Prediction of non-reassuring fetal status and umbilical artery acidosis by the maternal characteristic and ultrasound prior to induction of labor.

OBJECTIVE: To investigate the predictive value of pre-induction digital examination, sonographic measurements and parity for the prediction of non-reassuring fetal status and cord arterial pH < 7.2 prior to the induction of labor (IOL). METHOD: This was a prospective observational study, including 384 term pregnancies undergoing IOL. Before the IOL, the Bishop score (BS) by digital examination, sonographic Doppler parameters and the estimated fetal weight (EFW) was assessed. The fetal cord arterial was sampled to measure the pH at delivery. Multivariate logistic regression analysis was performed to identify independent predictors of non-reassuring fetal status and low cord arterial pH. RESULTS: Forty four cases (11.5%) had non-reassuring fetal status, and 76 cases (19.8%) had fetal cord arterial pH < 7.2. In the non-reassuring fetal status group, the incidence of cord arterial pH < 7.2 was significantly higher than that in the normal fetal heart rate group (χ2 = 6.401, p = 0.011). Multivariate analysis indicated that significant independent predictors of non-reassuring fetal status were nulliparity (adjusted odds ratio [AOR]: 3.746, p = 0.003), EFW < 10th percentile (AOR: 3.764, p = 0.003) and cerebroplacental ratio (CPR) < 10th centile (AOR:4.755, p < 0.001). In the prediction of non-reassuring fetal status, the performance of the combination of nulliparity and EFW < 10th percentile was improved by the addition of CPR < 10th percentile (AUC: 0.681, (95%CI: 0.636 to 0.742) vs 0.756, (95%CI:0.713 to 0.795)), but the difference was not significant (DeLong test: z = 1.039, p = 0.053).. None of the above variables were predictors of cord arterial pH < 7.2. CONCLUSION: The risk of fetal acidosis has increased in cases of non-reassuring fetal status. Nulliparity, small for gestational age and CPR < 10th centile are independent predictors for non-reassuring fetal status in term fetuses, though the addition of CPR < 10th centile could not significantly improve the screening accuracy.

Editor's Highlight: Ethylene Glycol Teratogenicity: A Role for Embryonic Acidosis?

Ethylene glycol (EG) is a developmental toxicant in pregnant rats and mice. A suggested mechanism for this toxicity is that the EG metabolite, glycolic acid (GA), causes acidosis which may affect the embryonic heart rate (HR). This inhibition would cause periods of embryonic bradycardia and arrhythmia resulting in increased embryonic death and malformation in surviving embryos. This hypothesis was investigated using gestational day (GD) 11 and 13 rat embryos in vitro. Increasing concentrations of GA or lactic acid in the incubation medium caused a decrease in external pH (pHe) and a concentration-dependent decrease in embryonic HR. Increased concentrations of GA or lactic acid with pHe corrected to normal levels did not affect HR. Severely decreased pHe, caused by reduced NaHCO3 in the incubation medium, had little effect on the HR of GD 13 embryos but substantially reduced the HR of GD 11 embryos. These results suggest that increased monocarboxylate concentration (glycolate or lactate) needs to be in combination with increased H+ concentration (low pHe) to influence the embryonic HR. These results implicate the monocarboxylate transporter reported to be present in the early postnatal rat heart, the chick embryonic heart throughout development, and the chorioallantoic placenta. The results showed some evidence that the adverse effect of GA and reduced pHe on the embryonic HR increased with duration of exposure and hence lends support to the suggested mechanism of embryotoxicity for EG.

Accuracy of intrapartum fetal blood gas analysis by scalp sampling: A retrospective cohort study.

Fetal blood gas analysis (FBGA) using scalp blood is commonly used to identify serious fetal distress. However, there is a lack of data regarding its accuracy and reliability. The aim of this study was to determine the positive predictive value (PPV) and negative predictive value (NPV) of FBGA for predicting postpartum acidosis in case of nonreassuring fetal heart rate tracings (NRFHRT). To this end, we conducted a retrospective cohort study of singleton term deliveries with NRFHRT according to Fédération Internationale de Gynécologie et d'Obstétrique and Fisher cardiotocography scores undergoing FBGA in a university hospital. The PPV and NPV of FBGA regarding neonatal acidosis (defined as a pH value ≤ 7.15 in arterial or venous umbilical cord blood) and Apgar scores indicating neonatal depression (defined as a 5-min Apgar score ≤5) were evaluated. Multivariate analysis was used to determine the influence of cardiotocography variations and the time delay between FBGA and delivery on the accuracy of FBGA. We analyzed 343 deliveries with NRFHRT. In 32 (9%) of these cases, fetal acidosis was confirmed by a postpartum umbilical cord blood pH value ≤ 7.15. In 308/343 (90%) cases, FBGA identified NRFHRT as false positive (as confirmed by nonacidotic postpartum pH values) and thus avoided unnecessary interventions such as operative delivery. The overall test accuracy of FBGA was 91%. FBGA accurately predicted postpartum cord blood pH values with a margin of ±0.2 in 319/343 (93%) cases. On the other hand, the false negative rate of FBGA was 8% (29/343). The PPV and NPV of FBGA for predicting postpartum acidosis were 50% and 91%, respectively. The sensitivity was 9% and the specificity was 99%. In a multivariate logistic regression analysis, maternal body mass index (odds ratio [OR] 1.1; 95% confidence interval [CI] 1.01-1.17; P = .029) and cardiotocography variations (OR 0.80; 95% CI 0.66-0.98; P = .029) independently affected the predictive value of FBGA. The PPV of FBGA regarding neonatal depression according to Apgar scores was low with only 17%. We conclude that FBGA may be used in clinical practice to rule out, but not to rule in, neonatal acidosis in parturients with NRFHRT. It can avoid unnecessary interventions such as cesarean section or operative vaginal delivery in up to 90% of cases, but cannot reliably detect fetal acidosis.

