Trends in incidence of recorded diagnosis of osteoporosis, osteopenia, and fragility fractures in people aged 50 years and above: retrospective cohort study using UK primary care data

Summary This study used primary care data to estimate the incidence of recorded diagnosis of osteoporosis, osteopenia, and fragility fracture in the UK during 2000–2018 accounting for age, sex, calendar year and social deprivation. More than 3 million people aged 50–99 years were included. We found that men living in the most deprived areas had a 45% higher risk of being diagnosed with osteoporosis and 50% higher risk of fragility fracture compared to men living in the least deprived areas. Purpose a) To estimate the incidence trends of a recorded diagnosis of osteoporosis, osteopenia, and fragility fracture in the UK over time; b) to describe differences according to age, sex, and social deprivation. Methods This is a longitudinal population-based cohort study using routinely collected primary care data obtained via IQVIA Medical Research Database (IMRD). All patients aged 50–99 years registered with a practice participating in THIN (The Health Improvement Network) between 2000–2018 were included. The first recorded diagnosis of osteoporosis, osteopenia, or fragility fracture was used to estimate incidence rates (IR) per 10,000 person-years at risk. Poisson regression was used to provide Incidence Rate Ratios (IRR) adjusted by age, sex, social deprivation, calendar year, and practice effect. Results The year-specific adjusted IRR of recorded osteoporosis was highest in 2009 in women [IRR 1.44(95%CI 1.38–1.50)], whereas in men it was highest in 2013–2014 [IRR 1.94(95%CI 1.72–2.18)] compared to 2000. The year-specific adjusted IRR of fragility fracture was highest in 2012 in women [IRR 1.77(95%CI 1.69–1.85)], whereas in men it was highest in 2013 [IRR 1.64(95%CI 1.51–1.78)] compared to 2000. Men in the most deprived areas had a higher risk of being diagnosed with osteoporosis [IRR 1.45(95%CI 1.38–1.53)], osteopenia [IRR 1.17(95%CI 1.09–1.26)], and fragility fracture [IRR 1.50(95%CI 1.44–1.56)] compared to those living in the least deprived areas, but smaller differences were seen in women. Conclusion Use of fracture risk assessment tools may enhance the detection of osteoporosis cases in primary care. Further research is needed on the effect of social deprivation on diagnosis of osteoporosis and fractures. Supplementary Information The online version contains supplementary material available at 10.1007/s00198-023-06739-1.


Introduction
Osteoporosis leads to nearly 9 million fractures annually worldwide [1], and over 300,000 fragility fractures in the UK every year [2]. Fragility fractures result from mechanical forces that would not ordinarily result in fracture, known as low-level trauma. The most common sites of osteoporotic fractures are the hip, vertebrae, forearm, but also the pelvis, humerus, and ribs [3]. The impact of hip fractures alone is high, with a 30-day mortality rate of 6.5% [4] and costing an estimated £3.5 billion in the UK in 2010, projected to rise to £5.5 billion per year by 2025 [5]. The total direct cost of osteoporotic fractures in the EU was €56.9 billion in 1 3 2019, with hip fractures estimated to account for 57%, vertebral fractures for 10%, distal forearm fractures for 2% and others for 32% of the total costs [6].
Despite the availability of effective treatments [7][8][9][10], a great challenge remains the early diagnosis of osteoporosis and timely detection and management of increased risk of fragility fracture before a fracture occurs. According to UK NICE guidelines [11], General Practitioners (GPs) are expected to identify people at high risk of fragility fractures. Although recommended screening tools (e.g. QFracture [12] and FRAX [13]) to estimate the 10-year risk of osteoporotic fracture, as well as Bone Mineral Density (BMD) scans using DXA (dual-energy X-ray absorptiometry), are used in clinical practice, there is no nationwide systematic screening programme for osteoporosis in primary care in the UK, and implementation of fracture risk assessment may vary across practices and geographical regions. GPs' increasingly busy workload in combination with a lack of public awareness [14] can lead to underdiagnosis and undertreatment of osteoporosis, and subsequent fragility fractures, some of which could be prevented.
The incidence of fragility fractures and in particular hip fractures, which are associated with the highest mortality and disability rates [6], has been a subject of epidemiological research, with considerably heterogeneous results reported in different countries globally [10,15]. Research on the epidemiology of recorded osteoporosis diagnosis however is scarce and there is no recently published population-based data on the incidence of osteoporosis diagnosis not defined by fracture. Furthermore, there is a lack of data on the incidence of osteopenia from cohort studies, which may reflect a lack of focus on prevention. Although female sex and older age are well-known risk factors for osteoporosis, the role of other demographic characteristics is less known. A recent systematic review demonstrated an association between social deprivation and fragility fractures [16], but the link between social deprivation and a diagnosis of osteoporosis or osteopenia has not been investigated. Hence, we carried out this research study using routinely collected primary care data, aiming to understand how osteoporosis, osteopenia and fragility fractures are recorded in UK primary care and explore trends in observed incidence rates by sociodemographic characteristics. Understanding the patterns of recorded diagnosis of osteoporosis is essential for the design and delivery of public health and community interventions for the prevention of fragility fractures in older people.
The objectives of the present study were: a) to estimate the incidence of a recorded diagnosis of osteoporosis, osteopenia, and fragility fracture in people aged ≥ 50 in the UK; b) to explore time trends in the recording of osteoporosis, osteopenia, and fragility fracture in the UK; c) to describe any differences in incidence rates according to age, sex, and social deprivation.

