ArticlePDF Available

Malaria prevalence, anemia and baseline intervention coverage prior to mass net distributions in Abia and Plateau States, Nigeria

Authors:

Abstract and Figures

Nigeria suffers the world's largest malaria burden, with approximately 51 million cases and 207,000 deaths annually. As part of the country's aim to reduce by 50% malaria-related morbidity and mortality by 2013, it embarked on mass distribution of free long-lasting insecticidal nets (LLINs). Prior to net distribution campaigns in Abia and Plateau States, Nigeria, a modified malaria indicator survey was conducted in September 2010 to determine baseline state-level estimates of Plasmodium prevalence, childhood anemia, indoor residual spraying (IRS) coverage and bednet ownership and utilization. Overall age-adjusted prevalence of Plasmodium infection by microscopy was similar between Abia (36.1%, 95% CI: 32.3%-40.1%; n = 2,936) and Plateau (36.6%, 95% CI: 31.3%-42.3%; n = 4,209), with prevalence highest among children 5-9 years. P. malariae accounted for 32.0% of infections in Abia, but only 1.4% of infections in Plateau. More than half of children <=10 years were anemic, with anemia significantly higher in Abia (76.9%, 95% CI: 72.1%-81.0%) versus Plateau (57.1%, 95% CI: 50.6%-63.4%). Less than 1% of households in Abia (n = 1,305) or Plateau (n = 1,335) received IRS in the 12 months prior to survey. Household ownership of at least one bednet of any type was 10.1% (95% CI: 7.5%-13.4%) in Abia and 35.1% (95% CI: 29.2%-41.5%) in Plateau. Ownership of two or more bednets was 2.1% (95% CI: 1.2%-3.7%) in Abia and 14.5% (95% CI: 10.2%-20.3%) in Plateau. Overall reported net use the night before the survey among all individuals, children <5 years, and pregnant women was 3.4%, 6.0% and 5.7%, respectively in Abia and 14.7%, 19.1% and 21.0%, respectively in Plateau. Among households owning nets, 34.4% of children <5 years and 31.6% of pregnant women in Abia used a net, compared to 52.6% of children and 62.7% of pregnant women in Plateau. These results reveal high Plasmodium prevalence and childhood anemia in both states, low baseline coverage of IRS and LLINs, and sub-optimal net use--especially among age groups with highest observed malaria burden.
Content may be subject to copyright.
R E S E A R C H A R T I C L E Open Access
Malaria prevalence, anemia and baseline
intervention coverage prior to mass net
distributions in Abia and Plateau States, Nigeria
Gregory S Noland
1*
, Patricia M Graves
1,9
, Adamu Sallau
2
, Abel Eigege
2
, Emmanuel Emukah
3
, Amy E Patterson
1,10
,
Joseph Ajiji
4
, Iheanyichi Okorofor
5
, Oji Uka Oji
5
, Mary Umar
4
, Kal Alphonsus
2
, James Damen
6
, Jeremiah Ngondi
1
,
Masayo Ozaki
1
, Elizabeth Cromwell
1
, Josephine Obiezu
3
, Solomon Eneiramo
2
, Chinyere Okoro
7
,
Renn McClintic-Doyle
1
, Olusola Oresanya
8
, Emmanuel Miri
2
, Paul M Emerson
1
and Frank O Richards Jr
1
Abstract
Background: Nigeria suffers the worlds largest malaria burden, with approximately 51 million cases and 207,000
deaths annually. As part of the countrys aim to reduce by 50% malaria-related morbidity and mortality by 2013, it
embarked on mass distribution of free long-lasting insecticidal nets (LLINs).
Methods: Prior to net distribution campaigns in Abia and Plateau States, Nigeria, a modified malaria indicator
survey was conducted in September 2010 to determine baseline state-level estimates of Plasmodium prevalence,
childhood anemia, indoor residual spraying (IRS) coverage and bednet ownership and utilization.
Results: Overall age-adjusted prevalence of Plasmodium infection by microscopy was similar between Abia (36.1%,
95% CI: 32.3%40.1%; n = 2,936) and Plateau (36.6%, 95% CI: 31.3%42.3%; n = 4,209), with prevalence highest
among children 5-9 years. P. malariae accounted for 32.0% of infections in Abia, but only 1.4% of infections in
Plateau. More than half of children 10 years were anemic, with anemia significantly higher in Abia (76.9%, 95% CI:
72.1%81.0%) versus Plateau (57.1%, 95% CI: 50.6%63.4%). Less than 1% of households in Abia (n = 1,305) or
Plateau (n = 1,335) received IRS in the 12 months prior to survey. Household ownership of at least one bednet of
any type was 10.1% (95% CI: 7.5%13.4%) in Abia and 35.1% (95% CI: 29.2%-41.5%) in Plateau. Ownership of two or
more bednets was 2.1% (95% CI: 1.2%3.7%) in Abia and 14.5% (95% CI: 10.2%20.3%) in Plateau. Overall reported
net use the night before the survey among all individuals, children <5 years, and pregnant women was 3.4%, 6.0%
and 5.7%, respectively in Abia and 14.7%, 19.1% and 21.0%, respectively in Plateau. Among households owning nets,
34.4% of children <5 years and 31.6% of pregnant women in Abia used a net, compared to 52.6% of children and
62.7% of pregnant women in Plateau.
Conclusions: These results reveal high Plasmodium prevalence and childhood anemia in both states, low baseline
coverage of IRS and LLINs, and sub-optimal net useespecially among age groups with highest observed malaria
burden.
Keywords: Malaria, Plasmodium, Falciparum, Malariae, Anemia, Net use, Net ownership, Nigeria, LLIN, Bed net
* Correspondence: gnoland@emory.edu
1
The Carter Center, 453 Freedom Parkway, Atlanta, GA 30307, USA
Full list of author information is available at the end of the article
© 2014 Noland et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative
Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and
reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain
Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article,
unless otherwise stated.
Noland et al. BMC Infectious Diseases 2014, 14:168
http://www.biomedcentral.com/1471-2334/14/168
Background
In Nigeria, approximately 97% of the estimated 160 mil-
lion inhabitants are at risk of Plasmodium infection [1],
resulting in an estimated 51 million cases and 207,000
deaths annuallymore than any other country in the
world and approximately 25% of the total malaria burden
within Africa [2]. Malaria reportedly accounts for an esti-
mated 60% of outpatient visits in Nigeria, 30% of hospitali-
zations, 30% of under-five mortalities, 25% of infant
mortalities and 11% of maternal mortalities [3]. Beyond
the impact on human health, malaria exerts a large eco-
nomic burden on individuals and households, with the
loss due to protection, treatment and indirect costs esti-
mated to consume an estimated 132 billion Naira ($835
million) [4].
In 2008, the Nigerian Ministry of Health committed to
an ambitious goal of reducing by 50% malaria-related
morbidity and mortality by 2013 [5]. This is to be achieved
through scale-up for impact (SUFI) of World Health
Organization (WHO)-recommended prevention and con-
trol measures in order to provide protection for all at-risk
Nigerians. Specific targets set by the National Malaria
Control Strategic Plan for 2009-2013 include: at least 80%
of households own two or more insecticide treated nets
(ITN) by 2010; at least 80% of pregnant women and chil-
dren under five years of age sleep under an ITN nightly by
2010; at least 8% (by 2010) and 20% (by 2013) of house-
holds in targeted areas receive indoor residual spraying
(IRS); and 100% of pregnant women attending antenatal
care clinics receive two doses of intermittent preventative
therapy (IPTp) by 2013.
Use of ITNs is considered one of the most cost-effective
interventions against malaria in highly endemic areas [6].
ITNs are associated with significant reductions in malaria
morbidity and mortality [7], reduced complications associ-
ated with malaria in pregnancy [8], and reduced all cause
mortality [7]. In 2008, 8.0% of households in Nigeria
owned at least one ITN and only 2.7% owned two or more
ITNs, while use of ITNs was 6% among children under five
years and 5% among pregnant women [3]. Beginning in
2009, the National Malaria Control Programme launched
a two-pronged strategy for distribution of long lasting
insecticidal nets (LLINs) across the countrys 36 states
and Federal Capital Territory (FCT). The first catch-up
phase aimed to rapidly scale up LLIN ownership through
mass campaigns targeting the distribution of 64 million
LLINs (2 nets for each of 32 million households). The sec-
ond keep-upphase involves the expansion of routine dis-
tribution channels in order to sustain the high-level
coverage attained through universal mass distribution.
Routine channels, which include antenatal care clinics,
immunization clinics, school-based distributions, and the
commercial sector, had been utilized under previous na-
tional strategic plans to provide nets to pregnant women
and children under five yearspopulations considered
most vulnerable to malaria.
Administratively, Nigerias 36 states are divided into six
geo-political zones (Figure 1). The national demographic
and health surveys (DHS) of 2003 [9] and 2008 [3] pro-
vided net coverage estimates at the national and geo-
political zone level, while the national malaria indicator
survey (MIS) of 2010 [1] provided national and zonal esti-
mates of malaria intervention coverage as well as parasite
prevalence in children under five years. However, surveys
designed to evaluate the scale-up of malaria interventions
and parasite prevalence amongst all age groups with state-
level precision are lacking.
The Carter Center has helped to support net distribu-
tion efforts in Nigeria since 2004. This began with inte-
grated ITN distribution during mass drug administration
(MDA) for lymphatic filariasis and onchocerciasis [10].
Since anopheline mosquitoes can transmit both Plasmo-
dium and Wuchereria bancrofti parasites, nets provide
protection and reduce transmission of both diseases
simultaneously, while enabling programmatic efficiency
and cost savings [11,12]. In order to help evaluate the
impact of mass LLIN distribution in Abia and Plateau
States, The Carter Center coordinated a modified mal-
aria indicator survey on behalf of the state ministries of
health in September 2010, prior to the statesplanned
mass distribution campaigns. The goal of this survey
was to determine baseline state-level estimates of net
ownership and utilization, Plasmodium prevalence in all
age groups and anemia prevalence in children less than
11 years old in Abia and Plateau States, Nigeria.
Methods
Study area and sample selection
This study was conducted in September 2010 in Abia
State (population est. 3.2 million) located in the South
East Zone and Plateau State (population est. 3.6 million)
located in North Central Zone (Figure 1). Malaria trans-
mission in Abia is predicted to typically last ten months
or longer (March-December), while in Plateau, a shorter
seven-month seasonal transmission period predomi-
nates (May-November) [13].
A random cluster sampling design was used to select a
state-level representative sample in each state. The re-
quired sample size was based on detection of a 50% preva-
lence of malaria in children under five years with 5%
precision, α= 0.05 and a design effect of 2. Assuming a
70% response rate and that 80% of households include at
least one child less than five years of age, approximately
1400 households were required per state. Clusters were
defined as a census enumeration area (EA), or a randomly
selected segment of large EAs, with an expected average
of 25 households per cluster. Using a list of all EAs within
each state obtained from the Nigerian National Population
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 2 of 13
http://www.biomedcentral.com/1471-2334/14/168
Commission, 60 clusters per state were selected in system-
atic (equal interval) fashion with a random start. Survey
teams made a rough listing and sketch map of household
locations within each cluster, and if the number of house-
holds exceeded pre-defined thresholds, the cluster was
randomly divided into segments and one segment ran-
domly selected according to the Multiple Indicator Cluster
Survey (MICS) methods [14]. All households within se-
lected clusters were eligible for inclusion in the study. If
no one was home at the time of first visit, interviewers
returned later in the day in an attempt to include all eli-
gible households.
