Prevalence and immediate outcomes of low birth weight neonates born of pre-eclamptic women at Moi Teaching and Referral Hospital, Kenya
Lina Sigei, Emily Muthoni Nyaga, Benson Milimo
Corresponding author: Emily Muthoni Nyaga, School of Nursing and Midwifery, Moi University, Eldoret, Kenya
Received: 25 Oct 2022 - Accepted: 01 Jan 2023 - Published: 17 Jan 2023
Domain: Obstetrics and gynecology,Neonatology
Keywords: Low birth weight, preeclampsia, immediate birth outcomes
©Lina Sigei et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Lina Sigei et al. Prevalence and immediate outcomes of low birth weight neonates born of pre-eclamptic women at Moi Teaching and Referral Hospital, Kenya. Pan African Medical Journal. 2023;44:31. [doi: 10.11604/pamj.2023.44.31.37975]
Available online at: https://www.panafrican-med-journal.com//content/article/44/31/full
Research
Prevalence and immediate outcomes of low birth weight neonates born of pre-eclamptic women at Moi Teaching and Referral Hospital, Kenya
Prevalence and immediate outcomes of low birth weight neonates born of pre-eclamptic women at Moi Teaching and Referral Hospital, Kenya
&Corresponding author
Introduction: pre-eclampsia has been linked to poor neonatal outcomes such as; stillbirth, low birth weight (LBW), prematurity and neonatal morbidities owing to utero-placental insufficiency. The study objective was to determine the prevalence of LBW and immediate (within 24 hours) birth outcomes of LBW neonates born to pre-eclamptic women at Moi Teaching and Referral Hospital (MTRH), Kenya.
Methods: a descriptive cross-sectional study was conducted among 364 participants (346 singletons and 9 twins) born to pre-eclamptic women at MTRH. A study tool was used to gather data on birth weight and neonatal outcomes. Data was cleaned, coded and entered into SPSS version 22 for analysis. Descriptive statistics were computed for the prevalence of LBW and immediate neonatal outcomes.
Results: the study found an LBW prevalence of 180(49.5%) and prematurity of 81(45%). Of the LBW neonates (n=180), 162(90%) were alive and 18(10%) were stillbirths. Their immediate morbidities were, birth asphyxia 51(28.7%), neonatal jaundice 38(21%), hypothermia 18(7.9%) and neonatal sepsis 1(0.7%). Of the neonates that were born alive; 107(59.2%) were admitted to level II nursery care, 53(29.5%) were rooming in with their mothers and 20(11.3%) died within 24 hours.
Conclusion: preeclampsia contributes to LBW, nursery admissions and morbidity/mortality of neonates necessitating the need for neonatal units' preparedness for prompt and appropriate management to avert death.
Birth weight is the first weight recorded after birth, ideally measured within the first hours after birth, prior to the significant weight loss that occurs after birth. Low birth weight (LBW) is a birth weight of less than 2500 grams (up to and including 2499grams) and is further categorized into very low birth weight (VLBW, <1500grams) and extremely low birth weight (ELBW, <1000grams) [1]. The LBW is a crucial indicator of child´s vulnerability to mortality, morbidity, delayed growth and development, chronic diseases later in life, and chances of survival [2,3]. The increased neonatal mortality among LBW neonates has been attributed to susceptibility to hypoglycemia, hypothermia, birth asphyxia, trauma, respiratory disorders, and neonatal sepsis [4]. For instance, Tshehla et al. (2019) [3] reported a mortality rate twenty times higher among LBW compared to normal birth weight neonates. Notably, the global prevalence of LBW in 2015 stood at 15.5% (20.5 million neonates) with the majority (91%) arising from low and middle-income countries, 24% from sub-Saharan Africa, and 11% from Kenya [5,6].
