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1.
JAC Antimicrob Resist ; 4(1): dlac014, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35237755

RESUMO

BACKGROUND: Combination antibiotic therapy with an antitoxin agent, such as clindamycin, is included in some guidelines for severe, toxin-mediated Staphylococcus aureus infections. The evidence to support this practice is currently limited to in vitro, animal and observational human case-series data, with no previous randomized controlled trials (RCTs). OBJECTIVES: This pilot RCT aimed to determine the feasibility of conducting a clinical trial to examine if adjunctive clindamycin with standard therapy has greater efficacy than standard therapy alone for S. aureus infections. METHODS: We performed an investigator-initiated, open-label, multicentre, pilot RCT (ACTRN12617001416381p) in adults and children with severe S. aureus infections, randomized to standard antibiotic therapy with or without clindamycin for 7 days. RESULTS: Over 28 months, across nine sites, 127 individuals were screened and 34 randomized, including 11 children (32%). The primary outcome-number of days alive and free of systemic inflammatory response syndrome ≤14 days-was similar between groups: clindamycin (3 days [IQR 1-6]) versus standard therapy (4 days [IQR 0-8]). The 90 day mortality was 0% (0/17) in the clindamycin group versus 24% (4/17) in the standard therapy group. Secondary outcomes-microbiological relapse, treatment failure or diarrhoea-were similar between groups. CONCLUSIONS: As the first clinical trial assessing adjunctive clindamycin for S. aureus infections, this study indicates feasibility and that adults and children can be incorporated into one trial using harmonized endpoints, and there were no safety concerns. The CASSETTE trial will inform the definitive S. aureus Network Adaptive Platform (SNAP) trial, which includes an adjunctive clindamycin domain and participants with non-severe disease.

3.
Intern Med J ; 44(12b): 1389-97, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25482747

RESUMO

Healthcare-associated fungal outbreaks impose a substantial economic burden on the health system and typically result in high patient morbidity and mortality, particularly in the immunocompromised host. As the population at risk of invasive fungal infection continues to grow due to the increased burden of cancer and related factors, the need for hospitals to employ preventative measures has become increasingly important. These guidelines outline the standard quality processes hospitals need to accommodate into everyday practice and at times of healthcare-associated outbreak, including the role of antifungal stewardship programmes and best practice environmental sampling. Specific recommendations are also provided to help guide the planning and implementation of quality processes and enhanced surveillance before, during and after high-risk activities, such as hospital building works. Areas in which information is still lacking and further research is required are also highlighted.


Assuntos
Microbiologia do Ar , Aspergilose/prevenção & controle , Aspergillus/crescimento & desenvolvimento , Infecção Hospitalar/prevenção & controle , Exposição Ambiental/prevenção & controle , Arquitetura Hospitalar/normas , Antifúngicos , Aspergilose/transmissão , Lista de Checagem , Consenso , Infecção Hospitalar/microbiologia , Ambiente Controlado , Filtração/instrumentação , Guias como Assunto , Humanos , Hospedeiro Imunocomprometido , Controle de Infecções , Educação de Pacientes como Assunto
4.
J Clin Microbiol ; 49(8): 3078-81, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21653770

RESUMO

Prototheca spp. are environmental algae that may cause serious infection in the immunocompromised patient. Clinical manifestations may mimic other diseases. We present a case of fatal infection in a 78-year-old cardiac transplant recipient and discuss pitfalls in the clinical and laboratory diagnoses.


Assuntos
Doenças Transmissíveis/etiologia , Prototheca/classificação , Prototheca/isolamento & purificação , Idoso , Doenças Transmissíveis/patologia , Meios de Cultura/química , Técnicas Citológicas , Evolução Fatal , Feminino , Transplante de Coração/efeitos adversos , Histocitoquímica , Humanos , Hospedeiro Imunocomprometido , Técnicas Microbiológicas , Microscopia , Dados de Sequência Molecular , Análise de Sequência de DNA , Transplante
7.
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