Abstract
Background
Malaria remains a major public health problem in Sub Saharan Africa, where widespread poverty also contribute to the burden of the disease. This study was designed to investigate the relationship between the prevalence of childhood fever and socioeconomic factors including poverty in Nigeria, and to examine these effects at the regional levels.
Methods
Determinants of fever in the last two weeks among children under five years were examined from the 25004 children records extracted from the Nigeria Demographic and Health Survey 2008 data set. A two-level random effects logistic model was fitted.
Results
About 16% of children reported having fever in the two weeks preceding the survey. The prevalence of fever was highest among children from the poorest households (17%), compared to 15.8% among the middle households and lowest among the wealthiest (13%) (p<0.0001). Of the 3,110 respondents who had bed nets in their households, 506(16.3%) children had fever, while 2,604(83.7%) did not. (p=0.082). In a multilevel model adjusting for demographic variables, fever was associated with rural place of residence (OR=1.27, p<0.0001, 95% CI: 1.16, 1.41), sex of child: female (OR=0.92, p=0.022, 95% CI: 0.859, 0.988) and all age categories (>6months), whereas the effect of wealth no longer reached statistical significance.
Conclusion
While, overall bednet possession was low, less fever was reported in households that possessed bednets. Malaria control strategies and interventions should be designed that will target the poor and make an impact on poverty. The mechanism through which wealth may affect malaria occurrence needs further investigation.
Background
Malaria is one of the most important challenges to public health with about 300 to 500 million cases reported annually. More than 1 million people die from the disease, most of them children under age 5 years. Over 90.0% of the cases and 75% of the deaths occur in sub-Saharan Africa (SSA). These childhood deaths, resulting mainly from cerebral malaria and anaemia, constitute somewhere between 20% and 25% of child mortality in Africa [1,2].
African countries south of the Sahara bear the heaviest burden of malaria. These countries are among the poorest in the world and widespread poverty on the continent continues to play a role in the burden of the disease. Malaria cases and deaths have risen steadily in sub-Saharan Africa since the late 1970s, especially in Nigeria. The emergence of resistance to insecticides and chloroquine, the cheap anti-malarial treatment widely used for clinical management of uncomplicated malaria, has been held as a major factor in this trend, aided by a general weakening of health systems. This effect was exacerbated by economic stagnation and decline, which has implications for growth and welfare. For instance, malaria is responsible for about a 1.3 per cent reduction in the average annual rate of economic growth for those countries with the highest burden. In Nigeria, malaria is the major cause of morbidity and mortality, especially among children below age five [3]. Malaria is a social and economic problem, which consumes about US$3.5 million in government funding and US$2.3 million from other stakeholders in the form of various control attempts in 2003[4].
Given the above scenarios, the drive of the government to achieve the targets of the National Economic Empowerment and Development Strategy (NEEDS), Seven-Point Agenda and the MDGs is currently threatened by the seemingly intractable trend of the ancient scourge which has compounded national and household poverty through intensive loss of productive time to attack and death in extreme cases. This is compounded by the development of resistance to the traditional first-line drug (chloroquine), while the newly introduced therapy (ACT) would be largely beyond the reach of many due to poverty, if it was not heavily sponsored by international organizations. Given that malaria is endemic throughout Nigeria, and that over 50.0% of the country's population are living below poverty line, malaria incidence may increase significantly in Nigeria because many may not be able to afford the newly introduced drugs due to poverty.
There are quite a good number of attempts to analyse the economic effects of malaria in the literature [2,3,5-7]. Most of the studies are limited to determining the mathematical significance of malaria. However, a comprehensive analysis of malaria and poverty remains scarce. The links between malaria and poverty are multiple and complex. Therefore a better understanding of the direction and magnitude of the causal relationship is needed, along with better understanding of the nature of poverty that is related to malaria. For example, understanding whether the relationship between malaria and poverty is related to household factors, community, or larger regional factors would help to identify whether further investigation and action is needed at one or more of these levels. Poverty sustains the conditions where malaria thrives, and malaria impedes economic growth and keeps communities in poverty. With a potential dual relationship between poverty and malaria, where poor households experience high malaria prevalence that in turn maintains them in poverty, these households are trapped in reinforcing cycles [8,2].
