Skip to main content

Variation in malariometric and red cell indices in children in the Mount Cameroon area following enhanced malaria control measures: evidence from a repeated cross-sectional study



Following enhanced malaria control measures, such as nationwide free distribution of insecticide-treated bed nets (ITN) by the government of Cameroon, its impact on malariometric and red cell indices in children ≤14 years in Muea, in the Mount Cameroon area was evaluated.


Two cross-sectional studies were conducted during the malaria transmission season (March-July) in 2006 (baseline) and 2013 (follow-up), respectively. The investigative methods included the use of a questionnaire to assess ITN use and coverage, clinical evaluation and laboratory investigations. Blood sample collected from each child was used for the preparation of blood films for detection of malaria parasites and density as well as full blood count determination using standard procedures and also an automated haematology analyzer.


The majority of children (81.5%) possessed an ITN in 2013. The proportion of effective users of ITN increased significantly from 20.9% (CI = 17.3-25%) in 2006 to 35.2% (CI = 31–39.7%) in 2013. The highest relative risk reduction in prevalence during the follow-up study was observed in malaria anaemia (79%, CI = 58.0-69.1% [69.1 to 14.5%]), followed by gametocytaemia (71.6%, CI = 58.9-80.3% [25.6 to 7.3%]), anaemia (64%, CI = 58.0-69.1% [80.1 to 28.9%]), and malaria parasitaemia (57.2%, CI = 51.4-62.3% [85.4 to 36.6%]). In the baseline survey, the prevalence of splenomegaly was significantly highest (χ2 = 18.3, P <0.001) in the youngest group of children while in the follow-up study, it was highest in the oldest (χ2 = 6.03, P = 0.049). The overall prevalence of mild, moderate and severe anaemia in the study population at baseline (59.6, 14.9, 6.3%) decreased significantly (P <0.001) to 24.4, 2.7 and 1.3%, respectively during the follow-up with the highest relative risk reduction in prevalence occurring in moderate anaemia (82.1%, CI = 67.3-90.2% [14.9 to 2.7%]). Microcytic anaemia also decreased significantly (P <0.001) from 56 to 7.7% during the follow-up survey.


Following interventions, anaemia (moderate to severe) was a more sensitive measure to changes in malaria exposure and children between 11–14 years of age experienced a significant increase in malaria-related morbidity.


The estimates of malaria burden are based on malariometric indices, such as prevalence of malaria parasitaemia, spleen rate and anaemia in defined risk groups [1]. Childhood anaemia may be a useful indicator of the burden of malaria and of the progress in malaria control [2]. As an intra-erythrocytic parasite of blood, Plasmodium induces haematological alterations. It is essential to monitor these alterations in order to assess the impact of malaria control interventions.

There are many preventive measures of malaria both at community and individual level, with the most promising being insecticide-treated bed nets (ITNs) [35]. The use of ITNs may be easier to implement and sustain than available alternative vector control methods, such as environmental sanitation. This is because of the immediate perceptible benefits to the user in personally preventing them from the nuisance of mosquitoes, as well as their killing effect on head lice [6] and bed bugs [7]. In order to be protected, individuals must not only own ITNs but also use them. As high coverage rates are needed to realize the full potential of vector control, the World Health Organization (WHO) recommends that in areas targeted for malaria prevention, and for which ITNs are selected as the vector control method, they should be made available to all people at risk, i.e., universal access [8]. In Cameroon, a high (>70%) percentage of the population potentially covered by ITNs distributed in 2011 was reported, yet no decrease in admissions and deaths were registered [9].

A strong association between interventions and their impact on malaria morbidity and mortality has been reported in Sao Tome and Principe [9]. When full coverage is achieved, ITNs have been reported to reduce clinical episodes of malaria caused by Plasmodium falciparum and Plasmodium vivax infection by 50% on average (range 39-62%), as well as reducing the prevalence of high density parasitaemia [3]. Despite efforts made by the National Malaria Control Programme (NMCP) to curb the disease burden, the prevalence is seemingly not on the increase but still a public health problem. Following substantial investments by the government of Cameroon in malaria control, coupled with the lack of population-based surveys or specific studies of the impact of interventions, the need for evaluation of intervention is critical. The objective of this study was to evaluate the impact of enhanced malaria control measures by the free distribution of ITNs on malariometric and red cell indices in children ≤14 years in Muea, in the Mount Cameroon area.


Study area and participants

The study was carried out in Muea village, a semi-rural setting in the Mount Cameroon area. The coordinates of the study area ranged from altitude 540 m, latitude 04°10.464′N, longitude 009°18.168′E to 556 m, 04°10.015′N and 009°18.009′E. The study area has been described in detail by Sumbele et al.[10]. The children from the community who participated in the study weighed >5 kg, were ≤14 years old, free from other clinical conditions not related to malaria and sickle test negative. Children who presented with fever, joint pains, headache, malaise, abdominal pain, nausea, and vomiting were considered to be symptomatic (clinical malaria).

