Recommendation 5: Either antepartum or intrapartum deinfibulation can be considered to facilitate vaginal birth in women with Type III FGM.

 World Health Organization (WHO)

Recommendation 5

Strength of recommendation: Conditional (very-low-certainty evidence)

Women and girls living with FGM are more likely to have a mental health disorder, such as anxiety, depression and/or post-traumatic stress disorder (PTSD), compared with women and girls who have not undergone FGM. 

- Summary of the evidence -

The evidence review for this recommendation, which updated a previous review, considered whether the timing of deinfibulation, i.e. antepartum versus intrapartum, made any difference in terms of obstetric or newborn outcomes among women living with Type III FGM. Four studies were identified in the systematic review. These included a retrospective cohort study conducted in Norway by Taraldsen et al., and three studies conducted in the United Kingdom: one prospective cohort study by Bikoo et al., one non-randomized controlled study by Paliwal et al. using hospital-based controls drawn from medical records at the hospitals, and one retrospective cohort study by Albert et al. in which antepartum and intrapartum deinfibulation were directly compared. The study participants were predominantly African women who had migrated to Norway or the United Kingdom. No RCTs were identified and the certainty of the evidence from all four of the studies for all outcomes was considered very low. Evidence from these studies suggested that antepartum deinfibulation may lead to a shorter duration of labour, compared with intrapartum deinfibulation. However, the effects of antepartum deinfibulation vary, and it is possible that antepartum deinfibulation makes little or no difference to the risk of prolonged labour. One study by Paliwal et al. (n = 253 women with Type III FGM) found that antepartum deinfibulation was associated with higher rates of postpartum haemorrhage and caesarean births in pregnant women with Type III FGM, compared with intrapartum deinfibulation. It is therefore, unclear whether antepartum deinfibulation compared with intrapartum deinfibulation increases or decreases the likelihood of perineal tears, rate of episiotomies, birth asphyxia and perinatal deaths. Another study, by Albert et al. (n = 59), showed no significant difference in the odds of prolonged labour among women who received antepartum versus intrapartum deinfibulation. All four of the studies (n = 632) found that the odds of perineal tears did not significantly vary based on the timing of deinfibulation. Evidence from two of these studies, by Albert et al. and Taraldsen et al. (n = 597), also found that the likelihood of postpartum haemorrhage was significantly higher in pregnant women who were deinfibulated during pregnancy compared with those deinfibulated during labour. Two studies, by Albert et al. and Paliwal et al. (n = 77), found no overall difference in the likelihood of requiring an episiotomy between women in the antepartum deinfibulation group and those in the intrapartum deinfibulation group. Finally, three studies, by Bikoo et al., Paliwal et al. and Taraldsen et al. (n = 912), found that the odds of caesarean delivery were significantly higher among women who had received antepartum deinfibulation compared with intrapartum deinfibulation. Similarly, three studies (n = 288) found no overall difference in the likelihood of birth asphyxia (Apgar scores of < 7 at 1 minute and 5 minutes) between women in the antepartum deinfibulation group and those in the intrapartum deinfibulation group. Evidence from one study by Taraldsen et al. (n = 869) found no difference between the antepartum deinfibulation and intrapartum deinfibulation groups with regard to the risk of perinatal death. One study by Albert et al. found no statistically significant difference between the groups on the need for blood transfusion, antibiotics and/or syntocinon.

- Rationale -

The GDG noted that contextual and health systems factors influence decision-making about the timing of deinfibulation, for women who request it during pregnancy. In most settings with a high prevalence of FGM, many pregnant women don’t attend ANC until late in pregnancy, and in some settings, the rates of facility-based births attended by skilled health personnel are low and the competence of health workers to offer and perform deinfibulation varies. Given the very low certainty of the available evidence and after assessing the benefits and harms, values and preferences, equity, acceptability, feasibility and resource needs, the GDG decided to retain the existing recommendation on the timing of deinfibulation without recommending a preferred timing. In making this decision, GDG members considered the following contextual factors that may influence the decision on the timing of deinfibulation. 1. Preference of the woman: Women should be consulted on their preferences. For example, if a woman prefers to avoid an additional intrapartum procedure, or if she suffers from urinary complications, she is likely to prefer antepartum deinfibulation since this allows adequate healing time before childbirth to prevent additional complications. 2. Access to health facilities and commodities: In settings where women may encounter unintended delays in physically reaching health facilities (e.g. challenges with related costs) and where there may be issues with the availability of health commodities (e.g. type of analgesia to conduct the procedure), antepartum deinfibulation may be
preferred to ensure the procedure is done, in case there are delays in reaching the facility at the time of labour/delivery. 3. Place of delivery: Given that deinfibulation should be carried out by a trained health worker at a health facility, antepartum deinfibulation may be prioritized in contexts where home births are common. The same applies to settings where the health facility has a high patient load. 4. Health worker’s skill level: Anatomical conditions like tissue oedema and distortion during labour, as well as the size of the opening of the infibulation – including whether a vaginal exam is possible or not – may pose difficulties for less-experienced health workers performing intrapartum deinfibulation. In this case, antepartum deinfibulation would likely be preferable. In settings with experienced, well trained providers, intrapartum deinfibulation is an acceptable procedure. The GDG noted that during intrapartum deinfibulation, it may be clinically useful to conduct the intervention during the first stage of labour as opposed to later for better neonatal outcomes and better monitoring of labour. The GDG also noted the advantages of antepartum deinfibulation: less oedematous tissue than during labour, more time to heal prior to giving birth, and more time for women to adjust to the changes in the functioning and appearance of their genitals.

