- Meeting report
- Open Access
Challenges for achieving safe and effective radical cure of Plasmodium vivax: a round table discussion of the APMEN Vivax Working Group
Malaria Journalvolume 16, Article number: 141 (2017)
The delivery of safe and effective radical cure for Plasmodium vivax is one of the greatest challenges for achieving malaria elimination from the Asia–Pacific by 2030. During the annual meeting of the Asia Pacific Malaria Elimination Network Vivax Working Group in October 2016, a round table discussion was held to discuss the programmatic issues hindering the widespread use of primaquine (PQ) radical cure. Participants included 73 representatives from 16 partner countries and 33 institutional partners and other research institutes. In this meeting report, the key discussion points are presented and grouped into five themes: (i) current barriers for glucose-6-phosphate deficiency (G6PD) testing prior to PQ radical cure, (ii) necessary properties of G6PD tests for wide scale deployment, (iii) the promotion of G6PD testing, (iv) improving adherence to PQ regimens and (v) the challenges for future tafenoquine (TQ) roll out. Robust point of care (PoC) G6PD tests are needed, which are suitable and cost-effective for clinical settings with limited infrastructure. An affordable and competitive test price is needed, accompanied by sustainable funding for the product with appropriate training of healthcare staff, and robust quality control and assurance processes. In the absence of quantitative PoC G6PD tests, G6PD status can be gauged with qualitative diagnostics, however none of the available tests is currently sensitive enough to guide TQ treatment. TQ introduction will require overcoming additional challenges including the management of severely and intermediately G6PD deficient individuals. Robust strategies are needed to ensure that effective treatment practices can be deployed widely, and these should ensure that the caveats are outweighed by the benefits of radical cure for both the patients and the community. Widespread access to quality controlled G6PD testing will be critical.
In November 2014, the governments of the Asia–Pacific nations reconfirmed their commitment to the regional elimination of malaria by 2030. Although major gains in malaria control have been made over the last two decades, these successes have been far less apparent for Plasmodium vivax than for Plasmodium falciparum. Once regarded as a relatively benign disease, vivax malaria is now acknowledged as an important public health concern leading to life-threatening complications, miscarriage, chronic infection and increased mortality [1–3]. P. vivax poses specific difficulties to elimination, mainly due to its ability to relapse weeks to months after the initial infection . The propensity of P. vivax to form dormant liver stages (hypnozoites) leading to recurrent infections, requires specific strategies to achieve its elimination, including the provision of radical cure to treat both the blood and dormant liver stages of the parasite.
The only widely available drug to treat hypnozoites is primaquine (PQ), a drug which can cause haemolysis when administered to patients with a glucose-6-phosphate-dehydrogenase (G6PD) enzyme deficiency . G6PD deficiency (G6PDd) is the most common enzymopathy worldwide, with more than 185 clinically relevant G6PD variants reported , conferring varying degrees of phenotypic deficiency. The gene encoding the G6PD enzyme is located on the X-chromosome, hence males can be hemizygous normal (wildtype) or deficient, whereas women can be homozygous-, heterozygous-deficient or normal for the G6PD variants. Heterozygous females harbour two distinct populations of red blood cells (RBCs), a G6PD normal and a G6PDd fraction. In heterozygous females the distribution of G6PDd and G6PD normal RBCs is determined at random through a process called lyonization . Accordingly, heterozygous females with the same G6PD alleles can manifest different degrees of deficiency.
As a result of these factors, the risk of haemolysis varies with the dose of PQ administered, the level of G6PD enzyme activity and the genetic variant of G6PDd. The World Health Organization’s (WHO) malaria treatment guidelines recommend that PQ is administered over 14 days to reduce the risk of severe haemolysis , but such a prolonged treatment course poses significant issues regarding adherence that limits the regimens’ effectiveness. Tafenoquine (TQ), another 8-aminoquinoline compound which is currently at the end of it's Phase 3 clinical programme has a significantly longer half-life than PQ, allowing it to be administered as a single dose regimen. Like PQ, TQ can cause severe haemolysis in G6PDd individuals, and it will therefore be crucial to determine the G6PD status prior to prescribing the drug to mitigate the risk of sustained haemolysis (Justin Green, pers. comm.).
Currently only 7 malaria-endemic countries in the Asia–Pacific region and Sri Lanka, which is malaria free, recommend G6PD testing prior to PQ treatment (Table 1) . However few countries have introduced G6PD testing into routine practice due to considerable barriers for its public health deployment .