Study design

Following several control programmes, including the free distribution of ITNs (Figure 1) by the government of Cameroon through the NMCP, two cross-sectional studies were conducted during the malaria transmission season (March-July) in Muea, a semi-rural community in the Mount Cameroon area. The first cross-sectional study (baseline) was carried out in 2006 following the free distribution of ITNs to malaria-vulnerable groups (pregnant women and children under five years) only, in selected regions of the country. A second cross-sectional study (follow-up) was conducted in 2013 following an upscale systematic distribution of ITN and long-lasting, insecticidal nets (LLINs) to all households in all health districts and the institution of free malaria treatment for children under five years of age.

Figure 1

Relevant malaria control interventions in Cameroon.

At the start of each study, the parents, guardians and children were educated at their various neighbourhoods. During education, the study protocol was explained and the benefits of participating in the study highlighted. Children were enrolled into the study only when parent or guardian signed the assent form or gave a verbal consent. Thereafter the children were clinically evaluated and their parent/caregivers interviewed using a semi-structured questionnaire to obtain information on ITN possession and use. Blood samples were collected for thick and thin smear microscopy as well as a standard full blood count. Labelled blood samples were transported on ice in a cool box of temperature between 8-10°C to the University of Buea Malaria Research Laboratory for further analyses.


A semi-structured questionnaire was administered to the participant/parent/guardians/caregiver to obtain information about ITN/LLINs use, its state, various malaria control measures and occurrence of malaria since they started using the nets. Children, who had good nets (potent ITN/LLINs, without hole/tears) that were used regularly, were considered effective users while children who had good nets but used them irregularly or had torn nets were considered as ineffective users.

Clinical evaluation

The clinical evaluation carried out by trained medical personnel in their homes consisted in part by the measurement of body temperature and examination of the spleen. Axillary body temperature was measured using a digital thermometer. A child with a body temperature ≥37.5°C was considered febrile. Ages of the children were obtained from their mothers and verified from their birth certificates. The tip of the spleen was felt by pressing the abdomen under the left coastal border and splenomegaly was graded according to the classification of Hackett [11].

Laboratory methods

Approximately 4–5 ml of blood sample was collected from the children by venipuncture into 5 ml sterile disposable syringes and dispensed into micro-containers or vacutainers containing ethylenediaminetetraacetate (EDTA) solution. Drops of whole blood were dispensed immediately on slides to prepare blood films. The thick and thin blood smears prepared on glass slides at the time of blood sampling were stained with Giemsa and examined following standard protocols [12]. Parasite density was determined on the basis of number of parasites per 200 leukocytes on thick blood film with reference to subjects’ white blood cell counts (WBC). If gametocytes were seen, the count was extended to 500 leukocytes [13]. In 2006, haemoglobin (Hb) concentration was measured in the field using a Stanbio STAT-SiteR Test Kit (STAT-site MHgb Meter, Stanbio Laboratory, Texas, USA) following the manufacturer’s instructions. Also WBC and red blood cell counts (RBC) were determined using the improved Neubauer haemocytometer as described by Cheesbrough [12] and Dacie and Lewis [14]. In 2013, a complete blood count: RBC, WBC, Hb, haematocrit (Hct), platelet, mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), and mean corpuscular haemoglobin concentration (MCHC) was run following the manufacturer’s instructions using an automated haematology analyzer, the Beckman Coulter counter (URIT 3000).

Definitions and end points

  •  Fever was defined as temperature ≥37.5°C;

  •  Asymptomatic malaria (AM) was defined as the presence of Plasmodium with an axillary temperature of <37.5°C;

  •  Clinical malaria (CM) was defined as the presence of any species of Plasmodium, with an axillary temperature of ≥37.5°C or reported fever in previous 48 hours;

  •  Parasitaemia was categorized as low (<1,000 parasite/μL blood), moderate (1,000-4,999 parasites/μL blood) and high (≥5,000 parasites/μL blood);

  •  A Hb level of <11 g/dL was classified as anaemic and further categorized as mild (Hb between 10.1 and 10.9 g/dL), moderate (Hb between 7.0 and 10.0 g/dL) and severe (Hb <7 g/dL) anaemia [12, 15];

  •  Malarial anaemia (MA) was defined as children with Hb <11 g/dL and malaria parasite positive [16];

  •  Microcytosis was defined as MCV of less than 73 fl [17];

  •  Hypochromasia was defined as a MCHC of less than 320 g/L [18].