Data source
We used de-identified data provided by patients as a part of their routine primary care (IQVIA Medical Research Database (IMRD), incorporating data from THIN (The Health Improvement Network), a Cegedim database. Approximately 98% of the UK population is registered with a GP [17]. THIN is a primary care database of over 20 million patients in the UK [18]. GPs record medical diagnoses and symptoms using the Read classification system [19]. Diagnostic Read codes are entered by GPs for conditions that can be diagnosed either in primary care or in secondary care. For example, osteoporosis and osteopenia are often diagnosed in primary care based on DXA bone density scan, and the diagnosis is entered to the patient's record following review of the result by the GP. They can also (less often) be diagnosed in secondary care (for example if a patient is on medication that increase their risk of osteoporosis and are being monitored by a specialist). In the latter case a diagnostic Read code will be entered to the patient's primary care record by reviewing the information provided in the clinic letter sent to the GP. Fragility fractures are usually diagnosed in Emergency Departments (as they are often acute, and an x-ray is required), and this information is sent electronically to the patient's GP and it is subsequently entered as a Read code upon review of the discharge letter. Similarly, if a patient is hospitalised for a major osteoporotic fracture (e.g. hip fracture) the discharge summary containing the Read code is shared with the patient's GP, and the code is subsequently entered on to the primary care record.
All data in THIN are fully anonymized and they are considered to be representative of the UK population in terms of age, sex, practice size and geographical distribution [20]. A measure of social deprivation recorded as quintiles of Townsend scores is also provided. The

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Townsend deprivation score is an area-based measure, incorporating unemployment, non-car ownership, nonhome ownership and household overcrowding combined, based on an individual's post (zip) code [21]. We excluded practices that had no linked Townsend data to reduce missing data.

Study design
Longitudinal population-based cohort study.

Study population and period
All patients aged 50-99 years registered with participating practices in the THIN database between 1/1/2000 and 31/12/2018 were included. We excluded practices that did not meet criteria for standard quality indicators used in the database, i.e. Acceptable Mortality Reporting (AMR) [22] and Acceptable Computer Usage (ACU) recording [23] during the study period. Study entry was defined as the latest date of patient's registration with the practice, when they turned 50 years old, or 1/1/2000. The end of the study period was the earliest of the patient's date of death, the patient's transfer out of the practice or the last date the practice contributed data to THIN.

