Abstract
Purpose
The gracilis tendon (GT) is a commonly used autologous graft in Orthopaedic surgery. The majority of information on knee function and outcomes after hamstring harvest is related to both semitendinosus and GT harvest. Little is known regarding isolated harvest of a GT. It was hypothesized that isolated GT harvest would lead to altered gait patterns (e.g. augmented anterior-posterior translation or rotation in the tibiofemoral joint) and consequently a higher prevalence of cartilage lesions and meniscal tears in knees.
Methods
GT harvesting was performed on patients with chronic acromioclavicular joint instability without previous knee injuries or surgeries. MRI of both knees and thighs were performed. Knee MRI were evaluated using the Whole-Organ Magnetic Resonance Imaging Score (WORMS). Inter- and intraobserver reliabilities, cross-sectional areas of different muscles, fatty infiltration of the gracilis muscle (GM) and GT regeneration were evaluated. The contralateral limb served as reference. The observers were blinded towards the identity of the patients and the operatively treated side.
Results
After a mean time of 44 months after surgery testing was performed on 12 patients. No significant side-to-side differences were found using WORMS, although there was a trend towards increased cartilage lesions after GT harvest (median healthy knee 4.8 and GT harvested knee 7.8 p = 0.086). Inter- and intraobserver repeatability was high with 0.899 (95% confidence interval (CI) 0.708–0.960) and 0.988 (95% CI 0.973–0.995), respectively. A significant hypotrophy of the GM with a mean decrease of 25.3%, 18.4% and 16.9% occurred at 25% (p = 0.016), 50% (p = 0.007) and 75% (p = 0.002) of the length of the femur from distal. No compensatory hypertrophy of other thigh muscles or increased fatty infiltration of the GM was found. Tendon regeneration took place in eight out of 12 patients. In case of regeneration, the regenerated tendon inserted in a more proximal place.
Conclusion
Isolated harvest of the GT for shoulder procedures did not affect knee MRI significantly indicating therefore in general suitable graft utilization for surgeries outside of the knee. GT regenerated in most patients with just a more proximal insertion and a hypotrophy of the muscle belly.
Keywords: Gracilis, Autograft, Tendon harvest, MRI, Radiologic outcome
Background
The gracilis tendon (GT) is a popular graft source for reconstructive procedures in orthopedic surgery [5, 17, 19, 29]. To our knowledge, the consequences of isolated GT harvesting in healthy knees remains unclear. Patients were only examined with torn ACL and reconstruction with isolated ST or combined ST and GT graft. Consequently, the outcome parameters were influenced by several factors: injury to the knee with damage of further structures (menisci, collateral ligaments), additional harvest of the ST tendon, surgery (ACL reconstruction), and rehabilitation of the knee. In studies on patients after rupture and reconstruction of the ACL with ST or ST and GT graft a substantially higher risk for developing osteoarthritis (OA) of the knee joint was shown [7, 18, 36]. Although it remains unclear whether development of OA was primarily because of the persisting rotational instability after ACL reconstruction [36] or also because of insufficient rotational control after harvest of hamstrings autograft [7]. The regenerative potential of ST and GT after harvesting for ACL reconstruction was for the first time reported by Cross et al. in 1992 [6]. Strength deficits were found after harvesting of the GT and ST tendon and as a consequence a compensatory hypertrophy of the hamstrings muscles [3, 10, 16]. But, it remains unclear whether deficits in thigh muscle strength were created by isolated harvesting of the GT. Only mild fatty infiltration was described after hamstrings tendon harvesting. It was hypothesized that further fatty infiltration did not take place because the functionality of the muscles was at least partially preserved [32, 37]. To sum up, the consequences of hamstrings tendon harvesting on the ipsilateral knee joint were analyzed by several studies. However, all of them presented a large number of factors influencing the outcome. Thus, the aim of the present study was to analyze the radiologic consequences of isolated GT harvest of otherwise healthy, uninjured knees.
As a primary outcome it was hypothesized that altered kinematics after GT harvesting would lead to a higher prevalence of cartilage lesions and meniscal tears in knees after GT harvest and therefore show a higher WORMS. As secondary outcomes it was hypothesized that after harvesting the GT, a tendon-like structure would regenerate, but lead to a hypotrophy and fatty infiltration of the gracilis muscle (GM). In addition, a compensatory hypertrophy of the other hamstrings muscles was hypothesized.
Methods
In this retrospective cohort pilot study patients with chronic ACJ instability who underwent stabilization with autologous GT graft, in our clinic between 2007 and 2014, were considered for testing. The study was approved by the ethics committee of our institution (no. EA2/104/12). The study was registered at the German clinical trial register (no. DRKS00007100).
Written consent was given by all patients who met the inclusion criteria. Criteria for inclusion were: 1) stabilization of their ACJ with isolated GT at least 1 year before follow-up, 2) aged between 18 and 60 years, 3) no history of previous surgeries or injuries on both knees, and 4) ability to perform the MRI analysis (e.g. no claustrophobia).
