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BMJ open · 2025

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

Протокол клинического исследованияСтатьяНазвание и аннотация: Перевод в очереди
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Ouedraogo Rachida, Alves Aline, Bruant Amélie, Sy Oumar, Tabra Osorio Cécilia, Schortgen Frédérique, Chenal Amélie, Contou Damien, Krzyzaniak Laurence, Fartoukh Muriel, Le Joncour Marianne, Mongardon Nicolas, Ait Benaissa Latifa, Da Silva Daniel, Bouguerra Meriem, Demeret Sophie, Tanguy Dubois Stéphanie, Starczala Eric, Petyt Chirine, Schmidt Matthieu, Dezellus Séverine, Georger Jean Francois, Pallud Ann-Cécile, Carras Damien, Boussely Fabien, Audureau Etienne, Mekontso Dessap Armand

Аннотация

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.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты