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Background of Tendon Repair

Tendon surgery is done most commonly when injuries involving the tendon occur. Tendon injuries that frequently require surgery are:

  1. Acute tendon ruptures Repairing the ruptured tendon has numerous suture techniques with most demonstrating adequate strength to maintain the repair. Tendon allografts, autogenous tendon grafts, or tendon transfers are well described to augment the repair. The advent of biomaterials to augment the repair have been popularized to supplement the repair more recently. These techniques are especially used when gaps within the tendon are present. This graft supplementation is best documented in Achilles tendon ruptures, but it is also being used for repair of the posterior tibial tendon and other acute ruptures.

  2. Chronic tendon injuries Surgical intervention for these injuries is more common in the chronic degenerative process of the posterior tibial tendon when treating posterior tibial tendon dysfunction or in chronic and recalcitrant Achilles tendinosis. The technique for repairing the chronic degenerative process usually involves excision of the degenerative tendon with some suture technique to repair the remaining tendon. Again, augmentation of the repair has been popularized with the new graft materials available.

OrthoWrap™ Bioresorbable Protective Sheet

The OrthoWrap™ Bioresorbable Protective Sheet can be utilized for the management and protection of tendon injuries where there has been no substantial loss of tendon tissue. The OrthoWrap™ sheet minimizes soft tissue attachments to the device in case of direct contact with other tissues. It can be cut with sterile scissors, shaping the material according to the preference of the surgeon for the anatomic considerations of the patient and surgical procedure. The OrthoWrap™ sheet is then sutured into place using absorbable suture. This clear sheet allows for good visualization of the tissues to ensure proper placement. However, the mechanical integrity and handling of the material is simple and allows for repositioning as often as necessary to ensure proper placement is achieved.

Discussion

Whether the tendon is repaired with suturing techniques or with suturing and graft supplementation, post-operative complications can occur. Fibrosis leading to soft tissue attachments or scar tissue between the repaired tendon and neighboring tissues are most concerning and limiting during the rehabilitation period. In addition, the period of immobilization immediately following the procedure lends itself to developing fibrosis and attachments. Scar tissue and subsequent soft tissue attachments have both been shown to limit the potential for complete recovery. At a minimum, these complications can delay the success of the rehabilitation secondary to negative effects on the tendon, muscle, joint and ligaments. Immobilization causes intra-substance fibrosis of the tendons increasing the risk of re-rupture. The muscle weakens with stiffness, more rapid fatigue and decreased metabolic capacity. Joints have stiffness and increased joint compression and lastly, ligaments have decreased strength and mass with increased stiffness.

Minimizing the occurrence of fibrosis and soft tissue attachments may greatly improve the success of the tendon repair, whether the repair involved an acute rupture or a chronic degenerative process using any repair technique preferred by the surgeon. By using the OrthoWrap™ Bioresorbable Protective Sheet around the tendon as demonstrated below, it is less likely that fibrosis from adjacent bleeding bone or from surrounding soft tissues will attach to the tendon.

The OrthoWrap™ sheet is made from 70:30 Poly (L-lactide-co-D,L-lactide), more commonly known as PLA. This material has been used in other podiatric and orthopedic devices such as fixation implants. This material has a non-porous hydrophobic nature that resists attachments. The degradation of PLA weakens the OrthoWrap™ sheet, however it is impermeable throughout the critical healing period and up to 8 weeks, retaining nearly 80% of the original mechanical strength for the 0.02mm sheet and nearly 100% of the mechanical strength for the 0.05mm sheet. Loss of 50% of the mechanical strength is not seen in either size until after 20 weeks. The retention of mechanical strength is adequate since it functions during the main period of scar tissue formation. Normal tendon healing occurs over a period of months. However the inflammatory process and infiltration of fibroblasts occurs within the first two weeks; then for the next few weeks, cross linking of the collagen fibrils and scar tissue formation occurs. While this can be minimized with motion, Achilles tendon repair has documented that with the usual length of immobilization, scar tissue forms in approximately 11% of cases. The use of the OrthoWrap™ Sheet can assist in minimizing the soft tissue attachments to the device, thus helping to alleviate the effects of the immobilization.

