Skip to main content
PLOS Global Public Health logoLink to PLOS Global Public Health
. 2022 Nov 2;2(11):e0001220. doi: 10.1371/journal.pgph.0001220

Prevalence of low birth weight and its associated factors: Hospital based cross sectional study in Nepal

Pratibha Thapa 1, Amod Poudyal 1, Rajan Poudel 1, Dipak Prasad Upadhyaya 2, Ashish Timalsina 1, Rama Bhandari 1, Jijeebisha Baral 1, Rabindra Bhandari 1, Prakash Chandra Joshi 3, Pratiksha Thapa 4, Nabin Adhikari 5,*
Editor: Zohra S Lassi6
PMCID: PMC10021178  PMID: 36962657

Abstract

Low birth weight is still an important public health problem worldwide. It is a major contributor to neonatal death in developing countries, including Nepal. The government of Nepal has developed and implemented different programs to improve maternal and neonatal health, including baby’s birth weight. However, low birth weight is a major maternal and child health challenge. Maternal factors determining the birth weight of neonates have been poorly assessed in previous studies in Nepal. Thus, this study aims to assess the prevalence and risk factors associated with low birth weight in Nepal. An institution-based descriptive cross-sectional study was carried out in Paropakar Maternity Hospital and Tribhuvan University Teaching Hospital of Kathmandu district among 308 postnatal mothers. The data was collected through the face-to-face interview technique. The data was entered in EpiData 3.1 and exported to Statistical Package and Service Solutions version 21 for analysis. Multivariate logistic regression was used to obtain an adjusted odds ratio, while p-value < 0.05 with 95% Confidence Interval (CI) was considered significant. The findings showed that 15.3% of the children had low birth weight. The mean and standard deviation of childbirth weight was 2.96±0.59 kg. Mothers belonged to Dalit ethnic (AOR = 2.9, 95% CI = 1.2–7.1), Antenatal Care visited three or fewer (AOR = 2.6, 95%CI = 1.0–6.6) and did not comply with Iron and Folic Acid supplementation (AOR = 2.1, 95% CI = 1.0–4.4) were significantly associated with low birth weight. Nearly one in every six children had low birth weight. Maternal health services such as antenatal care and compliance with a recommended dose of maternal micronutrients significantly impact on birth weight. Maternal and neonatal health programs should consider these factors to reduce adverse birth outcomes in Nepal.

Introduction

Birth weight has been one of the predictors of child mortality and morbidity. According to the World Health Organization (WHO), Low birth weight (LBW) live-born infants with a birth weight of less than 2500 grams, irrespective of the gestational age [1]. Epidemiological observations reflect that LBW babies have 20 times higher odds of dying than heavier infants [2]. Globally, LBW contributes to 40–60% of newborn mortality [3]. The baby’s birth weight is a sensitive indicator of the overall health situation of the population. LBW babies are at risk of cognitive deficits, motor delays, cerebral palsy, and other behavior and psychological problems [4, 5]. Furthermore, it is an indirect indicator of maternal health and a predictive indicator of potential neonatal death, the child’s malnutrition and cardiovascular disease risks in later life [6].

The global prevalence of low birth weight is estimated to be 15% to 20% of all births representing over 20 million births in a year [7]. There is wide variation in the prevalence of low birth weight across regions; however, evidence shows the nearly half of low births weight occurs in low and middle-income countries and especially in the most vulnerable population [8]. The regional estimates of low birth weight show 28% in south Asia, 6% east Asia and the Pacific, 13% in sub-Saharan Africa and 9% in Latin America [9]. According to Nepal Demographic Health Survey 2016, the prevalence of low birth weight in Nepal was 12%, which has stagnant since 2011 [10]. Similarly, most hospital-based cross-sectional studies conducted in Nepal show the prevalence of LBW varies from 12% to 39.6% [1114].

Evidence suggests that factors such as iron folic acid intake [15], maternal weight gain during pregnancy [16], preterm birth [17], mothers having inadequate antenatal care visits [18], anemic mothers [19] and smoking habits [20] were associated with low birth weight. Previous studies conducted in Nepal have shown that maternal education, maternal weight, maternal height, maternal age and lack of consumption of nutritious food during pregnancy were significantly associated with low birth weight [16, 21, 22]. The government of Nepal has recognized nutrition as a priority program of Nepal. Nepal aims to reduce LBW to less than 1.4% by 2030 [23]. To reduce low birth weight government has taken different strategies such as counseling during ANC visits, routine supplementation of IFA to pregnant women, providing nutritious food such as super cereals to pregnant women residing in highly food insecure areas and awareness of early pregnancy, smoking and alcohol during pregnancy [23]. Despite these efforts, the prevalence of low birth weight remains a major public health problem in Nepal [10].

