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Mass drug administration for the control and elimination of Plasmodium vivax malaria: an ecological study from Jiangsu province, China
Malaria Journal volume 12, Article number: 383 (2013)
Recent progress in malaria control has caused renewed interest in mass drug administration (MDA) as a potential elimination strategy but the evidence base is limited. China has extensive experience with MDA, but it is not well documented.
An ecological study was conducted to describe the use of MDA for the control and elimination of Plasmodium vivax in Jiangsu Province and explore the association between MDA and malaria incidence. Two periods were focused on: 1973 to 1983 when malaria burden was high and MDA administered to highly endemic counties province-wide, and 2000 to 2009, when malaria burden was low and a focal approach was used in two counties. All available data about the strategies implemented, MDA coverage, co-interventions, incidence, and adverse events were collected and described. Joinpoint analysis was used to describe trends in incidence and the relationship between MDA coverage and incidence was explored in negative binomial regression models.
From 1973 to 1983, MDA with pyrimethamine and primaquine was used on a large scale, with up to 30 million people in target counties covered in a peak year (50% of the total population). Joinpoint analyses identified declines in annual incidence, -56.7% (95% CI -75.5 to -23.7%) from 1973–1976 and -12.4% (95% CI -24.7 to 2.0%) from 1976–1983. Population average negative binomial models identified a relationship between higher total population MDA coverage and lower monthly incidence from 1973–1976, IRR 0.98 (95% CI 0.97 to 1.00), while co-interventions, rainfall and GDP were not associated. From 2000–2009, incidence in two counties declined (annual change -43.7 to -14.0%) during a time when focal MDA using chloroquine and primaquine was targeted to villages and/or individuals residing near passively detected index cases (median 0.04% of total population). Although safety data were not collected systematically, there were rare reports of serious but non-fatal events.
In Jiangsu Province, China, large-scale MDA was implemented and associated with declines in high P. vivax malaria transmission; a more recent focal approach may have contributed to interruption of transmission. MDA should be considered a potential key strategy for malaria control and elimination.
Mass drug administration (MDA) is a core strategy used for the control and elimination of many tropical diseases, including trachoma, lymphatic filariasis, schistosomiasis and onchocerciasis. For malaria eradication in the 1950s and 60s, MDA was advocated by the World Health Organization (WHO) as a strategy in situations where more conventional control measures such as indoor residual spraying (IRS) with dichlorodiphenyltrichloroethane (DDT) had failed to end residual transmission. Defined as empiric administration of a therapeutic regimen to an entire population or well-defined sub-population at the same time, MDA campaigns worldwide utilized a variety of different drugs, regimens and dosing intervals. Most were associated with declines in incidence or parasite prevalence during the intervention but did not focus on species-specific impact and were not designed to show interruption of transmission[3–5]. Due to concerns about efficacy, operational feasibility, sustainability, and emergence of drug resistance, MDA fell eventually out of favour.
Recent progress in malaria control has caused renewed enthusiasm and interest in MDA as a potential strategy for elimination and eradication[6, 7]. MDA has also been considered as a strategy to contain the recent emergence of artemisinin resistance at the Cambodia-Thai and Thai-Myanmar borders[8, 9]. However, recent evidence to guide MDA as a public health intervention for malaria remains sparse. Since the eradication era, studies of MDA have been limited[10–12] and large-scale use of drugs in communities has been focused on targeted therapies in specific populations such as in intermittent preventative therapy and seasonal malaria chemoprevention[13, 14]. Furthermore, there has been less attention on MDA specifically for Plasmodium vivax, the species which becomes the ultimate challenge for most eliminating countries because it is more resilient than Plasmodium falciparum to standard interventions outside Africa. Plasmodium vivax is able to persist in a dormant liver (hypnozoite) stage and relapse over long intervals of months to years. Primaquine, the only drug widely available for radical cure has variable efficacy and poor adherence due to the long treatment course required and concerns about potential life-threatening haemolysis in persons with underlying glucose-6-phosphate dehydrogenase (G6PD) deficiency. An argument for MDA, versus screening and treatment, is that diagnosis is hampered by the lack of biomarkers for the liver stage, and limitations of microscopy or rapid diagnostic tests (RDTs) to detect blood stage infections which are characteristically of lower density than P. falciparum. Furthermore, anopheline mosquito species that transmit P. vivax tend to be outdoor biting and resting making standard vector control measures such as bed nets and IRS less effective.
China has extensive experience with MDA, including for P. vivax, but this historical experience focusing specifically on MDA has not been well documented[3, 4, 19, 20]. After the eradication era of the 1950s and 60s, falciparum malaria was eliminated from large parts of the country. But, the challenge of P. vivax persisted, particularly in the form of resurgences in central China occurring approximately every decade[21–27]. In the 1970s and 80s large-scale MDA was used to control these epidemics. In the 1990s and thereafter, a focal approach was used. The goal of this study was to document this MDA experience with P. vivax, focusing on Jiangsu Province for two time periods for which detailed records were available. The first period from 1973-1983 began with large P. vivax outbreaks which had been occurring since the Cultural Revolution (1965–68), during which time civil disturbances resulted in the abandonment of anti-malarial activities[21, 22]. Mass drug administration was performed on a large scale involving millions of people. The second period focuses on 2000-2009, which began with an outbreak of P. vivax malaria in nearby Anhui Province and bordering areas of Jiangsu. Focal MDA was performed on a smaller scale, targeted to close contacts, households and villages of index cases. The impact of MDA on incidence is also explored, acknowledging limitations of an ecological study design, which can show associations and generate hypotheses but cannot prove causality.
