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Diagnostic performance of CareStart™ malaria HRP2/pLDH (Pf/pan) combo test versus standard microscopy on falciparum and vivax malaria between China-Myanmar endemic borders
Malaria Journal volume 12, Article number: 6 (2013)
Rapid diagnostic test (RDT) is becoming an alternative way of establishing quickly the diagnosis of malaria infections, by detecting specific malaria antigens in suspected patients’ blood between the China-Myanmar endemic borders areas, towards achieving the National Malaria Elimination programme by 2020. The objective of this study is to evaluate the performance of CareStart™ Malaria Pf/Pan RDT kit for the diagnosis of malaria infections in suspected patients. Blood examination by microscopy was taken as gold standard to evaluate CareStart™ kit’s sensitivity, specificity and predictive value and corrected with PCR assay.
Overall 126 of 241 (52.28%) malaria cases were detected by microscopy compared to 115 of 241(47.72%) CareStart™ kit and 128 of 241 (53.11%) PCR corrected assay. CareStart™ kit’s sensitivity and specificity for the diagnosis of malaria were 89.68% and 98.26% respectively, compared to standard microscopy, whereas the sensitivity and specificity for falciparum malaria were 88.52% and 98.26%, and for vivax malaria: 90.77% and 100%. The CareStart™ positive predictive values were 98.26% (93.88-99.52%, 95% CI) compared to 100% (96.77-100%, 95% CI) for PCR-corrected, and the negative predictive values of 89.68% (83.15-93.87%, 95% CI) were the same in microscopy as PCR-corrected. The diagnostic accuracy of CareStart™ kit versus microscopy and PCR were 93.78% (89.99-96.19%, 95% CI) and 94.61% (90.99-96.82%, 95% CI) respectively. The likelihood of diagnostic of malaria positive was almost similar between microscopy and CareStart™ kit, with an entropy reduction of 60.0% compared to a weak likelihood of misdiagnosis of 0.10 (0.09-0.12, 95% CI), with an entropy reduction of 36.01%.
The accuracy of CareStart™ kit is comparable to gold standard microscopy in these areas, it is easy to perform and suitable for cross-border diagnosis and monitoring of local or imported malaria patterns by any local health staff in endemic remotes.
Malaria remains unevenly endemic across Yunnan The CareStart™ P.f/P.v Combo province, Southeast China. Within Yunnan, malaria occurs mainly at the border areas, in the drainage areas of the Yuanjiang River and amongst the high population of motile ethnic minority groups at risk living in forests and on forest fringes for economic reasons, on the China-Myanmar borders . While parasite-based diagnosis is increasing, most suspected cases of malaria are not properly identified, with accurate diagnosis and disease monitoring consequently remaining elusive .
Although malaria cases and deaths have dropped substantially over the past decade, efforts must be intensified in the malaria-endemic communities to abolish the public threat of malaria by prompt diagnosis and effective treatment . However, limitations of comparative field trials and the heterogeneous nature of malaria transmission has limited the availability of good quality performance diagnostic that the National Malaria Elimination programme requires for a surveillance response system and to make informed decisions and implementation towards malaria elimination by 2020.
