Longitudinal study of urban malaria in a cohort of Ugandan children: description of study site, census and recruitment
© Davis et al; licensee BioMed Central Ltd. 2006
Received: 22 December 2005
Accepted: 21 March 2006
Published: 21 March 2006
Studies of malaria in well-defined cohorts offer important data about the epidemiology of this complex disease, but few have been done in urban African populations. To generate a sampling frame for a longitudinal study of malaria incidence and treatment in Kampala, Uganda, a census, mapping and survey project was conducted.
All households in a geographically defined area were enumerated and mapped. Probability sampling was used to recruit a representative sample of children and collect baseline descriptive data for future longitudinal studies.
16,172 residents living in 4931 households in a densely-populated community (18,824 persons/km2) were enumerated. A total of 582 households were approached with at least one child less than 10 years of age in order to recruit 601 children living in 322 households. At enrollment, 19% were parasitaemic, 24% were anaemic, 43% used bednets, and 6% used insecticide-treated nets. Low G6PD activity (OR = 0.33, P = 0.009) and bednet use (OR = 0.64, P = 0.045) were associated with a decreased risk of parasitaemia. Increasing age (OR = 0.62 for each year, P < 0.001) and bednet use (OR = 0.58, P = 0.02) were associated with a decreased risk of anaemia
Detailed surveys of target populations in urban Africa can provide valuable descriptive data and provide a sampling frame for recruitment of representative cohorts for longitudinal studies. Plans to use a multi-disciplinary approach to improve the understanding of the distribution and determinants of malaria incidence and response to therapy in this population are discussed.
Malaria remains one of the most serious global health problems. There are an estimated one million deaths each year, with nearly 75% occurring in children living in sub-Saharan Africa . Malaria control in resource poor countries has been severely affected by growing resistance to commonly used anti-malarial drugs and low utilization of preventative measures. New tools, such as highly effective artemisinin-based combination-therapy (ACT) and long-acting insecticide-treated nets (ITNs), offer great hope for Africa [2, 3]. However, a better understanding of the epidemiology of malaria is needed to maximize the impact of these interventions.
Complex interactions between the host, parasite, and mosquito vector leads to wide variability in the risk of malaria and its clinical manifestations, ranging from asymptomatic parasitaemia to severe disease . In highly endemic areas, malaria can cause repeated episodes of disease, especially in less immune younger children. This can lead to both short-term health impacts, such as response to antimalarial therapy, and long-term impacts, such as chronic anaemia and the impairment of cognitive development [5, 6]. The burden of malaria can best be assessed using longitudinal studies with extended follow-up and comprehensive evaluation of outcomes. These studies also offer the opportunity to use a multi-disciplinary approach to explore these complex interactions . Well-defined cohorts from the Gambia, Senegal, Kenya, Tanzania, and Mozambique have been instrumental in characterizing the epidemiology of malaria, exploring the acquisition of immunity, and demonstrating the effectiveness of control interventions such as insecticide-treated bednets, intermittent preventative treatment and vaccines [6, 8–11].
Longitudinal studies of malaria have typically been conducted in rural communities with stable populations and relatively homogeneous transmission intensities and age-specific disease risk. However, sub-Saharan Africa currently has the highest rates of urbanization in the developing world . These rapidly growing low-income urban communities differ from rural populations demographically, in socio-economic and cultural composition, and in access to treatment . Urban malaria is usually defined by relatively low transmission intensity (entomologic inoculation rates less than 5 per person per year) with focal larval breeding sites, reduced mosquito dispersal and variable parasite prevalence rates . A number of studies have demonstrated in densely-populated cities that malaria transmission, parasite prevalence, and malaria incidence may be centered in "micro-environments" [15–17]. Urban areas provide a unique opportunity for malaria control given existing infrastructure, technologic capabilities and greater access to high quality health services [18, 19]. Quantitative assessment of the malaria burden in urban areas can help to specifically target integrated and cost-effective strategies to improve control and treatment .
