No functional differences in anatomic reconstruction with one vs. two suture anchors after non-simultaneous bilateral distal biceps brachii tendon rupture: a case report and review of the literature.

BACKGROUND: Surgical reattachment of the tendon is still the gold standard for ruptures of the distal biceps brachii tendon. Several fixation techniques have been described in the literature, with suture anchors being one of the most common fixation techniques. Currently, there is no data available on how many anchors are required for a safe and stable refixation. In this case report clinical data of a patient with non-simultaneous bilateral distal biceps tendon ruptures treated with a different number of suture anchors for each side (one vs. two) are demonstrated. CASE PRESENTATION: A 47-year-old factory worker suffered a rupture of the distal biceps tendon on both arms following two different occasions. The left side was fixed using a single suture anchor, while refixation on the right side was performed with two anchors. The patient was prospectively followed for one year. Functional outcome was assessed using the Andrews Carson Score (ACS), the Oxford Elbow Score (OES), and the Disabilities of Arm, Shoulder and Hand (DASH) Score after six, twelve, 24 and 48 weeks. Furthermore, an isokinetic strength measurement for flexion strength was performed after 24 and 48 weeks. After 48 weeks the patient presented with excellent functional outcome scores and no follow-up complications. During the follow-up period, no differences in the functional scores nor in the isokinetic flexion strength measurement could be detected. Furthermore, no radiological complications (like heterotopic ossifications) could be detected in the postoperative radiographs after one year. CONCLUSIONS: Anatomic reattachment of the distal biceps tendon is a successful operative treatment option for distal biceps tendon ruptures. Suture anchor fixation remains one of the most common techniques, as it allows fast surgery and provides good results with respect to range of motion (ROM) and functional scoring according to the current literature. However, the number of anchors required for a stable fixation remains unclear. As indicated by our presented case, we hypothesize, that there are no significant differences between a one-point or a two-point fixation. In the presented case report, no intraindividual differences between the usage of one versus two suture anchors were evident in the short-term follow-up.

Comparison of the efficacy of a distal clavicular locking plate with and without a suture anchor in the treatment of Neer IIb distal clavicle fractures.

BACKGROUND: To compare the clinical outcomes between the use of a distal clavicular locking plate alone and the combined use of a plate and a coracoclavicular suture anchor in the treatment of Neer IIb distal clavicle fractures and to discuss the application procedure of suture anchors. METHODS: This is a retrospective study. Thirty-four patients with unilateral Neer IIb distal clavicle fractures who underwent open reduction and internal fixation with a distal clavicular locking plate only (16 patients) or with both a plate and a coracoclavicular suture anchor (18 patients) were evaluated. The main observation data included the Constant-Murley Shoulder Function Score (CMS), rate of postoperative complications, and union time. RESULTS: The distal clavicular locking plate and coracoclavicular suture anchor combination group had better outcomes in the Constant-Murley score (94.6 ± 4.5 vs. 90.1 ± 9.5) (P < 0.05) and a shorter union time (13.9 ± 2.3 vs. 16.1 ± 3.0) (P < 0.05) than the locking plate only group did, and the rate of complications showed no significant difference, 16.7% vs. 31.2% (5/16) (P>0.05). CONCLUSIONS: Both methods achieved good results in the treatment of Neer IIb distal clavicle fractures; however, the use of both locking plates and coracoclavicular suture anchors can provide more stability in the early stage after operation than can the use of locking plates alone, which can make the sped of union quicker and result in better clinical outcomes. For elderly patients with comminuted Neer IIb distal clavicle fractures, a locking plate combined with a suture anchor is recommended to provide more stability in the early stage after the operation.

Bone and soft tissue palatal morphology and potential anchorage sides in cleft palate patients.

