Abstract
Purpose of Review
Over the last two to three decades, a growing body of research has shown that vaginal childbirth is more traumatic to mothers than generally assumed. Apart from obstetric anal sphincter tears which have been extensively studied, trauma to the levator ani muscle is a form of maternal injury that is less well recognised and often undiagnosed. In the context of an increasing push towards vaginal birth, this article will review the recent literature to better inform health care providers regarding the significance of pelvic floor trauma.
Recent Findings
Imaging studies have shown that levator avulsion, where the puborectalis muscle has detached from the os pubis, occurs in up to 1/3 of vaginally primiparous women, depending on demographic factors and obstetric management. Forceps is a well-established risk factor for levator avulsion with an odds ratio of 4–5 compared to vacuum, which does not seem to convey additional risk over unassisted vaginal birth. Levator injuries are significantly associated with pelvic organ prolapse and treatment failure. Such trauma can also lead to significant psychological morbidity, up to and including post-traumatic stress disorder. Antenatal prediction does not appear feasible. Modification of obstetric practice by abandoning forceps would significantly reduce pelvic floor trauma and the future need for prolapse surgery.
Summary
Vaginal childbirth is more traumatic than commonly assumed. Levator trauma is associated with significant physical and psychological morbidity. Perinatal health care providers need to understand and recognise the significance of maternal birth trauma and its potential impact on women’s health.
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Avoid common mistakes on your manuscript.
Introduction
Childbirth is an important experience in a woman’s life. This life event is often described as joyful and empowering. Vaginal delivery is generally considered to be more physiological, natural and hence a superior way to give birth compared to caesarean section (CS). As a result, the rising CS rate seen worldwide is considered problematic and has led to increasing pressure on clinicians to modify clinical practice.
Epidemiological studies have shown that childbirth is an important risk factor for pelvic floor disorders [1,2,3,4]. Parous women are more likely to experience pelvic organ prolapse (POP) and to suffer from urinary and faecal incontinence than nulliparous women. While both the hormonal and mechanical effects of pregnancy may contribute to pelvic floor dysfunction [5], mode of delivery plays a central role, mediated by childbirth-related mechanical trauma. Women after vaginal birth are more commonly found to suffer from pelvic floor dysfunction than women after CS [6]. The accumulating scientific evidence in this field over the last two to three decades has helped us understand the etiological link between vaginal birth and pelvic floor disorders. It is now evident that vaginal delivery is more traumatic than generally assumed.
What Is Pelvic Floor Trauma?
What we call the pelvic floor usually refers to the muscles of the pelvic diaphragm. It consists of the levator ani and the coccygeus muscle; pelvic floor trauma commonly refers to trauma to the levator ani. While there is a lack of agreement in regard to the components of the levator ani and their nomenclature, the V-shaped muscle sling that attaches to the os pubis bilaterally and runs posteriorly around the anorectum seems to be of most relevance in the context of maternal birth trauma. We call this part of the levator ani the ‘puborectalis muscle’.
The puborectalis muscle together with the pubic bone encloses the levator hiatus, the largest potential hernia portal in the human body. Traversing through the hiatus are the urethra anteriorly, the vagina in the middle and the anorectum posteriorly (Fig. 1). The levator ani plays a role in supporting various body functions in a woman’s life including controlled evacuation of body wastes, support of pelvic organs against displacement due to the pressure differential between inside and outside and due to gravity, as well as reproductive function. Childbirth is a particular challenge to the pelvic floor in view of the relative size of the baby’s head.
Levator Trauma
In 1943, Howard Gainey, a Kansas City Obstetrician, reported a study on 1000 patients in a postnatal clinic where about 20% of women were diagnosed with a detachment of the pubococcygeus muscle (which we would call the puborectalis muscle), a condition we now describe with the term ‘levator avulsion’ [8]. Unfortunately, Gainey’s report was ignored until the late 1990s. Recent advances in imaging technologies using magnetic resonance (MR) and ultrasound (US) have confirmed these 70-year-old observations. Levator avulsion has been demonstrated on MR [9, 10], on three-dimensional US [11, 12], in the delivery suite [13] and in cadavers [14]. Figure 2 shows ultrasound images of a patient diagnosed of levator avulsion before and after a first vaginal birth.
In a computer modelling study using MR data of a healthy nulliparous woman, Lien et al. showed that the most ventro-medial aspect of the levator ani muscle has to stretch the most (by a factor of 3.26) and over the shortest period of time during vaginal delivery [15]. In a retrospective observational study using 3D US data of 224 pregnant nulliparous women, the required muscle distension during vaginal delivery of a baby of average size was shown to vary widely in the general population, i.e. from 25 to 245% [16]. Given the degree of muscle distension, it is not surprising that vaginal delivery frequently leads to pelvic floor muscle trauma.
Studies using US and MR have now shown levator avulsion rates of 2–36% in primiparous women after vaginal delivery [9, 17,18,19,20,21,22,23,24], depending on demographics and obstetric practice [25]. Imaging before and after childbirth has confirmed vaginal delivery as the direct cause of such trauma [11]. The condition is not found in women after CS [11, 23, 26].
Levator avulsion is usually occult, likely due to greater distensibility of vaginal tissues compared to the muscle-bone interface of the puborectalis muscle. This explains the lack of progress in understanding the condition after Gainey’s first report. Occasionally however, an avulsion is directly visible due to a large vaginal tear. Figure 3 shows levator avulsion as seen through a large vaginal tear after vaginal delivery, on US and on MR 3 months after vaginal delivery. Recent studies have shown that vaginal and 3rd/4th degree perineal tears are clinical markers for levator avulsion and may help detection of the condition [27, 28].
While avulsion can be palpated digitally [29], the diagnostic gold standard at present is tomographic translabial ultrasound (multislice imaging or TUI) [30]. Figure 4 shows a TUI representation of a full unilateral avulsion. Anatomical improvement over time has been documented in imaging studies; however, it is much less common than persistence of the condition [31,32,33].