Various factors were explored to identify the cause of low birth weight in different countries [16, 24, 25]. The majority of these studies focused on sociodemographic, cultural and nutritional factors. However, other factors such as ANC visit, consumption of IFA, maternal knowledge and tobacco/alcohol consumption have not been well studied. Hence this study would help to better understand the associated risk factors of low birth weight of babies in our context. This study’s finding also help generate local evidence for informed planning of the intervention to address the problem of low birth weight.

Methods

Study design

A cross-sectional study was conducted among two tertiary hospitals from September 2019 to August 2020 by using quantitative methods.

Study population

Our study population was postnatal mothers. We included mothers who had singleton pregnancy and recently delivered liv- birth baby admitted in the postnatal ward of Tribhuvan University Teaching Hospital (TUTH) and Paropakar Maternity and Women’s Hospital (PMWH). We excluded the mothers with any serious obstetric or medical conditions, mothers who did not have ANC cards, who had multiple pregnancies, whose last menstrual period was not exactly known, who had a history of some complications like antepartum hemorrhage and neonates with congenital malformations, had medical conditions like Diabetes, Hypertension, cardiac diseases or chronic infections and who required constant medical support and monitoring.

Study site

The study sites were Tribhuvan University Teaching Hospital (TUTH) and Paropakar Maternity and Women’s Hospital (PMWH) of Kathmandu district, Nepal. Kathmandu district is located in Kathmandu Valley, Bagmati Province of Nepal. It covers an area of 413.69 km2 (153 sq mi), and is the most densely populated district. It’s headquarter is Kathmandu Metropolitan City [26]. Kathmandu district has many tertiary hospitals, which is the catchment area for most people from several regions of Nepal. TUTH and PMWH are both public tertiary health centers as well as referral centers. These hospitals have a substantial caseload, with PMWH being the main public maternity hospital in Kathmandu and TUTH being a University hospital providing all kinds of maternity services to a large group of women inside and outside Kathmandu valley. People attending these hospitals have diverse ethnicity, culture and lifestyle, so that more information can be obtained.

Sample size and sampling method

A total of 308 mothers were interviewed with equal samples (154) taken from each hospital which was calculated using the formula n = z2pq/d2, considering the prevalence of low birth weight as 23.6% from the previous study conducted at Bharatpur Nepal [27], at 95% CI, 5% tolerable error and 10% non-response rate. Two tertiary level hospitals were selected purposively. Equal samples were taken from each hospital. The list of mothers was obtained from the postnatal wards of the respective hospital. The number of beds occupied was obtained from a ward in charge and the number was almost similar (TUTH 312 vs PMWH 304). Samples were selected through a systematic random sampling method in each hospital. The random number was generated, and the research participants were sorted in ascending bed numbers. The first participant’s bed number was selected by lottery method. Then, each study participant was selected by using systematic random sampling. The sampling interval(K) was 2. Data was collected on the day of discharge of participants before leaving the facility.

Data collection tools and techniques

We conducted face-to-face interviews among postnatal mothers using a semi-structured questionnaire. We also used the ANC card and Maternity register to confirm the information. The tools were developed based on study objectives through extensive literature review and pretested among 10% of non- sampled population in postnatal ward of TU Teaching hospital. PT, NA and two trained enumerators were involved in data collection from February 20, 2020 to April 7, 2020.

Dependent variables

Birth weight was reported in grams which was operationalized as a continuous variable. We constructed a binary variable for low birth weight based on the weight of birth <2500 gm as defined by WHO [28].

Independent variables

Independent variables were selected based on previously published studies [23, 27, 2931]. Independent variables were broadly classified into socio-demographic factors, maternal factors, health service-related factors, maternal knowledge and compliance to iron and folic acid supplementation.

