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. Author manuscript; available in PMC: 2015 Jun 19.
Published in final edited form as: Birth Defects Res A Clin Mol Teratol. 2013 Sep 2;97(10):664–672. doi: 10.1002/bdra.23165

Table 2.

Timely versus Late Detection of Critical Congenital Heart Disease (CCHD) among Florida Live-Born Infants (n =3603), 1998 to 2007

CCHD condition Timely detecteda n (%) Late detected
n (%) Median age (range) at detection, daysb
All (n=3603) 2778 (77.1) 825 (22.9) 88 (2–364)
Single CCHD
 AI/A (n=96) 70 (72.9) 26 (27.1) 71 (4–364)
 COA (n=747) 472 (63.2) 275 (36.8) 41 (2–347)
 DORV (n=109) 77 (70.6) 32 (29.4) 90 (6–327)
 d-TGA (n=260)c 234 (90.0) 26 (10.0) 46 (6–122)
 EA (n=87) 76 (87.4) 11 (12.6) 56 (15–216)
 HLHS (n=223)c 196 (87.9) 27 (12.1) 18 (3–280)
 PA (n=96)c 74 (77.1) 22 (22.9) 47 (8–228)
 SV (n=32) 24 (75.0) 8 (25.0) 140 (40–264)
 TA (n=101)c 69 (68.3) 32 (31.7) 46 (10–229)
 TAPVC (n=92)c 55 (59.8) 37 (40.2) 62 (3–289)
 TOF (n=745)c 561 (75.3) 184 (24.7) 108 (2–358)
 TRA (n=122)c 102 (83.6) 20 (14.0) 162 (11–235)
Multiple CCHD (n=893) 768 (86.0) 125 (14.0) 51 (2–356)
a

Timely detection at the birth hospital =Any ICD-9-CM code for CCHD noted on inpatient birth hospital discharge record.

b

Age in days assessed as the day of first hospital admission on which a congenital heart disease ICD-9-CM code appeared in the discharge record.

c

Conditions identified as primary targets for pulse oximetry screening (Mahle et al., 2009; Kemper et al., 2011).

AI/A, aortic interruption/atresia / hypoplasia; COA, coarctation / hypoplasia of aortic arch; DORV, double-outlet right ventricle; d-TGA dextro-transposition of the great arteries; EA Ebstein anomaly; HLHS hypoplastic left heart syndrome; PA pulmonary atresia; SV single ventricle; TA truncus arteriosus; TAPVC total anomalous pulmonary venous connection; TOF tetralogy of Fallot;TRA tricuspid atresia.