Background
Intrapartum fetal hypoxia which is one of the leading causes of neonatal morbidity and mortality is a preventable cause. Over the past years, many methods have been employed to diagnose fetal distress, a sign of fetal hypoxia, among these, cardiotocography (CTG) is the most widely used method. Diagnosis of fetal distress based on CTG can have high inter and intraobserver variation leading to either delayed or inessential intervention henceforth increasing maternal morbidity and mortality. Fetal cord arterial blood pH is an objective method to diagnose intrapartum fetal hypoxia, hence by observing the incidence of acidemia in cord blood pH among those newborns born through cesarean section (CS) in view of non-reassuring CTG can help make a judicious decision.
Methods
In this single institutional observational study, patients admitted for safe confinement were subjected to CTG in the latent and active phases of labor. Non-Reassuring traces were further classified based on NICE guideline CG190. The cord blood of these neonates born through CS in view of non-reassuring CTG was drawn and sent for ABG analysis.
Results
Among the 87 neonates delivered through CS in view of fetal distress, 19.5% had acidosis. Among those with pathological traces, 16(28.6%) had acidosis and one (100%) which was categorized as the need for urgent intervention showed acidosis. This result showed a statistically significant association (p value-0.003). No statistically significant association was obtained when variation in baseline characters of CTG when taken independently.
Conclusions
In our study, neonatal acidemia which is the objective evidence of fetal distress was seen in 19.5% of our study population who underwent cesarean in view of non-reassuring CTG. Among these, acidemia was significantly associated with pathological CTG trace compared to suspicious trace. We also observed that abnormal FHR features when taken independently showed no significant association with acidosis. Acidosis among newborns certainly increased the requirement for active resuscitation and additional hospital stay. Hence, we conclude that by recognizing specific fetal heart rate patterns associated with acidosis in a fetus, a more judicious decision can be made, thereby preventing both delayed as well as inessential intervention.
Keywords : Caesarean section · Cardiotocography · Fetal distress · pH · Academia
In developing countries, birth asphyxia accounts for around seven deaths per 1000 births. The majority of deaths occur soon after birth, while few during the intrapartum period.
Birth asphyxia is an important cause of neonatal mortality and serious morbidities such as hypoxic-ischemic encephalopathy (HIE), seizures, intraventricular hemorrhage, cerebral palsy, and delayed development. The main aim of intrapartum fetal monitoring is to identify fetal hypoxia at right time to prevent subsequent acidemia and associated cell damage [1].
The ultimate goal of a health care provider is a safe mother and baby. Accurate perinatal fetal assessment is the key to safety.
CTG is one of the commonly employed methods for the detection of fetal distress by monitoring fetal heart rate and uterine contractions [2]. Accurate CTG interpretation and timely intervention ensure better neonatal outcomes.
APGAR is the most commonly used method for the assessment of newborn conditions. However, prematurity and meconium-stained liquor can alter the APGAR even in the absence of birth asphyxia. Hence, there is a need for more objective tests for the evaluation of neonates.
Neonatal cord blood acid–base analysis is one such objective tool that can reflect birth asphyxia. When the oxygen supply to the fetus is significantly disrupted, tissue oxygen deprivation with consequent acidosis occurs, and acidaemia results. The development of metabolic acidosis in the fetus is reflected in the low pH of the blood obtained from the umbilical artery soon after birth hence the most useful umbilical cord blood parameter is pH.
The identification of hypoxic cases may guide giving oxygen to these neonates to prevent the development of cerebral lesions. The incidence of cesarean section is rising these days and one of the commonest indications cited for the same is fetal distress. The diagnosis of fetal distress is commonly clinical in resource-constrained settings.
As the cesarean section is associated with a higher incidence of maternal morbidity and mortality, the indication for the same should be justifiable. Hence, proving the correlation between CTG showing fetal distress with umbilical artery blood pH showing acidosis can provide us evidence concerning precise diagnosis and subsequent management at the appropriate time.
The present study is an institutional ethical and scientific committee review board-approved single institutional prospective observational study conducted over 1 year. (September 2020–September 2021).
