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    Catheter-related bloodstream infections in intensive care units:a systematic review with meta-analysis

    Prabha Ramritu, Kate Halton, David Cook, Michael Whitby & Nicholas Graves

    Accepted for publication 28 August 2007

    Correspondence to N. Graves:

    e-mail: [email protected]

    Prabha Ramritu MN RN

    Project Officer

    The Centre for Healthcare Related Infection

    Surveillance & Prevention, Princess

    Alexandra Hospital, Brisbane, Qld, Australia

    Kate Halton MSc

    Project Officer

    The Centre for Healthcare Related Infection

    Surveillance & Prevention, Princess

    Alexandra Hospital, Brisbane, Qld, Australia

    Institute of Biomedical and Health

    Innovation, Brisbane, Qld, Australia

    David Cook MBBS PhD

    Medical Officer

    Intensive Care Unit, Princess Alexandra

    Hospital, Brisbane, Qld, Australia

    Michael Whitby FRACP MPH

    Director of Infectious Diseases

    The Centre for Healthcare Related Infection

    Surveillance & Prevention, Princess

    Alexandra Hospital, Brisbane, Qld, Australia

    Nicholas Graves PhD

    Senior Research Fellow in Health Economics

    The Centre for Healthcare Related Infection

    Surveillance & Prevention, Princess

    Alexandra Hospital, Brisbane, Qld, Australia

    Institute of Biomedical and Health

    Innovation, Brisbane, Qld, Australia

    R A M RI T U P . , H A L T O N K . , C O O K D . , W H I T B Y M . & G R AV E S N . ( 2 0 08 )R A M RI T U P . , H A L T O N K . , C O O K D . , W H I T B Y M . & G R AV E S N . ( 2 0 08 ) Catheter-

    related bloodstream infections in intensive care units: a systematic review with

    meta-analysis. Journal of Advanced Nursing 62(1), 321

    doi: 10.1111/j.1365-2648.2007.04564.x

    AbstractTitle. Catheter-related bloodstream infections in intensive care units: a systematic

    review with meta-analysis.Aim. This paper is a report of a systematic review and meta-analysis of strategies,

    other than antimicrobial coated catheters, hypothesized to reduce risk of catheter-

    related bloodstream infections and catheter colonization in the intensive care unit

    setting.

    Background. Catheter-related bloodstream infections occur at a rate of 5 per 1000

    catheter days in the intensive care unit setting and cause substantial mortality and

    excess cost. Reducing risk of catheter-related bloodstream infections among inten-

    sive care unit patients will save costs, reduce length of stay, and improve outcomes.

    Methods. A systematic review of studies published between January 1985 and

    February 2007 was carried out using the keywords catheterization central venous

    with combinations of infection*, prevention* and bloodstream*. All included

    studies were screened by two reviewers, a validated data extraction instrument was

    used and data collection was completed by two blinded independent reviewers. Risk

    ratios for catheter-related bloodstream infections and catheter colonization were

    estimated with 95% confidence intervals for each study. Results from studies of

    similar interventions were pooled using meta-analyses.

    Results. Twenty-three studies were included in the review. The strategies that

    reduced catheter colonization included insertion of central venous catheters in the

    subclavian vein rather than other sites, use of alternate skin disinfection solutions

    before catheter insertion and use of Vitacuff in combination with polymyxin, neo-

    mycin and bacitracin ointment. Strategies to reduce catheter-related bloodstream

    infection included staff education multifaceted infection control programmes and

    performance feedback.Conclusion. A range of interventions may reduce risks of catheter-related blood-

    stream infection, in addition to antimicrobial catheters.

    Keywords: bloodstream infection, central venous catheters, intensive care unit,

    meta-analysis, nursing, prevention, systematic review

    R E V I E W P A P E RJAN

    2008 The Authors. Journal compilation 2008 Blackwell Publishing Ltd 3

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    Introduction

    Catheter-related bloodstream infections (CRBSI) occur at a

    rate of 50 per 1000 catheter days in the intensive care unit

    (ICU) setting (McLaws & Taylor 2003, Anonymous, 2004).

