The aim of this study was to inform the epidemiology and treatment of slipped capital femoral epiphysis (SCFE).
This was an anonymized comprehensive cohort study, with a nested consented cohort, following the the Idea, Development, Exploration, Assessment, Long-term study (IDEAL) framework. A total of 143 of 144 hospitals treating SCFE in Great Britain participated over an 18-month period. Patients were cross-checked against national administrative data and potential missing patients were identified. Clinician-reported outcomes were collected until two years. Patient-reported outcome measures (PROMs) were collected for a subset of participants.
A total of 486 children (513 hips) were newly affected, with a median of two patients (interquartile range 0 to 4) per hospital. The annual incidence was 3.34 (95% confidence interval (CI) 3.01 to 3.67) per 100,000 six- to 18-year-olds. Time to diagnosis in stable disease was increased in severe deformity. There was considerable variation in surgical strategy among those unable to walk at diagnosis (66 urgent surgery vs 43 surgery after interval delay), those with severe radiological deformity (34 fixation with deformity correction vs 36 without correction) and those with unaffected opposite hips (120 prophylactic fixation vs 286 no fixation). Independent risk factors for avascular necrosis (AVN) were the inability of the child to walk at presentation to hospital (adjusted odds ratio (aOR) 4.4 (95% CI 1.7 to 11.4)) and surgical technique of open reduction and internal fixation (aOR 7.5 (95% CI 2.4 to 23.2)). Overall, 33 unaffected untreated opposite hips (11.5%) were treated for SCFE by two-year follow-up. Age was the only independent risk factor for contralateral SCFE, with age under 12.5 years the optimal cut-off to define ‘at risk’. Of hips treated with prophylactic fixation, none had SCFE, though complications included femoral fracture, AVN, and revision surgery. PROMs demonstrated the marked impact on quality of life on the child because of SCFE.
The experience of individual hospitals is limited and mechanisms to consolidate learning may enhance care. Diagnostic delays were common and radiological severity worsened with increasing time to diagnosis. There was unexplained variation in treatment, some of which exposes children to significant risks that should be evaluated through randomized controlled trials.
Cite this article: Bone Joint J 2022;104-B(4):519–528.
Take home message
Diagnostic delays in the treatment of slipped capital femoral epiphysis (SCFE) are common and associated with worse radiological deformity.
The experience of individual hospitals is limited, and mechanisms to consolidate care and learning throughout geographical regions may enhance care.
There are several uncertainties, relating to severe disease, unstable SCFE, and the unaffected hip, that warrant the consideration of definitive randomized controlled trials.
Slipped capital femoral epiphysis (SCFE) is a disease of the adolescent hip joint that affects one in 1,300 adolescents.1,2 The mechanism is principally failure of the physis in response to load. Childhood obesity appears to be the primary cause of SCFE.1,2 In the short term, it always requires urgent surgery to stabilize the physis, and typically results in deformity of the hip. In the short term, this leads to damage to the acetabular cartilage.3 In the long term, SCFE accelerates the development of osteoarthritis, and many patients have disability necessitating hip arthroplasty in early adulthood.4 SCFE typically has an insidious onset, presenting to the family doctor, emergency department, or physiotherapist with knee, thigh, or hip pain, and/or a limp.1 In many patients the diagnosis is overlooked, and it is common for the diagnosis to take several months.1,5
While SCFE is the most frequent hip disease of adolescence, robust evidence to support effective management and intervention is poor, with no clinical trials to guide treatment decisions. Information regarding outcomes is almost universally limited to retrospective case series arising from single centres. Poor-quality evidence has contributed to considerable differences in surgical practice internationally.6-8 This has prompted members of the British Society of Children’s Orthopaedic Surgery to prioritize questions pertaining to SCFE among the top five research priorities in children’s orthopaedic surgery.9,10
Criticism within The Lancet of the poor quality of evidence in surgery11 prompted the development of a framework to guide surgical research, called the Idea, Development, Exploration, Assessment, Long-term study (IDEAL) framework.12-14 We describe a national cohort study of SCFE that follows the IDEAL recommendations (IDEAL Stage 2b, ‘Exploration’), to explore the disease frequency, case mix, technical intervention variables, surgeon- and patient-reported outcomes, and safety.
We prospectively identified a cohort of skeletally immature children with a new radiological diagnosis of SCFE undergoing surgery in Great Britain. Children were identified between 4 April 2016 and 30 September 2017. Data were collected through a national surveillance programme, called the British Orthopaedic Surgery Surveillance (BOSS) study. This used a bespoke electronic platform. A full protocol detailing the BOSS study platform and details of the SCFE study has been previously published.15,16 All but one hospital in Britain that routinely treated SCFE agreed to participate in the study (n = 143). The denominator population was defined as six- to 18-year-olds, within the geographical boundaries of Great Britain.
