Skip to main content
BioMed Research International logoLink to BioMed Research International
. 2018 Apr 23;2018:8169615. doi: 10.1155/2018/8169615

Determinants of Low Birth Weight among Deliveries at a Referral Hospital in Northern Ethiopia

Lema Desalegn Hailu 1, Deresse Legesse Kebede 2,
PMCID: PMC5937567  PMID: 29850570

Abstract

Background

Low birth weight is the leading cause of infant and child mortality and contributes to several poor health outcomes. Proper knowledge of risk factors of low birth weight is important for identifying those mothers at risk and thereby for planning and taking appropriate actions. This study investigates factors predicting occurrence of low birth weight among deliveries at Debreberhan Referral Hospital.

Methods

Facility-based unmatched case-control study was conducted among deliveries that took place at Debreberhan Referral Hospital. Birth records and mothers' ANC files were reviewed from April to June 2016. The study participants were selected by consecutive sampling technique. Data analysis was performed by SPSS version 20. Binary logistic regression analysis was performed to identify predictors of low birth weight.

Result

A total of 147 birth records of babies with low birth weight (cases) and 294 birth records of babies with normal birth weight (controls) were reviewed. The birth weight of low birth weight babies (cases) ranged from 1000 grams to 2400 grams with median (±IQR) of 2200 grams (±300 grams), whereas it ranged from 2500 grams to 4500 grams with median (±IQR) of 3100 grams (±525 grams) among controls. Preterm birth (AOR = 5.32; CI = 2.959–9.567), history of any physical trauma experienced during pregnancy (AOR = 13.714; CI = 2.382–78.941), and history of any pregnancy complication (AOR = 2.708; CI = 1.634–4.487) were predictors of low birth weight. On the other hand, cesarean delivery (AOR = 0.415; CI = 0.183–0.941) and instrumental (AOR = 0.574; CI = 0.333–0.987) modes of delivery as well as maternal history of chronic diabetes (AOR = 0.275; CI = 0.090–0.836) had preventive effect of low birth weight.

Conclusion

Preterm birth, history of experiencing any physical trauma during pregnancy, and history of any pregnancy complication were predictors of low birth weight, whereas cesarean and instrumental delivery had positive effect to preventing low birth weight.

1. Background

Birth weight or size at birth is an important indicator of the child's vulnerability to the risk of childhood illnesses and to predict the child's future health, development, and the chances of survival [1]. Low birth weight (LBW) is defined by the World Health Organization (WHO) as weight at birth of less than 2,500 grams. This is based on epidemiological observations that infants weighing less than 2,500 grams are at higher risk of neonatal mortality when compared with heavier babies [2]. Low birth weight is considered as the single most important predictor of infant mortality, especially of deaths within the first months of life [3]. Globally, 60–80% of neonatal deaths occur among low birth weight infants [1]. In developing countries, a birth weight below 2,500 grams is the leading cause of infant and child mortality and contributes to several poor health outcomes [2]. It is associated with poor neurological and cognitive development, childhood morbidity, growth impairment, a range of poor health outcomes, and chronic diseases later in life. It is a cause of both short-term and long-term consequences leading to adverse social and economic impacts [4, 5].

