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Journal of Experimental Orthopaedics
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Strength of the porcine proximal femoral epiphyseal plate: the effect of different loading directions and the role of the perichondrial fibrocartilaginous complex and epiphyseal tubercle – an experimental biomechanical study

Journal of Experimental Orthopaedics volume 1, Article number: 4 (2014) Cite this article

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Abstract

Background

The high loads on adolescent athletes’ musculoskeletal system are known to cause morphological and degenerative changes in bone, intervertebral discs and joints. It has been suggested that the cam deformity of the proximal femoral head originates from a subclinical slipped capital femoral epiphysis (SCFE) as a result of non-physiological loading. The perichondrial fibrocartilaginous complex (PFC) and the epiphyseal tubercle are believed to stabilise the proximal femoral epiphysis, but their role is still unclear. The aim of the present study was to develop an experimental, biomechanical model to evaluate the strength of the porcine proximal femoral epiphysis in different loading directions and, furthermore, to investigate the stabilising role of the PFC and the epiphyseal tubercle.

Methods

A descriptive laboratory study. An in-vitro model was developed and nine young (5 months) porcine proximal femoral epiphyses were loaded to failure; three in the anterior-posterior direction, three in the lateral-medial direction and three in the vertical direction. The injured proximal femoral epiphyses were then examined both macroscopically and histologically.

Results

Anterior and lateral loading of the proximal femoral epiphysis resulted in failure of the epiphyseal plate, while vertical loading resulted in a fracture epiphyseolysis. The epiphysis was weakest when exposed to a lateral load and strongest when exposed to a vertical load. Despite histological epiphyseolysis, the PFC was intact in 15 of 27 (56%) slices. In histological examinations, the epiphyseal tubercle appears to halt the slide of the epiphysis.

Conclusions

We have developed an experimental, biomechanical model to measure the strength of the proximal femoral epiphyseal plate in different loading directions. The strength of the proximal femur was weakest through the epiphyseal plate. The epiphysis was weakest when exposed to a lateral load and strongest when exposed to a vertical load. The epiphyseal tubercle and the PFC stabilise the epiphysis when the epiphyseal plate is damaged. The findings in the present study indicate that overloading the hips in growing individuals can disrupt the epiphyseal plate. These findings may have implications when it comes to understanding the pathogenesis of cam deformity of the hip.

Background

The skeleton of the growing individual is susceptible to mechanical injuries, but the growing bone is also capable of adapting to varying stresses [[1]]. Some physiological load is needed for normal bone growth, [[2]] but exceeding this physiological load can lead to unwanted morphological changes and different pathologies of the bone and joints [[3],[4]].

Adolescent athletes in sports where high demands are imposed on the back have been shown to have a high frequency of abnormalities in the vertebral endplates, apophyseal ring and intervertebral discs [[5],[6]]. A systematic review of sports-related growth plate injuries reported similar results for the upper and lower extremities [[3]].

The cam deformity is a non-spherical extension of the femoral head at the antero-superior head-neck junction of the proximal femur. It is more common in adolescent athletes, participating in high-load sports, compared with an age-matched control group [[7]] and it is thought to be a frequent cause of hip pain in athletes [[8]]. The etiology of the cam deformity is not known. One suggested explanation is that it is caused by a subclinical epiphysiolysis of the proximal femoral epiphysis [[9]–[11]].

In 1976, Chung et al. reported that the perichondrial fibrocartilaginous complex (PFC) was an important stabiliser of the human epiphyseal plate. When the PFC was excised, the shear strength of the plate decreased significantly [[12]]. Other researchers have proposed that a defect in the PFC or thinning of the periosteum may precipitate subclinical slipped capital femoral epiphysis (SCFE) [[13],[14]]. The epiphyseal tubercle is also believed to stabilise the proximal femoral epiphyseal plate. It is a tuberosity, eccentrically and inferiorly placed on the capital epiphysis, projecting into an appropriately shaped socket in the metaphysis. The tubercle is believed to hold the epiphysis in place in a chronic SCFE [[15]–[17]].

