Published online Aug 19, 2026. doi: 10.5498/wjp.117791
Revised: March 30, 2026
Accepted: May 7, 2026
Published online: August 19, 2026
Processing time: 153 Days and 0.8 Hours
Traditional low forceps midwifery requires lateral episiotomy, which affects the delivery experience of the parturient, impairs the recovery of postpartum pelvic floor muscle strength, and is associated with complications such as perineal pain and infection. These factors impose physical and psychological burdens and may increase postpartum depression. Non-invasive low forceps midwifery controls the delivery speed of the fetal head and applies traction during intervals between uterine contraction to assist gradual delivery without lateral episiotomy, thereby facilitating recovery of postpartum pelvic floor muscle strength.
To investigate the effect of non-invasive low forceps midwifery on postpartum pelvic floor muscle strength and postpartum depression in singleton full-term pregnant women.
Clinical data from 70 parturients who underwent forceps-assisted delivery at Suzhou Ninth People’s Hospital (Affiliated with Soochow University) from Ja
There were no significant differences in baseline data, number of forceps tractions, or duration of the second stage of labor between groups (P > 0.05). However, the observation group had less intrapartum bleeding and lower bleeding at 24 hours postpartum than the control group (P < 0.05). Postpartum pain intensity was also lower in the observation group, with reduced Visual Analogue Scale scores at 12 hours and 24 hours (P < 0.05). Regarding complications, the severity of perineal tears was greater in the control group (Z = -2.368, P = 0.018) and the incidence of postpartum urinary retention was higher in the control group than in the observation group (χ2 = 3.968, P = 0.046). Compared with the control group, the observation group reported better delivery experience scores (P < 0.05). Follow-up at six weeks, three months, and six months postpartum revealed higher pelvic floor muscle strength and lower Edinburgh Postpartum Depression Scale scores in the observation group than in the control group (P < 0.05).
Compared with traditional low forceps midwifery with episiotomy, non-invasive low forceps midwifery effec
Core Tip: Traditional low forceps-assisted delivery requires episiotomy, which may negatively affect childbirth experience and recovery of postpartum pelvic floor muscle strength, potentially contributing to postpartum depressive symptoms. This study highlights that non-invasive low forceps-assisted delivery facilitates the recovery of postpartum pelvic floor muscle strength and helps alleviate postpartum depressive symptoms compared with traditional low forceps-assisted delivery with episiotomy.
- Citation: Zhong YJ, Zhang XY, Shi Y, Chen X, Jin DD, Huang YY. Effect non-invasive low forceps delivery on pelvic floor muscle strength and postpartum depression in singleton full-term pregnant women. World J Psychiatry 2026; 16(8): 117791
- URL: https://www.wjgnet.com/2220-3206/full/v16/i8/117791.htm
- DOI: https://dx.doi.org/10.5498/wjp.117791
Vaginal delivery is a natural mode of childbirth, and its smooth progression depends on rhythmic and effective myo
In this retrospective study, clinical data from 70 parturients assessed to require forceps-assisted delivery at Suzhou Ninth People’s Hospital (Affiliated with Soochow University) from January 2024 to June 2025 were collected. According to the midwifery method, patients were divided into a control group (n = 35) and an observation group (n = 35). The control group received traditional low forceps midwifery with episiotomy, whereas the observation group underwent non-invasive low forceps midwifery.
Inclusion criteria: (1) Age ≥ 20 years; (2) Singleton pregnancy; (3) Full-term pregnancy; (4) No obstetric complications; (5) Met indications for forceps midwifery: Viable fetus, fully dilated cervix, occipital or vertex presentation, the bony part of the fetal head is ≤ 3 cm below the spine, and ruptured fetal membrane; and (6) Receipt of routine standardized rehabilitation guidance after lochia clearance.
Exclusion criteria: (1) Pregnancy via assisted reproductive technology; (2) Scarred uterus; (3) Head basin disproportion; (4) Fetal malformation or death; (5) Abnormal birth canal; (6) Severe fetal head deformation; (7) Estimated fetal weight ≥ 4.0 kg; (8) Diagnosed mental illness before delivery; and (9) Inability to communicate normally.
The control group underwent traditional low forceps midwifery with episiotomy. During the first stage of labor, midwives guided correct breathing and closely monitored fetal heart rate and labor progress. During the second stage, episiotomy-assisted low forceps midwifery was performed. The parturient was placed in a semi-reclining position on a multifunctional delivery bed, followed by routine disinfection of the external genitalia and sterile draping. Cervical dilation and fetal head position (≤ 3 cm below the spinous process) were confirmed. Then, the parturient was positioned in the lithotomy position, and local anesthesia at the episiotomy site or bilateral perineal nerve block anesthesia was administered, followed by electrocardiogram monitoring and lateral episiotomy. The midwife carefully placed the left and right lobes of the forceps, ensuring no maternal soft tissue or umbilical cord was entrapped, and then locked. Traction was applied along the pelvic axis during uterine contraction. After exposure of the fetal forehead, the forceps were released and removed. In occiput posterior position, traction was adjusted laterally, and the forceps were removed when the nasal root or forehead reached the lower edge of the phalangeal joint (the right lobe forceps were removed first before the left lobe forceps). The fetus was then delivered with uterine contractions and abdominal pressure, followed by umbilical cord clamping (2 cm), placental delivery, and assessment of maternal and neonatal status.
The observation group underwent non-invasive low forceps midwifery. Management during the first stage was the same as in the control group. In the second stage, the parturient was positioned similarly, and standard routine disinfection and draping were performed. After confirming cervical dilation and fetal head position (3 cm below the spinous process), catheterization was performed, and the forceps were checked and lubricated. The left and right leaf forceps were placed sequentially and locked, ensuring no umbilical cord or soft tissue entrapment. Traction force and speed was adjusted according to perineal tension. Midwives controlled the speed of fetal head delivery (lightly holding the fetal head) while providing moderate perineal protection and verbal encouragement. Closely monitoring of contractions and labor progress was maintained. Once the fetal head crowned, the forceps were promptly removed and slowly slid out along the fetal head. Delivery was completed with uterine contractions and abdominal pressure, followed by umbilical cord clamping (2 cm), placental delivery, and assessment of maternal and neonatal status.
Perioperative indicators: These included the number of forceps tractions, the amount of intrapartum bleeding, the duration of the second stage of labor, the amount of bleeding 24 hours postpartum, and postpartum perineal pain. Postpartum perineal pain was assessed using the Visual Analogue Scale (VAS) at 12 hours and 24 hours postpartum (0-10 points; higher scores indicate greater pain).
Complications: Maternal complications included cervical laceration and perineal tear (grade I: Vaginal mucosa and perineal skin tear with minimal bleeding; grade II: Involvement of perineal muscles and vaginal mucosa with increased bleeding; grade III: Deep perineal and external anal sphincter laceration), postpartum urinary retention, and postpartum perineal infection. Neonatal complications included skin abrasions, scalp hematoma, and neonatal asphyxia.
Childbirth experience: One day before discharge, the Childbirth Experience Questionnaire (2.0)[8] was used to assess delivery experience. The questionnaire includes self-ability (6 items), professional support (6 items), safety perception (4 items), and participation (3 items), with scores ranging from 19 points to 76 points; higher scores indicate better childbirth experience.
Postpartum pelvic floor muscle strength: At six weeks, three months, and six months postpartum, pelvic floor muscle strength and electromyography were assessed by the same experienced obstetrician using standardized instruments. Type I pelvic muscle fiber endurance was graded from 0 (0 second) to 5 (≥ 5 seconds), and type II pelvic floor muscle fiber contractions were graded by repetition count. A level ≤ 3 indicated reduced muscle strength. Electromyography was measured using a vaginal electrode: Resting values were recorded under relaxation, and maximal values were obtained during rapid contractions (five repetitions at 10-seconds intervals). Normal values were 2-4 V (resting) and 35-45 V (maximum).
Postpartum depression: At six weeks, three months, and six months postpartum, depression was evaluated using the Edinburgh Postnatal Depression Scale (EPDS)[9]. The scale includes 10 items scored on four levels, namely: Never, 0 points; occasionally, 1 point; often, 2 points; and always, 3 points. The total score was 0-30 points; higher scores indicate more severe depression.
IBM SPSS Statistics version 25.0 was used for data analysis. Measurement data were analyzed to for normality using the Shapiro-Wilk test and expressed as mean ± SD. Between-group comparisons were performed using the independent samples t-test. Repeated measures within groups were analyzed using analysis of variance. Count data are presented as n (%) and were compared using the χ2 test. Ranked data were analyzed using the rank-sum (Z) test. A significance level of α = 0.05 was applied, with P < 0.05 indicating statistical significance.
