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Journal of Cosmetic and Laser Therapy, 2011; 13: 142–153

ORIGINAL ARTICLE

Evaluation of mesotherapeutic injections of three different


combinations of lipolytic agents for body contouring

ZEKAYI KUTLUBAY

Lazerart Clinics, Division of Dermatology, Istanbul, Turkey


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Abstract
Background: There has been significant interest recently in the technique of mesotherapy as a method of ‘melting fat’ for
body contouring. Objective: The aim of this study was to evaluate the safety, efficacy and lipolytic potential of several com-
pounds commonly used in cosmetic mesotherapy. Methods: A total of 75 women (mean age: 33 years) were separated
randomly into three mesotherapy groups. Injections were performed for 15 treatments once a week. The main component
of each cocktail was phosphatidylcholine/deoxycholic acid for group 1, caffeine for group 2, and Conjonctyl® for group 3.
Outcome was evaluated by weight, body fat percentage (BFP), circumference measurements, and patient questionnaires.
Results: Seventy-two of all the patients (96%) showed a circumference loss. An average circumference reduction of 4.41 cm
per site for group 1, 2.99 cm for group 2, and 2.10 cm for group 3 was achieved. Mean body circumference loss was
statistically significant, with p ⬍ 0.00. Weight loss was 5.33 ⫾ 1.09 kg for group 1, 3.74 ⫾ 1.51 kg for group 2, and 2.82 ⫾ 1.43 kg
for group 3. Seventy-four subjects (98.7%) showed a BFP decrease. A questionnaire indicated high patient satisfaction (63%).
For personal use only.

No patient showed irregularities, dimples or any serious side effects after treatment. Conclusion: Mesotherapy is a well-tolerated
and effective alternative treatment modality for reducing the diameter of body circumference.

Key Words: body contour, cosmetic dermatology, lipolysis, mesotherapy

Introduction Mesotherapy is a minimally invasive technique


that consists of the intra- or subcutaneous injection of
Mesotherapy is a recently introduced treatment that
variable mixtures of natural plant extracts, allopathic
involves the delivery of pharmacologic drugs or sub-
medicines, homeopathic agents, pharmaceuticals, vita-
stances into the mesoderm, which is the layer of fat and
connective tissue under the skin (1). Mesotherapy using mins, enzymes, nutrients, antibiotics, hormones, and
different substances has been advocated by some to other bioactive substances in microscopic quantities
treat a variety of conditions as varied as chronic pain, through dermal multipunctures (1,5,6).
psoriasis, cellulite, weight loss, and local obesity con- Mesotherapy has been used for several years in
trol. In particular, mesotherapy has been advocated by Europe and South America for body contouring.
some physicians and used as a nonsurgical alternative Its introduction and application is about 10–15 years
to liposuction for several years. The pharmacologic in Turkey.
substances most frequently injected for body contour- Mesotherapy describes a technique by which mix-
ing are phosphatidylcholine (PC), deoxycholate (DC), tures of medications and other compounds are injected
isoproterenol, aminophylline, caffeine, L-carnitine, directly into a diseased area so that the systemic effects
buflomedil, calcitonin, and others. Despite the num- of oral or intravenous medications can be avoided (7).
ber of anecdotal reports and data suggesting that the The composition of common mesotherapy formu-
components of traditional mesotherapy formulations lations is selected and mixed in a ‘cocktail’ before
might be effective, this study performed a clinical trial injection (8).
to determine the effect of different mesotherapy cock- Mesotherapy is a non-surgical, relatively painless
tails on body contouring (2–4). injection technique with a broad range of applications.

Correspondence: Zekayi Kutlubay, Lazerart Güzellik Merkezi, Aytar cad. Aydın sok. Fırat i merkezi, D:10 1. Levent, Istanbul, Turkey. Fax: 90 212 3259676.
E-mail: zekayikutlubay@hotmail.com; zekayikutlubay@gmail.com

(Received 13 December 2010 ; accepted 14 May 2011)


ISSN 1476-4172 print/ISSN 1476-4180 online © 2011 Informa UK, Ltd.
DOI: 10.3109/14764172.2011.594059
Mesotherapeutic injections for body contouring 143

The true mechanism of mesotherapy remains unknown. hormone therapy or exercise plans were given to the
Mesotherapy promotes the body’s circulatory, lym- patients. They continued routine social activities. No
phatic, and immune system to create a biological res- other type of treatment of fat deposits (e.g. liposuction,
ponse and reverse abnormal physiology. Mesotherapy ultrasound, vigorous massaging) was allowed during
is a safe and effective alternative for the treatment of the study period.
cellulite, weight loss, hair loss (alopecia), and face and Exclusion criteria were pregnancy, breast-feeding,
neck rejuvenation. Mesotherapy is virtually painless, insulin-dependent diabetes, a history of strokes, recent
and requires no postoperative recovery time. Patients cancer, thromboembolic phenomena, patients on med-
notice an improvement in skin quality, less dimpling ications such as aspirin, warfarin, and heparin, patients
of the skin, and weight reduction, including a loss of with lymphedema or periodic swellings due to lym-
one to two clothing sizes (9). phatic problems, and an unrealistic expectation of the
The use of mesotherapy for body contouring, spot patient.
weight loss, and overall weight reduction typically Patients were separated randomly into three meso-
involves multiple injections of lipolytic agents into the therapy groups. Each group was composed of 25 patients.
area selected for contouring. Dermatologists have been Patients in each group were injected with different
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using similar injection techniques to treat alopecia mesotherapy cocktails (Table I). Group 1 patients were
areata, keloids and hypertrophic scars with steroids given a 15-ml cocktail made up of 5 ml of Lipostabil®
(3,6). Lipolytic stimulants are usually used for lipoly- N, 5 ml of normal saline, 3 ml of L-carnitene, and 2 ml
sis and the treatment of ‘cellulite’, which may be described of 2% procaine. The Lipostabil N brand (Artesan
as the cutaneous dimpling of the thighs, buttocks, and Pharma, Lüchow, Germany) contains 5% PC (50 mg/
hips seen predominantly in women. Each session may ml) and 4.75% deoxycholic acid (DC) (47.5 mg/ml)
involve up to several hundred injections administered with 0.9% benzoyl alcohol and saline. Group 2 patients
at various skin levels (epidermis, dermis, subcutaneous were given an 11-ml solution containing 5 ml of Cel-
layer) by syringe (5,8). lucare®, 5 ml of normal saline, and 1 ml of 2% procaine.
Despite the fact that there is very little scientific The Cellucare brand (Revitacare Laboratory, Saint
evidence sustaining its widespread use, the field of meso- Ouen l’Aumône, France) contains 250 mg of caffeine
For personal use only.

