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Exact(5)
Women bearing abnormal fetuses were not consented for study.
Subjects were not consented for release to public databases.
Participants in HUFS and NHAAN were not consented for wide data release (such as in a publicly-available database), but data can be made available for collaborative research.
However, for many cohorts, especially those developed before the advent of the genomics era, participants were not consented for open access of genome-wide data.
The reasons that 19 patients were not consented for the study ranged from medical deterioration (3) or improvement (1), preference for standard exercise (4), feeling that the study was not of interest or too burdensome (6), and follow-up and communication difficulties with study coordinator (5).
Similar(55)
The stigmatisation of people living with HIV is a reason for not consenting for screening.
Patients who were not responsible for their own medication taking (i.e. relied on a carer) or could not consent for themselves were not eligible to participate.
Specific guidelines, however, have been developed that describe how HPs can share information with relatives without breaking confidentiality or even when service users do not consent for information to be shared [ 60– 63].
Patients who receive treatment on an outpatient basis during the intensive phase and those who do not consent for HIV screening are more likely to interrupt their antituberculosis treatment.
Acceptance of a compliment is not consent for entering into my personal space.
Patients were excluded if they had a history of prior treatment for tuberculosis, did not consent for HIV testing, were less than 18 years of age and had clinical evidence of liver damage prior to starting medication.
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