- Research article
- Open Access
- Open Peer Review
Estimating the magnitude of female genital mutilation/cutting in Norway: an extrapolation model
BMC Public Health volume 16, Article number: 110 (2016)
With emphasis on policy implications, the main objective of this study was to estimate the numbers of two main groups affected by FGM/C in Norway: 1) those already subjected to FGM/C and therefore potentially in need for health care and 2) those at risk of FGM/C and consequently the target of preventive and protective measures. Special attention has been paid to type III as it is associated with more severe complications.
Register data from Statistics Norway (SSB) was combined with population-based survey data on FGM/C in the women/girls’ countries of origin.
As of January 1st 2013, there were 44,467 first and second-generation female immigrants residing in Norway whose country of origin is one of the 29 countries where FGM/C is well documented. About 40 pct. of these women and girls are estimated to have already been subjected to FGM/C prior to immigration to Norway. Type III is estimated in around 50 pct. of those already subjected to FGM/C. Further, a total of 15,500 girls are identified as potentially at risk, out of which an approximate number of girls ranging between 3000 and 7900 are estimated to be at risk of FGM/C.
Reliable estimates on FGM/C are important for evidence-based policies. The study findings indicate that about 17,300 women and girls in Norway can be in need of health care, in particular the 9100 who are estimated to have type III. Preventive and protective measures are also needed to protect girls at risk (3000 to 7900) from being subjected to FGM/C. Nevertheless, as there are no appropriate tools at the moment that can single these girls out of all who are potentially at risk, all girls in the potentially at risk group (15,500) should be targeted with preventive measures.
The World Health Organization (WHO) defines Female Genital Mutilation/Cutting (FGM/C) as ‘all procedures that involve partial or total removal of the external female genitalia, or other injury to the female genital organs for non-medical reasons’ . FGM/C is associated with series of immediate and long-term physical and psychological health consequences [2–7].
It is estimated that 133,000,000 girls and women in 29 countries have undergone FGM/C, and that 3,600,000 girls are at risk annually . Immigration from these countries to other parts of the world has made FGM/C a global concern. As a response, many governments in host countries have established preventive, protective and prosecutive measures alongside health care provision to tackle the issue [9–21]. The target group for preventive and protective measures is girls at risk, while health care provision targets girls and women already subjected to the procedure. Efficient planning and allocation of resources for the different sets of measures require precise estimates of total numbers of women and girls in each of the two target groups.
Currently, the most accurate estimates on the prevalence of FGM/C and those at risk are derived from population-based survey data such as Demographic Health Survey (DHS) and Multiple Indicator Cluster Survey (MICS) in 29 countries where FGM/C is traditionally practiced . To employ similar methods in diaspora, where FGM/C is only common among immigrant minorities, would be methodologically, ethically and financially difficult. Therefore, alternative models and data-sources have been explored. The most commonly used alternative model in Europe extrapolates prevalence data from countries of origin to the corresponding resident female immigrant population . Other models include surveys among health professionals [23–25] and non-representative samples of FGM/C practicing communities [23, 26, 27]. Even though the results from these surveys cannot be generalized, it still provides important insight into how FGM/C is evolving in the diaspora.
In Norway, a previous risk estimate was published in 2008 by the Norwegian Institute for Social Research (ISF) . The estimate was a small part of a larger study that focused on incidence of FGM/C and included only women and girls between 0 and 19 years of age from six African countries .
To give a more comprehensive estimate on the number of women and girls in Norway living with FGM/C and girls at risk of FGM/C we included in this study both first and second generation immigrants from the 29 FGM/C prevalent countries. An earlier and less refined version of this study was published by DAMVAD and NKVTS in 2014 . The earlier version did not take into account differences in prevalence when estimating the number of girls at risk for FGM/C; neither did it include data on typology. The present paper controls for both these factors, as well as employing updated national prevalence data.
We adopted the extrapolation model to estimate the number of girls and women living in Norway by January 1st 2013 who were at risk of FGM/C and those who most likely already have been subjected to FGM/C. We combined data on FGM/C from the 29 FGM/C prevalent countries with register data on first- and second-generation female immigrants from these countries.
In 2012, a consortium of researchers were commissioned by the European Institute for Gender Equality (EIGE) to map the current situation on FGM/C in the European Union (EU) and Croatia . The study identified lack of harmonized approach to generate reliable data on the magnitude of FGM/C as one of the main challenges facing the development of effective policies on FGM/C in the EU [23, 30]. The study also found that even when the extrapolation model was adopted, the variation in definitions and data sources have generated incomparable data [23, 30].
