Frequency and factors associated with infusion-related local complications of vancomycin on peripheral venous catheters

Author:

Ammar Helmi12ORCID,Rolland Simon3,Jouffroy Romain4567,Dubert Marie23,Le Beller Christine1,Podglajen Isabelle28,Lillo-Lelouet Agnès1,Lebeaux David239,Bensaid Samuel3

Affiliation:

1. Centre Régional de Pharmacovigilance, Hôpital Européen Georges Pompidou, AP-HP , Paris , France

2. Université Paris Cité , Paris 75006 , France

3. Service de Microbiologie, Unité Mobile d’Infectiologie, AP-HP, Hôpital Européen Georges Pompidou , 20 rue Leblanc, Paris 75015 , France

4. Intensive Care Unit, Ambroise Paré Hospital, Assistance Publique Hôpitaux Paris and Paris Saclay University , Boulogne Billancourt , France

5. EA7329, Institut de Recherche bioMédicale et d’Epidémiologie du Sport, INSEP, Paris University , Paris , France

6. U1018, Centre de recherche en Epidémiologie et Santé des Populations, INSERM, Paris Saclay University , Paris , France

7. EA 7525, Université des Antilles , Fort de France 97261 , France

8. Service de Microbiologie, AP-HP, Hôpital Européen Georges Pompidou , 20 rue Leblanc, Paris 75015 , France

9. FHU PROTHEE , Paris , France

Abstract

AbstractBackgroundVancomycin is a reference antibiotic against methicillin-resistant staphylococci. Its administration is associated with infusion-related local complications (IRLC). To reduce this risk, it has been proposed to increase vancomycin dilution in the IV bag and to perform continuous infusion using the volumetric pump. The aim of our study was to assess the safety of peripheral infusion of vancomycin with the volumetric pump.ObjectivesTo compare the frequency of IRLC between patients receiving vancomycin and those receiving β-lactam (BL) antibiotics. Our secondary objective was to assess factors associated with the occurrence of IRLC.Patients and methodsWe conducted a prospective observational study in a French tertiary hospital. Between February 2021 and November 2021, we included all patients receiving continuous infusions of vancomycin or BL through a peripherally inserted venous catheter (PIVC). The primary endpoint was the occurrence of IRLC on Day 1 (D1).ResultsWe included 168 patients (56 vancomycin, 112 BL). At D1, 14 patients (25%) presented IRLC in the vancomycin group versus 11 patients (10%) in the BL group (P = 0.01). There was significantly more IRLC in the group receiving vancomycin at an infused concentration above 5 mg/mL than those receiving BL (8/15, 53.3% versus 11/112, 10%, respectively, P < 0.01). However, no significant difference was observed between patients receiving infused vancomycin concentration ≤5 mg/mL and patients receiving BL (P = 0.4).ConclusionOur data support safe administration of vancomycin if infused at a concentration under 5 mg/mL, through the volumetric pump on PIVC.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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