- Open Access
Cost analysis of school-based intermittent screening and treatment of malaria in Kenya
© Drake et al; licensee BioMed Central Ltd. 2011
- Received: 6 May 2011
- Accepted: 20 September 2011
- Published: 20 September 2011
The control of malaria in schools is receiving increasing attention, but there remains currently no consensus as to the optimal intervention strategy. This paper analyses the costs of intermittent screening and treatment (IST) of malaria in schools, implemented as part of a cluster-randomized controlled trial on the Kenyan coast.
Financial and economic costs were estimated using an ingredients approach whereby all resources required in the delivery of IST are quantified and valued. Sensitivity analysis was conducted to investigate how programme variation affects costs and to identify potential cost savings in the future implementation of IST.
The estimated financial cost of IST per child screened is US$ 6.61 (economic cost US$ 6.24). Key contributors to cost were salary costs (36%) and malaria rapid diagnostic tests (RDT) (22%). Almost half (47%) of the intervention cost comprises redeployment of existing resources including health worker time and use of hospital vehicles. Sensitivity analysis identified changes to intervention delivery that can reduce programme costs by 40%, including use of alternative RDTs and removal of supervised treatment. Cost-effectiveness is also likely to be highly sensitive to the proportion of children found to be RDT-positive.
In the current context, school-based IST is a relatively expensive malaria intervention, but reducing the complexity of delivery can result in considerable savings in the cost of intervention.
(Costs are reported in US$ 2010).
- Rapid Diagnostic Test
- Intermittent Preventative Treatment
- Malaria Parasitaemia
There is a growing appreciation that malaria not only impacts on the health of infected individuals but also has broader social and economic consequences [1, 2]. Recent evidence suggests that non-severe malaria can affect the cognition, attention and ultimately educational achievement of school children [3–7]. Reaching this population is most effectively achieved via the school infrastructure, and with increasing enrolment in schools by African school-age children , schools provide a natural access point for malaria control among this age group. Notwithstanding this potential, the optimal approach to controlling malaria in schools remains unclear [4, 9]. Recent studies in Africa have demonstrated the potential of intermittent preventative treatment (IPT) - the administration of curative doses of anti-malarial treatment at predefined intervals regardless of infection status - in reducing malaria parasitaemia, clinical disease and anaemia and improving cognitive performance [3, 10, 11]. Moreover, modelling work demonstrates that IPT administered among school-age children can also help reduce malaria transmission in the wider community, particularly in areas of low to moderate transmission . However, recent changes in national drug policies in many African countries preclude the use of sulphadoxine-pyrimethamine and amodiaquine, some of the drugs previously used in IPT, thereby limiting its potential implementation.
An alternative school-based malaria control strategy is intermittent screening and treatment (IST), using rapid diagnostic tests (RDTs) to screen and treat asymptomatic children. Recent studies in Ghana found IST in pregnant women to be equally efficacious as IPT  and acceptable to patients . The present analysis examines the costs of IST of school children in two districts in coastal Kenya as part of an ongoing trial investigating the impact IST has on the health and education of school children . The analysis explores how variation in the design of the intervention, including different component prices, affects programme cost.
Description of the IST trial
A factorial, cluster randomized trial is currently investigating the impact of school-based malaria control and enhanced literacy instruction on the health and educational achievement of school children in Kenya. The study design and description of the intervention are detailed elsewhere . In brief, the trial is being implemented, 2010-2012, in 101 primary schools on the coast of Kenya where continuous precipitation supports moderately intense malaria transmission (predominantly Plasmodium falciparum). Typically, there are two seasonal peaks in malaria cases reflecting the bimodal rainfall pattern; the heaviest rainfall typically occurring between April and June and a smaller peak in October and November each year. Under nutrition, especially anaemia, is common . In terms of education, the area is one of the poorest performing in Kenya, having the lowest mean national examination scores since 2005 .
The interventions being evaluated are (i) intermittent screening and treatment of malaria in schools by public health workers and (ii) training workshops and support for teachers to promote explicit and systematic literacy instruction (not evaluated here). The primary outcomes are educational achievement and anaemia. Secondary outcomes include malaria parasitaemia, school attendance, sustained attention and other cognition abilities. Randomly selected children from classes 1 and 5 are included in the evaluation. Baseline health and education surveys were conducted in intervention and control schools between January and March 2010, with 12 and 24-month follow-up surveys scheduled.
