Selected article for: "informed consent give and study participate"

Author: Andrews, Denise; Chetty, Yumela; Cooper, Ben S.; Virk, Manjinder; Glass, Stephen K; Letters, Andrew; Kelly, Philip A.; Sudhanva, Malur; Jeyaratnam, Dakshika
Title: Multiplex PCR point of care testing versus routine, laboratory-based testing in the treatment of adults with respiratory tract infections: a quasi-randomised study assessing impact on length of stay and antimicrobial use
  • Document date: 2017_10_10
  • ID: 1sdt9zz8_16
    Snippet: The inclusion criteria were that patients were ≥16 years of age, with mental capacity to give written informed consent and presenting with URTI/ILI defined as symptoms including fever or feeling feverish (chills), cough, sore throat, runny or stuffy nose, muscle-aches or body-aches, headaches, fatigue (tiredness) and possibly vomiting or diarrhoea [13] +/− LRTI. Patients who did not meet inclusion criteria or with evidence or suspicion of bac.....
    Document: The inclusion criteria were that patients were ≥16 years of age, with mental capacity to give written informed consent and presenting with URTI/ILI defined as symptoms including fever or feeling feverish (chills), cough, sore throat, runny or stuffy nose, muscle-aches or body-aches, headaches, fatigue (tiredness) and possibly vomiting or diarrhoea [13] +/− LRTI. Patients who did not meet inclusion criteria or with evidence or suspicion of bacterial infection affecting sites other than the respiratory tract were excluded from the opportunity to participate in the study. Patients who requested withdrawal from the study were excluded from the analysis.

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