    The mortality attributable to these infections may be as high

    as 246% and length of stay is extended by between 7 and

    191 days; the cost per case has been estimated to be

    $US4888 (c. 2448) and 16,356 (c. 11,139) (Orsi et al.

    2002, Rosenthal et al. 2003a). Reducing risk of CRBSI

    among ICU patients will save costs, reduce length of stay and

    improve mortality and morbidity.

    The risk of CRBSI in the ICU setting depends on many

    factors. Although many relate to patient diagnosis and

    underlying health state, others are associated with discre-

    tionary decisions made by healthcare professionals. Many

    studies have focused on the use of anti-microbial catheters

    to reduce rates in this clinical context and a number of

    meta-analyses have been published that describe the effec-tiveness of different types of anti-microbial catheters for

    the ICU setting (Veenstra et al. 1999, Marin et al. 2000,

    Mermel 2000, Walder et al. 2002, Geffers et al. 2003).

    However, a multitude of other interventions used at various

    points in the catheter insertion and management pathway

    are available. There are currently no systematic reviews

    summarizing the evidence for these other interventions

    specifically in relation to their effectiveness in the adult

    ICU setting, or attempting to bring this information together

    in one coherent summary (Halton & Graves 2007).

    The review

    Aim

    The aim of the review was to evaluate strategies, other than

    antimicrobial coated catheters, hypothesized to reduce risk of

    CRBSI and catheter colonization in the ICU setting.

    Design

    A systematic review was conducted according to the methods

    described by the Centre for Reviews and Dissemination,University of York (Centre for Reviews and Dissemination,

    2001).

    Search methods

    Databases and search terms

    A search was conducted of the following electronic data-

    bases for research published between January 1985 and

    February 2007: MEDLINE; Cumulative Index of Nursing

    and Allied Health Literature (CINAHL); Current Contents;

    Current Contents Connect; Australian Medical Index; Bio-

    logical Abstracts; EMBASE; Science Citation; National

    Library of Medicine; PubMed; Dissertation Abstracts;

    Database of Review of Abstracts of Effectiveness; Cochrane

    Library; Health Services Technology (National Health

    Service, United Kingdom and United States of America);

    National Clearing House (Agency for Healthcare Research

    and Quality); Center for Disease Control guideline and

    reports; Bandolier and Clinical Evidence (Wales BMJ

    Publishing group). The broad MeSH search term, cathe-

    terization central venous with combinations of keywords

    infection*, prevention* and bloodstream* was used. The

    reference lists of all relevant guidelines, systematic reviews,

    and full articles of all studies included were hand-checked

    for additional studies. Details of the inclusion and exclu-

    sion criteria are presented in Table 1. Observational and

    randomized controlled trial (RCT) designs were included.Studies were included if a definition of CRBSI was pro-

    vided that required the isolation of the same organism from

    the culture of a catheter segment and peripheral blood

    cultures. Catheter colonization results were reported if the

    study used a recognized definition of a positive catheter

    colonization of either 15 colony forming units (CFU) by

    semi-quantitative culture (Maki et al. 1977) or 103 CFU/

    mL by quantitative technique from culture of the distal end

    of the catheter (Brun-Buisson et al. 1987).

    Table 1 Inclusion and exclusion criteria

    Inclusion criteria

    Full report of observational study or randomized controlled trial

    Investigate short-term (

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    Search outcome

    Five hundred and sixty-nine abstracts were reviewed and 513

    excluded. The remaining 56 articles were read in full and

    judged explicitly against the inclusion criteria. Twenty-seven

    were excluded and 29 met the inclusion criteria. Complete

    data sets were obtained from twenty-three studies, published

    between 1985 and February 2007: 13 RCTs, two trials and

    nine observational cohort studies, see Table 2. Six were

    excluded as part of the quality assessment exercise because

    we could not obtain all the necessary data despite attempts to

    contact the authors, see Table 3 for all exclusion criteria. The

    process is illustrated by Figure 1.

