Evaluation and Association of Meconium-Stained Amniotic Fluid With Fetal Distress
Nilesh S Karpe, Manjusha B Tagad, Rahul R Holkar, Vibha S More

TL;DR
This study examines how meconium-stained amniotic fluid relates to fetal distress during childbirth and identifies associated risk factors.
Contribution
The study provides new insights into the association between meconium-stained amniotic fluid and fetal distress, highlighting its role as an obstetric risk factor.
Findings
26% of cases had moderate meconium-stained amniotic fluid linked to fetal distress.
Fetal distress was significantly associated with meconium-stained amniotic fluid.
No significant link was found between meconium-stained amniotic fluid and umbilical cord pH or labor stage.
Abstract
Background Meconium-stained amniotic fluid (MSAF) often leads to complicated deliveries ranging from instrumental delivery, cesarean delivery, and neonatal complications like fetal distress, neonatal intensive care unit (NICU) admission, and neonatal death. Therefore, this study aimed to evaluate the prevalence of MSAF in fetal distress, to determine the clinical profile of newborns in terms of risk factors, and to study the association between antenatal or intra-natal risk factors with MSAF, between umbilical cord pH and MSAF, between stage of labor and MSAF, and between fetal distress and MSAF. Methods A total of 200 cases were enrolled after the diagnosis of fetal distress in the intrapartum period in this observational, non-interventional, and cross-sectional study. The inclusion criteria involved pregnant women who had intrapartum fetal distress diagnosed by the abnormal fetal…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
| Sociodemographic characteristics (N = 200) | Frequency (n) | Percentage (%) | |
| Age | <20 years | 15 | 7.5% |
| 21-25 years | 84 | 42% | |
| 26-30 years | 74 | 37% | |
| 31-35 years | 22 | 11% | |
| 36-40 years | 5 | 2.5% | |
| Gravida | Primigravida | 107 | 53.5% |
| Multigravida | 93 | 46.5% | |
| Gestational age | 30-32 weeks | 1 | 0.5% |
| 32.1-36 weeks | 16 | 8% | |
| 36.1-38 weeks | 55 | 27.5% | |
| 38.1-40 weeks | 65 | 32.5% | |
| Obstetrics factor (n = 200) | Frequency | Percentage (%) |
| Moderate MSAF | 52 | 26% |
| Post term | 34 | 17% |
| Post LSCS | 30 | 15% |
| Oligohydramnios | 24 | 12% |
| IUGR | 20 | 10% |
| PROM | 16 | 8% |
| Cord around the neck | 14 | 7% |
| Thick meconium | 16 | 34% |
| Cord prolapse | 1 | 0.5% |
| Preterm labor | 1 | 0.5% |
| Abruptio placenta | 1 | 0.5% |
| Placenta previa | 1 | 0.5% |
| Antenatal and intra-natal risk factors | Meconium-stained amniotic fluid | Chi-square test | p-value | |
| Yes (%) | No (%) | |||
| Obstetrics | 66 (33%) | 98 (49%) | 14.2707 | 0.0007* |
| Maternal | 0 (0%) | 25 (12.5%) | ||
| Both | 2 (1%) | 9 (4.5%) | ||
| Total | 68 (34%) | 132 (66%) | ||
| Umbilical cord analysis | Meconium-stained amniotic fluid | Chi-square test | p-value | |
| Yes (%) | No (%) | |||
| <7 | 0 (0.0%) | 6 (3%) | 1.2563 | 0.2623 |
| ≥7 | 68 (34%) | 126 (63%) | ||
| Total | 68 (34%) | 132 (66%) | ||
| Stage of labor | Meconium-stained amniotic fluid | Chi-square test | p-value | |
| Yes (%) | No (%) | |||
| First stage | 64 (32%) | 127 (63.5%) | 0.458 | 0.499 |
| Second stage | 4 (2%) | 5 (2.5%) | ||
| Total | 68 (34%) | 132 (66%) | ||
| Fetal distress | Meconium-stained amniotic fluid | Chi-square test | p-value | |
| Yes (%) | No (%) | |||
| Bradycardia | 0 (0%) | 28 (14%) | 14.6219 | 0.005* |
| Late deceleration | 20 (10%) | 30 (15%) | ||
| Loss of variability | 3 (1.5%) | 5 (2.5%) | ||
| Persistent fetal tachycardia | 4 (2%) | 9 (4.5%) | ||
| Variable deceleration | 41 (20.5%) | 60 (30%) | ||
| Total | 68 (34%) | 132 (66%) | ||
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsNeonatal Respiratory Health Research · Assisted Reproductive Technology and Twin Pregnancy · Neonatal and fetal brain pathology
Introduction
The fluid that surrounds the fetus in the uterus is called amniotic fluid, providing a low-resistance and safe environment for the fetus. Meconium is a dark green fluid that the newborn baby passes naturally and comprises epithelial cells, mucus, and bile. Meconium enters the amniotic fluid when the fetus is under stress. It leads to higher perinatal morbidity and death and is an indication of fetal impairment [1]. A higher incidence of instrumental delivery, cesarean delivery, low birth weight, fetal distress, neonatal intensive care unit (NICU) admission rate, and neonatal death is linked to meconium-stained amniotic fluid (MSAF) [2].
