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Great advances have been made in developing rapid diagnostic tests (RDTs) for diagnosing malaria. To date, RDTs present an exceedingly practical format for malaria diagnosis that outperforms traditional microscopy and more experimental next generation devices in the development pipeline. However, although use of such tests is accepted in principle, their actual use has lagged. Furthermore, study of how these tests perform, what their limitations are, and how to work with these limitations to still use them effectively has stagnated. We propose that the study and implementation of such RDTs should be aggressively advanced and propose a series of questions that can guide efforts.
Received April 20, 2009. Accepted for publication August 27, 2009.
Disclosure: Michael T. Makler and Robert C. Piper are co-owners of Flow Inc., in Portland, Oregon. Flow Inc. produces monoclonal antibodies to Plasmodium lactate dehydrogenase.
* Address correspondence to Robert C. Piper, Physiology Department, University of Iowa, 5660 Bowen Science Building, Iowa City, IA 52242. E-mail: robert-piper{at}uiowa.edu
Authors addresses: Michael T. Makler, Flow Inc., 6127 SW Corbett Avenue. Portland, OR 97239, E-mail: mikeatflow{at}aol.com. Robert C. Piper, Physiology Department, University of Iowa, 5660 Bowen Science Building, Iowa City, IA 52242, E-mail: robert-piper{at}uiowa.edu.
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