A longitudinal cohort study in 300 children aged 6 months to 5 years followed for 1 year was previously completed in Kampala, Uganda. Malaria was common in this cohort, with over two treatments per person year in children under the age of five years. This study provided valuable data on malaria incidence and response to therapy, but was limited by a relatively small sample size and duration of follow-up, and the use of convenience sampling, which limited the ability to generalize results . In July 2004, a second longitudinal cohort study designed to enroll, by probability sampling, 600 children between one and 10 years of age from a geographically defined urban slum of Kampala was initiated. Described below are the methods used to enroll this cohort and characterize the study area, census population and study participants.
Description of study site
Kampala is the capital of Uganda with an estimated 1.2 million persons living in 306,000 households according to a 2002 national census. Malaria is considered meso-endemic in this region, occurring throughout the year with peaks during rainy seasons from March-May and September-November.
The study was conducted in the Mulago III parish, which is a typical urban slum located near our study clinic at Mulago Hospital, Uganda's main tertiary referral center. The area is primarily residential, characterized by high population density with low-income single- or two-roomed housing units. The local economy is primarily dependent on petty commercial activities and small-scale farming. The parish has a large swamp area with poor drainage and frequent flooding during the rainy seasons. The principal mosquito vector is Anopheles gambiae sensu stricto. A study conducted in an adjacent parish showed 0.1 to 2.9 A. gambiae (11% infective) per house .
Census and demographic survey
The goal was to recruit a representative cohort of 600 children aged 1–10 years to participate in a three-year longitudinal study to measure malaria incidence and compare the efficacy of three different combination therapies. To generate a sampling frame of households with appropriate aged children for recruitment and gather basic demographic information about the target population, a census and brief survey was conducted from July to October 2004. Prior to the start of the study, investigators met with elected government representatives to inform them of the census project and explain the methodology.
Over a four month period, teams of three study personnel systematically covered the entire area of Mulago III parish on foot to identify and enumerate all households. The households were without addresses and scattered along unnamed dirt roads and foot paths. A household was defined as any single permanent or semi-permanent structure acting as the primary residence for a person or group of people. Households were assigned sequential unique numbers, written on a visible label fixed above the doorway, and residents were given a household identification card. After enumeration, study personnel asked an adult resident (18 years of age or older) from each household for verbal consent to participate in a brief demographic survey. Using a standardized questionnaire, information was gathered on households, including construction materials and number of rooms, and the age, gender and bednet practices of each resident. A resident of a household was defined as a person who intended to sleep primarily at that location for the subsequent 6 months . If no adult resident was available, households were revisited up to four times to complete the survey. The house was considered vacant if no residents were present at the household after four visits.
Mapping the study area
To create a map of households and other points of interest, Mulago III Parish was charted using Pathfinder Pocket Global Positioning System (GPS) Receivers (Trimble Navigation Ltd., Sunnyvale, CA, USA) equipped with TerraSync 2.40 software (Trimble Navigation Ltd., Sunnyvale, CA, USA) connected to handheld personal digital assistants (PDA). A minimum of 12 satellite readings, with an accuracy goal of ~1 m, were taken from the door of each household. These values were average to obtain the final GPS reading (Easting, Northing, and Altitude) for each household in UTM units. Similar readings were taken for the boundaries of the parish and potential mosquito breeding sites such as swamps, cement drains, water channels, springs, closed water taps, and wells. A swamp was defined as a wet marsh-like field with papyrus plants. Large drains and water channels were defined as >1 meter wide. A protected spring was defined as a water source with a continuous flow of water through a pipe from a sheltered cement access point. A natural spring was defined as continuous flow of water from soil, rock, or pool. Closed water taps were defined as outdoor closed faucets with or without hose attachments, and wells were defined as large volume water storage containers. Additional readings were recorded for health care facilities (drug shops, pharmacies, public and private clinics, and hospitals) and other points of interest (schools, abattoirs). GPS data were transferred from the handheld PDA devices and synchronized with a Microsoft Access database using GPS Pathfinder Office version 2.90 (Trimble Navigation Ltd., Sunnyvale, CA, USA). Arc View version 3.3 (ESRI, Buckinghamshire, UK) was used to analyse geographical data and create a detailed map of the study area.
