This rule prescribes the procedures that apply if, upon
screening of a specimen, the bureau of public health laboratory determines that
the result indicates potential risk for one or more of the screened
disorders.
(A) The
director
shall
will
communicate the results to the following
person, as applicable:
(1) If a child was born in a hospital or
freestanding birthing center, the director shall
will
communicate the results to the child's attending physician, child's primary
medical provider, pediatrician, certified nurse midwife, certified nurse
practitioner or clinical nurse specialist. If the director is unable to contact
the attending physician, child's primary medical provider, pediatrician,
certified nurse midwife, certified nurse practitioner or clinical nurse
specialist, the director shall
will communicate the results to the newborn
screening coordinator at the facility where the child was born.
(2) If the child was not born in a
hospital
or
freestanding birthing center, the
director shall
will
communicate the results to the
person designated in paragraph (A)(2) or (A)(3)
of rule
3701-55-05 of the Administrative
Code, as applicable.
(B)
The
person notified of the results by the
director under paragraph (A) of this
rule
shall
will communicate the results to the child's parent,
legal guardian, or legal custodian and
shall
will obtain and
submit a repeat blood specimen for screening or diagnostic testing in
accordance with the following procedures:
(1)
When the result indicates potential risk for a disorder listed in
paragraphs
paragraph (A)
(1) to
(A)(36) of rule
3701-55-02 of the Administrative
Code, a screening or diagnostic test
shall
will be obtained in accordance with paragraph
(B)(3) of this rule as soon as possible, but no later than ten days after
notification by the
director.
(2)
When the results are abnormal for a hemoglobin disease or hemoglobin trait, a
diagnostic test shall
will be obtained in accordance with paragraph
(B)(3) of this rule before the child reaches two months of age.
(3) Diagnostic specimens obtained under
paragraphs (B)(1) and (B)(2) of this rule
shall
will be
submitted for testing to a laboratory certified under the
current version Clinical Laboratory Improvement
Act, 42 USC
263a
as amended
January 24, 2004, that reports results with normal pediatric reference
ranges. That laboratory
shall
will promptly transmit the results of the
diagnostic test to the
person who submitted the specimen.
(C) If after ten business days, the
person
responsible for obtaining and submitting the
repeat specimen and/or diagnostic
tests under paragraph (B) of this rule is unable to obtain a specimen from a
newborn child with an initial screen result of a potential risk despite making
a reasonable effort, he or she
shall
will notify the
health commissioner of the
health
district in which the mother, legal guardian, or legal custodian resides.
The health commissioner shall
will make a
reasonable effort to locate the child and cause a second
repeat
specimen and/or diagnostic tests to be obtained.
If the health commissioner is not able to locate that child within thirty days,
he or she may close the file.
(D) The health commissioner
shall
will
submit a report to the director, upon case closure, listing the names and other
identifiers of newborns the health commissioner was unable to locate.
Notes
Ohio Admin. Code
3701-55-07
Effective:
7/1/2023
Five Year Review (FYR) Dates:
2/27/2023 and
05/05/2028
Promulgated
Under: 119.03
Statutory
Authority: 3701.501
Rule
Amplifies: 3701.501
Prior
Effective Dates: 02/15/1999, 03/17/2003 (Emer.), 06/15/2003, 08/16/2004,
02/13/2009, 02/13/2014