|
|
OJHAS Vol. 6, Issue 3: (2007
Jul-Sep) |
|
|
Studies on
the Predisposing Factors of Protein Energy Malnutrition Among Pregnant
Women in a Nigerian Community |
|
Okwu GN,
Ukoha AI, Nwachukwu N, Agha NC, Department
of Biochemistry, Federal University
of Technology, Owerri |
|
|
|
|
|
|
|
|
|
Address For Correspondence |
Gloria
N. Okwu Department
of Biochemistry, Federal University
of Technology,
P.O. Box 2572, Owerri, Imo
State, Nigeria.
E-mail:
gnokwu@yahoo.com |
|
|
|
|
Okwu GN, Ukoha AI, Nwachukwu N, Agha NC. Studies on
the Predisposing Factors of Protein Energy Malnutrition Among Pregnant
Women in a Nigerian Community.
Online J Health Allied Scs. 2007;3:1 |
|
Submitted Aug 18, 2007; Accepted Dec
17, 2007; Published: Jan 24, 2008 |
|
|
|
|
|
|
|
|
Abstract: |
Protein Energy
Malnutrition (PEM) continues to be a major public health problem in
developing countries and affects mostly infants, young children, pregnant
and lactating mothers. This study was carried on some of the factors
that predispose pregnant women to PEM and hence identify groups at greater
risk. A total of 1387 pregnant women (910 in the urban area and 477
in the rural areas) were recruited for the study. Anthropometric indices
of weight, height and Body Mass Index (BMI) of the pregnant women were
measured and semi structured questionnaires were used to elicit information
on possible predisposing factors such as age, level of education, parity,
child spacing etc. Results obtained showed that the mean weight and
height of the rural pregnant women, were significantly (p<0.0001)
lower than those of the urban pregnant women. The mean BMI of the rural
subjects, was also significantly (p< 0.0027) lower than that of the
urban subjects. Analysis of the effect of age showed that the younger
age category (24 years and below) had significantly (p<0.0001) lower
mean BMI and higher prevalence of PEM while the effect of level of education
showed significantly (p<0006) lower mean BMI and higher PEM
prevalence among the less educated (no formal and primary education).
Those with parity of two, one and primipara showed significantly (p<0.0175)
lower mean BMI while child spacing did not have any significant effect
on both mean BMI and prevalence of PEM. The implications of these findings
are discussed and recommendations made on how to tackle the problem.
Key Words:
Protein Energy Malnutrition, Pregnant Women, Predisposing Factors, Owerri,
Nigeria |
|
Worldwide,
an estimated 852 million people are undernourished with most (815 million),
living in developing countries.1,2 Poverty is the main underlying
cause of malnutrition and its determinants.3 The degree and
distribution of Protein Energy Malnutrition (PEM) in a given population
depends on many factors – the political and economic situation, level
of education and sanitation, the season and climate conditions, food
production, cultural and religious food customs, breastfeeding habits,
prevalence of infectious diseases, the existence and effectiveness of
nutrition programmes and the availability and quality of health services.2,4
Malnutrition
continues to be a major health burden in developing countries. It is
globally the most important risk factor for illness and death with hundreds
of millions of pregnant women and young children particularly affected.5
Poor nutrition in pregnancy in combination with infections is a common
cause of maternal and infant mortality and morbidity, low birth weight
and intrauterine Growth Retardation (IUGR).6 In Nigeria,
maternal death per 100,000 births is put at 800 while percentage low
birth weight stands at twenty.7
Low birth weight
babies have increased risk of mortality, morbidity and development of
malnutrition. Children who suffer from malnutrition are more likely
to have slowed growth, delayed development, difficulty in school and
high rates of illness and they may remain malnourished to adulthood.8,9 IUGR is associated with poor cognitive and neurological development
for the infant and in adulthood, susceptibility to cardiovascular disease,
diabetes and renal disease.10
Malnutrition
remains one of the world’s highest priority health issues not only
because its effects are so widespread and long lasting but also because
it can be eradicated. Eradication is best carried out at the preventive
stage. Hence the need to identify groups of pregnant women at greater
risk of developing PEM. Such high-risk groups can be targeted in any
planned intervention programme.