Technical support for malaria prevention and control in China is provided at national level by the National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention (CDC), based in Shanghai. The strategies of the National Malaria Elimination programme 2010–2020 include greater access to early diagnosis and prompt treatment coverage in remote areas, free distribution of long-lasting, insecticide-treated bed nets (LLINs), strengthening quality and regulatory mechanisms for anti-malarial drugs, strengthening malaria surveillance and information systems, epidemic preparedness, increasing the awareness of malaria, involvement and empowerment, basic and applied research on Plasmodium vivax and Plasmodium falciparum, whilst monitoring the indicators for malaria elimination . Moreover, World Health Organization (WHO) recommends that malaria case management be based on parasite-based diagnosis in all cases, with the exception of young children in areas of high transmission and where lack of resources or need for urgent response temporarily limits its applications [1–4] The use of antigen-detecting rapid diagnostic tests (RDTs) forms a vital part of this strategy, providing the possibility of parasite-based diagnosis in areas where good quality microscopy cannot be maintained . There are numerous malaria RDTs that are commercially available in many formats, including plastic cassettes, cards or dipsticks, and quality depends on manufacturer as well as storage conditions . The variation depends on malaria antigen targeted for detection in blood flowing along a membrane containing specific anti-malaria antibodies. Previous studies from clinical trials have found that HRP-2 based P. falciparum-specific tests generally have greater sensitivity (over 90%) than the pLDH-based tests when compared with microscopy in clinical cases, whilst sensitivity of pLDH tests for non-P. falciparum species was low [6, 7]. Specificity of both types of tests was reported to be good (>85%). Despite the encouraging results from the RDT trials in clinical cases, there is limited information about the sensitivity, specificity and predictive value in the endemic China-Myanmar malaria population where laboratory facilities are not available. Reports of wide variation in accuracy of malaria RDTs in published field trials usually compared with light microscopy as a gold standard [8–10]. The CareStart™ P.f/P.v combo test (detecting histidine-rich protein (pHRP-2) and P. vivax-specific lactate dehydrogenase (pLDH) has been evaluated in a few field settings, including higher sensitivities for P. falciparum (99.4%) reported in Ethiopia with P. falciparum samples with parasite densities above 100/μl, , sensitivities for P. falciparum low values at parasite densities <100/μl (60.0%) and increasing sensitivity at higher parasite densities (100% at >500/μl) reported in Madagascar , and sensitivities for the detection of P. vivax were significantly higher than those found in Ethiopia with pLDH (pan) (91.0%), but similar results for the CareStart™ malaria pLDH (pan/Pf) reported in Myanmar . Similarly, some studies evaluating other RDTs in non-endemic countries reported similar sensitivities as those found for the CareStart™ malaria HRP-2/pLDH (Pf/pan) combo test but a different degree of sensitivity and specificity for P. falciparum ranging from 87.5-99.0% [6–14] and for P. vivax, RDTs detecting pan-pLDH showed sensitivities ranging from 62.0-95.0%, [10–15] compared to 46.0%-93.0% for those RDTs targeting aldolase . The increase of sensitivities at higher parasite densities is a well known phenomenon with breakpoints around 100/μl (P. falciparum) and 500/μl (P. vivax) [6, 13, 17, 18].
The aim of the study was to evaluate the performance of CareStart™ malaria Pf/pan test kit in early diagnosis for prompt effective case management of malaria.
The CareStart™ malaria HRP-2/pLDH (Pf/pan) combo test was evaluated in suspected patients attending TengChong CDC, China and Health Unlimited clinic in Laiza City, Kachin State, Myanmar, near the China-Myanmar border. Standard microscopy method was done for all thick smears corrected by polymerase chain reaction (PCR) assay. The assessment of the diagnostic performance was performed in comparison the CareStart™ (CS) kit with gold standard microscopic results, corrected by PCR assay.
Blood sample collection
The study was conducted in July to December, 2011 in TengChong CDC, China and Health Unlimited clinic in Laiza City, Kachin State, Myanmar, near the China-Myanmar border on all suspected patients. Individual biodata and malaria history in the previous one year were documented from each suspected case as well as an informed consent. All patients had venous blood samples collection for microscopy and CS kit evaluation and also samples were collected in EDTA and stored at −20°C condition for PCR analysis.
The study was reviewed and approved by the Ethical Committee of Yunnan Institute of Parasitic Diseases, Yunnan province and Health Ministry of Kachin State of Myanmar. All patients provided informed consent before admission into the study.
Standard microscopy evaluation
Duplicate thin and thick slides were made from all blood, stained using 5% Giemsa stain and dyed for 30 minutes, read under x100 electron microscopy. The malaria microscopic examination was performed by two independent experienced microscopists, for identification of the malaria parasite species. The number of parasites was counted against 200 leucocytes and quantification of parasite density was estimated by assuming 8,000 leucocytes/μl blood. Samples were considered negative when no parasite was detected after examining 100 microscopic fields . In order to check for interobserver difference, a double-blind cross reading of a random 50 blood slides was performed by a senior microscopist.