Data analysis

Data were entered into spreadsheets using Microsoft Excel and analysed with the IBM Statistical package for Social Sciences (SPSS) version 19 (SPSS Inc., Chicago, IL, USA). Data were summarized into means and standard deviations (SD), and percentages were used in the evaluation of the descriptive statistics. Proportions were compared using the Chi-square test (χ2). Parasitaemia was log transformed before analysis. Means were compared using independent sample t-test and analysis of variance (ANOVA) where appropriate. The 95% confidence interval (CI) for the difference between two proportions and relative risk reduction were calculated using a Microsoft Excel confidence interval calculator as described by the Newcombe-Wilson method [19, 20]. The relative risk reduction and its confidence limits were obtained as one minus the relative risk and the values presented as percentages (%) by multiplying by a hundred (100).

Ethical considerations

Before commencement of each study, administrative clearance was obtained from the South West Regional Delegation of Public Health. The institutional review board hosted by the Faculty of Health Sciences, University of Buea issued the ethical clearance document. Additional authorization was obtained from the local health committee and the village chief. Children participated in the study if a parent or guardian signed the informed consent/assent form. The parents or guardians and their children were informed that their participation in the study was voluntary and they could withdraw at any time without explanation.


Characteristics of study populations

In 2006, a total of 411 children (215, 52.3% males and 196, 47.7% females) ≤14 years with a mean age of 6.4 (7.4) years were examined for the presence of malaria parasites and some malaria-related indices. Two-hundred and twenty (53.5%) of the children were age ≤ five years while 134 (32.6%) and 57 (13.9%) belonged to the six to ten and 11–14 years age groups, respectively. A total of 129 (31.4%, CI = 27.1-36%) children possessed or used an ITN. Only 86 (20.9%, CI = 17.3-25%) of them used them effectively. The proportion of effective users in the different age groups was comparable (P = 0.82).

In the follow-up study in 2013, 454 children (211, 46.5% males and 243, 53.5% females) ≤14 years with a mean age of 6.7 (3.4) years were examined. Of these, 177 (39.0%), 205 (45.2%) and 72 (15.9%) of the children were in the ≤ five, six to ten and 11–14 years age groups, respectively. The majority of the children (81.5%, CI = 77.7-84.8%) in the community possessed or used an ITN. The proportion of effective users of ITN in 2013 increased significantly from 20.9% (86, CI = 17.3-25%) in 2006 to 35.2% (160, CI = 31–39.7%). The proportion of effective users was significantly highest (χ2 = 9.52, P = 0.01) in the < five years age group (42.4%, CI = 35.3-49.7%) when compared with the six to ten (33.7%, CI = 27.5-40.4%) and the 11–14 years (22.2%, CI = 14.2-33.1%) age groups.

Variation in malariometric indices

The prevalence of fever, malaria parasitaemia, gametocytaemia, splenomegaly, CM, AM, anaemia, and MA decreased significantly (P <0.05) in 2013 when compared with the baseline data in 2006 (Table 1). In decreasing order, the highest relative risk reduction in prevalence during the follow-up study in 2013 was observed in MA (79%, CI = 58.0-69.1%), where MA prevalence decreased from 69.1 to 14.5%. This was followed by gametocytaemia (71.6%), anaemia (64%), CM (62.2%), AM (60.6%), malaria parasitaemia (57.2%), and splenomegaly (39.3%) as shown on Table 1. The prevalence of fever showed the least relative risk reduction in prevalence (23.5%).

Table 1 Variation in prevalence of malariometric indices

The trends in prevalence of fever and gametocytaemia in the different age groups were comparable at baseline and in the follow-up study. Although not statistically significant, the highest prevalence of malaria parasite was observed in children between 11–14 years of age in the follow-up study (40.3%, CI = 29.7-51.8%), while in the baseline study children in the six to ten years age group had the highest prevalence (88.1%, CI = 81.5-92.5%) as indicated in Table 2.

Table 2 Effect of age on the prevalence of malariometric indices

In the baseline survey, the prevalence of splenomegaly was significantly highest (χ2 = 18.3, P <0.001) in the youngest group of children while in the follow-up study, the highest prevalence of splenomegaly that approached significance (χ2 = 6.03, P = 0.049) was observed in the oldest group of children (Table 2). The prevalence of splenomegaly in children in the 11–14 years age group was higher (χ2 = 3.71, P = 0.054) in the follow-up study (23.6%, CI = 15.3-36.5%) than at the baseline (10.5%, CI = 4.9-21.1%) with an odds ratio of 2.63 (CI = 0.96-7.18).

The prevalence of anaemia in both study periods decreased significantly (P <0.05) with increased age (Table 2). The highest relative risk reduction in prevalence occurred in the 11–14 years age group (89.9%, CI = 75.9-95.7%) when compared with the < five years (55.0%, CI = 45.2-63.1%) and six to ten years (63.3%, 53.6-70.9%) age groups.

