Please use this identifier to cite or link to this item: https://doi.org/10.1053/j.ajkd.2014.04.022
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dc.titleInitial and Extended Use of Femoral Versus Nonfemoral Double-Lumen Vascular Catheters and Catheter-Related Infection During Continuous Renal Replacement Therapy
dc.contributor.authorChua, H.-R.
dc.contributor.authorSchneider, A.G.
dc.contributor.authorSherry, N.L.
dc.contributor.authorLotfy, N.
dc.contributor.authorChan, M.J.
dc.contributor.authorGaltieri, J.
dc.contributor.authorWong, G.R.
dc.contributor.authorLipcsey, M.
dc.contributor.authorMatte, C.d.A.
dc.contributor.authorCollins, A.
dc.contributor.authorGarcia-Alvarez, M.
dc.contributor.authorBellomo, R.
dc.date.accessioned2016-07-08T09:26:39Z
dc.date.available2016-07-08T09:26:39Z
dc.date.issued2014-12-01
dc.identifier.citationChua, H.-R., Schneider, A.G., Sherry, N.L., Lotfy, N., Chan, M.J., Galtieri, J., Wong, G.R., Lipcsey, M., Matte, C.d.A., Collins, A., Garcia-Alvarez, M., Bellomo, R. (2014-12-01). Initial and Extended Use of Femoral Versus Nonfemoral Double-Lumen Vascular Catheters and Catheter-Related Infection During Continuous Renal Replacement Therapy. American Journal of Kidney Diseases 64 (6) : 909-917. ScholarBank@NUS Repository. https://doi.org/10.1053/j.ajkd.2014.04.022
dc.identifier.issn02726386
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/125406
dc.description.abstractBackground: The risk of catheter-related infection or bacteremia, with initial and extended use of femoral versus nonfemoral sites for double-lumen vascular catheters (DLVCs) during continuous renal replacement therapy (CRRT), is unclear. Study Design: Retrospective observational cohort study. Setting & Participants: Critically ill patients on CRRT in a combined intensive care unit of a tertiary institution. Factor: Femoral versus nonfemoral venous DLVC placement. Outcomes: Catheter-related colonization (CRCOL) and bloodstream infection (CRBSI). Measurements: CRCOL/CRBSI rates expressed per 1,000 catheter-days. Results: We studied 458 patients (median age, 65 years; 60% males) and 647 DLVCs. Of 405 single-site only DLVC users, 82% versus 18% received exclusively 419 femoral versus 82 jugular or subclavian DLVCs, respectively. The corresponding DLVC indwelling duration was 6 ± 4 versus 7 ± 5 days (P = 0.03). Corresponding CRCOL and CRBSI rates (per 1,000 catheter-days) were 9.7 versus 8.8 events (P = 0.8) and 1.2 versus 3.5 events (P = 0.3), respectively. Overall, 96 patients with extended CRRT received femoral-site insertion first with subsequent site change, including 53 femoral guidewire exchanges, 53 new femoral venipunctures, and 47 new jugular/subclavian sites. CRCOL and CRBSI rates were similar for all such approaches (P = 0.7 and P = 0.9, respectively). On multivariate analysis, CRCOL risk was higher in patients older than 65 years and weighing >90 kg (ORs of 2.1 and 2.2, respectively; P < 0.05). This association between higher weight and greater CRCOL risk was significant for femoral DLVCs, but not for nonfemoral sites. Other covariates, including initial or specific DLVC site, guidewire exchange versus new venipuncture, and primary versus secondary DLVC placement, did not significantly affect CRCOL rates. Limitations: Nonrandomized retrospective design and single-center evaluation. Conclusions: CRCOL and CRBSI rates in patients on CRRT are low and not influenced significantly by initial or serial femoral catheterizations with guidewire exchange or new venipuncture. CRCOL risk is higher in older and heavier patients, the latter especially so with femoral sites. © 2014 National Kidney Foundation, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1053/j.ajkd.2014.04.022
dc.sourceScopus
dc.subjectAcute kidney injury (AKI)
dc.subjectacute renal failure (ARF)
dc.subjectcatheter-related bloodstream infection (CRBSI)
dc.subjectcatheter-related colonization
dc.subjectcatheter-related infection
dc.subjectcontin
dc.subjectdouble lumen vascular catheter
dc.subjectline infection
dc.subjectline sepsis
dc.subjectnontunneled dialysis catheter
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.1053/j.ajkd.2014.04.022
dc.description.sourcetitleAmerican Journal of Kidney Diseases
dc.description.volume64
dc.description.issue6
dc.description.page909-917
dc.description.codenAJKDD
dc.identifier.isiut000345404200013
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