Preeclampsia is a known part of hypertensive disorders of pregnancy and is classically defined as hypertension and proteinuria or hypertension with end-organ damage after 20 weeks of gestation. Majorly presents with visual disturbances, headaches, swelling, excessive weight gain, and abdominal pain. Preeclampsia remains a common health problem with a global incidence of between 2 to 10%. Of concern, the health problem often goes under-recognized and undertreated impacting greatly on birth weight [7-9]. Owing to acute or chronic uteroplacental insufficiency, preeclampsia has been associated with intrauterine growth restriction, LBW, prematurity, stillbirth, admission to neonatal intensive care unit, and perinatal death [10-12]. A systematic review and meta-analysis conducted in Ethiopia reported an LBW prevalence of 39.7% among neonates born to pre-eclamptic women [13]. In addition, a retrospective study in Jamaica by McKenzie et al. (2019) [14] reported pre-eclamptic women as more likely to give birth to LBW (OR = 2.8; CI: 2.2 - 3.5), small for gestational age (OR = 2.3; CI: 1.9-2.9) or preterm neonates (OR = 2.5; CO: 2.0-3.0) than normotensive women.
Although Moi Teaching and Referral Hospital (MTRH), Kenya, has had a lower prevalence of LBW neonates than the national figure of 22% [15], the figures have been rising for the past three years from 2018 with a prevalence of 8.9%, 10.7% and 11.6% (hospital statistics, 2021). The cost implication to the hospital, families, and society in the care of LBW neonates remains a burden, especially in developing countries. This study's objective was to determine the prevalence and immediate (within 24 hours) outcomes of LBW neonates born to pre-eclamptic women at MTRH, Kenya.
Study design and setting: a descriptive cross-sectional study was conducted at MTRH, the second largest referral hospital in Kenya located in Uasin Gishu County.
Sample size: a sample size of 355 was arrived at using the formula for estimating single population proportion described by Lwanga et al. (1990) [16] and a prevalence of LBW of 36.2% from a similar study conducted in Ethiopia by Legesse et al. 2019, [17].
Population: the target population was all neonates born of women diagnosed with preeclampsia at MTRH during the study period. Approximately 310 neonates are born to pre-eclamptic women every month. The study targeted a study population of 1550 for the five months of data collection.
Sampling procedure: four trained research assistants (nursing staff on off-duty working at MTRH) recruited study participants. Women diagnosed with preeclampsia and birthing at the labor ward or maternity theatre had their neonates recruited into the study after delivery. Systematic sampling was employed where every 4th neonate (target population of 1550/sample size of 355) was recruited into the study until the desired sample size was reached. A total of 364 participants (346 singletons and 9 twins) were recruited into the study between 21st March and 20th August 2021.
Eligibility criteria: neonates were included in the study if they were; a) born to pre-eclamptic women during the study period, b) delivered within the last 24 hours, and c) delivered at MTRH. Neonates born of women diagnosed with eclampsia were excluded from the study due to the need to terminate the pregnancy.
Data collection procedures: a study tool developed by the first author (Lina Sigei) following a thorough review of related literature was reviewed for content by four experts in the field of maternal and neonatal health resulting in the editing of two items in the study tool. In addition, a pilot study was conducted at MTRH among 30 participants a month prior to data collection occasioning a rephrasing of one item and content revision of two items. A Cronbach´s alpha coefficient of 0.7 was obtained for the pre-test population making the tool sufficient for reliability. Participants in the pilot study were excluded from the main study. The study tool obtained data on BWT, gestational age at birth, gender, mode of delivery and neonatal appearance, pulse, grimace, activity, and respirations (APGAR) score. Also obtained were immediate outcomes (state of the neonate at birth including medical diagnosis all obtained from neonates file) such as congenital malformation, need for resuscitation, and morbidities for LBW neonates.
Statistical analysis: data collected were coded and entered into Statistical Package for the Social Sciences (SPSS) version 22 database for analysis. The analysis aimed at determining; a) the prevalence of LBW and b) neonatal social demographic factors and immediate birth outcomes of the LBW neonates. Descriptive statistics were computed for neonatal social demographic factors, the prevalence of LBW, and immediate birth outcomes. The results were presented in tables.
