Acute Malnutrition PDF

Download as pdf or txt
Download as pdf or txt
You are on page 1of 10

Gizaw et al.

Italian Journal of Pediatrics (2018) 44:21


DOI 10.1186/s13052-018-0457-1

RESEARCH Open Access

Acute malnutrition among children aged


6–59 months of the nomadic population in
Hadaleala district, Afar region, northeast
Ethiopia
Zemichael Gizaw1*, Wondwoson Woldu2 and Bikes Destaw Bitew1

Abstract
Background: Acute malnutrition to be a major health burden in the world, particularly in the developing world.
Acute malnutrition is associated with more than one third of the global disease burden for children. Malnourished
children are physically, emotionally and intellectually less productive and suffer more from chronic illnesses and
disabilities. The nature, magnitude and determinants of acute malnutrition are determined among the general
populations; however, there is a lack of evidence in the nomadic communities.
Methods: A cross-sectional study was conducted to assess the magnitude and factors associated with acute
malnutrition among children aged 6–59 months in Hadaleala district, Afar Region. A total of 591 under-five
children were included in this study, and subjects were recruited by the multistage cluster sampling
technique. Data were collected by a pre-tested questionnaire and a simple anthropometric index so called
mid-upper arm circumference (MUAC). The multivariable binary logistic regression analysis was used to
identify factors associated with acute malnutrition on the basis of adjusted odds ratio (AOR) with 95%
confidence interval (CI) and p < 0.05.
Results: The prevalence of acute malnutrition was 11.8% (95% CI = 9.3, 14.8%). The highest prevalence (50%)
of acute malnutrition occurred among children aged between 12.0–23.0 months. Childhood acute malnutrition was
associated with the presence of two (AOR = 2.49, p < 0.05) and three (AOR = 12.87, p < 0.001) children in each
household, unprotected drinking water sources (AOR = 3.78, p < 0.05), absence of the latrine (AOR = 5.24, p < 0.05),
hand washing with soap (AOR = 0.21, p < 0.05), childhood diarrheal disease (AOR = 2.72, p < 0.05), and child vaccination
(AOR = 0.15, p < 0.001).
Conclusion: The prevalence of acute malnutrition among children aged 6-59 months was was higher than the
national prevalence. The number of children in each household, drinking water sources, latrine availability,
hand washing practice before food preparation and child feeding, childhood diarrheal disease, and child
vaccination were identified as factors affecting the childhood acute malnutrition in the nomadic community.
Protecting drinking water sources from possible contaminants, improving hand washing practices, utilization
of latrine, preventing diarrheal diseases and vaccinating children integrated with the access of nutrition
education is important to improve nutrition of children of the nomadic people.
Keywords: Acute malnutrition, Children aged 6–59 months, Nomads, Afar region, Ethiopia

* Correspondence: [email protected]
1
Department of Environmental and Occupational Health and Safety,
University of Gondar, Gondar, Ethiopia
Full list of author information is available at the end of the article

© The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
the Creative Commons license, and indicate if changes were made. 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.
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 2 of 10

Background Ababa, the capital city of Ethiopia. It has an area of


Under nutrition continues to be a major health burden 1272 km2 divided into 11 rural kebeles (the smallest ad-
in the world, particularly in the developing world [1–3]. ministrative units in Ethiopia) with a total population of
Globally, children with moderate and severe acute under 42,845 as projected for the year 2015. It has 7516 house-
nutrition are approximately 60 million and 13 million holds with an average household size of 5.7 persons per
respectively [1, 2]. Under nutrition is globally the most house. Under-five children account for 10.1% (4328) of
important risk factor for illness and death, with hun- the total population. As the population lives in a very
dreds of millions of young children particularly affected scattered manner, the average population density is 14
[4, 5]. It is associated with more than one third of the persons/km2. Furthermore, the economy of the district is
global disease burden for children [6]. Between 8 to 11 based on livestock and crop production [48].
million under-five children die each year globally [2, 7],
and more than 35% of these deaths are attributed to Sample size determination
under nutrition [3]. The sample size was determined using the single population
Under nutrition among children is a critical problem. Its proportion formula by considering the following assump-
effects are long lasting [1, 8]. Under nourished children tions: p = 10.0% (prevalence of malnutrition among children
are physically, emotionally and intellectually less product- aged 6–59 months in Bule Hora district, South Ethiopia
ive and suffer more from chronic illnesses and disabilities [49]), 95% confidence interval, and a 4% margin of error (d),
[9–12]. Malnutrition affects child performance, health,
2
and survival [13, 14]. In the long term, early nutritional zα =2 pð1−pÞ ð1:96Þ2 0:1ð1−0:1Þ
deficits are linked to impairments of intellectual perform- n¼ 2 ¼ ¼ 217
d 0:042
ance; work capacity, reproductive outcomes and overall
health during adolescence and adulthood [14–18]. The Considering the design effect of 2 and 10% non response
immediate consequences of poor nutrition during the rate, the final sample size was 478 mother-child pair.
early years include significant morbidity and mortality and
delayed mental and motor developments. Malnutrition at Sampling procedure
the early stages of life can lower child resistance to The multistage cluster sampling technique was used to se-
infections [19]. Moreover, the potential negative impact of lect study participants from the nomadic population. The
child malnutrition goes beyond the individual, affecting clusters were villages with defined geographical boundar-
society and future generations [20, 21]. ies. Out of a total of 11 kebeles, 6 were selected by the
In Ethiopia, under nutrition among children is still a com- simple random sampling technique. The 6 selected
mon problem. Ethiopia is one of the countries with very kebeles were clustered into 39 villages, and 17 villages
high burden of under nutrition. In the country, under nutri- were selected by the systematic random sampling tech-
tion is the underlying cause of 57% of child deaths [22–25]. nique. All the households (591) found in the selected 17
Under nutrition among children depends on complex in- villages with children aged 6–59 months were included in
teractions of various factors, like socio-demographic [24–30], the study. For households which had more than one child
drinking water quality [26, 28, 29, 31–35], hygiene of each, the younger one was selected for the study.
complementary foods [24, 28], environmental sanitation
[26, 31, 32, 36–38], child co-morbidities [19, 39–44], and Data collection tools and procedures
child vaccination [45–47]. Though, the nature, magnitude A structured questionnaire and anthropometric meas-
and determinants of under nutrition are determined urement were used to collect data. The questionnaire
among the general populations, there is lack of evidence was pre-tested out of the study area in a community
in the nomadic communities. This cross-sectional study which had similar characteristics prior to the actual data
was therefore conducted to assess the magnitude and fac- collection. Eight diploma graduate nurses and two envir-
tors associated with acute malnutrition among children onmental health officers who were fluent enough in both
aged 6–59 months in Hadaleala district, Afar Region, Amharic and Afarigna (local languages) and working in
northeast Ethiopia. the district were involved in the data collection process.
Training was given for the data collectors and supervi-
Methods sors. The data collectors visited all households in the
Study design and settings selected clusters. When the data collectors found the
A community - based cross-sectional study was con- target groups during the visits, they interviewed the
ducted among the nomadic populations in Hadaleala mothers about the variables and measured the circum-
district, Afar Region, northeast Ethiopia in May, 2015. ference of the upper arm of the child. Finally, the
Hadaleala district is located at 341 km southwest of the collected data were checked and corrected by the data
regional capital, Semera, and 268 km north of Addis collectors immediately after finalizing the questionnaire.
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 3 of 10