During routine daily activities, the hip joint is mainly loaded vertically [[18]–[21]]. The way the load is distributed in the hip joint in deep flexion or during sport is largely unknown.

The purpose of the present study was to create a porcine model in order to estimate the difference in strength of the proximal femoral epiphysis in relation to different loading directions. Furthermore, the aim was to explore the stabilising roles of the PFC and epiphyseal tubercle, utilising a histological analysis.

The hypothesis was that the epiphyseal plate would be the weakest link in the proximal femur and that its strength would be greatest during vertical loading.

Methods

Experimental animals and procedures

The proximal femur from nine young (5 months) porcine hips were dissected and cleaned of soft tissue, muscle and capsular attachments. The porcine subjects were male domestic pigs, obtained from the local abattoir, with a median weight of 90 kg (range 85–95). The diameter of the femoral heads was measured in the coronal and sagittal planes with a measurement error of less than 1 mm using a slide caliper [[22]].

Mechanical test procedures

Nine femurs were used in pilot tests of the model in order to establish a correct fixation method; the remaining nine femurs were used for the study.

The prepared proximal femurs were fixed with cement in a metal fixture and attached to the actuator of a servo hydraulic universal testing machine (MTS Test Star, Minneapolis, MN, USA). A custom-made aluminium rod with a small plastic cup (25 mm in diameter), contoured to the shape of the femoral head, was attached to the upper crosshead of the testing machine. The deformation control mode was set at a rate of 0.05 mm/sec. Force and deformation were recorded continuously and failure was defined as a sudden decrease in force, which could be seen on the force/deformation diagram on the computer. Furthermore the failure was visual and audible to the researchers (the first and second authors) in all test cases. Loading was stopped immediately after the first sign of failure.

The physeal line was clearly visible on the surface of the femoral head and was used as a guide for the placement of the plastic cup, which was proximally to the line. The proximal epiphysis was then loaded to failure in one of three directions. Three femurs were loaded from the lateral side in the coronal plane, three femurs were loaded from the anterior side in the sagittal plane and three femurs were loaded vertically (Figures 1, 2 and 3). On those loaded from the lateral side, the major trochanter was removed to facilitate access for the loading rod with the plastic cup. After failure, the size of the footprint left by the plastic cup on the femoral head and its distance from the physeal line were measured. Any signs of epiphyseolysis or fracture, visual or palpable, were registered if present.

Figure 1
figure1

Set-up for lateral loading of the specimens. The major trochanter was removed to facilitate access for the loading rod.

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Figure 2
figure2

Set-up for vertical loading of the specimens.

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Figure 3
figure3

Set-up for anterior loading of the specimens.

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Macroscopic and histological examinations

The specimens were then stored in a −20°C freezer until completely frozen. When frozen, they were sawn into four equally thick primary slices in the loading plane using a bandsaw. The slices were decalcified, dehydrated, fixed in paraffin and cut in 4 μm slices using a microtome. Four slices from each specimen were then stained with hematoxylin-eosin and alcian blue solution. The histological slices were examined microscopically for injuries by the first and the second author (an orthopedic surgeon and a research engineer respectively).

The histological presence of epiphyseolysis, the percentage of the epiphyseal plate that was damaged, the epiphyseal zone that was damaged and a Salter-Harris classification were registered for each slice. The integrity of the PFC and the presence of the epiphyseal tubercle were also noted and registered.

Results

Anterior load

Imposing an anterior load on all three specimens resulted in failure at a median load of 1,750 N (range 1,679-1,756). On histological examination, subtotal epiphyseolysis was present in two specimens and total epiphyseolysis was present in one specimen. The damage wandered erratically between the resting and the ossifying zones of the epiphyseal line (Figure 4). PFC damage could not be assessed in one slice and was seen on only one slice of the remaining eleven (Figure 5). Macroscopically, a small cleavage was seen proximal to the footprint over the epiphyseal line (Figure 6). On palpation, no movement could be detected between the epiphysis and metaphysis after failure.