Recruitment of the cohort
To recruit a representative cohort of children between 1–10 years of age for participation in the longitudinal study, probability sampling at the level of the household was used. Household level recruitment was chosen to meet the practical objective of enrolling all eligible children from each household and because residents, but not houses, may change between the census and recruitment periods. From a database of all households enumerated in the census, a random list of households with at least one child less than 10 years of age was generated. From November 2004 to April 2005, experienced home visitors approached households for recruitment sequentially from the randomized list, using handheld GPS receivers to locate households by previously recorded coordinates. Interviews were conducted to confirm that households had at least one child age 1 to 10 years. A brief description of the study was provided in the appropriate language to parents and/or guardians. For parent/guardian(s) interested in the study, an appointment was made for a screening interview at our study clinic. Residents not at home during the initial visit were revisited up to three times over the next six weeks to assess interest in the study.
Screening and enrollment
Interested households were screened sequentially until 601 children were enrolled. All eligible children from each household screened were enrolled. Initial assessment of eligibility was conducted by study physicians for the following selection criteria; 1) age one to 10 years; 2) agreement to come to study clinic for any febrile episode or illness; 3) agreement to avoid medications administered outside the study; 4) agreement to remain in Kampala; 5) absence of known chronic disease or history of side effects to the study medications, and 6) written informed consent provided by parent or guardian. Children who passed initial screening were assigned study numbers and underwent a history and physical examination including temperature, height and weight. Children with weight < 10 kg, or severe malnutrition, as defined by weight-for-height or height-for-age Z-score < -3, were excluded. Blood was collected by venipuncture for thick blood smear, complete blood count, creatinine, alanine aminotransferase, bilirubin, haemoglobin electrophoresis, glucose-6-phosphate dehydrogenase (G6PD) activity, and storage for future molecular studies. Children returned to review results of screening labs, generally within 72 hours. Children who were homozygous for haemoglobin SS or had life-threatening screening laboratory abnormalities (based on toxicity grading scales developed by the World Health Organization and the National Institutes of Health) were excluded. Children with symptomatic malaria (fever and a positive thick blood smear) at the time of initial screening were treated with quinine (10 mg/kg tid × 7 days). Follow-up began when children fulfilled all of our selection criteria and were free of symptomatic malaria.
Within two weeks of enrollment, an appointment was scheduled for administration of a household survey to the primary caregiver for each enrolled household. The primary caregiver was defined as the person primarily responsible for daily care of the child. The questionnaire was administered at the home and collected basic demographic information about the study participant, primary care giver, and household, including use of prevention measures. Reported bednet use was verified by direct observation.
Thick blood smears were stained with 2% Giemsa for 30 minutes. Parasite density was estimated by counting the number of asexual parasites per 200 white-blood cells and calculating parasites per μL, assuming a white blood cell count of 8,000 cells per μL. A smear was judged to be negative if no parasites were seen after review of 100 high-powered fields. A second microscopist, who was unaware of the results of the first reading, re-read all slides. A third reviewer resolved discordant results.
Data management and analysis
Census data were collected in the field on written forms and transferred to an electronic data collection (EDC) system using Visual CE 8.1 software (Syware Inc, Cambridge, MA, USA) on a handheld PDA. The data were downloaded to Microsoft Access and then transferred into an Epi-Info version 6.04 database at the end of each day. Double entry verification from paper questionnaires was performed to assure accuracy. Given the success of the census EDC system, direct entry EDC questionnaire was used during the household survey, eliminating need for double entry verification. Categorical variables were compared using the chi-square test and continuous variables using a two-sample t-test. Independent predictors of anaemia and parasitaemia were identified using multivariate logistic regression. A p-value < 0.05 (two-tailed) was considered statistically significant. Analysis was done using SPSS version 10.0 (SPSS, Chicago, IL, USA) and Stata version 8.0 (Stata, College Station, TX, USA).
Verbal consent was obtained for the brief census survey described above. Written informed consent was obtained from the parent/guardian(s) of children for their participation in the cohort study and for the future use of biological specimens. The study was approved by the Institutional Review Boards at the University of California, San Francisco and Makerere University School of Medicine, and by the Ugandan National Council of Science and Technology.
Census and mapping
Comparison of census population and enrolled households and children.