Globally, more than 20 million infants, representing 15.5% of all births, are born with low birth weight; 95.6% of them lived in developing countries, accounting for 17% of all births in developing countries [6, 7]. According to a hospital-based study among institutional deliveries in Iran, the prevalence of low birth weight was 40%, and gestational age less than 37 weeks, maternal age less than 20 years, irregular antenatal checkup, mother's height less than 150 cm, mother's weight less than 50 kg, hemoglobin less than 10 gm/dl, severe physical work, and tobacco chewing were significant determinants of low birth weight [8]. An epidemiological survey from China showed that low birth weight was associated with maternal age of less than 20 years, low level of maternal education, previous histories of adverse pregnancies, and pregnancy comorbidities and complications, such as hypertensive disorders during pregnancy, anemia, oligohydramnios, premature rupture of membranes, and gestational diabetes [9]. In a study from Lombok, Indonesia, determinants of LBW included infant's sex, woman's education, season at birth, mothers' residence, household wealth, maternal mid-upper arm circumference (MUAC), maternal height, birth order, and pregnancy interval [1]. According to the World Health Organization (WHO), factors contributing to LBW in developing countries include inadequate weight gain during pregnancy, low prepregnancy weight, short stature, malaria and other infectious diseases, hard physical work during pregnancy, social factors such as lower status of women, malnutrition, and lack of antenatal care [10]. In Ethiopia, the prevalence of LBW is as high as more than 10% according to reports from different regions of the country. A recent study reported from Tigray region, northern Ethiopia, showed that 10.5% of live births in the region were underweight [4]. According to a study conducted in Gondar University Hospital, northern Ethiopia, 11.2% of deliveries that were performed in the hospital were LBW [11], and in another hospital-based study from Tigray region, northern Ethiopia, the prevalence of low birth weight was 14.6% [7]. According to the national Ethiopian Demography and Health Survey 2011 (EDHS 2011), among babies who had reported birth weight in the country, 11% (17% in rural and 9% in urban) were born with low birth weight (weighed less than 2.5 kilograms), with variations among regions. Apart from regional variations, low birth weight was more common among children of the youngest mothers (age less than 20 years) and older mothers (age 35–49 years). Furthermore, first-order births, children of mothers with no education, and children born to mothers in the lowest wealth quintile were the most likely to be reported as very small [12]. On the other hand, factors like lack of antenatal follow-up, preterm delivery, chronic medical illness, lack of formal education, young age of the mother, and so forth were reported to be associated with low birth weight from different studies [4, 7, 13].

Having proper knowledge of risk factors for low birth weight is important to identification and giving appropriate attention to those mothers at risk. Despite few studies available to show factors associated with low birth weight across the country, it is not investigated in the study area. Therefore, this study investigates factors related to low birth weight particularly among deliveries at Debreberhan Referral Hospital. Findings from this study add to the current knowledge of risk factors of low birth weight particularly regarding mode of delivery, maternal chronic diabetes, pregnancy complication, and physical trauma during pregnancy which has not been well explained by other studies. This will have great relevance in identifying mothers and children at risk, designing appropriate measures, and undertaking timely interventions.

2. Methods and Materials

2.1. Study Design, Setting, and Population

Facility-based unmatched case-control study was conducted from April to June 2016 among deliveries that were performed at Debreberhan Referral Hospital. The hospital is found in Debreberhan town, located 130 kilometers to the North East of Addis Ababa. It is one of the most popular health facilities in the town rendering a range of medical, maternal, and child health services including delivery services, and various inpatient and outpatient healthcare services for a catchment population of over 95 thousand coming from the town as well as surrounding rural areas. Deliveries that take place at Debreberhan hospital were the source population. A case (low birth weight) was defined as a live birth baby born with birth weight of <2500 grams; and a control was defined as a live birth baby born with birth weight of ≥2500 grams.

2.2. Sample Size and Sampling Technique

Assuming odds ratio of 2 desired to detect, 95% confidence level, 80% power, and control to case ratio of 2, the sample size was calculated by Open Epi version 2.3 using the formula for unmatched case control and found to be 441, 147 cases and 294 controls. Birth records were selected by consecutive sampling technique. For each low birth weight (birth weight < 2500 grams), the next two delivery cases with birth weight ≥ 2500 grams were considered as controls.

2.3. Data Collection and Analysis

Data were collected by review of birth records and mothers' ANC files. Relevant data were extracted from the birth records as well as corresponding mothers' ANC files using a structured checklist. Sociodemographic as well as maternal and obstetric variables were extracted from birth records, while gestational age of the fetus and data about history of pregnancy complications were obtained from the mothers' ANC files. Data processing and analysis were performed by using Statistical Package for Social Sciences (SPSS) version 20. Having the average age and the relative proportion of mothers in each age category under consideration as well as other literatures for comparison purpose, age of the mothers was categorized into three as 15–24 years, 25–34 years, and 35 years or above. Birth weight was categorized into two as low birth weight (birth weight < 2500 grams), considered as cases, and normal birth weight (birth weight ≥ 2500 grams), considered as controls or the reference birth weight. Multicollinearity diagnostics was performed to check for collinearity among independent variables and evaluated that each of the independent variables in the multiple analysis had tolerance value >0.1 against every other independent variable. Multiple binary logistic regression analysis was performed to identify independent predictors of low birth weight. Adjusted odds ratio (AOR) with 95% confidence interval (CI) and p value ≤ 0.05 were used to claim statistical significance.

