- Research article
- Open Access
- Open Peer Review
How many preterm births in England are due to excision of the cervical transformation zone? Nested case control study
© Wuntakal et al. 2015
- Received: 5 February 2015
- Accepted: 18 September 2015
- Published: 29 September 2015
Preterm births (as a proportion of all births) have been increasing in many countries. There is growing evidence of increased risk of preterm birth following excisional treatment of the cervix. We estimate the number of preterm births attributable to excisional treatments with a length of 10 mm or more in England.
Case–control study nested in a record linkage cohort of women with a histological sample at 13 hospitals in England. We combined observed age at first excisional treatment in our cohort with the weighted distribution of excision length from the case–control study to estimate the length distribution by age at first treatment among the cohort. The number of births after excision for each 5-year age group was estimated using national fertility data; published absolute risks of preterm (<37 gestational weeks) and very preterm birth (<32 weeks) were applied to these to estimate the number of preterm births per 100 women treated. Excess preterm births were estimated assuming all treatments were small. The attributable risk of preterm birth following excisional treatment in England was estimated.
The majority of first excisional treatments at colposcopy were small (47.5 %) or medium (39.1 %), 9.5 % were large and 4.1 % were very large excisions. 4.0 % of women treated before birth had more than one excisional treatment. Thus based on our cohort of 10,711 treated women and the length of treatment observed in the case control study we estimate an excess of 240 preterm births (including 57 very preterm) or 2.2 (including 0.5 very preterm) per 100 women treated. At a population level (for England) we estimate that 39,101 women aged 20–39 would be treated each year and that these treatments will lead to an excess of 840 preterm births (including 196 very preterm) in England each year.
Assuming associations between preterm birth and treatment for cervical disease are causal; we estimate that an excess 840 (2.5 %) preterm birth in England each year are due to excisional treatments of 10 mm or more. Those that go on to become pregnant should be closely monitored during antenatal period to reduce their risk of preterm birth.
- Preterm birth
- Cervical treatment
- Attributable risk
A growing body of literature suggests that women who undergo treatment for cervical disease are at increased risk of preterm birth, particularly when the length of the tissue excised is greater than or equal to 10 mm [1–8]. In England, the absolute risk of preterm birth among treated women increased with the length of excision from 7.5 % (with length <10 mm) to 18 % in those with excisions greater than 20 mm .
Although the risk of preterm birth following excision is often cited as a reason for not offering cervical screening to young women, we are not aware of any papers formally calculating the risk associated with screening per se. Further whilst preterm births (as a proportion of all births) have been increasing in many countries [9, 10] it is unclear what proportion may be attributable to prior treatment for cervical disease.
In this study, we estimate the number of preterm births among women with cervical excisional treatments, accounting for age at excision and length of excision, in order to estimate the number and proportion of preterm births in England attributable to cervical tissue excision of 10 mm deep or more.
From this cohort we identified women who had at least one singleton live birth with a gestational age of 20–42 weeks. We then selected the first singleton preterm birth (gestational age of 20–36 completed weeks) in each woman and frequency matched these to singleton term births (38–42 completed weeks) in women with no preterm births. Births at 37 weeks gestational age were excluded when performing the matching to allow a clear divide between term and preterm births. Full details on the study design have been published previously [8, 12]. From HES records we obtained detailed obstetric information. Hospitals entered colposcopy details into a study database and additionally submitted anonymised pathology reports to Barts Health NHS Trust. Pathology reports were entered into the study database by two trained individuals (AP and TP) to ensure measurements were entered in a standardised way, facilitating the identification of the length, thickness and circumference of specimens. Participating pathology departments confirmed that usual practice was to record the length of the specimen first on the pathology reports. Individuals searching for and coding colposcopy information were blind to the case–control status of the women.
Women were not eligible for the case–control study if detailed colposcopy information was not available, if colposcopy records were known to be incomplete, if the only pathology sample reported was non-cervical or if the woman was diagnosed with cervical cancer at any time. We also excluded one woman who was recorded as being sterilized whilst pregnant. Details of women excluded from the case–control study have been published previously . Here we further exclude the following women: those attending colposcopy but not receiving excisional treatment, those who had their first treatment aged 40 and over and those with unknown length of their only excisional treatment (see Fig. 1). In our previous publication births as a result of a high risk pregnancy (defined elsewhere ) were excluded; however they are included here to determine the age at first excisional treatment, to ensure the sample is representative of the general population.