therapy and nonsurgical lipolysis has grown enormously and 20 mg of hyaluronic acid and trace elements:
in the past few years, becoming a common method in Mn-Zn-Co in a vial of 5 ml. Group 3 patients were given
cosmetic medicine. It gained recognition primarily in a 17-ml solution containing 5 ml of conjonctyl, 5 ml
pain management, sports medicine, and rheumatology. of chophytol, 2.5 ml of buflomedil, 2.5 ml of L-carnitene
Its use in cosmetic medicine to “eliminate cellulite, and 2 ml of 2% procaine.
reduce and contour fat, promote weight loss, treat aging Before the procedure, the patients did not use local
skin and redundant (sagging) skin, reduce acne scars anesthetic cream or an ice massage to reduce the level
and stretch marks and rejuvenate the hands and neck” of pain. The solutions were injected into the dermis
is gaining in popularity and acceptance (5). and subcutaneous layer – between 6 mm and 13 mm in
depth. The treatment was repeated in the same man-
ner once a week for 15 weeks.
In addition, weight and body fat percentages (BFP)
Materials and methods
were analyzed by Gaia 359 Plus™ (body composition
This randomized, prospective, clinical trial was carried analyzer; Jawon Medical, Kyungsan-City, Korea).
out on volunteers who had localized obesity and fat The size and location of the fat deposits were examined
deposits.The study included 75 women seeking weight and the circumference was measured. Perimetric cir-
loss and slimming (mean age: 33 years; range: 20–60 cumferential thickness measurements of 10 body sites
years) at a private clinic, between June 2007 and (i.e. upper belly, lower belly, waist, hip, right thigh,
February 2009. All the volunteers provided written left thigh, right calf, left calf, right knee and left knee)
informed consent and accepted the possibility of side were obtained before the application and 1 month after
or adverse effects, including infections, pain, bruising the 15th session of treatment. Measurements were
and an ineffective result associated with the procedure. obtained at a specific and consistent distance from an
Dietary modification, hormone replacement ther- anatomic bony landmark to ensure a consistent loca-
apy, exercise, and nutritional supplements are often tion, and the total and mean changes in body circum-
used in conjunction with mesotherapy. No specific diet, ference were calculated.To eliminate any interobserver

Table I. List of contents of the mesotherapy cocktails tested according to the groups.
Groups Content Total volume

Group 1 5 ml of Lipostabil® N 5 ml of normal saline 3 ml of L-carnitene 2 ml of procaine-2% 15 ml


Group 2 5 ml of Cellucare® 5 ml of normal saline 1 ml of procaine-2% 11 ml
Group 3 5 ml of Conjonctyl® 5 ml of chophytol-2% 2.5 ml of buflomedil-1% 2.5 ml of 2 ml of 17 ml
L-carnitene-20% procaine-2%
144 Z. Kutlubay

differences, the same nurse, who was blinded to this at the hips (5.35 cm), whereas the minimum loss was
study, measured the circumferences before treatment obtained at the left knees (1.89 cm) in all three groups
and at 1 month after the last mesotherapy session. Fur- (Tables II and III). The differences between the base-
thermore, a mean body circumference loss was deter- line and the after-treatment mean total body circum-
mined for each area, and these 10 parameters were then ferences were statistically significant for all three
averaged into a mean index of average overall loss. groups with p ⬍ 0.00.
In addition, photographs were taken before and after Circumferential reductions at the hip were achieved
the procedure to document the changes resulting from as 7.66 ⫾ 1.18 cm (minimum 5.8 cm and maximum
treatment. 10.4 cm loss) for group 1. It was 4.57 ⫾ 1.73 cm for
The surfaces were cleaned with alcohol before and group 2 and 3.83 ⫾ 1.81 cm for group 3.
after treatment. All the injections were performed man- Average circumference reductions of 4.41 cm per
ually by means of needles and syringes appropriate for site for group 1, 2.99 cm for group 2, and 2.10 cm for
mesotherapy. Each patient was treated by the same group 3 were achieved when comparing all of the mea-
dermatologist. sured body sites (Figures 1, 2 and 3).
The injections were performed in an outpatient set- After completing all of the sessions, 72 patients
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ting with the patient lying on the operating table. Using (96%) had lost weight and three patients (one in group
30-gauge needles of 13 mm in length, the cocktails 2 and two from group 3) had gained weight (mean gain:
were injected into the fat deposit following a multi- 1.1 kg) (Table III). Weight loss was 5.33 ⫾ 1.09 kg for
injection pattern. The amounts of cocktail injected group 1, 3.74 ⫾ 1.51 kg for group 2, and 2.82 ⫾ 1.43 kg
into each site ranged between 0.1 ml and 0.4 ml per for group 3.
application according to the individual needs of the
patient. The number of injections varied according Table II. ANOVA post-hoc pairwise comparisons.
to the size of the treatment area. Each session involved
up to 100 injections administered at various skin lev- D Paired
Group Before After (mean) SD p-values ANOVA
els with a separation distance of 2–4 cm.
Care was taken to respect the locations of the vas- Weight 1 66.07 60.70 5.33 1.22 0.00∗ 1–3∗
For personal use only.