CareStart™ malaria kit assessment
The CS RDT kit contains a membrane strip, which is pre-coated with two monoclonal antibodies as two separate lines across a test strip. One monoclonal antibody (test line 2) is pan-specific to lactate dehydrogenase (pLDH) of the Plasmodium species (P. falciparum, P. vivax, Plasmodium malariae and Plasmodium ovale) and the other line (test line 1) consists of a monoclonal antibody specific to histidine-rich protein 2 (HRP2) of the P. falciparum species. The conjugate pad is dispensed with monoclonal antibodies, which are pan-specific to pLDH and P. falciparum specific to HRP2. The CS RDT kit is designed for the differential diagnosis between P. falciparum and other pan-specific species. The CS RDT kit was supplied by the China-England Advanced Communication Project and is produced by American Access Bio Company; batch number C201R, period of validity to February 2012. The test reproducibility was evaluated by testing 15 samples representing all species at variable parasite densities on three consecutive occasions in Teng Chong CDC.
CareStart™ malaria test procedures
Tests were performed according to manufacturer’s instructions. Readings were carried out at daylight, assisted by a standard electric bulb, by three health worker-observers performing and interpreting the test results. The first observer performed readings at 20 minutes, reading time recommended by the manufacturer, followed by observers 2 and 3 within the next 10 minutes. The observers were blinded to each other’s readings and to the results of microscopy and PCR assay.
In the case when no control line appeared, the test was considered invalid and was repeated. To score line intensities, a scoring system of five categories was used as defined previously : none (no line visible), faint (barely visible line), weak (paler than the control line), medium (equal to the control line) or strong (stronger than the control line).
The test results were based on consensus agreement, which meant that an identical result read by at least two out of three health worker-observers was withheld. In the case of no consensus, the results of the first reader were considered. To assess inter-observer agreement, results of positive and negative readings as well as line intensities were considered.
Test detection and validation
The sensitivity and specification of CS RDT kit were performed by random selection of P. falciparum and P. vivax cases, and negative blood samples for 10 times repeat tests, and the results estimated following the manufacturer specification.
Plasmodium species identification
All cases were identified by microscopy and analysed by real-time PCR for detection of the 18 s rRNA of malaria parasite for confirmation, species identification and determination of parasite density, as described previously . In the case of discordant results between microscopy and PCR, the results of PCR were used as the standard method.
All data were processed using Excel to build database and Wilson score software was used for analysis. Sensitivity, specificity and predictive values were calculated separately for P. falciparum and the non-falciparum species with 95% CI.
The Pearson Chi-square test was used to determine significance of results, or in the case of a small sample size, a two-tailed Fisher’s exact test. A p-value <0.05 was considered statistically significant.
General characteristics of patients
A total of 241 blood samples from suspected patients were analysed for malaria parasites by the CS RDT kit and the results were compared with results from gold standard microscopy, corrected by PCR assay. The male: female ratio was 3.54:1. The mean age was 29.62 ± 11.21 years (range 3–58 years old) of which the majority 89.21% (215) were older than 18 years and only four patients (1.66%) were under five years. The microscopic results indicated that 52.28% (126 of 241) of patients were infected with malaria. Among the malaria-positive patients, 51.58% (65 of 126) harboured P. vivax, 43.63% (55 of 126) had P. falciparum, and 4.76% (six of 126) mixed infections of P. vivax and P. falciparum. There were only two cases of missed diagnosis observed by microscopy.
The geometric mean parasite density was 5,990, ranged (48~377143/μl. The parasite density distribution showed that 3.18% cases were <100 parasites/μl, 11.90% cases were between 100~1000/μl and 84.95% cases were >1,000 parasites/μl.
The median parasite density in 13 missed cases by CS was 348/μl, ranged from 48 ~ 22,688/μl, of which four cases were <100 μl, three cases between 100~1,000/μl and six cases were >1,000 parasites/μl (see Table 1).
