Field evaluation of an automated RDT reader and data management device for Plasmodium falciparum/Plasmodium vivax malaria in endemic areas of Colombia

被引:32
作者
Herrera, Socrates [1 ,2 ]
Vallejo, Andres F. [1 ,2 ]
Quintero, Juan P. [1 ,2 ]
Arevalo-Herrera, Myriam [1 ,2 ,3 ]
Cancino, Marcela [4 ]
Ferro, Santiago [4 ]
机构
[1] Caucaseco Sci Res Ctr, Cali, Colombia
[2] Latin Amer Ctr Malaria Res, Cali, Colombia
[3] Univ Valle, Fac Hlth, Cali, Colombia
[4] Fio Corp, Toronto, ON, Canada
关键词
DekiReader; Malaria rapid diagnostic test; PCR; mHealth; RAPID DIAGNOSTIC-TESTS; MONOCLONAL-ANTIBODIES; FALCIPARUM; MICROSCOPY; QUALITY; PCR; PERFORMANCE; INFECTIONS; CHILDREN; PROTEIN;
D O I
10.1186/1475-2875-13-87
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Massive implementation of malaria diagnostics in low-resource countries is regarded as a pivotal strategy in control and elimination efforts. Although malaria rapid diagnostic tests (RDTs) are considered a viable alternative, there are still obstacles to the widespread implementation of this strategy, such as reporting constraints and lack of proper quality assurance of RDT-based programmes at point-of-care (POC). Methods: A prospective cohort of patients, seeking routine care for febrile episodes at health centres in malaria-endemic areas of Colombia, was used to assess the diagnostic performance of a device based on smartphone technology (Deki Reader (TM), former codename "GenZero"), that assists users at POC to process RDTs. After informed consent, patients were enrolled into the study and blood samples were collected for thick blood smear (TBS) and RDT. The RDT results were interpreted by both visual inspection and Deki Reader device and concordance between visual and device interpretation was measured. Microscopy corrected by real-time polymerase chain reaction (PCR) and microscopy were "gold standard" tests to assess the diagnostic performance. Results: In total, 1,807 patients were enrolled at seven health centres in malaria-endemic areas of Colombia. Thirty-three Plasmodium falciparum and 100 Plasmodium vivax cases were positive by corrected microscopy. Both sensitivity and specificity were 93.9% (95% CI 69.7-95.2) and 98.7% (95% CI 98.5-99.4) for P. falciparum, and 98.0% (95% CI 90.3-98.9) and 97.9% (95% CI 97.1-98.5) for P. vivax. Percentage concordance between visual and device interpretation of RDT was 98.5% and 99.0% for P. vivax and P. falciparum, respectively. The RDT, when compared to TBS, showed high sensitivity and specificity for P. falciparum in both visual and device interpretation, and good overall diagnostic performance for P. vivax. Comparison between PCR as gold standard and visual and device interpretation showed acceptable overall performance for both species. Conclusions: The diagnostic performance of the Deki Reader was comparable to visual interpretation of RDTs (without significant differences) for both malaria species. Providing standardized automated interpretation of RDTs at POC in remote areas, in addition to almost real-time reporting of cases and enabling quality control would greatly benefit large-scale implementation of RDT-based malaria diagnostic programmes.
引用
收藏
页数:10
相关论文
共 38 条
  • [21] Quality Assurance of Rapid Diagnostic Tests for Malaria in Routine Patient Care in Rural Tanzania
    McMorrow, Meredith L.
    Masanja, M. Irene
    Kahigwa, Elizeus
    Abdulla, Salim M. K.
    Kachur, S. Patrick
    [J]. AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2010, 82 (01) : 151 - 155
  • [22] Monoclonal Antibodies Against Recombinant Histidine-Rich Protein 2 of Plasmodium falciparum and Their Use in Malaria Diagnosis
    Merwyn, Samuel
    Gopalan, Natarajan
    Singh, Anil Kumar
    Rai, Ganga Prasad
    Agarwal, Gauri Shanker
    [J]. HYBRIDOMA, 2011, 30 (06): : 519 - 524
  • [23] Treatment guided by rapid diagnostic tests for malaria in Tanzanian children: safety and alternative bacterial diagnoses
    Mtove, George
    Hendriksen, Ilse C. E.
    Amos, Ben
    Mrema, Hedwiga
    Mandia, Victor
    Manjurano, Alphaxard
    Muro, Florida
    Sykes, Alma
    Hildenwall, Helena
    Whitty, Christopher J. M.
    Reyburn, Hugh
    [J]. MALARIA JOURNAL, 2011, 10
  • [24] Mukadi P, 2012, MALAR J S1, V11, pP65
  • [25] Treatment of malaria restricted to laboratory-confirmed cases: a prospective cohort study in Ugandan children
    Njama-Meya, Denise
    Clark, Tamara D.
    Nzarubara, Bridget
    Staedke, Sarah
    Kamya, Moses R.
    Dorsey, Grant
    [J]. MALARIA JOURNAL, 2007, 6 (1)
  • [26] Submicroscopic Infection in Plasmodium falciparum-Endemic Populations: A Systematic Review and Meta-Analysis
    Okell, Lucy C.
    Ghani, Azra C.
    Lyons, Emily
    Drakeley, Chris J.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2009, 200 (10) : 1509 - 1517
  • [27] Comparative Diagnosis of Malaria Infections by Microscopy, Nested PCR, and LAMP in Northern Thailand
    Poeschl, Birgit
    Waneesorn, Jarurin
    Thekisoe, Oriel
    Chutipongvivate, Salakchit
    Panagiotis, Karanis
    [J]. AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2010, 83 (01) : 56 - 60
  • [28] Minimising human error in malaria rapid diagnosis: clarity of written instructions and health worker performance
    Rennie, Waverly
    Phetsouvanh, Rattanaxay
    Lupisan, Socorro
    Vanisaveth, Viengsay
    Hongvanthong, Bouasy
    Phompida, Sarnlane
    Alday, Portia
    Fulache, Mila
    Lumagui, Richard
    Jorgensen, Pernille
    Bell, David
    Harvey, Steven
    [J]. TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2007, 101 (01) : 9 - 18
  • [29] Detection of four Plasmodium species in blood from humans by 18S rRNA gene subunit-based and species-specific real-time PCR assays
    Rougemont, M
    Van Saanen, M
    Sahli, R
    Hinrikson, HP
    Bille, J
    Jaton, K
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (12) : 5636 - 5643
  • [30] Schellenberg D, 2011, PLOS MED, V8