Figure 4
figure4

Photomicrograph showing damaged epiphyseal plate. In the anterior and lateral loaded specimens, the damage wandered between the resting and ossifying zones. Sample stained with hematoxylin-eosin solution. Magnification X25. Scale bar equals 1 mm.

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Figure 5
figure5

Epiphysiolysis with a damaged PFC (arrow). Sample stained with hematoxylin-eosin solution. Scanned slide, no magnification.

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Figure 6
figure6

A small cleavage (arrow) over the epiphyseal line can be seen after failure.

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Lateral load

Imposing a lateral load on all three specimens resulted in failure at a median load of 920 N (range 918–1,148). On histological examination, subtotal epiphysiolysis was found in all specimens, with the damage wandering erratically between the resting and ossifying zones (Figure 4). On those slices in which the epiphyseal tubercle was present, it appeared as though it was partially dislodged and was pressing against the medial wall of the metaphyseal socket (Figure 7). PFC integrity could not be assessed in two slices and the PFC was damaged on eight of the remaining ten slices. Macroscopically, a small cleavage was seen proximal to the footprint, over the epiphyseal line. On palpation, no movement could be detected between the epiphysis and metaphysis.

Figure 7
figure7

The epiphyseal tubercle (arrow) pressing against the medial wall of the metaphyseal socket. The PFC is damaged. Sample stained with hematoxylin-eosin solution. Scanned slide, no magnification.

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Vertical load

Imposing a vertical load on all three specimens resulted in failure at a median load of 7,397 N (range 7,008-7,413). On histological examination, all specimens showed signs, to a varying degree, of epiphyseolysis and fracture epiphyseolysis Salter Harris type 2. The epiphyseolysis was primarily in the ossifying zone. The epiphyseal tubercle was present in one slice in every specimen and the fractures tended to originate laterally to the epiphyseal tubercle and extend through the medial cortex of the femoral neck. The integrity of the PFC could not be assessed in six slices, but the PFC was damaged in three of the remaining six slices. Macroscopically, a cleavage was seen laterally over the epiphyseal line and an obvious fracture, medially on the femoral neck, was seen. On palpation, movement over the fracture could easily be detected.

General

Loading of all the specimens (9 of 9) resulted in an epiphyseolysis (anterior load and lateral load) or a fracture epiphyseolysis. The epiphyseal plate showed the greatest strength in response to vertical loading (mean 7,273 N (SD 229)) and the least strength in response to lateral loading (mean 995 N (SD 132)), with the strength in response to anterior loading falling in between (mean 1,728 N (SD 43)).

The femoral heads were of similar size and the plastic cup on the rod left a shallow footprint on the femoral head after loading. The size of the indentation from the plastic cup was clearly detectable on the femoral head and the size of the footprint was related to the load – larger footprints at higher load failures. The macroscopic characteristics of the porcine hips, the footprint size and distance from the physeal line and the load and deformation at failure are presented in Table 1. A sample loading/deformation curve is presented in Figure 8.

Table 1 Macroscopic characteristics with load and deformation at failure for all specimens
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Figure 8
figure8

Anterior loaded specimen sample load/deformation curve.

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On nine of thirty-six slices, PFC integrity could not be estimated. During preparation of the slices, the metaphyseal part of the PFC disappeared, making judgement of its integrity impossible. The PFC was damaged on 12 of the remaining 27 slices. All specimens loaded laterally showed some damage to the PFC. The epiphyseal tubercle was identified on 12 of 36 slices. Its presence was confirmed in all specimens apart from one loaded anteriorly. The microscopic characteristics are presented in Table 2.

Table 2 Microscopic characteristics of the specimens
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The force/deformation graphs for lateral, anterior and vertical loads are presented in Figures 2, 3 and 4 respectively.

