The Effect of Graft Strength on Knee Laxity and Graft In-Situ Forces after Posterior Cruciate Ligament Reconstruction

Abstract

Surgical reconstruction is generally recommended for posterior cruciate ligament (PCL) injuries; however, the use of grafts is still a controversial problem. In this study, a three-dimensional finite element model of the human tibiofemoral joint with articular cartilage layers, menisci, and four main ligaments was constructed to investigate the effects of graft strengths on knee kinematics and in-situ forces of PCL grafts. Nine different graft strengths with stiffness ranging from 0% (PCL rupture) to 200%, in increments of 25%, of an intact PCL’s strength were used to simulate the PCL reconstruction. A 100 N posterior tibial drawer load was applied to the knee joint at full extension. Results revealed that the maximum posterior translation of the PCL rupture model (0% stiffness) was 6.77 mm in the medial compartment, which resulted in tibial internal rotation of about 3.01°. After PCL reconstruction with any graft strength, the laxity of the medial tibial compartment was noticeably improved. Tibial translation and rotation were similar to the intact knee after PCL reconstruction with graft strengths ranging from 75% to 125% of an intact PCL. When the graft’s strength surpassed 150%, the medial tibia moved forward and external tibial rotation greatly increased. The in-situ forces generated in the PCL grafts ranged from 13.15 N to 75.82 N, depending on the stiffness. In conclusion, the strength of PCL grafts have has a noticeable effect on anterior-posterior translation of the medial tibial compartment and its in-situ force. Similar kinematic response may happen in the models when the PCL graft’s strength lies between 75% and 125% of an intact PCL.

About the Authors:

Yu-Shu Lai

Current address: Orthopaedic Device Research Center, National Yang-Ming University, Taipei, Taiwan

Affiliation: Orthopaedic Device Research Center, National Yang-Ming University, Taipei, Taiwan

Wen-Chuan Chen

Affiliation: Orthopaedic Device Research Center, National Yang-Ming University, Taipei, Taiwan

Chang-Hung Huang

Affiliation: Department of Medical Research, Mackay Memorial Hospital, New Taipei City, Taiwan

Cheng-Kung Cheng

Affiliation: Department of Biomedical Engineering, National Yang-Ming University, Taipei, Taiwan

Kam-Kong Chan

Affiliation: Department of Orthopaedics, Cardinal Tien Hospital, New Taipei City, Taiwan

Ting-Kuo Chang

* E-mail: [email protected]

Current address: Mackay Medical College, New Taipei City, Taiwan

Affiliations Department of Orthopedics, Mackay Memorial Hospital, Taipei, Taiwan, Mackay Medical College, New Taipei City, Taiwan

Introduction

Surgical reconstruction of damaged ligaments is a relatively new but rapidly developing option for the treatment of knee conditions. Most of these surgical treatments were originally developed for anterior cricuate ligament (ACL) reconstruction and then adapted to the posterior cruciate ligament (PCL). This is primarily due to the far greater incidence of injury to the ACL, but this does not withdraw from the severity of damage to the PCL. When the PCL is injured, progressive knee damage resulting from abnormal loading and joint laxity could lead to further knee pain, swelling, instability, and the onset of degenerative osteoarthrosis [1–4].

Limited medical data on PCL damage and a low number of studies performed to investigate such injuries greatly complicates the treatment of PCL ruptures [5]. Despite treatment of the PCL being a controversial issue, surgical reconstruction is recommended for patients with PCL-deficient knees [6–7]. However, the reconstruction of an isolated PCL tear can decrease tibial posterior laxity, but may not sufficiently restore the kinematics [8–10], which is believed to in connection with graft choice, graft fixation, tunnel creation, initial graft tension, etc. Because of insufficient clinical and biomechanical data, the selection of the appropriate graft for PCL reconstruction is still controversial. Some factors implicated in the failure of PCL reconstruction are similar to those identified in ACL failures, such as bone tunnel placement, pretensioning, size, strength and fixation method [11–14]. Weak graft anchorage during the remodeling phase has also been considered as another cause of failure [15]. Hence, information regarding graft strength and in-situ forces is important for a successful postoperative rehabilitation.

