| Literature DB >> 32587283 |
David A Larsen1, Anne Martin2, Derek Pollard2, Carrie F Nielsen3, Busiku Hamainza4, Matthew Burns2, Jennifer Stevenson5,6, Anna Winters2,7.
Abstract
Although transmission of malaria and other mosquito-borne diseases is geographically heterogeneous, in sub-Saharan Africa risk maps are rarely used to determine which communities receive vector control interventions. We compared outcomes in areas receiving different indoor residual spray (IRS) strategies in Eastern Province, Zambia: (1) concentrating IRS interventions within a geographical area, (2) prioritizing communities to receive IRS based on predicted probabilities of Anopheles funestus, and (3) prioritizing communities to receive IRS based on observed malaria incidence at nearby health centers. Here we show that the use of predicted probabilities of An. funestus to guide IRS implementation saw the largest decrease in malaria incidence at health centers, a 13% reduction (95% confidence interval = 5-21%) compared to concentrating IRS geographically and a 37% reduction (95% confidence interval = 30-44%) compared to targeting IRS based on health facility incidence. These results suggest that vector control programs could produce better outcomes by prioritizing IRS according to malaria-vector risk maps.Entities:
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Year: 2020 PMID: 32587283 PMCID: PMC7316765 DOI: 10.1038/s41598-020-66968-w
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
Figure 1A map of the study area showing the allocation of different spray strategies.
Figure 2Zoom-level view of communities and different IRS allocation strategies. When allocating based on health facility-level incidence, communities within catchment areas would be sprayed or not, depending on the numbers of cases per the nearest health center. When allocating based on predicted An. funestus habitat, communities within lighter squares would be sprayed or not. Sub-geographic concentration would be to spray all communities within an arbitrary boundary.
Number of spray areas targeted and average spray area size across trial arm districts.
| District | Trial arm | Number of spray areas targeted (buffer) | Total number of spray areas in district | Median number of houses per spray area | Mean number of houses per spray area (standard deviation) |
|---|---|---|---|---|---|
| Chadiza | Health facility-targeting | 232 (41) | 347 | 17 | 57.37 (115.33) |
| Katete | Geographic concentration | 148 (40) | 474 | 19 | 103.53 (411.23) |
| Lundazi | Ecological-targeting | 988 (208) | 1,695 | 19 | 32.75 (133.67) |
| Mambwe | Ecological-targeting | 85 (15) | 157 | 26 | 108.82 (334.34) |
| Nyimba | Geographic concentration | 112 (99) | 242 | 16.5 | 63.52 (177.02) |
| Vubwi | Health facility-targeting | 105 (1) | 142 | 29 | 74.01 (119.86) |
| Total | 1,670 (409) | 3,057 | 10 | 54.78 (217.34) |
Targeted spray area adherence by district and trial arm.
| District | Trial arm | Percentage of structures sprayed that were targeted | Percentage of structures targeted (primarily) that were sprayed |
|---|---|---|---|
| Chadiza | Health facility-targeted | 99.1% | 90.0% |
| Katete | Geographic concentration | 96.1% | 66.7% |
| Lundazi | Ecological-targeted | 95.5% | 78.8% |
| Mambwe | Ecological-targeted | 99.3% | 86.5% |
| Nyimba | Geographic concentration | 98.0% | 94.2% |
| Vubwi | Health facility-targeted | 92.1% | 90.1% |
Spray coverage within sprayed communities by district and trial arm.
| District | Group | Spray coverage < 25% | Spray coverage 25–50% | Spray coverage 50–75% | Spray coverage 75–100% | Total communities sprayed |
|---|---|---|---|---|---|---|
| Chadiza | Health Facility | 0 | 2 | 9 | 261 | 272 |
| Katete | Blanket | 0 | 11 | 18 | 125 | 154 |
| Lundazi | Ecological | 7 | 39 | 71 | 871 | 988 |
| Mambwe | Ecological | 0 | 0 | 2 | 97 | 99 |
| Nyimba | Blanket | 0 | 2 | 1 | 180 | 183 |
| Vubwi | Health Facility | 1 | 0 | 4 | 87 | 92 |
| Total | 8 | 54 | 105 | 1,621 | 1,788 |
Figure 3Unadjusted median trends of various malaria indicators at health facilities in the study area over time.
Figure 4Adjusted coefficients of difference-in-differences analysis showing change in malaria incidence between pre- and post- periods and by trial arm.