Discussion

The main finding in the present study is that the epiphyseal plate is the weakest point in the young porcine proximal femur. Loading to failure resulted in epiphyseolysis or fracture epiphyseolysis in all the specimens. The model was consistent and easy to set up.

Load at failure was lowest for the laterally loaded specimens (995 N) and highest for the vertically loaded specimens (7,273 N). The load set-up in the present model resulted primarily in a tensile load over the epiphyseal plate in the laterally loaded specimens, a shear load in the anteriorly loaded specimens and a compressive load in those loaded vertically. The highest strength was therefore to be expected in the vertically loaded specimens, where the loading direction is comparable to the loading direction in vivo [[18]–[21]].

The vertical load mainly caused failure in the ossifying zone of the epiphyseal plate, while a more random pattern of failure between different epiphyseal zones was seen in the other groups. In a study of cattle, Moen et al. reported that compressive forces tended to cause failure in the ossifying zone [[23]].

Chung et al. [[12]] reported a significant decrease in shear strength when the PFC was excised. They loaded their specimens anteriorly. In the present study, all but one slice from the anteriorly loaded specimens showed an undamaged PFC (figure 9), while some PFC damage was seen in all laterally loaded specimens. This indicates that the PFC performs a stabilising function, at least when the epiphysis is loaded anteriorly. In the vertically loaded specimens, the integrity of the PFC could not be assessed in six of 12 slices. The disappearance of the metaphyseal part during the preparation of the slices might indicate that the PFC was damaged.

Figure 9
figure9

Photomicrograph showing microscopic epiphyseolysis (arrowhead) with the PFC (arrow) intact. Sample stained with hematoxylin-eosin solution. Magnification X20. Scale bar equals 1 mm.

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The epiphyseal tubercle was identified in all specimens apart from one of the anteriorly loaded specimens. On the slices from the laterally loaded specimens where the tubercle was identified, the tubercle can be seen pressing against the metaphyseal socket, stopping the slide of the epiphysis (Figure 7). The same finding was seen on the slices from the vertically loaded specimens, where the tubercle appears to stop the epiphysis in its slide. Due to the compressive forces applied in the vertically loaded specimens, the tubercle compresses the medial wall of the socket, resulting in a fracture of the metaphysis through the medial cortex instead of dislodging the tubercle from the socket. This implies that the tubercle performs a stabilising function during vertical and lateral loading.

On microscopic examination of the vertically loaded specimens, the epiphyseal plate was damaged laterally to the epiphyseal tubercle. The cam deformity is usually located antero-superiorly on the femoral head [[24]] and therefore laterally to the epiphyseal tubercle. It is possible to speculate that the cam deformity develops from a partial epiphyseolysis, where the epiphyseal tubercle prevents total epiphyseolysis or dislodges partially in total epiphyseolysis. Rotation of the epiphysis around the eccentric epiphyseal tubercle has also been suggested as a possible cause of chronic SCFE [[16],[17]].

Anterior and lateral loading forces around the femoral head are small during routine activities [[18]–[21]]. The way loading occurs during sports and in deep flexion is unknown. Muscle action and ligament constraints around the hip joint most probably prevent the joint being loaded from an anterior direction in vivo. In reality, the hip joint is probably loaded somewhere between the vertical and anterior loading directions in deep flexion. A posterior slope of the femoral epiphysis increases the anterior load on the epiphyseal plate and is a known predictor of SCFE [[25]] and anterior load also appears to increase in deep flexion [[26]]. It is possible to speculate that the strength of the epiphyseal plate is therefore lower when the hip is in flexion.

Limitations

Using an in-vitro porcine model can be regarded as a limitation when it comes to understanding human hip joint diseases, but many studies of hip biomechanics and hip conditions use a porcine model, especially in pediatric orthopedics, [[27]–[34]] and, in a phenomenological study like the present one, it is thought to be appropriate.

During the preparation of the specimens, all the soft tissues were removed. The muscles and ligaments of the hip most certainly play a major role in dynamic hip biomechanics. Our conclusions are not affected by this fact, as we are only investigating semi-static strength.