This study was approved by the Brompton, Harefield, and NHLI research ethics committee, Charing Cross Hospital, London (study reference number: 09/h0708/65). Since this was a retrospective linkage study using routinely recorded data, informed consent was not required by the research ethics committee. All data received by the researchers were anonymous.
To assess the concordance between dates at first colposcopy procedure recorded in the cohort and the case–control study we selected all women recorded in the case–control study as having an excisional treatment as their first colposcopic procedure. We used a paired sample t-test to compare the age at first colposcopic appointment in the case–control study and the cohort study.
Length of excision was defined as the distance from the distal or external margin to the proximal or internal margin of the excised specimen, as defined by the IFCPC nomenclature . The length of treatment was coded as per the pre-specified statistical analysis plan: excision with a length of <10 mm (small), 10–14 mm (medium), 15–19 mm (large) and ≥20 mm (very large). When the excision was piecemeal, the largest fragment length was used. For women with more than one excisional treatment (n = 106), if the treatments were within a year (n = 40), the lengths were summed, as is it is extremely unlikely there would be a birth between the two treatments. Length of treatments that were more than a year apart (n = 66) were summed at the time of the later treatment.
The distribution of length of excisional treatment was calculated using all available data for each age group (<20, 20–24, 25–29, 30–34, 35–39) in the case–control study, weighted using the inverse probability of selection into the case–control study to reflect the distribution of cases and eligible controls in the cohort. These data were combined with cohort data on the number of women in each age group who underwent an excisional treatment between April 1988 and December 2011. Using these data we estimate by age group the number of women in the cohort who had an excisional treatment in each length category. We assume that single excisions with unknown length have the same distribution as those with known length in the same age group. Women with an unknown length of first treatment but known length of second treatment within a year were assigned the median length observed among women who had multiple treatments within a year for the unknown length. For women with multiple treatments which were at least a year apart, if either treatment had an unknown length they were proportionally assigned to the length categories of treated women who had multiple treatments within the same age group.
Using age-specific fertility rates for England from 2010,  we estimated the expected number of future births per woman in 5-year age groups. We have previously shown that the increased risk of preterm birth remains for all future births, not just the first birth after colposcopy . Therefore we applied published absolute risks  of preterm (20–36 gestational weeks) and very preterm (20–31 gestational weeks) births for each length category to the expected number of future births for women in each age group. The absolute risks of a preterm birth were 7.5 % following small excisions, 9.6 % following medium, 15.3 % following large and 18.0 % following very large excisions (for very preterm they were 2.0 %, 2.3 %, 3.6 % and 6.4 % respectively) . Women with multiple excisional treatments not within a year of each other were assigned the absolute risk appropriate for their first treatment length from the age at their first excisional treatment to their second treatment, and the absolute risk associated with the two treatment lengths summed from the age at the second treatment. The expected number of preterm births was then estimated assuming that all treatments were small, to allow estimation of the excess risk of preterm birth caused by deeper excisions.
To estimate the number of preterm births associated with excisional treatments in England, it was necessary to estimate the number of women per year who have excisional treatments. For this we sourced the number of tests taken and the result of these tests from routinely published screening data for England in the financial year 2013/14 . We then used previously published methodology  to estimate (from the published data) the total number of women aged 20–39 who had an excisional treatment in financial year 2013/14. Full details on how this was estimated can be found in Additional file 1, and the results in Additional file 2: Tables S1 and Additional file 3: Table S2.
Analyses were carried out in STATA 12 (StataCorp. College Station, Texas, USA).