Definition of variables
The outcome variables were: osteoporosis; osteopenia; fragility fracture (defined by a diagnostic Read code entered on the patient's record) (Appendix Tables 4, 5, and 6). Additional subgroup analyses of first occurrence of a fragility fracture were conducted by site: a) hip; b) vertebrae; c) other, including wrist/radius, pelvic, humerus, ribs, or unspecified site generically coded as fragility fracture. The covariates age, sex and Townsend quintile of social deprivation were included in the analyses as categorical variables.

Incidence
The date of the first recording of the event in the medical records was used as the date of diagnosis, and therefore incidence rates were estimated based on the number of first recorded episodes. We performed a Lewis plot [24], based on which we excluded events that were diagnosed in the first 6 months from registration with the practice, as they were more likely to represent prevalent cases.

Statistical analysis
The incidence rate (IR) of osteoporosis, osteopenia, and fragility fractures was estimated per 10,000 person-years (PY) at risk. This was calculated by adding the number of patients with a first recording of diagnostic Read code for osteoporosis, osteopenia, or fragility fracture during the period 2000-2018, and then dividing this number by the total person-years of follow-up for all patient records for this period. We determined incidence rates per age group, sex, social deprivation, and calendar year of diagnosis. Poisson regression was used to compare incidence rates and provide adjusted Incidence Rate Ratios (IRR) by age, sex, social deprivation, and calendar year. Likelihood ratio (LR) tests were performed to explore interactions between covariates. A fixed effects Poisson model was compared against a mixed effects Poisson model using GP practice as a random intercept to assess potential clustering by practice. Statistical analyses were conducted using statistical software Stata 17 (StataCorp).

Ethical approval
The study protocol was approved by IQVIA Scientific Review Committee (SRC) (Ref. 21SRC011).

Results
A cohort of more than 3 million people aged 50-99 years from a total of 688 GP practices participating in THIN were included in the analysis. Across all three outcomes, there was a significant interaction between age and sex (p < 0.001) (Suppl. Graph S1, S2, S3), therefore results are presented separately in men and women. Clustering by practice had a significant effect and was therefore included in the adjusted model (Tables 1, 2, 3).

Osteoporosis
The overall crude incidence of osteoporosis diagnosis was significantly higher in women, 79.82 vs. 15.28 in men per 10,000 PY. A peak of recorded osteoporosis diagnosis was observed in 2009 in women, followed by a period of increased incidence between 2013-2015 in both men and women ( Fig. 1. Graph 1A). The incidence of osteoporosis diagnosis increased with age: it was lowest in the age group 50-54 in both men and women, and it was highest in men 90-99y and in women 85-89y. The overall adjusted risk of osteoporosis diagnosis across all ages was 4.9 times

Osteopenia
Women were more likely to be diagnosed with osteopenia compared to men, at any age. The overall IR of osteopenia diagnosis was 45.10 in women vs. 8.65 in  the least deprived areas, whereas there was no significant effect of deprivation on osteopenia diagnosis in women ( Table 2).

Fragility fractures
The incidence of recorded fragility fractures increased with age and an increasing trend was observed during the study period. The overall crude IR in men was 28  Additional analyses by fracture site demonstrated a crude IR of hip fracture 10.44 in men and 27.30 in women per 10,000 PY. The recorded diagnosis of hip fracture was stable during the study period, and the risk of suffering a hip fracture was extremely high in the oldest old (90-99y), compared to 50-54y [men IRR 60. 16 Table S1).
Rates of first recorded vertebral fracture were very low compared to fractures at other sites, with an overall IR of vertebral fracture 4.60 in men and 9.47 in women per 10,000 PY. There was however a slight increase in incidence time trend for older age groups (Fig. 2