Characteristics of the household from census data
All Households (n = 4931)
Households with children aged 1 to 10 years not included in the study (n = 1672)
Households with children aged 1 to 10 years included in the study (n = 322)
Median number of persons (range)
Median number of rooms (range)
Construction of home
Cement or Concrete
Mud and wattle
Mud or clay brick
Use of at least one bednet
Use of at least one ITN
Characteristics of the individual
Census Population (n = 16,172)
Children aged 1 to 10 years in census (n = 3590)
Children aged 1 to 10 years enrolled in study (n = 601)
Mean age in years (SD)
Gender (% female)
Use of bednet
Use of ITN
Recruitment and enrollment of study participants
Of the 582 households that were approached for recruitment, 209 were excluded prior to screening for the following reasons: children aged 1 to 10 years no longer living in the household (20%), parents not interested in the study (11%), and homes vacated or destroyed since the time of census (5%). A total of 743 children from 373 households were screened in the clinic (Figure 1). The most common reasons for exclusion during screening included: parent/guardian unwilling to provide informed consent (6%), plans to move out of Kampala (4%), and weight < 10 kg (4%).
When the census database was analysed, there were no differences between households with children aged 1 to 10 years that were enrolled and those not enrolled in the study (Table 1). A similar proportion of enrolled households had at least one bednet when data collected during the household survey (using direct observation) was compared to data reported during the census (60% vs. 63%, P = 0.47). However, the proportion of enrolled households with at least one ITN that was directly observed during the household survey was lower than the proportion based on data reported during the census (10% vs. 16%, P < 0.01). Compared to children aged 1 – 10 years from the census, enrolled children were slightly older (5.8 years vs. 5.3 years, P < 0.01), probably because young children weighing less than 10 kg were excluded. Based on direct observation, enrolled children were less likely to use a bednet and less likely to use an ITN compared to data from children aged 1–10 years collected during the census (43% vs. 48%, P = 0.03 and 6% vs. 13%, P < 0.01, respectively).
Baseline characteristics of study cohort
Baseline characteristics of study cohort (n = 601).
Summary (No. (%))
Relationship to primary caregiver
Born and raised in Kampala
Mean height for age Z-score (SD, range)
-0.63 (1.2, -2.9 – 6.1)
Mean weight for height Z-score (SD, range)
-0.29 (0.9, -2.8 – 5.3)
Height for Age < -2SD
Weight for Height < -2SD
Low G6PD activity*
Mean haemoglobin at enrollment (SD, range)
11.8 (1.4, 6.8–15.7)
Anaemia (Hb<11 g/dl)
Moderate anaemia (Hb<8 g/dl)
Use of bednets
Additional details about bednet use were collected during the household survey for enrolled children. Only 6% of enrolled children used an ITN and 68% of these ITNs were either new or retreated within the last 6 months. Observed bednets were generally in poor condition with 56% having visible holes.
Longitudinal studies in well-defined cohorts are critical to improving our understanding of the complex epidemiology of malaria in urban areas. In Africa, longitudinal studies of malaria have traditionally been conducted in rural villages where stable populations are well-suited to participate. However, malaria risk in urban environments has been recognized as a growing problem, and data from rural settings may not be applicable to urban settings. It has been estimated that half of Africa's population will live in urban areas by 2025 . Compared to rural areas, intense focal transmission near urban breeding sites leads to clustering of malaria incidence, resulting in a smaller proportion of households carrying most of the malaria burden [16, 18]. In addition, urban populations often demonstrate a delayed acquisition of immunity which could lead to a higher risk of disease in older age groups . The lack of longitudinal studies of malaria control in urban areas may be due to lower disease incidence, the effort required to sample from rapidly growing and densely populated communities, and the transient nature of urban residents. In this study, the methodology used to enroll a representative cohort of children from an urban environment was described and some of the advantages of this type of study are highlighted, together with the difficulties encountered.
