“…Available data was not always representative of the country [ 32 , 40 ], and was unable to support the estimation of underreported cases or change in incidence and prevalence following an intervention, leading to underestimation of costs and/or benefits [ 20 , 41 , [45] , [46] , [47] ]. Reasons for unreliable data reported were that not all cases seek healthcare [ 20 ], some diseases studied are not notifiable and therefore, are not recorded or result in asymptomatic infections [ 48 ]. If no national data is available, studies use data from similar-context country studies [ 31 , 49 ], secondary data [ 23 , 50 ] or depend largely on expert opinion [ 37 , 51 , 52 ].…”