Fetal ECG waveform for intrapartum monitoring.
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Biomedical subjects
Publications and source records attributed to K R Greene.
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It is possible to record the fetal electrocardiographic waveform (ECG) from the scalp electrode used in labour for detection of fetal heart rate. Animal and observational studies of changes in the ST waveform of the ECG during hypoxia suggest that a combination of heart rate and ST waveform analysis might improve the predictive value of intrapartum monitoring. In a randomised trial, we have studied intervention rates and neonatal outcome for high-risk labours monitored either by conventional cardiotocography (CTG) or by ST waveform analysis plus CTG. 1200 women with pregnancy of at least 34 weeks' gestation were assigned to the groups when the decision to apply a fetal scalp electrode was made. Neonatal outcome was assessed by umbilical-cord blood gas analysis, Apgar scores, resuscitation needed, and postnatal course. All recordings were retrospectively viewed by an observer unaware of clinical details to check adherence to the trial protocol. The addition of ST waveform monitoring to CTG substantially reduced the proportion of deliveries for fetal distress (ST + CTG 27/615 vs CTG 58/606; p less than 0.001). The groups did not differ in rate of operative delivery for other reasons, incidence of asphyxia at birth, or neonatal outcome. Metabolic acidosis and low 5 min Apgar scores were less common in the ST + CTG than the CTG group, but not significantly so. The only case of birth asphyxia in the ST + CTG group was identified by both heart rate and ST changes. The review of recordings showed that the reduction in intervention rate was among cases with CTG patterns classified as normal or intermediate, whereas there was no difference in intervention rates among cases with abnormal recordings. Our findings confirm that ST waveform analysis discriminates CTG changes in labour and that our protocol for interpretation is safe. Further randomised studies are warranted.
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As the limitations of heart-rate based intrapartum monitoring have become apparent, there is renewed interest in analysis of the fetal electrocardiographic waveform as obtained from a fetal scalp electrode. A high quality ECG signal is necessary for waveform analysis. This study examined the suitability of five commonly available scalp electrodes for collecting this signal by examining their physical and electrical characteristics, together with a randomised clinical trial in which the ECG trace quality was assessed in 50 patients. The frequency response of Copeland electrodes was such that they attenuate the ECG signal more than the baseline noise. Difficulties were experienced in obtaining optimum attachment and the long, semi-rigid design increased movement artefact resulting in significantly poorer quality ECG signals. Whilst the Hewlett-Packard double spiral electrode had a near ideal frequency response, certain design features made it difficult to apply and remain secure so the clinical signals were of intermediate quality. The Corometrics and Cetro single spirals had the most stable attachment to the scalp and a near ideal frequency response, so produced significantly better signal quality in the clinical trial. Currently, single spiral electrodes are the most suitable for electrocardiographic data collection.
The experimental evaluation of the fetal ECG waveform as a method of fetal surveillance has been based largely on experimentally induced hypoxia. The present data, obtained from chronically instrumented fetal lambs, includes three fetuses monitored throughout spontaneous labour, six fetuses with spontaneously developed long-term ST waveform changes and another three fetuses which died in the post-operative period. Uterine contractions could by themselves cause an increase in T wave height (T/QRS ratio greater than 0.30). If the ST elevation was normalised between contractions the fetus seemed to compensate to a moderate degree of hypoxia. When oxygenation was further reduced the T wave remained elevated between contractions and a progressive increase occurred in the T/QRS ratio (greater than 0.60) during the final stages of labour, in parallel with increasing blood lactate levels. Long-term ST changes with T/QRS consistently exceeding 0.30 were found to be related to low haemoglobin levels and/or fetal hypotension. Subsequently, all these fetuses died during labour as compared with a survival rate of 40% in fetuses showing a normal ST waveform. In this group negative T waves are reported as a sign of failing myocardial response to hypoxia. Death in utero, whatever the cause (bleeding, infection or spontaneous hypoxia) was always preceded by marked ST waveform changes. It is concluded that ST elevation with high peaked T waves can appear on a long-term basis in fetuses with intrauterine complications.
Different portions of the ECG waveform are influenced differently. The QRS waveform is influenced principally by ventricular muscle mass but may be influenced by differences in ventricular filling which occur with cardiac failure or transiently with cord compression. The PR interval normally has a positive correlation with the R-R interval but this correlation becomes negative, probably as a result of catecholamines, when the fetus is stressed. This difference between PR/RR correlation may help distinguish vagally mediated decelerations from those associated with hypoxia. The ST waveform becomes elevated when myocardial oxygen delivery is insufficient to maintain aerobic metabolism to meet the energy demands of the myocardium, and anaerobic metabolism occurs with the production of lactate; this is a dynamic situation and may occur at different levels of oxygenation in different fetuses, depending on their ability to compensate and the workload on the myocardium. It is very likely that changes in PR/RR relationships and the ST waveform will be useful in intrapartum monitoring in the future, and this contention is supported by recent analysis of PR/RR and ST segment shifts (Figure 16). It seems clear that the detailed study of the ECG waveform provides more, and perhaps clinically more useful, information from the same signal and electrode as heart rate, and it is no longer reasonable to ignore it. However, as clinicians we have an extraordinary ability to move with disenchantment from one method of fetal monitoring to another of no proven value, with a firm but unreasoned conviction that it is better. ECG analysis is by no means ready for clinical use if we are to avoid the same pitfalls as continuous FHR monitoring. Further clinical assessment will not be easy. In modern obstetric practice asphyxiated infants are fortunately not common, so there are practical difficulties in monitoring sufficient numbers of patients to evaluate new indices of asphyxia, as well as the difficulties of defining an objective endpoint. Thorough clinical (probably multicentre) studies are needed with well defined endpoints and this is beginning. Further fetal lamb studies are also needed, particularly to examine the interrelationships between changes in heart rate, PR interval and ST waveform; it is hoped that this chapter has emphasized the importance of such animal studies in understanding the physiological and therefore clinical background to any change.(ABSTRACT TRUNCATED AT 400 WORDS)
Waveform changes in the fetal electrocardiogram (ECG) are under reassessment as a means of fetal surveillance. The purpose of the study was to identify ST waveform changes from the fetal scalp lead during labour and to compare any change with conventional signs of fetal distress. Two scalp electrodes provided a sufficiently stable signal from which ST waveform changes could be identified and measured as the T/QRS ratio. No infant was clinically hypoxic. Only 26% of the 46 patients studied had a continuously normal CTG whereas 67% had no ST waveform abnormalities. A relation was found between the two variables as the mean T/QRS ratio increased from 0.20 (SD 0.11) during epochs of normal CTG to 0.27 (SD 0.17) with CTG changes. A linear correlation (r = 0.58, P less than 0.01) was found between the T/QRS ratio before birth and the cord plasma lactate values.
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