Considering the degree of muscle distension required for vaginal delivery, it is plausible that vascular, neuromuscular and connective tissue changes, that is, other forms of damage apart from gross avulsion injury may occur. From muscle physiology research, it can be assumed that substantial ultrastructural trauma, up to and including disruption of sacromeres, may occur if skeletal muscle is stretched to beyond 1.5 times its original length [34]. It is plausible that muscle atrophy, impairment of muscle function and alterations in pelvic floor distensibility may occur as a result of vaginal delivery. However, as no evidence of permanent denervation and muscle atrophy was found in women suffering from obstetric fistula, denervation seems unlikely as an important pathophysiological mechanism in child birth-related pelvic floor muscle injury [35].
In a prospective imaging study comparing the hiatal area before and after a first vaginal birth at a mean of 5 months postpartum, 19% of women with an intact levator were found to have > 20% peripartum increase in hiatal area on Valsalva together with ballooning, i.e. an abnormally distensible hiatus defined as a hiatal area on Valsalva = > 25 cm2 based on previous studies in non-pregnant nulliparae [36] and in the symptomatic population [37]. These findings suggest that the levator may have been overstretched [38]. On comparing imaging data on hiatal area obtained at 3–6 months and 2–3 years after the first birth, no evidence of regression or healing was found suggesting that over-distension of the puborectalis or levator ‘micro-trauma’ may be irreversible [31] (Fig. 5).
Risk Factors
Levator avulsion and micro-trauma are largely the consequences of the 1st vaginal birth [39, 40]. Older maternal age at first birth is an established antenatal risk factor [9, 22, 41,42,43] for levator trauma as well as for OASI. An odds ratio of 1.064 for overall risk of injury was noted for each increasing year of age past age 18 years [43] (Fig. 6). This has important implications since women in many societies increasingly delay child bearing.
Other antenatal risk factors shown to be associated with avulsion include a lower maternal body mass index and reduced bladder neck descent, a measure that may reflect a stiffer pelvic floor [22, 44]. A family history of CS was found to be associated with micro-trauma [22].
Foetal head circumference, foetal head position other than occipito-anterior and a prolonged 2nd stage of labour have variously been shown to be associated with levator trauma [18, 38, 45, 46]. Forceps delivery, however, is the most important and best-established risk factor for avulsion. In a recently published meta-analysis, forceps was shown to carry an OR for avulsion of 6.94 (4.93–9.78) compared to NVD and an OR of 4.57(3.21–6.51) compared to vacuum birth [47••]. The excess risk of avulsion in forceps delivery cannot be fully explained by an increase in space requirement during delivery. The shortened time to maximum distension and increased overall force during forceps are likely the main factor in the excess risk observed due to forceps [48].
It has been hypothesised that low forceps and non-rotational forceps may be less traumatic to the pelvic floor than mid forceps and rotational forceps. The literature regarding this issue is controversial [49, 50].
The indication for forceps may be associated with avulsion risk. Forceps delivery performed for second stage arrest as compared to delivery for foetal distress with short second stage was found to be associated with a higher major levator defects rate (63 versus 42%) though this did not reach statistical significance (P = 0.07), likely due to a power issue [51]. Vacuum is not a risk factor for avulsion [47••].
The role of episiotomy in the pathogenesis of levator avulsion is intriguing. Some authors have shown a positive correlation with avulsion [9, 52] while others failed to show any association [38, 46, 53]. A positive correlation between avulsion and episiotomy may of course reflect a difficult vaginal delivery rather than a cause and effect relationship. Epidural anaesthesia may be protective against levator injury [18, 54] by preventing premature maternal pushing and/or by paralysing the pelvic floor muscle.
Consequences of Levator Trauma
The pelvic floor is important for pelvic organ support and the levator hiatus is a potential hernia portal through which POP may develop, and it also plays a role in the maintenance of anal and urinary continence and sexual function. Trauma to the pelvic floor, not surprisingly, can lead to various morbidities.
Pelvic Organ Prolapse
POP is highly prevalent with women’s lifetime risk for POP surgery in the order of 10–20% [55, 56]. Given its high prevalence, it is obvious that improved understanding of levator trauma should have a high priority. Both levator avulsion and ballooning, i.e. an abnormally distensible hiatus, are independent risk factors for both symptoms and signs of POP [12, 57,58,59,60,61]; the latter is associated with a 6–11% increase in the risk of symptoms and signs of prolapse for each square centimetre of hiatal area on Valsalva [59].
Avulsion has been shown to be associated with ballooning or an abnormally distensible hiatus, increased muscle distensibility and a weaker muscle [62, 63]. These mechanisms may underlie the obvious epidemiological association between avulsion and POP. Women with avulsion were about twice as likely to have POP of stage II or higher than those without; the effect is mainly on the anterior and central compartment [57, 61]. Interestingly levator avulsion is associated with Green type III cystoceles (cystoceles with an intact retrovesical angle) rather than cystourethroceles (cystoceles with an open retrovesical angle or Green II) contradicting the commonly held belief that Green type III cystoceles are caused by central rather than by lateral fascial defects [64].
The effect of avulsion on the posterior compartment is less, though an association of rectal intussusception and hiatal ballooning has been reported [65].
It is unclear why women tend to present with symptoms of POP decades after pelvic floor trauma though forceps delivery and older age at first birth are associated with a shorter time to presentation [66]. John Delancey’s ‘Ship in the dock’ hypothesis may be a plausible explanation [67]. Though levator avulsion was found to be associated with more advanced POP stage, it is not associated with symptoms severity, symptoms bother or quality of life scores [41, 68, 69].
Levator trauma is not only significant as a cause of POP but also a risk factor for treatment failure. Avulsion was associated with a higher risk of vaginal pessary expulsion [70]. In a recent meta-analysis, avulsion carried an OR of 2.76 for POP recurrence after surgical repairs; hiatal area on Valsalva conveyed an OR of 1.06 for each square centimetre [71••]. Depending on the status of the pelvic floor, the risk of prolapse recurrence can be up to 90% in some women [72•] (Fig. 7).