AIM: The aim of this study was to evaluate palatal vertical bone thickness and density in relation to soft tissue on the hard palate for better selection of adequate bone regions for the insertion of orthodontic mini-implants (MIs) in cleft palate patients. MATERIALS AND METHODS: Cone beam computed tomography scans (CBCT) were obtained from 60 patients (mean age range 9-12). The study population included patients with isolate right side cleft palate formation (n = 20; 6 females; 14 males), left side cleft palate formation (n = 20; 9 females; 11 males) and without cleft formation as control group (n = 20; 15 females; 5 males). Bone and soft tissue measurements were performed vertical at a 90° angle to the bone surface, on previously defined measurement points (n = 88) on the hard palate. Bone density was measured on ten vertical layers in caudo-cranial direction. RESULTS: In non-cleft patient the highest bone thickness was in the anterior palate and decreased significantly in posterior direction. In patients with right and left cleft palate, the highest vertical bone level could be observed at the palatal premaxillary border opposite to the cleft side. Patients in the control group showed a significantly lower vertical soft tissue thickness than patients with palatal cleft formation. The evaluation of bone density showed no significant differences in all three groups. CONCLUSION: The results suggest that the favorable region for orthodontic MI placement is in the similar anatomical region compared to non-cleft patients, but differs from one side in each group. In unilateral cleft palate patients, the highest bone level was found on the anterior palate side opposite to the cleft side, indicating the most effective region for MIs placement.

Patella incarceration with associated patella fracture: a rare case of a paediatric patient with no associated femoral fracture.

We describe the case of a 15-year-old girl who presented to the Accident and Emergency Department with right knee pain and a tense effusion following a twist and fall directly onto her right knee. An MRI scan demonstrated that she had an incarcerated dislocated patella with an associated patella avulsion fracture. This required open reduction. Open reduction and fixation was performed using suture anchors. We feel that this case is particularly pertinent since nearly all previous case reports describe an incarcerated patella with an associated femur fracture. Furthermore, no previous case reports have been published in a child.

Evaluation of retroauricular skin mobility for bone-anchored solutions.

BACKGROUND: A subset of patients with bone-anchored hearing aids develop skin reactions that may be related to excess skin mobility around the skin-penetrating abutments. However, there is a lack of reports on the extent of skin mobility within the retroauricular space, typical for the implant location. METHODS: This study was based on photographic analysis of the relative shifts between the skull and soft tissue of the head in the retroauricular region, detected under the physiological conditions of head support and facial muscle contraction. RESULTS: The mean calculated value for skin shifts at the implant site was 5.1 mm. In 84 per cent of cases, the extent of skin shift was greater with the head at rest, by an average of 3.1 mm. The extent of skin movement during facial muscle contraction ranged between 0 mm and 8.9 mm. No direct correlations were detected between the extent and direction of skin shifts and patients' age, gender or body mass index. CONCLUSION: There are no objective data that can predict individual skin movement at the osseointegrated implant site. The study confirmed high variability in terms of the direction and extent of skin shift, which should be discussed when managing related skin problems.

Novel ultrasound assisted suture anchor system using the BoneWelding® technology yields a comparable primary stability in osteopenic and healthy human humeri as a benchmark anchor.

INTRODUCTION: The aim of this biomechanical study was to evaluate the primary stability of the SportWelding® Sombrero 3.6 mm suture anchor system in osteopenic and healthy cadaveric humeri. METHODS: The Sombrero® and BioCorkscrew® anchors were deployed in 8 osteopenic and 4 healthy cadaver humeri after the bone mineral density (BMD) measurements of the 32 specimens. Both anchors were loaded with a USP Nr. 2 FiberWire® suture. An established cyclic testing protocol was performed. The maximum failure load (Fmax), the system displacement and the modes of failure were recorded. RESULTS: The Fmax and system displacement of the Sombrero® in osteopenic and healthy humeri was equivalent to the Bio-Corkscrew® benchmark anchor; there were no significant differences in the maximum failure loads and system displacement values. Only anchor and suture dislocations were observed; suture ruptures did not occur. CONCLUSION: This study shows that the Sombrero® yields similar maximum failure loads and system displacement values as the established Bio-Corkscrew® benchmark anchor. The primary stability of the Sombrero® and Bio-Corkscrew® seems to be independent of the bone mineral quality. This relatively small-sized polymer anchor is independent of the BMD and may be an alternative to established suture anchors in rotator cuff repair.

Biomechanical Analysis of Suture Anchor vs Tenodesis Screw for FHL Transfer.