Harner et al. [16] used human cadaveric knees to investigate the in-situ forces in the PCL and the changes of knee kinematics under different load types. They found a strong relationship between the PCL in-situ force, load type, and tibial translation. Markolf et al. [15] used a load cell to measure the force generated in the PCL with a bone-patellar tendon-bone graft in human cadaveric knees. Their results indicated that the forces in a graft are slightly greater than in an intact PCL under a constant tibial loading. On the other hand, Lenschow et al. [17] reported a lower in-situ force in a hamstring tendon graft than an intact PCL. Thus, it implies that different graft strengths develop different in-situ forces, which may affect the initial graft fixation and post-operative knee kinematics. However, cadaveric studies, due to individual differences, are difficult to quantify with a specific graft and the effect of graft strengths on knee kinematics and PCL in-situ forces. To overcome these limitations, three-dimensional finite element models of the human knee joint have been used to analyze the biomechanical behavior [18].

Hence, the purpose of this study was to determine the effects of different PCL graft strengths on the knee kinematics and in situ forces of PCL grafts at knee extension.

Materials and Methods

Model Reconstruction

A three-dimensional finite element model was constructed from magnetic resonance imaging (MRI) scans of the left knee joint of a healthy male (with written consent to participate in this study. IRB approval by Mackay Memorial Hospital. Approval number: 12MMHIS209). The model meshes were generated using the MSC/PATRAN software (MacNiel-Schwindler Corp., Santa Ana, CA). Non-linear analysis and post-processing were performed with MSC/Mentat 2005 software (MacNiel-Schwindler Corp., Santa Ana, CA). This model consisted of three bony structures (femur, tibia and fibula), articular cartilage layers, menisci, and four main ligaments (collateral and cruciate ligaments). Non-linear cable elements were used to represent all ligaments, including four cable elements for both the ACL and PCL, and three cable elements for the LCL. The MCL was formed by eight cable elements, four were represented the proximal portion attaching the femur to the medial meniscus, and the other four represented the distal portion attaching the meniscus to the tibia (Fig 1) [18]. The global coordinate system defined the X, Y and Z axes as pointing in the directions of medial-lateral, posterior-anterior and proximal-distal respectively. Contact elements were assumed between the femoral cartilage and meniscus, the meniscus and tibial cartilage, and the femoral cartilage and tibial cartilage for both the lateral and medial areas. The model included six contact-surface pairs and the contact status was defined as ‘touching (sliding and rolling)’ in the software. Each contact surface was also modeled as frictionless [19]. The anterior and posterior horns of the menisci were fixed on the tibial cartilage to simulate an ‘unconstrained’ movement of the meniscus periphery. The gap between each contact element was adjusted to less than 0.15 mm to simulate the initial contact between femoral cartilage, tibial cartilage and meniscus [18]. Convergence tests was performed using six mesh densities in element sizes ranging from 6 mm2 down to 1 mm2 on the tibial cartilage and menisci. Under a compressive load of 890 N at knee extension, the boundary conditions on the top surface of the femur were set to be ‘fixed’, and the bottom surface of the tibia was set to be ‘constrained’ except for in proximal-distal (Z axis) translation. The calculated mean contact pressures on the medial and lateral compartments were used to check for model convergence. To take into account the elements’ aspect ratio and calculative efficiency of the computer, the solution was considered to converge with an element size of 2 mm2 on the meniscus and tibial cartilage and an element size of 4 mm2 on the other contact structures (Table 1). Thereby, the convergence model was composed of 110,294 tetrahedral elements (110,197 nodes) (Fig 1).

[Figure omitted. See PDF.]

Fig 1. Finite element model of human knee including the femur, tibia, fibula, articular cartilage layers, menisci, and four main ligaments.

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Table 1. The mean contact pressure in medial and lateral tibial cartilage and meniscus at 890 N for the six finite element mesh densities.

