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site_file$interventions

Interventions contains the historical intervention information for a site. It is also the section of the site file that you would modify with intervention information for future scenarios. Details, references and methods for individual interventions are shown below:

ITNs

ITN use

site_file$interventions$itn_use

Due to differences in the availability of data sources the approach for countries within sub-Saharan Africa differs to countries outside of sub-Saharan Africa:

Within sub-Saharan Africa

The population at risk weighted mean ITN use estimates for each site are taken from the malaria atlas project raster entitled: “Insecticide treated bednet (ITN) use version 2020”. This, and other elements of the netz R package are based on work by Bertozzi-Villa et al1

Outside of sub-Saharan Africa

ITN use is much more heterogeneous outside of SSA and data are less systematically collected. As a result, there are strong assumptions associated with the historical scale and magnitude of ITN distributions. We make the assumption that any reported ITN distributions (as detailed by the world malaria report2) are tarted to areas that have > 1% PfPr or > 1% PvPr at baseline. Annual distributions in these regions are then scaled so that that number of ITNs distributed is aligned with the world malaria report.

Missing years

Available data on ITN use (via MAP3 or the world malaria report @ WMR) will not extend to the present year. Missing ITN use estimates to present are filled assuming a constant, continuing level of coverage. To respect the multi-year cyclical nature of ITN distribution cycles any missing estimates are filled in assuming that coverage is constant with respect to 3 years prior. For example if years 2019, 2020 and 2021 are missing then 2019 == 2016, 2020 == 2017 and 2021 == 2018.

Net type

site_file$interventions$net_type

It is assumed that all nets distributed prior to 2025 are standard pyrethroid (pyrethroid_only) bed nets. Current available net types are: pyrethroid_only, pyrethroid_pbo and pyrethroid_pyrrole.

Net input distribution

site_file$interventions$itn_input_dist

We need to estimate the annual ITN distributions that would cumulatively result in our observed timeseries of ITN usage. For the we use the fit_usage() function from the netz R package. We an impose 3 year cyclical limits to the number of nets that are distributed to avoid unrealistic over-distribution.

Pyrethroid resistance

site_file$interventions$pyrethroid_resistance

For each site we include an estimated level of pyrethroid insecticide resistance. This has been estimated by Tom Churcher and colleagues using spatio-temporally distributed bioassay mortality data. This work is not yet published. Therefore for attribution/citation and further information on the methods used please contact Pete Winskill or Tom Churcher.

ITN efficacy parameters

site_file$interventions$dn0 site_file$interventions$rn0 site_file$interventions$gamman site_file$interventions$rnm

Given an ITN type and level of pyrethroid insecticide resistance, we can link to the corresponding estimates of the key ITN efficacy parameters. These have been estimated by Ellie Sherrard-Smith et al4. Please note that gamman is provided in units of years here, these will need to be converted to days for use in malariasimulaiton.

IRS

IRS coverage

site_file$interventions$irs_cov

As with ITNs, due to differences in the availability of data sources the approach for countries within sub-Saharan Africa differs to countries outside of sub-Saharan Africa:

Within sub-Saharan Africa

The population at risk weighted mean IRS coverage estimates for each site are taken from the malaria atlas project raster entitled: “Indoor Residual Spraying (IRS) coverage version 2020”3. Coverage estimates are rescaled such that the country-level estimate of the number of persons protected by IRS matches the number reported in the world malaria report2.

Outside of sub-Saharan Africa

IRS coverage is much more heterogeneous outside of SSA and data are less systematically collected. As a result, there are strong assumptions associated with the historical scale and magnitude of IRS campaigns. We make the assumption that any reported IRS campaigns (as detailed by the world malaria report2) are tarted to areas that have > 1% PfPr or > 1% PvPr at baseline. Coverage in these regions are then scaled so that that number of persons protected by IRS is aligned with the world malaria report.

IRS insecticide

site_file$interventions$irs_insecticide

It is assumed that a DDT-type insecticide is used prior to 2017, after which there is a switch to an actellic-like insecticide.

Current available IRS insecticide options are: ddt, actellic, bendiocarb, sumishield.

