CC BY-NC-ND 4.0 · Rev Bras Ortop (Sao Paulo) 2019; 54(02): 190-197
DOI: 10.1016/j.rbo.2017.11.008
Original Article | Artigo Original
Sociedade Brasileira de Ortopedia e Traumatologia. Published by Thieme Revnter Publicações Ltda Rio de Janeiro, Brazil

Biomechanical Evidence on Anterior Cruciate Ligament Reconstruction[*]

Article in several languages: português | English
António Completo
1   Departamento de Engenharia Mecânica, Universidade de Aveiro, Aveiro, Portugal
,
José Carlos Noronha
2   Hospital da Ordem da Trindade, Porto, Portugal
,
Carlos Oliveira
1   Departamento de Engenharia Mecânica, Universidade de Aveiro, Aveiro, Portugal
,
Fernando Fonseca
3   Serviço de Ortopedia, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
4   Faculdade de Medicina, Universidade de Coimbra, Coimbra, Portugal
› Author Affiliations
Further Information

Address for correspondence

Fernando Fonseca
Serviço de Ortopedia
Centro Hospitalar e Universitário de Coimbra, Coimbra
Portugal   

Publication History

06 September 2017

28 November 2017

Publication Date:
17 April 2019 (online)

 

Abstract

Objective Anterior cruciate ligament (ACL) reconstruction is recommended in athletes with high physical demands. Several techniques are used in reconstruction; however, the most relevant question still is the best biomechanical positioning for the graft. The present study aimed to analyze the biomechanical effect of the position of bone tunnels on load distribution and joint kinetics, as well as the medium-term functional outcomes after ACL reconstruction.

Methods A biomechanical study using a finite element model of the original knee (without anterior cruciate ligament rupture) and reconstruction of the ACL (neoACL) was performed in four combinations of bone tunnel positions (central femoral-central tibial, anterior femoral-central tibial, posterosuperior femoral-anterior tibial, and central femoral-anterior tibial) using the same type of graft. Each neo-ACL model was compared with the original knee model regarding cartilaginous contact pressure, femoral and meniscal rotation and translation, and ligamentous deformation.

Results No neo-ACL model was able to fully replicate the original knee model. When the femoral tunnel was posteriorly positioned, cartilage pressures were 25% lower, and the mobility of the meniscus was 12 to 30% higher compared with the original knee model. When the femoral tunnel was in the anterior position, internal rotation was 50% lower than in the original knee model.

Conclusion Results show that the femoral tunnel farther from the central position appears to be more suitable for a distinct behavior regarding the intact joint. The most anterior position increases rotational instability.


#

Introduction

Anterior cruciate ligament (ACL) lesions are very frequent in sports (70%)[1] However, the medium and long-term success of the reconstruction of the ACL (neoACL) is directly related to the alignment/positioning of the bony tunnels, as well as to the tension of the ligament graft. The positioning of the bony tunnels is critical to knee kinetics and biomechanics,[2] and it influences surgical outcomes. Finite elements models simulate knee biomechanical characteristics both at the ligament level and at the cartilage level; moreover, these models allow the calculation of the different tensions generated either without ACL rupture or with ligament reconstruction. In the present study, neoACL was simulated based on finite element models. The ligament was replaced by four bone-tendon-bone (BTB) grafts.[3] The positioning of the bone tunnels was reproduced from the cadaveric study developed by one of the authors of the present paper (JCN), which simulated several positional possibilities, always with the same type of reconstruction, and compared them with the original model. Some biomechanical conditions, cartilaginous contact pressures, femoral posterior translation and rotation, meniscal translation, and maximum ligamentous main strains (tension) generated by the various positions could be calculated, allowing us to predict the medium and long-term risks incurred by an operated knee.


#

Materials and Methods

The original knee model was developed in a computer from the 3D Open-Knee Model, which was prepared from magnetic resonance imaging (MRI) of the left knee of a 77-year-old cadaver[4] [5] and consisted of distal femur, proximal tibia, cartilage, intact menisci, collateral ligaments, cruciate ligaments, and proximal fibula ([Fig. 1]). The tibial slope was 5° posterior.

Zoom Image
Fig. 1 Geometric model of the intact knee (Open Knee Model).