3. Result

3.1. Maternal Characteristics

A total of 147 birth records of babies with low birth weight (cases) and 294 birth records of babies with normal birth weight (controls) were reviewed in this study. The age of mothers ranged from 15 to 42 years with mean (±SD) of 25.37 (±4.99) years. Overall, majority of the mothers were in the age group of 15–24 years, followed by 25–34 years, accounting for 203 (46.0%) and 202 (45.8%), respectively. The median (±IQR) age of mothers was 24 (±7) years among cases, while it was 25 (±6) among controls. Among cases, 77 (52.4%) of mothers were in the age group of 15–24 years, while 146 (49.7%) of maternal age among controls were found in the age group of 25–34 years. The proportion of mothers aged 35 years and above were relatively small both in cases and in controls: 14 (9.5%) and 22 (7.5%), respectively. Maternal gravidity ranged from 1 to 6 with primigravida accounting for the larger proportion of mothers both in cases and in controls: 86 (58.5%) and 156 (53.1%), respectively. Maternal parity ranged from 0 to 5 with primipara accounting for the larger proportion of mothers both in cases and in controls: 90 (61.2%) and 172 (58.5%), respectively. ANC follow-up status of mothers was almost similar among cases and controls. Among cases, 54 (36.7%) of mothers had ANC visit, while the remaining 93 (63.3%) had no ANC visit. Among controls, 107 (36.4%) of mothers had ANC visit, while 187 (63.6%) had no ANC visit. The hemoglobin level of mothers ranged from 6.9 g/dl to 19.3 g/dl among cases with mean (±SD) of 13.6 g/dl (±1.93 g/dl), whereas in controls it ranged from 6.0 g/dl to 41.0 g/dl with mean (±SD) of 13.8 g/dl (±2.58 g/dl). The proportion of mothers who ever experienced any physical trauma during pregnancy was relatively higher among cases. Among cases, 5 (3.4%) of mothers had ever experienced any physical trauma during pregnancy, while the proportion was only 2 (0.7%) among controls. Among cases, 76 (51.7%) of mothers experienced any one or more signs of pregnancy complications (any one or more of bleeding, gush, headache, blurred vision, fever, and severe abdominal pain) during pregnancy, whereas among controls, 106 (36.1%) of mothers had any sign of pregnancy complications during pregnancy (Table 1).

Table 1.

Frequency distribution of maternal and newborn characteristics among cases and controls, Debreberhan Referral Hospital, northern Ethiopia, June 2016.

Variable Cases (n = 147) Controls (n = 294)
Frequency % Frequency %
Sex of newborn
 Female 69 46.9% 158 53.7%
 Male 78 53.1% 136 46.3%
Mothers' age category
 15–24 77 52.4% 126 42.9%
 25–34 56 38.1% 146 49.7%
 35–42 14 9.5% 22 7.5%
Mother's gravidity
 Primigravida 86 58.5% 156 53.1%
 Multigravida 61 41.5% 138 46.9%
Mother's parity
 Primipara 90 61.2% 172 58.5%
 Multipara 57 38.8% 122 41.5%
Mother's history of abortion
 No 137 93.2% 274 93.2%
 Yes 10 6.8% 20 6.8%
Gestational age at birth
 Full-term 82 55.8% 231 78.6%
 Preterm 47 32.0% 25 8.5%
 Postterm 4 2.7% 11 3.7%
 Unknown 14 9.5% 27 9.2%
Mode of delivery
 SVD 106 72.1% 172 58.5%
 Instrumental 30 20.4% 86 29.3%
 CS 11 7.5% 36 12.2%
Mother's ANC visit
 No 93 63.3% 187 63.6%
 Yes 54 36.7% 107 36.4%
Iron supplementation during pregnancy
 No 129 87.8% 251 85.4%
 Yes 18 12.2% 43 14.6%
Mother's history of chronic hypertension
 No 118 80.3% 239 81.3%
 Yes 29 19.7% 55 18.7%
Pregnancy-induced hypertension (PIH)
 No 131 89.1% 276 93.9%
 Yes 16 10.9% 18 6.1%
Mother's history of anemia
 No 117 79.6% 241 82.0%
 Yes 30 20.4% 53 18.0%
Mother's history of chronic DM
 No 126 85.7% 238 81.0%
 Yes 21 14.3% 56 19.0%
Experience of physical trauma during pregnancy
 No 142 96.6% 292 99.3%
 Yes 5 3.4% 2 0.7%
Any sign of pregnancy complications
 No 71 48.3% 188 63.9%
 Yes 76 51.7% 106 36.1%