Subjects
A total of
1,387 pregnant women took part in the study, 910 in Owerri urban area
and 477 in the rural area surrounding Owerri. The study was carried
out at the antenatal clinics of government hospitals and private clinics
in Owerri urban area and antenatal clinics of health centres in rural
areas surrounding Owerri and covered a period of 11 months.
Approval to
carry out the study was obtained from the appropriate health authorities
and informed consent obtained from the subjects before the commencement
of the study. Pregnant women who had complications such as pregnancy
induced hypertension, infections, malaria, metabolic disorders etc (as
indicated in their medical records) were excluded from the study. All
the pregnant women in the study received routine prescriptions of iron,
multivitamins, folic acid and daraprim (as antimalaria prophylaxis).
Data on age, educational level, parity, child spacing, etc were obtained
from the pregnant women through a semi-structured questionnaire.
Sampling
Technique And Sample Size
For the Owerri
urban area, proportionate cluster sampling method was used. Five clusters
were identified and one was randomly selected. All the hospitals and
clinics in the selected cluster were included in the study. For the
rural areas surrounding Owerri a total of 12 health centres were randomly
selected from the 55 health centres belonging to 55 autonomous communities.
Sample size
n, for random sampling was calculated using the relationship
n = (Z1-α/δ)2
p(1-p)11
Prevalence,
P was taken to be 50, which gives the largest sample size.
Sampling error,
was 5%
Confidence
coefficient 1- α = 95% (Z1- α = 1.96)
Accordingly
a minimum sample size of 384 was calculated for the rural areas. To
take into account the cluster design effect, the calculated random sampling
size, n is multiplied by two.12 Hence a minimum sample size
of 768 was obtained for the Owerri urban area.
Anthropometric
Indices
Anthropometric
measurements of the pregnant women were performed with the help of trained
assistants. Body weights were measured without shoes and with light
clothing to the nearest 0.1kg on a weight scale. Standing height was
measured without headgear using a stadiometer to the nearest 0.1cm.
Body mass index (BMI) was calculated as weight (kg) divided by height
(m) squared (kg/m2). According to UN classification, BMI
< 18 is considered severely malnourished, 18-20 is moderately malnourished,
21-24 is normal, 25-27 is overweight and > 27 is obese.13
Statistical
Analysis
Data was analysed
using the software package SAS version 8. (SAS Institute Inc, Cary,
North Carolina). Pearson chi Square, Anova and post Hoc Duncan’s multiple
range test were used to identify statistically significant differences.
Data was considered significant for p <0.05 at 95% confidence limit.
A total of
1,387 pregnant women were included in the study (910 in the urban area
and 477 in the rural areas). The mean weight and height of the pregnant
women in the rural areas, 63.65 ± 14.80kg and 1.58 ± 0.07m respectively
were significantly lower than those of the urban subjects, 68.92 ±
10.23kg and 1.67 ± 0.08m respectively, p<0.0001 in each case. The
mean BMI of the rural subjects, 25.28 ± 4.60kg/m2 was also
significantly lower than that of the urban subjects, 26.41 ± 3.36kg/m2, p<0.0027.
In the urban area, 35% of the pregnant women were public servants, 43%
were involved in some business activity and 22% were housewives/students
not holding any jobs. In the rural sub sample, 8% were public servants,
22% were involved in some business activity and 70% were engaged in
subsistence farming as a means of livelihood.
Table
1: Mean BMI
And Prevalence Of PEM According To Age Of The Pregnant Women.
