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National Project Implementation Plan - NVBDCP

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chloroquine in P. falciparum cases is widespread in India 2 . The share of P.<br />

falciparum malaria has been increasing in India since 1980s, and is<br />

currently about 45 percent of reported malaria cases. At present different<br />

treatment policies are applied in different parts of the country based on the<br />

chloroquine resistance level, so that ACT (artemisinin+sulfadoxinepyremethamine)<br />

is used as first line treatment for P.falciparum malaria only<br />

in clusters of PHC areas, where reported chloroquine resistance is above<br />

25%. The experience from other countries such as Cambodia, Thailand and<br />

Vietnam indicates that a rising share of P. falciparum malaria is a sign of<br />

chloroquine treatment failure, and that this trend can be reversed by<br />

treating all P. falciparum cases with Artemisinin-based Combination Therapy<br />

(ACT).<br />

Furthermore, millions of fever patients who do not have malaria are given<br />

presumptive treatment with a single, sub-curative dose of 10 mg/kg<br />

chloroquine (600 mg in adults) by the government health services. This can<br />

increase drug pressure, cause unnecessary side-effects, is wasteful and<br />

reduces confidence of the public in the services. Progressively, all fever<br />

patients suspected of malaria should be tested to confirm the diagnosis of<br />

treatment before treatment is given. The JMM recommended<br />

discontinuation of presumptive treatment with chloroquine 10 mg/kg.<br />

According to JMM, several important changes in the policy on diagnosis and<br />

treatment of malaria are required; the most important of these include the<br />

following 3 :<br />

(i) Use ACT as the first line treatment for all confirmed falciparum malaria<br />

cases. Introduce this policy in a phased manner to cover nation-wide –<br />

according to a prioritized plan including diagnostics, training, quality<br />

assurance, supply chain management and information to the public.<br />

(ii) Reform the surveillance of malaria by expanding the coverage of<br />

passive case detection. The target should be prompt blood slide or RDK test<br />

for all suspected malaria cases. Strengthened and expanded PCD should<br />

help the programme to achieve the target of about 10% annual blood<br />

examination rate. Active Case Detection (ACD) should be restricted to<br />

pockets of problem areas particularly areas with poor access to PCD or used<br />

during focal outbreaks.<br />

(iii) Testing all suspected malaria cases 4 before treatment: The main<br />

challenge in terms of training, logistics and funding for implementing the<br />

2 Since 2001, 64 studies of resistance to chloroquine have been conducted following WHO<br />

protocol. Only five of these 64 studies found that the level of resistance to chloroquine was<br />

less than 10%. Seventeen studies showed levels of resistance between 10% and 25%, and 42<br />

studies showed levels of resistance greater than 25%. WHO recommendation is to use 10% as<br />

the cut off level for drug resistance.<br />

3 <strong>National</strong> Vector Borne Disease Control Programme: Joint Monitoring Mission Report, February<br />

2007<br />

4 Precise guidelines on criteria for suspicion of malaria should be prepared by <strong>NVBDCP</strong> at<br />

central level according to following principles: Malaria should be suspected in patients who<br />

present with fever or anemia living in malaria- risk areas (e.g. PHC) or having visited an<br />

endemic area within the last month. A malaria-endemic area could for example be defined as<br />

11

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