An ecological study was performed to describe the use of mass drug administration for control and elimination of P. vivax malaria in Jiangsu Province, China (Figure 1A), and to explore the impact on malaria incidence. While MDA had been used since the 1950s, two periods identified by the provincial malaria programme as having detailed records available were focused on: a) 1973 to 1983 with MDA to target counties in the province, and b) 2000 to 2009 with focal MDA to villages and close contacts of index cases in select counties during a P. vivax epidemic. As individual level data on malaria cases and compliance with MDA and other interventions were not available, population level figures were utilized.
MDA methodology, 1973–1983
The goal of seasonal MDA with pyrimethamine and primaquine was to treat potential reservoirs of P. vivax blood and liver stage infection before the start of the malaria transmission season. Plasmodium falciparum had nearly been eliminated from Jiangsu Province by this time, accounting for fewer than 140 annual cases reported (Table 1).
Villagers were notified prior to the annual campaign. Community health workers and local public health officers administered medications daily by directly observed therapy (Figure 2A). MDA was administered before or at the start of the malaria transmission season that typically begins in April. From 1973 to 1976, seasonal MDA using pyrimethamine and primaquine was directed at all rural counties, and from 1977 to 1983, a stratified approach using chloroquine and primaquine was implemented (Table 2).
MDA methodology, 2000–2009
From 2000–2009, focal “spring treatment” was administered in counties on the western border as response to a P. vivax epidemic due to larger outbreaks in nearby Anhui Province. Initially, entire natural villages (population ~20 persons, the division below an administrative village) were targeted. As incidence declined, more focal approaches were taken based on the provincial mandate (Table 2). Exclusion criteria included: age < one year, pregnancy, serious heart, liver or kidney disease, fever, and history of cyanosis, systemic bleeding, or dark coloured urine.
MDA was conducted by local hospital and health bureau workers in the homes of targeted individuals. Informed consent was conducted verbally and through a handout. Villagers were instructed to have food before taking the medication. The administration of drugs was by directly observed therapy (Figure 2B) and documented by collecting patient signatures. Medication was stopped if serious adverse effects such as dark urine, cyanosis, or haemolysis occurred. The goal was for 85% of individuals infected in the previous year to complete the full course and for 80% of other individuals (family, neighbours, etc.) to complete the full course. All medication administration and data collection were to be completed by the end of March of that year.
Aggregate data from all 11 prefectures of Jiangsu Province were collected including monthly and annual incidence of reported malaria cases, annual number of people reached with MDA using pyrimethamine and primaquine prior to the malaria transmission season, annual prefecture population (based on annual census data), annual quantities of drug salts and other prophylactic medications administered, and vector control measures. Protocols and reports on haemolysis or other adverse events relating to MDA were reviewed.
Aggregate data were gathered from two counties (the administrative level below prefecture) in the western part of Jiangsu where focal MDA was implemented and detailed records were available: Sihong in Suqian prefecture and Xuyi in Huaian prefecture (Suquian and Huaian previously combined and known as Huaiyin prefecture)[31, 32]. The data included monthly and annual incidence, as well as number of subjects that were targeted and successfully completed a MDA course. Data on adverse events and coverage of vector control measures were only available from Sihong. Annual population was available for all townships (administrative level below county) within Sihong and 22 of 28 in Xuyi[33, 34]. For missing data, populations were imputed based on average township population that year. Published literature as well as county and provincial records were reviewed for any data on haemolysis or other adverse effects relating to focal MDA.
For both time periods, gross domestic product (GDP) data from China were collected from the World Bank and deflated to year 2000 US$ to account for inflation. All monthly rainfall data were collected from the International Research Institute for Climate and Society. For the 1978 to 1983 period, monthly rainfall data were calculated as the average from 14 weather stations throughout Jiangsu Province. For the 2000 to 2009 period, average monthly rainfall data were collected from two weather stations closest by coordinates to the selected counties.
Data management and analysis
Data were extracted from paper records with support of a translator, and then double entered into Microsoft Excel (Microsoft Corp, Seattle, USA). Data were cleaned and analysed in R (Foundation for Statistical Computing, Vienna, Austria) and Stata 11.0 (Stata Corp, College Station, TX, USA).
Total MDA coverage was defined as per cent of the total population covered by MDA (total population coverage). This value did not take into account the fact that only high-risk or target villages and individuals received MDA. Therefore, target population coverage, or per cent of the target population covered by MDA for the 2000-2009 dataset (data not available for 1973-1983 dataset) was also presented. Also, as a functional measure that has relevance to operations and implementation, particularly for focal MDA where only villages or household members and neighbours are treated, the ratio of population receiving MDA to incident case was also calculated.
Given that incidence rate appeared to vary over the study time period, trends were analysed using joinpoint regression analysis, a statistical method that fits a series of joined straight lines to rates over time and chooses best-fitting points or joinpoints where the rate of increase or decrease changes significantly. The grid search method was used to detect segments best describing the data. This method creates a “grid” of all possible locations for joinpoints and tests the error sum of squares at each one to find the best possible fit. Joinpoints were identified as years in which a significant change in trend was detected over the study period. Annual per cent change with 95% CI for each segment are reported to describe linear trends by period.