3.2. Newborn Characteristics

The birth weight of babies ranged from 1000 grams to 2400 grams among cases with median (±IQR) of 2200 grams (±300 grams), whereas in controls it ranged from 2500 grams to 4500 grams with median (±IQR) of 3100 grams (±525 grams). Male age accounted for the larger proportion of cases, 78 (53.1%), while female age accounted for the larger proportion of controls, 158 (53.7%). Regarding gestational age at birth, 82 (55.8%) of cases were delivered at their full term, while 47 (32.0%) were delivered preterm or premature. Among controls, 231 (78.6%) of deliveries were full term, while 25 (8.5%) were preterm or premature. With regard to mode of delivery, the proportion of spontaneous vaginal delivery (SVD) was higher among cases as compared to controls. Among cases, 106 (72.1%) of the mode of delivery was SVD, whereas SVD accounted for 172 (58.5%) of the mode of delivery among controls. In contrast, the proportion of cesarean section (CS) and other instrumental deliveries were lower among cases as compared to controls (Table 1).

3.3. Bivariate Analyses

From binary logistic regression analyses of each variable with low birth weight, maternal age, gestational age at birth, mode of delivery, and experience of any sign of pregnancy complications were found to have significant association with low birth weight. Moreover, maternal experience of any physical trauma during pregnancy had remarkable effect on low birth weight. Independent samples t-test showed that there is no significant difference in the mean hemoglobin level of mothers between cases and controls (p = 0.349). Both maternal gravidity and parity in its continuous scale as birth order as well as the categorized forms had no significant association with low birth weight (Table 2).

Table 2.

Bivariate analyses of different variables with low birth weight, Debreberhan Referral Hospital, northern Ethiopia, June 2016.

