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1.
Malar J ; 12: 240, 2013 Jul 12.
Article in English | MEDLINE | ID: mdl-23849053

ABSTRACT

BACKGROUND: Despite recent advances in malaria diagnosis and treatment, many isolated communities in rural settings continue to lack access to these life-saving tools. Community-case management of malaria (CCMm), consisting of lay health workers (LHWs) using malaria rapid diagnostic tests (RDTs) and artemisinin-based combination therapy (ACT) in their villages, can address this disparity. METHODS: This study examined routine reporting data from a CCMm programme between 2008 and 2011 in Saraya, a rural district in Senegal, and assessed its impact on timely access to rapid diagnostic tests and ACT. RESULTS: There was a seven-fold increase in the number of LHWs providing care and in the number of patients seen. LHW engagement in the CCM programme varied seasonally, 24,3% of all patients prescribed an ACT had a negative RDT or were never administered an RDT, and less than half of patients with absolute indications for referral (severe symptoms, age under two months and pregnancy) were referred. There were few stock-outs. DISCUSSION: This CCMm programme successfully increased the number of patients with access to RDT and ACT, but further investigation is required to identify the cause for over-prescription, and low rates of referrals for patients with absolute indications. In contrast, previous widespread stock-outs in Saraya's CCMm programme have now been resolved. CONCLUSION: This study demonstrates the potential for CCMm programmes to substantially increase access to life-saving malarial diagnostics and treatment, but also highlights important challenges in ensuring quality.


Subject(s)
Case Management/organization & administration , Malaria/diagnosis , Malaria/drug therapy , Adolescent , Adult , Aged , Aged, 80 and over , Antimalarials/therapeutic use , Artemisinins/therapeutic use , Child , Child, Preschool , Community Health Workers , Diagnostic Tests, Routine/methods , Drug Therapy, Combination/methods , Female , Health Services Accessibility/statistics & numerical data , Health Services Research , Humans , Infant , Infant, Newborn , Lactones/therapeutic use , Male , Middle Aged , Pregnancy , Senegal , Young Adult
2.
Malar J ; 12: 137, 2013 Apr 23.
Article in English | MEDLINE | ID: mdl-23617576

ABSTRACT

BACKGROUND: In sub-Saharan Africa, malaria is the leading cause of morbidity and mortality especially in children. In Senegal, seasonal malaria chemoprevention (SMC) previously referred to as intermittent preventive treatment in children (IPTc) is a new strategy for malaria control in areas of high seasonal transmission. An effectiveness study of SMC, using sulphadoxine-pyrimethamine (SP) plus amodiaquine (AQ), was conducted in central Senegal from 2008 to 2010 to obtain information about safety, feasibility of delivery, and cost effectiveness of SMC. Here are report the effect of SMC delivery on the prevalence of markers of resistance to SP and AQ. METHODS: This study was conducted in three health districts in Senegal with 54 health posts with a gradual introduction of SMC. Three administrations of the combination AQ + SP were made during the months of September, October and November of each year in children aged less than 10 years living in the area. Children were surveyed in December of each year and samples (filter paper and thick films) were made in 2008, 2009 and 2010. The prevalence of mutations in the pfdhfr, pfdhps, pfmdr1 and pfcrt genes was investigated by sequencing and RTPCR in samples positive by microscopy for Plasmodium falciparum. RESULTS: Mutations at codon 540 of pfdhps and codon 164 of pfdhfr were not detected in the study. Among children with parasitaemia at the end of the transmission seasons, the CVIET haplotypes of pfcrt and the 86Y polymorphism of pfmdr1 were more common among those that had received SMC, but the number of infections detected was very low and confidence intervals were wide. The overall prevalence of these mutations was lower in SMC areas than in control areas, reflecting the lower prevalence of parasitaemia in areas where SMC was delivered. CONCLUSION: The sensitivity of P. falciparum to SMC drugs should be regularly monitored in areas deploying this intervention. Overall the prevalence of genotypes associated with resistance to either SP or AQ was lower in SMC areas due to the reduced number of parasitaemia individuals.


Subject(s)
Antimalarials/pharmacology , Chemoprevention/methods , Drug Resistance , Genetic Markers , Plasmodium falciparum/drug effects , Plasmodium falciparum/genetics , Amodiaquine/pharmacology , Amodiaquine/therapeutic use , Antimalarials/therapeutic use , Child , Child, Preschool , Drug Combinations , Drug Therapy, Combination/methods , Female , Humans , Infant , Malaria, Falciparum/epidemiology , Malaria, Falciparum/parasitology , Malaria, Falciparum/prevention & control , Male , Mutation Rate , Plasmodium falciparum/isolation & purification , Prevalence , Pyrimethamine/pharmacology , Pyrimethamine/therapeutic use , Senegal/epidemiology , Sulfadoxine/pharmacology , Sulfadoxine/therapeutic use
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