Comparison of CareStart™ kit, standard microscopy and polymerase chain reaction results
Two (1.58%) positive cases initially misdiagnosed by microscopy were identified by PCR assays and CS RDT kit. There was no significant difference between the sensitivity of PCR and standard microscopy, however the specificity of PCR assay was 100% against 98.26% for microscopy. The diagnostic accuracies of both diagnostic methods were comparable. The likelihood of ratio of a positive test and negative test were 51.57 (19.32-137.7) and 0.11 (0.09, 0.12) respectively. The negative entropy after a positive microscopic test was 60.44%, whereas the microscopy and PCR entropy reduction after a negative test were 36.1% and 35.96% respectively. There was no significant difference between the Cohen’s kappa values of microscopy compared to PCR assay (see Table 2).
CareStart™ malaria test results
The CS kit results indicated that 47.72% (115/241) of the patients were infected with malaria. Among the positive samples, malaria species identified showed that P. vivax represented 51.30% (59/115), P. falciparum or P. falciparum mixed other species was present 48.70% (56/115). Two cases microscopically negative were CS kit P. falciparum positive whereas 13 cases (six cases of P. vivax and seven cases of P. falciparum) originally detected by microscopy were not detected by CS RDT kit. The summary results of microscopy and CS kit results are showed in Table 3.
Sensitivity, specificity and predictive values of CareStart™ malaria kit
The CareStart™ P.f/P.v Combo test sensitivity ranged between 88.55 - 90.77% and specificity ranged 98.26 - 100% (95%CI) when compared to gold standard microscopic blood films for detection of malaria. The mean CS malaria P.v/P.f rapid kit sensitivity was 89.68% (83.15-93.97%, 95% CI) and mean specificity was 98.26% (93.88-100%, 95% CI). The positive predictive value was 98.26% (93.88-99.52, 95% CI) and negative predictive value of 89.68% (89.68-3.87%, 95% CI) when compared to traditional blood films for falciparum and vivax malaria detection. The diagnostic accuracy of CS compared to microscopy was 93.78% (89.99-96.19%) (see Table 3).
Results of polymerase chain reaction assay
Real-time PCR for diagnosis of malaria, and identification of parasite species showed a difference in P. falciparum and P. vivax sensitivity of 88.89% and 90.77%, but similar specificity species identification of 100%. The assay confirmed 128 Plasmodium cases of which 49.22% (63/128) were falciparum against the predominant 50.72% (65/128) vivax malaria in the areas. In contrast, CS diagnosis had a lower specificity to P. vivax of 98.26%, but same specificity for P. falciparum when compared with corrected PCR assay results, as shown in Table 3.
The important finding of this study was that the CS kit had sensitivity of 89.68% and specificity of 98.26% compared to the gold standard microscopy method for detection of malaria. The CS sensitivity for the detection of P. falciparum was 98.3% and 99.3% in samples with parasite densities above 100/μl and 1,000/μl respectively whereas the sensitivity for P. vivax was 97.6% for parasite densities above 500/μl. No positive result occurred among the Plasmodium-negative samples, which is consistent with the recent study of CS kit in Ethiopia . RDTs detecting P. vivax-specific pLDH CS kit based on specific monoclonal antibody, detected histidine-rich protein 2(HRP-2, test line 1) and four kinds of lactic acid dehydrogenase of Plasmodium in human blood (pLDH, test line 2) in a card detection device, aseptic and single packing. The comparison of the sensitivity and specificity of the CS-RDTs versus microscopy corrected by PCR assay (Table 3) indicated that the detection rate was relatively similar for P. vivax and P. falciparum, indicating that the microscopic training performed had a high efficiency on the performance microscopists. This kit showed no need of sophisticated equipment and facilities, and was easy to operate. Its applicability and rapidity in diagnosis could be of additional value for both falciparum and vivax malaria detection and prompt case management as well as cross borders malaria monitoring in the China-Myanmar endemic areas in the National Malaria Elimination programme.
In total, 241 kits, and 20 kits for quality assurance and control, were used in this study without the invalid case, specificity and sensitivity of this batch kit was 100%, which implied the quality was stable. However, the false negative rate of (10.4%) 13/126 documented in the study can be explained only partly by the CS threshold level of >100 parasites/μl and probably the CS storage conditions and duration in the field resulted in loss of sensitivity, since the quality assurance and control testing was 100%.