Typically, 13% to 16% of childbirths are complicated by MSAF [3]. About 2% to 10% of all cases of MSAF involve meconium aspiration syndrome (MAS), which happens when the newborn aspirates the meconium [4]. In approximately 12% of newborns with MAS, neonatal mortality occurs [1]. MSAF could be a sign of the gastrointestinal tract's typical maturation. It could also exist when there is fetal distress brought on by an acute or ongoing hypoxic episode [4,5]. There has been much discussion over the biology of aberrant amniotic fluid staining, and its clinical implications are still unclear [6]. The green coloration associated with meconium and its consistency leads to a meconium plug and the ability to trigger inflammation in MSAF, a typical anomaly of amniotic fluid staining [7].
The prenatal transfer of meconium from the fetal digestive tract to the amniotic fluid is the subject of several theories. Meconium passing is thought to be a normal physiological phenomenon of the fetus's and its gastroenteric nerve system's growth [5]. However, the contrasting theory states that meconium ejection is a reaction to fetal discomfort. Hypoxia triggers the vagal reflex and vasoconstriction, which in turn causes hyperperistalsis [7]. With conflicting findings, studies have tried to confirm the link between meconium transit in pregnancy and fetal discomfort. According to several studies, MSAF and fetal hypoxia/acidosis are interlinked [8,9]; however, others have not found a connection, indicating that meconium passing during pregnancy is not likely to be linked to worse perinatal outcomes [10,11]. Hence, this study aimed to evaluate the prevalence of MSAF in fetal distress, to determine the clinical profile of newborns in terms of risk factors, and to study the association between antenatal or intra-natal risk factors with MSAF, between umbilical cord pH and MSAF, between stage of labor and MSAF, and between fetal distress and MSAF.
Materials and methods
This observational, non-interventional, cross-sectional study is part of a large research project performed at the department of obstetrics and gynecology of a tertiary care hospital from January 2018 to December 2019 after obtaining approval from the Institutional Ethical Committee with reference number EC/24/2018. The patients were enrolled after diagnosis of fetal distress in the intrapartum period for the data collection. The diagnosis of fetal distress was made by the abnormal fetal heart rate monitoring findings on cardiotocography (CTG), and the interpretation of CTG, adapted from the National Institute for Health and Care Excellence (NICE) Clinical Guideline 190, was used to classify CTG as abnormal. The inclusion criteria involved singleton pregnancy, gestational age at term (≥30 weeks), cephalic presentation, mode of delivery by cesarean section, as well as term delivery, abnormal fetal heart rate monitoring findings suggestive of fetal distress, and women who were willing to participate. The exclusion criteria included multiple gestations, breech presentation, known fetal anomalies, gestational age less than 30 weeks, intrauterine fetal demise, antepartum hemorrhage, and women who did not want to participate in the present study. The patients were counseled, and those willing to participate in the study were recruited after obtaining their informed consent after the patient delivered the neonate and was shifted to the ward. Based on the eligibility criteria and sample size calculation, a total of 200 cases were enrolled for the present study. The sample size was calculated assuming a desired effect size of 0.3, a significance level (α error) of 0.05, power (1-β error) of 0.92, and degree of freedom (df) of 5. It derived the sample size of 196 participants with actual power of 0.9212 and critical χ² of 11.07, which was rounded off to 200 participants.
The retrospective and prospective data were collected from the labor room records in the data collection sheet and recorded in an Excel sheet (Microsoft Corporation, Redmond, WA). The data were analyzed using SPSS version 17 (SPSS Inc., Chicago, IL). All the parameters were assessed using descriptive statistics, and qualitative data were represented as frequency and percentage. The association was determined using a chi-square test, and a p-value equal to or less than 0.05 was considered significant.
