Volume 18, Number 5—May 2012
A Spatial Analysis of Individual- and Neighborhood-Level Determinants of Malaria Incidence in Adults, Ontario, Canada
Malaria, once endemic in Canada, is now restricted to imported cases. Imported malaria in Canada has not been examined recently in the context of increased international mobility, which may influence incidence of imported and autochthonous cases. Surveillance of imported cases can highlight high-risk populations and help target prevention and control measures. To identify geographic and individual determinants of malaria incidence in Ontario, Canada, we conducted a descriptive spatial analysis. We then compared characteristics of case-patients and controls. Case-patients were significantly more likely to be male and live in low-income neighborhoods that had a higher proportion of residents who had emigrated from malaria-endemic regions. This method’s usefulness in clarifying the local patterns of imported malaria in Ontario shows its potential to help identify areas and populations at highest risk for imported and emerging infectious disease.
Malaria is a parasitic, vector-borne disease that causes ≈1 million deaths each year and substantial global public health costs (1,2). The disease was previously endemic in North America, with transmission in most of the United States and parts of southern Canada (3). The malaria parasite, Plasmodium spp., was introduced into North America during the 16th–17th centuries through the arrival of European colonists and African slaves (3). Malaria was eliminated in North America by the 1950s through several different interventions, including vector control by changes in vector habitat, introduction of new antimalarial medications (such as quinine) for improved treatment, and decreased contact between humans and mosquitoes, in part because of changes in housing conditions (3).
Cases of locally acquired, mosquito-transmitted (autochthonous) malaria still occur in the United States, particularly in the Northeast. Most recently, reported autochthonous cases in the United States have occurred in suburban or urban areas (3). Although no confirmed cases of autochthonous malaria have been recorded in Canada in recent years, ≈400 cases of imported malaria are identified in Canada each year, a significantly higher prevalence than in the United States (4,5). Increased international travel and immigration have the potential to change the probability of autochthonous transmission in Canada and the United States, where competent vectors and suitable regional climates already exist (3,6).
Malaria incidence is affected by socioeconomic inequality and human movement (7). Malaria transmission in Canada was associated historically with socioeconomic inequality and migration; in particular, malaria transmission surged among migrant workers on the Rideau Canal in Ontario during 1826–1832 (8). Regional and international travel and migration patterns have also been implicated in malaria incidence across the globe, including reports of so-called airport malaria, refugee outbreaks, and cases in migrant populations (9–12). Rates of transmission in highly traveled areas have been found to affect rates of imported malaria cases (13). Length and type of travel and travel behavior are associated with risk for malaria transmission (14–16). At particularly high risk of acquiring malaria and importing it to their country of residence are travelers who visit friends and relatives (VFRs) in countries where malaria is endemic (16–21). Research has recently shown that VFRs are also at risk for multidrug-resistant malaria because of the inappropriate use of antimalarial drugs available over the counter in malaria-endemic countries (22).
Emerging and reemerging disease risk interacts with socioeconomic vulnerability to determine the populations at highest risk for infection and those most likely to import pathogens into the country. In the context of changing patterns in international travel, immigration, and global disease spread, understanding the socioeconomic determinants of existing disease risks is prudent.
In this study, we first conducted a descriptive spatial analysis to identify the geographic and individual determinants of malaria incidence in Ontario, Canada. We then tested the hypothesis that malaria case-patients do not differ significantly from controls in terms of their individual and geographic characteristics.
The study location was Ontario, Canada. Data on positive and negative malaria tests conducted in Ontario were used to assign persons to 1 of 2 groups: case-patients (persons who tested positive for Plasmodium spp. by standard microscopy using Giemsa stain) and controls (persons who tested negative for Plasmodium spp.). First, descriptive statistics, mapping, and space–time cluster analysis were used to examine the spatial patterns of malaria incidence in Ontario and associated individual and geographic risk factors. Second, logistic regression was used to test the hypothesis that malaria case-patients and controls did not differ significantly in their individual and geographic determinants.
