Fla. Admin. Code Ann. R. 64D-3.042 - STD Testing Related to Pregnancy
(1)
Practitioners attending a woman for prenatal care shall cause the woman to be
tested for chlamydia, gonorrhea, hepatitis B, HIV and syphilis as follows:
(a) At initial examination related to her
current pregnancy; and again.
(b)
At 28 to 32 weeks gestation.
(2) Exceptions to the testing outlined in
subsection (1), above, are as follows:
(a) A
woman, who tested positive for hepatitis B surface antigen (HbsAg) during the
initial examination related to her current pregnancy, need not be re-tested at
28-32 weeks gestation.
(b) A woman,
with documentation of HIV infection or AIDS need not be re-tested during the
current pregnancy.
(3)
Women who appear at delivery or within 30 days postpartum with:
(a) No record of prenatal care, or
(b) Prenatal care with no record of
testing;
(c) Prenatal care with no
record of testing after the 27th week of gestation shall be considered at a
high risk for sexually transmissible diseases and shall be tested for hepatitis
B surface antigen (HBsAg), HIV and syphilis prior to
discharge.
(4) Emergency
Departments of hospitals licensed under Chapter 395, F.S., may satisfy the
testing requirements under this rule by referring any woman identified as not
receiving prenatal care after the 12th week of gestation, to the county health
department.
(a) The referral shall be in
writing; and,
(b) A copy shall be
submitted to the county health department having jurisdiction over the area in
which the emergency department is located.
(5) Prior to any testing required by this
rule, practitioners shall:
(a) Notify the
woman which tests will be conducted;
(b) Inform the woman of her right to refuse
any or all tests;
(c) Place a
written statement of objection signed by the woman each time she refuses
required testing in her medical record specifying which tests were refused. If
the woman refuses to sign the statement, the provider shall document the
refusal in the medical record. No testing shall occur for the infections
specified in the refusal statement of objection.
(6) Women who had a serologic test for
syphilis during pregnancy that was reactive, regardless of subsequent tests
that were non-reactive shall be tested as soon as possible at or following
delivery.
(7)
(a) Specimens shall be submitted to a
laboratory certified by the Centers for Medicare and Medicaid Services under
the federal Clinical Laboratory Improvement Amendments and the federal rules
adopted thereunder to perform tests for chlamydia, gonorrhea, hepatitis B
surface antigen (HBsAg), HIV and syphilis.
(b) The practitioner submitting the specimens
for testing to a certified laboratory shall state that these specimens are from
a pregnant or postpartum woman.
(8) Practitioners required by law to prepare
birth and stillbirth certificates shall document on the certificate if
chlamydia, gonorrhea, hepatitis B, HIV, syphilis infections or genital herpes
or genital human papilloma virus were present and/or treated during this
pregnancy.
(9) Nothing in this rule
shall prohibit a practitioner from testing these women for other sexually
transmissible diseases in accordance to prevailing national standards,
community disease distribution or the professional judgment of the
practitioner.
Notes
Rulemaking Authority 381.003(2), 384.25, 384.33 FS. Law Implemented 381.0011, 381.003(1)(c), 381.004(3), 384.31 FS.
New 11-20-06, Amended 3-9-20.
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