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Aesthetic procedures have gradually become more mainstream and popular over the past 15 years, largely led by the significant increase in minimally invasive procedures since the US Food and Drug Administration (FDA) approval of Botox Cosmetic treatment for glabellar rhytids in 2002. In 2014, more than 15.6 million cosmetic procedures were performed, of which 13.9 million were minimally and noninvasive procedures (ASPS 2014 statistics). Of the minimally invasive procedures, more than 6.6 million botulinum toxin type-A (BoA) procedures were performed, representing a 748% increase since 2000. More than 2.3 million soft tissue filler injections were performed, representing a 253% increase since 2000.
A complete discussion of minimally and noninvasive cosmetic procedures would also include adipose tissue transfer/injections, chemical peels, laser skin resurfacing and other laser treatments, intense pulsed light (IPL), ultrasound and radiofrequency devices, sclerotherapy, microdermabrasion, and other procedures. This chapter will focus on the two most frequent noninvasive cosmetic procedures that prospective aesthetic patients seek: BoA neuromodulator injections and soft tissue filler injections. For simplicity, the BoA injections will be referred to as Botox (OnabotulinumtoxinA, Allergan), but it applies to other commercially available botulinum toxin-A products in the United States: Dysport (AbobotulinumtoxinA, Galderma) and Xeomin (IncobotulinumtoxinA, Merz; Table 160.1 ). The discussion of soft tissue filler injections will be limited to the hyaluronic acid (HA) product lines: Juvéderm (Allergan) injection procedure described can be applied to other HAs used in the United States: Restylane/Lyft/Silk (Galderma) and Belotero (Merz). The technique of Botox and filler injection procedures is summarized in FDA-approved anatomic locations, as well as in more advanced, off-label areas.
Year of FDA Approval | Product Trade Name (Manufacturer) |
---|---|
2002 | Botox (OnabotulinumtoxinA) (Allergan) |
2009 | Dysport (AbobotulinumtoxinA) (Galderma) |
2011 | Xeomin (IncobotulinumtoxinA) (Merz) |
Pending | PurTox (Mentor) |
Pending | RT001 (Topical and Injectable) (Revance) |
The importance of the doctor-patient relationship in aesthetic surgery and medicine should not be diminished, despite the increasing popularity of medi-spas, corporate aesthetic practices, Botox “parties,” and the ease at which some minimally and noninvasive cosmetic procedures can be delivered. A patient who is interested in nonsurgical injectable procedures should have a consultation with a physician/surgeon specializing in aesthetic interventions/cosmetic procedures. During the consultation, the physician can ascertain the patient’s concerns and goals and be able to offer appropriate recommendations and treatment options.
Patient concerns and goals
Personal preferences
Gender, social, cultural, ethnic considerations
Work and/or family considerations
Downtime
Cost
General health
Aesthetic treatment history
Past medical history
Systemic disease
Autoimmune/collagen vascular disease
Bleeding tendencies/hematologic conditions
Reaction to anesthesia
Localized disease/condition
Ocular conditions
Herpes simplex virus (HSV)/cold sores
Facial nerve weakness/disorders
History of allergic reactions
Severe allergies/anaphylaxis
Food allergies: milk and egg products
Current medications
Steroids and other immunosuppressive agents, muscle relaxants, pain medications, anticoagulants (Coumadin or Plavix), psychiatric medications
Over-the-counter medications and supplements
NSAIDs, other blood thinning products
Females: Pregnancy and breast feeding
Social history: Smoking and alcohol use
Psychiatric history and conditions
Bipolar disorder
Body dysmorphic disorder (BDD)
Family history: Cardiovascular, psychiatric, hematologic disorder
Occupation/work history
Skin quality and texture
Facial sagging and laxity
Loss of volume/contour deficiencies
Dynamic and static rhytids
Examination of face/neck at rest and with dynamic expression
Scars and/or acne scars
Pre-existing facial asymmetries/irregularities
Eyebrow/upper eyelid complex ptosis
Lower eyelid and cheek complex
Facial nerve evaluation/facial weakness
Cranial nerve examination
Muscles of facial expression: Assess strength and size.
