Tynor Leg Traction Brace is basically designed to provide traction to the leg. It works well even on the weak or geriatric skin. It ensures proper compression of the leg and provides traction. It is made of three layered polyurethane fabric which makes it soft and comfortable to use. The innermost layer gives the required friction for faster recovery.
It is augmented with hook and loop closures to make it convenient to put on and remove. It does not require any adhesion. It provides cushion like support to the leg and relieves it from pain. It also prevents the bone from getting fractured and any muscle pull. It does not cause any peeling of skin and any rash or allergy on skin. It distributes the pressure exerted on the leg evenly.
Tynor Leg Traction Brace
Leg traction brace is a traction halter applied to the leg for below knee traction. It offers a distinct advantage of a very large holding surface area, ease of application and removal, reuse and patient comfort.
Easy application & removal.
Can be used for geriatric/ weak skin.
Ideal for sensitive skins.
Easy monitoring.
Distributes pressure evenly.
Tynor Leg Traction Brace Features
Three-layered PU bonded fabric offers:
Soft feel and plush looks through the top layer.
Comfortable cushioning through the middle
Polyurethane layer.
Inner layer provides good frictional characteristics.
Multiple hook loop closures
Ensure controlled compression.
Easy application and removal
No loosening, less monitoring
Large skin contact area
Ensures no vaso-constriction.
Eliminates need of an adhesive.
Convenient and quick to apply
Ensures no skin peeling.
Ideal for weak or geriatric skins
Tynor Rib Belt
Rib belt is applied to the thoracic and upper abdominal region to compress and bind the rib cage during rib fractures and postoperative care, while allowing sufficient flexibility for comfortable breathing.
Extra porous.
With splinting pad.
No buckling or rolling over.
Controlled compression
Tynor Wrist & Forearm Splint Right/Left is designed to provide comfortable and firm support to the wrist as well as to the forearm. It effectively works during various orthopedic conditions. It will keep the wrist in the functional position and speed up the recovery process. It will feel comfortable and relieved after applying this wrist and forearm support.
The PUF fused fabric provide comfortable and smooth feel which does not cause any rashes on the skin. It allows proper ventilation system to the skin area and also the skin to breathe properly. It has aluminum splints which are easy to remove and apply as well as offers a better grip and a snug fit. It also has long length that will permit the easy movement. This brace enables free finger movement. It has a hook loop closure system which provides optimal compression and it can easily adjust it as per the requirement. Its brace has an in-built thumb opening which keeps the thumb relaxed and free from pressure.
Tynor Wrist & Forearm Splint (Right/Left)
Wrist and Forearm Splint is designed to immobilize and provide firm and comfortable support to hand and wrist in various orthopedic conditions. It maintains the wrist in the functional position.
Aesthetically appealing.
Customizable splint.
Perfect immobilization.
Controlled compression.
Anatomical thumb opening.
Tynor Wrist & Forearm Splint (Right/Left) Features
Made out of PUF fused Matty fabric
Breathable
Excellent aesthetics
Improved comfort
Enhanced life.
Removable, Aluminum Splints
Customized fitting
Required degree of dorsi-flexion can be achieved
Very good grip and immobilization
Design features
Long length of the brace, ensures enhanced immobilization
Brace abuts the Palmer crease , allows free finger movement.
Elegant tabs , allow easy application and removal
Elegant tabs, also enhance the aesthetics of the product.
Black Color, enhances the aethetics
Hook loop closures
Easy to apply and remove
Ensures optimal compre
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Pneumonia is a typical symptom of COVID-19 infection, while acute respiratory distress syndrome (ARDS) and multiple organ failure are common in severe COVID-19 patients
NETs are important for preventing pathogen invasion, their excessive formation can result in a slew of negative consequences, such as autoimmune inflammation and tissue damage
SARS-CoV-2 infection has also been linked to increased neutrophil-to-lymphocyte ratios, which is associated with disease severity and clinical prognosis
NETosis is a special form of programmed cell death in neutrophils, which is characterized by the extrusion of DNA, histones, and antimicrobial proteins in a web-like structure known as neutrophil extracellular traps (NETs)
increased generation of reactive oxygen species (ROS) is a crucial intracellular process that causes NETosis
Another indirect route of SARS-CoV-2-induced NET production is platelet activation
When NETs are activated in the circulation, they can also induce hypercoagulability and thrombosis
In COVID-19, major NET protein cargos of NETs (i.e., NE, MPO, and histones) are significantly elevated.