Ethics approval and consent to participate: the study was approved by the Institutional Research and Ethics Committee (IREC) of Moi Teaching and Referral Hospital; approval number 0003815. In addition, written informed consent was obtained from the mothers prior to data collection. The authors declare that all methods were carried out in accordance with relevant guidelines and regulations for research.
The findings of the 364 participants revealed an LBW prevalence of 49.5%. An analysis of the LBW participants (n = 180) found that 81(45%) were preterm, 102(56.7%) were males, 18(10%) were twins and 107(59.44%) were delivered via caesarean section. The mean BWT was 2017 (± 417.539) grams, and APGAR scores were 6.4 (± 2.8), 7.2 (±3.1) and 7.7 (±3.1) at one, five and ten minutes respectively (Table 1).
An analysis of the immediate outcome of the LBW neonates found that at birth 162(90%) participants were alive, 17(9.4%) were fresh still births while 1(0. 6%) was macerated still birth. Notably, 12(7%) participants had congenital anomalies while 67(37%) were resuscitated after birth. The neonatal morbidities found were; 51(28.7%) birth asphyxia, 38(21%) neonatal jaundice, 18(7.9%) hypothermia, 3(1.7%) multiple morbidities and 1(0.7%) neonatal sepsis. At the end of 24 hours following delivery, the study found that 107(59.2%) of the participants were admitted at special care nursery, 53(29.5%) were rooming in with their mothers and 20(11.3%) had died (Table 2).
The study findings revealed an LBW prevalence of 49. Five percent (5%) similar to findings reported in Nigeria by Yilgwan et al. (2020) [18], Ethiopia by Legesse et al. (2019) [17], and Brazil by Anselmini et al. (2018) [19] found a prevalence of 42.2%, 36.2%, and 32.7% respectively. Ours though is on the higher side underscoring the importance of measures to mitigate this. Similar to the current study, McKenzie et al. (2019) [14] reported a significantly lower mean BTW (2.2±0.9 kilograms) among neonates born to pre-eclamptic women compared to neonates born to normotensive women (2.2±0.9 kilograms). The low birth weight among pre-eclamptic women has been attributed to fetal under-nutrition as a result of uteroplacental vascular insufficiency [20]. Congruent to our study findings, a study in Brazil by Anselmini et al. (2018) [19] found 46.2% of neonates were born prematurely by pre-eclamptic women while contrast findings from South Africa by Nathan et al. (2018) [21] and Ethiopia by Belay et al. (2020) [22] reported prematurity of 70% and 19.5% respectively. That about two-thirds of the LBW neonates were delivered via caesarean section owing to non-reassuring fetal status and worsening preeclampsia or impending eclampsia was congruent with other studies that have reported caesarian section as the most common mode of delivery among pre-eclamptic women in the quest to mitigate adverse perinatal outcomes [23-25].
The mean APGAR scores for the participants were consistent with other studies that have reported low APGAR scores in LBW neonates at one and five minutes compared to normal weight neonates [AOR = 0.52 (95%CI: 0.37-0.73)] [26-28]. Moreover, 10% of the LBW participants in the current study were stillbirths comparable to findings of 17.7% in South Africa [21], 8.9% in Ethiopia [13], and 6.7% in Brazil [19]. Preeclampsia has been reported to pose a significant risk for intrauterine fetal demise due to placental insufficiency contributing to 2.1% of stillbirths [29]. In addition, our study found that 37% of the participants were resuscitated after birth similar to the findings of 42.7% in Thailand by Kongwattanakul et al. (2018) [30].