Apart from the usual demographic data the Marx Activity Rating Scale was collected to describe our study population [20].
Surgical technique
GT was harvested under general anesthesia and a single shot perioperative antibiotic. The tendon harvesting was performed by different well-experienced knee and shoulder surgeons. The patients were placed in the beach chair position because of the following intervention on the ACJ. After full relaxation a tourniquet was applied to the thigh. An approximately 2,5 cm longitudinal incision was made over the pes anserine. Then the sartorius aponeurosis was identified and an incision was made proximal to the GT over the length of approximately 4 cm. The GT was identified and released at its musculotendinous junction with an open tendon stripper. Finally the distal attachment was dissected and released from the bone [29].
MRI examination
MRI of both knees and thighs were performed in dedicated multi-channel knee and surface coils using a 1.5 Tesla system (Avanto, Siemens, Erlangen, Germany). Sequences allowing a good evaluation of the cartilage, menisci and ligaments were chosen for the knee and of the tendons and muscles for the thighs (Supplement 1). MR images were evaluated using the Osirix software (Pixmeo, Bernex, Switzerland).
First, it was checked if the GT was harvested and not accidentally the ST. Knee MRIs were evaluated separately by three different researchers allowing the calculation of the interobserver repeatability. A second evaluation was performed 6 weeks later by the third researcher in order to calculate the intraobserver repeatability. The observers were blinded with regard to the identity of the patients and the operatively treated side. For the evaluation the Whole-Organ Magnetic Resonance Imaging Score (WORMS) was used [26]. Fourteen features of the knee joint were scored independently. Five of these features (cartilage, subarticular bone marrow abnormality, subarticular cysts, subarticular bone attrition, marginal osteophytes) were evaluated in 15 different regions (Table 1). Consequently, a total combined score as well as scores for the different features and regions were calculated. A healthy knee joint was scored 0. The higher the score the more abnormalities presented the knee joint. The worst possible score was 332. The contralateral healthy knee of each patient served as reference for the gracilis tendon harvested knee. Furthermore, a correlation analysis between the WORMS of the knee and time of follow-up was performed. In the T1-weighted axial images of the thigh, the cross-sectional area (CSA) of different muscles was measured at four different heights; the distal femoral growth plate, 25%, 50% and 75% of the length of the femur from distal. The CSA was measured using the closed polygon tool of OSIRIX (Fig. 1a and b, Table 2). In addition to CSA of the muscles, the fatty infiltration of the GM was evaluated as described by Engelken et al. [9]. These measurements were conducted using the ImageJ software [30]. Therefore, a slice at the transition from the middle to the distal third of the length of the femur in an axial t1-weighted sequence was chosen. First, reference measurements of pure fat and pure muscle tissue were performed in an oval region of interest (ROI) with approximately 200 counts. The intensity ranges in which all pixels represent pure fat or pure muscle were determined as the means ±2 standard deviations (SD). Next, the GM was defined as ROI with the freehand selection tool and intensity profiles were created for each pixel in this ROI. Then the pixels in the fat intensity and those in the muscle intensity range were added and a ratio (fat/muscle) was calculated. As reference, the same measurements were conducted at the contralateral thigh.
Table 1.
Features | Regional Subdivision | |
---|---|---|
articular cartilage integrity* | Patellofemoral joint (PFJ) | medial patella (MP) |
subarticular bone marrow abnormality* | lateral patella (LP) | |
subarticular cysts* | anterior medial femoral condyle (MFa) | |
subarticular bone attrition* | anterior lateral femoral condyle (LFa) | |
marginal osteophytes* | Medial tibiofemoral joint (MTFJ) | posterior femoral condyle (MFp) |
medial meniscal integrity | central medial femoral condyle (MFc) | |
lateral meniscal integrity | anterior medial tibial plateau (MTa | |
anterior cruciate ligament integrity | central medial tibial plateau (MTc) | |
posterior cruciate ligament integrity | posterior medial tibial plateau (MTp) | |
medial collateral ligament integrity | Lateral tibiofemoral joint (LTFJ) | central lateral femoral condyle (LFc) |
lateral collateral ligament integrity | posterior lateral femoral condyle (LFp) | |
synovitis/effusion | anterior lateral tibial plateau (LTa) | |
intraarticular loose bodies | central lateral tibial plateau (LTc) | |
periarticular cysts/bursitis | posterior lateral tibial plateau (LTp) | |
Subspinous region | portion of the tibial plateau beneath the tibial spines (S-region) |
Table 2.