No significant differences were observed between the two groups in age, body mass index, parity, education level, gestational age at delivery, indications for forceps-assisted delivery, or neonatal sex and birth weight (P > 0.05; Table 1).
| Baseline data | Control group (n = 35) | Observation group (n = 35) | t/χ2 value | P value |
| Age (years) | 0.324 | 0.569 | ||
| < 35 | 28 (80.00) | 26 (74.29) | ||
| ≥ 35 | 7 (20.00) | 9 (25.71) | ||
| Body mass index (kg/m2) | 25.43 ± 1.65 | 25.63 ± 1.71 | 0.498 | 0.620 |
| Type of maternity | 0.357 | 0.550 | ||
| Primipara | 29 (82.86) | 27 (77.14) | ||
| Multipara | 6 (17.14) | 8 (22.86) | ||
| Educational level | 0.651 | 0.722 | ||
| Junior high school and below | 11 (31.43) | 8 (22.86) | ||
| Secondary/high school | 15 (42.86) | 17 (48.57) | ||
| College degree or above | 9 (25.71) | 10 (28.57) | ||
| Delivery gestational week (weeks) | 38.72 ± 1.03 | 38.95 ± 1.26 | 0.836 | 0.406 |
| Types of forceps delivery required | 0.253 | 0.969 | ||
| Fetal distress | 13 (37.14) | 14 (40.00) | ||
| Uterine atony | 8 (22.86) | 9 (25.71) | ||
| Abnormal position of the fetal head | 6 (17.14) | 5 (14.29) | ||
| Prolonged second stage of labor | 8 (22.86) | 7 (20.00) | ||
| Gender of newborn | 0.233 | 0.629 | ||
| Baby boy | 19 (54.29) | 21 (60.00) | ||
| Baby girl | 16 (45.71) | 14 (40.00) | ||
| Newborn birth weight (kg) | 3.55 ± 0.42 | 3.43 ± 0.39 | 1.239 | 0.219 |
There were no significant differences in the number of forceps tractions or the duration of the second stage of labor between the two groups (P > 0.05). However, the amount of bleeding intrapartum and 24 hours postpartum were lesser in the observation group than in the control group (P < 0.05). Postpartum pain intensity was also lower in the observation group, with reduced VAS scores at 12 hours and 24 hours postpartum (P < 0.05; Table 2).
| Perioperative observation indicators | Control group (n = 35) | Observation group (n = 35) | t value | P value |
| Number of forceps traction (times) | 1.26 ± 0.18 | 1.34 ± 0.21 | 1.711 | 0.092 |
| Amount of bleeding during delivery (mL) | 267.19 ± 19.76 | 221.47 ± 17.28 | 10.301 | < 0.001 |
| Second stage of labor duration (minute) | 87.04 ± 7.55 | 88.59 ± 8.85 | 0.788 | 0.433 |
| Postpartum 24-hour bleeding volume (mL) | 314.87 ± 25.48 | 268.92 ± 23.51 | 7.881 | < 0.001 |
| VAS score at 12 hours postpartum (points) | 7.24 ± 0.73 | 5.38 ± 0.51 | 5.713 | < 0.001 |
| VAS score at 24 hours postpartum (points) | 5.19 ± 0.45 | 3.56 ± 0.37 | 6.398 | < 0.001 |
The severity of perineal tears was greater in the control group than in the observation group (Z = -2.368, P = 0.018), and the incidence of postpartum urinary retention was higher in the control group than in the observation group (χ2 = 3.968, P = 0.046). There were no significant differences in cervical laceration, postpartum perineal infection, or neonatal complications between the two groups (P > 0.05; Table 3).
| Complications situation | Control group (n = 35) | Observation group (n = 35) | χ2/Z value | P value |
| Cervical laceration | 2 (5.71) | 1 (2.86) | 0.348 | 0.555 |
| Perineal tear | -2.368 | 0.018 | ||
| I degree | 14 (40.00) | 9 (25.71) | ||
| II degree | 11 (31.43) | 5 (14.29) | ||
| III degree | 1 (2.86) | 0 (0.00) | ||
| Postpartum uroschesis | 6 (20.00) | 1 (2.86) | 3.968 | 0.046 |
| Postpartum perineal infection | 1 (2.86) | 0 (0.00) | 1.014 | 0.314 |
| Skin abrasions in newborns | 3 (8.57) | 2 (5.71) | 0.215 | 0.643 |
| Neonatal scalp hematoma | 3 (8.57) | 1 (2.86) | 1.061 | 0.303 |
| Neonatal asphyxia | 4 (11.43) | 2 (5.71) | 0.729 | 0.393 |
Compared with the control group, the observation group had higher scores across all dimensions of the delivery experience (self-ability, professional support, security awareness, and participation), as well as a higher total score (P < 0.05; Table 4).