At baseline a comparison of MA prevalence within the age groups showed no significant difference (P >0.05) while in 2013, the prevalence decreased significantly (P <0.001) with an increase in the age group with children in the 11–14 years age group having a 97.7% (CI = 83.5-99.7%) relative risk reduction in prevalence (Table 2).

Although not statistically significant, the asexual geometric mean parasite density (GMPD)/μL of blood in 2013 was higher (834.8) than the baseline value (789.9). As shown in Table 3, the decrease in GMPD with increased age was statistically significant (P <0.01) at baseline, while in the follow-up study, no significant difference in neither GMPD with age group nor a trend was observed.

Table 3 Comparison of geometric mean parasite density per μL of blood within the age groups and study period

The disparity in prevalence of low, moderate and high asexual malaria parasite at baseline (60.1%, CI = 54.9-65.1% [210]; 27.6%, CI = 23.2-32.5% [97]; 12.3%, CI = 9.2-16.1% [43]) and follow-up (56.5%, CI = 48.8-63.9% [91]; 29.8%, CI = 23.3-37.3% [48] and 13.7% CI = 9.2-19.8% [22], respectively) was not significant (P = 0.74).

Variation in red cell indices

Between the baseline survey and the follow-up study, the overall mean Hb concentration significantly increased (t = 17.08, P <0.001) from 9.5 (1.7) g/dL (CI = 9.3-9.7 g/dL) to 11.6 (1.9) g/dL (CI = 11.4-11.8 g/dL) with a mean difference of 2.1 g/dL (CI = 1.9-2.4 g/dL). Children who were malaria parasite positive in the follow-up study had significantly higher (P <0.001) mean Hb, Hct, MCH, MCHC, and MCV when compared with their baseline counterpart. On the other hand, the mean RBC was significantly lower in malaria parasite positive children in the follow-up study than those at baseline (Table 4).

Table 4 A comparison of mean red cell indices in malaria parasite positive children at baseline and follow-up

The overall prevalence of mild, moderate and severe anaemia in the study population at baseline (59.6, 14.9, 6.3%) decreased significantly (P <0.001) to 24.4, 2.7 and 1.3%, respectively during follow-up as shown in Table 5. The highest relative risk reduction in prevalence of anaemia was observed in moderate anaemia (82.1%, CI = 67.3-90.2% [14.9 to 2.7%]).The prevalence of microcytosis, hypochromasia and microcytic anaemia (MCV <73 fl and Hb <11 g/dL) decreased significantly (P <0.001) from >55% in 2006 to <29% in 2013 (Figure 2). The occurrence of microcytic anaemia in children in the follow-up survey had the highest reduction in relative risk (86.3%, CI = 80.5-90.3%) when compared with microcytosis (80.5%, CI = 75–84.8%) and hypochromasia (59.1%, CI = 51.6-65.4%).

Table 5 Variation in the different categories of anaemia in the study populations
Figure 2

Prevalence of microcytosis, hypochromasia and microcytic anaemia at baseline and during follow-up.


Most parts of Cameroon have approached or met the Roll Back Malaria (RBM) household ITN coverage of at least 60% as reported by previous studies [9]. However, malaria still remains a public health concern even though LLINs were distributed freely in 2011. This study aimed at assessing the impact of ITN use as one of the enhanced malaria control measures on malariometric and red cell indices in children in Muea, in the Mount Cameroon area.

Parasitaemia is one of the indices used in estimating the burden of malaria and the impact of interventions. The prevalence of malaria parasitaemia is on the decline in the Mount Cameroon area as revealed by the study. Overall, the prevalence of malaria parasite obtained in the follow-up study (36.6%) was lower than those obtained at baseline (85.4%) and a similar study conducted in 2012 (44.3%) in this part of the Mount Cameroon area by Kimbi et al. [21]. The achievement of a relative risk reduction in malaria parasite prevalence of 57.2% may be credited to all the control efforts implemented by the Cameroon government, through the NMCP in the Ministry of Public Health. Some of the measures included the free distribution of LLINs to all age groups, as well as free treatment of malaria among children less than five years of age. Also, the government introduced several educative health campaigns on malaria prevention in public and private media (radio and television channels). Such messages included the recognition of common signs and symptoms of malaria and the need to get prompt and effective treatment following diagnosis. Other protective measures encouraged included eliminating breeding sites by drainage of pools in which water collects, regular collection of household refuse by designated authorities to reduce container breeding of mosquitoes, filling up of pot-holes, chemical killing of mosquito larvae in well defined and limited breeding sites and compulsory monthly clean up of the environment by communities.

