During the second stage of labor, women augment the force of uterine contractions by bearing down. They are often instructed to begin pushing soon after contraction onset and to make sustained efforts to continue until the contraction wanes.1 Although the pattern of pushing varies, this typically results in one push before, one during and one after peak uterine contraction force. In contrast, when women push spontaneously, they do not initiate the bearing down effort until near the middle of the uterine contraction, with most effort directed at contraction peak.1 Several studies have started to explore the biomechanics of pushing during the second stage. These include factors that affect intrauterine pressure during pushing and the amplitude of intercostal muscle myoelectric signal,2–3 but the theoretical effects of different pushing patterns remains unclear.
Pushing requires significant maternal effort to be expended during the second stage. The mean second stage duration in nulliparous women has been reported as 70 minutes, with 27% of patients having a second stage duration exceeding 2 hours.4 During prolonged labor, some women become so exhausted that they cannot generate sufficient force to deliver without instrumented assistance with forceps or vacuum, interventions that can pose potential complications for mother and fetus.5,6 Therefore, understanding factors that might reduce maternal exhaustion may lead to a higher likelihood of spontaneous delivery and reduction of potential fetal or maternal injury.
The goal of this theoretical study, therefore, was to estimate how different patterns of maternal effort might affect progress during the second stage of labor. We developed a biomechanical model to simulate the second stage of labor such that the efficacy of different patterns of maternal effort could be quantitatively compared and analyzed.
MATERIALS AND METHODS
The initial geometry of female pelvic floor at the beginning of the second stage of labor was based on magnetic resonance (MR) images of a healthy woman taken from an earlier study (Fig. 1A).7 Using this MR geometry, a simplified three-dimensional biomechanical model was then developed in Matlab (The MathWorks, Natich, MA) and solved using its Simulink software (Fig. 1B). Six levator ani muscle bands were used to represent the iliococcygeal, pubovisceral, and puborectal portions of the levator ani muscle (Fig. 1C). The muscle bands were simulated by U-shaped viscoelastic slings wrapped around the fetal head to form the birth canal and were interconnected by springs representing the iliococcygeal raphe (Fig. 1C). The material properties of these structures are described in more detail later in this section.
After taking into account the 10% reduction in size resulting from the effect of molding,8 the premolded fetal head was simulated with a 9-cm-diameter rigid sphere representing the 50th percentile fetal head.9 During the simulation, the fetal head was constrained to move along a specific trajectory given by the dashed line in Figure 1D, which represents the curve of Carus. As a first-order approximation, the body of the fetus was neglected, and the fetal head was considered to carry the whole inertial mass of the fetus.
The time history profiles of the intrauterine pressure and the pressure on fetal head during the second stage of labor were taken from the literature.10,11 Rempen and Kraus10 showed that the mean pressure on the fetal head in the amniotic cavity was 8.5 kPa during a uterine contraction, whereas a voluntary push increased the pressure to 19 kPa. The average basal tone during the rest interval was 2.6 kPa. As a first-order approximation, the expulsive force was simulated by applying uniform expulsive pressure to the “cranial” hemisphere of the fetal head, the equator of which was constrained to lie perpendicular to the curve of Carus as the head progressed through the pelvic floor. The curve of Carus was defined as a locus of points lying 6 cm dorsal to the posterior margin of the pubic symphysis (Fig. 1D). The resulting expulsive pressure was integrated and applied as a force to move the fetal head along its path of progression during labor (see below).
Maternal behavior during the directed pushing was implemented as described in the literature.11,12 In directed pushing, the birthing mother is commonly asked to begin pushing when the coach senses a uterine contraction has started, being asked to hold the effort for 10 seconds, to take a rest and resume the effort. Therefore, we simulated directed pushing by superposing three 10-second voluntary pushes timed to occur at 25%, 50%, and 75% of the uterine contraction duration (Fig. 2A). In contrast, during spontaneous pushing, the maternal “bearing down” efforts occur when each uterine contraction is well established. Spontaneous pushing was therefore simulated with one voluntary push timed at the contraction peak (Fig. 2B). The duration of the uterine contraction and the duration of the rest interval between two contractions were set to be 1 minute and 2 minutes, respectively. Other possible voluntary pushing patterns during birth were also simulated, including double voluntary pushes timed at 25% and 50% of the uterine contraction duration, double voluntary pushes timed at 50% and 75% of the uterine contraction duration, a single voluntary push occurring before the peak uterine contraction duration, and a single voluntary push occurring after the peak uterine contraction duration (Fig. 2C–F).