Height | Muscles | ||||||
---|---|---|---|---|---|---|---|
G | ST | SM | BF | Q | RF | VL/VM/VI | |
growth plate | x | x | |||||
25% | x | x | x | x | |||
50% | x | x | x | x | x | x | x |
75% | x | x | x | x | x |
G M. gracilis, ST M. semitendinosus, SM M. semimembranosus, BF M. biceps femoris, Q M. quadriceps, RF M. rectus femoris, VL/VM/VI Sum of the Mm. vastus medialis, vastus lateralis and vastus intermedius
In addition, the observer checked whether the GT regenerated. It was distinguished between “no regeneration“, “tendon-like regeneration“, and “muscle-like regeneration “at the joint line, height of the distal femoral growth plate and at 25% of the length of the femur from distal.
Statistical analyses
This was a pilot study, which is why an a priori power analysis was not performed but it was attempted to included all available patients operated at our institution. To test the Gaussian distribution of the population, the D’Agostino & Pearson omnibus normality test was used. To analyze for side-to-side differences the dependent t-test was used for parametric data and the Wilcoxon signed-rank test for non-parametric data. Parametric data are presented as mean and SD or 95% confidence interval (CI), whereas non-parametric data are presented as median and interquartile range (IQR). If applicable, the range was added e.g. for follow-up time and age. For correlation analyses the Pearson correlation coefficient was used for parametric data and otherwise the Spearman correlation coefficient. Predictive values were calculated as an approximation using r2.
The level of significance was 5% (p < 0.05) Intra- and interclass correlations were calculated using the Intraclass Correlation Coefficient (ICC) for absolute agreement [27]. All statistical analyses were performed using GraphPad Prism Version 6.01 (GraphPad Software, Inc., San Diego, CA, U.S.A.).
Results
Sixteen patients were evaluated (14 male, 2 female). Retrospectively four patients had to be excluded because the MRIs showed accidental harvest of the ST tendon instead of the GT (Fig. 2). Demographic data is shown in Table 3. The gracilis tendon was harvested in equal parts from the right and left limb (six each).
Table 3.
Mean | Standard Deviation | Range | |
---|---|---|---|
Age [years] | 43 | 13 | 20–56 |
Follow-up Time [months] | 44 | 25 | 20–93 |
Body Mass Index [kg/m2] | 26.5 | 4.5 | 19.9–33.6 |
Marx Activity Rating Scale [points] | 4 | 5 | 0–13 |
The total combined WORMS showed a median of 6.3 points (IQR 2.5 to 10) for the healthy limb and 10 points (IQR 5.4 to 15.5) for the limb with GT harvest (p = 0.095). The evaluation of the articular cartilage integrity of the knee joint showed a median of 4.8 (IQR 1.4 to 7.4) for healthy limbs and 7.8 (IQR 4.3 to 10.8) for limbs with GT harvest reaching almost statistical significance (p = 0.086). For all other features, statistical differences were higher (Table 4). Evaluation of the WORMS of the regions patellofemoral joint (PFJ), medial tibiofemoral joint (MTFJ) and lateral tibiofemoral joint (LTFJ) showed a median of 2.3 (IQR 0 to 3.8), 3.0 (IQR 0 to 3.9) and 0 (IQR 0) for the healthy limb and 3.3 (IQR 0.3 to 7.3), 3.5 (IQR 0.8 to 6.0) and 0 (IQR 0) for the GT harvested limb with a level of significance of p = 0.438, p = 0.234 and p > 0.05 respectively.
Table 4.
Mean/Median Healthy | 95%-CI/IQR Healthy | Mean/median Gracilis Harvest | 95%-CI/IQR Gracilis Harvest | p-value | |
---|---|---|---|---|---|
Total combined score | 6.3 | 2.5–10 | 10 | 5.4–15.5 | 0.095 |
Cartilage | 4.8 | 1.4–7.4 | 4.3–10.8 | 4.3–10.8 | 0.086 |
Bone marrow abnormality | 0 | 0–0 | 0 | 0–0 | 0.375 |
Subarticular cysts | 0 | 0–0 | 0 | 0–0 | ♦ |
Subarticular bone attrition | 0 | 0–0 | 0 | 0–0 | ♦ |
Osteophytes | 0 | 0–0 | 0 | 0–0 | > 0.999 |
Menisci | 0 | 0–0 | 0 | 0–2.5 | 0.125 |
Ligaments (cruciates and collaterals) | 0 | 0–0 | 0 | 0–0 | ♦ |
Synovitis/effusiona | 0.3 | −0.1 - 0.5 | 0.3 | −0.1 - 0.5 | > 0.999 |
Loose bodies | 0 | 0–0 | 0 | 0–0 | ♦ |
Periarticular cysts / bursitis | 0.5 | 0.0–1.0 | 0.5 | 0.0–1.0 | > 0.999 |
♦no difference between the two limbs, cannot calculate a paired t-test or Wilcoxon test. aGaussian distribution. CI confidence interval, IQR Interquartile range
Articular cartilage integrity in the PFJ, MTFJ and LTFJ showed a median of 1.5 (IQR 0 to 3.6), 3.0 (IQR 0 to 3.8) and 0 (IQR 0) for the healthy limb and 3.3 (IQR 0 to 4.8), 3.5 (IQR 0.8 to 6.0) and 0 (IQR 0) for the limb with GT harvest with a level of significance of p = 0.5, p = 0.141 and p > 0.05 respectively. For all other features and regions, no differences between the mean or median of the healthy and GT harvested limb were found.
