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      Reduction in the proportion of fevers associated with Plasmodium falciparum parasitaemia in Africa: a systematic review

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      Malaria Journal
      BioMed Central

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          Malaria is almost invariably ranked as the leading cause of morbidity and mortality in Africa. There is growing evidence of a decline in malaria transmission, morbidity and mortality over the last decades, especially so in East Africa. However, there is still doubt whether this decline is reflected in a reduction of the proportion of malaria among fevers. The objective of this systematic review was to estimate the change in the Proportion of Fevers associated with Plasmodium falciparum parasitaemia (PFPf) over the past 20 years in sub-Saharan Africa.


          Search strategy. In December 2009, publications from the National Library of Medicine database were searched using the combination of 16 MeSH terms.

          Selection criteria. Inclusion criteria: studies 1) conducted in sub-Saharan Africa, 2) patients presenting with a syndrome of 'presumptive malaria', 3) numerators (number of parasitologically confirmed cases) and denominators (total number of presumptive malaria cases) available, 4) good quality microscopy.

          Data collection and analysis. The following variables were extracted: parasite presence/absence, total number of patients, age group, year, season, country and setting, clinical inclusion criteria. To assess the dynamic of PFPf over time, the median PFPf was compared between studies published in the years ≤2000 and > 2000.


          39 studies conducted between 1986 and 2007 in 16 different African countries were included in the final analysis. When comparing data up to year 2000 (24 studies) with those afterwards (15 studies), there was a clear reduction in the median PFPf from 44% (IQR 31-58%; range 7-81%) to 22% (IQR 13-33%; range 2-77%). This dramatic decline is likely to reflect a true change since stratified analyses including explanatory variables were performed and median PFPfs were always lower after 2000 compared to before.


          There was a considerable reduction of the proportion of malaria among fevers over time in Africa. This decline provides evidence for the policy change from presumptive anti-malarial treatment of all children with fever to laboratory diagnosis and treatment upon result. This should insure appropriate care of non-malaria fevers and rationale use of anti-malarials.

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          Effect of a fall in malaria transmission on morbidity and mortality in Kilifi, Kenya

          Summary Background As efforts to control malaria are expanded across the world, understanding the role of transmission intensity in determining the burden of clinical malaria is crucial to the prediction and measurement of the effectiveness of interventions to reduce transmission. Furthermore, studies comparing several endemic sites led to speculation that as transmission decreases morbidity and mortality caused by severe malaria might increase. We aimed to assess the epidemiological characteristics of malaria in Kilifi, Kenya, during a period of decreasing transmission intensity. Methods We analyse 18 years (1990–2007) of surveillance data from a paediatric ward in a malaria-endemic region of Kenya. The hospital has a catchment area of 250 000 people. Clinical data and blood-film results for more than 61 000 admissions are reported. Findings Hospital admissions for malaria decreased from 18·43 per 1000 children in 2003 to 3·42 in 2007. Over 18 years of surveillance, the incidence of cerebral malaria initially increased; however, malaria mortality decreased overall because of a decrease in incidence of severe malarial anaemia since 1997 (4·75 to 0·37 per 1000 children) and improved survival among children admitted with non-severe malaria. Parasite prevalence, the mean age of children admitted with malaria, and the proportion of children with cerebral malaria began to change 10 years before hospitalisation for malaria started to fall. Interpretation Sustained reduction in exposure to infection leads to changes in mean age and presentation of disease similar to those described in multisite studies. Changes in transmission might not lead to immediate reductions in incidence of clinical disease. However, longitudinal data do not indicate that reductions in transmission intensity lead to transient increases in morbidity and mortality. Funding Wellcome Trust, Kenya Medical Research Institute.
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            Rapid diagnostic tests compared with malaria microscopy for guiding outpatient treatment of febrile illness in Tanzania: randomised trial.

