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      Factors for Hospitalizations and Neurologic Complications in Zika Virus Infection in the Department of Veterans Affairs (VA)

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          Abstract

          Background

          Zika virus (ZIKV) is an important flavivirus, but severity of infection is poorly described in adults. We investigated factors associated with hospitalization and neurologic complications as measures of severity.

          Methods

          ZIKV cases from December 1, 2015 to October 31, 2016 were identified from clinical samples tested in VA, state and commercial laboratories, and patients were followed until 3/31/2017. ZIKV positive patients (RT-PCR or screening IgM positive confirmed by a plaque-reduction neutralization test [PRNT] IgM positive for ZIKV alone or including dengue virus) were reviewed for demographic and clinical factors. Logistic regression analysis was performed to evaluate factors associated with 1) hospitalization and 2) neurologic complications in VA ZIKV positive patients.

          Results

          736 of 1,538 (48%) patients tested were ZIKV positive; 655 (89%) were male and 683 (93%) were diagnosed at the VA Caribbean Healthcare System (VACHCS). In total, 94 (13%) were hospitalized with 91 (12%) at VACHCS. 19 (3%) patients, all at VACHCS, died from any cause after ZIKV diagnosis. Hospitalization was more likely with increased age, co-morbidities, neurologic symptoms, thrombocytopenia, or preadmission glucocorticoid use, and less likely if rash was present (Table 1). Hospitalization, prior cerebrovascular disease and dementia were associated with neurologic complications.

          Conclusion

          Older Veterans with multiple comorbidities or presenting with neurologic symptoms were more likely to be hospitalized after ZIKV infection, and those with a prior history of cerebrovascular disease and dementia were at increased risk for neurological complications.

          Table 1. Factors associated with hospitalization and neurologic complications among Veterans with ZIKV infection, December 1, 2015–October 31, 2016.

          Hospitalization Factors OR adj 95% CI
          Age group (10 years) 1.3 1.0, 1.8
          Charlson co-morbidity index (age-adjusted) 1.2 1.1, 1.4
          Connective tissue disease 15.0 1.7, 130.7
          Congestive heart failure 4.9 1.8, 13.5
          Neurological symptoms 5.3 2.4, 11.7
          Thrombocytopenia (<155 platelets/μL) 4.7 2.2, 10.0
          Glucocorticoid use (within 30 days of ZIKV testing) 16.8 1.8, 157.0
          Rash 0.23 0.11, 0.47
          Neurologic complication factors
          Hospitalized 5.9 2.9, 12.2
          Cerebrovascular disease 4.9 1.7, 14.4
          Dementia 2.8 1.2, 6.6

          Oradj, adjusted odds ratio; CI , confidence interval.

          Disclosures

          All authors: No reported disclosures.

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          Author and article information

          Journal
          Open Forum Infect Dis
          Open Forum Infect Dis
          ofid
          Open Forum Infectious Diseases
          Oxford University Press (US )
          2328-8957
          Fall 2017
          04 October 2017
          04 October 2017
          : 4
          : Suppl 1 , ID Week 2017 Abstracts
          : S319
          Affiliations
          [1 ] Public Health Surveillance and Research, Department of Veterans Affairs , Palo Alto, California
          [2 ] Biostatistics and Epidemiology, University of Oklahoma Health Sciences Center , Oklahoma City, Oklahoma
          [3 ] Stanford University , Stanford, California
          [4 ] VA Caribbean Healthcare System , San Juan, Puerto Rico
          Author notes

          Session: 139. Adult Viral Infection

          Friday, October 6, 2017: 12:30 PM

          Article
          ofx163.750
          10.1093/ofid/ofx163.750
          5631974
          932cfd8b-29ae-4a3c-997b-b47336902a9b
          © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

          This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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