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Repetitive strain injuries (RSIs) are a common classification of injuries that can impede a patient’s career, hobbies, quality of life, and much more. According to the most recent data from the United States Bureau of Labor Statistics, 36% of all cases of worker absence were a result of workplace-related sprains and strains and the leading type of injury in the manufacturing sector. In Canada, repetitive strain injuries are estimated to affect approximately 4.5 million people, or 15% of the country’s population, at any given time, according to data from Statistics Canada.
While time and rest can help heal these injuries, repetition of the same behaviors that caused them can make the diagnosis and intervention much more severe. Here, we outline the common causes, symptoms, and treatments for repetitive strain injuries to accurately diagnose and deliver optimal treatment outcomes to these prospective patients.
Carpal tunnel syndrome, tendonitis, and tennis elbow are just a small sampling of the long list of repetitive strain injuries. Simply put, an RSI is a traumatic injury that results from cumulative damage caused by repetitive movements. In many cases, repetition occurs over a prolonged period of time and on a regular basis. As a result, nerves, muscles, and tendons suffer micro-injuries that eventually lead to pain, numbness, weakness, and alterations in one’s posture, motor control, or movements.
To dive a little deeper, consider the RSI carpal tunnel syndrome as a result of prolonged computer work. Over time, the fine hand movements required to type and use a mouse for eight hours or more each day leads to strain and tension in the muscles and tendons located in the fingers, wrists, and forearms. This strain causes tiny tears in soft tissue and muscles, causing them to contract and limiting range of motion. Abrasion also occurs between tissue and tendons, leading to inflammation that presses on nerves, causing sensations of pain and numbness from the elbow down through the wrist and into the hands.
Generally speaking, the three basic causes of RSIs boil down to poor posture and technique in combination with overuse as a result of repetition. Careers or hobbies requiring the completion of repetitive tasks put a patient most at risk of developing an RSI, particularly if the person neglects to take regular breaks, doesn’t perform tasks in a way that best supports proper posture, or overlooks the importance of incorporating regular stretching and exercise to prevent soft tissue trauma and/or support proper soft tissue healing if trauma does occur.
Pain is the most common symptom of an RSI that occurs after damage has already been done, making prevention ideal. Pain may present in different degrees and may be described as local (in a defined area, such as the fingertips) or diffuse (in a larger area surrounding the injured tissue, such as the forearm). However, diagnosing an RSI can be a little tricky as it’s possible that pain may not be a presenting symptom. For those cases, and even when pain is present, the following symptoms may occur:
Patients may report continuous symptoms or those that worsen the longer they complete the repetitive task causing the RSI. Specific symptoms can also range from mild to severe, though a severe case of RSI may not present all of the above-listed symptoms.
For the most part, patients presenting with an RSI may recover in three to six months if proper rest is given to the damaged tissues. Without proper treatment and rest, symptoms may persist and worsen to become debilitating over time. Fortunately, certain measures can be taken that may speed up recovery time or prevent further damage, preventing more long-term complications. The following are just some of the more common ways you may treat a patient diagnosed with an RSI, in addition to some of the top advances in the treatment of soft tissue injuries.
If you suspect the injury has been caused as a result of repetitive duties at work or hobbies at home, suggest that the patient modify those activities to minimize repetition or, if at work, that they seek new duties from their employer for health reasons. For practicing physicians, a physician’s note to the employer may be required. If the patient is unable to avoid the activity, recommend small, frequent breaks and a set of stretches they may be able to use to improve healing and reduce pain and tension. While these small changes may assist patients in minimizing pain and offering damaged tissue the opportunity to better heal, the road to recovery may be longer and tissue may not heal properly without proper treatment.
The short-term use of anti-inflammatory medications may help to reduce inflammation and better support the healing of damaged tissue. Pain may be managed by simple pain medications like ibuprofen. Further, the injection of steroids into the affected tissue can help to minimize more severe cases of inflammation to reduce pain and better allow tissue to heal naturally. Medications may be combined with other treatments for improved outcomes and better pain management throughout treatment.