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Material Properties

The material behavior of the cortical bone, cancellous bone, cartilage and meniscus were all assumed homogeneous and linearly elastic. The elastic modulus and Poisson’s ratio were adopted from literature (Table 2) [18–19]. Both the ACL and PCL were assumed as two-bundle structures (ACL: anterior-medial bundle and posterior-lateral bundle; PCL: anterior-lateral bundle and posterior-medial bundle). The material properties of the two bundles of the ACL were identical, but each bundle of the PCL was given different material properties (Table 2) [18–21]. The stress-strain relationship of nonlinear ligament elements was described using the following equations:Where σ is stress, κ is the elastic modulus of ligaments, and ει is assumed to be 0.03 as reference strain [22]. The aforementioned material properties were edited using Compaq Visual FORTRAN 6 (Compaq Computer Corp., CA) as a supplement to the MSC/Marc 2005 (MacNiel-Schwindler Corp., Santa Ana, CA) software. From the MRI data, the total cross-section areas were found to be 42, 62, 20, and 26 mm2 for the ACL, PCL, LCL, and MCL, respectively.

[Figure omitted. See PDF.]

Table 2. The elastic modulus and Poisson’s ratio of cortical bone, cancellous bone, cartilage, meniscus and four ligaments.

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Boundary Conditions

In clinical settings, common grafts used for PCL reconstruction include hamstring tendons and bone-patellar tendon-bone (BPTB), and the elastic moduli of these grafts falls between 87 to 354 MPa, which is approximately 0.5 to 2 times that of an intact PCL [23]. Other detrimental factors such as insufficient graft strength during remodeling [15] may further reduce the graft’s effectiveness. Therefore, the strengths of different PCL grafts used in this study were defined from 0%-200% of an intact PCL’s elastic modulus, increasing in increments of 25%. A posterior drawer force of 100 N was applied to the tibial tubercle, and the boundary conditions on the top surface of the femur were set to be fixed in all directions, while the bottom surface of the tibia remained unconstrained except in flexion-extension [18]. These conditions assured a stable motion of the knee joint under a drawer force [18]. The kinematic response at knee extension was recorded, which included anterior-posterior tibial translation in medial and lateral compartments, internal-external rotation of the knee joint and changes of in-situ forces in PCL grafts with different strengths.

Results

The results of validation, kinematic response and the graft’s in-situ forces in different models at full extension are described separately as follows.

Model Validation

When the knee was at full extension and sustained a 100 N posterior drawer force, Fox et al. [24] used robotic technology to determine the forces in a human PCL and found that an intact PCL has a mean in-situ force of 35.6 N. This is very similar to our finding of 39.91 N in this study. Tibial posterior translation has been reported to range from 2 to 5 mm in an intact knee [18–19,25–26] and from 3 to 11 mm in a PCL-ruptured knee [18–19,27–29]. In our finite element analysis, the maximum tibial posterior translation was 3.60 mm in the intact knee (100%) and 6.77 mm in the knee with a ruptured PCL (0%). Previous studies have also reported noticeable posterior translation in medial tibial coupling with an abnormal internal tibial rotation in patients with a ruptured PCL [30,31]. Logan et al. [32] used open-access magnetic resonance imaging to investigate the tibiofemoral motion of PCL-deficient patients and indicated that the medial tibia was located 5 mm posterior to a normal knee at full extension. It indicated that the medial tibia shifted to a posterior position in PCL-ruptured knees. In our finial element analysis, a similar tendency was found for the PCL rupture model.

