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and forefinger during local anesthesia infiltration,

laser energy delivery, and lipoaspiration. Limiting

exogenous water infiltration to 3 mL minimizes

distortion of the anatomy during treatment and fa-

cilitates endpoint identification but also limits

thermal confinement. The fatty tissue ablation

efficiency of the micropulsed 1444-nm Nd:YAG

interstitial fiber laser, however, enables sufficient

local tissue effect with preserved thermal confine-

ment within the suggested total energy usage

parameters.

The local anesthetic mixture that the author fa-

vors includes 0.5% lidocaine; 0.25% Bupivacaine

hydrochloride; and 1:200,000 epinephrine and

hyaluronidase, 2 to 4 IU per mL (eg, Hylenex re-

combinant, Halozyme Therapeutics, San Diego,

CA, USA). Initially, approximately 1.0 mL of this

local anesthetic mixture is used to provide anes-

thesia to the percutaneous entry site and the

intervening tissue toward the LAFC treatment

zone as well as a field block that includes the tis-

sue for debulking and contouring. A narrow (eg,

21-gauge) multihole infiltration cannula is then

used to deliver 3 mL of local anesthetic to the

LAFC treatment area.

With the thermally confined micropulsed

1444-nm Nd:YAG interstitial fiber laser, energy de-

livery occurs via a 600-

m

m silica multimode fiber

with the fiber used either free (bare) or assembled

with a disposable or nondisposable cannula. Prior

studies have demonstrated general safety guide-

lines for energy delivery during LAFC of the lower

face when using the micropulsed 1444-nm

Nd:YAG interstitial fiber laser and minimal volume

local anesthesia (dry technique)—typical parame-

ters include power 5.4 W, pulse energy 180 mJ,

pulse duration 100

m

s (fixed), pulse rate 30 Hz,

and total energy delivered 200 to 300 J.

1,7

Although the unique thermal signature of the

micropulsed 1444-nm Nd:YAG interstitial fiber

laser enables safe treatment without the need for

internal or external temperature monitoring, it is

important to keep the fiber continuously moving

through the tissue during active lasing—this facili-

tates even distribution of laser energy and limits

the potential for clinical thermal confinement fail-

ure. Certainly some latitude exists with regard to

these treatment parameters; however, in a prior

study of mid- and lower face LAFC, complications,

such as prolonged inflammatory edema and over-

correction, were associated with faster energy de-

livery (40 Hz) and with a doubling of the total

energy delivered (eg, 500 J).

1

Immediately after

energy delivery, a similar volume (eg, 3 mL) of

room temperature sterile saline is infiltrated into

the treatment area as a postcooling or thermal

quenching step that attempts to minimize collat-

eral thermal spread to adjacent tissues as well as

reduce PIE.

Removal of emulsified tissue and liquefied fat via

manual lipoaspiration with a small dual port aspira-

tion cannula (eg, 19 gauge) and a 6-mL syringe

(prefilled with 1-mL sterile saline) enables definitive

tissue contouring.

Fig. 2

shows the full minimal

instrumentation requirement for LAFC. It is not un-

common for a small-diameter aspiration cannula

to become blocked with fibrous tissue during

lipoaspiration—when this occurs, the cannula is

Fig. 1.

(

A

) Preoperative view of LAFC treatment area with lower facial fullness and jowling in a 58-year-old

woman in upright seated position. (

B

) Intraoperative view of LAFC treatment area in the same patient in 20

reverse Trendelenburg position. LAFC treatment zone is outlined with purple marker. LAFC entry site is located

approximately 2 cm posterior to inked posterior extent of LAFC treatment zone and 2 cm above the caudal

mandibular margin. The 600-

m

m bare laser fiber is present at the LAFC entry point and the red aiming beam

at the fiber tip is seen faintly between the surgeon’s gloved thumb and index finger. Note that the laser fiber

is engaged in fatty tissue at the superior extent of the jowl fat compartment.

Holcomb