Inter- and intraobserver repeatability was high with 0.899 (95% CI 0.708 to 0.96) and 0.988 (95% CI 0.973 to 0.995), respectively. A correlation between the total combined WORMS and time of follow-up could not be established (p > 0.05).
A tendon-like regeneration of the GT at the joint line was observed for five patients. At the height of the femoral growth plate, eight patients showed a tendon-like regeneration of the harvested GT. At 25% of the length of the femur from distal, a muscle-like regeneration was observed for four, a tendon-like regeneration for seven and no regeneration for one patient.
The CSA of the different muscles showed a statistically significant hypotrophy of the GM at all heights apart from the growth plate where the CSA on the operated side was not measurable because of the more proximal insertion of the tendon (Table 5, Fig. 3). The mean decrease of the CSA of the GM was 25.3%, 18.4% and 16.9% at 25%, 50% and 75% of the length of the femur from distal compared to the contralateral limb. A compensatory hypertrophy of the other thigh muscles was not observed, neither for all the patients nor in the subgroup where no regeneration of the tendon took place.
Table 5.
Mean/Median Healthy (cm2) | 95%-CI / IQR Healthy | Mean/Median Gracilis Harvest (cm2) | 95%-CI/IQR Gracilis Harvest | p-value | |
---|---|---|---|---|---|
25% | 1.87 | 1.50–2.33 | 0.96 | 0.15–1.71 | 0.016* |
50%a | 4.54 | 3.76–5.31 | 3.70 | 2.68–3.76 | 0.007* |
75% | 3.71 | 2.69–4.33 | 2.82 | 2.18–3.54 | 0.002* |
*reached statistical significance. aGaussian distribution. CI confidence interval, IQR Interquartile range
An increased fatty infiltration of the GM after harvesting of its tendon was not observed. The fatty infiltration of healthy GM was 0.006 (IQR 0.001 to 0.01), whereas it was 0.015 (IQR 0 to 0.028) (p > 0.05) for the ones with the harvested tendon.
Discussion
The main finding of this study was that no statistical differences in the WORMS between the GT harvested thighs and the contralateral thighs were found. A trend towards increased cartilage lesions in the GT harvested thigh was shown in the WORMS. These lesions occurred especially in the PFJ and the MTFJ but without reaching statistical significance. The MTFJ and the lateral part of the PFJ represent also the regions in healthy knee joints with the biggest changes in cartilage thickness during loading and have therefore, irrespective of GT harvesting, a higher risk for developing OA [8]. Furthermore, changes in knee joint kinematics may be caused by harvesting of the GT and lead to early OA (e.g. smaller peak knee flexion angle, greater tibial rotation excursion, lower peak knee flexion moments) [7]. However, smaller knee flexion angles during stance phase of gait were also observed in uninjured patients with early patellofemoral OA because the surface through which patellofemoral loads are distributed is limited [7, 12]. Greater tibial rotation excursion after ACL reconstruction is potentially due to insufficient rotational control after hamstrings autograft and might be part of the mechanism after GT harvest too [7]. The small number of patients and the short time of follow-up might be an explanation for the missing statistical significance in the present study. However, a correlation between the total combined WORMS and time of follow-up was not found in the present study either. Thus, it remains unclear whether the tendency towards early cartilage lesions is a coincidence or due to tendon harvest.
High inter- and intraobserver repeatability in this study show good applicability of the WORMS in clinical use and the quality of the assessment.
Measurements of the cross-sectional area of the GM showed hypotrophy irrespective of regeneration of its tendon. However, no hypertrophy of the other thigh muscles, and especially the other hamstrings muscles, was seen. Hypotrophy of the GM in patients with GT and ST tendon harvest for ACL reconstruction was confirmed in the past [2, 15, 16, 28, 39]. On the other side, no decrease of the CSA of the G and ST muscle after harvesting for ACL reconstruction was found 10 cm above the joint, but this is distal to the main portion of the muscle bellies of most patients [31]. The findings of the present study contradict with prior published data showing a hypertrophy of the BF and SM muscles if no regeneration of the GT had occurred [3, 10, 14]. Hypertrophy of the SM muscle and long head of the BF muscle was even found irrespective of ST tendon and GT regeneration [16]. However, most of them harvested both, the ST and GT, tendons of muscles that have similar functions and therefore might lead to a higher deficit in muscle strength and a compensatory hypertrophy of the other hamstrings muscles. Findings of Eriksson et al. contradict this theory. After isolated harvesting of the ST patients without tendon regeneration showed hypertrophy of the SM muscle [10]. Factors that may implicate a compensatory hypertrophy of the SM and BF muscles are harvesting of multiple tendons (ST and GT) and if no regeneration of the harvested tendons takes place.