Kinematics of the Knee Joint

Under the 100 N posterior drawer load, the normal PCL knee reached a maximum posterior translation of 3.60 mm in the lateral compartment (Fig 2) and a tibial external rotation of 2.60° (Fig 3). The maximum posterior translation of the knee with a ruptured PCL (0%) was 6.77 mm in the medial compartment (Fig 2), which resulted in tibial internal rotation of about 3.01° (Fig 3). The PCL rupture led to increase the sagittal laxity in the medial compartment of the tibia. After PCL reconstruction with any graft strength, the laxity of the medial tibial compartment was noticeably improved. When the 25% strength graft was used, the posterior translation of the medial tibia was only 1.05 mm, showing a decrease of about 5.62 mm in comparison to the PCL-ruptured knee, while external tibial rotation was 1.52° (Fig 3). The laxity of the medial tibia was reduced after PCL reconstruction, with increasing graft strengths offering further joint constraint. Tibial translation and rotation were similar to the intact knee after PCL reconstruction with graft strengths falling from 75% to 125% (Fig 2 and Fig 3). When the graft strength exceeded 150% of an intact PCL, the medial tibia moved forward; it translated anteriorly by 0.3 mm in the 150%, 175%, and 200% models. Also, when the strength surpassed 150%, external tibial rotation increased to 3.01°, 3.05° and 3.06° in the 150%, 175%, and 200% models, respectively (Fig 3).

[Figure omitted. See PDF.]

Fig 2. Anterior-posterior translations of medial and lateral tibial compartments in the reconstructed knee joint with different graft strengths.

The anterior-posterior translations of the medial tibial compartment are noticeably affected by the graft strength.

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Fig 3. Tibial rotations in the reconstructed knee joint with different graft strengths.

Internal tibial rotation occurred in the PCL fully-ruptured knee model. In all PCL reconstruction cases the tibia rotated externally.

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Graft In-Situ Forces

With a 100 N posterior force applied to the tibia, a 39.91 N in-situ force was generated in the normal intact PCL at full extension. The force generated in the PCL grafts ranged from 13.15 N to 75.82 N; the in-situ force was related to the graft strength, with the lower strength grafts having a lower force. The force generated in the 25% strength graft was 13.15 N, representing on only 33% of an intact PCL (Fig 4). The in-situ forces for the 125%, 150%, 175%, and 200% strength graft models were 52.18 N, 59.01 N, 68.45 N, and 75.82 N, respectively (Fig 4).

[Figure omitted. See PDF.]

Fig 4. The in-situ forces in the grafts with different strengths under a 100 N posterior tibial force.

The in-situ forces and graft strengths represented a proportional relationship.

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Discussion

The strength of PCL grafts is an important factor that affects the postoperative kinematics of the knee joint and the graft’s in-situ force. The aim of this study was to investigate the effects of different PCL graft strengths on knee kinematics and in-situ forces at knee full extension. To accomplish this study, a three-dimensional finite element model of a human knee joint was constructed with an atomic PCL.

There are a few limitations in this study that should be noted. First, the bone and soft tissues were assumed as homogeneous and isotropic, which is not representative of an anatomical knee. Hence, creep and stress relaxation could not be investigated in our model. Second, the special bundled structures of ligaments was not reconstructed accurately, but were simplified to be represented by cable elements. Although the interaction between different bundles of ligaments was not evaluated, it may still be important for knee stability [18]. Third, the joint capsule and other soft tissues around the knee joint were not reconstructed in this model and the effect of ligament position and ligament pre-straining were also not considered. Fourth, the graft strength of PCL reconstruction is affected by graft length, graft fixation and tunnel location in clinical. In this study, we ignored these variations and assumed they have equal initial graft length, fixation technique and tunnel location.

The strength of a PCL graft has a considerable effect on knee kinematics. The PCL grafts with 75% ~ 125% strength had a similar kinematic response to the intact PCL model. When the graft strength dropped below 50%, normal rotation of the tibia could not be restored. The graft with 25% strength caused a decrease in external tibial rotation and an increase in posterior translation of the medial tibia. However, if the graft strength exceeded 150%, the posterior translation of the medial compartment of the tibia became over-constrained and instead moved forward. In addition, the corresponding graft tensions were 48% greater than the tension in the intact PCL (Fig 4). Suggs et al. [33] found that using ACL grafts with higher stiffness than an intact ACL resulted in an over-constrained knee joint. Covey et al. [34] also indicated that PCL grafts with stronger mechanical properties caused tightening of the knee joint. Over-constraining the medial tibia would increase the tibiofemoral contact force, and the external rotation of tibia would further affect the “roll-back” mechanism. Thus the strength of PCL grafts not only affects the laxity of the medial tibia compartment but also plays an important role in controlling tibial rotation.