Intermittent screening and treatment (IST)
Each school term, all children are tested for malaria using a RDT. The RDT used is a ParaCheck-Pf device (Orchid Biomedical Systems, Goa, India) which is able to detect P. falciparum and other (unspecified) Plasmodium species. Children (with or without malaria symptoms) found to be RDT-positive are treated with artemether-lumefantrine, AL (Coartem®, Novartis), an artemisinin-based combination therapy. Testing and treatment is administered by district health workers and supported by the Division of Malaria Control (DoMC), Ministry of Public Health and Sanitation (MoPHS).
On day 1, children are screened by a laboratory technician using a RDT. Those children found to be RDT-positive are given milk and bread and then given the first dose of AL. Parents or older siblings of children are called and a nurse explains that their child is infected with malaria parasites and requires treatment (assuming they are not already taking medication). The parents/older siblings are given the second dose of AL and told that this should be taken in the evening with food. On day 2, the nurse returns to the school, gives the third AL dose to children and provides the parent/older sibling with the fourth dose. Children absent from school are followed up at their home and provided with the doses. On day 3, the procedures are the same as day 2. During follow-up visits nurses monitor for potential side effects of treatment.
The analysis is undertaken from the perspective of the Government of Kenya, as a public service provider. Only costs to the provider are included as costs to the patient of accessing the intervention are likely to be low since it is delivered in schools and there is no fee to receive the intervention. The costs of accessing IPT have previously been considered negligible on the same basis [18, 19]. The comparison (null) for this evaluation is no intervention. The total economic cost is calculated based on an initial 5 year programme implementation. The decreased value placed on future costs and annualization of capital costs is calculated using a 3% discount rate, in line with WHO recommendations . The financial costs are the unadjusted funds required to finance the intervention and the economic cost reflects the total resource burden, taking into account the value of donated goods or unpaid workers.
Programme costing was guided by a three-step process: resource identification, resource measurement and resource valuation. In this process, relevant unit costs were collected according to an ingredients based approach , the quantity or usage of each ingredient was determined and combined with cost information to produce a monetary valuation of total resources used, or economic cost. Costs were separated into those that required new funds, such as the purchase of additional RDTs and antimalarials, and those that involved the redeployment of existing resources, including use of health workers who would otherwise have duties at the local health facility.
Data collection was undertaken in 2010, with unit costs established from the project accounting system and from interviews with purchasing officers. Where information was unavailable or unrepresentative, unit costs were sourced from the Ministry of Public Health and Sanitation (MoPHS) or wholesale market prices. Ingredient usage was established from direct observation of the intervention, interviews with trial co-ordinators, from health worker time sheets and driver mileage survey. The majority of costs were collected in Kenyan Shillings (KES) and then converted to US$ using the average exchange rate from the preceding 12 months (01.08.09 to 31.07.10): US$ 1 = KES 79.9 . Costs derived from other years were inflated or deflated to 2010, using a compound inflation factor based on the year by year consumer price index . The World Health Organization CHOosing Interventions that are Cost-Effective (WHO CHOICE)  was used to determine the country specific item lifespan of capital items: vehicle 8 years, personal computer 10 years, printer 10 years. Costs relating to activities solely for research purposes were excluded. To account for resource waste through faulty goods, mishandling or accidents, a wastage factor of 10% was applied to all relevant items.
Components of the intermittent screening and treatment in school children in coastal Kenya
1. Community sensitisation
Sensitization consisted of a meeting with parents and teachers at every school to describe the intervention and answer questions. It occurs once and comprises the set-up costs of the intervention, thus costs are annualized across the five-year programme.
A half-day training on the intervention delivery and a refresher of relevant clinical practice is given to all staff at every screening round.
3. Screening day
A mobile health team travels to the school. Children are screened by a laboratory technician using a RDT and those found to be RDT-positive are given milk and bread and the first dose of treatment. The evening dose is given to the child or if the child is too young to take responsibility the parents or older sibling are called.
4. Treatment Follow-up
On days two and three a nurse returns to the school to supervise the morning treatment dose and deliver the evening dose.
Supervising health officers join two intervention teams for observation at each round.
This includes coordinator time, office use and the cost of distributing significant extra quantities of RDTs and anti-malarials to district hospitals.