SARS-CoV-2 can also infect host cells through noncanonical receptors such as C-type lectin receptors
Immunopathological manifestations, including cytokine storms and impaired adaptive immunity, are the primary drivers behind COVID-19, with neutrophil infiltration being suggested as a significant cause
NETosis and NETs are increasingly recognized as causes of vascular injury
SARS-CoV-2 and its components (e.g., spike proteins and viral RNA) attach to platelets and increase their activation and aggregation in COVID-19, resulting in vascular injury and thrombosis, both of which are linked to NET formation
Connects SARS-CoV-2 to TLR on Platelets to NETosis to metastasis.
NET formation may be caused by activated platelets rather than SARS-CoV-2 itself
NETosis, leading to aberrant immunity such as cytokine storms, autoimmune disorders, and immunosuppression.
early bacterial coinfections were more prevalent in COVID-19 patients than those infected with other viruses
NETosis and NETs may also have a role in the development of post COVID-19 syndromes, including lung fibrosis, neurological disorders, tumor growth, and worsening of concomitant disease
NETs and other by-products of NETosis have been shown to act as direct inflammation amplifiers. Hyperinflammation
“cytokine storm”
SARS-CoV-2 drives NETosis and NET formation to allow for the release of free DNA and by-products (e.g., elastases and histones). This may trigger surrounding macrophages and endothelial cells to secrete excessive proinflammatory cytokines and chemokines, which, in turn, enhance NET formation and form a positive feedback of cytokine storms in COVID-19
NET release enables self-antigen exposure and autoantibody production, thereby increasing the autoinflammatory response
patients with COVID-19 who have higher anti-NET antibodies are more likely to be detected with positive autoantibodies [e.g., antinuclear antibodies (ANA) and anti-neutrophil cytoplasmic antibodies (ANCA)]
COVID-19 NETs may act as potential inducers for autoimmune responses
have weakened adaptive immunity as well as a high level of inflammation
tumor-associated NETosis and NETs promote an immunosuppressive environment in which anti-tumor immunity is compromised
NETs have also been shown to enhance macrophage pyroptosis in sepsis
facilitating an immunosuppressive microenvironment
persistent immunosuppression may result in bacterial co-infection or secondary infection
can enhance this process by interacting with neutrophils through toll-like receptor 4 (TLR4), platelet factor 4 (PF4), and extracellular vesicle-dependent processes
NET-induced immunosuppression in COVID-19 in the context of co-existing bacterial infection
Following initial onset of COVID-19, an estimated 50% or more of COVID-19 survivors may develop multi-organ problems (e.g., pulmonary dysfunction and neurologic impairment) or have worsening concomitant chronic illness
NETs in the bronchoalveolar lavage fluid of severe COVID-19 patients cause EMT in lung epithelial cells
COVID-19 also has a long-term influence on tumor progression
Patients with tumors have been shown to be more vulnerable to SARS-CoV-2 infection and subsequent development of severe COVID-19
patients who have recovered from COVID-19 may have an increased risk of developing cancer or of cancer progression and metastasis
awaken cancer cells
NETs have been shown to change the tumor microenvironment
enhance tumor progression and metastasis
vitamin C has been tested in phase 2 clinical trials aimed at reducing COVID-19-associated mortality by reducing excessive activation of the inflammatory response
vitamin C is an antioxidant that significantly attenuates PMA-induced NETosis in healthy neutrophils by scavenging ROS
vitamin C may also inhibit NETosis and NET production in COVID-19