Summary

The OrthoWrap™ Bioresorbable Protective Sheet has proven to be a cost effective and inert product. It can be wrapped around the various tendons in acute and chronic repairs to help manage and protect injured tendons while minimizing soft tissue attachments to the device that may impede the recovery of the patient. While early success has been observed, further investigation is required to determine the efficacy of the OrthoWrap™ sheet in tendon surgery of the foot and ankle as well as in other foot and ankle surgery procedures.

OrthoWrap™ Bioresorbable Protective Sheet

The OrthoWrap™ Bioresorbable Protective Sheet can be utilized for the management and protection of tendon injuries where there has been no substantial loss of tendon tissue. The bioresorbable protective sheet minimizes soft tissue attachments to the device in case of direct contact with other tissues.

 

 


 

   
 

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Background of Foot and Ankle Tendon Disorders

Plantar fibromatosis is a connective tissue disorder that involves proliferation of fibroblasts. Excision is frequently done when the mass has become painful to bear weight or when entrapment of the plantar medial neurovascular bundle occurs. The fibromas are located within the plantar fascia, adjacent to the superficial layer of the intrinsic musculature and during the excision these muscles are exposed. In addition, the neurovascular bundle of the plantar medial foot is also frequently exposed. It is typical to remain nonweight bearing after the excision secondary to the plantar incision, which provides maximum exposure to the mass. The effects of immobilization have been shown to impact the fibrosis and scarring that can occur following any surgical procedure, especially when surgery involves well vascularized tissue such as skeletal muscle.

OrthoWrap™ Bioresorbable Protective Sheet

The OrthoWrap™ Bioresorbable Protective Sheet can be utilized for the management and protection of tendon injuries where there has been no substantial loss of tendon tissue. The OrthoWrap™ sheet minimizes soft tissue attachments to the device in case of direct contact with other tissues. It can be cut with sterile scissors, shaping the material according to the preference of the surgeon for the anatomic considerations of the patient and surgical procedure. The OrthoWrap™ sheet is then sutured into place using absorbable suture. This clear sheet allows for good visualization of the tissues to ensure proper placement. However, the mechanical integrity and handling of the material is simple and allows for repositioning as often as necessary to ensure proper placement is achieved.

Discussion

When excising a plantar fibroma, a section of the plantar fascia is removed. Wide margins are desired to help prevent recurrence. This leaves direct contact between the subcutaneous tissue in the plantar arch and the superficial layer of the intrinsic musculature. The highly vascular muscle layer and the vascularity of the subcutaneous tissues lend itself to forming fibrotic tissue. This coupled with the period of immobilization following the surgery increases the risk of forming scar tissue. Fibrosis in this area may lead to other complications as well. Since the plantar medial neurovascular bundle is located between the abductor hallucis and flexor digitorum brevis muscles in the superficial muscle layer, fibrosis can cause neuritic symptoms. This complication is more likely in the procedures involving recurrent fibromas secondary to the more extensive dissection and greater exposure of the first layer of intrinsic muscles. Limiting the chance of fibrosis and subsequent soft tissue attachments may increase the overall success of the fibroma excision.

The OrthoWrap™ Bioresorbable Protective Sheet is made from 70:30 Poly (L-lactideco- D,L-lactide), more commonly known as PLA. This material has been used in other podiatric and orthopedic materials such as fixation implants. The OrthoWrap™ sheet has a non-porous hydrophobic nature that resists attachments. The degradation of PLA weakens the OrthoWrap™ sheet, however it is impermeable throughout the critical healing period and up to 8 weeks, retaining nearly more than 80% of the original mechanical strength for the 0.02mm sheet and nearly 100% of the mechanical strength for the 0.05mm sheet. Loss of 50% of the mechanical strength is not seen in either size until after 20 weeks. The retention of mechanical strength is adequate since it functions during the main period of scar tissue formation.

By using the OrthoWrap™ sheet to cover the intrinsic muscles, as demonstrated in the cases above, formation of fibrotic tissue and subsequent soft tissue attachments between the tissue layers is less likely. This is important when the disorder being treated is one of exuberant fibrotic tissue in an area that is likely to develop soft tissue attachments.

Summary

The OrthoWrap™ Bioresorbable Protective Sheet has proven to be a cost effective and inert product. It can be used as a protective sheet overlying the intrinsic muscles and neurovascular bundle potentially exposed during plantar fibroma excision to prevent soft tissue attachments to the device. While early success has been observed with this technique, further investigation is required to determine the efficacy of the OrthoWrap™ sheet in plantar fibroma excision and in other foot and ankle surgery procedures.