Univariate sensitivity analysis was conducted to determine how sensitive costs are to variation in input parameters, including commodity prices, the design of the delivery strategy, and evaluation methodology. Results are displayed graphically using a tornado diagram. For anti-malarials and RDTs, the highest and lowest prices of equivalents available in Kenya were chosen. Other variables examined include salary levels (± 20%); discount rate (0%, 5%), and wastage factor (0%, 20%). To investigate the marginal cost of supervising treatment, health worker attendance on days 2 and 3 were removed, with parents/older siblings being given a full treatment course and instructions on how to administer treatment on the screening day. The second intervention change was the removal of technicians from the screening teams, with nurses from local health facilities carrying out RDT testing. The current estimates for time spent at schools includes preparation of blood slides and collection of research information. For the sensitivity analysis is it estimated that nurses could carry implement IST without a technician under non-research conditions.
A final parameter investigated was the prevalence of Plasmodium falciparum in the target population, a factor that will determine the quantity of anti-malarial treatments used. Simulations using bespoke scripting in Microsoft Excel (2007) were performed, whereby variation in prevalence of infection was simulated through repeated sampling of programme cost at random prevalences. One thousand repetitions were performed in order to cover the full prevalence range. The cost per child screened and cost per child treated are plotted to present variation in programme cost and cost-effectiveness (the number of children treated is a proxy measure of effect).
Ethical and scientific approval for the present study is provided as part of the wider trial by the Kenya Medical Research Institute and National Ethics Review Committee (SSC No. 1543), the London School of Hygiene and Tropical Medicine (LSHTM) Ethics Committee (5503), and the Harvard University Committee on the Use of Human Subjects in Research (F17578-101). Sponsorship and insurance is provided by the LSHTM's Clinical Trials Sub-Committee (QA225).
Financial and economic costs of malaria intermittent screening and treatment in schools in coastal Kenya by resource category (US$ 2010)
Annual Economic Cost
Economic cost per child screened
Cost Profile (%)6
The costs of malaria intermittent screening and treatment in schools in coastal Kenya by resource category and intervention activity (US$ 2010)
Sensitivity analysis of the costs of malaria intermittent screening and treatment in schools in coastal Kenya
Parameter Baseline Value
Variation and Justification
Cost Per Child Screened
First Response: $0.61
NOW Malaria: $3.21
The cheapest and most expensive high performing alternatives considered by the Kenyan government.
AL: $0.31 - 1.23 depending on child weight
AQ + SP: $0.125
Dihydroartemisinin Piperaquine (DP) is an alternative ACT while Amodiaquine Sulphadoxine-Pyrimethamine (AQ + SP) is a cheap alternative that might be used in an area where SP is still effective.
Treatment Follow Up
Treatment follow up carried out by nurses as described
Health Team Personnel
Technicians used by trial to carry out RDT and blood slide.
Nurses implement IST without technicians.
Personnel may be reduced by removing research tasks such as taking blood slides and anthropometry.
Midpoint of relevant pay scales.
Salaries are likely to vary by region or over time
0% and 5%
0% reflects un adjusted programme costs. Some argue that time preferences for delay of costs are not necessarily rational and should not be included in decision-making. 5% represents a greater time preference, argued by some to be more relevant to developing country contexts.
0% and 20%
No empirical evidence. Based on literature precedent.
The current analysis estimates that the financial cost of IST is US$ 6.61 per child screened. The economic cost is US$ 6.24 although the difference is largely due to discounting of costs incurred in the future. The largest cost components were RDTs and salaries. Almost half (47%) of the costs comprised of the redeployment of existing resources including health worker time and use of hospital vehicles. While this may reduce the new funds required to finance the intervention it also highlights the potential for additional strain to be placed on existing resources, depending on the current working capacity. Sensitivity analysis highlighted that changes to the delivery strategy, such as using different RDTs, removing treatment follow-up and only including nurses in the screening team, can reduce overall costs by 40%, increasing the affordability of the intervention.