Sociodemographic factors included age of postnatal mother (categorized into 15 to 19, 20 to 24, 25 to 29, 30 to 34, 35 and above), ethnicity (categorized into Dalit and non-Dalit), education of mother (categorized into illiterate, informal, primary, secondary and higher education), occupation (categorized into agriculture, service, business and housewife). Maternal obstetric factors included the height of mother (categorized into less than 145 cm and more than 145 cm), weight gain during pregnancy (categorized into less than 10 kg, 10 kg or more), gestational age at birth (categorized into less than 37 weeks, 37 or more weeks), parity (categorized into primiparous, multiparous and grand multiparous), birth interval (categorized into less than 2 years and more than 2 years), pregnancy intention (categorized into unintended and intended), history of abortion Behavioral factors included tobacco and alcohol use. Diet-related factors included dietary patterns, food taboos during pregnancy. Health service-related factors included ANC visit (categorized into less than 4 visits and more than or 4 visits), intake of deworming (categorized into Yes and No), hemoglobin level recorded at first ANC visit (categorized into less than 11 gm/dl and 11gm/dl or more). Maternal compliance with compliance to iron-folic acid was also assessed. Compliance was defined as the uptake of IFA supplementation by pregnant women daily. The mother was determined to have compliance if she uptakes at least 80% of the recommended dose (categorized into non-compliance if uptake less than 144 tablets and compliance if uptake more than or equal to 144 tablets) [32, 33]. Maternal knowledge of anemia and IFAS variables was categorized into adequate and inadequate based on the mean score.

Statistical analysis

Data was entered in EpiData version 3.1. After confirming the completeness, data were exported to IBM SPSS Version 21 for further analysis. Univariate analysis was conducted using frequencies, percentages, mean and standard deviation. Multi-collinearity was assessed before logistic regression using the variance inflation factor (VIF). The decision criterion for excluding of variable from the regression model was set out as those with VIF values greater than 10. The goodness of fit the regression model was tested by applying the of Hosmer and Lemeshow chi-square test. Those variables significantly associated in the univariate analysis at 95% confidence level, p-value less than 0.05 were included in the multivariate model. We applied Multivariate logistic regression analysis adjusting for covariates such as ethnicity, IFA compliance, and ANC visit to identify the factors associated with low birth weight. The unadjusted and adjusted odds ratio with 95% confidence intervals were reported. P-value less than 0.05 was considered statistically significant.

Ethics statement

The ethical review committee approved the study at the Institute of Medicine (approval no: 258(6–11) E2 076/077) and Nepal Health Research Council (approval no: 22/2020 MT). Permission was taken from both hospitals. Participants provided verbal and written consent to participate in the study, which was voluntary and anonymous.

Results

Distribution of participants by socio-demographic factors, maternal health service and birth weight-related factors

Table 1 describes the sociodemographic characteristics of the research participants. The majority of the participants belonged to age group 20–24 years of age (35.7%). The mean age of the respondent was 25.7 ± 4.8. The response rate in this study was 100%. Majority of the participants (43.5%) were Brahmin/Chhetri. Almost half of the participants (46.1%) had a higher educational level. More than three-fourths (77.6%) of the participants were homemakers. The majority (96.1%) of the participants had a height of more than and equal to 145cm. About two-third (61.7%) of the respondents had the weight gain of at least 10 kg during the pregnancy. The average weight gain during the pregnancy was 11.04 ± 4.15kg. Majority of the participants (90.6%) had more than 37 weeks of gestation. Majority (91.6%) of participants had attended four or more ANC visits during their pregnancy. More than half (58.4%) of the respondents did not consume deworming tablet during pregnancy. More than four-fifths (87.7%) of the respondents were non-anemic compared to 12.3% who were anemic. The mean hemoglobin level recorded at first ANC visits was 12.27 ± 1.28 gm/dl. Majority (97.4%) of participants consumed IFA tablets during pregnancy. More than three-fourths (77.6%) of the respondents had compliance to IFA supplementation. Most of the respondents (84.7%) had given birth to at least 2.5 kg of baby, while 15.3% had given birth to less than 2.5 kg of a baby. The mean birth weight was 2.96 ±0.59 kg.

Table 1. Distribution of participants by sociodemographic factors, maternal health service and birth weight-related factors.