Supervisors daily checked the completeness, quality, and interquartile range was 25-35 years. Almost all, 577
consistency of information collected. (97.6%) of the mothers were married at the time of data
collection. The great majority, 514 (87.0%) of mothers
Measurement of outcome variable were illiterate. Almost all, 559 (94.6%) of the mothers
Childhood malnutrition, the primary outcome variable were housewives by occupation. Five hundred thirty –
of this study, is determined by a simple anthropometric seven (90.9%) mothers were Afar by ethnicity. More
index the so called mid-upper arm circumference than half, 339 (57.4%) of the households had more than
(MUAC). Nutritional status of children was take as acute five family members. Three hundred eighty – two
malnutrition if MUAC value is lower than 125 mm [50]. (64.6%) households were economically poor. Two hun-
Childhood diarrheal disease, one of the predictor vari- dred twenty – nine (38.7%) of the children were aged
ables is defined as having three or more loose or watery above 35 months. The median age of children was
stools in 24 h [51, 52]. Household economic status, 28 months and the interquartile range (IQR) was 16-
which was the other predictor variable was calculated by 40 months. More than half, 338 (57.2%) of the house-
using tropical livestock unit (TLU). Tropical livestock holds had only one child aged 6-59 months, and 317
unit was determined by multiplying the number of spe- (53.6%) of the children were male (Table 1).
cific species with the TLU conversion factor assigned to
that specific species. Camels, cattle, sheep, goats, horses, Drinking water and hygiene of complementary foods
mules, asses, and chickens were common in the study Three hundred fifty – four (59.9%) households collected
area. Generally, TLU was determined as (1.0*Number of drinking water from unimproved sources and the greater
camels) + (0.8*Number of horses) + (0.7* Number of majority, 522 (88.3%) of the water sources were seasonal.
mules) + (0.7*Number of cattle) + (0.5*Number of asses) Very few, 20 (3.4%) households treated drinking water at
+ (0.1*Number of sheep) + (0.1*Number of goats) home. Cow or goat milk was the commonest, 337
+ (0.01*Number of chickens). Household economic sta- (57.0%) complementary food for the children. Three
tus was determined by comparing the TLU scores with hundred thirty – three (56.3%) households served un-
the standard score. A below 5 TLU score indicated that cooked foods for the children, and the greater majority,
the household was poor. A TLU score of 5 to 12.99 551 (93.2%) of the households used unclean utensils to
showed the household was medium in economic status, serve foods. Three – forth, 447 (75.6%) of the house-
and rich households scored 13 and above TLU [53]. holds fed the children soon after the food is prepared,
and the overwhelming majority, 539 (91.2%) used left-
Data management and statistical analysis over foods. Three hundred twenty - four (54.8%)
Data were entered using the EPI-INFO version 3.5.3 stat- mothers washed hands with only water (Table 2).
istical package and exported to SPSS version 20 for further
analysis. Cross tabulation was used to describe socioeco- Personal hygiene and environmental sanitation
nomic, environmental sanitation, health, and nutritional Nearly one – tenth, 56 (9.5%) of the mothers had good
characteristics of children. Categorical data were pre- personal hygiene. More than threefold, 483 (81.7%), and
sented as frequency counts or percentages and compared 490 (82.9%) of the households practiced open defecation
using the Pearson chi-square. Continuous data were sum- and indiscriminate solid waste disposal respectively. The
marized as mean or median with ± standard deviation and living environment of 464 (78.5%) households was poor
interquartile range. The univariable binary logistic regres- condition, and vector infestation was observed among
sion analysis was used to choose variables for the multi- 483 (81.7%) households. Three hundred thirty (55.8%)
variable binary logistic regression analysis, and variables households had only one room, and very few, 91 (15.4%)
which had less than 0.2 p – values by the univariable ana- households had cemented or plastered floor (Table 3).
lysis were then analyzed by the multivariable binary logis-
tic regression for controlling the possible effects of Health condition of mothers and children
confounders, and finally, variables which had significant Sixty (10.2%) mothers and 172 (29.1%) children had
association were identified on the basis of adjusted odds diarrheal disease in the 2 week period prior to the sur-
ratio (AOR) with 95% CI and p < 0.05. vey. A majority, 416 (70.4%) of the mothers didn’t know
the causes of diarrhea. Three hundred twenty – seven
Results (55.3%) and 377 (63.8%) mothers didn’t know that flies
Socio-demographic information and child excreta can cause diarrheal diseases, respect-
A total of 591 mothers - child pair participated in this ively. The great majority, 477 (80.7%) of the children had
study with a 100% response rate. More than half, 311 ever been vaccinated. However, significant number or
(52.6%) of the mothers were aged 25-34 years. The me- proportion, 254 (43.0%) and 418 (70.7%) of the children
dian age of the mothers was 30 years, and the had no measles and rotavirus vaccination respectively.
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 4 of 10