The Asia Pacific Malaria Elimination Network and the Vivax Working Group
The Asia Pacific Malaria Elimination Network (APMEN) in conjunction with the Asia Pacific Malaria Alliance (APLMA) is a regional network of National Malaria Control Programmes (NMCPs) and research partners working together to overcome the challenges for the regional elimination of malaria. At the initial APMEN meeting in 2009, P. vivax was identified as a key challenge for the regional malaria elimination. The Vivax Working Group (VxWG) was established to identify key knowledge gaps impeding the control of vivax malaria . The VxWG provides a forum for its members to prioritise research activities that will provide the necessary evidence for policy makers to change policy and impact on health outcomes. The group comprises representatives from 18 NMCPs, a wide range of research partner institutes, the WHO, as well as a variety of consortia and industry representatives. The working group follows a cyclical process as described in detail previously . Annual workshops, meetings and consultations are a critical part of the groups work to build consensus, set common agendas and foster partnerships.
Round table discussion “Incorporation of G6PD testing for P. vivax case management, how and when to use it”
The annual VxWG meeting was held in October 2016 in Bali Indonesia with 73 representatives from 16 partner countries and 33 institutional partners and other research institutes. During this meeting a round table discussion was held to discuss the incorporation of G6PD testing for P. vivax case management and how and when to use it. The specific questions posed to the forum are listed in Table 2. The key discussion points arising from this session are grouped into five overarching issues: (i) current barriers for G6PD testing for PQ radical cure, (ii) necessary properties of G6PD tests for wide scale deployment, (iii) the promotion of G6PD testing, (iv) improving the adherence to a complete PQ treatment course and (v) challenges for future TQ roll out.
Topic 1: current barriers for G6PD testing for PQ radical cure
The WHO malarial treatment guidelines were revised recently, including a statement that good practice requires that the G6PD status of patients should be ascertained prior to administration of PQ . Implementing routine testing for G6PDd is challenging in the absence of a robust, affordable point of care (PoC) test and is not yet universally accepted. Hence the WHO guidelines also state that if testing is unavailable, an individual risk–benefit assessment should guide the decision on whether or not to prescribe PQ (Table 3) .
National policies vary considerably from country to country, with only 7 of the 20 malaria-endemic countries in the Asia–Pacific region and Sri Lanka, which is malaria free, currently recommending testing for G6PDd prior to prescribing PQ (Table 1) . In some countries it was acknowledged that the actual clinical practise differs from the guidelines. Identifying and addressing the barriers for the introduction of G6PD testing will help to promote the safe delivery of PQ. Furthermore, since G6PD testing will likely be a prerequisite for TQ prescription, which may demand far more stringent criteria, ensuring the widespread implementation of G6PD testing will greatly facilitate the roll out of this new treatment once it becomes available.
Many participants questioned the need for routine G6PD testing prior to PQ radical cure, perceiving the risk of drug induced severe haemolysis to be low, and citing extensive experience in treating patients with PQ with very few reports of severe adverse events. This perception was echoed in a more formal study undertaken in four of the APMEN partner countries . Many participants proposed that in certain populations and locations it would be safe to prescribe PQ without prior G6PD testing.
A counter argument to this approach was raised that, since there was a lack of formal pharmacovigilance systems the occurrence of severe adverse events would be rarely recognised or recorded. A comprehensive review of reported PQ induced toxicity documented an overall risk of mortality as 1 in 621,428 . However there are several reports of severe PQ toxicity and in some cases these were fatal [13, 14]. Most of these reports were not accompanied by corresponding denominators for the number of patients exposed and hence there is a degree of uncertainty about the absolute risk of haemolysis and how this varies with different G6PD variants. The Mediterranean and Mediterranean-like G6PDd variants are of particular concern because of severe PQ induced haemolytic anaemia that is not self-limiting .
The perceived need for G6PD testing therefore depends on a balance of the population-level risk of drug induced haemolysis and the benefits of achieving radical cure. The healthcare priority for managing a patient with acute malaria is the reduction in asexual parasitaemia and achieving symptom resolution. In this context the prescriber and/or patient may not perceive the immediate expediency of preventing future relapse which occur in only a proportion of patients and often do not manifest clinically for weeks or even months . Each recurrent bout of parasitaemia is associated with parasite induced haemolysis and haemopoietic suppression resulting in a cumulative risk of severe anaemia . The morbidity and mortality associated with recurrent infections will vary between geographical populations, access to healthcare, and the prevailing relapse patterns . Hence the risk–benefit assessment varies, depending on the clinical setting and the specific application of PQ, such as the treatment of symptomatic patients, terminal prophylaxis in healthy but exposed individuals and even mass drug administration [19, 20]. The risk–benefit also depends on the progress of malaria elimination in the respective setting. In countries with low endemicity close to malaria elimination the risk of reinfection is low and reappearance of parasites is mainly caused by relapses rendering radical cure highly beneficial. The ability of the health system to ensure adherence to treatment is an additional variable that should be included in the risk–benefit assessment, since incomplete treatment only provides the risks, but not the benefits of radical cure.