While there has been a heated debate in regard to the use of transvaginal mesh in prolapse repairs [73, 74], POP in some women may be incurable without mesh implants [72•]. Transvaginal mesh has been shown to reduce risk of POP recurrence in women with avulsion compared with native tissue repair [72•, 75•, 76]. It however is not beneficial to women without avulsion [72•, 76]. In the modelling study by Rodrigo et al., it was implied that the risk of POP recurrence may be lowered by hiatal reduction surgery [72•]. It is obvious that a full pelvic floor assessment, preferably by imaging, should be part of the investigation of POP to allow full patient counselling and proper management; and especially in any POP treatment trials, given that both are significant confounders of recurrence risk.
Urinary Incontinence
It is a commonly held opinion that the levator ani muscle is important in urethral support and for urinary continence. However, levator avulsion was not found to be associated with either symptoms of stress urinary incontinence (SUI) or urodynamic stress incontinence (USI) [12, 60, 77,78,79]. This observation is counterintuitive given that pelvic floor muscle exercises are commonly employed in the management of SUI and USI. It is plausible that pelvic floor muscle exercises ‘train’ not just the levator ani but also other muscles that are important for maintenance of urinary continence, in particular the urethral rhabdosphincter. Furthermore, while levator avulsion was found significantly associated with increased bladder neck mobility, it is mobility of the mid-urethra that is most strongly associated with symptoms of SUI and USI [80, 81].
Faecal Incontinence
Faecal continence is achieved by the structural and functional integrity of the anorectal unit that includes the puborectalis muscle. It is plausible, therefore, that levator trauma may contribute to anal incontinence. Current evidence in this area, however, is conflicting with some showing levator avulsion as an independent risk factor for anal incontinence after primary repair of OASI [82] while other studies failed to show an association between avulsion or hiatal area and faecal incontinence [60, 83]. Again, this seems to contradict the common practice of referring patients for pelvic floor muscle exercises after OASI and for treatment of faecal incontinence; however, the same explanation as for SUI/USI may apply. Pelvic floor physiotherapy may strengthen other muscle groups that are important for anal continence apart from the puborectalis, in particular the external anal sphincter.
Sexual Function
The puborectalis muscle is sometimes called the ‘love muscle’. It is responsible for maintenance of the vaginal high pressure zone [84]. Not surprisingly, levator trauma may impact on sexual function. Women with avulsion seem to notice the effect of avulsion as a reduction in pelvic floor muscle contraction strength [85] and as increased vaginal laxity and reduced tone on intercourse [86, 87]. Sexual dysfunction as a result can impact on women’s relationship with partners and may lead to marital disharmony [88]. The significance of the levator ani muscle in sexual function may become an important consideration given the resurgence of cosmetic genitoplasty procedures aiming at tightening the vagina.
Psychological Consequences
Apart from physical morbidities, women may also suffer from psychological morbidities secondary to pelvic floor trauma. In a qualitative study on 40 women with known levator avulsion, 27 reported symptoms of post-traumatic stress disorder [88]. In this study, participants had experienced multiple barriers in seeking help and commonly felt abandoned by the system. Health care providers were reported to be dismissive, or they trivialised women’s complaints. A lack of knowledge and understanding of levator trauma among health service providers may contribute to this attitude [89] which may further impact on women’s mental health [88].
Prediction
Though a number of antenatal risk factors for levator trauma have been identified, maternal age at delivery is the only firmly established risk factor [9, 22, 41, 42]. Risk assessment to identify women at high risk of levator trauma so as to allow preventative intervention does not currently seem feasible.
Prevention
Levator trauma is a consequence of vaginal birth; hence, it is evident that CS prevents levator avulsion, childbirth-related levator over-distension and OASI. However, CS is not without risks. It is also considered more costly than vaginal birth though there is some evidence that this may not be the case [90]. If one takes into consideration the economic cost associated with loss of productivity and treatment of physical and psychological morbidities secondary to maternal trauma, CS may turn out to appear more favourable from the perspective of health economics, especially in women who intend to have only one or two children. Elective CS without medical indication is a topic of heated debate which is likely to continue [91,92,93,94,95].
It has been hypothesised that by changing the biomechanical characteristics of the pelvic floor muscle antenatally with a birth trainer, the EpiNo® device may prevent pelvic floor trauma. However in a large randomised control trial on the antepartum use of the device, no beneficial effect could be demonstrated [19].
Forceps is a well-established risk factor for pelvic floor trauma and the most important modifiable obstetric factor for prevention. Dropping forceps delivery will result in less pelvic floor injuries and will reduce the subsequent need for treatment as observed in Denmark and in the USA [96,97,98]. If assisted vaginal delivery is indicated, vacuum should be the instrument of choice.
It remains to be determined if limiting the length of 2nd stage or use of epidural/pudendal block to paralyse the pelvic floor muscle is protective against pelvic floor trauma.
Treatment
Attempts at primary repair of levator avulsion in the delivery suite have been unsuccessful [13]. It may be difficult to effect a solid repair since the muscle is likely friable after major injury, and necessarily overdistended and elongated. Secondary repair of avulsion has been tested in a surgical trial in women with symptomatic POP deemed for surgery, but its effects on prolapse recurrence and hiatal dimensions were unsatisfactory in the majority of patients [99]. It appears that reattachment of the muscle may only make sense in a subset of patients with good muscle function and mild or absent ballooning.
Over a decade ago, a surgical procedure involving the placement of a mesh sling in the ischiorectal fossa, from one obturator foramen to the anococcygeal raphe and back to the contralateral side, was trialled in patients with faecal incontinence [100]. We have adapted this technique to develop the ‘Puborectalis Sling’ (PR Sling), aiming to reduce the size of the levator hiatus. In this procedure the ends of the mesh sling are anchored to the periosteum of the inferior pubic ramus bilaterally. Results of a pilot study showed that the PR Sling significantly reduced the levator hiatus by almost 30% with no major long-term complications [101]. A randomised control study of the PR Sling is ongoing.