Relationship between fetal heart rate patterns and a time course for evaluation of fetal well-being: "the 30 minutes rule" for decision of mechanical delivery.

OBJECTIVE: To predict acidosis in fetus showing deceleration associated with non-reassuring fetal status during delivery, we examined the relationship between duration of the deceleration and umbilical arterial pH. MATERIALS AND METHODS: A total of 19,907 deliveries in eight facilities of the Juntendo Perinatal Care Group, 895 cases of vaginal deliveries with level 3 decelerations were selected for the subjects of this study. The cut-off point of time when the umbilical arterial pH fell below 7.20 in all cases of level 3 and for each deceleration type were examined. The explanatory variables were the pH and pO2 of umbilical arterial gas and the time from onset of the level 3 pattern to delivery. From receiver operating characteristic (ROC) analysis using these variables, the critical point indicating low Apgar score was set at an umbilical arterial pH < 7.20. RESULTS: The cut-off point of time when the umbilical arterial pH fell below 7.2 was 33.5 min for all cases of level 3, and 604 cases of severe variable decelerations with normal baseline variability and normal baseline heart rates, the cut-off point was 33.5 min as well. For 108 cases of late decelerations, there was no significant cut-off point for either the mild or severe cases. Mild prolonged deceleration showed the cut-off point of 34.5 min. CONCLUSIONS: We confirmed the time indices for predicting and preventing acidosis in fetuses showing decelerations. To prevent fetal acidosis, the decision related to proper timing for performing assisted delivery by considering the time course is important.

Fetal heart rate patterns during delivery complicated by hypoxia and acidosis - a computer-aided analysis.

BACKGROUND: Using the naked eye, evaluation of fetal heart-rate (FHR) patterns remains difficult and is not complete. Computer-aided analysis of the FHR offers the opportunity to analyse FHR patterns completely and to detect all changes possibly due to hypoxia and acidosis. It was the goal of this study to make these hypoxic changes of the FHR visible and to compare them directly with normal tracings. METHODS: During a period of 11 years the FHR signals (i. e., R-R intervals of the F-ECG) of 646 fetuses were recorded simultaneously also by a computer. The computer files were analysed thereafter, i. e., the obtained results had no immediate influence on the clinical management itself. To enter the study all fetuses must have been delivered by the vaginal route - in consequence without a significant loss of FHR signals. During forceps or vacuum deliveries recordings were continued. If necessary a new electrode was inserted. Recordings of fetuses with chorioamnionitis, tracings of malformed neonates and tracings shorter than 30 min were also excluded. No additional drugs were given to the mother during the time of recording. Thus 484 recordings were left. In this study only the last 30 min of each record were analysed off-line using our own computer programs written in MATLAB. Only 3 parameters were determined electronically: i) the mean fetal frequency (FRQ, bpm), ii) the number of turning points (N/min, see Fig. 1) in the FHR, which we called 'microfluctuation' (MIC) and iii) the oscillation amplitude of the FHR (OA, bpm, Fig. 1). Routine measurements of the acid-base variables from umbilical arterial (UA) and venous (UV) blood were performed using RADIOMETER equipments (ABL500) and trained personnel. To compare acidotic and non-acidotic FHR tracings, 2 pH groups were chosen: fetuses with a small non-acidotic "pH window" (pHUA=7.290-7.310) and 5 fetuses with severe acidosis, i. e., pHUA values <= 7.103. RESULTS: Using this narrow "pH-window" (7.290-7.310) shows that FRQ, MIC and OA belong together. The 3 variables are strongly associated with each other in a linear manner. All 3 correlation coefficients (r) are highly significant (P<0.001); in this context all 3 regressions seem to be linear. The mean pHUA in this special group amounts to 7.300±0.008 (N=50). In severe fetal acidosis (mean pHUA=7.051±0.060, N=5) MIC and OA are diminished significantly (P << 0.001) whereas the mean frequency is increased (ca.+6 bpm). Microfluctuation (MIC) seems to be the most sensible FHR parameter for the diagnosis of hypoxia and acidosis followed by OA and the fetal frequency niveau. CONCLUSIONS: In non-acidotic fetuses MIC, OA and FRQ belong together and their association can be described by the 3 basic principles presented above. Fetal reaction patterns during hypoxia and severe acidosis differ significantly when compared with tracings of non-acidotic fetuses. Computer-analysis reveals that MIC is the most sensitive FHR variable concerning hypoxia and acidosis followed by OA and the mean FRQ niveau. (Some of the acidotic recordings together with the WAS-score can be observed in full length at www.fhr-monitoring.org.).