The logistics of delivering diagnostics in many malaria endemic areas are substantial. At the round table discussions participants raised concerns regarding the cost-effectiveness of G6PD testing in areas with low risk of PQ induced haemolysis. In countries with limited public health resources this issue becomes crucial for implementation routine G6PD testing and policy makers must be convinced that G6PD testing adds value and is good use of available funding. Economic studies to address this are currently underway in a number of Asian countries . Preliminary modelling data from the Thai-Myanmar border suggests that there is a potential reduction in total healthcare costs when using G6PD testing prior to PQ compared to PQ treatment without testing. These savings result from averting drug induced haemolytic episodes and the cumulative impact of P. vivax relapses .
Participants from NMCPs highlighted the financial challenges, and the barriers of ensuring appropriate training and quality control practices. Furthermore the logistical challenges of maintaining a supply chain and suitable storage facilities are paramount in order to use tests within their expiry dates. This is especially important for low endemic settings where only a few vivax patients are seen, but stocks would need to be kept up to date.
Wide-scale introduction of G6PD testing for vivax patients will require the availability of easy to use, reliable PoC tests with robust performance indicators . Several participants discussed the difficulties of introducing malaria Rapid Diagnostic Tests (RDTs) including the practice of adhering to guidelines when the RDT result was negative [23–25] and the variable utilization in some settings [26–30]. Although the lessons learnt from the introduction of malaria RDTs are relevant to G6PD testing, the former are required for diagnosing an acute infection, whereas the latter are required for safety and prevention of future infections , and thus the experience and challenges are often different.
Topic 2: necessary properties of G6PD test for wide scale deployment
Most endemic countries where G6PD testing is carried out routinely rely on the fluorescent spot test (FST) as the primary diagnostic tool. In some cases the FST is backed up by spectrophotometer based quality control systems (e.g. Malaysia). Whilst the FST is widely used, it has a number of limitations including difficulties in its interpretation, the need for basic laboratory infrastructure and an extended time to result of at least 30–45 min, rendering the test unsuitable for PoC testing . The FST has a cut-off enzyme activity at approximately 30% of the adjusted male median . Whilst this threshold is currently widely believed to be suitable to guide PQ treatment, it is not sufficient to guide TQ treatment and the manufacturers recommendations will likely require an individual’s enzyme activity to be greater than 70% [5, 33].
The FST provides a qualitative test result and is unable to diagnose heterozygous females who can have G6PD activity between 30 and 70%. In heterozygous females the fraction of RBCs with G6PD normal activity produces a G6PD normal result, however following PQ administration, the fraction of G6PDd RBCs will be subject to drug induced haemolysis, which can result in a substantial drop in haemoglobin. In settings where the FST is already used as a routine diagnostic, there is no immediate need for a change of practice to other tests as long as medical staff is aware of the test’s shortcomings in heterozygous females.
Two test formats have been introduced to the market within recent years. One of these is a lateral flow assay based on a colorimetric reaction that provides a qualitative G6PD result within less than 15 min. The most widely used lateral flow assay is the CareStart G6PD RDT (Accessbio, USA) with operational characteristics suitable for application in the field . The test has been evaluated thoroughly and in most cases found to perform comparably to the FST [34–38]. It has a similar cut-off activity to the FST and hence it is not suitable for guiding treatment with TQ  however its superior operational characteristics and price [6, 37] make it a useful alternative to the FST prior to PQ treatment.
The second test format is a quantitative biosensor (Accessbio, USA). The Biosensor measures electrochemical properties of a blood sample and provides a quantitative G6PD activity reading that requires normalizing by a haemoglobin measurement or RBC count. While the performance of the current biosensor is not yet sufficient to replace the FST, the format addresses two important shortcomings of all other currently available PoC tests . The machine can provide a quantitative reading making it adaptable to different test-and-treat scenarios in which drug therapy may be based on different enzyme cut-offs. Unlike the lateral flow format the biosensor can identify heterozygous females with G6PD activities between 30 and 70% of the adjusted male median . Some participants had concerns that the quantitative outcome was too complex for basic field applications. However it may be possible to convert the biosensor outcome into a qualitative reading according to predefined absolute cut-off activities.
