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Reactivation of Cytomegalovirus Following Left Ventricular Assist Device Implantation: A Case-Control Study
Scott W Lundgren1, Diana F Florescu2, Ronald Zolty1
1From the Department of Internal Medicine, Division of Cardiology, University of Nebraska Medical Center, Omaha, NE.
Insights
Cytomegalovirus (CMV) reactivation after left ventricular assist device (LVAD) implantation is more common than previously thought. Early detection and treatment in at-risk patients may improve outcomes.
Area of Science:
- Infectious Diseases
- Cardiology
- Critical Care Medicine
Background:
- Cytomegalovirus (CMV) reactivation is known to occur in critically ill patients, but its incidence post-left ventricular assist device (LVAD) implantation is poorly documented.
- Left ventricular assist devices (LVADs) are crucial for end-stage heart failure management, but potential complications like viral reactivation require investigation.
Purpose of the Study:
- To determine the incidence of cytomegalovirus (CMV) reactivation in patients following left ventricular assist device (LVAD) implantation.
- To identify risk factors associated with CMV reactivation in the post-LVAD population.
Main Methods:
- Retrospective chart review of 349 patients who underwent LVAD implantation between 2004 and 2018.
- Matched case-control study (1:2) comparing patients with CMV reactivation to those without.
- Statistical analyses included Fisher's exact test, paired sample t-tests, and Kaplan-Meier survival analysis.
Main Results:
- CMV reactivation occurred in 3.8% (8/208) of CMV-seropositive patients post-LVAD implantation, with a median time to reactivation of 21.5 days.
- Patients with CMV reactivation had higher creatinine, elevated Red Cell Distribution Width (RDW), recent steroid use, and concurrent bacterial infections compared to controls.
- The study identified CMV viremia in 75% of cases; others presented with colitis or pneumonia without viremia.
Conclusions:
- CMV reactivation following LVAD implantation is more frequent than anticipated.
- Risk factors for CMV reactivation include renal failure, steroid use, elevated RDW, and concurrent bacterial infections.
- Prompt testing, diagnosis, and treatment for CMV in at-risk LVAD patients may enhance clinical outcomes.
Abstract:
While cytomegalovirus (CMV) reactivation occurs in immunocompetent patients who are critically ill and has been associated with worse outcomes, very few cases of CMV reactivation have been reported following left ventricular assist device (LVAD) implantation. We aimed to evaluate the incidence and risk factors for CMV reactivation following LVAD implantation. Retrospective chart review of patients who had undergone LVAD implantation between July 2004 and December 2018 was performed. Cases with CMV reactivation post-LVAD were randomly matched (1:2) by sex, LVAD type, and implant year with controls utilizing SAS macros. Fisher's exact and paired sample t-tests were performed to evaluate for differences between categorical and continuous variables, respectively. Days to reactivation post-LVAD implantation were calculated in cases, and the corresponding times post-LVAD implantation were determined in control patients for variable comparisons. Survival analysis was performed using the Kaplan-Meier method. Of the 349 patients reviewed, 208 (59.6%) patients were seropositive for CMV before LVAD implantation. Of these 208 patients, eight (3.8%) had CMV reactivation following LVAD implantation. The median time to CMV reactivation following LVAD implantation was 21.5 days (range, 6-177). Six (75%) patients had CMV viremia, and the other two had colitis and pneumonia without viremia. In comparison to controls, patients with CMV had higher creatinine levels (p = 0.039) and higher RDW (p = 0.05) and were more likely to have received steroids within the previous week (p = 0.028) and to have concurrent bacterial infection (p = 0.001). CMV reactivation following LVAD implantation is more frequent than expected. Early testing, diagnosis, and treatment in at-risk patients (i.e., renal failure, steroid use, elevated RDW) might improve clinical outcomes.
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