The CareStart™ P.f/P.v Combo (detecting HRP-2 and P. vivax-specific pLDH) test has been evaluated in Ethiopia [11–25] compared to this study which reported higher sensitivity for P. falciparum (99.4%). No clear reason could be given for increasing sensitivity and possibly included exclusively P. falciparum samples with parasite densities above 100/μl, which is above the detection threshold of most RDTs . Also, CareStart™ malaria pLDH (Pf/pan) combo test has been evaluated in a field study in Madagascar which reported sensitivities for P. falciparum low values at parasite densities <100/μl (60.0%) and increasing sensitivity at higher parasite densities (100% at >500/μl) .
The two products (CareStart™ malaria pLDH (Pf/pan) combo test) and CareStart™ brand (malaria pLDH (pan)), evaluated in Myanmar, reported sensitivities for the detection of P. vivax were significantly higher than those found in Ethiopia with pLDH (pan) (91.0%), but results were similar for the CareStart™ malaria pLDH (pan/Pf) [13–25].
A study in The Philippines compared the results of the ICT malaria P.f/P.v RDT with microscopy and found a high discordant rate involving cases positive for P. falciparum by the RDT, but negative by microscopy .
The CareStart™ malaria pLDH (Pf/pan) combo test field study in Madagascar reported sensitivities for P. falciparum that are comparable to the present study, but there were only nine P. vivax samples included, making comparison difficult . Moreover, the CareStart™ brand (malaria pLDH (pan)) has also been evaluated in Myanmar with similar results obtained across the China-Myanmar malaria endemic borders .
When PCR was the reference method, the microscopic method showed a low specificity (88.2%). The P. vivax and P. falciparum positive and negative predictive values of CS were 100% and 94.96% compared to 100% and 94.17% respectively. In addition, P. vivax diagnostic accuracy of CS was 96.67% compared to 94.89% for P. falciparum. The differential explanation could be the lack of differentiation of other species of Plasmodium species as reported in Thailand . However, the two blood slides from the samples could not show malaria parasites microscopically. The negative predictive values of CS observed could not be directly explained but may be attributed to possible genetic heterogeneity of HRP2 as well as possible geographic variations in malaria antigens.
This study recorded two misdiagnosed microscopic cases, corrected using PCR assay, whereas 13 cases were not detected by CS kit. The reported sensitivities for the detection of P. vivax were significantly higher than those found in the present study in case of the CareStart™ malaria pLDH (Pf/pan) (88.52%), but for the CareStart™ malaria pLDH (Pv/pan) they were in line with the previous findings (90.77%) [10, 11].
Studies evaluating other RDTs in non-endemic countries report similar sensitivities as those found for the CareStart™ malaria HRP-2/pLDH (Pf/pan) combo test in this study for P. falciparum where they ranged from 87.5-99.0%, with one exception of 76.2%, whereas for P. vivax, RDTs detecting pan-pLDH showed sensitivities of 33.5% and 62.0%-95.0% [6–9]. The detection rates as demonstrated by WHO/FIND are slightly higher as compared to the sensitivities found in this study, but the differences were not statistically significant .
The specificity and sensitivity of CS kit were 89.68% and 98.26%, a difference not statistically significant than previous CS results in southwest Ethiopia (see Table 2) . The sensitivity and specificity documented in this study can be accounted for by the long historical trends of anti-malarial usage, counterfeit, substandard and counter prescription contributing to the progression of selective pressure of malaria parasites in the blood stream and hence low parasitaemia below the CS kit detection threshold. The findings showed that CS usefulness in detection and case management of malaria in remote areas and on motile populations across borders has implications in the search for more efficient and sensitive diagnostic tools for parasite detection and case management in areas of low endemicity, as well as targeting gametocyte detection towards blocking the transmission, and monitoring malaria elimination.
The study demonstrated that the CareStart™ malaria HRP-2/pLDH (Pf/pan) combo test performs satisfactory well for the detection of P. falciparum and P. vivax malaria infections in cross-border malaria. Hence, providing a rationale surveillance response system for malaria cross-border control and elimination programmes in conjunction with national malaria programmes is urgently needed for China’s National Malaria Elimination programme for 2020.
