Table 1.
Source | Setting and time period of the intervention | Time horizon for the benefits | Discount rate | Cost year | Cost of the intervention | Total economic benefitb | Net present value | Internal rate of return |
---|---|---|---|---|---|---|---|---|
Benton & Skinner 67 | OCP (1974–2004) | 1974–2023 | 5–10% | 1985 US$ |
|
US$148 million (10% discount rate) to US$543 million (5% discount rate). | US$8 million (10% discount rate) to US$312 million (5% discount rate). | 11–13% |
Kim & Benton 58 | OCP (1974–2002) | 1974–2012 | 3–10% | 1987 US$ |
|
Not stated. | US$485 million (10% discount rate) to US$3729 million (3% discount rate). | 20% |
McFarland & Murray 124, a | OCP (10‐year project time period) | 1974–2023 | 5% | Not available |
|
Not available. | US$8 million. | ‐ |
Benton 125 | APOC (1996–2007) | 1996–2017 | 10% | 1996 US$ |
|
Not stated. | US$53.7 million. | 17% |
Haddix 69, a | APOC (1996–2007) | 1996–2017 | 3–10% | 1996 US$ |
|
Not available. | US$87.6 million (10% discount rate) to US$307.4 million (3% discount rate). | 24% |
Kim et al. 60 | Potential benefits of achieving elimination scenarios in Africa | 2013–2045 | 3% | 2013 US$ | NA | Compared with the control scenario, the Elim I and II scenariosc would generate US$5.96 (2.53–7.28) billion and US$6.46 (2.83–8.09) billion in economic benefits respectively. | NA | NA |
Redekop et al. 59 | Potential economic benefits of achieving the WHO 2020 targets | 2011–2030 | 3% | 2005 US$ | NA | US$3.3 (2.4–5.11) billion. | NA | NA |
Turner et al. 95 | Potential impact of moxidectin on onchocerciasis elimination in African savannah settingsd | 50 years | 3% | 2012 US$ |
|
Annual moxidectin treatment would achieve similar reductions in programme duration as using biannual ivermectin treatment. If the moxidectin tablets were donated its use would lead to substantial in‐country cost savings. |
NA | NA |
APOC, African Programme for Onchocerciasis Control; NA, not applicable; OCP, Onchocerciasis Control Programme in West Africa; pOTTIS, provisional operational thresholds for treatment interruption followed by surveillance.
Information for this study was taken from Waters et al. 18.
The estimated economic benefits are outlined in further detail in Table 3.
The Control, Elim I and Elim II scenarios are described in Kim et al. 99.
Assumed that MDA would be stopped (determining the programme duration) once the pOTTIS would have been achieved (defined as the modelled microfilarial prevalence being <1.4%, measured just before the next treatment round).