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Economic considerations support C-reactive protein testing alongside malaria rapid diagnostic tests to guide antimicrobial therapy for patients with febrile illness in settings with low malaria endemicity
Malaria Journal volume 18, Article number: 442 (2019)
Malaria is no longer a common cause of febrile illness in many regions of the tropics. In part, this success is a result of improved access to accurate diagnosis and effective anti-malarial treatment, including in many hard-to-reach rural areas. However, in these settings, management of other causes of febrile illness remains challenging. Health systems are often weak and other than malaria rapid tests no other diagnostics are available. With millions of deaths occurring annually due to treatable bacterial infections and the ever increasing spread of antimicrobial resistance, improvement in the management of febrile illness is a global public health priority. Whilst numerous promising point-of-care diagnostics are in the pipeline, substantial progress can be made in the interim with existing tools: C-reactive protein (CRP) is a highly sensitive and moderately specific biomarker of bacterial infection and has been in clinical use for these purposes for decades, with dozens of low-cost devices commercially available. This paper takes a health-economics approach to consider the possible advantages of CRP point-of-care tests alongside rapid diagnostic tests for malaria, potentially in a single multiplex device, to guide antimicrobial therapy for patients with febrile illness. Three rudimentary assessments of the costs and benefits of this approach all indicate that this is likely to be cost-effective when considering the incremental costs of the CRP tests as compared with either (i) the improved health outcomes for patients with bacterial illnesses; (ii) the costs of antimicrobial resistance averted; or (iii) the economic benefits of better management of remaining malaria cases and shorter malaria elimination campaigns in areas of low transmission. While CRP-guided antibiotic therapy alone cannot resolve all challenges associated with management of febrile illness in remote tropical settings, in the short-term a multiplexed CRP and malaria RDT could be highly cost-effective and utilize the well-established funding and distribution systems already in place for malaria RDTs. These findings should spark further interest amongst industry, academics and policy-makers in the development and deployment of such diagnostics, and discussion on their geographically appropriate use.
Challenges and opportunities in the management of patients testing negative for malaria
The global malaria burden has halved since the turn of the century, mainly due to improved access to diagnosis, treatment and insecticide-treated nets. Progress, however, has stalled, with no reduction in cases between 2015 and 2017 . In 2017, funding for malaria reached a new high, exceeding US$3 billion, and worldwide there is appetite to eliminate malaria [2, 3]. Consequently, substantial economic opportunity exists for interventions that can capitalize on the global commitment to eradicate malaria, although a protracted era of a low but persistent burden could see this momentum lost. Coupled with the insidious spread of artemisinin resistance, this could have dire consequences in the form of resurgent drug resistant malaria.
Nearly 250 million malaria rapid diagnostic tests (RDTs) were distributed in 2017, almost quadruple the number distributed in 2010 . In Asia, Latin America and increasingly in Africa, most patients tested with an RDT have a negative result (Fig. 1) . In the Asia-Pacific, only 3% of over 25 million RDTs were positive for malaria in 2016. For the vast majority of patients in whom malaria has been ruled out, no other diagnostic tools are available, and clinical algorithms for their management have shown moderate and inconsistent performance [5, 6], although improvement has been shown to occur with their adaptation to an electronic format [7, 8]. Utilization of the malaria RDT infrastructure—both the devices themselves, as well as their funding and distribution networks, could offer an efficient and scalable pathway to improved management of febrile illness.
There are increasingly urgent reasons for such a strategy . First, are the potentially adverse health outcomes for the increasingly large proportion of patients testing negative for malaria: fever studies in Southeast Asia demonstrate that up to a third of febrile patients with a bacterial infection go unrecognized [10, 11], some with pathogens associated with high mortality when untreated [12, 13]. Second, is the increasing proportion of patients with a viral infection receiving antibiotics, promoting spread of antimicrobial resistance (AMR) [11, 14,15,16]. Finally, as malaria declines patients have little incentive to seek care from health workers that cannot test or treat other diseases; integrated management of febrile illnesses has been shown to increase patient attendance at formal health providers, contributing to improved malaria case detection and elimination efforts .