Current Trends in Obstetrics
Pregnant women tend to be older and have a higher BMI today as compared to previous decades. In 2016, the average age of first-time mother in Australia was 29 years compared to 28.1 years in 2006 and 26.6 years in 1996 [102,103,104]. Almost half of mothers are overweight or obese at their first antenatal visit. Given this change in demographic characteristics, it should not be surprising that women are more likely to suffer medical complications and to require emergency operative delivery. One in three births in Australia is now by CS compared to 30.8% in 2006 [104].
The optimal CS rate is unknown and the WHO no longer recommends a maximum CS rate [105]. Nonetheless, the perception is that the current CS rate is unnecessarily high, driven by ill-informed public activism. Consequently, there has been increasing pressure on professional bodies, hospitals and individual practitioners to reduce their CS rates. One example was a policy directive by New South Wales Health in 2010 where a reduction of CS rates to 20% or less by 2015 was mandated [106]. Another example was the joint consensus document by the Society for Maternal-Fetal Medicine and the American College of Obstetrics and Gynecology in 2014 where the definitions of labour dystocia was revised, aiming to reduce primary caesarean delivery [107]. This document also recommends operative vaginal delivery, including forceps, in order to reduce CS in the second stage of labour.
In spite of a lack of safety data, such interventions have led to changes in obstetric practice. In some centres, longer labours are being tolerated [108] and in others dedicated efforts are made to promote vaginal birth after CS (VBAC) [109]. In some jurisdictions like the UK and Australia, we are seeing an increase in forceps use since forceps is more likely to achieve vaginal delivery than vacuum. In Australia, for instance, the forceps rate has risen from 3.5% in 2006 to 5.3% in 2016 [103, 104]. In one large Australian teaching hospital, trainees are required to become competent in forceps delivery before they are allowed to use vacuum [110].
These trends in Obstetrics are worrying and dangerous. While a policy change to tolerate longer labours may reduce the primary CS rate, this is likely to result in a higher rate of operative vaginal deliveries in nulliparae, higher risk of unplanned CS, higher rates of OASI, shoulder dystocia, postpartum haemorrhage, and a higher rate of arterial cord pH below 7.0 as well as admission to the neonatal intensive care unit [108, 111]. In a study on outcomes in a dedicated VBAC clinic, the authors reported more than 50% emergency operative deliveries, two perinatal deaths with one secondary to uterine rupture out of 160 VBAC cases [109]. Using modelling, doubling the forceps rate in UK between 2004 and 2014 may have resulted in over 100,000 additional major cases of levator trauma and OASI [112]. A change in training policy in instrumental delivery over a 5-year period as mentioned above was estimated to result in approximately 750 additional forceps deliveries and at least 150 additional cases of major maternal trauma [109, 113].
Where Do We Go from Here?
Medicine is supposed to be scientific and evidence-based. Any change in medical practice should be supported by solid evidence and safety data, not ideology. Otherwise, we are at risk of causing harm to our patients as exemplified above. Obstetrics should be no different. As in other fields of Medicine, Obstetric patients are entitled to unbiased and full disclosure of options of management and material risks. This is both an ethical/moral and a legal requirement in many jurisdictions.
Antenatal consent for an attempt at normal vaginal delivery has recently been a subject of debate [114, 115]. Opponents of antenatal consent argue that childbirth is a natural process, not a procedure or treatment and hence antenatal consent is not indicated [115]. However in the 2015 case of Montgomery v Lanarkshire Health Board in the UK [116] and in a recent case in Australia [117], the courts were clear that clinicians have a duty to warn patients of all material risks, defined as all matters a patient is either known to, or would be likely to; consider important in their circumstances [118]. It has recently been shown that only about 1/3 of primiparous women aiming at vaginal delivery at two tertiary Australian obstetric units achieved a normal vaginal delivery without sustaining levator or anal sphincter injuries [119]. Women should be made aware of the degree of personal risk in an attempt at natural birth and the overall and relative risks of interventions that might be indicated through a proper informed consent process, and they should be involved in obstetric decision-making. They need to be treated as adults [114].
Conclusion
Our fixation on the CS rate has driven changes in Obstetric practice that are dangerous. It is evident that vaginal birth is more traumatic than is generally assumed. Maternal birth trauma encompasses not just obstetric anal sphincter tears but also levator avulsion and hiatal over-distension. These forms of musculo-skeletal trauma can have long-term physical and psychological consequences. In the face of increasing pressure and interference from political activists ill-informed policy makers, professional bodies and peers, perinatal health care providers need to understand and recognise the significance of somatic birth trauma and its potential impact on women’s health.
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
Mant J, Painter R, Vessey M. Epidemiology of genital prolapse: observations from the Oxford Family Planning Association Study. Br J Obstet Gynaecol. 1997;104(5):579–85.
Swift S, Woodman P, O'Boyle A, Kahn M, Valley M, Bland D, et al. Pelvic Organ Support Study (POSST): the distribution, clinical definition, and epidemiologic condition of pelvic organ support defects. Am J Obstet Gynecol. 2005;192(3):795–806.
Hendrix S, Clark A, Nygaard I, Aragaki A, Barnabei V, McTiernan A. Pelvic organ prolapse in the Women’s Health Initiative: gravity and gravidity. Am J Obstet Gynecol. 2002;186:1160–6.
Rortveit G, Hannestad YS, Daltveit AK, Hunskaar S. Age- and type-dependent effects of parity on urinary incontinence: the Norwegian EPINCONT study. Obstet Gynecol. 2001;98(6):1004–10.
Shek K, Kruger J, Dietz H. The effect of pregnancy on hiatal dimensions and urethral mobility: an observational study. Int Urogynecol J. 2012;23:1561–7.
Blomquist J, Muñoz A, Carroll M, Handa V. Association of delivery mode with pelvic floor disorders after childbirth. JAMA. 2018;320(23):2438–47.
Dietz H. Pelvic floor trauma in childbirth. Aust NZ J Obstet Gynaecol. 2013;53:220–30.
