
Routine collection, analysis, publication, and interpretation of health data is a key part of public health surveillance (Brookmeyer and Stroup 2004), and the foundation for timely and effective public health interventions. With the emergence of a substantial literature documenting social inequalities in health across a wide range of diseases and environments, and national and international ethical concerns about potential health inequities (WHO Commission on Social Determinants of Health 2008), there is a pressing need to extend monitoring and surveillance systems to health inequalities.
Author(s): Sam Harper and Nicholas B. King
Volume 91, Issue 1
(pages 205–209)
DOI: 10.1111/milq.12009
Published in 2013