BACKGROUND: Chronic Achilles injury is often treated with flexor hallucis longus (FHL) tendon transfer to the calcaneus using 1 or 2 incisions. A single incision avoids the risks of extended dissections yet yields smaller grafts, which may limit fixation options. We investigated the required length of FHL autograft and biomechanical profiles for suture anchor and biotenodesis screw fixation. METHODS: Single-incision FHL transfer with suture anchor or biotenodesis screw fixation to the calcaneus was performed on 20 fresh cadaveric specimens. Specimens were cyclically loaded until maximal load to failure. Length of FHL tendon harvest, ultimate load, stiffness, and mode of failure were recorded. RESULTS: Tendon harvest length needed for suture anchor fixation was 16.8 ± 2.1 mm vs 29.6 ± 2.4 mm for biotenodesis screw ( P = .002). Ultimate load to failure was not significantly different between groups. A significant inverse correlation existed between failure load and donor age when all specimens were pooled (ρ = -0.49, P < .05). Screws in younger specimens (fewer than 70) resulted in significantly greater failure loads ( P < .03). No difference in stiffness was found between groups. Modes of failure for screw fixation were either tunnel pullout (n = 6) or tendon rupture (n = 4). Anchor failure occurred mostly by suture breakage (n = 8). CONCLUSION: Adequate FHL tendon length could be harvested through a single posterior incision for fixation to the calcaneus with either fixation option, but suture anchor required significantly less graft length. Stiffness, fixation strength, and load to failure were comparable between groups. An inverse correlation existed between failure load and donor age. Younger specimens with screw fixation demonstrated significantly greater failure loads. CLINICAL RELEVANCE: Adequate harvest length for FHL transfer could be achieved with a single posterior incision. There was no difference in strength of fixation between suture anchor and biotenodesis screw.

[Injuries of major tendons : Review of current diagnostic and surgical standards]. / Verletzung großer Sehnen : Übersicht über die Diagnostik und Therapie der Sehnenverletzungen.

Chronic degenerative tendon injuries as well as injuries due to acute high-energy trauma and incisional injuries are a significant aspect in the emergency surgery department. As a result of anatomical characteristics and exposure certain tendons are particularly vulnerable to injury. These include the biceps brachialis, quadriceps femoris, patella, achilles and tibialis anterior tendons. Besides the broad spectrum of non-surgical treatment, surgeons should have knowledge of the various surgical techniques including suturing, anchor refixation and reconstruction techniques. The indications for surgery are of particular importance for the clinical outcome of tendon injuries. The therapeutic approach should consider the patients biological age, functional requirements and pre-existing comorbid pathologies. Finally, adequate aftercare has been shown to significantly determine the surgical outcome.

Tratamiento quirúrgico de las roturas del tendón distal del bíceps con anclajes óseos por abordaje anterior único / Surgical treatment of distal biceps tendon ruptures with bone anchors using a single anterior approach

Objetivo. Valorar los resultados clínicos de la reinserción del tendón distal del bíceps con anclajes óseos por vía anterior. Material y métodos. Estudio retrospectivo de 79 pacientes en los que se realizó la reinserción del tendón distal del bíceps con anclajes metálicos óseos por vía anterior. El promedio de edad fue de 46 años (rango, 32-64). En el 57% de los casos se utilizaron dos anclajes y en el 43% un anclaje. Todos los pacientes realizaron el mismo protocolo postoperatorio. Se hizo una valoración funcional con la escala funcional MEPS. El promedio de tiempo de seguimiento fue de 20 meses (rango: 12-28). Resultados. La puntuación final media de la escala MEPS fue de 95,2 pts (DE 6,8). El 94% de los pacientes tuvieron resultado excelente y bueno y en el 6% el resultado fue aceptable y pobre. No se observaron diferencias al comparar el resultado funcional entre los pacientes en los que se utilizó un anclaje (96 puntos) con aquellos en los que se utilizaron dos anclajes (95 puntos), p = 0,5. El tiempo promedio de baja laboral fue de 14 semanas (rango, 5-56) pudiendo reincorporarse a su trabajo el 100% de los pacientes. La incidencia de complicaciones fue del 13%, siendo la más frecuente la neuroapraxia del nervio cutáneo antebraquial lateral. Conclusiones. La reinserción anatómica del tendón distal del bíceps con anclajes óseos por vía anterior única es una técnica segura que ofrece resultados funcionales excelentes y buenos a mediano plazo (AU)

