KEY NOTES CHAPTER 1: GENERAL PRINCIPLES (I) Lasers and Microsurgery Flashcards

1
Q

What does LASER stand for?

A

Light Amplification by Stimulated Emission of Radiation

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2
Q

What wavelength is the visible part of the electromagnetic spectrum?

A

Visible part of electromagnetic spectrum = 400nm (blue) to 700nm (red).

Invisible wavelengths:
∘ Shorter wavelengths (higher energy) – UV, X-rays, γ-rays.
∘ Longer wavelengths (lower energy) – infrared, microwaves, radio waves.

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3
Q

What is stimulated emission?

A
  • An atom in its resting state is composed of a nucleus and circulating electrons in their ground state.
  • Adding energy to an atom causes electrons to shift into a higher energy, unstable orbit.
  • The excited electron falls back to more stable ground state, and releases a photon of light of specific wavelength to that atom.
  • If that photon collides with another excited electron, that electron returns to its ground state, releasing another photon.
  • The original photon is not absorbed, so there are now two photons of the same frequency.
  • These photons are in phase.
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4
Q

What is light amplification?

A
  • As photons hit other excited electrons, more photons are released and the light energy increases.
  • Population inversion occurs when majority of the molecules in the laser exist in an excited state.
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5
Q

What is the structure of a basic laser?

A
  1. An external power source, e.g. flash lamp, diode, radiofrequency emission.
  2. A lasing medium:
    – Solid, e.g. ruby crystal, Neodymium:YAG, Erbium:YAG, KTP.
    – Gas, e.g. CO2, argon.
    – Liquid, in dye lasers.
  3. Reflective mirrors at each end of a laser tube.
    – Photons hit mirrors and are reflected back into lasing medium, number of photons that travel back and forth between mirrors increases, parallel to the tube.
    – 1 mirror is only partially reflecting. Light is allowed to escape from the tube as a beam of laser (can be focused with a lens).
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6
Q

What is Q-switching?

A
  • Q-switched laser uses two fully reflective mirrors.
  • Stimulated emission of light cannot escape and high power is generated because of a large population inversion.
  • Q-switch dumps entire contents of the chamber, producing a short pulse of high intensity.

∘ A normal laser releases its energy like water escapes from a bath through the plughole.
∘ A Q-switched laser releases its energy like if the bottom of the bath was suddenly removed, dumping all the water at once.

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7
Q

What are the properties of laser light?

A
  1. Collimated: minimal divergence
  2. Monochromatic: 1 wavelength.
  3. Coherent: peaks and troughs of laser light waves are in phase.
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8
Q

How does laser react with tissue?

A

• Causes thermal, chemical, or photoacoustic effects.

When laser light hits tissue it can be:
∘ Reflected
∘ Scattered
∘ Absorbed (& causes biological effects)
∘ Transmitted.

A specific wavelength of laser light will be preferentially absorbed by a target chromophore e.g. water, Hb, melanin.

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9
Q

What are the thermal effects of laser?

A
  1. Coagulation
    – Light absorbed by a target chromophore is converted to heat.
    – Coagulation occurs when tissue containing the chromophore reaches 60 ∘C.
  2. Vaporisation
    – Tissue heated to 100 ∘C will vaporise.
  3. Selective photothermolysis
    – Thermal damage is induced in a tissue target that absorbs light of a specific wavelength.
    – Selectivity occurs when exposure time of tissue to laser light is shorter than thermal relaxation time (TRT).
    – TRT = time taken by a specific volume of tissue to dissipate 51% of the energy absorbed.
    – Heat energy dissipated to surrounding non-target tissues can cause collateral effects.
    – Once the TRT has elapsed, another pulse can be delivered to the target without generating
    thermal damage to surrounding non-target tissue.
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10
Q

What effect does cooling have on laser treatment?

A
  • Cooling protects superficial non-target tissue, e.g. epidermis, from collateral thermal damage.
  • Allows higher energy levels to be used.

• Four basic methods:

  1. Bulk pre-cooling – epidermis and dermis cooled prior to pulse delivery.
  2. Dynamic pre-cooling - epidermis cooled prior to pulse delivery.
  3. Parallel cooling – epidermis cooled during pulse delivery.
  4. Post-cooling – epidermis and dermis cooled after pulse delivery.

• e.g. cryogen spray, gliding window handpiece, cold handpiece, cold air, cooling gel.

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11
Q

What variables are used to control lasers?

A
  1. Wavelength
    – Measured in nanometres (nm); specific to lasing medium.
  2. Power
    – Measured in Watts (W) or Joules per second (J/s).
  3. Spot size
    – Measured in cm2.
    – Larger spot sizes show less scatter and penetrate deeper.
  4. Duration of action (pulse width)
    – Measured in fractions of a second.

Variables 2-4 used to calculate:
∘ Power density: energy delivered per unit area of incident tissue (W/cm2).
∘ Fluence: product of power density and exposure time (J/cm2).

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12
Q

What are the clinical applications of laser?

A
Vascular lesions (Oxyhaemoglobin) 
Pulsed Yellow Dye Laser 585
KTP 532
Nd:YAG 1064
IPL* N/A

Skin resurfacing (Water)
Er:YAG 2940
CO2 10,600

Pigmented lesions (Melanin)
Diode 800
Ruby 694
IPL* N/A

Hair removal (Melanin) 
Alexandrite 755
Diode 800
Nd:YAG 1064
Ruby 694
IPL* N/A

Tattoo removal
- Black/blue/green
Q-switched ruby 694
Q-switched alexandrite 755

  • Black
    Q-switched Nd:YAG 1064
  • Red/orange/brown
    Q-switched Nd:YAG 532
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13
Q

What are the key points in laser safety?