Sociodemographic Frequency Percentage
Age (in years)
<20 years 24 7.7
20–29 years 217 70.4
≥30 years 67 21.9
Ethnicity
Dalit 44 14.3
Non Dalit 264 85.7
Educational status
Illiterate 11 3.6
Informal education 16 5.2
Formal 281 91.2
Occupational status
Employed 69 22.4
Homemaker 239 77.6
Weeks of gestation
<37 29 9.4
≥37 279 90.6
Height of mother
< 145 cm 12 3.9
≥145cm 296 96.1
Weight gain during pregnancy
<10kg 118 38.3
≥10 kg 190 61.7
Mean ± SD 11.04 ± 4.15 kg
Weeks of gestation
<37 weeks of gestation 29 9.4
≥37 weeks of gestation 279 90.6
Parity
Primiparous 161 52.3
Multiparous 142 46.1
Grand multiparous 5 1.6
Birth Interval (n = 147)
Less than 2 years 12 8.2
More than 2 years 135 91.8
Type of delivery
Cesarean Section 109 35.4
Normal Delivery 199 64.6
Number of ANC visit
less than 4 times 26 8.4
4 or more times 282 91.6
Intake of deworming tablet
Yes 128 41.6
No 180 58.4
Hemoglobin level at first ANC visit
<11 gm/dl 38 12.3
≥11 gm/dl 270 87.4
Mean ± SD 12.27±1.28 gm/dl
Consumption of IFA tablet
Yes 300 97.4
No 8 2.6
Number of IFA tablet intake
≥180 tablets 216 70.1
<180 tablets 92 29.9
Mean ± SD 153.25±43.06
Compliance with IFA supplementation
Non-compliance 69 22.4
Compliance 239 77.6
Birth weight of baby
<2.5kg 47 15.3
≥2.5kg 261 84.7
Mean ± SD 2.96±0.59 kg
Knowledge of anemia and IFA intake
Inadequate knowledge 292 94.8
Adequate Knowledge 16 5.2
Tobacco use during pregnancy
Yes 4 1.2
No 304 98.8
Alcohol intake during pregnancy
Yes 4 1.2
No 304 98.8
Food taboos
Yes 196 63.6
No 112 36.4

Association of study variables with risk of low birth weight

Table 2 shows the factors associated with low birth weight. The result from regression analysis showed that the risk of low birth weight baby was more likely for mothers who belonged to Dalit ethnicity (AOR = 2.9, 95% CI = 1.2–7.1), mothers with IFA compliance (AOR = 2.1, 95% CI = 1.0–4.4), and Mothers who had four or more ANC (AOR = 2.6, 95%CI = 1.0–6.6).

Table 2. Factors associated with low birth weight.

Variables Unadjusted OR 95% CI P- value Adjusted OR 95% CI P- value
Ethnicity
Dalit 3.6 1.5–8.5 0.003 2.9 1.2–7.1 0.017*
Non Dalit 1 1
IFA Compliance
Non Compliance 2.8 1.4–5.5 0.002 2.1 1.0–4.4 0.031*
Compliance 1 1
ANC visit
Less than four times 4.1 1.7–9.8 0.001 2.6 1.0–6.6 0.045*
Four or more times 1 1

*Statistically significant (p< 0.05) at 95% CI

COR = Crude Odds Ratio, AOR = Adjusted Odds Ratio, Ref = Reference category

Discussion

Our study found that about one in every seven children had a birth weight of less than 2500 gm. The three factors: (1) ethnicity, (2) Compliance with IFA, and (3) Maternal Antenatal care visits were significantly associated with birth weight of children. The prevalence of low birth weight (15.3%) was slightly lower than the study conducted in Dhulikhel hospital (21.6%) [34], Janakpur zonal hospital (21.5%) [35], Bharatpur teaching hospital (23.6%) [27] and higher than the National prevalence of (12.9%) [10] reported by Nepal Demographic Health Survey 2016. The prevalence of low birth weight was also higher in different regions or countries other than Nepal, such as in India (18%) [36], Ethiopia (17.3%) [37], Bangladesh (22%) [38], and in sub Saharan African countries (16.4%) [39]. But, the reported prevalence is higher than the study conducted in china (2.8%) [40], Jordan (13.8%) [29], and Malawi (12.1%) [41]. This difference could occur due to variation in study setting, socioeconomic and demographic characteristics of study participants.

Maternal age is considered as a key factor for the healthy outcome of pregnancy. This study reveals no statistical association between maternal age and low birth weight, which contradicts the study done in tertiary hospitals of Nepal that shows higher risk of delivering low birth weight babies by mothers of age less than 20 years [22, 30]. This might be because most of the participants were from age group 20–30 years, and the mean age was 25.75 years.