A household was defined as: a married man, his wives
and all of his dependents who currently live with him (in-
cluding biological children, adoptive children, domestic
workers, other family members for whom he is respon-
sible); an unmarried (widowed, divorced, never married)
woman who is recognized as the head of household and
Plateau
Abia
Legend
Figure 1 Study areas and Plasmodium prevalence by cluster. Plasmodium prevalence, diagnosed by microscopy, by survey cluster site in Abia and
Plateau States, Nigeria. State maps outline their constituent local government areas (LGAs), while the national map highlights the six geo-political zones
within Nigeria.
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 3 of 13
http://www.biomedcentral.com/1471-2334/14/168
all of her dependents who currently live with her; or two
or more unmarried adult persons who sleep in the same
dwelling unit and who share meals (e.g. university stu-
dents who share an apartment).
Survey questionnaire
The survey questionnaire was based on the Roll Back
Malaria Monitoring & Evaluation Reference Group
(MERG) Malaria Indicator Survey household and womens
questionnaires, modified for local conditions [15]. The
questionnaires were translated and printed in Hausa and
Igbo languages, and field tested prior to the survey.
Household interviews were conducted with consenting
heads of households or another resident adult if the head
of household was absent or unable to respond. Respon-
dents were asked about demographic information of usual
residents, standard socio-economic indicators, educational
level, household construction, indoor residual spraying as
well as mosquito net ownership, utilization, condition and
care (verified by direct observation). One woman of repro-
ductive age (1549 years) from each household was se-
lected at random to answer the womens questionnaire,
which included questions relating to malaria knowledge,
attitudes, practice, and exposure to malaria health mes-
sages. Geo-coordinates of each household were recorded
using handheld global positioning system units (Garmin
eTrex H, Garmin International).
Blood testing
All children ten years of age or younger as well as indi-
viduals of all ages in every third household were eligible
for malaria parasite testing by rapid diagnostic test
(RDT) and microscopy. RDT testing from finger prick
samples was used for on-site diagnosis and treatment of
malaria. CareStart Malaria HRP2/pLDH combo RDTs
(Access Bio, Inc., model G0131), which can discriminate
non-P. falciparum infections from pan-Plasmodium in-
fections, were used according to the manufacturers in-
structions. Thick and thin blood films were prepared by
laboratory technologists on a single slide, air dried and
stained with Giemsa on the day of collection. Blood films
were read by certified laboratory scientists in The Carter
Center laboratory in Owerri, Imo State (for Abia samples)
and The Carter Center laboratory in Jos, Plateau State (for
Plateau samples). A WHO-certified microscopist then re-
read all positive slides and 10% of the negatives from both
states for quality control. Individuals with positive RDT
results were offered on-site treatment according to na-
tional guidelines: artesunate-amodiaquine (Sanofi-Aventis
Groupe) or artemether-lumefantrine (Coartem, Novartis
AG) for non-pregnant individuals older than four months
of age, or sulfadoxine-pyrimethamine for self-reported
pregnant women. Individuals younger than four months
with a positive RDT test were referred to the nearest
health facility for further evaluation, as were RDT-negative
individuals with self-reported fever or other overt signs of
clinical illness. To enable maximum participation for
blood sampling, households with absentees were revisited
later the same day to recruit individuals missing at the first
visit.
Blood samples were also used for anemia testing in all
children under 11 years of age using handheld spectro-
photometers (Hb201+, HemoCue, Inc.). Anemia was
classified according to WHO guidelines [16] using altitude-
adjusted hemoglobin (Hb) values: mild (10.0 g/dL Hb
< 11.0 g/dL), moderate (7.0 g/dL Hb < 10.0 g/dL), severe
(Hb <7.0 g/dL) for children less than five years; and mild
(11.0 g/dL Hb < 11.5 g/dL), moderate (8.0 g/dL Hb
< 11.0 g/dL), severe (Hb <8.0 g/dL) for children 511 years.
Individuals with moderate anemia were provided treat-
ment according to national guidelines: presumptive
anti-malarial chemotherapy (artesunate-amodiaquine or
artemether-lumefantrine), iron supplementation (iron
syrup for those between four months and five years or
iron-folate tablets for children less than five years), and
a single dose 400 mg albendazole for children less than
two years. Individuals with severe anemia were referred
directly to the nearest health facility for evaluation and
treatment.
Data analysis
Completed questionnaires were checked by supervisors in
the field and inconsistencies verified with the respondents.
Data were double entered by different clerks in each state
and compared for consistency using EpiInfov3.5.3 (Cen-
ters for Disease Control and Prevention). Statistical analysis
was conducted using Stata v11.2 (StataCorp LP). Point esti-
mates and confidence intervals were derived using the
SURVEY (SVY) commands in Stata to account for cluster-
ing and sampling weights. Logistic regression models under
the SVY command were used to calculate Plasmodium
prevalence estimates for each state adjusted for age, cluster-
ing and sampling weights.
A household wealth index was constructed using the
methods of Vyas and Kumaranayake [17]. This index
was based on possession of assets (having electricity in
the household, a functioning radio and/or a functioning
television), type and location of usual water source, pos-
session of and type of latrine, house construction mate-
rials (wall, roof and floor), number of rooms and density
of people per room. The first principal component was
used to generate the asset index, which was then di-
vided into quintiles. The indicators percent of house-
hold with at least one net for every two peopleand
percent of population with access to a net within a
householdwere calculated using the methods of Kilian
and colleagues [18].
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 4 of 13
http://www.biomedcentral.com/1471-2334/14/168
Ethics considerations
This protocol received ethical clearance from the Emory
University Institutional Review Board (IRB#00044684),
and the Nigeria Health Research Ethics Committee
[NHREC/01/01/2007]. Verbal informed consent to partici-
pate in the household and womens interviews was sought
from heads of household or eligible women, respectively.
For blood testing, verbal informed consent was sought
from all eligible individuals older than 18 years of age or
from the parents of minors (017 years of age), as well as
additional verbal assent from minors over the age of six
years.
Results
Characteristics of study population
A total of 116 out of the selected 120 clusters were sam-
pled in Abia and Plateau States (Figure 1). Two clusters
each in Abia and in Plateau were not accessible due to
civil unrest or insecurity. Missing clusters were not re-
placed. Sampled clusters contained 1,426 households in
Abia (mean number of households per cluster: 24.6; range:
940) and 1,382 households in Plateau (mean number of
households per cluster: 23.8; range: 738). Of eligible
households, 121 (8.5%) in Abia and 47 (3.4%) in Plateau
were excluded from final analysis because no one was
present or because of refusal. This resulted in a study
population of 1,305 households in Abia and 1,335 in
Plateau.
Characteristics of surveyed households and individuals
are shown in Table 1. The mean number of individuals
per household and number of rooms used for sleeping
were lower in Abia than in Plateau. The mean elevation of
surveyed households was also significantly lower in Abia
(108.0 m; range: 11 m351 m) versus Plateau (815.0 m;
range: 117 m1344 m). Households in Abia were most
commonly (34.3%) classified in the highest wealth index
category, while households in Plateau were most com-
monly (28.0%) classified in the lowest wealth classification.
Most houses in Abia were made of cement or stone
block (81.4%), with a minor proportion built of mud and
sticks (14.2%) or mud bricks (2.8%), whereas in Plateau, a
greater diversity of construction types was observed be-
tween cement or stone blocks (40.9%), mud bricks
(33.7%), mud and stick construction (16.7%), and solid
brick construction (8.6%). The majority of roofs in both
Abia and Plateau were made of zinc or metal (87.4%,
70.9%, respectively) with the remained thatch/palm leaf
roofs (9.1%, 27.5%, respectively) or concrete/cement roofs
(1.0%, 1.1%, respectively).
Demographic data for the 14,057 individuals living in
the study households is also shown in Table 1. Age distri-
bution of individuals in surveyed households was generally
similar between states, as were the proportions of males,
females and self-reported pregnant women. There were
significantly more females (53.6%) than males (49.6%) in
Abia, but not in Plateau (49.5% and 50.5%, respectively).
Plasmodium prevalence
All children less than eleven years of age and individuals
of all ages in every third household were eligible for mal-
aria parasite testing by microscopy and rapid diagnostic
test (RDT). Microscopy results were available from 2,936
individuals in Abia and 4,209 individuals in Plateau. Over-
all age-adjusted prevalence of Plasmodium as detected by
microscopy was similar between Abia (36.1%, 95% CI:
32.3%40.1%) and Plateau (36.6%, 95% CI: 31.3%42.3%).
Crude prevalence by cluster ranged from 14.8% to 66.1%
in Abia and from 1.8% to 86.4% in Plateau (Figure 1).
Cluster prevalence was negatively, but poorly, associated
with elevation in Abia (r
2
=0.014)andPlateau(r
2
=0.142).
Table 1 Characteristics of study households and individuals
in Abia and Plateau states, Nigeria, September 2010
Abia Plateau
Number of clusters sampled 58 58
Household characteristics
Number of households sampled 1,305 1,335
Mean (SD) number of people per household 4.4 (2.7) 6.3 (3.1)*
Mean (SD) number of sleeping
rooms per household
1.9 (1.1) 2.4 (1.2)*
Altitude
100 m (%) 55.1 0.0*
1001000 m (%) 44.8 46.3
>1000 m (%) 0.2 53.7*
Household wealth index, quintiles
Poorest (%) 6.9 28.0*
Second (%) 11.8 25.7*
Third (%) 21.2 17.0
Fourth (%) 25.9 18.0
Richest (%) 34.3 11.3*
Individual characteristics
Number of persons in sampled households 5,754 8,303
Age
<5 yrs (%) 14.7 16.4
5-9 yrs (%) 12.0 16.0*
10-14 yrs (%) 9.9 11.9
15-19 yrs (%) 9.3 9.8
20-49 yrs (%) 35.5 36.7
50 yrs (%) 18.6 9.3*
Proportion female (%) 53.6 49.6
Pregnant women, self-reported
(% of all individuals/% of women)
2.5/4.6 2.1/4.3
*Asterisk indicates statistically significant difference between states
(non-overlapping 95% confidence intervals).
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 5 of 13
http://www.biomedcentral.com/1471-2334/14/168
In Abia, 68.1% of infections were identified as Plasmo-
dium falciparum, 32.0% were Plasmodium malariae with
one instance of P. falciparum-P. malariae co-infection. In
Plateau, 98.7% of infections were P. falciparum,1.4%
P. malariae and two instances of co-infection. No Plasmo-
dium ovale infections were identified in either state. Preva-
lence of Plasmodium infection was significantly associated
with age in both Abia (χ
2
= 136.62, P < 0.001) and Plateau
(χ
2
= 326.45, P < 0.001), with prevalence highest in the 5
9 year age group and lowest in those aged 50 years and
older (Figure 2). Infection was non-significantly higher
in males in both states, and significantly and inversely
associated with wealth in Abia (χ
2
= 122.96, P < 0.001)
and Plateau (χ
2
= 318.25, P < 0.001).
Blood samples were tested by RDT for on-site provision
of treatment for positive individuals. Concordant results
were obtained from 6,502 of 6,771 samples with valid
results for both microscopy and RDT (96.0% agreement;
κ= 0.919). Overall age-adjusted prevalence of Plasmodium
as determined by RDT was similar between Abia (30.4%,
95% CI: 25.7%35.4%) and Plateau (32.4%, 95% CI:
26.6%38.9%), with a significantly higher proportion of
non-P. falciparum infections in Abia (40.0%) than in Plat-
eau (0.7%), in line with microscopy results.