Macroscopically, the porcine hip is comparable to the human hip, the main difference being a more prominent major trochanter and a shorter femoral neck (Figure 10). Ipsen et al. reported that, in one-year-old pigs, the proximal femoral epiphysis is similar in size to that in adolescent humans and its shear strength is comparable to that reported by Chung et al. [[12],[35]]. The specimens in the present study are of comparable size to those in a 10-year-old child and the shear strength of the anteriorly loaded specimens was comparable to the values reported by Chung et al. [[12]]. The microscopic characteristics of the porcine epiphyseal plate are identical to those of the human epiphyseal plate, with the different epiphyseal growth zones clearly visible (Figure 11).

Figure 10
figure10

Porcine proximal femur split coronally. The major trochanter is relatively larger than in a human and the femoral neck shorter. The growth plate and the epiphyseal tubercle are clearly visible in this specimen (arrow).

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Figure 11
figure11

The different zones of the porcine epiphyseal plate. Sample stained with hematoxylin-eosin solution. Magnification X40. Scale bar equals 1 mm.

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Conclusion

This model is consistent and simple. The weakest part in the young porcine proximal femur was the epiphyseal plate. This location of weakness may explain the cam deformity found in young athletes. The epiphyseal plate is strongest when exposed to vertical load, weaker when exposed to anterior load and weakest when exposed to lateral load. The epiphyseal tubercle and the PFC are important stabilisers of the epiphysis.

References

  1. 1.

    Arkin AM, Katz JF: The effects of pressure on epiphyseal growth; the mechanism of plasticity of growing bone. J Bone Joint Surg Am 1956,38-A(5):1056–1076.

  2. 2.

    Malina RM: Exercise as an influence upon growth. Review and critique of current concepts. Clinical pediatrics 1969,8(1):16–26.

  3. 3.

    Caine D, DiFiori J, Maffulli N: Physeal injuries in children's and youth sports: reasons for concern? Br J Sports Med 2006,40(9):749–760. 10.1136/bjsm.2005.017822

  4. 4.

    Strobino LJ, French GO, Colonna PC: The effect of increasing tensions on the growth of epiphyseal bone. Surgery, gynecology & obstetrics 1952,95(6):694–700.

  5. 5.

    Lundin O, Hellstrom M, Nilsson I, Sward L: Back pain and radiological changes in the thoraco-lumbar spine of athletes. A long-term follow-up. Scand J Med Sci Sports 2001,11(2):103–109. 10.1034/j.1600-0838.2001.011002103.x

  6. 6.

    Sward L, Hellstrom M, Jacobsson B, Nyman R, Peterson L: Disc degeneration and associated abnormalities of the spine in elite gymnasts. A magnetic resonance imaging study. Spine (Phila Pa 1976) 1991,16(4):437–443. 10.1097/00007632-199104000-00009

  7. 7.

    Siebenrock KA, Ferner F, Noble PC, Santore RF, Werlen S, Mamisch TC: The cam-type deformity of the proximal femur arises in childhood in response to vigorous sporting activity. Clin Orthop Relat Res 2011,469(11):3229–3240. 10.1007/s11999-011-1945-4

  8. 8.

    Murray RO, Duncan C: Athletic activity in adolescence as an etiological factor in degenerative hip disease. J Bone Joint Surg Br 1971,53(3):406–419.

  9. 9.

    Murray RO: The aetiology of primary osteoarthritis of the hip. The British journal of radiology 1965,38(455):810–824. 10.1259/0007-1285-38-455-810

  10. 10.

    Harris WH: Etiology of osteoarthritis of the hip. Clin Orthop Relat Res 1986, 213: 20–33.

  11. 11.

    Goodman DA, Feighan JE, Smith AD, Latimer B, Buly RL, Cooperman DR: Subclinical slipped capital femoral epiphysis. Relationship to osteoarthrosis of the hip. J Bone Joint Surg Am 1997,79(10):1489–1497.

