Non-surgical Procedure
Injectables
Bellafill®
Bellafill® is an FDA-approved dermal filler designed for the correction of nasolabial folds, commonly known as smile lines. Over time, factors such as aging, genetics, weight fluctuations, UV exposure, and repetitive facial movements contribute to the development of facial wrinkles and folds.
Bellafill® offers a durable solution for those seeking to diminish smile lines, combining immediate results with long-term facial rejuvenation.
Key Benefits of Bellafill®:
- Long-Lasting Results: Bellafill® is unique among dermal fillers, providing results that can last up to five years, reducing the need for frequent re-treatments.
- Immediate Improvement: Patients often notice a visible enhancement in facial volume and wrinkle reduction shortly after the procedure.
- Convenient In-Office Procedure: The treatment is performed in a clinical setting, typically requiring only one or two sessions to achieve optimal results.
- Proven Safety Profile: Clinical studies have demonstrated the safety and efficacy of Bellafill® for the correction of nasolabial folds.
Considerations:
- Skin Testing: A skin test is necessary before treatment to identify any potential allergic reactions.
- Gradual Enhancement: While some improvement is immediate, the full effect develops over several months as Bellafill® stimulates the body’s natural collagen production.
Juvéderm®
Juvéderm® is an FDA-approved hyaluronic acid dermal filler designed to restore facial volume and smooth away wrinkles and folds, such as nasolabial folds—the lines running from the nose to the corners of the mouth.
Juvéderm® offers a reliable option for those seeking to diminish facial wrinkles and restore volume, providing smooth and natural-looking results.
Key Features of Juvéderm:
- Smooth Gel Consistency: Juvéderm is formulated as a smooth gel, allowing for natural-looking results and a more comfortable injection experience.
- Hyaluronic Acid-Based: Composed of hyaluronic acid, a substance naturally found in the skin, Juvéderm helps maintain hydration and add volume.
- Safety Across Skin Types: Clinical studies have demonstrated that Juvéderm is safe and effective for individuals of all skin types, including persons of color, with no increased risk of hyperpigmentation or hypertrophic scarring.
Treatment Overview:
The procedure involves injecting Juvéderm® gel into targeted areas to enhance facial contours and reduce the appearance of wrinkles.
Considerations:
- Longevity of Results: The effects of Juvéderm can last up to one year, depending on the treatment area and individual factors.
- Side Effects: Common side effects may include temporary redness, swelling, or bruising at the injection site. These effects are generally mild and resolve on their own.
Radiesse®
Radiesse® is an FDA-approved dermal filler designed to replenish soft tissue volume and smooth moderate to severe facial wrinkles and folds, such as nasolabial folds—the lines extending from the nose to the mouth corners.
Radiesse® offers a durable and effective solution for individuals seeking to address facial wrinkles, folds, and volume loss in the hands, with the added benefit of collagen stimulation for prolonged improvement.
Composition and Mechanism:
Radiesse consists of synthetic calcium hydroxylapatite (CaHA) microspheres suspended in a gel carrier. Upon injection, it provides immediate volume and stimulates the body’s natural collagen production, promoting long-term skin rejuvenation.
FDA-Approved Uses:
- Facial Wrinkles and Folds: Radiesse effectively corrects moderate to severe facial wrinkles and folds, including nasolabial folds.
- Hand Augmentation: It is approved for restoring volume loss in the back of the hands, improving the appearance of tendons and veins.
Off-Label Uses:
While not FDA-approved for these purposes, Radiesse has been utilized in procedures such as gluteal (buttocks) enhancement, especially in patients lacking sufficient fat for transfer. However, the safety and efficacy of such applications have not been established.
Common Side Effects:
Adverse events may include bruising, redness, swelling, pain, itching, and the formation of nodules or lumps at the injection site. Individuals with a history of herpes may experience a recurrence following treatment.
Duration of Results:
The effects of Radiesse can last approximately 12 to 18 months, outlasting many hyaluronic acid-based fillers, which typically last 6 to 12 months.
Procedure Comfort:
Radiesse injections are generally well-tolerated, with patients experiencing mild and temporary discomfort during the procedure. The sensation is often described as a slight pinching and pressure.
Post-Treatment Care:
Patients are advised to avoid massaging or applying pressure to the treated areas for 4 to 6 hours post-injection and to refrain from sleeping on the treated side(s) for the next 2 to 3 days to ensure optimal results.
Radiesse offers a durable and effective solution for individuals seeking to address facial wrinkles, folds, and volume loss in the hands, with the added benefit of collagen stimulation for prolonged improvement.
Restylane®
Restylane® is an FDA-approved hyaluronic acid-based dermal filler designed to restore volume and smooth moderate to severe facial wrinkles and folds, such as nasolabial folds—the lines extending from the nose to the mouth corners. It is also utilized for lip enhancement, providing a fuller and more defined appearance.
Restylane® offers a versatile and effective solution for individuals seeking to address facial wrinkles, folds, and volume loss, with the added benefit of hyaluronic acid to maintain skin hydration and elasticity.