Meanwhile, four geometric models with neoACL were developed based on the studies of Noronha.[5] These four models were prepared with the CATiA CAD software (Dassault Systèmes, Vélizy-Villacoublay, France) by replacing the ACL with a BTB graft with a cross-section equivalent to the intact ligament. Since the different positions of the tibia and femur tunnels reproduced those described in the experimental cadaveric work from Noronha,[5] which were the positions closest to the original ACL isometry, the same nomenclature was used ([Fig. 2]). Acronyms FC and TC represent the central-natural ACL positions in the femur (FC) and in the tibia (TC), respectively; acronyms FA and TA represent the most anterior tunnels with respect to the central-natural positions of the femur (FA) and of the tibia (TA), respectively; acronym FPS represents a femoral tunnel in posterosuperior position (FPS), and acronym TAI represents a tibial tunnel in the anterointernal position (TAI). Based on the different positions of the tibial and femoral tunnels, four combinations of neoACL were analyzed: FC-TC, FA-TC, FC-TA, and FPS-TAI ([Fig. 2]). The different geometries of each model were imported to the Abaqus software, version 6.13 (Dassault Systèmes, Vélizy-Villacoublay, France), in which the finite element mesh was generated ([Fig. 3]) and simulations were made. The type of element, the number of elements and the number of knots at each structure from the different joint models are shown in [Table 1]. Although all of the materials from the different joint structures present a viscoelastic behavior, the short time of articular load application during knee flexion (t = 1 second) approximates their behavior to linear elastic[6] with elastic moduli (E) and Poisson ratio (í),[7] [8] [9] [10] [11] [12] detailed in [Table 2]. The interaction-attachment conditions between the different joint structures attempted to approach the physiological condition, considering that the tibia and the femur are solidary in the neoACL models reconstructed with BTB grafts. Interactions between bone surfaces and ligamentous and cartilaginous attachment zones were modeled as rigid connections. The remaining interactions between the different structures were modeled with frictionless contact.[6] The fixation of the meniscal horns was modeled with 10 springs (350 N/mm) per horn ([Fig. 3]). Numerical models, forces, and moments developed in the knee during a 75 kg-person gait cycle were applied to the models.[13] [14] The joint flexion resulted only from the application of forces and momentum in the femur, since the fibula and the tibia were fixed in the distal zone ([Fig. 3]). The tibial-femur joint force (Fy), the patellofemoral anteroposterior joint force (Fx), and an abduction-adduction momentum at the frontal plane (Mx) were applied to the femur ([Fig. 3]). The evolution of the Fy and Fx forces and of the Mx in the joint during flexion, lasting 1 second, are shown in [Table 3].[13] [14] A test was performed up to a flexion angle of 100°, higher than the 60° normally developed in the gait cycle. The parameters analyzed were contact pressure in the cartilage; femoral translation and rotations; meniscal translations at AL, PL, AM and PM ([Fig. 3]); and maximum main deformations (traction) in the ligaments and in the neoACL.

Zoom Image
Fig. 2 Position of the bone tunnels in the analyzed tibia and femur. FC-TC, central femur and tibia; FA-TC, anterior femur and central tibia; FC-TA, central femur and anterior tibia; FPS-TAI, posterior-superior femur and anterior-internal tibia.
Zoom Image
Fig. 3 A, Finite element model of the knee (posterior view); B, Schematic representation of the forces and momentum applied to the joint; C, Location of the points AL, PL, AM, PM in which menisci displacements were measured.
Table 1

Structure

Element type

Elements number

Knots number

Femur

S3R

40,628

20,316

Tibia

S3R

25,130

12,567

Fibula

S3R

1,528

766

Menisci

C3D4

25,573

5,952

Tibial cartilage

C3D10M

13,992

24,782

Femoral cartilage

C3D10M

24,094

6,405

ACL

C3D4

1,601

510

PCL

C3D4

2,381

721

MCL

C3D4

3,847

1,165

LCL

C3D4

2,453

774

NeoACL FC-TC

C3D4

6,139

1,420

NeoACL FC-TA

C3D4

5,633

1,357

NeoACL FA-TC

C3D4

3,020

734

NeoACL FPS-TAI

C3D4

5,496

1,374

Table 2

Material

Reference

Young modulus (MPa)

Poisson ratio

Bone

[7]

