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. Author manuscript; available in PMC: 2012 Mar 1.
Published in final edited form as: Am J Obstet Gynecol. 2010 Dec 8;204(3):228.e1–228.10. doi: 10.1016/j.ajog.2010.09.024

Noninvasive Uterine Electromyography For Prediction of Preterm Delivery*

Miha L UCOVNIK 1,2, William L MANER 1, Linda R CHAMBLISS 1, Richard BLUMRICK 1, James BALDUCCI 1, Ziva NOVAK-ANTOLIC 2, Robert E GARFIELD 1
PMCID: PMC3090039  NIHMSID: NIHMS242650  PMID: 21145033

Abstract

Objective

Power spectrum (PS) of uterine electromyography (EMG) can identify true labor. EMG propagation velocity (PV) to diagnose labor has not been reported. The objective was to compare uterine EMG against current methods to predict preterm delivery.

Study design

EMG was recorded in 116 patients (preterm labor, n=20; preterm non-labor, n=68; term labor, n=22; term non-labor, n=6). Student’s t-test was used to compare EMG values for labor vs. non-labor (P<0.05 significant). Predictive values of EMG, Bishop-score, contractions on tocogram, and transvaginal cervical length were calculated using receiver-operator-characteristics analysis.

Results

PV was higher in preterm and term labor compared with non-labor (P<0.001). Combined PV and PS peak frequency predicted preterm delivery within 7 days with area-under-the-curve (AUC) = 0.96. Bishop score, contractions, and cervical length had AUC of 0.72, 0.67, and 0.54.

Conclusions

Uterine EMG PV and PS peak frequency more accurately identify true preterm labor than clinical methods.

Keywords: prediction, preterm labor, propagation velocity, uterine electromyography

INTRODUCTION

Other than childbirth, “threatened preterm labor” is the most common diagnosis that leads to hospitalization during pregnancy.1 Up to 50% of patients admitted for threatened preterm labor are, however, not in true labor, and will eventually deliver at term.2 20% of symptomatic patients that are diagnosed as not being in preterm labor, on the other hand, will deliver prematurely.3 This leads to unnecessary treatments, missed opportunities to improve neonatal outcome, and largely biased research of treatments.

Myometrial activation, required for effective contractions and true labor, is characterized by molecular changes leading to an increase in coupling and excitability of cells.4-7 Electrical activity of the myometrium, which can be monitored non-invasively by measuring the uterine electromyography (EMG), changes at delivery as a result of these events.8-14 ‘Bursts’ of electrical signals responsible for contractions have been reported to be more frequent and their duration more constant in labor15,16. An increase in peak amplitude and frequency of EMG signals, assessed by power-spectrum (PS) analysis, has also been observed prior to labor.15,17,18 Propagation velocity (PV) of electrical signals in the myometrium has been shown in-vitro to increase before delivery when gap junctions are increased.19,20 As a result, it has been suggested that EMG could be used to assess the PV in vivo. Previous studies mainly focused on methods for assessing EMG signal propagation.21-28 However, the prognostic capability of PV for predicting labor (term or preterm) has not been evaluated yet.

This study investigates whether uterine EMG can be used to evaluate PV of uterine electrical signals in labor and non-labor patients at term and preterm and compares diagnostic accuracy of various EMG parameters, including PV, to methods currently used in the clinic to predict preterm delivery.

MATERIALS AND METHODS

Patients

116 pregnant women were included in the study at a single institution (St. Joseph’s Hospital and Medical Center, Phoenix, Arizona). From previous EMG studies, there has been reported difference in means of EMG PS peak frequency in labor vs. non-labor patients of (0.4708 − 0.3982 = 0.0726 Hz), and an average standard deviation of [(0.0459 + 0.0231)/2 = 0.0345 Hz].16 Using power of 0.80, and alpha − 0.05, with t-test, gives a desired sample size of 5 per group minimum.

88 consecutive preterm patients were included. They were admitted with the diagnosis of preterm labor at less than 34 weeks of gestational age. The cut-off of 34 weeks was chosen because the risk of death and handicap is mainly increased if delivery occurs prior to this time point, and attempts to stop preterm labor are very rarely done at later gestations.29 Preterm labor was diagnosed clinically as at least 6 contractions in 60 minutes assessed by TOCO and/or maternal perception and a cervical dilatation of at least 2 cm or effacement of at least 80% assessed by digital cervical examination. Calculation of gestational age was based on the last menstrual period or, when it differed by ≥ 7 days from the ultrasonographic estimation (calculated by crown-rump length measured within the first trimester), on ultrasound. Women delivering within 7 days from the EMG measurement were classified in the preterm labor group and those delivering outside of 7 days from the measurement in the preterm non-labor group.

