Botox Workshop2003.pdf

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    Botox WorkshopBy:

    Moustafa AbouzaidProf. Dermatology & Andrology

    Faculty of medicineAzhar University

    Cairo Egypt2011

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    Clostridium Botulinium

    A gram positive,

    Spore-forming,

    Obligate anaerobic bacillus

    Produces the most potent neurotoxins ,causing Botulism.Latin name: Botulus (black sausage)

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    There are seven distinct antigenic toxins.:

    1. BTX A,2. B , C ( C & C ),3. D,4. E,5. F &6. G

    BTX-A is the most potent.

    All are produced by different strains of clostridiumbotulinum.

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    There are three forms of human botulism:

    1. Food-borne (improperly preserved food containing

    the preformed neurotoxin).

    2. Infantile (ingestion of spores and production of thetoxin in infant's intestine).

    3. Wound infection

    Botulism

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    History

    1820.

    First

    collected

    data onbotulism

    1895.

    Theanaerobicbacterium

    was isolated

    1922.

    Theextracellular

    toxin (crudeform) wasisolated

    1930

    Thecrystalline

    (purifiedform) wasdeveloped

    1946

    BTX(clinicalproduct )

    1973Animal

    experiments

    onstrabismus(Published).

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    The cosmetic useof botulinium

    toxinBy Jean Carruthers

    in 1987.

    FDA approved use

    in adultstrabismus andblepharospasm in

    1989.

    BTX for blockingcholinergic

    innervations tosweat glands forhyperhidrosis

    1994 .

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    2) Ophthalmological use1- Strabismus2- Blepharospasm3- Nystagmus

    Clinical uses of Botox:

    Hemifacial spasm Facial asymmetry Oromandibular dystonia Spasmodic dystonia Cervical dystonia

    BTX-A was found safe and effective for:

    Spasmodic torticollis Achalasia Gustatory sweating Hyperlacrimation Synkinesia

    1) Neurologic use and excessive muscle activity

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    3) Dermatologic use Hyper functional glabellar frown lines,

    crow's feet & f orehead lines Brow ptosis and brow position Nasal scrunch and flare Upper lip wrinkles Marionette (sad lines ) Platysmal bands Palmar and axillary hyperhidrosis

    4)Others uses: Anal fissures Pain management

    Headache

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    Glabellar frown lines

    Crow's feetForehead lines

    Marionette (sad lines )

    Platysmal bands

    Nasal scrunch and flare

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    Temporary improvement in

    the appearance of moderate to severe Glabellar lines

    Fore head line

    Crows feet

    Adults 65 years

    Indications for

    Botulinum Toxin Type A

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    Administering physicians1. Be well trained

    2. Have knowledge of muscles controlling facialexpression

    3. Should know the dynamics of aging

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    The face and ageing

    Ageing

    Skin loseselasticity and

    becomesthinner

    Habitualexpressions &

    constantmusclecontraction or

    relaxation

    Wrinklesand

    creases

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    Cosmetic Uses of BTX

    Basic applications Horizontal

    forehead lines Glabellar frown

    lines Lateral and

    medial brow lifts Crows feet

    Advanced and otherapplications

    Nasal scrunch and flare

    Upper lip wrinkles Marionette (sad) lines Neck lines Platysmal bands Facial asymmetry Hyperhidrosis

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    Why Botulinum Toxin?

    Botulinum Toxin Type A is a therapeutic agentthat improves dynamic facial lines by targetingthe underlying responsible muscles

    Mechanism of Action It works by blocking acetylcholine impulses that

    trigger hyperactive muscle contractionsResult: CHEMICAL DENERVATION

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    Neurotransmission

    Neurons are specialized cells that

    receive and transmit nerve impulses.

    Dendrite

    Soma/cell

    Axon terminaland synapse

    Axon

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    Neurotransmission

    Nerve impulses are conducted betweenadjacent cells across synapses, via the release of neurotransmitters.