Next generation biosensors are being developed which will have improved performance and if successful these will facilitate greatly the transition from PQ to TQ based radical cure. This advance in diagnostics is likely to come at greater financial costs since the biosensor and corresponding supplies are significantly more expensive (500 USD/machine, 2.50 USD/test) than the CareStart G6PD RDT (1.50 USD/test) and the FST (<$1/test) .
Topic 3: promoting the roll out of G6PD testing
Participants discussed the criteria that need to be met before NMCPs can endorse G6PD testing to support PQ based radical cure. These were: (i) a clear risk–benefit and cost-effectiveness assessment of G6PD testing, (ii) the availability of a robust tests that is reliable in field settings with limited infrastructure, (iii) a competitive and affordable price for the test and (iv) secured and sustainable funding for the test, for training of health care staff and associated quality control processes. The first three points were discussed in topics 1 and 2 above.
Appropriate training of health care workers and laboratory personnel is needed at all relevant levels of the health system, with an emphasis on the management of G6PDd patients and appropriate monitoring on adherence to guidelines. Successful introduction and scale up of testing will require a system of quality assurance and monitoring mechanisms that should start at the moment of sample collection. This would also need to encompass the correct recording and reporting of results and subsequent adherence to respective treatment algorithms.
Country partners mentioned significant logistical challenges regarding the introduction of routine G6PD testing and emphasised the lack of evidence on how routine G6PD testing could be achieved nationally. Several participants called for pilot projects where efforts could be made to identify and address logistical bottlenecks and provide reassurance of feasibility. In a pilot project in Thailand CareStart™ G6PD RDTs were deployed in 62 selected malaria clinics in 16 provinces (personal communication Suravadee Kitchakam). The main challenges encountered were around the procurement process, the training of staff, the interpretation of test results and following treatment algorithms. Lessons learned from this kind of pilot studies will be help NMCPs to focus resources to achieve widespread deployment.
Topic 4: improving the adherence to a full course of primaquine treatment
Adherence to the currently recommended 14 day PQ regimen is challenging. Previous studies have shown that adherence to a full course of 14 days is often low [40–43] and, whilst this may be mitigated by a shorter treatment course , even unsupervised 7 days regimens may be compromised by poor adherence . On the other hand, the experience with tuberculosis (TB) and HIV suggests that extended treatment courses are feasible. Directly observed treatment (DOT) is used to improve adherence to TB treatment and has been shown to improve outcomes for malaria as well [41, 42]. Many participants commented on the importance of context specific solutions, rather than a “one size fits all” approach. For example, in a very low endemic setting such as Malaysia with a relatively well sourced health system, it is feasible to admit all patients with malaria for treatment and this ensures close supervision and maximal treatment efficacy. In countries with greater case numbers, less well funded health systems or impoverished populations that rely on a daily income admitting all malaria patients to hospital is not feasible. DOTs programmes delivered by village workers might be an option in some settings as was recently discussed at a meeting in Cambodia , however this approach is not formally endorsed by WHO. Some participants suggested that incentives for village health workers would encourage them to remind patients to adhere to their treatment.
Adequate patient communication and simple messaging have been shown to overcome poor adherence in settings with low education and literacy rates . Where P. vivax and P. falciparum are co-endemic some participants thought that it was important that patients were aware of the biomedical difference between the two species. Explaining the long-term risk of P. vivax repeated infections due to its propensity to recur and the beneficial effects of radical cure was considered essential in encouraging patients and their carers to complete a full course of treatment.
Alternative solutions were discussed including modern communication technologies such as messaging through mobile phones (SMS) or using specifically developed apps. Results from trials using SMS to increase adherence to malaria treatment and to treatment for other diseases such as HIV and TB have shown mixed results [47–50]. Content and type of messaging need to be well developed, tested and refined and locally adapted for their implementation to be successful [51, 52]. Mobile applications have been developed to improve adherence to a range of other diseases however there is little knowledge on whether they actually impact on adherence .