Gainey HL. Post-partum observation of pelvic tissue damage. Am J Obstet Gynecol. 1943;46:457–66.
Kearney R, Miller J, Ashton-Miller J, Delancey J. Obstetric factors associated with levator ani muscle injury after vaginal birth. Obstet Gynecol. 2006;107(1):144–9.
Tunn R, DeLancey JO, Howard D, Thorp JM, Ashton-Miller JA, Quint LE. MR imaging of levator ani muscle recovery following vaginal delivery. Int Urogynecol J. 1999;10(5):300–7.
Dietz H, Lanzarone V. Levator trauma after vaginal delivery. Obstet Gynecol. 2005;106:707–12.
Dietz HP, Steensma AB. The prevalence of major abnormalities of the levator ani in urogynaecological patients. BJOG Int J Obstet Gynaecol. 2006;113(2):225–30.
Dietz H, Gillespie A, Phadke P. Avulsion of the pubovisceral muscle associated with large vaginal tear after normal vaginal delivery at term. Aust NZ J Obstet Gynaecol. 2007;47:341–4.
Wallner C, Wallace C, Maas C, Lange M, Lahaye M, Moayeri N, et al. A high resolution 3D study of the female pelvis reveals important anatomical and pathological details of the pelvic floor. Neurourol Urodyn. 2009;28(7):668–70.
Lien KC, Mooney B, DeLancey JO, Ashton-Miller JA. Levator ani muscle stretch induced by simulated vaginal birth. Obstet Gynecol. 2004;103(1):31–40.
Svabik K, Shek K, Dietz H. How much does the levator hiatus have to stretch during childbirth? Br J Obstet Gynaecol. 2009;116:1657–62.
Dietz H, Lanzarone V. Levator trauma after vaginal delivery. Obstet Gynecol. 2005;106(4):707–12.
Shek K, Dietz H. Intrapartum risk factors of levator trauma. Br J Obstet Gynaecol. 2010;117:1485–92.
Kamisan Atan I, Shek K, Langer S, Guzman-Rojas R, Caudwell-Hall J, Daly J, et al. Does the Epi-No birth trainer prevent vaginal birth-related pelvic floor trauma? A multicentre prospective randomised controlled trial. BJOG. 2016;123(6):995–1003.
Chan SSCCR, Yiu AKW, Lee LLL, Pang AWL, CHoy KW, Leung TY, et al. Prevalence of levator ani muscle injury in Chinese women after first delivery. UOG. 2012;39:704–9.
Valsky DV, Lipschuetz M, Bord A, Eldar I, Messing B, Hochner-Celnikier D, et al. Fetal head circumference and length of second stage of labor are risk factors for levator ani muscle injury, diagnosed by 3-dimensional transperineal ultrasound in primiparous women. Am J Obstet Gynecol. 2009;201:91e1–7.
Caudwell-Hall J, Kamisan Atan I, Brown C, Guzman Rojas R, Langer S, Shek KL, et al. Can pelvic floor trauma be predicted antenatally? Acta Obstet Gynecol Scand. 2018;97(6):751–7.
Abdool Z, Lindeque B, Dietz H. The impact of childbirth on pelvic floor morphology in primiparous Black South African women: a prospective longitudinal observational study. Int Urogynecol J. 2018;29(3):369–75.
Durnea C, O’Reilly B, Khashan A, Durnea U, Smyth M, Dietz H. Status of the pelvic floor in young primiparous women. Urosound Obstet Gynecol. 2015;46(3):356–62.
Turel F, Caagbay D, Dietz H. The prevalence of major birth trauma in Nepali women. J Ultrasound Med. 2018;37:2803–9.
Chan S, Cheung R, Yiu K, Lee L, Chung T. Pelvic floor biometry in Chinese primiparous women 1 year after delivery: a prospective observational study. Ultrasound Obstet Gynecol. 2014;43:466–74.
Shek KL, Green K, Caudwell-Hall J, Guzman-Rojas R, Dietz H. Perineal and vaginal tears are clinical markers for occult levator ani trauma: a retrospective observational study. Ultrasound Obstet Gynecol. 2016;47(2):224–7.
Valsky DV, Cohen SM, Lipschuetz M, Hochner-Celnikier D, Daum H, Yagel I, et al. Third- or fourth-degree intrapartum anal sphincter tears are associated with levator ani avulsion in primiparas. J Ultrasound Med. 2016;35(4):709–15.
Dietz HP, Hyland G, Hay-Smith J. The assessment of levator trauma: a comparison between palpation and 4D pelvic floor ultrasound. Neurourol Urodyn. 2006;25(5):424–7.
Dietz H, Bernardo M, Kirby A, Shek K. Minimal criteria for the diagnosis of avulsion of the puborectalis muscle by tomographic ultrasound. Int Urogynecol J. 2010;22(6):699–704.
Shek K, Chantarasorn V, Langer S, Dietz H. Does levator trauma ‘heal’? Ultrsound Obstet Gynecol. 2012;40:570–5.
Branham V, Thomas J, Jaffe T, Crockett M, South M, Jamison M, et al. Levator ani abnormality 6 weeks after delivery persists at 6 months. Am J Obstet Gynecol. 2007;197(1):65.e1–6.
Chan S, Cheung R, Lee L, Choy R, Chung T. Longitudinal follow-up of levator ani muscle avulsion: does a second delivery affect it? Ultrasound Obstet Gynecol. 2017;50(1):110–5.
Brooks S, Zerba E, Faulkner J. Injury to muscle fibres after single stretches of passive and maximally stimulated muscle in mice. J Physiol. 1995;488(2):459–69.
Dietz HP, Tekle H, Williams G. Pelvic floor structure and function in women with vesicovaginal fistula. J Urol. 2012;188(5):1772–7.
Dietz H, Shek K, Clarke B. Biometry of the pubovisceral muscle and levator hiatus by three-dimensional pelvic floor ultrasound. Ultrasound Obstet Gynecol. 2005;25:580–5.
