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Assessment of malaria burden
Source: TropIKA
Title of the session: Assessment of malaria burden Date: 03 November 2009 Agenda item: Scientific session 13 Session theme: Epidemiology Meeting room: Tsavo Ballroom 2 Chair(s):
Presenters:
TropIKA rapporteur: Daniel Kiboi Major topics:
Keywords: Scope: The session covered on epidemiology of malaria, immunity and pregnancy associated malaria (PAM) prevalence in varying transmission setting of Africa. Effects of intervention strategies such a use of antimalarial drugs or use of Insecticides Treated Nets (ITNs) on the epidemiology of malaria was assessed. REPORT ON ORIGINAL SESSIONOverviewThe true burden of malaria in Diemo Senegal was higher that already recorded, Diagne shows that decreased susceptibility to malaria infection was associated with increasing age. Studies in KEMRI-Wellcome Trust also reflected the same scenario showing progression of febrile malaria to asymptomatic malaria with increasing age. A Trimethoprim-sulfamethoxazole (TS) prophylaxis study in Tororo, Uganda was associated with 40% increased protection against malaria in HIV exposed children under 5 years. This is the first reported study on prophylactic potential of TS in HIV exposed children. Report on increased risk of treatment failure on the use of amodiaquine-sulfadoxine-pyrimethamine (AQ-SP) in Kampala Uganda, The treatment failure was associated with low immunity as opposed to expected SP resistance. CONTEXT AND ISSUEMalaria burden in Diemo Senegal higher that reported, Diemo Senegal, to assess the prevalence of malaria in high transmission region Diemo Senegal, follow up study for 18 years, children under 5 years to 18 years old Does TS prophylaxis protect HIV-infected children against malaria? Tororo Uganda, Observational studies suggest Trimethoprim-sulfamethoxazole protects HIV-infected children against malaria Inconsistencies in febrile malaria in relation to immunity in children, Kenya, Motivation of population to use antimalarial drugs, Dakar Senegal, high use of antimalarial drugs despite being low transmission areas Efficacy of Amodiaquine—sulfadoxine/pyrimenthamine (AQ-SP) combination, Amodiaquine-artesunate (AQ-ASN) and Artemether-lumefantrine (AL), Kampla Uganda, to assess the efficacy of AQ-ASN, AQ-SP and AL combination therapies, children under 5 years Key facts and figuresMalaria burden in Diemo Senegal is higher that currently estimated, all 86 enrolled children presented with at least 2 malaria attacks within the follow up period A Trimethoprim-sulfamethoxazole (TS) prophylaxis protects HIV exposed children under 5 years against malaria by 40% Over diagnosis of malaria in Dakar Senegal results to self medication and overuse of antimalarial drugs, documented prevalence rate in Dakar is below 10% Treatment failure is associated with AQ-SP in Kampala Uganda, 14.1% treatment failure recorded for the combination, Initiatives on the ground; experience/s derivedCross-sectional and longitudinal studies were carried out, Report by Diagne from Senegal analyzed data of 81 children (20 months) and were followed at least ten years. Taylor Sandison, conducted the first randomized clinical trial of Trimethoprim-sulfamethoxazole (TS) protective efficacy among HIV-exposed children. Research FindingsDiemo Senegal daily surveillance of endemic populations shows that the malaria burden is much higher than previously believed and that the susceptibility to the disease varies considerably according to individuals (Diagne). Antibodies to the infected red cell surface were associated with acquiring asymptomatic infection rather than febrile malaria or remaining uninfected (Philip Bejon) Over use of antimalarial drugs in Dakar Senegal associated with self diagnosis (Diallo) Risk of treatment failure of associated with AQ-SP in Kampala Uganda (Denise Njama-Meya) Lessons learnedFirst report on prophylactic potential of Trimethoprim-sulfamethoxazole in HIV positive children Decreased susceptibility to malaria episodes with increasing age associated with development of immunity due to exposure to malaria infections. Immunoglobulin G 4 associated with increased risk of developing severe malaria. Immunity against malaria varies between individual in high transmission due to variant antigens associated with Plasmodium falciparum. Children in low transmission areas have higher malaria episodes than children in high transmission areas Issues raised, obstacles, difficultiesFuture plansEffects of SP resistance on the efficacy of TS combination in HIV positive children under 5 years Regulated use of antimalarial drugs to curb against self medication, FINDINGS AND CONCLUSIONSFrom formal presentationsTranslational Research ImpactImplementation of TS in prophylaxis of malaria episodes in children under 5 years Knowledge gap createdRelationship between Immunoglobulin G4 associated with increased risk of developing severe malaria. From open discussions/debatesReasons for increased malaria prevalence in Diemo Senegal, is it because of resistance or vector factors? The effects of HIV on malaria episodes in HIV positive children in relation to increased protective effects of Trimethoprim-sulfamethoxazole Identified conclusionsMain points of agreementPotential of Trimethoprim-sulfamethoxazole in prophylaxis against malaria of HIV exposed children Main points of divergenceIncreased prevalence of malaria in Dakar Senegal could be due to changes in vector behavior. Sulfadoxine-pyrimethamine resistance still varying in different areas Recommendations
CommentsPersonal observations from rapporteurEffectiveness of antimalarial drugs depended on various reasons such as immunity, nutritional status of the patients and proper adherence of the prescription. Comments |
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