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The Evolving Role of Perlane® in Healthcare: A Guide for Providers

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Image of woman receiving an injection of Perlane. Featured in the Evolving Role of Perlane®

Dermal fillers have been one of the cornerstones in aesthetic and medical treatments, providing patients with minimally invasive techniques for various conditions.  Of these, Perlane® stands out due to its efficacy and safety record. 

Perlane® is an FDA-approved hyaluronic acid-based dermal filler notably indicated for adding volume and smoothening deep wrinkles, bringing natural-looking, long-lasting results. It has been used extensively in aesthetic medicine modalities to treat facial aging and volume loss.

This all-inclusive guide aims to give healthcare administrators an overview of Perlane® and the benefits associated with this particular line of treatment—providing Perlane®—to enhance patient satisfaction, expand services, and underscore a commitment to advanced healthcare solutions.

Note: The IAPAM recommends that healthcare providers have received accredited Botox® training and feel comfortable and confident in their ability to work with botulinum toxin injections before attempting any type of dermal filler injections.

Understanding Perlane®

Perlane® is one of the most popular dermal fillers primarily composed of non-animal stabilized hyaluronic acid, or NASHA. Hyaluronic acid (HA) is a naturally occurring substance found in the skin, responsible for maintaining moisture, volume, and elasticity. Through the use of NASHA technology with Perlane®, there is a significant amount of purity and consistency involved, which
makes this material entirely trustworthy for many aesthetic and medical uses.

This filler has larger gel particles than other fillers, so it has an advantage in treating deeper
wrinkles and filling huge volumes. Perlane is injected into the middle to deep dermal level and allows easy integration of its material with the natural hyaluronic acid in the skin, filling and
smoothening wrinkles while promoting hydration and elasticity that gives a natural, youthful appearance.

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Historical Development and Approval by Regulatory Bodies

Perlane® traces its development back to advanced biotechnological research and innovation. The first introduction was made by Q-Med, a Swedish biotech company well known for inventing an innovative non-animal stabilized hyaluronic acid technology. More specifically, the development of Perlane® represented an extremely significant advancement in dermal fillers, presenting an effective, safe, and long-lasting product.

The European Union initially licensed Perlane® in the early 2000s and by the United States FDA in 2007. These licenses were based on an extensive clinical trial program, assessing safety and efficacy for treating moderate to severe facial wrinkles and folds, including nasolabial folds.

How Perlane® Works Beneath the Skin

Perlane® works based on the powerful properties of hyaluronic acid (HA), a naturally occurring substance in the skin that can hold moisture. [5] When introduced, the Perlane® integrates with the naturally existing HA in the skin and instantaneously provides hydration and volumization.

The larger gel particles make Perlane® more appropriate for deeper dermal layers, where filling of significant wrinkles and folds is possible, thereby smoothing them out. Once injected, the HA molecules in Perlane® associate with water molecules in the body to create a cushioning effect that supports the skin’s structure and delivers a natural, youthful plumpness.

The process will not only reduce the appearance of these wrinkles but also improve skin elasticity and texture. The low risk of forming any allergic reaction due to the biocompatibility of Perlane® makes it a potent and safe option for the broadest array of patients.

Common Indications

Perlane® is FDA-approved for correcting moderate to severe facial wrinkles and folds. It is most commonly used to treat:

Long-Term Effects and Benefits

Perlane® offers several long-term benefits, making it a valuable addition to aesthetic and medical practices:

Downtime After Treatment

Another significant advantage associated with Perlane® is that there is minimal, if any, downtime involved in its use. On average, most patients can resume all daily activities immediately after the procedure. However, a few considerations ensure optimal results with the least potential for side effects:

Safety Profile and Biocompatibility of Perlane®

Perlane® has an absolutely perfect safety profile, thanks to intensive clinical research and decades of practical application in aesthetic medicine. Its NASHA technology minimizes cases of allergic reactions and side effects, making it amply secure for many patients.

The safety profile of Perlane® contains:

Clinical Applications of Perlane®

Perlane® has made a name for itself as both a versatile and very effective dermal filler used in:

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Why Offer Perlane® to Your Patients

With the increasing need and popularity of non-surgical cosmetic procedures, healthcare practices looking to fulfill this demand can help in improving patient satisfaction with Perlane®. Underneath are some benefits:

Training and Expertise in Perlane® Administration

Professional Perlane® training is of prime importance for the administration of Perlane® to both safety and efficacy. The anatomy of facials, injection techniques, and patient assessment are deeply intertwined with the precise nature of dermal filler injections. Proper Perlane® training provides a health professional with the necessary knowledge and skills for excellent results and minimizing risks.

Patient Management and Care

Pre-Treatment Considerations and Consultation

Successful management of the patient begins with careful pre-treatment considerations and consultations. Assessing the patient’s medical history, medications, and former cosmetic treatments is essential in considering Perlane ® suitability.

An excellent facial aesthetic analysis defines the areas to treat in pursuit of aesthetic goals. The likely outcome, benefits, and side effects can be elaborated with official visual props like before-and-after pictures to set realistic expectations.