To enhance the comparability of our findings with other study findings in the region, we have therefore adhered as close as possible to the definitions, models and methodological approaches recommended by the aforementioned consortium of researchers in their 2103  and 2015  reports, as well as other key articles [23, 32, 33].
The extrapolation model combines prevalence data from countries of origin with data on resident population in the diaspora with origins from these countries . So far national prevalence rates have been predominantly used in prevalence studies using this model  with the exception of a Dutch study . One of the limitations of using national prevalence rates is that it obscures the variation in prevalence levels among different ethnicities and/or regions in the different countries [22, 23, 33]. Not adjusting for ethnicity could lead to bias in form of under- or over- estimation. In most European countries, including Norway, the National Registry offices do not provide information on ethnicity for ethical and legal reasons . Nevertheless, as there is a close correlation between ethnicities and sub-regions within countries of origin , adjusting for regional differences could be a viable alternative . A study carried out in the Netherland has therefore used data on places of birth to regroup the female immigrants according to regions within their countries of origin . In Norway, additional data on place of birth could be requested from Statistics Norway. Unfortunately, since this recommendation was first published after we had requested and acquired our dataset, we were unable to adjust for neither ethnicity nor regional differences. This could therefore lead to a possible bias in our results in the form of under- or over- estimation. This bias could still be insignificant for countries with small numbers of immigrants and countries of high national prevalence. However, for countries with low national prevalence but larger immigrant groups such bias is more likely to affect the overall estimate. In this study Iraq is such an example. The national prevalence of FGM/C in Iraq is 8 pct. whereas it is as high as 42.8 pct. among the Kurdish population. According to estimates from the Norwegian office of immigration (UDI), a little over 40 pct. of the Iraqi residents in Norway are of Kurdish origin. If this factor is taken into account, the total number of Iraqis affected by FGM/C in Norway will be much higher than our current estimates.
Another limitation of the extrapolation of national prevalence level is that it does not address the selection process of immigrants . Ortensi et al.  argue that migration is a selective process and that immigrants are usually younger, wealthier, and more educated than their counterpart that did not migrate. Since younger age and higher levels of wealth and education often are correlated with lower prevalence levels of FGM/C, the authors emphasize that the application of the national prevalence levels without adjustment for age, wealth and education is likely to bias the indirect estimates of FGM/C prevalence . Again, it was unfortunate that this recommendation was published after finalization of the data analysis and subsequent deletion of dataset (stratified by age) as stipulated by Statistics Norway. The suggested improved model will nevertheless be incorporated in any future follow-up studies.
Leye et al.  defined the prevalence of FGM/C in any EU member state as ‘the number of women and girls in that country who have undergone FGM at a certain point in time expressed as the proportion of the total number of women living in the country, but originating from countries where FGM is practiced’.
In this article, we adopted a similar definition for the prevalence of FGM/C in Norway: The proportion of girls and women estimated to have undergone FGM/C at a certain point in time out of the total number of women and girls with origins from the 29 FGM/C prevalent countries.
Identifying the relevant populations and sub-populations is central to both prevalence and risk estimation of FGM/C. The total resident population originating from the 29 FGM/C prevalent countries in Norway consists of first- and second-generation immigrants. In this article, we use the term first- generation immigrants to refer to girls and women who migrated from one of the 29 countries where FGM/C is concentrated, whereas second- generation immigrants refers to girls born in Norway to two parents who have migrated from one of these 29 countries. Girls with only one parent from a FGM/C practicing country were excluded, as the risk is very uncertain and most likely low.
The first-generation immigrants consist of those who have been subjected to FGM/C prior to arrival in host countries, those who have been subjected to FGM/C post arrival, those who have not been subjected to FGM/C because they/their families do not practice or have abandoned the practice, and those who have not been subjected to FGM/C but still are at risk.
The second-generation group consists of those who have been subjected to FGM/C at one point of time, those who have not been subjected to FGM/C and are not at risk as their families do not practice or have abandoned the practice and those who have not been subjected to FGM/C but still at risk.
Thus the relevant groups for estimation of FGM/C prevalence would be:
First-generation immigrants who have been subjected to FGM/C prior to arrival in host countries and those who have been subjected to FGM/C post arrival.
Second-generation immigrants who have been subjected to FGM/C at one point of time.
In countries of origin, there is usually a customary age within which FGM/C is performed . Thus, it would be safe to assume that those of first-generation immigrants who were older than that age upon arrival in host countries, had already been subjected to FGM/C in corresponding proportion to the prevalence rates in their countries of origin.