Age among women whose first attendance to colposcopy resulted in excisional treatment. Comparison of cohort and case–control data
Age at treatment
Treated at first colposcopy in cohort among those included in the case–control study
Treated at first colposcopy
Treated at first colposcopy
Estimated (weighted) age at first excisional treatment by length of tissue removed among women in the cohort study
20 + mm
Estimated preterm births due to excisional treatment of the cervical transformation zone
Estimated births after first treatment (N)
Very preterm births
(<37 gestational weeks)
(20–31 gestational weeks)
Age at first treatment
Women with excisional treatment
Estimated births taking into account length distribution*
Estimated births assuming all excisions ≥10 mm were small
Excess births due to treatments
Estimated births taking into account length distribution
Estimated births assuming all excisions ≥10 mm were small
Excess births due to treatments
<20 single excision
20–24 single excision
25–29 single excision
30–34 single excision
35–39 single excision
Estimated number of women referred and treated at colposcopy due to cervical intraepithelial neoplasia grade 2 (CIN2+) or worse diagnosis and the resulting excess preterm births each year in England
N screening tests:
N referred to colposcopy:
N referred with mild
N referred with mod+
N with CIN2+:
Estimated excess number of future preterm births
Estimated excess number of future very preterm births
per woman treated
in women treated
per woman treated
in women treated
Based on the observed age at first excisional treatment at colposcopy in women under age 40, the observed length of tissue removed, age specific fertility rates and the length specific absolute risks of preterm birth we have estimated that treatment for cervical disease leads to 2.2 preterm (0.5 very preterm) births per 100 women treated under age 40. At a national level this corresponds to 840 preterm births per year in England.
Strengths and limitations
Our results are based on the assumption that the association between preterm birth and treatment for cervical disease is causal. However lifestyle factors (such as smoking) were not adjusted for when estimating the risks used in this study, thus it is possible that residual confounding remains.
The distribution of age at first excisional treatment for women in England is extrapolated from that observed in our study and may not be representative of all women currently being treated in England. For example, women aged 20–24 are no longer invited for cervical screening in England, so we expect the number of preterm births due to excisional treatment among women in this age group to be lower than the number estimated here. Only 2.7 % of all treatments in the study were carried out before age 25, so the impact on the number of preterm birth is likely to be small.
Although the NHS hospital trusts providing data to this study were self selected they did not differ (on the basis of published data) from other colposcopy clinics in England . We therefore think it is justified to assume that the observed distribution of excised tissue length can be extrapolated to all women in England.
Due to the lack of routinely reported data, it was necessary to estimate the number of women treated each year at colposcopy in England. Our estimate (n = 39,101) is based on routinely reported cytology and histology data, however it is worth noting that the results are similar to twice the number of CIN3 diagnoses in women under age 40 (n = 40,750) . Diagnoses of CIN2 are not routinely recorded or reported, but we think it sensible to assume that the number diagnosed is similar to that of CIN3 and that most of these women would have an excisional treatment as a result. This gives us confidence that our estimate of women treated at colposcopy each year is robust.
We have made assumptions regarding the length of excision among samples where the measurements are unknown, including those with multiple treatments. The risk in those with unknown length was found to be similar to those with medium excisions  suggesting that factors other than length (such as piecemeal excisions) are responsible for missing values.
We have applied absolute risks of preterm birth to all future births, not just the first following excisional treatment. We believe this is justified since we have shown that an increased risk of preterm birth remains for all future births, not just the first birth following treatment .
We have estimated the excess number of preterm birth attributable to excisional by comparing the observed length distribution in our study to a scenario where all excisions have a length of less than 10 mm (equivalent to the baseline risk in those attending colposcopy). We are not suggesting that clinical practice should change to force all excisions to be small, we are purely estimating the excess risk attributable to excisions with a length greater than 10 mm.
Relative risks of preterm birth following large (17 + mm) treatments compared to small treatments (≤10 mm) have been reported to be between 1.74  and 1.79  in Scandinavian populations and up to 2.4 in an English population . A meta-analysis  comparing untreated women to those with excisions deeper than 10 mm found the relative risk of preterm delivery to be 2.61 (95 % CI 1.28–5.34), though a study from Belgium  found even higher risks (RR = 4.55, 95 % CI:1.32–15.65). The study in England  found that the absolute risk of preterm birth among those who receive a diagnostic biopsy (7.2 %, 95 % CI: 5.9 %–8.5 %) is similar to that of women with small treatments (7.5 %, 95 % CI: 6.0 %–8.9 %). Nevertheless women attending colposcopy following an abnormal cytology result are at a higher risk of preterm birth than the general population in England, where the preterm rate in England is 6.7 % . This is most likely due to the shared risk factors for preterm delivery and cervical disease.
