Table 4.
Parameter | Best estimate (low-high) | Source for range (if different to PSA range) | 5% PfPR | 50% PfPR | ||||||||||
TS-N | TS-T | TS-U | TS-N | TS-T | TS-U | |||||||||
Low | High | Low | High | Low | High | Low | High | Low | High | Low | High | |||
Base case ICER | (Best estimates for each parameter) | (See table 2, online supplementary file S2) | 482 | 115 | D | 44 | 45 | D | ||||||
Discount rate | 0.03 (0.01–0.10) | Assumptions | 290 | 1372 | 73 | 309 | D | D | 27 | 120 | 28 | 122 | D | D |
Proportion of patients under 5 years | 0.40 (0.30–0.50) | (See table 2) | 636 | 389 | 128 | 105 | D | D | 51 | 38 | 53 | 39 | D | D |
Patients receiving RDT (‘uptake’)* | 0.41 (0.08–0.72) | (See table 2) | 1401 | 316 | 109 | 121 | D | D | 38 | 49 | 82 | 33 | D | D |
Positive RDT gets antimalarial | (See online supplementary file S4) | D | 154 | 280 | 72 | D | D | 76 | 30 | 87 | 30 | D | D | |
Antimalarial with positive RDT result that is ACT | 709 | 362 | 128 | 105 | D | D | 47 | 41 | 49 | 42 | D | D | ||
Negative RDT gets antibiotic | D | 47 | 233 | 31 | D | 196 | 45 | 37 | 47 | 37 | D | D | ||
Initial treatment parameters for intervention with no test unchanged from control | 492 | 268 | 868 | 107 | 59 | 210 | ||||||||
Reduction in ACT effectiveness due to reduced API consumed | Low transmission: 0.15 (0.00–0.30) Med/high transmission: 0.10 (0.00–0.30) |
Assumptions | 103 | D | 90 | 159 | D | D | 30 | 129 | 39 | 57 | D | D |
Reduction in other antimalarial effectiveness due to reduced API consumed | D | 131 | 123 | 109 | D | D | 59 | 31 | 47 | 42 | D | D | ||
Malaria case progresses to severe with no (or not effective) treatment* | (See PSA ranges in table 2 for <5 and >5 years, low and medium/high transmission settings) | D | 40 | 701 | 34 | D | D | 129 | 5 | 111 | 6 | D | D | |
Severe case receives further (inpatient) care* | 0.75 (0.19–0.88) | (See table 2) | 93 | 16 013 | 48 | 172 | D | D | 22 | 58 | 23 | 59 | D | D |
CFR of severe malaria receiving inpatient care * | 0.10 (0.05–0.15) | 5170 | 259 | 144 | 97 | D | D | 56 | 36 | 56 | 38 | D | D | |
CFR of severe malaria with no further care * | (See PSA ranges in table 2 for <5 and >5 years, low and medium/high transmission settings) | D | 216 | 236 | 91 | D | D | 87 | 29 | 81 | 31 | D | D | |
RDT exmanufacturer price * | 0.22 (0.17–0.28) | (See table 2) | 471 | 495 | 112 | 119 | D | D | 43 | 45 | 44 | 46 | D | D |
ACT exmanufacturer price* | 0.68 (0.51–1.56) | 472 | 535 | 117 | 106 | D | D | 42 | 50 | 45 | 44 | D | D | |
Supporting intervention cost per febrile patient | 0.43 (0.21–2.54) | Min: −25%; Max: assumption based on18 | 294 | 2330 | 62 | 638 | D | D | 26 | 217 | 24 | 247 | D | D |
Cost-effective at all six country-specific thresholds (Madagascar, Uganda, Nigeria, Tanzania, Ghana and Kenya) | ||||||||||||||
Cost-effective for at least one country-specific threshold (but not all six) | ||||||||||||||
Not cost-effective at any of six country-specific thresholds, but not dominated | ||||||||||||||
Dominated |
*Parameters where range of uncertainty in deterministic sensitivity analysis is the same as the PSA range. D: dominated, that is, intervention is more costly and less effective than the control.
ACT, artemisinin combination therapy; API, active pharmaceutical ingredient; CFR, case fatality rate; DALY, disability-adjusted life year; ICER, incremental cost-effectiveness ratio; PfPR, Plasmodium falciparum positivity rate; PSA, probabilistic sensitivity analysis; RDT, rapid diagnostic test.