Comparison of CareStart™ HRP2/pLDH COMBO rapid malaria test with light microscopy in north-west Ethiopia
© Moges et al.; licensee BioMed Central Ltd. 2012
Received: 18 May 2012
Accepted: 20 July 2012
Published: 20 July 2012
In Ethiopia, light microscopy is the gold standard for malaria diagnosis although it is not available in most peripheral health facilities. It is time consuming, requires trained personnel and needs careful preparation and application of reagents to ensure quality results. This study was aimed at testing the diagnostic performance of CareStart™ malaria rapid diagnostic test (RDT) with reference to light microscopy for the diagnosis of falciparum and vivax malaria in Ethiopia.
Blood samples were collected from 254 patients suspected to have malaria at Kola Diba Health Center in the late malaria transmission peak season from November 2011 to December 2011. The samples were examined immediately by light microscopy and the RDT (CareStart™ Malaria HRP2/pLDH COMBO Test kit). Statistical analysis was performed using SPSS version 16 and the JavaStat two-way contingency table analysis.
The overall sensitivity and specificity of CareStartTM RDT was found to be 95% (90–97.9%, 95% CI) and 94.2% (90.9–96%, 95% CI), respectively. The sensitivity of the CareStartTM RDT for Plasmodium falciparum or mixed infection was calculated to be 92.9% (82.5–98%, 95%CI) while a sensitivity of 90.9% (74.1–98.4%, 95%CI) was found for non-falciparum species. The specificity for P. falciparum or mixed infections was found to be 95.4% (92.5–96.8%, 95%CI) while it was 97.3% (94.8–98.4%, 95%CI) for non-falciparum species. There was an excellent agreement between the two tests with a kappa value of 0.918.
The CareStartTM RDT test showed good sensitivity and specificity with an excellent agreement to the reference light microscopy. The RDT could therefore be used in place of light microscopy, which in poor set-ups cannot be used routinely.
KeywordsCareStart™ Light microscopy Malaria Rapid diagnostic test Ethiopia
Malaria is ranked as the leading communicable disease in Ethiopia, accounting for about 30% of the overall Disability Adjusted Life Years lost. Approximately 68% of the total population of 78 million lives in areas at risk of malaria . According to Ethiopia’s Federal Ministry of Health (FMOH), in 2008/2009, malaria was the leading cause of outpatient visits, health facility admissions and inpatient deaths, accounting for 12% of reported outpatient visits and nearly 10% of admissions. Because a large proportion of the population does not have access to health care services, these figures probably under-estimate the true burden of malaria in the country . In Ethiopia, Plasmodium falciparum and Plasmodium vivax are the major parasites accounting for about 70% and 30% of infections, respectively, during peak transmission periods [2, 3].
The malaria transmission pattern in Ethiopia is highly seasonal and unstable . Because of this unstable transmission and infrequent exposure to infection, immunity is generally under-developed and all age groups are at risk of malarial disease. Although pregnant women and children under five years of age are the most vulnerable groups, the population at age five and older is also high risk .
In the prevention and control of malaria, prompt and accurate diagnosis is the key to effective disease management . However, in Ethiopia, clinical diagnosis and empirical treatment has been the mainstay of malaria management in areas where laboratory facilities are not available. Due to the non-specific nature of signs and symptoms of malaria, clinical diagnosis is unreliable [3, 5, 6]. In many countries malaria is still being diagnosed clinically, an unreliable method leading to over-diagnosis and over-treatment . Light microscopy (LM) remains preferred and standard for laboratory diagnosis of malaria although it is not accessible and affordable in most peripheral health facilities in the country. Moreover, microscopy is time consuming, requires trained personnel and needs careful preparation and application of reagents to ensure quality results [6, 8]. For a better and sustainable control, malaria diagnosis requires a more rapid, easy, sensitive and specific method.