Children were identified prospectively by treating clinical teams. Following admission to hospital, nominated clinicians completed an electronic patient record form providing anonymous details related to the patient, disease presentation, and surgery. Patients who were potentially missed were identified monthly by cross-referencing collected data with routinely collected administrative data available from Hospital Episode Statistics (HES) for England, Patient Episode Database for Wales (PEDW), and the Information Services Division (ISD) for Scotland. Missing patient records were also available from an independent network of trainee surgeons. Each month an automated email was sent to nominated reporting clinicians in each hospital to ask them to verify and confirm the completeness of their monthly case uploads (including verification of a null report). In addition, the email highlighted potential missed patients identified through administrative data or by trainees, and invited reporting clinicians to upload the missing records or indicate these as a false identification. The email also identified when follow-up was due. Surgeon follow-up from routine care records was sought at three months and two years post-surgery to identify complications, principally the development of avascular necrosis (AVN), chondrolysis, reoperations, and contralateral disease.
Patient-reported outcome measures (PROMs) were collected for a subset of hospitals recruiting patients to the study. While surgeons entered patient data to collect anonymized outcomes from the time of diagnosis, patients could be enrolled to provide PROMs at any time during the two years of follow-up. Regardless of when patients were enrolled, PROMs were collected following the schedule related to the date of surgery. The PROMs collected were the Paediatric Quality of Life Inventory (PedsQL),17 the youth version of the EuroQol five-dimension three-level questionnaire (EQ-5D-Y),18 and the Wong-Baker FACES Pain Rating Scale.19
The study was registered on the ISCTRN registry (ISRCTN54477575). The study is reported in accordance with the IDEAL reporting guidelines.20 Parents and representatives from STEPS Worldwide, the primary charitable support group for children and young people with limb disorders, coproduced the work from prefunding until publication with involvement in producing patient-facing materials and defining outcomes and outcome timepoints. A parent representative participated in the Study Management Group throughout the five-year study period. The Alder Hey NIHR Young Person’s Advisory Group (YPAG), a group of children and young people involved in improving the conduct of research in children, were also involved throughout the progress of the study. The YPAG have assisted in the development of the paper and digital participant information materials, advised on conduct during interval study updates, and are engaged in the dissemination of this work to patients and the public through animations and infographics.
The statistical analysis was finalized prior to data lock. Incidence rates for new SCFE (no prior diagnosis in either hip) were calculated using patients identified between 1 June 2016 and 31 August 2017, which allowed for a ‘run-in period’ in terms of case ascertainment and discounted the final month of data collection for which national administrative data were unavailable. Rates were calculated by country, region, age, and sex. Denominators were taken to be the 2016 mid-year Office for National Statistics population estimates.21 Poisson 95% confidence intervals (CIs) were calculated.
Cohort characteristics were summarized, as well as medical history, timeline prior to surgery, imaging availability, and presentation of affected hip(s). Patients were classified according to the commonly used definition of clinical stability (i.e. ‘stable’ is when a child is able to walk at the time of admission, with or without the use of crutches),22 and hips were classified by the radiological severity of SCFE determined by the treating surgeon according to their usual practice (i.e. mild, moderate, or severe). Further detail was summarized regarding presentation, the use of prophylactic surgery in the unaffected (opposite) hip, fixation techniques, and postoperative planning. Full details of pre-planned analysis related to cohort characteristics is available in Supplementary Material.
Over the course of a two-year follow-up, we summarized the complications for affected hips, and unaffected (opposite) hips. Random effects logistic regression was used to model the risk of AVN in all affected hips, adjusting for stability of hip at presentation and use of open reduction, and in open reduction, adjusting for surgeon experience. The results of multivariable modelling, in line with the statistical analysis plan, can be found in the full statistical analysis report (Supplementary Material).
The effects of patient and treatment factors on the risk of contralateral SCFE, in unilateral first presentations without prophylactic surgery, were explored using survival analysis (Kaplan-Meier graphs and Cox proportional hazards modelling). Recursive partitioning was also used to generate an understanding of key binary predictors of this outcome. A separate analysis was carried out investigating PROMs. Given the low numbers of patients for this analysis, results are presented using descriptive statistics. We have chosen to calculate percentages throughout, excluding missing data. Tables in the full BOSS statistical analysis report indicate numbers missing for each variable (Supplementary Material).
Overall, 486 children had a new radiological diagnosis of SCFE identified during the 18-month recruitment period. Patients were identified from 100 of the 143 recruiting hospitals, with the median number of patients in each hospital being two (interquartile range (IQR) 0 to 4). Of these, 17 children were excluded from follow-up analyses as baseline case report forms were not completed beyond initial case confirmation, leaving a cohort of 469 children (513 hips).
The annual incidence of SCFE was 3.34 (95% CI 3.01 to 3.67) patients per 100,000 six- to 18-year-olds throughout the incident period. Rates were broadly similar across England, Scotland, and Wales (Table I).
|Variable||Population, n||First presentation|
|n||Incidence (95% CI)|
|All||9,499,724||397||3.34 (3.01 to 3.67)|
|England||8,301,394||357||3.44 (3.08 to 3.80)|
|London/surrounding boroughs||1,851,204||81||3.5 (2.78 to 4.35)|
|South||1,696,467||69||3.25 (2.53 to 4.12)|
|Northern||2,280,272||99||3.47 (2.79 to 4.16)|
|Central||2,473,451||108||3.49 (2.83 to 4.15)|
|Wales||454,551||7||1.23 (0.50 to 2.54)|
|Scotland||743,779||33||3.55 (2.44 to 4.98)|
|6 to 10 yrs||3,850,071||79||1.64 (1.30 to 2.05)|
|11 to 18 yrs||5,649,653||318||4.5 (4.01 to 5.00)|
|Male||4,867,679||225||3.7 (3.21 to 4.18)|
|Female||4,632,045||172||2.97 (2.53 to 3.41)|
Six- to 18-year-olds in England, Scotland, and Wales (2016 mid-year estimate from the Office for National Statistics).
CI, confidence interval.
Sensitivity analysis using administrative data
International Classification of Diseases-1023 and OPCS Classification of Interventions and Procedure codes24 within routine hospital administrative data from England, Scotland and Wales identified 596 admission records of SCFE within the incident period. Welsh data was not provided after 1 April 2017. Of these 596 records, clinicians confirmed that 222 of these records were not new disease episodes (i.e. previously diagnosed disease undergoing secondary procedures) and six records were duplicates. In total, 336 (91.3%) of the remaining 368 codes matched to new patients within the database using the predefined parameters (i.e. month and year of birth, sex, date of surgery, and hospital), leaving 32 unmatched. There were an additional 61 patients confirmed by clinicians, for which there was no record within administrative data. Within the administrative data, the 32 unmatched codes were unresolved at the time that the database closed for case ascertainment. Assuming that the 32 patients who were all missed were true, the incidence would rise to 3.61 (95% CI 3.27 to 3.95) cases per 100,000 six- to 18-year-olds.
The median age of children was 12.7 years (IQR 11.4 to 13.8), with a slight preponderance in males (Table I). Of the 486 participants, 149 were recorded as having at least one comorbidity. The principal comorbidity being obesity (123 children; 26.3%), with others including hypothyroidism (nine children; 1.9%), other endocrinopathies (seven children; 1.5%), Down’s syndrome (four children; 0.9%), and prior treatment with radiotherapy (one child; 0.2%).
A total of 102 children (21%) were described to have a clinically unstable SCFE, with the child unable to walk with or without the use of crutches at diagnosis. Among the 380 children (402 hips) with stable SCFE, the deformity was described as mild in 215 hips (53%), moderate in 109 (27%), and severe in 75 (19%).
In 344 of the 486 individuals, clinicians indicated more than one week elapsed from the onset of symptoms to admission for treatment. There were 311 free-text entries describing events during this time interval: 98 highlighted delays by the family in seeking healthcare; 96 identified multiple healthcare attendances with an initial diagnosis of “groin sprain”, “growing pains”, or similar; 28 reported radiographs were initially believed to be normal; and 26 noted that the radiologically confirmed disease was referred on a non-urgent basis. Other delays included delays accessing radiographs or delays in accessing specialist opinions prior to a definitive diagnosis. Among stable slips, the disease severity increased as the median time to diagnosis increased (Table II).
|Variable||Stable at presentation||Unstable at presentation|
|Median time to diagnosis, mths (IQR)||1 (0 to 2)||2 (1 to 8)||3 (0 to 7)||1 (0 to 2)|
IQR, interquartile range.
Surgical fixation involved the use of a single screw to stabilize the physis in 433 hips (85%), with multiples screws used in 61 hips (12%). Ten hips (2%) were stabilized without screws, while 25 hips were treated with modified screws designed to permit growth at the physis. Among patients for whom the slip was classified stable, surgery was generally undertaken as planned surgery on the next available routine trauma list (299/380; 79.9%). Among patients for whom the slip was classified unstable, a planned delay to surgery occurred in 37/96 (38.5%), at a median of 8.5 days (IQR 5.5 to 10.0). Open reduction to reduce the severity of the SCFE was undertaken in 95 hips (53 unstable, 41 stable, 1 unreported), of which 39 were performed through a surgical dislocation and 51 performed without dislocating the hips. The technique was unreported in five hips. The clinical stability and radiological severity of the hip strongly influenced the surgical strategy (Figure 1).
There were 406 unaffected hips (i.e. patients for whom the opposite hip was not, or had not previously been affected, by SCFE). Of these, 120 (30%) underwent prophylactic fixation to prevent SCFE, leaving 286 (70%) at risk of SCFE. Of those undergoing prophylactic fixation, surgeons identified this as their standard protocol in 57 hips (48%), while others cited risk factors of obesity, younger age, or ‘other’ as the reason for fixation.
Outcomes were recorded for 89% of hips at three months and 79% at two years. Data were missing either because patients were identified as lost to follow-up (20 hips at three months and 62 hips at two years), or because patient record forms were not returned by clinicians (34 hips at three months, 47 hips at two years).