Histidine-rich protein 2
Pan Plasmodium-specific parasite lactate dehydrogenase
Polymerase chain reaction
Foundation for innovative new diagnostics
Plasmodium falciparum-specific parasite lactate dehydrogenase
Plasmodium-specific parasite lactate dehydrogenase
Plasmodium vivax-specific parasite lactate dehydrogenase
Rapid diagnostic test
World health organization.
World Health Organization: Malaria rapid diagnostic test performance. Results of WHO product testing of malaria RDTs. 2010, Geneva: World Health Organisation
McMorrow ML, Masanja MI, Abdulla SM, Kahigwa E, Kachur SP: Challenges in routine implementation and quality control of rapid diagnostic tests for malaria-Rufiji District, Tanzania. Am J Trop Med Hyg. 2008, 79: 385-390.
Ministry of Health: Annual malaria reports. 2010, Beijing, People’s Republic of China
World Health Organization: Malaria rapid diagnostic test performance. Results of WHO product testing of malaria RDTs: round 1. 2009, Geneva: World Health Organization
Moody A: Rapid diagnostic tests for malaria parasites. Clin Microbiol Rev. 2002, 15: 66-78. 10.1128/CMR.15.1.66-78.2002.
Wongsrichanalai C, Barcus MJ, Muth S, Sutamihardja A, Wernsdorfer WH: A review of malaria diagnostic tools: microscopy and rapid diagnostic test (RDT). Am J Trop Med Hyg. 2007, 77: 119-127.
Hopkins H, Kambale W, Kamya MR, Staedke SG, Dorsey G, Rosenthal PJ: Comparison of HRP2- and pLDH-based rapid diagnostic tests for malaria with longitudinal follow-up in Kampala, Uganda. Am J Trop Med Hyg. 2007, 76: 1092-1097.
Tjitra E, Suprianto S, Dyer M, Currie BJ, Anstey NM: Detection of histidine-rich protein 2 and pan-malarial ICT MALARIA P.v. test antigens after chloroquine treatment of uncomplicated falciparum malaria does not reliably predict treatment outcome in eastern Indonesia. J Clin Microbiol. 1999, 37: 2412-2417.
Mason DP, Kawamoto F, Lin K, Laoboonchai A, Wongsrichanalai C: A comparison of two rapid field immunochromatographic tests to expert microscopy in the diagnosis of malaria. Acta Trop. 2002, 82: 51-59. 10.1016/S0001-706X(02)00031-1.
Maltha J, Gillet P, Bottieau E, Cnops L, van Esbroeck M, Jacobs J: Evaluation of a rapid diagnostic test (CareStart™ malaria HRP-2/pLDH (Pf/pan) combo test) for the diagnosis of malaria in a reference setting. Malar J. 2010, 9: 171-10.1186/1475-2875-9-171.
Mekonnen Z, Ali S, Belay G, Suleman S, Chatterjee S: Evaluation of the performance of CareStart™ Malaria Pf/Pv Combo rapid diagnostic test for the diagnosis of malaria in Jimma, southwestern Ethiopia. Acta Trop. 2010, 113: 285-288. 10.1016/j.actatropica.2009.12.001.
Ratsimbasoa A, Randriamanantena A, Raherinjafy R, Rasoarilalao N, Menard D: Which malaria rapid test for Madagascar? Field and laboratory evaluation of three tests and expert microscopy of samples from suspected malaria patients in Madagascar. AmJTrop Med Hyg. 2007, 76: 481-485.
Ashley EA, Touabi M, Ahrer M, Hutagalung R, Htun K, Luchavez J, Dureza C, Proux S, Leimanis M, Lwin MM, Koscalova A, Comte E, Hamade P, Page AL, Nosten F, Guerin PJ: Evaluation of three parasite lactate dehydrogenase-based rapid diagnostic tests for the diagnosis of falciparum and vivax malaria. Malar J. 2009, 8: 241-10.1186/1475-2875-8-241.
Gillet P, Bosselaers K, Cnops L, Bottieau E, Van Esbroeck M, Jacobs J: Evaluation of the SD FK70 malaria Ag plasmodium vivax rapid diagnostic test in a non-endemic setting. Malar J. 2009, 8: 129-10.1186/1475-2875-8-129.