            To compare rapid diagnostic tests (RDTs) for malaria with routine microscopy in guiding treatment decisions for febrile patients. Randomised trial. Outpatient departments in northeast Tanzania at varying levels of malaria transmission. 2416 patients for whom a malaria test was requested. Staff received training on rapid diagnostic tests; patients sent for malaria tests were randomised to rapid diagnostic test or routine microscopy Proportion of patients with a negative test prescribed an antimalarial drug. Of 7589 outpatient consultations, 2425 (32%) had a malaria test requested. Of 1204 patients randomised to microscopy, 1030 (86%) tested negative for malaria; 523 (51%) of these were treated with an antimalarial drug. Of 1193 patients randomised to rapid diagnostic test, 1005 (84%) tested negative; 540 (54%) of these were treated for malaria (odds ratio 1.13, 95% confidence interval 0.95 to 1.34; P=0.18). Children aged under 5 with negative rapid diagnostic tests were more likely to be prescribed an antimalarial drug than were those with negative slides (P=0.003). Patients with a negative test by any method were more likely to be prescribed an antibiotic (odds ratio 6.42, 4.72 to 8.75; P<0.001). More than 90% of prescriptions for antimalarial drugs in low-moderate transmission settings were for patients for whom a test requested by a clinician was negative for malaria. Although many cases of malaria are missed outside the formal sector, within it malaria is massively over-diagnosed. This threatens the sustainability of deployment of artemisinin combination treatment, and treatable bacterial diseases are likely to be missed. Use of rapid diagnostic tests, with basic training for clinical staff, did not in itself lead to any reduction in over-treatment for malaria. Interventions to improve clinicians' management of febrile illness are essential but will not be easy. Clinical trials NCT00146796 [ClinicalTrials.gov].
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              The Limits and Intensity of Plasmodium falciparum Transmission: Implications for Malaria Control and Elimination Worldwide