A

Control of Artificial Optical Radiation at Work Regulations 2010: medical lasers are class IV.

Risks: retinal and cutaneous burns.

∘ Risk awareness through risk assessment.
∘ Cover reflective surfaces.
∘ Eye protection.
∘ Laser key stored away from machine.
∘ Corneal eye shields if Rx around eyes.
∘ Laser-safe ET tube with CO2 laser.
∘ Plume evacuators for e.g. CO2 laser, to prevent inhalation of live virus particles.

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14
Q

How is collateral damage of surrounding tissue prevented?

A

Duration of exposure of the laser must be equal to or shorter than the thermal relaxation time of the chromophore target.

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15
Q

How do you classify lasers in terms of mechanism of action?

A

Ablative and non-ablative.

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16
Q

What are the 2 main types of ablative lasers and what are their effects on the skin?

A

CO2 laser
Erbium:YAG laser

The goal is to

  • vaporize superficial epidermal tissues and
  • cause thermal coagulation deeper tissues
  • without causing scarring.

• Areas of irreversible and reversible damage are produced, both of which produce inflammation and wound healing.

17
Q

How does CO2 laser work?

A
Wavelength: 10,600nm
Chromophore: water
Depth of ablation: depends on:
- no. of passes
- cooling time b/t passes.
Clinical endpoint: pale yellow skin surface (midreticular dermis)
Risks
• 3-6mths erythema
• hypopigmentation
• erythema
• hyperpigmentation (reduced by adding hydroquinone, kojic acid and sunscreen postop)
• Milia
• Acne exacerbation
• Superficial infection
• Stimulation of herpes simplex flare-ups
• Hypertrophic scarring 
• Ectropion
18
Q

What are the absolute contraindications?

A

Active viral, bacterial, fungal infection.

Isotretinoin use within 12mths.

19
Q

How does fractionated CO2 laser work?

A
  • Combines fractional photothermolysis with ablation.
  • Pulse delivered in evenly spaced “pixilated” pattern (microthermal zones - MTZ).
    • Supplies dermal coagulative energy without confluent epidermal damage
    • Rapid reepithelialization and dermal reconstruction occurs from unaffected cells within
    punctate zones of injury.

Indications

  • facial rhytids
  • actinic damage
  • scarring

Therapy is guided by proper selection of coverage density and energy settings, not clinical
endpoints as with CO2 laser.

20
Q

How does the Erbium:YAG laser work?

A

Wavelength 2940nm
Chromophore: water
Less thermal diffusion than CO2
Energy absorbed 12-18x more efficiently than CO2
Provides 3-5 mm of ablation per pass
Generates 20-50 mm of thermal damage
Clinical endpoint: punctate bleeding, fragmented dermis appearance.

Indications: epidermal/dermal lesions, mild acne scars and AK, subtle dyspigmentation.

  • less depth of penetration
  • shorter recovery time
  • 5.5 days to re-epithelialise
  • 3-4wks erythema
21
Q

What are the non-ablative lasers?

A

Fractional resurfacing
Nd: YAG
IPL

22
Q

How do non-ablative lasers work?

A

Heat generated in dermis causes inflammation, collagen reorganization, and new collagen generation, thus tightening and rejuvenating skin
Does NOT vaporise epidermis.

23
Q

What is fractional resurfacing?

A

Wavelength: 1.5 microm
Penetration: 300 microm
Chromophore: Blue dye is pixilated onto skin and this acts as target (MTZ).
About 13-17% of face is treated each time.
Requires 4-5 treatments
Less downtime, but less noticeable results than ablative.
Suitable for: dyschromia, fine wrinkles (neck, chest, hands, face).

24
Q

What is Nd:YAG laser?

A

Neodymium:yttrium-aluminum-garnet laser

Wavelength 1064nm
Non-specific absorption and heating of tissue
Chromophores: Proteins (Blood vessels, RBC, collagen, and melanin) and water
Due to scattering of laser, area of greatest photon density is 1-2mm below skin (in dermis)

1320 nm Nd:YAG laser targets water.
- Requires cooling to prevent blistering

Overall collagen remodelling and neocollagenesis is less than ablative, but there is no crusting, oedema and prolonged erythema.

25
Q

What post treatment care is required?

A
Warn patients about appearance.
Moist wound healing:
- liquid based ointments
- acyclovir
- antibiotics
\+/- antifungals, steroids
\+/- Vit C cream
\+/- Hydroquinone, kojic acid, and sunscreen to prevent hyper pigmentation.
26
Q

What is IPL?

A
  • IPL is not laser
  • It emits photons 500-1300 nm
  • Chromophore: water and hemoglobin at 550-580 nm, superficial pigment at
    550-570 nm, and deeper pigment at 590-755 nm (filters used to exclude other wavelengths).
  • Apply topical anaesthesia
  • Downtime 24hrs
  • Sunblock.
27
Q

What are the indications and contraindications of IPL?

A

Indications
• Hypervascularity (flushing, telangiectasias, or rosacea) - 50-75% success rate.
• Hyperpigmentation (solar lentigines, melasma, or freckling) - 40-60% success rate.
• Improvement of skin texture
• Decrease pore size

Contraindications
• Unrealistic expectations
• Tanned skin
• Hypersensitivity to sunlight
• Photosensitizing medications
• Active isotretinoin (Accutane) treatment
• Therapeutic anticoagulation medications
• Pregnancy
• Active lupus
• History of wound-healing problems
• Skin cancer
• Fitzpatrick VI skin type (Fitzpatrick V is a relative contraindication.)
28
Q

What are the potential side effects of IPL?

A
prolonged redness, 
transient speckling of pigmentation, 
scabbing, 
edema, 
hair loss, 
purpura, 
hyperpigmentation, 
hypopigmentation, 
herpes eruption, 
infection, and 
scarring