The challenge would be to estimate the number of second-generation immigrants who have been subjected to FGM/C, as well as those of the first-generation immigrants who have been subjected to FGM/C post migration (those who were younger than the customary age upon arrival but older than that age by the time of analysis/estimation). This challenge arises from the lack of reliable FGM/C incidence rates in host countries and the expected overestimation if extrapolation of prevalence rates from countries of origin were to be used. There is growing evidence on attitude change toward FGM/C in host countries that would indicate FGM/C is practiced at much lower rates than in countries of origin [34–37]. Therefore, we have decided to assume that none of the first-generation immigrants who were younger than the customary age of FGM/C in their countries of origin upon arrival in Norway or the second-generation immigrants has been subjected to FGM/C.
FGM/C risk estimation
The 2015 EIGE report  emphasized the difference between girls potentially at risk and girls at risk.
Girls potentially at risk are defined as ‘minor girls (in the age range of 0–18) who come from FGM risk countries, or were born to parents (or one parent) who originate from countries where female genital mutilation is commonly practiced’ . We found it necessary to modify this definition as including all first-generation girls under the age of 18 would imply including girls who could already have been subjected to FGM/C prior to migration. As a consequence we considered only first-generation girls who were younger upon arrival in Norway than the customary age of FGM/C in their countries of origin to be potentially at risk; whereas for second-generation girls, all those under 18 were considered to be potentially at risk. Further for the second-generation girls, only those with BOTH parents originating from one of the 29 countries were included. Therefore it is more apt to say that our definition for girls potentially at risk is: ‘first-generation girls who were younger upon arrival in Norway than the customary age for FGM/C in their countries of origin and second-generation girls who at the time of data collection (reference year/date) were younger than 18’. Preventive measures should target all girls potentially at risk.
On the other hand, girls at risk is not defined per se in the 2015 EIGE report . Instead the report provides a definition for the FGM/C risk estimation as:
‘minor girls (either born in, or born to mothers from, FGM risk countries) living in an EU Member State who might actually be at risk of female genital mutilation, expressed as a proportion of the total number of girls living in an EU country who originate from or are born to a mother from FGM risk countries’ .
The corresponding recommended model presents the risk estimation as an interval between low and high risk scenarios that takes into consideration the effect of migration through ‘migration and acculturation impact factor’ . In this model the national FGM/C prevalence rate for the age cohort 15–19 is multiplied by the total number of first and second generation immigrant girls who are younger than the customary age for cutting at their/their parents countries of origin. Here, unlike the estimation of girls potentially at risk, the customary age for cutting is taken into consideration. We do agree that the customary age for FGM/C in the countries of origin is important to exclude first-generation girls who could have been subjected to FGM/C prior to migration. However, we are skeptical to the exclusion of first-generation girls who have been younger than the customary age in their countries of origin upon arrival but older than that age at the time of data collection/reference year. The same applies to second-generation girls who were older than the customary age. This skepticism stems from the emerging evidence that customary age for cutting in countries of origin has less relevance in the migration context, where the ‘opportunity to cut’ seems to be more significant . Consequently, we have only excluded first-generation girls who were older than the customary age upon arrival, first-generation girls who were younger than the customary age upon arrival but older than 18 at the reference year, and second generation girls who were also older than 18 at the reference year.
Other than this modification on the exclusion criteria, we have followed the rest of the steps described in the recommended model.
The recommended model expresses the migration and acculturating impact factor as binary variable with values as either ‘0’ or ‘1’ and is assessed through qualitative research. The ‘0’ value signifies that migration has no impact on attitudes and behaviors toward FGM/C in the migration context. That is to say that the risk of FGM/C would be the same as if migration never took place. The ‘1’ value signifies on the other hand that migration has such an impact on attitudes and behaviors toward FGM/C that the level of risk is reduced to zero.
In the high FGM/C risk scenario, it is assumed that migration has no effect whatsoever (migration and acculturation impact factor equal ‘0’) and that the number of first and second generation girls at risk of FGM/C would be the same as if they/their parents have never migrated .
In the low FGM/C risk scenario, it is assumed that migration has an impact on attitudes and behaviors toward FGM/C and that second-generation girls experience a lower risk. In contrast, the first-generation girls are considered to be at risk (migration and acculturation impact factor equal ‘0’). Even though for purposes of calculation the migration and acculturation impact factor for second-generation girls in this scenario is given the value ‘1’, the authors caution against interpreting this estimation in the strictest sense that no second-generation girl would be at risk .
