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. Author manuscript; available in PMC: 2019 Aug 22.
Published in final edited form as: Public Health Genomics. 2008 Sep 14;12(2):67–72. doi: 10.1159/000156115

Table 1.

Assumption in modelling newborn screening for CAH

Parameter definition (notation in fig. 1) Point estimatea Range Reference
Incidence of CAH 13
  SW and SV combined (incidence) 1 in 17,800 1 in 25,000,
1 in 12,000
  Proportion of SW among SW and SV (prop_sw) 0.65
Sensitivity of early clinical recognition 11, 12, 14
  SW (sen_cl_sw) 55% 45–65%
  SV (sen_cl_sv) 45% 15–75%
Screen false positive rate (false_pos) 0.5% 0.1–1.0% 13
Sensitivity of detection with screening 11
  SW (sen_sw) 1.0
  SV (sen_sv) 0.40 0.3–0.9
Cost of screening per one specimen (c_test), USD 4.15 2.30–6.00 8, 12
Cost of follow-up and confirmatory test per screen positive (c_follow), USD 216 130–637 12
Reduced cost of hospitalization per male SW case (c_hosp), USD 6,000 12, 17
SW mortality without screening (mr_sw) 4.2% 2.0–9.0% 7, 16, 18, 26
Reduction in SW mortality with screening (mr_reduce) 80% 74–86%
a

Also used as a mode in a triangle distribution in probabilistic analysis. All cost values were in 2005 USD.

CAH = Congenital adrenal hyperplasia; SW = salt wasting; SV = simple virilizing.