Overall, 29 hips (7.1%) were affected by AVN by two years. Nine patients with AVN occurred within the group of 316 clinically stable hips with SCFE. Among stable hips for which open reduction was performed, 4/34 (11.8%) developed AVN, whereas AVN occurred in 5/276 (1.8%) stable hips that did not undergo open reduction. AVN occurred in 20/90 hips (23.0%) presenting with ‘unstable’ SCFE. The ORs of AVN were 4.4 (95% CI 1.7 to 11.4) for unstable versus stable hips, and 7.5 (95% CI 2.4 to 23.2) for hips undergoing open reduction versus not (Table III). Surgeon-reported experience in the technique of open reduction did not appear to mitigate the risk of AVN (Table IV).
|Covariate||Hips, n||Any AVN, n (%)||OR (95% CI)|
|Stability of hip at presentation|
|Stable||310||9 (2.9)||1.0 (reference)|
|Unstable||87||20 (23.0)||4.4 (1.7 to 11.4)|
|Open reduction carried out at baseline|
|Yes||79||21 (26.7)||7.5 (2.4 to 23.2)|
|No||318||8 (2.5)||1.0 (reference)|
|Hips excluded from model||116|
|Stability/open reduction status missing||11|
|Followed up, but AVN status unknown||85|
|Lost to follow-up||20|
AVN, avascular necrosis; CI, confidence interval; OR, odds ratio.
|Covariate||Hips, n||Any AVN, n (%)||OR (95% CI)|
|Experience of most senior surgeon*||72||19 (26.4)||1.0 (0.8 to 1.2)|
|5 to 10||13||2 (15)|
|> 10||19||6 (32)|
|Hips excluded from model||23|
|Experience of surgeon missing||12|
|Followed up, but AVN status unknown||7|
|Lost to follow-up||4|
Number of similar procedures using the open reduction technique performed in past year by the senior surgeon.
AVN, avascular necrosis; CI, confidence interval; OR, odds ratio.
Chondrolysis occurred in three hips (0.8%) by two years. Other complications included surgical site infection (n = 4; 0.9%), osteomyelitis (n = 1; 0.2%), periprosthetic fracture (n = 2; 0.4%), implant penetration into the joint (n = 6; 1.3%), and screw failure or movement resulting in disease recurrence (n = 5; 1.1%). Following the initial surgery, 74 hips (16%) were known to have undergone secondary surgery by two years, with a further 43 (11%) scheduled to have surgery in the period after completion of the study. Most notably, 11 (2.5%) had undergone (or were scheduled to undergo) total hip arthroplasty, and ten (2.2%) had undergone, or were scheduled to undergo, major realignment surgery involving corrective osteotomies.
A preplanned analysis using α angle to describe hip shape was undertaken, though yielded little usable information. These are available within the Supplementary Material.
Opposite (unaffected) hips
Among the 120 hips that underwent prophylactic fixation, follow-up was available in 117 (97.5%) at three months and 106 (88.3%) at two years. By three months, four (3.6%) developed a surgical site infection, one (0.9%) was revised for a periprosthetic fracture, and one (0.9%) for implant penetration into the joint. By two years, one (1.0%) developed AVN, and one (1.0%) developed osteomyelitis, with additional surgery undertaken on a further eight hips, composed of two (1.7%) exchange/adjustment of screws, one (0.9%) failed removal of screw, and five (4.3%) removal of screws. No hips that had been prophylactically fixed developed a subsequent SCFE.
In total, 286 hips unaffected by SCFE did not undergo prophylactic fixation. Among these, 33 operations for SCFE were recorded during the two-year follow-up period (11.5% (95% CI 7.8% to 15.2%)). The Kaplan-Meier plot illustrates the time from the start of the at-risk period (the time of first SCFE surgery) to diagnosis, stratified by sex and age (Figures 2a to c). A univariate analysis demonstrated that age appeared to be an important determinant of disease, with younger children at greater risk of SCFE. Other baseline predictors (sex, BMI, SCFE severity) were not predictors of subsequent contralateral disease.
A decision tree analysis, using recursive partitioning, showed that age alone was the most useful predictor of contralateral disease: the optimal partition was at 12.5 years, with 23 patients from 124 hips (18.5%) below this age, and nine patients from 164 hips (5.6%) above this age.
A nested cohort of participants (n = 144) consented to complete PROMs and could be recruited at any point during the follow-up period. In total, 50 of the 143 sites agreed to collect PROMs: 47 participants completed PROMS at baseline, from 49 participants enrolled at this timepoint. However, only 59 patients completed outcomes at two years (41% of those enrolled). The baseline demographic data of those completing PROMs were broadly similar in terms of age, sex, ethnicity, BMI, and clinical stability to those in the surveillance cohort (Supplementary Material). However, a slightly larger proportion of those completing PROMs were classified as having more severe SCFE, with 26/59 (44%) having severe deformity and 14/59 ( 24%) moderate deformity.
At diagnosis, SCFE had a marked impact on health, which was particularly evident within the domain of physical health (PedsQL median total score 52.7 (IQR 43.5 to 66.3) and median physical health score 31.3 (IQR 15.6 to 50.0)). At two years, the median total score was 82.6 (IQR 63.0 to 92.4) and median physical health score was 83.3 (IQR 62.5 to 90.6). Overall, 51% participants (30/59) reported ‘very good or excellent’ health by two years, compared to 4.3% (2/47) at baseline (Figure 3).25 This was reflected in the EQ-5D-Y scores, which were 0.1 (IQR -0.2 to 0.6) at baseline, improving to 0.9 (IQR 0.8 to 0.1) at final follow-up. Similarly, there were improvements in pain. However, questionnaire completion was insufficient to investigate the association between PROMs and baseline factors.