Anemia
Mean unadjusted hemoglobin among children less than
11 years of age was significantly lower in Abia (9.9 g/dL,
95% CI: 9.710.1 g/dL) versus Plateau (10.9 g/dL, 95%
CI: 10.611.2 g/dL). After adjusting for age and altitude,
more than half of children were anemic (any type) in
both states (Table 2), with anemia significantly more
prevalent in Abia (76.9%, 95% CI: 72.1%81.0%) than in
Plateau (57.1%, 95% CI: 50.6%63.4%). In Abia, there
was a significantly greater proportion of children with
both moderate anemia and severe anemia compared to
Plateau. Anemia was significantly more prevalent among
children less than 5 years (64.7%, 95% CI: 58.3%70.6%)
compared to children five years and older (50.3%, 95%
CI: 43.0%57.6%) in Plateau, with a similar trend ob-
served in Abia (80.5%, 95% CI: 75.1%84.9%; 73.1%, 95%
CI: 67.4%78.2%).
Malaria prevention measures
Less than one percent of households in Abia (0.4%) and
Plateau (0.6%) reported that indoor residual spraying
(IRS) with insecticide had been performed in the past
12 months (Table 3).
Household ownership of at least one bednet (of any type)
was 10.1% in Abia and 35.1% in Plateau. Only 2.1% of
households in Abia and 14.5% of households in Plateau
owned two or more nets. Likewise, 1.4% and 6.3% of all
households in Abia and Plateau, respectively, owned at least
one net for every two household members and 14.2% and
18.1% of households that owned nets in Abia and Plateau,
respectively, had enough nets for every two persons. While
net ownership was greatest among the highest wealth index
category in both states, there was not a significant associ-
ation between net ownership and quintiles of household
wealth index in either Abia (χ
2
= 9.01, P = 0.28) or Plateau
(χ
2
= 17.29, P = 0.17).
The mean number of nets per household was signifi-
cantly lower in Abia versus Plateau, whether considering
all households (0.1 nets versus 0.6 nets) or only those
households that owned at least one net (1.2 nets versus
1.7 nets), Table 3. The most frequently reported reasons
for not owning a net in households without nets include:
nets not available (56.3% in Abia, 44.3% in Plateau), nets
0
10
20
30
40
50
60
70
<5 5-9 10-14 15-19 20-49 >=50
Percent positive (%)
Age group (years)
Abia Plateau
Figure 2 Plasmodium prevalence. Proportion of individuals testing positive for Plasmodium infection by microscopy, by age group, Abia and
Plateau States, Nigeria, September 2010. In Abia, 68.1% of all infections were P. falciparum, 32.0% P. malariae with one co-infection; in Plateau,
98.7% of infections were P. falciparum, 1.4% P. malariae with two co-infections. Error bars are 95% confidence intervals.
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 6 of 13
http://www.biomedcentral.com/1471-2334/14/168
are too expensive (25.4%; 35.9%). Very few people re-
ported not liking nets (0.9% in Abia, 1.7% in Plateau) or
no mosquitoes (5.2%, 1.7%) as reasons for not owning
nets. Overall, 8.2% of the population in Abia and 23.8% of
the population in Plateau had access to a net within a
household, assuming a net is used by two people (Table 3).
As shown in Table 4, reported net use the night prior to
the survey among all individuals in all households was sig-
nificantly lower in Abia (3.4%, 95% CI: 2.1% 5.5%) versus
Plateau (14.7%, 95% CI: 11.3% 18.9%). Reported net use
was positively associated with wealth in Plateau (χ
2
=
172.67, P = 0.002), but not Abia (χ
2
=40.64, P=0.17). Re-
ported net use was also significantly associated with age in
both Abia (χ
2
= 29.93, P = 0.007) and Plateau (χ
2
=101.22,
P < 0.001), with net use highest among children less than
five years in both states (Figure 3). Reported net use was
significantly lower in Abia for all age groups except those
1519 years. Reported net use among pregnant women
was also lower in Abia (5.7%) versus Plateau (21.0%).
There was no difference in net use between males and
females in either Abia (χ
2
= 1.35, P = 0.30) or Plateau (χ
2
=
1.92, P = 0.12).
The same trends were observed when restricted only to
households owning at least one net. Net use was lower in
Abia versus Plateau among all individuals (27.6%, 95% CI:
20.1%36.6%; vs. 41.1%, 95% CI: 36.5%45.9%, respect-
ively), children under five years (34.4% vs. 52.6%) and preg-
nant women (31.6% vs. 62.7%) (Table 4). In this smaller
subset, associations between net use and age (χ
2
= 11.25,
P = 0.14), gender (χ
2
= 1.30, P = 0.26) and wealth (χ
2
=
10.80, P = 0.50) were not evident in Abia. In Plateau, signifi-
cant associations with age (χ
2
= 143.79, P < 0.001) and
wealth (χ
2
= 67.09, P = 0.009), but not gender (χ
2
= 3.17,
P = 0.10) were observed.
Characteristics of nets observed in Abia (n = 150) and
Plateau (n = 807) are summarized in Table 5 along with
confidence intervals for all point estimates. The majority
of nets in both states were identified as LLINs, with a sig-
nificantly lower proportion in Abia (65.6%) versus Plateau
(89.5%). Baby nets (nets on a folding free standing wire
frame, suitable for placing over a sleeping infant) com-
prised a significantly greater proportion of all nets in Abia
(17.4%) compared to Plateau (0.5%). Approximately half of
all nets in Abia (49.4%) and Plateau (50.7%) were report-
edly obtained less than 12 months prior to the survey. In
Abia, nets were most frequently obtained from health fa-
cilities (37.0%) and markets (32.2%). Other sources include
shops (14.4%), received as a gift (8.7%), mass distribution
campaigns (4.4%), and community health worker apart
from mass distribution (2.2%). In Plateau, nets were also
most frequently obtained from markets (38.4%) and health
facilities (30.3%). The remainder were obtained from mass
distribution campaigns (17.4%), received as a gift (6.5%),
shops (2.4%), various other source (2.4%) and community
health worker (1.9%). Around half of all nets in both Abia
(49.0%) and Plateau (47.5%) were reportedly purchased.
The majority of nets in Abia (74.7%) and Plateau
(86.1%) were reportedly used at least once. The propor-
tion of nets hanging at the time of survey was signifi-
cantly lower in Abia (52.3%) compared to Plateau
(79.2%). Nearly all of the hanging nets in both states
Table 2 Anemia prevalence in children less than 11 years
of age in Abia and Plateau states, Nigeria, September 2010
Abia (n = 1,556) Plateau (n = 2,823)
% (95% CI) % (95% CI)
Normal
1
23.2 (19.027.9) 45.0 (38.252.0)*
Mild
2
16.1 (14.018.3) 18.5 (16.720.4)
Moderate
3
53.1 (47.858.3) 33.6 (28.139.5)*
Severe
4
7.8 (5.810.3) 3.0 (2.33.8)*
1
For age <5 years: hemoglobin [Hb] 11.0 g/dL; for age
511 years: Hb 11.5 g/dL.
2
For age <5 years: 10.0 g/dL < Hb < 11.0 g/dL; for age
511: 11.0 g/dL < Hb < 11.5 g/dL.
3
For age <5 years: 7.0 g/dL < Hb < 10.0 g/dL; for age
511: 8.0 g/dL < Hb < 11.0 g/dL.
4
For age <5 years: Hb <7.0 g/dL; for age 511: Hb <8.0 g/dL.
*Asterisk indicates statistically significant difference between states
(non-overlapping 95% confidence intervals).
Table 3 Household malaria prevention measures, Abia and Plateau states, Nigeria, September 2010
Abia (n = 1,305) Plateau (n = 1,335)
Percent of households that received IRS in past 12 months (95% CI) 0.4% (0.11.4) 0.6% (0.31.5)
Percent of households owning at least one net (95% CI) 10.1% (7.513.4) 35.1% (29.241.5)*
Percent of households owning two or more nets (95% CI) 2.1% (1.23.7) 14.5% (10.220.3)*
Percent of households with at least one net for every two people (95% CI) all households 1.4% (0.82.1) 6.3% (3.88.8)*
Percent of households with at least one net for every two people (95% CI) households
with at least one net
14.2% (8.819.6) 18.1% (13.323.0)
Mean number of nets per household (95% CI) all households 0.1 (0.10.2) 0.6 (0.40.7)*
Mean number of nets per household (95% CI) households with at least one net 1.2 (1.11.3) 1.7 (1.51.8)*
Percent of population with access to net within a household (assuming net used by two people) (95% CI) 8.2% (3.7-6.9) 23.8% (14.5-24.1)*
*Asterisk indicates statistically significant difference between states (non-overlapping 95% confidence intervals).
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 7 of 13
http://www.biomedcentral.com/1471-2334/14/168
(95.2%; 97.7%, respectively) were hung at an appropriate
heighti.e. able to be tucked in under sleeping mat on
floor or mattress on bed. The most commonly reported
reasons for not hanging nets in each state included: re-
spondent did not want to use net (40.0% in Abia, 28.4%
in Plateau), have not yet hung it (14.6%; 12.9%), were too
tired to hang it last night (9.1%; 5.6%) and dont know how
to hang it (10.9%; 2.2%). Various other reasons were re-
ported by less than 10% of respondents as shown in Table 5.
Themajorityofnetswerereportedlyusedbyahousehold
member the previous night in Abia (60.6%) and Plateau
(80.4%), with use significantly higher in Plateau. Reasons
why nets were not used last night are listed in Table 5. No
single reason was reported by more than 18% of respon-
dents. The proportions of nets with holes were similar in
Abia (17.7%) and Plateau (16.5%), as were the proportions
of nets with mends (10.7%; 5.4%, respectively).
Additional reported methods used for protection
against mosquitoes or other nuisance insects include:
mosquito coils (used by 37.7% and 27.8% of households
in Abia and Plateau, respectively), canned insect spray
(31.4%; 22.9%), Otapiapia, an organophosphate-based
pesticide in liquid form (dichlorvos), approved for use in
grain storage areas but widely available locally from shops
and traders (19.5%; 38.6%; significantly higher in Plateau),
Piff Puff, a synthetic pyrethroid-containing insecticide
powder (9.9%; 12.8%). Other reported methods such as
burning leaves (<6% of households) and using repellent
soaps or creams (<1%) were uncommon in either state.
Discussion
This study was conducted in September 2010 prior to
planned mass distribution campaigns in Abia and Plateau
States, which took place in August 2012 and December
2010, respectively. The results document high levels of
Plasmodium infection and anemia in both states, extremely
low (<1%) IRS coverage and low bed net ownership and
use. Low IRS coverage across the sampled population is not
unexpected, as IRS in Nigeria is limited to targetareas in-
cluding: densely populated municipalities, areas with short
malaria transmission seasons, areas where LLINs are diffi-
cult to implement, and institutional locations [5].
Table 4 Reported net use, Abia and Plateau states, Nigeria, September 2010
Abia Plateau
n% (95% CI) n% (95% CI)
All households
All individuals 5,754 3.4 (2.15.5) 8,303 14.7 (11.318.9)*
Children <5 years 853 6.0 (3.79.6) 1,384 19.1 (14.225.0)*
Pregnant women (self-reported) 129 5.7 (1.915.8) 186 21.0 (14.329.8)
Households owning at least 1 net
All individuals 648 27.6 (20.136.6) 3,161 41.1 (36.545.9)
Children <5 years 135 34.4 (24.246.2) 534 52.6 (44.260.9)
Pregnant women (self-reported) 19 31.6 (12.061.0) 72 62.7 (49.274.4)
*Asterisk indicates statistically significant difference between states (non-overlapping 95% confidence intervals).
0
5
10
15
20
25
30
<5 5-9 10-14 15-19 20-49 >=50
Percent (%)
A
g
e
g
roup (years)
Abia Plateau
Figure 3 Net use. Proportion of individuals who reported sleeping under a net the night prior to survey, by age group, Abia and Plateau States,
Nigeria, September 2010. Error bars are 95% confidence intervals.