28 consecutive patients presenting with regular uterine contractions with intact membranes at term (>37 weeks of gestation) were also included. Women delivering within 24 hours from the EMG measurement were defined as being in labor (term labor group) and those delivering outside of 24 hours from the measurement as not being in labor (term non-labor group).

Different cut-off measurement-to-delivery intervals for term and preterm labor vs. non-labor groups were chosen based on previous studies, which showed, that an increase in uterine EMG activity occurs within approximately 24 hours from delivery at term, and within several days from delivery preterm.17

All women included provided written informed consent for study participation. Data from patients who ultimately underwent cesarean-section were not used for analysis (Figure 1). We chose to exclude the cesarean-section patients because the decision on when exactly the surgery will be performed is based on several considerations, including those on fetal well-being and the subjective assessment of labor progress. This decision is therefore too subjective and arbitrary to include in a proper receiver-operating-characteristics (ROC) analysis in which one wants to also accurately determine the mean measurement-to-delivery-interval.

Figure 1.

Figure 1

Flow sheet diagram for better visualization of study groups.

We chose to include PPROM patients because our objective was to evaluate whether uterine EMG measurements can differentiate between true preterm labor, i.e. patients who are going to deliver spontaneously within a short period of time, and those who are not in true preterm labor, when the clinical evaluation does not allow us to make this differentiation.

The St. Joseph’s Hospital and Medical Center Institutional Review Board approved the study.

Uterine EMG Signal Recordings

Uterine EMG measurements were performed by 5 different researchers within 24 hours from patient’s admission to the hospital. We standardized the electrode arrangement to the following: 2.5 cm electrode-electrode vertical and horizontal separation distances (measured from center-to-center) in a square-shaped pattern about the navel, and with each electrode positioned in the vertex of each of the 4 corners of the share. Uterine EMG was measured for 30 minutes from each patient using a custom-built uterine EMG patient-monitoring system. Patients were asked to remain still while supine without disturbing any of the probes and wires for the recordings.

Signal Analysis

Analog EMG signals were digitally filtered to yield a final band-pass of 0.34 to 1.00 Hz, in order to exclude most components of motion, respiration, and cardiac signals from the analysis. Data were sampled at 100 Hz (this high sampling rate was chosen so as to increase the resolution of PS analysis later).

Previously Described EMG Parameters

EMG parameters were chosen from previous publications.17,30 The definition of these parameters, as well as the rationale for their use, can also be found in those publications.

Propagation Velocity Analysis

PV can be calculated by dividing the distance (D) that the propagating wave travels by the amount of time (T) required for the propagating wave to traverse this distance. All the time differences in corresponding action potential peaks for each burst of action potentials were calculated, and the average of absolute values of all time differences for bursts in a patient’s uterine EMG recording was used to calculate the PV.

Only those pairs of peaks on different channels (electrode pairs) with congruent shapes and within 2 seconds temporal separation of one another were included in the analysis, insuring that any peak observed on one channel during any 2-second window “matched” the associated peak on the other channel (Figure 2).

Figure 2.

Figure 2

Propagation velocity of electromyographic (EMG) signals was calculated from the time difference of the signal arrival at adjacent electrodes (t). Top trace shows a sample recording from two electrode pairs (channels 1&2). Note the excellent temporal correspondence between EMG and mechanical contractile events (measured by TOCO). Bottom trace shows the expanded EMG burst, with the individual voltage peaks clearly distinguishable.

For our EMG instrument, we use differential, bipolar electrode pairs. The advantage of a differential bipolar setup over a mono-polar setup is signal quality, allowing us to more accurately identify individual uterine voltage peaks. Only those bursts for which the mean voltage peak value was > 2 times the mean baseline voltage peak value were used in these calculations, in order to clearly see and compare uterine voltage peaks at adjacent electrodes. Within each of these electrical contractile bursts, there were found anywhere from about 30 to 60 voltage peaks (associated with propagating voltage waves) which were analyzed (Figure 2). More than 25 000 voltage peaks pairs were analyzed, with an average of approximately 215 peaks per patient.

Common Obstetric Measures

Presence or absence of contractions on TOCO at the time of EMG measurement was documented by the researcher recording the EMG. Transvaginal cervical length and Bishop scorewere also documented, but only when they were assessed no more than 24 hours before or after the EMG measurement. Bishop score has not been developed as a predictor of preterm birth. Nevertheless, it gives a metric evaluation of digital cervical examination, which is commonly used to diagnose preterm labor and predict delivery. That is why we chose to compare predictive values of Bishop score to those of uterine EMG. Transvaginal cervical length was measured by one of 5 board certified perinatologists or one of 4 certified ultrasound technicians. Digital examination was performed by one of 26 resident physicians involved in the care of the patients included in the study.

