Healthcare-associated infections in a multidisciplinary children’s hospital: results of a ten-year monitoring

2019 ◽  
Vol 17 (2) ◽  
pp. 53-60
Author(s):  
E.A. Kriger ◽  
◽  
О.V. Samodova ◽  
S.Yu. Nazarenko ◽  
N.L. Rogushina ◽  
...  
2020 ◽  
Vol 7 (Supplement_1) ◽  
pp. S693-S694
Author(s):  
Lauren Sommer ◽  
Jesus G Vallejo ◽  
Kristina G Hulten ◽  
Sheldon L Kaplan ◽  
Jonathon C McNeil

Abstract Background The emergence of community-acquired methicillin-resistant Staphylococcus aureus (MRSA) in the late 1990s-early 2000s complicated the empiric management of suspected staphylococcal infection in children. Rising clindamycin resistance rates in many communities adds further to management challenges. Ceftaroline, an anti-MRSA cephalosporin, represents an attractive therapy option. Little data are available, however, regarding the frequency of reduced susceptibility (RS) to ceftaroline among MRSA isolates from a general pediatric population. Methods Isolates were selected from an ongoing S. aureus surveillance study at Texas Children’s Hospital. Invasive MRSA isolates from 2015-2018 were included. Isolates were initially screened for ceftaroline RS with E-test; all isolates with a ceftaroline E-test MIC ≥ 1.5µg/ml underwent ceftaroline broth dilution. Ceftaroline RS was regarded as an MIC ≥ 2 µg/ml; full ceftaroline resistance was defined as an MIC ≥ 8 μg/ml. Accessory gene regulator (agr) groups were characterized by PCR. Results 201 viable isolates were included. The ceftaroline MIC50 and MIC90 were 0.5 and 1 µg/ml, respectively (Figure 1). Six isolates had MIC ≥ 2 µg/ml (2.9%) with two having MIC ≥ 8 µg/ml (0.9%). All ceftaroline RS isolates were from healthcare associated infections. Ceftaroline RS isolates were more often associated with clindamycin-resistance and agr group II (Figure 2). Infections with ceftaroline RS were associated with central venous lines, recent ICU admission, preceding antibiotic exposure (specifically cephalosporins) and prior MRSA infection. One subject with MRSA CLABSI had a ceftaroline susceptible MRSA infection followed < 1 month later by a ceftaroline resistant infection (MIC =32 μg/ml); the isolates were identical by PFGE. Only 3 subjects had previously received ceftaroline, none of which subsequently developed a ceftaroline RS isolate. Figure 1. Ceftaroline MIC Distribution Figure 2. Clinical And Microbiologic Associations with Reduced Ceftaroline Susceptibility Conclusion Ceftaroline RS occurs in 2.9% of invasive MRSA isolates in children and is most prominent among healthcare-associated infections. These isolates were associated with clindamycin resistance and agr group II. While ceftaroline RS is rare among invasive MRSA infections, the lack of preceding ceftaroline exposure is concerning and warrants careful surveillance. Disclosures Sheldon L. Kaplan, MD, Allergan (Research Grant or Support)Pfizer (Grant/Research Support) Jonathon C. McNeil, MD, Allergan (Research Grant or Support, Allergan provided ceftaroline powder for use in studies described in this abstract)


Author(s):  
EV Belyaeva ◽  
GB Ermolina ◽  
EV Boriskina ◽  
IS Shkurkina ◽  
VS Kropotov