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 8 of 13
http://www.biomedcentral.com/1471-2334/14/168
Around the same time (October 2010), the first national
malaria indicator survey (MIS) was conducted throughout
Nigeria in order to evaluate the scale-up of malaria pre-
vention and control measures [1]. While the MIS provides
national and zone-level estimates for interventions, state-
level evaluation is also critical as mass net distribution
campaigns are done on a state-by-state basis. In addition,
since state campaigns have been conducted in different
years, many of the 2010 MIS aggregate zonal estimates
combine data from states that had already completed mass
LLIN distribution with others that had not. As far as we are
aware, this study is the first to report baseline estimates of
malaria prevention measures, malaria prevalence and
anemia in individual Nigerian states prior to scaledup
mass distribution campaigns targeting universal coverage.
Overall age-adjusted Plasmodium prevalence by mi-
croscopy (all ages) was similar between Abia (36.1%)
and Plateau (36.6%) with almost one third of infections in
Abia state being P.malariae. These represent some of the
only modern estimates of Plasmodium prevalence across
all age groups in Nigeria, as recent surveys including 2010
MIS tend to focus on specific sub-populations like chil-
dren [1,19,20], neonates [21,22], pregnant women [23], or
those infected with HIV [24-26]. Prevalence estimates for
children under five years by microscopy were similar for
Plateau (43.5%, 95% CI: 36.6%50.7%) compared to the
2010 MIS estimate for the larger area of the North Central
zone in which it is located (49.4%, CI not reported), but
likely different in Abia (42.0%, 95% CI: 35.7%48.6%) com-
pared to the 2010 MIS South East zone estimate (27.6%, CI
not reported) [1]. One recent study conducted among all
aged individuals during the dry season in Lagos State,
South West zone, estimated an overall prevalence of 14.7%,
Table 5 Net characteristics in sampled households, Abia
and Plateau states, Nigeria, September 2010
Abia
(n = 150)
Plateau
(n = 807)
% (95% CI) % (95% CI)
Net type
LLINs 65.6 (54.075.5) 89.5 (84.293.1)*
Pre-treated net 0.8 (0.15.8) 0.4 (0.11.4)
Untreated net 5.8 (1.125.0) 3.3 (1.95.7)
Other 0 0.3 (0.11.0)*
Dont know or missing 27.8 (19.338.3) 6.5 (3.611.6)*
Proportion baby nets 17.4 (9.330.3) 0.5 (0.21.5)*
Net age
6 months 26.6 (18.536.5) 28.5 (20.238.6)
6-12 months 22.8 (13.735.4) 22.2 (16.928.5)
> 12 months 43.2 (32.854.1) 47.2 (39.655.0)
Dont know or missing 7.5 (3.913.9) 2.1 (1.23.6)*
Source of nets
Market 32.2 (20.546.4) 38.4 (28.749.3)
Health facility 37.0 (24.251.9) 30.3 (22.140.1)
Mass distribution 4.4 (1.412.8) 17.4 (9.030.9)
Shop 14.4 (4.736.5) 2.4 (1.15.4)
Gift 8.7 (4.615.9) 6.5 (3.910.6)
Community health
worker (non-campaign)
2.2 (0.76.2) 1.9 (1.03.8)
Other 0.9 (0.23.6) 2.4 (1.06.0)
Proportion of nets purchased 49.0 (37.560.6) 47.5 (37.657.7)
Proportion of nets ever used 74.7 (64.582.7) 86.1 (80.090.5)
Proportion nets observed hanging 52.3 (40.963.5) 79.2 (72.584.7)*
Proportion of hanging nets
hung at appropriate height
95.2 (82.098.9) 97.7 (94.599.0)
Reasons why net was not hung
(multiple responses possible)
Do not want to use net 40.0 (22.560.5) 28.4 (16.244.8)
Have not yet permanently hung 14.6 (7.526.5) 12.9 (5.029.5)
Too tired to hang 9.1 (3.223.1) 5.6 (1.618.2)
Dont know how to hang 10.9 (4.424.5) 2.2 (0.86.0)
Inconvenient 3.6 (1.012.6) 7.3 (3.414.8)
Too hard to hang 7.3 (1.825.6) 3.3 (1.29.2)
No space for net 5.5 (0.927.8) 2.8 (0.89.2)
Person responsible
for hanging absent
1.8 (0.212.4) 0.6 (0.14.3)
Other 20.0 (8.839.3) 31.4 (21.443.6)
Proportion nets used last night 60.6 (49.970.4) 80.4 (73.286.0)*
Reasons why net was not used last
night (multiple responses possible)
Usual user did not
sleep here last night
17.4 (8.233.3) 1.6 (0.55.3)*
Net not needed last night 4.4 (1.214.5) 14.1 (9.121.2)
Table 5 Net characteristics in sampled households, Abia
and Plateau states, Nigeria, September 2010 (Continued)
Cannot hang net 12.0 (6.122.3) 6.4 (3.013.1)
No mosquitoes 8.7 (3.918.4) 9.4 (3.423.7)
Net too old or torn 13.0 (6.225.5) 4.7 (1.910.9)
Net not available last
night (washing)
3.3 (0.421.2) 12.5 (6.223.8)
Too hot 10.9 (3.926.7) 3.3 (1.29.1)
Feel closed in or afraid 6.5 (1.821.3) 5.3 (1.219.9)
No malaria 0 5.7 (1.519.6)*
Net too dirty 4.4 (1.413.1) 0.6 (0.13.6)
Dont like smell 2.2 (0.314.5) 2.6 (0.97.5)
Other 20.7 (11.434.5) 24.7 (14.838.3)
Dont know 4.4 (0.919.4) 7.9 (2.820.4)
Proportion nets with holes 17.7 (10.129.2) 16.5 (12.022.2)
Proportion nets with mends 10.7 (4.124.8) 5.4 (3.58.4)
*Asterisk indicates statistically significant difference between states
(non-overlapping 95% confidence intervals).
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 9 of 13
http://www.biomedcentral.com/1471-2334/14/168
with prevalence highest in the 514 year age group [27].
This trend with age is consistent with our results, where
prevalence was highest in the 59and1014 age groups in
both Abia and Plateau.
A high level of concordance was observed in Plasmo-
dium prevalence between microscopy and RDT, though
RDT-estimates were slightly lower than microscopy. This
contrasts with observations from other large surveys that
consistently observe higher RDT-prevalence attributed to
antigen persistence following treatment or submicroscopic
infections [28]. Differences between this study and MIS
2010 results in RDT-prevalence estimates for children
under five years were less pronounced than for micros-
copy results. However, unlike our study, which utilized a
Pf/Pan combination RDT, the MIS 2010 utilized Para-
check PF®, an RDT that only detects P. falciparum-specific
histidine-rich protein-2. MIS RDT results thus likely
underestimated the overall Plasmodium prevalence in
some areas through undiagnosed non-falciparum infec-
tions, as nearly one third of malaria infections in Abia in
the present study were identified as P. malariae by mi-
croscopy. A significant proportion of non-falciparum in-
fections were also identified by microscopy in South East
and North Central zones in the MIS 2010 [1]. Historically,
a significant proportion of P. malariae and P. ovale infec-
tions were also reported by The Garki Project, in Kano
State, North West zone, from 1969 to 1976 [29]. Taken to-
gether, these results demonstrate that non-falciparum in-
fections are prevalent in parts of Nigeria and highlight the
importance of utilizing multi-species RDTs to monitor
trends of all Plasmodium parasites. In addition to variation
in prevalence between species, our study highlights large
heterogeneity in prevalence between clusters within states
that deserves further investigation to improve malaria risk
stratification of all species in Nigeria.
In this study, more than half of children less than 11 years
in both states were found to be anemic (mild, moderate or
severe), with prevalence higher in Abia than in Plateau and
also higher among children less than 5 years. Our results
are consistent with WHOs estimate that two-thirds of
preschool-age children in Africa are anemic [30], and
within Nigeria, are similar to those from the 2010 MIS,
which found 71.7% anemia prevalence in South East zone
and 56.0% in North Central zone among children under
five [1]. Malaria is a major cause of childhood anemia in
malaria endemic areas where it accounts for approximately
half of pediatric admissions for severe anemia [31,32].
Given the similar malaria prevalence between the two
states, it is not immediately clear why anemia was signifi-
cantly higher in Abia. Perhaps the higher prevalence of
P. malariae or the slightly longer malaria transmission sea-
son may contribute. Other causes of anemia include iron
and other nutritional deficiencies, blood disorders, inflam-
mation and other acute and chronic diseases [16]. Thus
differences in diet and genetic composition may also con-
tribute to higher anemia in Abia. However, we hypothesize
that repeated statewide MDA in Plateau, but not Abia, of
deworming drugs from 20032012 for the elimination of
lymphatic filariasis, as well as since 2008 for treatment of
schistosomiasis in school-age children [33,34], may have
reduced the prevalence of helminth infections that have
been shown to interact with malaria infection to worsen
anemia [35]. Indeed, a recent survey of school-aged chil-
dren has confirmed a higher prevalence of hookworm in-
fection in Abia compared to Plateau (D. Evans, personal
communication).
Prior to 2009, Nigerias policy was to provide free net
distribution to children under five and pregnant women
(vulnerable groups) only. As part of Nigerias aim to re-
duce by 50% malaria-related morbidity and mortality by
2013, the country embarked in 2009 on a strategy of
scaled-up mass distribution of universal coverage with free
long-lasting insecticidal net (LLINs) across the 36 states
and Federal Capital Territory. The new policy goal is to
reach at least 80% of households with an average of two
nets per household but the delivery of nets for these
scaled-up distributions, supported by The Global Fund
and other donors, took place over a five year period
(2009-2013) on a state-by-state basis.
The net ownership figures estimated here for both states
in 2010 are much lower than the current ministry target,
reflecting previous policy. In order to place our state-level
results in the context of previous net distribution strategy
and coverage estimates, we reviewed results from the
DHS 2003 [9] the study of Oresanya et al [36], the DHS
2008 [3], and the MIS 2010 [1] that reported zonal level
estimates. In the South East zone (a group of five states in-
cluding Abia, Figure 1), household net ownership of at
least one net of any type was 5.8% in 2003, reportedly in-
creased after scale up to 36.5% in 2005, decreased to
13.4% in 2008 and was up to 35% in MIS 2010. Our esti-
mate of ownership for Abia state only in 2010 (10.1%) was
surprisingly low, given that many more than 10% of
households would have a vulnerable group member. It
could be explained by 1) lack of net replacement since
2005, although we note that half of the nets in Abia in the
present study were less than one year old; or 2) inter-state
differences between Abia and other states within the
South East zone, perhaps mainly reflecting the mass distri-
bution in Anambra State that took place in 2009. Similar
review of net ownership in North Central zone (a group of
six states including Plateau, Figure 1), showed it to be
14.9% in 2003 [9], 19.0% in 2005 [36], 15.9% in 2008 [3]
and 32.7% in MIS 2010 [1]. The latter estimate was similar
to results of the current study in Plateau State only
(35.1%) and suggests a large increase in net ownership
from 2008 to 2010. Despite these similar estimates for
state and zone, intra-zonal differences between states also
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 10 of 13
http://www.biomedcentral.com/1471-2334/14/168
likely exist in North Central zone; for example scale up to
universal coverage occurred in 2009 in Niger State and
likely biased the zone estimate upwards. The higher own-
ership overall in Plateau may be partly due to efforts by
The Carter Center to increase and maintain net ownership
by integrating distribution with MDA for onchocerciasis
and lymphatic filariasis [10]. As in Abia, approximately half
of nets observed in Plateau were less than one year old.
The wide variation between states in both baseline coverage
and in past and future timing of scale up distribution high-
lights the importance of state-level surveys in evaluating
the impact of Nigeriasmassnetdistributionstrategy.
