Clinical application of skin antisepsis using aqueous olanexidine: a scoping review

Yutaro Shinzato1, Eiryu Sakihara1, Yuki Kishihara1

  • 1Department of Emergency and Critical Care Medicine Jichi Medical University Saitama Medical Center Saitama Japan.

Acute Medicine & Surgery
|January 14, 2022
PubMed

Insights

Olanexidine gluconate (OLG) shows promise in combating resistant bacteria, potentially outperforming chlorhexidine gluconate (CHG) and povidone-iodine (PVP-I) for surgical site infections (SSIs). However, more clinical research is needed to confirm its efficacy for SSIs and catheter-related bloodstream infections (CRBSIs).

Area of Science:

  • Antimicrobial efficacy and infection prevention strategies.
  • Pharmacology and clinical applications of novel disinfectants.

Background:

  • Increasing rates of surgical site infections (SSIs) and catheter-related bloodstream infections (CRBSIs) due to bacterial resistance to traditional disinfectants like chlorhexidine gluconate (CHG) and povidone-iodine (PVP-I).
  • Development of olanexidine gluconate (OLG) in Japan (2015) as a potential alternative for preventing SSIs and CRBSIs caused by resistant bacteria.

Purpose of the Study:

  • To conduct a scoping review to identify the existing knowledge and knowledge gaps regarding the disinfection efficacy of OLG.
  • To evaluate OLG's effectiveness against resistant bacterial strains and its clinical utility in preventing healthcare-associated infections.

Main Methods:

  • Comprehensive literature search across multiple databases (PubMed, CINAHL, Cochrane, ClinicalTrials.gov, etc.) up to July 18, 2021.
  • Inclusion of 47 studies categorized into pharmacological/spectral effects (29 studies) and clinical/adverse effects (18 studies).
  • Manual reference searches were performed to supplement database findings.

Main Results:

  • OLG demonstrated bactericidal activity against methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE), and common Gram-positive and Gram-negative bacteria.
  • Preliminary clinical evidence suggests 1.5% OLG may be more effective than 10% PVP-I and 1% CHG in SSI prevention, though data is limited.
  • Significant limitations exist due to a scarcity of clinical studies, particularly concerning CRBSI prevention.

Conclusions:

  • OLG exhibits broad-spectrum bactericidal activity, including against key resistant pathogens.
  • While initial findings suggest potential superiority over existing agents for SSI prevention, the clinical usefulness of OLG remains uncertain due to limited evidence.
  • Further rigorous clinical trials are essential to establish the efficacy and safety of OLG for both SSI and CRBSI prevention.

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