Table 1 Test level prior authorization request outcomes.

From: Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics

 

Total

 

(n = 4,535)

Time (days) between prior authorization request and decision

 Mean (SD)

11.97 (64.79)

 Median (Q1, Q3)

5.0 (2.0, 12.0)

Patient age (years) at prior authorization submission

 Mean (SD)

6.02 (4.69)

 Median (Q1, Q3)

4.7 (2.2, 9.0)

Insurance type

 Public

2,893 (63.8%)

 Private

1,642 (36.2%)

Prior authorization outcome

 Approve

3,235 (71.3%)

 Deny

908 (20.0%)

 Prior authorization not required

392 (8.6%)

Genetic test type

 Cytogenetic and moleculara

2,224 (49.0%)

 Single-gene or multigene panel

1,411 (31.1%)

 Exome

773 (17.0%)

 Epigenetic

86 (1.9%)

 Mitochondrial

41 (0.9%)

Diagnostic codes

 Autism ICD-10-CM codes (F84.0)

688 (15.2%)

 Developmental delay ICD-10-CM codes (F80.4, F82, F88, F80.9, R62.50)

1,418 (31.3%)

 Intellectual disability ICD-10-CM codes (F79, F70–78, F81.9)

323 (7.1%)

 Seizures or epilepsy ICD-10-CM codes (G40–40.919)

121 (2.7%)

 Multiple congenital anomalies ICD-10-CM codes (Q89.7)

136 (3.0%)

  1. ICD-10-CM International Classification of Diseases, Tenth Revision, Clinical Modification.
  2. aIncludes cytogenetic tests, chromosome microarray, and FMR1 repeat expansion analysis for fragile X syndrome and excludes single-gene or multigene panels.