Introduction: Staphylococcal infections rank high among healthcare-associated infections. Coagulase-negative staphylococci, especially S. epidermidis and S. haemolyticus, often induce inflammatory processes in newborns. In this regard, it is important to study the persistence of these microorganisms in pediatric hospitals using intraspecific differentiation based on the comparison of spectra of their extracellular proteins. Our objective was to study circulation of S. epidermidis and S. haemolyticus strains in a children’s hospital by electrophoretyping of their extracellular proteins. Materials and methods: We studied 277 strains of S. haemolyticus and 267 strains of S. epidermidis isolated from patients and various objects of the hospital environment by obtaining extracellular proteins of the isolates, analyzing them using polyacrylamide gel electrophoresis, and determining their antibiotic resistance and ability to form biofilms. Results: The analysis of electrophoregrams of extracellular proteins of staphylococci revealed groups of identical strains. Isolates from different patients were combined into 21 S. haemolyticus groups comprising of 69 strains and 13 groups of S. epidermidis comprising of 38 strains. All the cultures were methicillin-resistant, with the exception of one group of two S. haemolyticus strains. More than half of the cultures grouped by spectra of extracellular proteins were multidrug resistant. The absolute majority of S. haemolyticus strains (97.2 %) and three quarters of S. epidermidis strains (76.0 %) were able to form biofilms. The average values of the degree of film formation in S. haemolyticus strains were significantly higher than those in S. epidermidis. Conclusions: Of all the studied cultures of staphylococci, 25 % of strains and 14 % of S. epidermidis strains persisted and were endemic in the children’s hospital, including 88.4 % of hemolytic and 42.1 % of epidermal staphylococcus strains for more than a month, and 21.7 % of S. haemolyticus and 21.1 % of S. epidermidis strains for almost a year. The strains were resistant to methicillin, and the isolates of S. haemolyticus had a high ability to form biofilms.


2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Catherine E. Foster ◽  
Paula A. Revell ◽  
Judith R. Campbell ◽  
Lucila Marquez

2019 ◽  
Vol 6 (Supplement_2) ◽  
pp. S853-S854
Author(s):  
Catherine Foster ◽  
Paula Revell ◽  
Judith R Campbell ◽  
Lucila Marquez

Abstract Background Cutaneous mucormycosis in children is a rare fungal infection which primarily occurs in patients with underlying medical conditions and is associated with significant morbidity. We describe characteristics of pediatric patients with healthcare-associated (HCA) cutaneous mucormycosis at Texas Children’s Hospital (TCH) and results of an outbreak investigation. Methods Patients at TCH were identified retrospectively through review of the TCH Microbiology Laboratory mycology culture reports from 1/1/2012–2/18/2019. Pediatric patients <21 years of age with cutaneous mucormycosis that developed during a hospitalization or was associated with a medical device were included. Demographic information was collected through review of the electronic medical record. Randomly amplified polymorphic DNA (RAPD) analysis were performed by the Fungus Testing Laboratory, University of Texas Health Science Center at San Antonio. This study was approved through the Baylor College of Medicine Institutional Review Board. Results We identified 12 patients with HCA cutaneous mucormycosis. The characteristics of these patients are detailed in the table. Six cases of Rhizopus infection occurred over a narrow 7 month period from March through September of 2017 prompting an outbreak investigation. Genotyping results revealed 4 molecular types from 5 available isolates suggesting that the isolates were not clonally related. Adhesive products were suspected as a potential source. Infection Control activities included site visits to the hospital supply warehouse and linen facility. Tape practices throughout the hospital were assessed through a nursing survey. Samples of adhesive products were cultured at an environmental microbiology laboratory and no Rhizopus spp. were isolated. A source was not identified. Conclusion Mucormycosis is a life-threatening infection in children. Providers should have a low threshold of suspicion for cutaneous mucormycosis in patients with underlying medical conditions (malignancies and extreme prematurity) that develop skin lesions near medical device dressings or securement sites. Disclosures All authors: No reported disclosures.


2008 ◽  
Vol 18 (2) ◽  
pp. 76-86 ◽  
Author(s):  
Lauren Hofmann ◽  
Joseph Bolton ◽  
Susan Ferry

Abstract At The Children's Hospital of Philadelphia (CHOP) we treat many children requiring tracheostomy tube placement. With potential for a tracheostomy tube to be in place for an extended period of time, these children may be at risk for long-term disruption to normal speech development. As such, speaking valves that restore more normal phonation are often key tools in the effort to restore speech and promote more typical language development in this population. However, successful use of speaking valves is frequently more challenging with infant and pediatric patients than with adult patients. The purpose of this article is to review background information related to speaking valves, the indications for one-way valve use, criteria for candidacy, and the benefits of using speaking valves in the pediatric population. This review will emphasize the importance of interdisciplinary collaboration from the perspectives of speech-language pathology and respiratory therapy. Along with the background information, we will present current practices and a case study to illustrate a safe and systematic approach to speaking valve implementation based upon our experiences.


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