By enumerating a census population from a geographically defined residential area near the study clinic, it was possible to characterize a target population and generate a sampling frame for recruitment of a representative cohort of children. The census depicted a community with high population density (nearly double that of New York City) and high household occupancy, where the majority of homes were permanent, cement, single-room structures. The difficulty of enumerating homes without addresses densely concentrated along unpaved roads and foot paths was overcome by labeling homes with identification numbers and recording GPS coordinates. Eliciting local elected officials to participate as part of the census contributed to the success of the project due to their familiarity with the community. One obstacle encountered was that adult residents were frequently not home during daytime hours, reflective of a working class adult population.
Compared to rural areas, where households are typically inhabited by large extended families, the census population had smaller household sizes with over 40% inhabited by a single adult resident or one or more adult residents without children . Only 40% of the census population was under 18 years of age, compared to nearly 60% in rural Uganda . In this census, 45% of households reported owning at least one bednet, which was higher than urban areas (33%) and considerably higher than rural areas (9%) previously reported in Uganda . Bednet use was highest in the youngest age groups, declined during adolescence and then increased in the adult population over the age of 18 years, when females were significantly more likely than males to use a bednet.
Probability sampling of households enumerated during the census was used to recruit a cohort of 601 children one to 10 years of age for our longitudinal study. Only 44% of households enumerated in the census had at least one child one to 10 years of age and were eligible for recruitment. This age range was chosen because one of the study regimens (artemether-lumefantrine) was not approved for use in children less than 10 kg when the study was designed. In addition, the relatively delayed development of acquired malaria-specific immunity in low endemicity areas like urban Kampala puts older children at risk. Recruitment was conducted at the household level because households enumerated during the census would likely remain constant, although residents may change. Only 45% of the households approached contributed at least one child to the study. Therefore, using random selection at the household-level, it was necessary to approach nearly double the number of households needed to enroll the proposed sample of 600 children. This was primarily due to children no longer residing in the household when it was approached for recruitment, likely secondary to the common practice of sending children to less expensive boarding schools outside of Kampala. The efficiency of the recruitment process was also reduced by a large proportion of households with future intentions to move from Kampala and a considerable proportion of households that were uninterested in the study, often stating that the offer of free health care was not an incentive given their access to health insurance. GPS technology afforded a significant advantage, enabling home visitors to relocate eligible households in the densely populated community from previously recorded coordinates. Experience with the census and recruitment process in this study population suggests that a broad study area and sizeable recruitment strategy is needed to carry out population-based random sampling for paediatric clinical studies in urban areas.
Cross-sectional analysis of anaemia and parasitaemia in the enrolled cohort of children revealed some risk factors for malaria in this community. The prevalence of mild anaemia was low (24%) and, consistent with prior studies, significantly more common in younger children and less common in children using bednets . Mild anaemia in children in the cohort between one to five years of age (44%) was lower than that reported from national surveillance data for children of that age group in urban and rural areas of Uganda (51% and 67%, respectively) . Malaria endemicity is classically defined by surveys of parasite prevalence. The Mulago III parish would be considered meso-endemic, defined as parasite prevalence of 11–50% in children of two to nine years of age, given a parasite prevalence of 20% in this age group. Increasing age showed a non-significant trend for an increased risk of parasitaemia, but low G6PD activity and use of bednets appeared to be protective. In addition, children with parasitaemia were significantly more likely to have mild anaemia. These predictors of anaemia and parasitaemia identified by cross-sectional analysis are applicable to other meso-endemic urban African environments.
Given the feasibility of deployment and the impact of ITNs on reducing malaria transmission and child mortality, high coverage rates should be sought in urban areas . Use of any bednet by enrolled children less than five years of age (57%) was higher than previously reported in urban (21–34%) and considerably higher than rural areas (6–18%) in Uganda . In addition, ITN use in enrolled children less than five years of age (15%) was higher than ITN use reported in urban areas (1–6%) and rural areas (0.2–2%) in Uganda . It was also found that census surveys based on subjective reporting may overestimate the actual use of bednets given the significantly lower use of bednets and ITNs noted when nets were directly observed for the enrolled children during the household survey. Although measures of socioeconomic status were not controlled, cross-sectional analysis in this cohort suggests that use of bednets lowers the risk of parasitaemia and anaemia, reinforcing the well-known benefit of bednet use in children. To improve malaria control, increased ITN use was prioritized by African leaders at the Roll Back Malaria Summit in Abuja with a goal of 60% of those at risk of malaria, especially children under five years of age and pregnant women, to have access to ITNs by 2005. Despite the high level of bednet use in the census population, the use of ITNs in this community still remains far below the Abuja target.