Statistics

Student’s t-test and Mann Whitney U-test (when appropriate, due to non-normal distribution of variables) were used to compare delivery within, vs. outside of, 24 hours from the measurement in term patients, and 7 days from the measurement in preterm patients. Statistical comparison between preterm and term patients was performed to determine whether gestational age impacts EMG PV. Data were analyzed by ANOVA and Dunn’s test was used for pair-wise comparisons among groups. Pearson’s correlation analysis was used to determine whether demographic and/or clinical parameters influence the PV. A P value of < 0.05 was considered significant.

Receiver-operating-characteristics (ROC) curves were used to estimate the predictive values of EMG parameters that were significantly higher in preterm patients delivering within 7 days, and to assess the diagnostic accuracy of Bishop score, contractions on TOCO, and trans-vaginal cervical length for predicting preterm delivery within 7 days. Diagnostic accuracy of EMG, Bishop score, TOCO and trans-vaginal cervical length were then compared.

The ROC analysis was also performed on the cohort of patients for whom the results of all the examined methods were available. ROC curves constructed on this cohort were compared by Student’s t-test.

Repeatability and reproducibility measures

The PV analysis was re-performed on a subset of the data to determine intra-observer and inter-observer agreement. Approximately 175 voltage spikes from patients in term labor, term non-labor, preterm labor and preterm non-labor groups were re-analyzed. The intra-observer and inter-observer agreements were calculated according to the statistical methods proposed previously.31

RESULTS

116 patients were evaluated in the study. The data regarding the preterm and term groups will be presented in separate sections.

Preterm patients

General

The study population consisted of 88 pregnant women admitted at our institution between September, 2009 and February, 2010 with the diagnosis of preterm labor at less than 34 weeks gestation. Uterine EMG was initially recorded in 98 preterm patients, but 10 patients who underwent cesarean section were subsequently excluded from the analysis. Patients were included in the study at a median of 28 5/7 weeks of gestational age (range 21 5/7 to 33 6/7 weeks). 9 (10%) patients were <24 weeks’, 31 (35%) 24-28 weeks’, 33 (38%) 28-32 weeks’ and 15 (17%) > 32 weeks’. Delivery within 7 days from the EMG measurement occurred in 23% (20/88) of the cases. Out of 68 patients who did not deliver within 7 days from admission, 23 delivered at term (after 37 weeks), and 45 delivered before 37 weeks of gestation. Clinical background variables are summarized in Table 1. Note that at the time of EMG measurement (no more than 24 hours after admission to the hospital) the contractions were detected by TOCO in only 30% (26/88) of patients, although they were all initially admitted for preterm labor. In spite of this, uterine EMG signals were being produced and easily detected in these patients. This confirms that EMG is a much more sensitive technology for assessing contractile activity than is the TOCO.

Table 1.

Clinical Background Variables in Women Delivering Preterm Within, as Compared to After, 7 Days from the Uterine Electromyography Measurement

Variable Women Delivering Within
7 days (n=20)
Women Delivering
After 7 days (n=68)
P-Value
Maternal age (years) 24 (18-40) 27 (18-43) 0.59
Nulliparous 5 16 0.99
Number of previous
gestations
1 (0-8) 1 (0-11) 0.64
Previous preterm
delivery or late abortion
2 13 0.54
Twin gestations 1 8 0.65
Gestational age at
measurement
27 5/7
(22 6/7 to 33 4/7)
28 6/7
(21 5/7 to 33 6/7)
0.51
Preterm premature
rupture of membranes
3 2 0.42
Smoking 1 9 0.58
BMI (kg/m2) 28 (24 to 47) 27 (20 to 45) 0.15
Illicit drug abuse 1 7 0.72
Tocolytic treatment 16 53 0.89
Antenatal
corticosteroids
11 54 0.09
Contractions on TOCO 7 19 0.64
Bishop score 7 (2-13) 5 (1-10) 0.01*
Transvaginal cervical
length (cm) (n=59)
2.0 (0.5 – 3.5)
(n=7)
2.8 (0.3 – 4.8)
(n=52)
0.16

Data are median (range) and n. P value calculated by Mann-Whitney U-test and Student’s T-test.* represents statistical significance (P<0.05); BMI body mass index

Transvaginal cervical length was measured in 67% (59/88) of patients. Cervical length was not significantly shorter in women who delivered within 7 days (median 2.0 cm) compared with that in women who did not (median 2.8 cm) (P = 0.16).

EMG Parameters

EMG PV was significantly higher in patients delivering within 7 days from the measurement (52.56 ± 33.94 cm/s) compared to those who delivered after 7 days (11.11 ± 5.13 cm/s) (P<0.001; Figure 3). No statistically significant correlation was found between PV and the following demographic/clinical variables: maternal age, body mass index, number of previous gestations, number of previous preterm births, gestational age, twin gestations, PPROM, smoking, drug abuse, tocolytic treatment, and antenatal corticosteroids.