    Acetylcholine

    Muscle

    Axon

    Axon branch

    Muscle cell

    Motor end plate

    Axonterminal

    Axon terminal

    Axon

    Neuro-muscular

    junction

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    The facial muscles muscle basics

    Nerve impulse

    Relaxed

    Contracted

    Body Muscles to

    Move

    Facial Muscles toGive our Features

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    Botulinum Toxin

    Type A :Mechanism of Action

    Adapted from: dePaiva et al. PNAS 1999, 96:3200

    1 2 3

    4 5

    Binding Internalisation Blocking

    formation of thecollateral nerve sprouts

    The sprouts retract andthe original nerve end

    starts to work normally

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    Diffusion Description

    Particles of greater molecularweight diffuse more slowlythrough an aqueous mediumthan do smaller molecules so

    long as charge and temperatureis the same

    (Ficks first law, Fick 1855)

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    Why is diffusion important?

    Desired (larger molecule size) Needed for maximum local effect Access motor nerve terminal (NMJ)

    Distribution within target muscle to reach nerve

    terminal Not desired (smaller molecular size)

    Excess local weakness Pharmacological effect on adjacent muscle

    Distal weakness / dry mouth etc. Leakage from target muscle leads to spread via

    blood stream

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    BOTOX: Vial Dilutions

    Saline diluentvolume

    U/mL U/0.1 mL

    1.0 mL 100.0 10.0

    1.5 mL 66.7 6.72.0 mL 50.0 5.02.5 mL 40.0 4.03.0 mL 33.3 3.34.0 mL 25.0 2.5

    5.0 mL 20.0 2.0Only in axillary hyperhidrosis

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    Dosage and Administration

    Reconstitution Reconstitute with 0.9% sterile , non-preserved saline

    Use 2.5 cc 5 cc syringe to draw saline solution

    Insert at 45 angle and inject saline into Botulinum ToxinType A vial

    Discard vial if vacuum doesnt pull diluent into vial Record date of reconstitution

    Store reconstituted Botulinum Toxin Type A in a refrigeratorand use within 2 hours in room temperature

    All details above refer to BOTOX

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    Administration

    Remove syringe used for reconstitution and useinsulin syringe with built-in 30-gauge needle.

    Draw 0.5 mL into syringe and expel air bubbles

    NOTE: In practice, it has been reported that:

    Refrigerated vial without diluent remainseffective indefinitely

    Efficacy maintained following reconstitution

    Refrigerated and use it

    for up to 4 weeks

    Dosage and Administration (cont)

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    Considerations for Treatment Botulinum Toxin Type A is contraindicated for the

    following patients: Patients with infection at proposed injection site

    Patients with known hypersensitivity to any ingredient in Botulinum Toxin A

    Administration of Botulinum Toxin Type A is

    not recommended during pregnancy

    Co-administration with aminoglycosides or other agents interferingwith neuromuscular transmission should be performed with caution

    The most common side effect s are injection-related andare transient are localized pain, tenderness &/or bruising

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    Injection Considerations

    Photograph the patient before injection. Instruct patient to animate to show

    muscle activity Mark injection sites Use 30-gauge needle for comfort Inject into relaxed muscle Instruct patient to animate repeatedly

    post-injection to maximise toxin absorption(2 - 4 hours) Provide patient with post treatment

    instructions

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    Follow-up

    Pre-injection photos

    Inform patients to return in 1-2 weeks forevaluation Compare results with Pre-injection photos

    Correct any asymmetries / complains Set re-injection schedule

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    Anatomy of the face

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    Frontalis

    Depressor supercilii Corrugatorsupercili

    Procerus

    Orbicularis oculi

    Depressor labii inferiorus

    Depressoranguli oris

    Orbicularis oris

    Zygomaticus minor

    MentalisPlatysma

    BuccinatorRisorius

    Zygomaticus major

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    CorrugatorSupercilii

    Procerus

    Frontalis

    Orbicularis

    Oculi

    Key Muscles of the Upper Face

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    Glabellar Aesthetics

    Depression of the central

    brow appears angry, sad,

    Brow elevation appearsserene and calm

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    Sites for Glabellar Injection

    X

    X X

    X X XX

    Saline diluent U/mL U/0 1 mL

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    5 injection sites: 1 in procerus 2 in each corrugator

    Total dose: 20 U (4 U/injection

    site) 0.1 mL/injection

    site (in case of 2.5mL dilution)

    Carruthers A, Lowe NJ

    CorrugatorSupercilii

    Procerus

    volumeU/mL U/0.1 mL

    1.0 mL 100.0 10.01.5 mL 66.7 6.72.0 mL 50.0 5.02.5 mL 40.0 4.03.0 mL 33.3 3.34.0 mL 25.0 2.5