Table 1 Socioeconomic information of households (n = 591) Table 2 Drinking water and hygiene of complementary
in Hadaleala district, Afar region, northeast Ethiopia, April to foods of households in Hadaleala district, Afar region,
May, 2015 northeast Ethiopia, April to May, 2015
Variables Frequency Percentage Environmental variables Frequency Percentage
Age of mothers in years Drinking water sources
15–24 131 22.2 Improved 237 40.1
25–34 311 52.6 Unimproved 354 59.9
≥ 35 149 25.2 Seasonality of water sources
Marital status of mothers Permanent 69 11.7
Currently married 577 97.6 Temporarily 522 88.3
Currently not married 14 2.4 Home based water treatment
Educational level of mothers Yes 20 3.4
No formal education 514 87.0 No 571 96.6
Formal education 77 13.0 Types of complementary foods for the children
Occupational status of mothers Cow or goat milk 337 57.0
Housewife 559 94.6 Adults’ food 133 22.5
Employed 32 5.4 Gruel 112 19.0
Ethnic group of mothers Infant formula/Powder milk 9 1.5
Afar 537 90.9 Using unclean utensils to serve foods
Oromo 44 7.4 Yes 551 93.2
Amhara 10 1.7 No 40 6.8
Family size Serving uncooked food for the children
≤ 5. 252 42.6 Yes 333 56.3
>5 339 57.4 No 258 43.7
Household economic status Feeding children soon after food prepared
Poor 382 64.6 Yes 447 75.6
Medium 209 35.4 No 144 24.4
Age group of children Children ate leftover foods
6.0–11.0 72 12.2 Yes 539 91.2
12.0–23.0 152 25.7 No 52 8.8
24.0–35.0 138 23.4 How do you wash your hand
> 35.0 229 38.7 With plain water 324 54.8
Sex of children With soap 267 45.2
Male 317 53.6
Female 274 46.4
Number of children (95% CI = 9.3, 14.8%). Female children were more mal-
One 338 57.2 nourished than males. Out of 70 malnourished children,
42 (60%) females and 28 (40%) males were malnourished
Two 218 36.9
respectively. The highest prevalence of acute malnutri-
Three 35 5.9
tion occurred among children aged 12-23 months, which
accounted 35 (50%) (Fig. 1).
Four hundred eighty- eight (82.6%) of the children re-
ceived vitamin A supplementation (Table 4). Factors associated with nutritional status
Table 5 presents the results of the binary logistic
Nutritional status regression analysis on socioeconomic, water and hy-
The MUAC value of 70 children was below 125 mm. giene of complementary foods, personal hygiene and
Therefore, the prevalence of acute malnutrition among environmental sanitation, and health related variables.
children aged 6 - 59 months in the nomadic population Childhood acute malnutrition was statistically associ-
of Hadaleala district, Afar Region was found to be 11.8% ated with the number of children in the household.
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 5 of 10

Table 3 Personal hygiene and environmental sanitation of Table 4 Health conditions of mothers and children in Hadaleala
households in Hadaleala district, Afar region, northeast Ethiopia, district, Afar region, northeast Ethiopia, April to May, 2015
April to May, 2015 Health related information Frequency Percentage
Environmental variables Frequency Percentages Two week history of maternal diarrhea
Personal hygiene of mothers Yes 60 10.2
Poor 535 90.5 No 531 89.8
Good 56 9.5 Childhood diarrhea
Latrine availability Yes 172 29.1
Yes 108 18.3 No 419 70.9
No 483 81.7 Mothers know the causes of diarrheal disease
Solid waste management Yes 175 29.6
Controlled 101 17.1 No 416 70.4
Open field 490 82.9 Mothers know flies transmit diarrheal disease
Environmental sanitation Yes 264 44.7
Poor 464 78.5 No 327 55.3
Good 127 21.5 Mothers know excreta of children can cause disease
Infestation of insects Yes 214 36.2
Yes 483 81.7 No 377 63.8
No 108 18.3 Child ever been vaccinated
Number of rooms Yes 477 80.7
One 330 55.8 No 114 19.3
Two 231 39.1 Measles vaccination
Three 30 5.1 Yes 337 57.0
Housing floor material No 254 43.0
Earth/sand 500 84.6 Rota virus vaccination
Cemented 91 15.4 Yes 173 29.3
No 418 70.7
Acute malnutrition was 2.49 times more likely to be Vitamin A supplementation
higher among households with two children compared Yes 488 82.6
with households with only one child [AOR = 2.49, 95% CI
No 103 17.4
= (1.06, 5.85)]. Similarly, the likelihood of acute malnutri-
tion was also 12.87 times higher among households with
three children compared with households who had one
child [AOR = 12.87, 95% CI = (4.04, 41.00)]. diarrhea and vaccination. Childhood acute malnutrition
Acute malnutrition among children aged 6 - 59 months was 2.72 times more likely to be higher among children
was associated with drinking water sources, availability of who had diarrheal disease [AOR = 2.72, 95% CI = (1.15,
latrine, and hand washing practices. It was 3.78 times 6.40)]. This study indicated that child vaccination has a
more likely to be higher among households that collected protective effect on childhood acute malnutrition.
drinking water from unprotected sources [AOR = 3.78, Children who ever been vaccinated were 85% less
95% CI = (1.07, 13.34)]. The likelihood of childhood acute likely to be malnourished, compared with their coun-
malnutrition was 5.24 times to be higher among house- terparts [AOR = 0.15, 95% CI = (0.07, 0.31)].
holds who had no latrine compared with their counter-
parts [AOR = 5.24, 95% CI = (1.19, 23.19)]. Children Discussion
whose mothers washed their hands before food prepar- The prevalence of acute malnutrition among children
ation and feeding with soap were less likely to be malnour- aged 6-59 months was 11.8% (95% CI = 9.3, 14.8%).
ished. Hand washing with soap before food preparation Childhood acute malnutrition was statistically associated
and child feeding can prevent childhood acute malnutri- with the number of children in each household, drinking
tion by 79% [AOR = 0.21, 95% CI = (0.05, 0.81)]. water sources, latrine availability, hand washing practice
Childhood acute malnutrition was also statistically asso- before food preparation and child feeding, childhood
ciated with the health status of children, like childhood diarrheal disease, and child vaccination. The prevalence
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 6 of 10