In response to a 100 N posterior tibial load, the in-situ force of the PCL grafts with different strengths ranged from 13.15 N to 75.82 N, becoming more severe with each successive increase in graft strength. The greater in-situ forces may cause higher stress concentrations at the graft fixation site and increase the risk of postoperative failure. Weiler et al. [35] used a sheep model to investigate the fixation strength of biodegradable interface screws in ACL reconstruction with tendon-to-bone grafts and reported graft failure at the screw insertion site. The mean failure forces were 44.8 N and 105.6 N at 6 and 9 weeks postoperatively. In our study, when the graft strength exceeded 125%, the in-situ forces were greater than 44.8 N, which would heighten the risk of graft fixation failure. However, the lower strength grafts produce a lower in-situ force to a posterior tibial load. Chen et al. [36] evaluated the fixation strength and failure types of three grafts (bone-patellar tendon-bone, hamstring tendon, and Achilles tendon) and the result indicated that the tendon-bone junction and the suture-tendon fixation site were the weakest points. The highest tensile stress values are often located at the graft’s femoral insertion zones. This is a common site of PCL rupture for a reconstructed PCL, as observed in some clinical cases [37]. Ramaniraka [37] et al. indicated that the tensile stresses in a high-stiffness PCL graft structure (double graft reconstruction) were greater than those of a single graft reconstructed PCL, and the high tensile stress within the graft may be the cause of fixation failure. Hence, grafts with high internal forces generated in response to muscle loading could accelerate graft failure. This study found that the strength of PCL grafts should lie between 75% and 125% of an intact PCL, which could decrease the risks of abnormal tibial rotation and early failure after PCL reconstruction.

Our results showed reported on changes of in-situ forces and knee joint kinematics due to different PCL graft strengths under the same loading conditions. This data may provide useful information on the biomechanical functions of the PCL, artificial tendon designs, and improve the selection of different PCL grafts.

Conclusion

The structural strength of a graft plays an important role in determining the outcome of PCL reconstruction. This study showed that PCL graft strength noticeably affects the anterior-posterior translation of the medial tibial compartment but has little effect on the lateral tibial compartment. Similar kinematic response may happen in the models when the PCL grafts strength lies between 75% and 125% of an intact PCL. However, further study is needed to determine the effect of graft strength after PCL reconstruction at flexion position to be more relevant to PCL biomechanics.

Author Contributions

Conceived and designed the experiments: YSL CKC KKC TKC. Performed the experiments: WCC CHH. Analyzed the data: YSL WCC CHH. Contributed reagents/materials/analysis tools: YSL WCC CHH CKC. Wrote the paper: YSL WCC.

Citation: Lai Y-S, Chen W-C, Huang C-H, Cheng C-K, Chan K-K, Chang T-K (2015) The Effect of Graft Strength on Knee Laxity and Graft In-Situ Forces after Posterior Cruciate Ligament Reconstruction. PLoS ONE 10(5): e0127293. https://doi.org/10.1371/journal.pone.0127293

References

1. Burns WC 2nd, Draganich LF, Pyevich M, Reider B (1995) The effect of femoral tunnel position and graft tensioning technique on posterior laxity of the posterior cruciate ligament-reconstructed knee. Am J Sports Med. 23:424–30. pmid:7573651

2. Dejour H, Walch G, Peyrot J, Eberhard P (1988) The natural history of rupture of the posterior cruciate ligament. Rev Chir Orthop Reparatrice L’Appareil Mot. 74:35–43

3. Keller PM, Shelbourne KD, McCarroll JR, Rettig AC (1993) Nonoperatively treated isolated posterior cruciate ligament injuries. Am J Sports Med. 21:132–6. pmid:8427355