Figure 3.

Figure 3

Comparison of uterine electromyography propagation velocity values for preterm patients delivering within 7 days of measurement vs. those delivering more than 7 days from measurement. Means and standard deviations shown; * represents statistical significance (P<0.05).

PS peak frequencies were also significantly higher in women who delivered within 7 days (0.56 ± 0.15 Hz) compared to those who did not (0.44 ± 0.07 Hz) (P=0.002; Figure 4). All other EMG parameters analyzed did not differ significantly among groups. (Table 2).

Figure 4.

Figure 4

Comparison of uterine electromyography power spectrum (PS) peak frequency values for preterm patients delivering within 7 days of measurement vs. those delivering more than 7 days from measurement. Means and standard deviations shown; * represents statistical significance (P<0.05).

Table 2.

Comparison of Diagnostic EMG Parameters for Preterm Delivery Within, as Compared to After, 7 Days from the Uterine Electromyography Measurement

EMG Parameter Women Delivering
Within 7 days
Women Delivering
After 7 days
P-value
PS Peak Frequency * 0.56 ± 0.15 Hz 0.44 ± 0.07 Hz 0.002
Propagation Velocity * 52.56 ± 33.94 cm/s 11.11 ± 5.13 cm/s <0.001
PS Median Frequency 0.64 ± 0.12 Hz 0.68 ± 0.05 Hz 0.11
PS Peak Amplitude 50.98 ± 84.70 μV2 70.56 ± 134.64 μV2 0.63
PS Median Amplitude 16.27 ± 44.14 μV2 10.16 ± 16.29 μV2 0.58
Mean Burst Duration 35.53 ± 9.00 s 39.32 ± 12.26 s 0.21
SD of Burst Duration 7.44 ± 5.85 s 10.16 ± 7.0 s 0.07
Mean Inter-burst
Interval
307.5 ± 178.38 s 348.96 ± 227.27 s 0.65
SD of Inter-burst
Interval
184.14 ± 136.68 s 149.76 ± 157.92 s 0.26

PS power spectrum; SD standard deviation; P value calculated by Mann-Whitney U-test and Student’s T-test.* represents statistical significance (P<0.05).

Predictive values of EMG PV, PS peak frequency, and the combination (rescaled sum) of these parameters for predicting preterm delivery at various time points were calculated (Table 3). PV and PS peak frequency were then combined, by looking at the sum of their rescaled values. Specifically, PS peak frequency was multiplied by 100 and added to the corresponding PV value. The combination of these two parameters yielded the best predictive values at 7 days to delivery. These values were higher than for any parameter alone at any time point. A similar combination (product) using PV and PS peak frequency yielded no better results.

Table 3.

Predictive Measures ofUterine Electromyography Propagation Velocity, Power Spectrum Peak Frequency and Their Rescaled Sum, at 1, 2, 4, 7, and 14 Days to Delivery

1 day to delivery 2 days to delivery 4 days to delivery 7 days to delivery 14 days to delivery
PV PFr PV
+
PFr
PV PFr PV
+
PFr
PV PFr PV
+
PFr
PV PFr PV
+
PFr
PV PFr PV
+
PFr
AUC 0.91 0.61 0.90 0.92 0.66 0.90 0.96 0.74 0.95 0.95 0.78 0.96 0.89 0.71 0.89
Best cut-
off
22.13
cm/s
0.87
Hz
191.96 28.00
cm/s
0.87
Hz
191.96 24.88
cm/s
0.64
Hz
95.33 22.88
cm/s
0.64
Hz
84.48 26.6
cm/s
0.64
Hz
84.48
Sensitivity
(%)
100 14 14 77 8 8 82 18 53 85 15 70 70 13 61
Specificity
(%)
80 100 100 92 100 100 93 100 100 94 100 100 99 100 100
PPV (%) 30 100 100 63 100 100 74 100 100 81 100 100 94 100 100
NPV (%) 100 92 92 96 83 84 69 80 88 96 78 90 90 71 85

PV- propagation velocity; PFr – power spectrum peak frequency; AUC - area under the curve; PPV - positive predictive value; NPV - negative predictive value; Best cut-off values are presented as cm/s and Hz. Their rescaled sum has no units.

The sum of PV and PS peak frequency increased as the measurement-to-delivery interval decreased, as shown in Figure 5. Based on this figure it is possible to speculate that the EMG activity increases even before 7 days from delivery and it may be useful to identify patients in preterm labor even prior to this cut-off.

Figure 5.

Figure 5

Uterine electromyography propagation velocity (PV) + power spectrum peak frequency (PS) increases as the measurement-to-delivery interval decreases. □ Preterm labor – delivery ≤ 7 days from the measurement; ● delivery > 7 days from the measurement.

