Section 410 IAC 3-3-3 - Screening for certain disorders; collection proceduresAuthority: IC 16-19-3-4; IC 16-41-17-9
Affected: IC 16-41-17
Sec. 3.
(a) Except as provided for in section 2(b) of this rule, all newborns and infants born in the state of Indiana shall be screened for the following: (1) The following endocrine disorders: (A) Congenital adrenal hyperplasia (CAH).(2) The following hemoglobinopathies:(A) Sickle cell anemia Hb SS.(C) Hb S/beta-thalassemia.(D) Other Hb variant including genetic trait.(3) The following metabolic conditions:(A) The following amino acid (AA) disorders (including urea cycle disorders): (i) Arginase deficiency (Argininemia).(ii) Argininosuccinic aciduria (Arginosuccinase deficiency).(iii) Biopterin cofactor defects.(iv) Citrullinemia, type I.(v) Citrullinemia, type II (also called Citron deficiency).(vi) Homocystinuria (HCY).(vii) Hypermethioninemia.(viii) Hyperphenylalaninemia.(ix) Maple syrup urine disease (MSUD).(x) Phenylketonuria (PKU).(xii) Tyrosinemia type II.(xiii) Tyrosinemia type III.(B) The following fatty acid oxidation (FAO) disorders:(i) 2, 4-dienoyl-CoA reductase deficiency.(ii) Carnitine-Acylcarnitine translocase deficiency (CACT).(iii) Carnitine palmitoyltransferase deficiency I (CPT IA).(iv) Carnitine palmitoyltransferase deficiency II (CPT II).(v) Carnitine uptake defect (CUD).(vii) Long chain hydroxyacyl-CoA dehydrogenase deficiency (LCHAD).(viii) Medium chain acyl-CoA dehydrogenase deficiency (MCAD).(ix) Medium/short chain acyl-CoA dehydrogenase deficiency (M/SCHAD).(x) Trifunctional enzyme deficiency.(xi) Very long chain acyl-CoA dehydrogenase deficiency (VLCAD).(xii) Medium-chain ketoacyl-CoA thiolase deficiency (MCAT).(C) The following organic acidemia (OA):(i) 2-Methylbutyrylglycinuria (2-MBG).(ii) 3-Hydroxy-3-methyl glutaric aciduria (HMG).(iii) 3-Methylcrotonyl-CoA carboxylase deficiency (3-MCC deficiency).(iv) 3-Methylglutaconic acidemia (3-MGA).(v) Beta-ketothiolase deficiency.(vi) Glutaric acidemia type I (GA type I).(vii) Isobutyrylglycinuria (IBG).(viii) Isovaleric acidemia (IVA).(ix) Malonic aciduria (MAL).(x) Methylmalonic acidemia (MUT or methylmalonyl-CoA mutase).(xi) Methylmalonic acidemia with cobalamin disorders (CblA and CblB).(xii) Methylmalonic acidemia with homocystinuria (CblC and CblD).(xiii) Multiple-CoA carboxybutyric aciduria (2M3HBA).(xiv) Propionic acidemia.(xv) 2-Methyl-3-hydroxybutyric aciduria (2M3HBA).(4) The following other inborn errors of metabolism:(A) Biotinidase deficiency.(B) Galactosemia (classic galactosemia or G/G, galactosemia D/G variant and other galactosemia variants).(5) The following other genetic conditions:(B) Severe combined immunodeficiencies (SCID).(C) Spinal muscular atrophy.(D) Beginning July 1, 2020, Krabbe disease.(E) Beginning July 1, 2020, Pompe disease.(F) Beginning July 1, 2020, Mucopolysaccaridosis type 1 (MPS1).(G) Beginning July 1, 2021, adrenoleukodystrophy. (6) Other genetic conditions that are detectable at birth via newborn screening methods, including, but not limited to, the following:(A) Tandem mass spectrometry: amino acid and acylcarnitine analysis.(B) High performance liquid chromatography.(C) Isoelectric focusing.(D) Time resolved fluoroimmunoassay.(G) Immunoreactive trypsin (IRT).(I) DNA mutation analysis.(b) The responsible physician, midwife, birthing center, or hospital shall collect a specimen of the newborn or infant's blood on a filter paper kit approved by the department. The specimen shall consist of capillary blood obtained by heel puncture and applied directly to the special filter paper. All circles shall be saturated with blood from one (1) side of the filter paper only. All information requested on the form attached to the special filter paper shall be provided. The specimen shall be air dried and then inserted into the protective envelope with complete data. If multiple specimens are forwarded in one (1) envelope, care must be taken to avoid cross-contamination. Completed specimens shall be forwarded to a designated laboratory within twenty-four (24) hours after collection.