Fetal sheep left ventricle is more sensitive than right ventricle to progressively worsening hypoxemia and acidemia.

OBJECTIVE: In a sheep model we tested the hypothesis that the fetal left ventricle is less tolerant to worsening acidemia than the right ventricle. STUDY DESIGN: At 106-124/145 days of gestation, 12 fetuses were instrumented. After a 4-day recovery, placental vascular resistance was increased by fetal angiotensin (AT) II infusion. After a 2h ATII infusion, to further deteriorate fetal oxygenation, maternal hypoxemia was induced. Fetal cardiac function and hemodynamics were assessed by tissue Doppler imaging (TDI) and pulsed Doppler imaging. Ultrasonography was performed at baseline, at 1 and 2h after the beginning of ATII infusion and during the ATII+hypoxemia phase. RESULTS: Fetal pH and pO2 decreased significantly and progressively during the experiment. Left ventricular TDI-derived isovolumic relaxation velocity (IVRV) was lower during ATII 2h and ATII+hypoxemia phases than at baseline. The IVRV deceleration was significantly less during the ATII+hypoxemia phase than at baseline. Right ventricular IVRV was significantly lower during the ATII+hypoxemia phase than at baseline. IVRV deceleration did not change. Only left ventricular IVRV deceleration correlated with fetal pO2 (R=0.36, p<0.05). Fetal right and left ventricular cardiac outputs, as well as umbilical artery, aortic isthmus and ductus venosus pulsatility indices remained unchanged during the experiment. CONCLUSION: Our results show that signs of cardiac dysfunction develop earlier in the left ventricle than in the right ventricle. The fetal left ventricle seems to be more sensitive to progressively worsening hypoxemia and acidemia than the right ventricle.

The reliability of foetal blood sampling as a test of foetal acidosis in labour.

OBJECTIVES: To establish whether foetal blood sampling for pH is a reliable test of foetal acidosis in labour by comparing paired foetal blood samples taken at a single procedure. STUDY DESIGN: We conducted a prospective study assessing 293 consecutive attempts at foetal blood sampling in labour over a four month period from February to May 2012. A total of 100 paired samples were suitable for analysis. We compared the consistency of pH results of paired foetal blood samples, evaluated cases where inconsistent results would result in conflicting clinical decisions, and explored factors associated with discordant results. RESULTS: There was a statistically significant difference between the mean pH of the two samples: 7.297 (SD 0.065) versus 7.315 (SD 0.059), p<0.0005. Of the 100 paired samples, 43 had a difference greater than the laboratory acceptable maximum analytical difference of 0.038. There was discordance between the samples in 16 cases with results crossing a decision threshold, and in 11 cases (69%) delivery was by emergency caesarean section. Inconsistent results were not associated with specific clinical factors and occurred more often with senior operators. CONCLUSION: Foetal blood sampling is considered by many as the gold standard in assessing intrapartum foetal wellbeing. We have demonstrated inconsistency of paired foetal blood pH results which suggests that foetal blood sampling should not be considered infallible.

Effect of angiotensin II on the left ventricular function in a near-term fetal sheep with metabolic acidemia.

We tested the hypothesis that, in acute metabolic acidemia, the fetal left ventricle (LV) has the capacity to increase its contractility in response to angiotensin II infusion. Eleven ewes and their fetuses were instrumented at 127-138/145 days of gestation. The effect of angiotensin II on fetal LV function was assessed using intraventricular pressure catheter and tissue Doppler imaging (TDI). Angiotensin II increased fetal arterial blood pressure, whereas pH and pO(2) decreased. The heart rate and systemic venous pressure were not affected significantly. The LV end-diastolic and end-systolic pressures, as well as dP/dt(max), increased. The TDI-derived LV longitudinal myocardial isovolumic contraction velocity and its acceleration and velocity during early filling were higher than those at baseline. The incidence of absent isovolumic relaxation velocity was greater during angiotensin II infusion. In summary, during acute metabolic acidemia, the fetal left ventricle could increase its contractility in response to inotropic stimulus even in the presence of increased afterload. The diastolic LV function parameters were altered by angiotensin II.

