17 research outputs found

    Epidemiological data on health care-associated infections (HAIs) reported in Brazil

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    As Infecções Relacionadas à Assistência à Saúde (IRAS) constituem um grande problema à saúde pública mundial, já que estão relacionadas ao aumento de morbidade e mortalidade, aumentando custos hospitalares. Além disso, grande parte destas infecções estão relacionadas à microrganismos que apresentam resistência aos antimicrobianos (RM), dificultando o tratamento. Conhecer o perfil epidemiológico destas infecções contribui para o desenvolvimento de estratégias para o controle de IRAS/RM. Neste sentido, o presente trabalho realizou uma revisão bibliográfica de dados epidemiológicos das IRAS no Brasil publicados entre 2017-2022. Foram selecionadas 27 publicações científicas. 13 destas apresentaram prevalência/incidência geral de IRAS, com apenas um estudo multicêntrico, multisetorial e multietário. Os demais estudos reportaram taxas de IRAS a partir de dados epidemiológicos oriundos de infecções de corrente sanguínea, infecções de sítio cirúrgico e infecção urinária, entre outras. Quando disponíveis, os perfis microbiológicos/resistência a antimicrobianos foram incluídos, sendo compatíveis com o que reporta a literatura científica. A partir dos dados desta revisão, observou-se que, apesar dos avanços na área, os estudos que reportam taxas de IRAS ainda são escassos e limitados a um contexto específico no Brasil, evidenciando a necessidade de mais estudos multicêntricos e contínuos. Conhecer melhor a epidemiologia de IRAS a nível nacional e público possibilita um melhor planejamento, desenvolvimento de estudos científicos e implementação de estratégias de controle e mitigação destas infecções

    Local Diversification of Methicillin- Resistant Staphylococcus aureus ST239 in South America After Its Rapid Worldwide Dissemination

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    The global spread of specific clones of methicillin-resistant Staphylococcus aureus (MRSA) has become a major public health problem, and understanding the dynamics of geographical spread requires worldwide surveillance. Over the past 20 years, the ST239 lineage of MRSA has been recognized as an emerging clone across the globe, with detailed studies focusing on isolates from Europe and Asia. Less is known about this lineage in South America, and, particularly, Brazil where it was the predominant lineage of MRSA in the early 1990s to 2000s. To gain a better understanding about the introduction and spread of ST239 MRSA in Brazil we undertook a comparative phylogenomic analysis of ST239 genomes, adding seven completed, closed Brazilian genomes. Brazilian ST239 isolates grouped in a subtree with those from South American, and Western, romance-language-speaking, European countries, here designated the South American clade. After an initial worldwide radiation in the 1960s and 1970s, we estimate that ST239 began to spread in South America and Brazil in approximately 1988. This clone demonstrates specific genomic changes that are suggestive of local divergence and adaptational change including agrC single-nucleotide polymorphisms variants, and a distinct pattern of virulence-associated genes (mainly the presence of the chp and the absence of sea and sasX). A survey of a geographically and chronologically diverse set of 100 Brazilian ST239 isolates identified this virulence genotype as the predominant pattern in Brazil, and uncovered an unexpectedly high prevalence of agr-dysfunction (30%). ST239 isolates from Brazil also appear to have undergone transposon (IS256) insertions in or near global regulatory genes (agr and mgr) that likely led to rapid reprogramming of bacterial traits. In general, the overall pattern observed in phylogenomic analyses of ST239 is of a rapid initial global radiation, with subsequent local spread and adaptation in multiple different geographic locations. Most ST239 isolates harbor the ardA gene, which we show here to have in vivo anti-restriction activity. We hypothesize that this gene may have improved the ability of this lineage to acquire multiple resistance genes and distinct virulence-associated genes in each local context. The allopatric divergence pattern of ST239 also may suggest strong selective pressures for specific traits in different geographical locations

    Prevalence, associated factors and outcomes of pressure injuries in adult intensive care unit patients: the DecubICUs study