Although IST is principally a strategy of treatment rather than prevention of malaria, it can be compared to preventive interventions such as IPT in that it seeks to prevent malaria associated anaemia and its consequences in school children [3, 10]. Studies in western Kenya found the yearly cost of school-based IPT to be US$ 3.17 per child  (Unless otherwise stated costs are adjusted to US$ 2010 using national CPI). Notwithstanding inflationary differences, the yearly cost of three rounds of IST at US$ 18.72 per child is considerably higher than IPT. It should be noted however, that the low cost of IPT hinges on the ability to use SP or amodiaquine, which is no longer possible in Kenya due to changes in national drug policy withdrawing SP and amodiaquine monotherapy. The ACT dihydroartemisinin-piperaquine (DP) has been considered as an alternative for IPT in school children , but would increase IPT costs . The cost of IPT for children (IPTc) aged between 1 and 5 years in Ghana is estimated to be US$ 11.38 to US$ 14.79  while a comparison of strategies for delivering IPTc in the Gambia estimated costs of US$ 3.85 and US$ 1.81 if delivered by village health workers or reproductive and child health trekking teams respectively . This illustrates the opportunities for cost reduction depending on delivery strategy and highlights the potential difference in cost between settings. Multi-site studies of IPT for infants (IPTi) and for insecticide-treated bed net (ITN) distribution found respective yearly costs to be in the region of US$ 1.36 to US$ 4.03 per child (US$ 2007)  and US$ 1.38 and US$ 1.90 per child (US$ 2005) . Studies are also beginning to consider screening strategies for targeting asymptomatic malaria infection in the wider community [28, 29], although estimates of cost are not yet available.
The sensitivity analysis provides an indication of how the costs of IST may be reduced in the future. A variety of malaria RDTs are currently available, but have varying diagnostic performance and any cost savings in using different RDTs or an alternative diagnostic tool will need to be balanced against performance. In the current study, the cheaper RDT considered in the sensitivity analysis performs slightly better than the trial RDT according to studies by the World Health Organization . RDT diagnosis performs similarly to or even better than routine microscopy in health centres , although a lower mean parasite density in asymptomatic infection may affect diagnostic performance. A study of school children with and without fever in Benin found that while PCR diagnosis led to a considerable increase in identified Plasmodium infection compared to microscopy or RDT, there was little or no clinical benefit in treating sub-microscopic infection . Moreover, the costs of screening programmes using microscopy or PCR diagnosis would likely be prohibitively expensive. While cost-effectiveness of RDTs compared to microscopy in health centres depends on the local setting [33–36], the logistical disadvantage of microscopy as a mobile diagnostic tool means it is unlikely to be cost-effective for school-based IST.
The change to unsupervised treatment is justified on (i) findings from previous clinical trials indicating that supervised treatment and unsupervised treatment are equivalent in terms of efficacy [37, 38] and (ii) that national guidelines permit unsupervised treatment . In addition to the likely reduction in health worker personnel time on implementation, there may be scope for teachers to assist or even lead screening. Studies in Zambia and the Democratic Republic of Congo have shown that RDTs can be used effectively by non-medical personnel [40–42]. The wider regional or national roll out of IST may result in reduced RDT cost from bulk purchasing and improved efficiency from familiarity with the intervention. However, as coverage expands to include those in more remote areas, increased transport and therefore personnel time may increase marginal cost. In addition, integration with other school-based or community health programmes provides further potential cost reduction through economies of scope. For example, school health programmes currently provide children with de-worming and micronutrient supplementation . The UNICEF led Child Health Day programme can cost-effectively deliver multiple health services to younger children  and bed net distribution has been successfully integrated with routine or campaign vaccination strategies . IST implementation would need to be tailored to the epidemiological context and take into account infrastructural capacity and local geography. The cost, and ultimately cost-effectiveness, will crucially depend on the prevalence of Plasmodium infection, with overall costs decreasing with decreasing prevalence but costs per child treated increasing exponentially. However, this does not incorporate potentially crucial cost savings associated with reducing malaria transmission. That is, this strategy may indeed be cost-effective at low to moderate prevalence if elimination, or even reduction in transmission, is achieved.
