Supplemental Bibliography

  • book and penAlassia LN, Benítez S, Luna DR, Bernaldo de Quiros FG. Validating the Access to an Electronic Health Record: Classification and Content Analysis of Access Logs. In Sarkar IN, Georgiou A, Mazzoncini de Azevedo Marques P., eds., Studies in Health Technology and Informatics, Vol. 216: MEDINFO 2015: eHealth-enabled Health, 2015, pp. 3-6. Available at; accessed 1 June 2020.
  • Caires B, Lopes MC, Vancini Campanaro CR, Batista R. Knowledge of Healthcare Professionals About Rights of Patient’s Images. Einstein (São Paulo). 2015;13(2): 255-259. Available at; accessed 2 June 2020.
  • De Castro P, Marsili D, Poltronieri E, Calderon C. Dissemination of Public Health Information: Key Tools Utilized by the NECOBELAC Network in Europe and Latin America. Health Information and Library Journals. 2012; 29(2): 119-130. Available at:; accessed 2 June 2020.
  • Gomez Cordoba A. Informed Consent for Genetic Information Management in Colombian Law. Revista Derecho Genoma Humano. 2011;35: 183-223. Available at:; accessed 2 June 2020. 
  • Mc Naughton H, Hernandez E, Mitchell E, Padilla K, Blandon M. Patient Privacy and Conflicting Legal and Ethical Obligations in El Salvador: Reporting of Unlawful Abortions. American Journal of Public Health. 2006;96(11): 1927-1933. Available at:; accessed 2 June 2020. 
  • Sanchez Henarejos,A, Fernandez Aleman,J, Toval A, Hernandez I et al,. A guide to Good Practice for Information Security in the Handling of Personal Health Data by Health Personnel in Ambulatory Care Facilities. Atención Primaria. 2014;46(4): 214-222. Available at:; accessed 2 June 2020.