Discussion
In this study we report the incidence of a diagnosis of osteoporosis, osteopenia and fragility fracture as recorded in primary care. Osteoporosis and fragility fractures were found to be more commonly diagnosed in women and older age groups. The incidence of recorded osteopenia was in general lower than expected, although it was higher in women, and it decreased with advanced age in both sexes. Social deprivation was independently associated with higher risk of osteoporosis and osteopenia diagnosis and fragility fractures in men, whereas smaller differences were seen in women.
We were unable to identify any comparable population-based studies reporting the incidence of osteoporosis diagnosis not defined by a fracture, based on routinely collected primary care data. The available literature reports prevalence and not incidence of osteoporosis. The prevalence of osteoporosis varies across studies, depending on the country, population sample, age, and case finding method [25]; it has been reported 10.3% in people aged ≥ 50 in the US [26], 24% in women in their 7 th decade in a UK study [27], and 30-40% in women and 10-20% in men aged > 50 in China [28]. Prevalence of osteopenia (based on DXA) was reported to be higher, 43.9% [26] and 49% [27] from US and UK studies respectively. In our study we found lower than expected rates of osteopenia diagnosis, given that in other studies the prevalence of osteopenia was higher than that of osteoporosis, and we would therefore expect incidence rates of osteopenia to be respectively higher. However, these studies have a different design compared to our study, as they have used screening to define osteoporosis or osteopenia in smaller population samples, whereas we have studied the incidence of recorded osteoporosis and osteopenia based on diagnostic Read codes in a very large dataset of routinely collected data.
Our study found that the incidence of osteoporosis diagnosis and fragility fractures increased from 2009 onwards in women, and from 2012 onwards in men. This could be explained by the introduction of fracture risk assessment tools around that time. More specifically, the FRAX score was introduced in 2008 [13], whereas the validation paper of the original QFracture was published in 2009 [29]. Importantly, the introduction of fracture risk assessment tools was part of the comprehensive guidelines on the prevention and treatment of osteoporosis (The National Osteoporosis Guideline Group), which were first introduced in 2008 [30], followed by later updates in subsequent years. Publicity of the new fracture risk screening tools might have triggered an interest of GPs in using those, leading to identification of more cases. QFracture was subsequently updated in 2012 [12], and osteoporosis was introduced to the Quality and Outcomes Framework for GPs in 2012-13 [31]. As part of this incentives' scheme, GPs are rewarded with points for people aged ≥ 50 with a diagnosis of osteoporosis confirmed on DXA, who have not sustained a fragility fracture before the age of 75, and people aged ≥ 75 with a record of fragility fracture and a diagnosis of osteoporosis [32]. Nevertheless, despite the peak in the recorded diagnosis, we did not see a corresponding reduction in subsequent fractures in the following years. We therefore need to understand if diagnosis is triggering appropriate treatment. A review of quality measures and quality improvement initiatives for osteoporosis in the US found a gradual improvement in osteoporosis screening, identification and treatment following fragility fracture (2006-2016), although according to data from population-based studies, performance for these quality measures was lower when reporting was not mandatory [33]. Systematic reviews have shown that the Fracture Liaison Service (FLS) model of care is associated with improvements in rates of bone mineral density testing, initiation of osteoporosis treatment and adherence with treatment in people with fragility fractures [34].
The lower incidence of recorded osteopenia and osteoporosis diagnosis in older men contrasts with the high incidence of fragility fractures in this group. This finding implies that there is a gap in prevention, which is more prominent in men. Traditionally osteoporosis screening has been targeted at women, and bone health is a domain commonly overlooked in men. Similarly, the oldest old seem to have very low rates of osteopenia diagnosis, but very high rates of fragility fractures. This is likely to represent a very low number of referrals for DXA scans in the oldest old, possibly due to a reluctance of patients, relatives, or healthcare professionals, on the grounds of other health priorities, multimorbidity and frailty. There is also debate about the value of treatment in people with a low life expectancy and quality of life, e.g. people with dementia, polypharmacy, and greater risk of adverse effects.