4. Torg JS, Barton TM, Pavlov H, Stine R (1989) Natural history of the posterior cruciate ligament-deficient knee. Clin Orthop. 246:208–16. pmid:2766608

5. Cosgarea AJ, Jay PR (2001) Posterior cruciate ligament injuries: evaluation and management. J Am Acad Orthop Surg. 9:297–307. pmid:11575909

6. Bach BR, Daluga DJ, Mikosz R, Andriacchi TP, Seidl R (1992) Force displacement characteristics of the posterior cruciate ligament. Am J Sports Med. 20:67–72. pmid:1554076

7. Hughston JC, Degenhardt TC (1982) Reconstruction of the posterior cruciate ligament. Clin Orthop. 164:59–77. pmid:7073822

8. Clancy WG Jr, Shelbourne KD, Zoellner GB, Keene JS, Reider B, Rosenberg TD (1983) Treatment of knee joint instability secondary to rupture of the posterior cruciate ligament: Report of a new procedure. J Bone Joint Surg Am. 65:310–22. pmid:6826593

9. Lipscomb AB Jr, Anderson AF, Norwig ED, Hovis WD, Brown DL (1993) Isolated posterior cruciate ligament reconstruction: Long-term results. Am J Sports Med. 21:490–6. pmid:8368406

10. Richter M, Kiefer H, Hehl G (1996) Primary repair for posterior cruciate ligament injuries. Am J Sports Med. 24:298–305. pmid:8734879

11. Johnson DL, Swenson TM, Irrgang JJ, Fu FH, Harner CD (1996) Revision anterior cruciate ligament surgery: experience from Pittsburgh. Clin Orthop. 325:100–9. pmid:8998862

12. Noyes FR, Barber-Westin SD, Roberts CS (1994) Use of allografts after failed treatment of rupture of the anterior cruciate ligament. J Bone Joint Surg Am. 76:1019–31. pmid:8027109

13. Uribe JW, Hechtman KS, Zvijac JE, Tjin-A-Tsoi EW (1996) Revision anterior cruciate ligament surgery: experience from Miami. Clin Orthop. 325:91–9. pmid:8998902

14. Wirth CJ, Kohn D (1996) Revision anterior cruciate ligament surgery:experience from Germany. Clin Orthop. 325:110–5. pmid:8998863

15. Markolf KL, Slauterbeck JR, Armstrong KL, Shapiro MS, Finerman GA (1997) A biomechanical study of replacement of the posterior cruciate ligament with a graft. Part II: Forces in the graft compared with forces in the intact ligament. J Bone Joint Surg Am. 79:381–6. pmid:9070527

16. Harner CD, Höher J, Vogrin TM, Carlin GJ, Woo SL (1998) The effects of a popliteus muscle load on in situ forces in the posterior cruciate ligament and on knee kinematics. A human cadaveric study. Am J Sports Med. 26:669–73. pmid:9784814

17. Lenschow S, Zantop T, Weimann A, Lemburg T, Raschke M, Strobel MJ, et al. (2006) Joint kinematics and in situ forces after single bundle PCL reconstruction: a graft placed at the center of the femoral attachment does not restore normal posterior laxity. Arch Orthop Trauma Surg. 126:253–9. pmid:16273379

18. Moglo KE, Shirazi-Adl A (2003) On the coupling between anterior and posterior cruciate ligaments, and knee joint response under anterior femoral drawer in flexion: a finite element study. Clin Biomech. 18:751–9. pmid:12957562

19. Bendjaballah MZ, Shirazi-Adl A, Zukor DJ (1998) Biomechanical response of the passive human knee joint under anterior-posterior forces. Clin Biomech. 13:625–33. pmid:11415842

20. Bendjaballah MZ, Shirazi-Adl A, Zukor DJ (1995) Biomechanics of the human joint in compression: reconstruction, mesh generation and finite element analysis. Knee. 2:69–79. pmid:8770447

21. Jilani A, Shirazi-Adl A, Bendjaballah MZ (1997) Biomechanics of human tibio-femoral joint in axial rotation. Knee. 4:203–13.