cular and nervous systems to diminish the possibility (kg) 2 62.95 59.17 3.74 1.51 0.00∗ 1–2∗
of hematoma formation. 3 65.78 62.84 2.82 1.43 0.00∗ 2–3∗
BFP 1 29.43 24.76 4.66 1.09 0.00∗ 1–3∗
A questionnaire was given to the subjects to
2 28.40 25.13 3.28 1.20 0.00∗ 1–2∗
enquire about their experiences with mesotherapy. 3 30.41 28.26 2.16 0.86 0.00∗ 2–3∗
Results also were assessed subjectively by the patients Upper 1 90.60 85.82 4.78 1.21 0.00∗ 1–3∗
who completed a questionnaire that assessed the toler- belly 2 86.78 83.21 3.57 1.15 0.00∗ 1–2∗
ability and efficacy of the treatment. All of the women 3 88.07 85.53 2.54 0.98 0.00∗ 2–3∗
replied as to how much they were satisfied with the Lower 1 96.71 91.19 5.52 0.97 0.00∗
belly 2 88.93 85.22 3.70 1.56 0.00∗ 1–3∗
final results. A patient satisfaction score (A ⫽ not satis- 1–2∗
3 90.56 87.70 2.91 1.18 0.00∗
fied, B ⫽ somewhat satisfied, and C ⫽ highly satisfied) Waist 1 88.12 83.09 5.30 1.08 0.00∗ 1–3∗
was recorded after completion of treatment.The women 2 80.73 77.16 3.56 1.22 0.00∗ 1–2∗
were also asked whether they would recommend meso- 3 81.28 78.77 2.50 1.19 0.00∗ 2–3∗
therapy to others. At every visit any adverse effects Hip 1 105.36 97.70 7.66 1.18 0.00∗
2 100.06 95.48 4.57 1.73 0.00∗ 1–3∗
were recorded.
3 103.48 99.63 3.83 1.81 0.00∗ 1–2∗
Data are presented as means ⫾ SD. Pretreatment Right 1 61.25 57.27 3.98 0.62 0.00∗ 1–3∗
and post-treatment mean values for perimetric circum- thigh 2 55.80 52.92 2.88 1.01 0.00∗ 1–2∗
ferential thicknesses were calculated and then com- 3 59.60 57.56 2.04 0.84 0.00∗ 2–3∗
pared using the paired samples t-test. A value for Left 1 61.13 57.45 3.68 0.78 0.00∗ 1–3∗
p ⬍ 0.05 was considered statistically significant. The sta- thigh 2 55.61 52.81 2.79 0.98 0.00∗ 1–2∗
3 59.32 57.16 1.98 0.95 0.00∗ 2–3∗
tistical analysis was done by using ANOVA post-hoc
Right 1 50.41 46.91 3.50 0.62 0.00∗ 1–3∗
pairwise comparison and analysis of variance tests. calf 2 48.86 46.59 2.27 0.78 0.00∗ 1–2∗
3 50.61 49.07 1.54 0.56 0.00∗ 2–3∗
Left 1 50.48 46.82 3.65 0.73 0.00∗ 1–3∗
Results calf 2 48.68 46.25 2.44 0.92 0.00∗ 1–2∗
Seventy-two of all the patients (96%) included in our 3 50.67 49.28 1.40 0.78 0.00∗ 2–3∗
Right 1 39.60 36.63 2.97 0.77 0.00∗ 1–3∗
study showed a circumference loss, and the mean knee 2 38.41 36.38 2.03 0.61 0.00∗ 1–2∗
body circumference loss was statically significant for 3 40.09 38.94 1.14 0.58 0.00∗ 2–3∗
every measured body site, with p ⬍ 0.00. A body circum- Left 1 39.59 36.38 3.21 0.67 0.00∗ 1–3∗
ference increase was determined in only one patient knee 2 38.20 36.90 1.30 0.71 0.00∗ 1–2∗
in group 2 and two patients in group 3. The reason for 3 40.09 38.93 1.16 0.63 0.00∗ 2–3∗
this different response could be a lower sensibility of ∗Indicates significant differences.
the fat cells of these patients to these drug mixtures. D ⫽ difference; SD ⫽ standard deviation; BFP ⫽ body fat percentage.
The maximum mean circumference loss was obtained p ⬍ 0.05.
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Table III. Patient summary, overall treatment results.

Initials Group Age Weight (kg) – d bfp – d u belly – d l belly – d waist – d hip – d R thigh – d L thigh – d R calf – d L calf – d R knee – d L knee – d