Topic 5: anticipated challenges for rolling out Tafenoquine
TQ is currently at the end of its phase 3 development programme. Phase 3 read out anticipated in 2017 and subsequent licensing expected to follow in endemic countries as approvals are gained. If marketed, TQ as a single dose radical cure will be a major advance in improving the adherence issues associated with PQ regimens. However, TQs long elimination half-life means that if drug induced signs of haemolysis occur treatment can’t be curtailed by ceasing further drug administration as is currently the case with PQ. This is likely to be particularly important for patients with the Mediterranean variant in whom haemolysis continues without compensatory effect, but less important for those with mild or moderate variants.
Patients with G6PDd, particularly those with Mediterranean variants, may be at risk of an extended period of haemolysis and for this reason prior testing for G6PDd is likely to be mandatory. Until more information has been gathered from heterozygous females with intermediate G6PDd (enzyme activity between 30 and 70%) the licence holder will restrict its use to those with a minimum G6PD enzyme activity of 70%. Identification of patients at risk through a reliable quantitative PoC test will therefore be one of the greatest challenges for access to TQ . Alternative solutions need to be considered in case no appropriate PoC test is available in time. Participants suggested that patients could be referred to centres where quantitative testing, for instance using spectrophotometry, could be assured. It seems likely that the licence holder will insist on such safety precautions to ensure an acceptable risk–benefit ratio. However restricting the availability of TQ to tertiary centres with quantitative G6PD measurement facilities will significantly limit the number of patients receiving TQ treatment, and thus the public benefits.
Other challenges that need to be addressed prior to the introduction of TQ were also discussed. Current testing and treatment of malaria is generally undertaken by healthcare and laboratory workers with limited training. Given the risk of sustained haemolysis following TQ, medical and laboratory personnel will require enhanced training on testing, interpretation of the results and treatment protocols, as well as ensuring appropriate quality control processes are in place. Alternatively, higher levels of care may need to be provided, including more physician involvement, however this is unlikely to be feasible for many NMCPs.
Once appropriate PoC G6PD tests are available, these will need to be introduced at all outlets where administration of TQ is envisaged. One option to facilitate this is to assess every vivax patient routinely prior to TQ treatment. Another option is to test patients only once, assuming no major changes in enzyme activity occur over a life-time, and to record the patient’s results on a register or patient card, which could be used to base decisions on treatment in the future. Whether records should be kept as hard or soft copy and whether results should remain with the patient or in a centralized repository will depend largely on the capacity of the NMCPs and the health care system in general. In Malaysia and the Philippines new-borns have their G6PD activity measured. The carers of the babies are provided with cards indicating the results. Those tested normal will need to be tested again later in life to confirm their status, as G6PD levels are physiologically elevated in new-borns [55, 56]. The potential loss of cards over time, may limit the usefulness of the system for many NMCPs . In the absence of electronic patient record systems and ongoing uncertainty regarding the stability of enzyme activity over time in heterozygous females, it is likely that most control programs will opt for repeated testing.
Adherence to test results and clear decision trees for adequate treatment of G6PDd patients will need to be developed and staff will require training and regular assessment on how well they are adhering to these protocols. Training of staff will need to include quality assurance issues, appropriate handling of samples for testing, as well as adequate communication to patients about the prescription of TQ, its benefits and risks and alternate treatment options when TQ is contraindicated.
There are significant challenges for achieving safe and effective radical cure in the communities at greatest risk of malaria. NMCPs, researchers and funders need to address these challenges and create a viable strategy to achieve their goals, providing novel solutions for overcoming critical bottle-necks. This process needs to begin now to enhance treatment practice for PQ based radical cure. Highlighting the benefits of radical cure for the patient and community will improve prescription practice and patient adherence. Coupling this with improved access to adequate G6PD testing will pave the way for the introduction of TQ, with huge potential to accelerate the elimination of P. vivax.
Baird JK. Evidence and implications of mortality associated with acute Plasmodium vivax malaria. Clin Microbiol Rev. 2013;26:36–57.
Baird JK. Neglect of Plasmodium vivax malaria. Trends Parasitol. 2007;23:533–9.
Barcus MJ, Basri H, Picarima H, Manyakori C, Sekartuti Elyazar I, et al. Demographic risk factors for severe and fatal vivax and falciparum malaria among hospital admissions in northeastern Indonesian Papua. Am J Trop Med Hyg. 2007;77:984–91.
RBM. The Asia Pacific Malaria Elimination Network (APMEN) supporting the common goal of a malaria-free Asia Pacific (Progress & impact series, 11). Geneva: Roll Back Malaria Parternship Secreteriat; 2014.
von Seidlein L, Auburn S, Espino F, Shanks D, Cheng Q, McCarthy J, et al. Review of key knowledge gaps in glucose-6-phosphate dehydrogenase deficiency detection with regard to the safe clinical deployment of 8-aminoquinoline treatment regimens: a workshop report. Malar J. 2013;12:112.
