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Utility of passive malaria surveillance in hospitals as a surrogate to community infection transmission dynamics in western Kenya
© The Author(s). 2018
- Received: 15 February 2018
- Accepted: 15 June 2018
- Published: 26 July 2018
Malaria continued to be the major public health concern in sub-Sahara Africa, thus for better planning of control activities, periodic surveillance of both clinical and asymptomatic cases remains important. However, the usability of routinely collected malaria data in Kenyan hospitals as a predictor of the asymptomatic malaria infection in the community amidst rapid infection resurgence or reduction in different areas of disease endemicities remains widely unstudied. This study was therefore aimed to evaluate the utility of passive surveillance of malaria in health facilities as a proxy of infection transmission of the surrounding community in different transmission intensities.
Prospective multiple cross-sectional surveys were done in three villages in western Kenya. Monthly asymptomatic malaria positivity among school children, number of outpatient (OPD) confirmed malaria cases and abundancy of indoor resting malaria vectors were surveyed from June 2015 to August 2016. Community surveys on antimalarial drug use among adults and children were also done. Detection of malaria parasitaemia was done using thick and thin Giemsa stained blood slide microscopy for both clinical and school participants. A questionnaire was used to collect information on self-use of antimalarial drugs from randomly selected households.
The overall OPD blood slide positivity from all study sites was 26.6% (95%CI 26.2–27.0) and highest being among the 5–14 years (41.2% (95% CI 40.1–42.3). Asymptomatic malaria positivity among the school children were 6.4% (95%CI 5.3–7.5) and 38.3% (95%CI 36.1–40.5) in low and high transmission settings respectively. A strong correlation between overall monthly OPD positivity and the school age children positivity was evident at Marani (low transmission) (rho = 0.78, p = 0.001) and at Iguhu (Moderate transmission) (rho = 0.61, p = 0.02). The high transmission setting (Kombewa) showed no significant correlation (rho = − 0.039, p = 0.89).
Hospital malaria data from low and moderate malaria transmission predicted the infection transmission dynamics of the surrounding community. In endemic sites, hospital based passive surveillance didn’t predict the asymptomatic infection dynamics in the respective community.
- Outpatient department (OPD)
- Malaria blood slide positivity
- School age children
Malaria infection in tropical and sub-tropical countries continued to be a major public health concern . In 2015 alone, about 429,000 deaths were due to malaria globally, 92% of them were in Africa . Approximately 70% of Kenyan population were at risk of malaria infection with an immense threat in the coast and lake endemic areas of the country . The introduction of intense distribution and use of interventions against malaria has emanated to a decrease of both mortality and morbidity [3, 4]. However, despite the intensive use of malaria intervention measures, some areas in Kenya have witnessed persistence of asymptomatic infection and clinical cases [5–7]. This scenario has been as well observed elsewhere [8–10].
Monitoring of malaria transmission dynamics require both local and nationwide surveillance mechanisms. Malaria control programs conduct regular indicator surveys for nationwide planning and decision making [2, 11]. The Kenya malaria control strategy (2009–2018) recommend that all malaria indicators to be local, routinely monitored and evaluated . The local health authorities were therefore required to have the capacity to detect and respond in a timely manner to malaria outbreaks . Surveillance of malaria in schools is one of the recommend approaches to monitor local transmission dynamics . In western Kenya, the asymptomatic malaria positivity rate among primary school pupils has been correlated with that of the respective communities . Moreover, asymptomatic blood slide positivity rates among under-five children or pregnant mothers attending antenatal clinic in Tanzania correlated with the overall outpatient blood slide positivity rates . The introduction of long lasting insecticide treated nets, artemisinin based combination therapy and indoor residual spray in sub-Saharan Africa has resulted to a significant reduction malaria morbidity and mortality . Active surveillance of asymptomatic infections and hospital based passive surveillance have therefore been used to monitor the impact of the disease in Kenya [2, 5, 16, 17]. However, accuracy of the passive malaria surveillance in hospitals as a predictor of community transmission dynamics in the context of different infection intensities has not been widely contemplated. In the midst of a changing infection dynamics, exploration of the reliability of passive malaria surveillance in health facilities as a predictor of infection transmission rate in surrounding communities is therefore imperative. This study therefore aimed to evaluate the utility of the routine passive malaria surveillance in health facilities as a proxy of the infection transmission dynamics of the surrounding catchment population.
This study involved multiple cross-sectional surveys conducted monthly from June 2015 to August 2016. Surveillance of asymptomatic malaria among primary school children, OPD confirmed malaria and indoor resting malaria vectors for 15 observations. Moreover community based cross-sectional surveys on the use and source of anti-malarial were done in June and December 2016. A snap shot additional study to determine accuracy of blood slide malaria microscopy examination was conducted at Iguhu hospital (moderate transmission site).