Congruent to our study findings, other studies have reported birth asphyxia as the leading cause of neonatal morbidity among neonates born to pre-eclamptic women owing to lung immaturity and insufficient surfactant production [23,25,31]. In contrast, some studies have reported preeclampsia as being protective of respiratory morbidity by accelerating fetal lung maturation [32-34]. The study also found that neonatal jaundice occurred in 21% of the participants similar to findings in Iran by Boskabadi et al. (2020) [35] that reported a prevalence of 30.9%. Similarly, other studies have reported an increased risk of developing jaundice among LBW born to pre-eclamptic women [36,37]. Our study findings on the state of the participants at the end of 24 hours after birth are congruent with a study by McKenzie et al. (2019) [14] that established that 60% of the LBW neonates born to pre-eclamptic women were admitted to the neonatal unit, 24.2% were rooming in with their mothers and 15.8% had died.
Limitations: this study was carried out at a national referral hospital that had a possible bias of admitting high-risk pregnancies referred from other regions in the country hence the findings may not be generalizable. In addition, the study included twins who may not share the same risk factors as the singletons.
This study was carried out at a national referral hospital that had a possible bias of admitting high-risk pregnancies referred from other regions in the country hence the findings may not be generalizable. In addition, the study included twins who may not share the same risk factors as the singletons. Preeclampsia contributes to LBW, nursery admissions, and morbidity/mortality of neonates necessitating the need for neonatal units’ preparedness for prompt and appropriate management to avert death.
What is known about this topic
- Preeclampsia contributes to stillbirth, low birth weight, prematurity, and morbidity due to uteroplacental insufficiency.
What this study adds
- The findings of low birth weight (49%), prematurity (45%), and fresh stillbirth (9%) among pre-eclamptic women at MTRH, Kenya.
The authors declare no competing interests.
All authors participated in proposal development, result analysis, discussion and conclusion. In addition, all the authors read and approved the final manuscript.
The authors thank Geofrey Bartei and Evans Mutai for their assistance in data collection.
Table 1: neonatal characteristics (n=180)
Table 2: immediate outcomes of the low birth weight neonates (n=180)
- World Health Organization. International statistical classification of diseases and related health problems. 2nd ed. Geneva: World Health Organization; 2004. Google Scholar
- Rao J, Fan D, Wu S, Lin D, Zhang H, Ye S et al. Trend and risk factors of low birth weight and macrosomia in south China, 2005-2017: a retrospective observational study. Sci Rep. 2018 Feb 21;8(1):3393. PubMed | Google Scholar
- Tshehla RM, Coetzee M, Becker PJ. Mortality and morbidity of very low-birthweight and extremely low-birthweight infants in a tertiary hospital in Tshwane. S Afr J Child Health. 2019;13(2):89-97. Google Scholar
- Lee JH, Noh OK, Chang YS; Korean Neonatal Network. Neonatal outcomes of very low birth weight infants in Korean neonatal network from 2013 to 2016. J Korean Med Sci. 2019 Jan 28;34(5):e40. PubMed | Google Scholar
- Ekubagewargies DT, Kassie DG, Takele WW. Maternal HIV infection and preeclampsia increased risk of low birth weight among newborns delivered at University of Gondar specialized referral hospital, Northwest Ethiopia, 2017. Ital J Pediatr. 2019 Jan 10;45(1):7. PubMed | Google Scholar