| Group | n | Self-ability | Professional support | Security awareness | Participatory nature | Total score |
| Control group | 35 | 15.48 ± 2.19 | 11.56 ± 1.49 | 12.47 ± 1.72 | 6.97 ± 1.09 | 46.48 ± 5.25 |
| Observation group | 35 | 16.79 ± 2.47 | 12.35 ± 1.06 | 13.48 ± 1.94 | 8.15 ± 1.26 | 50.77 ± 5.79 |
| t value | 2.348 | 2.556 | 2.305 | 4.190 | 3.247 | |
| P value | 0.021 | 0.013 | 0.024 | < 0.001 | 0.002 |
Pelvic floor muscle strength (type I and type II muscle fibers) increased gradually at six weeks, three months, and six months postpartum (P < 0.05). At each time point, pelvic floor muscle strength levels were significantly higher in the observation group than in the control group (P < 0.05; Table 5). The pelvic floor electromyographic values (resting average and maximum fast muscle values) also increased in both groups (P < 0.05). These parameters were significantly higher in the observation group at all follow-up time points than in the control group (P < 0.05; Table 6).
| Group | n | Type I muscle fibers | Type II muscle fiber | ||||||||
| 6 weeks postpartum | 3 months postpartum | 6 months postpartum | F value | P value | 6 weeks postpartum | 3 months postpartum | 6 months postpartum | F value | P value | ||
| Control group | 35 | 2.97 ± 1.32 | 3.23 ± 1.36 | 3.95 ± 1.42 | 4.825 | 0.011 | 3.02 ± 1.18 | 3.39 ± 1.41 | 4.07 ± 1.51 | 5.261 | 0.007 |
| Observation group | 35 | 3.60 ± 1.12 | 3.98 ± 1.17 | 4.63 ± 1.28 | 6.684 | 0.002 | 3.72 ± 1.29 | 4.13 ± 1.35 | 4.84 ± 1.32 | 6.448 | 0.002 |
| t value | 2.153 | 2.473 | 2.104 | 2.369 | 2.243 | 2.271 | |||||
| P value | 0.035 | 0.016 | 0.039 | 0.021 | 0.028 | 0.026 | |||||
| Group | n | Resting average electromyographic value | Maximum electromyographic value of fast muscle | ||||||||
| 6 weeks postpartum | 3 months postpartum | 6 months postpartum | F value | P value | 6 weeks postpartum | 3 months postpartum | 6 months postpartum | F value | P value | ||
| Control group | 35 | 2.42 ± 0.51 | 2.97 ± 0.64 | 3.25 ± 0.62 | 17.760 | < 0.001 | 25.02 ± 2.71 | 27.45 ± 3.08 | 32.07 ± 4.12 | 39.840 | < 0.001 |
| Observation group | 35 | 2.79 ± 0.38 | 3.34 ± 0.48 | 3.63 ± 0.53 | 29.150 | < 0.001 | 30.25 ± 2.25 | 32.64 ± 3.32 | 35.13 ± 4.32 | 17.990 | < 0.001 |
| t value | 3.442 | 2.736 | 2.756 | 8.784 | 6.780 | 3.033 | |||||
| P value | 0.001 | 0.008 | 0.008 | < 0.001 | < 0.001 | 0.003 | |||||
The EPDS scores in both groups increased slightly at six weeks, three months, and six months postpartum, but the differences were not statistically significant (P > 0.05). At each time point, the EPDS scores were lower in the observation group than in the control group (P < 0.05; Table 7).
| Group | n | EPDS rating | ||||
| 6 weeks postpartum | 3 months postpartum | 6 months postpartum | F value | P value | ||
| Control group | 35 | 7.06 ± 2.54 | 8.12 ± 2.68 | 8.26 ± 2.62 | 2.205 | 0.115 |
| Observation group | 35 | 5.37 ± 1.73 | 6.13 ± 1.65 | 6.39 ± 2.13 | 2.877 | 0.061 |
| t value | 3.253 | 3.741 | 3.276 | |||
| P value | 0.018 | < 0.001 | 0.002 | |||
Low forceps delivery has clear advantages in managing difficult deliveries, such as cephalic dystocia and fetal distress, as it can shorten the second stage of labor and effectively solve cephalic dystocia. It is therefore widely used in clinical practice[10]. However, traditional low forceps delivery typically requires lateral episiotomy to expand the vaginal outlet, which may cause physical injury[11]. Moreover, perineal protection during traction increases operational difficulty and may be associated with greater intraoperative blood loss[12]. Therefore, it is necessary to optimize forceps delivery techniques in clinical practice to reduce maternal trauma.