Variable Cases (n = 147) Controls (n = 294) COR (95% CI) p value
Frequency (%) Frequency (%)
Sex of newborn
 Female 69 (46.9%) 158 (53.7%) 1.000
 Male 78 (53.1%) 136 (46.3%) 1.313 (0.883, 1.953) 0.178
Mothers' age category
 15–24 77 (52.4%) 126 (42.9%) 1.595 (1.048, 2.422) 0.029
 25–34 56 (38.1%) 146 (49.7%) 1.000
 35–42 14 (9.5%) 22 (7.5%) 1.659 (0.794, 3.469) 0.178
Mother's gravidity β = −0.039 0.962 (0.827, 1.118) 0.614
Gravidity in category
 Primigravida 86 (58.5%) 156 (53.1%) 1.000
 Multigravida 61 (41.5%) 138 (46.9%) 0.802 (0.537, 1.196) 0.279
Mother's parity β = −0.035 0.965 (0.826, 1.128) 0.657
Parity in category
 Primipara 90 (61.2%) 172 (58.5%) 1.000
 Multipara 57 (38.8%) 122 (41.5%) 0.893 (0.596, 1.339) 0.583
History of abortion
 No 137 (93.2%) 274 (93.2%) 1.000
 Yes 10 (6.8%) 20 (6.8%) 1.000 (0.456, 2.195) 1.000
Gestational age at birth
 Term 82 (55.8%) 231 (78.6%) 1.000
 Preterm 47 (32.0%) 25 (8.5%) 5.296 (3.066, 9.149) 0.000
 Postterm 4 (2.7%) 11 (3.7%) 1.024 (0.317, 3.306) 0.968
 Unknown 14 (9.5%) 27 (9.2%) 1.461 (0.731, 2.921) 0.284
Mode of delivery
 SVD 106 (72.1%) 172 (58.5%) 1.000
 Instrumental 30 (20.4%) 86 (29.3%) 0.566 (0.350, 0.916) 0.020
 CS 11 (7.5%) 36 (12.2%) 0.496 (0.242, 1.016) 0.055
ANC visit
 No 93 (63.3%) 187 (63.6%) 1.000
 Yes 54 (36.7%) 107 (36.4%) 1.015 (0.673, 1.531) 0.944
Iron supplementation
 No 129 (87.8%) 251 (85.4%) 1.000
 Yes 18 (12.2%) 43 (14.6%) 0.814 (0.452, 1.469) 0.495
Chronic hypertension
 No 118 (80.3%) 239 (81.3%) 1.000
 Yes 29 (19.7%) 55 (18.7%) 1.068 (0.647, 1.762) 0.797
PIH
 No 131 (89.1%) 276 (93.9%) 1.000
 Yes 16 (10.9%) 18 (6.1%) 1.873 (0.926, 3.789) 0.081
History of anemia
 No 117 (79.6%) 241 (82.0%) 1.000
 Yes 30 (20.4%) 53 (18.0%) 1.166 (0.708, 1.921) 0.547
Chronic DM
 No 126 (85.7%) 238 (81.0%) 1.000
 Yes 21 (14.3%) 56 (19.0%) 0.708 (0.410, 1.223) 0.216
Trauma during preg.
 No 142 (96.6%) 292 (99.3%) 1.000
 Yes 5 (3.4%) 2 (0.7%) 5.141 (0.985, 26.823) 0.052
Any sign preg. comp.
 No 71 (48.3%) 188 (63.9%) 1.000
 Yes 76 (51.7%) 106 (36.1%) 1.898 (1.270, 2.837) 0.002

3.4. Multivariable Analyses

From the multiple binary logistic regression analyses, gestational age at birth (preterm), mode of delivery, maternal history of chronic diabetes mellitus, experience of any physical trauma during pregnancy, and experience of any sign of pregnancy complications (any one or more of bleeding, gush, headache, blurred vision, fever, and severe abdominal pain) were found to be independent predictors of low birth weight. Babies who were born preterm (premature babies) were five times more likely to have low birth weight as compared to those born at their full term (AOR = 5.321; CI = 2.959–9.567). With regard to mode of delivery, babies born via cesarean delivery were 58% less likely to have low birth weight (AOR = 0.415; CI = 0.183–0.941) and babies born via instrumental delivery (vacuum delivery, forceps delivery, etc.) were 43% less likely to have low birth weight (AOR = 0.574; CI = 0.333–0.987) when compared to babies born via spontaneous vaginal delivery. On the other hand, babies born to mothers who had history of any physical trauma experienced during pregnancy were about fourteen times more likely to have low birth weight as compared to babies born to mothers who did not have such history (AOR = 13.714; CI = 2.382–78.941). And similarly, babies born to mothers who had history of any sign of pregnancy complications (any one or more of bleeding, gush, headache, blurred vision, fever, and severe abdominal pain) were about three times more likely to have low birth weight as compared to babies born to mothers who did not have such history (AOR = 2.708; CI = 1.634–4.487). Maternal history of chronic diabetes was found to have negative relationship with low birth weight. In this regard, babies born to mothers having history of chronic diabetes mellitus were 72% less likely to have low birth weight as compared to those born to mothers with no history of chronic diabetes mellitus (AOR = 0.275; CI = 0.090–0.836). The variables such as sex of the newborn, maternal age category, maternal parity (birth order), ANC visit, and maternal hemoglobin level had no significant association with low birth weight (Table 3).

Table 3.

Multiple logistic regression analyses of different variables with low birth weight, Debreberhan Referral Hospital, northern Ethiopia, June 2016.