In both Abia and Plateau, household members had
taken the initiative to purchase about half of the nets cur-
rently owned, despite differences in wealth profiles be-
tween the two states. Around one-third of nets in both
Abia (37.0%) and Plateau (30.3%) had been obtained
through health facilities, although not all such nets were
provided free-of-charge: 9.8% and 19.4% of nets obtained
from health facilities in Abia and Plateau, respectively,
were reportedly purchased. One third of all nets were ob-
tained from markets or shops, indicating significant exist-
ing demand for nets prior to statewide mass distribution,
as was also observed in Enugu State, South East zone [37].
Unlike the present results, other studies of net ownership
in Nigeria have observed inequity prior to mass distribu-
tion campaigns, though with conflicting trendssome re-
port highest ITN ownership among wealthiest households
[3,38], while an earlier report found inverse associations
with wealth [9]. It will be important to document whether
demand for nets translates into sustained net use in
Nigeria once the access to free nets increases, as studies
from other African countries have revealed declines in net
use among households owning nets following mass distri-
bution campaigns [39,40].
Net use estimates follow similar trends to ownership.
Overall net use in 2010 estimated in this study for children
under five years and pregnant women in Abia (6.0%; 5.7%,
respectively) and Plateau (19.1%; 21.0%) was far below
ministry target of 80% for both populations. Past trends in
the South East zone for net use by children under five in
all households show it was 4.4% in 2003 [9], 16.0% in 2005
[36], 14.3% in 2008 [3] and 17.4% in MIS 2010 [1]. For
pregnant women in South East (not assessed in 2005) the
corresponding figures were 2% in 2003, 10.2% in 2008 and
12% in MIS 2010. These indicate substantial heterogeneity
in net use within the South East zone and that Abia was
lower than its zone average in 2010, although this is to be
expected given the low net ownership. In North Central
zone, trends in net use by under fives were fairly stable at
8.9% in 2003 [9], 7.3% in 2005 [36] and 9.7% in 2008 [3]
but doubled to 18.9% by MIS 2010 [1]. Pregnant women
showed a similar trend at 9.2% in 2003 and 9.4% in 2008
but greater increase by MIS 2010 to 36.7%. Thus Plateau
state was above average in net use by children under five
(19.1%) and below average for pregnant women (21.0%)
compared to its surrounding zone.
Among households that owned nets, net use by children
under five and pregnant women was five-fold higher in
Abia and 2.5- to 3-fold higher in Plateau compared to all
households; however, only about one third (in Abia) and
one half (in Plateau) of vulnerable groups reported sleep-
ing under a net the previous night. Yet 61.3% of nets in
Abia and 80.4% of nets in Plateau were reportedly used by
a household member last night, indicating that nets are
being used by persons other than children under five and
pregnant women within households, especially in Abia.
Use by other members is not surprising given that the
mean number of individuals per household in each state
exceeds by a factor of 3.7 the number of nets currently
available per household. Analysis of the early scale-up of
malaria prevention measures across sub-Saharan Africa
has shown that the primary driver of net use is the relative
availability of nets within households [41], and recent ap-
plication of additional MERG-recommended net indica-
tors to 2010 MIS data demonstrates that 61% and 71% of
households with an ITN in South East and North Central
zones, respectively, did not have enough nets for each
household member (defined as one ITN per two persons)
[18]. Using the same indicator, we found that 86% and 82%
of households with a net (of any type) in Abia and Plateau,
respectively, did not have sufficient number of nets.
Previous studies [38,41] have observed that net use
among children is not significantly associated with
household wealth after net distributions. In the present
study, which was conducted prior to mass distributions,
net use was positively associated with wealth in Plateau,
but not in Abia. Interestingly, DHS 2008 and MIS 2010
both reported inverse associations between wealth and
net use at the national level [1,3]. Also in contrast to
other studies, which reveal a female bias in net use in
Nigeria [1,42], significant differences between the sexes
were not observed in either state in the present study.
Age was significantly associated with net use among all
households in Abia and Plateau, which was highest in chil-
dren under five and those over 20 years. This is in agree-
ment with other surveys from Nigeria [1,38,42], which
consistently observe that net usage is lowest among older
children and young adults. This finding is very important
given that older children are the group with highest preva-
lence of Plasmodium infection. In addition to improving
access to nets, this points to a significant need for educa-
tion regarding malaria prevention and net use, including by
children over five years old. That this is needed even among
those who own nets is illustrated by the finding that not
wanting to use netwas the most common reason for nets
not being hung last night and that 25% of nets in Abia had
never been used.
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 11 of 13
http://www.biomedcentral.com/1471-2334/14/168
In an effort to address these gaps, The Carter Center has
developed behavior change communication (BCC) mate-
rials that emphasize strategies for increasing net use that
were identified among consistent net users during focus
group discussions conducted in Plateau State. In addition,
BCC materials incorporate health education about lymph-
atic filariasis and malaria. This innovative, integrated
health messaging approach was driven by the fact that
both diseases share the same Anopheles vector and the be-
lief that heightened awareness of LF-associated sequelae,
which include swelling of the limbs (lymphedema, ele-
phantiasis) and genital organs (hydrocele), is likely to pro-
mote increased net usage, particularly among adolescents
and males.
As with any survey, there are limitations to note. Re-
sults from this study represent a single cross-sectional
sample, which was collected during peak malaria sea-
son. We compared results with the 2010 MIS survey,
which was conducted approximately one month after
our survey. However, the DHS surveys of 2003 and 2008
were conducted during the months of March to August
and June to October, respectively, which overlap periods
of typically lower malaria transmission. Care should thus
be taken when comparing our results with the DHS, par-
ticularly malaria parasite prevalence estimates, as well as
utilization of malaria prevention measures, since net use
has been observed to decline during dry seasons [43-45].
Studies of this type are also reliant upon self-reported data
for many questions. In an effort to verify net ownership
and ever-use of nets, survey teams visually inspected nets
within households and observed whether the net was still
sealed in its original packaging. However, it was not
possible to verify use of net the previous night or other
self-reported data. The survey was also conducted by inde-
pendent groups of survey teams in each state, and uniden-
tified sources of systematic error between teams may have
biased state level estimates and the inferred differences be-
tween states. Likewise, slides from Abia and Plateau were
read in separate laboratories. Although quality control was
conducted by the same individual for slides from both
states, systematic differences in initial slide reading be-
tween states could have occurred. Nonetheless, RDT data
closely matched the overall microscopy prevalence esti-
mates for each state, suggesting that gross errors between
states, and overall, did not exist.
Conclusions
Results from this study, which was conducted in September
2010 prior to planned mass distribution campaigns in Abia
and Plateau States, document high levels of Plasmodium
infection and anemia in both states, extremely low IRS
coverage and low bed net ownership and use. Mass LLIN
campaigns are expected to significantly improve access to
bednets for all at-risk Nigerians and follow-up surveys are
planned after distributions to evaluate progress toward
ministry targets for prevention measures and impact on the
disease burden of malaria.
Abbreviations
CI: Confidence interval; DHS: Demographic and health survey;
EA: Enumeration area; FCT: Federal capital territory; Hb: Hemoglobin;
IPTp: Intermittent preventative therapy in pregnancy; IRS: Indoor residual
spraying with insecticide; ITN: Insecticide-treated net; LLIN: Long-lasting
insecticidal net; MDA: Mass drug administration; MERG: Monitoring & evaluation
reference group; MICS: Multiple indicator cluster survey; MIS: Malaria indicator
survey; RDT: Rapid diagnostic test; SUFI: Scale-up for impact.
Competing interests
The authors declare that they have no competing interests.
Authorscontributions
AE, EE, EM, FOR, PME and PMG conceived the study. AS, AE, AEP, CO, EC, EE,
JD, OO and PMG trained survey teams. AE, AEP, AS, EE, IO, JA, KA, OUO, MU
and PMG conducted and supervised the survey. JN, JO, MO, PMG and SE
managed survey databases. JD supervised reading of blood films and
performed slide quality control, with assistance from KA. GSN, JN and PMG
analyzed data. RMD produced the map. GSN drafted the manuscript. AEP,
FOR and PMG contributed significant revisions to the manuscript. All authors
read and approved the final manuscript.
Acknowledgements
We thank all participants, survey staff, village volunteers and community
leaders for their assistance. We appreciate the efforts of all data entry staff
especially Ms Okpala Theresa. We also recognize the Nigerian National
Population Commission for assistance.
This study was funded by The Carter Center.
We are saddened by the recent untimely death of one of our co-authors,
Mr. Kal Alphonsus. He will be greatly missed.
Author details
1
The Carter Center, 453 Freedom Parkway, Atlanta, GA 30307, USA.
2
The
Carter Center, Jos, Plateau State, Nigeria.
3
The Carter Center, Southeast
Owerri, Imo State, Nigeria.
4
Plateau State Ministry of Health, Jos, Nigeria.
5
Abia State Ministry of Health, Umuahia, Nigeria.
6
University of Jos, Jos,
Nigeria.
7
Federal Medical Centre, Owerri, Imo State, Nigeria.
8
Federal Ministry
of Health, Abuja, Nigeria.
9
Current address: School of Public Health, Tropical
Medicine and Rehabilitation Sciences, James Cook University, Cairns, QLD,
Australia.
10
Current address: Agnes Scott College, Decatur, GA, USA.
Received: 27 November 2013 Accepted: 21 March 2014
Published: 26 March 2014
References
1. National Population Commission (NPC) [Nigeria], National Malaria Control
Programme (NMCP) [Nigeria], ICF International: Nigeria Malaria Indicator
Survey 2010. Abuja, Nigeria: NPC, NMCP and ICF International; 2012.
2. WHO: World Malaria Report 2012. Geneva: World Health Organization; 2012.
3. National Population Commission (NPC) [Nigeria], ICF Macro: Nigeria
Demographic and Health Survey 2008. Abuja, Nigeria: NPC and ICF Macro; 2009.
4. WHO: Progress & Impact Series: Focus on Nigeria. Geneva, Switzerland: World
Health Organization; 2012.
5. Federal Ministry of Health: Strategic Plan for Malaria Control in Nigeria 2009-
2013. Abuja, Nigeria: FMOH; 2008.
6. WHO: Insecticide-Treated Mosquito Nets: A WHO Position Statement. Geneva,
Switzerland: World Health Organization; 2007.
7. Lengeler C: Insecticide-treated bed nets and curtains for preventing
malaria. Cochrane Database Syst Rev 2004, 2:CD000363.
8. Gamble C, Ekwaru JP, Ter Kuile FO: Insecticide-treated nets for preventing
malaria in pregnancy. Cochrane Database Syst Rev 2006, 2:CD003755.
9. National Population Commission (NPC) [Nigeria], ORC Macro: Nigeria
Demographic and Health Survey 2003. Abuja, Nigeria: NPC and ORC Macro; 2004.
10. Blackburn BG, Eigege A, Gotau H, Gerlong G, Miri E, Hawley WA, Mathieu E,
Richards F: Successful integration of insecticide-treated bed net
distribution with mass drug administration in Central Nigeria. Am J Trop
Med Hyg 2006, 75(4):650655.
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 12 of 13
http://www.biomedcentral.com/1471-2334/14/168
11. Richards FO, Emukah E, Graves PM, Nkwocha O, Nwankwo L, Rakers L,
Mosher A, Patterson A, Ozaki M, Nwoke BE, Ukaga CN, Njoku C, Nwodu K,
Obasi A, Miri ES: Community-wide distribution of long-lasting insecticidal
nets can halt transmission of lymphatic filariasis in Southeastern Nigeria.
Am J Trop Med Hyg 2013, 89(3):578587.
12. van den Berg H, Kelly-Hope LA, Lindsay SW: Malaria and lymphatic
filariasis: the case for integrated vector management. Lancet Infect Dis
2013, 13(1):8994.