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    Funder: European Society of Intensive Care Medicine; doi: http://dx.doi.org/10.13039/501100013347Funder: Flemish Society for Critical Care NursesAbstract: Purpose: Intensive care unit (ICU) patients are particularly susceptible to developing pressure injuries. Epidemiologic data is however unavailable. We aimed to provide an international picture of the extent of pressure injuries and factors associated with ICU-acquired pressure injuries in adult ICU patients. Methods: International 1-day point-prevalence study; follow-up for outcome assessment until hospital discharge (maximum 12 weeks). Factors associated with ICU-acquired pressure injury and hospital mortality were assessed by generalised linear mixed-effects regression analysis. Results: Data from 13,254 patients in 1117 ICUs (90 countries) revealed 6747 pressure injuries; 3997 (59.2%) were ICU-acquired. Overall prevalence was 26.6% (95% confidence interval [CI] 25.9–27.3). ICU-acquired prevalence was 16.2% (95% CI 15.6–16.8). Sacrum (37%) and heels (19.5%) were most affected. Factors independently associated with ICU-acquired pressure injuries were older age, male sex, being underweight, emergency surgery, higher Simplified Acute Physiology Score II, Braden score 3 days, comorbidities (chronic obstructive pulmonary disease, immunodeficiency), organ support (renal replacement, mechanical ventilation on ICU admission), and being in a low or lower-middle income-economy. Gradually increasing associations with mortality were identified for increasing severity of pressure injury: stage I (odds ratio [OR] 1.5; 95% CI 1.2–1.8), stage II (OR 1.6; 95% CI 1.4–1.9), and stage III or worse (OR 2.8; 95% CI 2.3–3.3). Conclusion: Pressure injuries are common in adult ICU patients. ICU-acquired pressure injuries are associated with mainly intrinsic factors and mortality. Optimal care standards, increased awareness, appropriate resource allocation, and further research into optimal prevention are pivotal to tackle this important patient safety threat

    The multifaceted resources and microevolution of the successful human and animal pathogen methicillin-resistant Staphylococcus aureus

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    Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most important bacterial pathogens based on its incidence and the severity of its associated infections. In addition, severe MRSA infections can occur in hospitalised patients or healthy individuals from the community. Studies have shown the infiltration of MRSA isolates of community origin into hospitals and variants of hospital-associated MRSA have caused infections in the community. These rapid epidemiological changes represent a challenge for the molecular characterisation of such bacteria as a hospital or community-acquired pathogen. To efficiently control the spread of MRSA, it is important to promptly detect the mecA gene, which is the determinant of methicillin resistance, using a polymerase chain reaction-based test or other rapidly and accurate methods that detect the mecA product penicillin-binding protein (PBP)2a or PBP2’. The recent emergence of MRSA isolates that harbour a mecA allotype, i.e., the mecC gene, infecting animals and humans has raised an additional and significant issue regarding MRSA laboratory detection. Antimicrobial drugs for MRSA therapy are becoming depleted and vancomycin is still the main choice in many cases. In this review, we present an overview of MRSA infections in community and healthcare settings with focus on recent changes in the global epidemiology, with special reference to the MRSA picture in Brazil

    Culture-independent genotyping, virulence and antimicrobial resistance gene identification of staphylococcus aureus from orthopaedic implant-associated infections

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    Our culture-independent nanopore shotgun metagenomic sequencing protocol on biopsies has the potential for same-day diagnostics of orthopaedic implant-associated infections (OIAI). As OIAI are frequently caused by Staphylococcus aureus, we included S. aureus genotyping and virulence gene detection to exploit the protocol to its fullest. The aim was to evaluate S. aureus genotyping, virulence and antimicrobial resistance genes detection using the shotgun metagenomic sequencing protocol. This proof of concept study included six patients with S. aureus-associated OIAI at Akershus University Hospital, Norway. Five tissue biopsies from each patient were divided in two: (1) conventional microbiological diagnostics and genotyping, and whole genome sequencing (WGS) of S. aureus isolates; (2) shotgun metagenomic sequencing of DNA from the biopsies. Consensus sequences were analysed using spaTyper, MLST, VirulenceFinder, and ResFinder from the Center for Genomic Epidemiology (CGE). MLST was also compared using krocus. All spa-types, one CGE and four krocus MLST results matched Sanger sequencing results. Virulence gene detection matched between WGS and shotgun metagenomic sequencing. ResFinder results corresponded to resistance phenotype. S. aureus spa-typing, and identification of virulence and antimicrobial resistance genes are possible using our shotgun metagenomics protocol. MLST requires further optimization. The protocol has potential application to other species and infection types