Ley B, Luter N, Espino FE, Devine A, Kalnoky M, Lubell Y, et al. The challenges of introducing routine G6PD testing into radical cure: a workshop report. Malar J. 2015;14:377.
Cappellini MD, Fiorelli G. Glucose-6-phosphate dehydrogenase deficiency. Lancet. 2008;371:64–74.
WHO. Guidelines for the treatment of malaria. 3rd ed. Geneva: World Health Organization; 2015.
WHO. World Malaria Report 2016. Geneva: World Health Organization; 2016. http://www.who.int/malaria/publications/world-malaria-report-2016/report/en/.
Ley B, Thriemer K, Jaswal J, Poirot E, Alam MS, Phru CS, et al. Perceptions of P. vivax malaria and barriers to routine G6PD testing prior to its treatment with primaquine. Malar J. 2017. (under review).
Vivax Working Group. Targeting vivax malaria in the Asia Pacific: The Asia Pacific Malaria Elimination Network Vivax Working Group. Malar J. 2015;14:484.
Recht J, Ashley E, White NJ. Safety of 8-aminoquinoline antimalarial medicines. Geneva: World Health Organization; 2014.
Monteiro WM, Moura-Neto JP, Recht J, Bassat Q, Lacerda MV. Fatal primaquine-induced hemolysis in a patient with Plasmodium vivax malaria and G6PD A(-) variant in the Brazilian Amazon. Clin Infect Dis. 2016;62:1188.
Ashley EA, Recht J, White NJ. Primaquine: the risks and the benefits. Malar J. 2014;13:418.
Beutler E, Duparc S. G6PD deficiency working group. Glucose-6-phosphate dehydrogenase deficiency and antimalarial drug development. Am J Trop Med Hyg. 2007;77:779–89.
White NJ. Determinants of relapse periodicity in Plasmodium vivax malaria. Malar J. 2011;10:297.
Douglas NM, Anstey NM, Buffet PA, Poespoprodjo JR, Yeo TW, White NJ, et al. The anaemia of Plasmodium vivax malaria. Malar J. 2012;11:135.
Price RN, Douglas NM, Anstey NM. New developments in Plasmodium vivax malaria: severe disease and the rise of chloroquine resistance. Curr Opin Infect Dis. 2009;22:430–5.
Louicharoen C, Patin E, Paul R, Nuchprayoon I, Witoonpanich B, Peerapittayamongkol C, et al. Positively selected G6PD-Mahidol mutation reduces Plasmodium vivax density in Southeast Asians. Science. 2009;326:1546–9.
Leslie T, Briceno M, Mayan I, Mohammed N, Klinkenberg E, Sibley CH, et al. The impact of phenotypic and genotypic G6PD deficiency on risk of Plasmodium vivax infection: a case-control study amongst Afghan refugees in Pakistan. PLoS Med. 2010;7:e1000283.
IMPROV Study Group. Improving the radical cure of vivax malaria (IMPROV): a study protocol for a multicentre randomised, placebo-controlled comparison of short and long course primaquine regimens. BMC Infect Dis. 2015;15:558.
Devine A, Parmiter M, Chu C, Bancone G, Nosten F, Price RN et al. Using G6PD tests to enable the safe treatment of Plasmodium vivax infections with primaquine on the Thailand-Myanmar border: a cost-effectiveness analysis. PLoS Neglect Trop Dis. Under review. 2017.
Reyburn H, Mbakilwa H, Mwangi R, Mwerinde O, Olomi R, Drakeley C, et al. Rapid diagnostic tests compared with malaria microscopy for guiding outpatient treatment of febrile illness in Tanzania: randomised trial. BMJ. 2007;334:403.
Hamer DH, Ndhlovu M, Zurovac D, Fox M, Yeboah-Antwi K, Chanda P, et al. Improved diagnostic testing and malaria treatment practices in Zambia. JAMA. 2007;297:2227–31.
Uzochukwu BS, Onwujekwe E, Ezuma NN, Ezeoke OP, Ajuba MO, Sibeudu FT. Improving rational treatment of malaria: perceptions and influence of RDTs on prescribing behaviour of health workers in southeast Nigeria. PLoS ONE. 2011;6:e14627.
