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A  COMPARATIVE  STUDY  ON  EFFICACY   AND  ADVERSE  EFFECTS  OF  ANTIMALARIALS   WITH  SPECIAL  EMPHASIS  ON  PARASITE  CLEARANCE  TIME Dr. Tanoy  Bose Co-Authors: Laskar B, Kalita BC, Das S, Dutta A Department of Medicine Assam Medical College, Dibrugarh
Introduction & Epidemiology ~ 2 million laboratory confirmed cases/yr but case incidence is 30 fold or more underestimated. †  40-50% is P.falciparum. † P. falciparum: Majority parasite (>60%) in NE India: hot spot for proliferation and corridor for spread of drug-resistant malaria to rest of peninsular India. ‡ NVBDC still depends on Chloroquine to combat malaria ; RESULT: Pf has taken deep roots in malaria endemic regions. § Continuation of an outdated drug in Rx of all P.f cases : counterproductive in fighting drug res malaria & containment of Pf.  § Trends of malaria transmission and species composition in the Sonapur Primary Health Centre, Kamrup district, Assam for the years (1991-2007). Pf, Plasmodium falciparum; Pv, Plasmodium vivax; SPR, slide positivity rate.‡ † NATIONAL ANTI MALARIA DRUG POLICY (2007)  ‡ Rolling back malaria is possible.V. Dev, G.C. Doley & A. P. Dash: Indian J Med Res 128, July 2008, pp 82-83 § Battling malaria iceberg with chloroquine in India Vinod P Sharma :Malaria Journal 2007,6:105
Objectives: To  study  the  efficacy  of  enteral  and parenteralantimalarials on parasite density and   parasite  clearance  time Their  short  term  adverse  effects   in  patients  admitted  with malaria  in  a  teaching  hospital  of  a  malaria  endemic  region.
Methodology A hospital based nonrandomised observational study Study Duration: August 2006 to July 2007, Assam Medical College & Hospital 165  patients  were  selected  from OPD & Indoor on  the  basis  of  slide  positivity  for  Plasmodium  falciparum  malaria by multiple observers. Divided  into  3  groups,  each  group  receiving  Chloroquine	(Group A)  Oral: 25 mg/Kg over 3 days Quinine 	(Group B)  I.V: 20mg/Kg load X 4hrs f/b 10mg/Kg 8hourly until oral Rx ( Total 7 d)    Artesunate 	(Group C) I.V: 2.4mg/Kg  f/b 1.2mg/Kg at 12h,24h & daily X 5days Clinical  assessment  and  parasitological  assessment  was  done  before  the  initiation  of  treatment  and  at  day  1,  2,  3,  7,  and  14  of  treatment  and  followed  up  at  day  21  and  28 Resistant cases were treated as per WHO Malaria 2006 Guidelines   Data analysed and interpreted by a single observer
Inclusion & Exclusion Criteria: Exclusion Criteria ,[object Object]
 Coexistent other Systemic illness revealed on Clinical and laboratory evidence
 Intake of any antimalarials in past 6 weeks
 PregnancyInclusion Criteria ,[object Object]
 Axillary Temperature ≥37.5ºC
 Uncomplicated malaria
 Not receiving any antimalarial prior to hospitalisation

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A COMPARATIVE STUDY ON EFFICACY AND ADVERSE EFFECTS OF ANTIMALARIALS WITH SPECIAL EMPHASIS ON PARASITE CLEARANCE TIME

  • 1. A COMPARATIVE STUDY ON EFFICACY AND ADVERSE EFFECTS OF ANTIMALARIALS WITH SPECIAL EMPHASIS ON PARASITE CLEARANCE TIME Dr. Tanoy Bose Co-Authors: Laskar B, Kalita BC, Das S, Dutta A Department of Medicine Assam Medical College, Dibrugarh
  • 2. Introduction & Epidemiology ~ 2 million laboratory confirmed cases/yr but case incidence is 30 fold or more underestimated. † 40-50% is P.falciparum. † P. falciparum: Majority parasite (>60%) in NE India: hot spot for proliferation and corridor for spread of drug-resistant malaria to rest of peninsular India. ‡ NVBDC still depends on Chloroquine to combat malaria ; RESULT: Pf has taken deep roots in malaria endemic regions. § Continuation of an outdated drug in Rx of all P.f cases : counterproductive in fighting drug res malaria & containment of Pf. § Trends of malaria transmission and species composition in the Sonapur Primary Health Centre, Kamrup district, Assam for the years (1991-2007). Pf, Plasmodium falciparum; Pv, Plasmodium vivax; SPR, slide positivity rate.‡ † NATIONAL ANTI MALARIA DRUG POLICY (2007) ‡ Rolling back malaria is possible.V. Dev, G.C. Doley & A. P. Dash: Indian J Med Res 128, July 2008, pp 82-83 § Battling malaria iceberg with chloroquine in India Vinod P Sharma :Malaria Journal 2007,6:105
  • 3. Objectives: To study the efficacy of enteral and parenteralantimalarials on parasite density and parasite clearance time Their short term adverse effects in patients admitted with malaria in a teaching hospital of a malaria endemic region.
  • 4. Methodology A hospital based nonrandomised observational study Study Duration: August 2006 to July 2007, Assam Medical College & Hospital 165 patients were selected from OPD & Indoor on the basis of slide positivity for Plasmodium falciparum malaria by multiple observers. Divided into 3 groups, each group receiving Chloroquine (Group A) Oral: 25 mg/Kg over 3 days Quinine (Group B) I.V: 20mg/Kg load X 4hrs f/b 10mg/Kg 8hourly until oral Rx ( Total 7 d) Artesunate (Group C) I.V: 2.4mg/Kg f/b 1.2mg/Kg at 12h,24h & daily X 5days Clinical assessment and parasitological assessment was done before the initiation of treatment and at day 1, 2, 3, 7, and 14 of treatment and followed up at day 21 and 28 Resistant cases were treated as per WHO Malaria 2006 Guidelines Data analysed and interpreted by a single observer
  • 5.
  • 6. Coexistent other Systemic illness revealed on Clinical and laboratory evidence
  • 7. Intake of any antimalarials in past 6 weeks
  • 8.
  • 11. Not receiving any antimalarial prior to hospitalisation
  • 12.
  • 13.
  • 14. A parasitemia >15000/cumm of blood was associated with similar S/S & biochemical profile
  • 15.
  • 16. Chloroquine & Artesunate arm were relatively free from adverse effects except for hyperbilirubinemia in artesunate arms
  • 17. Tinnitus & Hypoglycemia were noticed in 6.66% of patients receiving Quinine
  • 18.
  • 19. Take Home Message Artesunate is the most efficacious and least toxic antimalarial and is associated with early recovery & discharge from hospital Parenteral Quinine though almost equally efficacious as artesunate, it’s use is associated with important adverse effects and needs close monitoring In management of uncomplicated falciparum malaria, the high prevalence of chloroquine resistance should be kept in mind by the clinicians
  • 20. THANK YOU The Department Of Medicine, Assam Medical College,Dibrugarh