Selection and Description of ParticipantsAntenatal women with a gestational age of >34 weeks singleton pregnancy, and cephalic presentation were included in the study, while those with multifetal gestation, gestational age <34 weeks, malpresentation, and those who underwent cesarean section for indications other than fetal distress were excluded from the study. Convenience sampling was done.
Based on the proportion (53.6%) of neonatal acidemia in fetal distress observed in an earlier publication (International Journal of Reproduction, Contraception, Obstetrics, and Gynaecology) and with 20% allowable error, 95% confidence, the minimum sample size was 83 (Figs. 1 and 2).
The primary objective of the study was to determine the incidence of acidaemia in cord blood pH among those neonates delivered through CS in view of non-reassuring CTG. The secondary objective is to study the association between acidaemia in cord blood PH and neonatal outcomes of those neonates born through CS performed in view of fetal distress.
All antenatal women > 34 weeks were admitted for further management or safe confinement, and CTG monitoring was done. The CTG machine used in the study was BPL Diva with the paper speed being 1 cm/min with an external transducer. The CTG was interpreted and classified based on NICE guideline CG 190. (Appendix 1). The average time taken from the diagnosis to the delivery of the baby was 35 min. Either spinal or spinal-epidural anesthesia was used.
The arterial cord blood of the newborn was collected using a preheparinized 2 cc syringe soon after birth. In our hospital setting, the sample is transported through a pneumatic tube system within 5 min of sample collection. Radiometer ABL 800 Basic was used to analyze the arterial blood gas, the average time to report the analysis was 15 min. A pH value of < 7.2 according to the institutional protocol was considered acidosis. APGAR score of each newborn was calculated 5 min after birth was.
Other neonatal outcomes including the need for active resuscitative measures, bag and mask ventilation, chest compressions, and medications as well as neonate requiring NICU admission and further interventions were collected (Tables 1, 2, 3 and 4).
StatisticsStatistical analysis was performed using IBM SPSS version 20.0 software; categorical variables are expressed by frequency and percentage. Continuous variables are presented by mean, median, SD 25 the percentile, and 75 the percentile. To test the statistical significance of the association of categorical variables with acidosis, Chi-square test was used. To test the statistical significance of the difference in the median hospital stay for acidosis, Mann–Whitney U test was used.
The most common and routinely practiced method to diagnose fetal distress is CTG, which most other studies have concluded has a high false-positive rate leading to an increased frequency of inessential intervention. This is due to high inter- and intraobserver variation. Hence, it calls for an objective method for analyzing the CTG and timely decision-making. Henceforth, various guidelines have been proposed for cardiotocography interpretation. In this study, NICE guideline CG 190 has been used for CTG interpretation. There has been previous literature validating these guidelines. Eighty-seven patients who underwent cesarean section because of non-reassuring CTG were included in the study. CTG Interpretation was later correlated to cord blood pH and significant perinatal outcomes. Cord blood pH was used, as it has shown to provide objective evidence of hypoxia during labor and is found to be more resourceful than APGAR alone.
Disagreements concerning the ability of abnormal fetal heart rate patterns to predict fetal well-being still exist. While many authors found abnormal fetal heart rate patterns significantly associated with adverse outcomes [3–6], others did not. However, most studies have concluded that these abnormal FHR patterns led to increased intervention in terms of operative vaginal deliveries or cesarean sections [7, 8].In our study, fetal monitoring was done in latent and active phase labor. Abnormal CTG was further classified, into suspicious (34.5%), pathological (64.4%), and need for immediate intervention tracing (1.1%) before subjecting to cesarean section.
In this study, pH < 7.2 was taken as a cutoff value to define acidosis in a neonate according to institutional protocol, Kaban et al. used the cutoff value for defining acidosis as cord blood pH < 7.2.
However, Modarressnejad V used a cutoff value of pH < 7.1.7 to define acidosis. Of 87 neonates included in the study,17 (19.5%) neonates had acidosis (pH < 7.2) while the remaining 70 (80.5%) neonates were born healthy and without acidosis. As most fetuses were shown to tolerate acidaemia during labor with a pH cutoff of 7.0 without experiencing neurologic impairment, [9, 10], the clinical importance of these findings is debatable.