    Epidemiological data on health care-associated infections (HAIs) reported in Brazil

    Get PDF
    As Infecções Relacionadas à Assistência à Saúde (IRAS) constituem um grande problema à saúde pública mundial, já que estão relacionadas ao aumento de morbidade e mortalidade, aumentando custos hospitalares. Além disso, grande parte destas infecções estão relacionadas à microrganismos que apresentam resistência aos antimicrobianos (RM), dificultando o tratamento. Conhecer o perfil epidemiológico destas infecções contribui para o desenvolvimento de estratégias para o controle de IRAS/RM. Neste sentido, o presente trabalho realizou uma revisão bibliográfica de dados epidemiológicos das IRAS no Brasil publicados entre 2017-2022. Foram selecionadas 27 publicações científicas. 13 destas apresentaram prevalência/incidência geral de IRAS, com apenas um estudo multicêntrico, multisetorial e multietário. Os demais estudos reportaram taxas de IRAS a partir de dados epidemiológicos oriundos de infecções de corrente sanguínea, infecções de sítio cirúrgico e infecção urinária, entre outras. Quando disponíveis, os perfis microbiológicos/resistência a antimicrobianos foram incluídos, sendo compatíveis com o que reporta a literatura científica. A partir dos dados desta revisão, observou-se que, apesar dos avanços na área, os estudos que reportam taxas de IRAS ainda são escassos e limitados a um contexto específico no Brasil, evidenciando a necessidade de mais estudos multicêntricos e contínuos. Conhecer melhor a epidemiologia de IRAS a nível nacional e público possibilita um melhor planejamento, desenvolvimento de estudos científicos e implementação de estratégias de controle e mitigação destas infecções

    Rapid nanopore-based dna sequencing protocol of antibiotic-resistant bacteria for use in surveillance and outbreak investigation

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    Outbreak investigations are essential to control and prevent the dissemination of pathogens. This study developed and validated a complete analysis protocol for faster and more accurate surveillance and outbreak investigations of antibiotic-resistant microbes based on Oxford Nanopore Technologies (ONT) DNA whole-genome sequencing. The protocol was developed using 42 methicillin-resistant Staphylococcus aureus (MRSA) isolates identified from former well-characterized outbreaks. The validation of the protocol was performed using Illumina technology (MiSeq, Illumina). Additionally, a real-time outbreak investigation of six clinical S. aureus isolates was conducted to test the ONT-based protocol. The suggested protocol includes: (1) a 20 h sequencing run; (2) identification of the sequence type (ST); (3) de novo genome assembly; (4) polishing of the draft genomes; and (5) phylogenetic analysis based on SNPs. After the sequencing run, it was possible to identify the ST in 2 h (20 min per isolate). Assemblies were achieved after 4 h (40 min per isolate) while the polishing was carried out in 7 min per isolate (42 min in total). The phylogenetic analysis took 0.6 h to confirm an outbreak. Overall, the developed protocol was able to at least discard an outbreak in 27 h (mean) after the bacterial identification and less than 33 h to confirm it. All these estimated times were calculated considering the average time for six MRSA isolates per sequencing run. During the real-time S. aureus outbreak investigation, the protocol was able to identify two outbreaks in less than 31 h. The suggested protocol enables identification of outbreaks in early stages using a portable and low-cost device along with a streamlined downstream analysis, therefore having the potential to be incorporated in routine surveillance analysis workflows. In addition, further analysis may include identification of virulence and antibiotic resistance genes for improved pathogen characterization
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