Bill Text: NY S07345 | 2017-2018 | General Assembly | Introduced
Bill Title: Requires healthcare practitioners to provide a written or an alternative format of up to date and evidence based information on Down syndrome to pregnant women and parents of infants who test positive for Down syndrome.
Spectrum: Partisan Bill (Republican 2-0)
Status: (Introduced - Dead) 2018-06-20 - COMMITTED TO RULES [S07345 Detail]
Download: New_York-2017-S07345-Introduced.html
STATE OF NEW YORK ________________________________________________________________________ 7345 IN SENATE January 8, 2018 ___________ Introduced by Sen. ORTT -- read twice and ordered printed, and when printed to be committed to the Committee on Mental Health and Develop- mental Disabilities AN ACT to amend the mental hygiene law, in relation to Down syndrome diagnosis awareness The People of the State of New York, represented in Senate and Assem- bly, do enact as follows: 1 Section 1. The mental hygiene law is amended by adding a new section 2 13.43 to read as follows: 3 § 13.43 Down syndrome diagnosis awareness. 4 (a) For purposes of this section, the following terms shall have the 5 following meanings: 6 (1) "Health care practitioner" means a medical professional that 7 provides prenatal or postnatal care and administers or requests adminis- 8 tration of a diagnostic or screening test to a pregnant woman or infant 9 that detects for Down syndrome; and 10 (2) "Down syndrome" means a chromosomal condition caused by an error 11 in cell division that results in the presence of an extra or partial 12 copy of chromosome twenty-one. 13 (b) A health care practitioner who orders tests for a pregnant woman 14 or infant to screen for Down syndrome shall provide the following infor- 15 mation to such pregnant woman or the infant's parent if such test 16 reveals a positive result: 17 (1) Up-to-date and evidence-based information about Down syndrome that 18 has been reviewed by medical experts and national Down syndrome organ- 19 izations. The information must be provided in a written or an alterna- 20 tive format and must include the following: 21 (i) expected physical, developmental, educational, and psychosocial 22 outcomes; 23 (ii) life expectancy; 24 (iii) the clinical course description; 25 (iv) expected intellectual and functional development; 26 (v) treatment options available for the particular syndrome for which 27 the test was positive; and EXPLANATION--Matter in italics (underscored) is new; matter in brackets [] is old law to be omitted. LBD14126-02-8S. 7345 2 1 (vi) any other information the office deems necessary. 2 (2) Contact information for nonprofit organizations that provide 3 information and support services for Down syndrome including but not 4 limited to: 5 (i) information hotlines specific to Down syndrome; 6 (ii) relevant resource centers or clearinghouses; and 7 (iii) national and local Down syndrome organizations. 8 (c) (1) The commissioner shall provide written information to health 9 care practitioners necessary to implement subdivision (b) of this 10 section. 11 (2) Additionally, the commissioner shall post such information on the 12 office's website. 13 (3) The commissioner shall follow existing practices to ensure that 14 the information is culturally and linguistically appropriate for all 15 recipients. 16 (4) Any local or national organization that provides education or 17 services related to Down syndrome, may request that the commissioner 18 include the organization's informational material and contact informa- 19 tion on the office's website. Once a request is made, the commissioner 20 may add the information to the website. 21 § 2. This act shall take effect on the ninetieth day after it shall 22 have become a law. Effective immediately, the addition, amendment and/or 23 repeal of any rule or regulation necessary for the implementation of 24 this act on its effective date are authorized to be made and completed 25 on or before such effective date.