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Anogenital Distance and Perineal Measurements of the Pelvic Organ Prolapse POP Quantification System
Published on: September 20, 2018
Pregnancy, labour and delivery as risk factors for pelvic organ prolapse: a systematic review
Laura Cattani1,2, Judit Decoene2, Ann-Sophie Page1
1Department Development and Regeneration, Cluster Urogenital Surgery, Biomedical Sciences, KU Leuven, Leuven, Belgium.
Insights
First vaginal delivery and forceps delivery significantly increase the risk of pelvic organ prolapse (POP). Cesarean birth is protective against POP symptoms and clinical findings.
Area of Science:
- Obstetrics and Gynecology
- Pelvic Floor Disorders
- Women's Health Research
Background:
- Pregnancy and childbirth are recognized risk factors for pelvic organ prolapse (POP).
- The long interval between obstetric events and POP symptoms complicates establishing direct causal links.
- Intermediate outcomes like organ descent and levator avulsion (LA) offer new insights.
Purpose of the Study:
- To evaluate the impact of obstetric events on symptoms and signs of POP.
- To assess the association between obstetric events and levator avulsion (LA).
Main Methods:
- Systematic literature review of PubMed/MEDLINE, Embase, and Cochrane Library.
- Inclusion of studies on women examining obstetric events and POP/LA outcomes.
- Meta-analysis of eligible studies to determine odds ratios (OR) and confidence intervals.
Main Results:
- First vaginal delivery is a significant risk factor for POP symptoms (sPOP), clinical findings (cPOP), and LA.
- Forceps delivery also increases the risk for sPOP, cPOP, and LA.
- Exclusive cesarean birth demonstrates a protective effect against sPOP and cPOP.
Conclusions:
- A strong etiological relationship exists between vaginal birth and POP.
- The first vaginal delivery and forceps delivery are key determinants of POP.
- Cesarean delivery appears to be protective against POP development.
Introduction:
Pregnancy and childbirth are considered risk factors for pelvic organ prolapse (POP). The long latency between obstetric events and morbidity hinders the establishment of cause-effect relationships. Recently, intermediate outcomes such as organ descent and levator avulsion (LA) have been identified. We aimed to assess the effect of obstetric events on symptoms and signs of POP and on LA.
Methods:
We systematically reviewed the literature by searching PubMed/MEDLINE, Embase and Cochrane Library. We included studies in women examining associations between obstetric events and symptoms and signs of POP and LA, assessed through questionnaires, clinical examination and pelvic floor imaging. Two reviewers evaluated the studies for eligibility and for methodological quality/susceptibility to bias. We extracted study results and clustered them by outcome: symptoms of POP (sPOP), clinical findings of POP (cPOP) and LA. When appropriate, we performed a random-effect meta-analysis and reported the summary odds ratios (OR) with 95% confidence intervals. Heterogeneity across studies was assessed using the I2 statistic.
Results:
The first vaginal delivery was a risk factor for POP as measured by sPOP (OR: 2.65 [1.81-3.88]), cPOP (OR: 4.85 [2.15-10.94]) and in association with LA (OR: 41.6 [4.13- 419.41]). Forceps delivery was a risk factor for POP as measured by sPOP (OR: 2.51 [1.34-4.69]), cPOP (OR: 1.68 [1.21-2.34]) and in association with LA (OR: 5.92 [3.75-9.34]). Birth exclusively by caesarean was protective for sPOP (OR: 0.38 [0.29-0.51]) and for cPOP (OR: 0.29 [0.20-0.41]) and it did not confer any additional risk compared to nulliparity.
Conclusions:
This review confirms a strong aetiological link between vaginal birth and POP, with the first vaginal and forceps delivery being the main determinants.
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