A method for processing initial measured values A(n) corresponding to results of biological analyses of the same patient from one or more laboratories, said analyses each relating to the same biological parameter, the method comprising:
- a) using for each initial value A(n), measured and expressed by a given laboratory according to a unit of measurement proposed by said laboratory and a normal range (BI(n), BS(n)), provided by the same laboratory, materialised by a range delimited between a lower bound BI(n) and an upper bound BS(n), or by a range lower than the upper bound BS(n) only, or by a range higher than the lower bound BI(n) only;
- b) recording data, encrypted or not, sent by a messaging system, advantageously secure, for consolidation on a server, advantageously secure, according to a format determined based on heterogeneous presentations specific to each of these laboratories, this format further comprising the measured value A(n), metadata attached to it indicating the corresponding normal range and, opportunely, a certain number of data relating in particular to the corresponding laboratory, specifically to the conditions for carrying out the examination and/or analysis and indications on the identity of the patient and/or that of the prescriber;
- c) using at least one mathematical model, with or without the aid of computer processing, to transform each of the initial values A(n) obtained from each laboratory into a normalised value Anorm(n), a single laboratory is capable of providing several initial values A(n) over time for the same patient;
- d) associating with all these normalised values Anorm(n), the common normalised normal range (BInorm, BSnorm) determined, said range being defined by a common simple normalised lower bound BInorm or by a common simple normalised upper bound BSnorm or by a common normalised upper bound BSnorm associated with a common homogenised lower bound BInorm, knowing that the normal ranges (BI(n),BS(n)) or the values BI(n) and/or BS(n) provided by the same laboratory may vary over time;
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- e) subsequently proposing, by a method of chronological or synthetic graphic representation appropriate to the user and/or to the user and/or to the data medium, a display comprising the successive different normalised values Anorm(n) for the given biological parameter in combination with at least one element of data, visible, permanent or ephemeral, but always accessible, relating to the common normalised normal range (BInorm,BSnorm) adopted.