In the present study a fatty infiltration of the GM using MRI was not observed. Mild fatty infiltration (Goutallier Grade 1 or 2) of both ST and GM was shown in previous studies after harvesting both tendons in patients with ACL reconstruction [32, 37]. Histological analysis of the ST muscle of rabbits three, 6 and 12 months after harvesting their tendon ipsilateral showed no significant differences in fatty infiltration between both thighs (contralateral thigh was control). They hypothesized that low fatty infiltration was a sign that the muscle remained functional after tendon harvest [38].
Regeneration of the tendon of the GM took place in eight out of 12 patients. For these eight patients a tendon was detected at the distal femoral growth plate, but for only five of them a tendon was observed at the knee joint line, which lets us deduce that the regenerated tendons do not insert in their original localization, the pes anserinus superficialis, but in a more proximal position. This is in accordance with the findings of the majority of the previous studies after single ST tendon harvest or combined harvest of ST and GT. A more proximal insertion was shown in MRI [6, 28, 31, 34, 39], sonography [25] and surgical exploration [13]. Few authors, however, found in MRI or macroscopically during surgical exploration regenerated tendons at its normal insertion [1, 24]. Even a tibial insertion distal of the original point of insertion of the harvested tendon was detected, but with a more proximal musculotendinous junction [4]. Latter was confirmed by several authors [15, 21, 37]. It was hypothesized that the more proximal tibial insertion and musculotendinous junction had functional consequences and would lead to strength deficits especially for deep knee flexion angles (≥ 70°) [1, 4, 22, 23, 33, 35]. It was hypothesized that the more proximal tibial insertion and retraction of the muscle belly would lead to a shorter knee flexion moment arm and that therefore the concerned muscles are not able to produce the same amount of force [34, 35, 39]. At lower grades of knee flexion, the BF and SM muscles are the main producers of knee flexion strength and able to compensate here a loss of ST (and G) muscle strength [6, 39]. After ACL reconstruction with ST and GT autograft a correlation between the number of regenerated tendons and the strength deficit was shown [4]. Microscopically a fibrous structure appeared after 6 months, which evolved to a structure similar to the preharvest tendon after 2 years [11, 13], but some small areas with scar tissue persisted [13]. To summarize, scientific knowledge remains controversial if it comes to tendon regeneration and functionality of the regenerated tendons.
Limitations
The present study has some limitations. First of all, more included patients would be favorable. Nevertheless, this was a pilot study looking for trends, where GT harvest might influence knee degeneration and muscle morphology of the thigh. All patients since starting with use of GT for chronic ACJ stabilization with a minimum follow-up of 1 year were tried to be included. Obviously, the risk of a type-II-statistical error was well-known. Unfortunately, the initial cohort was further decimated because of accidental harvest of the ST tendon.
A second limitation is the cross-sectional study design. Comparisons were only made between the surgical and contralateral limb. No presurgical comparisons existed and we had no data about the evolution of cartilage lesions, CSA of the thigh muscles and tendon regeneration over time. The present study cohort included only two female patients and therefore separate analyses on gender differences could not be performed. Some patients also presented short times of follow-up, which could make it difficult to detect degenerative changes or tendon regeneration. A correlation between the total combined WORMS and time of follow-up, however, could not be established. However, analysis of the radiologic consequences of isolated GT harvest in uninjured knee joints represent a novel and valuable addition to the literature.
Conclusions
Isolated harvest of the GT for shoulder procedures did not affect knee MRI significantly indicating therefore in general suitable graft utilization for surgeries outside of the knee. GT regenerated in most patients with just a more proximal insertion and a hypotrophy of the muscle belly.
Supplementary information
Acknowledgements
Not applicable.
Abbreviations
- GT
Gracilis tendon
- WORMS
Whole-Organ Magnetic Resonance Imaging Score
- GM
Gracilis muscle
- CI
Confidence interval
- ACL
Anterior cruciate ligament
- MPFL
Medial patellofemoral ligament
- ACJ
Acromioclavicular joint
- OA
Osteoarthritis
- PFJ
Patellofemoral joint
- MP
Medial patella
- LP
Lateral patella
- MTFJ
Medial tibiofemoral joint
- MFa
Anterior medial femoral condyle
- MFc
Central medial femoral condyle
- MFp
Posterior medial femoral condyle
- MTa
Anterior medial tibia plateau
- MTc
Central medial tibia plateau
- MTp
Posterior medial tibia plateau
- LTFJ
Lateral tibiofemoral joint
- LFa
Anterior lateral femoral condyle
- LFc
Central lateral femoral condyle
- LFp
Posterior lateral femoral condyle
- LTa
Anterior lateral tibia plateau
- LTc
Central lateral tibia plateau
- LTp
Posterior lateral tibia plateau
- CSA
Cross-sectional area
- G
Gracilis
- ST
Semitendinosus
- SM
Semimembranosus
- BF
Biceps femoris
- Q
Quadriceps
- RF
Rectus femoris
- VL
Vastus lateralis
- VM
Vastus medialis
- VI
Vastus intermedius
- ROI
Region of interest
- SD
Standard deviation
- ICC
Intraclass Correlation Coefficient
- BMI
Body mass index
Authors’ contributions
Author AF performed the examinations of the study. SK, TD and AF analyzed the data and performed the statistical analysis. NK helped with the patient recruitment. All authors substantially revised the work. The authors read and approved the final manuscript.
