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Table 3 Values for fixed parameters

From: Potential public health impact of RTS,S malaria candidate vaccine in sub-Saharan Africa: a modelling study

Parameter

Value

Source

 Vaccine efficacy after 1 dose

None

Assumption

 Vaccine efficacy after 2 doses

One quarter of the vaccine efficacy of a full course (see Table 2)

Assumption

 Maternal protection, % of infants protected

95 %

Assumption

 Waning of maternal protection, wm

3 months half-life

Similar to previous models

 Probability of recovery from clinical disease, r

1/3

Half recover after 15 days

Assumption for a context of good access to care

 Access to ACT treatment

Ghana: 55 %, Kenya: 45 %, Tanzania: 62 % and country surveys for 22 countries

Average of 31 % for the remaining 17 countries

Sicuri [15] and Demographic and Health Surveys and Malaria Indicators Surveys

 % of severe cases hospitalized

54 %

Assumed same as access to ACT in public health facilities in Ghana, Kenya and Tanzania

 Relative risk for an untreated uncomplicated episode becoming severe (compared with a treated uncomplicated episode)

1.84 (95 % CI 1.68, 2.01)

Calculated from the modelled number of severe cases, the  % of severe cases hospitalized, and access to treatment [16]

 % of severe malaria cases resulting in sequelae

1.7 % (range 0.85–2.54 %)

Calculated from the % of cerebral malaria cases with sequelae from WHO report [21], and the  % of severe cases that are cerebral malaria [20]

Case-fatality rate, CFR (% of severe cases)

 Treated

13.6 % (95 % CI 8.4, 18.8 %)

Thwing [22]

 Untreated

3 × treated cases

40.8 % (95 % CI 25.2, 56.4 %)

Thwing [22]

  1. ACT artemisinin-based combination therapy, CI confidence interval