A potential solution: host biomarker-guided antibiotic therapy in febrile illness
One strategy with the potential to address all three of these issues is the use of host biomarker testing to identify patients most likely to benefit from antibiotic treatment. Use of such tests in conjunction with up-to-date aetiological surveillance data could further enhance the impact and cost-effectiveness of this approach . An ideal biomarker of bacterial infection would be robust to temporal and spatial heterogeneity in causes of fever , and will, therefore, have been studied in a broad range of populations.
Numerous biomarkers to identify bacterial infections have been proposed , but none have perfect sensitivity and specificity. The most studied is C-reactive protein (CRP), a marker of inflammation that has been in clinical use for decades . While in some populations it has underperformed, particularly at the severe end of the clinical spectrum , in many studies CRP has been found to be appropriately sensitive and moderately specific to identify patients with a bacterial infection [22, 23]. Low-cost and accurate rapid CRP tests appropriate for use in remote tropical settings are widely available [24,25,26].
A 2014 Cochrane review confirmed the utility of CRP-guided antibiotic therapy in patients with non-severe acute respiratory infections (ARIs) . This approach is routine in Scandinavian countries and the Netherlands, and recommended in guidelines from the National Institute for Clinical Excellence (NICE) in England and Wales . A recent clinical trial in Vietnam demonstrated a 20% point reduction in antibiotic prescription in primary care patients with non-severe ARIs , and a secondary analysis of a clinical trial in Tanzanian children with non-severe ARIs demonstrated that when deployed together with a clinical algorithm, CRP-guided treatment can reduce antibiotic prescriptions and improve clinical outcomes . Fewer studies investigate the utility of CRP-guided antibiotic therapy in the general febrile population. A retrospective analysis of 1300 febrile patients across Southeast Asia found CRP to be a sensitive marker of bacterial infection . A clinical trial of CRP-guided treatment in patients with non-severe febrile illnesses in primary care in Thailand and Myanmar demonstrated reductions in antibiotic prescribing .
This paper provides preliminary, ‘broad brush’ economic analyses of the impact of CRP tests to guide antibiotic prescription in patients with febrile illness, considering (i) direct benefit to individual patients with bacterial illnesses; (ii) societal benefits in terms of the costs of AMR averted; and (iii) the impact on malaria case detection and elimination efforts. A combined rapid test for malaria and CRP could harness existing infrastructure and funding already in place to support distribution of malaria RDTs, with one such test commercially-available and undergoing analytical field validation . Access related factors favouring combined malaria-CRP tests are also explored, namely synergistic procurement pathways, and the large market share which could make such tests attractive to developers, ensuring long-term sustainability, independent of international donor funding.
It is important to emphasize that the analyses are kept deliberately simple for non-economist readers and the data to support them are often scarce and drawn from a variety of settings. Further adaptation and contextualized analyses will be required if such multiplex devices are to be considered as replacements for malaria RDTs in different geographical settings.
Direct health benefits for patients with bacterial illnesses
To consider the potential impact of better identification and treatment of bacterial infections data from the World Malaria Report is drawn on to estimate the number of RDTs negative for malaria . A simple decision tree (Fig. 2) is used to incorporate the proportion likely due to bacterial infection, estimated at 5% [15, 34, 35]; and the probability these are diagnosed and treated based on clinical judgement, set at 57% . The sensitivity of a CRP test with a threshold of 20 mg/l to detect bacterial infections, is estimated at 86% . For untreated bacterial infections a conservative mortality rate of 3% (half the median estimate from a Delphi survey on this topic) is assumed . The added cost of a combined malaria-CRP test is estimated at $1 on top of that of a malaria RDT, and this additional cost is applied to all patients, irrespective of the malaria test result.
With these assumptions applied to the 25 million febrile episodes in which malaria RDTs were used in the Asia-Pacific in 2016, CRP-guided antibiotic treatment in the 97% of malaria negative cases could avert approximately 10,500 deaths per year due to better identification of patients with bacterial infections. Assuming an additional cost of $1 per combination test, the incremental cost effectiveness ratio (ICER) per disability adjusted life year (DALY) averted would be $28, therefore considered a highly cost-effective intervention.