Dietz H, De Leon J, Shek K. Ballooning of the levator hiatus. Ultrasound Obstet Gynecol. 2008;31:676–80.
Caudwell-Hall J, Kamisan Atan I, Martin A, Guzman Rojas R, Langer S, Shek KL, et al. Intrapartum predictors of maternal levator ani injury. Acta Obstet Gynecol Scand. 2017;96:426–31.
Kamisan Atan I, Lin S, Herbison P, Dietz H, Wilson PD, ProLong Study Group. It is the first birth that does the damage: a cross-sectional study 20 years after delivery. Int Urogynecol J. 2018;29(11):1637–43.
Kamisan Atan I, Gerges B, Shek K, Dietz H. The association between vaginal parity and hiatal dimensions: a retrospective observational study in a tertiary urogynaecological. BJOG. 2015;122:867–72.
Oversand S, Staff A, Sandvik L, Volloyhaug I, Svenningsen R. Levator ani defects and the severity of symptoms in women with anterior compartment pelvic organ prolapse. Int Urogynecol J. 2018;29(1):63–9.
Dietz H. Does delayed childbearing increase the risk of levator injury in labour? Aust NZ J Obstet Gynaecol. 2007;47:491–5.
Rahmanou P, Caudwell-Hall J, Kamisan Atan I, Dietz H. The association between maternal age at first delivery and risk of obstetric trauma. Am J Obstet Gynecol. 2016;215:451.e1–7.
Shek K, Chantarasorn V, Dietz H. Can levator avulsion be predicted antenatally? Am J Obstet Gynecol. 2010;202(6):586.e1–6.
Valsky D, Lipschuetz M, Bord A, Eldar I, Messing B, Hochner-Celnikier D, et al. Fetal head circumference and length of second stage of labor are risk factors for levator ani muscle injury, diagnosed by 3-dimensional transperineal ultrasound in primiparous women. Am J Obstet Gynecol. 2009;201:91.e1–7.
Speksnijder L, Oom M, Van Bavel J, Steegers E, Steensma A. Association of levator injury and urogynecological complaints in women after their first vaginal birth with and without mediolateral episiotomy. Am J Obstet Gynecol. 2019;220:93.e1–9.
•• Friedman T, Eslick G, Dietz H. Delivery mode and the risk of levator muscle avulsion: a meta-analysis. Int Urogynecol J. 2019. https://doi.org/10.1007/s00192-018-3827-8 This meta anaiysis establishes forceps an important risk factor for levator avulsion).
Caudwell-Hall J, Weishaupt J, Dietz H. Contributing factors in forceps associated pelvic floor trauma. Int Urogynecol J. 2019. https://doi.org/10.1007/s00192-019-03869-1.
García Mejido J, Aquise Pino A, Fernández Palacín A, de la Fuente VP, Ramos Vega Z, Sainz BJ. The correlation between the type of forceps application and the rate of levator ani muscle avulsion: a prospective cohort study. Neurourol Urodyn. 2018;37(5):1731–6.
Ortega I, Dietz HP, Medina-Castellano M, Laseca-Modrego M, Perez-Morales ME, Fernández-Mederos A, et al. Kielland rotational forceps: is it safe for the mother? EUGA 11th Annual Congress 2018.
Kearney R, Fitzpatrick M, Brennan S, Behan M, Miller J, Keane D, O'Herlihy C., DeLancey J.O.L. Levator ani injury in primiparous women with forceps delivery for fetal distress, forceps for second stage arrest, and spontaneous delivery. Int J Gynaecol Obstst 2010;111(1):19–22.
Lammers K, Fütterer JJ, Inthout J, Prokop M, Vierhout ME, Kluivers KB. Correlating signs and symptoms with pubovisceral muscle avulsions on magnetic resonance imaging. Am J Obstet Gynecol. 2013;208(2):148.e1–7.
Cassadó J, Pessarrodona A, Rodriguez-Carballeira M, Hinojosa L, Manrique G, Márquez A, et al. Does episiotomy protect against injury of the levator ani muscle in normal vaginal delivery? Neurourol Urodyn. 2014;33(8):1212–6.
Kruger J, Budgett S, Wong V, Nielsen P, Nash M, Smalldridge J, et al. Characterizing levator-ani muscle stiffness pre- and post-childbirth in European and Polynesian women in New Zealand: a pilot study. Acta Obstet Gynecol Scand. 96:1234–42.
Olsen AL, Smith VJ, Bergstrom JO, Colling JC, Clark AL. Epidemiology of surgically managed pelvic organ prolapse and urinary incontinence. Obstet Gynecol. 1997;89(4):501–6.
Smith F, Holman C, Moorin R, Tsokos N. Lifetime risk of undergoing surgery for pelvoc organ prolapse. Obstet Gynecol. 2010;116:1096–100.
Dietz H, Simpson J. Levator trauma is associated with pelvic organ prolapse. Br J Obstet Gynaecol. 2008;115:979–84.
DeLancey J, Morgan D, Fenner D, Kearney R, Guire K, Miller J, et al. Comparison of levator ani muscle defects and function in women with and without pelvic organ prolapse. Obstet Gynecol. 2007;109(2):295–302.
Dietz HP, Franco AV, Shek KL, Kirby A. Avulsion injury and levator hiatal ballooning: two independent risk factors for prolapse? An observational study. Acta Obstet Gynecol Scand. 2012;91(2):211–4.
Handa V, Blomquist J, Roem J, Munoz A, Dietz H. Pelvic floor disorders after obstetric avulsion of the levator ani muscle. Female Pelvic Med Reconstr Surg. 2019;25:3–7.
Volløyhaug I, Mørkved S, Salvesen K. Association between pelvic floor muscle trauma and pelvic organ prolapse 20 years after delivery. Int Urogynecol J. 2016;27:39–45.
Abdool Z, Shek K, Dietz H. The effect of levator avulsion on hiatal dimensions and function. Am J Obstet Gynecol. 2009;201:89.e1–5.