Variable AOR (95% CI) p value
Sex of newborn
 Female 1.000
 Male 1.246 (0.795, 1.954) 0.337
Mothers' age category
 15–24 1.454 (0.897, 2.357) 0.128
 25–34 1.000
 35–42 1.662 (0.692, 3.990) 0.256
Mother's parity 0.961 (0.790, 1.169) 0.690
History of abortion
 No 1.000
 Yes 0.974 (0.391, 2.425) 0.955
Gestational age at birth
 Term 1.000
 Preterm 5.321 (2.959, 9.567) 0.000
 Postterm 1.418 (0.413, 4.866) 0.579
 Unknown 1.565 (0.735, 3.335) 0.246
Mode of delivery
 SVD 1.000
 Assisted 0.574 (0.333, 0.987) 0.045
 CS 0.415 (0.183, 0.941) 0.035
ANC visit
 No 1.000
 Yes 0.864 (0.522, 1.430) 0.570
Mother's hemoglobin level (g/dl) 0.955 (0.863, 1.058) 0.378
Iron supplementation
 No 1.000
 Yes 0.607 (0.285, 1.290) 0.194
Chronic hypertension
 No 1.000
 Yes 1.226 (0.445, 3.380) 0.694
PIH
 No 1.000
 Yes 1.473 (0.625, 3.470) 0.376
History of anemia
 No 1.000
 Yes 2.172 (0.776, 6.074) 0.139
Chronic DM
 No 1.000
 Yes 0.275 (0.090, 0.836) 0.023
Trauma during pregnancy
 No 1.000
 Yes 13.714 (2.382, 78.941) 0.003
Any sign of preg. complications
 No 1.000
 Yes 2.708 (1.634, 4.487) 0.000

Statistically significant with p value ≤ 0.05.

4. Discussion

This study investigated some maternal and pregnancy related factors associated with low birth weight. Preterm birth was found to be a risk factor for low birth weight; babies born preterm were more likely to be of low birth weight when compared to their full term counterparts. This is supported by a study from Ardabil, Iran, in which preterm birth was reported to be a risk factor of low birth weight [14] and a study conducted in Kuala Lumpur, Malaysia, in which premature delivery was among predictors of low birth weight [5]. It is also in line with report from a study in Gondar University Hospital, northwest Ethiopia, in which preterm births were about six times more likely to be of low birth weight when compared to full term ones [11], and also supported by reports from hospital-based studies conducted in Tigray region, northern Ethiopia, where premature delivery (gestational age less than 37 weeks) was one of the important predictors of low birth weight [4, 7]. It is clear that babies born premature before completing their term due to any gynecological, medical, or other causes are not completing their normal physical development in the womb and at higher risk to have low weight at birth. In this regard, it could be important that any gynecological, medical, or other condition that could be possible cause of premature delivery should be timely recognized and properly managed during pregnancy.

In the current study, mode of delivery was found to be associated with low birth weight. It was observed that babies born via cesarean section as well as instrumental deliveries (vacuum delivery, forceps delivery, etc.) were less likely to be of low birth weight when compared to those born via spontaneous vaginal delivery. This means that low birth weight is less common among cesarean as well as instrumental deliveries while it is more common among spontaneous vaginal deliveries. It could be due to the natural mechanism that cesarean and instrumental procedures are more likely to be indicated for larger sized babies (the rates of cesarean and instrumental deliveries are lower for low birth weight babies), while relatively smaller sized babies with low birth weight are likely to be born spontaneously. Apart from this, the natural procedure in the case of spontaneous vaginal delivery could have impact on the birth weight of the baby. That is, series of physical compressions due to the labor process and the procedure during spontaneous vaginal delivery could have been resulting in significant weight loss to the baby during delivery. Although cesarean section and minor instrumental procedures like vacuum or forceps deliveries are applied for different reasons, they would have positive effect in maintaining birth weight of the baby. Those babies born via cesarean section and other instrumental procedures are prevented from potential compressions at birth and hence attributable weight loss during delivery, yet the association with mode of delivery needs further investigation.