17,000

0.36

Cartilage

[6]

15

0.45

Meniscus

[8]

59

0.45

ACL

[9]

280

0.42

PCL

[10]

300

0.42

MCL

[11]

372

0.42

LCL

[10]

332

0.42

NeoACL

[12]

320

0.42

Table 3

Flexion angle

Fy (N)

Fx (N)

Mx (Nm)

0

0

0

10°

950

300

7.5

20°

1,520

480

15

30°

1,330

420

10.5

40°

1,520

480

12

50°

1,900

600

13.5

60°

950

300

6

70°

760

240

4.5

80°

570

180

4.5

90°

570

180

4.5

100°

570

180

4.5


#

Results

Maximum contact pressures in the femoral and tibial cartilages are presented in [Fig. 4] for the intact model (without neoACL) and for the neoACL models in flexion of up to 60° (gait cycle). The highest value of contact pressure occurred in the intact model in the medial tibial cartilage (12 MPa). The neoACL FPS-TAI model was the most different from the mean pressure values of the intact model, while the remaining neoACL models presented values 25% lower than the intact model. Maximum femoral rotations in the transverse (internal rotation) and frontal planes are shown in [Fig. 5]. The FA-CT model was the one with the lowest rotational values in both planes, with a mean value 50% lower than the other models for the flexion of up to 60°. The 70° to 100° flexion interval presented nominal values of maximum rotation in the inverse direction to the other models. Regarding the posterior translation of the femur (rollback) in flexion of up to 60° ([Fig. 6A]), all of the analyzed models presented similar values, ∼ 16 mm. The movements in the anterior (AL and AM) and posterior (PL and PM) points of the meniscus ([Fig. 6B]) presented different values among the analyzed models. The neoACL FA-CT model presented the lowest values of posterior translation, with a value 30% lower than the intact model. The neoACL FPS-TAI model presented the highest values, with translational values 12 and 30% higher than the intact model. The deformations in the different joint ligaments are presented in [Fig. 7]. In flexion of up to 60° (gait cycle), the posterior and anterior cruciate ligaments presented more distinct behaviors among the neoACL models. In the posterior cruciate ligament, the FA-CT model presented 40% lower deformation values than the intact model, while the neoACL FC-TC and FPS-TAI models presented 30% higher values. In the anterior cruciate ligament, the neoACL FA-CT model showed a deformation value 100% higher than the intact model, while the FPS-TAI model presented a 30% lower value. In the flexural complement between 70° and 100°, the neoACL FA-CT model showed deformation values 2 to 3 times higher than the intact model, whereas the FPS-TAI model showed 3 times lower deformation values.

Zoom Image
Fig. 4 A, Contact pressure gradients at the femoral and tibial cartilage; B, Maximum contact pressure at the femoral and tibial cartilage (0-60o flexion).
Zoom Image
Fig. 5 Maximal femoral rotations in cross-sectional and frontal planes during a movement in flexion up to 60o
Zoom Image
Fig. 6 A, Posterior femoral translation in up to 60o flexion; B, Posterior meniscal translation at points AM, PM, AL and PL (Fig. 3) in up to 60o flexion
Zoom Image
Fig. 7 Maximal main deformity (tension) on knee ligaments and neoACL in up to 60o and 70o to 100o flexion