Toronto, the largest city in the province and country, experiences a high volume of international travel, with 3.5 million passengers arriving at Toronto’s Pearson International Airport in 2007 (23). Toronto is a major immigration destination, globally and within Canada (24). One fifth of Canadians were born outside of Canada, and in the census metropolitan area of Toronto, the proportion is more than twice the national rate, with 45.7% of the population born outside Canada (25). Locations where immigrants choose to settle within the greater Toronto area (GTA) show the strongest growth of cities outside the city of Toronto (25).
Data on malaria cases were obtained from the Malaria Reference Laboratory, Public Health Laboratories (PHL), Ontario Agency for Health Protection and Promotion (Toronto). These data included results of malaria tests conducted in the 12-month period from May 2008 through April 2009, and they identified patients as either positive (case-patients) or negative (controls) by reference thick and thin blood films. PHL receives blood specimens from other laboratories throughout the province and from hospitals and clinics. The data include the results of any test conducted at PHL for malaria diagnosis, confirmation, or malaria parasite speciation. PHL conducts ≈75% of the malaria testing for Ontario. An ethics certificate was obtained from the McGill University Research Ethics Board, and the de-identified data were stored in a confidential and secure manner.
The dataset from the Ontario Agency for Health Protection and Promotion contained 990 specimens. A specimen represented a blood sample that was tested for malaria. Specimens from persons for whom home postal code information was not available and those for whom home addresses were outside of Ontario were excluded, leaving 770 specimens. Data were converted from specimens to observations (persons) to avoid duplication in the dataset because some persons had results for multiple tests. Conversion from specimen to person was based on home postal code, birth date, and sex. This conversion resulted in 562 observations (persons). Malaria can be more severe in children, and symptoms in children are similar to those of other diseases (26,27); these facts may prompt a higher index of suspicion and different patterns of diagnostic testing for children and adults. The dataset included many negative test results for children, and combined with a low number of child case-patients, stratified analysis of malaria in children was not feasible; persons <18 years of age were thus excluded.
The final dataset included 354 observations of individual adults who tested positive or negative for Plasmodium spp. These persons were categorized as case-patients (n = 94) and controls (n = 260). A travel history was reported for 151 of these persons. Data on immigration status were not available. Such information would have been a valuable component of the analysis.
Census data describing population size, residents’ immigration status, and median household income were compiled for all Ontario census tracts. Census tracts were used as a proxy for neighborhoods (28), and population density was calculated for each area. Proportion of residents who are immigrants from malaria-endemic countries for each neighborhood was calculated by dividing the number of respondents reporting immigration from an area where malaria is endemic (Southeast Asia, South Asia, East Africa, Central Africa, West Africa) by the number of census respondents. Geographic boundaries of both census tracts (population size ≈2,000–8,000 persons) and dissemination areas (population size ≈400–700 persons) were used for mapping, area calculation, and spatial reference.
All cartography was carried out by using ArcGIS version 9.3 software (ESRI, Redlands, CA, USA). Several key variables were used in the descriptive mapping of malaria case-patients: case-control status, parasite species, and age and sex of participant. For case–control data, observations were placed at the geographic center of the postal code recorded as the home address. Six-digit postal codes were used for all observations retained in the dataset, and those without appropriate postal codes were removed. Placing the observation at the geographic center of the postal code ensured accurate representation of location while maintaining participant privacy. Week codes (a numerical designation by the US Centers for Disease Control and Prevention for each week of the year, 1–52) were assigned to observations in the dataset to facilitate temporal graphing. Timeline graphs were created for evaluating the seasonal and temporal distribution of malaria observations. Incidents were stratified by parasite species.
Travel history was categorized by using the regional groupings provided in the 2006 Canadian census. Univariate tests and graphing were performed for the variables of travel, neighborhood immigration characteristics, case or control status, and parasite species. For travel and immigration analysis, observations that noted a parasite species other than P. falciparum and P. vivax (n = 9) were excluded.