Costs of antimicrobial resistance averted
The same decision tree structure is used to consider reductions in unnecessary antibiotic prescribing, averting both direct antibiotic costs and, more importantly, indirect health and economic costs of emergence and spread of AMR. A recent analysis provided rudimentary estimates for the cost of AMR per antibiotic consumed . In the Thai context the consumption of a course of broad spectrum beta-lactam antibiotics was associated with a cost of AMR of approximately $10. In this analysis, this is adjusted downwards to $3.8 using the ratio of GDP per capita (PPP) for all endemic countries in the Asia-Pacific compared with that of Thailand, weighted by the volume of RDTs used in each country . The costs of AMR averted are then estimated if all patients with low CRP test results (a CRP level of less than 20 mg/L) were not prescribed an antibiotic. These estimates for the costs of AMR averted are then applied alongside direct purchase costs of the antibiotics and the incremental costs of CRP tests, to calculate the net-benefit of CRP-guided antibiotic therapy.
Under current practice, amongst the 24.5 million patients with a negative malaria RDT, 59% would be prescribed an antibiotic (corresponding closely with a recent review on the topic ). With CRP guidance, antibiotic prescribing in patients with a negative malaria test would reduce to 36%, averting approximately 5.6 million courses of antibiotics annually in the Asia-Pacific. Considering the costs of CRP tests and the direct and indirect costs of antibiotics, combined malaria-CRP tests would be expected to be cost-saving, with a net-benefit of over USD $9.5 million.
Higher malaria detection and treatment to support malaria elimination
Finally, the benefit of improved malaria case detection in areas targeting elimination is considered. This was demonstrated in the context of community health workers (CHWs) in Myanmar, initially introduced only to diagnose and treat malaria. Over time, malaria testing rates steadily declined as febrile patients benefitted little from having malaria excluded without other treatment for their illness. Medical Action Myanmar, an organization supporting a network of CHWs, extended the role of the CHWs to include a broader range of basic health services . This was followed by an immediate and sustained increase in testing rates (Fig. 3).
The health benefits for patients with bacterial illnesses were described above, but in addition to these are the direct health benefits for patients with malaria, due to the higher testing (and treatment) rates. A simple cost-effectiveness calculation for the potential benefits of better malaria case detection, by virtue of increasing the probability that a febrile patient will present to a health worker, demonstrates that malaria-CRP rapid tests would be cost-effective ($36 per DALY averted), even when considering only the improved outcomes for the small proportion of patients with malaria (Table 1).
In addition to direct benefits to patients with malaria are the implications of higher case detection rates on time to interruption of transmission. This is illustrated by a previously described model  for which a web-based interface is available for further simulation. Increasing malaria case detection rates is predicted to reduce subsequent malaria incidence and prevalence, implying faster time to interruption of transmission, resulting in shorter malaria elimination campaigns and further cost-savings (Fig. 4).
Market incentive for global investment
The above health and economic benefits could be achieved with commercially available rapid CRP tests. However, while this is a workable approach, long-term success is more likely if existing malaria control infrastructure (for example, training, procurement channels and supply chains) are leveraged using a combined malaria-CRP test; the anticipated market opportunity for such a device is explored below.
Unitaid’s annual global forecast estimates that 15.8 billion febrile episodes occur amongst individuals living in malaria endemic low- and middle-income countries (LMICs) . This indicates a large potential available market (PAM) for a malaria-CRP test. From the PAM, the total available market (TAM) can be calculated, which accounts for the number of febrile patients likely to seek care. Treatment seeking rates from household surveys indicate an annual TAM of 1.48 billion tests. Within the TAM, the currently accessible market, termed the Serviceable Available Market (SAM), is determined by the yearly number of malaria RDTs and microscopy slides performed within LMICs where malaria is prevalent . In 2016, the SAM comprised approximately 467 million tests (Fig. 5).