Funding
This work was supported by the AGA - Society for Arthroscopy and Joint Surgery under research grant No. 63.
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
All procedures performed in this study were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study was approved by the ethics committee of our institution (no. EA2/104/12) and all patients gave written consent. The study was registered at the German clinical trial register (no. DRKS00007100).
Informed consent was obtained from all individual participants included in the study. Additional informed consent was obtained from all individual participants for whom identifying information is included in this article.
Competing interests
Author M. T. Provencher received IP royalties and speaker fees from Arthrex Inc. as well as consulting fees from Slack Inc. and Joint Research Foundation. All other authors declare that they have no conflict of interest.
Footnotes
Research performed at Charité – University Medicine Berlin
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Supplementary information accompanies this paper at 10.1186/s40634-020-00236-8.
References
- 1.Ahlen M, Liden M, Bovaller A, Sernert N, Kartus J. Bilateral magnetic resonance imaging and functional assessment of the semitendinosus and gracilis tendons a minimum of 6 years after ipsilateral harvest for anterior cruciate ligament reconstruction. Am J Sports Med. 2012;40:1735–1741. doi: 10.1177/0363546512449611. [DOI] [PubMed] [Google Scholar]
- 2.Burks RT, Crim J, Fink BP, Boylan DN, Greis PE. The effects of semitendinosus and gracilis harvest in anterior cruciate ligament reconstruction. Arthroscopy. 2005;21:1177–1185. doi: 10.1016/j.arthro.2005.07.005. [DOI] [PubMed] [Google Scholar]
- 3.Carofino B, Fulkerson J. Medial hamstring tendon regeneration following harvest for anterior cruciate ligament reconstruction: fact, myth, and clinical implication. Arthroscopy. 2005;21:1257–1265. doi: 10.1016/j.arthro.2005.07.002. [DOI] [PubMed] [Google Scholar]
- 4.Choi JY, Ha JK, Kim YW, Shim JC, Yang SJ, Kim JG. Relationships among tendon regeneration on MRI, flexor strength, and functional performance after anterior cruciate ligament reconstruction with hamstring autograft. Am J Sports Med. 2012;40:152–162. doi: 10.1177/0363546511424134. [DOI] [PubMed] [Google Scholar]
- 5.Coughlin MJ, Matt V, Schenck RC., Jr Augmented lateral ankle reconstruction using a free gracilis graft. Orthopedics. 2002;25:31–35. doi: 10.3928/0147-7447-20020101-13. [DOI] [PubMed] [Google Scholar]
- 6.Cross MJ, Roger G, Kujawa P, Anderson IF. Regeneration of the semitendinosus and gracilis tendons following their transection for repair of the anterior cruciate ligament. Am J Sports Med. 1992;20:221–223. doi: 10.1177/036354659202000223. [DOI] [PubMed] [Google Scholar]
- 7.Culvenor AG, Perraton L, Guermazi A, Bryant AL, Whitehead TS, Morris HG, et al. Knee kinematics and kinetics are associated with early patellofemoral osteoarthritis following anterior cruciate ligament reconstruction. Osteoarthr Cartil. 2016;24:1548–1553. doi: 10.1016/j.joca.2016.05.010. [DOI] [PubMed] [Google Scholar]
- 8.Eckstein F, Lemberger B, Gratzke C, Hudelmaier M, Glaser C, Englmeier KH, et al. In vivo cartilage deformation after different types of activity and its dependence on physical training status. Ann Rheum Dis. 2005;64:291–295. doi: 10.1136/ard.2004.022400. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Engelken F, Wassilew GI, Kohlitz T, Brockhaus S, Hamm B, Perka C, et al. Assessment of fatty degeneration of the gluteal muscles in patients with THA using MRI: reliability and accuracy of the Goutallier and quartile classification systems. J Arthroplast. 2014;29:149–153. doi: 10.1016/j.arth.2013.04.045. [DOI] [PubMed] [Google Scholar]
- 10.Eriksson K, Hamberg P, Jansson E, Larsson H, Shalabi A, Wredmark T. Semitendinosus muscle in anterior cruciate ligament surgery: morphology and function. Arthroscopy. 2001;17:808–817. doi: 10.1016/S0749-8063(01)90003-9. [DOI] [PubMed] [Google Scholar]