Malaria rapid diagnostic test (RDT) was introduced in the 1990s and has undergone many improvements . The CareStart™ Malaria HRP-2/ pLDH (Pf/PAN) Combo Test is a three-band RDT detecting HRP-2 and PAN-pLDH. RDTs for detection of P. falciparum and other species have been used by health extension workers (HEWs) at health posts in Ethiopia since 2005 [10–14]. It is a new tool for the rapid qualitative determination of malaria histidine-rich protein 2 (HRP2) and lactate dehydrogenase in human blood, aiding the diagnosis of malaria infection.
This study was conducted to evaluate the sensitivity and specificity of CareStart™ rapid malaria test in reference to the conventional LM in north-west Ethiopia.
Study area and period
The cross-sectional study was conducted at Kola Diba Health Center in Dembia District from November to December 2011, which was a peak transmission season in Ethiopia. The district is malarious and covers an area of 1,270 km2. The altitude of the district ranges between 1,750 and 2,100 m above sea level. It has a population of more than 300,000 and the majority of its population depends on subsistence farming. Kola Diba Health Center is one of the health centres in the district where people with symptoms suggestive of malaria obtain free services for diagnosis and treatment. Despite the presence of different control activities in the area, it remained endemic for both P. vivax and P. falciparum malaria despite a strong control effort.
Two hundred and fifty four malaria suspected patients attending the medical and paediatric out-patient departments of Kola Diba Health Center during the study period were included and screened for malaria infection using LM and the CareStart™ RDT. Patients who had received anti-malarial drugs during the past four weeks and critically ill patients who were unable to give blood were excluded from the study.
Specimen collection and processing
The socio-demographic characteristics and clinical data of the participants were collected using a structured and pre-tested questionnaire. Finger-prick samples were collected and placed in a grease-free, clean, glass slide. The same finger-prick blood sample was used to carry out the RDT in parallel, following manufacturer’s instructions. In a single slide, both thick and thin films were prepared. The thin films were fixed in methanol after air-drying, the slides were stained in 10% Giemsa solution for 15 min. Thin and thick films were read at the health centre by an experienced laboratory technician and the result was considered negative if no parasites were seen after examination of 200 fields at 1,000x magnification. The technician was blinded to the results of the RDT. All blood films were re-read a second time by an experienced microscopist at Gondar University Hospital laboratory who was also blinded to initial microscopy and RDT results. In cases where the results were discordant, a third expert reader was used. The results of the third expert reader were considered final. All the microscopists were from Gondar University Hospital laboratory. The laboratory is labelled as three star laboratory during the national pre-accreditation assessment by the Ethiopian Health and Nutrition Research Institute (EHNRI) which is on the final stages of accreditation by the WHO-AFRO. The laboratory is involved in external quality assurance (EQA) at EHNRI and the Amhara Regional Research and Diagnostic Laboratory. All the microscopists involved in the study had pre-study training and were qualified.
The collected data were computerized using Excel program, exported and analysed by SPSS version 16 and JavaStat two-way contingency table analysis. Sensitivity, specificity, and positive and negative predictive values were determined for both tests and compared with one another. Kappa value was determined to see the consistency of the results among the diagnostic tools. A P value of less than 0.05 was considered significant in all comparisons.
Ethical clearance was obtained from the Institutional Review Board (IRB) of the University of Gondar, College of Medicine and Health Sciences. Verbal consent was taken from all study participants and mothers/guardians of all children under 18 after explaining the purpose and objective of the study. Participants who were diagnosed to have malaria were given the appropriate treatment at the health centre.
Parasite positivity as detected by light microscopy among different socio-demographic factors of patients using logistic regression analysis
Parasite positivity by the LM
Age group in years
Parasite positivity detected by light microscopy based on patient signs and symptoms using logistic regression analysis
Myalgia and arthralgia
Malaria parasite positivity based on light microscopy and CareStart TM RDT
P.falciparum Number (%)
P. vivax(PAN only) Number (%)
Mixed (pf+PAN) Number (%)
Negative Number (%)
Total Number (%)
Performance characteristics of CareStart TM by species identified in comparison to the standard reference light microscopy*
Sensitivity% (95% CI)
Specificity% (95% CI)
PPV% (95% CI)
NPV% (95% CI)
Agreement between tests Kappa (95% CI)
Pf or mixed by LM vs pf/pan by RDT
Non-Pf (by LM) vs Pan only (by RDT)
All positive by LM vs all positive by RDT
Since both the Pf-specific and the ‘PAN’ antigen used by the CareStartTM RDT are detected in P. falciparum infections, giving the result “Pf plus PAN” even for non-mixed P. falciparum infections, it was not possible to directly compare the performance of the test against P. falciparum single infections detected by LM. Therefore, the sensitivity and specificity of “Pf or mixed” (by LM) to “Pf plus PAN” (by RDT) were compared, whilst non-falciparum infections detected by LM were compared directly to the “PAN only” RDT results (Table 4). Accordingly, the sensitivity of the CareStartTM RDT for P. falciparum or mixed infection compared to LM was calculated to be 92.9% (82.5–98%, 95%CI) while a sensitivity of 90.9% (74.1–98.4%, 95%CI) was found for non- falciparum species. The specificity for P. falciparum or mixed infections was found to be 95.4% (92.5–96.8%, 95%CI) while it was 97.3% (94.8–98.4%, 95%CI) for non-falciparum species (Table 4).
Of note in the present study was an excellent agreement between CareStartTM RDT and LM with a Kappa value of 0.918. There was also a very good agreement between the RDT and LM in detecting different species of Plasmodium: Kappa value of 0.853 for P. falciparum or mixed infection and Kappa value of 0.849 for non-falciparum species.
The present study revealed a high sensitivity and specificity of the CareStartTM RDT (Table 4). The high sensitivity of the RDT in this study was in line with other studies from south-west Ethiopia  and Madagascar . The current study revealed a higher sensitivity and a slightly lower specificity than reports from Myanmar . Overall, the CareStartTM RDT showed good sensitivity when compared to the LM. In set ups where health personnel rely on their clinical judgment, using RDT for the diagnosis of malaria can be helpful for early institution of treatment.
This study had also tried to evaluate the performance of the CareStartTM RDT in detecting different species of malaria parasite. The finding in the current study was higher than that reported by Ashton et al from Oromia Regional State of Ethiopia . The sensitivity of the RDT in the current study for P. falciparum or mixed infection was also higher than that by Maltha et al (78.5%) . However, the sensitivity in this study was found to be lower than reports from south-west Ethiopia , south Ethiopia  and Madagascar . These differences could be due to observer variation, difference with malaria species circulating at different localities or host factors .
The specificity of the CareStartTM in the present study for P. falciparum or mixed infections was higher than the reports from Oromia Regional State in Ethiopia and Madagascar [15, 17] and lower than the reports from southern  and south-west Ethiopia . The specificity for the non-falciparum species in the current study was comparable to the reports of some studies , higher in some others  and lower in elsewhere [11, 12]. The differences in the specificity of the RDT could be due to the aforementioned reasons .
The RDT had high NPV, meaning that it was reliable in ruling out malaria. Similarly, the higher PPV means that patients will be correctly diagnosed as positive for malaria and avoids unnecessary treatment.
The overall prevalence of malaria in the study area was very high, as detected by either the CareStartTM RDT (39.4%) or the LM (40.9%). The result was higher than the report from Oromia Regional State in Ethiopia (23.2%)  while it was in agreement with a report from three regions in Ethiopia . The high prevalence could be partly explained by the fact that the study was conducted in a peak malaria transmission season in the country. Also, the malaria transmission pattern in Ethiopia is highly seasonal and unstable. Because of this unstable transmission and infrequent exposure to infection, immunity is generally under-developed and all age groups are at risk of malarial disease . On the other hand, it might be due to development of anti-malarial or insecticide resistance in the area . The knowledge, attitude and practice of the participants could also be a factor . However, these assumptions should be evaluated with further studies. The high prevalence of malaria, despite the tremendous effort to distribute bed nets and apply outdoor insecticides, heralds the need to evaluate the malaria control system in the area and beyond.
Current subjective or objective fever (axillary temperature of >37.50c) was the most common presenting symptom by the participants (Table 2). Fever detects only 40.9% malaria. This could be explained by the fact that individuals may carry parasites without symptoms. On the other hand, the significant overlap of malaria symptoms with other tropical diseases might have impaired the specificity of fever and encouraged the indiscriminate use of anti-malarials for managing febrile conditions in endemic areas. Studies of fever cases in Philippines, Sri Lanka, Thailand, Mali, Chad, Tanzania and Kenya have shown high percentages of malaria over-diagnosis when using fever as a clinical diagnostic tool [21–27]. Comprehensive investigation to identify the etiologic agents of febrile illnesses could be helpful in the study area and beyond. Defining the malaria-attributable fraction to estimate the frequency of true febrile malaria among all febrile cases, by fitting the risk of fever as a function of parasite density using a logistic regression model, would be of paramount importance .
The CareStartTM RDT test showed good sensitivity and specificity with an excellent agreement to the reference LM. The RDT could therefore be used in place of LM, which in poor set-ups cannot be used routinely.
Health Extension Workers
Histidine-Rich Protein 2
Institutional Review Board
Negative Predictive Value
Positive Predictive Value
Rapid Diagnostic Test
World Health Organization.
The authors are grateful to Kola Diba Health Center for their support during the study period. We are thankful to the North Gondar Zonal Health Bureau for supplying the RDT kits and the participant patients without whom this study could not have been realised. Finally, our special gratitude goes to the staff of Department of Microbiology, Immunology, and Parasitology, College of Medicine and Health Sciences, University of Gondar for the full support during the study.
- Malaria Operational Plan Ethiopia FY. 2011
- Tulu NA: Malaria. The Ecology of Health and Disease in Ethiopia 2nd edition. Edited by: Kloos H, Zein AZ. 1993, Westview Press Inc, Boulder, USA, 341-352.Google Scholar
- World Malaria report. 2011, WHO
- Ministry of Health (MOH) [Ethiopia]: Health and health related indicators. 2006, Ministry of Health, Addis Ababa, EthiopiaGoogle Scholar
- Malaria diagnosis and treatment guidelines for health workers in Ethiopia 2nd edition. 2004
- World Health Organization: New Perspectives: Malaria Diagnosis, Report of a Joint WHO/USAID. Informal Consultation held on 25–27 October 1999. 2000, World Health Organization, Geneva, Switzerland, 4-48.Google Scholar
- Reyburn H, Redempta M, Chris D, Ilona C, Emmanuel M, Ombeni M, Kapalala S, John S, Andrew K, Raimos O, Brian MG, Christopher JMW: Over diagnosis of malaria in patients with severe febrile illness in Tanzania: a prospective study. BMJ. 2004, 329: 1212-10.1136/bmj.38251.658229.55.PubMed CentralView ArticlePubMedGoogle Scholar
- Haditsch M: Quality and reliability of current malaria diagnostic methods. Trav Med Infect Dis. 2004, 2: 149-160. 10.1016/j.tmaid.2004.03.001.View ArticleGoogle Scholar
- Moody A: Rapid diagnostic tests for malaria parasites. Clin Microbiol Rev. 2002, 15: 66-78. 10.1128/CMR.15.1.66-78.2002.PubMed CentralView ArticlePubMedGoogle Scholar
- Federal Democratic Republic of Ethiopia MoH: National Five Year Strategic Plan for Malaria Prevention and Control in Ethiopia. 2006, Addis Ababa, EthiopiaGoogle Scholar
- 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.View ArticlePubMedGoogle Scholar
- 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.View ArticlePubMedGoogle Scholar