Purpose. To evaluate the clinical results of reinsertion of the distal biceps tendon with anterior bone anchors. Material and methods. A retrospective study was conducted on 79 patients who underwent reinsertion of the distal biceps tendon with anterior bone anchors. The mean age was 46 years (range, 32-64). Two anchors were used in 57% of cases, and one anchor in 43%. The same postoperative protocol was performed in all patients. Functional assessment was made using a Motor evoked potentials (MEPS) functional scale. The mean of follow-up time was 20 months (range, 12 -28 months). Results. The final mean of MEPS score was 95.2 points (SD 6.8). Almost all (94%) patients had excellent and good results, and 6% a bad result. No differences were observed when comparing functional outcome among patients in whom one anchor was used (96 points) with those in whom two anchors were used (95 points), p = 0.5. The mean time off work was 14 weeks (range, 5-56) and 100% of patients were able to return to work. The incidence of complications was 13%. The most frequent was neuropraxia of the lateral antebrachial cutaneous nerve. Conclusion. The anatomic re-attachment of the distal biceps tendon with bone anchors using a single anterior approach is a safe technique that offers excellent and good functional results in the medium term (AU)

Effect of configuration on the biomechanical performance of three suture materials used in combination with a metallic bone anchor.

OBJECTIVE: To determine whether different suture configurations could improve the biomechanical performance of 3 suture materials used with bone anchors. SAMPLES: 3 suture materials (60-lb test nylon leader line, size 2 polyblend polyethylene composite suture, and 150-lb test ultrahigh-molecular weight spun polyethylene). PROCEDURES-Each suture material was looped through the eyelet of a metallic bone anchor and constructs were evaluated by use of an acute uniaxial load. Three configurations were tested for each suture material: single stranded (SS), double stranded (DS), and single stranded plus plastic insert (SSP). Force at failure, extension at failure, force at 3 mm of extension, stiffness, and site of failure of the suture were recorded for each test. RESULTS: For all sutures, the DS configuration was the stiffest and yielded significantly higher forces at failure and forces at 3 mm of extension. The SS configuration had the lowest forces at failure. The SSP configuration yielded greater forces at failure for all suture materials, compared with the SS configuration, with a comparable stiffness. All sutures failed at the eyelet in the SS and DS configurations. In the SSP configuration, 60-lb test nylon leader line and 150-lb test ultrahigh-molecular weight spun polyethylene failed at the eyelet less frequently than did the polyblend composite suture. CONCLUSIONS AND CLINICAL RELEVANCE: Among the tested constructs, a DS suture configuration used in combination with the metallic bone anchor gave the best biomechanical results for all suture materials. Considering that the SSP configuration yielded greater forces at failure, compared with the SS configuration, covering metallic edges in bone anchors with softer materials might protect sutures and result in increased forces at failure.

Mechanical properties of isolated loops of nylon leader material, polyethylene cord, and polyethylene tape and mechanical properties of those materials secured to cadaveric canine femurs via lateral femoral fabellae, toggles placed through bone tunnels, or bone anchors.

OBJECTIVE: To determine mechanical properties of various prosthetic materials secured to cadaveric canine femurs via various methods and to compare results with those for isolated loops of prosthetic material. SAMPLE: 80 femurs obtained from cadavers of skeletally mature large-breed dogs. PROCEDURES: 10 femoral constructs in each of 8 groups (single circumfabellar loop of polyethylene cord, double loop of polyethylene tape secured via a bone anchor [BAPT], single or double circumfabellar loops of nylon leader material [CNL] or polyethylene tape [CPT], or single or double loops of polyethylene tape secured via a toggle placed through a bone tunnel [BTPT]) and 10 isolated loops of prosthetic material in each corresponding configuration were tested. Stress relaxation, creep, elongation, load at 3 mm of displacement, stiffness, and peak load at failure were determined. RESULTS: 5 single CNL constructs failed before completion of testing. Double CNL and single circumfabellar polyethylene cord constructs had the lowest loads at 3 mm of displacement. Single and double CPT constructs had the highest stiffness. Double BTPT and CPT constructs had the highest peak loads at failure. Double BTPT, double CPT, and BAPT constructs were mechanically superior on the basis of lower creep and stress relaxation and higher stiffness and load at 3 mm of displacement versus other constructs. Stiffness of femoral constructs was 28% to 69% that of corresponding isolated prosthetic loops. CONCLUSIONS AND CLINICAL RELEVANCE: Double BTPT, double CPT, and BAPT constructs were mechanically superior to other constucts. Mechanical properties and methods of anchorage and securing of free ends of prostheses contributed to mechanical properties of constructs.

Adult bone anchored hearing aid services in the United Kingdom: building a consensus for development.

