureus/drug effects , Off-Label Use , Soft Tissue Infections/drug therapy , Staphylococcal Infections/drug therapy , Teicoplanin/analogs & derivatives , Adult , Female , France , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Retrospective Studies , Surveys and Questionnaires , Teicoplanin/therapeutic use , Treatment Outcome , Vancomycin/therapeutic use
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