2% chlorhexidine gluconate aqueous versus 2% chlorhexidine gluconate in 70% isopropyl alcohol for skin disinfection prior to percutaneous central venous catheterisation: the ARCTIC randomised controlled feasibility trial.

Infectious Disease Medicine Microbiology Neonatology Sepsis

Journal

Archives of disease in childhood. Fetal and neonatal edition
ISSN: 1468-2052
Titre abrégé: Arch Dis Child Fetal Neonatal Ed
Pays: England
ID NLM: 9501297

Informations de publication

Date de publication:
31 Oct 2023
Historique:
received: 25 05 2023
accepted: 08 09 2023
medline: 1 11 2023
pubmed: 1 11 2023
entrez: 31 10 2023
Statut: aheadofprint

Résumé

Catheter-related sepsis (CRS) is a major complication with significant morbidity and mortality. Evidence is lacking regarding the most appropriate antiseptic for skin disinfection before percutaneous central venous catheter (PCVC) insertion in preterm neonates. To inform the feasibility and design of a definitive randomised controlled trial (RCT) of two antiseptic formulations, we conducted the Antiseptic Randomised Controlled Trial for Insertion of Catheters (ARCTIC) feasibility study to assess catheter colonisation, sepsis, and skin morbidity. Feasibility RCT. Two UK tertiary-level neonatal intensive care units. Preterm infants born <34 weeks' gestation scheduled to undergo PCVC insertion. Skin disinfection with either 2% chlorhexidine gluconate (CHG)-aqueous or 2% CHG-70% isopropyl alcohol (IPA) before PCVC insertion and at removal. Proportion in the 2% CHG-70% IPA arm with a colonised catheter at removal. Rates of: (1) CRS, catheter-associated sepsis (CAS), and CRS/CAS per 1,000 PCVC days; (2) recruitment and retention; (3) data completeness. Daily skin morbidity scores recorded from catheter insertion until 48 hours post-removal. 116 babies were randomised. Primary outcome incidence was 4.1% (95% confidence interval: 0.9% to 11.5%). Overall catheter colonisation rate was 5.2% (5/97); CRS 2.3/1000 catheter days; CAS 14.8/1000 catheter days. Recruitment, retention and data completeness were good. No major antiseptic-related skin injury was reported. A definitive comparative efficacy trial is feasible, but the very low catheter colonisation rate would make a large-scale RCT challenging due to the very large sample size required. ARCTIC provides preliminary reassurance supporting potential safe use of 2% CHG-70% IPA and 2% CHG-aqueous in preterm neonates. ISRCTN82571474.

Identifiants

pubmed: 37907266
pii: archdischild-2023-325871
doi: 10.1136/archdischild-2023-325871
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Paul Clarke (P)

Neonatal Intensive Care Unit, Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK paul.clarke@nnuh.nhs.uk.
Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.

Aung Soe (A)

Neonatal Intensive Care Unit, Medway Maritime Hospital, Gillingham, Kent, UK.

Amy Nichols (A)

Neonatal Intensive Care Unit, Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Helen Harizaj (H)

Neonatal Intensive Care Unit, Medway Maritime Hospital, Gillingham, Kent, UK.

Mark A Webber (MA)

Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.
Quadram Institute Bioscience, Norwich, Norfolk, UK.

Louise Linsell (L)

National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Jennifer L Bell (JL)

National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Catherine Tremlett (C)

Department of Microbiology, Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Priyadarsini Muthukumar (P)

Neonatal Intensive Care Unit, Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Santosh Pattnayak (S)

Neonatal Intensive Care Unit, Medway Maritime Hospital, Gillingham, Kent, UK.

Christopher Partlett (C)

National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Andrew King (A)

National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Ed Juszczak (E)

National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Paul T Heath (PT)

Centre for Neonatal and Paediatric Infection, Infection and Immunity, Saint George's University of London, London, UK.

Classifications MeSH