The use of 8-cm 22G Seldinger catheters for intravenous access in children with cystic fibrosis

Sarah Y Qian; Matthias Horn; Richard Barnes; David Stuart Armstrong

doi:10.5301/jva.5000274

The use of 8-cm 22G Seldinger catheters for intravenous access in children with cystic fibrosis

Sarah Y Qian, Matthias Horn, Richard Barnes, David Stuart Armstrong

Paediatrics Monash Health

Research output: Contribution to journal › Article › Research › peer-review

14 Citations (Scopus)

Abstract

Long intravenous catheters are an effective and economical choice of vascular access for intravenous antibiotic therapy in children with cystic fibrosis (CF). This prospective audit assesses the use of Vygon Leaderflex 22G ? 8 cm catheters in an Australian tertiary centre. Key outcomes included catheter lifespan, ability to complete antibiotic therapy and complication rates.

Original language	English
Pages (from-to)	415 - 417
Number of pages	3
Journal	The Journal of Vascular Access
Volume	15
Issue number	5
DOIs	https://doi.org/10.5301/jva.5000274
Publication status	Published - 2014

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10.5301/jva.5000274

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abstract = "Long intravenous catheters are an effective and economical choice of vascular access for intravenous antibiotic therapy in children with cystic fibrosis (CF). This prospective audit assesses the use of Vygon Leaderflex 22G ? 8 cm catheters in an Australian tertiary centre. Key outcomes included catheter lifespan, ability to complete antibiotic therapy and complication rates.",

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AB - Long intravenous catheters are an effective and economical choice of vascular access for intravenous antibiotic therapy in children with cystic fibrosis (CF). This prospective audit assesses the use of Vygon Leaderflex 22G ? 8 cm catheters in an Australian tertiary centre. Key outcomes included catheter lifespan, ability to complete antibiotic therapy and complication rates.

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DO - 10.5301/jva.5000274

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JO - The Journal of Vascular Access

JF - The Journal of Vascular Access

IS - 5

ER -

The use of 8-cm 22G Seldinger catheters for intravenous access in children with cystic fibrosis

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