- Implementation remarks -

Given that both antepartum and intrapartum deinfibulation appear to be comparable in terms of obstetric and neonatal outcomes, the decision about the timing of the procedure should be based on the contextual factors outlined above. The GDG noted a lack of clarity on the responsibility for various tasks along the continuum of care among health workers caring for women living with FGM in many settings, which may represent a barrier to identifying women who need deinfibulation to prevent FGM-related obstetric and neonatal risks. In this regard, the GDG emphasized the importance of establishing a clear referral pathway for pregnant women living with Type III FGM, and encouraged efforts to define the roles and responsibilities of different health workers within the client continuum of care from antenatal care to the postpartum period, including local requirements regarding which types of health workers can perform the deinfibulation procedure.

- Research gaps -

 Many research gaps remain with regard to women’s preferences around the timing of deinfibulation, health system readiness to carry out deinfibulation during the antepartum period, and feasibility of antepartum deinfibulation. Current research provides conflicting evidence around clinical outcomes, demonstrating the need for additional studies that prioritize women’s preferences while considering contextual factors, with the aim of informing recommendations on the timing of deinfibulation.


Women with Type III FGM should be offered counselling before undergoing deinfibulation, and partners and other family members can be included at the request of the woman, particularly in settings where reinfibulation is commonly requested.


- Summary of the evidence -

A systematic review was conducted to explore the outcomes of counselling before undergoing deinfibulation as compared with no counselling, with or without inclusion of a male partner or family member during counselling. No studies were identified to assess the outcomes of interest, which were increased uptake of deinfibulation and reduced rate of requests for reinfibulation. Evidence on the values and preferences of women who underwent deinfibulation suggests that some women may report initial discomfort with the post-operative appearance of deinfibulated labia. Therefore, in addition to obtaining preoperative consent, when counselling women with a history of FGM, health workers should always provide balanced, unbiased information on expected benefits and potential risks associated with a procedure in a clear preoperative briefing. In the context of deinfibulation, this briefing should include information regarding the anatomical and physiological changes that can be expected after deinfibulation (e.g. faster micturition, increased vaginal discharge).

- Rationale -

Counselling and consent prior to any medical procedure is a clinical best practice and an important aspect of person-centred care, which is a cornerstone of good clinical care. As explained in WHO’s clinical handbook on the care of girls and women living with FGM, it is important to recognize that women often feel conflicted in how they manage their sociocultural values and the expectations of their families. Without counselling, some women may request reinfibulation because of fear of repercussions if they go against their family’s wishes, especially if they are dependent on their family for social or financial support. Clear and respectful communication while ensuring confidentiality is essential in enabling women to make decisions.

- Implementation remarks -

 The GDG emphasized the importance of informed decision-making prior to the deinfibulation procedure, regardless of whether it is during the antepartum or intrapartum period. They noted that in many settings this decision-making might include the involvement of a male partner or another person, such as a woman’s mother or mother in-law. The GDG also noted the potential for unintended negative consequences if the involvement of a partner or family member is not arranged sensitively and with a woman’s consent. For girls living with Type III FGM, no paediatric evidence currently exists on the benefits of deinfibulation. However, expert opinion suggests that deinfibulation would prevent urological and gynaecological complications regardless of the presence of symptoms. Health workers can wait for girls to reach the age of assent and until their genitals have estrogenized before suggesting deinfibulation, unless a girl is experiencing urological or gynaecological complications. 

- Research gaps-

 Given the importance of pre-operative counselling prior to any surgical procedure and the need to ensure that counselling considers contextual factors, potential risks or unintended outcomes, and individual concerns, additional research should aim to identify effective communication and counselling models. These efforts should inform decision-making in contexts where decisions might be influenced by partners and family members, and where sociocultural beliefs around FGM and body image present barriers to deinfibulation. Greater understanding and acknowledgement of women’s preferences and concerns related to body image would contribute to improvements in provider–client interactions, improved uptake of deinfibulation, and reduced requests for reinfibulation. 

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