Circulatory collapse during wound closure in spine surgery with an unknown cause: a possible adverse effect of

Xiaoqing Zhang1, Wenwen Zhai1, Min Li1

  • 1Department of Anesthesiology, Peking University Third Hospital, No. # 49, Huayuan Rd; Haidian Dist, Beijing, China.

BMC Anesthesiology
|January 7, 2021
PubMed
Abstract

Insights

Topical vancomycin (VCM) powder in orthopedic surgery may cause anaphylaxis. This study found VCM-associated shock and hypotension, highlighting the need for vigilance during and after its application.

Area of Science:

  • Anesthesiology
  • Orthopedic Surgery
  • Pharmacology

Background:

  • Vancomycin (VCM) is effective against Gram-positive bacteria and used topically in orthopedic surgery to prevent infections.
  • However, VCM can induce anaphylaxis through direct histamine release, independent of antibodies or complement.
  • This reaction is infusion rate-dependent.

Purpose of the Study:

  • To investigate potential adverse events associated with topical vancomycin (VCM) powder in orthopedic surgery.
  • To identify the characteristics and clinical presentation of VCM-induced anaphylaxis in this context.

Main Methods:

  • Retrospective analysis of seven cases presenting with severe hypotension and shock during or after orthopedic surgery.
  • Cases were evaluated based on clinical manifestations and timing of shock onset, with differential diagnosis used due to lack of laboratory data.

Main Results:

  • All seven cases were linked to the local application of VCM powder during wound closure.
  • Two patients experienced sudden cardiac arrest, and six cases showed circulatory collapse.
  • Most patients recovered without severe sequelae, but one case with 3g VCM developed cardiac arrest and coma.

Conclusions:

  • Local vancomycin (VCM) application in orthopedic surgery may pose safety risks, including anaphylaxis.
  • VCM-induced anaphylaxis can manifest as delayed, severe hypotension and circulatory collapse.
  • Surgeons and anesthesiologists must exercise caution during and after VCM application due to potential non-IgE mediated anaphylactic reactions.

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