{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T02:48:07Z","timestamp":1792723687274,"version":"4.5.0"},"reference-count":40,"publisher":"American Society for Microbiology","issue":"6","license":[{"start":{"date-parts":[[2014,6,1]],"date-time":"2014-06-01T00:00:00Z","timestamp":1401580800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Clin Microbiol"],"published-print":{"date-parts":[[2014,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            <jats:named-content content-type=\"genus-species\">Plasmodium knowlesi<\/jats:named-content>\n            causes severe and fatal malaria in Malaysia. Microscopic misdiagnosis is common and may delay appropriate treatment.\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            can cross-react with \u201cspecies-specific\u201d parasite lactate dehydrogenase (pLDH) monoclonal antibodies used in rapid diagnostic tests (RDTs) to detect\n            <jats:named-content content-type=\"genus-species\">P. falciparum<\/jats:named-content>\n            and\n            <jats:named-content content-type=\"genus-species\">P. vivax<\/jats:named-content>\n            . At one tertiary-care hospital and two district hospitals in Sabah, we prospectively evaluated two combination RDTs for malaria diagnosis by using both a pan-\n            <jats:named-content content-type=\"genus-species\">Plasmodium<\/jats:named-content>\n            -pLDH (pan-pLDH)\/\n            <jats:named-content content-type=\"genus-species\">P. falciparum<\/jats:named-content>\n            -specific-pLDH (\n            <jats:italic>Pf<\/jats:italic>\n            -pLDH) RDT (OptiMAL-IT) and a non-\n            <jats:named-content content-type=\"genus-species\">P. falciparum<\/jats:named-content>\n            VOM-pLDH\/\n            <jats:italic>Pf<\/jats:italic>\n            -HRP2 RDT (CareStart). Differential cross-reactivity among these combinations was hypothesized to differentiate\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            from other\n            <jats:named-content content-type=\"genus-species\">Plasmodium<\/jats:named-content>\n            monoinfections. Among 323 patients with PCR-confirmed\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            (\n            <jats:italic>n<\/jats:italic>\n            = 193),\n            <jats:named-content content-type=\"genus-species\">P. falciparum<\/jats:named-content>\n            (\n            <jats:italic>n<\/jats:italic>\n            = 93), and\n            <jats:named-content content-type=\"genus-species\">P. vivax<\/jats:named-content>\n            (\n            <jats:italic>n<\/jats:italic>\n            = 37) monoinfections, the VOM-pLDH individual component had the highest sensitivity for nonsevere (35%; 95% confidence interval [CI], 27 to 43%) and severe (92%; CI, 81 to 100%)\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            malaria. CareStart demonstrated a\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            sensitivity of 42% (CI, 34 to 49%) and specificity of 74% (CI, 65 to 82%), a\n            <jats:named-content content-type=\"genus-species\">P. vivax<\/jats:named-content>\n            sensitivity of 83% (CI, 66 to 93%) and specificity of 71% (CI, 65 to 76%), and a\n            <jats:named-content content-type=\"genus-species\">P. falciparum<\/jats:named-content>\n            sensitivity of 97% (CI, 90 to 99%) and specificity of 99% (CI, 97 to 100%). OptiMAL-IT demonstrated a\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            sensitivity of 32% (CI, 25 to 39%) and specificity of 21% (CI, 15 to 29%), a\n            <jats:named-content content-type=\"genus-species\">P. vivax<\/jats:named-content>\n            sensitivity of 60% (CI, 42 to 75%) and specificity of 97% (CI, 94 to 99%), and a\n            <jats:named-content content-type=\"genus-species\">P. falciparum<\/jats:named-content>\n            sensitivity of 82% (CI, 72 to 89%) and specificity of 39% (CI, 33 to 46%). The combination of CareStart plus OptiMAL-IT for\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            using predefined criteria gave a sensitivity of 25% (CI, 19 to 32%) and specificity of 97% (CI, 92 to 99%). Combining two RDT combinations was highly specific for\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            malaria diagnosis; however, sensitivity was poor. The specificity of pLDH RDTs was decreased for\n            <jats:named-content content-type=\"genus-species\">P. vivax<\/jats:named-content>\n            and\n            <jats:named-content content-type=\"genus-species\">P. falciparum<\/jats:named-content>\n            because of\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            cross-reactivity and cautions against their use alone in areas where\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            malaria is endemic. Sensitive\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            -specific RDTs and\/or alternative molecular diagnostic tools are needed in areas where\n            <jats:named-content content-type=\"genus-species\">P. knowlesi<\/jats:named-content>\n            malaria is endemic.\n          <\/jats:p>","DOI":"10.1128\/jcm.00181-14","type":"journal-article","created":{"date-parts":[[2014,4,3]],"date-time":"2014-04-03T06:17:43Z","timestamp":1396505863000},"page":"2053-2060","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":52,"title":["Combining Parasite Lactate Dehydrogenase-Based and Histidine-Rich Protein 2-Based Rapid Tests To Improve Specificity for Diagnosis of Malaria Due to Plasmodium knowlesi and Other Plasmodium Species in Sabah, Malaysia"],"prefix":"10.1128","volume":"52","author":[{"given":"Matthew 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