This is the most comprehensive study to investigate SCFE, with almost complete involvement of hospitals throughout Britain. We identified the rarity of SCFE in hospitals, with the median number of patients encountered over the study period per hospital of two. We found an association between time to diagnosis and the severity of disease, coupled with recognizing the barriers to making a prompt diagnosis. We also demonstrated marked differences in surgical decisions regarding the treatment of similar patients with SCFE, with evidence that this has important effects on patient outcomes and the complications that affected children encounter.
The comprehensive case-finding mechanism enabled a reliable estimate of incidence, with few patients being identified within routine nationwide hospital administrative data unaccounted for. The slightly lower rate of disease in Wales may be accounted for with incomplete access to administrative data in the later period.
The study particularly highlights the variation in practice. Uncertainty was notably related to three areas of surgical practice: clinically unstable hips, with 60% having urgent surgery, while 40% had surgery that was deliberately delayed by at least one week; clinically stable hips with severe deformity, for which half of the children had correction of the deformity and half had fixation of the deformity without correction; and unaffected opposite hips, of which 30% were operated on to prevent SCFE, and 70% were not. This variation is in part due to a lack of evidence from randomized controlled trials (RCTs) to support any element of practice in SCFE surgery, with interventions often having major variation in the magnitude and complexity of surgery.
This cohort confirms the high risk of AVN among unstable hips, the magnitude of which was broadly in keeping with other studies.26 Among unstable hips, a particular difference in practice was that some surgeons enforced a period of ‘bed rest’ prior to surgery, in the belief that there is a time window (between 24 hours and one to two weeks) during which surgery heightens the risk of AVN.27,28Among those patients with severe deformity, surgeons are generally divided on whether to perform open reduction to normalize the anatomy, albeit risking AVN, or to accept deformity and the symptoms and potential sequelae associated with it. A review by the UK National Institute for Health and Care Excellence noted the safety risk related to AVN, and concluded that the procedure should only be undertaken with special arrangements for governance, consent, audit, and research.29 We have demonstrated that open reduction carries a high risk of AVN in SCFE, independent of stability at baseline, with no evidence that this risk is mitigated by the experience of the surgeon. However, the benefit of surgery on the physical function of the child may be sufficient to outweigh the risks, the answer to which is not available from this study.
For the unaffected (opposite) hip, we have also shown that the importance of age in the risk of SCFE, which appears likely to be related to the ‘at risk period’ (i.e. years of growth) remaining. Prophylactic surgery did prevent the development of SCFE but also had several major complications, including one patient who developed AVN and a subtrochanteric fracture, which must be balanced against the risk of SCFE in this group. A sensible approach appears to be one that considers individual risk; however, the only baseline predictor contributing to future risk was age, with younger children having greater risk, especially younger than 12.5 years old. Other factors, such as sex, BMI, clinical stability, or radiological severity, did not contribute to the risk. We are aware that there may be other factors to consider that we did not record, such as biochemical measures (i.e. leptin) or specific radiological measures (i.e. epiphyseal tubercle anatomy).30,31
The collection of PROMs demonstrated the profound impact of SCFE on affected children in the immediate aftermath of disease, with the impact on life still persisting two years after the diagnosis. The biggest impact to the children was on their physical health, although all health domains were impacted by disease.
As well as highlighting areas of controversy within surgical practice, this study highlighted areas with little controversy, such as the need to use a single conventional screw for the majority of patients. In addition, we identified obesity as the major comorbidity among those with SCFE. Other comorbid diseases that are commonly believed to be risk factors (i.e. hyopthyroidism) were rare in this population.1,2
Challenges in receiving a prompt diagnosis were evident. There was poor awareness of the disease among healthcare professionals and families. Furthermore, even when a diagnosis was made, treatment was not always recognized to be urgent, with missed diagnostic opportunities evident among physiotherapists, radiologists, family doctors, emergency doctors, and orthopaedic surgeons. Delay was important, because we identified that an increasing delay was associated with a worsening radiological severity of disease at diagnosis. While education will inevitably be the mainstay of raising awareness of SCFE and its treatments, the use of technology may offer opportunities. Diagnostic prompts may be used in electronic health records to flag ‘at risk’ children with relevant symptoms, and machine vision may be used to flag radiographs that the computer identifies to show SCFE.
A strength of this study was the completeness of case ascertainment, which minimized the likelihood of selection bias. The incidence of disease appears likely to be reliable, with only one small hospital not contributing to the study, where there were no patients with SCFE identifed from their hospital administrative data. Elements of the study were deliberately pragmatic, seeking to reflect real-world clinical practice, such as surgeon determination of radiological severity. The study is limited in some respects by missing follow-up data. Automated reminders and an easy web-based data collection tool resulted in a 79% return rate from clinicians. However, PROM follow-up rates were generally low, reflecting the challenges faced in introducing multicentre research within a research-naïve clinical speciality. The completed PROMs demonstrated some evidence of selection bias, identified through a greater disease severity among those completing PROMs. We were also unable to investigate baseline predictors of outcome (i.e. disease severity) with PROMs. Nevertheless, this does not lessen the value of the PROMs in illustrating the impact of the disease on affected children.
