Sec. 10.18.02.01. Scope  


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  • A. This chapter establishes the requirements for:

    (1) Physician reporting of a:

    (a) Case of human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS); and

    (b) Birth of an infant whose mother has tested positive for HIV;

    (2) Institution reporting of a case of HIV or AIDS;

    (3) Laboratory reporting of a test result for:

    (a) HIV detection;

    (b) HIV viral load;

    (c) CD4+ cell count or percentage; or

    (d) HIV genotype sequence; and

    (4) Follow-up of:

    (a) A physician's report of HIV or AIDS;

    (b) A physician's report of an infant whose mother has tested positive for HIV;

    (c) An institution's report of HIV or AIDS; and

    (d) A laboratory’s report of a test result for:

    (i) HIV detection;

    (ii) HIV viral load;

    (iii) CD4+ cell count or percentage; or

    (iv) HIV genotype sequence infection or CD4+ count.

    B. Except as noted in §C of this regulation, this chapter applies to all instances of laboratory testing of specimens from a human body for:

    (1) HIV detection;

    (2) HIV viral load;

    (3) CD4+ cell count or percentage; or

    (4) HIV genotype sequence.

    C. This chapter does not apply if the specimen from a human body is:

    (1) Not tested for:

    (a) HIV detection;

    (b) HIV viral load;

    (c) CD4+ cell count or percentage; or

    (d) HIV genotype sequence;

    (2) Tested for HIV detection solely for the purpose of determining the suitability of the source individual as a prospective donor of blood, semen, or tissue;

    (3) Taken from a patient at a designated anonymous HIV test site solely for the purpose of performing an anonymous HIV test;

    (4) Tested for HIV detection as part of research conducted by an institution within Maryland under the following conditions:

    (a) All personal identifiers are removed from the specimen before testing;

    (b) The specimen cannot be linked to the individual from whom the specimen was taken;

    (c) The result cannot be linked to the individual from whom the specimen was taken; and

    (d) The research protocol has been approved by an institutional review board;

    (5) Tested for HIV detection as part of research conducted under a research protocol approved by an institutional review board of an institution located outside of Maryland;

    (6) Taken from a patient known to reside outside of the United States; or

    (7) Tested for HIV detection as part of a research project that has been approved under Regulation .02 of this chapter for an exemption.