The study brings to light a change in morbidity in children in the follow-up survey. Although not statistically significant, the asexual GMPD/μL of blood in 2013 was higher (834.8) than the baseline value (789.9). Furthermore, in the follow-up study, children in the 11–14 years age group had a significantly higher (P = 0.04) GMPD/μL of blood than their baseline equivalent. The highest prevalence of malaria parasite and the significant increase in parasite density observed in children 11–14 years old, unlike in the baseline study, probably reflects the manner of usage of ITNs by children in the study area. Results from the study indicate that while the effective use of ITNs in 2006 was comparable in the different age groups, in 2013 children in the 11–14 years age group registered a significant decrease in usage. Consequently, they were more exposed to infective mosquito bites than the other age groups. This may have resulted in the high prevalence and density of malaria parasite observed in this age group. Hence, children in the 11–14 years age group most likely did not acquire immunity to parasitization per se but may have acquired immunity that prevented the development of febrile disease as the study revealed an increase in asymptomatic malaria in the age group (Table 2). This is in line with Bejon et al. [22] who reported a shift away from febrile malaria to acquiring asymptomatic parasitaemia with increasing age. The asymptomatic parasitaemia may be beneficial in inducing and sustaining partial immunity against malaria [23], although a significant drawback is the suppression of Hct levels [24].

It is not surprising that children under five years recorded the highest parasitaemia when compared with the older children in spite of their effective use of ITNs. Children under five years are more vulnerable to the disease in areas of high transmission [21, 25] as naturally acquired immunity builds up in older children following repeated exposure to the parasite. In another study [22], the use of ITNs was associated with remaining infection-free rather than acquiring asymptomatic infection or febrile malaria. The high effective use of ITNs in this age group, culminating in a lack of exposure to infective mosquito bites, could have prevented the development of blood stage immunity, the protective effect of living in a high-transmission area [22], hence, the high parasitaemia observed.

The prevalence of Plasmodium gametocytes, the sexual, non-proliferating blood stage in the life cycle, significantly reduced in the follow-up study. It is plausible that the implementation of a highly gametocytocidal, artemisinin-based combination therapy (ACT) [26], namely amodiaquine-artesunate, as first-line treatment for uncomplicated malaria by the government of Cameroon, may have contributed to the reduction in gametocyte prevalence. However, malaria transmission is dependent on mosquito vector dynamics, the proportion of humans with peripheral gametocytaemia, and the infectiousness of circulating gametocytes to mosquitoes. The reduction in prevalence of peripheral gametocytaemia observed in the follow-up survey is of utmost importance as this probably attests to a decline in malaria transmission following a reduction in the infectiousness of Anopheles mosquitoes.

Splenomegaly is the main clinical marker of endemicity in P. falciparum transmission areas [27]. The minimal reduction in the prevalence of splenomegaly when compared with other malariometric indices indicates malaria is still meso-endemic [28] in the study area. Worthy of note is the significant change in morbidity with age when both surveys were compared. Contrary to the baseline trend, the follow-up study showed an increase in splenomegaly prevalence with age. Persistent parasitaemia from treatment failure [29] and a pronounced immunological response especially in children ≤ five years [25] are known to contribute to splenic enlargement. However, with the introduction of ACT as the first-line treatment for malaria in Cameroon, the widespread use of ITNs and prompt access to effective treatment in children, especially those aged under five, the spleen rate is expected to decline. While the increased prevalence of splenomegaly in children age over ten years may be the consequence of increased presence of malaria parasite and density in this age group, the lowered spleen rate in children under five years may be ascribed to the benefits of the therapeutic actions of ACT and the effective use of ITNs. ACT is given in all hospitals in Cameroon to children aged under five with malaria, free of cost, a policy the government instituted in 2010. The beneficial features of ACT include rapid and substantial reduction of the parasite biomass, rapid parasite clearance and effective action against multidrug resistant P. falciparum[30], thus preventing recrudescence and multiple infections which may over work the spleen, consequently leading to splenomegaly. Studies indicate that the spleen-specific pitting function accounts for a large fraction of parasite clearance in artemisinin-treated patients [31].

The increase in mean Hb concentration from 9.4 (1.8) in the baseline study to 11.3 (1.9) g/dL in the follow-up study, regardless of the status, signifies a great improvement in the health of children in this study area. WHO and RBM recommend that anaemia be used as an additional indicator to monitor malaria burden at community level as interventions are nationally scaled-up [32]. The significant reduction in anaemia and MA at follow-up suggests a substantial diminution in malaria-related morbidity in the community. On the other hand, the significant decline in morbidity related to malaria is not unexpected in a community which benefits from free ITNs, LLINs and ACT in the vulnerable group. In addition, non-malaria-related intervention, such as regular deworming of school-age children carried out by the health authorities and parents, may have contributed to the improved Hb levels and health of the children. Furthermore, the acquisition of knowledge by caregivers/parents on the health and nutritional status of their children following the education on the outcome of the baseline study, may have played a significant role in improving health and well being in the community.