    Quality appraisal

    Validated data extraction instruments for experimental and

    observational studies chosen for clarity, comprehensiveness

    and use in previous central venous catheter (CVC)-related

    reviews [specifically the Evidence-based Practice Infection

    Control (EPIC) project] were pilot tested and used (Prattet al. 2001). This instrument and the Scottish Intercollegiate

    Guidelines Network (SIGN) checklist were used to assess

    study quality (SIGN 2001). As in the EPIC project, studies

    were grouped into three quality categories (Pratt et al. 2001):

    category 1, well-designed study, findings can be generalized

    to most hospitals; category 2, acceptable experimental study,

    conclusions may be generalized and in absence of category 1

    evidence, study accepted into review; category 3, study

    methodology fatally flawed and rejected from review. Details

    of the data extracted are provided in Appendix 1.

    Data abstraction

    All studies were screened by two reviewers using the abstract

    or full paper. Data were extracted independently by two

    reviewers (PR and either NG or DC or KH), blinded to the

    author, date of publication and author affiliations, with

    inconsistencies resolved by consultation. If required, corre-

    sponding authors were contacted by e-mail, twice in 4 weeks,

    to obtain missing information or clarify ambiguity.

    Synthesis

    For each study, the risk ratios (RR) with 95% confidence

    intervals (CI) were calculated for the outcomes of CRBSI andcatheter colonization. A RR is a measure of relative risk

    derived from two proportions. Relative risk is the risk of

    developing a disease relative to exposure. Data from studies

    investigating the same intervention were pooled. The DerSi-

    monian & Laird method was used to calculate summary RR

    with 95% CI for both outcomes via a random effects model

    (Petitti 2000), normally distributed errors were assumed. This

    method incorporates an assumption that the different studies

    are estimating different, yet related, treatment effects. Sta-

    tistical heterogeneity was assessed using the MantelHaenzel

    test statistic. Studies brought together in any systematic

    review will differ and these differences are known as statis-

    tical heterogeneity. STATASTATA 9TM software package (StataCorp,

    College Station, TX, USA) was used for all the statistical

    analysis. No sensitivity or subgroup analysis was undertaken

    due to the small number of studies anticipated to be available

    for any one type of intervention.

    Results

    Study characteristics and a summary of results are presented

    in Tables 3 and 4. Studies were grouped into eight categories:

    site of CVC insertion; choice of skin disinfectant; catheter

    replacement at a new site vs. exchange over a guidewire;

    connectors and hubs; attachable cuffs; number of lumens on

    the CVC; educational programme to increase healthcare

    professional awareness of strategies to prevent infection; andcombined interventions. All 23 reported rates of CRBSI and

    16 studies reported catheter colonization. The range of

    definitions used in the studies are summarized in Table 5.

    Site of insertion (two studies)

    Short-term non-tunnelled CVC are inserted into the internal

    jugular, subclavian, femoral or axillary veins and the risk of

    CRBSI is believed to vary by site. One RCT (Merrer et al.,

    2001) found a higher proportion of catheters inserted in the

    femoral vein were colonized compared to the subclavian (RR

    64; 95% CI: 19212; P < 0001) but there was no

    difference in CRBSI rates (RR 2 02; 95% CI: 019221;

    P = 06). A prospective comparative open study (Martin et al.

    1998) found a similar colonization rate for internal jugular

    vs. axillary vein (RR 106; 95% CI: 034332; P = 05) and

    no significant difference in the CRBSI rate (RR 0 42; 95% CI:

    004398; P = 041).

    Skin disinfectant solutions (three studies)

    The skin can be a source of CRBSI, with skin flora believed to

    migrate along the subcutaneous insertion tract. The use ofskin disinfectants prior to insertion and ongoing management

    of the catheter may be an important risk reducing strategy.

    Three studies compared different types of skin disinfectants.