13. MARA: Mapping mlaria risk in Africa. In http://www.mara.org.za/.
14. UNICEF: Multiple Indicator Cluster Survey Manual 2005. New York, NY:
UNICEF; 2006.
15. Roll Back Malaria Monitoring and Evaluation Reference Group, World Health
Organization, United Nations Childrens Fund, MEASURE DHS, MEASURE
Evaluation, US Centers for Disease Control and Prevention: Malaria Indicator
Survey: Basic documentation for survey design and implementation. Calverton,
Maryland: MEASURE Evaluation; 2005.
16. WHO: Haemoglobin concentrations for the diagnosis of anaemia and
assessment of severity. Geneva, Switzerland: World Health Organization; 2011.
17. Vyas S, Kumaranayake L: Constructing socio-economic status indices: how
to use principal components analysis. Health Pol Plan 2006, 21(6):459468.
18. Kilian A, Koenker H, Baba E, Onyefunafoa EO, Selby RA, Lokko K, Lynch M:
Universal coverage with insecticide-treated nets - applying the revised
indicators for ownership and use to the Nigeria 2010 malaria indicator
survey data. Malar J 2013, 12(1):314.
19. Samdi LM, Ajayi JA, Oguche S, Ayanlade A: Seasonal variation of malaria
parasite density in paediatric population of Northeastern Nigeria. Glob J
Health Sci 2012, 4(2):103109.
20. 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 a rural setting. Mal Res Treat 2013, 2013: 716805.
21. Okoli CA, Okolo SN, Collins JC: Plasmodium falciparum infection among
neonates in the North Central region of Nigeria. J Infect Dev Ctries 2013,
7(5):365371.
22. Omalu IC, Mgbemena C, Mgbemena A, Ayanwale V, Olayemi IK, Lateef A,
Chukwuemeka VI: Prevalence of congenital malaria in minna, north
central Nigeria. J Trop Med 2012, 2012:274142.
23. Agu PU, Ogboi JS, Akpoigbe K, Okeke T, Ezugwu E: Impact of Plasmodium
falciparum and hookworm infections on the frequency of anaemia in
pregnant women of rural communities in Enugu, South East Nigeria.
Pan Afr Med J 2013, 14:27.
24. Olowookere SA, Adeleke NA, Abioye-Kuteyi EA, Mbakwe IS: Use of insecticide
treated net and malaria preventive education: effect on malaria parasitemia
among people living with AIDS in Nigeria, a cross-sectional study. Asia Pac
Fam Med 2013, 12(1):2.
25. Omoti CE, Ojide CK, Lofor PV, Eze E, Eze JC: Prevalence of parasitemia and
associated immunodeficiency among HIV-malaria co-infected adult
patients with highly active antiretroviral therapy. Asian Pac J Trop Med
2013, 6(2):126130.
26. Iroezindu MO, Agaba EI, Okeke EN, Daniyam CA, Obaseki DO, Isa SE, Idoko JA:
Prevalence of malaria parasitaemia in adult HIV-infected patients in Jos,
North-Central Nigeria. Niger J Med 2012, 21(2):209213.
27. Aina OO, Agomo CO, Olukosi YA, Okoh HI, Iwalokun BA, Egbuna KN, Orok
AB, Ajibaye O, Enya VN, Akindele SK, Akinyele MO, Agomo PU:
Malariometric survey of Ibeshe community in Ikorodu, Lagos state: dry
season. Malar Res Treat 2013, 2013:487250.
28. McMorrow ML, Aidoo M, Kachur SP: Malaria rapid diagnostic tests in
elimination settingscan they find the last parasite? Clin Microbiol Infect
2011, 17(11):16241631.
29. Molineaux L, Gramiccia G: The Garki Project. Research on the Epidemiology
and Control of Malaria in the Sudan Savanna of West Africa. Geneva,
Switzerland: World Health Organization; 1980.
30. WHO: Worldwide prevalence of anaemia 19932005: WHO global database on
anaemia. Geneva, Switzerland: World Health Organization; 2008.
31. 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(2):165178.
32. Menendez C, Kahigwa E, Hirt R, Vounatsou P, Aponte JJ, Font F, Acosta CJ,
Schellenberg DM, Galindo CM, Kimario J, Urassa H, Brabin B, Smith TA, Kitua AY,
Tanner M, Alonso PL: Randomised placebo-controlled trial of iron supple-
mentation and malaria chemoprophylaxis for prevention of severe anaemia
and malaria in Tanzanian infants. Lancet 1997, 350(9081):844850.
33. Richards FO, Eigege A, Miri ES, Kal A, Umaru J, Pam D, Rakers LJ, Sambo Y,
Danboyi J, Ibrahim B, Adelamo SE, Ogah G, Goshit D, Oyenekan OK,
Mathieu E, Withers PC, Saka YA, Jiya J, Hopkins DR: Epidemiological and
entomological evaluations after six years or more of mass drug
administration for lymphatic filariasis elimination in Nigeria. PLoS Negl
Trop Dis 2011, 5(10):e1346.
34. Gutman J, Richards FO Jr, Eigege A, Umaru J, Alphonsus K, Miri ES: The
presumptive treatment of all school-aged children is the least costly
strategy for schistosomiasis control in Plateau and Nasarawa states,
Nigeria. Ann Trop Med Parasitol 2009, 103(6):501511.
35. Pullan RL, Gitonga C, Mwandawiro C, Snow RW, Brooker SJ: Estimating the
relative contribution of parasitic infections and nutrition for anaemia
among school-aged children in Kenya: a subnational geostatistical
analysis. BMJ Open 2013, 3(2):e001936.
36. Oresanya O, Hoshen M, Sofola O: Utilization of insecticide-treated nets by
under-five children in Nigeria: assessing progress towards the Abuja
targets. Malar J 2008, 7(1):145.
37. Onwujekwe O, Chima R, Shu E, Nwagbo D, Okonkwo P: Hypothetical and
actual willingness to pay for insecticide-treated nets in five Nigerian
communities. Trop Med Int Health 2001, 6(7):545553.
38. Ye Y, Patton E, Kilian A, Dovey S, Eckert E: Can universal insecticide-treated
net campaigns achieve equity in coverage and use? The case of
northern Nigeria. Malar J 2012, 11(1):32.
39. Shargie EB, Ngondi J, Graves PM, Getachew A, Hwang J, Gebre T, Mosher AW,
Ceccato P, Endeshaw T, Jima D, Tadesse Z, Tenaw E, Reithinger R, Emerson PM,
Richards FO, Ghebreyesus TA: Rapid increase in ownership and use of
long-lasting insecticidal nets and decrease in prevalence of malaria in three
regional States of Ethiopia (2006-2007). JTropMed2010, 2010:750978.
40. Toe LP, Skovmand O, Dabire KR, Diabate A, Diallo Y, Guiguemde TR,
Doannio JM, Akogbeto M, Baldet T, Gruenais ME: Decreased motivation in
the use of insecticide-treated nets in a malaria endemic area in Burkina
Faso. Malar J 2009, 8:175.
41. Eisele TP, Keating J, Littrell M, Larsen D, Macintyre K: Assessment of
insecticide-treated bednet use among children and pregnant women
across 15 countries using standardized national surveys. Am J Trop Med
Hyg 2009, 80(2):209214.
42. Garley A, Ivanovich E, Eckert E, Negroustoueva S, Ye Y: Gender differences
in the use of insecticide-treated nets after a universal free distribution
campaign in Kano State, Nigeria: post-campaign survey results. Malar J
2013, 12(1):119.
43. Binka FN, Adongo P: Acceptability and use of insecticide impregnated
bednets in northern Ghana. Trop Med Int Health 1997, 2(5):499507.
44. Damien GB, Djenontin A, Rogier C, Corbel V, Bangana SB, Chandre F,
Akogbeto M, Kinde-Gazard D, Massougbodji A, Henry MC: Malaria infection
and disease in an area with pyrethroid-resistant vectors in southern
Benin. Malar J 2010, 9:380.
45. Okrah J, Traoré C, Palé A, Sommerfeld J, Müller O: Community factors
associated with malaria prevention by mosquito nets: an exploratory
study in rural Burkina Faso. Trop Med Int Health 2002, 7(3):240248.
doi:10.1186/1471-2334-14-168
Cite this article as: Noland et al.:Malaria prevalence, anemia and
baseline intervention coverage prior to mass net distributions in Abia
and Plateau States, Nigeria. BMC Infectious Diseases 2014 14:168.
Submit your next manuscript to BioMed Central
and take full advantage of:
Convenient online submission
Thorough peer review
No space constraints or color figure charges
Immediate publication on acceptance
Inclusion in PubMed, CAS, Scopus and Google Scholar
Research which is freely available for redistribution
Submit your manuscript at
www.biomedcentral.com/submit
Noland et al. BMC Infectious Diseases 2014, 14:168 Page 13 of 13
http://www.biomedcentral.com/1471-2334/14/168
... The study identified the prevalence of malaria infection and examined the socio-demographics, LLINs Usage and hematological parameters-based factors that determine the likelihood of malaria infection among adolescents aged 10-19 years in rural Southwestern Nigeria. The prevalence of malaria infection (71.1%) found in this study was comparable to a cross sectional study conducted among school aged participants in Abia Southeastern Nigeria which reported prevalence of 68.1% [27]. This may be due to the similarity in the study population, climatic factors, and the use of bed nets. ...
... In contrast, the prevalence of malaria in this study was high than 12.9% reported in a cross sectional study conducted in Kano Northwestern Nigeria [28]. It was also higher than 35.7% reported in another study conducted in Kaduna North-central Nigeria [29], and 36.6% reported in Plateaus North central Nigeria [27]. This could be due to the differences in the prevailing climatic conditions and environmental factors of our study area compared to other studies that were conducted in Northern Nigeria. ...
... This could be due to the differences in the prevailing climatic conditions and environmental factors of our study area compared to other studies that were conducted in Northern Nigeria. Previous study across the regions of Nigeria had reported a higher prevalence of malaria infection in the Southwestern Nigeria compared to the Northern Nigeria [27,30]. Thus, differences in settings, season variations, and environment factors conducive for malaria vectors to thrive might be responsible for this finding [27,30]. ...
Article
Full-text available
Background: There is increasing evidence suggesting that adolescents are contributing to the populations at risk of malaria. This study determined the prevalence of malaria infection among the adolescents and examined the associated determinants considering socio-demographic, Long Lasting Insecticide Nets (LLINs) usage, and hematological factors in rural Southwestern Nigeria. Methods: A hospital-based cross-sectional study was conducted between July 2021 and September 2022 among 180 adolescents who were recruited at a tertiary health facility in rural Southwestern Nigeria. Interviewer administered questionnaire sought information on their socio-demographics and usage of LLINs. Venous blood samples were collected and processed for malaria parasite detection, ABO blood grouping, hemoglobin genotype, and packed cell volume. Data were analyzed using SPSS version 20. A p-value <0.05 was considered statistically significant. Results: The prevalence of malaria infection was 71.1% (95% CI: 68.2%-73.8%). Lack of formal education (AOR = 2.094; 95% CI: 1.288-3.403), being a rural residence (AOR = 4.821; 95% CI: 2.805-8.287), not using LLINs (AOR = 1.950; 95% CI: 1.525-2.505), genotype AA (AOR = 3.420; 95% CI: 1.003-11.657), genotype AS (AOR = 3.574; 95%CI: 1.040-12.277), rhesus positive (AOR = 1.815; 95% CI:1.121-2.939), and severe anemia (AOR = 1.533; 95% CI: 1.273-1.846) were significantly associated with malaria infection. Conclusion: The study revealed the prevalence of malaria infection among the adolescents in rural Southwestern Nigeria. There may be need to pay greater attention to adolescent populations for malaria intervention and control programs.