Because of a high concentration of cases in the GTA, a subset of the malaria case dataset was created, with only observations in the GTA. For purposes of analysis, Canadian regional municipalities were used to delimit the dataset, and the GTA subset thus included Toronto, Halton, Peel, York, and Durham municipalities. Cluster analysis was performed on the GTA subset to assess the significance of any potential spatial clustering. A space–time scan statistic (29) was performed on case–control status and parasite species by using SaTScan version 8.1.1 software (M. Kulldorff, Boston, MA, USA). The scan statistic compares observed case counts within a range of alternate scan windows, in both space and time, to expected case counts derived from Monte Carlo random simulation. The scan window with the maximum likelihood ratio statistic is identified and compared with the null hypothesis of no significant clustering. Analyses assumed a binomial distribution in which the 2 possible outcomes were to be either a case-patient or a control. The maximum cluster size was 50%, so that no more than 50% of the observations could be classified as being part of the detected cluster.
The key variables in the logistic regression model were population density, median household income, proportion of residents who are immigrants from malaria-endemic countries, and sex. Predictor variables were chosen on the basis of individual and ecologic risk factors for travel-related disease and infectious disease. The outcome variable was case–control status. All statistical analyses were assessed for significance at the 95% CI. Univariate tests were conducted to assess the relationship between the individual predictor variables and case–control status. One observation was removed because no census data were available for the postal code geographic center. All variables were checked for co-linearity and normality, and the model was checked for notable interaction, outliers, confounding, predictive ability and accuracy, leverage, and goodness-of-fit. The best-fit model was chosen on the basis of the inclusion of the key variables related to imported malaria cases, given data availability and the results of the tests for goodness-of-fit and other postestimation procedures. The best-fit model was interpreted by using quartile values of each of the predictor variables, comparing the first and fourth quartiles. All statistical analyses were performed by using Stata version 11 software (StataCorp, College Station, TX, USA).
The general distributions of sex, age, and relative parasite proportions did not differ greatly between case-patients (n = 94) and controls (n = 260) for all of Ontario and the GTA subset (Table 1). The spatial distribution of the case-patients and controls was consistent with Ontario’s settlement patterns, with most of the observations located in southern Ontario and the GTA (Figure 1). The downtown core of Toronto had a large concentration of controls, whereas more case-patients lived in suburban areas.
Significant clustering of case-patients occurred in suburban Toronto during the summer months (Figure 1). A significant space–time cluster was identified during May 15, 2008–November 6, 2008, in the region northwest of Toronto near Brampton (p<0.01; relative risk 3.54). This area is near the main international airport in the GTA. In this area during the summer months, tested persons were 3.5× more likely to receive a diagnosis of malaria than were persons outside of this area and period. No significant clustering of individual parasite species (P. falciparum or P. vivax) was identified.
Cases were not significantly more likely to occur in the summer months (June–September) than in the nonsummer months for the GTA and for all of Ontario (χ2; p = 0.14 and p = 0.11, respectively). This result is consistent with that of the space–time cluster analysis, which found that the significant space–time cluster extended through summer into autumn. Visual observation of monthly incidence, however, did not indicate any strong or clear trends, possibly because of the influence of low observation numbers, and incidence and seasonality in malaria-endemic countries from which the disease is imported (Figure 2).
Population density was highly variable in the study area, with more densely populated areas located near the downtown core of the GTA. Median household income, in contrast, exhibited negligible clustering except for low-income suburbs east and west of the downtown core. The proportion of residents who were immigrants from malaria-endemic regions was highest in the suburban areas to the east and west of Toronto (Figure 3). More than 94% of case-patients for whom travel history was recorded indicated recent travel to Africa or Asia (Figure 4), with travel to Africa reported most frequently. These results are consistent with known spatial ranges of malaria-endemic areas (30).