Okebe JU, Walther B, Bojang K, Drammeh S, Schellenberg D, Conway DJ, et al. Prescribing practice for malaria following introduction of artemether–lumefantrine in an urban area with declining endemicity in West Africa. Malar J. 2010;9:180.
Juma E, Zurovac D. Changes in health workers’ malaria diagnosis and treatment practices in Kenya. Malar J. 2011;10:1.
Msellem MI, Martensson A, Rotllant G, Bhattarai A, Stromberg J, Kahigwa E, et al. Influence of rapid malaria diagnostic tests on treatment and health outcome in fever patients, Zanzibar: a crossover validation study. PLoS Med. 2009;6:e1000070.
Thiam S, Thior M, Faye B, Ndiop M, Diouf ML, Diouf MB, et al. Major reduction in anti-malarial drug consumption in Senegal after nation-wide introduction of malaria rapid diagnostic tests. PLoS ONE. 2011;6:e18419.
Skarbinski J, Ouma PO, Causer LM, Kariuki SK, Barnwell JW, Alaii JA, et al. Effect of malaria rapid diagnostic tests on the management of uncomplicated malaria with artemether–lumefantrine in Kenya: a cluster randomized trial. Am J Trop Med Hyg. 2009;80:919–26.
Malaria Consortium. Learning Brief-Successful roll out of RDTs in Uganda.
Domingo GJ, Satyagraha AW, Anvikar A, Baird K, Bancone G, Bansil P, et al. G6PD testing in support of treatment and elimination of malaria: recommendations for evaluation of G6PD tests. Malar J. 2013;12:391.
Llanos-Cuentas A, Lacerda MV, Rueangweerayut R, Krudsood S, Gupta SK, Kochar SK, et al. Tafenoquine plus chloroquine for the treatment and relapse prevention of Plasmodium vivax malaria (DETECTIVE): a multicentre, double-blind, randomised, phase 2b dose-selection study. Lancet. 2014;383:1049–58.
Brito MA, Peixoto HM, Almeida AC, Oliveira MR, Romero GA, Moura-Neto JP, et al. Validation of the rapid test Carestart(tm) G6PD among malaria vivax-infected subjects in the Brazilian Amazon. Rev Soc Bras Med Trop. 2016;49:446–55.
Espino FE, Bibit JA, Sornillo JB, Tan A, von Seidlein L, Ley B. Comparison of three screening test kits for G6PD enzyme deficiency: implications for its use in the radical cure of vivax malaria in remote and resource-poor areas in the Philippines. PLoS ONE. 2016;11:e0148172.
Henriques G, Raut S, Phommasone K, Adhikari B, Pongvongsa T, Ley B, et al. Prevalence of glucose-6-phosphote dehydrogenase deficiency among a rural and remote population of Lao PDR (Laos). Atlanta: ASTMH Annual Meeting; 2016.
Baird JK, Dewi M, Subekti D, Elyazar I, Satyagraha AW. Noninferiority of glucose-6-phosphate dehydrogenase deficiency diagnosis by a point-of-care rapid test vs the laboratory fluorescent spot test demonstrated by copper inhibition in normal human red blood cells. Transl Res. 2015;165:677–88.
Satyagraha AW, Sadhewa A, Elvira R, Elyazar I, Feriandika D, Antonjaya U, et al. Assessment of point-of-care diagnostics for G6PD deficiency in malaria endemic rural eastern Indonesia. PLoS Neglect Trop Dis. 2016;10:e0004457.
Ley B, Alam MS, O’Donnell JJ, Hossain MS, Kibria MG, Jahan N, et al. A comparison of three quantitative methods to estimate G6PD activity in the Chittagong Hill tracts, Bangladesh. PLoS ONE. 2017;12:e0169930.
Pereira EA, Ishikawa EA, Fontes CJ. Adherence to Plasmodium vivax malaria treatment in the Brazilian Amazon Region. Malar J. 2011;10:355.
Maneeboonyang W, Lawpoolsri S, Puangsa-Art S, Yimsamran S, Thanyavanich N, Wuthisen P, et al. Directly observed therapy with primaquine to reduce the recurrence rate of Plasmodium vivax infection along the Thai-Myanmar border. Southeast Asian J Trop Med Public Health. 2011;42:9–18.
Takeuchi R, Lawpoolsri S, Imwong M, Kobayashi J, Kaewkungwal J, Pukrittayakamee S, et al. Directly-observed therapy (DOT) for the radical 14-day primaquine treatment of Plasmodium vivax malaria on the Thai-Myanmar border. Malar J. 2010;9:308.
