Current through Register Vol. XLI, No. 45, November 8, 2024
Section 64-7-11 - Electronic Laboratory Reporting11.1. Laboratories participating in WVHIN shall report laboratory data to WVHIN by HL-7 messaging. Until the laboratory is designated by the bureau as a validated submitter, the laboratory shall submit laboratory reports to the Bureau by paper in the time frame required. When the laboratory is designated as a validated submitter by the Commissioner, the laboratory may substitute electronic reporting to WVHIN or WVEDSS through HL-7 in real time for the required paper reporting. When the laboratory is designated a validated submitter they shall report the conditions listed in this subsection through a real time electronic feed. These conditions are in addition to conditions reportable in this rule. Reports from laboratories shall include the patient's name, address, telephone number, date of birth, sex, race and ethnicity; the name of the person or agency submitting the specimen for testing; the specimen source and date of specimen collection; the date of result, name of the test, test result, normal value or range; and the name, address, phone and fax number of the laboratory. Conditions to be reported include: 11.1.a. Adenovirus, laboratory evidence of acute infection;11.1.b. Enterovirus (non-polio), laboratory evidence of acute infection;11.1.c. Human metapneumovirus, laboratory evidence of acute infection;11.1.d. Influenza, laboratory evidence of acute infection, including type and subtype, as available;11.1.e. Parainfluenza virus, laboratory evidence of acute infection;11.1.f. Respiratory syncitial virus, laboratory evidence of acute infection; and11.1.g. Rotavirus, laboratory evidence of acute infection.