In our study we found a slightly lower incidence rate of fragility fracture and hip fracture compared to that reported in a UK study using Clinical Practice Research Datalink (CPRD) data (1988-2012) [35]. Interestingly, the incidence rate of vertebral fracture in people above 50 in that study [35] was the same as in our study. It is worth noting that the actual incidence of vertebral fractures is likely to be higher, as they are often asymptomatic, they can therefore be missed from diagnosis, although recent techniques can improve detection [36,37]. The majority of other studies reporting the incidence of hip and vertebral fractures have been conducted in women, using convenience, and not population-based samples [38], and with case finding in secondary care [38,39] or via surveys [40]. The incidence of hip fractures has been found to be lower in Eastern countries [38,39,[41][42][43], whereas it has been reported to be higher in Northern Europe [6,37,44].
Temporal trends in the incidence of hip fracture in Portugal were found to be affected by socioeconomic inequalities which were more marked in women aged 65-79 [45]. A systematic review of observational studies showed that low socioeconomic status measured at the individual level (education, income, occupation, co-habiting) was associated with an increased risk of both hip and non-hip fragility fracture [RR 1.27 (95%CI 1.12-1.44)], whereas the use of area-based measures of deprivation did not provide a statistically significant association [16]. In our study social deprivation measured using the area-based Townsend index was significantly and independently associated with osteoporosis diagnosis and fragility fractures in both sexes and with osteopenia diagnosis in men.
The present study has strengths and limitations. The main strength is the rigorous methodology, using nationally representative, real-world data. This is, to our knowledge, the first population-based study estimating incidence of recorded diagnosis of osteoporosis in primary care. A limitation is that analyses were based on Read codes as they were recorded by GPs, which can be influenced by various factors, e.g. GP workload, length of consultation, allocation of additional time for administrative tasks, and different coding behaviours amongst GPs or across different practices. It is therefore possible that some cases of osteoporosis are identified and treated without a diagnosis being formally coded. We did not have access to DXA results to explore this, and the incidence of osteoporosis, and especially osteopenia, is likely to be underestimated. Despite the fact that the actual osteopenia incidence rates in this population of people above 50 are probably much higher, the under-recording and under-diagnosis of osteopenia in primary care records is an important finding. Although fragility fractures are generally more likely to be identified (with the exception of vertebral fractures) and therefore coded in patients' electronic records, it is still possible that a proportion of these fractures may not be coded in the primary care records, for example if data is not transcribed fully from secondary care correspondence onto the primary care record or if a fragility fracture occurs in the community but a diagnostic Read code is not inserted at the time. Moreover, while analysis of prescriptions of anti-osteoporotic medication was beyond the scope of this project, it is possible that, had prescription data been included in this analysis, we might have identified some additional cases of osteoporosis or fragility fractures which were not captured by diagnostic coding.
There are significant implications arising from this study. Despite the increased incidence of recorded osteoporosis after the introduction of fracture risk screening tools, the incidence of fragility fractures increased over time in men and women, even after accounting for age. Osteopenia appears to be under-diagnosed, which highlights an important gap in early detection and missed opportunity for intervention. We need further research on management and the prescription of treatments to understand why age-adjusted fragility fracture rates are rising and examine if increased recording of osteoporosis translates into better management. The association of the area-based Townsend index of deprivation with osteoporosis and fragility fractures, which is more pronounced in men, warrants further research to understand the reasons for this. More specifically we need to explore any socioeconomic inequalities in screening for osteoporosis and subsequent management, as well as prescription of bone-sparing medication for older people with fragility fractures.

