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The Origin of Information: Registers and Health Information Systems

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Abstract

Let us go back to Chap. 1 and in particular to Sect. 1.2 and have another look at the Register of Consultations of a Commune Health Station. In order to explain the basic ideas we reproduce below, as Table 11.1, a very simplified version of a page of this register. The columns “Insured or free of charge”, “Profession”, “Ethnicity”, “Place of treatment”, “Person consulted” and “Remarks” were omitted and others modified; in particular the entries for “symptoms” and “treatments” were drastically shortened.

This lesson describes permanent sources of data and of epidemiologic indicators that are derived from data, in contrast to non-permanent data collection organized for a particular purpose within a particular study. It starts with a section on the underlying basic concepts.

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Krickeberg, K., Van Trong, P., Thi My Hanh, P. (2019). The Origin of Information: Registers and Health Information Systems. In: Epidemiology. Statistics for Biology and Health. Springer, Cham. https://doi.org/10.1007/978-3-030-16368-6_11

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