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MALARIA

MALARIA. What is Malaria?. You know it. Well done. And for those who think they know little about malaria, follow us for next 35 minutes and go through your book at home. MALARIA. THE PARASITE. Plasmodium falciparum Plasmodium vivax Plasmodium ovale Tropical Africa

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MALARIA

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  1. MALARIA

  2. What is Malaria? • You know it. Well done. • And for those who think they know little about malaria, follow us for next 35 minutes and go through your book at home.

  3. MALARIA THE PARASITE

  4. Plasmodium falciparum • Plasmodium vivax • Plasmodium ovale • Tropical Africa • Plasmodium malariae • Karnataka

  5. MALARIA THE VECTOR

  6. Some species • An. culicifacies • An. fluviatilis • An. stephensi • An. minimus • An. philippinensis • An. sundaicus • An. maculatus

  7. Factors which determine vectorial importance of mosquitoes • DENSITY • Critical density- below which effective transmission cannot be maintained in a community • An. culicifacies- high density • An. fluviatilis- low density • LIFE SPAN

  8. CHOICE OF HOST • Anthrophilic species like An. fluviatilisare better vectors of malaria than zoophilic species • RESTING HABITS • Endophily • Exophily • BREEDING HABITS • TIME OF BITING • RESISTANCE TO INSECTICIDES

  9. MALARIA THE DISEASE

  10. Reservoir of infection • Human reservoir • Harbors the sexual forms (gametocytes) of the parasite • P. malariae • Chimpanzees in tropical Africa

  11. A patient can be a carrier of several plasmodia species at the same time • Children are more likely to be gametocyte carriers than adults. The child is thus epidemiologically a better reservoir than the adult.

  12. Conditions that must be met before a person can serve as a reservoir • Both male and female gametocytes are present in blood • Gametocytes are mature • Gametocytes are viable • Gametocytes are present in sufficient density to infect mosquitoes (at least 12/cumm of blood)

  13. Period of communicability • As long as mature, viable gametocytes exist in circulating blood in sufficient density

  14. Mode of transmission • Vector transmission • Direct transmission • Congenital malaria

  15. Incubation period • Falciparum • 12 (9-14) • Vivax • 14 (8-17) • Ovale • 17 (16-18) • Malariae • 28 (18-40)

  16. Clinical features • Signs and symptoms • Complications • Cerebral malaria • ARF • Liver damage • GI symptoms • Dehydration • Collapse • Anemia • Blackwater fever

  17. Anemia • Splenomegaly • Enlargement of liver • Herpes • Renal complications

  18. MALARIA GLOBAL SCENARIO

  19. Every minute 2 people die of malaria. By the time we will finish this lecture malaria would have killed180 more people.

  20. MALARIA SOUTH-EAST ASIA REGION

  21. MALARIA PREVENTION & control

  22. A. Malaria Vector Control • Integrated Vector Management (IVM) • Indoor Residual Spraying (IRS) • Insecticide Treated Nets (ITNs) • Other methods • Larviciding • Environmental management approaches to vector control • Personal protection measures (includes ITNs) • Fogging or area spraying Integrated vector management (IVM) is a rational decision-making processfor the optimal use of resourcesin the management of vector populations, so as to reduce or interrupt transmission of vector-borne diseases.

  23. INSECTICIDES Organo-Chlorines DDT Organo-Phosphates Malathion,Abate, Fenthion, Chlorpyrifos Carbamates Propoxur, Carbaryl Synthetic pyrethroids Tetramethrin, Resmethrin, Allethrin

  24. B. Diagnosis • Direct Microscopy • RDTs (Rapid diagnostic tests)

  25. Histidine-rich protein-2 (HRP2) • Parasite-specific lactate dehydrogenase (pLDH)

  26. C. Treatment Chloroquine25 mg/Kg over 3days PLUS Primaquine0.25 mg/kg BW daily for 14 days CQ Sensitive Vivax ACT PLUS Primaquine0.25 mg/kg BW daily for 14 days CQ Resistant ACT PLUS Primaquine0.75 mg/kg BW single dose Falciparum Severe Malaria ParenteralArtemesinin derivatives/Quinine Followed by full course of ACT

  27. Plasmodium vivax cases • Day 0: T. Chl 10 mg/kg BW (600 mg adult dose) • Day 1: T. Chl 10 mg/kg BW (600 mg adult dose) • Day 2: T. Chl 5 mg/kg BW (300 mg adult dose) • PLUS • T. Primaquin 0.25 mg/kg BW daily for 14 days

  28. ACT (Artesunate Combination Therapy) • T. Artesunate 4mg/kg BW daily X 3days • PLUS • T. Sulphadoxine 25 mg/kg BW and T. Pyrimethamin 1.25 mg/kg BW on the first day • Resistance to Chloroquine and ACT • Oral Quinine 10 mg/kg BW and T. Doxycycline 100 mg daily for 3 days THEREAFTER T. Primaquin 0.75 mg/kg BW single dose

  29. Artesunate 2.4 mg/Kg BW IV or IM at 0, 12 & 24 hrs, then daily • Artemether 3.2 mg/Kg BW at 0, then 1.6 mg.Kg BW per day • Quinine 20 mg salt/Kg BW at 0 (IV infusion), then 10 mg/Kg BW every 8 hrs

  30. D. Intermittent Preventive Treatment

  31. E. Malaria vaccines

  32. Pre-erythrocytic vaccines • Blood-stage vaccines • Transmission-blocking vaccines • Pfs25 • Cocktail vaccines • SPf66

  33. F. Chemoprophylaxis • Travelers from non-endemic areas • Soldiers serving in highly endemic areas • Migrant labourers • Should be complemented by personal protection and environmental measures • Intermittent preventive treatment in pregnancy

  34. For short-term prophylaxis (< 6 weeks) • Doxycycline 100 mg X OD in adults or 1.5 mg/kg BW for children >8 years old. • Started 2 days before travel and continued for 4 weeks after leaving the malarious area. • Contraindicated in pregnant females and children <8 years. • For long-term prophylaxis (>6 weeks) • Mefloquine 5 mg/kg BW (upto 250 mg) weekly • Started 2 weeks before travel and continued till 4 weeks of leaving the malarious area. • Contraindicated in cases with H/O convulsions, neuropsychiatric problems and cardiac conditions.

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