I.A. 1 28.0 2.4 3.8 2.2 3.7 2.9 5.8 3.9 3.1 3.4 3.4 1.9 2.7
B.G. 1 29.0 4.6 4.3 4.2 5.6 4.6 7.6 3.6 2.8 2.2 3.5 2.8 2.3
F.T. 1 39.0 5.2 3.8 5.3 5.8 7.5 7.5 3.5 3.5 3.2 3.2 3.4 3.6
C.M. 1 46.0 4.9 6.8 3.3 4.3 4.6 6.4 3.2 3.2 2.6 4.5 3.3 3.6
A.V. 1 32.0 5.5 4.7 4.2 7.3 5.6 9.4 3.4 3.6 2.6 3.6 3.2 3.7
B.E. 1 34.0 4.5 4.3 6.4 6.8 6.6 10.4 3.2 3.0 2.6 3.8 4.4 2.7
G.A 1 35.0 5.2 6.4 5.3 4.8 4.6 9.7 4.3 4.3 4.6 2.5 2.6 3.5
A.B. 1 28.0 4.6 4.5 4.6 4.9 3.8 7.7 3.8 2.4 2.6 3.3 3.3 3.7
C.S. 1 27.0 8.5 5.7 6.3 6.3 5.4 7.1 4.2 3.7 4.2 4.7 2.7 4.3
A.K. 1 28.0 5.2 4.4 4.3 4.9 4.9 6.9 4.3 3.2 3.5 4.5 2.2 3.8
E.G. 1 33.0 5.6 3.6 3.8 5.6 5.2 7.2 3.3 2.7 3.7 3.9 2.5 3.5
S.K. 1 28.0 5.5 3.4 3.1 4.9 4.4 6.1 3.8 3.1 3.6 2.8 2.7 2.6
H.B. 1 40.0 5.2 4.6 5.2 5.1 5.1 8.3 3.6 4.2 3.9 3.3 3.3 2.6
Y.G. 1 36.0 6.3 3.5 3.8 4.1 3.6 7.6 5.2 4.2 4.2 3.5 3.2 1.6
M.D. 1 40.0 4.2 3.6 5.4 5.6 5.1 6.6 3.9 3.3 3.8 2.5 4.7 2.6
E.K. 1 28.0 5.4 3.8 2.3 3.8 3.5 6.7 4.4 3.2 3.4 3.4 2.8 2.8
A.B. 1 37.0 4.2 4.1 4.8 6.7 6.0 6.7 3.2 4.5 4.2 4.3 2.1 2.8
B.B. 1 30.0 5.3 5.3 5.3 6.6 6.1 8.3 4.4 3.2 3.6 3.8 2.5 3.5
A.E. 1 33.0 5.8 5.2 5.2 6.3 6.4 7.5 4.2 3.8 3.2 4.3 3.5 3.8
Y.T. 1 25.0 5.2 5.5 5.7 5.2 4.9 6.6 4.3 3.5 3.5 2.8 1.6 3.1
S.G. 1 52.0 6.2 4.6 6.2 5.7 4.6 9.6 4.4 5.1 3.2 2.9 2.4 2.4
K.O. 1 60.0 6.5 4.2 6.2 6.8 5.6 8.8 4.9 4.6 3.7 3.8 2.6 3.5
N.G. 1 34.0 4.8 4.5 5.3 5.5 4.3 7.4 3.1 3.4 3.9 3.1 3.5 3.7
S.K. 1 48.0 6.4 4.2 4.8 5.6 4.2 7.5 3.9 4.8 3.7 5.3 2.5 3.5
S.D. 1 35.0 6.1 7.8 6.4 6.2 6.3 8.1 5.4 5.5 4.4 4.6 4.5 4.4
N.K. 2 29.0 4.3 3.5 3.7 3.5 3.5 4.4 2.3 2.5 2.3 2.9 2.6 2.6
A.N. 2 36.0 3.2 2.9 4.2 4.8 3.9 6.3 3.8 3.2 2.3 2.1 2.1 1.8
M.A. 2 31.0 3.8 2.3 3.6 4.5 5.3 4.2 3.1 2.9 2.6 2.9 2.1 2.8
S.E. 2 39.0 3.9 4.4 4.1 5.5 4.1 4.6 3.3 2.6 2.2 2.4 2.5 2.5
M.O. 2 25.0 4.5 4.2 4.3 4.7 4.0 5.3 3.5 1.9 2.1 2.3 2.6 2.3
E.A. 2 25.0 3.3 3.5 4.2 4.3 3.2 5.0 3.3 2.3 3.6 3.5 2.3 2.5
F.E. 2 48.0 5.2 5.1 6.5 5.2 4.1 6.4 5.2 4.6 2.7 2.4 2.1 2.8
N.F. 2 26.0 4.3 3.5 4.8 4.3 4.1 4.4 3.3 3.4 2.2 3.1 2.7 2.7
N.Y. 2 36.0 4.2 5.5 3.3 4.4 4.6 5.2 3.4 3.2 3.2 3.4 2.6 3.3
S.O. 2 34.0 4.9 4.4 3.6 4.8 5.4 6.4 3.1 3.8 2.5 3.1 2.2 2.5
Y.O. 2 25.0 4.3 3.6 3.4 4.4 3.6 5.2 3.4 3.1 2.2 2.5 2.0 2.6
Y.A. 2 39.0 5.3 3.6 4.5 4.1 4.6 5.4 3.7 3.8 3.5 3.7 3.2 2.8
G.Y. 2 35.0 5.1 4.3 3.3 4.2 4.4 5.4 3.0 2.9 2.5 2.4 2.3 2.6
S.B. 2 35.0 6.8 4.1 2.9 3.8 4.4 5.9 3.3 3.2 2.3 2.9 2.2 2.6
S.S. 2 35.0 4.6 4.2 4.1 5.5 4.9 6.6 4.2 4.5 3.2 4.0 2.4 2.5
G.K. 2 54.0 2.3 2.5 2.6 2.7 3.2 2.4 1.2 2.3 2.9 2.8 1.5 1.2
Mesotherapeutic injections for body contouring

Y.G. 2 27.0 2.4 1.7 3.4 2.4 3.1 3.6 2.1 2.3 1.4 1.4 1.5 1.7

(Continued)
145
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146

Table III. (Continued)


Z. Kutlubay

Initials Group Age Weight (kg) – d bfp – d u belly – d l belly – d waist – d hip – d R thigh – d L thigh – d R calf – d L calf – d R knee – d L knee – d

Y.A. 2 34.0 3.6 2.9 3.6 4.9 3.1 4.4 2.7 2.9 2.9 2.6 2.3 1.4
J.B. 2 39.0 4.4 3.2 4.2 3.2 3.6 3.4 2.1 2.3 2.3 1.0 1.2 1.5
H.H. 2 40.0 3.2 2.8 3.5 4.0 3.4 5.2 3.4 3.2 2.2 2.6 2.0 1.5
A.H. 2 30.0 –0.8 0.3 0.2 –1.4 0.3 –1.9 0.3 –0.4 0.3 0.5 0.9 0.2
O.T. 2 29.0 1.3 0.9 1.8 1.2 0.8 3.1 1.6 1.7 1.1 0.8 0.9 0.5
P.A. 2 24.0 2.4 2.7 3.2 1.5 2.4 3.4 2.2 2.5 1.5 1.1 1.0 1.4
T.C. 2 23.0 2.7 2.6 2.1 2.3 2.1 4.7 2.1 2.5 1.1 1.6 1.2 1.5
T.K. 2 38.0 4.3 3.2 4.1 3.8 2.9 5.3 2.5 2.6 1.7 2.9 2.3 2.6
A.C. 3 27.0 3.1 2.4 2.3 2.5 3.2 4.4 2.2 2.8 1.4 1.2 1.7 0.9
M.S. 3 42.0 3.6 2.2 3.4 4.6 4.6 5.2 2.4 2.5 0.7 1.1 1.4 1.2
N.C. 3 36.0 3.6 3.2 3.5 3.1 2.2 3.6 2.7 2.2 1.9 1.2 0.9 1.3
S.E. 3 30.0 2.4 2.7 2.3 1.9 2.2 3.1 2.3 2.4 1.9 2.1 1.3 0.6
P.G. 3 24.0 3.2 2.3 2.8 3.0 3.4 4.6 1.6 1.5 1.1 1.1 1.0 1.2
T.A. 3 29.0 2.3 2.1 2.7 2.4 1.9 4.3 1.5 1.8 1.5 1.1 0.8 1.0
S.C. 3 36.0 3.3 3.1 2.4 3.5 3.4 4.9 3.4 2.4 1.7 2.9 2.4 1.3
T.K. 3 28.0 4.2 2.3 2.5 3.5 2.8 4.5 3.2 2.3 2.6 1.5 1.0 0.9
N.E. 3 25.0 4.7 2.9 3.6 4.0 3.2 5.9 2.3 3.0 2.2 2.5 1.4 1.5
D.M. 3 24.0 –1.1 0.5 0.3 –0.6 0.7 –1.4 0.3 –0.6 1.0 –1.1 0.2 –0.6
S.D. 3 27.0 2.9 2.3 2.7 3.6 2.6 3.1 1.4 1.2 1.2 1.7 1.2 0.9
F.K. 3 32.0 2.7 1.1 2.0 1.8 2.4 3.1 1.1 1.1 1.4 1.3 0.9 0.6
E.F. 3 46.0 3.1 2.6 2.6 2.0 2.3 3.6 1.2 1.3 1.6 0.9 0.8 0.6
E.K. 3 24.0 3.8 2.6 2.3 3.5 2.7 4.8 2.0 3.2 1.1 1.4 1.3 0.8
N.K. 3 36.0 –1.4 –0.8 –0.8 0.5 –1.6 –2.0 0.3 0.1 0.2 0.3 –0.2 0.4
S.C. 3 31.0 3.4 2.1 2.5 2.6 1.7 4.2 1.7 0.7 13.0 1.0 0.8 1.2
T.S. 3 30.0 0.9 2.5 3.6 3.1 2.4 4.6 3.2 2.5 2.1 2.3 1.8 2.1
U.Y. 3 20.0 3.2 2.5 2.5 3.2 3.4 4.4 2.7 2.2 1.5 1.3 1.4 1.0
Z.G. 3 27.0 3.1 2.4 2.7 4.0 3.3 4.1 3.3 2.7 1.9 2.2 2.6 2.5
S.Z. 3 32.0 2.4 1.5 2.3 3.0 2.2 4.5 1.7 1.8 2.8 2.0 1.1 1.6
N.V. 3 48.0 3.2 1.9 3.4 3.4 2.8 5.1 2.5 2.9 1.3 1.8 0.9 1.2
E.A. 3 32.0 3.1 2.8 2.2 3.5 1.8 4.0 1.7 1.5 1.4 1.4 1.2 1.4
H.F. 3 46.0 4.4 2.7 3.3 4.8 4.3 5.5 2.6 3.2 1.3 0.8 0.9 1.8
G.G. 3 23.0 3.2 1.6 3.2 2.3 2.5 3.6 2.2 2.6 1.4 1.5 0.8 1.5
A.A. 3 30.0 3.2 2.4 3.2 3.5 2.2 4.1 1.5 2.3 1.9 1.4 1.0 2.1