There are certain limitations associated with economic evaluations of randomized trials. In this case, the intervention is designed with the trial objectives in mind and not maximisation of cost-effectiveness, for example only two classes per school were screened. In the base case scenario all research only costs were removed but intervention alterations were not modelled. The intention is to maximize the level certainty in the base case estimate, providing a solid estimate of cost from which to model variation in setting or intervention design. Findings can be generalized for settings with similar social, economic and epidemiological conditions, such as Western or Nyanza provinces . Although specific figures will change, options for cost reduction, issues around scale-up and discussion of consequences are likely to remain relevant. A degree of socio-economic, epidemiological and environmental consistency is assumed and the analysis does not account for significant exogenous variation. In particular, it is assumed that the prevalence of malaria remains constant year on year. It is noted that this is unlikely to be the case in the study setting since transmission is currently in decline .
The hypothesized consequences of malaria intermittent screening and treatment in schools in coastal Kenya
Justification of Consequence
48% reduction of moderate anaemia was found from IPT in Kenyan school children and improved haemoglobin in Ugandan children using IPT.
Reduced clinical malaria
Reductions of between 42% and 67% reported by seasonally targeted IPT trials in schools in Mali.
Reduced malaria transmission
Modelling studies of community based IST and school based IPT suggests potential for considerable impact on transmission of malaria due to treatment of asymptomatic disease reservoir
Potential of school malaria surveys for community surveillance of malaria.
Early detection systems for malaria in the Kenyan highlands were found to cost US$15,512 per district.
Modelling studies highlight the increased resistant parasite selection pressure due to treatment of asymptomatic infection.
Improved educational achievement
Improvement in attendance, cognitive ability and educational attainment found from IPT or chemoprophylaxis in school children.
Local household cost burden reduced by US$ 2.52 per malaria episode.
With regard to impact on malaria transmission, Kern et al  found that intermittent community screening campaigns using RDTs followed by treatment of asymptomatic carriers has greatest impact in areas of high transmission but that the rate of infection returned to its normal level in the subsequent year, unless the intervention was repeated, highlighting the potential of community-based IST in reducing malaria transmission. In areas of low transmission, the reduction in infection was sustained for over three years following a single round of intervention. The impact of screening and treating only school children on the overall level of transmission in the wider community remains to be established, but Aguas et al find that IPT in school children has the potential to reduce transmission particularly in areas of low or moderate endemicity . Kern et al also found that screening campaigns scheduled in close succession (monthly intervals) at the start of the dry season had the greatest impact on the success of the intervention. Such findings have relevance for the optimal delivery of school-based IST.
In addition to the impact on health and malaria control, school-based IST has the potential to improve education and reduce household costs. Malaria is considered to impact children's educational achievement through reduced school attendance due to illness and through impaired concentration and cognition [3–7]. Recent work by Chuma et al estimated the average cost to the household per episode of malaria in the study districts, Kwale and Msambweni, to be US$ 2.52  [Jane Chuma, personal communication]. The above breadth of potential consequences of school-based IST necessitates that a broad perspective to economic evaluation is adopted. A possible approach is cost-consequence analysis (CCA), a framework which presents, but does not aggregate, multiple outcomes. Coast et al  and Williams et al  support CCA as a clear and comprehensive approach to economic evaluation whilst Weatherley et al  recommend a CCA framework be used in the evaluation of intersectoral costs and consequences.
This analysis shows that in the current setting IST in schools is a relatively expensive intervention, primarily due to the RDT costs and the follow-up visits to observe treatment on day 2 and 3. However, many of the costs represent redeployment of existing resources and future alteration in the design of the intervention can reduce costs by 40%. Future research will evaluate impact of IST in schools and how this might vary in different transmission and operational settings.
The authors are grateful to Kara Hanson for comments on a draft of the manuscript and to Jane Chuma for sharing data on the household cost of malaria. We are also grateful for the guidance and support provided by the Division of Malaria Control, Kenya Ministry of Public Health and Sanitation, for various aspects of the study. The work is funded by the International Initiative for Impact Evaluation and the World Bank, through the Norwegian Education Trust Fund, the multi-donor Education Programme Development Fund (EPDF) and the Spanish Impact Evaluation Fund. The results reported here contributed to the World Bank Africa Programme for Education Impact Evaluation and the Malaria Impact Evaluation Programme. Additional funding is provided by the Wellcome Trust through a Masters Training Fellowship to George Okello (092765) and a Research Career Development Fellowship to Simon Brooker (081673). The artemether-lumefantrine for the intervention trial is provided by the Division of Malaria Control, Ministry of Public Health and Sanitation, Nairobi, Kenya. None of the funding agencies had any role in the preparation or submission of this manuscript.
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