DHS 115.03(6)
(6) “Screening" means checking each member of a population to identify presumptive medical conditions that indicate that diagnostic testing for congenital or metabolic disorders is needed.
DHS 115.03 History
History: Cr.
Register, May, 1993, No. 449, eff. 6-1-93; correction in (2) made under s.
13.92 (4) (b) 6., Stats.,
Register January 2009 No. 637;
CR 14-074: am. (3)
Register July 2015 No. 715, eff. 10-1-15.
DHS 115.04
DHS 115.04 Congenital disorders. Pursuant to s.
253.13 (1), Stats., blood samples taken from each newborn shall be tested for all of the following conditions:
DHS 115.04(4)
(4) Hemoglobinopathies, including all of the following:
DHS 115.04(6)
(6) Congenital adrenal hyperplasia, ICD-10-CM-E25.0.
DHS 115.04(8)
(8) Fatty acid oxidation disorders, including all of the following:
DHS 115.04(8)(a)
(a) Medium-chain acyl-CoA dehydrogenase deficiency, ICD-10-CM-E71.311.
DHS 115.04(8)(b)
(b) Long-chain L-3-Hydroxy acyl-CoA dehydrogenase deficiency, ICD-10-CM-E71.318.
DHS 115.04(8)(c)
(c) Very long-chain acyl-CoA dehydrogenase deficiency, ICD-10-CM-E71.310.
DHS 115.04(8)(cm)
(cm) Carnitine palmitoyltransferase IA deficiency, ICD-10-CM-E71.318.
DHS 115.04(8)(d)
(d) Carnitine palmitoyltransferase II deficiency, ICD-10-CM-E71.318.
DHS 115.04(8)(e)
(e) Carnitine-acylcarnitine translocase deficiency, ICD-10-CM-E71.318.
DHS 115.04(8)(i)
(i) Medium/short-chain hydroxy CoA dehydrogenase deficiency, ICD-10-CM-E71.318.
DHS 115.04(8)(j)
(j) Medium-chain ketoacyl-CoA thiolase deficiency, ICD-10-CM-E71.318.
DHS 115.04(11)
(11) Tyrosinemia types I, II, and III, ICD-10-CM-E70.21.
DHS 115.04(14)
(14) Severe Combined Immunodeficiency and related conditions of immunodeficiency, ICD-10-CM-D81.9.
DHS 115.04(15)
(15) Organic acidemias, including all of the following:
DHS 115.04(15)(c)
(c) Methylmalonic acidemia (CBL A, B, C, D; MUT), ICD-10-CM-E71.120.
DHS 115.04(16)
(16) Critical congenital heart disease, including all of the following:
DHS 115.04(16)(g)
(g) Single ventricle heart disease variants other than HLHS, including all of the following:
DHS 115.04(16)(g)3.
3. Congenital malformations of the tricuspid valve unspecified, ICD-10-CM-Q22.9.
DHS 115.04 History
History: Cr.
Register, May, 1993, No. 449, eff. 6-1-93; emerg. am. (5) and (6), cr. (7), eff. 1-31-95; correction in (intro.) made under s. 13.93 (2m) (b) 7., Stats.,
Register, July, 1995, No. 475; am. (5) and (6), cr. (7),
Register, July, 1995, No. 475, eff. 8-1-95; am. (intro.) and (1) to (6), cr. (8),
Register, December, 1999, No. 528, eff. 1-1-00; emerg. cr. (9) to (13), eff. 10-12-02;
CR 02-136: cr. (9) to (13)
Register March 2003 No. 567, eff. 4-1-03; emerg. cr. (14), eff. 1-1-08;
CR 08-005: cr. (14)
Register June 2008 No. 630, eff. 7-1-08;
CR 14-074: am. (intro.), cr. (15), (16)
Register July 2015 No. 715, eff. 8-1-15, and renum. (1) to (1) (a) and am., cr. (1) (b), am. (2), (3), r. and recr. (4), am. (5) to (7), r. and recr. (8), am. (9) to (14), r. and recr. (15), am. (16)
Register July 2015 No. 715, eff. 10-1-15; correction in (15) (g) made under s. 35.17, Stats.,
Register September 2015 No. 717;
EmR1920: emerg. am. (title), (intro.), cr. (8) (cm), (15m), eff. 10-15-19;
CR 19-064: am. (title), (intro.), cr. (8) (cm), (15m)
Register December 2019 No. 768, eff. 1-1-20;
EmR2131: emerg. cr. (17), eff. 1-10-22; CR 21-051: cr. (17) Register May 2022 No. 797, eff. 6-1-22. DHS 115.05(1)(1)
Procedures. The state laboratory shall establish procedures, with the approval of the department, for obtaining blood specimens for the testing required under s.
253.13 (1), Stats., and this chapter, performing tests and reporting results of tests performed to the infant's physician and the department as required under s.
253.13 (4), Stats.
DHS 115.05(2)
(2)
Additional tests for research and evaluation purposes. The department may direct the state laboratory to perform other tests on specimens for research and evaluation purposes related to congenital and metabolic disorders or laboratory procedures. In directing that additional testing be performed, the department shall ensure that all applicable laws relating to protection of human subjects of research are observed.
DHS 115.05 History
History: Cr.
Register, May, 1993, No. 449, eff. 6-1-93; corrections in (1) made under s. 13.93 (2m) (b) 7., Stats.,
Register, July, 1995, No. 475;
CR 12-025: cr. (3)
Register May 2013 No. 689, eff. 6-1-13;
CR 14-074: (3) renum. to 115.055 and am.
Register July 2015 No. 715, eff. 8-1-15.
DHS 115.055
DHS 115.055 Fees. The newborn screening sample collection card fee for testing a newborn under s.
253.13 (1), Stats., and this chapter shall be $109 to cover the costs of testing and to fund follow-up services and other activities under s.
253.13 (2), Stats.
DHS 115.055 History
History: CR 14-074: renum. from 115.05 (3) and am.
Register July 2015 No. 715, eff. 8-1-15.
DHS 115.06
DHS 115.06 Criteria for adding or deleting conditions. In determining which disorders are to be added or deleted from s.
DHS 115.04, the department shall seek the advice and guidance of medical consultants, staff of the state laboratory and other persons who have expertise and experience in dealing with congenital and metabolic disorders. Criteria to be considered in adding or deleting disorders shall include all of the following:
