Background
Malaria remains a major public health threat, particularly in sub-Saharan Africa, where about 191 million new infections and 395,000 deaths were reported in 2015 [
1]. The World Health Organization (WHO) now recommends a confirmatory diagnosis of malaria using microscopy and/or RDT before initiation of treatment, partly influenced by the fear of the development of drug resistance and to enable the identification of malaria-negative patients, for which further investigations need to be sought for appropriate treatment [
2]. Accurate diagnosis of malaria is thus vital for effective management and control of malaria while avoiding the wrong use of anti-malarial drugs. In most malaria-endemic countries, malaria is usually diagnosed by microscopy or rapid diagnostic tests (RDT) and clinical evidence.
The traditional practice by health care workers (HCW) in malaria-endemic countries has been to diagnose malaria based on a history of fever (clinical diagnosis) [
3‐
6]. The specificity of clinical diagnosis of malaria is reduced by the overlap of malaria symptoms with other tropical diseases, such as typhoid fever, respiratory tract infections, bacterial disease and viral infections. The accuracy of clinical diagnosis may vary with the level of malaria endemicity, malaria transmission season and age group. Malaria microscopy is complex, which includes different species and blood stages of the
Plasmodium parasite and requires a competent microscopist. Also, the presence of sub-microscopic parasitaemia greatly reduces the accuracy of malaria diagnosis by TFM. Unlike TFM, RDT detect malaria antigens, not malaria parasites, which gives them an added advantage in the ability to diagnose malaria in patients with low-grade parasitaemia below the detection limit of TFM [
7,
8]. However, the specificity of the commonly used RDT that detects histidine rich protein–II (HRP-II) of
P. falciparum, is limited when the parasite is cleared and antigens remain in circulation for about 28 days (false positive) [
2].
As malaria-endemic countries move towards malaria elimination, there is a need for rapid and accurate diagnostic tools for malaria. Active monitoring of the performance of various diagnostic methods for malaria at the country level is necessary to guide policy on the diagnostic methods to use for malaria diagnosis and elimination. In this study, the performance of RDT, TFM and PCR in the diagnosis of malaria in Cameroon was compared in order to illustrate the number of cases missed by traditional methods (clinical diagnosis, RDT and TFM) of diagnosis.
Methods
Study area
This study was conducted in three Regions of Cameroon, Far North, Centre and North West with varied climatic conditions and altitudes (Table
1). In the Far North Region with seasonal malaria transmission the study was conducted in Maroua (10.5925°N, 14.3210°E) in October 2014. In the Central Region, which is holoendemic for malaria, the study was carried out in Nkolbisson (a neighbourhood in Yaoundé (3.8480°N, 11.5021°E) from February 2014 to April 2014. In the North West Region, which is holoendemic for malaria, the study was conducted in Bamenda (5.9631°N, 10.1591°E) in February 2015.
Table 1
General characteristics of study population, study sites and environmental factors
Gender
|
Male | 64 (52) | 168 (53) | 33 (29) | 265 (48) |
Female | 60 (48) | 147 (47) | 79 (71) | 286 (52) |
Total | 124 | 315 | 112 | 551 |
Age group (years)
|
0–5 | 81 (65) | 180 (57) | 34 (30) | 295 (54) |
6–10 | 15 (12) | 86 (27) | 5 (4) | 106 (19) |
11–16 | 9 (7) | 49 (16) | 4 (4) | 62 (11) |
≥ 17 | 19 (15) | 0 (0) | 69 (61) | 88 (16) |
Climate | Sahel | Tropical | Tropical | |
Average annual temperature (°C) | 28.3 | 23.7 | 21.5 | |
Average annual rainfall (mm) | 794 | 1643 | 2145 | |
Elevation (m) | 384 | 750 | 1614 | |
Weather condition at time of specimen collection | End of rainy season | Rainy season | Dry season | |
Study design
A cross-sectional study was conducted in selected health facilities in Maroua, Nkolbisson, and Bamenda. Inclusion criteria were age > 6 months and axillary temperature >37.5 °C at the time of recruitment or fever within 24 h preceding recruitment. A written informed consent was obtained from all study participants ≥ 18 years of age. Parents or legal guardians of children < 18 years gave a written informed consent on behalf of their children.
Ethical considerations
Ethical approvals were obtained from the Committee on Human Subjects of the University of Hawaii (protocol number CHS 21724) and the National Research Ethics Committee of the Ministry of Public Health, Cameroon (protocol number 2014/04/442/CE/CNERSH/SP). Administrative approvals were obtained from the Ministry of Public Health, Cameroon and the Directors of the participating facilities.
Study procedures
An easy-to-read questionnaire was used for the collection of demographic and clinical data. After obtaining informed consent, the research or clinic staff took axillary temperatures and recorded the reported signs and symptoms. Venous blood, 2–5 mL, was collected from each participant, dispensed into ethylenediaminetetraacetic acid (EDTA) tubes and stored in cold boxes until transported to the research laboratory where they were stored at 4–8 °C. TFM and RDT for malaria were conducted for all participants, and both results were presented to the consulting health care worker (HCW). At the end of the hospital visit, an exit survey was conducted to obtain information on (1) the clinical diagnosis made by the HCW, and (2) determine if anti-malarial drugs had been prescribed. This information was used to determine how frequent anti-malarial drugs were used to treat malaria-negative patients. When exit survey information was not available, the hospital record was consulted for the information.
Laboratory investigations
Malaria TFM
Thick blood films were prepared and stained using 10% Giemsa for 15 min. A slide was considered positive if at least one asexual blood-stage P. falciparum parasite was identified. Parasitaemia was determined by counting the number of parasites per 200 white blood cells and assuming that each subject had 8000 white blood cells/μL of blood. Two readings were conducted for each slide and discrepancies greater than 10% were resolved by a third reading by an independent trained microscopist. The slides for this study were read by well-trained and experienced scientists who have worked in malaria-research for a number of years.
Malaria RDT
Approximately 5 μL of blood was used to diagnose malaria using the Ag Pf/Pan malaria RDT kit (Standard Diagnostic Inc., South Korea), following the manufacturer’s instructions. This RDT is a qualitative immunochromatographic test that detects P. falciparum HRP-II and Plasmodium lactate dehydrogenase, which is a glycolytic enzyme common to P. falciparum, Plasmodium ovale, Plasmodium vivax and Plasmodium malariae asexual-stage parasites.
Malaria PCR
DNA was extracted from 200 μL of whole blood using the mini-prep spin-column technique (Macherey-Nagel, Germany) following the manufacturer’s instructions. Detection of malaria parasite DNA was based on nested PCR amplification of the 18 s rRNA gene in a reaction that used 2 μL of the extracted DNA, 10 μL of GoTaq polymerase and master mixes (Promega, USA), 0.25 μM each of upstream and downstream primers, and 6 μL of nuclease free water in a total reaction volume of 20 μL. The first PCR encompassed genus-specific primers and the second nested PCR run encompassed the species-specific primers for
P. falciparum, as previously described [
9]. The presence of a characterizing band of ~ 205-bp for
P. falciparum visualized on a UV transilluminator after electrophoresis on a 2% agarose gel stained with ethidium bromide.
Statistical analysis
Data were entered into Microsoft Office Excel and analysed using StatPlus 5.9.80 (AnalystSoft Inc., Walnut, CA) and Prism 6.0 (Graphpad Software, San Diego, CA) for descriptive statistics. Diagnostic test performance for clinical diagnosis, TFM and RDT for the diagnosis of malaria was analysed using MedCalc 16.8 (Ostend, Belgium). Descriptive statistics are represented as frequencies and medians. Sensitivity, specificity, positive and negative predictive values, accuracy and percentage of agreement (kappa value) were calculated with confidence intervals by age groups. Multivariable logistic regression was conducted to identify correct diagnosis comparing other test methods (TFM and RDT) to PCR. P < 0.05 was considered statistically significant. All the other analyses were conducted using SAS version 9.4 (SAS Institute Inc., Cary, NC). The figure was generated using R version 3.4.2.
Discussion
Accurate and prompt diagnosis of malaria is the only way to effectively treat, manage and eventually eliminate the disease. This study was conducted to determine the proportion of malaria cases missed by conventional malaria diagnostic methods, namely, TFM, RDT, clinical diagnosis, but detected by PCR.