Finally, to produce a pragmatic demand forecast reflective of probable market consumption, the serviceable and obtainable market (SOM) must be estimated, by identifying and analysing factors that might affect in-country adoption, including malaria prevalence, existing market size for substitutes, planned procurement mechanisms, government commitment to universal health care, malaria financing and price of diagnostics. These factors must be explored in detailed discussions with procurement and government agencies. A simple SOM estimate can be calculated by considering two key factors; countries with a low proportion of malaria infections amongst the febrile population (less than 10%); and those with strong existing malaria RDT markets, as opposed to reliance on blood film microscopy. Although incorporating additional factors would reduce the SOM, considering these two factors identifies more than 23 LMICs (mainly in Southeast Asia and sub-Saharan Africa), in which more than 55 million malaria RDTs were sold in 2016.
While multiple approaches exist to improving care for patients with febrile illness, the strategy described in this paper could be rolled out in the near-term using existing infrastructure and capitalizing on current global appetite for malaria elimination. The rudimentary analyses presented here provide a general indication that integrating CRP-guided antibiotic therapy with malaria RDTs is likely to be highly cost-effective considering either (and of course all) the potential benefits in the different analyses, although further refinement and context-specific adaptations to these analyses are required to verify their conclusions. While CRP-guided antibiotic therapy is not without limitations it could offer considerable advantages over current practice, and pave the way for rapid implementation of improved technologies as they become available. In the longer term better biomarkers and multiplexed pathogen-specific tests, deployed with the support of electronic clinical decision algorithms, could replace CRP-guided therapy, but the timeline for this is likely to be long, with substantial preventable mortality, morbidity and erosion of antibiotic resources in the interim. To avoid this, low-cost CRP tests could be deployed alongside malaria RDTs or incorporated into a combination point-of-care test.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
acute respiratory infection
community health worker
disability adjusted life year
gross domestic product
incremental cost effectiveness ratio
low- and middle-income country
non-malarial febrile illness
National Institute for Clinical Excellence
potential available market
purchasing power parity
rapid diagnostic test
serviceable available market
serviceable and obtainable market
total available market
United States dollar
WHO. World malaria report. Geneva: World Health Organization; 2018.
WHO. Global technical strategy for malaria 2016–2030. Geneva: World Health Organization; 2015.
Asia Pacific Malaria Elimination Network. https://www.apmen.org.
WHO. World malaria report. Geneva: World Health Organization; 2017.
Nguyen DTK, Leung KK, McIntyre L, Ghali WA, Sauve R. Does integrated management of childhood illness (IMCI) training improve the skills of health workers? A systematic review and meta-analysis. PLoS ONE. 2013;8:e66030.
Gouws E, Bryce J, Habicht J-P, Amaral J, Pariyo G, Schellenberg JA, et al. Improving antimicrobial use among health workers in first-level facilities: results from the multi-country evaluation of the integrated management of childhood illness strategy. Bull World Health Organ. 2004;82:509–15.
Rambaud-Althaus C, Shao AF, Kahama-Maro J, Genton B, D’acremont V. Managing the sick child in the era of declining malaria transmission: development of ALMANACH, an electronic algorithm for appropriate use of antimicrobials. PLoS ONE. 2015;10:e0127674.
Keitel K, Kagoro F, Samaka J, Masimba J, Said Z, Temba H, et al. A novel electronic algorithm using host biomarker point-of-care tests for the management of febrile illnesses in Tanzanian children (e-POCT): a randomized, controlled non-inferiority trial. PLoS Med. 2017;14:e1002411.
McDonald CR, Weckman A, Richard-Greenblatt M, Leligdowicz A, Kain KC. Integrated fever management: disease severity markers to triage children with malaria and non-malarial febrile illness. Malar J. 2018;17:353.
Mayxay M, Castonguay-Vanier J, Chansamouth V, Dubot-Pérès A, Paris DH, Phetsouvanh R, et al. Causes of non-malarial fever in Laos: a prospective study. Lancet Glob Health. 2013;1:46–54.
Lubell Y, Althaus T, Blacksell SD, Paris DH, Mayxay M, Pan-ngum W, et al. Modelling the impact and cost-effectiveness of biomarker tests as compared with pathogen-specific diagnostics in the management of undifferentiated fever in remote tropical settings. PLoS ONE. 2015;11:e0152420.
Taylor AJ, Paris DH, Newton PN. A systematic review of the mortality from untreated leptospirosis. PLoS Negl Trop Dis. 2015;9:e0003866.
