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Published on: June 23, 2020
Minimum inhibitory concentration changes in relapsed left ventricular assist device driveline infections
Tara H Lines1, Leah A Sabato1, Whitney J Nesbitt1
1Department of Pharmacy, Nashville, TN, USA.
Abstract:
Driveline infection is the most common infectious complication in patients with left ventricular assist devices. Minimum inhibitory concentration changes are not well described in relapsed driveline infections. This retrospective descriptive epidemiology study of patients with left ventricular assist device implantation between January 1, 2013, and August 1, 2017, who developed driveline infection with positive cultures aimed to describe minimum inhibitory concentration changes. Of the 330 patients underwent left ventricular assist device implantation, 30 (9%) met criteria for driveline infection. Median duration of follow-up was 26 months (interquartile range 16, 39) and time to first driveline infection was 171 days (interquartile range 83, 403). There were 74 driveline infections: 40 new and 34 relapsed. Staphylococcus aureus was most common in new and relapsed driveline infection. Thirteen patients comprised the 34 relapsed infections, 9 of which experienced a minimum inhibitory concentration change. Median time to first minimum inhibitory concentration change was 56 days (interquartile range 36-88), and type of minimum inhibitory concentration change was an increase in five cases, decrease in two cases, and both increase and decrease in two cases. Minimum inhibitory concentration changes did not result in resistance in S. aureus but did in Pseudomonas aeruginosa and Mycobacterium fortuitum relapsed driveline infection. Time to first relapse from initial infection was longer in those who received suppressive therapy, 60 days versus 83 days, p = 0.047. Relapsed driveline infections were most common with S. aureus. Minimum inhibitory concentration changes were quite variable and may not be the major contributor to relapsed infection in gram-positive driveline infection.
Insights
Minimum inhibitory concentration changes in relapsed driveline infections after left ventricular assist device implantation are variable. These changes did not always lead to resistance, suggesting other factors contribute to recurrent infections.
Area of Science:
- Cardiology
- Infectious Diseases
- Medical Device Technology
Background:
- Driveline infection is a frequent complication in patients with left ventricular assist devices (LVADs).
- Understanding minimum inhibitory concentration (MIC) changes in relapsed driveline infections is crucial for effective management.
- Limited data exists on MIC variability in recurrent LVAD driveline infections.
Purpose of the Study:
- To describe minimum inhibitory concentration (MIC) changes in patients with LVADs who experienced relapsed driveline infections.
- To investigate the relationship between MIC changes and the development of resistance in relapsed infections.
- To identify factors associated with relapsed driveline infections.
Main Methods:
- Retrospective descriptive epidemiology study.
- Analysis of patients with LVAD implantation between January 1, 2013, and August 1, 2017, who developed driveline infection with positive cultures.
- Evaluation of MIC changes in relapsed driveline infections, particularly focusing on Staphylococcus aureus, Pseudomonas aeruginosa, and Mycobacterium fortuitum.
Main Results:
- Out of 330 LVAD patients, 30 developed driveline infection, with 34 relapsed infections observed.
- Staphylococcus aureus was the most common pathogen in both new and relapsed driveline infections.
- Nine of 13 patients with relapsed infections showed MIC changes; these changes did not cause resistance in S. aureus but did in Pseudomonas aeruginosa and Mycobacterium fortuitum.
Conclusions:
- Minimum inhibitory concentration (MIC) changes in relapsed driveline infections are variable and may not be the primary driver of recurrence in gram-positive infections.
- Suppressive therapy may be associated with a longer time to first relapse.
- Further research is needed to fully elucidate the mechanisms behind relapsed driveline infections in LVAD patients.
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