    Dosing

    T i l B t li T i T A (BOTOX )

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    Typical Botulinum Toxin Type A (BOTOX )Doses for the Female Glabellar

    4

    444 4

    Corrugator

    Supercilii

    Procerus

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    Procerus injection - massage

    Firm upward pressure is used to move the BotulinumToxin Type A upward & outward toward depressor

    supercillii

    Flynn 2001

    Gl b ll I j i T h i

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    Glabellar Injection Techniques

    Thumb of non-injectinghand protects orbital rim

    Hand rests on patients faceto control the injection

    Injections must be 1 cmaway from orbital rim

    Flynn 2001

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    Decrease in Glabellar Lines after Treatmentwith Botulinum Toxin Type A

    Baseline Day 30

    Unretouched clinical trial photos taken while frowning beforeBotulinum Toxin Type A and after Botulinum Toxin Type A . Individual

    results may vary .

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    The frontalis muscle ends

    midway between thelateral and mid-brow.The orbicularis - oculi

    depresses the portion of

    the brow lateral to this.Injection of 2- 4 Mu of

    Botox just below thelateral brow and lateralto the temporal fusionline can raise the lateralbrow, giving the patient a"chemical" brow-lift of

    up to 2mm.

    Lateral Brow Lifting

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    Complications of glabellar injections

    Brow ptosis, occurs when toxin affects the frontalis, asthe toxin spread 1-1.5cm (2-3cm in diameter)

    Avoid injecting the glabella and whole forehead in one sessionespecially in patients with low-set brows, mild brow ptosis andpatients over 50 years (preinject the brow depressors).

    Patient is advised to remain upright for 2 hours .To exercise muscles for the first 2 hours.Avoid rubbing or massaging for 2 hours.Responds to apraclonidine ( -adrenergic agonist) ophthalmiceye drops (2 drops / hour).

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    Eyelid ptosis, when toxin migrates to

    upper eyelid levator muscle, producing aweak paralytic effect as early as 48 hours oras late as 14 days and persisting for 2-12

    weeks.

    Avoid injection no closer than 1cm above thecentral eyebrow .Bothersome ptosis is treated byapraclonidine.

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    Crows Feet

    Superficial rhytides radiatingfrom the region of the lateralcanthus

    Represents dynamichypertrophy of the orbicularisoculi coupled with static skinchanges

    Coordinates with the smi le

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    BOTOX: Crows Feet (cont)

    xx

    xx

    Optimum dose 10 to 12 units per side

    Saline diluentvolume

    U/mL U/0.1 mL

    1.0 mL 100.0 10.01.5 mL 66.7 6.7

    2.0 mL 50.0 5.02.5 mL 40.0 4.03.0 mL 33.3 3.34.0 mL 25.0 2.5

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    BOTOX: Crows Feet

    Optimum dose 10 to 12 units per side

    Second treatment gave greater improvementand longer duration

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    BTX: Crows Feet

    After BOTOX

    Before BOTOX

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    BOTOX : Infraorbital Creases

    Test skin laxity with asnap test

    1-2 U of BOTOX

    Lid margin in linewith the pupil

    Lid margin slightlylateral to themidpoint betweenpupil and lateralcanthus

    xx

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    A more wide-eyed look can be obtained by injecting thelower eyelid at the lash margin by 2MU at mid pupil and2MU midway between pupil and outer canthus, some use

    the first injection only.

    This also helps smooth out fine lines under eyes.Do not do if patient exhibits a significant degree of scleralshow pretreatment, or had significant surgery under the eye,or if has a great deal of redundant skin under eye asexhibited by the snap test of the lower eyelid

    X X

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    Infraorbital Creases

    Before BOTOX After BOTOX

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    Reported complications of this area are :

    Diplopia (cover eye) and send to ophthalmologist

    Ectropion or a drooping lateral lower eyelid

    Strabismus (send to ophthalmologist)Bruising

    An asymmetric smile caused by the toxin diffusingto the zygomaticus major

    Transient lymph edema

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    Horizontal Forehead Lines

    Horizontal lines andwrinkles across theforehead

    Produced by excessive

    contractions of thefrontalis

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    BOTOX: Horizontal Forehead Lines

    x x x x

    For forehead 4-6 injections (a total of 10-20MU ) are placedacross the forehead in a uniform grid, visible blebs are temporarilyproduced. The lateral most injection should be vertically above themid-pupil, although with a wider forehead this can be extendedbeyond the pupil to the iris.