The study site for this project has extensive resources to conduct a longitudinal clinical trial. Mulago Hospital complex is a tertiary care hospital open 7 days a week, including a paediatric acute care unit open 24 hours a day. On-site laboratory testing and comprehensive health services staffed by qualified physicians and scientists, provides access to prompt diagnosis and strict quality control standards. Future multidisciplinary investigations within the longitudinal study to identify predictors of malaria incidence and response to therapy include the impact of environmental risk factors, household characteristics and measures of socioeconomic status, and molecular studies investigating the role of immune responses and genetic polymorphisms in the host and parasite. In addition, probability sampling from the census used for enrolling the representative cohort of children will allow generalization of these results to growing urban populations.
The challenge of decreasing the malaria burden in endemic areas is rooted in the complex epidemiology of this disease. Due to underlying differences between rural and urban areas, prevention and treatment strategies may need to be adapted to urban settings . Fortunately, with the existing infrastructure available in most cities and the focal nature of transmission, urban malaria may be uniquely amenable to control interventions. For example, greater access to formal health care facilities may allow for more accurate diagnosis and appropriate therapy, while high population densities may facilitate increased bednet coverage . Performing a census in a defined study area allows researchers to characterize their target population and generate a sampling frame for recruitment of representative cohorts. Such cohorts are critical for undertaking more comprehensive longitudinal studies in urban areas to identify environmental, household and individual-level predictors of malaria incidence and help to target control strategies aimed at reducing malaria morbidity and mortality in this increasingly important population.
Financial support was provided from the National Institutes of Allergy and Infectious Disease (AI052142) and Fogarty International Center/National Institutes of Health (TW00007)
We would like to thank the clinical study team of Charles Ocan, Arthur Mpimbaza, Bridget Nzarubara, Catherine Maiteki, Moses Musinguzi, John Patrick Mpindi, Basaliza M. Karakire, Naome Kilama, Norah Asaba. We would also like to thank Tabua Francis Butagira, Jacob Kaleebi, Fredrick Mudangha, Osaliya Richard, Kigongo Sulamiman, Awuzu Wilson, Namposia Yaledi, Kalyani McCullough, Neil Sachs and Damon Francis for their tireless work during the census and mapping; Sam Nsobya, Regina Nakafeero, Moses Kiggundu, Christopher Bongole, Maxwell Kilama, Felix Jurua for providing quality laboratory control; Marx Dongo, William Musoke, Caroline Bako for their work in the community; Peter Padilla, Sara Kibirango and Kenneth Mwebaze for administrative support; Nuhu Kibampawo for logistical support; Jonathan Cox for his expertise with GPS technology and Alta Tseng for her graphics skills; and all the parents/guardians and study participants for their cooperation.