Khantikul N, Butraporn P, Kim HS, Leemingsawat S, Tempongko MA, Suwonkerd W. Adherence to antimalarial drug therapy among vivax malaria patients in northern Thailand. J Health Popul Nutr. 2009;27:4–13.
Grietens KP, Soto V, Erhart A, Ribera JM, Toomer E, Tenorio A, et al. Adherence to 7-day primaquine treatment for the radical cure of P. vivax in the Peruvian Amazon. Am J Trop Med Hyg. 2010;82:1017–23.
CNM. Meeting report. Meeting on Diagnosis and Treatment in the context of elimination. Phnom Penh: CNM2016.
Leslie T, Rab MA, Ahmadzai H, Durrani N, Fayaz M, Kolaczinski J, et al. Compliance with 14-day primaquine therapy for radical cure of vivax malaria–a randomized placebo-controlled trial comparing unsupervised with supervised treatment. Trans R Soc Trop Med Hyg. 2004;98:168–73.
Mohammed S, Glennerster R, Khan AJ. Impact of a daily SMS medication reminder system on tuberculosis treatment outcomes: a randomized controlled trial. PLoS ONE. 2016;11:e0162944.
Nsagha DS, Lange I, Fon PN, Nguedia Assob JC, Tanue EA. A randomized controlled trial on the usefulness of mobile text phone messages to improve the quality of care of HIV and AIDS patients in Cameroon. Open AIDS J. 2016;10:93–103.
Steury EE. Mobile phone short message service to improve malaria pharmacoadherence in Zambia. J Nurs Scholarsh. 2016;48:354–61.
Talisuna AO, Oburu A, Githinji S, Malinga J, Amboko B, Bejon P, et al. Efficacy of text-message reminders on paediatric malaria treatment adherence and their post-treatment return to health facilities in Kenya: a randomized controlled trial. Malar J. 2017;16:46.
Liu JX, Modrek S. Evaluation of SMS reminder messages for altering treatment adherence and health seeking perceptions among malaria care-seekers in Nigeria. Health Policy Plan. 2016;31:1374–83.
Githinji S, Jones C, Malinga J, Snow RW, Talisuna A, Zurovac D. Development of a text-messaging intervention to improve treatment adherence and post-treatment review of children with uncomplicated malaria in western Kenya. Malar J. 2015;14:320.
Haase J, Farris KB, Dorsch MP. Mobile applications to improve medication adherence. Telemed J E Health. 2017;23:75–9.
Price RN, Nosten F. Single-dose radical cure of Plasmodium vivax: a step closer. Lancet. 2014;383:1020–1.
Travis SF, Kumar SP, Paez PC, Delivoria-Papadopoulos M. Red cell metabolic alterations in postnatal life in term infants: glycolytic enzymes and glucose-6-phosphate dehydrogenase. Pediatr Res. 1980;14:1349–52.
Konrad PN, Valentine WN, Paglia DE. Enzymatic activities and glutathione content of erythrocytes in the newborn: comparison with red cells of older normal subjects and those with comparable reticulocytosis. Acta Haematol. 1972;48:193–201.
WHO. World Malaria Report. Geneva. Switzerland: World Health Organization; 2015. p. 2015.
KT, BL and RP conceived the idea and questions for the round table discussion; AB, LS, MSA, AP, EL, GD and JS facilitated the discussions; BL, SA, RC, JM, AD, EJ and GD acted as note-takers during the discussions; all authors participated on the round table discussion; KT, BL, RP wrote the first draft of the manuscript. All authors read and approved the final manuscript.
We would like to thank all participants of the annual meeting and the Indonesian NMCP for hosting this event. We thank Justin Green (GlaxoSmithKline) for his critical review of the paper and helpful comments regarding the development of tafenoquine.
The meeting was funded by Medicines for Malaria Venture (MMV). Major funding for the Asia Pacific Malaria Elimination Network (APMEN) Vivax Working Group (VxWG) was provided by the Australian Government Department of Foreign Affairs and Trade. The working group is currently funded by The Bill and Melinda Gates Foundation (OPP1164105).
SD is full time employee at Medicines for Malaria Ventures, that has funded the meeting and co-develop tafenoquine with GlaxoSmithKline. GJD is a full time employee of PATH, that is advancing the development of G6PD tests to support radical cure of vivax malaria. YSH is a full time employee of Access Bio Inc, US, that manufactures G6PD diagnostics.
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