Our study showed that ethnicity significantly affects a baby’s birth weight. The mothers who belongs to Dalit ethnicity were nearly three times more likely to have low birth weight baby. This finding was consistent with another study conducted in Chitwan, which revealed that mothers belonging to Dalit and Madhesi ethnicity were more likely to have low birth weight baby [23]. Similarly, another study conducted in California showed African American women had 2 times more likely to have low birth weight compared to white women [42]. This might be due to the poor health care utilization, poor socio economic condition, and other social disparities faced by these ethnic groups in Nepal.

Our study revealed that mothers who did not attend four times or more antenatal services were 2.6 times higher change of low-birth-weight baby compared to those who attend four or more times. In support with this finding, another study conducted in Nepal using nationally representative survey data in 2011 showed that mothers who attend three or fewer ANC visits only were two times more likely to have low birth weight babies [31]. This finding was also consistent with the other studies conducted in sub Saharan Africa [39], Ethiopia [40], India [43], and the United States [44]. This might be due to during Antenatal visits, pregnant mothers are likely to receive health services such as nutrition counseling to improve dietary practices, encourage recommended weight gain during pregnancy, health assessment and receive nutrient supplement which is key to improving birth outcome [45].

Our study showed that 77.6% of mothers had compliance to iron-folic acid supplementation. A lower finding was seen in a study in Pokhara, Nepal that showed the compliance rate of 58% [32]. The studies in Karnataka and Senegal had similar findings, with 71% and 69% of the IFA compliance [46, 47]. However, only 18% of the compliance was seen in a study in Ethiopia [48]. These differences could be the result of different cut-offs for determining the IFA compliance in different countries. This study has considered 80% or above the intake of recommended dose as compliance, while different studies have used cut-off of 100 or the mean value.

Low iron intake causes the poor delivery of iron to the fetus, impair in proper hormonal and neuronal regulation of pregnancy and poor oxygenation of the fetus leading to poor growth and development [49]. Our study reflects that there is significant association of compliance to Iron folic acid supplementation with baby’s birth weight. Mothers who did not comply with iron-folic acid were two times more likely to have low birth weight babies. This finding is consistent with the findings of other studies [22, 50, 51], which revealed that IFA compliance has a positive association with baby’s birth weight. Every pregnant woman are recommended to take a total of 180 IFA tablets to reduce the risk of maternal anemia, and adverse outcomes including low birth weight. This is also supported by other studies’ findings, which showed higher odds of delivering low birth weight baby among non-compliant mothers [22, 50, 52].

Smoking and alcohol consumption negatively affects the fetus’s growth and development because of their chemical substances [53]. However, no significant association was seen with low birth weight in bivariate analysis. This is because of the very small portion of participants (only 8) who smoked and consumed alcohol. There may be possible social desirability bias because of social stigma.

This study has certain limitations that should be addressed in future research. The study was based on the health institutions limiting its generalizability in the community setting. Also, the other potential risk factors for low birth weight including micronutrient deficiencies among mothers and exposure to toxins like pesticides and indoor air pollution, were not evaluated, which may have affected the result.

Conclusion

This study concluded that about one in seven children had low birth weight. The mothers who belong to Dalit ethnicity, who did not have antenatal visits as per recommended protocol (4 or more times) and mothers who did not comply with iron-folic acid supplementation were likelier to have low birth weight babies. This suggests that disadvantageous ethnic groups should be a focus in national preventive programs for the prevention of risk of delivering low birth weight baby. During ANC visits, priority should be given for providing nutrition education and motivating pregnant women towards IFA compliance focusing on complete ANC visits. Further studies such as case-control, cohort studies might help to bring forward the information on factors associated with the birth weight of children.

Supporting information

S1 Data

(SAV)

S1 File. Questionnaire in English.

(DOCX)

Acknowledgments

We would like to acknowledge all the people who directly or indirectly contributed to the present study and the participants who shared their valuable time with us.

Data Availability

All data are in the manuscript and/or supporting information files.

Funding Statement

The authors received no specific funding for this work.