Conclusion
The identification and recording of a diagnosis of osteoporosis, osteopenia, or fragility fracture may have improved due to the introduction of osteoporotic fracture risk assessment tools as well as incentivization schemes in primary care. As expected, female sex and advanced age were associated with higher incidence of osteoporosis and fragility fractures in this study. We also found significantly increased risk of osteoporosis, osteopenia and fragility fractures in men living in deprived areas. This work has identified that further research is needed on the effect of social deprivation on diagnosis of osteoporosis and fractures. Osteoporosis-treatment response 66aB.00 Osteoporosis-no treatment response 9hP..00 Exception reporting: osteoporosis quality indicators N330.00 Osteoporosis N330000 Osteoporosis, unspecified N330100 Senile osteoporosis N330200 Postmenopausal osteoporosis N330300 Idiopathic osteoporosis N330400 Dissuse osteoporosis N337000 Disuse atrophy of bone N330600 Postoophorectomy osteoporosis N330700 Postsurgical malabsorption osteoporosis N330800 Localized osteoporosis-Lequesne N330900 Osteoporosis in multiple myelomatosis N330A00 Osteoporosis in endocrine disorders N330C00 Osteoporosis localized to spine N330D00 Osteoporosis due to corticosteroids N331D00 Collapsed vertebra NOS N331200 Postoophorectomy osteoporosis with pathological fracture N331300 Osteoporosis of disuse with pathological fracture N331400 Postsurgical malabsorption osteoporosis with pathological fracture N331500 Drug-induced osteoporosis with pathological fracture N331600 Idiopathic osteoporosis with pathological fracture N331800 Osteoporosis + pathological fracture lumbar vertebrae N331900 Osteoporosis + pathological fracture thoracic vertebrae N331A00 Osteoporosis + pathological fracture cervical vertebrae N331B00 Postmenopausal osteoporosis with pathological fracture N331H00 Collapse of cervical vertebra due to osteoporosis N331J00 Collapse of lumbar vertebra due to osteoporosis N331K00 Collapse of thoracic vertebra due to osteoporosis N331L00 Collapse of vertebra due to osteoporosis NOS NyuB000 [X]Other osteoporosis with pathological fracture NyuB100 [X]Other osteoporosis NyuB200 [X]Osteoporosis in other disorders classified elsewhere NyuB800 [X]Unspecified osteoporosis with pathological fracture 66a..00 Osteoporosis monitoring 66a2.00 Osteoporosis treatment started 66a5.00 Osteoporosis-no treatment 66a6.00 Osteoporosis-dietary advice 66a7.00 Osteoporosis-dietary assessment 66a8.00 Osteoporosis-exercise advice 9Od0.00 Attends osteoporosis monitoring 9Od2.00 Osteoporosis monitoring default 66aE.00 Refer to osteoporosis specialist 9N0h.00 Seen in osteoporosis clinic 8HTS.00 Referral to osteoporosis clinic Excepted from osteoporosis quality indicators: patient unsuitable 9hP1.00 Excepted from osteoporosis quality indicators: informed dissent N330z00 Osteoporosis NOS N330500 Drug-induced osteoporosis N374600 Osteoporotic kyphosis 58EG.00 Hip DXA scan result osteoporotic 58EM.00 Lumbar DXA scan result osteoporotic 58EV.00 Femoral neck DEXA scan result osteoporotic N330B.00 Vertebral osteoporosis  Revision to bedrest stabilisation of spinal fracture 7J42D00 Revision to collar stabilisation of spinal fracture 7J42G00 Revision to external fixation stabilisation of spinal fracture 7J42J00 Primary closed reduction spinal fracture alone 7J42L00 Primary closed reduction spinal fracture and bedrest stabilisation 7J42M00 Primary closed reduction spinal fracture and skull traction stabilisation 7J42y00 Other specified other reduction of fracture of spine 7J42z00 Other reduction of fracture of spine NOS 7J43.00 Fixation Revision to open reduction spinal fracture and internal fixation with rod system 7J43C00 Revision to open reduction spinal fracture and internal fixation with internal fixator 7J43E00 Removal of fracture fixation device from spine 7J43y00 Other specified fixation of fracture of spine 7J43z00 Fixation of fracture of spine NOS 7K1D000 Primary open reduction and internal fixation of proximal femoral fracture with screw/nail and plate device 7K1D600 