#

Discussion

We have decided to consider only knees with intact meniscus, normal cartilage, mechanical axis of 180° and tibial inclination of 5°, and only kinematics variations and joint pressures introduced by the different bone tunnels were studied. The introduction of more variables would increase noise and difficult the interpretation of our objectives. The cartilage contact pressure gradients exhibited by the intact model (natural ACL) closely follow the normal asymmetrical load distribution on the natural knee, resulting in contact pressures in the upper medial tibial cartilage of about between 30 and 40% of those observed on the flexural lateral side during the gait cycle.[14] [15] Similarly, the kinematic results of the intact model regarding femoral rotations and posterior translation (rollback), as well as the posterior meniscal movements during flexion, were in the same range obtained in the natural knee.[2] [16] [17] [18] This ability of the intact model to approximate the behavior of the natural knee in terms of load distribution and of femoral and meniscal kinematics during flexion shows its validity for the comparative study of neoACL , which was the main object of the present study. In the comparison of the contact pressure in the tibial cartilage of the different models with neoACL, all of the models presented peak values within the physiological range, between 8.2 and 12 MPa.[15] However, the FPS-TAI model was the most distant from the behavior of the intact model and from the normal load distribution in the joint, since it presented higher pressure values in the lateral tibial cartilage than in the medial one. Apparently, the combination of the posterosuperior femoral tunnel with an anterointernal tibial tunnel alters the load distribution in the joint in a more significant way. Regarding the maximum femoral rotations, the FA-CT reconstruction model, with a more anterior femoral tunnel and a central-natural positioned tibial tunnel, showed the lowest values of femoral rotation in the transverse plane (internal rotation) and in the frontal plane rotation in up to 60° flexion, with values 40% lower than the intact model and other neoACL models. This same FA-CT model presented peak rotational values in the opposite direction to the other models at 70° to 100° flexion, indicating that the most anterior position of the femoral tunnel (FA) changes more significantly the femoral rotational kinematics in this range of joint flexion. Regarding posterior femur translation during flexion, all of the neoACL reconstruction models presented values identical to the intact model; apparently, the different locations of femoral and tibial tunnels did not alter the femoral rollback effect in the range of flexion of the gait cycle. Regarding the movement of the menisci in their anterior and posterior regions, the neoACL reconstruction models that presented values more distinct from the intact model were the FPS-TAI, which showed a tendency for a greater posterior displacement of both menisci, and the FA-TC, which exhibited the smallest displacement of the menisci of all of the analyzed models. In this case, the removal of the tunnels from their natural central positions in the femur, either anteriorly (AF) or posteriorly (FPS), appears to have the greatest influence on meniscal mobility. As for the state of deformation of the ligament and neoACL traction, in up to 60° flexion (gait cycle), it was verified that the models FA-TC and FPS-TAI presented the most different values of deformation compared with the intact model, especially in the cruciate ligaments. The model with the most anterior femoral tunnel, FA-CT, showed the lowest deformation in the posterior cruciate ligament. On the other hand, the femoral tunnel model in the most posterior position, FPS-TAI, showed the lowest deformation value in the neoACL between all of the analyzed models, whereas the model with the most anterior femoral tunnel, FA-CT, presented the highest deformation values, two times higher than in the intact model. This confirms that the positioning of bone tunnels during neoACL affects both the load distribution at the joint and the kinematics of its structures. The neoACL models closer to the structural and kinematic behavior of the intact model were those with more central-natural positioned femoral tunnels, namely FC-CT and FC-TA. Both models with femoral tunnel farthest from the center, either in the anterior direction, FA-CT, or in the posterior direction, FPS-TAI, presented the most distinct behaviors from the intact model for most of the analyzed parameters.

In agreement with the literature reports,[19] the positioning of the femoral tunnel is important for joint mobility and the clinical outcome. However, we know that after neoACL, there is still the possibility of developing arthrosis, even without meniscectomy associated with the procedure. In the long-term, which corresponds to 10 years, this development is associated with loss of full extension and joint mobility.[20] In 20 years of follow-up, the described risk factors for developing arthrosis were loss of full extension, meniscectomy (medial or lateral), cartilage disease, and aging of the patient.[21] The present study shows that after neoACL, there is no return to the biomechanical state prior to the rupture of the ACL and, that by positioning the femoral tunnel more posteriorly, the surgeon contributes to a change in the load exerted at the cartilage level of about 25% compared with the knee without rupture of the ACL; in the medium/long-term, this can lead to degenerative cartilage changes. These experimental data compel us to reflect and try to find a femoral tunnel position that does not significantly change cartilage pressures, but that allows good knee stability after neoACL.

There are limitations associated with the present study. One of them is related to the simplification of the load state in the joint. However, the most preponderant joint forces during the gait cycle were considered. In addition, the viscoelastic behavior of different structures was not considered. Nevertheless, due to the short time of force application (t = 1 second), it is reasonable to consider an elastic behavior of these structures. Moreover, all of the structures were considered homogeneous, a situation different from the real one. However, due to the comparative nature of the present study, in which only the positioning of the bone tunnels was distinct between the models, it is assumed that this simplification does not alter the relative outcomes from different models.


