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

Chen Yuan Chiang, P. Glaziou, D. A. Enarson, F. Cobelens, W. J. Lew

Research output: Contribution to journalArticle

1 Citation (Scopus)

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.

Original languageEnglish
Pages (from-to)27-31
Number of pages5
JournalInternational Journal of Tuberculosis and Lung Disease
Volume13
Issue number1
Publication statusPublished - Jan 2009
Externally publishedYes

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Keywords

  • Patient rights
  • Prevalence survey
  • Quality assurance
  • Safety

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Infectious Diseases

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