Handa VL, Blomquist JL, Roem J, Muñoz A, Dietz HP. Levator morphology and strength after obstetric avulsion of the levator ani muscle. Female Pelvic Med Reconstr Surg. 2018. https://doi.org/10.1097/SPV.0000000000000641.
Eisenberg V, Chantarasorn V, Shek K, Dietz H. Does levator ani injury affect cystocele type? Ultrasound Obstet Gynecol. 2010;36(5):618–23.
Rodrigo N, Shek K, Dietz H. Rectal intussusception is associated with abnormal levator structure and morphometry. Tech Coloproctol. 2011;15:39–43.
Thomas V, Shek KL, Rojas RG, Dietz HP. Temporal latency between pelvic floor trauma and presentation for prolapse surgery: a retrospective observational study. Int Urogynecol J. 2015;26(8):1185–9.
Delancey JO. Anatomy. In: Cardon L, Staskin D, editors. Textbook of female urology and urogynaecology. London, UK, 2001.
Endress E, Shek KL, Dietz HP. Levator avulsion is not associated with symptom bother of female pelvic organ prolapse. Arch Gynecol Obstet. 2015;292(3):629–33.
Yu CH, Chan SSC, Cheung RYK, Chung TKH. Prevalence of levator ani muscle avulsion and effect on quality of life in women with pelvic organ prolapse. Int Urogynecol J. 2018;29(5):729–33.
Cheung R, Lee J, Lee L, Chung T, Chan SSC. Levator ani muscle avulsion is a risk factor for expulsion within 1 year of vaginal pessary placed for pelvic organ prolapse. Ultrasound Obstet Gynecol. 2017;50:776–80.
•• Friedman T, Eslick G, Dietz H. Risk factors for prolapse recurrence: systematic review and meta-analysis. Int Urogynecol J. 2018;29:13–21 This meta analysis showed that levator avulsion is an important risk factor for prolpase recurrence.
• Rodrigo N, Wong V, Shek KL, Martin A, Dietz H. The use of 3-dimensional ultrasound of the pelvic floor to predict recurrence risk after pelvic reconstructive surgery. ANZJOG. 2014;54(3):206–11 This modelling study showed the recurrence risk of pelvic organ prolapse in relation to pelvic floor muslce status and hiatal ballooning.
Wong V, Shek K. The mesh debate: transvaginal anterior anchored mesh should not be abandoned. Aust NZ J Obstet Gynaecol. 2017;57(1):105–7.
Mowat A, Maher C. Transvaginal mesh: let's not repeat the mistakes of the past. Aust NZ J Obstet Gynaecol. 2017;57(1):108–10.
• Svabik K, Martan A, Masata J, El Haddad R, Hubka P. Comparison of vaginal mesh repair with sacrospinous vaginal colpopexy in the management of vaginal vault prolapse after hysterectomy for patients with levator ani avulsion: randomized controlled trial. UOG. 2014;43(4):365–71 This RCT clearly showed the efficacy of transvaginal mesh repair in patients with high risk of levator avulsion and were at high risk of recurrence.
Wong V, Shek KL, Goh J, Krause H, Martin A, Dietz H. Cystocele recurrence after anterior colporrhaphy with and without mesh use. Eur J Obstet Gynecol Reprod Biol. 2014;172:131–5.
Morgan D, Cardoza P, Guire K, Fenner D, DeLancey J. Levator ani defect status and lower urinary tract symptoms in women with pelvic organ prolapse. Int Urogynecol J. 2010;21(1):47–52.
Dietz H, Kirby A, Shek K, Bedwell P. Does avulsion of the puborectalis muscle affect bladder function? Int Urogynecol J. 2009;20:967–72.
García Mejido JA, Valdivieso Mejias P, Fernández Palacín A, Bonomi Barby MJ, De la Fuente VP, Sainz Bueno JA. Evaluation of isolated urinary stress incontinence according to the type of levator ani muscle lesion using 3/4D transperineal ultrasound 36 months post-partum. Int Urogynecol J. 2017;28(7):1019–26.
Shek K, Dietz H, Kirby A. The effect of childbirth on urethral mobility. J Urol. 2010;184(2):629–34.
Pirpiris A, Shek K, Kay P, Dietz H. Urethral mobility and urinary incontinence. Ultrasound Obstet Gynecol. 2010;36:507–11.
Shek K, Guzmán Rojas R, Dietz HP. Residual defects of the external anal sphincter following primary repair: an observational study using transperineal ultrasound. Ultrasound Obstet Gynecol. 2014;44(6):704–9.
Chantarasorn V, Shek K, Dietz H. Sonographic detection of puborectalis muscle avulsion is not associated with anal incontinence. Aust NZ J Obstet Gynaecol. 2011;51(2):130–5.
Jung S, Pretorius D, Padda B, Weinstein M, Nager C, den Boer D, et al. Vaginal high-pressure zone assessed by dynamic 3-dimensional ultrasound images of hte pelvic floor. Am J Obstet Gynecol. 2007;197(1):52.e1–7.
Dietz H, Shek K, Chantarasorn V, Langer S. Do women notice the effect of childbirth-related pelvic floor trauma? Int Urogynecol J. 2011;22(S1):S66–7.
Thibault-Gagnon S, Yusuf S, Langer S, Shek KL, Dietz HP. Do women notice the impact of childbirth-related levator trauma on pelvic floor and sexual function? Int Urogynecol J Pelvic Floor Dysfunct. 2014;25:1389–98.
van Delft K, Sultan AH, Thakar R, Schwertner-Tiepelmann N, Kluivers K. The relationship between postpartum levator ani muscle avulsion and signs and symptoms of pelvic floor dysfunction. BJOG. 2014;121(9):1164–71.
Skinner E, Barnett B, Dietz HP. Psychological consequences of pelvic floor trauma following vaginal birth: a qualitative study from two Australian tertiary maternity units. Archives of Women’s Mental Health. 2018;21:341–51.
