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CATheter Infections in CHildren (CATCH): a randomised controlled trial and economic evaluation comparing impregnated and standard central venous catheters in children. / Harron, Kate; Mok, Quen; Dwan, Kerry et al.
In: Health Technology Assessment, Vol. 20, No. 18, 03.2016.

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Harron, K, Mok, Q, Dwan, K, Ridyard, C, Mott, T, Millar, M, Ramnarayan, P, Tibby, SM, Muller-Pebody, B, Hughes, D, Gamble, C & Gilbert, RE 2016, 'CATheter Infections in CHildren (CATCH): a randomised controlled trial and economic evaluation comparing impregnated and standard central venous catheters in children', Health Technology Assessment, vol. 20, no. 18. https://doi.org/10.3310/hta20180

APA

Harron, K., Mok, Q., Dwan, K., Ridyard, C., Mott, T., Millar, M., Ramnarayan, P., Tibby, S. M., Muller-Pebody, B., Hughes, D., Gamble, C., & Gilbert, R. E. (2016). CATheter Infections in CHildren (CATCH): a randomised controlled trial and economic evaluation comparing impregnated and standard central venous catheters in children. Health Technology Assessment, 20(18). https://doi.org/10.3310/hta20180

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Harron K, Mok Q, Dwan K, Ridyard C, Mott T, Millar M et al. CATheter Infections in CHildren (CATCH): a randomised controlled trial and economic evaluation comparing impregnated and standard central venous catheters in children. Health Technology Assessment. 2016 Mar;20(18). doi: 10.3310/hta20180

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RIS

TY - JOUR

T1 - CATheter Infections in CHildren (CATCH)

T2 - a randomised controlled trial and economic evaluation comparing impregnated and standard central venous catheters in children

AU - Harron, Kate

AU - Mok, Quen

AU - Dwan, Kerry

AU - Ridyard, Colin

AU - Mott, Tracy

AU - Millar, Michael

AU - Ramnarayan, Padmanabhan

AU - Tibby, S.M.

AU - Muller-Pebody, Berit

AU - Hughes, Dyfrig

AU - Gamble, Carol

AU - Gilbert, Ruth E.

N1 - This project was funded by the NIHR Health Technology Assessment programme

PY - 2016/3

Y1 - 2016/3

N2 - Children who are admitted to hospital for intensive care often need to have medicines given directly into their veins, through a small plastic tube called a central venous catheter (CVC). CVCs avoid the need for repeated injections, but their disadvantage is an increased risk of bloodstream infection (BSI), which can result in prolonged treatment and time in hospital. In adults, CVCs coated with medicine to kill bacteria (antibiotics) or prevent clots (heparin) help reduce the risk of BSI. However, we do not know if coating the much narrower CVCs used for children would work in the same way. The only way to find out which type of CVC (standard non-coated, antibiotic coated or heparin coated) works best was to carry out a randomised controlled trial. Children aged < 16 years who needed a CVC for intensive care treatment participated within 14 hospitals in England. Consent was provided for all participants in the trial. Each child had an equal chance of receiving one of the three CVC types. Bloodstream infection occurred in 4% of children with standard CVCs and 2% of those with impregnated CVCs. Rates of BSI were lowest in the antibiotic CVC group (1%) but these children had slightly higher health-care costs for the 6 months after trial participation. Although doubt remains whether or not antibiotic CVCs would result in cost savings for the NHS in England, our results suggest that using antibiotic CVCs could help reduce BSI rates for children in intensive care.

AB - Children who are admitted to hospital for intensive care often need to have medicines given directly into their veins, through a small plastic tube called a central venous catheter (CVC). CVCs avoid the need for repeated injections, but their disadvantage is an increased risk of bloodstream infection (BSI), which can result in prolonged treatment and time in hospital. In adults, CVCs coated with medicine to kill bacteria (antibiotics) or prevent clots (heparin) help reduce the risk of BSI. However, we do not know if coating the much narrower CVCs used for children would work in the same way. The only way to find out which type of CVC (standard non-coated, antibiotic coated or heparin coated) works best was to carry out a randomised controlled trial. Children aged < 16 years who needed a CVC for intensive care treatment participated within 14 hospitals in England. Consent was provided for all participants in the trial. Each child had an equal chance of receiving one of the three CVC types. Bloodstream infection occurred in 4% of children with standard CVCs and 2% of those with impregnated CVCs. Rates of BSI were lowest in the antibiotic CVC group (1%) but these children had slightly higher health-care costs for the 6 months after trial participation. Although doubt remains whether or not antibiotic CVCs would result in cost savings for the NHS in England, our results suggest that using antibiotic CVCs could help reduce BSI rates for children in intensive care.

U2 - 10.3310/hta20180

DO - 10.3310/hta20180

M3 - Article

VL - 20

JO - Health Technology Assessment

JF - Health Technology Assessment

SN - 1366-5278

IS - 18

ER -