Even though both studies had as a limitation a small number of children in the 11–14 years age group, it is unlikely that the difference in numbers may have introduced a bias as the mean difference in age was of no consequence. The higher prevalence of anaemia in the ≤ five years group with decreasing severity with age is in line with previous studies that anaemia due to malaria is more severe in younger children in areas of intense transmission [25]. Children in this age group are more vulnerable to infection with malaria than others with severe and potentially fatal complications.

Studies by Korenromp et al. [2] reported the impact of ITNs on anaemia to be more pronounced than that for parasitaemia prevalence and CM, with moderate to severe anaemia being a more sensitive measure to changes in malaria exposure due to increasing coverage of malaria interventions. Findings from the study attest to this as the highest relative risk reduction in prevalence was observed in moderate and severe anaemia indicating that the nationwide free distribution of ITNs and use had a major impact on the health of the children. Nonetheless, although the proportion of effective users of ITNs in the population was low, the non-effective users probably benefitted from the reduction in mosquito vector population achieved in the community from nets of effective users, hence the reduction in anaemia and severity.

Results from the baseline survey indicated a prevalence of 56% for microcytic anaemia to be a common finding in the children examined when compared with 7.7% at follow-up. Microcytic anaemia, a surrogate marker of iron deficiency, is also a characteristic feature of anaemia due to malaria [33]. The anaemia of P falciparum malaria is typically normocytic and normochromic, with a notable absence of reticulocytes, although microcytosis and hypochromia may be present due to the very high frequency of alpha- and beta-thalassaemia traits and/or iron deficiency in many endemic areas [34]. However, Premji et al. [35] reported a majority of children infected with P. falciparum to be iron deficient. In a related study in the same area, 28% of the children with P. falciparum infections were iron deficient albeit the majority had microcytic anaemia [10]. It is therefore reasonable to state that the significant decline in microcytic anaemia observed in children at follow-up was the result of a reduction in prevalence of malaria parasitaemia. This consequently lends support to the fact that malaria is a major contributor to microcytic anaemia in the study population.

The primary limitation of the study is the lack of information on the variation in consultations with children under five years in health facilities following the commencement of free treatment of malaria as inferences have been made. However, irrespective of the age group, all the children benefitted in the same way from the environmental management instituted to control the breeding of the mosquito vector and the distribution of LLINs.


The results from the studies suggest that even though a greater majority of the population is in possession of an ITN, less than half of the population use them effectively. Although malaria is still meso-endemic, most malariometric indices declined and the red cell indices markedly improved. Following interventions, anaemia (moderate to severe) was a more sensitive measure to detect changes in malaria exposure. Children in the 11–14 years age group experienced a significant increase in malaria-related morbidity, and microcytic anaemia was no longer a common finding in children in the area.



Artemisinin-based combination


Asymptomatic malaria


Clinical malaria


95% Confidence interval


Geometric mean parasite density






Insecticide-treated bed nets


Long-lasting, insecticide-treated net


Malarial anaemia


Mean corpuscular haemoglobin


Mean corpuscular haemoglobin concentration


Mean corpuscular volume


National Malaria Control Programme


Roll Back Malaria


Red blood cell


White blood cell.


  1. 1.

    WHO: World Malaria Report, WHO, HTM/MAL/2005.11. 2005, Geneva, Switzerland: WHO

    Google Scholar 

  2. 2.

    Korenromp EL, Armstrong-Schellenberg JRM, Williams BG, Nahlen BL, Snow RW: Impact of malaria control on childhood anaemia in Africa – a quantitative review. Trop Med Int Health. 2004, 9: 1050-1065. 10.1111/j.1365-3156.2004.01317.x.

    Article  PubMed  Google Scholar 

  3. 3.

    Lengeler C: Insecticide-treated bed nets and curtains for preventing malaria. Cochrane Database Sys Rev. 2004, 2: CD000363-

    Google Scholar 

  4. 4.

    WHO: Malaria Date accessed: 13 August 2014

  5. 5.

    Atkinson JM, Fitzgerald L, Toaliu H, Taleo G, Tynan A, Whittaker M, Riley I, Vallely A: Commmunity participation for malaria elimination in Tafea Province, Vanuatu: Part I. Maintaining motivation for prevention practices in the context of disappearing disease. Malar J. 2010, 9: 93-10.1186/1475-2875-9-93.

    PubMed Central  Article  PubMed  Google Scholar 

  6. 6.

    Sampath TR, Yadav RS, Sharma VP, Adak T: Evaluation of lambdacyhalothrin impregnated bednets in a malaria endemic area of India. Part 1. Implementation and acceptability of the trial. J Am Mosq Control Assoc. 1998, 14: 431-436.