Herron-Marx S, Williams A, Hicks C. A Q methodology study of women’s experience of enduring postnatal perineal and pelvic floor morbidity. Midwifery. 2007;23:322–34.
Bost B. Caesarean delivery on demand: what will it cost? Obstet Gynecol. 2003;188(6):1418–23.
Duperron L. Should patients be entitled to caesarean section on demand? Can Fam Physician. 2011;57:1246–8.
Shek KL, Dietz HP. Elective caesarean delivery—the right choice for whom? Current Women’s Health Reviews. 2013;9:50–5.
Robson SJ, de Costa CM. Thirty years of the World Health Organisation’s target caesarean section rate: time to move on. Med J Aust. 2017;206(4):181–5.
Nygaard I. Should women be offered elective cesarean section in the hope of preserving pelvic floor function?[comment]. Int Urogynecol J. 2005;16(4):253–4.
Sand PK. Should women be offered elective cesarean section in the hope of preserving pelvic floor function?[see comment]. Int Urogynecol J. 2005;16(4):255–6.
Lisonkova S, Lavery JA, Ananth CV, Chen I, Muraca G, Cundiff GW, et al. Temporal trends in obstetric trauma and inpatient surgery for pelvic organ prolapse: an age-period-cohort analysis. Am J Obstet Gynecol. 2016;215:208.e1–12.
Dietz HP. Comments on Løwenstein et al.: incidence and lifetime risk of pelvic organ prolapse surgery in Denmark from 1977 to 2009. Int Urogynecol J. 2015;26(7):1089.
Løwenstein E, Ottesen B, Gimbel H. Incidence and lifetime risk of pelvic organ prolapse surgery in Denmark from 1977 to 2009. Int Urogynecol J. 2015;26(1):49–55.
Dietz HP, Shek KL, Daly O, Korda A. Can levator avulsion be repaired surgically? A prospective surgical pilot study. IUGJ. 2013;24:1011–5.
Rosenblatt P. Trans-obturator post-anal sling (TOPAS) procedure for fecal incontinence. HJournal of Minimally Invasive Gynecology. 2007;14(S152).
Dietz HP, Korda A, Benness C, Wong V, Shek KL, Daly O. Surgical reduction of the levator hiatus. Neurourol Urodyn. 2012;31(6):862–3.
Anonymous. Australia’s mothers and babies 1996. Available at https://www.aihw.gov.au. Accessed on 30th Jan 2019.
Anonymous. Australia’s mothers and babies 2006. Available at https://www.aihw.gov.au. Accessed on 30th Jan 2019.
Anonymous. Australia’s mothers and babies 2016. Available at https://www.aihw.gov.au. Accessed on 30th Jan 2019.
Department of Reproductive Health and Research, World Health Organization. WHO statement on caesarean section rates: WHO/RHR/15.02. Geneva: WHO, 2015.
Anonymous. Maternity-towards normal birth in NSW, in PD 2010-045, N. Health, Editor. Sydney: NSW Health, 2010. [Accessed on 23 June 16.] Available from URL: www0.health.nsw.gov.au/policies/pd/2010/pdf/PD2010_045.pdf
American College of Obstetricians and Gynecologists (College); Society for Maternal-Fetal Medicine, Caughey AB, Cahill AG, Guise JM, Rouse DJ. Safe prevention of the primary caesarean delivery. Obstet Gynecol. 2014;123:693–711.
Zipori Y, Grunwald O, Ginsberg Y, Beloosesky R, Weiner Z. The impact of extending the second stage of labor to prevent primary cesarean section on maternal and neonatal outcomes. Am J Obstet Gynecol. 2019:191.e1–7.
Gardner K, Henry A, Thou S, Davis G, Miller T. Improving VBAC rates: the combined impact of two management strategies. Aust NZ J Obstet Gynaecol. 2014;54:327–32.
Skinner S, Davies-Tuck M, Wallace E, Hodges R. Perinatal and maternal outcomes after training residents in forceps before vacuum instrumental birth. Obstet Gynecol. 2017;130(1):151–8.
Lipschuetz M, Cohen S, Lewkowicz A, Amsalem H, Haj Yahya R, Levitt L, et al. Prolonged second stage of labor: causes and outcomes. Harefuah. 2018;157(11):685–90.
Dietz H, Campbell S. Toward normal birth—but at what cost. Am J Obstet Gynecol. 2016;15(4):439–44.
Dietz H, Shek K, Callaghan S. Letter to the editor: perinatal and maternal outcomes after training residents in forceps before vacuum instrumental birth. Obstet Gynecol. 2017;130:910.
Dietz HP, Callaghan S. We need to treat pregnant women as adults: women should be consented for an attempt at normal vaginal birth as for operative delivery, with risks and potential complications explained. ANZJOG. 2018;58(6):701–3.
Petersen RW. Vaginal delivery: an argument against requiring consent. ANZJOG. 2018;58(6):704–6.
Anonymous. Montgomery v Lanarkshire Health Board. London: Supreme Court of the United Kingdom, 2015.
KS and XT v Calvary Health Care ACT trading as Calvary Hospital and Dr Andrew Foote [2018] ACTSC 84 (5 April 2018).
Anonymous. Roger v Whitaker. Aust Law J. 1993;67:47–55.
Caudwell-Hall J, Kamisan Atan I, Guzman Rojas R, Langer S, Shek KL, Dietz HP. Atraumatic normal vaginal delivery: how many women get what they want? Am J Obstet Gynecol. 2018;219:379.e1–8.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of Interest
Ka Lai Shek reports an unrestricted educational grant from GE Medical during the time of this study and Peter Hans Dietz also reports honoraria and flight costs from GE Medical. Otherwise, the authors declare no other conflict of interest.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This article is part of the Topical Collection on Urogynecology
Rights and permissions
About this article
Cite this article
Shek, K.L., Dietz, H.P. Vaginal Birth and Pelvic Floor Trauma. Curr Obstet Gynecol Rep 8, 15–25 (2019). https://doi.org/10.1007/s13669-019-0256-8
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13669-019-0256-8