Number of rounds of IRS per year

site_file$interventions$irs_spray_rounds

We assume a single IRS spray round per year.

IRS efficacy parameters

site_file$interventions$ls_theta site_file$interventions$ls_gamma site_file$interventions$ks_theta site_file$interventions$ks_gamma site_file$interventions$ms_theta site_file$interventions$ms_gamma

Given an IRS insecticide type we can link to the corresponding estimates of the key IRS efficacy parameters. These have been estimated by Ellie Sherrard-Smith et al5.

IRS households sprayed

It is often helpful to convert the number of persons protected by IRS into an estimate of the number of households covered. To aid this conversion we have included country-levels estimates of the average household size obtained from the UN6.

site_file$interventions$hh_size

Missing years

Available data on IRS coverage (via MAP3 or the world malaria report2) will not extend to the present year. Missing IRS coverage estimates to present are filled assuming a constant, continuing level of coverage.

Treatment

Coverage

site_file$interventions$tx_cov

The population at risk weighted mean treatment coverage of an effective antimalarial for each site are taken from the malaria atlas project raster entitled: “Effective treatment with an Antimalarial drug version 2020”3.

Drug type

site_file$interventions$prop_act

We estimate the proportion of treatments that are with an ACT from DHS StatCompiler data7, using the indicator: “Children who took any ACT” (ID: ML_AMLD_C_ACT). For SSA estimates by year are expanded by linear interpolation between data points and an assumption of constant coverage after the most recent data point. We assume that ACT coverage is zero before 2006, when the WHO recommendation was first issued. For outside of SSA the DHS indicator is confounded by treatment for Plasmodium vivax, and we therefore assume the mean values by year from data within SSA.

Drug provider

site_file$interventions$prop_public

We include an estimate of the proportion of treatments that are from the public sector prop_public. This is useful for costing. We use the DHS StatCompiler7 indicator “Children with fever for whom advice or treatment was sought, the source was a public sector facility” (ID: ML_FEVA_C_PUB). We assume a constant proportion over time by country, estimated as the mean from all country survey estimates since 2010. For countries without survey data, we assume the median across all estimates.

Seasonal malaria chemoprevention (SMC)

SMC coverage

site_file$interventions$smc_cov

Historical SMC implementation and coverage estimates are fragmented. We identify historical SMC implementation areas from maps presented by both Access SMC8 and more recently SMC alliance9. We assume a linear increase in coverage post implementation initiation up to a maximum of 80% to capture an increasing number of smaller sub-national units being targeted over time.

SMC drug

site_file$interventions$smc_drug

We assume that SP-AQ is used for SMC. This is currently the only available drug option.

Number of SMC rounds delivered annualy

site_file$interventions$smc_n_rounds

We assumed that historical SMC is delivered over 4 rounds smc_n_rounds.

SMC age range

site_file$interventions$smc_min_age site_file$interventions$smc_max_age

We assume SMC is delivered to children aged between 3 months and 5 years.

RTS,S vaccine

site_file$interventions$rtss_cov

We include historical RTS,S coverage that has occurred as part of the MVIP implementation trial, sub-nationally in Malawi, Ghana and Kenya. The spatial distribution is informed from an MVIP briefing presentation10

Perennial malaria chemoprevention (PMC).

This intervention has been known in the past as intermittent preventative treatment of infants (IPTi).

PMC coverage

site_file$interventions$pmc_cov

Due to the very limited (non-trial setting) implementation of PMC historically, we assume 0 coverage.

PMC drug

site_file$interventions$pmc_drug

We assume PMC would be implemented with SP. This is currently the only available drug option.

Citations

1.
Bertozzi-Villa, A. et al. Maps and metrics of insecticide-treated net access, use, and nets-per-capita in africa from 2000-2020. Nature Communications 12, 1–12 (2021).
2.
World Health Organization. World malaria report. (2021).
3.
4.
Sherrard-Smith, E. et al. Optimising the deployment of vector control tools against malaria: A data-informed modelling study. The Lancet Planetary Health 6, e100–e109 (2022).
5.
6.
7.
8.
9.
10.
World Health Organization. MVIP briefing.