Monitoring fetal electrocortical activity during labour for predicting worsening acidemia: a prospective study in the ovine fetus near term.

BACKGROUND: Severe fetal acidemia during labour with arterial pH below 7.00 is associated with increased risk of hypoxic-ischemic brain injury. Electronic fetal heart rate (FHR) monitoring, the mainstay of intrapartum surveillance, has poor specificity for detecting fetal acidemia. We studied brain electrical activity measured with electrocorticogram (ECOG) in the near term ovine fetus subjected to repetitive umbilical cord occlusions (UCO) inducing FHR decelerations, as might be seen in human labour, to delineate the time-course for ECOG changes with worsening acidemia and thereby assess the potential clinical utility of fetal ECOG. METHODOLOGY/PRINCIPAL FINDINGS: Ten chronically catheterized fetal sheep were studied through a series of mild, moderate and severe UCO until the arterial pH was below 7.00. At a pH of 7.24 ± 0.04, 52 ± 13 min prior to the pH dropping <7.00, spectral edge frequency (SEF) increased to 23 ± 2 Hz from 3 ± 1 Hz during each FHR deceleration (p<0.001) and was correlated to decreases in FHR and in fetal arterial blood pressure during each FHR deceleration (p<0.001). CONCLUSIONS/SIGNIFICANCE: The UCO-related changes in ECOG occurred in advance of the pH decreasing below 7.00. These ECOG changes may be a protective mechanism suppressing non-essential energy needs when oxygen supply to the fetal brain is decreased acutely. By detecting such "adaptive brain shutdown," the need for delivery in high risk pregnant patients may be more accurately predicted than with FHR monitoring alone. Therefore, monitoring fetal electroencephalogram (EEG, the human equivalent of ECOG) during human labour may be a useful adjunct to FHR monitoring.

Normalized spectral power of fetal heart rate variability is associated with fetal scalp blood pH.

BACKGROUND: Spectral power of fetal heart rate variability is related to fetal condition. Previous studies found an increased normalized low frequency power in case of severe fetal acidosis. AIMS: To analyze whether absolute or normalized low or high frequency power of fetal heart rate variability is associated with fetal scalp blood pH. STUDY DESIGN: Prospective cohort study, performed in an obstetric unit of a tertiary care teaching hospital. SUBJECTS: Consecutive singleton term fetuses in cephalic presentation that underwent one or more scalp blood samples, monitored during labour using ST-analysis of the fetal electrocardiogram. Ten-minute continuous beat-to-beat fetal heart rate segments, preceding the scalp blood measurement were used. OUTCOME MEASURES: Absolute and normalized spectral power in the low frequency band (0.04-0.15 Hz) and in the high frequency band (0.4-1.5 Hz). RESULTS: In total 39 fetal blood samples from 30 patients were studied. We found that normalized low frequency and normalized high frequency power of fetal heart rate variability is associated with fetal scalp blood pH. The estimated ß of normalized low frequency power was -0.37 (95% confidence interval -0.68 to -0.06) and the relative risk was 0.69 (95% confidence interval 0.51-0.94). The estimated ß of normalized high frequency power was 0.33 (95% confidence interval 0.01-0.65) and the relative risk was 1.39 (95% confidence interval 1.01-1.92). CONCLUSIONS: Normalized low and normalized high frequency power of fetal heart rate variability is associated with fetal scalp blood pH.

Predictors of outcome at 2 years of age after early intrauterine growth restriction.

OBJECTIVE: To examine the relative importance of antenatal and perinatal variables on short- and long-term outcome of preterm growth restricted fetuses with umbilical artery (UA) Doppler abnormalities. METHODS: This was a cohort study of 180 neonates with birth weight < 10(th) percentile, gestational age at delivery < 34 weeks and abnormal Doppler ultrasound examination of the UA. Various antenatal and perinatal variables were studied in relation to short- and long-term outcome. RESULTS: Neonatal and overall mortality (up to 2 years of age) were predicted by low gestational age at delivery. Neonatal mortality was additionally predicted by absent or reversed UA end-diastolic flow, while the presence of severe neonatal complications and placental villitis were additional predictors of both infant (between 28 days and 1 year of postnatal life) and overall mortality. Placental villitis was found to be the only predictor of necrotizing enterocolitis. Low gestational age at delivery, male sex, abnormal cardiotocography, absent or reversed UA end-diastolic flow and the HELLP syndrome predicted respiratory distress syndrome. Abnormal neurodevelopmental outcome at 2 years was predicted by low birth weight (< 2.3(rd) percentile), fetal acidosis (UA pH < 7.00), and placental villitis. CONCLUSION: Less advanced gestation at delivery remains an important predictor of short-term outcome in growth-restricted fetuses. In addition, the presence of placental villitis may aid neonatologists in the early identification of infants at increased risk of necrotizing enterocolitis, death and abnormal neurodevelopment at 2 years of age. Abnormal neurodevelopment was related to low weight and acidosis at birth, indicating that the severity of malnutrition and fetal acidosis affect long-term outcome.