Fogg C, Twesigye R, Batwala V, Piola P, Nabasumba C, Kiguli J, Mutebi F, Hook C, Guillerm M, Moody A, Guthmann JP: Assessment of three new parasite lactate dehydrogenase (pan-pLDH) test for diagnosis of uncomplicated malaria. Trans R Soc Trop Med Hyg. 2008, 102: 25-31. 10.1016/j.trstmh.2007.09.014.
Marx A, Pewsner D, Egger M, Nuesch R, Bucher HC, Genton B, Hatz C, Juni P: Meta-analysis: accuracy of rapid tests for malaria in travelers returning from endemic areas. Ann Intern Med. 2005, 142: 836-846.
Sharew B, Legesse M, Animut A, Jima D, Medhin G, Erko B: Evaluation of the performance of CareStart™ malaria Pf/Pv combo and paracheck Pf® tests for the diagnosis of malaria in wondo genet, southern Ethiopia. Acta Trop. 2009, 111: 321-324. 10.1016/j.actatropica.2009.05.014.
Craig MH, Bredenkamp BL, Williams CH, Rossouw EJ, Kelly VJ, Kleinschmidt I, Martineau A, Henry GF: Field and laboratory comparative evaluation of ten rapid malaria diagnostic tests. Trans R Soc Trop Med Hyg. 2002, 96: 258-265. 10.1016/S0035-9203(02)90092-1.
WHO/TDR: Determining cost effectiveness of malaria rapid diagnostic tests in rural areas with high prevalence. 1996, Geneva: World Health Organization
Rougemont M, Van Saanen M, Sahli R, Hinrikson HP, Bille J, Jaton K: Detection of four plasmodium species in blood from humans by 18S rRNA gene subunit-based and species-specific real-time PCR assays. J Clin Microbiol. 2004, 42: 5636-5643. 10.1128/JCM.42.12.5636-5643.2004.
Moges B, Amare B, Belyhun Y, Tekeste Z, Gizachew M, Workineh M, Gebrehiwot A, Woldeyohannes D, Mulu A, Kassu A: Comparison of CareStart™ HRP2/pLDH COMBO rapid malaria test with light microscopy in north-west Ethiopia. Malar J. 2012, 11: 234-10.1186/1475-2875-11-234.
Ashton RA, Takele K, Gezahegn T, Helen C, Damtew Y, Bonnie C, Richard R, Jan HK: Performance of three multi-species rapid diagnostic tests for diagnosis of plasmodium falciparum and plasmodium vivax malaria in oromia regional state. Ethiopia. Malar J. 2010, 9: 297-10.1186/1475-2875-9-297.
Bell D, Wongsrichanalai C, Barnwell JW: Ensuring quality and access for malaria diagnosis: how can it be achieved?. Nat Rev Microbiol. 2006, 4: 682-695. 10.1038/nrmicro1474.
Murray CK, Gasser RA, Magill AJ, Miller RS: Update on rapid diagnostic testing for malaria. Clin Microbiol Rev. 2008, 21: 97-110. 10.1128/CMR.00035-07.
Singh N, Saxena A: Usefulness of a rapid on-site Plasmodium falciparum diagnosis (Paracheck PF) in forest migrants and among the indigenous population at the site of their occupational activities in central India. Am J Trop Med Hyg. 2005, 72: 26-29.
Thanks go to all staff of TengChong CDC and Dehong Health, Rose Health Center, Myanmar and all patients for their cooperation.
The authors declare that they have no competing interests.
ET, SX and XZ participated in the design of the study, execution, statistical analysis and drafted the manuscript. WC, CZ, ET and DY performed the PCR assays. WJ, WJ collected the blood sample. All authors read and approved the manuscript.
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Xiaodong, S., Tambo, E., Chun, W. et al. Diagnostic performance of CareStart™ malaria HRP2/pLDH (Pf/pan) combo test versus standard microscopy on falciparum and vivax malaria between China-Myanmar endemic borders. Malar J 12, 6 (2013) doi:10.1186/1475-2875-12-6