  12. 12.

    Chung SM, Batterman SC, Brighton CT: Shear strength of the human femoral capital epiphyseal plate. J Bone Joint Surg Am 1976,58(1):94–103.

  13. 13.

    Pritchett JW, Perdue KD: Mechanical factors in slipped capital femoral epiphysis. J Pediatr Orthop 1988,8(4):385–388. 10.1097/01241398-198807000-00001

  14. 14.

    Billing L, Bogren HG, Henrikson B, Wallin J: Slipped capital femoral epiphysis. The mechanical function of the periosteum: new aspects and theory including bilaterality. Acta radiologica Supplement 2004, 431: 1–27. 10.1080/03655950410009733

  15. 15.

    Liu RW, Armstrong DG, Levine AD, Gilmore A, Thompson GH, Cooperman DR: An anatomic study of the epiphyseal tubercle and its importance in the pathogenesis of slipped capital femoral epiphysis. J Bone Joint Surg Am 2013,95(6):e341–348. 10.2106/JBJS.L.00474

  16. 16.

    Tayton K: Does the upper femoral epiphysis slip or rotate? J Bone Joint Surg Br 2007,89(10):1402–1406. 10.1302/0301-620X.89B10.19563

  17. 17.

    Tayton K: The epiphyseal tubercle in adolescent hips. Acta Orthop 2009,80(4):416–419. 10.3109/17453670903153550

  18. 18.

    Correa TA, Crossley KM, Kim HJ, Pandy MG: Contributions of individual muscles to hip joint contact force in normal walking. J Biomech 2010,43(8):1618–1622. 10.1016/j.jbiomech.2010.02.008

  19. 19.

    Bergmann G, Deuretzbacher G, Heller M, Graichen F, Rohlmann A, Strauss J, Duda GN: Hip contact forces and gait patterns from routine activities. J Biomech 2001,34(7):859–871. 10.1016/S0021-9290(01)00040-9

  20. 20.

    Bergmann G, Graichen F, Rohlmann A: Hip joint contact forces during stumbling. Langenbeck's archives of surgery/Deutsche Gesellschaft fur Chirurgie 2004,389(1):53–59. 10.1007/s00423-003-0434-y

  21. 21.

    Brand R: Forces on the femoral head during activities of daily living. Iowa Orthop J 1982, 2: 43–49.

  22. 22.

    Kosashvili Y, Backstein D, Safir O, Ran Y, Loebenberg MI, Ziv YB: Hemiarthroplasty of the hip for fracture-what is the appropriate sized femoral head? Injury 2008,39(2):232–237. 10.1016/j.injury.2007.05.021

  23. 23.

    Moen CT, Pelker RR: Biomechanical and histological correlations in growth plate failure. J Pediatr Orthop 1984,4(2):180–184. 10.1097/01241398-198403000-00006

  24. 24.

    Rakhra KS, Sheikh AM, Allen D, Beaule PE: Comparison of MRI alpha angle measurement planes in femoroacetabular impingement. Clin Orthop Relat Res 2009,467(3):660–665. 10.1007/s11999-008-0627-3

  25. 25.

    Barrios C, Blasco MA, Blasco MC, Gasco J: Posterior sloping angle of the capital femoral physis: a predictor of bilaterality in slipped capital femoral epiphysis. J Pediatr Orthop 2005,25(4):445–449. 10.1097/01.bpo.0000158811.29602.a5

  26. 26.

    Sparks DR, Beason DP, Etheridge BS, Alonso JE, Eberhardt AW: Contact pressures in the flexed hip joint during lateral trochanteric loading. J Orthop Res 2005,23(2):359–366. 10.1016/j.orthres.2004.08.019

  27. 27.

    Baranto A, Ekstrom L, Hellstrom M, Lundin O, Holm S, Sward L: Fracture patterns of the adolescent porcine spine: an experimental loading study in bending-compression. Spine (Phila Pa 1976) 2005,30(1):75–82.

  28. 28.