In this study, TFM missed 23% of PCR-positive malaria infections. In a previous meta-analysis based on data from 42 studies, microscopy missed about 50% of PCR-positive malaria infections [
11]. Also, in a large epidemiological study in Cambodia a significant proportion of microscopy-negative samples were detected by PCR (289/7491; 3.85%) [
12]. False-negative microscopy results are known to increase as parasite density decreases [
13]. Moreover, the detection threshold of Giemsa-stained TFM varies considerably between 50–500 parasites/μl of blood. However, TFM predicted the presence of malaria parasite in 99% of the study participants making TFM a good “rule in” test for malaria. This means that a positive TFM result for malaria can be trusted; meanwhile, a negative result does not exclude the presence of malaria infection.
Malaria RDT missed 12% of PCR-positive malaria infections. However, the accuracy of malaria RDT was good as compared to PCR. The sensitivity and specificity of malaria RDT in this study was 78% and 94% respectively, which is consistent with a recent study in Kenya [
14] that evaluated the same RDT. Several factors have been demonstrated to affect the sensitivity of RDTs based on detection of HRP-II, including an inherent limitation of the device, mutation or deletion of the gene encoding the HRP-II, and storage conditions [
13,
15]. Interestingly, RDT detected 15% of malaria cases that were missed by TFM. This is because RDT detects antigens, not parasites, which gives it an added advantage over microscopy in its ability to diagnose malaria in patients with low parasitaemia below the detection threshold of microscopy [
7,
8]. However, there is the possibility of false positive RDT results when the malaria parasite is cleared, and antigens remain in circulation. In the present study, malaria RDT could predict the presence of malaria parasite in 94% of the study participants making it a good “rule in” test for malaria. Therefore, in the absence of PCR, malaria RDT can be used to improve the quality of care by ensuring appropriate treatment of confirmed malaria cases while avoiding indiscriminate administration of anti-malarial drugs for malaria-negative patients. However, because a substantial proportion of infections were missed by RDT, it is therefore not sufficiently sensitive for mass screening programmes as recommended by the WHO [
16].
This study found high rates of clinical diagnosis and overtreatment of malaria, in all three Cameroonian study sites, which is consistent with previous studies [
17‐
20]. Even though the sensitivity of clinical diagnosis of malaria was high, the overall accuracy of clinical diagnosis was poor with 41% of malaria-negative patients erroneously treated for malaria. Moreover, clinical diagnosis of malaria could predict the presence of malaria parasite in only 59% of study participants. Clearly, many patients that were treated for malaria had other causes of fever. Therefore, clinical diagnosis of malaria cannot be relied upon as a “rule in” test for malaria due to overlapping malaria symptoms with other tropical febrile illnesses.
Results of this study also provide information on the prevalence of malaria in three Regions of Cameroon. The prevalence of malaria was high in Nkolbisson and Maroua, but low in Bamenda. These three regions are characterized by different climatic variables (Table
1), which have been shown to affect the prevalence of malaria in a given region [
21‐
25]. A previous study in Tanzania reported malaria prevalence proportions of 79–90%, 27–46% and 8–16% in low, intermediate and high altitudes, respectively [
26]. Results of this study thus provide information on the prevalence of malaria in three climatically different regions of Cameroon, which is important to guide malaria control interventions.
This study has a limitation in that quantitative PCR was not conducted in order to quantify parasitaemia. Thus, it was not possible to stratify the infections that were missed by TFM and RDT by level of parasite density in order to determine the variation in sensitivity across parasite density levels.
Conclusions
Results of this study suggest that the conventional diagnostic methods for malaria (TFM, RDT,) are not adequate when accurate epidemiological data are needed to monitor malaria control and elimination interventions. PCR permitted the detection of 23% of malaria cases missed by TFM and RDT further, confirming it as a valuable tool for epidemiological surveys, mass screening, and the assessment of interventions for malaria elimination. Therefore, the development and standardization of a rapid and sensitive molecular-based test capable of detecting sub-microscopic malaria infection are warranted for the global elimination of malaria. Furthermore, continual training and proficiency testing should be instituted for laboratory technicians on malaria microscopy and post-market surveillance to assure the quality of malaria RDT since high-performance microscopy and quality assured RDTs will suffice for the clinical management of patients with suspected malaria.
Authors’ contributions
KOM, VRN, RGL and OAA designed the study. KOM, OAA, MC, ONB, LFE collected the samples, and conducted the laboratory studies. KG, KOM, VRN, DWT contributed to data analysis. KOM wrote the draft manuscript, DWT, VRN edited the manuscript, and all authors reviewed the final manuscript. RGL, DWT and VRN supervised the study. All authors read and approved the final manuscript.