The size of the SCFE population and variation in surgical pathways, coupled with an obvious difference in procedural safety and profound impact on the quality of life of the child, means that more definitive research is necessary. The research delivery network within UK paediatric orthopaedics has grown considerably since the initiation of this study, though this needs continued nurturing to ensure the feasibility of such research. In particular, a clinical trial must address the clear uncertainty related to severe stable SCFE to ascertain whether open reduction to correct deformity results in better patient outcomes than fixation without deformity correction. Furthermore, clinical trials and risk prediction models to guide the treatment of the opposite hip are needed, though given the paucity of events, this effort may need to be global to derive clinically meaningful results. In light of this study, we are pleased that the National Institute for Health Research have recently funded our group to conduct a RCT identifying the optimal treatment for severe stable SCFE.
In conclusion, this is a comprehensive cohort study of SCFE which has demonstrated that diagnostic delays were common and were associated with worse radiological deformity, also that education and innovative tools are a potential solution in order to maximize diagnostic opportunities. The experience of individual hospitals treating SCFE was limited, but mechanisms to consolidate care and learning throughout geographical regions may enhance care. We also found that there are several key aspects of treatment which may expose children to significant risk of complications and consideration should be given to them in the context of definitive RCTs to determine their efficacy.
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D. C. Perry: Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Investigation, Data curation, Visualization, Writing – original draft.
B. Arch: Methodology, Investigation, Formal analysis, Writing – review & editing.
D. Appelbe: Methodology, Software, Investigation, Writing – review & editing.
P. Francis: Project administration, Data curation.
J. Craven: Project administration, Writing – review & editing
F. P. Monsell: Conceptualization, Supervision, Writing – review & editing.
P. Williamson: Formal analysis, Investigation, Writing – review & editing.
M. Knight: Conceptualization, Methodology, Supervision, Writing – review & editing.
The author(s) disclose receipt of the following financial or material support for the research, authorship, and/or publication of this article: this work presents independent research funded by the National Institute for Health Research (NIHR) through an NIHR Clinician Scientist Fellowship (CS-2014-14-012) awarded to D. C. Perry. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, or the Department of Health.
We would like to thank all those involved in making BOSS a success, including the patients and their parents/carers, the research associates at all the research sites, the multidisciplinary teams including nurses, radiographers, physiotherapists and orthopaedic surgeons from different hospitals in the UK. Thanks to the BOSS steering committee which included Prof. Xavier Griffin (Barts Health NHS Trust), Prof. Mike Pearson (University of Liverpool), Emma Morely (Patient representative, STEPS charity) and was chaired by Prof. James Wright (Hospital for Sick Children, Toronto). Further thanks to Jenny Preston for her facilitation of patient and public engagement and The children and young people of the Generation R Liverpool Young Person’s Advisory Group (YPAG). In particular, we would like to thank Cath Spowart and Emma Cwiklinski for their commitment in trial coordination and management.
Thank you to the individuals who led data collection at each site:
A. Kitching, Airedale NHS Foundation Trust; C. Bruce, Alder Hey Children's NHS FoundationTrust; S. Lewis, Aneurin Bevan University Health Board; K. Vemulapalli and A. Acharya, Barking, Havering and Redbridge University Hospitals NHS Trust; S. Sharma, Barnsley Hospital NHS Foundation Trust; M. Ramachandran, Barts Health NHS Trust; M. Tiruveedhula and S. Symons, Basildon & Thurrock University Hospital NHS Foundation Trust; P. Edge, Bedfordshire Hospitals NHS Foundation Trust; K. Azurza and D. A. V. O'Kelly, Betsi Cadwaladr University Health Board; E. Bache, Birmingham Women's and Children's NHS Foundation Trust; A. Anand, Blackpool Teaching Hospitals NHS Foundation Trust; S. Livingston, Borders General Hospital; D. Shaw, Bradford Teaching Hospitals NHS Foundation Trust; S. N. Maripuri, Brighton and Sussex University Hospitals NHS Trust; J. Hicks, Buckinghahire Healthcare NHS Trust; S. Burgess, Calderdale