Vincent Batwala
Mbarara University of Science and Technology
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Featured researches published by Vincent Batwala.
Malaria Journal | 2010
Vincent Batwala; Pascal Magnussen; Fred Nuwaha
BackgroundPrompt, accurate diagnosis and treatment with artemisinin combination therapy remains vital to current malaria control. Blood film microscopy the current standard test for diagnosis of malaria has several limitations that necessitate field evaluation of alternative diagnostic methods especially in low income countries of sub-Saharan Africa where malaria is endemic.MethodsThe accuracy of axillary temperature, health centre (HC) microscopy, expert microscopy and a HRP2-based rapid diagnostic test (Paracheck) was compared in predicting malaria infection using polymerase chain reaction (PCR) as the gold standard. Three hundred patients with a clinical suspicion of malaria based on fever and or history of fever from a low and high transmission setting in Uganda were consecutively enrolled and provided blood samples for all tests. Accuracy of each test was calculated overall with 95% confidence interval and then adjusted for age-groups and level of transmission intensity using a stratified analysis. The endpoints were: sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV). This study is registered with Clinicaltrials.gov, NCT00565071.ResultsOf the 300 patients, 88(29.3%) had fever, 56(18.7%) were positive by HC microscopy, 47(15.7%) by expert microscopy, 110(36.7%) by Paracheck and 89(29.7%) by PCR. The overall sensitivity >90% was only shown by Paracheck 91.0% [95%CI: 83.1-96.0]. The sensitivity of expert microscopy was 46%, similar to HC microscopy. The superior sensitivity of Paracheck compared to microscopy was maintained when data was stratified for transmission intensity and age. The overall specificity rates were: Paracheck 86.3% [95%CI: 80.9-90.6], HC microscopy 93.4% [95%CI: 89.1-96.3] and expert microscopy 97.2% [95%CI: 93.9-98.9]. The NPV >90% was shown by Paracheck 95.8% [95%CI: 91.9-98.2]. The overall PPV was <88% for all methods.ConclusionThe HRP2-based RDT has shown superior sensitivity compared to microscopy in diagnosis of malaria and may be more suitable for screening of malaria infection.
Malaria Journal | 2011
Vincent Batwala; Pascal Magnussen; Kristian Schultz Hansen; Fred Nuwaha
BackgroundCurrent Uganda National Malaria treatment guidelines recommend parasitological confirmation either by microscopy or rapid diagnostic test (RDT) before treatment with artemether-lumefantrine (AL). However, the cost-effectiveness of these strategies has not been assessed at rural operational primary care centres.MethodsThree health centres (HCs) were randomized to three diagnostic arms (microscopy, RDT and presumptive diagnosis) in a district of low and another of high malaria transmission intensities in Uganda. Some 22,052 patients presenting with fever at outpatients departments were enrolled from March 2010 to February 2011. Of these, a random sample of 1,627 was selected to measure additional socio-economic characteristics. Costing was performed following the standard step-down cost allocation and the ingredients approach. Effectiveness was measured as the number and proportion of patients correctly diagnosed and treated. Incremental Cost-Effectiveness Ratios (ICERs) were estimated from the societal perspective (http://Clinicaltrials.gov, NCT00565071).ResultsOverall RDT was most cost-effective with lowest ICER US
Journal of Community Health | 2006
Sarah K. Nabukera; Kim Witte; Charles Muchunguzi; Francis Bajunirwe; Vincent Batwala; Edgar Mulogo; Celeste Farr; Souleymane Barry; Hamisu M. Salihu
5.0 compared to microscopy US
Malaria Journal | 2011
Vincent Batwala; Pascal Magnussen; Fred Nuwaha
9.61 per case correctly diagnosed and treated. In the high transmission setting, ICER was US
International Health | 2010
Vincent Batwala; Pascal Magnussen; Fred Nuwaha
4.38 for RDT and US
PLOS Neglected Tropical Diseases | 2008
Philippe J Guerin; Lisbeth M. Næss; Carole Fogg; Einar Rosenqvist; Loretxu Pinoges; Francis Bajunirwe; Carolyn Nabasumba; Ray Borrow; Leif O. Frøholm; Salah Ghabri; Vincent Batwala; Rogers Twesigye; Ingeborg S. Aaberge; John-Arne Røttingen; Patrice Piola; Dominique A. Caugant
12.98 for microscopy. The corresponding ICERs in the low transmission setting were US
PLOS ONE | 2016
Richard Mangwi Ayiasi; Patrick Kolsteren; Vincent Batwala; Bart Criel; Christopher Garimoi Orach
5.85 and US
International Journal of Medical Education | 2018
Achille Bapolisi; Katherine Crabtree; Jana Jarolimova; Caitrin Kelly; Katherine Kentoffio; Palka Patel; Geren S. Stone; Vincent Batwala
7.63 respectively. The difference in ICERs between RDT and microscopy was greater in the high transmission area (US
Advances in Public Health | 2018
Jonathan Izudi; Pontius Apangu; Francis Bajunirwe; Edgar Mulogo; Vincent Batwala
8.9) than in low transmission setting (US
Journal of Public Health in Africa | 2017
Nadege Goumkwa Mafopa; Gianluca Russo; Raoul Emeric Guetiya Wadoum; Emmanuel Iwerima; Vincent Batwala; Marta Giovanetti; Antonella Minutolo; Patrick Turay; Thomas B. Turay; Brima Kargbo; Massimo Amicosante; Mattei Maurizio; Carla Montesano
1.78). At a willingness to pay of US