INTRODUCTION: In practice, the use of a whip stitch versus a locking stitch in anterior cruciate ligament (ACL) graft preparation is based on surgeon preference. Those who prefer efficiency and shorter stitch time typically choose a whip stitch, while those who require improved biomechanical properties select a locking stitch, the gold standard of which is the Krackow method. The purpose of this study was to evaluate a novel suture needle design that can be used to perform two commonly used stitch methods, a whip stitch, and a locking stitch, by comparing the speed of graft preparation and biomechanical properties. It was hypothesized that adding a locking mechanism to the whip stitch would improve biomechanical performance but would also require more time to complete due to additional steps required for the locking technique. METHODS: Graft preparation was performed by four orthopaedic surgeons of different training levels where User 1 and User 2 were both attendings and User’s 3 and 4 were both fellows. A total of 24 matched pair cadaveric knees were dissected and a total of 48 semitendinosus tendons were harvested. All grafts were standardized to the same size. Tendons were randomly divided into 4 groups (12 tendons per group) such that each User performed analogous stitch on matched pair: Group 1, User 1 and User 3 performed whip stitches; Group 2, User 1 and User 3 performed locking stitches; Group 3, User 2 and User 4 performed whip stitches; Group 4, User 2 and User 4 performed locking stitches. For instrumentation, the two ends of tendon grafts were clamped to a preparation stand. A skin marker was used to mark five evenly spaced points, 0.5 cm apart, as a guide to create a 5-stitch series. The stitches were performed with EasyWhip, a novel two-part suture needle which allows one to do both a traditional whip stitch and a locking whip stitch, referred to as WhipLock (Figure 1). The speed for graft preparation was timed for each User. Biomechanical testing was performed using a servohydraulic testing machine (MTS Bionix) equipped with a 5kN load cell (Figure 2). A standardized length of tendon, 10 cm, was coupled to the MTS actuator by passing it through a cryoclamp cooled by dry ice to a temperature of -5°C. All testing samples were pre-conditioned to normalize viscoelastic effects and testing variability through application of cyclical loading to 25-100 N for three cycles. The samples were then held at 89 N for 15 minutes. Thereafter, the samples were loaded to 50-200 N for 500 cycles at 1 Hz. If samples survived, they were ramped to failure at 20 mm/min. Displacement and force data was collected throughout testing. Metrics of interest were peak-to-peak displacement (mm), stiffness (N/mm), ultimate failure load (N) and failure mode. Data are presented as averages and standard deviations. A Wilcoxon signed-rank test was used to evaluate the groups for time to complete stitch and biomechanical performance. Statistical significance was set at P = .05. RESULTS SECTION: In Group 1, the time to complete the whip stitch was not significantly different between User 1 and User 3, where the average completion time was 1 min 13 sec. Similarly, there were no differences between Users when performing the WhipLock (Group 2) with an average time of 1 min 49 sec. In Group 3 (whip stitch), User 2 took 1 min 48 sec to complete the whip stitch, whereas User 4 took 1 min 25 sec (p=.033). The time to complete the WhipLock stitch (Group 4) was significantly different, where User 2 took 3 min and 44 sec, while User 4 only took 2 min 3 sec (p=.002). Overall, the whip stitch took on average 1 min 25 sec whereas the WhipLock took 2 min 20 sec (p=.001). For whip stitch constructs, no differences were found between Users and all stitches were biomechanically equivalent. Correspondingly, for WhipLock stitches, no differences were found between Users and all suture constructs were likewise biomechanically equivalent. Averages for peak-to-peak displacement (mm), stiffness (N/mm), and ultimate failure load (N) are presented in Table 1. Moreover, when the two stitch methods were compared, the WhipLock constructs significantly increased stiffness by 25% (p <.001), increased ultimate failure load by 35% (p<.001) and reduced peak-to-peak displacement by 55% (p=.001). The common mode of failure for grafts with whip stitch failed by suture pullout from tendon (18/24), where a few instances occurred by suture breakage (6/24). Tendon grafts with WhipLock stitch commonly failed by suture breakage (22/24), where two instances of combined tendon tear and suture breakage were noted. DISCUSSION: The WhipLock stitch significantly increased average construct stiffness and ultimate failure load, while significantly reducing the peak-to- peak displacement compared to the whip stitch. These added strength benefits of the WhipLock stitch took 55 seconds more to complete than the whip stitch. No statistically significant difference in biomechanical performance was found between the Users. Data suggests equivalent stitch performance regardless of the time to complete stitch and surgeon training level. SIGNIFICANCE/CLINICAL RELEVANCE: Clinically, having a suture needle device available which can be used to easily perform different constructs including one with significant strength advantages regardless of level of experience is of benefit.