and Huddersfield NHS Foundation Trust; K. Stohr and A. Rehm, Cambridge University Hospitals NHS Foundation Trust; C. Carpenter and P. Thomas, Cardiff and Vale University Local Health Board; S. Evans, Chelsea and Westminster Hospital NHS Foundation Trust; J. Cashman, Chesterfield Royal Hospital NHS Foundation Trust; G. DeKiewiet and I. Talkhani, City Hospitals Sunderland NHS Foundation Trust; V. S. Shanker and V. Mula, Colchester Hospital University NHS Foundation Trust; K. Thomason and M. Nixon, Countess of Chester Hospital NHS Foundation Trust; J. Page, County Durham and Darlington NHS Foundation Trust; J. Murray, Cwm Taf Health Board; M. Mohan Utukuri and S. Tafazal, Derby Hospitals NHS Foundation Trust; R. Kucharski and S. Madan, Doncaster and Bassetlaw Hospitals NHS Foundation Trust; N. Savva, Dorset County Hospital NHS Foundation Trust; A. Hawkins, Dumfries and Galloway Royal Infirmary; N. De Roeck, East and North Hertfordshire NHS Trust; M. Cornell, East Kent Hospitals University NHS Foundation Trust; R. Paton, East Lancashire Hospitals NHS Trust; A. Butler-Manuel, East Sussex Healthcare NHS Trust; E. Oakley, Epsom and St Helier University Hospitals NHS Trust; F. Norman-Taylor, Evelina London Children’s Hospital; B. Murray, Forth Valley Royal Hospital; A. Jalgaonkar and T. Jacob, Frimley Park Hospital NHS Foundation Trust; D. Rowland, Glasgow Royal Infirmary; M. Henderson, Gloucestershire Hospitals NHS Foundation Trust; A. Roposch and Y. Jabbar, Great Ormond Street Hospital for Children NHS Foundation Trust; S. Irby, Great Western Hospitals NHS Foundation Trust; M. Kokkinakis and D. Reed, Guys and St Thomas NHS Foundation Trust; I. Macleod and N. Rossiter and K. Conn, Hampshire Hospitals NHS Foundation Trust ; D. Lavalette, Harrogate and District NHS Foundation Trust; R. Dimitriou, Heart Of England NHS Foundation Trust; H. Bhatt, Hillingdon Hospitals NHS Foundation Trust; A. Patel and S. Jiwanmall, Hinchingbrooke Health Care NHS Trust; T. Baring, Homerton University Hospital NHS Foundation Trust; S. Hobson and E. Moulder, Hull University Teaching Hospitals NHS Trust; R. Bhattacharya and K. Sarraf, Imperial College Healthcare NHS Trust; D. Donaldson, Inverclyde Royal Hospital; G. Carlile, Ipswich Hospital NHS Trust; S. Shyamsundar and S. Siddiqui, Kettering General Hospital NHS Foundation Trust; O. Lahoti and I. Reichert, Kings College Hospital NHS Foundation Trust; T. McEvoy and P. Kasliwal, Lancashire Teaching Hospitals NHS Foundation Trust; C. Holton, Leeds Teaching Hospitals NHS Trust; M. Abdus-Samee and S. Bajaj, Lewisham and Greenwich NHS Trust; S. Verma, Luton and Dunstable Hospital NHS Foundation Trust; M. Katchburian, J. Dartnell, Maidstone and Tunbridge Wells NHS Trust; M. Kenawey, Manchester University NHS Foundation Trust (Manchester Children's Hospital); B. Singh and M. Bhat, Medway NHS Foundation Trust; D. Machin and H. Kazi, Mid Cheshire Hospitals NHS Foundation Trust; P. Buddhdev and J. Tuite, Mid Essex Hospital Services NHS Trust; N. Tulwa, Mid Yorkshire Hospitals NHS Trust; J. Flynn and M. Khalik, Milton Keynes Hospital NHS Foundation Trust; D. Campbell and J. MacLean, NHS Tayside; A. P. Sanghrajka and R. Hutchinson, Norfolk and Norwich University Hospitals NHS Foundation Trust; C. Brignall, North Cumbria University Hospitals NHS Trust; V. Asopa, North Middlesex University Hospital NHS Trust; I. Holloway, North West London Hospitals NHS Trust; R. Natarajan and K. Muthusamy, Northampton General Hospital NHS Trust; L. Brunton, Northern Devon Healthcare NHS Trust; F. Howell, Northern Lincolnshire and Goole Hospitals NHS Foundation Trust; M. Reed and R. Critchley, Northumbria Healthcare NHS Foundation Trust; K. Price and J. Hunter, Nottingham University Hospitals NHS Trust; R. Buckingham and A. Wainwright, Oxford University Hospitals NHS Trust; A. Bonshahi and E. Yates, Pennine Acute Hospitals NHS Trust ; P. Mitchell, Peterborough and Stamford Hospitals NHS Foundation Trust; B. Holroyd and J. Aird, Plymouth Hospitals NHS Trust; R. Richards, Portsmouth Hospitals University NHS Trust; P. Renshaw and K. Mcleod, Raigmore Hospital; R. Freeman, Robert Jones and Agnes Hunt Orthopaedic and District Hospital NHS Trust; S. Barker and L. Mills, Royal Aberdeen Children’s Hospital; R. B Abu-Rajab and J. Smith, Royal Alexandria Hospital; N. Davies, Royal Berkshire NHS Foundation Trust; R. Hawkins, Royal Cornwall Hospitals NHS Trust; P. Cox and J. Howell, Royal Devon and Exeter NHS Foundation Trust; O. Malaga Shaw, Royal Free London NHS Foundation Trust; J. Saksena, Royal Free London NHS Foundation Trust (Barnet and Chase Farm Hospitals); E. Baird and M. Gaston, Royal Hospital for Sick Children, Edinburgh; N. Wilson, Royal Hospital for Sick Children, Glasgow; D. Eastwood