Changes in the ST-interval segment of the fetal electrocardiogram in relation to acid-base status at birth.

OBJECTIVE: To assess the occurrence of ST-interval segment changes of the fetal electrocardiogram (ECG) and cardiotocographic (CTG) abnormalities preceding acidaemia at birth. DESIGN: Case-control study. SETTING: University hospital labour ward. SAMPLE: Newborns with severe cord artery metabolic acidaemia (pH < 7.00 and lactate > or = 10 mmol/l; n= 24), moderate metabolic acidaemia (pH 7.00-7.09 and lactate > or = 10; n= 48), acidaemia (pH 7.00-7.09; n= 52), pre-acidaemia (pH 7.10-7.19; n= 265), and controls (pH > or = 7.20; n= 117). METHODS: Monitoring traces were assessed blinded to outcome. MAIN OUTCOME MEASURES: CTG and ST changes. RESULTS: Any ST event occurred significantly more often among cases with severe (79%) and moderate (75%) metabolic acidaemia than among controls (50%). The difference was restricted to baseline T/QRS rises and to the second stage of labour, during which any event only occurred significantly more often among cases with severe metabolic acidaemia (62%) than among controls (38%). ST events coincided with abnormal CTG patterns in 67, 44, 40, and 28% of cases with severe and moderate metabolic acidaemia, acidaemia, and pre-acidaemia, respectively, and in 12% of controls. ST events with intermediary CTG were similarly frequent in the case groups (0-6%) as in the controls (4%). The ST guidelines stated intervention in 96, 62, 73, and 49% of case groups and 23% of controls. CONCLUSIONS: Only two of three cases with severe and less than half of cases with moderate metabolic acidaemia were preceded by ST events coinciding with CTG abnormalities. It is therefore important to intervene for long-lasting, rapidly deteriorating or marked (preterminal) CTG abnormalities, also in the absence of ST events.

Linear and nonlinear fetal heart rate analysis of normal and acidemic fetuses in the minutes preceding delivery.

Linear and nonlinear fetal heart rate (FHR) indices, namely mean FHR, interval index (II), very low, low and high frequencies, approximate (ApEn) and sample entropy (SampEn), were computed, immediately before delivery, in the initial and final FHR tracing segments, from 48 normal, 10 mildly acidemic and 10 moderate-to-severely acidemic fetuses. Progression of labor was associated with a significant increase in linear frequency domain indices whereas nonlinear indices were significantly decreased. Moderate-to-severe fetal acidemia was associated with a significant decrease in nonlinear indices. The best discrimination between moderate-to-severe acidemic fetuses and the remaining cases was obtained combining II and ApEn(2,0.15), with a specificity of 71% and a sensitivity of 80%. These findings support the hypothesis of increased autonomic nervous system activity in the final minutes of labor and of decreased central nervous system activity, both in the final minutes of labor and in moderate-to-severe acidemic fetuses.

[Quantitative Cardiotocography--what does it look like and what can we expect]. / Quantitative Kardiotokographie -- wie sieht sie aus und was dürfen wir von ihr erwarten?