The resulting estimates of the low and high risk scenarios are then presented as an interval; in which the estimates from the two scenarios demarcate its boundaries. The scenario that is more likely to apply in the local context is finally selected according to the findings from the qualitative component . We have not carried out a qualitative study as recommended to accompany our estimation analysis. Still, there are several recent studies on change of attitude and behavior among Somalis in Norway [34–36] that helped to guide us as to which of the two scenarios is more relevant.
Finally, it is important to mention that despite the great potential of this model, the binary nature of the migration and acculturation impact factor is a significant limitation. To assume that migration would have either ‘no impact’ or ‘a huge impact’ on attitudes and behaviors towards FGM/C is in contrast to findings from several studies that indicate much more fluid opinions and variations in the depth or intensity of conviction [22, 38–41]. The migration and acculturation impact factor can be significantly improved by future research that can help to assign values between ‘0’ and ‘1’ dependent on scores given to identified determinants for change.
Estimation of type III
We extrapolated the prevalence of the different types of FGM/C in countries of origin to the different groups to estimate the number of those expected to have already been subjected to the most severe form of FGM/C (infibulation) and those at risk of infibulation.
In this study, we used two main data sources: 1) DHS and MICS and 2) Statistics Norway (SSB).
DHS and MICS are broad population and health surveys using a statistically representative sample of the population. In both DHS and MICS surveys, the percentage of girls and women aged 15 to 49 reporting to have experienced any form of FGM/C is used to indicate how prevalent the practice is in a particular country . Great consistency of data over time, as well as comparability to other studies, suggest that data on national prevalence is reliable [22, 42]. Still, it is important to acknowledge some of the inherent limitations of the DHS and MICS surveys such as reporting bias and the inability to reflect recent FGM/C trends in practicing countries [26, 32].
The DHS and MICS data used in this article are openly available and are published online in form of country reports on the respective web-sites for the responsible organizations. We used the most recent DHS and MICS reports for each of these 29 countries [43, 44] to ensure that we have the latest data on prevalence, typology and customary age for FGM/C (Tables 1 and 2). In two countries, Egypt and Sudan, the latest reports (DHS 2008 and MICS 2010 respectively) did not provide information on typologies. For these two countries we instead used data from the latest available report that has information on typology, e.g. for Egypt we used the DHS 1995 instead of DHS 2008.
Data on the most extensive form of FGM/C, type III, (Table 2) was available for most of the countries with a large immigrant group in Norway. However, typology data are missing for Liberia, Iraq, Uganda and Yemen. Therefore we assumed a zero prevalence of type III in these four countries. Generally, available data on types of FGM/C is found to be much less reliable than prevalence data, with a tendency to under-report type III [45, 46].
The dataset for this study was requested and obtained from our second data source i.e. Statistics Norway (SSB) which provides micro-data for research projects. Using this dataset required exemption from the duty of confidentiality and was further handled with utter adherence to SSB ethical requirements. The dataset is population register data that covers all female residents in Norway that, by the reference date (January 1st 2013), have migrated or their parents have migrated from one of the aforementioned 29 countries (Table 3). This includes refugees, whereas women and girls visiting Norway for less than six months, asylum seekers and illegal immigrants are not included. The dataset includes information on countries of origin, age at arrival in Norway and current age. It also comprises information on parents’ countries of origin for second-generation immigrants.
As of 1st January 2013 there were 44,467 girls and women who have either immigrated or their parents have immigrated from one of the 29 FGM/C prevalent countries (Table 3). We first divided these 44,467 girls and women into two main groups: 1) first-generation immigrants and group 2) second-generation immigrants. We further divided the first group into three groups (1a, 1b and 1c) taking into account the following variables: customary age for FGM/C in the country of origin, age at arrival in Norway and current age.
Group 1a consisted of 28,202 girls and women who upon arrival in Norway were older than the customary age for FGM/C in their countries of origin (Table 3). Hence, a corresponding proportion to the 15–49 prevalence rates in countries of origin is most likely to have already been subjected to the practice.
Group 1b consisted of 4763 girls who upon arrival in Norway were younger than or within the customary age for FGM/C in their countries of origin, and who by 1st January 2013 were older than the customary age but younger than 18. Group 1c, consisted of 1456 girls who upon arrival in Norway were younger than or within the customary age for FGM/C in their countries of origin, and who were still within the customary age or younger by January 1st 2013. Both groups were assumed not to have been subjected to FGM/C. Instead, these two groups were considered to be potentially at risk, and that a proportion of this group corresponding to that of girls in countries of origin in the age group 15–19, are at risk of FGM/C.