After-Treatment Care and Follow-up

Adequate care post-treatment is needed to show the desired results and acquire patient satisfaction. Patients need to be told that mild side effects like swelling and redness will be present but will only last for days. Other specific aftercare measures include avoiding strenuous activities, sun exposure, and alcohol consumption. The cold compress relieves discomfort.

A follow-up visit assures good results, takes care of problems, and makes sure that the patient is satisfied, thus gaining their trust and loyalty.

Managing Patient Expectations and Outcomes

Good communication during consultation: clear expectations. Discuss what Perlane® can and cannot do. Initial effects can be seen immediately. The final result may be attained within days to weeks because the swelling is absorbed in the first few days and with the integration of the filler.

Educate patients that the longevity of Perlane® is 6–12 months, guiding treatment planning and managing patient expectations.

Comparison with Other Dermal Fillers

When considering the integration of Perlane® into healthcare practice, it is essential to understand how it compares to other leading dermal fillers such as Restylane® and Juvederm®. [12]

Below is a detailed comparison of these products, highlighting key attributes and differentiators.

  • Perlane®
  • Restylane®
  • Juvederm®
Feature Perlane®Restylane®Juvederm®
Feature
Main ComponentHyaluronic Acid (HA)Hyaluronic Acid (HA)Hyaluronic Acid (HA)
Particle SizeLargerMediumSmaller to medium
Cross-linking TechnologyNon-animal stabilized HANon-animal stabilized HAVycross™ technology (in some products) [13]
Consistency/ViscosityThicker gelMedium consistencySmooth gel
Primary UsesDeep facial wrinkles, folds, and volume restorationFine lines, moderate wrinkles, and lip augmentationSmooth moderate to severe wrinkles and folds, volume enhancement
Longevity of Results6 to 8 months6 to 12 months6 to 12 months (varies by product)
Injection DepthDeep dermis and subcutaneousMid to deep dermisMid to deep dermis
Common Treatment AreasNasolabial folds, marionette lines, cheeks, chinNasolabial folds, lips, tear troughs, cheeksNasolabial folds, marionette lines, lips, cheeks
FDA ApprovalYesSome formulationsYes
Contains LidocaineSome formulationsVersatile, good for various applicationsMost formulations
Unique AdvantagesLong-lasting for deeper lines and volumeSmooth consistency, excellent for superficial lines
Start Your Practice NowBuy NowBuy NowBuy Now

Future Trends and Latest Advancements in Perlane® Technology

Perlane® continues to evolve with formulation and delivery advancements. Most recently, innovations seem to be concentrated on improving the filler’s consistency for more straightforward injection and more predictable results. Advancements in syringe technology have also made a big difference in allowing delivery to happen more precisely, thus achieving finer control over the injection process.

These innovations make Perlane® last longer, with results upward of 12 months or more depending on the character of the treatment areas and individual factors. [14] The availability of such long-lasting medication will enhance patient satisfaction by decreasing the frequency of touching-up with treatments to keep looking youthful for a more extended period.

Integration of Lidocaine for Enhanced Comfort

One of the technological developments associated with Perlane is that it contains lidocaine, a local anesthetic. [15] This additive in the formulation reduces the overall pain and discomfort during actual injections for the patient and thus enhances the experience considerably. Its presence means treatments will then be more comfortable, which alleviates anxiety in patients and consequently leads to increased satisfaction with the procedure.

How Healthcare Practices Benefit from Staying Ahead of Trends

Staying up-to-date with new trends or innovative dermal filler technology introductions is significant for healthcare practices. If a provider is up-to-date, then they will be able to help patients with the finest and most current treatments, significantly improving patient satisfaction and practice reputation.

Further, with knowledge of the trends, healthcare providers make informed decisions on the integration of new techniques and products into services for better patient outcomes and growing a practice.

Conclusion

Offering Perlane® takes your practice to new heights by broadening your service offerings, meeting increased demand from patients looking for the most innovative treatments, and positioning you as a leader in cutting-edge aesthetic and medicinal therapies. With its advanced formula for wrinkle removal, proven to work with a high satisfaction rate among patients, Perlane® genuinely becomes of value added to the repertoire of any healthcare provider.

It is recommended that healthcare administrators incorporate Perlane® into their practice, and they must pursue professional training regarding the use of Perlane to enable a safe and effective way of administering this versatile dermal filler.

Frequently Asked Questions – FAQs

What is Perlane®, and how does it differ from other dermal fillers?

Perlane is an HA-based dermal filler that corrects facial wrinkles and folds of moderate to severe degrees, restoring volume to lost contour in the face. Unlike other fillers, it has larger particles, so it gives one a more significant lift and is more long-lasting.

Perlane® is effective for treatments that last from six to eight months, depending on the area that has been treated, along with patient specifics. Regular maintenance treatments help in sustaining results.

The expected common side effects include redness, bruising, swelling, and tenderness around the injected area, which all usually resolve within a few days. Severe complications are rare when a trained professional performs the procedure.