    One RCT (Maki et al. 1991) compared 2% aqueous

    chlorhexidine (Chl) gluconate to 10% povidone iodine (PI)

    and 70% isopropyl alcohol. The 2% aqueous Chl solution

    compared to 10% PI reduced colonization by 69% (RR 031;

    95% CI: 017088; P = 001) but there was no statistically

    JAN: REVIEW PAPER Catheter-related bloodstream infections in intensive care units

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    Table2

    Studycharacteristics

    Strategy&Author

    Year

    Studydesign

    Setting(no.

    ICUs)

    Interventions

    Sample

    size

    Participants

    Durationof

    study(months)

    Mean

    age(years)

    %

    Males

    Siteofinsertion

    Merrer

    2001

    RCT

    M,

    S(8)

    Subclavianvs.

    femoral

    136

    134

    59

    7

    61

    9

    6270

    93

    2

    Martin

    1998

    OBS

    Mixed(1)

    Axillaryvs.

    internaljugular

    62

    79

    54

    59

    7975

    24

    Insertionsiteskindisinfectings

    olution

    Humar

    2000

    RCT

    M/S;M,

    NS(4)

    10%

    PIvs.

    0

    5%

    Chl

    117

    125

    62

    2

    58

    3

    615

    625

    12

    Maki

    1991

    RCT

    S(1)

    10%PIvs.

    70%

    alcoholvs.

    2%

    Chl

    77

    32

    67

    53

    53

    51

    NRNRNR

    7

    Parienti

    2004

    CORT

    M

    (2)

    5%

    PI/70%

    ethanolvs.

    10%

    aqueousPI

    106*

    117

    54

    4

    61

    5

    NRNR

    12

    Catheterreplacement

    Bach

    1992

    RCT

    CS(1)

    Newsitevs.

    guidewireexchange

    80

    79

    68

    64

    6661

    NR

    Devices:connectors

    Luna

    2000

    RCT

    ICU(1)&surgicalunits

    Standardhubvs.

    SegurLock

    27*

    24*

    NR

    NR

    NRNR

    18

    Leon

    2003

    RCT

    M,

    S(7)

    Standardhubvs.

    SegurLock

    114

    116

    59

    6

    58

    1

    649

    586

    15

    Lucet

    2000

    RCT

    M,

    S(3)

    Hubprotectionboxandstandardhub

    vs.

    needle-lessclosedconnectorwithmultiflohub

    37

    40

    NR

    NR

    NRNR

    3

    Yebenes

    2004

    RCT

    Mixed(1)

    Standard3-waystopcockvs.

    disinfecta

    ble

    needle

    freeconnector

    139*

    139*

    58

    7

    55

    3

    755

    705

    NR

    Devices:cuff

    Flowers

    1989

    RCT

    S(1)

    Nocuff&PNBvs.

    vitacuff&PNB

    29*

    26*

    49

    1

    42

    5

    812

    790

    9

    Hasaniya

    1996

    NRT

    S(2)

    Nocuffvs.

    vitacuff

    64

    90

    47

    57

    NRNR

    13

    Lumens

    Gupta

    1995

    RCT

    NR(1)

    Singlevs.

    double

    25

    25

    NR

    NR

    NRNR

    12

    Gil

    1989

    OBS

    M

    (1)

    Singlevs.

    triple

    63*

    157*

    NR

    NR

    NRNR

    15

    Hilton

    1988

    OBS

    Mixed(4)

    Singlevs.

    triple

    99*

    309*

    NR

    NR

    NRNR

    6

    Farkas

    1992

    RCT

    M/S(1)

    Singlevs.

    triple

    51

    54

    63

    5

    65

    5

    NRNR

    22

    P. Ramritu et al.

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    Table2

    (Continued)

    Strategy&Author

    Year

    Studydesign

    Setting(no.