Taylor AJ, Paris DH, Newton PN. A Systematic review of mortality from untreated scrub typhus (Orientia tsutsugamushi). PLoS Negl Trop Dis. 2015;9:e0003971.
Arunkumar G, Ravi V, Laserson K. Acute febrile illness and acute encephalitis surveillance in India in the context of the global health security agenda: unveiling emerging pathogens and informing disease prioritization. Baltimore: ASTMH; 2017.
D’Acremont V, Kahama-Maro J, Lengeler C, Genton B, Cherpillod P, Kaiser L, et al. Beyond malaria—causes of fever in outpatient Tanzanian children. N Engl J Med. 2014;370:809–17.
Mueller TC, Siv S, Khim N, Kim S, Fleischmann E, Ariey F, et al. Acute undifferentiated febrile illness in rural Cambodia: a 3-year prospective observational study. PLoS ONE. 2014;9:e95868.
McLean ARD, Wai HP, Thu AM, Khant ZS, Indrasuta C, Ashley EA, et al. Malaria elimination in remote communities requires integration of malaria control activities into general health care: an observational study and interrupted time series analysis in Myanmar. BMC Med. 2018;16:183.
Chandna A, White LJ, Pongvongsa T, Mayxay M, Newton PN, Day NPJ, et al. Accounting for aetiology: can regional surveillance data alongside host biomarker-guided antibiotic therapy improve treatment of febrile illness in remote settings? Wellcome Open Res. 2019;4:1.
Kapasi AJ, Dittrich S, González IJ, Rodwell TC. Host biomarkers for distinguishing bacterial from non-bacterial causes of acute febrile illness: a comprehensive review. PLoS ONE. 2016;11:e0160278.
Cals JW, Ebell MH. C-reactive protein: guiding antibiotic prescribing decisions at the point of care. Br J Gen Pract. 2018;68:112–3.
Díez-Padrisa N, Bassat Q, Machevo S, Quintó L, Morais L, Nhampossa T, et al. Procalcitonin and C-reactive protein for invasive bacterial pneumonia diagnosis among children in Mozambique, a malaria-endemic area. PLoS ONE. 2010;5:e13226.
Nijman RG, Moll HA, Smit FJ, Gervaix A, Weerkamp F, Vergouwe Y, et al. C-reactive protein, procalcitonin and the lab-score for detecting serious bacterial infections in febrile children at the Emergency Department. Pediatr Infect Dis J. 2014;33:e273–9.
Thompson M, Van den Bruel A, Verbakel J, Lakhanpaul M, Haj-Hassan T, Stevens R, et al. Systematic review and validation of prediction rules for identifying children with serious infections in emergency departments and urgent-access primary care. Health Technol Assess. 2012;16:1–100.
Phommasone K, Althaus T, Souvanthong P, Phakhounthong K, Soyvienvong L, Malapheth P, et al. Accuracy of commercially available c-reactive protein rapid tests in the context of undifferentiated fevers in rural Laos. BMC Infect Dis. 2016;16:61.
Brouwer N, van Pelt J. Validation and evaluation of eight commercially available point of care CRP methods. Clin Chim Acta. 2015;439:195–201.
Minnaard MC, van de Pol AC, Broekhuizen BDL, Verheij TJM, Hopstaken RM, van Delft S, et al. Analytical performance, agreement and user-friendliness of five C-reactive protein point-of-care tests. Scand J Clin Lab Invest. 2013;73:627–34.
Aabenhus R, Jensen J, Jørgensen KJ, Hróbjartsson A, Bjerrum L. Biomarkers as point-of-care tests to guide prescription of antibiotics in patients with acute respiratory infections in primary care. Cochrane Database Syst Rev. 2014;11:CD010130.
Prina E, Ranzani OT, Torres A. Community-acquired pneumonia. Lancet. 2015;386:1097–108.
Do NTT, Ta NTD, Tran NTH, Than HM, Vu BTN, Hoang LB, et al. Point-of-care C-reactive protein testing to reduce inappropriate use of antibiotics for non-severe acute respiratory infections in Vietnamese primary health care: a randomised controlled trial. Lancet Glob Health. 2016;4:e633–41.