Figure 6 and Table 4 present ROC analysis results. The ROC curve for uterine EMG differed significantly from the ROC curve for Bishop score (P=0.02), transvaginal cervical length (P=0.03), and TOCO (P<0.001), even when the ROC analysis was performed on the same group of patients for which the results of all the methods were available.

Figure 6.

Figure 6

Comparison of receiver-operating-characteristics (ROC) curves for uterine electromyography (EMG) parameters (rescaled sum of propagation velocity [PV] and power spectrum [PS] peak frequency) and currently used clinical methods to predict preterm delivery within 7 days.

Table 4.

Predictive Measures ofUterine Electromyography Para meters (Combination of Propagation Velocity and Power Spectrum Peak Frequency) Compared to Currently Used Methods to Predict Preterm Delivery Within 7 Days.

Method AUC Best cut-off Sensitivity Specificity PPV NPV
EMG (PV +
PS Peak
Frequency)
(N=88)
0.96 84.48 70% 100% 100% 90%
Bishop Score
(N=88)
0.72 10 18% 100% 100% 81%
Transvaginal
Cervical
Length
(N=59)
0.67 0.7 cm 14% 98% 50% 90%
Contractions
on TOCO
(N=88)
0.54 N/A 35% 72% 27% 79%

EMG uterine electromyography; PV propagation velocity; PS power spectrum; TOCO tocodynamometer; AUC area under the curve; PPV positive predictive value; NPV negative predictive value; N number of patients included in the analysis.

Term Patients

Uterine EMG was recorded in 36 term patients and 8 patients who underwent caesarean-section were subsequently excluded from the analysis. Gestational age at inclusion did not differ significantly between the two groups (P=0.216). The median gestational age for labor patients was 39 2/7 (range 38 0/7 to 40 6/7 weeks) and for non-labor patients 38 5/7 (range 37 1/7 to 41 1/7 weeks). The median measurement to delivery interval for non-labor patients was 8 days (range 3 to 14 days) and in labor group 4 hours (range 2 to 14 hours). PV was significantly higher (P<0.001) in labor (31.25 ± 14.91 cm/s) compared with non-labor patients (11.31 ± 2.89 cm/s). (Figure 7). In an ROC analysis to distinguish between term patients in true vs. false labor, PV had an area under the curve (AUC) of 0.98. For predicting delivery within 24 hours, a PV > 13.19 cm/s had 100% sensitivity, 83% specificity, 96% positive predictive value (PPV) and 100% negative predictive value (NPV).

Figure 7.

Figure 7

Propagation velocity was significantly higher (P < 0.001) in labor groups compared to non-labor groups. The differences between term vs. preterm labor and term vs. preterm non-labor groups were not significant (P > 0.05). Data are presented as box plots and not vertical bar charts due to non-normal distribution in term labor group. Term Labor – delivery within 24 hours; Term Non-labor – delivery after 24 hours; Preterm Labor – delivery within 7 days; Preterm Non-labor – delivery after 7 days.* represents statistical significance.

Comparison between preterm and term patients

PV was significantly higher in labor at term and preterm compared with non-labor patients at term and preterm. The differences between term and preterm labor and term and preterm non-labor groups were not significant (P > 0.05). (Figure 7)

Repeatability and reproducibility measures

Intra-observer and inter-observer agreements were 99.92 ± 0.04 % and 99.67 ± 0.20 %, respectively. The technique to assess the PV of uterine EMG signals, described in the methods, is therefore highly repeatable and reproducible.

COMMENT

Noninvasive measurement of uterine EMG propagation and frequency can identify true preterm labor more accurately than the currently used methods. It can therefore identify those patients who will really benefit from early institution of tocolytic therapy, transport to a hospital with facilities for neonatal intensive care, and administration of steroids. At the same time, uterine EMG also identifies patients in false preterm labor who are not going to deliver within the next 7 days. This can help to avoid substantial economic costs associated with unnecessary hospitalization, the maternal risks associated with tocolytics, and the potential fetal risks associated with steroids. In the case of low PV and peak frequency values, it therefore stands to reason that it would be safe not to admit, treat, or transfer the patient, regardless of the presence of contractions on TOCO, and regardless of digital cervical exam and transvaginal cervical length results, since all of the changes in the myometrium required for labor are not yet fully established.