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This content will become publicly available on February 11, 2026
Evaluation of Whip Stitch Reinforcement in Cadaveric Semitendinosus Grafts
INTRODUCTION: Repair and reconstruction of torn ligaments and tendons are commonly performed surgical procedures by orthopaedic surgeons, occurring at multiple locations in the body, such as the elbow or the knee for anterior cruciate ligament (ACL). Suturing is a critical step in the procedure, and although advancements in suturing have been made, residual laxity and graft failure at the suture site are challenges that still prevail. The whip stitch is one of the most popular suturing methods. However, a major drawback with this technique is that it concentrates the force along the central axis of the tissue, making it prone to failure due to suture pull-through and tissue shredding. New whip stitch reinforcement techniques have been developed, and the introduction of suture tape augmentation or “tags” have become popular to minimize tissue damage. However, the introduction of additional foreign material has increased concerns of suture burden. The purpose of this study was to assess the biomechanical performance of different whip stitch reinforcement techniques by comparing elongation, stiffness, and failure load across products developed by two different manufacturers. METHODS: This was a controlled biomechanical study that utilized 21 matched pair cadaveric knees. Specimens were dissected, and 40 semitendinosus tendons were harvested in preparation for stitching. All tendons were standardized to the same length and were randomized into six test groups varying in reinforcement techniques based on company (Arthrex [A], Winter Innovations [W]), number of reinforcements (0, 1, 2), and type of reinforcement (locking method [L], material [M]). Baseline groups had no reinforcements and consisted of a standard whip stitch (WS) method with products from both companies. For single reinforcement groups, the material consisted of a thicker suture tape that was laid on top of the tissue and stitched through. The locking method groups employed a WhipLock pattern, which creates a locking suture mechanism (like a Krackow) but requires half as many needle passes through the tissue (like a whip stitch). The final group combined both reinforcement techniques (locking method and material). Stitching was performed by a fellowship-trained orthopaedic surgeon and a physician assistant. For instrumentation, tendons were clamped to a graft preparation stand and five evenly placed stitches were completed at the proximal end. Cyclical testing was performed using a servohydraulic testing machine (MTS Bionix) equipped with a 5kN load cell. Each sample was coupled to the MTS actuator by passing it through a cryolamp cooled by dry ice to -5ᵒC. All testing samples were pre-conditioned to normalize viscoelastic effects by cyclical loading to 25-100 N for three cycles, followed by static hold at 50N for 1 min. Samples were then loaded to 50-200 N at 1 Hz for 500 cycles. If samples survived, they were ramped to failure at 20 mm/min. Displacement and force data were collected throughout testing. Metrics of interest were stiffness (N/mm), ultimate failure load (N), peak-to-peak displacement (mm), elongation (mm), and failure displacement (mm), and failure mode (tissue pull-through vs. suture break). To characterize suture material burden, three independent synthetic grafts were prepared for each of the 0 and 1 reinforcement groups. Sutures were trimmed at the end of the tissue and then removed from the tendon. The weight of each suture construct was taken, and a pooled weight was recorded and then averaged across the 3 samples to obtain the suture weight (g) for each group. Data are presented as averages plus/minus standard deviation. A one-way ANOVA with a Tukey HSD for post hoc analysis was used to evaluate differences between groups. Statistical significance was set at P = .05. RESULTS: For the zero reinforcement groups, no significant differences were observed between W0 and A0 for elongation (p=.479), stiffness (p=.769), ultimate failure load (p=.387), or failure displacement (p=.899). However, it was determined that A0 had significantly larger peak-to-peak displacement compared to W0 (p=.00156). The addition of suture material reinforcement (A1-M) significantly improved biomechanical performance across all metrics compared to A0, where elongation was reduced (p=.001), peak-to-peak displacement decreased (p=.001), stiffness increased (p=.001), ultimate failure load increased (p=.001), and failure displacement decreased (p=.001). While the biomechanical performance of W0 improved with the addition of suture material (W1-M), only the decrease in failure displacement was found to be significantly different (p=.008). The reinforcement locking method W1-L resulted in a significant increase in