Protecting patients' rights, ensuring safety and quality assurance in tuberculosis prevalence surveys

Int J Tuberc Lung Dis. 2009 Jan;13(1):27-31.

Abstract

The conduct of biomedical studies is guided by statements of internationally recognised principles of human rights. The first principle of the Nuremberg Code was the centrality of voluntary participation of subjects with informed consent. All prevalence surveys should be reviewed by the appropriate ethics review committees. Each potential survey participant should be adequately informed of the aims, methods and sources of funding of the survey, any possible conflicts of interest, the institutional affiliations of the researchers, the anticipated benefits and potential risks of the study, and any discomfort it may entail. Attention should be paid to safety in each component of the survey. Test procedures that require particular attention are chest radiography (CXR) and bacteriological examination. Quality assurance should be applied to all aspects of research and, in particular, to any measurements undertaken, including CXR assessments, laboratory examinations and questionnaire and data management. Furthermore, to ensure comparability of data from different surveys, it is important to apply the same survey design and methodology and to use the same reporting format.

MeSH terms

  • Confidentiality
  • Health Surveys*
  • Humans
  • Patient Rights
  • Prevalence
  • Quality Assurance, Health Care
  • Tuberculosis / epidemiology*