There are many pathways through which the relationship between malaria and poverty operates. At the household level, poor housing can expose people to contact with infective mosquitoes. Simple preventive measures such as insecticide-treated bed nets are unaffordable to the poorest if they must pay for them. Lack of resources prevents people from seeking timely health care. Often, peak malaria transmission coincides with harvesting time, which is a factor that affects risks at the village level. A few days of work lost to illness can mean food insecurity for the entire family.
A meaningful relationship between malaria and poverty should consider the effect of both individual and cluster where individual belongs. This approach requires a multilevel analysis incorporating variables at different levels of aggregation. In this report, the relationship between poverty and malaria in Nigeria was analyzed using a multi-level logistic model. The independent variables considered were bed net ownership, type of place of residence, sex and age of child, and literacy level of mother.
Methods
This report utilizes secondary data from the Nigerian Demographic and Health Survey [9]. Demographic and health surveys are an international series of nationally representative surveys conducted in middle and lower income countries [10].
The study population in this analysis was the 25,004 under five children extracted from the records of 104,808 respondents who responded to the household questionnaire. The outcome measure in this analysis was occurrence of fever in children less than five years of age in the last two weeks preceding the survey. The explanatory variables were sex of child, age of child, whether or not household possess a bed net, whether child slept under bed net night before survey, type of bed net (treated or untreated), type of place of residence (rural/urban) and wealth index; a measure of poverty. This index serves as a proxy for measuring the long-term standard of living. It was based on data from the household's ownership of consumer goods; dwelling characteristics; type of drinking water source; toilet facilities and other characteristics that are related to a household socio-economic status such as car, radio, television, gas cooker, iron, boat/ship, telephone, source of water, electricity supplies, and type of wall, floor and roof, etc. To construct the index, each of these assets was assigned a weight (factor score) generated through principal component analysis, and the resulting asset scores were standardized in relation to a standard normal distribution with a mean of zero and standard deviation of one [11]. Each household was then assigned a score for each asset, and the scores were summed for each household. Individuals were ranked according to the total score of the household in which they resided. The sample was then divided into quintiles from one (lowest) to five (highest). A single asset index was developed on the basis of data from the entire country sample and this index was used in the analysis. The data were analyzed using Stata 10.0 [12].
Frequency tables were generated for relevant variables. Descriptive statistics such as means, medians and standard deviations were used to summarize continuous variables. Relationships between the outcome measure (occurrence of fever) and each explanatory variable was first explored using the chi squared test in bivariable analysis before a multilevel logistic regression was carried out. Explanatory variables found to be associated with the outcome were included in the logistic model based on the magnitude of the chi squared values. Odd ratios and 95% CIs were computed. A random effect logistic model was fitted that included fixed effects and group-level intercepts as random effects [13]. This allowed for a two-level, inherently nested nature of the data: individuals (children) nested within clusters/regions. Nigeria has six geopolitical zones and there is variation in all characteristics including fever patterns in all the zones.
Multi-level models allow the additional information provided by knowing which cluster a child comes from to be taken into account in modeling the relationship between independent and dependent variables. This model was run using the GLLAMM routine in Stata. In using this approach, the correlation between children from the same cluster or region arises from their sharing specific but unobserved properties of the respective regions. A random effect logistic regression model for the data is given by
Where b1, b2, b3 and b4 represents fixed effects and Ui represents a random effect. Ui is a random variable with a mean of zero and constant variance. Ui, is the estimation of the variance across all of the regions involved in the study. If the variance is large then the outcome of interest is dependent on the region, if the variance is small then the variations in outcome of interest may be explained by the measured characteristics alone.
