Prevalence of and Risk Factors Associated with Polymerase Chain Reaction-Determined Plasmodium falciparum Positivity on Day 3 after Initiation of Artemether-Lumefantrine Treatment for Uncomplicated Malaria in Bagamoyo District, Tanzania

被引:9
作者
Mwaiswelo, Richard [1 ,2 ]
Ngasala, Billy [1 ,3 ]
Jovel, Irina [4 ]
Xu, Weiping [4 ]
Larsson, Erik [4 ]
Malmberg, Maja [5 ,6 ]
Gil, Jose Pedro [3 ,7 ]
Premji, Zul [8 ]
Mmbando, Bruno P. [9 ]
Martensson, Andreas [3 ]
机构
[1] Muhimbili Univ Hlth & Allied Sci, Dept Parasitol & Med Entomol, POB 65011, Dar Es Salaam, Tanzania
[2] Hubert Kairuki Mem Univ, Dept Microbiol & Parasitol, Dar Es Salaam, Tanzania
[3] Uppsala Univ, Dept Womens & Childrens Hlth, Int Maternal & Child Hlth IMCH, Uppsala, Sweden
[4] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Stockholm, Sweden
[5] Swedish Univ Agr Sci, Virol Sect, Dept Biomed Sci & Vet Publ Hlth, Uppsala, Sweden
[6] Swedish Univ Agr Sci, Dept Anim Breeding & Genet, SLU Global Bioinformat Ctr, Uppsala, Sweden
[7] Karolinska Inst, Div Pharmacogenet, Dept Physiol & Pharmacol, Drug Resistance Unit, Stockholm, Sweden
[8] Aga Khan Univ Hosp, Nairobi, Kenya
[9] Natl Inst Med Res, Tanga Ctr, Dept Stat & Epidemiol, Tanga, Tanzania
基金
瑞典研究理事会;
关键词
ARTEMISININ RESISTANCE; COMBINATION THERAPY; CHILDREN; CHLOROQUINE; CLEARANCE; PARASITES; AMODIAQUINE; ARTESUNATE; ALLELES; GENE;
D O I
10.4269/ajtmh.18-0729
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Prevalence of and risk factors associated with polymerase chain reaction (PCR)-determined Plasmodium falciparum positivity were assessed on day 3 after initiation of treatment, pre-implementation and up to 8 years post-deployment of artemether-lumefantrine as first-line treatment for uncomplicated malaria in Bagamoyo district, Tanzania. Samples originated from previously reported trials conducted between 2006 and 2014. Cytochrome b-nested PCR was used to detect malaria parasites from blood samples collected on a filter paper on day 3. Chi-square and McNemar chi-squared tests, logistic regression models, and analysis of variance were used as appropriate. Primary outcome was based on the proportion of patients with day 3 PCR-determined P. falciparum positivity. Overall, 256/584 (43.8%) of screened patients had day 3 PCR-determined positivity, whereas only 2/584 (0.3%) had microscopy-determined asexual parasitemia. Day 3 PCR-determined positivity increased from 28.0% (14/50) in 2006 to 74.2% (132/178) in 2007-2008 and declined, thereafter, to 36.0% (50/139) in 2012-2013 and 27.6% (60/217) in 2014. When data were pooled, pretreatment microscopy-determined asexual parasitemia >= 100,000/mu L, hemoglobin < 10 g/dL, age < 5 years, temperature >= 37.5 degrees C, and year of study 2007-2008 and 2012-2013 were significantly associated with PCR-determined positivity on day 3. Significant increases in P. falciparum multidrug resistance gene 1 N86 and P. falciparum chloroquine resistant transporter K76 across years were not associated with PCR-determined positivity on day 3. No statistically significant association was observed between day 3 PCR-determined positivity and PCR-adjusted recrudescence. Day 3 PCR-determined P. falciparum positivity remained common in patients treated before and after implementation of artemether-lumefantrine in Bagamoyo district, Tanzania. However, its presence was associated with pretreatment characteristics.
引用
收藏
页码:1179 / 1186
页数:8
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