An excess of 2.2 preterm births per 100 women treated may not seem like much, however the average number of births in England between 2000 and 2009 was 510,660 each year and the preterm rate during this period was 6.7 % (or 33,168 births) . Extrapolating the results observed in this study to the whole of England, we would expect 840 preterm births a year (equivalent to 2.5 % of preterm births in England) to be due to excisional treatments of length ≥10 mm.
The risk of preterm birth following treatment for cervical disease can be considered a harm of cervical cancer screening. Nevertheless it needs to be considered against the 20,375 women under age 40 diagnosed and treated for carcinoma in situ of the cervix uteri (CIN3) in 2012 , many of whom would have gone on to develop cervical cancer without intervention.
Colposcopists will need to carefully consider whether the benefits of a small excision outweigh the potential risk of leaving diseased tissue on the cervix (i.e. positive margins), risking the need for further treatment. Patients who need a large excision of the cervix should be informed about the risk of preterm birth. Close obstetric monitoring is warranted for women who undergo large excisional treatment and subsequently become pregnant, particularly since recently published evidence suggests that preterm birth in high risk pregnancies can be substantially reduced by measuring fibronectin levels and assessing cervical length . The extra costs of close obstetric monitoring of these women will easily be offset by the saving made in the reduction of preterm births, which cost on average 1.47 % more than term babies up to age 18 .
We estimate that 840 or 2.5 % of preterm births in England each year are due to excisional treatments of 10 mm or more. Clinicians (and in particular obstetricians) need to be aware of whether women in their care have undergone treatment of the cervical transformation zone. Those who have must undergo close monitoring and further investigations with the aim of reducing the number of preterm births among these women.
Peter Brocklehurst, Heather Evans, Donald Peebles, Naveena Singh, Patrick Walker and Julietta Patnick. Pathology report data entry for the study was done by Anna Parberry and Tim Pyke (Barts Health NHS Trust). Members of PaCT study group (participating hospitals) are responsible for the collection of data included in this study. They include: Hollingworth A and Wuntakal R (Whipps Cross University Hospital London), Singh N and Parberry A (Barts Health NHS Trust), Palmer J (Royal Hallamshire Hospital, Sheffield), Das N, Andrew A and Russ L (Royal Cornwall Hospital), China S, Lenton H and Raghavan R (Worcestershire Acute Hospitals NHS Trust), Wood N and Preston S (Royal Preston Hospital Lancashire), Hannemann M and Fuller D (Royal Devon and Exeter NHS Foundation Trust), Lincoln K, Wheater G and Rolland P (The James Cook University Hospital, South Tees), Ghaem-Maghami S and Soutter P (Hammersmith Hospital, Imperial College), Hutson R (St James University Hospital, Leeds), Senguita P and Dent J (North Durham County and Darlington Trust), Lyons D (St Mary’s Hospital, Imperial College), N Gul and A Miles (Wirral University Teaching Hospital). All contributors were paid for their contribution to the data collection in this study.
This manuscript presents independent research funded by the National Institute for Health Research (NIHR) under its Research for Patient Benefit (RfPB) Programme (Grant Reference Number PB-PG-1208-16187). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. The funder had no input in the design, conduct, collation, analysis or interpretation of the data or the preparation, review or approval of the manuscript.