22. Wismans J, Veldpaus F, Janssen J, Huson A, Struben P (1980) A three-dimensional mathematical model of the knee-joint. J Biomech. 13:677–85. pmid:7419534

23. Wilson TW, Zafuta MP, Zobitz M (1999) A biomechanical analysis of matched bone-patellar tendon-bone and double-looped semitendinosus and gracilis tendon grafts. Am J Sports Med. 27:202–7. pmid:10102102

24. Fox RJ, Harner CD, Sakane M, Carlin GJ, Woo SL (1998) Determination of the in situ forces in the human posterior cruciate ligament using robotic technology. A cadaveric study. Am J Sports Med. 26:395–401. pmid:9617402

25. Butler DL, Noyes FR, Grood ES (1980) Ligamentous restraints to anteriorposterior drawer in the human knee. J. Bone Joint Surg. Am. 62:259–70. pmid:7358757

26. Gollehon DL, Torzilli PA, Warren RF (1987) The role of the posterolateral and cruciate ligaments in the stability of the human knee. J Bone Joint Surg Am. 69:233–42. pmid:3805084

27. Grood ES, Stowers SF, Noyes FR (1988) Limits of movement in the human knee: effect of sectioning the posterior cruciate ligament and posterolateral structures. J Bone Joint Surg Am. 70:88–97. pmid:3335577

28. Race A, Amis A (1996) Loading of the two bundles of the posterior cruciate ligament: an analysis of bundle function in a posterior drawer. J Biomech. 29:873–9. pmid:8809617

29. Vogrin TM, Höher J, Arøen A, Woo SL, Harner CD (2000) Effects of sectioning the posterolateral structures on knee kinematics and in situ forces in the posterior cruciate ligament. Knee Surg Sports Traumatol Arthrosc. 8:93–8. pmid:10795671

30. Li G, Suggs J, Gill T (2002) The effect of anterior cruciate ligament injury on knee joint function under a simulated muscle load: A three-dimensional computational simulation. Ann Biomed Eng. 30: 713–20. pmid:12108845

31. Fukubayashi T, Torzilli PA, Sherman MF, Warren RF (1982) An in-vitro biomechanical evaluation of anterior-posterior motion of the knee. Tibial displacement, rotation, and torque. J Bone Joint Surg Am. 64:258–64. pmid:7056781

32. Logan M, Williams A, Lavelle J, Gedroyc W, Freeman M (2004) The effect of posterior cruciate ligament deficiency on knee kinematics. Am J Sports Med. 32:1915–22. pmid:15572321

33. Suggs J, Wang C, Li G (2003) The effect of graft stiffness on knee joint biomechanics after ACL reconstruction—a 3D computational simulation. Clin Biomech. 18:35–43. pmid:12527245

34. Covey DC, Sapega AA, Sherman GM (1996) Testing for isometry during reconstruction of the posterior cruciate ligament. Anatomic and biomechanical considerations. Am J Sports Med. 24:740–6. pmid:8947394

35. Weiler A, Peine R, Pashmineh-Azar A, Abel C, Südkamp NP, Hoffmann RF (2002) Tendon healing in a bone tunnel. Part I: Biomechanical results after biodegradable interference fit fixation in a model of anterior cruciate ligament reconstruction in sheep. Arthroscopy. 18:113–23. pmid:11830804

36. Chen CH, Chou SW, Chen WJ, Shih CH (2004) Fixation strength of three different graft types used in posterior cruciate ligament reconstruction. Knee Surg Sports Traumatol Arthrosc. 12:371–5. pmid:14586492

37. Ramaniraka NA, Terrier A, Theumann N, Siegrist O (2005) Effects of the posterior cruciate ligament reconstruction on the biomechanics of the knee joint: a finite element analysis. Clin Biomech. 20: 434–42. pmid:15737452