d ⫽ difference; bfp ⫽ body fat percentage; u ⫽ upper; l ⫽ lower; R ⫽ right; L ⫽ left.


Mesotherapeutic injections for body contouring 147
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For personal use only.

Figure 1. A patient from group 1 seen (A) before and (B) 1 month after the 15th session.

Of all the patients, only one (1.3%) in group 3 and erythema, which typically lasted for 2–3 days.
showed a BFP increase. Two patients gained weight yet Pain was typically minimal during and after the injec-
achieved some decrease in body fat. BFP losses were tions. The injected sites might bleed transiently and
statistically significant in all three groups, with p ⬍ 0.00. exhibited signs of inflammation, which resolved within
The highest decrease was obtained as 4.66 ⫾ 1.09 in several days. Seventeen of 75 patients (23%; 12
group 1 (Table II). patients from group 2) had mild ecchymotic areas
Regarding the level of satisfaction with the effect situated primarily on the thighs which faded away
of mesotherapy, all of the patients answered with a within 7–10 days. Nineteen of 25 patients (25% of all)
questionnaire. In terms of the subjective scales regard- in group 1 complained of immediate burning (typically
ing the effectiveness of mesotherapy, most of the patients lasting less than 30 minutes), transient urticaria and
expressed positive thoughts about mesotherapy but variable degrees of pruritus. Postinflammatory hyper-
three patients (4%: one patient from group 2, two pigmentation, prolonged swelling, ulceration, and
patients from group 3) were not satisfied with the cos- hematoma formation were not determined in our
metic outcome of this therapy. Highly satisfied patients patients. No patients in any of the groups had sub-
were from group 1: 80% (20 of 25 patients). This was cutaneous postinflammatory nodules at the injection
63% (47 of 75 patients) when taken from all three groups sites. During the study time, no re-enlargement of fat
(Table IV). Almost all of the patients would recom- deposits was reported (Table V).
mend this treatment to others as a body-contouring
procedure.
Cosmetic improvement was seen in every patient
Discussion
(Figure 4): no irregularities or dimples were seen; no
serious side effects or complications were noted. Some Mesotherapy qualifies at present as one of the ‘hot-
of the patients reported a little bit of pain, swelling test’ topics in cosmetic medicine.
148 Z. Kutlubay
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Figure 2. A patient from group 2 seen (A) before and (B) 1 month after the 15th session.

Mesotherapy is most commonly employed today quantity injected at a specified subcutaneous tissue
for the reduction of fat and cellulite. Specifically cre- depth. What components are combined and in what
ated formulas are claimed to reduce fat content in proportions tends to be based on anecdotal reports or
the cellulite, improve impaired circulation, and break the physician’s experience, rather than empirical data.
down damaged connective tissue, thereby smooth- For this reason, in this study we aimed to find which
ing the skin surface. Such formulas are said also to formula was the most effective. Of course it was not
prevent cells from storing fat and help break down possible to try all of the protocols. We chose the for-
existing fat cells apparently by inducing rupture and mulas that are commonly used in our country and maybe
cell death of adipocytes. Nevertheless, despite the in the world. Isoproterenol, conjonctyl, yohimbine,
lack of supporting literature and despite the fact that and aminophylline are all well-recognized lipolytic
the use of mesotherapy solutions to induce local stimulants for mesotherapy. Moreover, combinations
lipolysis is based primarily on empirical observations of lipolytic stimulators seem to produce greater stim-
and long-term clinical use, mesotherapy techniques ulation of lipolysis than each of the individual com-
are increasingly being applied to treat fat in the face, ponents alone (10).
neck, and elsewhere in the body and are the primary Traditional European mesotherapy does not incor-
application of mesotherapy in Turkey, as in other porate PC and/or DC into its formulations. There is
countries (7,10). not one standardized formulation for body contour-
Mesotherapists traditionally have resorted to polyp- ing and cellulite, a number of common ingredients are
harmacy, combining several lipolytic stimulators with advocated at training seminars and are readily available
the goal of enhancing lipolysis. There are a large num- over the internet.
ber of protocols or treatment formulas used in meso- It is possible that the mechanism of action involves
therapy. Because each protocol differs from doctor to enhancing lipase activity and thereby lipolysis. When
doctor, it is not possible to test the effect of each for- body-contouring procedures are skillfully applied to
mula as a standard protocol (2). Currently, there is the appropriate patient, the results are pleasing to both
no standardization of dosage and no treatment algo- the physician and the patient. The promise of a simple,
rithm to enable a prediction of how much tissue or fat permanent method of weight loss, spot weight reduction,
will be ‘dissolved’ with a specific solution in a defined or cellulite improvement is obviously very appealing.
Mesotherapeutic injections for body contouring 149
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Figure 3. A patient from group 3 seen (A) before and (B) 1 month after the last session.