(c) The newborn or infant's blood for these tests shall be collected not earlier than twenty-four (24) hours after birth and not later than forty-eight (48) hours after birth, except as stated in subsections (f) and (g).(d) When a live birth occurs in a hospital or birthing center, the responsible physician or midwife shall have a specimen of the newborn or infant's blood taken prior to the newborn or infant's discharge from the hospital. If the newborn is discharged from the hospital before twenty-four (24) hours after birth, a blood specimen shall be collected regardless, but collection shall be repeated after forty-eight (48) hours and not later than one hundred twenty (120) hours after birth. The hospital or birthing center shall provide a written notice to the parents, at or before discharge, of the requirements for the newborn to be tested again prior to one hundred twenty (120) hours after birth.(e) When a live birth occurs in a facility other than a licensed hospital or birthing center, it shall be the responsibility of the physician or midwife in attendance at the birth to assure that the newborn or infant is referred to an appropriate facility, such as a physician office, hospital, birthing center, or local health department, and to make the arrangements to obtain and submit a satisfactory blood specimen in accordance with this section. In the absence of an attending physician or midwife, the registrar of births shall refer the newborn or infant immediately to the parent's physician or to the local health department for submission of a specimen in accordance with this section and notify the MCH/NBS immediately.(f) For preterm or low birth weight (less than two thousand (2,000) grams) newborns or infants, the initial specimen shall be taken not earlier than twenty-four (24) hours after birth and not later than forty-eight (48) hours after birth. A repeat specimen collection shall be taken not earlier than fourteen (14) days and not later than thirty (30) days after birth or the day of discharge, whichever comes first. Prematurity and transfusion status shall be noted on the request form in the space provided. If the newborn or infant is to receive total exchange transfusion, then the specimen for the newborn screening test is to be obtained prior to transfusion, which represents the newborn or infant's own blood. If the pre-transfusion collection occurred before twenty-four (24) hours after birth, a repeat collection shall be taken not earlier than twenty-four (24) hours post transfusion start time. A second repeat collection shall be taken at thirty (30) days or day of discharge, whichever comes first.(g) Except for newborns and infants described in subsection (f), for newborns or infants within the neonatal intensive care unit (NICU), the initial collections shall be taken not earlier than twenty-four (24) hours after birth and not later than forty-eight (48) hours after birth. A repeat collection shall be taken at thirty (30) days or day of discharge, whichever comes first. Indiana State Department of Health; 410 IAC 3-3-3; filed Nov 7, 1986, 3:30 p.m.: 10 IR 416; filed Sep 17, 1999, 10:42 a.m.: 23 IR 324; errata filed Nov 19, 1999, 9:31 a.m.: 23 IR 814; readopted filed Jul 11, 2001, 2:23 p.m.: 24 IR 4234; readopted filed May 22, 2007, 1:44 p.m.: 20070613-IR-410070141RFA; filed Apr 25, 2012, 3:46 p.m.: 20120523-IR-410100504FRAFiled 9/28/2018, 2:04 p.m.: 20181024-IR-410180158FRAFiled 11/5/2020, 9:46 a.m.: 20201202-IR-410200311FRAReadopted filed 11/5/2021, 8:22 a.m.: 20211201-IR-410200607FRA