It was found in the current study that occurrence of any sign of pregnancy complications (any one or more of bleeding, gush, headache, blurred vision, fever, and severe abdominal pain) was a risk factor for low birth weight. This is consistent with the finding from a study conducted in Ardabil, Iran, in which bleeding or spotting during pregnancy was reported to be a risk factor for low birth weight [14]. It was also supported by an epidemiological survey conducted in China [9], as well as a hospital-based study from Bale zone, southeast Ethiopia [13]. The signs and symptoms of pregnancy complications are indicative of some kind of disorder during pregnancy which could have negative impact on the birth weight of the baby. It is therefore recommended that pregnant women should be aware of danger signs during pregnancy and possible cause of such complications during pregnancy should be timely recognized and properly managed during pregnancy. To this end, regular antenatal follow-up by pregnant women might help for early detection and appropriate management of such disorders during pregnancy.

It was observed that babies born to mothers who had experienced any physical trauma during pregnancy were more likely to be born with low birth weight. The physical trauma could have directly resulted from an accidental injury which occurred during pregnancy or it could have resulted from a forceful hard work performed indoor or outdoor during pregnancy. According to a study conducted at a tertiary care hospital in Uttar Pradesh, severe physical work was one of the significant determinants of low birth weight [8]. In line, WHO reported that hard physical work during pregnancy is one of the factors contributing to occurrence of low birth weight in developing countries [11]. Any physical trauma encountered during pregnancy might have been accompanied by internal bleeding or soft tissue injury to the mother or the conception in the womb and could have significant impact on the birth weight of the outcome. As any physical trauma during pregnancy might have such negative impact on the birth weight of the outcome, avoiding hard work and preventing physical trauma are important during pregnancy.

According to this study, babies born to mothers having history of chronic diabetes mellitus were less likely to be born with low birth weight when compared to those born to mothers with no history of chronic diabetes mellitus. This could be explained by the medical effect that such mothers are medically likely to give birth to “giant babies” or the observed association could be just incidental. However, it is in contrary to the finding from a hospital-based study in Tigray, northern Ethiopia, which reported that presence of any chronic medical illness increased the risk of low birth weight [7]. The discrepancy could be related to the specific type of disease observed as evidenced from studies in northern Tanzania [15] as well as Gondar, Ethiopia [11], in which mother's chronic hypertension was observed to be associated with low birth weight or it could be related to variations in clinical stages of the diseases.

Generally, this study has identified risk factors of low birth weight particularly those pertaining to the study area and most of which has not been identified by other previous studies. Despite employing case-control design which we consider as the strength of this study, it is yet not without limitation. As variables related to maternal nutrition and biomedical or anthropometric variables of the mother such as height, weight, and body mass index might have effect on the birth weight of the pregnancy outcome, lack of these variables from secondary data is limitation of the study.

5. Conclusion

Preterm birth, history of experiencing any physical trauma during pregnancy, and history of any pregnancy complication were predictors of low birth weight, whereas cesarean and instrumental modes of delivery had preventive effect of low birth weight. Prompt identification of causes and prevention of premature delivery, proper knowledge of signs and symptoms of pregnancy complications, and preventing any physical trauma or its potential causes are recommended during pregnancy to prevent low birth weight. Identification of high risk mothers and early detection and management of the risk factors would reduce incidence of low birth weight and related short-term and long-term consequences.

Ethical Approval

Ethical clearance was obtained from Addis Ababa University Research Ethics and Publication Committee before conducting the study. Further permission was obtained from Debreberhan Referral Hospital administration for utilization of the birth records. Any information related to personal identification of the study participants was not recorded to maintain confidentiality of the study.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Authors' Contributions

Lema Desalegn Hailu conceived the study, developed the proposal, and managed the data collection. Deresse Legesse Kebede and Lema Desalegn Hailu performed the data analysis. Deresse Legesse Kebede drafted the manuscript. Both Deresse Legesse Kebede and Lema Desalegn Hailu read and approved the manuscript.