With the rise in the number of overweight individu- membrane. It is a naturally occurring phospholipid
als in our society, it is likely that the demand will and has three important functions: (i) it emulsifies
increase for body-contouring procedures, including dietary fat; (ii) it is an essential component of the
mesotherapy. The use of mesotherapy for body con- apolipoproteins that regulate cholesterol metabolism;
touring in the English language medical literature is and (iii) it is an essential component of cell mem-
limited to a few clinical trials (1). branes. The mechanism by which injectable PC may
Lipolysis is regulated by α2 and β-adrenoreceptors result in decreased localized fat collections to improve
on the adipocyte cell surface: β-receptor activity increases the body contour is not well understood. One hypoth-
lipolysis; α2-receptor activity inhibits β-receptors. So, esis is that PC injected subcutaneously emulsifies fat,
β-adrenergic activation and α2-adrenergic inhibition allowing tissue lipases to hydrolyze fat, producing
increase lipolysis in fat cells (11). glycerol and free fatty acids (1,12).
PC, caffeine, organic silicium and buflomedil, Caffeine increases lipolysis, raises cyclic adenos-
L-carnitene, chophytol, and procaine were used in this ine monophosphate (cAMP) by inhibiting phos-
clinical trial because they were commonly used in phodiesterase (PDE), increasing catecholamine
mesotherapy by mesotherapists. release (epinephrine) by the sympathetic nervous
Phosphatidylcholine (PC) is a soybean lecithin extract system. A significant increase in free fatty acid
and the main phospholipid component of the cell (FFA) oxidation over physiologic levels is deter-
mined at rest and during exercise after ingestion
of caffeine (3,4,7).
Table IV. Patient satisfaction questionnaire results.
Conjoctyl (organic silicium, salicylate of monomethyl-
Average satisfaction score silanetriol) is an anti-oxidant effective drug. Silicon is
Somewhat Highly an element in the structure of elastic connective tissue.
Groups n Not satisfied satisfied satisfied It acts as a coenzyme in the synthesis of the macro-
molecules of the interstitial matrix. In the microcir-
Group 1 25 0 5 patients 20 patients
culation, it modifies the venous capillary and lymphatic
(20%) (80%)
Group 2 25 1 patients 8 patients 16 patients permeability, and in the adipose tissue it stimulates
(4%) (32%) (64%) the synthesis of the cAMP and the hydrolysis of trig-
Group 3 25 2 patients 12 patients 11 patients lycerides. Organic silicium increases collagen produc-
(8%) (48%) (44%) tion (3,4,6).
Total 75 3 patients 25 patients 47 patients
Buflomedil (Fonzylane) opens the precapillary sphinc-
(4%) (33%) (63%)
ter, improving microcirculation. It is considered to
150 Z. Kutlubay
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For personal use only.

Figure 4. (A) Before and (B) 1 month after the 15th session. Notice the improvement in cellulite appearance.

have a lipolytic or mesodrainage effect by inhibiting When used for body contouring, a ‘typical’ dosage
the α-adrenoceptors (3,4). of PC of 100 mg per 5 ⫻ 5-cm area is recommended
l-Carnitene is an amino acid that constitutes an and often three to six treatments are administered 2
essential cofactor in the metabolism of fatty acids act- weeks apart. Reported cosmetic results obtained with
ing to diminish triglycerides and total cholesterol by Lipostabil are impressive (17). We also used Lipostabil
improving lipid metabolism. Lack of L-carnitine impedes in group 1 patients and obtained the best results; 15
fat transport. Carnitine augments lipid oxidation. Car- treatments, 250 mg per session, once a week. More-
nitine increases the delivery rate of long-chain FFAs over, there is no general agreement on its mode of
into mitochondria for β-oxidation (7). action in cosmetic applications even though it is
Chophytol (extract of artichoke, Cynara scolymus) thought to work as a detergent causing nonspecific
increases the volume of bile secreted. It increases the fat-cell membrane lysis (1,5). It is theorized that the
antitoxic and glycogenic function of the liver. It also has reduction of subcutaneous fat likely follows inflamma-
lipolytic, choloretic and anti-edema effects (3,4). It aug- tion-mediated necrosis and resorption (15,18). Recent
ments circulation and directly potentiates the release of data suggest that cell lysis may be due to the action of
nitric oxide which is a potent vasorelaxant (7). DC, a natural detergent used in these formulations to
Procaine is best known for its anesthetic property. keep PC soluble in water. Irrespectively, the chemical
Procaine is used in mesotherapy in the form of chlo- effects of PC/DC, either through direct detergent
rhydrate of procaine, 1–2%. It is anti-arrhythmic and effects upon the adipocyte cell membrane or an indi-
a vasodilator (3,4). rect response following inflammatory-cell-mediated
PC injections have recently become a popular treat- chemotaxis to the area, result in an increase in acute
ment for localized fat removal. A number of clinical and chronic inflammation within the septae and lob-
studies and recent presentations have demonstrated ules of the subcutaneous fat. Eventually, the inflam-
localized fat loss in multiple anatomic sites after subcu- matory response may abate with ingrowth of fibrocytes
taneous injections of a formula containing PC. PC is a and collagen production (18–20). Fibroplasia and an
precursor to acetylcholine (8,13–16). Long-term fol- associated reduction in adipocyte number and volume
low-up of patients treated with PC injections to reduce could contribute to the tightening and possible retrac-
local fat deposits indicate that the reduction of fat tion of skin. In Brazil, PC has been used extensively
deposits is permanent, provided weight gain is low or as an off-label cosmetic treatment of unwanted fat
none (13). deposits (5).
Mesotherapeutic injections for body contouring 151

Table V. Side effects and complications.