    ICUs)

    Interv

    entions

    Sample

    size

    Participants

    Durationof

    study(months)

    Mean

    age(years)

    %

    Males

    Educationalprogramme

    Warren

    2003

    OBS

    M,S

    (2)

    Preintervention(nodetails)vs.

    interventioneduc

    ation,

    posters,factsheetspostedinICU;10-pageself-study

    modulecompleted

    674

    541

    71

    71

    5252

    29

    Multipleinterventions

    Bonawitz

    1991

    RCT

    S(1)

    Gp1

    cuff&CVCremovedat3days

    Gp2

    cuff&CVCremovedat7days

    Gp3

    nocuff&CVCremovedat3days

    Gp4

    nocuff&CVCremovedat7days

    40*

    35*

    45*

    39*

    NR

    NR

    NR

    NR

    NRNRNRNR

    14

    Cobb

    1992

    RCT

    M,

    S(2)

    Gp1

    CVCreplacedevery3days+insertionatnewsite

    Gp2

    CVCreplacedevery3days+exchangeoverguidewire

    Gp3

    CVCreplacedwhenclinically

    indic

    ated+insertionatnewsite

    Gp4

    CVCreplacedwhenclinically

    indic

    ated+exchangeoveraguidewire

    35

    40

    41

    44

    57

    59

    55

    59

    685059 52

    16

    Civetta

    1996

    OBS

    Trauma(1)

    Phase

    1:PIforskinpreparation

    Ph2:

    triplelumenChg/ssdCVCs

    Phase

    3chlorhexidineskincleanser,changeincriteria

    forg

    uidewireexchange;extensionofsafeperio

    d

    forc

    atheterextensionfrom2to4days

    147

    34

    156

    NR

    NR

    NR

    NRNRNR

    15

    Lobo

    2005

    OBS

    M

    (1)

    Phase

    1pretest,

    observationofCVC

    Phase

    2effectofeducationprogram,

    standardizedcathetercarepractices

    Phase

    3monthlyCRBSIratefeedback,

    provision

    ofCRBSI

    preventionguidetoallmedicalresidents

    316

    190

    266

    NR

    NR

    NR

    NRNR NR

    23

    Higuera

    2005

    OBS

    M/SNS(2)

    Phase

    1activesurveillancewithoutprocesscontrol

    Phase

    2infectioncontroleducationprogram;process

    controlofCVCcare;compliancewithinfection

    controlpracticesandCVCcare

    132

    338

    44

    3

    45

    9

    45

    5

    48

    2

    11

    Rosenthal

    2003

    OBS

    M/SC(4)

    Phase

    1surveillanceofCRBSIrates

    Phase

    2trainingandeducation

    Phase

    3performancefeedbackoncompliance

    with

    infectioncontrolprogrammeandCVCcare

    NR

    NR

    NR

    71

    71

    71

    48

    8

    53

    6

    53

    6

    28

    CRBSI,

    catheter-relatedbloodstreaminfection;ICU,

    intensivecareunit;C

    VC,

    centralvenouscatheter;NR,

    notrepo

    rted;RCT,

    randomizedcontrolledtrial;O

    BS:cohortobservational

    study;CORT,

    cross-overunit-randomizedtrial;NRT,

    non-randomizedtrial;M,

    medical;M/S,

    medical/surgical;C,cardiac;S,surgical;CS,cardiacsurgical;NS,neuro-surgical.

    *NumberofCVCsreportedon

    ly.

    JAN: REVIEW PAPER Catheter-related bloodstream infections in intensive care units

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    significant reduction for CRBSI (RR 023; 95% CI: 003

    192; P = 014). Compared to the 70% alcohol solution the

    2% Chl showed no statistically significant difference in

    colonization (RR 038; 95% CI: 011133; P = 011) or

    CRBSI rates (RR 024; 95% CI: 002254; P = 024).

    Another RCT (Humar et al. 2000) compared 10% PI

    solution with 05% tincture of Chl solution and found no

    difference in rates of colonization or CRBSI (RR 0 8; 95% CI:

    052126; P = 022; RR 107; 95% CI: 027417; P = 06

    respectively). The third study (Parienti et al. 2004) used a

    cross-over unit-randomized trial to compare 10% aqueous PI

    solution with 5% PI in 70% ethanol based aqueous solution.