              Introduction The magnitude of the public health burden posed by malaria worldwide [1] and its connection to poverty [2] has galvanized the international donor community to put malaria control high on the development agenda and helped leverage unprecedented additional financing for malaria endemic countries [3]. Progress toward agreed targets of intervention coverage has been slow [4–6], but recent evidence indicates a precipitous increase in access to effective drugs and prevention strategies in several countries [7–10]. In part, this renaissance in malaria control has served as a catalyst to revisit the possibility of malaria elimination in many regions and countries [11–14]. A changing malaria landscape requires an accurate spatial and dynamic description of malaria risk that maps the spatial extent and need for control and elimination over the coming decades. Such a map is conspicuous by its absence [15]. Here, we present the first detailed description of the global distribution of P. falciparum risk in 40 y [16,17] by using geopositioned assemblies of national surveillance of malaria risk, medical intelligence, biological models of transmission suitability, and surveys of parasite prevalence. The paper focuses on detailing the data sources and their adaptation for the malaria cartography necessary to guide current disease control, with an emphasis on how we define the spatial limits of stable and unstable P. falciparum risk worldwide. Methods Using Medical Intelligence to Define the Limits of P. falciparum Risk Many countries have information assembled from medical intelligence on the distribution of malaria risk within their national borders. This information is documented primarily in reports from national health information systems that define the annual numbers of confirmed parasite-specific local malaria infections by geographic unit, referred to classically as the annual parasite incidence (API) [18–21]. The API is generated from various combinations of active (fever surveys in communities where every person presenting with a fever is tested for parasite infection) and passive (reports from febrile patients attending the local health services) case detection, and usually expresses the combined results as the number infected per 1,000 people per annum (pa) [18–21]. The precision of these estimates of malaria incidence are highly variable, and with the exception of some countries where case identification is a primary control tool [22], these data cannot be used confidently to derive the public health burden posed by malaria [1,23–26]. They can, however, be a useful indicator of where local parasite species-specific malaria risk is likely or absent, and are particularly plausible when triangulated with other sources of medical intelligence, reported in international travel health guidelines or by national malaria control programmes. Malaria coordinating officers in the regional offices of the World Health Organization (WHO), responsible for the collation of national API data from member countries were contacted to obtain data reported nationally to the highest possible geographic administrative unit level on populations at risk and numbers of confirmed P. falciparum cases, for as many years as were available between 2002 and 2006. Among the countries in the American Regional Office, P. falciparum–specific API (PfAPI) data from national surveillance systems in Brazil, Colombia, Peru, and Honduras were obtained directly from personal communication with malaria specialists. The reported cases of confirmed P. falciparum malaria per 1,000 resident population were computed for each year by administrative level and averaged over the number of reporting years. Summary data were categorized as no autochthonous P. falciparum cases reported, <0.1 autochthonous P. falciparum cases per 1,000 people pa, and ≥0.1 autochthonous P. falciparum cases per 1,000 people pa. The threshold around 0.1 cases per thousand pa was used to provide some indication of unstable conditions versus more stable transmission. This threshold is consistent with previous uses of PfAPI during the Global Malaria Eradication Programme [27] and balanced against the confidence in the precision of reported PfAPI values (Protocol S1). Each PfAPI summary estimate was mapped by matching it to its corresponding first-, second-, or third-level administrative unit in a geographic information system (GIS; ArcView GIS 3.2, ESRI, 1999). Mapped PfAPI data were then compared to other sources of medical intelligence, notably national malaria control presentations at regional malaria meetings obtained from regional WHO malaria coordinators and from Web sites, published sources that described national malaria epidemiology, and international travel and health guidelines [28,29]. These combined approaches were particularly useful to identify mapped descriptions of risk defined at higher spatial resolution than those described by the PfAPI reported across large first-level administrative units. Details of all sources used are provided in Protocol S1. Defining the Biological Limits of P. falciparum Transmission Within the limits of risk described through PfAPI, environmental conditions suitable for transmission vary enormously. These variations can be captured at much higher spatial resolution than it is possible to define by stratifying risk at administrative unit levels. Climate-based determinants of parasite and vector development and survival were developed that impose biological constraints on the geographical limits of P. falciparum transmission. First, we used a combination of the temperature-dependant relationship between P. falciparum