    CAS  PubMed  Google Scholar 

  7. 7.

    Pates HV, Curtis CF: Mosquito behaviour and vector control. Annu Rev Entomol. 2005, 50: 53-70. 10.1146/annurev.ento.50.071803.130439.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    WHO: Insecticide-treated Mosquito Nets: a WHO Position Statement. Geneva: Global Malaria Programme,,

  9. 9.

    WHO: Seasonal Malaria Chemoprevention (SMC) for Plasmodium falciparum malaria control in highly seasonal transmission areas of the Sahel sub region in Africa. 2012, Geneva, Switzerland: WHO,,

    Google Scholar 

  10. 10.

    Sumbele IUN, Nkuo-Akenji T, Samje M, Ndzeidze T, Ngwa EM, Titanji VPK: Haematological changes and recovery associated with treated and untreated Plasmodium falciparum infection in children in the Mount Cameroon Region. J Clin Med Res. 2010, 2: 143-151.

    Google Scholar 

  11. 11.

    Gilles HM: Pathology of Malaria: Handbook of Malaria Infection in the Tropics. 1997, Italy: Italian Association Amicidi Raoul Follerau (AIFO)

    Google Scholar 

  12. 12.

    Cheesbrough M: District Laboratory Practice in Tropical Countries. Part 1 & 2. 1998, Edinburg Building UK: Cambridge University Press

    Google Scholar 

  13. 13.

    Trape JF: Rapid evaluation of malaria parasite density and standardization of thick smear examination for epidemiological investigations. Trans R Soc Trop Med Hyg. 1985, 79: 181-184. 10.1016/0035-9203(85)90329-3.

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Dacie JV, Lewis SM: Red Cell Count in Practical Haematology. 1995, Michigan: Churchill Livingstone

    Google Scholar 

  15. 15.

    Mogensen CB, Sørensen JE, Bjorkman A: Pallor as a sign of anaemia in small Tanzanian children at different health care levels. Acta Trop. 2006, 99: 113-118. 10.1016/j.actatropica.2005.12.010.

    Article  PubMed  Google Scholar 

  16. 16.

    Ong’echa JM, Keller CC, Were T, Ouma C, Otieno RO, Landis-Lewis Z, Ochiel D, Slingluff JL, Mogere S, Ogonji GA, Orago AS, Vulule JM, Kaplan SS, Day RD, Perkins DJ: Parasitemia, anemia, and malarial anemia in infants and young children in a rural Holoendemic Plasmodium Falciparum transmission area. Am J Trop Med Hyg. 2006, 74: 376-385.

    PubMed  Google Scholar 

  17. 17.

    Calis JCJ, Phiri KS, Faragher BE, Brabin BJ, Bates I, Cuevas LE, de Haan RJ, Phiri AI, Malange P, Khoka M, Hulshof PJM, van Lieshout L, Beld MGHM, Teo YY, Rockett KA, Richardson A, Kwiatkowski DP, Molyneux ME, van Hensbroek MB: Severe anaemia in Malawian children. N Engl J Med. 2008, 358: 888-899. 10.1056/NEJMoa072727.

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    WHO: Iron Deficiency anaemia. Assessment Prevention and Control. A Guide for Programme Managers. 2001, Geneva, Switzerland: World Health Organization Publication

    Google Scholar 

  19. 19.

    Newcombe RG: Interval estimation for the difference between independent proportions: comparison of eleven methods. Stat Med. 1998, 17: 873-890. 10.1002/(SICI)1097-0258(19980430)17:8<873::AID-SIM779>3.0.CO;2-I.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Armitage P, Berry G: Statistical Methods in Medical Research (3rd ed.). 1994, London: Blackwell, 131-

    Google Scholar 

  21. 21.

    Kimbi HK, Keka FC, Nyabeyeu HN, Ajeagah HU, Tonga CF, Lum E, Gah HA, Lehman LG: An update of asymptomatic falciparum malaria in school children in Muea, Southwest Cameroon. J Bacteriol Parasitol. 2012, 3: 154-

    Google Scholar 

  22. 22.

    Bejon P, Warimwe G, Mackintosh CL, Mackinnon MJ, Kinyanjui SM, Musyoki JN, Bull PC, Marsh K: Analysis of immunity to febrile malaria in children that distinguishes immunity from lack of exposure. Infect Immun. 2009, 77: 1917-1923. 10.1128/IAI.01358-08.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  23. 23.

    Baliraine FN, Afrane YA, Amenya DA, Bonizzoni M, Menge DM, Zhou G, Zhong D, Vardo-Zalik AM, Githeko AK, Yan G: High prevalence of asymptomatic Plasmodium falciparum infections in a highland area of Western Kenya: a cohort study. J Infect Dis. 2009, 200: 66-74. 10.1086/599317.