Case-patients were significantly more likely than controls to be male and live in low-income neighborhoods with a higher proportion of residents who immigrated from malaria-endemic regions (Table 2). The proportion of residents who were immigrants from malaria-endemic countries was, for example, >2× as high in neighborhoods with case-patients than in neighborhoods where controls were identified. The average income of case-patient neighborhoods was ≈$28,000, compared with ≈$31,000 in control neighborhoods (Student t test, p = 0.04). Case-patients with a travel history (n = 47) were more likely to report having traveled to Africa and to be living in a neighborhood with a higher proportion of residents who are immigrants from malaria-endemic countries than controls with a travel history (Table 3).
The regression results are consistent with univariate analyses: case-patients were more likely to be male (odds ratio [OR] 2.24, 95% CI 1.24–4.05) and live in neighborhoods with high levels of immigration from malaria-endemic countries (OR 1.09, 95% CI 1.06–1.12) (Table 4). Population density was a weak predictor, but was retained in the model to account for potential confounding with proportion of residents who are immigrants from malaria-endemic regions of Africa. This variable had a wide range (0%–58%) and showed the strongest effect on case status: for every 1% increase in the proportion of residents who are immigrants from malaria-endemic regions, the odds of being a case-patient increased by 7%. The odds of being a case-patient were >17× higher in neighborhoods in the top quartile of proportion of residents who are immigrants from malaria-endemic areas than in the neighborhoods in the lowest quartile. There were slight negative effects from median household income and population density. For every 1 unit increase in either, the odds of being a case-patient decreased by 1%.
The pseudo R2 of the model was 0.19, with a predictive accuracy of 70% correctly classified by using a cutoff of 0.25 (67% sensitivity, 71% specificity). The model fit the data well (Hosmer-Lemeshow test, p = 0.76), and leverage values did not indicate any outliers that required removal. Several high positive residuals were found, because of the low sensitivity of the model that used a default cutoff (0.5). This low sensitivity reflects the limited number of variables available for analysis. The model was developed, however, for explanatory rather than predictive purposes; low sensitivity reflects the small number of covariates and use of neighborhood-level variables.
The distribution of parasite species infection in case-patients reflects the patterning of global malaria; P. vivax cases are associated with travel to or immigration from Asia, and P. falciparum cases are associated with travel to Africa (Table 3). Globally, a significant spatial patterning of parasite species exists, with P. falciparum found predominantly in Africa and P. vivax found predominantly in Asia (30). Case-patients infected with P. falciparum, for example, were significantly more likely to report recent travel to Africa than case-patients infected with P. vivax (Fisher exact test, p<0.01). Conversely, case-patients infected with P. vivax were more likely to report travel to malaria-endemic regions of Asia (Fisher exact test, p<0.01). Case-patients with P. vivax lived in neighborhoods with a significantly higher proportion of residents who are immigrants from malaria-endemic regions (Mann-Whitney, p<0.01). In contrast, however, P. falciparum case-patients did not necessarily live in neighborhoods with a high proportion of residents who are immigrants from malaria-endemic regions of Africa (Mann-Whitney, p = 0.33). This finding may be due to the much lower overall level of immigration from Africa.
Malaria case-patients in Ontario were found predominantly in the GTA, with more case-patients in suburban areas outside the city center. Malaria case-patients were more likely to live in neighborhoods with a high proportion of residents who emigrated from malaria-endemic areas. Case-patients were more likely than controls to report travel to areas with endemic malaria, and there was concordance between the parasite species and the region of travel. The association between parasite species and geography held when neighborhood immigration was examined as well—cases of P. vivax malaria corresponded with immigration from malaria-endemic areas of Asia, and cases of P. falciparum malaria were found in areas with immigration from malaria-endemic areas of Africa.