    Colonization rates were significantly lower for alcoholic PI

    (RR 038; 95% CI: 022 to 065; P < 0001) but there was

    no significant difference in CRBSI rate (RR 03; 95% CI:

    00324; P = 021).

    Catheter replacement on new site vs. exchange over

    guidewire (one study)

    Catheters can be replaced by inserting a replacement

    catheter in a new site, or by replacing the catheter over

    a guide wire in the same insertion site. The one RCT

    included in this review that looked at this intervention

    found no significant difference in colonization rates withguidewire exchange relative to new site replacement (RR

    037; 95% CI: 01135; P = 010) and no cases of CRBSI

    were observed (Bach et al. 1992).

    Use of devices: connectors (four studies)

    Central venous catheter hubs may be a source of intralu-

    minal catheter colonization and CRBSI due to frequent

    manipulation and use of a PI connection shield might

    reduce risk. Two RCTs (Lucet et al. 2000, Leon et al.

    2003) compared the rate of CRBSI observed with use of a

    Segur-Lock (Inibsa Laboratories, Barcelona, Spain) connec-

    tor relative to that observed under use of a standard hub.

    Luna (Luna et al. 2000) included patients from ICU and

    surgical units and data from ICU participants only are

    included in the analysis. The pooled findings of these two

    studies indicated a non-significant reduction in risk of

    CRBSI with Segur-Lock, see Figure 2 (RR 027; 95% CI:

    007105). Lucet et al. (2000) compared antiseptic impreg-

    nated hub protection boxes to needle-less closed connectors

    in a RCT, and reported a non-significant difference in risk

    of catheter colonization and CRBSI (RR 1 25; 95% CI:

    0662

    37; P = 0

    3 and RR 0

    96; 95% CI: 0

    0614

    99;

    P = 074, respectively). The fourth RCT (Yebenes et al.

    2004) compared a disinfectable needle-free connector to the

    standard three-way stopcock. The rates of CRBSI and

    catheter colonization were lower in the needle-free connec-

    tor group, with this difference approaching statistical

    significance for CRBSI (RR 014; 95% CI: 002114;

    P = 003), but not for catheter colonization (RR 0 69; 95%

    CI: 0316; P = 037).

    Use of devices: cuffs (two studies)

    A biodegradable collagen cuff impregnated with bacterici-

    dal silver ions (Vitacuff; Vitaphore Corp, Menlo Park, CA,

    USA) has been suggested to prevent CVC colonization from

    skin organisms migrating along the subcutaneous tract.

    One RCT (Flowers et al. 1989) and one non-randomized

    trial (Hasaniya et al. 1996) investigated triple-lumen

    catheters with an attachable cuff (Vitacuff) relative to

    catheters with no cuff. In the RCT, colonization rates with

    Table 3 Reasons for excluding studies following full review

    Excluded papers Reasons for exclusion

    Roberts & Cheung (1998) Definition of CRBSI was not clear.

    Berenholtz et al. (2004) Insufficient information

    on inclusion criteria

    Carrer et al. (2005) Insufficient information

    on inclusion criteria

    Coopersmith et al. (2002) Insufficient information

    on inclusion criteria

    Warren et al. (2004) Insufficient information

    on inclusion criteria

    Badley et al. (1996) Insufficient data on proven CRBSI

    to calculate rate of CRBSI in the

    three comparison groups

    CRBSI, catheter-related bloodstream infection.

    Search strategy

    569 abstracts for review

    513 rejected

    27 excluded

    (did not meet inclusion criteria)

    6 excluded

    (complete data sets not available)

    56 articles for further review

    29 included for full review

    23 included

    Figure 1 Search strategy and study selection.