Burning Ulceration
Ecchymosis pruritus Pain Hyperpigmentation Hematoma nodule Infection Necrosis Irregularity

Group 1 3 19 1 0 0 0 0 0 0
Group 2 12 0 0 0 0 0 0 0 0
Group 3 2 0 0 0 0 0 0 0 0
Total 17 (23%) 19 (25%) 1 (1.3%) 0 0 0 0 0 0

In an open-label clinical trial by Rittes (13), 50 per session every 4–8 weeks for up to four treatments.
patients were injected subcutaneously in the trunk, Multiple anatomic sites (including chin, abdomen,
neck, and extremities with 5 ml Lipostabil (50 mg/ml buttocks, thighs) were injected subcutaneously with
PC) distributed over an 80-cm2 surface area. Thirty- 0.4 ml PC distributed every 1–1.5 cm. ‘Dramatic
five of 50 patients received four treatments, the rest improvement’ was reported in 13 patients; 29 patients
had one to two treatments, all sessions were spaced had ‘mild to moderate improvement’; one patient
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15 days apart. Improvement occurs in ‘all’ patients was a nonresponder. In our study, we obtained high
(no objective data); at the 4-year follow-up no recur- satisfaction in 80% of patients injected with a PC
rence was determined in treated areas unless weight cocktail.
was gained by patients. The pharmacologically active agents cited in the
In a study reported by Moy, the trunk, chin, and literature act on the adipose tissue, connective tissue,
extremities were injected with 0.5 ml/cm2 of a PC for- or microcirculation, and can be used transdermally.
mulation (50 mg/ml) for two treatments spaced monthly. In vitro studies show that methylxanthines (theo-
An average decrease of 7.45 mm was measured in phylline, aminophylline, caffeine) stimulate lipolysis
subcutaneous fat thickness 1 month after the last and a reduction in the size of adipocytes through the
treatment (8). inhibition of phosphodiesterase and an increase in
In a double-blinded clinical trial by Asaadi et al. cAMP (4,8).
For personal use only.

(21), 100 patients were divided evenly into five treat- In a study by Park et al. (2) the authors injected a
ment groups; each received either a vasodilator (buflo- mixed solution (i.e. aminophylline, buflomedil and
medil), lipolytic (compounded PC), homeopathic agents lidocaine) into the superficial dermis of the medial
(carnitine and Melilotus), an equal combination of all aspect of one thigh weekly and no treatment was given
medications, or placebo (normal saline). Each patient to the other thigh. There was no body contouring
had 0.1–0.2 ml of solution injected every 1–2 cm into observed in this study. There were no statistically sig-
the thighs, waist and flank weekly for 5 weeks, then nificant changes in thigh girth. In our study, all the
monthly for a maximum of 5 months. Eighteen of 20 results (including weight, BFP and body circumfer-
patients in the combination group versus 14 of 20 ences) in group 3 (containing buflomedil) are the low-
patients in the PC group experienced at least a 2.5-cm est among the three groups; but all the values were
decrease in thigh circumference.The mean waist circum- statistically significant (Tables II and III).
ference decreased 4.2 cm in the combination group. Two plastic surgeons performed a clinical study
No significant decrease in circumference was deter- to evaluate the use of mesotherapy for body contour-
mined in the vasodilator, homeopathic, or saline groups. ing. Forty patients were enrolled in a prospective
No weight change was experienced by any patients. study; a single-body region was treated by mesother-
In another clinical trial by Rullan and Hexsel, 50 apy on a weekly basis for 5 weeks, followed by monthly
patients received one to three injections of a ‘cocktail’ maintenance therapy. The patients were separated
(PC, aminophylline, carnitine, and lidocaine) in the jowls into four groups: group I (n ⫽ 10) received mesother-
and submental region every 2–4 weeks. No more than apy treatments unilaterally; group II (n ⫽ 10) received
0.2 m was delivered subcutaneously per 1 cm. All treatments bilaterally; group III (n ⫽ 10) received
patients had some degree of improvement: 50% had mesotherapy in association with dietary modification
‘minor improvement’, 40% had ‘significant improve- and exercise; and group IV (n ⫽ 10) received saline
ment’, and 10% had ‘dramatic improvement’; 85% placebo injections. Circumference measurements dec-
of patients surveyed were satisfied and desired more reased in the majority of treated patients. The average
treatments. Subcutaneous nodules developed in ‘most decrease in circumference was 2.6 cm at the waist
patients’ and all resolved spontaneously (8). We did and 1.8 cm at the thigh. When evaluating all three
not determine any subcutaneous nodules or granu- groups in our study, the decrease in circumference
lomas in group 1 patients injected with the formula at the waist was 3.78 cm in our patients. No major
containing PC or in those of the other two groups complications occurred, but several minor complica-
(Table V). tions were observed (1).
A study reported by Duncan and Hasengschwandt- A double-blinded clinical trial evaluating ‘mesoplasty’,
ner (19) included the outcome of a series of 43 patients which was recently presented at the American Society
treated with up to 100 ml of PC (maximum 2.5 g) of Plastic Surgery Annual Meeting, demonstrated
152 Z. Kutlubay

significant waist and thigh reductions restricted to we believe that ultrasound and magnetic resonance
patients receiving subcutaneous injections of a PC imaging that allow evaluation of subcutaneous tissue
formulation; the vasodilator (buflomedil) and homeo- should be added to these methods for more accurate
pathic (carnitine and Melilotus) treatments did not assessment. The potential limitations of the present
produce any effect (7). study are the lack of biopsies showing fat necrosis and
Localized mesotherapy complications include aller- the lack of more objective means of assessing treat-
gic reactions, urticaria, lichenoid drug eruptions, pso- ment success.
riasis, hematoma, ulceration, necrosis, and various The majority of patients experienced minimal dis-
bacterial infections. It is claimed that most adverse reac- comfort with mesotherapy. Some patients saw results
tions associated with mesotherapy lipolysis are mild and after one treatment session while others may require five
transient, and supporters of the procedure consider it or more treatments to begin to see results. Often the
a safer alternative to liposuction (4,5,8). patient’s clothing became looser and friends and family
Patients in the current study tolerated the treatment told the patient they looked thinner and smoother.
sessions without difficulty and serious adverse effects When examining statistical analysis of t-tests for
that could interrupt patient attendance were not seen. paired samples within each group before and after treat-
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Patients generally feel only slight pain during the pro- ment, all the results were determined as statistically
cedure. Only one (1.3%) of our patients in group 1 significant (p ⬍ 0.00) (Table II). When we look at anal-
complained of severe pain during the procedure. Park ysis of co-variance values (all statistical effects entered
et al. (2) reported that most of their patients (56%) simultaneously) among the groups, group 1 has the
experienced severe pain during the mesotherapy. It may most effective results. Group 1 is statistically more sig-
be due to the effect of different anesthetic drugs or nificant than both the other two groups when evalu-
technique. We added procaine to the mesotherapy ating all the parameters including weight, BFP and
cocktails, whereas they had added lidocaine to the solu- circumferential measurements of 10 body sites. So
tion. We observed bruising and ecchymotic areas in 12 we can claim that the mesotherapy cocktail contain-
patients from group 2 (16%) (caffeine cocktail). Simi- ing PC/DC is more effective than those containing
larly, pruritus and burning were only determined in 19 caffeine and traditional mesotherapy formulas. Group
For personal use only.