For the 1973-1983 Jiangsu Province dataset, the association between annual total population MDA coverage and incidence was estimated using population average negative binomial models. To control for background incidence trend as a potential confounder, an interaction term for time period was included based upon segments identified in the joinpoint analysis: early (1973-1976) vs later (1977-1983). A Poisson model was considered but not used as the negative binomial distribution provided a better fit for the data given the high amount of over-dispersion. The negative binomial analysis modelled monthly counts (monthly cases of P. vivax) as the outcome, taking into account prefecture population as an offset. Regression coefficients were computed as incidence rate ratios (IRRs). Total annual population MDA coverage was the primary exposure variable and other covariates controlled for including: annual chemoprophylaxis coverage, net coverage (defined as the number of nets distributed per population), rainfall lagged by one month, and deflated GDP. Drug salts were not included in the model due to non-significant effect and collinearity with chemoprophylaxis and bed nets. Generalized estimating equations with an autoregressive correlation structure were used to control for serial correlation within prefecture time series. Monthly and prefecture dummy terms were used to control for seasonality effects beyond rainfall and unobserved prefecture fixed effects, respectively. To control for potential spatial endogeneity between prefectures, the model included anomalies for intervention terms (computed as the difference between annual coverage and the local mean coverage over the study period for each prefecture). Rainfall and GDP values were standardized to represent one standard deviation (by subtracting the mean and dividing by the standard deviation).To evaluate the association between MDA and incidence during different time periods, a binary term for early (1973-1976) vs. later (1977-1983) years was interacted with the MDA term. Confidence intervals (CI) of 95% are presented based upon robust standard errors. Due to low total population coverage and incidence, the model was not applied to the 2000-2009 county datasets.
Human subjects’ approval was not indicated because the surveillance data utilised was existing, aggregate and without personal identifiers. The analysis protocol was reviewed by the Centers for Disease Control and Prevention IRB and received non-research determination.
1973–1983, MDA, Jiangsu province
Total population coverage of seasonal MDA increased from 24.5% in 1973 to 50% in 1975, then gradually declined to 7.4% in 1983 (Table 1). At peak coverage in 1975, almost 30 million people were treated. The median number of individuals who received MDA for every incident case of P. vivax malaria the previous year was 24, ranging from 2 in 1973 to 76 in 1976.
In almost all prefectures, intermittent chemoprophylaxis was used during the transmission season from June to October. The regimen consisted of either pyrimethamine 50 mg every two weeks or chloroquine 300 mg every ten days. Per cent population coverage of chemoprophylaxis increased from 3.3% in 1973 to 9.8% in 1976, then declined to 1.1% by 1983. At the height of the programme, up to 44 million cumulative doses were administered a year. From 1976 to 1983, a few prefectures also distributed salt fortified with pyrimethamine. From June to September, each person received a monthly average of 400 g salt containing 157.5 mg pyrimethamine. Population coverage was highest at 2.4% in 1982. Bed nets were utilized beginning in 1978, however population level coverage was very low. Indoor residual spraying was not part of the provincial malaria strategy.
Treatment for clinical malaria cases varied by county. The most commonly used regimen was chloroquine on days 1-3 (1.2 g total) with primaquine on days 1-4 (22.5 mg daily). One month later patients were treated with primaquine for another four days (22.5 mg daily) for a total primaquine dose of 180 mg. Another regimen used was chloroquine on days 1-3 (1.2 g total) with primaquine on days 1-8 (22.5 mg daily, 180 mg total). From 1973 to 1977, a five-day regimen was also used in some counties, chloroquine on days 1-3 (1.2 g total) with primaquine on days 1-5 (22.5 mg daily, 112.5 mg total). Subjects who were infected in the previous year were also individually targeted for seasonal MDA.
MDA and incidence
In the setting of large scale MDA, the incidence of P. vivax in Jiangsu Province declined from 113.6 in 1973 to 2.1 per 1,000 population in 1983 (Table 1, Figures 1B-1D,3). Joinpoint analysis on the aggregate provincial dataset identified two distinct periods: 1973-1976 when annual per cent change was -56.7% (95% CI -75.5 to -23.7%) and 1976-1983 when annual per cent change was -12.4% (95% CI -24.7 to 2.0%). At the prefecture level, no more than two distinct periods were identified, with joinpoint breaks occurring from 1976 to 1978. In most prefectures, annual per cent changes in incidence were negative (Table 3).
The population average negative binomial model confirmed that time period significantly impacted the relationship between total population MDA coverage and incidence: monthly incidence was significantly lower in the later period compared with the earlier period (IRR = 0.19; 95% CI 0.11 to 0.33), after controlling for potential confounding factors including chemoprophylaxis, bed nets, rainfall, and GDP (Table 4). Between 1973 and 1976, higher total population MDA coverage was associated with significantly lower monthly incidence (IRR = 0.98; 95% CI 0.97 to 1.00) after controlling for confounders, but in the later period, it was associated with higher incidence (IRR = 1.05; 95% CI 1.03 to 1.06). Other potential confounders were not significantly associated with monthly incidence.