#

Conclusion

The present study illustrates that the structural and kinetic behavior of the knee joint structures with neoACL varies according to the positioning of the bone tunnels. The best position seems to be central, that is, anatomical. The location of the femoral tunnel farthest from the central-neutral position is more predisposing to an unbalanced structural and kinematic behavior with altered cartilage load, and it may be the cause of the development of arthrosis in the long term.


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#

Conflitos de interesse

Os autores declaram não haver conflitos de interesse.

Acknowledgments

The present study was funded by Programa Compete, through projects POCI-01-0145-FEDER-016574, PTDC/EMS-TEC/3263/2014, and project 3599 - PPCDT, shared by the European Community Fund (FEDER).

* Work developed at the Departamento de Engenharia Mecânica of the, Universidade de Aveiro, Aveiro, Portugal.


  • References

  • 1 Carnes J, Stannus O, Cicuttini F, Ding C, Jones G. Knee cartilage defects in a sample of older adults: natural history, clinical significance and factors influencing change over 2.9 years. Osteoarthritis Cartilage 2012; 20 (12) 1541-1547
  • 2 Completo A, Fonseca F. Fundamentos de biomecânica musculoesquelética e ortopédica. Porto: Publindustria; 2011
  • 3 Erdemir A, Sibole S. A three-dimensional finite element representation of the knee joint. 2010. . In: User's Guide. Version 1.0.0
  • 4 Sibole S, Bennetts C, Maas S. Open knee: a 3 d finite element representation of the knee joint. In: 34th Annual Meeting of the American Society of Biomechanics, Providence, RI from Wednesday, August 18, 2010
  • 5 Noronha JC. Ligamento cruzado anterior [tese]. Porto: Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto; 2000
  • 6 Peña E, Calvo B, Martínez MA, Doblaré M. A three-dimensional finite element analysis of the combined behavior of ligaments and menisci in the healthy human knee joint. J Biomech 2006; 39 (09) 1686-1701
  • 7 Rho JY, Ashman RB, Turner CH. Young's modulus of trabecular and cortical bone material: ultrasonic and microtensile measurements. J Biomech 1993; 26 (02) 111-119
  • 8 Donahue TL, Hull ML, Rashid MM, Jacobs CR. A finite element model of the human knee joint for the study of tibio-femoral contact. J Biomech Eng 2002; 124 (03) 273-280
  • 9 Butler DL, Guan Y, Kay MD, Cummings JF, Feder SM, Levy MS. Location-dependent variations in the material properties of the anterior cruciate ligament. J Biomech 1992; 25 (05) 511-518
  • 10 Harner CD, Xerogeanes JW, Livesay GA, Carlin GJ, Smith BA, Kusayama T. , et al. The human posterior cruciate ligament complex: an interdisciplinary study. Ligament morphology and biomechanical evaluation. Am J Sports Med 1995; 23 (06) 736-745
  • 11 Quapp KM, Weiss JA. Material characterization of human medial collateral ligament. J Biomech Eng 1998; 120 (06) 757-763
  • 12 Shani RH, Umpierez E, Nasert M, Hiza EA, Xerogeanes J. Biomechanical comparison of quadriceps and patellar tendon grafts in anterior cruciate ligament reconstruction. Arthroscopy 2016; 32 (01) 71-75
  • 13 Bergmann G, Bender A, Graichen F, Dymke J, Rohlmann A, Trepczynski A. , et al. Standardized loads acting in knee implants. PLoS One 2014; 9 (01) e86035
  • 14 Morrison JB. The mechanics of the knee joint in relation to normal walking. J Biomech 1970; 3 (01) 51-61
  • 15 Van Rossom S, Smith CR, Zevenbergen L, Thelen DG, Vanwanseele B, Van Assche D. , et al. Knee Cartilage Thickness, T1ρ and T2 Relaxation Time Are Related to Articular Cartilage Loading in Healthy Adults. PLoS One 2017; 12 (01) e0170002
  • 16 Liu F, Kozanek M, Hosseini A, Van de Velde SK, Gill TJ, Rubash HE. , et al. In vivo tibiofemoral cartilage deformation during the stance phase of gait. J Biomech 2010; 43 (04) 658-665
  • 17 Vedi V, Williams A, Tennant SJ, Spouse E, Hunt DM, Gedroyc WM. Meniscal movement. An in-vivo study using dynamic MRI. J Bone Joint Surg Br 1999; 81 (01) 37-41
  • 18 Matsumoto H, Seedhom BB, Suda Y, Otani T, Fujikawa K. Axis location of tibial rotation and its change with flexion angle. Clin Orthop Relat Res 2000; (371) 178-182
  • 19 Khalfayan EE, Sharkey PF, Alexander AH, Bruckner JD, Bynum EB. The relationship between tunnel placement and clinical results after anterior cruciate ligament reconstruction. Am J Sports Med 1996; 24 (03) 335-341
  • 20 Shelbourne KD, Gray T. Minimum 10-year results after anterior cruciate ligament reconstruction: how the loss of normal knee motion compounds other factors related to the development of osteoarthritis after surgery. Am J Sports Med 2009; 37 (03) 471-480
  • 21 Shelbourne KD, Benner RW, Gray T. Results of after anterior cruciate ligament reconstruction with patellar tendon autografts: objective factors associated with thw development of osteoarthritis at 20 to 33 years after surgery. Am J Sports Med 2017; 45 (12) 2730-2738