Results
An observational cross-sectional study was conducted to evaluate the prevalence of MSAF in fetal distress, to determine the clinical profile of newborns in terms of risk factors, and to study the association between antenatal or intra-natal risk factors with MSAF, between umbilical cord pH and MSAF, between stage of labor and MSAF, and between fetal distress and MSAF. The sociodemographic characteristics of the enrolled women are demonstrated in Table 1.
Moreover, the distribution of women amongst various obstetric risk factors is demonstrated in Table 2.
The distribution of the women based on MSAF stated that 68 (34%) were affected by meconium and 132 (66%) were not affected by meconium. Moreover, the association between antenatal or intra-natal risk factors with MSAF is demonstrated in Table 3.
The association between umbilical cord pH and MSAF is demonstrated in Table 4.
The association between the stage of labor and MSAF is demonstrated in Table 5.
Moreover, the association between fetal distress with the sub-groups, mentioning the several criteria to classify fetal distress, including bradycardia, late deceleration, loss of variability, persistent fetal tachycardia, and variable decelerations on CTG and MSAF, is demonstrated in Table 6.
Discussion
The present study evaluated the prevalence of MSAF in fetal distress and determined the association of the clinical profile of newborns in women with fetal distress, having an age range of 21 to 25 years. Similarly, a previous study by Gangwar et al. [12] observed that fetal distress was common at 24.5 years of age, and Ajah et al. [13] reported that the average age of women with fetal distress was between 25 and 29 years. Hence, the findings from the above-mentioned studies correspond well with the results of the present study. Moreover, the majority of the patients in the present study were primigravida, which was found to be congruous with the findings of the studies by Gangwar et al. [12] and Ajah et al. [13].
Additionally, fetal distress was more commonly observed in 38.1-40 weeks of gestation, which correlated well with the findings provided by Ajah et al. [13], in which all of the pregnant women were at term with the mean gestational age of 39 ± 2 weeks whereas, in a study given by Ugwa et al. [14] the mean gestational age was 37.6 ± 2.4 weeks, which corresponded with the findings of the current results.
In the present study, moderate MSAF affected 26% of patients out of 200 patients, and in a study conducted by Tasew et al. [15], MSAF affected 23.9% of patients. However, in a study by Aslam et al. [16], there were 19.5% of patients with MSAF out of 123 patients. In the present study, premature rupture of membrane (PROM) affected 8% of 200 patients, whereas Aslam et al. [16] reported that the PROM affected 33.3% of cases out of 123 patients, and the confidence interval was 3.75 to 22.81. However, Gebreheat et al. [17] reported that the PROM affected 4.51 % of 421 patients. A total of 24% of oligohydramnios patients were reported in the present study. However, Tasew et al. [15] reported 4.2% out of 264 patients, and Aslam et al. [16] reported 7.3% cases out of 123 patients under the present findings. One patient (0.5%) reported antepartum hemorrhage out of 200 cases of obstetric high-risk factors in this study. Aslam et al. [16] reported 3.3% out of 123 patients, and Tasew et al. [15] reported 9.1% out of 264 patients. One patient (0.5%) reported cord prolapse out of 200 cases of obstetric high-risk factors in this study. However, Aslam et al. [16] reported 8.1% out of 123 patients, and Tasew et al. [15] reported 8% out of 264 patients. In Gebreheat et al.'s [17] study, cord prolapse affected 4.26% of 421 patients.
Tasew et al. [15] found that the risk of birth asphyxia was 7.9 times higher for newborns with meconium stains than for those without birth asphyxia and that it was 2.2 times more likely to occur in preterm infants than in term ones. Likewise, there was a noteworthy correlation between the neonate's weight and delivery asphyxia. The risk of asphyxia was 6.9 times higher for low birth weight than for normal weight (≥2500 g). This could be because maternal complications such as diabetes mellitus or hypertension, which occur before or during pregnancy, cause low birth weight. Compared to term newborns, preterm babies had a 2.2-fold higher risk of asphyxia. The present study reported no cases of MSAF with cord pH less than 7, indicating that severe fetal acidosis was not observed among these cases; however, 34% of cases were observed with a cord pH more than and equal to 7, hence, suggesting that a significant proportion of fetuses exposed to meconium-stained fluid maintained a normal or near-normal acid-base status at birth. This finding implies that the presence of MSAF alone may not reliably predict severe fetal hypoxia or acidosis. In Kumar et al.'s [18] study, umbilical cord blood pH was the best indicator of fetal hypoxemia during labor, and a pH less than 7 had a higher percentage of NICU transfer. Also, in the present study, it was found that the presence of thick meconium in amniotic fluid is associated with poor fetal outcome and acidosis in comparison to thin meconium-stained liquor.