ultimate failure load (p=.018) and decrease in failure displacement (p< .001) compared to W0. However, decreases in elongation, decreases in peak-to-peak displacement, and increases in stiffness were not statistically significant. When comparing across A0 and W1-L, it was determined that W1-L had significantly less elongation (p=.0019), less peak-to-peak displacement (p< .001), increased stiffness (p=.012), increased ultimate failure load (p< .001) and decreased failure displacement (p< .001). Comparing across all the reinforcement groups (W1-L, W1-M, A1-M, W2-L,M), no significant differences were concluded across elongation, peak-to-peak displacement, stiffness, ultimate failure load or failure displacement. Interestingly, no significant differences were observed across all metrics when comparing W1-L and the addition of the second reinforcement of suture material (W2-L,M). The failure mode for whip stich method with no reinforcement (W0, A0) was suture pull-through tissue across a majority of the grafts. Generally, additional reinforcement groups utilizing W1-L, W1-M, and W2- L,M failed from suture breakage, however A1-M still resulted in suture pull-through. Within 1 reinforcement groups, the locking method W1-L had approximately 40% less suture by weight (0.050g) than the material groups W1-M (0.093g) and A1-M (0.080g). DISCUSSION: The use of whip stitch reinforcement, whether it is by a locking method or additional suture material, may help reduce the rate of failure and damage to tissue. In this cadaveric semitendinosus tendon model, it was shown that performing a whip stitch without reinforcement offered limited biomechanical security. The addition of reinforcement material enhanced the biomechanical properties associated with the graft significantly minimizing the failure displacement, however the effects varied depending on manufacturer. SIGNIFICANCE/CLINICAL RELEVANCE: The WhipLock reinforcement method demonstrated similar biomechanical properties when compared to material-reinforced semitendinosus grafts but required less suture material. The novel two-part needle from company W shows promise as it enables both a traditional whip stitch and the reinforced WhipLock method, which provides reinforcement without added suture burden of reinforcement materials.
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- Award ID(s):
- 2304269
- PAR ID:
- 10640633
- Publisher / Repository:
- Orthopaedic Research Society
- Date Published:
- Format(s):
- Medium: X
- Location:
- Phoenix, Arizona
- Sponsoring Org:
- National Science Foundation
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INTRODUCTION: Quadriceps tendon autografts have experienced a rapid rise in popularity for anterior cruciate ligament (ACL) reconstruction due to advantages in graft sizing and potential improvement in biomechanics. While there is a growing body of literature on use of quadriceps tendon grafts, deeper investigation into the biomechanical properties of stitch techniques in this construct has been limited. The purpose of this study was to evaluate the performance of a novel suture needle against different conventional suture needles by comparing the biomechanical properties of two commonly used stitch methods, a whip stitch, and a locking stitch in quadriceps tendon. It was hypothesized that the new device would be capable of creating both whip stitches and locking stitches that are biomechanically equivalent to similar stitch techniques performed with conventional needle products. METHODS: This was a controlled biomechanical study. A total of 24 matched pair cadaveric knees were dissected and a total of 48 quadriceps tendons were harvested and tested. All tendon grafts were standardized to the same size. Samples were then randomized into the following groups, keeping the matched pairs together: (Group 1, n=16) consisted of Company W’s novel two-part suture needle design, (Group 2, n=16) consisted of Company A suture, and (Group 3, n=16) consisted of Company B suture. For each group, the matched pairs were categorized into subgroups to be instrumented with either a whip stitch or a locking stitch. Two fellowship-trained surgeons performed all stitching, where they each instrumented 8 tendon grafts per group. For instrumentation, the grafts were clamped to a preparation stand in accordance with the manufacturer’s recommendations for passing each suture needle. A skin marker was used to identify and mark five evenly spaced points, 0.5 cm apart, as a guide to create a 5-stitch series. For Group 1, the whip stitch as well as the locking whip stitch were performed with a novel 2-part needle. For Group 2, the whip stitch was performed with loop suture needle and the locking stitch was krackow with a curved needle. Similarly, for Group 3, the whip stitch was performed with loop suture needle and the locking stitch was krackow with a curved needle (Figure 1). Cyclical testing