    P. Ramritu et al.

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    Table4

    Summaryresultsofincludedstudies(groupedtogetheraccording

    topreventativestrategyexamined)

    Preventativestrategy/Author

    Year

    Intervention

    Proportionofcoloniza

    tionRR(95%

    CI)

    ProportionofCRBS

    IRR(95%

    CI)

    Siteofinsertion

    Merrer

    2001

    Subclavianvs.

    femoral

    3/136

    19/134

    RR(usingfemoralsite

    )6

    4

    (1

    92

    1

    2,

    P

    1CVC

    allowed

    Multipleinterventions

    Bonawitz

    1991

    SC;IJ

    M

    S,SG,

    SGl

    ,C,

    M

    NS

    Ga

    uzepad

    &

    Opsite

    2-3

    Gps1&33

    Gps2&47

    Yes

    Cobb

    1992

    SC,

    IJ

    3

    M,

    SG,SG

    l,SD

    10%PI

    G,

    AO

    2

    Gp13

    Gp23

    Gp36

    Gp47

    Yes

    Civetta

    1996

    NR

    3

    M,C,S

    G,SGl

    Phase1:PI

    Phase2:4%

    chl

    SG

    /AO

    PRN,

    3

    Phase

    14

    5

    Phase

    35

    4

    Yes

    Lobo

    2005

    SCmostly

    NS

    SG,S

    Gl,LD,

    C,M

    PI

    G

    PRN,

    daily

    NS

    NS

    Higuera

    2005

    NS

    S

    Fullbarrier

    precaution

    sometime

    s

    NS

    G

    NS

    7

    3*

    NS

    Rosenthal

    2003

    NS

    S

    NS

    NS

    G

    NS

    7

    07*

    NS

    NS,notspecified;NR,

    notrepo

    rted;CVC,

    centralvenouscatheter;A,

    axillary;F.

    femoral;IJ,

    internaljugular;J,jugular;NR,

    notreported;S,supraclavicular;SC,

    subclavian;NC,

    non-

    coatedCVCs;Chg/ssd,

    chlorhexidinegluconate/silversulfadiazinecoated

    CVCs;M,

    multiple;S,standard;SP,

    standardpolyurethaneCVC;D,

    drapes;LD,lar

    gedrape;MBP,

    maximal

    barrierprecaution;SD,

    steriledrape;LSD,

    largesteriledrape;G.

    gown;SG.

    sterilegown;SGl,sterilegloves;Gl,gloves;M,

    mask;C,

    cap;Alc,

    alcohol;AlcPI.alcoholicpovidoneiodine;Aq

    PI,aqueouspovidoneiodine;AO

    ,antibiotic/antimicrobialointment;Chlg,chlorhexidinegluconate;Chl,chlorhexidine;I,iodinetincture;PI,povidoneiodine;SSD,s

    tandardsteriledressing;

    TSD,

    transparentsteriledressing;TPU,

    transparentpolyurethanedressing;

    SG,

    sterilegauze;G,

    gauze;THD,

    transparenthydrocolloiddressing;SPU,

    standardpo

    lyurethanedressing;AO,

    antiseptic/antimicrobialointmentappliedoninsertionsite;PRN,

    changed

    asrequired;SP,

    studysitepreference.

    *Informationobtainedfromau

    thorsviae-mail.

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    error and bias can be minimized at all stages of the research.

    Other limitations of the available evidence include the

    inadequate power of many of the studies to detect a real

    difference in CRBSI and colonization rates. Where possible

    we combined evidence in meta-analyses, but the small

    number of studies available for which we could pool datastill precluded the provision of statistical support for the

    effectiveness of interventions. For example, colonization rates

    were lower but did not reach significance at the 5% level for a

    number of interventions such as 10% PI vs. 05% Chl

    (Humar et al. 2000) and new site vs. guidewire exchange for

    CVC replacement (Bach et al. 1992). We suggest future

    studies be designed with a sample size large enough to detect

    a real difference or to inform a subsequent meta-analysis.