References

  • 1.World Health Organization. International Statistical Classification of Diseases and Related Health Problems: tenth revision-Version for 2007. [PubMed]
  • 2.Badshah S, Mason L, McKelvie K, Payne R, Lisboa PJ. Risk factors for low birthweight in the public-hospitals at Peshawar, NWFP-Pakistan. BMC public health. 2008;8(1):1–10. doi: 10.1186/1471-2458-8-197 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.UNICEF (2009) The state of the world’s children 2009: maternal and newborn health: United Nations Children’s Fund. [Google Scholar]
  • 4.Mathewson KJ, Chow CH, Dobson KG, Pope EI, Schmidt LA, Van Lieshout RJ. Mental health of extremely low birth weight survivors: A systematic review and meta-analysis. Psychological bulletin. 2017;143(4):347. doi: 10.1037/bul0000091 [DOI] [PubMed] [Google Scholar]
  • 5.Al Hazzani F, Al-Alaiyan S, Hassanein J, Khadawardi E. Short-term outcome of very low-birth-weight infants in a tertiary care hospital in Saudi Arabia. Annals of Saudi medicine. 2011;31(6):581–5. doi: 10.4103/0256-4947.87093 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Arnold L, Hoy W, Wang Z. Low birthweight increases risk for cardiovascular disease hospitalisations in a remote Indigenous Australian community–a prospective cohort study. Australian and New Zealand Journal of Public Health. 2016;40(S1):S102–S6. [DOI] [PubMed] [Google Scholar]
  • 7.Desta M, Tadese M, Kassie B, Gedefaw M. Determinants and adverse perinatal outcomes of low birth weight newborns delivered in Hawassa University Comprehensive Specialized Hospital, Ethiopia: a cohort study. BMC research notes. 2019;12(1):1–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Unicef. United Nations Children’s Fund and World Health Organization, Low Birthweight: Country, regional and global estimates. New York: UNICEF. 2004. [Google Scholar]
  • 9.Marete I, Ekhaguere O, Bann CM, Bucher SL, Nyongesa P, Patel AB, et al. Regional trends in birth weight in low-and middle-income countries 2013–2018. Reproductive health. 2020;17(3):1–8. doi: 10.1186/s12978-020-01026-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Ministry of Health, New Era & ICF International (2017) Nepal Demographic and Health Survey 2016. Kathmandu: Ministry of Health, Government of Nepal. [Google Scholar]
  • 11.Christian P, Murray-Kolb LE, Tielsch JM, Katz J, LeClerq SC, Khatry SK. Associations between preterm birth, small-for-gestational age, and neonatal morbidity and cognitive function among school-age children in Nepal. BMC pediatrics. 2014;14(1):1–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Kayastha S, Tuladhar H. Study of low birth weight babies in Nepal Medical College. Nepal Med Coll J. 2007;9(4):266–9. [PubMed] [Google Scholar]
  • 13.World Health Organization. Multicentre study of low birth weight and infant mortality in India, Nepal and Sri Lanka: WHO Regional Office for South-East Asia; 1994. [Google Scholar]
  • 14.MIRA/UNICEF Nepal (2000) Low Birth Weight Prevalence and Associated Factors in Four Regions of Nepal. Kathmandu, Nepal: Mother Infant Research Activities (MIRA), UNICEF. [Google Scholar]
  • 15.Neufeld HJ, De‐Regil LM, Dowswell T, Rogers LM. Effects of preventive oral supplementation with iron or iron with folic acid for women following childbirth. The Cochrane Database of Systematic Reviews. 2017;2017(9). [Google Scholar]
  • 16.Bhaskar RK, Deo KK, Neupane U, Chaudhary Bhaskar S, Yadav BK, Pokharel HP, et al. A case control study on risk factors associated with low birth weight babies in Eastern Nepal. International journal of pediatrics. 2015;2015. doi: 10.1155/2015/807373 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Ahumada-Barrios ME, Alvarado GF. Risk Factors for premature birth in a hospital. Revista latino-americana de enfermagem. 2016;24. doi: 10.1590/1518-8345.0775.2750 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Khanal V, Zhao Y, Sauer K. Role of antenatal care and iron supplementation during pregnancy in preventing low birth weight in Nepal: comparison of national surveys 2006 and 2011. Archives of Public Health. 