Primary open reduction and internal fixation of proximal femoral fracture with screw/nail device alone 7K1H600 Revision to open reduction and internal fixation of proximal femoral fracture with screw/nail device alone Revision to open reduction and internal fixation of proximal femoral fracture with screw/nail and plate device 7K1J000 Closed reduction and internal fixation of proximal femoral fracture with screw/nail device alone 7K1J600 Primary internal fixation(without reduction) of proximal femoral fracture with screw/nail and intramedullary device 7K1J800 Revision to internal fixation(without reduction) of proximal femoral fracture with screw/nail device alone 7K1JB00 Primary closed reduction and internal fixation of proximal femoral fracture with screw/nail device alone 7K1JD00 Primary closed reduction and internal fixation of proximal femoral fracture with screw/nail and plate device 7K1L400 Closed reduction of fracture of hip 7K1LL00 Closed reduction of fracture of radius and or ulna 7K1LM00 Closed reduction of fracture of wrist 7P20100 Delivery of rehabilitation for hip fracture N1y1.00 Fatigue fracture of vertebra N331D00 Collapsed vertebra NOS N331F00 Collapse of thoracic vertebra N331G00 Collapse of lumbar vertebra N331200 Postoophorectomy osteoporosis with pathological fracture N331300 Osteoporosis of disuse with pathological fracture N331400 Postsurgical malabsorption osteoporosis with pathological fracture N331500 Drug-induced osteoporosis with pathological fracture N331600 Idiopathic osteoporosis with pathological fracture N331800 Osteoporosis + pathological fracture lumbar vertebrae N331900 Osteoporosis + pathological fracture thoracic vertebrae N331A00 Osteoporosis + pathological fracture cervical vertebrae N331B00 Postmenopausal osteoporosis with pathological fracture N331H00 Collapse of cervical vertebra due to osteoporosis N331J00 Collapse of lumbar vertebra due to osteoporosis N331K00 Collapse of thoracic vertebra due to osteoporosis N331L00 Collapse of vertebra due to osteoporosis NOS N331M00 Fragility fracture due to unspecified osteoporosis N331N00 Fragility fracture NyuB000 [X]Other osteoporosis with pathological fracture S10..00 Fracture of spine without mention of spinal cord injury S102.00 Closed fracture thoracic vertebra S102000 Closed fracture thoracic vertebra, burst S102100 Closed fracture thoracic vertebra, wedge S102200 Closed fracture thoracic vertebra, spondylolysis S102300 Closed fracture thoracic vertebra, spinous process S102400 Closed fracture thoracic vertebra, transverse process S102500 Closed fracture thoracic vertebra, posterior arch S102y00 Other specified closed fracture thoracic vertebra S102z00 Closed fracture thoracic vertebra not otherwise specified S104.00 Closed fracture lumbar vertebra S104000 Closed fracture lumbar vertebra, burst S104100 Closed fracture lumbar vertebra, wedge S104200 Closed fracture lumbar vertebra, spondylolysis S104300 Closed fracture lumbar vertebra, spinous process S104400 Closed fracture lumbar vertebra, transverse process S104500 Closed fracture lumbar vertebra, posterior arch S104600 Closed fracture lumbar vertebra, tricolumnar S106.00 Closed fracture sacrum S106000 Closed compression fracture sacrum Read code Description S106100 Closed vertical fracture of sacrum S108.00 Closed fracture pelvis, coccyx S10B.00 Fracture of lumbar spine and pelvis S10B000 Fracture of lumbar vertebra S10B100 Fracture of sacrum S10B200 Fracture of coccyx S10x.00 Closed fracture of spine, unspecified, S10z.00 Fracture of spine without mention of spinal cord lesion NOS S120.00 Closed fracture rib S120000 Closed fracture of rib, unspecified S120100 Closed fracture of one rib S120200 Closed fracture of two ribs S120300 Closed fracture of three ribs S127100 Cough fracture of ribs S120z00 Closed fracture of rib(s) NOS S127.00 Fracture of rib S120A00 Cough fracture S132.00 Closed fracture pubis S132000 Closed fracture pelvis, single pubic ramus S132100 Closed fracture pelvis, multiple pubic rami-stable S132200 Closed fracture pelvis, multiple pubic rami-unstable S132y00 Other specified