Adverse events from MDA were not systematically monitored as part of the programme, but five reports documenting G6PD deficiency-related severe adverse events from primaquine were identified (Table 5). Two case series were recorded in the setting of large-scale campaigns, one from 1975 and one from 1976. There were two cross-sectional studies, one among family members of patients with severe G6PD deficiency and one among high-risk groups. Additionally, there was a case report from 1979.
In the two case series, drugs were administered to 254,910 residents in Jinhu county and 44,589 residents of Liuhe county. The incidence of acute haemolysis was 3.5 and 9.3 per 100,000 population, respectively. Symptoms were typical for acute haemolytic reaction. Among the 40 patients from Liuhe county, G6PD deficiency testing was performed using the methaemoglobin reductive test, which had a sensitivity of 65% for detection of patients with acute haemolysis. In both studies, there were no deaths and all patients recovered with drug discontinuation and supportive care.
In one of the cross-sectional studies, methaemoglobin testing was performed in 94 family members of three patients who suffered from haemolysis after primaquine and 59.6% tested positive. In another study, methaemoglobin testing was performed in groups hypothesized to have higher prevalence of G6PD deficiency. The prevalence of a deficiency was 5.7% in a village with a high incidence of acute haemolysis versus 0.7-1.0% in the other groups (a village with past P. falciparum cases and a village with members of the Hui minority group) and 0% in a control group of patients with liver disease. The higher prevalence in the village with a high incidence of acute haemolysis was thought to be due to a genetic predisposition in this community.
2000–2009, focal MDA, Sihong and Xuyi counties
Focal MDA coverage
Utilizing the stratified strategy, total population coverage was low. In 2001, it was 1.21% in Sihong and 0.21% in Xuyi, then dropped to very low levels by 2003 (Figure 4). On the other hand, target population coverage was generally high. In Sihong, median 91.6% (range 59.5 to 99.2%) completed treatment and in Xuyi, median 92.0% (range 76.5 to 98.3%) completed treatment. The median number of individuals who completed MDA for each incident case of P. vivax malaria was 16 (range 5 to 39) in Sihong and 10 (range 4 to 22) in Xuyi (Table 6).
Unlike in the 1973-1983 time period, other prophylactic drugs were not utilized. In Sihong county, there was some use of vector control measures. Insecticide-treated bed nets covered 0 to 3% of the population between 2000 and 2004, 10% in 2005, and 4 to 8% between 2006 and 2009. Indoor residual spraying was performed in 2007 and 2009 in select townships. Coverage was recorded as 109.5 kg sprayed over 47,706 sq m in 2007 and 231 kg sprayed over 109,125 sq m in 2009. No information was available on proportion of structures sprayed. There was no recorded use of vector control measures in Xuyi. During this time period, clinical cases of P. vivax presenting to health facilities were treated with chloroquine for three days (1.2 mg total dose) and primaquine for eight days (180 mg total dose).
Focal MDA and incidence
Although the peak incidences were low at baseline, 0.79 and 0.29 per 1,000 population in Sihong and Xuyi, respectively, incidence declined further in the setting of focal MDA (Figure 4). Sihong and Xuyi counties saw declines the year after focal MDA was started. Low incidences were maintained even as focal MDA coverage declined. Joinpoint analysis identified two distinct periods in Xuyi and one in Sihong (Table 3). In Xuyi, the break correlated with a change in total population coverage of focal MDA (Figure 4). Annual per cent changes were negative and statistically significant in all segments. Temporally, other factors did not appear to contribute to decreasing incidence. Gross domestic product increased over the study period but the rate was steady. Rainfall was highest in 2000, 2005 and 2007 (Additional file1: Figures S1b and S2b). Vector control measures were used in Sihong, but the periods of highest coverage do not correspond with declines in incidence.
In Sihong, the number of subjects with adverse reactions was recorded in 2003 and 2007. Adverse reactions were few, occurring in five subjects (2.1/1,000) in 2003 and two (4.3/1,000) in 2007. Symptoms included haemolysis with primaquine, dizziness, gastrointestinal upset, nausea, and vomiting with chloroquine. Safety data were not available from Xuyi.
MDA is increasingly being considered in the battle against malaria yet few descriptions of its use for P. vivax exist in the published literature. This ecological study describes the methods and rationale behind the largest malaria MDA implementation experience documented to date. The potential impact of seasonal MDA on the incidence of vivax malaria in Jiangsu Province, China was explored. After controlling for potential confounders including economic growth, weather, and co-interventions, it was found that large-scale MDA from 1973-1976 was associated with declines in P. vivax malaria transmission. In the 2000-2009 data from two counties, joinpoint analyses showed significant declines in incidence that temporally appear related to focal MDA and not other factors. Safety data were not collected systematically but there were rare reports of serious but non-fatal events. More recent surveillance data indicate that the declines in malaria have been sustained. In 2011, 20 of China’s 31 provinces reported no locally acquired malaria cases. In 2012, Jiangsu was one of six additional provinces to report no locally acquired cases. Thus, the large-scale approach was associated with declines in high levels of transmission and the more recent focal approach may have contributed to interruption of transmission.