13.0% 14.0%

6 - 11 months

12 - 23 months
23.0%
24-35 months

>35 months

50.0%

Fig. 1 Prevalence of acute malnutrition with respect to age of children in Hadaleala district, Afar region, northeast Ethiopia, April to May, 2015

of acute malnutrition reported by this study is slightly that children who frequently affected by infections have
higher than the national prevalence of acute malnutrion mal-absorption of important nutrients [60–63].
(9%) [54] and findings of various studies conducted in This study indicated that acute malnutrition was associ-
Ethiopia like Bule Hora district, South Ethiopia, 10% ated with child hood diarrheal diseases. Children who had
[49] and it was also just two-fold higher than the preva- diarrheal disease were more likely to be acutely malnour-
lence reported in Aleta Chucko and Aleta Wondo dis- ished as compared with their counter parts. This finding
tricts, Sidama Zone, South Ethiopia, 5.6% [55]. Whereas, was supported by the findings of other similar studies [24,
the magnitude of acute malnutrition reported by this 28, 33, 36, 38, 64–66]. This may be due to the fact that
study was lower than the findings of studies conducted diarrheal disease due to poor hygiene and lack of sanita-
in Pagak district, South Sudan, 16.7% [56]. The differ- tion induces a gut disorder called environmental enterop-
ence in prevalence might be attributed to the difference athy (EE) characterized by blunted intestinal villi,
in the socio- demographic, environmental, and behav- increased intestinal permeability; fat and carbohydrate
ioral characteristics of households and the nomadic na- mal-absorption, and increased protein needs [67] that di-
ture of the population. verts energy from growth towards an ongoing fight against
This study showed that families who had two or above subclinical infection [68–71]. EE is a major cause of post-
children aged 6-59 months were more likely to have natal stunting and wasting [71–77].
childhood acute malnutrition than those who had only Child vaccination was also the other statistically associ-
one child. This probably attributed to less balanced diet ated variable with childhood acute malnutrition. Children
intake and accessibility of child healthcare decreased who ever vaccinated were less likely to be malnourished
with more number of children per household, especially compared with their counterparts. This finding is supported
in low income families [33, 34, 57, 58]. by the findings of other similar studies [36, 45–47, 78]. This
In this study, it was found that acute malnutrition can be justified as vaccinated children are less likely to be
was associated with unprotected drinking water frequently infected with vaccine preventable diseases such
sources, open defecation, and poor hand washing as diarrhea and respiratory infections, which are known in
practices of mothers. Different studies also reported depleting nutrients from the body [45, 79, 80].
that acute malnutrition was associated with drinking Finally, this paper determined acute malnutrition using
water sources [26, 28, 29, 31–35], availability of MUAC measurement. It didn’t measure weight and
latrine [26, 31, 32, 36–38] and hand washing practices height to determine global malnutrition. This paper also
[36, 59]. This may be so because poor water, hygiene didn’t consider the effect of food security and access to
and sanitation condition increase the risk of diversified foods on childhood malnutrition. Moreover,
infections. Infections affect nutrient absorption and com- the paper didn’t investigate demand side issues and sup-
promised nutritional status of children. Evidences show ply side issues of systems failures with respect to poverty
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 7 of 10

Table 5 Factors affecting acute malnutrition among children aged between 6 and 59 months in Hadaleala district, Afar region,
northeast Ethiopia, April to May, 2015
Variables Acute malnutrition COR with 95% CI AOR with 95% CI
Yes No
Number of children
One 13 325 1
Two 35 183 4.78 (2.47, 9.27) 2.49 (1.06, 5.85)*
Three 22 13 42.31 (17.52, 102.18) 12.87 (4.04, 41.00)**
Family size
≤5 37 215 1
>5 33 306 0.63 (0.38, 1.03) 1.99 (0.95, 4.18)
Wealth status
Poor 58 324 2.94 (1.54, 5.61) 1.68 (0.72, 3.94)
Medium 12 197 1
Mothers’ occupation
House wife 63 496 0.45 (0.19, 1.09) 0.20 (0.04, 1.05)
Employee 7 25 1
Water sources
Protected 4 233 1
Unprotected 66 288 13.35 (4.80, 37.16) 3.78 (1.07, 13.34)*
Latrine availability
Yes 4 104 1
No 66 417 6.61 (2.04, 21.40) 5.24 (1.19, 23.19)*
Hand washing** *
With water only 66 258 1
With soap 4 263 0.06 (0.02, 0.17) 0.21 (0.05, 0.81)*
Children eat leftover foods
Yes 61 478 0.61 (0.28, 1.31) 0.68 (0.23, 2.01)
No 9 43 1
Childhood diarrhea
No 11 408 1
Yes 59 113 19.37 (9.85, 38.10) 2.72 (1.15, 6.40)*
Children ever vaccinated
Yes 19 458 0.05 (0.03, 0.09) 0.15 (0.07, 0.31)**
No 51 63 1
Solid waste management
Controlled 15 62 2.02 (1.08, 3.79) 1.89 (0.62, 5.75)
Uncontrolled 55 459 1
*Statistically significant at p < 0.05 | **statistically significant at p < 0.001 | ***before food preparation and child feeding