Case-patients were more likely to be male than female. This finding is consistent with the literature on sex and travel-associated diseases, which finds that men are more likely than women to have vector-borne diseases, including malaria (31). Whether this finding is due to a biologic predisposition or to behavioral differences associated with increased transmission risk is not known (31). Whether potential differences in patterns of health care use between men and women could have affected the results in this study also is not known. Further research into how men and women seek pretravel and posttravel medical care in Ontario would improve the understanding of this result.
When assessing imported malaria cases, underreporting is a substantial issue. In Ontario, underreporting of malaria is likely to range from 10% to 40% (5,32). In Ontario, 226 malaria cases were documented by laboratories in 1998 (32). However, in that same year, only 160 cases in Ontario were reported to Health Canada (32). No recent published or quantified estimates of actual incidence are available, and the true level of current underreporting of malaria in Ontario and Canada more generally remains unclear. The data used in the study are strengthened by the inclusion of negative and positive malaria test results. The use of controls enables the factors that correlate with malaria cases to be better understood, unbiased by underlying patterns of malaria testing.
The odds of becoming infected and importing malaria to Canada were >17× higher for residents of neighborhoods with high immigration from malaria-endemic areas than those with low immigration from malaria-endemic countries. These results, combined with the geographic findings of the cluster analysis, are supported by census data on immigration. Brampton (the location of the significant space–time cluster of malaria cases), Markham, and Ajax all showed a significant increase in the proportion of residents born outside Canada in the 2006 census (25). As immigration to the neighborhoods in the suburbs of the GTA grows, more imported malaria cases could result. These results have implications for potential preventative measures that could be taken before persons travel abroad. The use of cluster detection methods has been proposed in other areas to target prevention methods (33,34). Targeted prevention could focus on hospitals and clinics found in the cluster area and in regions with a high proportion of residents who are immigrants from malaria-endemic areas, with the goal of implementing targeted travel medicine screenings and education regarding malaria prophylaxis.
Predeparture travel medicine services are not covered under Ontario’s provincial insurance plan (35). However, the use of travel clinics is not associated with income in Canada (36). As a high-risk group, VFRs are characterized by differing preventive care choices and lower use of pretravel medical services (37). In Canada, 1 study found that VFRs consulted family practitioners more often than travel clinics and that the family practitioners were more likely to prescribe inappropriate chemoprophylaxis (38). Another reason for the increased risk for imported malaria among VFRs could be differing perceptions of the risk for malaria, leading to different behavior in malaria-endemic areas (16,21,39). The recent growth of immigrants in Brampton and related Toronto suburbs may merit targeted programming by physicians and public health agencies, including translation of public health prevention materials (25).
Imported malaria in Canada is of public health significance given current, and likely substantially underestimated, cases of imported disease in Canada. Our characterization of imported malaria cases in Ontario highlights increased risk for infection in immigrant and low-income neighborhoods, with associations between immigration from countries where malaria transmission and particular pathogen types are endemic. These results suggest a pattern of inequality in tropical health outcomes in Ontario with implications for prevention and control of current incidence.
Imported malaria cases represent the potential for geographic emergence of a range of travel-associated diseases. The current landscape of emerging infectious diseases demands that we improve our understanding of the mechanisms by which diseases are imported and the characteristics of neighborhoods and populations at highest risk. The results of this study point to potential individual- and neighborhood-level risk factors that might be relevant to emerging infectious diseases more generally. As new infectious diseases emerge, identifying the processes of emergence and the areas and persons at greatest risk is critical. An analysis of the local patterns of imported malaria in Ontario can help the public health community better understand the ways in which global travel and immigration can affect the spatial distribution of other travel-related diseases.
Ms Eckhardt completed this study at McGill University in Montreal. She is currently affiliated with the Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto. Her research interests include the spatial epidemiology of infectious diseases, social determinants of infectious diseases, and international infectious disease epidemics.
- World Health Organization. Malaria. Fact sheet no. 94 [cited 2010 May 18]. http://www.who.int/mediacentre/factsheets/fs094/en/index.html
- Suh KN, Kain KC, Keystone JS. Malaria. CMAJ. 2004;170:1693–702.