Age (yrs) |
Frequency |
BMI (kg/m2) |
%*
PEM |
Range |
Mean |
s.d |
Overall |
< 20 |
68 |
16.94-30.30 |
25.07c
|
2.58 |
25.00 |
20-24 |
443 |
18.82-42.36 |
25.16c
|
3.21 |
11.74 |
25-29 |
454 |
17.80-41.80 |
26.50b
|
3.86 |
6.17 |
30-34 |
261 |
18.65-38.08 |
26.35b
|
3.77 |
5.36 |
35-39 |
130 |
18.37-38.08 |
26.92 b
|
4.86 |
4.62 |
>
40 |
31 |
22.48-36.57 |
29.04 a
|
3.84 |
0.00 |
Total |
1387 |
|
|
|
|
Urban |
< 20 |
35 |
22.22-30.30 |
27.25
b |
2.63 |
0.00 |
20-24 |
245 |
18.82-33.15 |
25.72 b
|
3.000 |
4.89 |
25-29 |
328 |
17.80-36.79 |
26.54 b
|
3.42 |
4.57 |
30-34 |
186 |
20.00-35.50 |
26.49 b
|
3.32 |
4.20 |
35-39 |
88 |
18.37-35.63 |
26.58 b
|
3.59 |
3.41 |
>40 |
28 |
25.00-36.57 |
29.54 a
|
4.32 |
0.00 |
Total |
910 |
|
|
|
|
Rural |
< 20 |
33 |
16.94-25.10 |
22.29
b |
2.52 |
51.52 |
20-24 |
198 |
18.99-42.36 |
24.33 b
|
3.72 |
20.20 |
25-29 |
126 |
19.37-41.80 |
26.36 a
|
4.19 |
10.31 |
30-34 |
75 |
18.65-38.09 |
25.94 a
|
4.77 |
8.00 |
35-39 |
42 |
19.04-38.08 |
27.75 a
|
6.53 |
7.14 |
>
40 |
3 |
22.48-26.49 |
23.51 b
|
2.83 |
0.00 |
Total |
477 |
|
|
|
|
Values with
different superscripts per column are statistically significant (p<0.05)
* % PEM: Overall
– p<0.0136, Urban – p<0.4194, Rural – p<0.0001 (Pearson
X2 used)
Table 1 shows
mean BMI and prevalence of PEM amongst the pregnant women according
to age. Overall the pregnant women below 20yrs and 20-24yrs age groups
showed significantly (p<0.0010) lower mean BMI and significantly
(p<0.0136) higher percentage of PEM than the older age categories.
In the urban sub-sample, both mean BMI of the 24 years and below
age category was significantly (p<0.0421) lower than that of above
the 40 years age group while prevalence of PEM did not show statistical
difference (p<0.4194) among the various age groups. In the rural
sub-sample, mean BMI of the 24 years and below age group was significantly
(p<0.0111) lower than the older age groups and their proportion of
PEM was significantly (p<0.0001) higher.
Table
2: Mean BMI
and Prevalence of PEM of the Pregnant Women According to Educational
Level
Level of education |
Frequency |
BMI
(kg/m2) |
%*
PEM |
Range |
Mean |
s.d |
Overall |
No Formal Education |
104 |
16.94-36-85 |
24.80c
|
2.57 |
12.50 |
Primary
Education |
362 |
17.80-40.03 |
24.76c
|
3.43 |
12.71 |
Secondary
Education |
621 |
20.48-42.36 |
25.86 b
|
3.98 |
7.25 |
Post
Secondary Education |
300 |
18.73-41.80 |
27.03 a
|
4.10 |
4.00 |
Total |
1387 |
|
|
|
|
Urban |
No Formal Education |
62 |
22.86-34.18 |
25.63
a |
3.00 |
4.84 |
Primary
Education |
188 |
17.80-35.86 |
25.80 a
|
2.94 |
4.79 |
Secondary
Education |
420 |
18.73-35.56 |
26.19 a
|
3.08 |
4.05 |
Post
Secondary Education |
240 |
18.36-36.79 |
27.45 a
|
3.70 |
3.75 |
Total |
910 |
|
|
|
|
Rural |
No Formal Education |
42 |
16.94-36.85 |
24.72b
|
2.33 |
23.81 |
Primary
Education |
174 |
19.04-40.03 |
24.35b
|
3.93 |
21.26 |
Secondary
Education |
201 |
20.48-42.36 |
26.64 a
|
4.58 |
13.93 |
Post
Secondary Education |
60 |
19.73-41.80 |
28.47 a
|
4.48 |
5.00 |
Total |
477 |
|
|
|
|
Values with
different superscripts per column are statistically significant (p<0.05)
* % PEM: Overall
– p<0.0104, Urban – p<0.0351, Rural – p<0.0476 (Pearson
X2 used)
Table 2 shows
mean BMI and prevalence of PEM amongst the pregnant women according
to level of education. Overall, the pregnant women with primary education
and no formal education had significantly (p<0.0006) lower mean BMI
and significantly (p<0.0104) higher prevalence of PEM. In the urban
area, although there was no statistical difference (p<0.6287)
in mean BMI, there was significant difference (p<0.0351) in prevalence
of PEM amongst the pregnant women according to level of education. In
the rural sub-sample the primary and no formal education groups had
significantly (p<0.0012) lower mean BMI and significantly (p<0.0476)
higher prevalence of PEM.