With the renewed interest and commitment to malaria elimination, there is growing interest in MDA using primaquine because it is the only drug available to treat the hypnozoite stage of P. vivax, as well as mature gametocytes of P. falciparum. Primaquine has been widely used for MDA, particularly during the eradication era, but detailed documentation on its use specifically for P. vivax has been sparse, there are no controlled studies, and few have demonstrated sustained impact[2, 3, 45–51]. This study had similar limitations in that it was an ecological study and not able to prove impact given the lack of a control. There is also the possibility of reverse causation. From 1977-1983, the model showed a positive association between MDA and incidence, but this is likely because total population coverage decreased as incidence declined during this distinct period. Also, in the later time period, total population coverage was lower and underestimated the true target population coverage to a greater degree. Other potential limitations include confounding and information bias. However, attempts were made to control for economic growth, weather and co-interventions. While it is possible that local officials reported inaccurate coverage and incidence figures, findings were consistent across several groups (prefecture and counties) and over a long time period.
Despite the limitations of an ecological study, the design enabled exploration of the impact of a population level intervention on a population level outcome, which is of obvious public health importance and should stimulate further scientific endeavours, both for intervention studies and the development of new drugs and diagnostics for use in MDA. This paper is among the few to systematically document the MDA experience from China, where the malaria experience is rich but poorly documented due to language barriers. It provides a rare focus on P. vivax, the most large-scale MDA experience documented (peak coverage reaching 30 million people), and is the first to describe China’s recent use of focal MDA.
The optimal timing, frequency, drug(s), target population, and target population coverage in MDA are not clear[8, 52]. In Jiangsu, the timing (before the transmission season) and drugs (antirelapse +/- blood schizonticide) were selected to decrease the reservoir, rather than to produce an immediate impact on disease burden as the target population was largely asymptomatic. An eight-day course of primaquine was chosen based on efficacy seen in clinical trials and concern that a longer treatment course would be operationally challenging to administer via directly observed therapy and less acceptable to the population. Also, although the treatment course was shorter than the standard 14-day course recommended by WHO, the daily dose was higher, and courses were repeated annually.
The target population was adapted to a changing epidemiology. During the higher burden period from 1973-1976, drugs were administered to entire high-risk counties and as transmission declined, a stratified approach was taken to target villages and households of passively identified index cases (assuming local transmission at the home residence) and eventually single, high-risk individuals (e g, subjects positive by indirect fluorescent antibody test (IFAT) testing). The stratified approach was undertaken as a way to decrease workload, but more importantly, to minimize risk and maximize acceptability in communities that no longer saw malaria as a major threat. Target population coverage data were not available for the 1973-1983 programme. However from 2000-2009, it was generally above 85% in Sihong and Xuyi. These goal coverage levels are similar to estimated necessary coverage for P. falciparum elimination. To help guide MDA operations for P. vivax, future field and modelling work should aim to determine the minimal coverage required to achieve an objective (control or elimination).
As an additional measure of coverage, the ratio of population receiving MDA to incident case was calculated. Although this measure has not been used in prior MDA reports, it is presented as a functional measure that has relevance to operations and implementation, particularly for targeted MDA where only villages or household members and neighbours are treated. From 1973-1983, when MDA was administered to entire counties, the range was 2 to 76, with the ratio increasing as incidence declined. With the focal approach used from 2000-2009, the range was 4 to 39. Operationally, lower numbers correspond roughly to the size of a household of an index case, while larger numbers correspond with the involvement of neighboring households. This ratio could be considered similar to the concept of number needed to treat (NNT) and future work is needed to better define the optimal ratio.
A major challenge of primaquine use for MDA is the risk of haemolysis in patients with underlying G6PD deficiency. In symptomatic cases, testing for G6PD deficiency is not recommended prior to administration of a single dose to target P. falciparum gametocytes but it is recommended for a 7- to 14-day regimen for radical cure of P. vivax and there are no guidelines for use in MDA of asymptomatic individuals. The reported prevalence of G6PD deficiency among Han, the predominant ethic group in Jiangsu is low, <5% among males. In one of the case series study, the reported incidence of haemolysis from mass primaquine administration was 9.3 per 100,000 population. The authors note that the incidence was higher than expected and this may have been because the daily primaquine dose of 30 mg was too high (subsequent campaigns used 22.5 mg) or because the timing of that year’s MDA campaign was later than previous years and coincided with peak seasonal fava bean consumption. The most comparable MDA to those reported here was conducted in 300,000 US soldiers returning from Korea on troopships in 1952-4 who received 210 mg of primaquine over two weeks. The severe haemolytic reaction rate was estimated at four per 100,000 in a population that would have been expected to have a greater prevalence of G6PD-deficient individuals than in China. No irreversible adverse events occurred in the Jiangsu reports, but the potential risks suggest that in other settings with similar rates of G6PD deficiency, close monitoring, which would be possible with daily direct observed therapy, could be considered. In addition services for urgent blood transfusion should be available for the few cases that do haemolyse to very low levels of haemoglobin. Testing for G6PD deficiency might be focused on patients with a personal or family history of favism or haemolysis (Table 5) or performed on a more wide scale once a point of care G6PD deficiency test becomes available.
There is growing interest for the use of MDA to control and eliminate malaria but the literature on use specifically for P. vivax is limited. While this study was retrospective and mainly descriptive, it adds to the evidence base for seasonal MDA. It presents a little documented experience from China, where seasonal MDA was practiced (first on a large scale and later in a focal fashion) and likely contributed to declines in vivax malaria transmission and rare reported adverse events. Ongoing research is needed to develop a safer and more effective drug, but there are likely settings where MDA using primaquine could be applied now with a logical and safe operational design and evaluated through a phased approach. MDA should be considered as a potential strategy to hasten and achieve malaria elimination, and not remain something of only historical interest.