References

  • 1.Sebayang S. K., Dibley M. J., Kelly P. J., Shankar A. V., Shankar A. H. Determinants of low birthweight, small-for-gestational-age and preterm birth in Lombok, Indonesia: analyses of the birthweight cohort of the SUMMIT trial. Tropical Medicine & International Health. 2012;17(8):938–950. doi: 10.1111/j.1365-3156.2012.03039.x. [DOI] [PubMed] [Google Scholar]
  • 2.Regional and Global Estimates. 2004. United Nations Children’s Fund, World Health Organization: Low Birth Weight Country. [Google Scholar]
  • 3.Zenebe K., Awoke T., Birhan N. Low birth weight and associated factors among newborns in Gondar Town, Northwest Ethiopia. Indo Global Journal of Pharmaceutical Sciences. 2014;4(2):74–80. [Google Scholar]
  • 4.Mengesha H. G., Wuneh A. D., Weldearegawi B., Selvakumar D. L. Low birth weight and macrosomia in Tigray, Northern Ethiopia: who are the mothers at risk? BMC Pediatrics. 2017;17(1, article 144) doi: 10.1186/s12887-017-0901-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Sutan R., Mohtar M., Mahat A. N., Tamil A. M. Determinant of low birth weight infants: a matched case control study. Open Journal of Preventive Medicine. 2014;4(3):91–99. doi: 10.4236/ojpm.2014.43013. [DOI] [Google Scholar]
  • 6.Bugssa G., Dimtsu B., Alemayehu M. Socio demographic and maternal determinants of low birth weight at mekelle hospital, northern ethiopia: a cross sectional study. American Journal of Advanced Drug Delivery. 2014;2(5):609–618. [Google Scholar]
  • 7.Gebremedhin M., Ambaw F., Admassu E., Berhane H. Maternal associated factors of low birth weight: a hospital based cross-sectional mixed study in Tigray, Northern Ethiopia. BMC Pregnancy and Childbirth. 2015;15(1, article 222) doi: 10.1186/s12884-015-0658-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Agarwal K., Agarwal A., Agrawal V. K., et al. Prevalence and determinants of "low birth weight" among institutional deliveries. Annals of Nigerian Medicine. 2011;5(2):48–52. doi: 10.4103/0331-3131.92950. [DOI] [Google Scholar]
  • 9.Chen Y., Li G., Ruan Y., Zou L., Wang X., Zhang W. An epidemiological survey on low birth weight infants in China and analysis of outcomes of full-term low birth weight infants. BMC Pregnancy and Childbirth. 2013;13, article 242 doi: 10.1186/1471-2393-13-242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Tema T. Prevalence and determinants of low birth weight in Jimma zone, southwest Ethiopia. East African Medical Journal. 2006;83(7):366–371. doi: 10.4314/eamj.v83i7.9448. [DOI] [PubMed] [Google Scholar]
  • 11.Adane A. A., Ayele T. A., Ararsa L. G., Bitew B. D., Zeleke B. M. Adverse birth outcomes among deliveries at Gondar University Hospital, Northwest Ethiopia. BMC Pregnancy and Childbirth. 2014;14(1, article 90) doi: 10.1186/1471-2393-14-90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Ethiopia Demographic and Health Survey 2011, Central Statistical Agency, Addis Ababa, Ethiopia, ICF International, Calverton, Maryland, Md, USA, 2012.
  • 13.Demelash H., Motbainor A., Nigatu D., Gashaw K., Melese A. Risk factors for low birth weight in Bale zone hospitals, South-East Ethiopia: a case–control study. BMC Pregnancy and Childbirth. 2015;15(1, article 264) doi: 10.1186/s12884-015-0677-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Mirzarahimi M., Hazrati S., Ahmadi P., Alijahan R. Prevalence and risk factors for low birth weight in Ardabil, Iran. Iranian Journal of Neonatology. 2013;4(1):18–23. [PMC free article] [PubMed] [Google Scholar]
  • 15.Siza J. E. Risk Factors Associated with Low Birth weight of neonates among pregnant women attending a referral hospital in northern Tanzania. Tanzania Journal of Health Research. 2008;10(1):1–8. doi: 10.4314/thrb.v10i1.14334. [DOI] [PubMed] [Google Scholar]

Articles from BioMed Research International are provided here courtesy of Wiley

RESOURCES