sporogony and the longevity of the main dominant vectors to estimate the proportion of vectors surviving parasite development (Protocol S2). Using mean monthly temperature records from a 30-arcsec (∼1 km) spatial resolution climate surface [30], the duration of P. falciparum sporogony was estimated for each synoptic calendar month, and those pixels where the duration of sporogony was 31 d or less were identified. The exception was small areas that potentially support the longer-lived Anopheles sergentii and A. superpictus, where 62 d were considered more appropriate biologically (Protocol S2). This resulted in 12 images with a binary outcome: P. falciparum sporogony could or could not be completed in the month. These images were then combined to identify the number of suitable months for P. falciparum transmission in a synoptic year. All pixels where the duration of sporogony exceeded 1 mo, or 2 mo for areas within the range of A. sergentii and A. superpictus, were masked since it was highly unlikely that transmission would occur. Second, there are areas within several malaria endemic countries where, despite temperature being suitable for sporogony, arid conditions restrict Anopheles development and survival [31]. Limited surface water reduces the availability of water bodies for oviposition. Moreover, low ambient humidity in arid environments further affects egg and adult survival through the process of desiccation [32]. The ability of adult vectors to survive long enough to contribute to parasite transmission and of preadult stages to ensure minimum population abundance is, therefore, dependent on the levels of aridity and species-specific resilience to arid conditions. To capture the influence of aridity on transmission we used the enhanced vegetation index (EVI) derived from the bidirectional reflectance-corrected MODerate-resolution Imaging Spectroradiometer (MODIS) sensor imagery, available at approximately 1-km spatial resolution [33,34] (Protocol S2). Temporal Fourier–processed, monthly EVI images were used to develop 12 monthly surfaces that reclassified EVI ≤ 0.1, assuming this corresponded to a good proxy for arid conditions [35,36]. Pixels were classified as suitable for transmission if their EVI values were higher than 0.1 for at least two consecutive months in an average year. This definition was based on the biological requirement, at optimum temperatures, of at least 12 d to complete vector development from egg to adult [37] and on the assumption that a second month is required for a sufficient vector population to establish and transmit malaria [38]. These reclassified aridity images were then overlaid in a GIS to produce 12 paired images. The 12 pairs were then combined to define pixels where conditions were suitable for transmission. The aridity mask was treated differently from the temperature-limiting mask to allow for the possibility, in arid environments, of highly over-dispersed transmission due to man-made water collection points and nomadic human populations transporting vectors and parasites [39–41]. A more conservative approach was taken, therefore, which down-regulated PfAPI risk by one class. In other words, extremely arid areas defined originally as at stable risk were stepped down to unstable risk and those classified initially as unstable to malaria free. Estimating Populations at P. falciparum Transmission Risk in 2007 The Global Rural Urban Mapping Project alpha version provides gridded population counts and population density estimates for the years 1990, 1995, and 2000, both adjusted and unadjusted to the United Nations' national population estimates [42]. We used the adjusted population counts for the year 2000 and projected them to 2007 by applying national, medium variant, intercensal growth rates by country [43], using methods previously described [44]. This resulted in a contemporary population density surface of approximately 1-km spatial resolution, which was combined with the climate-adjusted PfAPI risk surface to extract population at risk estimates using ArcView GIS 3.2 (ESRI, 1999). Describing Global Patterns of Parasite Prevalence We have described previously the rigorous process of identifying, assembling, and geolocating community-based survey estimates of parasite prevalence undertaken since 1985 [45]. These data were used here to define the ranges of P. falciparum parasite prevalence rates (PfPR) in areas of stable and unstable malaria risk by WHO region. We acknowledge that these geopolitical boundaries do not necessarily conform to ecological or biological spatial representations of malaria [46,47]. They do, however, represent coherent regions of collective planning and cooperation for malaria control. In an attempt to minimize epidemiologically unrealistic divides for summary purposes, we have combined the Southeast Asian (SEARO) and Western Pacific (WPRO), as well as the Eastern Mediterranean (EMRO) and European (EURO) regions. The American WHO region (AMRO) and the African WHO region (AFRO) were considered separately. PfPR estimates were reported in various age groupings. To standardize to a single, representative age range of 2–10 y, we applied an algorithm based on catalytic conversion models first adapted for malaria by Pull and Grab [48] and described in detail elsewhere [49]. The geolocated and age-standardized prevalence data (PfPR2−10) [45] were overlaid on the PfAPI risk surface to extract a corresponding PfAPI value. Results PfAPI Data and Medical Intelligence to Define Spatial Limits of Transmission The PfAPI data identified 87 countries at risk of P. falciparum transmission between 2002 and 2006, which we now consider as P. falciparum