The resistance to progress met by the fetal head is largely due to the resistance of the levator muscle bands to stretch. The resistance of each muscle band to stretch was represented mathematically by a five-parameter, viscoelastic model, consisting of a spring in series with two Kelvin-Voigt elements. The constitutive equation of the muscle was
where E0, E1, and E2 were the elastic parameters, and μ1 and μ2 were viscosity coefficients; ς and ϵ denote stress and strain, respectively, and their first and second time derivatives (dot and double dot notation, respectively). This equation states that levator muscle stress (defined as tensile force in the muscle divided by muscle cross-sectional area) and strain (increase in length divided by initial length) and their derivatives (ie, rates of change over time) are related by a series of terms involving the elastic and/or viscous behavior of the muscle in tension. The stress-strain equation of the hyperelastic ligament spring was
Equation (Uncited)Image Tools
where A and B are the material constants. This equation states that the tensile resistance to muscle stretch increases exponentially with elongation. Because no material properties of the human levator ani muscle are published, their properties were assumed to be represented by published properties for the pregnant human cervix13 whose palpated ripening parallels that observed in pelvic floor tissues. The parameters of the material properties used for the levator muscle bands are shown in Table 1.
The expulsive force was assumed to be evenly distributed on the cranial half of the sphere representing the fetal head, so it was integrated and represented by concentrated force acting at the center of the sphere. An additional normal force was applied at right angles to the path of progression to constrain the fetal head to move along the trajectory of the curve of Carus. The movement of the fetal head was then calculated from the equations of the motion:
where X and Y were the position of the center of the fetal head, M was the mass of the fetal head, F was the expulsive force, N was the normal force, and Nmi represented the equivalent reaction force from each muscle band (Fig. 1D). This is the application of Newton’s second law: F=ma.
Equation (Uncited)Image Tools
The progress of the fetal head descent during the second stage of labor was then computed with respect to different voluntary push profiles. The time histories of the change in levator ani muscle stretch ratio, and strain rates were also calculated. The approval of the University of Michigan Medical School Institutional Review Board was obtained for the human studies described in this article.
The estimated duration of the second stage of labor and the numbers of voluntary pushes needed with respect to each pushing pattern are shown in Fig. 3. The triple pushing method resulted in the shortest duration, 57.5 minutes (“triple” or pre-peak-post pattern). The longest duration was 75.8 minutes (prepush and postpush patterns). For the peak-push technique, the duration of the second stage of labor increased by 16%. The increments of the duration of labor for the other pushing patterns, namely pre and peak pushing, peak and post push, prepush and postpush, were 5%, 5%, 36%, and 32%, respectively. However, the estimated numbers of the maternal pushes required to deliver the fetus for the triple-push technique was 59, whereas the peak-push technique only required 23 voluntary pushes, a 61% reduction. The reductions in the numbers of voluntary pushes for the pre-and-peak push, peak-and-post push, prepush, and postpush patterns were 29%, 30%, 54%, and 56%, respectively.
To investigate the sensitivity of the duration of labor to the magnitude of the voluntary push, the magnitude of the voluntary push was varied by 25%. With the triple-push pattern, the duration of labor was found to be increased by 10% when the magnitude of the voluntary push was reduced by 25%. The duration of labor was reduced by 11% when the magnitude of the voluntary push was increased 25%. With the peak-push pattern, the duration of labor increased 9% when the magnitude of the voluntary push was reduced 25%, whereas the duration of labor was reduced by 14% when the magnitude of voluntary push was increased by 25%. An example of the progress in a simulated vaginal delivery and the changes in muscle stretch ratios over time during the second stage of labor with peak-push pattern is shown in Figure 4. The progress in the location of the fetal head between contractions was fairly uniform. However, the extra descent due to each voluntary push was small at the beginning of the second stage but increased rapidly before delivery. The estimated stretch ratio of the dorsal portion of the iliococcygeal muscle (IC6) was small during the whole second stage of labor, and its maximal stretch ratio was a modest 1.32. The stretch ratio of the pubovisceral muscle band (PV4) increased linearly through the second stage of labor and reached 1.59. The medial-most pubovisceral muscle band (PV2) exhibited the largest stretch ratio, 3.30, during the second stage of labor. The increment in the muscle stretch ratio was small at first but rose rapidly at the end of the second stage of labor. With the peak-push pattern, the strain rate of the medial-most pubovisceral muscle band, PV2, reached 3.33 per second. The maximal strain rate of the PV2 muscle band for the different push patterns is shown in Table 2.