In the present study, it was observed that there were more cases of MSAF with fetal distress in the second stage of labor (2%) than in the first stage of labor (32%). Lee et al. [19] reported that MSAF has more commonly occurred in the first stage of labor than in the second stage of labor in nulligravida. According to this study, the longer the duration of labor, the higher the chances of MSAF. The second stage of labor is characterized by an increasing number and intensity of uterine contractions compared to the first stage of labor, as well as an increase in maternal bearing down efforts, which leads to maternal fatigue and high fetal lactic acid levels. Maanongun et al. [20] found that out of 140 cases in both the first and second stages of labor, the normal fetal outcome was present in 133 and 123 in the first and second stages of labor, respectively.
Limitations of the study
The sample size could be estimated with broader geographical consideration for the population. The study represents a lack of randomization, providing sampling bias affecting the generalizability of the population. The study incorporated retrospective and prospective data, which could limit the data availability. The study duration can be expanded to determine the long-term association of fetal distress.
Conclusions
The study concluded that amongst the obstetric risk factors, moderate MSAF accounted for the maximum frequency of women. However, the association of MSAF with antenatal or intra-natal risk factors was significant concerning obstetric risk factors, but that with umbilical cord pH and stage of labor was insignificant. Also, the association between MSAF and fetal distress was significant, specifying that the presence of meconium in the amniotic fluid is a meaningful clinical sign of potential fetal compromise, even if not always accompanied by changes in cord blood pH. The study reports the association, whereas the future scope might inculcate the strength of the association using odds ratio or prevalence ratio.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Impact of meconium-stained amniotic fluid on neonatal outcome in a tertiary hospital Cureus Parween S Prasad D Poonam P Ahmar R Sinha A Ranjana R 014202210.7759/cureus.24464 PMC 913170735637798 · doi ↗ · pubmed ↗
- 2Study of risk factors and perinatal outcome in meconium stained deliveries from a district of Uttar Pradesh, India Int J Reprod Contracept Obstet Gynecol Rathoria R Rathoria E Bansal U Mishra M Jalote I Shukla NK Agarwal D 3605360972018
- 3Fetal outcome in meconium stained deliveries J Clin Diagn Res Mundhra R Agarwal M 2874287672013 https://pubmed.ncbi.nlm.nih.gov/24551662/2455166210.7860/JCDR/2013/6509.3781 PMC 3919335 · doi ↗ · pubmed ↗
- 4Meconium aspiration syndrome: a role for fetal systemic inflammation Am J Obstet Gynecol Lee J Romero R Lee KA Kim EN Korzeniewski SJ Chaemsaithong P Yoon BH 3663692142016 https://pubmed.ncbi.nlm.nih.gov/26484777/10.1016/j.ajog.2015.10.009PMC 562535226484777 · doi ↗ · pubmed ↗
- 5The aetiology of meconium-stained amniotic fluid: pathologic hypoxia or physiologic foetal ripening? (Review)Early Hum Dev Monen L Hasaart TH Kuppens SM 325328902014 https://pubmed.ncbi.nlm.nih.gov/24794302/2479430210.1016/j.earlhumdev.2014.04.003 · doi ↗ · pubmed ↗
- 6Consequences of meconium stained amniotic fluid: what does the evidence tell us?Early Hum Dev 10 2024 Hutton EK Thorpe J 333339902014 https://www.sciencedirect.com/science/article/abs/pii/S 03783782140008632479430510.1016/j.earlhumdev.2014.04.005 · doi ↗ · pubmed ↗
- 7Meconium-stained amniotic fluid and histologic signs of fetal distress in stillbirths Eur J Obstet Gynecol Reprod Biol Avagliano L Massa V Bulfamante G 556226620213459265010.1016/j.ejogrb.2021.09.016 · doi ↗ · pubmed ↗
- 8The effect of meconium thickness level on neonatal outcome Early Hum Dev 10 2024 Gluck O Kovo M Tairy D Herman HG Bar J Weiner E 1049531422020 https://www.sciencedirect.com/science/article/abs/pii/S 03783782193041043193561010.1016/j.earlhumdev.2020.104953 · doi ↗ · pubmed ↗