alleviation. The authors believed that other studies food preparation and child feeding, childhood diarrheal dis-
should be conducted to fill the above identified gaps. ease, and child vaccination were identified as factors affecting
the childhood acute malnutrition in the nomadic commu-
Conclusion nity. Protecting drinking water sources from possible con-
The prevalence of acute malnutrition among children aged taminants, improving hand washing practices, utilization of
6-59 months was higher than the national prevalence. The latrine, preventing diarrheal diseases and vaccinating children
number of children in each household, drinking water integrated with the access of nutrition education is important
sources, latrine availability, hand washing practice before to improve nutrition of children of the nomadic people.
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 8 of 10

Abbreviations 6. Huq M, Dasgupta S, Khaliquzzaman M, Pandey KD, Wheeler D. Indoor air


AOR: Adjusted Odds Ratio; CI: Confidence Interval; COR: Crude Odds Ratio; quality for poor families: new evidence from Bangladesh. World Bank Policy
EE: Environmental Enteropathy; IQR: Interquartile Range; Km: Kilometer; Research Working Paper. 2004(3393).
Km2: Kilometer square; MUAC: Mid-upper arm circumference; SPSS: Statistical 7. Singer PA, Ansett S, Sagoe-Moses I. What could infant and young child
Package for Social Sciences; TLU: Tropical Livestock Holding nutrition learn from sweatshops? BMC Public Health. 2011;11(1):276.
8. Abuya BA, Ciera J, Kimani-Murage E. Effect of mother’s education on child’s
Acknowledgments nutritional status in the slums of Nairobi. BMC Pediatr. 2012;12(1):1.
The authors are pleased to acknowledge data collectors, field supervisors, 9. Jesmin A, Yamamoto SS, Malik AA, Haque MA. Prevalence and determinants
study participants, Hadaleala District Health Office, Afar Regional Health of chronic malnutrition among preschool children: a cross-sectional study in
Bureau for their unreserved contributions to the success of this study. The Dhaka City, Bangladesh. J Health Popul Nutr. 2011:494–9.
authors would also like to extend their gratitude to Hadaleala district 10. Dewey KG, Begum K. Long-term consequences of stunting in early life.
administrators for their facilitation. Matern Child Nutr. 2011;7(s3):5–18.
11. Kar BR, Rao SL, Chandramouli B. Cognitive development in children with
Funding chronic protein energy malnutrition. Behav Brain Funct. 2008;4(1):1.
The authors of this study didn’t receive funds from any funding organization. 12. Lopez-Valcarzel A. Occupational safety and health in the construction work.
However, University of Gondar had covered questionnaire duplication and Afr Newsl Occup Health Safety. 2001;11(1):4–6.
data collection fees. 13. Ghosh AK, Bhattacherjee A, Chau N. Relationships of working conditions
and individual characteristics to occupational injuries: a case-control study
Availability of data and materials in coal miners. J Occup Health. 2004;46(6):470–80.
Data will be made available upon requesting the primary author. 14. Onis M, Dewey KG, Borghi E, Onyango AW, Blössner M, Daelmans B, et al. The
World Health Organization's global target for reducing childhood stunting by
Authors’ contributions 2025: rationale and proposed actions. Matern Child Nutr. 2013;9(S2):6–26.
All the authors actively participated during conception of the research issue, 15. Gillespie S, Haddad L, Mannar V, Menon P, Nisbett N, Maternal, et al. The
development of a research proposal, data collection, analysis and interpretation, politics of reducing malnutrition: building commitment and accelerating
and writing various parts of the research report. ZG had analyzed the data and progress. Lancet. 2013;382(9891):552–69.
had written the manuscript. WW had designed the study protocol and had 16. Bhutta ZA, Das JK, Rizvi A, Gaffey MF, Walker N, Horton S, et al. Evidence-
supervised the quality of data. BDB had revised the study protocol and based interventions for improvement of maternal and child nutrition: what
manuscript. All the authors read and approved the final manuscript. can be done and at what cost? Lancet. 2013;382(9890):452–77.
17. León-Cava N, Lutter C, Ross J, Martin L. Quantifying the benefits of
Ethics approval and consent to participate breastfeeding: a summary of the evidence. Pan American Health Organization,
Ethical clearance was obtained from the Institutional Review Board of the Washington DC. 2002. Available at http://www.paho.org/hq/index.
University of Gondar and an official letter was submitted to the district php?option=com_content&view=article&id=5654%3A2011-cuantificacion-
administrators. There were no risks due to participation in this research beneficios-lactancia-materna-resena-evidencia-2002&catid=3719%3Anutrition-
project, and the collected data were used only for this research purpose. publications&Itemid=4081&lang=en. Accessed 10 May 2017.
Verbal informed consent was obtained from the mothers. All information 18. Bhandari N, Mazumder S, Bahl R, Martines J, Black RE, Bhan MK, et al. An
collected from each household was treated with complete confidentiality. educational intervention to promote appropriate complementary feeding
During data collection, oral rehydration solution and Zinc tablets with clear practices and physical growth in infants and young children in rural
instructions were given to children who had diarrhea, and advice was given Haryana, India. J Nutr. 2004;134(9):2342–8.
to mothers to take their children to a nearby health institution for further 19. Rodríguez L, Cervantes E, Ortiz R. Malnutrition and gastrointestinal and
management diarrhea and malnutrition. respiratory infections in children: a public health problem. Int J Environ Res
Public Health. 2011;8(4):1174–205.
Consent for publication 20. Victora CG, Adair L, Fall C, Hallal PC, Martorell R, Richter L, et al. Maternal
This manuscript does not contain any individual person’s data. and child undernutrition: consequences for adult health and human capital.
Lancet. 2008;371(9609):340–57.
Competing interests
21. Grantham-McGregor S, Cheung YB, Cueto S, Glewwe P, Richter L, Strupp B,
The authors declare that they have no competing interests.
et al. Developmental potential in the first 5 years for children in developing
countries. Lancet. 2007;369(9555):60–70.
Publisher’s Note 22. Ethiopia demographic and health survey, 2011. Addis Ababa, Ethiopia and
Springer Nature remains neutral with regard to jurisdictional claims in Calverton, Maryland, USA: Central Statistical Agency and ICF International.
published maps and institutional affiliations. 2012;430. Availlable at https://dhsprogram.com/pubs/pdf/GF26/GF26.pdf.
Accessed on 16 May 2016.
Author details 23. Taylor L. From food crisis to nutrition: challenges and possibilities in
1
Department of Environmental and Occupational Health and Safety, Ethiopia’s nutrition sector’. Institute of Development Studies. 2012.
University of Gondar, Gondar, Ethiopia. 2Hadaleala District Health Office, 24. Teshome B, Kogi-Makau W, Getahun Z, Taye G. Magnitude and determinants
Hadaleala District, Afar Regional State, Ethiopia. of stunting in children underfive years of age in food surplus region of
Ethiopia: the case of west gojam zone. Ethiop J Health Dev. 2009;23(2).
Received: 27 November 2017 Accepted: 16 January 2018 25. Sisay Z. Magnitude and factors associated with malnutrition of children
under five years of age in rural Kebeles of Haramaya, Ethiopia Harar Bull
Health Sci Extracts 2012(2011):4.
References 26. Medhin G, Hanlon C, Dewey M, Alem A, Tesfaye F, Worku B, et al.
1. Glewwe P, Miguel EA. The impact of child health and nutrition on Prevalence and predictors of undernutrition among infants aged six and
education in less developed countries. Handb Dev Econ. 2007;4:3561–606. twelve months in Butajira, Ethiopia: the P-MaMiE birth cohort. BMC Public
2. Collins S, Dent N, Binns P, Bahwere P, Sadler K, Hallam A. Management of Health. 2010;10(1):1.
severe acute malnutrition in children. Lancet. 2006;368(9551):1992–2000. 27. Yimer G. Malnutrition among children in southern Ethiopia: levels and risk
3. Black RE, Allen LH, Bhutta ZA, Caulfield LE, De Onis M, Ezzati M, et al. factors. Ethiop J Health Dev. 2000;14(3):283–92.
Maternal and child undernutrition: global and regional exposures and 28. Demissie S, Worku A. Magnitude and factors associated with malnutrition in
health consequences. Lancet. 2008;371(9608):243–60. children 6-59 months of age in pastoral community of Dollo ado district,
4. Müller O, Krawinkel M. Malnutrition and health in developing countries. Can Somali region, Ethiopia. Sci J Public Health. 2013;1(4):175–83.
Med Assoc J. 2005;173(3):279–86. 29. Wondafrash M, Amsalu T, Woldie M. Feeding styles of caregivers of children
5. Black R. Micronutrient deficiency: an underlying cause of morbidity and 6-23 months of age in Derashe special district, southern Ethiopia. BMC
mortality. Bull World Health Organ. 2003;81(2):79. Public Health. 2012;12(1):1.
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 9 of 10