- Nigussie D, Legesse M, Animut A, H/Mariam A, Mulu A: Evaluation of Paracheck pf and Parascreen pan/pf tests for the diagnosis of malaria in an endemic area, South Ethiopia. Ethiop Med J. 2008, 46: 375-381.PubMedGoogle Scholar
- Lemma H, Byass P, Desta A, Bosman A, Costanzo G, Toma L, Fottrell E, Marrast AC, Ambachew Y, Getachew A, Mulure N, Morrone A, Bianchi A, Barnabas GA: Deploying artemether-lumefantrine with rapid testing in Ethiopian communities: impact on malaria morbidity, mortality and healthcare resources. Trop Med Int Health. 2009, 15: 241-250.View ArticlePubMedGoogle Scholar
- 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. Am J Trop Med Hyg. 2007, 76: 481-485.PubMedGoogle Scholar
- 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.PubMed CentralView ArticlePubMedGoogle Scholar
- 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-View ArticlePubMedGoogle Scholar
- Jessica M, Philippe G, Emmanuel B, Lieselotte C, Marjan vE, Jan 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. Malaria Journal. 2010, 9: 171-10.1186/1475-2875-9-171.View ArticleGoogle Scholar
- Ethiopia Demographic and Health Survey: 2005: Central Statistical Agency Addis Ababa, Ethiopia. 2006, ORC Macro Calverton, Maryland, USAGoogle Scholar
- Tekola E, Teshome G, Jeremiah N, Patricia MG, Estifanos BS, Yeshewamebrat E, Berhan A, Gedeon Y, Tesfaye T, Ayenew M, Mulat Z, Asrat G, Aryc WM, Paul ME, Frank OR: Evaluation of light microscopy and rapid diagnostic test for the detection of malaria under operational field conditions: a household survey in Ethiopia. Malar J. 2008, 7: 118-10.1186/1475-2875-7-118.View ArticleGoogle Scholar
- Bell D, Go R, Miguel C, Walker J, Cacal L, Saul A: Diagnosis of malaria in a remote area of the Philippines: comparison of techniques and their acceptance by health workers and the community. Bull World Health Organ. 2001, 79: 933-941.PubMed CentralPubMedGoogle Scholar
- van der Hoek W, Premasiri DAR, Wickremasinghe AR: Early diagnosis and treatment of malaria in a refugee population in Sri Lanka. Southeast Asian J Trop Med Public Health. 1997, 28: 12-17.PubMedGoogle Scholar
- Stephens JK, Phanart K, Rooney W, Barnish G: A comparison of three malaria diagnostic tests, under field conditions in North-west Thailand. Southeast Asian J Trop Med Public Health. 1999, 30: 625-630.PubMedGoogle Scholar
- Dicko A, Mantel C, Kouriba B, Sagara I, Thera MA, Doumbia S, Diallo M, Poudiougou B, Diakite M, Doumbo OK: Season, fever prevalence and pyrogenic threshold for malaria disease definition in an endemic area of Mali. Trop Med Int Health. 2005, 10: 550-556. 10.1111/j.1365-3156.2005.01418.x.View ArticlePubMedGoogle Scholar
- Othnigue N, Wyss K, Tanner M, Genton B: Urban malaria in the Sahel: prevalence and seasonality of presumptive malaria and parasitaemia at primary care level in Chad. Trop Med Int Health. 2006, 11: 204-210. 10.1111/j.1365-3156.2005.01551.x.View ArticlePubMedGoogle Scholar
- Reyburn H, Ruanda J, Mwerinde O, Drakeley C: The contribution of microscopy to targeting antimalarial treatment in a low transmission area of Tanzania. Malaria J. 2006, 5: 4-10.1186/1475-2875-5-4.View ArticleGoogle Scholar
- Mwangi TW, Mohammed M, Dayo H, Snow RW, Marsh K: Clinical algorithms for malaria diagnosis lack utility among people of different age groups. Trop Med Int Health. 2005, 10: 530-536. 10.1111/j.1365-3156.2005.01439.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Smith T, Schellenberg JA, Hayes R: Attributable fraction estimates and case definitions for malaria in endemic areas. Stat Med. 1994, 13: 2345-2358. 10.1002/sim.4780132206.View ArticlePubMedGoogle Scholar
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