- Blencowe H, Krasevec J, De Onis M, Black RE, An X, Stevens GA et al. National, regional, and worldwide estimates of low birthweight in 2015, with trends from 2000: a systematic analysis. Lancet Glob Health. 2019 Jul;7(7):e849-e860. PubMed | Google Scholar
- Nakimuli A, Starling JE, Nakubulwa S, Namagembe I, Sekikubo M, Nakabembe E et al. Relative impact of pre-eclampsia on birth weight in a low resource setting: A prospective cohort study. Pregnancy Hypertens. 2020 Jul;21:1-6. PubMed | Google Scholar
- Sibai BM, Stella CL. Diagnosis and management of atypical preeclampsia-eclampsia. Am J Obstet Gynecol. 2009 May;200(5):481.e1-7. PubMed | Google Scholar
- Wagnew M, Dessalegn M, Worku A, Nyagero J. Trends of preeclampsia/eclampsia and maternal and neonatal outcomes among women delivering in addis ababa selected government hospitals, Ethiopia: a retrospective cross-sectional study. Pan Afr Med J. 2016 Nov 26;25(Suppl 2):12. PubMed | Google Scholar
- Hassan M, Begum M, Haque SZ, Jahan N, Yasmeen BN, Mannan A et al. Immediate outcome of neonates with maternal hypertensive disorder of pregnancy at a neonatal intensive care unit. Northern International Medical College Journal. 2015;6(2):57-60. Google Scholar
- Say L, Chou D, Gemmill A, Tunçalp O, Moller A, Daniels J et al. Global causes of maternal death: a WHO systematic analysis. Lancet Glob Health. 2014 Jun;2(6):e323-33. PubMed | Google Scholar
- Berhe AK, Ilesanmi AO, Aimakhu CO, Mulugeta A. Effect of pregnancy induced hypertension on adverse perinatal outcomes in Tigray regional state, Ethiopia: a prospective cohort study. BMC Pregnancy Childbirth. 2019 Dec 31;20(1):7. PubMed | Google Scholar
- Getaneh T, Negesse A, Dessie G, Desta M. The impact of pregnancy induced hypertension on low birth weight in Ethiopia: systematic review and meta-analysis. Ital J Pediatr. 2020 Nov 26;46(1):174. PubMed | Google Scholar
- McKenzie KA, Trotman H. A retrospective study of neonatal outcome in preeclampsia at the university hospital of the west indies: A resource-limited setting. J Trop Pediatrs. 2019 Feb 1;65(1):78-83. PubMed | Google Scholar
- Kenya National Bureau of Statistics, Republic of Kenya. Kenya Demographic Health Survey. Ministry of Health Kenya and the DHS Program, ICF International Rockville, Maryland, USA; 2014.
- Lwanga SK, Lemeshow S, World Health Organization. Sample size determination in health studies: a practical manual: World Health Organization; 1991. Google Scholar
- Legesse AY, Berhe Y, Mohammednur SA, Teka H, Goba G. Prevalence and Determinants of Maternal and Perinatal Outcome of Preeclampsia at a Tertiary Hospital in Ethiopia. Ethiopian Journal of Reproductive Health. 2019;11(4):8. Google Scholar
- Yilgwan CS, Pam VC, Yilgwan G, Ige OO, Golit WN, Anzaku S et al. Comparing neonatal outcomes in women with preeclampsia and those with normal pregnancy. Nigerian Journal of Paediatrics. 2020 Aug 6;47(3):258-63. Google Scholar
- Anselmini M, Rodrigues LK, Balestrin B, de Paula Santana D, Freitas G, Rodrigues LK et al. Perinatal outcome of hypertensive pregnant women is related to the severity of preeclampsia. Clinical & Biomedical Research. 2018;38(2). Google Scholar
- Afeke I, Mac-Ankrah L, Jamfaru I, Amegan-Aho KH, Mbroh HK, Lokpo SY et al. Maternal age, low birth weight and early neonatal death in tertiary Hospital in the Volta Region of Ghana. Open Journal of Pediatrics. 2017;7(04):254. Google Scholar
- Nathan HL, Seed PT, Hezelgrave NL, De Greeff A, Lawley E, Conti-Ramsden F et al. Maternal and perinatal adverse outcomes in women with pre-eclampsia cared for at facility-level in South Africa: a prospective cohort study. J Glob Health. 2018 Dec;8(2):020401. PubMed | Google Scholar