Gross domestic product
Indirect fluorescent antibody test
Incidence rate ratio
Indoor residual spraying
Mass drug administration
Rapid diagnostic test
University of California, San Francisco
World health organization.
Hotez PJ: Mass drug administration and integrated control for the world’s high-prevalence neglected tropical diseases. Clin Pharmacol Ther. 2009, 85: 659-664. 10.1038/clpt.2009.16.
Onori E: Experience with mass drug administration as a supplementary attack measure in areas of vivax malaria. Bull World Health Organ. 1972, 47: 543-548.
von Seidlein L, Greenwood BM: Mass administrations of antimalarial drugs. Trends Parasitol. 2003, 19: 452-460. 10.1016/j.pt.2003.08.003.
Poirot E, Hwang J, Kachur SP, Slutsker L, Skarbinski J: Mass drug administration for malaria. Cochrane Database Syst Rev. 2010, CD008846-DOI: 008810.001002/14651858.CD14008846
Greenwood B: The use of anti-malarial drugs to prevent malaria in the population of malaria-endemic areas. Am J Trop Med Hyg. 2004, 70: 1-7.
The malERA Consultative Group on Drugs: A research agenda for malaria eradication: drugs. PLoS Med. 2011, 8: e1000402-
Cotter C, Sturrock HJW, Hsiang MS, Liu J, Phillips AA, Hwang J, Smith-Gueye C, Fullman N, Gosling RD, Feachem RGA: The changing epidemiology of malaria elimination: new strategies for new challenges. Lancet. 2013, 382: 900-911. 10.1016/S0140-6736(13)60310-4.
Maude RJ, Socheat D, Nguon C, Saroth P, Dara P, Li G, Song J, Yeung S, Dondorp AM, Day NP, White NJ, White LJ: Optimising strategies for Plasmodium falciparum malaria elimination in Cambodia: primaquine, mass drug administration and artemisinin resistance. PLoS One. 2012, 7: e37166-10.1371/journal.pone.0037166.
World Health Organization: Consideration of mass drug administration for the containment of artemisinin-resistant malaria in the Greater Mekong subregion, Report of a consensus meeting, 27-28 September 2010. 2011, Geneva, Switzerland: World Health Organization
Kaneko A, Taleo G, Kalkoa M, Yamar S, Kobayakawa T, Bjorkman A: Malaria eradication on islands. Lancet. 2000, 356: 1560-1564. 10.1016/S0140-6736(00)03127-5.
Song J, Socheat D, Tan B, Dara P, Deng C, Sokunthea S, Seila S, Ou F, Jian H, Li G: Rapid and effective malaria control in Cambodia through mass administration of artemisinin-piperaquine. Malar J. 2010, 9: 57-10.1186/1475-2875-9-57.
Von Seidlein L, Walraven G, Milligan PJ, Alexander N, Manneh F, Deen JL, Coleman R, Jawara M, Lindsay SW, Drakeley C, De Martin S, Olliaro P, Bennett S, Schim van der Loeff M, Okunoye K, Targett GA, McAdam KP, Doherty JF, Greenwood BM, Pinder M: The effect of mass administration of sulfadoxine-pyrimethamine combined with artesunate on malaria incidence: a double-blind, community-randomized, placebo-controlled trial in The Gambia. Trans R Soc Trop Med Hyg. 2003, 97: 217-225. 10.1016/S0035-9203(03)90125-8.
Bardaji A, Bassat Q, Alonso PL, Menendez C: Intermittent preventive treatment of malaria in pregnant women and infants: making best use of the available evidence. Expert Opin Pharmacother. 2012, 13: 1719-1736. 10.1517/14656566.2012.703651.
Meremikwu MM, Donegan S, Sinclair D, Esu E, Oringanje C: Intermittent preventive treatment for malaria in children living in areas with seasonal transmission. Cochrane Database Syst Rev. 2012, 2: CD003756
Feachem RG, Phillips AA, Hwang J, Cotter C, Wielgosz B, Greenwood BM, Sabot O, Rodriguez MH, Abeyasinghe RR, Ghebreyesus TA, Snow RW: Shrinking the malaria map: progress and prospects. Lancet. 2010, 376: 1566-1578. 10.1016/S0140-6736(10)61270-6.
John GK, Douglas NM, von Seidlein L, Nosten F, Baird KJ, White NJ, Price RN: Primaquine radical cure of Plasmodium vivax: a critical review of the literature. Malar J. 2012, 11: 280-10.1186/1475-2875-11-280.
Douglas NM, John GK, von Seidlein L, Anstey NM, Price RN:Chemotherapeutic strategies for reducing transmission of Plasmodium vivax malaria. Advances in parasitology. 2012, 80: 271-300.
Sattabongkot J, Tsuboi T, Zollner GE, Sirichaisinthop J, Cui L: Plasmodium vivax transmission: chances for control?. Trends Parasitol. 2004, 20: 192-198. 10.1016/j.pt.2004.02.001.
Dapeng L, Leyuan S, Xili L, Xiance Y: A successful control programme for falciparum malaria in Xinyang, China. Trans R Soc Trop Med Hyg. 1996, 90: 100-102. 10.1016/S0035-9203(96)90099-1.