Group 2, second-generation girls constituted 10,046 girls of which 9324 (group 2a) were under the age of 18 by January 1st 2013. We assumed that girls under 18 with both parents originally from one of the 29 countries (9324) were potentially at risk and that a proportion of this group corresponding to that of girls in countries of origin in the age group 15–19 are at risk of FGM/C. In limited cases where parents were from two different FGM/C practicing countries, subsequent estimation was based on prevalence levels from the mother’s country of birth. Girls with only one parent from FGM/C practicing country were excluded, as the risk is very uncertain and most likely low.
To calculate the total number of girls potentially at risk, we combined group 1b, 1c and 2a without adjusting for prevalence rates in their parents’ countries of origin. To estimate the FGM/C risk we adopted the EIGE model described earlier in this section.
Finally, to estimate the number of those who have already been infibulated and the number of girls at risk of infibulation, we extrapolated the prevalence of the different types of FGM/C as reported in DHS and MICS (Table 2) to the different groups.
In this study we have divided girls and women into three major categories: 1) first- and second- generation girls and women who most likely have been subjected to FGM/C prior to immigration, 2) first- and second- generation girls who are potentially at risk of FGM/C, and 3) first- and second- generation girls that are at risk of FGM/C.
As of January 1st 2013, around 17,300 girls and women are estimated to have already been subjected to FGM/C prior to immigration to Norway, constituting an approximate prevalence of 40 pct. (Table 4). 50 pct. of these 17,300 girls and women originate from Somalia (Fig. 1). Also, around 50 pct. of the 17,300 girls and women are estimated to have been infibulated (Table 5). The majority of those estimated to be infibulated originate from Somalia, Eritrea, Sudan and Ethiopia (Fig. 2). These numbers nevertheless need to be interpreted with caution as data on types are significantly less reliable than prevalence data.
On the other hand, 15,500 girls are estimated to be potentially at risk (Table 6), while an approximate number of girls ranging between 3000 and 7900 were estimated to be at risk (Table 7). Finally, out of the total number of girls at risk, a number of girls ranging between 1800 and 4800 are estimated to be at risk of infibulation (Table 8).
FGM/C prevalence and risk estimations are needed to guide effective policies and interventions on health care and prevention. Prevalence and risk estimates can help to adjust the allocation of resources to the actual needs, as well as to evaluate the results of various interventions.
Women and girls who have been subjected to FGM/C (estimated to be around 17,300 in this study) are in potential need of health care for related physical and psychological complications. Need for health care is expected to be particularly important for those who have undergone infibulation (approximately 9100 out of the 17,300). Prevalence estimates, together with data on service provision and utilization, could also be useful in the assessment of accessibility and acceptability of available services.
Risk estimates are necessary to guide preventive measures. Generally, the main objective of preventive measures is to prevent FGM/C among girls at risk, who we found in this study to be in the range of 3000 to 7900. Currently, there are no appropriate tools, such as prediction models, that can single out these girls from all who are potentially at risk. Therefore, all girls who are potentially at risk, 15,500 girls, are to be targeted with preventive measures. Still additional protective measures may be needed for the girls at risk. Further, when combined with incidence rates, estimates of girls at risk can be useful in the evaluation of preventive measures and assessment of change.
Prevalence and risk estimates can also help to compare the magnitude of FGM/C between different countries. Currently, there are about 16 studies from nine European countries that estimate the FGM/C prevalence and/or risk by extrapolating DHS and MICS data to their immigrant population [23, 32, 47]. However, beside Norway, only three other countries use register-based data (Italy, Netherlands and Belgium) which would lead to more accurate estimates [23, 32, 33, 48]. The rest rely on census data, that collect information on country of origin from about five percent of the citizens, to estimate their female population originating from FGM/C prevalent countries . Limitation of census data in such a context is that uneven residence patterns of migrants in most countries, and other challenges such as language barriers or resistance to participation, can give inaccurate numbers of residents.
It is not possible to directly compare our prevalence estimates to that in other European countries. That is as even when the extrapolation model is used, there is a wide variation regarding who is included. In a recent study from the UK, all female 15 years of age and above emigrating from FGM/C prevalent countries were considered to have already undergone FGM/C in proportion to the 15–49 prevalence in home countries . In Belgium, all immigrants, regardless of age upon arrival, are considered to have FGM/C but in proportion to the prevalence in countries of origin . The closest to our approach is a recent study from the Netherlands. In the Dutch study, all immigrant females who upon arrival were above the median age for FGM/C in their home countries were considered to have already been cut, but in proportion to the corresponding age cohort . In our study instead of using median age as in the Dutch study, we used the upper margin of the customary age as a cut-off point.