2014;72(1):1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Van den Broek NR, Jean-Baptiste R, Neilson JP. Factors associated with preterm, early preterm and late preterm birth in Malawi. PloS one. 2014;9(3):e90128. doi: 10.1371/journal.pone.0090128 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.He J-R, Ramakrishnan R, Lai Y-M, Li W-D, Zhao X, Hu Y, et al. Predictions of preterm birth from early pregnancy characteristics: born in guangzhou cohort study. Journal of clinical medicine. 2018;7(8):185. doi: 10.3390/jcm7080185 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Singh U, Ueranantasun A, Kuning M. Factors associated with low birth weight in Nepal using multiple imputation. BMC Pregnancy and Childbirth. 2017;17(1):1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Sharma SR, Giri S, Timalsina U, Bhandari SS, Basyal B, Wagle K, et al. Low birth weight at term and its determinants in a tertiary hospital of Nepal: a case-control study. PloS one. 2015;10(4):e0123962. doi: 10.1371/journal.pone.0123962 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Department of Health Services Annual Report(2077/78). Kathmandu: Ministry of Health and Population, Government of Nepal. [Google Scholar]
  • 24.Joshi H, Subba S, Dabral S, Dwivedi S, Kumar D, Singh S. Risk factors associated with low birth weight in newborns. Indian J Community Med. 2005;30(4):142–3. [Google Scholar]
  • 25.Monawar Hosain G, Chatterjee N, Begum A, Saha SC. Factors associated with low birthweight in rural Bangladesh. Journal of tropical pediatrics. 2005;52(2):87–91. doi: 10.1093/tropej/fmi066 [DOI] [PubMed] [Google Scholar]
  • 26.National Population and Housing Census 2011 –General and Social Characteristics Table. Government of Nepal Central Bureau of Statistics.
  • 27.Bansal P, Garg S, Upadhyay HP. Prevalence of low birth weight babies and its association with socio-cultural and maternal risk factors among the institutional deliveries in Bharatpur, Nepal. Asian Journal of Medical Sciences. 2019;10(1):77–85. [Google Scholar]
  • 28.Sachdev HPS. Low birth weight in South Asia. Int J Diab Dev Countries. 2001;21(1):13–33. [Google Scholar]
  • 29.Islam MM, Ababneh F, Akter T, Khan HR. Prevalence and risk factors for low birth weight in Jordan and its association with under-five mortality: a population-based analysis. East Mediterr Health J. 2020;26(10):1273–84. doi: 10.26719/emhj.20.096 [DOI] [PubMed] [Google Scholar]
  • 30.Kandel KP, Kafle S. Risk factors associated with low birth weight among deliveries at bharatpur hospital. Journal of Nepal Health Research Council. 2017;15(2):169–73. doi: 10.3126/jnhrc.v15i2.18208 [DOI] [PubMed] [Google Scholar]
  • 31.Khanal V, Sauer K, Karkee R, Zhao Y. Factors associated with small size at birth in Nepal: further analysis of Nepal Demographic and Health Survey 2011. BMC pregnancy and childbirth. 2014;14(1):1–9. doi: 10.1186/1471-2393-14-32 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Yadav KD, Yadav UN, Wagle RR, Thakur DN, Dhakal S. Compliance of iron and folic acid supplementation and status of anaemia during pregnancy in the Eastern Terai of Nepal: findings from hospital based cross sectional study. BMC research notes. 2019;12(1):1–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Rahmati S, Delpishe A, Azami M, Ahmadi MRH, Sayehmiri K. Maternal Anemia during pregnancy and infant low birth weight: A systematic review and Meta-analysis. International journal of reproductive biomedicine. 2017;15(3):125. [PMC free article] [PubMed] [Google Scholar]
  • 34.Prajapati R, Shrestha S, Bhandari N. Prevalence and associated factors of low birth weight among newborns in a tertiary level hospital in Nepal. Kathmandu Univ Med J. 2018;61(1):49–52. [PubMed] [Google Scholar]
  • 35.Yadav D, Chaudhary U, Shrestha N. Risk factors associated with low birth weight. Journal of Nepal Health Research Council. 2011;9(2):159–64. [PubMed] [Google Scholar]
  • 36.Agarwal K, Agarwal A, Agrawal V, Agrawal P, Chaudhary V. Prevalence and determinants of “low birth weight” among institutional deliveries. Annals of Nigerian medicine. 2011;5(2):48. [Google Scholar]