Common Side Effects:
Adverse events may include bruising, redness, swelling, pain, itching, and the formation of nodules or bumps at the injection site. Individuals with a history of herpes may experience a recurrence following treatment.
FDA-Approved Uses:
- Facial Wrinkles and Folds: Radiesse effectively corrects moderate to severe facial wrinkles and folds, including nasolabial folds.
- Hand Augmentation: It is approved for restoring volume loss in the back of the hands, improving the appearance of tendons and veins.
Duration of Results:
The longevity of Restylane results varies depending on the treatment area and individual factors:
- Nasolabial Folds: up to 12 months
- Cheeks: up to 12 months
- Lips: up to 6 months
- Hands: up to 6 months
Procedure Comfort:
Restylane® injections are generally well-tolerated, with patients experiencing mild and temporary discomfort during the procedure, often described as a slight pinching sensation and pressure.
Post-Treatment Care:
Patients are advised to avoid massaging or applying pressure to the treated areas for 4 to 6 hours post-injection and to refrain from sleeping on the treated side(s) for the next 2 to 3 days to ensure optimal results.
Restylane® offers a versatile and effective solution for individuals seeking to address facial wrinkles, folds, and volume loss, with the added benefit of hyaluronic acid to maintain skin hydration and elasticity.
Revanesse® Versa™+
Revanesse® Versa™+ is an FDA-approved hyaluronic acid dermal filler designed to treat moderate to severe facial wrinkles and folds, including nasolabial folds.
It can also enhance facial volume in areas such as the cheeks and lips. The smooth consistency of the gel provides natural-looking results with minimal swelling, leading to shorter downtime. Clinical studies have shown that Revanesse® Versa™+ causes approximately 24% less swelling than other hyaluronic acid fillers. Results typically last six months or longer, as the hyaluronic acid is gradually absorbed by the body.
Revanesse® Versa™+ offers a safe and effective option for those seeking to reduce facial wrinkles and enhance volume. Consult with a qualified healthcare provider to determine if this treatment aligns with your aesthetic goals.
Common Side Effects:
- Bruising
- Redness
- Swelling
- Pain
- Itching
These side effects are generally mild and resolve within a week. If symptoms persist beyond one week, consult your healthcare provider.
Contraindications:
- Pregnancy or breastfeeding
- History of hypertrophic scarring or keloid formation
- Active acne or other inflammatory skin conditions near the injection site
- Under 22 years of age
Individuals with a history of severe allergies, particularly to hyaluronic acid products, should avoid treatment.
Rare but Serious Risks:
Unintentional injection into a blood vessel can lead to serious complications, including vision abnormalities, blindness, stroke, skin necrosis, or permanent scarring. Seek immediate medical attention if you experience unusual pain, vision changes, white appearance of the skin near the injection site, or signs of a stroke.
Sculptra™
Sculptra™ (poly-L-lactic acid) is an FDA-approved injectable treatment designed to address facial wrinkles and restore volume loss due to aging. Unlike traditional fillers, Sculptra stimulates the body’s natural collagen production, gradually enhancing skin structure and thickness over time.
Mechanism of Action
Sculptra works by injecting poly-L-lactic acid into the deep dermis, where it acts as a scaffold, encouraging collagen synthesis. This process results in a gradual and natural-looking improvement in facial volume and the reduction of wrinkles.
Treatment Areas
Common areas treated with Sculptra include:
- Nasolabial folds (smile lines)
- Marionette lines
- Chin wrinkles
- Hollow temples
- Cheeks
By targeting these areas, Sculptra helps restore a more youthful facial contour.
Procedure Overview
The Sculptra treatment typically involves a series of injections scheduled over a few months to achieve optimal results. The procedure has minimal downtime, allowing most individuals to resume their daily activities shortly after treatment.
Duration of Results
While individual results may vary, the effects of Sculptra can last up to two years. This extended duration is due to the stimulation of natural collagen production, which provides a more enduring improvement compared to some other dermal fillers.
Potential Side Effects
Common side effects associated with Sculptra injections include:
- Redness
- Swelling
- Bruising
- Tenderness
- Formation of small lumps under the skin
These side effects are generally temporary and resolve on their own. However, if any adverse reactions persist or cause concern, it is important to consult with your healthcare provider.
Post-Treatment Care
Following Sculptra injections, it is advisable to adhere to these guidelines to help optimize treatment outcomes and reduce the likelihood of complications:
- Gently massage the treated areas as directed by your provider to promote even distribution.
- Avoid excessive sun or UV exposure until any initial swelling and redness have resolved.
- Refrain from strenuous activities for 24 hours post-treatment.
Consultation
Before undergoing Sculptra treatment, a thorough consultation with a qualified healthcare professional is essential. This discussion should cover your medical history, aesthetic goals, and any potential risks to determine if Sculptra is an appropriate option for you.
By understanding the benefits and considerations associated with Sculptra, patients can make informed decisions about their cosmetic treatment options.