endemic countries (PfMEC) in 2007 (Protocol S1). PfAPI data were mapped to first, second, or third administrative level units across 41 PfMECs covering a total of 8,789 unique polygons. These data incorporate complete years between 2002 and 2006, including summaries of three consecutive years for 16 countries, two consecutive years for eight countries, and the most recent complete year for 17 countries (Protocol S1). No information was available for 46 countries; mostly those in Africa. The spatial representation of no risk, unstable (PfAPI < 0.1 per 1,000 people pa), and stable risk (PfAPI ≥ 0.1 per 1,000 people pa) of P. falciparum transmission globally is shown in Figure 1, top panel. Figure 1 P. falciparum Malaria Risk Defined by Annual Parasite Incidence (top), Temperature, and Aridity (bottom) Areas were defined as stable (dark-red areas, where PfAPI ≥ 0.1 per thousand pa), unstable (pink areas, where PfAPI < 0.1 per thousand pa), or no risk (light grey). The few areas for which no PfAPI data could be obtained, mainly found in India, are coloured in dark grey. The borders of the 87 countries defined as P. falciparum endemic are shown. Highland areas where risk was excluded due to temperature appear in light grey. The aridity mask excluded risk in a step-wise fashion, reflected mainly in the larger extents of unstable (pink) areas compared to the top panel, particularly in the Sahel and southwest Asia (southern Iran and Pakistan). Temperature and Aridity Masks to Constrain Limits of Transmission Within the PfAPI limits of stable transmission (PfAPI ≥ 0.1 per 1,000 pa) on the African continent, the areas with no temperature-suitable months for transmission were congruent with the high altitude areas in Ethiopia, Eritrea, western Kenya, eastern Tanzania, Rwanda, Burundi, eastern Democratic Republic of the Congo, the Malagasy highlands, Mount Cameroon, and the eastern highland ranges in Zimbabwe (Figure 1, bottom panel). Outside of Africa, there was a close correspondence between the areas masked by the absence of reported autochthonous cases and areas classified as unsuitable for transmission based on low temperature in Andean and Himalayan areas (Figure 1, bottom panel). The application of the temperature mask provided a finer spatial resolution constraint to PfAPI data, particularly for the island of New Guinea and the highlands neighbouring the city of Sana'a, Yemen. Important reductions in the spatial areas of risk were also evident in some administrative units in Afghanistan, Bhutan, China, India, and Kyrgyzstan. The aridity mask constrained the mapped P. falciparum transmission risk to small pockets in large administrative boundaries from southern areas of Hilmand and Kandahar, in Afghanistan, the municipality of Djibouti, in Djibouti, and the south-eastern provinces of Iran. The risk areas along the Red Sea coast of Saudi Arabia were also reduced further using the aridity mask. Additional areas constrained within their spatial margins to no risk using the aridity mask included administrative units in India (n = 4), Pakistan (n = 9), Peru (n = 3), Kyrgyzstan (n = 2), Tajikistan (n = 1), and the low risk areas of Namibia bordering the Namib desert. Large areas covered by the aridity mask were reduced from stable (PfAPI ≥ 0.1 per 1,000 pa) to unstable risk (PfAPI < 0.1 per 1,000 pa) in the Sahel. The transmission reducing effects of aridity were also evidenced in Djibouti, Eritrea, northwest Kenya, northeast Ethiopia, northern Somalia, central and coastal areas of Yemen, and southern Pakistan. Importantly, these areas retained small pockets of higher, more-suitable transmission conditions, corresponding to river tributaries and irrigated land where higher transmission risk is supported [50]. Populations at Risk Table 1 provides a summary of the spatial extents and the projected 2007 populations at risk (PAR) within areas of assumed unstable (PfAPI < 0.1 per 1,000 pa) and stable P. falciparum transmission (PfAPI ≥ 0.1 per 1,000 pa) globally and by WHO region. Country PAR estimations are also provided (Table S1). We estimate that there are 2.37 billion people at risk of P. falciparum transmission worldwide, 26% located in the AFRO region and 62% in the combined SEARO-WPRO regions (Table 1). The definition of unstable risk outlined here is the predominant feature of exposure to transmission in the EMRO-EURO region (Table 1). Low-risk areas in AFRO were also coincident with arid, low population density areas. Globally, 42% of the population exposed to some risk of P. falciparum was classified as inhabiting areas of unstable transmission; the total population in these areas was 0.98 billion people. Table 1 Area and Population at Risk of P. falciparum Malaria in 2007 Global and Regional Summary of P. falciparum Parasite Prevalence The summary data on age-corrected PfPR are presented without adjustments for biological and climatic covariates, urbanization, congruence with dominant Anopheles vector species, or any sampling issues inherent in an opportunistic sample of this kind. This is the subject of ongoing work. The summarized data, however, do provide important new insights into the ranges of infection prevalence reported between regions of the world within the P. falciparum spatial limits of stable and unstable transmission. A total of 4,278 spatially unique cross-sectional survey estimates of PfPR were assembled as part of the activities of the Malaria Atlas Project (MAP) by 01 September 2007. These included 186 (4.4%) surveys that were not possible to geolocate and are not considered further in the analysis. Of the positioned survey data, 3,700 (90.4%) were derived from individual communities (about 10 km2 or less), 131 from wide areas (more than about 10 km2 and about 25 km2 or less), 145 from small polygons (more than about 25 km2 and about 100 km2 or less), and 116 from large polygons (more than about 100 km2) [45]. A total of 406 surveys were undertaken outside the defined spatial limits of P. falciparum transmission, of which 46 reported presence of P. falciparum infection in the populations surveyed and 360 reported zero prevalence after allowing for a 10-km buffer around the limits. Thus, the overall sensitivity adjusting for plausible positioning errors [51] was 98.5%. There were 611 surveys falling inside the limits that reported zero prevalence. Even using the 10-km buffer the specificity of the limits was low (37.1%). This reflects the difficulties in estimating zero prevalence without large sample sizes [52], as well as the over-dispersed nature of infection risks between communities within small spatial scales [53]. The global diversity of the age-corrected PfPR2–10 estimates within the limits of transmission is shown in Figures 2–5. A total of 253 surveys reported zero prevalence among 2,121 surveys undertaken in AFRO (Figure 2). Outside of Africa, 358 surveys reported zero prevalence among 1,565 surveys undertaken within the defined limits of transmission. Over 92% and 95% of surveys reporting PfPR2–10 ≥ 50% and ≥ 75%, respectively, were located in AFRO and concentrated mostly between 15° latitude north and south, areas inhabited by Anopheles gambiae s.s. [54] (Figure 2). Conversely lower estimates of PfPR2–10 were described among those surveys conducted in areas occupying the A. arabiensis–dominant regions along the Sahel, horn, and southern areas of Africa [54] (Figure 2). In AMRO (Figure 3) and EMRO-EURO (Figure 4), 87% and 65% of surveys reported PfPR2–10 below 10%, respectively, referred to classically as hypoendemic. Over 65% of PfPR2–10 survey estimates in the combined SEARO-WPRO region reported infection prevalence below 10% (Figure 5), including 218 surveys reporting zero prevalence. Figure 2 Community Surveys of P. falciparum Prevalence Conducted between 1985 and 2007 in AFRO Other regions are shown in Figures 3–5. Of the 4,278 surveys reported globally, 4,092 could be geopositioned of which 3,686, shown in these figures, fell within the predicted limits of P. falciparum malaria risk. A total of 406 records, not shown in the figures, were found outside the limits, of which 46 reported presence of P. falciparum. Data shown are age-standardized (PfPR2–10) and represented as a continuum from zero to 100%. Table 2 and Figure 6 present detailed descriptive statistics for these data. Figure 3 Community Surveys of P. falciparum Prevalence Conducted between 1985 and 2007 in AMRO Figure 4 Community Surveys of P. falciparum Prevalence Conducted between 1985 and 2007 in EMRO-EURO Figure 5 Community Surveys of P. falciparum Prevalence Conducted between 1985 and 2007 in SEARO-WPRO Table 2 Summaries of the P. falciparum Parasite Rate Data Reported between 1985 and 2007 and Mapped within the Spatial Limits of P. falciparum Malaria Figure 6 Box and Whisker Plots of PfPR2–10 by Period and WHO Regions Thick black lines are the medians, and the light-blue boxes represent interquartile ranges; whiskers show extreme, non-outlier observations. Empty circles represent mild and/or extreme outliers. Sample sizes correspond to those shown in Table 2. Despite notable gaps in the coverage of PfPR2–10 data in many areas (Figures 2–5), a summary of the ranges of prevalence survey estimates is provided in Table 2 and Figure 6. These data are presented for the whole time period (Figure 6, top panel) and stratified by time (Figure 6, middle and bottom panels). We stress that these data are not spatially congruent and therefore should not be viewed as representing secular changes in PfPR2–10 estimates by WHO region. The data used for the bottom panel of Figure 6 are potentially of greater value, however, when describing the endemicity characteristics of malaria within the spatial limits shown in Figure 1, as they represent the most contemporary summary of malaria endemicity judged by PfPR2–10. Discussion We have triangulated as much information as we could assemble from exhaustive searches to provide an improved evidence-based description of the limits of P. falciparum transmission globally. The spatial referencing of health statistics, medical intelligence, and national expert opinion represents, to our knowledge, the most complete, current framework to understand the global distribution of P. falciparum risk in 2007. The use of plausible biological constraints upon transmission, based on long-term temperature data and remotely sensed correlates of vegetation cover, improved the spatial precision of the limits and categories of risk. We estimate that there were 2.37 billion people at risk of P. falciparum worldwide in 2007, and 40.1 million km2 of the world might be able to support P. falciparum transmission. Assembling geographic information on disease risk is an iterative process, building on new data and identifying gaps in our knowledge. We have presented previously the distribution of P. falciparum using historical descriptions of risk [1,16] and through the reconciliation of information in multiple travel advisories [55,56]. None have been perfect representations of contemporary malaria distributions worldwide, but such work has initiated a dialogue on the importance of providing an evidence base to malaria cartography and in the sharing of this information [15]. We have not considered the spatial distribution of P. vivax in this paper for a number of methodological reasons. First, the accuracy