Comparing estimates of girls at risk is even more complex. Even though only few European countries have estimates on FGM/C risk so far, the variation in the definition of who is at risk is vast. Second-generation is considered to be at risk in proportion to the prevalence in parents’ country of origin in Belgium . In UK, it is the first-generation under 15 that is considered as at risk . In the Netherlands, there are three alternative estimates for girls at risk. Two out of the three alternatives consider the second-generation to be at no risk .
In addition, in this study we decided to include only girls whose both parents are from countries with a tradition of FGM/C. In contrast, most other studies include all girls, even those with only one parent from FGM/C prevalent countries [33, 47, 48]. We believe that our approach gives more accurate estimates, as the risk is expected to be significantly lower when one of the parents is from a non-practicing country.
Nevertheless, the results from the three recent studies from Ireland, Sweden and Portugal that have piloted the recommended model for risk estimation presented in the 2015 EIGE report  could, to some degree, be comparable to our findings. In Ireland, the girls potentially at risk in 2012 were 14,577, of which 70 pct. originated from Nigeria (a low prevalent country). Of these girls the number estimated to be at risk varied between 158 and 1632. In Norway, the estimates for girls potentially at risk in 2013 were very close to the estimates from Ireland (15,500). Nevertheless in the high risk scenario we can see a substantial difference between those expected to be at risk in Ireland (1632) and their counterpart in Norway (7900). A similar difference can also be observed between our study and those from Sweden and Portugal. In Sweden, 59,409 girls were potentially at risk in 2011. Of these girls the number estimated to be at risk varied between 2016 and 11,145. This substantial difference, between our estimates and those of the EIGE model’s pilot countries, can be attributed to the difference in the composition of the potentially at risk groups in the different countries. Unlike Ireland and Portugal, a large number of girls in Norway have origins from high prevalence countries such as Somalia, Eritrea and Ethiopia. The difference can also be attributed to the different inclusion criteria for both the potentially at risk and the at risk groups in our analysis and in the EIGE model. In our analysis, unlike the EIGE model, girls under 18 who upon arrival were older than the customary age in their countries of origin were excluded from the potentially at risk. This group was only excluded in the EIGE model while estimating the numbers of girls at risk. Further, we did not exclude from our estimates of girls at risk those under 18 who were older than the customary age for FGM/C in countries of origin per the reference year. Instead, taking as a point of departure the emerging evidence that ‘opportunity to cut’ is more relevant in countries of migration , we included in our estimation all second-generation girls under 18, as well as first-generation girls under 18 who were younger than the customary age for FGM/C upon arrival.
The three above mentioned studies had an accompanying qualitative component to assess change in attitudes and behaviors toward FGM/C among the affected groups following immigration. All three studies reported to find change and consequently concluded that the estimates in the low FGM/C risk could be more accurate . We have not conducted the recommended qualitative component. Still, there are several recent studies that have assessed attitudes and behaviors towards FGM/C among Somalis in Norway [34–36]. The reported change in these studies would indicate that similar to Ireland, Portugal and Sweden, the estimates in the low FGM/C risk scenario could be more accurate.
Reliable estimates on FGM/C are important for evidence-based policy making. Thus in the absence of population based representative surveys, the extrapolation model is currently the most viable way to estimate both prevalence and risk in diaspora.
In this study we aspired to estimate the number of two main groups with different policy implications: those who are already subjected to FGM/C and those at risk.
We calculated the number of girls and women who are expected to have already undergone FGM/C. Also, as type III is associated with higher health risks and health care needs, we identified the proportion of those expected to be infibulated. Our estimate suggests that around 50 pct. of the 17,300 girls and women estimated to have undergone FGM/C prior to immigration had type III. Of the girls at risk in both the low and high risk scenario, approximately 60 pct. were at risk of infibulation.
Demographic Health Survey
European Institute for Gender Equality
Female Genital Mutilation/Cutting
Norwegian Institute for Social Research
Multiple Indicator Cluster Survey
Norwegian Center for Violence and Traumatic Stress Studies
World Health Organization
Eliminating Female Genital Mutilation. An Interagency Statement. Geneva, Switzerland: World Health Organization; 2008.
Cook RJ, Dickens BM, Fathalla MF. Female genital cutting (mutilation/circumcision): ethical and legal dimensions. Int J Gynaecol Obstet. 2002;79(3):281–7.
Rahman A, Toubia N. Female genital mutilation: A practical guide to worldwide laws & policies: Zed Books; London. 2000.
Berg RC, Underland V, Odgaard-Jensen J, Fretheim A, Vist GE. Effects of female genital cutting on physical health outcomes: a systematic review and meta-analysis. BMJ Open. 2014;4(11):e006316.