Address for correspondence

Fernando Fonseca
Serviço de Ortopedia
Centro Hospitalar e Universitário de Coimbra, Coimbra
Portugal   

  • References

  • 1 Carnes J, Stannus O, Cicuttini F, Ding C, Jones G. Knee cartilage defects in a sample of older adults: natural history, clinical significance and factors influencing change over 2.9 years. Osteoarthritis Cartilage 2012; 20 (12) 1541-1547
  • 2 Completo A, Fonseca F. Fundamentos de biomecânica musculoesquelética e ortopédica. Porto: Publindustria; 2011
  • 3 Erdemir A, Sibole S. A three-dimensional finite element representation of the knee joint. 2010. . In: User's Guide. Version 1.0.0
  • 4 Sibole S, Bennetts C, Maas S. Open knee: a 3 d finite element representation of the knee joint. In: 34th Annual Meeting of the American Society of Biomechanics, Providence, RI from Wednesday, August 18, 2010
  • 5 Noronha JC. Ligamento cruzado anterior [tese]. Porto: Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto; 2000
  • 6 Peña E, Calvo B, Martínez MA, Doblaré M. A three-dimensional finite element analysis of the combined behavior of ligaments and menisci in the healthy human knee joint. J Biomech 2006; 39 (09) 1686-1701
  • 7 Rho JY, Ashman RB, Turner CH. Young's modulus of trabecular and cortical bone material: ultrasonic and microtensile measurements. J Biomech 1993; 26 (02) 111-119
  • 8 Donahue TL, Hull ML, Rashid MM, Jacobs CR. A finite element model of the human knee joint for the study of tibio-femoral contact. J Biomech Eng 2002; 124 (03) 273-280
  • 9 Butler DL, Guan Y, Kay MD, Cummings JF, Feder SM, Levy MS. Location-dependent variations in the material properties of the anterior cruciate ligament. J Biomech 1992; 25 (05) 511-518
  • 10 Harner CD, Xerogeanes JW, Livesay GA, Carlin GJ, Smith BA, Kusayama T. , et al. The human posterior cruciate ligament complex: an interdisciplinary study. Ligament morphology and biomechanical evaluation. Am J Sports Med 1995; 23 (06) 736-745
  • 11 Quapp KM, Weiss JA. Material characterization of human medial collateral ligament. J Biomech Eng 1998; 120 (06) 757-763
  • 12 Shani RH, Umpierez E, Nasert M, Hiza EA, Xerogeanes J. Biomechanical comparison of quadriceps and patellar tendon grafts in anterior cruciate ligament reconstruction. Arthroscopy 2016; 32 (01) 71-75
  • 13 Bergmann G, Bender A, Graichen F, Dymke J, Rohlmann A, Trepczynski A. , et al. Standardized loads acting in knee implants. PLoS One 2014; 9 (01) e86035
  • 14 Morrison JB. The mechanics of the knee joint in relation to normal walking. J Biomech 1970; 3 (01) 51-61
  • 15 Van Rossom S, Smith CR, Zevenbergen L, Thelen DG, Vanwanseele B, Van Assche D. , et al. Knee Cartilage Thickness, T1ρ and T2 Relaxation Time Are Related to Articular Cartilage Loading in Healthy Adults. PLoS One 2017; 12 (01) e0170002
  • 16 Liu F, Kozanek M, Hosseini A, Van de Velde SK, Gill TJ, Rubash HE. , et al. In vivo tibiofemoral cartilage deformation during the stance phase of gait. J Biomech 2010; 43 (04) 658-665
  • 17 Vedi V, Williams A, Tennant SJ, Spouse E, Hunt DM, Gedroyc WM. Meniscal movement. An in-vivo study using dynamic MRI. J Bone Joint Surg Br 1999; 81 (01) 37-41
  • 18 Matsumoto H, Seedhom BB, Suda Y, Otani T, Fujikawa K. Axis location of tibial rotation and its change with flexion angle. Clin Orthop Relat Res 2000; (371) 178-182
  • 19 Khalfayan EE, Sharkey PF, Alexander AH, Bruckner JD, Bynum EB. The relationship between tunnel placement and clinical results after anterior cruciate ligament reconstruction. Am J Sports Med 1996; 24 (03) 335-341
  • 20 Shelbourne KD, Gray T. Minimum 10-year results after anterior cruciate ligament reconstruction: how the loss of normal knee motion compounds other factors related to the development of osteoarthritis after surgery. Am J Sports Med 2009; 37 (03) 471-480
  • 21 Shelbourne KD, Benner RW, Gray T. Results of after anterior cruciate ligament reconstruction with patellar tendon autografts: objective factors associated with thw development of osteoarthritis at 20 to 33 years after surgery. Am J Sports Med 2017; 45 (12) 2730-2738

