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Prior to inclusion in the trial, roughly 27% of patients in both the oral and IV groups had prosthetic heart valves and 7.5% in the IV group and 10% in the oral group had pacemakers.3 Patients were included once they were determined to be clinically stable (defined as a temperature <38°C for >2 days, C-reactive protein ≤25% of peak level, white cell count <15 x 109/L).
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  • Healthcare 75.00%
    • Hospitals, doctors and medical care 100.00%
  • Science and technology 25.00%

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