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. 2017 Nov 22;177(1):133–144. doi: 10.1007/s00431-017-3046-1

Table 1.

Model inputs: morbidity probabilities used in base case and sensitivity analyses

Model input Base case value SA range for one-way sensitivity analysesa Distribution Source
Probability
Prediction rule
 High risk (> 10% RSV hospitalisation risk) 0.112 0.08–0.14 β (SD 0.01) Korsten et al.
RSV prophylaxis group
 Recurrent wheezing, no RSV hospitalisationb 0.19 0.15–0.24 β (SD 0.02) Blanken et al.
 Recurrent wheezing, RSV hospitalisationb 0.55 0.41–0.68 β (SD 0.05) Blanken
 RSV hospitalisation, given high risk 0.126 0.095–0.158 β (SD 0.01) Korsten
 PICU, given hospitalisationc 0.088 0.07–0.11 β (SD 0.01) Korsten
 Mortality, given PICU admissionc 0.01 0.008–0.013 β (SD 0.001) Supplement
Placebo group
 Recurrent wheezing, no RSV hospitalisation 0.19 0.15–0.24 β (SD 0.02) Blanken
 Recurrent wheezing, RSV hospitalisation 0.55 0.41–0.68 β (SD 0.05) Blanken
 RSV hospitalisation, given low risk 0.034 0.026–0.043 β (SD 0.005) Korsten
 PICU, given hospitalisation 0.088 0.07–0.11 β (SD 0.01) Korsten
Standard care
 Recurrent wheezing, no RSV hospitalisation 0.19 0.15–0.24 β (SD 0.02) Blanken
 Recurrent wheezing, RSV hospitalisation 0.55 0.41–0.68 β (SD 0.05) Blanken
 RSV hospitalisation 0.044 0.033–0.055 β (SD 0.005) Korsten
 PICU, given hospitalisation 0.088 0.07–0.11 β (SD 0.01) Korsten
Utility (positive)/disutility (negative)
 No RSV hospitalisation, baseline 0.95 0.71–1.00 Gamma (SD 0.1) Greenough et al.
 RSV hospitalisation − 0.07 − 0.05– -0.09 Gamma (SD 0.01) Greenough
 PICU admission§ − 0.15 − 0.17– -0.28 Gamma (SD 0.02) Jones et al.
 Wheezing, QALY reduction − 0.08 − 0.06– -0.1 Gamma (SD 0.01) RIVM
Prophylaxis effectiveness
 Reduction of RSV hospitalisation 0.82 0.62–1.03 β (SD 0.08) Blanken
 Reduction of recurrent wheezing 0.47 0.35–0.59 β (SD 0.05) Blanken

SA range sensitivity analysis range, SD standard deviation

aUnivariate sensitivity analysis ranges were derived by increasing and decreasing baseline values by 25%

bRecurrent wheezing following RSV GP visit in the RSV prophylaxis group was assumed equal to recurrent wheezing following RSV GP visit in the placebo group because the trial data suggested an inconsistent probability of 1.0 following RSV GP visit in the RSV prophylaxis group (n = 2)

cPotential utility loss and costs due to PICU admission and mortality were included in all RSV hospitalisation based on the probability of PICU admission and mortality following RSV hospitalisation