BACKGROUND: [corrected] Cardiotocography (CTG) seems to be a non-reliable, expensive but nevertheless practical method for fetal surveillance. Moreover, its diagnostic value is dependent on a long-standing experience of the obstetrician (midwife). It is difficult to define exact diagnostic criteria since nearly all CTG phenomena are lacking precise qualification by the naked eye. Therefore, the idea must be born in mind to analyze fetal heart frequency (FHF) by computer, first off-line then on-line, in order to evaluate its true diagnostic power objectively. METHODS: The FHF of 583 deliveries terminated by the vaginal route were registered prospectively using a PC and an RS422 interface. In 443 cases acid-base measurements (ABL 500, RADIOMETER, Copenhagen) in blood of the umbilical artery (UA) and vein (UV) were available and plausible. In this study only the last 30 min ante-partum were analyzed. The program for FHF analysis was written in MATLAB (The Mathworks Inc., USA). A CTG score was developed using three components of FHF: basal FHF, the deceleration area of all dips, and the micro-fluctuation (MF) of the basal fetal heart rate (FHR). MF denotes the true number of "turning-points" per minute of basal FHR. For each component a maximum of 6 scoring points could be assigned according to empirical cut-off values. These cut-off values were determined using correlation analysis with acid-base parameters in UA blood, especially the actual pH. The accordance between score and pH values was further demonstrated by assignment of 0.036 pH-units to each of the 19 (18 + zero) scoring points, thus covering a pH range between 6.700 and 7.350 (UA). A resulting variable, delta pH (pH measured, UA-pH assigned) was studied and used for further analysis. In order to define criteria for fetal mortality in utero only cases with pH, UA between 7.250 and 7.350 were accepted. RESULTS: Median basal FHF under normal conditions amounted to 138 bpm (mean: 137 +/- 14.9) in 4180 minutes of 372 fetuses. 120 bpm equals the 13.4(th) and 160 bpm the 94.6(th) centile of the distribution. Given fetal normacidity (UA) MF is 58/minute and the mean MF 57.9 +/- 13.4, respectively, with a 10 (th) centile of 41/minute. MF and basal FHF are correlated significantly (r = 0.410, P << 10(-4)). The declaration-area per fetus is significantly correlated with actual pH (UA), r = -0.473, P << 10(-4). the score itself is highly significantly correlated with actual pH (UA) (r = -0.559, P << 10(-4)) and the other parameters of fetal acid-base balance. Nevertheless, prediction variability for pH, especially in score = 1, 2 and zero (minimal CTG pathology) is still present: 80% of all predicted pH values lie in between -0.092 and + 0.071. It is strongly suggested that this score-related predictive pH variability is caused by maternal breathing habits during the last 30 minutes of delivery. CONCLUSION: Adequate quantification of only three variables of FHR using a score leads to fairly good correlations with parameters of the fetal acid-base balance. Thus actual pH (UA) can be predicted in reasonable clinical limits. Still present variability in prediction of pH seems to be, in part, of maternal origin. The maternal influence could be eliminated by continuous (transcutaneous) monitoring of maternal pCO(2). Along these lines the quantitative electronic monitoring of FHR will be realized and instrumented (off-line and on-line) by nexus/gmt, Frankfurt, a.M., Germany.

[Reliability of fetal pulse oximetry for the detection of fetal acidosis]. / Die Zuverlässigkeit der fetalen Pulsoxymetrie bei der Detektion einer fetalen Azidose.

Fetal pulse oximetry is a continuous method to exclude the lack of oxygen in cases of non-reassuring fetal heart rate. This study aims at the evaluation of the predictive value of this method concerning the development of fetal acidosis. 136 fetuses with non-reassuring heart rate were monitored by fetal pulse oximetry. In all cases fetal blood pH and base excess were determined repeatedly by fetal blood analysis (FBA). The pH value and base excess in the umbilical artery and scalp blood as well as the changes of pH and base excess were correlated to the duration of low, medium and high fetal oxygen saturation (FSpO (2)). Sensitivity, specificity, positive and negative predictive values were calculated for the assumption that "FSpO (2) < or = 30 % for at least 10 or 15 minutes" predicts a pH or base excess in the umbilical artery and in FBA of < 7.1/7.15/7.2 or < or = -4/8/12 mmol/L and a decline of pH (base excess) by more than 0.05 (0.1) pH units (4 mmol/L). A highly significant negative correlation was found between umbilical artery and FBA pH and base excess as well as the change of both and the duration of low oxygen saturation. Additionally the change of FBA pH depends on the duration of medium FSpO (2). A pH below 7.15 in FBA as well as base excess < or = -12 mmol/L were safely detected by a cut-off of "FSpO (2) < or = 30 % for at least 10 minutes" and pH < 7.1 and base excess < or = -12 mmol/l in FBA in 100 % and 75 %, respectively. A decline of pH by more than 0.1 pH units and of base excess by more than 4 mmol/L were excluded by a negative predictive value of 98 %. In conclusion, medium and progressive acidosis can be reliably excluded by fetal pulse oximetry.

Severe variable decelerations and fetal pulse oximetry during the second stage of labor.

OBJECTIVES: The aim of the study was to investigate the usefulness of fetal pulse oximetry in cases of severe variable decelerations in the second stage of labor. METHODS: It is a prospective study including 58 patients. Thirty-eight patients (group A) had a normal uncomplicated labor and 20 patients (group B) developed severe variable decelerations during the second stage of labor. All patients were primiparous with normal pregnancies and had electronic fetal monitoring of labor in conjunction with fetal pulse oximetry. An estimation of fetal pH and base deficit was performed at delivery in all patients. RESULTS: There was no statistically significant difference in relation to maternal age and gestational age between the two groups. Group A patients did not delivered neonates with metabolic acidosis. Six out of 20 (group B) patients delivered neonates with a pH <7.10 despite a fetal pulse oximetry reading of >30%. CONCLUSIONS: It appears that fetal pulse oximetry is not capable of detecting pre-acidotic or acidotic fetuses during the second stage of labor in patients with severe variable decelerations and the management of such patients should be supported by fetal scalp pH when indicated or otherwise the obstetrician should expedite delivery either with assisted operative delivery or cesarean section. Fetal heart rate monitoring was introduced into clinical practice over 30 years ago. It continues to be the predominant method of intrapartum fetal surveillance despite worries about its accuracy and efficacy.