30. Fentaw R, Bogale A, Abebaw D. Prevalence of child malnutrition in agro-pastoral 52. Black RE, Morris SS, Bryce J. Where and why are 10 million children dying
households in afar regional state of Ethiopia. Nutr Res Pract. 2013;7(2):122–31. every year? Lancet. 2003;361(9376):2226–34.
31. James P, Sadler K, Wondafrash M, Argaw A, Luo H, Geleta B, et al. Children 53. Jahnke HE. Livestock production systems and livestock development in
with moderate acute malnutrition with no access to supplementary feeding tropical Africa; Livestock Population in Tropical Africa by Species in
Programmes experience high rates of deterioration and no improvement: Numbers and in Tropical Livestock Units (TLU) 1979. P. 10. www. pdf.usaid.
results from a prospective cohort study in rural Ethiopia. PLoS One. 2016; gov/pdf_docs/PNAAN484.pdf. Accessed 10 May 2016.
11(4):e0153530. 54. Ethiopia Mini Demographic and Health Survey. Central Statistical Agency
32. Zewdie T, Abebaw D. Determinants of child malnutrition: empirical Addis Ababa. Ethiopia. 2014;2014:1–112. https://www.unicef.org/ethiopia/
evidence from Kombolcha District of eastern Hararghe zone, Ethiopia. Q J Mini_DHS_2014__Final_Report.pdf. Accessed on 17 May 2016
Int Agric. 2013;52(4):357–72. 55. ACF International. Maize Livelihood Belt of Aleta Chucko and Aleta Wondo
33. Taye A, Wolde T, Seid A. Under-nutrition and related factors among children Woredas, Sidama Zone, SNNPR Ethiopia final report 2014. By Jennifer
aged 6-59 months in Gida Ayana District, Oromiya region, West Ethiopia: a Holden, Action Contre La Faim (ACF): Analyst of Nutrition Causal Analysis.
community based quantitative study. J Nutr Food Sci. 2016;6(5):1–12. Available at http://www.ghadvocates.eu/wp-content/uploads/2015/08/
34. Masibo PK, Makoka D. Trends and determinants of undernutrition Nutrition-Causal-Analysis-Link-NCA-Sidama-Zone-Ethiopia-2014.pdf.
among young Kenyan children: Kenya demographic and health Accessed on 09 May 2016.
survey; 1993, 1998, 2003 and 2008–2009. Public Health Nutr. 2012; 56. NUTRITIONAL ANTHROPOMETRIC SURVEY CHILDREN UNDER 5 YEARS OLD
15(09):1715–27. PAGAK DISTRICT UPPER NILE (LATJOR STATE). ACF-USA.Available at https://
35. Kavosi E, Hassanzadeh Rostami Z, Kavosi Z, Nasihatkon A, Moghadami M, www.actionagainsthunger.org/sites/default/files/publications/ACF-NUT-
Heidari M. Prevalence and determinants of under-nutrition among children South-Sudan-Latjar-Pagak-2003-04-EN.pdf. Accessed on 12 May 2016.
under six: a cross-sectional survey in Fars province, Iran. Int J Health Policy 57. Sengupta P, Philip N, Benjamin A. Epidemiological correlates of under-
Manag. 2014;3:71–6. nutrition in under-5 years children in an urban slum of Ludhiana. Health
36. Ayana AB, Hailemariam TW, Melke AS. Determinants of acute malnutrition and Popul Perspect Issues. 2010;33(1):1–9.
among children aged 6–59 months in public hospitals, Oromia region, West 58. Mengistu K, Alemu K, Destaw B. Prevalence of malnutrition and associated
Ethiopia: a case–control study. BMC Nutri. 2015;1(1):1. factors among children aged 6-59 months at Hidabu Abote District, North
37. Sharghi A, Kamran A, Faridan M. Evaluating risk factors for protein-energy Shewa, Oromia Regional State. J Nutr Disord Ther. 2013;2013
malnutrition in children under the age of six years: a case-control study
59. Bantamen G, Belaynew W, Dube J. Assessment of factors associated with
from Iran. Int J General Med. 2011;4:607.
malnutrition among under five years age children at Machakel Woreda,
38. Tariku B, Mulugeta A, Tsadik M, Azene G. Prevalence and risk factors of child
Northwest Ethiopia: a case control study. J Nutr Food Sci. 2014;2014
malnutrition in community based nutrition program implementing and
60. Spears D. The nutritional value of toilets: How much international variation
nonimplementing districts from south East Amhara, Ethiopia. Open Access
in heights can sanitation explain? Discussion Paper, Delhi School of
Library J. 2014;1(03):1.
Economics, Delhi, India, 2013. Available at http://riceinstitute.org/wordpress/
39. Morris SS, Cogill B, Uauy R, Maternal, Group CUS. Effective international
wp-content/uploads/downloads/2013/07/Spears-height-and-sanitation-6-
action against undernutrition: why has it proven so difficult and what can
2013.pdf. Accessed on 05 May 2016.
be done to accelerate progress? Lancet. 2008;371(9612):608–21.
61. Langford R, Lunn P, Brick CP. Hand‐washing, subclinical infections, and
40. Blössner M, De Onis M, Prüss-Üstün A, Campbell-Lendrum D, Corvalán C,
growth: A longitudinal evaluation of an intervention in Nepali slums. Am J
Woodward A. Quantifying the health impact at national and local levels.
Hum Biol. 2011;23(5):621–9.
Geneva: WHO; 2005.