Zoom Image
Fig. 1 Modelo geométrico do joelho intacto (Open Knee Model).
Zoom Image
Fig. 2 Posição dos túneis ósseos na tíbia e no fêmur analisados. FC-TC, fêmur e tíbia centrais; FA-TC, fêmur anterior e tíbia central; FC-TA, fêmur central e tíbia anterior; FPS-TAI, fêmur posterossuperior e tíbia posição anterointerna.
Zoom Image
Fig. 3 A, modelo de elemento finitos do joelho (vista posterior); B, representação esquemática das forças e do momento aplicados à articulação; C, localização dos pontos AL, PL, AM, PM onde foram medidos os deslocamentos dos meniscos.
Zoom Image
Fig. 1 Geometric model of the intact knee (Open Knee Model).
Zoom Image
Fig. 2 Position of the bone tunnels in the analyzed tibia and femur. FC-TC, central femur and tibia; FA-TC, anterior femur and central tibia; FC-TA, central femur and anterior tibia; FPS-TAI, posterior-superior femur and anterior-internal tibia.
Zoom Image
Fig. 3 A, Finite element model of the knee (posterior view); B, Schematic representation of the forces and momentum applied to the joint; C, Location of the points AL, PL, AM, PM in which menisci displacements were measured.
Zoom Image
Fig. 4 A, gradientes de pressão de contato na cartilagem femoral e tibial; B, máxima pressão de contato nas cartilagens femoral e tibial (flexão 0-60∘).
Zoom Image
Fig. 5 Rotações máximas no plano transverso e plano frontal do fêmur durante o movimento durante o movimento de flexão até 60∘.
Zoom Image
Fig. 6 A, translação posterior do fêmur na flexão até 60∘; B, translação posterior dos meniscos nos pontos AM, PM, AL e PL (Fig. 3) na flexão até 60∘.
Zoom Image
Fig. 7 Deformação principal máxima (tração) nos ligamentos e neoligamento LCA do joelho na flexão até 60∘ e na flexão de 70∘ a 100∘.
Zoom Image
Fig. 4 A, Contact pressure gradients at the femoral and tibial cartilage; B, Maximum contact pressure at the femoral and tibial cartilage (0-60o flexion).
Zoom Image
Fig. 5 Maximal femoral rotations in cross-sectional and frontal planes during a movement in flexion up to 60o
Zoom Image
Fig. 6 A, Posterior femoral translation in up to 60o flexion; B, Posterior meniscal translation at points AM, PM, AL and PL (Fig. 3) in up to 60o flexion
Zoom Image
Fig. 7 Maximal main deformity (tension) on knee ligaments and neoACL in up to 60o and 70o to 100o flexion