... Malaria endemicity in Nigeria is alarming and affects mostly children aged under 5 years as well as pregnant women when compared to the remaining population group [2]. Malaria is a risk for 97% of Nigeria population accounting for 25% of death in children under five years of age and 11% of maternal death [3]. The transmission of malaria is higher in rural areas compared to urban centers [4,5]. ...
... Considering gender, although more males were infected compared to females (50.5% vs 29.4%), there was no significant difference in malaria prevalence between males and females, suggesting a sex uniformity in the pattern of infection [18]. This finding is in concordance with previous studies which established that malaria prevalence is homogenous in distribution between males and females [3,13]. In malaria-endemic areas, the most common prevention and control measures are the use of barrier systems such as insecticide-treated nets. ...
Article
Full-text available
Despite the huge resources committed to eradicating malaria globally, malaria remains endemic in Africa. Chronic malaria infection may be life-threatening in children due to increased susceptibility to anemia. This study was aimed at determining the prevalence of anemia among malaria-infected children and its possible association with socio-demographic attributes in children. This study is a cross-sectional study involving 225 children under 10 years attending Doka rural hospital. Giemsa-stained thick blood films were examined microscopically. Hematocrit levels were determined using standard methods. Results were analyzed using chi-square statistics to determine the association between malaria infection and anaemia. A total of 204 children representing 80% of the study participants were positive for malaria. The use of insecticide-treated net was low (7%) and did not significantly reduce the risk of infection and anemia. The general prevalence of anemia was 59.2%. There was a significantly higher prevalence of anemia among malaria-positive children (p<0.000). Malaria presents a strong factor for developing anemia (OR=15.09; 95% CI=6.43, 35.38; P<0.0001). There was no association between malaria parasitemia and gender or season of the year. The prevalence of malaria in Doka is quite high and is strongly associated with anemia. Surprisingly, the use of insecticide-treated nets did not reduce malaria infection. Hence, there is a need for effective malaria prevention schemes which may include education and the inclusion of routine anemia programs when evaluating children for malaria infection.
... Interestingly, prior research has documented low malaria infection rates, as determined by microscopy, in urban Lagos, with rates as low as 8% and 0.9% [45][46][47][48]. However, it remains somewhat unclear why lower test positivity rates were observed in the urban clusters of Rivers and Abia, especially when previous studies conducted in urban areas have indicated higher test positivity rates among the study populations [49][50][51]. It is important to note that two of these earlier studies were health facility studies, which did not differentiate participants based on whether their specific place of residence was urban or rural. ...
Article
Full-text available
Urban population growth in Nigeria may exceed the availability of affordable housing and basic services, resulting in living conditions conducive to vector breeding and heterogeneous malaria transmission. Understanding the link between community-level factors and urban malaria transmission informs targeted interventions. We analyzed Demographic and Health Survey Program cluster-level data, alongside geospatial covariates, to describe variations in malaria prevalence in children under 5 years of age. Univariate and multivariable models explored the relationship between malaria test positivity rates at the cluster level and community-level factors. Generally, malaria test positivity rates in urban areas are low and declining. The factors that best predicted malaria test positivity rates within a multivariable model were post-primary education, wealth quintiles, population density, access to improved housing, child fever treatment-seeking, precipitation, and enhanced vegetation index. Malaria transmission in urban areas will likely be reduced by addressing socioeconomic and environmental factors that promote exposure to disease vectors. Enhanced regional surveillance systems in Nigeria can provide detailed data to further refine our understanding of these factors in relation to malaria transmission.
... A decrease in the hemoglobin level was observed in all infected children and induced anemia in symptomatic patients, this is confirmed by the low average number of red blood cells of infected children. Although the etiology of anemia in tropical areas is multi-factorial, our data are consistent with several other studies showing that anemia during P. falciparum malaria is closely associated with malaria parasitemia [27][28][29]. Similarly, it has been shown that in children infected with P. falciparum a combination of hemolysis of parasitized and non-parasitized red blood cells and erythropoiesis depression inducing anemia are often observed [30]. ...
Article
Full-text available
Background Malaria remains a major public health issue in the world despite a decline in the disease burden. However, though symptomatic malaria is diagnosed and treated, asymptomatic infections remain poorly known and support transmission. This study assessed the prevalence of symptomatic and asymptomatic Plasmodium spp. infections in three areas in Gabon to monitor and evaluate the impact of malaria. Methods and Results A cross-sectional study was conducted in three areas of Gabon. Febrile and afebrile children aged 6 months to 15 years were included in this study. Malaria prevalence was determined by microscopy of and using rapid diagnostic test (RDT). Plasmodium spp. species were identified by PCR according to the Snounou method. The data were recorded in Excel, and the statistical analyses were performed using the software R version R 64 × 3.5.0. A total of 2381(333 asymptomatic and 107 symptomatic) children were included. The overall prevalence of malaria was 40% (952/2381), with the majority (77% symptomatic and 98% asymptomatic) of infections caused by Plasmodium falciparum . A high prevalence of malaria was found in infected children in rural and semi-rural areas. In these two areas, a higher prevalence of Plasmodium malariae was observed in asymptomatic. Furthermore, mixed infections were more prevalent in asymptomatic children than in symptomatic. Conclusion This study showed that the prevalence of Plasmodium spp. infection varied according to the regions. The main species was Plasmodium falciparum , but in asymptomatic children the prevalence of Plasmodium malariae was high in rural areas. To help fight malaria more effectively asymptomatic infections should be taken into account and treated.
... According to the World Malaria Report (WHO, 2012) 40% of the estimated cases of malaria worldwide occurred in India, Nigeria and DR Congo. Malaria has been reported to account for an estimated 60% of outpatient hospital visits in Nigeria, 30% of hospitalizations, 30% of under-five mortalities, 25% of infant mortalities and 11% of maternal mortalities (Noland et al., 2014). Malaria remains a major public health problem in Nigeria where it is endemic where it causes significant human suffering (Adedotun et al., 2013). ...
Article
Full-text available
Malaria and tuberculosis (TB) are two of the most prevalent endemic infections in Nigeria. Thus, a study on the co-infection of malaria parasites with tuberculosis was undertaken among patients attending State Specialist Hospital Gombe between November, 2010 and March, 2011. A total of 203 blood samples comprising of 103 samples from confirmed AFB-positive patients and 100 from AFB-negative patients (control) were collected and analysed for the presence of malarial parasites. All the samples were subjected to blood film using Giemsa Staining Technique and viewed under oil immersion Microscopy. The prevalence of malaria parasites among AFB- positive and negative patients were found to be 33% and 31% respectively. Malaria parasites were most prevalent among patients aged 41-64 years (39.0%). Male patients had the highest prevalence of 17.5%, while females had a prevalence rate of 15.5%. The higher prevalence reported may be of significance in the light of recent data, showing that malaria infection may exacerbate TB. Thus, adequate measures should be taken to free TB patients from malaria infection.
... In 2018, P. falciparum accounted for 99.7% of estimated malaria cases in Africa, while P. vivax predominated in America, accounting for 75% of the cases [6]. P. malariae was the third most frequent species, with a prevalence of up to 15-40% and an overlapping distribution with P. falciparum throughout tropical Africa and malaria-endemic regions of the world [5,7,8]. P. ovale is predominantly found in forests and humid savannah areas in West and Central Africa, with a prevalence of 4 to 10% [9]. ...
Article
Full-text available
Up-to-date knowledge of key epidemiological aspects of each Plasmodium species is necessary for making informed decisions on targeted interventions and control strategies to eliminate each of them. This study aims to describe the epidemiology of plasmodial species in Mali, where malaria is hyperendemic and seasonal. Data reports collected during high-transmission season over six consecutive years were analyzed to summarize malaria epidemiology. Malaria species and density were from blood smear microscopy. Data from 6870 symptomatic and 1740 asymptomatic participants were analyzed. The median age of participants was 12 years, and the sex ratio (male/female) was 0.81. Malaria prevalence from all Plasmodium species was 65.20% (95% CI: 60.10–69.89%) and 22.41% (CI: 16.60–28.79%) for passive and active screening, respectively. P. falciparum was the most prevalent species encountered in active and passive screening (59.33%, 19.31%). This prevalence was followed by P. malariae (1.50%, 1.15%) and P. ovale (0.32%, 0.06%). Regarding frequency, P. falciparum was more frequent in symptomatic individuals (96.77% vs. 93.24%, p = 0.014). In contrast, P. malariae was more frequent in asymptomatic individuals (5.64% vs. 2.45%, p < 0.001). P. ovale remained the least frequent species (less than 1%), and no P. vivax was detected. The most frequent coinfections were P. falciparum and P. malariae (0.56%). Children aged 5–9 presented the highest frequency of P. falciparum infections (41.91%). Non-falciparum species were primarily detected in adolescents (10–14 years) with frequencies above 50%. Only P. falciparum infections had parasitemias greater than 100,000 parasites per µL of blood. P. falciparum gametocytes were found with variable prevalence across age groups. Our data highlight that P. falciparum represented the first burden, but other non-falciparum species were also important. Increasing attention to P. malariae and P. ovale is essential if malaria elimination is to be achieved.
... Findings of the present study showed a similar prevalence rate among the male (47.77 %) and female (52.2 %), which is consistent with previous studies in Nigeria, Kenya, and Mozambique, which suggests that the distribution of malaria risk is varied (Noland et al., 2014), Temu et al., 2012) and (Brooker et al., 2004). There is no any scientific fact to prove the higher prevalence being related to gender as susceptibility to Malaria infection is not influenced by gender. ...
Article
Full-text available
Helminths are group of parasites causing neglected tropical diseases of public health concern. It is important to map out soil contaminated with helminth eggs in selected primary schools and to project which school need health. This study screen soil samples for the prevalence of helminth eggs in soils of selected public and private primary schools in Kaltungo. A total of 280 (two hundred and eighty) Soil samples were collected from the ten randomly selected schools and Chi-square test was used to test for associations. The overall prevalence was (73.93) of helminth eggs found in public and private primary schools. There was statistically significant different (p < 0.05) in prevalence of helminth eggs in soil samples of public and private schools. The highest species-specific prevalence was Ancylostomaduodenaleeggs with 285(26.71% prevalence) with a mean of 146.5 ± 69.25, while the least specie was Trichuristrichiuraeggs with 30(2.81% prevalence) There was a significant association between the occurrence of helminth egg and season (χ2 = .5.9031, p = 0.015). The result of the study therefore indicates that there is high prevalence rate of helminths eggs in the selected primary schools within Kaltungo Metropolis. Therefore, there is a need of regular deworming of the school children and sanitary majors of the school premises should all be improved. Keywords: Deworming, Helminth, Neglected Parasite, Prevalence
... The prevalence of anaemia (59.1%) in these children is close to the prevalence of 54.1% reported from Plateau State, higher than 47.3% from Okada in Edo State, but lower than 76.9% found in children from Abia State, and 74% to 88.2% from Burkina Faso. 5,8,9 Nutritional and immunity status vary from one child to another across the various geographical locations which could explain differences in the prevalence of anaemia found. 9,12,17 Using multivariate logistic regression, the age of these children and their gender were not found to be predictive of anaemia in our study. ...
Article
Full-text available
Malaria is a major public health disease, and severe malaria with anaemia could be life-threatening. A focused study on malaria with anaemia will provide information which may help in mitigating this problem among the population in sub-Saharan Africa. The objective of this study is to determine the prevalence of Plasmodium falciparumparasitemia in relation to anaemia among children under 5 years in a tertiary health center in South-West, Nigeria.
