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Epidemiology of device-associated infections related to a long-term implantable vascular access device

M J Sotir1, C Lewis, E W Bisher

  • 1Department of Medicine, Emory University School of Medicine, Atlanta, GA 30303, USA.

Insights

Approximately 25% of patients with implantable vascular access devices developed bloodstream infections (BSIs). The overall BSI rate was low, but varied by underlying illness, highlighting the need for targeted prevention strategies for device-associated infections.

Area of Science:

  • Infectious Diseases
  • Medical Devices
  • Epidemiology

Background:

  • Implantable vascular access devices are crucial for long-term patient care.
  • Device-associated infections pose a significant risk, particularly in immunocompromised populations.
  • Understanding infection incidence and risk factors is vital for patient safety.

Purpose of the Study:

  • To determine the incidence of device-associated infections in patients with implantable venous access devices.
  • To identify risk factors associated with these infections.
  • To analyze infection rates based on underlying patient conditions.

Main Methods:

  • A retrospective cohort study was conducted at Grady Health System.
  • 123 patients receiving PAS-Port implantable venous access devices were followed for over one year.
  • Data on bloodstream infections (BSIs) and patient demographics were collected and analyzed.

Main Results:

  • Twenty-five percent (31/123) of patients developed a primary or device-associated BSI.
  • The overall infection rate was 1.23 primary BSIs per 1,000 device days.
  • Infection rates were higher in patients with HIV infection compared to those with malignancy, though not statistically significant. Gram-positive pathogens were most common.

Conclusions:

  • A substantial proportion of patients experienced BSIs, despite a relatively low overall infection rate per device day.
  • Infection rates varied significantly based on the patient's underlying illness.
  • Further research into specific risk factors and targeted prevention for device-associated infections is warranted.
Abstract

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