- Zucker JR. Changing patterns of autochthonous malaria transmission in the United States: a review of recent outbreaks. Emerg Infect Dis. 1996;2:37–43.
- Public Health Agency of Canada. Frequently asked questions: malaria [cited 2010 Feb 8]. http://www.phac-aspc.gc.ca/media/advisories_avis/mal_faq-eng.php
- Kain KC, Harrington MA, Tennyson S, Keystone JS. Imported malaria: prospective analysis of problems in diagnosis and management. Clin Infect Dis. 1998;27:142–9.
- Berrang-Ford L, MacLean JD, Gyorkos TW, Ford JD, Ogden NH. Climate change and malaria in Canada: a systems approach. Interdiscip Perspect Infect Dis. 2009;2009:385487.
- Martens P, Hall L. Malaria on the move: human population movement and malaria transmission. Emerg Infect Dis. 2000;6:103–9.
- MacLean JD, Ward BJ. The return of swamp fever: malaria in Canadians. CMAJ. 1999;160:211–2.
- Rodger AJ, Cooke GS, Ord R, Sutherland CJ, Pasvol G. Cluster of falciparum malaria cases in UK airport. Emerg Infect Dis. 2008;14:1284–6.
- Osorio L, Todd J, Pearce R, Bradley DJ. The role of imported cases in the epidemiology of urban Plasmodium falciparum malaria in Quibdó, Colombia. Trop Med Int Health. 2007;12:331–41.
- Faulde MK, Hoffmann R, Fazilat KM, Hoerauf A. Malaria reemergence in northern Afghanistan. Emerg Infect Dis. 2007;13:1402–4.
- Pitt S, Pearcy BE, Stevens RH, Sharipov A, Satarov K, Banatvala N. War in Tajikistan and re-emergence of Plasmodium falciparum. Lancet. 1998;352:1279.
- Behrens RH, Carroll B, Smith V, Alexander N. Declining incidence of malaria imported into the UK from West Africa. Malar J. 2008;7:235.
- Provost S, Gagnon S, Lonergan G, Bui Y, Labbé A. Hepatitis A, typhoid and malaria among travelers—surveillance data from Québec (Canada). J Travel Med. 2006;13:219–26.
- Chen LH, Keystone JS. New strategies for the prevention of malaria in travelers. Infect Dis Clin North Am. 2005;19:185–210.
- Pavli A, Maltezou HC. Malaria and travellers visiting friends and relatives. Travel Med Infect Dis. 2010;8:161–8.
- McCarthy M. Should visits to relatives carry a health warning? Lancet. 2001;357:862.
- Millet JP, Garcia de Olalla P, Carrillo-Santisteve P, Gascón J, Treviño B, Muñoz J, Imported malaria in a cosmopolitan European city: a mirror image of the world epidemiological situation. Malar J. 2008;7:56.
- Smith AD, Bradley DJ, Smith V, Blaze M, Behrens RH, Chiodini PL, Imported malaria and high risk groups: observational study using UK surveillance data 1987–2006. BMJ. 2008;337:a120.
- Mathai S, Bishburg E, Slim J, Nalmas S. Severe malaria in immigrant population: a retrospective review. J Immigr Minor Health. 2010;12:921–4.
- Schilthuis HJ, Goossens I, Ligthelm RJ, De Vlas SJ, Varkevisser C, Richardus JH. Factors determining use of pre-travel preventive health services by West African immigrants in the Netherlands. Trop Med Int Health. 2007;12:990–8.
- Shahinas D, Lau R, Khairnar K, Hancock D, Pillai DR. Artesunate misuse and Plasmodium falciparum malaria in traveler returning from Africa. Emerg Infect Dis. 2010;16:1608–10.