Methods currently available to clinicians to diagnose preterm labor have several major drawbacks. Digital cervical examination is subjective, and does not provide accurate diagnosis of true preterm labor.32,33 In the present study, the predictive measures of Bishop score were high only at scores of > 10, which is not useful clinically, because at that point imminent delivery is already obvious. An interesting finding of this study was that the uterine EMG is better than transvaginal cervical length in predicting preterm birth within 7 days of evaluation. This raises an important aspect related to the clinical utility of the cervical length in predicting preterm delivery within a short time interval. There is compelling data to suggest that cervical length is a good predictive marker for preterm birth between 24 to 32 weeks of gestation, but on the long and not on the short time interval.34It can be argued that the cervical length was only measured in 67%of the patients included, and only in 7 patients who delivered within 7 days. In many of the patients who presented with advanced cervical dilatation, cervical length was not obtained, and those patients were more likely to deliver within 7 days. The predictive values would, therefore, most likely be better if the transvaginal cervical length of all patients were known. However, several patients with short cervices in this study did not deliver within one week, and some did not deliver preterm at all. Further studies are needed to determine if addition of the fetal fibronectin test can improve the predictive value of transvaginal cervical length alone. However, given that the cervical length has much lower predictive values compared to uterine EMG, we doubt that the fetal fibronectin test will significantly change the results.

Our results also confirm that monitoring uterine activity with TOCO is not helpful in identifying patients in preterm labor.35,36 Only 23% of patients with contractions on TOCO during the 30 minutes of EMG recording delivered within 7 days, and the absence of contractions apparently does not rule out preterm labor reliably, as the NPV was only 79%. Approximately 1 in 5 patients who exhibited no contractions registering on TOCO did, nevertheless, deliver preterm within one week.

We are highly encouraged that measuring uterine electrical activity is superior to TOCO. It does not only detect uterine contractions as does TOCO, but can also identify myometrial properties that distinguish physiological preterm contractions from true preterm labor.

PS peak frequency has been the most predictive of true labor in both human and animal studies.16,17 Our results confirm that shifts to higher uterine electrical signal frequencies occur during transition from a non-labor state to both term and preterm labor states, and can be reliably assessed by non-invasive trans-abdominal uterine EMG. In addition, we demonstrate that PV of EMG signals in the myometrium can not only be determined by EMG measurement, but also that PV predicts preterm delivery more accurately than any other EMG parameter investigated so far. Similar data was obtained with patients at term. Possible reasons for the increased PV during preterm and term labor are the presence of gap junctions, number of muscle cells recruited, ion channels (size and number), cellular resting potential, and cellular threshold potential, conduction pathways – all of these play a part in what types of EMG signals are ultimately received at the electrodes.

We evaluated many EMG parameters and their predictive values for preterm delivery among patients admitted for “threatened preterm labor”. EMG PV, PS peak frequency, and their combination (rescaled sum) identified which patients will deliver soon and which will not with highest PPV and NPV. It would be useful to do a prospective clinical trial to confirm our results. They may be extremely important clinically, but could also lead to more reliable analyses of treatments and eventually to more effective interventions to prevent preterm birth.

Condensation: Uterine Electromyography distinguishes between true and false preterm labor more accurately than methods used clinically today.

Acknowledgments

Sources of Funding: 1) NIH R01HD037480 2) St. Joseph’s Foundation, Phoenix, AZ

Footnotes

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*

Presented orally at the 57th Annual Scientific Meeting of the Society for Gynecologic Investigation; March 27th, 2010, Orlando, Florida.