    Saline diluentvolume

    U/mL U/0.1 mL

    1 0 L 100 0 10 0

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    x x

    xxx

    xxx x

    4-6 injections (A total of 10-20MU)

    1.0 mL 100.0 10.01.5 mL 66.7 6.72.0 mL 50.0 5.02.5 mL 40.0 4.03.0 mL 33.3 3.34.0 mL 25.0 2.5

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    x

    x x

    x

    x

    xx

    x

    4-6 injections (A total of 10-20MU)

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    BTX: Horizontal Forehead Lines

    Before BOTOX

    After BOTOX

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    Botox (Botulinum toxin Type -A),Myobloc ( Botulinum toxin Type- B),

    Dysport (Abobotulinumtoxin-A)

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    Follow-up

    New patients to return in 1-2 weeks for evaluation Compare results with pre-injection photos Correct any asymmetries / complains Set re-injection schedule

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    - Regardless of botulinum toxin is chosen;- Follow the following tips to reducethe risk of both pain and bruising

    Injection Pearls

    American Society of Dermatologic Surgery in Orlando, Florida,

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    THE MORE NEUTRAL PHAND THE BENZYL ALCOHOLDECREASE THE LESS THE STING OF

    INJECTION.

    1-Dilute with saline containing preservative

    By pulling the skin toward the needle and pinchingthe skin lightly between the thumb and first finger(because the pressure sensation of the pull

    overrides the sensation of pain).

    2-Reduce the pain of the needle stick

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    4-PLACE A WARM TOWELON THE FACE BEFORE

    APPLYING TOPICAL ANESTHETIC

    TO INCREASE THE ABSORPTION AND EFFICACY OF THEANESTHETIC.

    3-Limit injections tono more that 4 per needle, after which the needle

    starts to dull.

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    5-TO MINIMIZE BRUISING,

    Request that patients stop all Aspirin or Nonsteroidal anti-inflammatory drugs, Vitamin E, Ginkgo biloba, And garlic

    14 days before botulinum injections .

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    6- For periocular areas, Consider precooling to help vasoconstrict vesselsand thus reduce the chance of bruising.

    In addition, use a specialized vein light to helpvisualize vasculature and thus avoid disturbing it.

    7-To tamponade any oozing Use cotton-tipped applicators ; Apply ice

    packs afterward to minimize bruising risk .

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    Combination Therapy

    BOTOX can be combined with manycosmetic procedures:

    Fillers Ablative laser resurfacing Non-Ablative laser remodeling

    IPL Peels Facial Surgery

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    BOTOX + Ablative laser

    BOTOX decrease mechanical disruption of healingprocess post laser treatment, improving collagenremodeling.

    BOTOX

    will prolong the smoothing wrinklereduction effect of laser. Combination useful in crows feet, forehead and

    peri-oral areas. Inject BOTOX two weeks before ablative laser

    treatment.

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    BOTOX + Non-Ablative laser

    Specific lasers (1320nm, 1450nm & 1540nm). Existing lasers (erbium-YAG, ND-YAG, Q-switched,

    pulse-dye lasers) Radiofrequency technology (e.g. Thermage) BOTOX will improve and prolong the cosmetic

    smoothing results.

    Use BOTOX

    few days prior or post laser to preventincreasing diffusion due to thermal inflamation.

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    BOTOX + IPL

    IPL is used to stimulate collagen and elastinsynthesis, resulting in softening the facial finelines.

    Multiple sessions is needed to achieve this effect,usually 4-6 sessions. BOTOX will improve and prolong the cosmetic

    smoothing results. Use BOTOX few days after the first IPL session.

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    BOTOX + Peels

    Chemical peels produce controlled injury followedby the wound healing process which producessmoother skin.

    Selection of the right peel. Use BOTOX 2 weeks before peeling to prevent

    increasing diffusion due to inflammation. Microdermabrasion usually doesnt produce

    inflammation, so BOTOX can be injected rightafter this procedure.

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    BOTOX + Facial Surgery

    BOTOX and facial surgery have complementary effecton the aging face.