Chen W, Wu K, Lin M, Tang L, Gu Z, Wang S, Lan C, Lan X, Li H, Huang M, Chen X, Sheng H: [A pilot study on malaria control by using a new strategy of combining strengthening infection source treatment and health education in mountainous areas of Hainan province](in Chinese). Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 1999, 17: 1-4.
Tang LH, Qian HL, Xu SH: Malaria and its control in the People’s Republic of China. Southeast Asian J Trop Med Public Health. 1991, 22: 467-476.
Tang LH: Progress in malaria control in China. Chin Med J. 2000, 113: 89-92.
Huang F, Zhou S, Zhang S, Li W, Zhang H: Monitoring resistance of Plasmdium vivax: point mutations in dihydrofolate reductase gene in isolates from Central China. Parasit Vectors. 2011, 4: 80-10.1186/1756-3305-4-80.
Xu BL, Su YP, Shang LY, Zhang HW: Malaria control in Henan Province, People’s Republic of China. Am J Trop Med Hyg. 2006, 74: 564-567.
Huang GQ, Yuan FY, Jin XL, Zhao CL, Su YP, Shen YZ: To analyze epidemic situation and control of malaria in Jiangsu, Shandong, Henan, Anhui, and Hubei province. Chin J Vector Biol Control. 2007, 18: 398-401.
Sleigh AC, Liu XL, Jackson S, Li P, Shang LY: Resurgence of vivax malaria in Henan Province, China. Bull World Health Organ. 1998, 76: 265-270.
Zhou SS, Wang Y, Tang LH: [Malaria situation in the People’s Republic of China in 2006](in Chinese). Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2007, 25: 439-441.
Zhang W, Wang L, Fang L, Ma J, Xu Y, Jiang J, Hui F, Wang J, Liang S, Yang H, Cao W: Spatial analysis of malaria in Anhui province, China. Malar J. 2008, 7: 206-10.1186/1475-2875-7-206.
Sihong County Centers for Disease Control and Prevention: Malaria anti-relapse therapy guidelines. 2008, Sihong, Jiangsu, China: Sihong County Centers for Disease Control and Prevention
Jiangsu Institute of Parasitic Diseases: Jiangsu Province Malaria Records 1973-1983. 1984, Wuxi, Jiangsu, China: Jiangsu Institute of Parasitic Diseases
Xuyi County Centers for Disease Control and Prevention: Xuyi County Malaria Reports 2000-2009. 2010, Xuyi, Jiangsu, China: Xuyi County Center for Disease Control and Prevention
Sihong County Centers for Disease Control and Prevention: Sihong County Malaria Reports 2000-2009. 2010, Sihong, Jiangsu, China: Sihong County Centers for Disease Control and Prevention
Sihong County Centers for Disease Control and Prevention: Sihong Statistical yearbooks 2000-2009. 2010, Sihong, Jiangsu, China: Sihong County Bureau of Statistics
Xuyi County Centers for Disease Control and Prevention: Xuyi Statistical yearbooks 2000-2009. 2010, Xuyi, Jiangsu, China: Xuyi County Bureau of Statistics
International Research Institute for Climate and Society:http://iridl.ldeo.columbia.edu,
Stracci F, Canosa A, Minelli L, Petrinelli AM, Cassetti T, Romagnoli C, La Rosa F: Cancer mortality trends in the Umbria region of Italy 1978-2004: a joinpoint regression analysis. BMC Cancer. 2007, 7: 10-10.1186/1471-2407-7-10.
Jiangsu Institute of Parasitic Diseases: Jiangsu Eight Main Counties, Malaria Control Report. 1984, Wuxi, Jiangsu, China: Jiangsu Institute of Parasitic Diseases
Jiangsu Institute of Parasitic Diseases: Primaquine adverse reaction: 9 case reports, Jiangsu Province Schistosomiasis Prevention Research Center and Liuhe County Health and Immunization Station, in: Selected Malaria Records from 1974-1983. 1984, Wuxi, Jiangsu, China: Jiangsu Institute of Parasitic Diseases, 122-
Jiangsu Institute of Parasitic Diseases: Primaquine causing hemolysis, 40 cases report, Jiangsu Province Schistosomiasis Prevention Research Center and Liuhe County Health and Immunization Station, in: Selected Malaria Records from 1974-1983. 1984, Wuxi, Jiangsu, China: Jiangsu Institute of Parasitic Diseases, 104-107.
Jiangsu Institute of Parasitic Diseases: Survey of family members: 3 cases, Jiangsu Province Schistosomiasis Prevention Research Center and Liuhe County Health and Immunization Station, in: Selected Malaria Records from 1974-1983. 1984, Wuxi, Jiangsu, China: Jiangsu Institute of Parasitic Diseases, 116-
Bian S, Li C, Zhang X, Huang B, Wang Y, Zhao L: Jiangsu Province Liuhe Region Hereditary RBC G6PD Defect Preliminary Investigation Report, Jiangsu Province Schistosomiasis Prevention Research Center and Liuhe County Health and Immunization Station, in: Selected Malaria Records from 1974-1983. 1984, Wuxi, Jiangsu, China: Jiangsu Institute of Parasitic Diseases, 110-115.