Table
3: Mean BMI
And Prevalence Of PEM According To Parity Of The Pregnant Women
Parity |
Frequency |
BMI
(kg/m2) |
%
PEM* |
Range |
Mean |
s.d |
Overall
Primipara |
|
106 |
19.26-33.12 |
25.68b
|
3.24 |
5.66 |
1 |
251 |
17.44-36.79 |
25.31b
|
2.95 |
12.35 |
2 |
304 |
16.94-42.36 |
25.45b
|
3.85 |
7.89 |
3 |
354 |
18.64-41.80 |
26.45 a
|
4.32 |
6.50 |
4 |
205 |
19.53-35.56 |
27.13 a
|
4.08 |
7.32 |
>4 |
167 |
17.79-40.03 |
26.63 a
|
4.15 |
9.58 |
Total |
1387 |
|
|
|
|
Urban |
Primipara |
100 |
19.26-33.12 |
25.82c
|
3.43 |
6.00 |
1 |
185 |
18.82-36.79 |
25.12c
|
3.06 |
5.41 |
2 |
220 |
18.36-33.96 |
25.66c
|
3.35 |
5.45 |
3 |
240 |
19.84-35.62 |
26.79 b
|
3.02 |
2.08 |
4 |
112 |
20.89-35.49 |
27.58 a
|
3.58 |
2.68 |
>
4 |
53 |
17.80-36.57 |
27.84 a
|
4.45 |
3.77 |
Total |
910 |
|
|
|
|
Rural |
Primipara |
6 |
22.66-23.31 |
22.99
a |
0.45 |
0.00 |
1 |
66 |
17.44-27.88 |
23.59 a
|
2.89 |
31.82 |
2 |
84 |
16.94-42.36 |
24.80 a
|
4.68 |
14.29 |
3 |
114 |
18.64-41.80 |
25.61 a
|
5.63 |
15.79 |
4 |
93 |
19.53-35.56 |
26.49 a
|
4.13 |
13.68 |
>4 |
114 |
19.04-40.03 |
25.97 a
|
4.85 |
12.28 |
Total |
477 |
|
|
|
|
Values with
different superscripts per column are statistically significant (p<0.05)
* % PEM: Overall
– p<0.0136, Urban – p<0.0166, Rural – p<0.1942 (Pearson
X2 used)
Table 3 shows
mean BMI and prevalence of PEM according to parity. Overall the lower
mean BMI of parity of one, parity of two and primipara showed significant
(p<0.0175) differences from the other groups although their prevalence
of PEM was not significantly (p<0.0638) different. In the urban sub
sample, the lower mean BMI of parity of one, two and primipara showed
significant (p<0.0244) difference from those of the other groups.
Their prevalence of PEM was also significantly (p<0.0166) different.
In the rural sub-sample, although the mean BMI and prevalence of PEM
did not show statistical differences, the pregnant women with parity
of one presented the highest prevalence of PEM of 31.82%.