The maximal tensile stress in each muscle band during the delivery with the different pushing patterns was also estimated. The PV2 muscle band underwent the highest stress. The maximal stresses for the six push patterns are shown in Table 2.
Although the triple-push pattern resulted in a 16% shorter second stage, this came at the energetic expense of a 61% increase in the number of pushes required. These computer simulation results provide theoretical insights into how the maternal pushing pattern may affect the duration of the second stage of labor and the amount of effort required to deliver the fetal head. The standard three-push paradigm resulting in the shortest duration of labor, 9 minutes shorter than the peak-push pattern (ie, spontaneous pushing), is consistent with clinical studies of self-directed, spontaneous, pushing that reveal a 5- to 13-minute longer second stage.14 If one considers maternal effort as metabolically proportional to the summed area under the maternal expulsive force-time curve, the maternal bearing down effort required with the triple push was almost three times more than for the peak-push pattern. This raises the possibility that some women who push three times during each contraction could become exhausted before achieving delivery.
Our birth simulation results also showed that the efficiency of a voluntary push in advancing the fetal head along the curve of Carus is sensitive to the timing of that push. The fact that a voluntary push timed at peak uterine contraction was found to be the most efficient technique was due to the higher peak total push force, the higher peak tissue strain, and the higher residual strain in the (viscoelastic) pelvic floor muscles between contractions. These results suggest that pushing at the wrong time is not only inefficient but also may waste maternal effort.
The endurance of striated muscle performing repetitive contractions is known to be inversely proportional to the muscle contraction level, the ratio of contraction time to cycle time (the duty cycle), and the cycle time, with the first two factors being the most important.15 In labor, the cycle time is essentially fixed by a 3-minute uterine contraction interval, so if we assume that the muscle volitional contraction level is maximal, then minimizing the duty cycle is the obvious way to maximize endurance during delivery. In short, this means minimizing the muscle contraction time needed to deliver the neonate.
The ability to birth a neonate without requiring an instrumented delivery is important because a prolonged second stage of labor that ends with an instrumented delivery has been associated with pelvic floor injury (see the Introduction). It has been traditional in the United States to coach women to push three times, beginning at the onset of a uterine contraction, to shorten the duration of the second stage of labor. Whether alternative strategies result in less exhaustion and higher delivery rates will require clinical trials.
In terms of muscle injury risk in vivo, the magnitude of muscle stress in tension is a known predictor of striated muscle injury severity, and stretches greater than 50% strain are known to result in significant force deficits in passive muscle.16 Increasing the strain rate can increase the risk of strain-related injuries in a passive muscle-tendon unit subjected to high rates of stretch.17 During the simulated vaginal delivery, the medial-most pubovisceral muscle band (band 2) underwent the largest stretch and experienced the largest stress and highest strain rate in the final push of the delivery (Fig. 3). Therefore, this portion of muscle is at greatest risk of stretch-induced injury.7 A practical way to reduce its risk of injury would be to reduce its rate of stretch by slowing the descent rate of the baby’s head during that final push.
To validate the present computer simulation results, the time histories of simulated maximal anteroposterior (AP) vertex diameter from the model using the peak-pushing pattern was compared with the measured increase in the AP vertex diameter measured in vivo in six primipara (Jane Walder, RN, personal communication, March 14, 2002, Fig. 5). Despite the large variation in the AP diameter measurements, the overall trend of the simulation result was similar to the experimental measurements, helping to validate the model predictions.
This study has several methodologic limitations. First, stretch is not necessarily uniform along a muscle band, as assumed. For example, localized stretch variation may occur along and across a muscle band,18 especially if the thickness of the muscle varies.19 Therefore, the assumption of the uniform tissue stretch led to a conservative estimate of tissue stresses and stretch ratios. Second, this analysis focused on the longitudinal stretch in the muscle bands; transverse compression and biaxial stretch effects were neglected. However, the overall trend predicted by this model should still be valid.
Third, as a first-order approximation, the fetus was represented by a rigid sphere in this simulation. The variations in fetal head shape, the degree of molding during delivery, the fetal head orientation, the size and shape of the fetal body, and pelvic shape may also affect the muscle stretch ratios and stresses. However, these effects are beyond the scope of this report. Fourth, in this model, the levator ani muscle bands were assumed to form a continuous U-shaped sling wrapped around the fetal head and birth canal. However, the pubovisceral muscles insert into the intersphincteric groove and perineal body. Therefore, the stretch of the anal sphincter and perineal body may affect the accuracy of the estimation of the pubovisceral muscle stresses and stretch ratios.