Weight and height
Fitzpatrick skin type
Affect and psychologic presentation
Photo documentation
Informed consent process
Answer patient concerns/questions
Follow-up
Seeks nonsurgical options for rejuvenation
Has aging changes mostly related to volume loss and/or dynamic rhytids
Prefers minimal and/or no downtime
Understands value of periodic ongoing treatments to maintain and achieve best results
Dynamic rhytids
Static rhytids: Mild to moderate rhytids/younger patients
Brow shaping and sculpting
Facial sculpting
Wrinkle prevention
Known hypersensitivity to any botulinum toxin preparation components
Ongoing presence of infection at the proposed injection site(s)
Pre-existing neuromuscular disorders, such as peripheral motor neuropathic diseases, amyotrophic lateral sclerosis, or neuromuscular junction disorders (e.g., myasthenia gravis or Lambert-Eaton syndrome)
Pregnancy or lactation (category C)
Generalized muscle weakness
Uncontrolled systemic disease and/or patients in poor health
Pre-existing dysphagia or dysphonia
Breathing difficulties
Pre-existing cardiovascular disease
Presence of inflammation at the proposed injection site(s)
Baseline eyelid ptosis
Diplopia
History of excessive weakness or atrophy in the targeted muscle(s) to be injected
Unrealistic expectations
Psychiatric disease
Drug interactions: Aminoglycosides, calcium channel blockers
Recent administration of a different botulinum toxin preparation
Selection of neuromodulator (patient and physician preference, clinical situation)
Determine dose and volume to be injected
Reconstitution and preparation
Account for and/or limit other procedures performed at or around the time of injection (other nonsurgical injectable treatments, skin resurfacing procedures, surgical procedures).
Notification of any rash or infection near or at the planned injection site
Avoid blood thinning agents such as aspirin/NSAIDs, fish oils, vitamin E, herbal supplements, and/or alcohol a few days prior to treatment.
Continue prescribed medications, including medically necessary blood thinners.
Materials for mixing
21- to 25-gauge needles
Preservative-free normal saline
Digital camera
Wipes
Mirror
Topical anesthetic (benzocaine/lidocaine/tetracaine [BLT] or lidocaine mixture)
Gloves
30-gauge needle or tuberculin syringes
1-mL syringe
Alcohol pads (or other disinfectant skin preparations)
Bottle opener (to remove rubber stopper of vial)
Marking pen/pencil
Gauze pads (4 × 4 or 2 × 2)
Ice pack
Medical waste container
Vacuum-dried powder form in single-use 50-Unit or 100-Unit vials
2.5 mL of preservative-free 0.9% sodium chloride diluent to reconstitute each 100-Unit vial, yielding a concentration of 4 Units per 0.1 mL
Common off-label preparation
Preservative containing saline
Adjusting diluent quantity (1.0 to 4.0 mL) to yield the desired dose per 0.1 mL
Stored in refrigerator (2°C to 8°C) and administered less than 24 hours after reconstitution
Off-label storage: Multiple studies showing preservation of drug potency up to 2 weeks
Botox Cosmetic effect/timeline
Chemical denervation of the injected muscles within the first several days post injection
Clinical detectable relaxation of muscles from a few days to 14 days
Maximum clinical effect within the first 4 to 6 weeks
Duration of effect ranging from 3 to 4 months
FDA-approved indication/sites: glabella (2002), crow’s feet (CF)/lateral canthal lines (2013)
Off-label use in all remaining upper face, lower face, and neck areas
Potency units of different neuromodulators not interchangeable
Use 1:2.5 or 1:3 Unit conversion for Dysport and 1:1 Unit conversion for Xeomin.
Physician/injector preference
Recumbent
Semirecumbent
Sitting up
Topical anesthesia—lidocaine based
Nerve/intraoral blocks
Cooling devices—Zimmer
Possible vasovagal reaction
Muscles of facial expression and neck
Eyebrow position and shape
Bony orbit
Facial vessels
Injections of glabella/frown lines/11’s (corrugator/procerus muscles)
On-label FDA-approved glabellar indication: 4 Units injected intramuscularly into each of five sites, 2 in each corrugator muscle and 1 in the procerus muscle for a total dose of 20 Units ( Fig. 160.1 )
10- to 40-Unit range for desired clinical effect/relaxation of the glabella
Higher doses needed for active muscles and male patients
Injections of lateral canthal/CF lines (orbicularis oculi muscle):
On-label FDA-approved CF indication: 4 Units are injected intramuscularly into each of six sites, 3 on each side, into the orbicularis oculi muscle for a total dose of 24 Units ( Fig. 160.2 ).
Two variant patterns of injecting lateral canthal lines are provided in the trial (see Fig. 160.2 ).
10- to 30-Unit range for desired clinical effect/relaxation of the CF
Concurrent treatment of glabellar lines and lateral canthal lines can be performed with an on-label suggested dose of 44 Units.