Given Ui, the responses from the same regions are mutually independent that is the correlation between children from the same regions is completely explained by them having been observed in the same regions. The variance τ2 measures the degree of heterogeneity in the probability of experiencing fever that cannot be explained by the classification into the 2 categories (fever: yes Vs no)
An important measure that describes these dependences in the data is called the intra-class correlation coefficient (ICC); this statistic measures the extent to which individuals within the same group are more similar to each other than they are to individuals in different groups. The intraclass correlation (ICC), ρ was calculated using:
Where τ = estimated variance and π = 3.142
The Gllamm approach
This is a stata procedure for fitting generalized linear models, a class of regression models for univariate responses with density from an exponential family [14]. The logistic regression model was specified from the family of generalized linear model with the logit link and binomial distribution using the link ( ) and family ( ) options. The option i(region) specifies the desired within region correlation matrix. The eform produces the estimated odds ratios. The full syntax is given below:
xi: gllamm fever i.place of residence i.sex of child i.childsage i.wealthnw, i(region ) family(binomial) link(logit) adapt nip(5), eform
Results
Characteristics of the sample
The study sample consisted of 25,004 children. In this sample, 3,965(15.9%) children had fever in the two weeks prior to the survey. The mean age of the children was 27 months (SD = 17.2 months).
Bivariate findings
Table 1 shows the associations between fever and the hypothesized predictors. All of the predictors were significantly related to the occurrence of fever except 'having bed net", "whether children under 5 slept under bed net previous night" and "type of bed net that child slept under". A total of 414(9.2%) children had fever in the North Central, 1,145(20.2%) in the North East, while 269(8.8%) had fever in the South West. (p < 0.0001). Three thousand and fifty one (16.8%) had fever in the rural areas compared with 914(13.3%) in the urban areas. (p < 0.0001). Of the 3,110 respondents who had bed nets in their households, 506(16.3%) children had fever, while 2,604(83.7%) did not. (p = 0.082). Of the 3,697 children who slept under bed nets, previous night, 580(15.69%) had fever compared with 425(17.3%) who did not. (p = 0.085). Furthermore, of the 1380 children who slept under treated net, 222(16.1%) had fever compared with 283(16.4%) who did not. (p = 0.82).
Table 1.
Occurrence of Fever by Selected Variables
| Fever Occurrence in Child | |||||
|---|---|---|---|---|---|
| Yes | No | Total | Chi | P value | |
| Region | |||||
| North Central | 414(9.2) | 4066(90.8) | 4480(100.0) | ||
| North east | 1145(20.2) | 4512(79.8) | 5657(100.0) | 519.3 | <0.0001 |
| North West | 1017(15.12) | 5707(84.9) | 6724(100.0) | ||
| South east | 542(25.2) | 1606(74.8) | 2148(100.0) | ||
| South south | 578(19.7) | 2358(80.3) | 2936(100.0) | ||
| South West | 269(8.8) | 2790(91.2) | 3059(100.0) | ||
| Total | 3965(15.9) | 21039(84.1) | 25004(100.0) | ||
| Place of residence | |||||
| Urban | 914(13.3) | 5960(86.7) | 6874(100.0) | ||
| Rural | 3051(16.8) | 15079(83.2) | 18130(100.0) | <0.0001 | |
| Total | 3965(15.9) | 21039(84.1) | 25004(100.0) | ||
| Possession of bed net in household | |||||
| No | 3404(16.1) | 17689(83.9) | 21093(100.0) | ||
| Yes | 506(16.3) | 2604(83.7) | 3110(100.0) | 0.035 | 0.0.85 |
| Total | 3910(16.2) | 20293(83.8) | 24203(100.0) | ||
| Children <5 yrs slept under bed net last night | |||||
| No | 425(17.3) | 2027(82.7) | 2452(100.0) | 2.92 | 0.085 |
| Yes | 580(15.69) | 3117(84.3) | 3697(100.0) | ||
| Total | 1005(16.3) | 5144(83.7) | 6149(100.0) | ||
| Type of bed net child slept under | |||||
| Treated net | 222(16.09) | 1158(.9) | 1380(100.0) | ||
| Untreated net | 283(16.4) | 1443(83.6) | 1726(100.0) | 0.054 | 0.82 |
| Total | 505(16.3) | 2601(83.7) | 3106(100.0) | ||
| Sex of child | |||||
| Male | 206816.3 | 10588(83.7) | 12656(100.0) | 4.47 | 0.034 |
| Female | 189715.4) | 10451(84.6) | 12348(100.0) | ||
