Mich. Admin. Code R. 325.9082 - Reportable information
Rule 2.
(1)
Reportable information pertains to the analysis of blood samples submitted to
clinical laboratories and the results from portable blood lead
analyzers.
(2) Upon initiating a
request for blood lead analysis, the physician/provider or user ordering the
blood lead analysis shall collect the following information:
(a) All of the following information with
respect to the individual tested:
(i)
Name.
(ii) Sex.
(iii) The individuals ethnic
origin.
(iv) The individuals
race.
(v) Birthdate.
(vi) Address, including county.
(vii) Telephone number.
(viii) Social security number and Medicaid
number, if applicable.
(ix) If the
individual is a minor, the name of a parent or guardian.
(x) If the individual is an adult, the name
of his or her employer.
(xi) A
secondary contact for the individual tested or, if the individual is a minor, a
secondary contact for the individuals parent or guardian, including, to the
extent available, name and phone number of the secondary contact.
(b) The date of the sample
collection.
(c) The type of sample,
either capillary or venous.
(d) The
physicians/providers or users name, name of practice or agency, if applicable,
telephone number, fax number, email address, and mailing address.
(3) The information collected in
subrule (2) of this rule must be submitted with the sample for analysis to a
clinical laboratory that performs blood lead analysis or a user of a portable
blood lead analyzer.
(4) Upon
receipt of the blood sample for lead analysis, the clinical laboratory or user
of a portable blood lead analyzer shall collect the following additional
information:
(a) The name, address, and phone
number of the laboratory or testing entity.
(b) The date of analysis.
(c) The specimen number.
(d) The results of the blood lead analysis in
micrograms of lead per deciliter of whole blood. If the result is below the
limit of detection, report as less than the laboratorys limit of detection for
that analytical procedure.
Notes
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