James Sande Odera
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
James Sande Odera has a total of 16 co-authors. Here are the top co-authors by number of shared publications:
- Bernhards Ogutu
Malaria Clinical Trials Alliance (MCTA), INDEPTH Network, Accra, Ghana
2 shared publications - Colin Ohrt
Armed Forces Research Institute of Medical Science, Bangkok, Thailand
2 shared publications - Peter McEvoy
Armed Forces Institute of Pathology, Washington DC, USA
2 shared publications - Shon Remich
Malaria Diagnostics Centre for Excellence, Walter Reed Project; United States Army Medical Unit-Kenya, Centre for Clinical Research, Kenya Medical Research Institute, Kisumu, Kenya
2 shared publications - Wendy Prudhomme O'MEara
Fogarty International Center, National Institutes of Health, Bethesda, Maryland, USA
2 shared publications - Ampon Nanakorn
Armed Forces Research Institute of Medical Science, Rajvithi Road, Bangkok, Thailand
1 shared publication
Latest Publications
- Open Access
- 28 January 2008
- Published by Springer Nature in Malaria Journal
- Vol. 7 (1) , 22
Pilot assessment of the sensitivity of the malaria thin film
Malaria microscopy remains the reference standard for malaria diagnosis in clinical trials (drug and vaccine), new diagnostic evaluation, as well as in clinical care in much of the world today. It is known that microscopy is an imperfect gold standard, and that very low false positive rates can dramatically lower protective efficacy estimates in malaria prevention trials. Although new methods are now available, including malaria rapid diagnostic tests and PCR, neither is as yet validated in the clinical trial setting and both have limitations. Surprisingly, the sensitivity of thin smears is not well established and thin smears are not commonly used in the developing world.
- 28 January 2008
- Published by Springer Nature in Malaria Journal
- Vol. 7 (1) , 22
Open AccessPilot assessment of the sensitivity of the malaria thin film
Malaria microscopy remains the reference standard for malaria diagnosis in clinical trials (drug and vaccine), new diagnostic evaluation, as well as in clinical care in much of the world today. It is known that microscopy is an imperfect gold standard, and that very low false positive rates can dramatically lower protective efficacy estimates in malaria prevention trials. Although new methods are now available, including malaria rapid diagnostic tests and PCR, neither is as yet validated in the clinical trial setting and both have limitations. Surprisingly, the sensitivity of thin smears is not well established and thin smears are not commonly used in the developing world.
- Open Access
- 12 June 2007
- Published by Springer Nature in Malaria Journal
- Vol. 6 (1) , 79
Establishing a malaria diagnostics centre of excellence in Kisumu, Kenya
Malaria microscopy, while the gold standard for malaria diagnosis, has limitations. Efficacy estimates in drug and vaccine malaria trials are very sensitive to small errors in microscopy endpoints. This fact led to the establishment of a Malaria Diagnostics Centre of Excellence in Kisumu, Kenya. The primary objective was to ensure valid clinical trial and diagnostic test evaluations. Key secondary objectives were technology transfer to host countries, establishment of partnerships, and training of clinical microscopists.
- 12 June 2007
- Published by Springer Nature in Malaria Journal
- Vol. 6 (1) , 79
Open AccessEstablishing a malaria diagnostics centre of excellence in Kisumu, Kenya
Malaria microscopy, while the gold standard for malaria diagnosis, has limitations. Efficacy estimates in drug and vaccine malaria trials are very sensitive to small errors in microscopy endpoints. This fact led to the establishment of a Malaria Diagnostics Centre of Excellence in Kisumu, Kenya. The primary objective was to ensure valid clinical trial and diagnostic test evaluations. Key secondary objectives were technology transfer to host countries, establishment of partnerships, and training of clinical microscopists.