| Total | 3965(15.9) | 21039(84.1) | 25004(100.0) | ||
| Wealth quintile of household | |||||
| Lowest (poorest) | 1106(17.04) | 5385(82.96) | 6491(100.0) | ||
| Second(poorer) | 978(16.6) | 4903(83.4) | 5881(100.0) | 30.78 | <0.0001 |
| Middle | 770(15.8) | 4105(84.2) | 4875(100.0) | ||
| Fourth(richer) | 651(15.4) | 3585(84.6) | 4236(100.0) | ||
| Highest(richest) | 460(13.1) | 3061(87.0) | 3521(100.0) | ||
| Total | 3965(15.9) | 21039(84.1) | 25004(100.0) | ||
| Age (months) | |||||
| <6 | 274(9.42) | 2635(90.58) | 2909(100.0) | ||
| 6-11 | 566(19.96) | 2270(80.04) | 2836(100.0) | ||
| 12-23 | 1027(21.03) | 3857(78.97) | 4884(100.0) | ||
| 24-35 | 800(17.77) | 3703(82.23) | 4503(100.0) | 263.67 | <0.0001 |
| 36-47 | 681(14.32) | 4703(85.68) | 4754(100.0) | ||
| 48-59 | 558(13.06) | 3713(86.94) | 4271(100.0 | ||
| Total | 3906(16.17) | 20251(83.8) | 24157(100.0) | ||
Row percentages presented
A total of 2,068(16.3%) male children had fever compared to 1,897(15.4%) females. (p = 0.034). More children had fever in the rural areas compared with the urban areas (16.8% and 13.3% respectively) (p < 0.0001). Children aged 6-11 months and 12-23 months reported more fevers (19.9% and 21% respectively) than other children (p < 0.0001). In addition, fever prevalence decreased significantly as wealth quintile increased. A total of 1,106(17.04%) children from the poorest (lowest wealth quintile) household had fever, 978(16.6%) from poorer households (second wealth quintile) had fever, while 460(13.1%) from the richest households had fever (p < 0.0001).
Multivariate predictors of fever
After controlling for all the predictors simultaneously in a multi-level model, fewer predictors remained significant (Table 2). Only age, sex of child and type of place of residence predicted the occurrence of fever. Wealth index and all bed net variables dropped out as predictors. Respondents in rural areas were more likely to have fever than those in urban areas (OR = 1.27, p < 0.0001, 95%CI: 1.16, 1.41). Children aged seven months and above were more likely to have fever than those less than six months. (p < 0.0001) The female children were less likely to have fever than their male counterparts (OR = 0.923, p = 0.022, 95% CI: 0.859, 0.988). However, the significant association of fever with wealth index in the bivariable analysis disappeared in the multi level logistic regression analysis. The children in the highest wealth quintile (richest) appeared to be less likely to have fever than the poorest (OR = 0.898, p = 0.75, 95% CI: 0.837, 1.14), but this association did not reach statistical significance. The estimated between region variance was 0.22(SE = 0.113) giving an ICC of 0.1.
Table 2.
Multilevel Logistic Regression analysis for determinants of childhood fever
| Odds Ratios | P value | 95% CI | |
|---|---|---|---|
| Type of Place of Residence | |||
| Urban | |||
| Rural | 1.27 | <0.0001 | 1.16 - 1.41 |
| Child's age | |||
| <6 months | |||
| 6-11 | 2.45 | <0.0001 | 2.13 - 2.91 |
| 12-23 | 2.64 | <0.0001 | 2.28 - 3.04 |
| 24-35 | 2.14 | <0.0001 | 1.84 - 2.47 |
| 36-47 | 1.65 | <0.0001 | 1.42 - 1.92 |
| 48-59 | 1.49 | <0.0001 | 1.28 - 1.74 |
| Wealth index of household | |||
| Poorest | |||
| Poorer | 1.03 | 0.57 | 0.93 - 1.13 |
| Middle | 1.01 | 0.91 | 0.90 - 1.12 |
| Richer | 1.01 | 0.91 | 0.89 - 1.14 |
| Richest | 0.98 | 0.75 | 0.84 - 1.14 |
| Literacy status of mother | |||
| Not literate | |||
| Literate | 0.93 | 0.38 | 0.800 - 1.089 |
Discussion
The overall prevalence of fever found in this survey is quite high when compared with the prevalence of fever in other SSA countries. Studies have shown that the prevalence of fever is less than 4.2% in the developed countries [2]. However similar fever prevalence has been reported in studies in other parts of the countries [15]. The regional analyses revealed that fever is more prevalent in the north central, followed by north east. A study on fever prevalence in northern Nigeria documented a prevalence of 56.9% among under fives seen in a primary health care center [16]. This pattern is also obtainable at both village and household levels especially among the children under the age of 5.