Berg RC, Odgaard-Jensen J, Fretheim A, Underland V, Vist G. An updated systematic review and meta-analysis of the obstetric consequences of female genital mutilation/cutting. Obstet Gynecol Int. 2014;2014:542859.
Berg RC, Denison E, Fretheim A. Psychological, social and sexual consequences of female genital. Report from Kunnskapssenteret. 2010; (13).
Vloeberghs E, van der Kwaak A, Knipscheer J, van den Muijsenbergh M. Coping and chronic psychosocial consequences of female genital mutilation in The Netherlands. Ethnicity Health. 2012;17(6):677–95.
UNICEF. Female Genital Mutilation/Cutting: What might the future hold? New York: UNICEF; 2014.
Lundberg PC, Gerezgiher A. Experiences from pregnancy and childbirth related to female genital mutilation among Eritrean immigrant women in Sweden. Midwifery. 2008;24(2):214–25.
Andersson C. Female genital mutilation meets Swedish health care. Female genital mutilation is one of many forms of discrimination of women in the world. Lakartidningen. 2001;98(20):2470–3.
Caroppo E, Almadori A, Giannuzzi V, Brogna P, Diodati A, Bria P. Health care for immigrant women in Italy: are we really ready? A survey on knowledge about female genital mutilation. Ann Ist Super Sanita. 2014;50(1):49–53.
McCaffrey M, Jankowska A, Gordon H. Management of female genital mutilation: the Northwick Park Hospital experience. Br J Obstet Gynaecol. 1995;102(10):787–90.
Carcopino X, Shojai R, Boubli L. Female genital mutilation: generalities, complications and management during obstetrical period. J Gynecol Obstet Biol Reprod. 2004;33(5):378–83.
Bikoo M. Female genital mutilation: classification and management. Nurs Stand. 2007;22(7):43–9. quiz 50.
Collinet P, Sabban F, Lucot JP, Boukerrou M, Stien L, Leroy JL. Management of type III female genital mutilation. J Gynecol Obstet Biol Reprod. 2004;33(8):720–4.
Leye E, Powell RA, Nienhuis G, Claeys P, Temmerman M. Health care in Europe for women with genital mutilation. Health Care Women Int. 2006;27(4):362–78.
Vangen S, Hoffmann R, Flo K, Lorentzen B, Sand S. Female circumcision--complications and treatment. Tidsskrift for den Norske laegeforening: tidsskrift for praktisk medicin, ny raekke. 2006;126(4):475–7.
Sundby J, Austveg B. Genital mutilation of women. A new challenge for the health service. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 1993;113(21):2704–7.
Sundby J. Genital mutilation of women--is it a concern for gynecologists? Acta Obstet Gynecol Scand. 1996;75(6):513–5.
Leye E, Deblonde J, Garcia-Anon J, Johnsdotter S, Kwateng-Kluvitse A, Weil-Curiel L, et al. An analysis of the implementation of laws with regard to female genital mutilation in Europe. Crime Law Social Ch. 2007;47(1):1–31.
Powell RA, Leye E, Jayakody A, Mwangi-Powell FN, Morison L. Female genital mutilation, asylum seekers and refugees: the need for an integrated European Union agenda. Health Policy. 2004;70(2):151–62.
UNICEF. Female Genital Mutilation/Cutting: A statistical overview and exploration of dynamics of change. New York: Unicef; 2013.
Leye E, Mergaert L, Arnaut C, Green SOB. Towards a better estimation of prevalence of female genital mutilation in the European Union: interpreting existing evidence in all EU Member States. GENUS. 2014;70(1):99–121.
Leye E, Ysebaert I, Deblonde J, Claeys P, Vermeulen G, Jacquemyn Y, et al. Female genital mutilation: Knowledge, attitudes and practices of Flemish gynaecologists. Eur J Contracep Repr. 2008;13(2):182–90.
Andro A, Lesclingand M, Cambois E, Cirbeau C. Rapport final: volet quantitatif du projet Excision et Handicap (ExH). Excision et Handicap (ExH): Mesure des lésions et traumatismes et évaluation des besoins en chirurgie réparatrice, Institut National des Etudes Démographiques (INED)-Université Paris I, Paris. 2009.
Behrendt A. Listening to African voices, Female Genital Mutilation/Cutting among Immigrants in Hamburg: Knowledge, Attitudes and Practice, Plan International Deutschland e V, Hamburg. 2011.