    Baranto A, Ekstrom L, Holm S, Hellstrom M, Hansson HA, Sward L: Vertebral fractures and separations of endplates after traumatic loading of adolescent porcine spines with experimentally-induced disc degeneration. Clin Biomech (Bristol, Avon) 2005,20(10):1046–1054. 10.1016/j.clinbiomech.2005.06.014

  29. 29.

    Dodds MK, Lee J, McCormack D: Transarticular stabilization of the immature femoral head: assessment of a novel surgical approach to the dislocating pediatric hip in a porcine model. J Pediatr Orthop 2008,28(1):36–42. 10.1097/BPO.0b013e31815ff350

  30. 30.

    Hosalkar HS, Varley ES, Glaser DA, Farnsworth CL, Wenger DR: Intracapsular hip pressures in a porcine model: does position and volume matter? J Pediatr Orthop B 2011,20(5):278–283. 10.1097/BPB.0b013e328346c05b

  31. 31.

    Kishan S, Upasani V, Mahar A, Oka R, Odell T, Rohmiller M, Newton P, Wenger D: Biomechanical stability of single-screw versus two-screw fixation of an unstable slipped capital femoral epiphysis model: effect of screw position in the femoral neck. J Pediatr Orthop 2006,26(5):601–605. 10.1097/01.bpo.0000230328.06460.be

  32. 32.

    Pawaskar SS, Grosland NM, Ingham E, Fisher J, Jin Z: Hemiarthroplasty of hip joint: An experimental validation using porcine acetabulum. J Biomech 2011,44(8):1536–1542. 10.1016/j.jbiomech.2011.02.140

  33. 33.

    Upasani V, Kishan S, Oka R, Mahar A, Rohmiller M, Pring M, Wenger D: Biomechanical analysis of single screw fixation for slipped capital femoral epiphysis: are more threads across the physis necessary for stability? J Pediatr Orthop 2006,26(4):474–478. 10.1097/01.bpo.0000217732.24041.81

  34. 34.

    Wenger D, Miyanji F, Mahar A, Oka R: The mechanical properties of the ligamentum teres: a pilot study to assess its potential for improving stability in children's hip surgery. J Pediatr Orthop 2007,27(4):408–410. 10.1097/01.bpb.0000271332.66019.15

  35. 35.

    Ipsen BJ, Williams JL, Harris MJ, Schmidt TL: Shear Strength of the Pig Capital Femoral Epiphyseal Plate. An Experimental Model for Human Slipped Capital Femoral Epiphysis Fixation Studies, ᅟ; 2002.

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Affiliations

  1. Department of Orthopaedics, Institute of Clinical Sciences at Sahlgrenska Academy, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden
    • Páll Sigurgeir Jónasson
    • , Lars Ekström
    • , Jón Karlsson
    •  & Adad Baranto
  2. Orthocenter/IFK-KLINIKEN, Sports Medicine Clinic, Gothenburg, Sweden
    • Mikael Sansone
    •  & Mattias Ahldén
  3. Östersund Hospital, Östersund, Sweden
    • Anna Swärd
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Correspondence to Páll Sigurgeir Jónasson.

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The authors have no financial or non-financial competing interests.

Authors’ contribution

PJ and LE participated in designing the study, performing the experiments and writing the article. AS, MS and MA participated in writing the article. JK and AB participated in designing the study and writing the article. All authors read and approved the final manuscript.

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Jónasson, P.S., Ekström, L., Swärd, A. et al. Strength of the porcine proximal femoral epiphyseal plate: the effect of different loading directions and the role of the perichondrial fibrocartilaginous complex and epiphyseal tubercle – an experimental biomechanical study. J EXP ORTOP 1, 4 (2014). https://doi.org/10.1186/s40634-014-0004-y

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Keywords

  • Hip
  • Load
  • Epiphysiolysis
  • Epiphyseal plate
  • Porcine
  • Epiphyseal tubercle
  • Perichondrial fibrocartilaginous complex