- 11.Eriksson K, Kindblom LG, Hamberg P, Larsson H, Wredmark T. The semitendinosus tendon regenerates after resection: a morphologic and MRI analysis in 6 patients after resection for anterior cruciate ligament reconstruction. Acta Orthop Scand. 2001;72:379–384. doi: 10.1080/000164701753542041. [DOI] [PubMed] [Google Scholar]
- 12.Farrokhi S, O’Connell M, Fitzgerald GK. Altered gait biomechanics and increased knee-specific impairments in patients with coexisting tibiofemoral and patellofemoral osteoarthritis. Gait Posture. 2015;41:81–85. doi: 10.1016/j.gaitpost.2014.08.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Ferretti A, Conteduca F, Morelli F, Masi V. Regeneration of the semitendinosus tendon after its use in anterior cruciate ligament reconstruction: a histologic study of three cases. Am J Sports Med. 2002;30:204–207. doi: 10.1177/03635465020300021001. [DOI] [PubMed] [Google Scholar]
- 14.Irie K, Tomatsu T. Atrophy of semitzendinosus and gracilis and flexor mechanism function after hamstring tendon harvest for anterior cruciate ligament reconstruction. Orthopedics. 2002;25:491–495. doi: 10.3928/0147-7447-20020501-15. [DOI] [PubMed] [Google Scholar]
- 15.Janssen RP, van der Velden MJ, Pasmans HL, Sala HA. Regeneration of hamstring tendons after anterior cruciate ligament reconstruction. Knee Surg Sports Traumatol Arthrosc. 2013;21:898–905. doi: 10.1007/s00167-012-2125-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Konrath JM, Vertullo CJ, Kennedy BA, Bush HS, Barrett RS, Lloyd DG. Morphologic characteristics and strength of the hamstring muscles remain altered at 2 years after use of a hamstring tendon graft in anterior cruciate ligament reconstruction. Am J Sports Med. 2016;44:2589–2598. doi: 10.1177/0363546516651441. [DOI] [PubMed] [Google Scholar]
- 17.Lipscomb AB, Johnston RK, Snyder RB. The technique of cruciate ligament reconstruction. Am J Sports Med. 1981;9:77–81. doi: 10.1177/036354658100900201. [DOI] [PubMed] [Google Scholar]
- 18.Louboutin H, Debarge R, Richou J, Selmi TA, Donell ST, Neyret P, et al. Osteoarthritis in patients with anterior cruciate ligament rupture: a review of risk factors. Knee. 2009;16:239–244. doi: 10.1016/j.knee.2008.11.004. [DOI] [PubMed] [Google Scholar]
- 19.Maffulli N, Spiezia F, Testa V, Capasso G, Longo UG, Denaro V. Free gracilis tendon graft for reconstruction of chronic tears of the Achilles tendon. J Bone Joint Surg Am. 2012;94:906–910. doi: 10.2106/JBJS.K.00869. [DOI] [PubMed] [Google Scholar]
- 20.Marx RG, Stump TJ, Jones EC, Wickiewicz TL, Warren RF. Development and evaluation of an activity rating scale for disorders of the knee. Am J Sports Med. 2001;29:213–218. doi: 10.1177/03635465010290021601. [DOI] [PubMed] [Google Scholar]
- 21.Nakamae A, Deie M, Yasumoto M, Adachi N, Kobayashi K, Yasunaga Y, et al. Three-dimensional computed tomography imaging evidence of regeneration of the semitendinosus tendon harvested for anterior cruciate ligament reconstruction: a comparison with hamstring muscle strength. J Comput Assist Tomogr. 2005;29:241–245. doi: 10.1097/01.rct.0000153779.86663.92. [DOI] [PubMed] [Google Scholar]
- 22.Nakamura E, Mizuta H, Kadota M, Katahira K, Kudo S, Takagi K. Three-dimensional computed tomography evaluation of semitendinosus harvest after anterior cruciate ligament reconstruction. Arthroscopy. 2004;20:360–365. doi: 10.1016/j.arthro.2004.01.032. [DOI] [PubMed] [Google Scholar]
- 23.Ohkoshi Y, Inoue C, Yamane S, Hashimoto T, Ishida R. Changes in muscle strength properties caused by harvesting of autogenous semitendinosus tendon for reconstruction of contralateral anterior cruciate ligament. Arthroscopy. 1998;14:580–584. doi: 10.1016/S0749-8063(98)70053-2. [DOI] [PubMed] [Google Scholar]
- 24.Okahashi K, Sugimoto K, Iwai M, Oshima M, Samma M, Fujisawa Y, et al. Regeneration of the hamstring tendons after harvesting for arthroscopic anterior cruciate ligament reconstruction: a histological study in 11 patients. Knee Surg Sports Traumatol Arthrosc. 2006;14:542–545. doi: 10.1007/s00167-006-0068-z. [DOI] [PubMed] [Google Scholar]