was performed using a servohydraulic testing machine (MTS Bionix) equipped with a 5kN load cell. A standardized length of tendon, 7 cm, was coupled to the MTS actuator by passing it through a cryoclamp cooled by dry ice to a temperature of -5°C (Figure 2). All testing samples were then pre-conditioned to normalize viscoelastic effects and testing variability through application of cyclical loading to 25-100 N for three cycles. The samples were then held at 89 N for 15 minutes. Thereafter, the samples were loaded to 50-200 N for 500 cycles at 1 Hz. If samples survived, they were ramped to failure at 20 mm/min. Displacement and force data was collected throughout testing. Metrics of interest were total elongation (mm), stiffness (N/mm), ultimate failure load (N) and failure mode. Data are presented as averages plus/minus standard deviation. A one-way analysis of variance (ANOVA) with a Tukey pairwise comparison post hoc analysis was used to evaluate differences between the various stitching methods. Statistical significance was set at P = .05. RESULTS SECTION: For the whip stitch methods, the total elongation was found to be equivalent across all methods (W: 36 ± 10 mm; A: 32 ± 18 mm; B: 33 ± 8 mm). The stiffness of Company A (103 ± 11 N/mm) method was significantly larger than Company W (64 ± 8 N/mm; p=.001), whereas stiffness of whip stitch by Company W was equivalent to Company B (80 ± 32 N/mm). The ultimate failure load was equivalent across all whip stitch methods (W: 379 ± 31 mm; A: 412 ± 103 mm; B: 438 ± 63 mm). For the locking stitch method, the total elongation (W: 26 ± 10 mm; A: 14 ± 2 mm; B: 29 ± 5 mm), stiffness (W: 75 ± 11 N/mm; A: 104 ± 23 N/mm; B: 79 ± 10 N/mm) and ultimate load (W: 343 ± 22 N; A: 369 ± 30 N; B: 438 ± 63 N) were found to be equivalent across all methods. The failure mode for all groups is in Table 1. The common mode of failure across study groups and stitch configuration was suture breakage. However, the whip stitch from Company A and Company B had varied failure modes. DISCUSSION: Products from the three manufacturers were found to produce biomechanically equivalent whip stitches and locking stitches with respect to elongation and ultimate failure load. The only significant difference observed was that the whip stitch created with Company A’s product had a higher stiffness than Company W’s product, which could have been due to differences in the suture material. In this cadaveric quadriceps tendon model, it was shown that when using Company W’s novel two-part suture needle, users were capable of creating whip stitches and locking stitches that achieved equivalent biomechanical performance compared to similar stitch techniques performed with conventional needle products. A failure mode limited solely to suture breakage for methods completed with Company W’s needle product suggest a reliable suture construct with limited tissue damage. SIGNIFICANCE/CLINICAL RELEVANCE: Having a suture needle device with the versatility to easily perform different stitching constructs may provide surgeons an advantage needed to improve clinical outcomes. The data presented illustrates a strong new suture technique that has equivalent performance when compared to conventional needle devices and has promising applications in graft preparation for ligament and tendon reconstruction.more » « less
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Background:One challenge surgeons face when using certain suture knot techniques is where the forces concentrate along the central axis of the tissue, making the suture knot prone to failure due to suture pull-through and tissue shredding. New reinforcement techniques have been developed (suture tape augmentation) and are becoming popular to minimize tissue damage. Purpose:To assess biomechanical performance of whipstitch reinforcement techniques (locking stitch method or additional suture material) in human cadaveric semitendinosus tendons (STs). Study Design:Controlled laboratory study. Methods:A total of 42 STs were harvested and divided into 6 groups consisting of a standard whipstitch and varying reinforcement techniques based on stitch pattern (whipstitch [WS], whipstitch through tag [WT], locking whipstitch [WL], or locking whipstitch through tag [WLT]), and products from varying manufacturer samples were preconditioned and then loaded from 50 to 200 N at 1 Hz for 500 cycles, followed by load to failure. Elongation, stiffness, ultimate load, and failure mode were compared across groups. Results:No significant differences were observed between whipstitch groups WS1and WS2. Addition of suture material for reinforcement (WT2) significantly improved biomechanical performance across all metrics compared with WS2. Reinforcement using a new locking whipstitch method (WL) resulted in significant increase in ultimate load compared with WS1. All reinforcement groups (WL, WT1, WT2, and WLT) achieved a similar