National Malaria Drug Policy

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    NATIONAL DRUG POLICY

    ONMALARIA(2010)

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    Objectives of National Drug Policy

    Access: equitable availability and affordabilityof essential drugsQuality: safety and efficacy of all medicinesRational use: the promotion of therapeuticallysound and cost effective use of drugs by healthprofessionals and consumers.

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    National Drug Policy on Malaria

    The main purpose of National Drug Policy onMalaria is to provide a framework for the safe andeffective treatment of uncomplicated and severemalaria as well as prevention of malaria intravelers and vulnerable groups, such as pregnantwomen and young children.

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    National Drug Policy on Malaria

    First formulated in 1982Reviewed and revised periodically

    Aims at:Providing complete cure (clinical & parasitological).Preventing progression into severe malaria.

    Prevention of relapses.Interruption of transmission.Preventing development of resistance.

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    Criteria for change of Drug Policy

    Drug policy is changed for the area/Block PHCreporting 10% or more total treatment failure(ETF+LTF) to the tested drug i.e. the currently usedantimalarials in a sample of minimum 30P.falciparum test cases.

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    Diagnosis

    All fever cases suspected to be malaria should be investigated by:Microscopy:Sensitive, parasite load can be estimatedPossible to distinguish different speciesRapid Diagnostic Test (RDT):Detect malaria antigen (HRP-2/pLDH)Should be provided in remote locations

    In cases where parasitological diagnosis is not possible due to non-availability of microscopy or RDT, suspected malaria cases will be treatedwith full course of chloroquine till the result of microscopy are received.

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    Treatment of P. Vivax cases

    1. Chloroquine X 3 days 10 mg/kg on days 1 & 2followed by 5 mg/kg on day 3

    2. Primaquine X 14 days 0.25 mg/kg

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    Treatment of P. Vivax cases

    1. Chloroquine X 3 days 10 mg/kg on days 1 & 2followed by 5 mg/kg on day 3

    2. Primaquine X 14 days 0.25 mg/kg

    Presumptive treatment with Chloroquine is notrecommended

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    Treatment of P. Vivax cases

    1. Chloroquine X 3 days 10 mg/kg on days 1 & 2followed by 5 mg/kg on day 3

    2. Primaquine X 14 days 0.25 mg/kg

    Age inyears

    Tablet Chloroquine (150 mg base)

    Day 1 Day 2 Day 3

    TabletPrimaquine

    (2.5 mg base)

    Day 1 to Day 14

    < 1 01 - 4 1 1 1

    5 - 8 2 2 1 2

    9 - 14 3 3 1 4

    15 & above 4 4 2 6

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    Treatment of P. FalciparumArtemisinin based combination therapy (ACT)

    Day 1

    Artesunate4mg/kg BW

    Sulfadoxine(25mg/kg BW) +

    Pyrimethamine(1.25 mg/kg BW)

    Day 2

    Artesunate4mg/kg BW

    Primaquine0.25 mg/kg BW

    Day 3

    Artesunate4mg/kg BW

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    Age wise dosage schedule forP.Falciparum cases

    Age inyears

    Day 1 Day 2 Day 3

    Artesunate(50 mg)

    S+P(500+25)

    Artesunate(50mg)

    Primaquine(7.5mg base)

    Artesunate(50 mg)

    < 1 0

    1 4 1 1 1 1 1

    5 8 2 1 2 2 2

    9 14 3 2 3 4 3

    15 & above 4 3 4 6 4

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    Treatment of uncomplicatedP. Falciparum cases in pregnancy

    1 st Trimester

    Quinine10mg/kg BW

    tid X 7 days

    2nd Trimester

    ACT as perschedule

    3 rd Trimester

    ACT as perschedule

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    Treatment of severe Malaria cases

    Drug Dosage Route Remarks

    Artesunate 2.4 mg/kg BW IV / IM 0h,12h,24h od

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    Treatment of severe Malaria cases

    Drug Dosage Route Remarks

    Artesunate 2.4 mg/kg BW IV / IM 0h,12h,24h od

    Artemether3.2 mg/kg BW

    1.6 mg/kg BWIM od

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    Treatment of severe Malaria cases

    Drug Dosage Route Remarks

    Artesunate 2.4 mg/kg BW IV / IM 0h,12h,24h od

    Artemether3.2 mg/kg BW

    1.6 mg/kg BWIM od

    Arteether 150 mg IM od X 3 days

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    Treatment of severe Malaria cases

    Drug Dosage Route Remarks

    Artesunate 2.4 mg/kg BW IV / IM 0h,12h,24h od

    Artemether3.2 mg/kg BW

    1.6 mg/kg BWIM od

    Arteether 150 mg IM od X 3 days

    Quinine

    Quinine+Doxycyclin

    OrClindamycin

    20 mg/kg BW

    10 mg/kg BW

    10 mg/kg BW3mg / kg BW

    10mg/kg BW

    IV / IM

    Oral

    tid

    tid X 7 daysod X 7 days

    bd X 7 days

    ACT for 3 days after parenteral therapy

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    Chemoprophylaxis

    Only in selective groups in high pf endemic areas.Short term (up to 6 wks): Doxycyclin 100mg od 2days before travel & continued 4 weeks afterleaving malarious area.Long term (more than 6 wks) : Mefloquine 250 mgweekly 2 weeks before & 4 weeks after exposure.

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    THANK YOU

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    Epidemiological Profile : India (2008)

    Total Population : 1091 millionPopulation in malarious areas : 981.9 million

    No. of lab confirmed cases : 1.53 millionPf proportion : 50%No. of deaths due to malaria : 1061High transmission areas: 26%Low transmission areas: 64%Malaria free: 10%

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    Malaria Situation in India

    . . -----

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    Chloroquine Resistant Areas (1978-2008 August)