Table
4: Mean BMI
And Prevalence Of PEM According To Child Spacing Of The Pregnant Women
Child spacing |
Frequency |
BMI
(kg/m2) |
%
PEM* |
Range |
Mean |
s.d |
Overall
|
Primipara |
106 |
16.94-32.36 |
25.53a |
3.34 |
5.60 |
<1yr |
80 |
19.98-29.90 |
25.21 a |
3.56 |
10.00 |
1-1.5yrs |
354 |
17.79-35.56 |
26.38 a |
3.65 |
7.34 |
1.5-2yrs |
415 |
18.73-40.03 |
26.59 a |
4.26 |
6.70 |
2-2.5yrs |
197 |
20.00-32.29 |
25.74 a |
3.34 |
9.64 |
Above
2.5yrs |
235 |
18.36-42.36 |
26.10 a |
4.62 |
11.91 |
Total |
1387 |
|
|
|
|
Urban |
Primipara |
100 |
18.82-32.29 |
26.17
a |
3.24 |
6.00 |
<
1yr |
50 |
21.83-28.26 |
26.01 a |
2.09 |
6.00 |
1-1.5yrs |
250 |
17.80-34.89 |
26.40 a |
3.13 |
3.20 |
1.5-2yrs |
295 |
18.73-34.89 |
26.70 a |
3.48 |
3.05 |
2-2.5
yrs |
102 |
20.00-32.29 |
25.87 a |
2.86 |
5.88 |
Above
2.5yrs |
113 |
18.36-36.79 |
26.58 a |
4.33 |
5.31 |
Total |
910 |
|
|
|
|
Rural |
Primipara |
6 |
16.94-32.36 |
23.15
a |
4.00 |
0.00 |
<
1yr |
30 |
19.98-29.90 |
23.88 a |
4.14 |
16.67 |
1-1.5yrs |
104 |
19.15-35.56 |
26.30 a |
3.87 |
17.31 |
1.5-2yrs |
120 |
20.00-40.03 |
26.36 a |
4.60 |
16.67 |
2-2.5yrs |
95 |
20.96-32.03 |
24.69 a |
5.01 |
18.68 |
Above
2.5yrs |
122 |
18.65-42.36 |
25.51 a |
5.31 |
16.39 |
Total |
477 |
|
|
|
|
Values with
different superscripts per column are statistically significant (p<0.05)
* % PEM: Overall
– p<0.2192, Urban – p<0.1991, Rural – p<0.1081 (Pearson
X2 used)
Table 4 shows mean BMI and
prevalence of PEM according to child spacing. Overall no statistical
difference in mean BMI and prevalence of PEM was found among the pregnant
women according to child spacing. The same was the case in both the
urban and rural sub-samples.
Majority of
the subjects in the rural sub sample were subsistence farmers and as
is the case in most sub-Saharan African countries although they spend
long hours farming they still have limited access to food since the
men control the family resources.14 The rural women therefore
consumes systematically below their minimum daily calorie requirement.15
This would explain the lower mean weight, height and BMI of the rural
subjects compared to the urban subjects. A previous study by the authors
showed prevalence of PEM to be 3-4 times higher in the rural area compared
with the urban area (unpublished finding).
The effect
of age on the prevalence of PEM showed that the age groups, below 20years
and 20-24 years, presented the higher prevalence of PEM of 25% and 11.74%
respectively. Their mean BMIs were significantly lower than those of
the other age group. The 24 years and below age group is apparently the
group at greater risk for PEM especially in the rural areas. The age
effect although not seen in the urban area was quite prominent in the
rural areas.
The effect
of level of education on the prevalence of PEM showed that those with
no formal education and primary education had significantly lower BMI
and higher percentages of PEM than those of other groups. Hence it can
be concluded that the less educated are at greater risk of developing
PEM. Level of education did not show any effect in the urban area but
was a significant factor in the rural areas. The more educated pregnant
women in the rural areas are the ones that are likely to be engaged
in occupations other than farming which will fetch them more income
and hence greater food purchasing power. In the urban area on the other
hand, even the less educated pregnant woman is likely to be engaged
in some economic activity which will earn her some income and thus guarantee
her reasonable food purchasing power.
Parity of two,
one and primipara recorded mean BMIs that were significantly lower than
those of the other groups. This effect was more pronounced in the urban
area than the rural areas. This can be explained by the fact that weight
gain increases with increase in parity.16 Hence those with
lower parity are likely to have lower BMIs. However, in the rural areas,
this might not necessarily be the case since as has been pointed out
the rural women live physically arduous lives17 and so the
usual weight gain with increase in parity may not be observed.
Although the
nutritional demands of frequent cycles of pregnancy and lactation (child
spacing) have always been known to impact negatively on the nutritional
status of women17, results from the present study showed
that child spacing did not have any significant effect on both
the mean BMIs and the prevalence of PEM amongst pregnant women both
in the urban and rural areas. The reason for this is not immediately
obvious but it might be that the education intervention programmes (usually
a common feature of antenatal clinics) on birth control measures and
child spacing may be yielding dividends.