- Snow RW, Craig M, Deichmann U, Marsh K: Estimating mortality, morbidity and disability due to malaria among Africa's non-pregnant population. Bulletin of the World Health Organization. 1999, 77 (8): 624-635.PubMed CentralPubMedGoogle Scholar
- Guerin PJ, Olliaro P, Nosten F, Druilhe P, Laxminarayan R, Binka F, Kilama WL, Ford N, White NJ: Malaria: current status of control, diagnosis, treatment, and a proposed agenda for research and development. Lancet Infect Dis. 2002, 2 (9): 564-573. 10.1016/S1473-3099(02)00372-9.View ArticlePubMedGoogle Scholar
- Trape JF, Pison G, Spiegel A, Enel C, Rogier C: Combating malaria in Africa. Trends Parasitol. 2002, 18 (5): 224-230. 10.1016/S1471-4922(02)02249-3.View ArticlePubMedGoogle Scholar
- Breman JG: The ears of the hippopotamus: manifestations, determinants, and estimates of the malaria burden. Am J Trop Med Hyg. 2001, 64 (1-2 Suppl): 1-11.PubMedGoogle Scholar
- Holding PA, Snow RW: Impact of Plasmodium falciparum malaria on performance and learning: review of the evidence. Am J Trop Med Hyg. 2001, 64 (1-2 Suppl): 68-75.PubMedGoogle Scholar
- Trape JF, Rogier C, Konate L, Diagne N, Bouganali H, Canque B, Legros F, Badji A, Ndiaye G, Ndiaye P: The Dielmo project: a longitudinal study of natural malaria infection and the mechanisms of protective immunity in a community living in a holoendemic area of Senegal. Am J Trop Med Hyg. 1994, 51 (2): 123-137.PubMedGoogle Scholar
- Bloland PB, Ruebush TK, McCormick JB, Ayisi J, Boriga DA, Oloo AJ, Beach R, Hawley W, Lal A, Nahlen B, Udhayakumar V, Campbell CC: Longitudinal cohort study of the epidemiology of malaria infections in an area of intense malaria transmission I. Description of study site, general methodology, and study population. Am J Trop Med Hyg. 1999, 60 (4): 635-640.PubMedGoogle Scholar
- Alonso PL, Sacarlal J, Aponte JJ, Leach A, Macete E, Milman J, Mandomando I, Spiessens B, Guinovart C, Espasa M, Bassat Q, Aide P, Ofori-Anyinam O, Navia MM, Corachan S, Ceuppens M, Dubois MC, Demoitie MA, Dubovsky F, Menendez C, Tornieporth N, Ballou WR, Thompson R, Cohen J: Efficacy of the RTS,S/AS02A vaccine against Plasmodium falciparum infection and disease in young African children: randomised controlled trial. Lancet. 2004, 364 (9443): 1411-1420. 10.1016/S0140-6736(04)17223-1.View ArticlePubMedGoogle Scholar
- D'Alessandro U, Olaleye BO, McGuire W, Langerock P, Bennett S, Aikins MK, Thomson MC, Cham MK, Cham BA, Greenwood BM: Mortality and morbidity from malaria in Gambian children after introduction of an impregnated bednet programme. Lancet. 1995, 345 (8948): 479-483. 10.1016/S0140-6736(95)90582-0.View ArticlePubMedGoogle Scholar
- Phillips-Howard PA, Nahlen BL, Kolczak MS, Hightower AW, ter Kuile FO, Alaii JA, Gimnig JE, Arudo J, Vulule JM, Odhacha A, Kachur SP, Schoute E, Rosen DH, Sexton JD, Oloo AJ, Hawley WA: Efficacy of permethrin-treated bed nets in the prevention of mortality in young children in an area of high perennial malaria transmission in western Kenya. Am J Trop Med Hyg. 2003, 68 (4 Suppl): 23-29.PubMedGoogle Scholar
- Schellenberg D, Menendez C, Aponte JJ, Kahigwa E, Tanner M, Mshinda H, Alonso P: Intermittent preventive antimalarial treatment for Tanzanian infants: follow-up to age 2 years of a randomised, placebo-controlled trial. Lancet. 2005, 365 (9469): 1481-1483. 10.1016/S0140-6736(05)66418-5.View ArticlePubMedGoogle Scholar
- Division UNP: World Urbanization Prospects: The 2003 Revision. 2004, New York , United NationsGoogle Scholar
- Tanner M, Harpham T: Action and research in urban health development - progress and prospects. 1995, London , Earthscan Publications Ltd.Google Scholar
- Caldas de Castro M, Yamagata Y, Mtasiwa D, Tanner M, Utzinger J, Keiser J, Singer BH: Integrated urban malaria control: a case study in dar es salaam, Tanzania. Am J Trop Med Hyg. 2004, 71 (2 Suppl): 103-117.PubMedGoogle Scholar