of health reporting systems for P. vivax clinical cases in areas of coincidental P. falciparum risk is notoriously poor [57]. Second, the climatic constraints on parasite–vector survival are less well defined and thus harder to predict using standardized regional-specific vector bionomics [58]. Third, the combined effects of a prolonged liver stage and the consequences upon natural and drug-resistant recrudescence make the interpretation of prevalence data considerably harder for P. vivax compared to P. falciparum [59]. We are acutely aware that the spatial extent and disease burden of P. vivax merits more attention than it has received, but to achieve an informed evidence-based map similar to that of P. falciparum demands a more fundamental construction of the basic biology of transmission and clinical epidemiology before this can be attempted effectively. We have been cautious in the use of the PfAPI data reported at national levels, recognizing the inadequacies and incompleteness of malaria surveillance [1,23–26]. The intention has been to identify administrative reporting areas that had not detected cases of P. falciparum malaria between 2002 and 2006. It was also recognized that there existed a wide range of reported PfAPI estimates, from one case per 100,000 people pa to reports of confirmed cases in almost 50% of the population every year, which presents a problem for the classification of risk. We therefore applied threshold criteria that would distinguish areas of low clinical risk (i.e., those areas reporting few cases and likely to support unstable transmission conditions) from areas with higher reported case incidence and probably more stable in their P. falciparum transmission characteristics. Our use of a distinction between unstable and stable transmission at 0.1 per thousand pa, while conservative is not without precedent. During the era of the Global Malaria Eradication Programme, epidemiologists proposed a variety of criteria to describe malaria risk in concert with preparatory, active, consolidation, and maintenance phases of elimination and ultimate “eradication” [60–63]. Parasite prevalence was the metric of choice for defining baseline endemicity in the preparatory phase and was useful as an indicator of control progress in the attack phase [52,64], until it became impossible to measure with cost-efficient sampling at very low levels of endemicity. At this juncture, it was proposed that malaria risk be measured through incidence metrics such as the PfAPI [65]. We identified very few PfPR surveys (n = 233) undertaken in areas where reported PfAPI was below 0.1 per thousand pa, 70 (30%) of which reported zero prevalence (Figures 2–5); and the median parasite prevalence was 1.4% (Table 2). It seems appropriate, practical, and feasible to consider multiple metrics during the assembly of malaria risk maps, and we have combined two common malariometric measures of risk: the PfAPI and PfPR. The mathematical relationship between these measures and other traditional epidemiological measures, such as the basic reproduction rate of infection and the entomological inoculation rate, is the subject of ongoing research [61]. Stratification of these risk areas by dominant vector species to enable a more informed assessment of the appropriate suites of intervention measures is also being pursued actively [15]. The PfPR data have been assembled from peer-reviewed literature, unpublished ministry of health sources, postgraduate theses and provision of raw data from malaria scientists in all malaria endemic regions [45]. They do not derive from nationally representative, random-sample surveys. Their coverage might, therefore, be subject to bias toward areas thought to be more malarious. The inclusion of 971 geopositioned surveys reporting zero prevalence (including 523 [53.8%] from Africa), however, does not support this view. Future investigation of the ecological and climatic covariates of PfPR2–10 will need to move from the categorical descriptions of over-dispersed endemicity data presented here, to geostatistically robust estimates of risk that are cognisant of the many potential biases in these data across the entire limits of stable transmission shown in Figure 1. We note, however, that as infection prevalence responds to increased intervention coverage and access to effective medicines, the use of traditional biological covariates might prove less effective in predicting the distribution of P. falciparum transmission intensity. Spatial models of PfPR distribution are being developed and tested as part of MAP's ongoing research to more accurately reflect the ranges of malaria transmission intensity within the margins of stable endemicity. Moreover, the PfAPI and PfPR data described in the present paper will change with time, and future data assemblies need to be maintained in a world with a rapidly changing malaria epidemiology. The supporting geostatistical models used to predict the spatial distribution of endemicity must also therefore facilitate rapid updates. The annual revision of the spatial limits of stable and unstable malaria, based upon new medical intelligence, PfAPI summaries, and the increasingly available contemporary PfPR information will iteratively redefine the cartography of malaria and be hosted on the MAP website (http://www.map.ox.ac.uk) as a public domain resource [15]. Assuming some degree of fidelity in the descriptions of unstable malaria used here, we estimate that one quarter (∼26%) of the malaria-endemic areas of the world are exposed to some degree of unstable P. falciparum transmission and home to approximately one (0.98) billion people. Even within the regions with