Bill Text: MN HF483 | 2013-2014 | 88th Legislature | Engrossed
Bill Title: Newborn screening required for critical heart disease.
Spectrum: Moderate Partisan Bill (Democrat 10-2)
Status: (Introduced - Dead) 2013-03-18 - Second reading [HF483 Detail]
Download: Minnesota-2013-HF483-Engrossed.html
1.2relating to health; requiring screening of newborns for critical congenital heart
1.3disease;proposing coding for new law in Minnesota Statutes, chapter 144.
1.4BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MINNESOTA:
1.5 Section 1. [144.1251] NEWBORN SCREENING FOR CRITICAL CONGENITAL
1.6HEART DISEASE (CCHD).
1.7 Subdivision 1. Required testing and reporting. Each licensed hospital or
1.8state-licensed birthing center or facility that provides maternity and newborn care services
1.9shall provide screening for congenital heart disease to all newborns prior to discharge
1.10using pulse oximetry screening. This screening should occur before discharge from the
1.11nursery, after the infant turns 24 hours of age. If discharge prior to 24 hours after birth
1.12occurs, screening should occur as close as possible to the time of discharge. Results of this
1.13screening must be reported to the Department of Health.
1.14For premature infants (less than 36 weeks of gestation) and infants admitted to a
1.15higher-level nursery (special care or intensive care), pulse oximetry should be performed
1.16when medically appropriate, but always prior to discharge.
1.17 Subd. 2. Implementation. The Department of Health shall:
1.18(1) communicate the screening protocol requirements;
1.19(2) make information and forms available to the persons with a duty to perform
1.20testing and reporting, health care providers, parents of newborns, and the public on
1.21screening and parental options;
1.22(3) provide training to ensure compliance with and appropriate implementation of
1.23the screening;
2.1(4) establish the mechanism for the required data collection and reporting of
2.2screening and follow-up diagnostic results to the Department of Health according to the
2.3Department of Health's recommendations;
2.4(5) coordinate the implementation of universal standardized screening;
2.5(6) act as a resource for providers as the screening program is implemented, and in
2.6consultation with the Advisory Committee on Heritable and Congenital Disorders, develop
2.7and implement policies for early medical and developmental intervention services and
2.8long-term follow-up services for children and their families identified with a CCHD; and
2.9(7) comply with sections 144.125 to 144.128.
1.3disease;proposing coding for new law in Minnesota Statutes, chapter 144.
1.4BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MINNESOTA:
1.5 Section 1. [144.1251] NEWBORN SCREENING FOR CRITICAL CONGENITAL
1.6HEART DISEASE (CCHD).
1.7 Subdivision 1. Required testing and reporting. Each licensed hospital or
1.8state-licensed birthing center or facility that provides maternity and newborn care services
1.9shall provide screening for congenital heart disease to all newborns prior to discharge
1.10using pulse oximetry screening. This screening should occur before discharge from the
1.11nursery, after the infant turns 24 hours of age. If discharge prior to 24 hours after birth
1.12occurs, screening should occur as close as possible to the time of discharge. Results of this
1.13screening must be reported to the Department of Health.
1.14For premature infants (less than 36 weeks of gestation) and infants admitted to a
1.15higher-level nursery (special care or intensive care), pulse oximetry should be performed
1.16when medically appropriate, but always prior to discharge.
1.17 Subd. 2. Implementation. The Department of Health shall:
1.18(1) communicate the screening protocol requirements;
1.19(2) make information and forms available to the persons with a duty to perform
1.20testing and reporting, health care providers, parents of newborns, and the public on
1.21screening and parental options;
1.22(3) provide training to ensure compliance with and appropriate implementation of
1.23the screening;
2.1(4) establish the mechanism for the required data collection and reporting of
2.2screening and follow-up diagnostic results to the Department of Health according to the
2.3Department of Health's recommendations;
2.4(5) coordinate the implementation of universal standardized screening;
2.5(6) act as a resource for providers as the screening program is implemented, and in
2.6consultation with the Advisory Committee on Heritable and Congenital Disorders, develop
2.7and implement policies for early medical and developmental intervention services and
2.8long-term follow-up services for children and their families identified with a CCHD; and
2.9(7) comply with sections 144.125 to 144.128.
