Literature DB >> 16574123

Developing a Research base for Intravenous Peripheral cannula re-sites (DRIP trial). A randomised controlled trial of hospital in-patients.

Joan Webster1, Sophia Lloyd, Tracey Hopkins, Sonya Osborne, Maria Yaxley.   

Abstract

BACKGROUND: There is currently no high grade evidence on which to base decisions about the frequency of intravenous cannula re-sites.
OBJECTIVE: To assess the safety of changing peripheral venous cannulas when clinically indicated.
DESIGN: Randomised controlled trial.
SETTING: A tertiary referral hospital in Brisbane, Australia. PARTICIPANTS: Two hundred and six hospitalised patients from surgical, medical and orthopaedic wards.
INTERVENTIONS: Peripheral intravenous cannulas were re-sited only when complications occurred (intervention group) or every 3 days (control group). MAIN OUTCOME MEASURES: The primary endpoint was any unplanned cannula removal, the secondary outcome was cost.
RESULTS: Forty six patients had unplanned removals in the intervention group compared with 41 in the control group [relative risk 1.12, 95% confidence interval 0.81-1.55 (p=0.286)], a non-significant difference. Total duration of peripheral cannulation was similar in both groups (mean 123.3h in the intervention group and 125.9h in the control group: P=0.82) but significantly more re-sites occurred in the control group (167 in intervention group, 202 in the control group: p=0.022). Cost of cannula replacements in the intervention group was AUD$3,183.62 and in the control group AUD$3,837.56 (p=0.006).
CONCLUSION: Re-siting peripheral venous cannulas when clinically indicated compared with changing them routinely every 3 days does not lead to more complications and reduces costs.

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Mesh:

Year:  2006        PMID: 16574123     DOI: 10.1016/j.ijnurstu.2006.02.003

Source DB:  PubMed          Journal:  Int J Nurs Stud        ISSN: 0020-7489            Impact factor:   5.837


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