Keitel K, Samaka J, Masimba J, Temba H, Said Z, Kagoro F, et al. Safety and efficacy of C-reactive protein–guided antibiotic use to treat acute respiratory infections in Tanzanian children: a planned subgroup analysis of a randomized controlled noninferiority trial evaluating a novel electronic clinical decision algorithm (ePOCT). Clin Infect Dis. 2019;69:1926–34.
Lubell Y, Blacksell SD, Dunachie S, Tanganuchitcharnchai A, Althaus T, Watthanaworawit W, et al. Performance of C-reactive protein and procalcitonin to distinguish viral from bacterial and malarial causes of fever in Southeast Asia. BMC Infect Dis. 2015;15:511.
Althaus T, Greer RC, Swe MMM, Cohen J, Tun NN, Heaton J, et al. Effect of point-of-care C-reactive protein testing on antibiotic prescription in febrile patients attending primary care in Thailand and Myanmar: an open-label, randomised, controlled trial. Lancet Glob Health. 2019;7:e119–31.
UNITAID. Fever diagnostic technology landscape. Geneva: UNITAID; 2018.
Brent AJ, Ahmed I, Ndiritu M, Lewa P, Ngetsa C, Lowe B, et al. Incidence of clinically significant bacteraemia in children who present to hospital in Kenya: community-based observational study. Lancet. 2006;367:482–8.
Maze MJ, Bassat Q, Feasey NA, Mandomando I, Musicha P, Crump JA. The epidemiology of febrile illness in sub-Saharan Africa: implications for diagnosis and management. Clin Microbiol Infect. 2018;24:808–14.
Lubell Y, Staedke SG, Greenwood BM, Kamya MR, Molyneux M, Newton PN, et al. Likely health outcomes for untreated acute febrile illness in the tropics in decision and economic models; a Delphi survey. PLoS ONE. 2011;6:e17439.
Shrestha P, Cooper BS, Coast J, Oppong R, Do Thi Thuy N, Phodha T, et al. Enumerating the economic cost of antimicrobial resistance per antibiotic consumed to inform the evaluation of interventions affecting their use. Antimicrob Resist Infect Control. 2018;7:98.
World Bank. GDP per capita. http://data.worldbank.org/indicator/NY.GDP.PCAP.CD.
Hopkins H, Bruxvoort KJ, Cairns ME, Chandler CIR, Leurent B, Ansah EK, et al. Impact of introduction of rapid diagnostic tests for malaria on antibiotic prescribing: analysis of observational and randomised studies in public and private healthcare settings. BMJ. 2017;356:j1054.
Tun STT, von Seidlein L, Pongvongsa T, Mayxay M, Saralamba S, Kyaw SS, et al. Towards malaria elimination in Savannakhet, Lao PDR: mathematical modelling driven strategy design. Malar J. 2017;16:483.
UNITAID. Global Malaria Diagnostic and Artemisinin Treatment Commodities Demand Forecast. Geneva: UNITAID; 2018.
Capeding MR, Chua MN, Hadinegoro SR, Hussain IIHM, Nallusamy R, Pitisuttithum P, et al. Dengue and other common causes of acute febrile illness in Asia: an active surveillance study in children. PLoS Negl Trop Dis. 2013;7:e2331.
This work was funded by the Wellcome Trust core Grant (106698Z/14/Z) to the Thailand Africa and Asia Programme (Mahidol-Oxford Tropical Medicine Research Unit), as well as funding from the Department for International Development (DfID), UK (204074-101), and Department for Foreign Affairs and Trade (DfAT), Australia (70957) to FIND. The funders had no role in the design of the study, nor the collection, analysis and interpretation of data, nor in the writing of the manuscript.
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Lubell, Y., Chandna, A., Smithuis, F. et al. Economic considerations support C-reactive protein testing alongside malaria rapid diagnostic tests to guide antimicrobial therapy for patients with febrile illness in settings with low malaria endemicity. Malar J 18, 442 (2019). https://doi.org/10.1186/s12936-019-3059-5
- C-reactive protein
- Rapid diagnostic test
- Point-of-care test
- Febrile illness