- Khan K, Arino J, Calderon F, Chan A, Gardam M, Heidebrecht C, The BIO.DIASPORA Project: an analysis of Canada’s vulnerability to emerging infectious disease threats via the Global Airline Transportation Network. A report released by St Michael’s Hospital. Toronto (Canada): St. Michael’s Hospital; 2009. p. 1–122 [cited 2012 Mar 13]. http://www2.biodiaspora.com/low_res.pdf
- Benton-Short L, Price MD, Friedman S. Globalization from below: the ranking of global immigrant cities. Int J Urban Reg Res. 2005;29:945–59.
- Chui T, Tran K, Maheux H. Immigration in Canada: a portrait of the foreign-born population, 2006 Census. Statistics Canada. 2007. Catalogue no. 97–557:1–37.
- Stauffer W, Fischer PR. Diagnosis and treatment of malaria in children. Clin Infect Dis. 2003;37:1340–8.
- Kuhn SM, McCarthy AE. Paediatric malaria: what do paediatricians need to know? Paediatr Child Health (Oxford). 2006;11:349–54.
- Ross NA, Tremblay S, Graham K. Neighbourhood influences on health in Montréal, Canada. Soc Sci Med. 2004;59:1485–94.
- Kulldorff M, Athas WF, Feuer EJ, Miller BA, Key CR. Evaluating cluster alarms: a space–time scan statistic and brain cancer in Los Alamos, New Mexico. Am J Public Health. 1998;88:1377–80.
- Griffith KS, Lewis LS, Mali S, Parise ME. Treatment of malaria in the United States: a systematic review. JAMA. 2007;297:2264–77.
- Schlagenhauf P, Chen LH, Wilson ME, Freedman DO, Tcheng D, Schwartz E, Sex and gender differences in travel-associated disease. Clin Infect Dis. 2010;50:826–32.
- Watkins K, McCarthy AE, Molnar-Szakacs H, Kwak EJ, Bodie-Collins M. A survey of the accuracy of malaria reporting by the laboratories in Ontario and British Columbia. Can Commun Dis Rep. 2003;29:121–5.
- Hickey PW, Cape KE, Masuoka P, Campos JM, Pastor W, Wong EC, Local, regional, and national assessment of pediatric malaria in the United States. J Travel Med. 2011;18:153–60.
- Coleman M, Coleman M, Mabuza AM, Kok G, Coetzee M, Durrheim DN. Using the SaTScan method to detect local malaria clusters for guiding malaria control programmes. Malar J. 2009;8:68.
- Ontario Ministry of Health and Long-Term Care. Fact sheet: travel medicine services. 1998 [cited 2012 Mar 13]. http://www.health.gov.on.ca/english/providers/program/ohip/bulletins/4000/bul4317b.html
- Duval B, De Serre G, Shadmani R, Boulianne N, Pohani G, Naus M, A population-based comparison between travelers who consulted travel clinics and those who did not. J Travel Med. 2003;10:4–10.
- Baggett HC, Graham S, Kozarsky PE, Gallagher N, Blumensaadt S, Bateman J, Pretravel health preparation among US residents traveling to India to VFRs: importance of ethnicity in defining VFRs. J Travel Med. 2009;16:112–8.
- dos Santos CC, Anvar A, Keystone JS, Kain KC. Survey of use of malaria prevention measures by Canadians visiting India. CMAJ. 1999;160:195–200.
- Pistone T, Guibert P, Gay F, Malvy D, Ezzedine K, Receveur MC, Malaria risk perception, knowledge and prophylaxis practices among travellers of African ethnicity living in Paris and visiting their country of origin in sub-Saharan Africa. Trans R Soc Trop Med Hyg. 2007;101:990–5.
Suggested citation for this article: Eckhardt R, Berrang-Ford L, Ross NA, Pillai DR, Buckeridge DL. A spatial analysis of individual- and neighborhood-level determinants of malaria incidence in adults, Ontario, Canada. Emerg Infect Dis [serial on the Internet]. 2012 May [date cited]. http://dx.doi.org/10.3201/eid1805.110602
1Current affiliation: University of Calgary, Calgary, Alberta, Canada.