Computerized cardiotocography in the management of intrauterine growth restriction associated with Doppler velocimetry alterations.

OBJECTIVE: To verify the reliability of computerized cardiotocography (cCTG) in the prediction of the oxygen metabolism status of fetuses with growth restriction and Doppler velocimetry alterations. METHODS: From 24 third-trimester cesarean section performed because of intrauterine growth restriction (IUGR) and Doppler velocimetry alterations, there were 11 cases of fetal heart rate alterations (Dawes-Redman criteria were not satisfied) and 13 cases of reactive cCTG. Fetal lung maturity was detected by amniocentesis and blood samples for umbilical blood gas analysis (UBGA) were collected before the first neonatal breath from the umbilical artery in a double-clamped segment of the cord. RESULTS: Umbilical cord gas analysis showed arterial cord blood pH to be 7.20 or less in 11 newborns (45.8%), 7.10 or less in 6 (25%), and 7.00 or less in 3 (12.5%). Linear regression analysis showed short-term variation (STV) in the fetal heart rate to be significantly correlated with umbilical artery pH (r = 0.49; P = 0.01) and pCO2 (r = -0.50; P = 0.01). There were no significant correlations between cCTG and the other UBGA parameters considered. Receiver operator curves permitted to calculate the STV values at which pathological neonatal UBGA values can be expected (pH < 7.00 and pCO2 > 80 mmHg). A short-term variation less than 4.5 ms was found to predict acidemia with a sensitivity of 100% and a specificity of 70% (positive predictive value, 33%; negative predictive value, 100%), and hypercarbia with a sensitivity of 100% and a specificity of 77.8% (positive predictive value, 55.6%; negative predictive value, 100%). CONCLUSION: In view of the results of this study, 4.5 ms for STV may be a threshold below which timing of delivery should be decided in cases of fetal growth restriction.

[CTG: microfluctuation]. / CTG: Mikrofluktuation.

OBJECTIVE: Microfluctuation (MF) of fetal heart rate (FHR) is regarded as the most sensitive parameter for diagnosing the condition of the fetus. The MF can only be crudely quantified with the naked eye. Therefore the following questions arise: 1) How can MF be exactly measured numerically? 2) What interrelationships are there between the MF determined electronically, the basal FHR, the oscillation amplitude (OA) of the FHR and the beat-to-beat variability (beat-to-beat var.) 3) What are the effects of hypoxia and acidosis on these index parameters? METHODS: 387 intrapartal FHR tracings were registered directly (F-ECG) with the cardiotocograph (HP instruments) via an RS422 interface and stored on diskette. The data were processed further with a computer program we developed ourselves (MATLAB, the MathWorks Inc., USA). The parameters of the fetal acid-base balance were measured in the blood of the umbilical artery (UA) and umbilical vein (UV) with instruments from Radiometer, Copenhagen (ABL 500, ABL 5) and stored off-line with a selection of clinical data and processed further on a laptop (HP, Omnibook XE 3). The fluctuation of the basal FHR was determined on the basis of the following four parameters: the number of high and low points (extrema) per minute (EXT),the mean beat-to-beat variability per minute and the OA (bpm). In order to correlate the MF of the basal FHR with the parameters of the fetal acid-base balance, only the last 30 CTG minutes ante-partum of each tracing were included. All decelerations and optionally in addition all accelerations were electronically deleted from the FHR curve. RESULTS: Basic statistical values and the distribution of the four index parameters in 5486 minutes of basal FHR were studied: the median of EXT is at 59 and the mean value at 58.9 +/- 13.9 extrema/min. The distribution is normal. The median frequency amounts to 138 bpm, the median OA to 22.2 bpm and the median beat-to-beat variability to 161.7 bpm, respectively. The mean pH value in UA blood was 7.262 +/- 0.064. The acidotic risk (pH, UA < 7.100) reached 1.3 %. There were no pH values below 7.0. With increasing basal FHR, EXT increases highly significantly (r = 0.468, P << 0.0000). EXT decreases highly significantly (r = -0.432, P << 0.0000) with increasing OA. The mean basal frequency shows the best correlation with the base excess in UA blood (r = -0.263, P << 0.0000). Beat-to-beat variability and EXT alone correlate poorly with the actual, pH and BE values (UA). Multiplication of the index parameters leads to an increase of the correlation coefficients when compared with their single values. CONCLUSION: With increasing hypoxia and acidosis the four index parameters do show a complex pattern which is characterized by tachycardia, increase of EXT and opening of the OA. A loss of EXT and a reduction of OA seems to be the result of already severe acidosis (pH, UA < 7.000). Using the four parameters of basal FHR alone, there is no possibility to evaluate fetal jeopardization. Numerical combination (e. g., multiplication) of some index parameters ameliorates their prognostic power and should be used in future online scoring procedures.

