Safety of lumbar puncture for people who are treated with ADP receptor antagonists

Mary Nash1, Sivan Bloch1,2, Daniel Golan3,4

  • 1Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

Journal of Neurology
|February 22, 2023
PubMed

Insights

Performing lumbar puncture without stopping adenosine-diphosphate receptor antagonists (ADPra) appears safe. This finding suggests current guidelines may be revised, potentially improving patient care and reducing cardiovascular risks.

Area of Science:

  • Neurology
  • Cardiology
  • Clinical Practice Guidelines

Background:

  • Current guidelines recommend discontinuing adenosine-diphosphate receptor antagonists (ADPra) 7 days before lumbar puncture (LP).
  • This practice may delay diagnosis of neurological emergencies and increase cardiovascular risk.
  • This study evaluated LP safety without ADPra discontinuation.

Purpose of the Study:

  • To assess the safety of performing lumbar puncture (LP) without discontinuing adenosine-diphosphate receptor antagonists (ADPra).
  • To evaluate the incidence of complications, specifically traumatic taps, in patients undergoing LP while on ADPra.
  • To compare complication rates with control groups on aspirin or no antiplatelet therapy.

Main Methods:

  • Retrospective case series of patients undergoing LP with uninterrupted or briefly interrupted ADPra.
  • Medical records were reviewed for complications, with traumatic tap defined by cerebrospinal fluid red cell count ≥ 1000 cells/μL.
  • Incidence of traumatic tap was compared between patients on ADPra, aspirin, and no antiplatelet therapy.

Main Results:

  • 159 patients underwent LP under ADPra, with 116 procedures performed without interruption.
  • The incidence of traumatic tap was 5% in the ADPra group, 5.7% in the aspirin group, and 2.5% in the no antiplatelet group (P=0.35).
  • No spinal hematomas or neurological deficits were reported in any patient.

Conclusions:

  • Lumbar puncture can be safely performed without discontinuing adenosine-diphosphate receptor antagonists (ADPra).
  • These findings support a potential revision of current guidelines.
  • Further case series may provide additional evidence to support guideline changes.
Abstract

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