REFERENCES

  • 1.Bennett TA, Kotelchuck M, Cox CE, Tucker MJ, Nadeau DA. Pregnancy-associated hospitalizations in the United States in 1991 and 1992: a comprehensive view of maternal morbidity. Am J Obstet Gynecol. 1998;178:346–54. doi: 10.1016/s0002-9378(98)80024-0. [DOI] [PubMed] [Google Scholar]
  • 2.McPheeters ML, Miller WC, Hartmann KE, et al. The epidemiology of threatened preterm labor: a prospective cohort study. Am J Obstet Gynecol. 2005;192:1325–30. doi: 10.1016/j.ajog.2004.12.055. [DOI] [PubMed] [Google Scholar]
  • 3.Iams JD, Romero R. Preterm Birth. In: Gabbe SG, Niebyl JR, Simpson JL, editors. Obstetrics: Normal and Problem Pregnancies. 5th ed Churchill Livingstone Elsevier; Philadelphia, PA: 2007. pp. 668–712. [Google Scholar]
  • 4.Tezuka N, Ali M, Chwalisz K, Garfield RE. Changes in transcripts encoding calcium channel subunits of rat myometrium during pregnancy. Am J Physiol. 1995;269:1008–17. doi: 10.1152/ajpcell.1995.269.4.C1008. [DOI] [PubMed] [Google Scholar]
  • 5.Balducci J, Risek B, Gilula NB, Hand A, Egan JF, Vintzileos AM. Gap junction formation in human myometrium: a key to preterm labor. Am J Obstet Gynecol. 1993;168:1609–15. doi: 10.1016/s0002-9378(11)90806-0. [DOI] [PubMed] [Google Scholar]
  • 6.Garfield RE, Blennerhassett MG, Miller SM. Control of myometrial contractility: role and regulation of gap junctions. Oxf Rev Reprod Biol. 1988;10:436–90. [PubMed] [Google Scholar]
  • 7.Young RC. Tissue-level signaling and control of uterine contractility : the action potential-calcium wave hypothesis. J Soc Gynecol Investig. 2000;7:146–52. doi: 10.1016/s1071-5576(00)00041-1. [DOI] [PubMed] [Google Scholar]
  • 8.Buhimschi C, Boyle MB, Saade GR, Garfield RE. Uterine activity during pregnancy and labor assessed by simultaneous recordings from the myometrium and abdominal surface in the rat. Am J Obstet Gynecol. 1998;178:811–22. doi: 10.1016/s0002-9378(98)70498-3. [DOI] [PubMed] [Google Scholar]
  • 9.Buhimschi C, Garfield RE. Uterine contractility as assessed by abdominal surface recording of electromyographic activity in rats during pregnancy. Am J Obstet Gynecol. 1996;174:744–53. doi: 10.1016/s0002-9378(96)70459-3. [DOI] [PubMed] [Google Scholar]
  • 10.Garfield RE, Chwalisz K, Shi L, Olson G, Saade GR. Instrumentation for the diagnosis of term and preterm labour. J Perinat Med. 1998;26:413–36. doi: 10.1515/jpme.1998.26.6.413. [DOI] [PubMed] [Google Scholar]
  • 11.Garfield RE, Saade G, Buhimschi C, et al. Control and assessment of the uterus and cervix during pregnancy and labour. Hum Reprod Update. 1998;4:673–95. doi: 10.1093/humupd/4.5.673. [DOI] [PubMed] [Google Scholar]
  • 12.Devedeux D, Marque C, Mansour S, Germain G, Duchene J. Uterine electromyography: a critical review. Am J Obstet Gynecol. 1993;169:1636–53. doi: 10.1016/0002-9378(93)90456-s. [DOI] [PubMed] [Google Scholar]
  • 13.Marque C, Terrien J, Rihana S, Germain G. Preterm labour detection by use of a biophysical marker: the uterine electrical activity. BMC Pregnancy Childbirth. 2007;7(Suppl 1):S5. doi: 10.1186/1471-2393-7-S1-S5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Vinken MPGC, Rabotti C, Mischi M, Oei SG. Accuracy of frequency related parameters of the electrohysterogram for predicting preterm delivery. A review of the literature. Obstet Gynecol Surv. 2009;64:529–4. doi: 10.1097/OGX.0b013e3181a8c6b1. [DOI] [PubMed] [Google Scholar]
  • 15.Buhimschi C, Boyle MB, Garfield RE. Electrical activity of the human uterus during pregnancy as recorded from the abdominal surface. Obstet Gynecol. 1997;90:102–11. doi: 10.1016/S0029-7844(97)83837-9. [DOI] [PubMed] [Google Scholar]
  • 16.Maner WL, Garfield RE. Identification of human term and preterm labor using artificial neural networks on uterine electromyography data. Ann Biomed Eng. 2007;35:465–73. doi: 10.1007/s10439-006-9248-8. [DOI] [PubMed] [Google Scholar]
  • 17.Maner WL, Garfield RE, Maul H, et al. Predicting term and preterm delivery with transabdominal uterine electromyography. Obstet Gynecol. 2003;101:1254–60. doi: 10.1016/s0029-7844(03)00341-7. [DOI] [PubMed] [Google Scholar]
  • 18.Marque C, Duchene J, Leclercq S, Panczer G, Chaumont J. Uterine EHG Processing for Obstetrical Monitoring. IEEE Trans Biomed Eng. 1986;33(12):1182–7. doi: 10.1109/TBME.1986.325698. [DOI] [PubMed] [Google Scholar]