group 1 patients (25%) (Table V). All of them had to 2 is also statistically more efficient than group 3, except
take oral antihistamines. Most patients (96%) con- lower belly and hip.
cluded that, overall, the treatments were effective. Such researches like our study will help us to find
Information on mesotherapy in the English lan- the most effective mesotherapy formulas for body con-
guage medical literature is scant. There are few publi- touring and melting away fat. Mesotherapy for fat
cations regarding its safety, efficacy, and mechanism of reduction is more about losing inches than losing large
action. Information on formulations, technique, dos- amounts of weight. Products whose mechanism of action
ages, treatment protocols (including dose/injection, is well understood and whose adverse effects and doses
technique/injection, and interval times), and toxicology are well studied should be chosen.
is not available and scientific literature describing the
use of specific substances is limited (1,22). Although
the FDA has approved most of the ingredients used in Conclusion
mesotherapy, its constituents are being utilized for Our ultimate goal as doctors will always be to provide
unapproved indications and are being administered in safe, proven methods of medical care, guaranteeing the
a manner whose efficacy, safety, and pharmacokinetics best possible result for our patients with the minimum
are unknown (5,7). amount of morbidity. It is important to assess the ben-
This study demonstrates the effectiveness of meso- efits, safety, experience, and standardization of meso-
therapy for body contouring and slimming. Moreover, therapy, and as a method of body contouring; more
there are many reports showing unexpected infections studies are necessary before mesotherapy can be advo-
or adverse reactions to mesotherapy (23). More clini- cated as a safe and effective treatment. This painless
cal trials will be needed to demonstrate the effective- approach to body contouring will always be appealing
ness of mesotherapy. to many, but without scientific evidence to verify meso-
A loss in circumference measurement was seen in therapy’s usefulness, mesotherapists must be aware of
most of the patients (96%). When three groups were the risks of the treatments and the lack of FDA approval
compared with regard to mean body circumference of the ingredients used in the injections (5).
loss, patients in group 1 showed the best results. The Despite a number of anecdotal reports and exper-
difference in mean grades before and after treatment imental data suggesting that components of traditional
was statistically significant, with p ⬍ 0.00. We found mesotherapy formulations may be effective, there are
that weight, BFP and body circumference losses were presently few peer-reviewed clinical trials that critically
interrelated. evaluate the efficacy of these localized injections for
We performed circumference measurements of medical or cosmetic applications.
the selected body sites and used them to determine Mesotherapy treatments have been performed
improvements in body contours. On the other hand, through out Turkey for 10 – 15 years. The Turkish
Mesotherapeutic injections for body contouring 153

fascination with mesotherapy has been limited to its 8. Rotunda A, Kolodney MS. Mesotherapy and phosphatidyl-
aesthetic applications, which are becoming increasingly choline injections: Historical clarification and review. Derma-
tol Surg. 2006;32:465–480.
popular for body contouring and spot weight loss.
9. Rohrich RJ. Mesotherapy: What is it? Does it work? Plast
The shortness of scientific validation is not proof Reconstr Surg. 2005;115:1425.
that mesotherapy does not work. Even if there are some 10. Caruso MK, Roberts AT, Bissoon L, Self KS, Guillot TS,
reports showing that mesotherapy is not effective (2,24), Greenway FL. An evaluation of mesotherapy solutions for
this study declares that all of the three different meso- inducing lipolysis and treating cellulite. J Plast Reconstr Aes-
therapy cocktails are beneficial and statistically effective thet Surg. 2008;61:1321–1324.
11. Bernlohr DA, Jenkins AE, Bennaars AA. Adipose tissue and
for controlling local obesity and for body contouring. lipid metabolism. In: Bernardi G, Vance DE, Vance JE, editors.
The formula containing PC/DC injected into the Biochemistry of lipids, lipoproteins and membranes. 4th ed.
patients of group 1 is the most effective one. Meso- Amsterdam: Elsevier; 2002. p. 275.
therapy is recommended for body contouring because 12. Gryskiewicz JM, Adams WP Jr. Orlando 2006: Plastic surgeons
most patients (96%) are happy with mesotherapy rate the ‘hot topics’. Aesthet Surg J. 2006;26:479–484.
13. Rittes P. The use of phosphatidylcholine for correction of local-
results, and its side effects are minimal and negligible.
ized fat deposits. Aesthetic Plast Surg. 2003;27:315–318.
For those patients seeking fat loss and body con- 14. Hexsel D, Serra M, Mazzuco R, Dal’Forno T, Zechmeister
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touring, mesotherapy is a good treatment for losing D. Phosphatidylcholine in the treatment of localized fat.
localized fat. J Drugs Dermatol. 2003;2:511–518.
15. Rotunda AM, Suzuki H, Moy RL, Kolodney MS. Detergent
effects of sodium deoxycholate are a major feature of an
Declaration of interest: The author has no finan- injectable phosphatidylcholine formulation used for localized
cial interest in any of the products, or drugs men- fat dissolution. Dermatol Surg. 2004;30:1001–1008.
tioned in this article. 16. Young VL. Lipostabil: The effect of phosphatidylcholine on
subcutaneous fat. Aesthet Surg J. 2003;23:413–417.
17. Rittes PG. The use of phosphatidylcholine for correction of
lower lid bulging due to prominent fat pads. Dermatol Surg.
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