62. Spears D. How much international variation in child height can sanitation
41. Arinaitwe E, Gasasira A, Verret W, Homsy J, Wanzira H, Kakuru A, et al. The
explain? World Bank policy 10.1186/s13052-018-0457-1 research working
association between malnutrition and the incidence of malaria among
paper. 2013(6351). Available at http://documents.worldbank.org/curated/en/
young HIV-infected and-uninfected Ugandan children: a prospective study.
449651468191643600/How-much-international-variation-inchild-height-can-
Malar J. 2012;11(1):1.
sanitation-explain. Accessed on 04 May 2016.
42. Sackey ME. Intestinal parasitic infection: prevalence, risk factors and
63. Rah JH, Cronin AA, Badgaiyan B, Aguayo VM, Coates S, Ahmed S. Household
consequences for child growth, iron status and development in rural
sanitation and personal hygiene practices are associated with child stunting in
Ecuador. 2001.
rural India: a cross-sectional analysis of surveys. BMJ Open. 2015;5(2):e005180.
43. Hasanain F, Jamsiah M, Zaleha M, Azmi MTamil MA. Association between
64. Janevic T, Petrovic O, Bjelic I, Kubera A. Risk factors for childhood
drinking water sources and diarrhea with malnutrition among kindergarten's
malnutrition in Roma settlements in Serbia. BMC Public Health. 2010;10(1):1.
children in Baghdad city, Iraq. Malays J Public Health Med. 2012;12(1):45–8.
65. Fekadu Y, Mesfin A, Haile D, Stoecker BJ. Factors associated with nutritional
44. Njuguna J, Muruka C. Diarrhoea and malnutrition among children in a Kenyan
status of infants and young children in Somali Region, Ethiopia: a cross-
District: a correlational study. J Rural Tropical Public Health. 2011;10:35–8.
sectional study. BMC Public Health. 2015;15(1):1.
45. Ma’alin A, Birhanu D, Melaku S, Tolossa D, Mohammed Y, Gebremicheal K.
66. Alelign T, Degarege A, Erko B. Prevalence and factors associated with
Magnitude and factors associated with malnutrition in children 6–59
undernutrition and anaemia among school children in Durbete Town,
months of age in Shinille Woreda, Ethiopian Somali regional state: a cross-
northwest Ethiopia. Arch Public Health. 2015;73(1):1.
sectional study. BMC Nutr. 2016;2(1):44.
67. Kelly P, Menzies I, Crane R, Zulu I, Nickols C, Feakins R, et al. Responses of
46. Tadesse T, Kisi T, Mekonnen H. Malnutrition and its correlates among rural
small intestinal architecture and function over time to environmental factors
primary school children of Fogera District, Northwest Ethiopia. J Nutr Disord
in a tropical population. Am J Trop Med Hyg. 2004;70(4):412–9.
Ther. 2013;2013
68. Korpe PS, Petri WA. Environmental enteropathy: critical implications of a
47. Ahmed T, Roy S, Alam N, Hossain MI. Determinants of undernutrition in children
poorly understood condition. Trends Mol Med. 2012;18(6):328–36.
under 2 years of age from rural Bangladesh. Indian Pediatr. 2012;49(10):821–4.
48. Ethiopia. Hadaleala district. Finance and economic development office 69. Checkley W, Epstein LD, Gilman RH, Cabrera L, Black RE. Effects of acute diarrhea
annual report 2014, by Dawud Haji Alisadik and others, Hadaleala : Officer on linear growth in Peruvian children. Am J Epidemiol. 2003;157(2):166–75.
of finance and economic development Afar Region, Ethiopia, 2014. 70. Brown J, Cairncross S, Ensink JH. Water, sanitation, hygiene and enteric
49. Asfaw M, Wondaferash M, Taha M, Dube L. Prevalence of undernutrition and infections in children. Arch Dis Child. 2013;98(8):629–34.
associated factors among children aged between six to fifty nine months in 71. Bhutta ZA, Ahmed T, Black RE, Cousens S, Dewey K, Giugliani E, et al. What
Bule Hora district, South Ethiopia. BMC Public health. 2015;15(1):1. works? Interventions for maternal and child undernutrition and survival.
50. Grellety E, Golden MH. Weight-for-height and mid-upper-arm circumference Lancet. 2008;371(9610):417–40.
should be used independently to diagnose acute malnutrition: policy 72. Checkley W, Gilman RH, Black RE, Epstein LD, Cabrera L, Sterling CR, et al.
implications. BMC nutrition. 2016;2(1):10. Effect of water and sanitation on childhood health in a poor Peruvian peri-
51. UNICEF/WHO. Diarrhoea: Why children are still dying and what can be urban community. Lancet. 2004;363(9403):112–8.
done. The United Nations Children’s Fund/World Health Organization, 73. Lin A, Arnold BF, Afreen S, Goto R, Huda TMN, Haque R, et al. Household
Geneva, 2009. Available at www.unicef.org/.../Final_Diarrhoea_Report_ environmental conditions are associated with enteropathy and impaired
October_2009_final.pdf. Accessed 18 May 2016. growth in rural Bangladesh. Am J Trop Med Hyg. 2013;89(1):130–7.
Gizaw et al. Italian Journal of Pediatrics (2018) 44:21 Page 10 of 10