level of biomechanical performance, with no significant differences across any metric. Addition of a second reinforcement (WLT) did not significantly enhance biomechanics beyond those achieved with a single reinforcement (WL). The failure mode for no-reinforcement groups was tissue pull-through, while reinforcement groups utilizing either material or locking method failed from suture breakage. Conclusion:Whipstitch alone offers limited biomechanical security, but reinforcement with either a locking method or additional suture material significantly enhances biomechanical performance. Clinical Relevance:Reinforcement may help limit tissue damage. The locking whipstitch method offers a promising alternative to reinforce a stitch with relatively less suture material.more » « less
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PURPOSE To compare the biomechanical properties of quadriceps tendon (QT) graft stitch methods using 3 different suture systems for anterior cruciate ligament reconstruction. METHODS A total of 48 QTs were harvested from cadaveric knee specimens (age: 73 ± 7 years; range, 66-86 years). Samples were randomly divided into 3 groups where different suture needle systems were used to create 2 stitch methods: whipstitch (WS) and locking stitch (LS). Surgeons performed each technique to 5 stitches, each 0.5 cm apart. Stitching time was recorded. Samples were preconditioned and then underwent cyclic loading, followed by load to failure. Stiffness (N/mm), ultimate failure load (N), peak-to-peak displacement (mm), elongation (mm), and failure displacement (mm) were recorded. RESULTS WS and LS were equivalent across stiffness, ultimate load, and peak-to-peak displacement within groups 2 and 3. In group 1, the LS was stiffer than the WS, but the WS achieved a higher ultimate load. For all groups, the LS achieved lower elongation and failure displacement than the WS, with significant differences in groups 1 and 2. Within each stitching method, equivalence was determined for total elongation and ultimate failure load for all 3 suture system groups. For WS samples, group 1 all failed from suture breakage, and both groups 2 and 3 had instances of failure from suture pull-through. All LS samples failed from suture breakage. CONCLUSIONS Both LS and WS provide adequate mechanical properties in each of the 3 suture systems. Differences in performance do exist; however, each method shows equivalent total elongation and ultimate failure load for all 3 suture systems. LS may be preferred over WS due to lower mean elongation and failure displacement. CLINICAL RELEVANCE There is an increased use of QT grafts in for anterior cruciate ligament reconstruction. However, there have been a limited number of studies comparing various stitching methods and optimizing techniques for QT graft fixation. This study may provide important information to surgeons about which suture techniques have better biomechanical profiles.more » « less
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null (Ed.)Objectives/Hypothesis Novel laryngotracheal wound coverage devices are limited by complex anatomy, smooth surfaces, and dynamic pressure changes and airflow during breathing. We hypothesize that a bioinspired mucoadhesive patch mimicking how geckos climb smooth surfaces will permit sutureless wound coverage and also allow drug delivery. Study Design ex‐vivo. Methods Polycaprolactone (PCL) fibers were electrospun onto a substrate and polyethylene glycol (PEG) – acrylate flocks in varying densities were deposited to create a composite patch. Sample topography was assessed with laser profilometry, material stiffness with biaxial mechanical testing, and mucoadhesive testing determined cohesive material failure on porcine tracheal tissue. Degradation rate was measured over 21 days in vitro along with dexamethasone drug release profiles. Material handleability was evaluated via suture retention and in cadaveric larynges. Results Increased flocking density was inversely related to cohesive failure in mucoadhesive testing, with a flocking density of PCL‐PEG‐2XFLK increasing failure strength to 6880 ± 1810 Pa compared to 3028 ± 791 in PCL‐PEG‐4XFLK density and 1182 ± 262 in PCL‐PEG‐6XFLK density. The PCL‐PEG‐2XFLK specimens had a higher failure strength than PCL alone (1404 ± 545 Pa) or PCL‐PEG (2732 ± 840). Flocking progressively reduced composite stiffness from 1347 ± 15 to 763 ± 21 N/m. Degradation increased from 12% at 7 days to 16% after 10 days and 20% after 21 days. Cumulative dexamethasone release at 0.4 mg/cm2 concentration was maintained over 21 days. Optimized PCL‐PEG‐2XFLK density flocked patches were easy to maneuver endoscopically in laryngeal evaluation. Conclusions This novel, sutureless, patch is a mucoadhesive platform suitable to laryngeal and tracheal anatomy with drug delivery capability.more » « less
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