Clinical analysis and treatment of symptomatic intracranial hemorrhage after deep brain stimulation surgery

Xin Wang1, Jing Wang1, Haikang Zhao2

  • 1a Department of Neurosurgery , Tangdu Hospital, Fourth Military Medical University , Xi'an , China.

Insights

Symptomatic intracranial hemorrhage (ICH) after deep brain stimulation (DBS) surgery is a rare but serious complication. Early identification and effective treatment are crucial for preserving DBS leads and limiting neurological deficits.

Area of Science:

  • Neurosurgery
  • Neurology

Background:

  • Symptomatic intracranial hemorrhage (ICH) is a significant risk associated with deep brain stimulation (DBS) surgery, potentially causing permanent neurological disability.
  • The clinical application of DBS is hindered by the risk of ICH, necessitating research into its incidence, prevention, and management.

Purpose of the Study:

  • To investigate the incidence, clinical characteristics, and outcomes of symptomatic intracranial hemorrhage (ICH) following deep brain stimulation (DBS) surgery.
  • To inform strategies for the prevention and effective treatment of ICH in DBS patients.

Main Methods:

  • Retrospective analysis of 396 patients undergoing DBS with 691 leads from January 2009 to December 2014.
  • Detailed examination of 10 patients who experienced symptomatic ICH, including clinical data, imaging, and treatment outcomes.

Main Results:

  • Ten patients (2.5% of total) developed symptomatic ICH, with 7 cases occurring around implanted electrodes.
  • Hemorrhage typically occurred within 24 hours post-surgery, often in the frontal lobe, with some cases presenting with seizures.
  • Conservative management was effective for most patients; all electrodes were preserved, and neurological function improved, leading to successful Parkinson's disease symptom relief in nine patients.

Conclusions:

  • Prompt identification and management of symptomatic ICH are vital after DBS implantation.
  • Effective treatment strategies can limit neurological deficits and ensure the preservation of DBS leads for continued therapeutic benefit.
Abstract

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