Chlorhexidine gluconate or polyhexamethylene biguanide disc dressing to reduce the incidence of central-line-associated bloodstream infection: a feasibility randomized controlled trial (the CLABSI trial)

被引:23
作者
Webster, J. [1 ,2 ,3 ]
Larsen, E. [1 ,2 ,3 ]
Marsh, N. [1 ,2 ,3 ]
Choudhury, A. [2 ,4 ,5 ,6 ]
Harris, P. [1 ,5 ]
Rickard, C. M. [1 ,2 ,3 ,4 ]
机构
[1] Royal Brisbane & Womens Hosp, Level 2,Bld 34,Butterfield St, Herston, Qld 4029, Australia
[2] Griffith Univ, Menzies Hlth Inst Queensland, Alliance Vasc Access Teaching & Res, Brisbane, Qld, Australia
[3] Griffith Univ, Natl Ctr Res Excellence Nursing, Nathan, Qld, Australia
[4] Griffith Univ, Alliance Vasc Access Teaching & Res AVATATR, Brisbane, Qld, Australia
[5] Univ Sunshine Coast, Sch Hlth & Sports Sci, Inflammat & Healing Res Cluster, Brisbane, Qld, Australia
[6] Univ Queensland, Royal Brisbane & Womens Hosp, UQ Ctr Clin Res, Herston, Qld, Australia
关键词
Catheter-related infections; Randomized controlled trial; Feasibility studies; Chlorhexidine; Polyhexamethylene biguanide; PREVENTION;
D O I
10.1016/j.jhin.2017.04.009
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: A number of antimicrobial-impregnated discs to prevent central-lineassociated bloodstream infection (CLABSI) are marketed but it is unclear which disc is most effective. Aim: To investigate the feasibility and safety of comparing two antimicrobial-impregnated discs to prevent CLABSI. Methods: A single-centre, parallel group, randomized controlled trial was conducted in a 929-bed tertiary referral hospital. Hospital inpatients requiring a peripherally inserted central catheter were randomized to chlorhexidine gluconate (CHG) or polyhexamethylene biguanide (PHMB) disc dressing group. Dressings were replaced every seven days, or earlier, if clinically required. Participants were followed until device removal or hospital discharge. Feasibility outcomes included: proportion of potentially eligible participants who were enrolled; proportion of protocol violations; and proportion of patients lost to follow-up. Clinical outcomes were: CLABSI incidence, diagnosed by a blinded infection control practitioner; all-cause bloodstream infection (BSI); and product-related adverse events. Findings: Of 143 patients screened, 101 (71%) were eligible. Five (3.5%) declined participation. There was one post-randomization exclusion. Two (2%) protocol violations occurred in the CHG group. No patients were lost to follow-up. Three (3%) BSIs occurred; two (2%) were confirmed CLABSIs (one in each group) and one a mucosal barrier injuryrelated BSI. A total of 1217 device-days were studied, resulting in 1.64 CLABSIs per 1000 catheter-days. One (1%) disc-related adverse event occurred in the CHG group. Conclusion: Disc dressings containing PHMB are safe to use for infection prevention at catheter insertion sites. An adequately powered trial to compare PHMB and CHG discs is feasible. (C) 2017 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.
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收藏
页码:223 / 228
页数:6
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