... The prevalence of anaemia (59.1%) in these children is close to the prevalence of 54.1% reported from Plateau State, higher than 47.3% from Okada in Edo State, but lower than 76.9% found in children from Abia State, and 74% to 88.2% from Burkina Faso. 5,8,9 Nutritional and immunity status vary from one child to another across the various geographical locations which could explain differences in the prevalence of anaemia found. 9,12,17 Using multivariate logistic regression, the age of these children and their gender were not found to be predictive of anaemia in our study. ...
Article
Full-text available
Introduction: The use of insecticide treated nets among pregnant women is of public health significance to protect the pregnant women and their babies. This study is aimed at determining the knowledge and attitude of insecticide treated nets use in malaria prevention and its associated factors among pregnant women.
Article
Full-text available
Until recently only two indicators were used to evaluate malaria prevention with insecticide-treated nets (ITN): "proportion of households with any ITN" and "proportion of the population using an ITN last night". This study explores the potential of the expanded set of indicators recommended by the Roll Back Malaria Monitoring and Evaluation Reference Group (MERG) for comprehensive analysis of universal coverage with ITN by applying them to the Nigeria 2010 Malaria Indicator Survey data. The two additional indicators of "proportion of households with at least one ITN for every two people" and "proportion of population with access to an ITN within the household" were calculated as recommended by MERG. Based on the estimates for each of the four ITN indicators three gaps were calculated: i) households with no ITN, ii) households with any but not enough ITN, iii) population with access to ITN not using it. In addition, coverage with at least one ITN at community level was explored by applying Lot Quality Assurance Sampling (LQAS) decision rules to the cluster level of the data. All outcomes were analysed by household background characteristics and whether an ITN campaign had recently been done. While the proportion of households with any ITN was only 42% overall, it was 75% in areas with a recent mass campaign and in these areas 66% of communities had coverage of 80% or better. However, the campaigns left a considerable intra-household ownership gap with 66% of households with any ITN not having enough for every family member. In contrast, the analysis comparing actual against potential use showed that ITN utilization was good overall with only 19% of people with access not using the ITN, but with a significant difference between the North, where use was excellent (use gap 11%), and the South (use gap 36%) indicating the need for enhanced behaviour change communication. The expanded ITN indicators to assess universal coverage provide strong tools for a comprehensive system effectiveness analysis that produces clear, actionable evidence of progress as well as the need for specific additional interventions clearly differentiating between gaps in ownership and use.
Article
Full-text available
Lymphatic filariasis (LF) in rural southeastern Nigeria is transmitted mainly by Anopheles spp. mosquitoes. Potential coinfection with Loa loa in this area has prevented use of ivermectin in the mass drug administration (MDA) strategy for LF elimination because of potential severe adverse L. loa-related reactions. This study determined if long-lasting insecticidal net (LLIN) distribution programs for malaria would interrupt LF transmission in such areas, without need for MDA. Monthly entomologic monitoring was conducted in sentinel villages before and after LLIN distribution to all households and all age groups (full coverage) in two districts, and to pregnant women and children less than five years of age in the other two districts. No change in human LF microfilaremia prevalence was observed, but mosquito studies showed a statistically significant decrease in LF infection and infectivity with full-coverage LLIN distribution. We conclude that LF transmission can be halted in southeastern Nigeria by full-coverage LLIN distribution, without MDA.
Article
Full-text available
Malaria and HIV are major causes of morbidity and mortality in sub-Saharan Africa with both diseases highly endemic in Nigeria. This study was conducted to assess the effect of long lasting insecticide treated net (ITN) use and malaria preventive education on burden of malaria parasite among people living with AIDS (PLWHA) at Osogbo southwestern Nigeria METHOD: A descriptive cross-sectional study of newly recruited consenting PLWHA that were screened consecutively for malaria, those positive were treated with artemisinin combination therapy. All PLWHA were educated about malaria infection, given ITN and followed up monthly for three months when they were rescreened for malaria infection. Data collected was analyzed using descriptive and inferential statistics.Result: A total of 392 (92%) PLWHA completed the study. Mean age of the respondents was 33 +/- 11.6 years. They were 120 (31%) males and 272 (69%) females. Majority (80%) were married, over 33% completed secondary education while 21% had tertiary education. Most were traders (40%) and artisans (25%). About 60% had Plasmodium falciparum malaria parasitemia at baseline which drastically reduced to 5% at three months with ITN use and malaria prevention education. Malaria is a major preventable condition among PLWHA. Preventive education and ITN use reduced malaria parasite burden among this population.
Article
Full-text available
Malariometric surveys generate data on malaria epidemiology and dynamics of transmission necessary for planning and monitoring of control activities. This study determined the prevalence of malaria and the knowledge, attitude, and practice (KAP) towards malaria infection in Ibeshe, a coastal community. The study took place during the dry season in 10 villages of Ibeshe. All the participants were screened for malaria. A semistructured questionnaire was used to capture sociodemographic data and KAP towards malaria. A total of 1489 participants with a mean age of 26.7 ± 20.0 years took part in the study. Malaria prevalence was 14.7% (95% CI 13.0-16.6%) with geometric mean density of 285 parasites/μL. Over 97% of participants were asymptomatic. Only 40 (2.7%) of the participants were febrile, while 227 (18.1%) were anemic. Almost all the participants (95.8%) identified mosquito bite as a cause of malaria, although multiple agents were associated with the cause of malaria. The commonest symptoms associated with malaria were hot body (89.9%) and headache (84.9%). Window nets (77.0%) were preferred to LLIN (29.6%). Malaria is mesoendemic in Ibeshe during the dry season. The participants had good knowledge of symptoms of malaria; however, there were a lot of misconceptions on the cause of malaria.
Article
Full-text available
This cross-sectional study investigated the rate of congenital and neonatal malaria infections in patients attending our hospital. Thick and thin blood films of 288 neonates admitted in the Special Care Baby Unit of Jos University Teaching Hospital, Nigeria, were examined microscopically for malaria parasites. Babies' and mothers' demographic and clinical data were analyzed. Of 288 blood samples examined, 160 (55.6%) were from males, 115 (39.9%) were from babies 0 to 7 days old, and 173 (60.1%) were from babies 8 to 28 days old. In total, 91 (31.6%) babies had malaria parasitaemia, of whom 49 (53.8%) were males. Malaria was significantly higher in babies 8 to 28 days old (p < 0.001) and was independent of gender (p=0.692). Prevalence rates for congenital and neonatal malaria were 6.9% and 24.7% respectively. Clinical presentations on admission included fever, cough, pallor, jaundice, and inability to suck. A total of 145 (50.3%) babies had symptoms of malaria, of whom 56 (61.5%) had malaria parasitaemia. Symptoms of malaria were present in 35 (12.2%) babies of 59 (20.5%) mothers who had symptoms of malaria during pregnancy. Ten (11.0%) of these neonates had malaria parasitaemia, of whom 4 (0.4%) were 0 to -7days old. Plasmodium falciparum was the only specie identified. No mortality was recorded against malaria-infected babies. High prevalence of malaria in these neonates calls for high index of suspicion. Inclusion of malaria parasite test in the routine battery of tests for babies presenting with clinical signs and symptoms of neonatal infections is recommended.
Article
Full-text available
Background Recent expansion in insecticide-treated net (ITN) distribution strategies range from targeting pregnant women and children under five and distributing ITN at antenatal care and immunization programmes, to providing free distribution campaigns to cover an entire population. These changes in strategy raise issues of disparities, such as equity of access and equality in ITN use among different groups, including females and males. Analysis is needed to assess the effects of gender on uptake of key malaria control interventions. A recent post-universal free ITN distribution campaign survey in Kano State, Nigeria offered an opportunity to look at gender effects on ITN use. Methods A post-campaign survey was conducted three to five months after the campaign in Kano State, Nigeria from 19 October to 4 November, 2009, on a random sample of 4,602 individuals. The survey was carried out using a questionnaire adapted from the Malaria Indicator Survey. Using binary logistic regression, controlling for several covariates, the authors assessed gender effects on ITN use among individuals living in households with at least one ITN. Results The survey showed that household ITN ownership increased more than 10-fold, from 6% before to 71% after the campaign. There was no significant difference between the proportion of females and males living in households with at least one ITN. However, a higher percentage of females used ITNs compared to males (57.2% vs 48.8%). After controlling for several covariates, females remained more likely to use ITNs compared to males (OR: 1.5, 95% CI: 1.3-1.7). Adolescent boys remained the least likely group to use an ITN. Conclusions This study reveals gender disparity in ITN use, with males less likely to use ITNs particularly among ages 15–25 years. The uptake of the intervention among the most at-risk group (females) is higher than males, which may be reflective of earlier strategies for malaria interventions. Further research is needed to identify whether gender disparities in ITN use are related to traditional targeting of pregnant women and children with malaria interventions; however, results provide evidence to design gender-sensitive messaging for universal ITN distribution campaigns to ensure that males benefit equally from such communications and activities.
Article
Full-text available
Malaria contributes to high childhood morbidity and mortality in Nigeria. To determine its endemicity in a rural farming community in the south-south of Nigeria, the following malariometric indices, namely, malaria parasitaemia, spleen rates, and anaemia were evaluated in children aged 2-10 years. This was a descriptive cross-sectional survey among school-age children residing in a rubber plantation settlement. The children were selected from six primary schools using a multistaged stratified cluster sampling technique. They were all examined for pallor, enlarged spleen, or liver among other clinical parameters and had blood films for malaria parasites. Of the 461 children recruited, 329 (71.4%) had malaria parasites. The prevalence of malaria parasitaemia was slightly higher in the under fives than that of those ≥5 years, 76.2% and 70.3%, respectively. Splenic enlargement was present in 133 children (28.9%). The overall prevalence of anaemia was 35.7%. Anaemia was more common in the under-fives (48.8%) than in those ≥5 years (32.8%). The odds of anaemia in the under fives were significantly higher than the odds of those ≥5 years (OR = 1.95 [1.19-3.18]). Malaria is highly endemic in this farming community and calls for intensification of control interventions in the area with special attention to school-age children.
Article
Full-text available
Malaria and hookworm infections are common in sub-Saharan Africa and they increase the prevalence of anaemia in pregnancy with resultant poor pregnancy outcomes. This study was carried out to assess the impact of Plasmodium falciparum and hookworm infections on the frequency of anaemia among pregnant women in two rural communities in Enugu, South East Nigeria. A cross sectional descriptive study was carried out in a total of 226 women attending antenatal clinics at two rural Primary Health Centres (PHC) from April 2011 to July 2011(each PHC with 113 subjects). Socio-demographic data were collected through a structured questionnaire. Blood and stool samples were evaluated for haemoglobin estimation and malaria parasites, and stool samples examined for parasitic infection in all the women. Data was analyzed using STATA 10 software statistical analysis package. Student t-test was used for comparing mean values and chi square test for comparing categorical variables and level of significance set at p<0.05 and logistic regression was used to identify the risk factors associated with malaria in pregnancy. The mean age of the women was 27years with range 18 - 38years and SD of 5years. Most of the women were housewives and over 50% in their second trimester. 53% of them had malaria parasites while 27% had hookworm infection. About 40% of the women were anaemic (haemoglobin < 0.001). Similar association was found between hookworm infection and anaemia (p <0.001). Though both malaria and hookworm infections greatly increase the odds for anaemia (AOR 18.06, CI 18.15 -39.99, P<0.001) and (AOR 5.28, CI 2.26-12.38, P<0.001) respectively, the odds for having anaemia in pregnancy was higher for malaria than hookworm infections. Plasmodium falciparum and hookworm infections have significant impact on the high frequency of anaemia in pregnancy in our rural communities. There is need to strengthen the control program that has been in place with an integrated intervention to combat these parasitic infections in our rural communities, with mass distribution of antihelminthics as one of the included relevant methods, among others.