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- Albrechtsen S, Rasmussen S, Thoresen S, Irgens LM, Iversen OE. Pregnancy outcome in women before and after cervical conisation: population based cohort study. BMJ. 2008;337:a1343.View ArticlePubMedPubMed CentralGoogle Scholar
- Sadler L, Saftlas A, Wang W, Exeter M, Whittaker J, McCowan L. Treatment for cervical intraepithelial neoplasia and risk of preterm delivery. JAMA. 2004;291(17):2100–6.View ArticlePubMedGoogle Scholar
- Noehr B, Jensen A, Frederiksen K, Tabor A, Kjaer SK. Depth of cervical cone removed by loop electrosurgical excision procedure and subsequent risk of spontaneous preterm delivery. Obstet Gynecol. 2009;114(6):1232–8.View ArticlePubMedGoogle Scholar
- Noehr B, Jensen A, Frederiksen K, Tabor A, Kjaer SK. Loop electrosurgical excision of the cervix and subsequent risk for spontaneous preterm delivery: a population-based study of singleton deliveries during a 9-year period. Am J Obstet Gynecol. 2009;201(1):33. e31-36.View ArticlePubMedGoogle Scholar
- Kyrgiou M, Koliopoulos G, Martin-Hirsch PL, Arbyn M, Prendiville W, Paraskevaidis E. Obstetric Outcome after conservative treatment for intraepithelial or early invasive cervical lesions: systematic review and meta-analysis. Lancet. 2006;367:489–98.View ArticlePubMedGoogle Scholar
- Bruinsma FJ, Quinn MA. The risk of preterm birth following treatment for precancerous changes in the cervix: a systematic review and meta-analysis. BJOG. 2011;118(9):1031–41.View ArticlePubMedGoogle Scholar
- Jakobsson M, Gissler M, Paavonen J, Tapper AM. Loop electrosurgical excision procedure and the risk for preterm birth. Obstet Gynecol. 2009;114(3):504–10.View ArticlePubMedGoogle Scholar
- Castanon A, Landy R, Brocklehurst P, Evans H, Peebles D, Singh N, et al. Risk of preterm delivery with increasing depth of excision for cervical intraepithelial neoplasia in England: nested case–control study. BMJ. 2014;349:g6223.View ArticlePubMedPubMed CentralGoogle Scholar
- Zeitlin J, Szamotulska K, Drewniak N, Mohangoo AD, Chalmers J, Sakkeus L, et al. Preterm birth time trends in Europe: a study of 19 countries. BJOG. 2013;120(11):1356–65.View ArticlePubMedPubMed CentralGoogle Scholar
- Martin JA, Kirmeyer S, Osterman M, Shepherd RA. Born a bit too early: recent trends in late preterm births. NCHS Data Brief. 2009;24:1–8.PubMedGoogle Scholar
- What is HES? [http://www.hscic.gov.uk/hes]
- Castanon A, Brocklehurst P, Evans H, Peebles D, Singh N, Walker P, et al. Risk of preterm birth after treatment for cervical intraepithelial neoplasia among women attending colposcopy in England: retrospective-prospective cohort study. BMJ. 2012;345, e5174.View ArticlePubMedPubMed CentralGoogle Scholar
- Bornstein J, Bentley J, Bosze P, Girardi F, Haefner H, Menton M, et al. 2011 colposcopic terminology of the International Federation for Cervical Pathology and Colposcopy. Obstet Gynecol. 2012;120(1):166–72.View ArticlePubMedGoogle Scholar
- Office for National Statistics: Age–specific fertility rates (ASFRs), constituent countries of the UK, 2010. In: Fertility Summary, 2010 http://www.ons.gov.uk/ons/rel/fertility-analysis/fertility-summary/2010/uk-fertility-summary.html. 2010.
- Castanon A, Landy R, Brocklehurst P, Evans H, Peebles D, Singh N, et al. Is the increased risk of preterm birth following excision for cervical intraepithelial neoplasia restricted to the first birth post treatment?. BJOG 2015;122:1191–1199.Google Scholar
- Health and Social Care Information Centre: Cervical Screening Programme, England, Statistics for 2013–14. In., 25 November 2014 edn; 2014.Google Scholar
- Landy R, Birke H, Castanon A, Sasieni P. Benefits and harms of cervical screening from age 20 years compared with screening from age 25 years. Br J Cancer. 2014;110(7):1841–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Office for National Statistics: Cancer Statistics Registrations, England (Series MB1) No 43, 2012. In., 19 June 2014 edn; 2014.Google Scholar
- Simoens C, Goffin F, Simon P, Barlow P, Antoine J, Foidart JM, et al. Adverse obstetrical outcomes after treatment of precancerous cervical lesions: a Belgian multicentre study. BJOG. 2012;119(10):1247–55.View ArticlePubMedGoogle Scholar
- Foster C, Shennan AH. Fetal fibronectin as a biomarker of preterm labor: a review of the literature and advances in its clinical use. Biomark Med. 2014;8(4):471–84.View ArticlePubMedGoogle Scholar
- Mangham LJ, Petrou S, Doyle LW, Draper ES, Marlow N. The cost of preterm birth throughout childhood in England and Wales. Pediatrics. 2009;123(2):e312–327.View ArticlePubMedGoogle Scholar