Adjusted negative binomial regression predicting the outcome of confirmed malaria cases and using the estimated health facility catchment area population as the offset.
| Factor | Categorization | IRR (95% CI) | p-value |
|---|---|---|---|
| Trial arm | Geographically-concentrated | Reference | Reference |
| Health facility-targeted | 1.350 (1.212–1.504) | <0.001 | |
| Ecologically-targeted | 0.867 (0.788–0.954) | 0.004 | |
| Time period | Pre-2017 IRS operations | Reference | Reference |
| Post-2017 IRS operations | 0.680 (0.599–0.772) | <0.001 | |
| Trial arm by time period interaction | Geographically-concentrated by Post-2017 IRS operations | Reference | Reference |
| Health facility-targeted by Post-2017 IRS operations | 1.396 (1.235–1.578) | <0.001 | |
| Ecologically-targeted by post-2017 IRS operations | 0.873 (0.793–0.962) | 0.006 | |
| Type of health facility | Health center | Reference | Reference |
| Hospital | 2.536 (1.836–3.503) | <0.001 | |
| Health post | 2.100 (1.956–2.255) | <0.001 | |
| NDVI lagged 1 month | Quintile 1 (0.148–0.205) | Reference | Reference |
| Quintile 2 (0.205–0.275) | 1.166 (1.089–1.248) | <0.001 | |
| Quintile 3 (0.278–0.343) | 2.055 (1.923–2.190) | <0.001 | |
| Quintile 4 (0.362–0.430) | 2.671 (2.515–2.837) | <0.001 | |
| Quintile 5 (0.435–0.487) | 2.759 (2.593–2.936) | <0.001 | |
| Precipitation lagged 1 month | Quintile 1 (0.0 mm–0.9 mm) | Reference | Reference |
| Quintile 2 (0.9 mm–7.0 mm) | 1.037 (0.978–1.098) | 0.222 | |
| Quintile 3 (7.0 mm–75.8 mm) | 1.214 (1.147–1.284) | <0.001 | |
| Quintile 4 (76.0 mm–183.2 mm) | 1.262 (1.193–1.336) | <0.001 | |
| Quintile 5 (183.2 mm–402.2 mm) | 1.264 (1.189–1.344) | <0.001 | |
| Altitude | Quintile 1 (438 m–774 m) | Reference | Reference |
| Quintile 2 (790 m–988 m) | 0.706 (0.633–0.789) | <0.001 | |
| Quintile 3 (988 m–1043 m) | 0.498 (0.438–0.567) | <0.001 | |
| Quintile 4 (1043 m–1125 m) | 0.560 (0.505–0.621) | <0.001 | |
| Quintile 5 (1128 m–1398 m) | 0.543 (0.483–0.610) | <0.001 | |
| Yearly nighttime light | Continuous – increase of 1 on a scale from 0–63 (ranging from 0 to 2.0 in this dataset) | 0.385 (0.330–0.448) | <0.001 |
| Total confirmed malaria cases lagged 1 month | Continuous – increase of 100 cases | 1.049 (1.045–1.053) | <0.001 |
| Total malaria tests done (RDTs or microscopy) | Continuous – increase of 1000 tests | 1.039 (1.034–1.045) | <0.001 |
| Sine-function for time | Continuous | 0.981 (0.919–1.047) | 0.560 |
| Cosine-function for time | Continuous | 1.459 (1.319–1.615 | <0.001 |
| Time | Continuous – increase of one month | 1.022 (1.016–1.029) | <0.001 |
N = 149 facilities, 5,587 months.
Adjusted negative binomial regression predicting the outcome of total Anopheles mosquitoes collected during entomological surveillance.
| Factor | Categorization | IRR (95% CI) | p-value |
|---|---|---|---|
| Trial arm | Geographically-concentrated | Reference | Reference |
| Health facility-targeted | 1.020 (0.519–2.006) | 0.954 | |
| Ecological-targeted | 1.915 (1.053–3.485) | 0.033 | |
| IRS | No IRS in village | Reference | Reference |
| IRS in village | 0.729 (0.581–0.913) | 0.006 | |
| Type of eaves | Closed | Reference | Reference |
| Open | 1.700 (1.375–2.103) | <0.001 | |
| ITN | None | Reference | Reference |
| At least 1 hanging | 0.923 (0.638–1.334) | 0.669 | |
| Type of collection | Light trap | Reference | Reference |
| Prokopack | 0.197 (0.146–0.267) | <0.001 | |
| NDVI lagged 1 month | Continuous | 0.355 (0.171–0.735) | 0.005 |
| Precipitation lagged 1 month | Continuous | 1.001 (0.997–1.005) | 0.764 |
| Nighttime light | Continuous | 0.655 (0.155–2.774) | 0.566 |
| Altitude | Continuous | 1.000 (0.999–1.001) | 0.521 |
| Month | December | Reference | Reference |
| January | 1.825 (1.105–3.014) | <0.001 | |
| February | 2.544 (1.719–3.765) | <0.001 | |
| March | 4.409 (2.640–7.362) | <0.001 | |
| April | 7.373 (4.905–11.083) | <0.001 |
N = 25 sites, 863 houses.
Figure 5A diagram showing how spatial error differs when attributing risk to household locations.