P-9.0001 - Act respecting the sharing of certain health information

Section 29 Disposition versions

2013-06-20

29. The laboratory domain is made up of the following health information, if available:

(1)  the unique user identification number of the person concerned;

(2)  the sex and body weight of the person concerned;

(3)  the date on which the prescription was written or an analysis was requested;

(4)  the nature of the analysis;

(5)  the category of the analysis;

(6)  the measuring method used;

(7)  the type of specimen or the anatomical site;

(8)  the priority code for the analysis;

(9)  the identification code for the analysis;

(10)  the clinical information accompanying the prescription or the request for an analysis;

(11)  the name and unique provider number of the health professional who wrote the prescription or requested the analysis or, if the health professional has no such number, the number of the health professional’s licence to practise;

(12)  the name and unique identification number of the location where services are provided and where the health professional who wrote the prescription or requested the analysis practises;

(13)  the name, address, telephone number and unique identification number of the location where services are provided and where the biological specimen was collected;

(14)  the name, address, telephone number and unique identification number of the location where services are provided and where the biological specimen was analyzed;

(15)  the dates and times when the biological specimen was collected and analyzed;

(16)  the date and time when the biological specimen was received at the location where services are provided and where the biological specimen was analyzed;

(17)  the clinical information accompanying the biological specimen;

(18)  the registration number of the request for an analysis;

(19)  the date, time and processing status of the request for an analysis;

(20)  the date, time and status of the results of the analysis;

(21)  the results of the analysis;

(22)  the clinical information accompanying the results;

(23)  the categorization of analysis and laboratory examination results for a given prescription or request for analysis;

(24)  the clinical information accompanying the categorization of results;

(25)  the information shown in the report;

(26)  the clinical information accompanying the report;

(27)  the abnormality indicator;

(28)  the reference values; and

(29)  any other information prescribed by regulation of the Government.

2012, c. 23, s. 29.