Perlane® is generally safe for most patients. However, a thorough medical assessment is necessary to rule out contraindications, such as severe allergies, bleeding disorders, or active skin infections. Pregnant or breastfeeding women are also advised to avoid dermal filler treatments.

A Perlane® treatment session typically involves an initial consultation and administering the filler through injections. The procedure is relatively quick, usually taking about 30-45 minutes. Patients may experience mild discomfort, which can be minimized with topical anesthetics or lidocaine fillers.

Reference

  1. Muhn, Channy. “The Evolving Role of Hyaluronic Acid Fillers for Facial Volume Restoration and Contouring: A Canadian Overview.” Clinical, Cosmetic and Investigational Dermatology, Oct. 2012, p. 147, https://doi.org/10.2147/ccid.s30794
  2. “Perlane (Non-Animal Stabilized Hyaluronic Acid (NASHA) Gel): Side Effects, Uses, Dosage, Interactions, Warnings.” RxList, www.rxlist.com/perlane-drug.htm.  Accessed 21 June 2024.
  3. Q-Med. “The Q-Med Group Divests the North American Business Regarding the Esthetic Products RESTYLANE, RESTYLANE Fine Lines and PERLANE to Medicis for USD 160 Million.” GlobeNewswire News Room, 10 Feb. 2003, www.globenewswire.com/en/news-release/2003/02/10/294001/1036/en/The-Q-Med-Group-Divests-the-North-American-Business-Regarding-the-Esthetic-Products-RESTYLANE-RESTYLANE-Fine-Lines-and-PERLANE-to-Medicis-for-USD-160-million.html.  Accessed 21 June 2024.
  4. Perlane (Dermal Filler) FDA Approval History.” Drugs.com, www.drugs.com/history/perlane.html.  Accessed 21 June 2024.
  5. Papakonstantinou, Eleni, et al. “Hyaluronic Acid: A Key Molecule in Skin Aging.” Dermato-Endocrinology, vol. 4, no. 3, July 2012, pp. 253–258, www.ncbi.nlm.nih.gov/pmc/articles/PMC3583886/, https://doi.org/10.4161/derm.21923
  6. SUMMARY of SAFETY and EFFECTIVENESS DATA for a Supplemental Premarket Approval Application. 
  7. “Perlane® Dermal Fillers.” Forefront Dermatology, forefrontdermatology.com/services/perlane-dermal-fillers/.  Accessed 21 June 2024.
  8. Kaufman‐Janette, Joely, et al. “Efficacy and Safety of a New Resilient Hyaluronic Acid Dermal Filler, in the Correction of Moderate‐To‐Severe Nasolabial Folds: A 64‐Week, Prospective, Multicenter, Controlled, Randomized, Double‐Blind and Within‐Subject Study.” Journal of Cosmetic Dermatology, vol. 18, no. 5, 24 Aug. 2019, pp. 1244–1253, https://doi.org/10.1111/jocd.13100
  9. Swift, Arthur, et al. “The Facial Aging Process from the “inside Out.”” Aesthetic Surgery Journal, vol. 41, no. 10, 16 Dec. 2020, https://doi.org/10.1093/asj/sjaa339
  10. Wollina, Uwe, and Alberto Goldman. “Fillers for the Improvement in Acne Scars.” Clinical, Cosmetic and Investigational Dermatology, Sept. 2015, p. 493, www.ncbi.nlm.nih.gov/pmc/articles/PMC4598204/, https://doi.org/10.2147/ccid.s86478
  11. Pavicic, Tatjana, and David Funt. “Dermal Fillers in Aesthetics: An Overview of Adverse Events and Treatment Approaches.” Clinical, Cosmetic and Investigational Dermatology, vol. 6, Dec. 2013, p. 295, https://doi.org/10.2147/ccid.s50546
  12. Brandt, Fredric S., and Alex Cazzaniga. “Hyaluronic Acid Fillers: Restylane and Perlane.” Facial Plastic Surgery Clinics of North America, vol. 15, no. 1, Feb. 2007, pp. 63–76, https://doi.org/10.1016/j.fsc.2006.11.002.  Accessed 13 Aug. 2019.
  13. Calvisi, Lucia, et al. “Rejuvenation of the Perioral and Lip Regions with Two New Dermal Fillers: The Italian Experience with VycrossTM Technology.” Journal of Cosmetic and Laser Therapy, vol. 19, no. 1, 23 Nov. 2016, pp. 54–58, https://doi.org/10.1080/14764172.2016.1247960.  Accessed 6 Mar. 2022. 
  14. Fredric S Brandt. Hyaluronic Acid Fillers: Restylane and Perlane. 2007, www.researchgate.net/publication/6487810_Hyaluronic_Acid_Fillers_Restylane_and_Perlane
  15. Brandt, Fredric . A Lidocaine-Containing Formulation of Large-Gel Particle Hyaluronic Acid Alleviates Pain. 2010, www.researchgate.net/publication/51446038_A_Lidocaine-Containing_Formulation_of_Large-Gel_Particle_Hyaluronic_Acid_Alleviates_Pain

 

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