- 25.Papandrea P, Vulpiani MC, Ferretti A, Conteduca F. Regeneration of the semitendinosus tendon harvested for anterior cruciate ligament reconstruction. Evaluation using ultrasonography. Am J Sports Med. 2000;28:556–561. doi: 10.1177/03635465000280041901. [DOI] [PubMed] [Google Scholar]
- 26.Peterfy CG, Guermazi A, Zaim S, Tirman PF, Miaux Y, White D, et al. Whole-organ magnetic resonance imaging score (WORMS) of the knee in osteoarthritis. Osteoarthr Cartil. 2004;12:177–190. doi: 10.1016/j.joca.2003.11.003. [DOI] [PubMed] [Google Scholar]
- 27.Petrie A. Statistics in orthopaedic papers. J Bone Joint Surg Br. 2006;88:1121–1136. doi: 10.1302/0301-620X.88B9.17896. [DOI] [PubMed] [Google Scholar]
- 28.Rispoli DM, Sanders TG, Miller MD, Morrison WB. Magnetic resonance imaging at different time periods following hamstring harvest for anterior cruciate ligament reconstruction. Arthroscopy. 2001;17:2–8. doi: 10.1053/jars.2001.19460. [DOI] [PubMed] [Google Scholar]
- 29.Scheibel M, Ifesanya A, Pauly S, Haas NP. Arthroscopically assisted coracoclavicular ligament reconstruction for chronic acromioclavicular joint instability. Arch Orthop Trauma Surg. 2008;128:1327–1333. doi: 10.1007/s00402-007-0547-9. [DOI] [PubMed] [Google Scholar]
- 30.Schneider CA, Rasband WS, Eliceiri KW. NIH image to ImageJ: 25 years of image analysis. Nat Methods. 2012;9:671–675. doi: 10.1038/nmeth.2089. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Simonian PT, Harrison SD, Cooley VJ, Escabedo EM, Deneka DA, Larson RV. Assessment of morbidity of semitendinosus and gracilis tendon harvest for ACL reconstruction. Am J Knee Surg. 1997;10:54–59. [PubMed] [Google Scholar]
- 32.Snow BJ, Wilcox JJ, Burks RT, Greis PE. Evaluation of muscle size and fatty infiltration with MRI nine to eleven years following hamstring harvest for ACL reconstruction. J Bone Joint Surg Am. 2012;94:1274–1282. doi: 10.2106/JBJS.K.00692. [DOI] [PubMed] [Google Scholar]
- 33.Tadokoro K, Matsui N, Yagi M, Kuroda R, Kurosaka M, Yoshiya S. Evaluation of hamstring strength and tendon regrowth after harvesting for anterior cruciate ligament reconstruction. Am J Sports Med. 2004;32:1644–1650. doi: 10.1177/0363546504263152. [DOI] [PubMed] [Google Scholar]
- 34.Takeda Y, Kashiwaguchi S, Matsuura T, Higashida T, Minato A. Hamstring muscle function after tendon harvest for anterior cruciate ligament reconstruction: evaluation with T2 relaxation time of magnetic resonance imaging. Am J Sports Med. 2006;34:281–288. doi: 10.1177/0363546505279574. [DOI] [PubMed] [Google Scholar]
- 35.Tashiro T, Kurosawa H, Kawakami A, Hikita A, Fukui N. Influence of medial hamstring tendon harvest on knee flexor strength after anterior cruciate ligament reconstruction. A detailed evaluation with comparison of single- and double-tendon harvest. Am J Sports Med. 2003;31:522–529. doi: 10.1177/31.4.522. [DOI] [PubMed] [Google Scholar]
- 36.Tashman S, Collon D, Anderson K, Kolowich P, Anderst W. Abnormal rotational knee motion during running after anterior cruciate ligament reconstruction. Am J Sports Med. 2004;32:975–983. doi: 10.1177/0363546503261709. [DOI] [PubMed] [Google Scholar]
- 37.Tsifountoudis I, Bisbinas I, Kalaitzoglou I, Markopoulos G, Haritandi A, Dimitriadis A, et al. The natural history of donor hamstrings unit after anterior cruciate ligament reconstruction: a prospective MRI scan assessment. Knee Surg Sports Traumatol Arthrosc. 2017;25:1583–1590. doi: 10.1007/s00167-015-3732-3. [DOI] [PubMed] [Google Scholar]
- 38.Vourazeris JD, Lawless MW, Markert RJ, Stills HF, Boivin GP. Semitendinosus muscle fatty infiltration following tendon harvest in rabbits. J Orthop Res. 2013;31:1234–1239. doi: 10.1002/jor.22356. [DOI] [PubMed] [Google Scholar]
- 39.Williams GN, Snyder-Mackler L, Barrance PJ, Axe MJ, Buchanan TS. Muscle and tendon morphology after reconstruction of the anterior cruciate ligament with autologous semitendinosus-gracilis graft. J Bone Joint Surg Am. 2004;86-A:1936–1946. doi: 10.2106/00004623-200409000-00012. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.