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MALARIA ELIMINATION IN ZANZIBAR - Soper Strategies

MALARIA ELIMINATION IN ZANZIBAR - Soper Strategies

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The first objective of the responses triggered at level 1 is to avoid<br />

onward transmission. The second objective is to determine and/<br />

or confirm whether transmission is still ongoing. The mass<br />

screening proposed aims at identifying secondary cases, which<br />

will determine if moving to level 3 is warranted.<br />

When no secondary cases can be identified it is still recommended<br />

to remain cautious (especially when the index case was likely<br />

locally acquired). The active case detection should therefore be<br />

repeated twice with an interval of 4 weeks (more or less the time<br />

of the parasite cycle). When two consecutive mass screenings<br />

cannot identify any secondary cases, the outbreak can be declared<br />

over and the area can return to vigilance level 0. In a scenario<br />

where effective coverage of preventive vector control measures<br />

is kept at around 75%, our simulations indicate that secondary<br />

cases will almost never occur and the risk of epidemics is low.<br />

However, when prevention is called back, epidemics become a<br />

real risk, and the thresholds for moving towards level 3 should<br />

therefore be far more conservative. We propose three secondary<br />

cases; far less than what is used in the simulator (outbreak defined<br />

as 50 cases in 2 weeks).<br />

At level 3, the ZMCP (in collaboration with all its partners) should<br />

initiate a massive response that aims at interrupting transmission.<br />

We suggest considering mass treatment of fever cases if the<br />

organization of a mass campaign is likely to be delayed. House to<br />

house visits by a small team that does not need to have training<br />

to do an RDT, might be easier to rapidly start and in the case<br />

of a locally-acquired infection, the time gained could be crucial.<br />

Mass screening, regardless of the presence of fever, follows the<br />

same more cautious rationale and has the added advantage that<br />

some asymptomatic cases, when treated, are cleared of parasites.<br />

Requirements of Implementation<br />

District staff, with assistance from the ZMCP, will be responsible<br />

for initiating confirmation procedures within 24 hours of<br />

receiving a report. The response activities will be labor intensive<br />

and have the potential to overwhelm the DHMT. If necessary,<br />

district staff from non-health sectors should be made available<br />

to assist with personnel needs. The government may also want<br />

to establish dedicated surveillance teams in key districts as<br />

suggested above (minimum three teams per high risk district) to<br />

ensure sufficient capacity for and execution of this activity. The<br />

surveillance teams could be taken from existing district health<br />

staff. We recommend that the 2 districts that are considered<br />

to have a higher transmission potential employ five full time<br />

investigation teams while for medium risk districts four teams<br />

would be sufficient most of the time. When a more elaborate<br />

response is required in low risk districts, additional temporary<br />

staff will need to be hired. Numbers will depend on the size of<br />

the area to be screened.<br />

Ideally, each district would also have a car and an emergency<br />

fuel stock on stand-by for investigation and the initial phases of<br />

the rapid response. In addition, spraying equipment (including<br />

protective gear) and a small stock of insecticides could be made<br />

available at the district level. A small stock of RDTs for initial<br />

stages of mass screenings can be kept at the district level with<br />

larger stocks available at the central level where storage conditions<br />

40<br />

are likely to be more adapted (ideally < 350). The ZMCP will<br />

also need to ensure that the necessary forms (and stationary) are<br />

available at the health facility level (case notification forms) and<br />

the district level (outbreak investigation forms). The ZMCP is<br />

also responsible for the management of ACT stocks, and they<br />

should ensure that areas where a case has been notified has<br />

sufficient emergency stocks at their disposal. Over time, these<br />

outbreaks will become increasingly rare with each outbreak<br />

resulting in fewer secondary cases. This will make forecasting the<br />

necessary emergency stand-by stocks challenging. In the worstcase<br />

scenario, Zanzibar could be faced with a massive epidemic<br />

in a non-immune population which would require large amounts<br />

of ACTs. However, keeping large stocks only for this purpose<br />

would not be cost-efficient. Zanzibar will therefore need to set<br />

up a system with manufacturers or neighboring malaria endemic<br />

countries that would give them quick access to large amounts of<br />

ACTs in an emergency.<br />

Entomological Surveillance<br />

A robust entomological surveillance system is a crucial component<br />

of any malaria elimination program. Entomological surveillance<br />

is, in essence, the monitoring of the vector population to assess<br />

the effect of vector control interventions in these populations and<br />

to ensure that control methodologies are effective, targeted and<br />

proactive. As such, entomological surveillance plays a key role in:<br />

�� Monitoring the effectiveness of vector control interventions<br />

�� Identifying active transmission foci<br />

�� Monitoring potential transmission foci<br />

�� Helping to establish the receptivity of an area to malaria<br />

transmission<br />

At a basic level, routine vector collection and processing will<br />

define vector populations in terms of species, biting and resting<br />

behavior, immature and adult stage density, and infection rates.<br />

However, additional investigation can be used to define the levels<br />

of resistance to insecticides. Levels of resistance are especially<br />

important when evaluating the effectiveness of vector control<br />

interventions such as IRS and LL<strong>IN</strong>s. Insecticide resistance<br />

genes can develop rapidly when mosquitoes are exposed to<br />

similar chemical families (e.g., pyrethroids). These factors are<br />

important to monitor, especially when evaluating how the vector<br />

population reacts when intensive vector control measures, such<br />

as IRS, are scaled back.<br />

These population effects are extremely important when assessing<br />

the potential receptivity of an area to re-infection from outside.<br />

WHO states that the degree of receptivity of an area is, amongst<br />

others, defined by its malaria history (WHO, 2007), specifically:<br />

�� Original degree of endemicity: This can be obtained from<br />

case records and any entomological data from the specific<br />

area (see technical feasibility chapter).<br />

�� Vectorial capacity before the implementation of intensive<br />

control measures<br />

This will define the nature of the vector population and give<br />

a baseline for comparison after control measures are scaled

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