In more extreme cases, surgery may be required. Surgical interventions are often favored for correcting more severe problems in nerves and tendons that are past the point of healing by non-surgical methods alone. In addition, surgical interventions are more common among older patients, as the body’s natural ability to repair damaged tissue can decline with age.
Physiotherapy refers to the use of exercise, stretching, or massage therapy as a means to counteract the contractions caused by an RSI and promote improved flexibility and movement as the tissue heals. Heat therapy may also be applied here to loosen tense muscles for further movement and flexibility. Through the use of traditional treatment methodologies alongside different healing technologies, physiotherapy may be used to improve posture, increase flexibility, improve strength, and otherwise restore or improve the patient’s muscle function, mobility, and quality of life.
As mentioned earlier, a common myth surrounding the healing of an RSI is that with rest, the injury will heal itself. While this may be true for some, many patients also experience chronic symptoms, such as persistent pain, weakness, and a decline in function, flexibility, mobility, balance, and more. This is why the rehabilitation community continues to seek to elevate the standard of care, more recently utilizing energy-based modalities to further accelerate healing and promote optimal rehabilitation as compared to rest or traditional treatments used alone.
With its RP3 technology—a unique combination of Multi-Polar Radio Frequency (RF), Pulsed Electro Magnetic Fields (PEMF), and massage modalities—Venus Heal™ delivers synergistic benefits for addressing repetitive strain injuries and other soft tissue conditions. Venus Heal™ is an innovative non-invasive system for the treatment of acute and chronic disorders of the musculoskeletal system, such as muscle spasms, back pain, and soft tissue injuries. With this easy-to-use, compact, and portable medical device, the soft tissue injury treatments increase tissue temperature by converting RF energy to heat deep within the targeted tissue. Combined with PEMF and therapeutic massage, this results in pain relief, muscle relaxation, an increase in local blood circulation, and reduced inflammation with the possibility of noticeable pain relief in as little as one treatment session. The overall outcome is a faster, more complete recovery for your patients and a higher patient satisfaction rate for your clinic.
Interested in learning more about Venus Heal™ and the benefits of a Venus Concept partnership for your business? Contact an expert today using the button below.
For more information call: (888) 907-0115 // info@venusconcept.com // 235 Yorkland Blvd., Suite 900, Toronto, ON, M2J 4Y8 Canada
REGULATORY CLEARANCES [ More ]
Venus Bliss™ is cleared by the FDA and licensed by Health Canada for non-invasive lipolysis of the abdomen and flanks in individuals with a Body Mass Index (BMI) of 30 or less, with the diode laser applicators. The (MP)2 applicator is cleared by the FDA for temporary reduction in the appearance of cellulite, and licensed by Health Canada for temporary increase of skin tightening, temporary circumferential reduction, and temporary cellulite reduction. Venus Bliss™ has CE Mark as a non-invasive medical aesthetic device enabling a comprehensive approach leading to body contouring, addressing fat reduction, skin tightening, circumference reduction, and cellulite reduction.
Venus Versa™ is cleared by the FDA, licensed by Health Canada, and has CE Mark as a multi-application device intended to be used in aesthetic and cosmetic procedures. The SR515 and SR580 applicators are cleared by the FDA, licensed by Health Canada, and have CE Mark for the treatment of benign pigmented epidermal and cutaneous lesions and treatment of benign cutaneous vascular lesions. The HR650/HR650XL and HR690/HR690XL applicators are cleared by the FDA, licensed by Health Canada, and have CE Mark for the removal of unwanted hair and to effect stable long-term or permanent hair reduction for Fitzpatrick skin types I-IV. The AC Dual applicator is cleared by the FDA, licensed by Health Canada, and has CE Mark for the treatment of acne vulgaris. The DiamondPolar™ and OctiPolar™ applicators on the Venus Versa™ system are cleared by the FDA for non-invasive treatment of moderate to severe facial wrinkles and rhytides on females with Fitzpatrick skin types I-IV. The DiamondPolar™ applicator is licensed by Health Canada and has CE Mark for non-invasive treatment of moderate to severe facial wrinkles and rhytides on females with Fitzpatrick skin types I-IV. The OctiPolar™ applicator on the Venus Versa™ system is licensed by Health Canada and has CE Mark for temporary body contouring via skin tightening, circumferential reduction, and cellulite reduction. The NanoFractional RF™ (Viva) applicator is cleared by the FDA, licensed by Health Canada, and has CE Mark for dermatological procedures requiring ablation and resurfacing of the skin.