The effect of maternal fatigue was not simulated in this model. During the simulation, the magnitude of the voluntary push was assumed to be constant. However, muscle fatigue may develop gradually over time such that women can no longer maintain a given push force. As the result, the duration of labor may be underestimated. Finally, epidural anesthetic may influence pushing in two ways. First, the degree of abdominal muscle paralysis may decrease the pushing force, which would tend to lengthen the second stage, but it would also reduce the pelvic floor resistance to stretch, which might tend to shorten the duration of labor.
1. Sampselle CM, Hines S. Spontaneous pushing during birth. Relationship to perineal outcomes. J Nurse Midwifery 1999;44:36–9.
2. Buhimschi CS, Buhimschi IA, Malinow AM, Kopelman JN, Weiner CP. Pushing in labor: performance and not endurance. Am J Obstet Gynecol 2002;186:1339–44.
3. Demaria F, Porcher R, Sheik-Ismael S, Amarenco G, Benifla JL. Recording expulsive forces during childbirth using intercostal muscle electromyogram: a pilot study [in French]. Gynecol Obstet Fertil 2005;33:299–303.
4. Schiessl B, Janni W, Jundt K, Rammel G, Peschers U, Kainer F. Obstetrical parameters influencing the duration of the second stage of labor. Eur J Obstet Gynecol Reprod Biol 2005;118:17–20.
5. Christianson LM, Bovbjerg VE, McDavitt EC, Hullfish KL. Risk factors for perineal injury during delivery. Am J Obstet Gynecol 2003;189:255–60.
6. Kearney R, Miller JM, Ashton-Miller JA, DeLancey JO. Obstetric factors associated with levator ani muscle injury after vaginal birth. Obstet Gynecol 2006;107:144–9.
7. Lien KC, Mooney B, DeLancey JO, Ashton-Miller JA. Levator ani muscle stretch induced by simulated vaginal birth. Obstet Gynecol 2004;103:31–40.
8. Carlan SJ, Wyble L, Lense J, Mastrogiannis DS, Parsons MT. Fetal head molding. Diagnosis by ultrasound and a review of the literature. J Perinatol 1991;11:105–11.
9. Chitty LS, Altman DG, Henderson A, Campbell S. Charts of fetal size: 2. Head measurements. Br J Obstet Gynaecol 1994;101:35–43.
10. Rempen A, Kraus M. Pressures on the fetal head during normal labor. J Perinat Med 1991;19:199–206.
11. Allman AC, Genevier ES, Johnson MR, Steer PJ. Head-to-cervix force: an important physiological variable in labour. 2. Peak active force, peak active pressure and mode of delivery. Br J Obstet Gynaecol 1996;103:769–75.
12. Thomson AM. Pushing techniques in the second stage of labour. J Adv Nurs 1993;18:171–7.
13. Conrad JT, Ueland K. The stretch modulus of human cervical tissue in spontaneous, oxytocin-induced, and prostaglandin E2-induced labor. Am J Obstet Gynecol 1979;133:11–4.
14. Sampselle CM, Miller JM, Luecha Y, Fischer K, Rosten L. Provider support of spontaneous pushing during the second stage of labor. J Obstet Gynecol Neonatal Nurs 2005;34:695–702.
15. Iridiastadi H, Nussbaum MA. Muscle fatigue and endurance during repetitive intermittent static efforts: development of prediction models. Ergonomics 2006;49:344–60.
16. Brooks SV, Zerba E, Faulkner JA. Injury to muscle fibres after single stretches of passive and maximally stimulated muscles in mice. J Physiol 1995;488:459–69.
17. Lin R, Chang G, Chang L. Biomechanical properties of muscle-tendon unit under high-speed passive stretch. Clin Biomech (Bristol, Avon) 1999;14:412–7.
18. Best TM, McElhaney JH, Garrett WE Jr, Myers BS. Axial strain measurements in skeletal muscle at various strain rates. J Biomech Eng 1995;117:262–5.
19. Bernstein I, Juul N, Grønvall S, Bonde B, Klarskov P. Pelvic floor muscle thickness measured by perineal ultrasonography. Scand J Urol Nephrol Suppl 1991;137:131–3.
Figure. No caption available.
© 2009 by The American College of Obstetricians and Gynecologists.