more stable transmission, the available empirical evidence from contemporary PfPR2–10 survey data is that outside of AFRO, the intensity of transmission is best described as hypoendemic [66] (Figure 6). This observation has important implications for how we view malaria control and broader development goals at a global scale over the next decade. The provisional categorical descriptions of global P. falciparum malaria risk are shown in Figure 1 and suggest that, at a global scale, an aggressive approach to P. falciparum elimination might be reconsidered as a more ambitious and achievable objective in many areas. Regional initiatives aimed at elimination have begun [11–14]. In the Americas, elimination is considered in the most recent 5-y regional strategic plan [12]. In the European region, the two PfMECs (Tajikistan and Kyrgyzstan) are targeted for P. falciparum elimination within the next 5 y [11,13]. Detailed plans have been developed in the Eastern Mediterranean region to consider targeted P. falciparum elimination strategies in Iran and Saudi Arabia, while strengthening maintenance phases of elimination in currently P. falciparum–free countries [14]. With the exception of EURO, detailed maps of the spatial extents of risk in these various regions are not available. Where elimination is considered a viable strategy, resource requirements, targets, and maps become a regional and sub-regional public good and are no longer solely national concerns. Saudi Arabia is providing substantial financial support for the elimination of malaria in its neighbour, Yemen [67]. If this plan is successful, the reportedly high rates of population inflow from Somalia [68] will pose a continued concern due to the potential reintroduction of the parasite. This situation further highlights the need for a reproducible and evidence-based global map of malaria risk that is maintained as a dynamic platform to estimate and predict cross-border risk. Maintaining the detail necessary to map the spatial extent of malaria risk is paramount to the future of malaria control outside of Africa over the next 5 y. We would also argue, however, that Africa has been labelled inappropriately as a vast expanse of holoendemic transmission, intractable to control. Less than a third of all surveys retrieved from AFRO (29%) reported parasite prevalence above 50%, and, as has been described, these results followed closely the distribution of A. gambiae s.s. [54]. The conditions of hypoendemic and mesoendemic transmission were common in surveys conducted outside of this belt (which are not subject to the ravages of this most efficient vector) and are likely to benefit from approaches to prevention and control specific to the underlying ecologic and epidemiologic conditions [15,69,70]. The descriptions of transmission intensity are dynamic and the PfPR2–10 estimates in Africa (Figure 2) do not correspond to levels of endemicity described four decades ago [17]. In the AFRO region, there has been a recent expansion of insecticide-treated net coverage and provision of effective medicines. These programmatic successes are showing tangible impacts on mortality [8,9,71] and morbidity [8,9,72], and it would seem entirely plausible that similar effects will be operating at the level of transmission. If Africa is undergoing a malaria epidemiological transition, capturing this dynamic through mapped information on infection prevalence, and planning accordingly, should be high on the control agenda. The current focus of the Roll Back Malaria movement is, appropriately, in Africa, as this continent bears the brunt of malaria morbidity and mortality [73,74] and the descriptions presented here reinforce this view. P. falciparum transmission is a global problem, however, requiring a global strategy with regional targets and approaches tailored to what can be achieved within defined intervention periods [61]. This strategic planning demands an epidemiologically consistent map that is constantly updated. The assembly of risk data presented here represents the first attempt to combine disparate sources of malariometric data that should serve as a dynamic platform to define a global strategy and map its progress over the coming decades. The maps and national levels of population at unstable and stable risk are released in the public domain, with the publication of this paper, to further that global effort (MAP, http://www.map.ox.ac.uk). Supporting Information Protocol S1 Sources and Descriptions of Medical Intelligence Used to Describe the PfAPI (346 KB DOC) Click here for additional data file. Protocol S2 Developing Global Biological Limits for P. falciparum Transmission (1.3 MB DOC) Click here for additional data file. Table S1 National Estimates of Population at Risk of P. falciparum Malaria in 2007 (231 KB DOC) Click here for additional data file.

                Author and article information

                Malar J
                Malaria Journal
                BioMed Central
                22 August 2010
                : 9
                : 240
                [1 ]Swiss Tropical and Public Health Institute, P.O. Box, 4002 Basel, Switzerland
                [2 ]University of Basel, Basel, Switzerland
                [3 ]Department of Ambulatory Care and Community Medicine, Infectious Disease service, University Hospital, Lausanne, Switzerland
                Copyright ©2010 D'Acremont et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                : 11 May 2010
                : 22 August 2010

                Infectious disease & Microbiology
                Infectious disease & Microbiology


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