and A. Hashemi-Nejad, Royal National Orthopaedic Hospital NHS Trust; C. Coates, Royal Surrey County NHS Foundation Trust; A. McBride, Royal United Hospital Bath NHS Trust; P. Pettit, Salisbury NHS Foundation Trust; S. Roy, Sandwell and West Birmingham Hospitals NHS Trust; S. Joshy, Scarborough and North East Yorkshire Health Care NHS Trust; N. Nicolaou and S. Madan, Sheffield Children’s NHS Foundation Trust; J. Rhee, Shrewsbury and Telford Hospital NHS Trust; G. Wansbrough, South Devon Healthcare NHS Foundation Trust; R. Tate and D. Ferguson, South Tees Hospitals NHS Foundation Trust; H. Mackay, Southport and Orkirk Hospital NHS Trust; K. Dal, Y. Gelfer, and A. Yeo, St Georges Healthcare NHS Trust; S. Lipscombe, St Helens and Knowsley Hospitals NHS Trust; B. Morgan and S. Alshryda, Stockport NHS Foundation Trust; P. Williams, Swansea Bay University Health Board; W. Jamil, Tameside Hospital NHS Foundation Trust; A. Kelly and E. Mounsey, Taunton and Somerset NHS Foundation Trust; V. Spiteri, The Dudley Group NHS Foundation Trust; P. Henman, W. Bliss, and A. de Gheldere, The Newcastle Upon Tyne Hospitals NHS Foundation Trust; D. Manoukian, The Princess Alexandra Hospital NHS Trust; S. Giles and S. Weston-Simons, The Rotherham NHS Foundation Trust; R. Vadivelu, The Royal Wolverhampton NHS Trust; A. O'Gorman and C. Charalambides, The Whittington Hospital NHS Trust; I. Majid, The Bolton NHS Foundation Trust; R. Hopcroft, The James Cook University Hospital; T. Southorn and R. Asirvatham, United Lincolnshire Hospitals NHS Trust; M. Oddy and J. Witt, University College London Hospitals NHS Foundation Trust; R. Marian Short and M. Zgoda, University Hospital Crosshouse; N. Kurdy, University Hospital of South Manchester NHS Foundation Trust; A. Aarvold, M. Uglow, and K. Elliott, University Hospital Southampton NHS Foundation Trust; F. Monsell, S. Thompson, and G. Atherton, University Hospitals Bristol NHS Foundation Trust; S. Cooke and G. Pattison, University Hospitals Coventry and Warwickshire NHS Trust; A. Abraham and A. Kulkarni, University Hospitals of Leicester NHS Trust; K. Allison, University Hospitals of Morecambe Bay NHS Foundation Trust; B. Carsi, University Hospitals of the North Midlands; K. Periasamy, University Hospital Hairmyres; A. Murray and K. Ferguson, University Hospital Monklands; N. Marriott, Warrington and Halton Hospitals NHS Foundation Trust; K. Deierl, West Hertfordshire Hospitals NHS Trust; V. Babu and H. Zadeh, West Middlesex University Hospital NHS Trust; S. Deakin, West Suffolk NHS Foundation Trust; A. Predl, Western Isles Hospital; K. Sri-Ram, Whipps Cross University Hospital; G. Jackson, Wirral University Teaching Hospital NHS Foundation Trust; C. Docker, Worcestershire Acute Hospitals NHS Trust; A. Ajis, Worthing And Southlands Hospitals NHS Trust; H. Wynn-Jones, H. Divecha, and B. D. Coupe, Wrightington, Wigan and Leigh NHS Foundation Trust; I. Bissell, Wye Valley NHS Trust; and S. Hobson, York Teaching Hospital NHS Foundation Trust.
Thank you to the trainees who submitted data. The following trainees reliably submitted data for at least four consecutive months during the project:
A. Dick, A. J Grazette, A. Doorgakant, B. A. Marson, C. E. Hill, D. Shields, D. Hansom, I. McLaughlin-Simon, J. T. Bourne, L. H. Lee, M. Hughes, M. Mohamed, M. A. Akhtar, mnN. M. Ormsby, P. Buddhev, R. Gogna, R. J. Critchley, R. W. D. Pilling, T. Boutefnouchet, T. Wood, W. D. Harrison, M. Chamberlain, Z. Hashim, E. Davidson, and T. Koc.
Ethical review statement
This programme of work complies with the Declaration of Helsinki and was reviewed and approved by the National Research Ethics Service Committee London – City and East (REC ref: 15/LO/2202) and the Health Research Authority (ref: 190754). The release of National Administrative Data for this purpose was approved by the Public Benefit and Privacy Panel (PBPP) in Scotland (ref: 1617-0030) and the Data Access Advisory Group (DAAG) in England (ref: NIC-362142-K9C7P). There was no similar process in Wales.
Open access funding
Funded by the National Institute for Health Research (NIHR) through an NIHR Clinician Scientist Fellowship (CS-2014-14-012) awarded to D. C. Perry.
Open access statement
This article is distributed under the terms of the Creative Commons Attributions (CC BY 4.0) licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original author and source are credited.
Trial registration number
The study was registered on the ISCTRN registry (ISRCTN54477575).
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The full pre-planned statistical analysis concerning incidence and the initial care (Part 1), and treatment and two-year outcomes (Part 2).
This article was primary edited by S. P. F. Hughes.