Survellance of laboratory confirmed malaria
All patients attended the OPD and suspected to have malaria were examined by Giemsa stained blood slides and their results were recorded on daily basis on the specific registry as from June 2015 to August 2016. A total of 48,892 malaria suspected patients were examined by Giemsa stained blood slide in the three hospitals. A total of 17,231, 20,985 and 10,676 suspected patients were tested for malaria at Marani, Iguhu and Kombewa hospitals respectively.
Sample size calculation
Surveillance of asymptomatic infection in schools required minimum of 150 school age children per month per study site. The sample size was based on the local prevalence asymptomatic malaria infection ranging from 6.2 to 47.1% . A total of 30 randomly selected houses in each village were used to collect indoor resting vectors per site per month along with the school surveillance . This study also assessed malaria self-treatment practice in households where a minimum of 250 household were visited per site per survey . To determine accuracy of microscopic diagnosis of malaria in clinical setting, a total of 200 blood slides from one selected health facility were re-examined .
Surveillance of asymptomatic malaria among school age children
Multiple cross-sectional surveys were conducted among school children attending nine primary schools in the study areas. A finger prick blood sample was obtained from each school child, thick and thin blood smears prepared, stained with Giemsa and examined using light microscope. Sum of 1795, 1972 and 2430 blood slides were collected and examined from Kombewa, Marani and Iguhu respectively as from June 2015 to August 2016.
Survellance of indoor resting malaria vectors
A total of 30 randomly selected houses in each village were used to collect vectors per site per month as from June 2015 to August 2016. Pyrethrum Spray Catch (PSC) method as described elsewhere  was used to collect the indoor resting malaria vectors, morphological identification of vectors was performed using a dissecting microscope with an identification guide .
Household survey of anti-malarial drug use
The survey involved 756 and 1500 randomly selected participants from households who had used anti-malarial drugs prior to the interview in June 2016 and December 2016 respectively. Using a structured questionnaire, information on the use of anti-malarial drug within 2 weeks prior to the interview and type of dispensing unit were inquired.
Accuracy of malaria microscopic diagnosis
About 200 Giemsa stained thin and thick smear blood sides among malaria suspected patients from a hospital located in mesoendemic transmission setting were collected and re-examined by two qualified laboratory technicians at the Kenya Medical Research Institute in Kisumu. Malaria suspected patients were those with history of chills, body malaise, joint pain and other symptoms together with fever above 37.50 C. Malaria suspected found with parasitemia were termed as clinical malaria cases. Malaria parasites (asexual form) and gametocytes were counted at each 200 white cell fields. Technicians who re-examined the blood slides were blinded of the hospital microscopy results and of each other’s results.
The monthly and overall prevalence of malaria parasites per site among the school children and among the symptomatic patients were computed. The mean number of female Anopheline mosquitoes identified per house per night were calculated and compared between the villages. Variations of vector abundance was compared between the study sites using one way analysis of variance (ANOVA) and Tukey-Kramer post-hoc test. The frequency of household anti-malarial drug use per age group and per site was computed. Cohen’s kappa measurement of agreement was used to determine blood slide results concordance between hospital results and those re-examined at the research centre. Relationship between monthly asymptomatic malaria positivity among school children and clinical blood slide positivity was determined by using Spearman’s correlation test. Spearman’s correlation between abundance of indoor resting female Anopheline mosquitoes collected by PSC and the different clinical age groups malaria positivity was also done. Regression analysis between the abundance of indoor vectors and the clinical blood slide positivity rate was done to determine strength of association. Spearman’s correlation coefficient (rho) and regression analysis were used to determine strength of associations. The association strength was considered significant when the p-value was < 0.05. Strong correlation and modest correction were defined when the p-value was ≤0.001 and < 0.01 respectively. Graphic presentation of data, display of trend lines as well as predictor equations were computed. The correlation analyses were done by using SPSS® version 17 and determination of linearity computed using Microsoft excel® window 10.
Hospital malaria positivity
Summary of number of malaria suspected patient who underwent blood slide examination as from June 2015 to August 2016
Characteristic of malaria blood slide
Blood slides examined
Surveillance of asymptomatic malaria among school children
The blood slide positivity was consistently highest at the high transmission study area (Kombewa) with an overall prevalence of 38.3% (95%CI 36.1–40.5) and lowest at the low transmission setting (Marani) with 6.4% (95%CI 5.3–7.5) (see Additional file 2). The positivity rate within the first 12 months was 38.9% (95%CI 36.5–41.4) and 7.2% (95%CI 5.9–8.4) for Kombewa and Marani respectively.