    PubMed Central  Article  PubMed  Google Scholar 

  24. 24.

    Ekvall H, Arese P, Turrini F, Ayi K, Mannu F, Premji Z, Bjorkman A: Acute haemolysis in childhood falciparum malaria. Trans R Soc Trop Med Hyg. 2001, 95: 611-617. 10.1016/S0035-9203(01)90095-1.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Udoh EE, Oyo-Ita AE, Odey FA, Eyong KI, Oringanje CM, Oduwole OA, Okebe JU, Esu EB, Meremikwu MM, Asindi AA: Malariometric indices among Nigerian children in rural setting. Malaria Res Treat. 2013, 2013: 716805-doi:10.1155/2013/716805

    Google Scholar 

  26. 26.

    Stepniewska K, Price RN, Sutherland CJ, Drakeley CJ, von Seidlein L, Nosten F, White NJ: Plasmodium falciparum gametocyte dynamics in areas of different malaria endemicity. Malar J. 2008, 7: 249-10.1186/1475-2875-7-249.

    PubMed Central  Article  PubMed  Google Scholar 

  27. 27.

    Snow RW, Omumbo JA, Lowe B, Molyneux CS, Obiero JO, Palmer A, Weber MW, Pinder M, Nahlen B, Obonyo C, Newbold C, Gupta S, Marsh K: Relation between severe malaria morbidity in children and level of Plasmodium falciparum transmission in Africa. Lancet. 1997, 349: 1650-1654. 10.1016/S0140-6736(97)02038-2.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Hay SI, Smitha DL, Snow RW: Measuring malaria endemicity from intense to interrupted transmission. Lancet Infect Dis. 2008, 8: 369-378. 10.1016/S1473-3099(08)70069-0.

    PubMed Central  Article  PubMed  Google Scholar 

  29. 29.

    Singh N, Shukla MM, Chand SK: Forest malaria in Chhinwara, Madhya Pradesh, central India: a case study in a tribal community. Am J Trop Med Hyg. 2003, 68: 602-607.

    PubMed  Google Scholar 

  30. 30.

    WHO: Antimalarial Drug Combination Therapy. Report of a WHO Technical Consultation. 2001, Geneva, Switzerland: WHO, WHO/CDS/RBM/2001

    Google Scholar 

  31. 31.

    Buffet PA, Safeukui I, Deplaine G, Brousse V, Prendki V, Thellier M, Turner GD, Mercereau-Puijalon O: The pathogenesis of Plasmodium falciparum malaria in humans: insights from splenic physiology. Blood. 2011, 117: 381-392. 10.1182/blood-2010-04-202911.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  32. 32.

    WHO: Minutes MERG Anaemia Task Force Meeting: 27-28th. 2003,, Oct ,

    Google Scholar 

  33. 33.

    Abdalla SH: Hematopoiesis in human malaria. Blood Cells. 1990, 16: 401-416.

    CAS  PubMed  Google Scholar 

  34. 34.

    Newton CR, Warn PA, Winstanley PA, Peshu N, Snow RW, Pasvol G, Marsh K: Severe anaemia in children living in a malaria endemic area of Kenya. Trop Med Int Health. 1997, 2: 165-178. 10.1046/j.1365-3156.1997.d01-238.x.

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Premji Z, Hamisi Y, Shiff C, Minjas J, Lubega P, Makwaya C: Anaemia and Plasmodium falciparum infections among young children in an holoendemic area, Bagamoyo, Tanzania. Acta Trop. 1995, 59: 55-64. 10.1016/0001-706X(94)00079-G.

    CAS  Article  PubMed  Google Scholar 

Download references


The authors appreciate the support and cooperation of the parents and guardians of the children in the Muea community, the staff of the Muea health centre and medical students from the Faculty of Health Sciences, University of Buea who took part in the study. This work was supported by the staff development grant and special fund for research and modernization given to authors by the government of Cameroon.

Author information



Corresponding author

Correspondence to Irene UN Sumbele.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

IUNS was involved in all phases of the study, including study design, data collection, data analysis, interpretation, and write-up of the manuscript; RT participated in the collection of data and laboratory analysis; OSBM participated in supervision and revision of the manuscript; TNA supervised the study and revised the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

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 (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Sumbele, I.U., Ning, T.R., Bopda, O.S. et al. Variation in malariometric and red cell indices in children in the Mount Cameroon area following enhanced malaria control measures: evidence from a repeated cross-sectional study. Malar J 13, 334 (2014).

Download citation


  • Malaria
  • Anaemia
  • Children
  • Prevalence
  • Insecticide-treated nets
  • Microcytic anaemia