In conclusion,
Protein Energy Malnutrition among pregnant women remains a major public
health problem in Nigeria especially in the rural areas. Those who are
at greater risk are the teenage and young mothers, the less educated,
the primigravidae and those with parity of one or two especially in
the rural areas. In view of the adverse effects of PEM on both mother
and child it is recommended that appropriate intervention programmes
be instituted to tackle the problem and the following recommendations
are hereby made:
- Introduction of
feeding programmes in antenatal clinics and health centers or in the
alternative, provision of food subsidies to targeted groups,
- Counseling on dietary
intake and reduced energy expenditure before and during pregnancy.
- Nutrition education
and efficient nutrition monitoring systems at all levels of care.
- Subsidized agricultural
inputs and labour saving devices for women.
- Hygiene education,
improved access to potable water and adequate sanitation and health
care services
- Providing opportunities
for women’s involvement in development through access to education,
paid employment, assets such as land and credit facilities.
The authors
thank Miss Dorothy Nwaneri, Miss Maryjoe Keke and Miss Chinemerem Anyanwu
for their assistance in data collection. We also thank the numerous
proprietors of the private hospitals and clinics in Owerri and the nurses
at the Government hospitals in Owerri and health centers in the rural
areas for their co-operation
-
World
Health Organization (2002). World Health Report, Geneva: The
Organization, 2002.
-
Food and
Agriculture Organization of the United Nations.
Under Nourishment
Around the World. In The State of Food Insecurity in the World,
Rome, The Organization, 2004.
-
Sachs JD,
McArthur JW. The Millennium Project: A Plan for
Meeting the Millennium Development Goals Lancet 2005;365:347-53
-
Salama
P, Spiegel P, Talley L, Waldman R. Lessons Learned
From Complex Emergencies Over Past Decade. Lancet 2004;364:1801–13.
-
Muller
O, Krawinkel M. Malnutrition
and Health in Developing
Countries. CMAJ 2005;171(3):279-293.
-
Pena
M, Bacalao J. Malnutrition and Poverty. Ann Rev Nutr 2002;22:241-253.
-
Enwonwu CO,
Phillips RS, Ibrahim CD, Danfillo IS. Nutrition
and Oral Health in Africa. International Dental Journal 2004;54:344-351.
-
Scrimshaw NS. Malnutrition, Brain Development, Learning
and Behaviour. Nutrition Research
1998;18(2):351-379.
-
Abidoye RO, Eze DI. Comparative School Performance Through
Better Health and Nutrition in Nsukka, Enugu, Nigeria. Nutrition
Research 2000;20(5):609-620.
-
De Onis
M, Blossner M, Villar J. Levels and Patterns of Intrauterine
Growth Retardation in Developing Countries. European Journal of Clinical
Nutrition 1998;52:583-592
-
World
Health Organization Sample Size Determination: A User’s Manual,
Geneva WHO 1986 (WHO/HST/EMS/86.1).
-
Lwanga SK, Lemeshow S. Sample Size Determination in Health
Studies: A Practical Manual, Geneva, WHO, 1991.
-
United
Nations Administrative Committee on Coordination/Subcommittee
on Nutrition. Second Report on the World Nutrition Situation,
vol. 1, 1992. Global and Regional Results. Geneva; United Nations Administrative
Committee on Co-ordination/Subcommittee on Nutrition.
-
Folbre
N. Hearts and Spades: Paradigms
of Household Economics. World development 1986;14:245-255.
-
Food
and Agriculture Organization (FAO).
Food Requirements and
Population Growth. Technical Paper No 12, 1996. World Food Sumit,
FAO.
-
Ogbeide
O, Okojie O, Wagbatsoma V, Isah E.
Nutritional Status
of Lactating Mothers in Benin City, Nigeria. Nig. J. Nutr.
Sci. 1994;15(1&2):37-39.
-
Leslie
J, Clemins E, Essama SB.
Female Nutritional Status Across
Life-Span in Sub-Sahara Africa. I. Prevalence Patterns. Food Nutr
Bull 1997;18:20-43.
|