Injections of horizontal forehead rhytids/lines (frontalis muscle):
5 to 20 Units injected intramuscularly into the frontalis muscle
Variable pattern and number of injection sites—individualize treatment
Counsel patients before injection regarding the possibility of brow position changes and brow ptosis.
Use in conjunction with treatment of orbicularis oculi to alter brow shape and position.
Injections for chemical browlift (orbicularis oculi/corrugators/procerus muscle):
5 to 20 Units total injected into the superolateral portion of the orbicularis oculi in the lateral third of the brow
Keep injections superior and lateral to the orbital rim to minimize ptosis.
May need to treat brow elevator to achieve desired brow height and shape
Can achieve a modest nonsurgical browlift of up to a few millimeters
Treatment of bunny lines (overactive procerus muscle):
Indicated for patients with excessive horizontal nasal lines
Can be unmasked by Botox treatment and relaxation of glabellar rhytids
In addition to treating the procerus, use small doses (1 to 2 Units Botox or 3 to 5 Units Dysport per side) injected directly over the bunny lines.
Injecting too low and lateral can affect the levator labii superioris.
Injections for “jelly rolls” in the lower eyelid (hypertrophied orbicularis oculi)
1 to 2 Units injected into the lower eyelid pretarsal orbicularis muscle
Decreases hypertrophied orbicularis muscle and increases the palpebral aperture
Reduced blinking can lead to corneal exposure and related symptoms.
Other potential complications include epiphora and edema of the lower eyelid.
Treatment of perioral lip lines (orbicularis oris), oral commissures (depressor anguli oris), and medial chin rhytids (mentalis muscles)
Can be used in conjunction with dermal fillers
Results are usually less dramatic and duration of effect shorter than those in the upper face.
Discuss the possibility of oral incompetence with your patient.
Contraindicated for patients who depend on use of muscles in perioral region (i.e., singers, musicians who play wind instruments)
Injections of perioral (vertical) lip lines (orbicularis oris):
Inject the orbicularis oris muscle in small amounts, maximum 1 to 1.5 Units Botox or 3 Units Dysport per site, two to six sites in the upper lip and two to four sites in the lower lips.
Stay close (within 5 mm) to the vermilion border.
Injections of oral commissures (depressor anguli oris muscles):
One to two injections (2 to 3 Units Botox or 6 to 9 Units Dysport) each side directly into the depressor anguli oris muscle overlying the mandibular body
Avoid injecting medial to the perpendicular line to the oral commissure.
Avoid injecting close to the mouth to minimize complications related to oral incompetence and/or lower lip ptosis.
Improves marionette lines and lifts mouth corners ( Fig. 160.3 )
Treatment of dimpled chin (mentalis muscle):
Two injection sites in a paramedian position near the inferior mandibular border: total of 2 to 8 Units Botox or 6 to 20 Units Dysport
Avoid injecting too far lateral or superiorly.
Treatment of gummy smile (depressor septi muscle):
Indicated for patients with with “gummy smiles” gingival show upon smile
Use small doses (total 1 to 3 Units Botox or 3 to 9 Units Dysport) injected just below the nose into the lip elevator complex (one to two injections).
As a nonsurgical treatment option for dynamic ptotic noses
Treatment of nasolabial folds (NLFs; levator labii superioris alaeque nasi muscle)
Patients with short upper lips and/or strong elevation of upper lip upon smile are potential candidates.
Use small doses (maximum 1 Unit Botox or 3 Units Dysport per side) injected just below the nose into the lip elevator complex and the levator labii superioris alaeque nasi muscle.
Advise patients that their smile pattern may be altered.
The area is best treated with dermal fillers.
Treatment of neck bands (platysma muscle):
Consider in older patients who are not candidates for surgery
Younger patients who are not candidates yet for facelift surgery
Patients with good skin elasticity and minimal submental fullness
Botox has no effect on skin laxity or redundancy, laxity, or adipose tissue deposits
Requires higher dosages than the lower face
Use 10 Units Botox or 30 Units Dysport per platysmal band.
Can inject multiple sites per band from the mandible to the lower neck, or inject the band only at the cervicomental angle to recreate it
Treatment of square jaw (masseter muscle):
Injected into the masseter muscle to alter shape of the jawline
Popular application in East Asian countries
10 to 25 Units Botox or 30 to 75 Units Dysport used per side (two to four injections)
Treatment effect may require multiple sessions, and treatment onset is slower but effects tend to last longer.
Adverse effects include mastication difficulty, muscle pain, dysarthria, and awkwardness with smiling.
Patients with Temporomandibular Joint Disorders (TMJ) and/or grinding tendency may benefit.
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