ARTAS iX™ is cleared by the FDA, licensed by Health Canada and has CE Mark with indication for use for harvesting hair follicles from the scalp in men diagnosed with androgenic alopecia (male pattern hair loss) who have black or brown straight hair. ARTAS iX™ is intended to assist physicians in identifying and extracting hair follicular units from the scalp during hair transplantation; creating recipient sites; and implanting harvested hair follicles.
NeoGraft® is cleared by the FDA, licensed by Health Canada and has CE Mark with indication for use in suction-assisted follicular extraction and re-implantation. NeoGraft® is an auto-graft system and can be used on both male and female patients.
Venus Legacy™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides in females with Fitzpatrick skin types I-IV with the OctiPolar™ and DiamondPolar™ applicators, and temporary reduction in the appearance of cellulite with the 4D Body (LB2) and 4D Face (LF2) applicators. It is licensed by Health Canada and has CE Mark for the temporary increase of skin tightening, temporary circumferential reduction, temporary cellulite reduction, and temporary wrinkle reduction.
Venus Velocity™ is cleared by the FDA, licensed by Health Canada and has CE Mark for hair removal, permanent hair reduction (defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae for all Fitzpatrick skin types.
Venus Fiore™ received regulatory approval in Israel for aesthetic and functional treatment of the vagina, labia and mons pubis. Venus Fiore™ is available for sale in India, Hong Kong, and other selected Asian countries.
The Venus Viva™ MD is cleared by the FDA, licensed by Health Canada and has CE Mark for the use in dermatological procedures requiring ablation and resurfacing of the skin using the Viva™/Viva™ MD applicator, and the non-invasive treatment, reduction in the appearance of moderate to severe facial wrinkles and rhytides for females in Fitzpatrick skin types I-IV with the DiamondPolar™ applicator.
The Venus Viva™ MD is cleared by the FDA for the use in dermatological procedures requiring ablation and resurfacing of the skin, and the non-invasive treatment of moderate to severe facial wrinkles and rhytides for females in Fitzpatrick skin types I-IV with the DiamondPolar™ applicator.
Venus Epileve™ is cleared by FDA, licensed by Health Canada and has CE Mark for hair removal, permanent hair reduction (defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae for all Fitzpatrick skin types. Venus Epileve™ is also CE-Marked for hirsutism.
Venus Freeze Plus™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides in females with Fitzpatrick skin types I-IV. It is licensed by Health Canada for temporary skin tightening, and temporary reduction in the appearance of cellulite on the abdomen and flanks, using the DiamondPolar™ and OctiPolar™ applicators. The DiamondPolar™ applicator on Venus Freeze Plus™ has CE Mark for the non-invasive treatment of moderate to severe facial wrinkles and rhytides, and the increase of skin tightening, temporary circumferential reduction, and cellulite reduction with the OctiPolar™ applicator.
Venus Heal™ is licensed by Health Canada and can be used for the treatment of both acute and chronic disorders of the musculoskeletal system, such as muscle spasms, back pain, and soft tissue injuries, and results in effects such as pain relief, myorelaxation, increase of local blood circulation, and edema reduction. In the U.S., Venus Heal™ is cleared by the FDA for the relief of minor muscle aches and pain, relief of muscle spasm, and temporary improvement of local blood circulation. These indications enable the treatment of certain soft tissue injuries and conditions.
Venus Glow™ is cleared by the FDA as a Class I motorized dermabrasion device. It provides a dermal rejuvenation treatment that works to open up and deep-clean pores. Venus Concept is the exclusive distributor for Venus Glow™.
Venus Skin™ is a skin care line of various lotions and creams intended to improve different aspects of skin appearance, skin serums, and skin nourishment solutions.
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