Forceps-assisted delivery refers to a situation in which the bony part of the fetal head has descended below the ischial spine, allowing quick delivery and improved maternal and neonatal outcomes. However, traditional low forceps delivery involves episiotomy, and forceps are typically removed after exposure of the fetal forehead. Expansion of the operative space may increase the risk of perineal laceration, leading to significant postpartum perineal pain[13], while episiotomy is also associated with puerperal infection[14]. Kudish et al[15] noted that the combination of forceps delivery and epi
Bercovich et al[18] reported that forceps-assisted delivery with lateral episiotomy can enlarge the perineal opening, accelerate fetal delivery, shorten the second stage of labor, and reduce the risk of fetal hypoxia, brain damage, or even suffocation due to vaginal compression. This differs from our findings, as we no significant differences were observed between the observation and control groups in the duration of the second stage of labor or neonatal complications. This discrepancy may be explained by several factors. The duration of the second stage of labor is often influenced by maternal pelvic shape, uterine contraction intensity, and fetal head position; thus, even with lateral episiotomy, unfavorable conditions may still prolong the second stage of labor. Furthermore, lateral episiotomy during low forceps delivery may require greater perineal protection, which can increase resistance to traction and delay delivery speed. Maternal fear about expansion of the incision may also reduce effective pushing, further delaying delivery. Non-invasive low forceps-assisted delivery avoids additional procedures and is relatively simple to perform. When the fetal head crowns (i.e., the biparietal diameter of the fetal head crosses the pelvic outlet), the forceps are removed promptly, allowing the fetus to slide out naturally and reducing the risk of fetal skin abrasion from transitional traction. Encou
Given these advantages, non-invasive low forceps-assisted delivery may also improve maternal childbirth experience. In this study, delivery experience scores were higher in the observation group than in the control group. This may be attributed to reduced blood loss and fewer perineal injuries, and the absence of increased fetal risk, as well as fewer maternal complications and less postpartum pain, resulting in greater comfort and safety during delivery. Additionally, during delivery, prolonged compression of pelvic floor tissues can lead to stretching and injury of muscles, fascia, and nerves, significantly reducing pelvic floor muscle strength[19]. Without effective postpartum rehabilitation, stress urinary incontinence may occur[20]. Previous studies have shown that more severe perineal tears during childbirth are associated with a higher incidence of pelvic floor dysfunction[21,22]. In this study, follow-up at six weeks, three months, and six months postpartum demonstrated higher pelvic floor muscle strength and electromyographic parameters in the observation group than in the control group. This may be because lateral episiotomy during traditional forceps delivery causes direct injury to pelvic floor muscles and nerves, impairing nerve signal transduction of pelvic floor muscles. In addition, traction and compression from forceps on the pelvic floor muscles may further exacerbate pelvic floor damage, reducing overall function and muscle strength. In contrast, non-invasive forceps delivery minimizes tissue damage by reducing excessive traction and preserving perineal integrity, thereby exerting minimal impact on postpartum pelvic floor muscle strength. VanWiel et al[23] reported a close association between pelvic floor health and postpartum psychological health, while Zhao and Zhang[24] found that negative childbirth experiences increase the risk of postpartum depression. These findings indirectly support our results, in which EPDS scores at six weeks, three months, and six months postpartum were significantly lower in the observation group than in the control group. This may be related to reduced childbirth-related trauma and fewer functional impairments, leading to improved body image and psychological status. Additionally, decreased pelvic floor muscle strength and urinary dysfunction associated with forceps use may contribute to urinary incontinence, which can negatively affect self-esteem and increase postpartum depression. Fur
This study has several limitations. This study is a single-center retrospective cohort with a small sample size and short follow-up duration, which limits generalizability. Therefore, future studies should include prospective, multicenter designs with larger sample sizes and longer follow-up to further evaluate the benefits of non-invasive low forceps-assisted vaginal delivery.
Compared with traditional low forceps delivery with episiotomy, non-invasive low forceps delivery - characterized by timely removal of forceps after fetal head crowning and manual perineal protection - effectively reduces the amount of maternal bleeding, postpartum pain, and complications without increasing neonatal complications. It also improves childbirth experience, preserves postpartum pelvic floor muscle strength, and contributes to the alleviation of postpartum depressive symptoms.
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