- Staedke SG, Nottingham EW, Cox J, Kamya MR, Rosenthal PJ, Dorsey G: Short report: proximity to mosquito breeding sites as a risk factor for clinical malaria episodes in an urban cohort of Ugandan children. Am J Trop Med Hyg. 2003, 69 (3): 244-246.PubMedGoogle Scholar
- Thompson R, Begtrup K, Cuamba N, Dgedge M, Mendis C, Gamage-Mendis A, Enosse SM, Barreto J, Sinden RE, Hogh B: The Matola malaria project: a temporal and spatial study of malaria transmission and disease in a suburban area of Maputo, Mozambique. Am J Trop Med Hyg. 1997, 57 (5): 550-559.PubMedGoogle Scholar
- Trape JF, Lefebvre-Zante E, Legros F, Ndiaye G, Bouganali H, Druilhe P, Salem G: Vector density gradients and the epidemiology of urban malaria in Dakar, Senegal. Am J Trop Med Hyg. 1992, 47 (2): 181-189.PubMedGoogle Scholar
- Carter R, Mendis KN, Roberts D: Spatial targeting of interventions against malaria. Bull World Health Organ. 2000, 78 (12): 1401-1411.PubMed CentralPubMedGoogle Scholar
- Donnelly MJ, McCall PJ, Lengeler C, Bates I, D'Alessandro U, Barnish G, Konradsen F, Klinkenberg E, Townson H, Trape JF, Hastings IM, Mutero C: Malaria and urbanization in sub-Saharan Africa. Malar J. 2005, 4 (1): 12-10.1186/1475-2875-4-12.PubMed CentralView ArticlePubMedGoogle Scholar
- Keiser J, Utzinger J, Caldas de Castro M, Smith TA, Tanner M, Singer BH: Urbanization in sub-saharan Africa and implication for malaria control. Am J Trop Med Hyg. 2004, 71 (2 Suppl): 118-127.PubMedGoogle Scholar
- Dorsey G, Njama D, Kamya MR, Cattamanchi A, Kyabayinze D, Staedke SG, Gasasira A, Rosenthal PJ: Sulfadoxine/pyrimethamine alone or with amodiaquine or artesunate for treatment of uncomplicated malaria: a longitudinal randomised trial. Lancet. 2002, 360 (9350): 2031-2038. 10.1016/S0140-6736(02)12021-6.View ArticlePubMedGoogle Scholar
- Lindsey SW, Egwang T, Kabuye F, Mutambo T, Matwale GK: Community-based environmental management program for malaria control in Kampala and Jinja, Uganda final report. 2004, Washington D.C. , United States Agency for International DevelopmentGoogle Scholar
- Molyneux CS, Mung'Ala-Odera V, Harpham T, Snow RW: Maternal responses to childhood fevers: a comparison of rural and urban residents in coastal Kenya. Trop Med Int Health. 1999, 4 (12): 836-845. 10.1046/j.1365-3156.1999.00489.x.View ArticlePubMedGoogle Scholar
- Robert V, Macintyre K, Keating J, Trape JF, Duchemin JB, Warren M, Beier JC: Malaria transmission in urban sub-Saharan Africa. Am J Trop Med Hyg. 2003, 68 (2): 169-176.PubMedGoogle Scholar
- Holtz TH, Marum LH, Mkandala C, Chizani N, Roberts JM, Macheso A, Parise ME, Kachur SP: Insecticide-treated bednet use, anaemia, and malaria parasitaemia in Blantyre District, Malawi. Trop Med Int Health. 2002, 7 (3): 220-230. 10.1046/j.1365-3156.2002.00846.x.View ArticlePubMedGoogle Scholar
- Uganda Bureau of Statistics (UBOS) and ORC Macro: Uganda Demographic and Health Survey 2000-2001. 2001, Calverton , UBOS and ORC MacroGoogle Scholar
- Crawley J: Reducing the burden of anemia in infants and young children in malaria-endemic countries of Africa: from evidence to action. Am J Trop Med Hyg. 2004, 71 (2 Suppl): 25-34.PubMedGoogle Scholar
- Hawley WA, ter Kuile FO, Steketee RS, Nahlen BL, Terlouw DJ, Gimnig JE, Shi YP, Vulule JM, Alaii JA, Hightower AW, Kolczak MS, Kariuki SK, Phillips-Howard PA: Implications of the western Kenya permethrin-treated bed net study for policy, program implementation, and future research. Am J Trop Med Hyg. 2003, 68 (4 Suppl): 168-173.PubMedGoogle Scholar
- Organization WH: World Malaria Report. 2005, Geneva , World Health OrganizationGoogle Scholar
This article is published under license to 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.