Jiangsu Institute of Parasitic Diseases: Primaquine adverse event: 1 case report, Jiangsu Province Schistosomiasis Prevention Research Center and Liuhe County Health and Immunization Station, in: Selected Malaria Records from 1974-1983. 1984, Wuxi, Jiangsu, China: Jiangsu Institute of Parasitic Diseases, 121-
Yin JH, Yang MN, Zhou SS, Wang Y, Feng J, Xia ZG: Changing Malaria Transmission and Implications in China towards National Malaria Elimination Programme between 2010 and 2012. PLoS One. 2013, 8: e74228-10.1371/journal.pone.0074228.
White NJ: Primaquine to prevent transmission of falciparum malaria. Lancet Infect Dis. 2013, 13: 175-181. 10.1016/S1473-3099(12)70198-6.
Shanks GD: Control and elimination of Plasmodium vivax. Adv Parasitol. 2012, 80: 301-341.
Garfield RM, Vermund SH: Changes in malaria incidence after mass drug administration in Nicaragua. Lancet. 1983, 2: 500-503.
World Health Organization: Interregional workshop on the control of vivax malaria in East Asia, Shanghai, China, 2003. 2004, Regional Office for the Western Pacific: World Health Organization
WHO: Inter-regional meeting on vivax malaria in Asia. 2009, Regional Office for South-East Asia: World Health Organization
Simeons ATW: Follow-up of a mass treatment with injectable atebrin. Ind Med Gaz. 1938, 73: 713-715.
Caceres JL: Malaria before and after massive radical cure in Sucre state, Venezuela. Bol Malar Salud Ambi. 2008, 48: 83-90.
Gabaldon A, Guerrero L: An attempt to eradicate malaria by the weekly administration of pyrimethamine in areas of out-of-doors transmission in Venezuela. Am J Trop Med Hyg. 1959, 8: 433-439.
Greenwood BM: Control to elimination: implications for malaria research. Trends Parasitol. 2008, 24: 449-454. 10.1016/j.pt.2008.07.002.
Ho C: Studies on malaria in new China. Chin Med J. 1965, 84: 491-497.
Okell LC, Griffin JT, Kleinschmidt I, Hollingsworth TD, Churcher TS, White MJ, Bousema T, Drakeley CJ, Ghani AC: The potential contribution of mass treatment to the control of Plasmodium falciparum malaria. PLoS One. 2011, 6: e20179-10.1371/journal.pone.0020179.
White NJ, Qiao LG, Qi G, Luzzatto L: Rationale for recommending a lower dose of primaquine as a Plasmodium falciparum gametocytocide in populations where G6PD deficiency is common. Malar J. 2012, 11: 418-10.1186/1475-2875-11-418.
Jiang W, Yu G, Liu P, Geng Q, Chen L, Lin Q, Ren X, Ye W, He Y, Guo Y, Duan S, Wen J, Li H, Qi Y, Jiang C, Zheng Y, Liu C, Si E, Zhang Q, Tian Q, Du C: Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese population. Hum Genet. 2006, 119: 463-478. 10.1007/s00439-005-0126-5.
Alving AS: Clinical treatment of malaria. US Army Medical Science Publication No 4. 1954, 22: 210-218.
This work has been an output of the Asia Pacific Malaria Elimination Network (APMEN) as well as the Malaria Elimination Group (MEG). Funding for the work was provided through a grant from the Bill and Melinda Gates Foundation to the UCSF Global Heath Group (MSH, RGAF, RG) as well as a grant from the UCSF Pathways Funding Committee Research Fellowship program (ART). MSH is additionally funded by a National Institutes of Health/National Institute of Allergy and Infectious Diseases K23 grant (P0045532) and a Burroughs Wellcome Fund/American Society of Tropical Medicine and Hygiene Fellowship Award (P0049395). JH and SPK are funded by the Centers for Diseases Control and Prevention. YL, JC, and QG are funded by Jiangsu Province’s Medical High Tech Platform (ZX201108) and Jiangsu Science and Technology Department (BM2009902). AB is funded by a grant from the President’s Malaria Initiative. GDS is funded by the Australian Defence Force. The paper represents the views of the authors and not the opinion or policy of their organization or the funders.
We thank Huayun Zhou, Julin Li, Weiming Wang, Yaping Gu, Guizhi She, Song Xu, Yue Tang, and Zhaodong Wang for their support in data collection; Yuanyuan Cao for support on the maps; Andy Anglemeyer, Allen Hightower, Ann Lazar, and Jenny Liu for their input in data analysis; Edmund Seto and Hugh Sturrock for helping to gather weather data; Gavin Yamey for his review of the paper; and Michael Wang for translation support.
The authors declare that they have no competing interests.
MSH, QG, RGAF, and GDS conceived the study. MSH, QG and JH designed the study. ART, YL and MSH collected the data. AB, JH, and MSH analysed the data. RG, SPK and CJ contributed to the interpretation of the data. MSH, ART, JH, and AB drafted the paper. All authors reviewed early drafts and contributed to the final paper. All authors read and approved the final manuscript.
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Hsiang, M.S., Hwang, J., Tao, A.R. et al. Mass drug administration for the control and elimination of Plasmodium vivax malaria: an ecological study from Jiangsu province, China. Malar J 12, 383 (2013). https://doi.org/10.1186/1475-2875-12-383
- Malaria elimination
- Mass drug administration
- Plasmodium vivax