AIMS AND OBJECTIVES: In October 2009, a multi-disciplinary group of UK clinicians met to review issues relating to bone-anchored hearing-aid (BAHA) development. The aim was to help define a model for BAHA services and service development via a process of widespread consultation with UK BAHA professionals. METHODS: A modified Delphi technique was used. Statements were proposed by the lead group and sent out for consultation. Those with ≥90% agreement were approved without further discussion. Statements with 50-89% agreement were discussed by the lead group to determine whether they should be included in the final document. Any statement with <50% agreement was removed without discussion. A second consultation was then made, and the process repeated. This led to a final set of consensus statements. RESULTS: The final consensus comprises 33 statements validated by the modified Delphi process. All of these statements achieved >75% agreement, with only six statements having <90% agreement. When these statements were presented to the UK BAHA Professionals group at their annual conference there was 89% agreement from the group for the consensus statements to be accepted. DISCUSSION: The levels of agreement for the final questionnaire show that the mandate for the consensus statements was exceptionally high. Implementation of the consensus is discussed, as are each of the key areas of the consensus, such as funding and minimum assessment standards.

Anclaje esofágico de una autosutura esofágica, liberado con ayuda de un videolaringoscopio McGrath / No disponible

No disponible

Diseño y desarrollo de un modelo experimental para estudios biomecánicos de fracturas tipo B de Tile del anillo pélvico / Design and development of an experimental model for biomechanical studies of Tile type B1 fracture of the pervic ring

Objetivo: Diseñar un modelo estandarizado y reproducible para la realización de ensayos biomecánicos de fracturas tipo B1 de Tile del anillo pélvico. Metodología: Establecida en dos fases. Fase 1, determinación de requerimientos fundamentales del sistema. Fase 2, diseño, testado y elección de las piezas del modelo experimental. Se empleó una máquina universal de ensayos (MTS- 810), programas de diseño gráfico (Solid Edge Academic), fantomas, rail de carga deslizante y materiales industriales de Fabricación del Sistema de Fijación. Resultados: Se obtuvo un modelo constituido por dos sistemas de anclaje, superior e inferior, que permiten articular la pelvis a la máquina de ensayo tanto proximalmente, a través del sacro y L5, como a nivel distal con ambos fémures. El sistema permitió fijación adecuada de especímenes a máquina de ensayo, mantener la estática postural de bipedestación a la carga y reproductibilidad de lesión B1 de Tile. Conclusión: Es posible diseñar y fabricar un sistema estandarizado de fijación de pelvis humanas a una máquina de análisis de materiales para el estudio biomecánico de las fracturas tipo B1 de Tile del anillo pélvico (AU)

Objetive: The aim of the study is to design a standardized and reproducible procedure for biomechanical testing of Tile B1 fractures of the pelvic ring. Methodology: The methodology for this study was divided in two phases. In the first phase, the requirements to be covered by the system were determined, and in the second one experimental model pieces were designed and chosen. An Universal Testing Machine (MTS-810), Graphic Design Plans Program Software (Solid Edge Academic), Fantomas, Bearing, Sliding Rail and Manufacturing Material Fixing System were used. Results: A specific loading biomechanic system has been created, consisting on an upper and a lower anchor, which allows pelvis ring fix to the test machine both proximally through the sacrum and the last lumbar vertebra, and in terms of both femurs to the database of the testing machine. The procedure make a correct bone fixation, place the pelvis in a stand position, getting to align the upper and lower anterior iliac spines in the same plane and reproduce Tile B1 fracture. Conclusion: It is possible to design and manufacture a simple standard system for determining human pelvis to a testing machine for biomechanical studies of Tile type B1 pelvic ring fractures (AU)

Tensile and shear loading stability of all-inside meniscal repairs: an in vitro biomechanical evaluation.

