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      Efficacy of introducing a checklist to reduce central venous line associated bloodstream infections in the ICU caring for adult patients

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          Abstract

          Background

          Central line-associated bloodstream infections (CLABSI) are a major source of sepsis in modern intensive care medicine. Some years ago bundle interventions have been introduced to reduce CLABSI. The use of checklists may be an additional tool to improve the effect of these bundles even in highly specialized institutions. In this study we investigate if the introduction of a checklist reduces the frequency of CLABSI.

          Methods

          During the study period from October 2011 to September 2012, we investigated the effect of implementing a checklist for the placement of central venous lines (CVL). Patients were allocated either to the checklist group or to the control group, roughly in a 1:2 ratio. The frequency of CLABSI was compared between the two groups.

          Results

          During the study period 4416 CVL were inserted; 1518 in the checklist group and 2898 in the control group. The use of the checklist during CVL placement resulted in a lower CLABSI frequency. The incidence in the checklist group was 3.8 per 1000 catheter days as compared to 5.9 per 1000 catheter days in the control group (IRR = 0.57; p = 0.001). The use of the checklist also reduced the frequency of catheter colonisation significantly, 36.3 per 1000 catheter days in the checklist group vs 21.2 per 1000 catheter days in the control group, respectively (IRR = 0.58; p < 0.001).

          Conclusion

          The introduction of a checklist to improve the adherence to hygiene standards while placement of central venous lines reduced the frequency of infections significantly.

          Electronic supplementary material

          The online version of this article (10.1186/s12879-018-3178-6) contains supplementary material, which is available to authorized users.

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          Most cited references17

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          Epidemiology of severe sepsis

          Severe sepsis is a leading cause of death in the United States and the most common cause of death among critically ill patients in non-coronary intensive care units (ICU). Respiratory tract infections, particularly pneumonia, are the most common site of infection, and associated with the highest mortality. The type of organism causing severe sepsis is an important determinant of outcome, and gram-positive organisms as a cause of sepsis have increased in frequency over time and are now more common than gram-negative infections. Recent studies suggest that acute infections worsen pre-existing chronic diseases or result in new chronic diseases, leading to poor long-term outcomes in acute illness survivors. People of older age, male gender, black race, and preexisting chronic health conditions are particularly prone to develop severe sepsis; hence prevention strategies should be targeted at these vulnerable populations in future studies.
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            Optimal testing parameters for blood cultures.

            The effects of volume of blood, number of consecutive cultures, and incubation time on pathogen recovery were evaluated for 37,568 blood cultures tested with the automated BACTEC 9240 instrument (Becton Dickinson Diagnostic Instrument Systems) at a tertiary care center over the period of 12 June 1996 through 12 October 1997. When the results for this study were compared with previous data published for manual broth-based blood culture systems and patient samples obtained in the 1970s and 1980s, the following were found: (1) the percentage increase in pathogen recovery per milliliter of blood is less, (2) more consecutive blood culture sets over a 24-h period are required to detect bloodstream pathogens, and (3) a shorter duration of incubation is required to diagnose bloodstream infections. Guidelines developed in the 1970s and 1980s for processing and culturing blood may require revision.
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              Attributable mortality of central line associated bloodstream infection: systematic review and meta-analysis.

              To identify the attributable mortality of central line associated blood stream infections (CLABSI) through meta-analysis.
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                Author and article information

                Contributors
                +49 40 7410 57010 , d.wichmann@uke.de
                c.belmar-campos@uke.de
                sehrhard@jhsph.edu
                timo.kock@gmx.de
                claudiaweber@schoen-kliniken.de
                h.rohde@uke.de
                s.kluge@uke.de
                Journal
                BMC Infect Dis
                BMC Infect. Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                8 June 2018
                8 June 2018
                2018
                : 18
                : 267
                Affiliations
                [1 ]ISNI 0000 0001 2180 3484, GRID grid.13648.38, Department of Intensive Care Medicine, , University Medical Center Hamburg-Eppendorf, ; Martinistrasse 52, 20246 Hamburg, Germany
                [2 ]ISNI 0000 0001 2180 3484, GRID grid.13648.38, Institute for Medical Microbiology, Virology and Hygiene, , University Medical Center Hamburg-Eppendorf, ; Martinistrasse 52, 20246 Hamburg, Germany
                [3 ]ISNI 0000 0001 2171 9311, GRID grid.21107.35, Department of Epidemiology, , Johns Hopkins Bloomberg School of Public Health, ; 615 North Wolfe Street, Baltimore, MD 21205 USA
                [4 ]Schoen-Klinik Hamburg Eilbek, Dehnhaide 120, 22081 Hamburg, Germany
                Author information
                http://orcid.org/0000-0002-4334-7640
                Article
                3178
                10.1186/s12879-018-3178-6
                5994052
                29884118
                6cdb3a22-30c2-470e-b838-0e45f2594315
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 11 July 2017
                : 30 May 2018
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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