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Infrared illumination for difficult peripheral venous catheterisation in critically ill adult patients: the prospective, randomised, multicentre ICARE trial

医学 重症监护医学 随机对照试验 外科 急诊医学
作者
R. Ouedraogo,Aline da Silva Alves,Amélie Bruant,Oumar Sy,Cécilia Tabra Osorio,Frédérique Schortgen,Amélie Chenal,Damien Contou,Laurence Krzyzaniak,Muriel Fartoukh,Marianne Le Joncour,Nicolas Mongardon,L. Benaïssa,Daniel Da Silva,Meriem Bouguerra,Sophie Demeret,Stéphanie Dubois,Eric Starczala,Chirine Petyt,Matthieu Schmidt,Séverine Dezellus,Jean Francois Georger,Ann-Cécile Pallud,Damien Carras,Fabien Boussely,Étienne Audureau,Armand Mekontso Dessap
出处
期刊:BMJ Open [BMJ]
卷期号:15 (2): e090611-e090611
标识
DOI:10.1136/bmjopen-2024-090611
摘要

Introduction The insertion of a peripheral venous line is of paramount importance in the stabilisation of critically ill patients. It is a preferred method of venous access over more invasive techniques due to its immediacy and fewer complications. Difficulties of catheterisation can result in delays to treatment, increased complication risks and pain, and a waste of valuable time and healthcare resources. Our hypothesis is that infrared vein illumination could improve the success rate of peripheral venous catheterisation in critically ill patients at risk of difficult catheterisation. Methods and analysis This is a prospective, multicentre, randomised, open-label controlled trial. It will be conducted in France and will involve critically ill patients at risk of difficult peripheral catheterisation. Patients will be randomly assigned to usual care or infrared vein illumination. The primary outcome is the rate of successful peripheral venous catheterisation at first puncture. Secondary outcomes include time to placement, overall rate of successful peripheral venous catheterisation, number of punctures, quality (calibre of the catheter), replacement rate, need for central line and local complications (dysfunction, diffusion, haematoma and lymphangitis). Ethics and dissemination The study has been granted ethical approval (CPP Ile de France 1). Following the provision of informed consent, patients will be included in the study. The results will be submitted for publication in peer-reviewed journals. Trial registration number NCT03932214 .
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