Surveillance of indoor resting malaria vectors
The mean density of indoor resting vectors (for 15 months observations) were 0.59 ± 0.22, 0.68 ± 0.08 and 1.01 ± 0.28 female anopheline mosquitoes per house per night at Marani, Iguhu and Kombewa respectively. Moreover, for the first 12 months the mean densities were 0.52 ± 28, 0.63 ± 0.15 and 0.98 ± 0.33 female anopheline mosquitoes per house per night at Marani, Iguhu and Kombewa respectively. There was significant variation of the monthly abundance of indoor vectors between the study areas (F = 3.66, df = 2, p < 0.05). Post hoc Tukey-Kramer test however revealed existence of a significant variation of indoor vectors only between Marani and Kombewa (see Additional file 2).
Correlation between OPD malaria positivity and asymptomatic infection among school children
Abundance of indoor resting malaria vectors and OPD positivity
Household survey of anti-malarial drug use
Household survey on sources of anti-malarial drugs in areas with different infection transmission intensity in western Kenya in June and December 2016
Source of antimalarial drugs
< 5 age group
5–14 age group
≥15 age group
Proportion of malaria self-treatment
Accuracy of blood slide examination
A selected health facility located in the moderate malaria transmission setting revealed an agreement of 88% (175/199) of all examined blood slides between the hospital results and those by two microscopy technicians at the Research Centre (kappa = 0.703; p = 0.000). Therefore, a substantial agreement between the hospital blood slide examination results and that at the research Centre observed.
Accuracy of passively collected malaria data in health facilities as a true reflection of infection transmission dynamics in the surrounding communities may be affected by a number of factors including diagnostic and reporting accuracy as well as health seeking behaviour [2, 21–23]. This study aimed at determining the trustworthiness of passive surveillance of malaria in health facilities as a proxy to infection transmission of the catchment community. This study therefore analysed OPD malaria positivity rates and the asymptomatic infection positivity among school children residing in the hospital catchment area.
Approximately one out of four malaria suspected clients examined by blood slide at OPD in three hospitals in western Kenya were malaria parasite positive. Nevertheless, about half of the school children [5–14] examined at the OPD in the low and high infection transmission settings were blood slide positive. This particular age group consistently presented with the highest positivity rate as compared to other age groups and the highest blood slide positivity was in September 2015 at Marani Hospital where two-third among those (5–14 years) suspected of having malaria were blood slide positive. A study in Manicaland province in Zimbabwe reported a higher (48%) positivity rate among all outpatient suspected cases in 2014 , this area experienced malaria resurgence. In the Lake endemic setting of Kenya in 2016, malaria accounted for more than 35% OPD of all OPD cases of which also higher than that observed in this study . The study presented existence of higher clinical malaria vulnerability among the 5–14 children in all study areas and among under-fives in high transmission settings. This is due to the fact that under-five children got low sporozoite challenge due to high utilization of bed nets along with their mothers and therefore remain unchallenged throughout their childhood . However, low utilization of LLINs in context of changing infection transmission dynamics this group may be seriously affected because of their weak diseases specific sub-immunity especially in the epidemic prone areas [2, 25–27]. The recent Kenya malaria indicators survey also revealed highest asymptomatic infection susceptibility in this particular age group and therefore proved that the 5–14 age group may reliably be used to monitor transmission dynamics . The highest registered OPD positivity at Marani in September 2015 was preceded by an increased indoor resting vectors as well as highest prevalence of asymptomatic infection among same age group. The observed high blood slide positivity rate could be explained by existence of an outbreak during the study period .
The asymptomatic infection among the school children varied from very low at Marani (epidemic prone) to highest at Kombewa (hyperendemic area). Kombewa registered highest prevalence of asymptomatic infection (55%) in June 2015 and lowest in May 2016 after bed nets mass distribution in December 2015. Elsewhere, increasing malaria susceptibility among the school children has been also reported [25, 27, 28].
This study found a significant correlation between asymptomatic malaria positivity among the children and OPD positivity of all age groups at the low transmission setting. Whereas at the moderate transmission study site, the correlation was only observed with the all age groups OPD positivity and < 5 children but not with ≥15 years age group. The correlation between school children asymptomatic malaria positivity and OPD positivity rates for all age groups at the low transmission setting occurred due to fact that clinical malaria susceptibility was higher for all age groups in low transmission settings. Therefore, likelihood of seeking for medical attention is higher as compared to the high transmission settings . Indeed, utilization of health facilities for malaria treatment was higher among all age groups in the low transmission. The absence of correlation with the ≥15 years in moderate transmission settings can also be explained by their low utilization of health facilities. The absence correlation between the asymptomatic infection positivity among school children and the clinical positivity in high transmission settings may be explained also by low utilization of health facilities when seeking for medical attention. This could be due to their low susceptibility to severe form of malaria as compared to their counterparts in highland low transmission settings .