The prediction of fetal acidosis by means of intrapartum fetal pulse oximetry.

OBJECTIVES: The study's objectives were to verify a threshold value for fetal arterial oxygen saturation as the critical boundary for fetal compromise during labor and to investigate a method of predicting acidosis caused by hypoxemia. STUDY DESIGN: In a multicenter study involving 3 German obstetric centers, a total of 400 deliveries were monitored by fetal pulse oximetry (Nellcor-Puritan-Bennett Model N-400 Oxygen Saturation Monitor and FS-14 Sensor; Nellcor, Inc, Pleasanton, Calif). The durations of low (60%) fetal arterial oxygen saturations during the measurement were compared between neonates with a pH <7.15 versus >/=7.15 and a base excess <-12 mmol/L versus >-12 mmol/L in the umbilical artery post partum and in neonates with an Apgar score <7 versus >/=7 by Mann-Whitney U test. In 121 of the pulse oximetry measurements the durations of low, medium, and high fetal arterial oxygen saturations were measured from one fetal scalp blood sampling to the next and correlated with the change of scalp blood pH between samplings. Multiple regression analysis was performed to estimate the expected change of pH between 2 fetal scalp blood samplings, and receiver operating characteristic analysis was done to define a minimum duration of low fetal arterial oxygen saturation values to exclude or predict a significant decline of pH. RESULTS: Neonates with a 1-minute Apgar score <7 differed from those with 1-minute Apgar score >/=7 significantly in the duration of low fetal arterial oxygen saturation but not in the durations of medium and high fetal arterial oxygen saturations. The duration of low fetal arterial oxygen saturation had been significantly longer in children with pH <7.15 or base excess <-12 mmol/L in the umbilical artery compared with those with a pH >/=7.15 or base excess >/=-12 mmol/L. The duration of high fetal arterial oxygen saturation was significantly shorter for children with a pH <7.15 or base excess <12 mmol/L than for those with a pH >/=7.15 or base excess >/=12 mmol/L. There was no difference in the groups with respect to the duration of medium fetal arterial oxygen saturation values. The duration of low fetal arterial oxygen saturation proved to be the best predictor of a decline of scalp pH between 2 fetal scalp blood samples. The pH declined significantly with a longer duration of low fetal arterial oxygen saturation (0.02 per 10 minutes). No decrease of pH by more than 0.05 was observed unless fetal arterial oxygen saturation had remained at /=10 minutes. CONCLUSION: An arterial oxygen saturation of 30% was confirmed as the critical boundary for fetal compromise during labor. The development of acidosis seems to be predictable by the duration of hypoxemia, as indicated by fetal arterial oxygen saturation

Cerebral oxygen delivery is reduced during the acidaemia associated with prolonged hypoxaemia in the immature ovine fetus.

Our aim was to determine the effects of 12 h of hypoxaemia on cerebral blood flow (CBF) and cerebral O2 delivery in ovine fetuses at 0.6 gestation. During fetal hypoxaemia, induced by reduced uterine blood flow, fetal SaO2 and PaO2 were reduced (p < 0.01) from control values of 77.0 +/- 1.6% and 27.3 +/- 1.0 mm Hg, respectively, to 28.4 +/- 3.4% and 15.6 +/- 0.6 mm Hg; fetal pHa decreased from control values of 7.37 +/- 0.01 to 7.20 +/- 0.02 at 3 h, but returned to control values before 12 h. CBF (ml/min/100 g) was 2.0- to 2.6-fold higher (p < 0.01) than control values during hypoxaemia, but only 1.7-fold higher (p < 0.01) at 3 h when pHa was lowest. Cerebral O2 delivery (ml/min/100 g) was lower (p < 0.01) than control values of 3.15 +/- 0.29 at 1.5h (2.09 +/- 0.36) and 3h (1.84 +/- 0.22) of hypoxaemia and higher 1 h after hypoxaemia had ceased (3.81 +/- 0.22, p < 0.01). We conclude that the ovine fetus at 0.6 gestation is unable to sustain increased CBF and hence maintain cerebral O2 delivery during the first 6 h of hypoxaemia, a time which coincides with acidaemia; in contrast, at 6 and 12 h of hypoxaemia, when pHa was normal, cerebral O2 delivery was similar to control values. Reduced cerebral O2 delivery during the early, acidaemic, stages of hypoxaemia may lead to impaired neural development.