OrthoWrap™ Bioresorbable Protective Sheet

The OrthoWrap™ Bioresorbable Protective Sheet can be utilized for the management and protection of tendon injuries where there has been no substantial loss of tendon tissue. The bioresorbable protective sheet minimizes soft tissue attachments to the device in case of direct contact with other tissues.
 

  
 

 

  
     
 

Background

Compression neuropathy of the posterior tibial nerve and/or its terminal branches is a common problem. The posterior tibial nerve usually bifurcates within the third compartment of the flexor retinaculum, but it can divide proximal to the flexor retinaculum. The posterior tibial nerve or the terminal branches can be entrapped within the tarsal tunnel or at the more commonly implicated site distal to the tarsal tunnel at the abductor hiatus (porta pedis). Frequently the sometimes vague and clinically progressive symptoms respond to conservative care of corticosteroid injections custom molded orthotics, NSAIDs, and/or physical therapy.

When the conservative care fails surgical release of the nerve entrapment is necessary. The flexor retinaculum is released and any structures or fibrosis compressing the posterior tibial nerves are released or excised. Skin and subcutaneous closure is then done without closing the flexor retinaculum. One of the most common complications is recurrence, which is usually caused by fibrosis within the tarsal tunnel. Recurrence has been reported in the literature to be 5-20%.

OrthoWrap™ Bioresorbable Protective Sheet

The OrthoWrap™ Bioresorbable Protective Sheet can be utilized for the management and protection of tendon injuries where there has been no substantial Background loss of tendon tissue. The OrthoWrap™ sheet minimizes soft tissue attachments to the device in case of direct contact with other tissues. It can be cut with sterile scissors, shaping the material according to the preference of the surgeon for the anatomic considerations of the patient and surgical procedure. The OrthoWrap™ sheet is then sutured into place using absorbable suture. This clear sheet allows for good visualization of the tissues to ensure proper placement. However, the mechanical integrity and handling of the material is simple and allows for repositioning as often as necessary to ensure proper placement is achieved.

Discussion

When decompressing the affected nerve, there is a potential for bleeding from small capillaries, veins and potentially the presence of varicosities removed from around the posterior tibial nerve. While the flexor retinaculum is not repaired over the third compartment of the tarsal tunnel, additional scarring can occur. If this fibrosis is present it tends to increase the chance of recurrence of the same problem. This coupled with the short period of immobilization following the surgery increases the risk of forming scar tissue around the nerve. Limiting the chance of fibrosis and subsequent scar tissue may increase the overall success of the surgery. Other concepts have been used, such as corticosteroid within the tarsal tunnel after the release, however no other modalities have been clinically proven to reduce the recurrence rate of the problem.

The OrthoWrap™ Bioresorbable Protective Sheet is made from 70:30 Poly (L-lactide-co-D,L-lactide), more commonly known as PLA. This material has been used in other podiatric and orthopedic materials such as fixation implants. This material has a non-porous hydrophobic nature that minimizes attachments to the device. The degradation of PLA weakens the OrthoWrap™ sheet, however it is impermeable throughout the critical healing period and up to 8 weeks, retaining more than 80% of the original mechanical strength for the 0.02mm sheet and nearly 100% of the mechanical strength for the 0.05mm sheet. Loss of 50% of the mechanical strength is not seen in either size until after 20 weeks. The retention of mechanical strength is adequate since it functions during the main period of tissue healing. By placing the OrthoWrap™ sheet in the tarsal tunnel compartment, formation of undesirable scar tissue attachments within the tarsal tunnel is less likely. This is important to attempt to decrease the high recurrence rate for this procedure.

Summary

The OrthoWrap™ Bioresorbable Protective Sheet has proven to be a cost effective and inert product. It can be used to reinforce soft tissues and minimize tissue attachments to the device. While early success has been observed with this technique, further investigation is required to determine the efficacy of the OrthoWrap™ sheet in foot and ankle surgery procedures.

OrthoWrap™ Bioresorbable Protective Sheet

The OrthoWrap™ Bioresorbable Protective Sheet can be utilized for the management and protection of tendon injuries where there has been no substantial loss of tendon tissue. The bioresorbable protective sheet minimizes soft tissue attachments to the device in case of direct contact with other tissues.

   
     
       
       
 

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