The analyses also showed that fever is higher in rural than urban areas. This may be associated with the high level of poverty in the rural areas. Poor people live in dwellings prone to mosquito proliferation. It has been shown that the characteristics of wall construction are associated with malaria prevalence [2]. In another study on rural-urban differential in maternal responses to childhood fever [17]; urban mother's responses to fever seem to be better than that of rural mothers. This might explain or corroborate the high prevalence of fever in the rural areas reported in this analysis.
The results of this analysis suggest that the possession of bed nets is not associated with fever. In addition, no association exists between "whether child slept under bed net and type of bed net child slept under". However, households that had bed nets reported less fever than those who did not though the difference did not achieve significance. This result is in line with other findings in other parts of Africa on the use of insecticide treated bed nets, and their effectiveness when studied on a population basis. A study conducted by Lengeler and Snow [18] showed that childhood mortality due to fever reduced significantly in areas where high percentage of children slept under bed nets. In another study on bed net use and malaria, those who used bed nets had better knowledge of malaria than non-users; however, this usage did not influence malaria morbidity at the household level [19]. The low rate of the possession of bed nets (which might be as a result of inability to afford them) might have accounted for the high prevalence of fever especially in rural areas in particular, and in villages where poverty is more pronounced. Preventive measures such as insecticide-treated bed nets are unaffordable to the poor if they must pay for them.
In the bivariate analysis, fever was found to be highest among the poor, followed by middle group, followed by the wealthiest group. On the basis of country-level data it was estimated that 57.9% of all deaths from malaria in the world in 1990 occurred among the poorest 20% of the world's population [20], but within the poor countries, there is evidence that the costs of malaria fall more heavily on the very poor. In Malawi, for instance, households with very low income carried a disproportionate share of the economic burden of malaria, with total direct and indirect cost of malaria consuming 32% of annual household income, compared with 4.2% among households in the low-to-high income categories [21]. In Tanzania, mortality in children younger than 5 years after acute fever was 39% higher among the poorest than in the least poor. The poorest (20%) of people in selected developing countries were as much as 2.5 times less likely to receive basic public health services as the least-poor [22]. Also, in India, malaria was linked to poverty, with an increase in the trend of malaria in states with stagnant economy [23].
Conclusions
While, overall bed net possession was low, less fever was reported in households that possessed bed nets. Malaria control strategies and interventions should be designed that will target the poor and make an impact on poverty. The results suggest that regional factors in Nigeria may be more influential in the risk of developing childhood fever than risks related to household wealth status. The mechanism through which wealth may affect malaria occurrence needs further investigation.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
All the authors conceived the study. OO was the principal investigator for Nigeria. DP and DB were collaborators from John Hopkins School of Public Health and contributed to the revising of the manuscript. OY conducted the analysis, BA and OO, contributed to data analysis and interpretation. OY and BA prepared the initial draft. All authors contributed to the draft. All authors read and approved the final manuscript.
Contributor Information
Oyindamola B Yusuf, Email: bidemi_yusuf@yahoo.com.
Babatunde W Adeoye , Email: bw_adeoye@yahoo.com.
Oladimeji O Oladepo, Email: oladepod@yahoo.com.
David H Peters, Email: dpeters@jhsph.edu.
David Bishai, Email: dbishai@jhsph.edu.
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