Abstract:The use of intensive chemotherapy and central devices has improved patients survival, but it is associated with catheter-related blood-stream infections (CRBSI). An educational program was instituted for preventing CRBSI occurrence in acute leukemia pediatric patients having totally implanted central devices. The Centers of Disease Control and Prevention criteria were used as definition for CRBSI. Data collected were age, sex, diagnosis, chemotherapy, inpatient versus outpatient, microbiological data, risk fac… Show more
“…In contrast, they noted a statistically significant increased risk for CLABSI in patients with severe neutropenia at the time of the CVC placement. 22 This is why it has been recommended that CVC placement should be avoided when ANC is <0.5 9 10 9 /L. 1 In the present retrospective study the majority of patients (95%) had a tunneled external (TE) CVC and only two patients (5%) had a totally implantable design, therefore an association between catheter design and risk for CLABSI could not be made.…”
Section: Discussionmentioning
confidence: 69%
“…showed that ANC was not associated with an increased risk for developing CLABSI. In contrast, they noted a statistically significant increased risk for CLABSI in patients with severe neutropenia at the time of the CVC placement . This is why it has been recommended that CVC placement should be avoided when ANC is <0.5 × 10 9 /L …”
Section: Discussionmentioning
confidence: 99%
“…In a multicenter surveillance study of CLABSI in children with cancer, 36% (68/191) of the patients were not neutropenic at the time of CLABSI diagnosis . Moreover, Berrueco et al . showed that ANC was not associated with an increased risk for developing CLABSI.…”
Section: Discussionmentioning
confidence: 99%
“…More intensive chemotherapy regimens seem to be significantly associated with CLABSI in the pediatric oncology group. This is probably related to prolonged and severe myelotoxicity, especially during the first 6 months of chemotherapy, along with the fact that this period requires frequent hospitalizations and CVC procedures …”
Section: Discussionmentioning
confidence: 99%
“…19 In a multicenter surveillance study of CLABSI in children with cancer, 36% (68/191) of the patients were not neutropenic at the time of CLABSI diagnosis. 21 Moreover, Berrueco et al 22 showed that ANC was not associated with an increased risk for developing CLABSI. In contrast, they noted a statistically significant increased risk for CLABSI in patients with severe neutropenia at the time of the CVC placement.…”
Younger age, neutropenia, hematologic malignancy and longer catheterization are important risk factors for CLABSI, but further research is required for the prevention of catheter-related infection in children with malignancy.
“…In contrast, they noted a statistically significant increased risk for CLABSI in patients with severe neutropenia at the time of the CVC placement. 22 This is why it has been recommended that CVC placement should be avoided when ANC is <0.5 9 10 9 /L. 1 In the present retrospective study the majority of patients (95%) had a tunneled external (TE) CVC and only two patients (5%) had a totally implantable design, therefore an association between catheter design and risk for CLABSI could not be made.…”
Section: Discussionmentioning
confidence: 69%
“…showed that ANC was not associated with an increased risk for developing CLABSI. In contrast, they noted a statistically significant increased risk for CLABSI in patients with severe neutropenia at the time of the CVC placement . This is why it has been recommended that CVC placement should be avoided when ANC is <0.5 × 10 9 /L …”
Section: Discussionmentioning
confidence: 99%
“…In a multicenter surveillance study of CLABSI in children with cancer, 36% (68/191) of the patients were not neutropenic at the time of CLABSI diagnosis . Moreover, Berrueco et al . showed that ANC was not associated with an increased risk for developing CLABSI.…”
Section: Discussionmentioning
confidence: 99%
“…More intensive chemotherapy regimens seem to be significantly associated with CLABSI in the pediatric oncology group. This is probably related to prolonged and severe myelotoxicity, especially during the first 6 months of chemotherapy, along with the fact that this period requires frequent hospitalizations and CVC procedures …”
Section: Discussionmentioning
confidence: 99%
“…19 In a multicenter surveillance study of CLABSI in children with cancer, 36% (68/191) of the patients were not neutropenic at the time of CLABSI diagnosis. 21 Moreover, Berrueco et al 22 showed that ANC was not associated with an increased risk for developing CLABSI. In contrast, they noted a statistically significant increased risk for CLABSI in patients with severe neutropenia at the time of the CVC placement.…”
Younger age, neutropenia, hematologic malignancy and longer catheterization are important risk factors for CLABSI, but further research is required for the prevention of catheter-related infection in children with malignancy.
We found higher rates of Gram-negative organisms in adults and higher rates of polymicrobial in children. Because of the low rates of peripheral blood cultures and the low rates of CVC removal, CRBSI diagnosis could be challenging in pediatrics. A modified CRBSI definition relying more on clinical criteria may be warranted.
Staphylococcus epidermidis is the leading etiologic agent of device-related infections. S. epidermidis is able to bind, by means of the adhesins of its cell wall, the host matrix proteins filming the artificial surfaces. Thence, bacteria cling to biomaterials and infection develops. The effect of temperature on integrity, structure, and biological activity of the collagen-binding adhesin (SdrF) of S. epidermidis has been here investigated. By cloning in E. coli XL1-Blue, a recombinant of the SdrF binding domain B (rSdrFB), carrying an N-terminal polyhistidine, was obtained. Purification was by HiTrap(TM) Chelating HP columns. Assessment of purity, molecular weight, and integrity was by SDS-PAGE. The rSdrFB-collagen binding was investigated by ELISA. A full three-dimensional reconstruction of rSdrFB was achieved by small-angle X-ray scattering (SAXS). At 25 °C, rSdrFB bound to type I collagen in a dose-dependent, saturable manner, with a Kd of 2.48 × 10(-7) M. When temperature increased from 25 to 37 °C, a strong conformational change occurred, together with the abolition of the rSdrFB-collagen binding. The rSdrFB integrity was not affected by temperature variation. SdrFB-collagen binding is switched on/off depending on the temperature. Implications with the infection pathogenesis are enlightened.
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