  • 19.Miller SM, Garfield RE, Daniel EE. Improved propagation in myometrium associated with gap junctions during parturition. Am J Physiol. 1989;256:C130–41. doi: 10.1152/ajpcell.1989.256.1.C130. [DOI] [PubMed] [Google Scholar]
  • 20.Miyoshi H, Boyle MB, MacKay LB, Garfield GE. Gap junction currents in cultured muscle cells from human myometrium. Am J Obstet Gynecol. 1997;178:588–93. doi: 10.1016/s0002-9378(98)70443-0. [DOI] [PubMed] [Google Scholar]
  • 21.Duchene J, Marque C, Planque S. Uterine EMG Signal : Propagation Analysis. Conf Proc IEEE Eng Med Biol Soc. 1990;1990:831–2. [Google Scholar]
  • 22.Rabotti C, Mischi M, van Laar JOEH, Oei SG, Bergmans JWM. On the propagation analysis of electrohysterographic signals. Conf Proc IEEE Eng Med Biol Soc. 2008;2008:3868–71. doi: 10.1109/IEMBS.2008.4650054. [DOI] [PubMed] [Google Scholar]
  • 23.Rabotti C, Mischi M, van Laar JOEH, Oei SG, Bergmans JWM. Inter-electrode delay estimators for electrohysterographic propagation analy- sis. Physiol Meas. 2009;30:745–61. doi: 10.1088/0967-3334/30/8/002. [DOI] [PubMed] [Google Scholar]
  • 24.Mischi M, Rabotti C, Vosters LPJ, Oei SG, Bergmans JWM. Electrohysterographic conduction velocity estimation. Conf Proc IEEE Eng Med Biol Soc. 2009;2009:6934–7. doi: 10.1109/IEMBS.2009.5333636. [DOI] [PubMed] [Google Scholar]
  • 25.Terrien J, Marque C, Germain G, Karlsson B. Sources of bias in synchronization measures and how to minimize their effects on the estimation of synchronicity: Application to the uterine electromyogram. In: Naik GR, editor. Recent Advances in Biomedical Engineering. I-Tech Education and Publishing; Vienna, Autria: 2009. pp. 73–99. [Google Scholar]
  • 26.Euliano TY, Marossero D, Nguyen MT, Euliano NR, Principe J, Edwards RK. Spatiotemporal electrohysterography patterns in normal and arrested labor. Am J Obstet Gynecol. 2009;200:54.e1–7. doi: 10.1016/j.ajog.2008.09.008. [DOI] [PubMed] [Google Scholar]
  • 27.Hassan M, Terrien J, Karlsson B, Marque C. Spatial analysis of uterine EMG signals: evidence of increased in synchronization with term. Conf Proc IEEE Eng Med Biol Soc. 2009;2009:6296–9. doi: 10.1109/IEMBS.2009.5332795. [DOI] [PubMed] [Google Scholar]
  • 28.Hassan M, Terrien J, Karlsson B, Marque C. Synchronization between EMG at Different Uterine Locations Investigated Using Time-Frequency Ridge Reconstruction: Comparison of Pregnancy and Labor Contractions. EURASIP J Adv Signal Process. 2010;2010 Article ID 242493. [Google Scholar]
  • 29.Marlow N, Wolke D, Bracewell MA, Samara M. Neurologic and developmental disability at six years of age after extremely preterm birth. N Engl J Med. 2005;352:9–19. doi: 10.1056/NEJMoa041367. [DOI] [PubMed] [Google Scholar]
  • 30.Garfield RE, Maner WL, MacKay LB, Schlembach D, Saade GR. Comparing uterine electromyography activity of antepartum patients versus term labor patients. Am J Obstet Gynecol. 2005;193:23–9. doi: 10.1016/j.ajog.2005.01.050. [DOI] [PubMed] [Google Scholar]
  • 31.Bland JM, Altman DG. Statistical methods of assessing agreement between methods of clinical measurements. Lancet. 1986;1:307–10. [PubMed] [Google Scholar]
  • 32.Gomez R, Galasso M, Romero R, et al. Ultrasonographic examination of the uterine cervix is better than cervical digital examination as a predictor of the likelihood of premature delivery in patients with preterm labor and intact membranes. Am J Obstet Gynecol. 1994;171:956–964. doi: 10.1016/0002-9378(94)90014-0. [DOI] [PubMed] [Google Scholar]
  • 33.Jackson GM, Ludmir J, Bader TJ. The accuracy of digital examination and ultrasound in the evaluation of cervical length. Obstet Gynecol. 1992;79:214–18. doi: 10.3109/01443619209013646. [DOI] [PubMed] [Google Scholar]
  • 34.Iams JD, Goldenberg RL, Meis PJ, Mercer BM, Moawad A, Das A. The length of the cervix and the risk of spontaneous premature delivery. N Engl J Med. 1996;334:567. doi: 10.1056/NEJM199602293340904. [DOI] [PubMed] [Google Scholar]
  • 35.Iams JD, Newman RB, Thom EA, et al. Frequency of uterine contractions and the risk of spontaneous preterm delivery. N Engl J Med. 2002;346:250–5. doi: 10.1056/NEJMoa002868. [DOI] [PubMed] [Google Scholar]
  • 36.Maul H, Maner WL, Olson G, Saade GR, Garfield RE. Non-invasive transabdominal uterine electromyography correlates with the strength of intrauterine pressure and is predictive of labor and delivery. J Matern Fetal Neonatal Med. 2004;15:297–301. doi: 10.1080/14767050410001695301. [DOI] [PubMed] [Google Scholar]

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