  • 37.Endalamaw A, Engeda EH, Ekubagewargies DT, Belay GM, Tefera MA. Low birth weight and its associated factors in Ethiopia: a systematic review and meta-analysis. Italian journal of pediatrics. 2018;44(1):1–12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Khan JR, Islam M, Awan N, Muurlink O. Analysis of low birth weight and its co-variants in Bangladesh based on a sub-sample from nationally representative survey. BMC pediatrics. 2018;18(1):1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Tessema ZT, Tamirat KS, Teshale AB, Tesema GA. Prevalence of low birth weight and its associated factor at birth in Sub-Saharan Africa: A generalized linear mixed model. PloS one. 2021;16(3):e0248417. doi: 10.1371/journal.pone.0248417 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Jember DA, Menji ZA, Yitayew YA. Low Birth Weight and Associated Factors Among Newborn Babies in Health Institutions in Dessie, Amhara, Ethiopia. Journal of multidisciplinary healthcare. 2020;13:1839. doi: 10.2147/JMDH.S285055 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.He Z, Bishwajit G, Yaya S, Cheng Z, Zou D, Zhou Y. Prevalence of low birth weight and its association with maternal body weight status in selected countries in Africa: a cross-sectional study. BMJ open. 2018;8(8):e020410. doi: 10.1136/bmjopen-2017-020410 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Ratnasiri AW, Parry SS, Arief VN, DeLacy IH, Halliday LA, DiLibero RJ, et al. Recent trends, risk factors, and disparities in low birth weight in California, 2005–2014: a retrospective study. Maternal health, neonatology and perinatology. 2018;4(1):1–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Dharmalingam A, Navaneetham K, Krishnakumar C. Nutritional status of mothers and low birth weight in India. Maternal and child health journal. 2010;14(2):290–8. doi: 10.1007/s10995-009-0451-8 [DOI] [PubMed] [Google Scholar]
  • 44.Hueston WJ, Gilbert GE, Davis L, Sturgill V. Delayed prenatal care and the risk of low birth weight delivery. Journal of Community Health. 2003;28(3):199–208. doi: 10.1023/a:1022908307844 [DOI] [PubMed] [Google Scholar]
  • 45.White DE, Fraser-Lee NJ, Tough S, Newburn-Cook CV. The content of prenatal care and its relationship to preterm birth in Alberta, Canada. Health care for women international. 2006;27(9):777–92. doi: 10.1080/07399330600880335 [DOI] [PubMed] [Google Scholar]
  • 46.SG C, Prashantha B. Assessment of compliance with iron-folic acid therapy during pregnancy among postnatal mothers in a tertiary care centre, Mysuru. 2019. [Google Scholar]
  • 47.Seck BC, Jackson RT. Determinants of compliance with iron supplementation among pregnant women in Senegal. Public health nutrition. 2008;11(6):596–605. doi: 10.1017/S1368980007000924 [DOI] [PubMed] [Google Scholar]
  • 48.Tegegne M. Compliance to prenatal Iron and Folic acid supplement and associated factors among women during pregnancy in South East Ethiopia: A Cross-sectional study. Global Journal of Medical Research. 2017;7(2). [Google Scholar]
  • 49.Allen LH. Biological mechanisms that might underlie iron’s effects on fetal growth and preterm birth. The Journal of nutrition. 2001;131(2):581S–9S. doi: 10.1093/jn/131.2.581S [DOI] [PubMed] [Google Scholar]
  • 50.Chikakuda AT, Shin D, Comstock SS, Song S, Song WO. Compliance to prenatal iron and folic acid supplement use in relation to low birth weight in Lilongwe, Malawi. Nutrients. 2018;10(9):1275. doi: 10.3390/nu10091275 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Balarajan Y, Subramanian S, Fawzi WW. Maternal iron and folic acid supplementation is associated with lower risk of low birth weight in India. The Journal of nutrition. 2013;143(8):1309–15. doi: 10.3945/jn.112.172015 [DOI] [PubMed] [Google Scholar]
  • 52.Imdad A, Bhutta ZA. Routine iron/folate supplementation during pregnancy: effect on maternal anaemia and birth outcomes. Paediatric and perinatal epidemiology. 2012;26:168–77. doi: 10.1111/j.1365-3016.2012.01312.x [DOI] [PubMed] [Google Scholar]
  • 53.Zaren B, Lindmark G, Bakketeig L. Maternal smoking affects fetal growth more in the male fetus. Paediatric and perinatal epidemiology. 2000;14(2):118–26. doi: 10.1046/j.1365-3016.2000.00247.x [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

S1 Data

(SAV)

S1 File. Questionnaire in English.

(DOCX)

Data Availability Statement

All data are in the manuscript and/or supporting information files.


Articles from PLOS Global Public Health are provided here courtesy of PLOS

RESOURCES