74. Ejemot R, Ehiri J, Meremikwu M, Critchley J, LUBY SP, CURTIS V. Hand


washing for preventing Diarrhoea. Commentaries. Int J Epidemiol. 2008;
37(3):470–3.
75. Luby SP, Agboatwalla M, Painter J, Altaf A, Billhimer W, Keswick B, et al.
Combining drinking water treatment and hand washing for diarrhoea
prevention, a cluster randomised controlled trial. Tropical Med Int Health.
2006;11(4):479–89.
76. Bowen A, Agboatwalla M, Luby S, Tobery T, Ayers T, Hoekstra R. Association
between intensive handwashing promotion and child development in
Karachi, Pakistan: a cluster randomized controlled trial. Arch Pediatr Adolesc
Med. 2012;166(11):1037–44.
77. Ngure FM, Reid BM, Humphrey JH, Mbuya MN, Pelto G, Stoltzfus RJ. Water,
sanitation, and hygiene (WASH), environmental enteropathy, nutrition, and
early child development: making the links. Ann N Y Acad Sci. 2014;1308(1):
118–28.
78. Adeba A, Garoma S, Fekadu H, Garoma W. Prevalence's of Wasting and its
Associated Factors of Children among 6-59 Months Age in Guto Gida
District, Oromia Regional State, Ethiopia. J Food Process Technol. 2014;2014
79. Agustina R, Sari TP, Satroamidjojo S, Bovee-Oudenhoven IM, Feskens EJ, Kok
FJ. Association of foodhygiene practices and diarrhea prevalence among
Indonesian young children from low socioeconomic urban areas. BMC
Public Health. 2013;13(1):1.
80. Madhi SA, Cunliffe NA, Steele D, Witte D, Kirsten M, Louw C, et al. Effect of
human rotavirus vaccine on severe diarrhea in African infants. N Engl J Med.
2010;362(4):289–98.

Submit your next manuscript to BioMed Central


and we will help you at every step:
• We accept pre-submission inquiries
• Our selector tool helps you to find the most relevant journal
• We provide round the clock customer support
• Convenient online submission
• Thorough peer review
• Inclusion in PubMed and all major indexing services
• Maximum visibility for your research

Submit your manuscript at


www.biomedcentral.com/submit

You might also like