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Written informed consent was obtained from the patients or, for patients unable to provide consent, from their closest relatives.
Informed consent was obtained either from the patients or, when deemed incompetent to provide consent, from their next of kin.
Informed consent to examine resident documentation at the facility and collect outcome data will be obtained from the residents themselves, or if they are unable to provide consent, from their family or guardian.
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Written informed consent was obtained from adults who were competent to provide consent and from the parents or legal guardians of children and adults with cognitive impairment.
Students who were unwilling to participate in the study, or did not wish to provide consent, were excluded from the recruitment process.
Pregnant women presenting with features of chorioamnionitis (i.e. foul smelling lochia, uterine tenderness associated with fever) allergies to the antibiotics used in the study, or those who had used antibiotics in the 24 hours preceding the operation or unconscious patients who could not provide consent were excluded from the study.
For the woman and her baby, consent to enrol in the project will provide consent to access information from the maternal and neonatal clinical records.
Written informed consent was obtained from each patient; if patients were unable to provide consent, written consent was obtained from their attendant.
Written informed consent was obtained from parents/guardians providing consent for offspring up to age 16 years, with offspring providing consent thereafter.
In the most severe patients who were unable to provide consent, written consent was obtained from the patient's family.
For 916 (40.1%) students, either the student him/herself or his/her guardians did not provide consent and they were omitted from the sample.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com