BACKGROUND: Most biomechanical studies for evaluation of the structural properties of meniscal repairs have been performed in tensile loading scenarios perpendicular to the circumferential meniscal fibers. However, meniscal repair constructs are also exposed to shear forces parallel to the circumferential meniscal fibers during healing, particularly in the midportion of the meniscus. HYPOTHESIS: Material properties of meniscal repair devices cannot be extrapolated from tensile to shear load scenarios. STUDY DESIGN: Controlled laboratory study. METHODS: In 84 harvested and isolated bovine lateral menisci following removal of adjacent soft tissue, a standardized vertical lesion was set followed by repair using all-inside flexible (FasT-Fix, FasT-Fix AB, RapidLoc) and rigid (Meniscus Screw, Meniscus Arrow) meniscal repair devices. Vertical and horizontal 2.0 Ethibond sutures were used as controls. The repaired meniscal construct was tested in a tensile (parallel to the axis of the tested repair device) and shear load scenario (perpendicular to the axis of the tested repair device) at 5 mm/min and 37 degrees C environmental temperature. Maximum load to failure, stiffness, and failure mode were recorded. RESULTS: The absolute load to failure values of each repair device in the shear scenario were only marginally different from the tensile load scenario. However, the stiffness of several tested devices was markedly reduced in the shear scenario. In both scenarios, large differences of the load to failure and the stiffness between the implant types up to 5-fold were found (P < .05). The failure mode of several all-inside flexible repair devices was different in the shear versus tensile load scenario, while the failure mode of the rigid systems was similar in both scenarios. CONCLUSION: All-inside meniscal repair devices exposed to shear load scenarios have comparable maximum loads to failures as tensile load scenarios. However, the stiffness of the majority of the flexible meniscal repair implants in a shear load scenario is markedly reduced. The applied scenario also affects the failure mode in several flexible meniscal repair devices. CLINICAL RELEVANCE: Meniscal repair devices with sufficient stiffness and stability against shear loads may be favored for meniscal repair, especially within the midportion of the meniscus where shear loads occur during healing.

Laminoplasty using Twinfix suture anchors to maintain cervical canal expansion.

Open-door laminoplasty is a commonly performed procedure for the treatment of multiple level cervical spinal stenosis. One complication of this procedure is closure of the hinge and subsequent restenosis. Twinfix suture anchor was used in laminoplasty to stabilize cervical canal expansion. 53 patients with multiple level cervical spinal stenosis underwent laminoplasty. A unilateral open-door technique was performed for the lesion level and the elevated lamina was fixed to the lateral mass using Twinfix suture anchors. Radiography, magnetic resonance imaging, and computed tomography (CT) scanning were used for imaging studies. The Japanese Orthopedic Association score was adopted to compare clinical outcome before and after surgery. None of 53 patients who had the door secured with Twinfix suture anchors had closure of the hinge. Additionally, the suture anchors maintained their position without loosening or "pull-outs" on postoperative follow-up radiographs. The Japanese Orthopedic Association score increased significantly from 8.5 ± 3.2 before surgery to 14.2 ± 1.36 at final follow-up. Postoperative radiography and CT scan demonstrated significantly increased anteroposterior diameter of the spinal canal. There were four short-term complications: two were small dural-tears which were repaired intraoperatively without further sequelae, and the other 2 were both epidural hematomas that required emergent return to the operating room for evacuation. There were no Twinfix suture anchor-related complications. This Twinfix suture anchor can provide a firm and secure anchor for elevated open laminae in laminoplasty.

Effects of zone-specific superior labral detachment on biceps anchor stability.

PURPOSE: This study aimed to elucidate the degree of biceps anchor displacement that occurs when specific zones of the superior labrum are detached from the glenoid. STUDY DESIGN: Descriptive laboratory study. METHODS: Twelve cadaveric scapulae with intact labrums were prepared by removing the surrounding musculature with the labrum, biceps anchor, and biceps tendon carefully preserved. Pulleys were used to apply traction in 3 different directions- superior, lateral, and combined posterior/superior/lateral, to simulate the "peel-back" mechanism-while a continuous 1.13 kg of traction was applied to the biceps tendon. Labral tears were created by sharp incisions in isolation and in combinations of 3 zones defined relative to the glenoid fossa: anterior, posterior, or superior. The displacement of the biceps anchor (position of the marker after the simulated lesion relative to the marker position with the labrum intact) was measured relative to a rigid reference frame. RESULTS: The greatest degree of displacement occurred with the sectioning of all 3 zones, followed by the sectioning of 2 adjacent zones. Superior traction created the least displacement in all combinations, while lateral traction created maximal displacement, with one exception: in the setting of anterosuperior/superior lesions, maximal displacement was observed using the peel-back mechanism. CONCLUSION: Biceps anchor displacement, particularly the degree and direction of displacement, is affected by the labral detachment pattern. All 3 labral zones assessed in this study have important biomechanical contributions to biceps anchor displacement. CLINICAL SIGNIFICANCE: These findings have important implications relating to the clinician's arthroscopic assessment of superior labrum anterior and posterior (SLAP) tears, as well as the determination of need for stabilization. This information is particularly useful when treating SLAP tears in certain laborers and athletes, whose activities may cause specific biceps anchor displacement patterns.