    Recent reports suggested that BOTOX can reduce thetension exerted on the skin by the healing process,

    resulting in reduced scarring. With blepharoplasty, relaxation of the local muscles

    can allow for accurate resection of the skin and betterplacement of the incision during the surgicalprocedure.

    Use BOTOX one week after surgery or at least threemonths before surgery.

    Botox and Hyperhydrosis

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    Procedure:1) Documentation of the problem :

    1- Gravimetric measurement or.

    2- The minor starch iodine test.First wiping the skin with a colored iodine tincture (must be brown-orange).

    Several seconds are given to allow the iodine solution to dry (fan).The area is then lightly dusted with ordinary baking cornstarchpowder.

    Botox and Hyperhydrosis

    Th l i f h i i i

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    The exact location of the active sweating isthen mapped and outlined with a marking

    pen before beginning injections.

    N.B. perform the test before applying any regional nerve blocks ortopical anesthetics like eutectic mixture of lidocaine (EMLA)(cause a hyperemic and a vasoconstrictive responserespectively interfering with the amount of sweating and can givemisleading results).

    Take a photo.

    B t d H h d i

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    2) Anesthesia:The axillary, forehead and facial sweating can be treatedwithout anesthetic or by topical anesthesia.

    Palmar and plantar with topical anesthesia , but mostpatients require regional nerve block anesthesia, such aswrist or ankle block.

    Disadvantages of nerve blocks ------ causes reactivehyperemia thus increasing the tendency to bleed from

    each small injection site, which may increase the loss of material from injection site and decrease the relativeeffectiveness of each injection.

    Botox and Hyperhydrosis

    Botox and Hyperhydrosis

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    3) Injection technique:

    Dilution

    5 ml saline + 1 vial BTXUse 10 syringes ( 5 for each axillae i.e. 2.5 ml for Rt.

    Axillae and 2.5 ml for Lt. Axillae).

    Withdraw 0.5 ml for each syringe.

    Inject 20 25 injections to every axillae i.e. 2 units for

    each injection

    Botox and Hyperhydrosis

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    For axilla, usually involves placement of 10-20

    individual intradermal injections (raising tinywheals) about 2.5cm apart , beginning at the periphery

    of the hair-bearing skin and circling into the centre of

    the axillary vault, keeping the needle bevel up andmore parallel to the skin surface.

    Approximately 50U/axilla ,

    duration of effect is

    approximately 4-10 months .

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    Focal Axillary Hyperhidrosis

    Before BTX-A After BTX-A

    Naumann Arch Dermatol 134 1998

    Botox and Hyperhydrosis of Palm & Sole

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    Palmar injections are placed approximately every1.5cm across the palmar surface. On the fingers the volarpad of each phalanx receives its individual dose. The fingertips usually receive two: one in mid pad and another at thevery tip. The dominant hand receives an extra row of injection along the ulnar side.

    The palmar skin is comparatively stiffer and a wheal cannot

    be raised, it is desirable to produce a small zone

    of visible blanching , indicating that the material isin the deep dermis . Allow a second or two beforewithdrawing the needle or else the fluid flows back out of injection tract directly.

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    C t & F f t t t

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    Patients with large shoe size have correspondinglylarger hands and require more injections, e.g. aman with a size 43-45 shoe requires up to150U/palm whereas a woman with a size 36 shoerequires as little as 75U to cover the palm .

    Inject approximately 120U/palm , duration of effectis 3-12 months (approximately 6 months).

    Treatment is approximately twice a year.

    Costs & Frequency of treatment

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    . 37 shoes size requires 1.5 vials for both palmsi.e., 150 Us( 75U/ each palm).

    . 38- 42 shoes size requires up to 2 vials for bothpalms i.e., 200 Us (100/ each palm).

    . 43- 45 shoes size requires up to 3 vials for bothpalms i.e., 300 Us (150/ each palm)

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    Injection of the soles follows the same technique and

    pattern as the palms.

    N.B. it may take several treatments before patient recognize

    less than total response as successful.

    Almost every patient develops a transient period of weakness and instability of the lumbrical muscles of the

    hand, which is predictably spontaneously reversible, patient

    can write, type and eat without difficulty, but opening up a

    tight jar lid for example poses problems for a few weeks (3-

    5). So, ma ybe treat one hand first then the second.

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    Thank you