Koukkula M, Keskimäki I, Koponen P, Mölsä M, Klemetti R. Female genital mutilation/cutting among women of Somali and Kurdish origin in 2010–2012 in Finland. Eur J Public Health. 2014;24 suppl 2:cku162. 014.
Lidén H, Berntzen T. Kjønnslemlestelse i Norge. 2008.
DAMVAD, NKVTS. Utbredelse av kjønnslemlestelse i Norge: Registeranalyse. Oslo: DAMVAD & NKVTS; 2014. p. 48.
Av V, Middelburg M, Arnaut C, Leye E, Deblonde J, Mergaert L, et al. Female genital mutilation in the European Union and Croatia. 2013.
Mergaert L, Arnaut C, Exterkate M, O’Brien S, Strid S, Leye E. Estimation of Girls at Risk of Female Genital Mutilation in the European Union. 2015.
Ortensi LE, Farina P, Menonna A. Improving estimates of the prevalence of Female Genital Mutilation/Cutting among migrants in Western countries. Demogr Res. 2015;32(18):543–62.
Exterkate M. Female genital mutilation in the Netherlands: Prevalence, incidence and determinants: Pharos; Utrecht. 2013.
Gele AA, Johansen EB, Sundby J. When female circumcision comes to the West: Attitudes toward the practice among Somali Immigrants in Oslo. BMC Public Health. 2012;12(1):697.
Gele AA, Sagbakken M, Kumar B. Is female circumcision evolving or dissolving in Norway? A qualitative study on attitudes toward the practice among young Somalis in the Oslo area. Int J Women’s Health. 2015;7:933.
Gele AA, Kumar B, Hjelde KH, Sundby J. Attitudes toward female circumcision among Somali immigrants in Oslo: a qualitative study. International J Women’s Health. 2012;4:7.
Johnsdotter S, Moussa K, Carlbom A, Aregai R, Essén B. “Never my daughters”: A qualitative study regarding attitude change toward female genital cutting among Ethiopian and Eritrean families in Sweden. Health Care Women Int. 2009;30(1–2):114–33.
Shell-Duncan B, Herniund Y. Are There “Stages of Change” in the practice of Female Genital Cutting? Qualitative Research Finding from Senegal and the Gambia. Afr J Reprod Health. 2007;10(2):57–71.
Shell-Duncan B, Wander K, Hernlund Y, Moreau A. Dynamics of change in the practice of female genital cutting in Senegambia: Testing predictions of social convention theory. Soc Sci Med. 2011;73(8):1275–83.
Skramstad H. The Fluid Meanings of Female Circumcision in a Multiethnic Context in Gambia. Norway: DERAP, Chr Michelsen Institute; 1990.
Lien I-L, Schultz J-H. Internalizing knowledge and changing attitudes to female genital cutting/mutilation. Obstet Gynecol Int. 2013;2013:467028.
Yoder PS, Khan S. Numbers of women circumcised in Africa: The production of a total. 2008.
The DHS Program Demographic and Health Surveys [http://dhsprogram.com/]. Accessed date March 18, 2015.
MICS Surveys [http://mics.unicef.org/surveys]. Accessed date March 18, 2015.
Elmusharaf S, Elhadi N, Almroth L. Reliability of self reported form of female genital mutilation and WHO classification: cross sectional study. BMJ. 2006;333(7559):124.
Lunde IB, Sagbakken M. Female genital cutting in Hargeisa, Somaliland: is there a move towards less severe forms? Reprod Health Matters. 2014;22(43):169–77.
Alison Macfarlane B, Stat F. Female Genital Mutilation in England and Wales: Updated statistical estimates of the numbers of affected women living in England and Wales and girls at risk Interim report on provisional estimates. 2014.
Dubourg D, Richard F, Leye E, Ndame S, Rommens T, Maes S. Estimating the number of women with female genital mutilation in Belgium. Eur J Contracept Reprod Health Care. 2011;16(4):248–57.
We thank our colleagues at NKVTS, in particular Ingvild B. Lunde, for their feedback.
The study was funded by the Norwegian Ministry of Children, Equality and Social Inclusion within the framework of the action plan against forced marriage, female genital mutilation and severe restrictions on young people’s freedom 2013–2016.
The authors declare that they have no competing interests.
MMZ contributed substantially to the study design, performed secondary statistical analysis, substantial contribution to data interpretation and writing of manuscript. MNS contributed to the study design, acquisition of data from Norwegian Statistics, performed primary statistical analysis and revised the final draft. REBJ have made the greatest contribution to the conception and design of the study, substantial contribution to interpretation of data and writing of manuscript. All authors read and approved the final manuscript.