Clinical and radiologic outcomes of arthroscopic glenoid labrum repair with the BioKnotless suture anchor.

BACKGROUND: Although arthroscopic glenoid labrum repair using the BioKnotless anchor is common, the benefits and efficacy have not been fully evaluated. HYPOTHESIS: BioKnotless suture anchor is a clinically and radiologically suitable material for arthroscopic labral repair. STUDY DESIGN: Case series; Level of evidence, 4. METHODS: Ninety-seven patients underwent arthroscopic glenoid labrum repair with BioKnotless anchor between July 2004 and December 2005. Thirty-seven patients had traumatic anterior instability and 60 patients had an isolated superior labrum, anterior-posterior (SLAP) lesion. The mean age at surgery was 36.0 years (range, 15-66); the average follow-up was 34.1 months (range, 24-54). Clinical outcomes were evaluated using range of motion and various functional evaluation scores including sports activity. Pain and patient satisfaction were measured using a visual analog scale (VAS). Computed tomography arthrography was conducted in 73 patients at least 1 year after surgery for radiologic evaluation. RESULTS: In patients with instability, the Western Ontario Shoulder Instability index and Rowe score improved from 53.2 to 85.9 and from 68.7 to 92.7, respectively. Return to normal recreation and sports were possible in 30 patients (81.1%); the mean satisfaction VAS was 9.2. There was 1 postoperative dislocation, and the apprehension test was positive in 1 case. Postoperative range of motion including external rotation was not different. In patients with a SLAP lesion, the American Shoulder and Elbow Surgeons score and Constant score improved from 67.3 to 96.0 and 79.1 to 96.8, respectively. Pain VAS decreased from 6.0 to 0.4, and the mean satisfaction VAS was 9.4. Return to normal recreation and sports were possible in 50 patients (83.3%). All labra were found to have firmly healed to bony glenoid rim without anchor-related osteolysis in postoperative CT arthrography. CONCLUSION: Clinically and radiologically, the BioKnotless anchor appears to be an acceptable alternative for arthroscopic labrum repair, and a suitable material allowing the avoidance of certain troublesome drawbacks of the conventional knot-tying suture anchor.

Arthroscopic rotator cuff repair using the Opus knotless suture anchor fixation system.

BACKGROUND: The reported failure rate of arthroscopic rotator cuff repair varies widely. The influence of repair technique on failure rates and functional outcomes after arthroscopic cuff repair remains controversial. PURPOSE: To determine the functional outcome of arthroscopic knotless fixation using the Opus AutoCuff device for rotator cuff repair and to compare our results with those reported in the literature. STUDY DESIGN: Case series; Level of evidence, 4. METHODS: Fifty-six consecutive patients underwent arthroscopic rotator cuff repair using an Opus AutoCuff device (Arthrocare, Sunnydale, California) with greater than 2 years' follow-up. Subjective and objective clinical examinations were performed to include the University of California at Los Angeles (UCLA) shoulder score, the American Shoulder and Elbow Surgeons (ASES) rating scale, the visual analog scale (VAS), and the Tegner Activity Level scale. RESULTS: Forty-eight patients were evaluated at a mean follow-up of 26 months (range, 24-35 months). The mean UCLA shoulder score was 33.1 of 35 (SD, 2.89) possible points, and the mean ASES rating scale was 94.2 of 100 (SD, 7.76) compared with a mean preoperative score of 65.7 (P < .001). Postoperative UCLA shoulder scores had 42 of 45 (93.3%) patients with good and excellent results. The mean preoperative ASES pain score was 1.3 (SD, 1.0), and the mean postoperative score was 4.4 (SD, 1.0) (P < .001). The Tegner Activity Level scores demonstrated restoration of function to preinjury status. There were 3 failures (6.3%), 2 by anchor failure (1 with specific trauma), and 1 by rotator cuff retear, all requiring revision surgery. CONCLUSION: Arthroscopic knotless suture fixation with the Opus AutoCuff device results in good to excellent results similar to those reported in the literature with conventional suture anchors.