    The appraisal of evidence for reducing catheter coloniza-

    tion and CRBSI is further complicated by the fact that a

    number of different interventions are used concurrently inthe insertion and ongoing management of CVC. Unless all

    studies investigating a particular intervention control for the

    effect of these co-interventions it will be difficult to determine

    the interventions that are most effective in reducing coloni-

    zation and CRBSI, and if we can expect to achieve this effect

    in other settings. As shown in Table 7, there was much

    clinical heterogeneity in the studies and important confound-

    ing data was often not provided for some co-interventions

    such as site of insertion, use of barrier precautions and type

    of disinfecting solution. Other problems arise from the

    findings being influenced by the absence of a consistent

    definition for CRBSI, see Table 5, and inconsistent catheter

    management protocols across studies. In short, we still do

    not have a full understanding of the most effective ways to

    prevent CRBSI in the ICU context although this review and

    others can help to indicate where some of the largest gaps in

    our knowledge lie.

    Conclusion

    Interventions other than antimicrobial catheters may be

    useful for reducing risks of CRBSI in the ICU setting.

    Infection control is typically nurse-led within a wider multi-

    disciplinary team and nurses play a key role in the care of ICU

    patients, including assisting with the insertion and daily

    management of CVCs. Nurse awareness and implementation

    of appropriate risk reducing strategies is important. Thisreview is relevant to evidence-based nursing practice in many

    international settings. It highlights the strength of evidence

    underlying each intervention and the recent trend to use a

    combination of most effective interventions to manage the

    care of CVC. The strategies we recommend are relatively

    low-cost, pose minimal risks for patients and constitute good

    nursing practice. Finally, good decision-making requires that

    the cost-effectiveness of all interventions be assessed and

    compared, but understanding their effectiveness is an impor-

    tant first step.

    Acknowledgements

    Financial support for the study was provided by the National

    Health & Medical Research Council of Australia.

    Author contributions

    PR and NG were responsible for the study conception and

    design and PR, DC and NG were responsible for the drafting

    of the manuscript. PR, KH, DC and NG performed the data

    collection and PR performed the searches and data analysis.

    MW and NG obtained funding. PR, KH, DC and NG madecritical revisions to the paper. KH provided statistical advice.

    DC, MW and NG supervised the study.

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    Appendix 1

    Details of data extracted.

    Clinical data: experimental and observational studies

    Study aim/objective

    Definitions of study outcomes

    Study design: type, appropriateness to aim

    Study setting/characteristics of sample/inclusion criteria/sample size; study dates

    Details of intervention type, regimen, co-interventions

    Outcomes baseline measures, details of measurement, summary results

    Duration of follow-up

    Investigators conclusions, reviewer agreements and any reservations

    Hand search of reference list

    Data analysis

    Preintervention comparability table

    Similarity of subjects at start of study

    Quality: experimental studies

    Method of allocation, randomization; blinding

    Sample size power calculation

    Equal treatment of groups other than intervention

    Bias due to drop out, characteristics and reasons for withdrawalsAppropriateness of statistical analysis, intention to treat or as treated

    Dealing with confounding variables

    Quality

    Observational studies

    Method of sample selection

    Comparability of groups at baseline

    Drop-out rate

    Details of withdrawal

    Appropriateness of statistical analysis

    Summary of reviewers judgement for experimental and observational studies

    Soundness of methodology design

    Generalizability of findings

    Clinical importance of outcomes

    Harm/benefit analysisRisk of bias

    Need for author contact for further information/ statistical assessment required

    Acceptance of paper into review

    Study grading for experimental studies

    Category 1: study well designed experimental study; findings generalizable

    Category 2: acceptable design, in absence of category 1, accept study into review

    Category 3: methodologically fatally flawed, reject study.

    Study grading for observational studies

    Category 1: well designed observational study, findings generalizable

    Category 2: acceptable design, in absence of category 1, accept study into review

    Category 3: methodologically fatally flawed, reject study.

    Sources: (Scottish Intercollegiate Guidelines Network 2001) & (Pratt et al. 2001).

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