- Tolu LB, Yigezu E, Urgie T, Feyissa GT. Maternal and perinatal outcome of preeclampsia without severe feature among pregnant women managed at a tertiary referral hospital in urban Ethiopia. PLoS One. 2020 Apr 9;15(4):e0230638. PubMed | Google Scholar
- Khader YS, Batieha A, Al-Njadat RA, Hijazi SS. Preeclampsia in Jordan: incidence, risk factors, and its associated maternal and neonatal outcomes. J Matern Fetal Neonatal Med. 2018 Mar;31(6):770-776. PubMed | Google Scholar
- Lin YW, Lin MH, Pai LW, Fang JW, Mou CH, Sung FC et al. Population-based study on birth outcomes among women with hypertensive disorders of pregnancy and gestational diabetes mellitus. Sci Rep. 2021 Aug 30;11(1):17391. PubMed | Google Scholar
- Luyeko SS, Lilungulu A, Rweyemamu MA. Haematological Indices and Obstetric Outcomes among Pregnant Women with Preeclampsia at Iringa Regional Tanzania. Systematic Reviews in Pharmacy. 2021;12(11):3627-32. Google Scholar
- Afaya A, Afaya RA, Azongo TB, Yakong VN, Konlan KD, Agbinku E et al. Maternal risk factors and neonatal outcomes associated with low birth weight in a secondary referral hospital in Ghana. Heliyon. 2021 May 1;7(5):e06962. PubMed | Google Scholar
- Mitao M, Philemon R, Obure J, Mmbaga BT, Msuya S, Mahande MJ. Risk factors and adverse perinatal outcome associated with low birth weight in Northern Tanzania: a registry-based retrospective cohort study. Asian pacific journal of Reproduction. 2016;5(1):75-9. Google Scholar
- Bayoumi MA, Ali AA, Hamad SG, Ali AA, Elmalik EE, Elkalaf MM et al. Effect of maternal preeclampsia on hematological profile of newborns in Qatar. Biomed Res Int. 2020 Mar 12;2020:7953289. PubMed | Google Scholar
- Simpson LL. Maternal medical disease: risk of antepartum fetal death. Semin Perinatol. 2002 Feb;26(1):42-50. PubMed | Google Scholar
- Kongwattanakul K, Saksiriwuttho P, Chaiyarach S, Thepsuthammarat K. Incidence, characteristics, maternal complications, and perinatal outcomes associated with preeclampsia with severe features and HELLP syndrome. Int J Womens Health. 2018 Jul 17;10:371-377. PubMed | Google Scholar
- Melese MF, Badi MB, Aynalem GL. Perinatal outcomes of severe preeclampsia/eclampsia and associated factors among mothers admitted in Amhara Region referral hospitals, North West Ethiopia, 2018. BMC Res Notes. 2019 Mar 15;12(1):147. PubMed | Google Scholar
- Yoon JJ, Kohl S, Harper RG. The relationship between maternal hypertensive disease of pregnancy and the incidence of idiopathic respiratory distress syndrome. Pediatrics. 1980 Apr;65(4):735-9. PubMed | Google Scholar
- Langenveld J, Ravelli AC, Van Kaam AH, Van Der Ham DP, Van Pampus MG, Porath M et al. Neonatal outcome of pregnancies complicated by hypertensive disorders between 34 and 37 weeks of gestation: a 7 year retrospective analysis of a national registry. Am J Obstet Gynecol. 2011 Dec;205(6):540.e1-7. PubMed | Google Scholar
- Friedman SA, Schiff E, Kao L, Sibai BM. Neonatal outcome after preterm delivery for preeclampsia. Am J Obstet Gynecol. 1995 Jun;172(6):1785-8; discussion 1788-92. PubMed | Google Scholar
- Boskabadi H, Rakhshanizadeh F, Moradi A, Zakerihamidi M. Risk factors and causes of neonatal hyperbilirubinemia: a systematic review study. Journal of Pediatrics Review. 2020;8(4):211-22. Google Scholar
- Murekatete F. Social demographic, medical and maternal life style factors associated with low birth weight at selected Refferal Hospital in Rwanda. University of Rwanda; 2019.
- Ndwiga C, Odwe G, Pooja S, Ogutu O, Osoti AE, Warren C. Clinical presentation and outcomes of pre-eclampsia and eclampsia at a national hospital, Kenya: A retrospective cohort study. PLoS One. 2020 Jun 5;15(6):e0233323. PubMed | Google Scholar