In our study, there was no significant difference among either gender who developed acidosis. Conversely, previous studies like Lau et al. [11] showed that male fetuses were at higher risk for developing distress during labor. This discrepancy can be because of our small sample size, therefore, larger studies are required for more appropriate results.
In our study, intrauterine resuscitative measures as mentioned above were used in response to abnormal FHR, thereby confounding the analysis of the correlation between the outcome and the observed abnormality. However, patients with persistent abnormal FHR who underwent cesarean section were only included in the study leaving a smaller sample size.
In our study, it is evident that there is a significant association between the intrapartum CTG category and acidosis among neonates. This association was confirmed in a study by Aboulghar W et al. who also concluded that pathological CTG rather than suspicious CTG increased the risk of acidosis significantly. But none of the newborns had HIE, hence accurate interpretation and timely intervention can help reduce morbidity and mortality among newborns.
Apart from bradycardia, none of the FHR patterns in our study were independently associated with fetal acidosis. As confirmed by Lau TK et al., if decelerations are not accompanied by a rise in FHR baseline (or tachycardia) with worsening variability, they do not represent fetal hypoxia [12]. Prolonged deceleration in our study has shown to be substantially associated with acidosis as seen in 44% neonates.
As concluded by Lysander et al. they study that “There was no significant difference between those with MSL and those without MSL in terms of pH [13]”. In this study, 21.8% (n = 19) of deliveries were complicated with MSL of which only 10.5% (n = 2) were associated with acidosis. APGAR score, despite the controversy concerning its reliability as a measure for morbidity in newborns, is in wide practice to evaluate the newborn condition and the need for immediate resuscitation. In this study, newborns with acidosis certainly had poor APGAR scores. But among those with APGAR > 7 at 5 min, six neonates (8%) had acidosis. In a study conducted by Anyaegbunam A et Al., 20.7% had an abnormal pH (< 7.20) and normal Apgar (> 7). Respiratory acidosis unlike metabolic acidosis is of less concern and tends to settle soon after birth. Hence, many of these infants with low arterial cord pH may have a normal 5-min Apgar score. [14].In a study by Richa Gangwar et al., which included 146 neonates, poor outcomes were seen in 14% of cases which is comparable to our study where 12.7% of neonates had poor outcomes requiring further intervention. [15]. However, neonatal acidaemia is weakly associated with adverse outcomes. Most neonates with neurological morbidity have normal cord pH values. Other variables must influence adverse outcomes and account for more of these than acidaemia.
In the study by Sunitha et al., no significant association was found between abnormal CTG patterns with that of NICU admission (p value − 0.5). In a study conducted by Gupta et al., similar findings were noted [16]. In agreement with other studies, in this study, no significant association was found between the type of CTG trace and the requirement for NICU admission (p value = 0.106) In our study, 23 babies were admitted to NICU for observation and further management.
Strengths and LimitationsStrengths
Availability of CTG monitoring for all the in-labor patients
and round-the-clock availability of facilities for emergency
interventions. Every CTG in the study was followed by only
one observer, hence overcoming the inter-observer variation
in interpretation. During analyzing the arterial blood gases,
value error is minimized as the investigation is done in the
same standardized laboratory.
Limitations: Small sample size. Lack of facilities like fetal blood sampling (FBS), decisions had to be taken only based on CTG findings without adjuvant confirmatory test. The positive and negative predictive values of CTG could not be calculated since our study included only those with abnormal CTG traces. In this study, we could not perform long-term follow-up, hence long-term problems like mental retardation, cerebral palsy, and poor school performance could not be observed.
Declarations
Conflict of interest This is an original article based on a prospective
study performed at the Amrita Institute of Medical Sciences, Kochi,
Kerala, India. The authors declare that there is no conflict of interest
related to this work.
Ethical Approval This study was approved by the Institutional review board and ethics committee. The study was performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments.
Informed Consent Informed consent was taken from all the participants in the study.