In Uganda, a non-linear relationship was observed between clinical malaria attack rate and community asymptomatic malaria positivity in a defined population . In Lake Victoria basin of Tanzania (holoendemic), the OPD positivity was found to be correlated with the asymptomatic malaria positivity among pregnant women and < 5 children attending reproductive and child health clinics . Therefore, absence of the expected correlation between infection dynamics in school age and OPD positivity in high transmission setting could be indeed due to low utilization of health facilities. Moreover, the Kenya malaria indicators survey (2015) also found better health care seeking among febrile children in epidemic prone areas than the Lake endemic area . So poor utilization of health facilities could be a possible reason for this observation. Furthermore, in the moderate transmission study areas where children over also practice self-malaria treatment, the positivity among 5–14 years and the ≥5 years at the OPD showed no correlation with asymptomatic infection positivity among school children. Lack of correlation among these age groups at this site was also due to poor health seeking behaviour. Also there was lower clinical disease susceptibility among the over fives as they were exposed to a significant sporozoite challenge when transmission intensity was still high few years back [4, 6, 7].
Immunoepidemiology of malaria indicated that, population in high transmission setting carry high burden of asymptomatic malaria and only a proportion of the population develops clinical disease, mainly children under-five because of their high exposure to the parasites compared to population in epidemic prone areas [2, 16]. In this areas, majority of the population remains at high risk of ending up with clinical disease and are likely to adhere to treatment and attending health facilities. Also, the older members of the community in epidemic prone areas understand the impact of malaria epidemics, thus, in case they have a suspected malaria cases in the house, are likely to run to health facilities . Also, the impact of public health education on malaria offered during the past malaria epidemics could have an influence the health seeking behaviour.
The population of indoor resting malaria vector collected by PSC was not correlated with the OPD malaria blood slide positivity. This could be due to the reported increasing outdoor resting behaviour, outdoor biting behaviour and changing host preference of previously known anthropophilic vectors [30–34]. Studies from western Kenya shows that more than 90% of indoor host seeking vectors escape through windows and heaves . Moreover presence of resistant knockdown insecticide resistance gene determines on whether the vectors exhibit exophilly or endophilly . The sampled indoor resting vector collected by PSC may therefore not show a relationship with infection transmission rate but may still be used to show trends of vector abundance .
This study however had some limitation including lack of a defined catchment area of the selected hospitals. Possibly some patients came from different areas with different infection transmission intensity and thus might have affected the outcome of interest especially in relatively less populated areas. The correction of variables could have been affected by accuracy of microscopic examinations. However, the accuracy of malaria diagnosis has greatly improved over the recent years compared to the past . This has been attributed by continuing on job training and the general malaria diagnostic capacity building .
The hospital based malaria surveillance in low transmission settings strongly correlated with the asymptomatic infection transmission dynamics among school children. Only the ≤5 children OPD positivity correlated significantly with the asymptomatic infection among school age living in mesoendemic study area. No correlation observed between hospital OPD malaria positivity and asymptomatic malaria positivity at the endemic high transmission study site. The use of hospital malaria data in endemic setting as a reflection of the surrounding catchment area may be unreliable despite provision of free anti-malarial drugs at health facilities. Passive and active surveillance of clinical and asymptomatic malaria should be emphasized in endemic settings of Kenya especially in these moments when there are reports of changing infection transmission risks.
Authors are grateful to everybody who participated in this study in schools and hospitals for their time and patience. We also acknowledge the support from hospital administration and heads of schools for their time and patience during the whole process of data collection. We appreciate the contribution of all field research assistants throughout the time of data collection particularly Ms. Carolyn Okoth and Mr. Amos Ouko. The contribution given by Ms. Sally Mwongoyi and Ester Bosire during data collection is highly appreciated. The study was supported by grants from the National Institute of Health (RO1 AI050243, U19 AI129326 and D43 TW001505).
AK, EJK, EK, GZ, AKG and GY participated in the idea conception, design, and implementation of the study. AK collected data and HEA and AKG coordinated the data collection process. AK, EJK, SEN, HDM, GZ, EK and GY did the statistical analysis and interpretation of the data and AK drafted the manuscript. All authors reviewed and approved the manuscript.
Ethics approval and consent to participate
The study was approved by the Ethical Review board of Kenya Medical Research Institute (SSC protocol No.3005) and received authorization from local health and education authorities. An informed consent was sought from participants before they were involved in the study. School children assented for study participation and the form was countersigned by their parents before they were allowed to participate in the study.
The authors declare that they have no competing interests.
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