closed fracture pubis S132z00 Closed fracture pubis NOS S15..00 Fracture of thoracic vertebra S220.00 Closed fracture of the proximal humerus S220000 Closed fracture of proximal humerus, unspecified part S220100 Closed fracture proximal humerus, neck S220200 Closed fracture of proximal humerus, anatomical neck S220300 Closed fracture proximal humerus, greater tuberosity S220400 Closed fracture proximal humerus, head S220500 Closed fracture of humerus, upper epiphysis S220600 Closed fracture proximal humerus, three part S220700 Closed fracture proximal humerus, four part S220z00 Closed fracture of proximal humerus not otherwise specified S226.00 Fracture of upper end of humerus S234.00 Closed fracture of radius and ulna, lower end S240.00 Closed fracture of carpal bone S234000 Closed fracture of forearm, lower end, unspecified S234100 Closed Colles' fracture S234700 Closed Smith's fracture S234200 Closed fracture of the distal radius, unspecified S234300 Closed fracture of ulna, styloid process S234400 Closed fracture of ulna, lower epiphysis S234500 Closed fracture distal ulna, unspecified S234600 Closed fracture radius and ulna, distal S234B00 Closed fracture radial styloid S234C00 Closed fracture distal radius, intra-articular, die-punch S234D00 Closed fracture distal radius, extra-articular, other type S234E00 Closed fracture distal radius, intra-articular, other type S234z00 Closed fracture of forearm, lower end, NOS  Fracture of lower end of both ulna and radius S30..00 Fracture of neck of femur S300.00 Closed fracture proximal femur, transcervical S300000 Closed fracture proximal femur, intracapsular section, unspecified S300100 Closed fracture proximal femur, transepiphyseal S300200 Closed fracture proximal femur, midcervical section S300300 Closed fracture proximal femur, basicervical S300400 Closed fracture head of femur S300500 Closed fracture proximal femur, subcapital, Garden grade unspecified S300600 Closed fracture proximal femur, subcapital, Garden grade I S300700 Closed fracture proximal femur, subcapital, Garden grade II S300800 Closed fracture proximal femur, subcapital, Garden grade III S300900 Closed fracture proximal femur, subcapital, Garden grade IV S300A00 Closed fracture of femur, upper epiphysis S300y00 Closed fracture proximal femur, other transcervical S300z00 Closed fracture proximal femur, transcervical, not otherwise specified S302.00 Closed fracture of proximal femur, pertrochanteric S302000 Closed fracture of proximal femur, trochanteric section, unspecified S302100 Closed fracture proximal femur, intertrochanteric, two part S302200 Closed fracture proximal femur, subtrochanteric S302300 Closed fracture proximal femur, intertrochanteric, comminuted S302400 Closed fracture of femur, intertrochanteric S302z00 Closed fracture of proximal femur, pertrochanteric section, not otherwise specified S304.00 Pertrochanteric fracture S305.00 Subtrochanteric fracture S30w.00 Closed fracture of unspecified proximal femur S30y.00 Closed fracture of neck of femur NOS S31z.00 Fracture of femur, NOS S4B0100 Closed fracture-dislocation superior radio-ulnar joint S4C..00 Fracture-dislocation or subluxation of wrist S4C0.00 Closed fracture dislocation of wrist S4C0000 Closed fracture-dislocation distal radio-ulnar joint S4C0100 Closed fracture-dislocation radiocarpal joint S4C2.00 Closed fracture-subluxation of the wrist S4C2000 Closed fracture-subluxation, distal radio-ulnar jt S4C2100 Closed fracture-subluxation radiocarpal joint S4E..00 Fracture-dislocation or subluxation hip S4E0.00 Closed fracture-dislocation, hip joint S4E2.00 Closed fracture-subluxation, hip joint SC01.00 Late effect of fracture of spine and trunk without mention of cord lesion SC01100 Late effect of fracture of thoracic vertebra SC01200 Late effect of fracture of lumbar vertebra SC3D400 Sequelae of fracture of femur S31..00 Other fracture of femur 7K1Jd00 Closed reduction of intracapsular fracture of neck of femur and internal fixation using a dynamic hip screw 7K1Y000 Remanipulation of intracapsular fracture of neck of femur and fixation using nail or screw