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1. Introduction
The microwave body remodeling system constitutes a novel noninvasive technology for subcutaneous adipose tissue reduction [1, 2]. Designed for deep tissue heating, it provides treatment of localized adiposities, edematous fibro sclerotic panniculopathy (EFP), and skin laxity, among other body remodeling applications in the fields of dermatology, plastic surgery, and aesthetic medicine [1, 3]. A frequency of 2.45 GHz in a controlled microwave emission interacts with biomolecules and generates controlled, localized heat where 80% of the transferred energy is absorbed in a selective manner by adipocytes in the deepest layer of the skin through a biophysical process called “dielectric heating” [2, 4, 5]. The immediate consequence is a disarray of the adipocyte’s cytoplasm due to a metabolic increase with an outflow of the fatty content through the blebbing effect [2] producing physiologic macrophage activation that takes up this fat and eliminates it via lymphatic drainage, at the same time producing collagen solubilization, fibroblasts activation, and fibrous tissue remodeling, reducing adipose tissue, improving cellular metabolism, local circulation, and skin quality [2]. This way, the system induces thermic modifications in subcutaneous adipose tissue, preferably without affecting the dermo-epidermic layer, unlike other systems such as radiofrequency (RF) [1]. In fact, the selective microwaves (called Coolwaves) of the Onda device (which works at 2.45 GHz) thanks to this high frequency, make the skin tissue almost “transparent” to the passage of energy which is almost totally conducted over the subdermal fat layer specifically. This makes the superficial layers of the dermis to be preserved from unwanted heating to stay cool. 80% of this selective microwave energy targets the fat cells, and 20% of energy is absorbed by the epidermal and dermal layers (this is in any case counterbalanced by the cooling system integrated into the handpiece that limits the effects of such heat and protects the epidermis). The situation is quite different with RF handpieces with a high risk of skin damage. Moreover, as the RF energy remains close to the surface, it fails to reach the hypodermis where the fat cells are located, and whose membranes must be broken for the treatment to be effective. For these microwaves, the conductivity of the outermost layers of skin is at least 3.5 times higher than that of the commonly used RF irradiation systems in aesthetic medicine (Figure 1). That means that most of the RF energy gets stuck in the epidermis and dermis, heating them up to such an extent that there is a risk of tissue damage.
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The main application of this system is the management of EFP, commonly known as cellulite. This condition affects between 80 and 90% of the female postpubertal population [1], and it is manifested as an alteration in the skin surface consisting of depression and elevation that give an irregular appearance known as “orange skin”. Typically, it is found on the thighs, buttocks, arms, and abdomen causing aesthetic unconformity [1]. It is caused by soft tissue fibrosis and sclerosis induced by genetic and hormonal factors, alcohol ingestion, contraceptive use, and microcirculatory venous lymphatic dysfunction among others. These factors are persistent despite a healthy diet and exercise [4]. The predominance in females is due to the structural and anatomical characteristics of the subcutaneous septum, where the fibers are oriented perpendicular to the skin surface generating a thick division between fat lobules, unlike males where the septum has an interlaced pattern; additionally, estrogen favors fat accumulation, especially in the lower half of the body, and gives the characteristic female “pear-shaped” morphology [6].
Obesity is related to generalized adiposity, defined by the World Health Organization (WHO) as a body mass index superior to 30 kg/m2, and its management must be carried out with additional measures by a multidisciplinary team [7, 8]. Although cellulite can affect individuals with normal weight, it is worsened by overweight and obesity. In Colombia, the prevalence for adults in the year 2020 was 57.5%, of which 36.2% corresponded to being overweight and 21.3% to obesity, and it is two times more common in females (65.4%) than in males (34.6%) [9, 10].
In the last 30 years, minimally invasive technologies based on energy such as RF, low-frequency ultrasound, cryolipolysis, and combined infrared light therapy are on the rise; among them, the introduction of the microwave system for body remodeling, with reports of in vitro studies, animal models, and case series that show promising results such as those by Di Pietro et al. [1], which detailed the improvement after four 30 minute sessions in the cellulite severity scale and the findings by Bonan et al. [4], showed a median reduction in abdominal circumference of 3.9 cm eight weeks post treatment.
These published studies demonstrate the beneficial effect of microwave at 2.45 GHz on the reduction of subcutaneous fat and for skin laxity and cellulite improving in Caucasian populations. In this study, we present for the first-time clinical data on the effect of the Onda (DEKA M.E.L.A, Florence, Italy) for localized adiposity reduction in a Latin American population.
2. Materials and Methods
2.1. Study Design
Cross-sectional analytical study data were collected from a medical aesthetic center in Bogotá between January 2019 and April 2022.
2.2. Population
Adults older than 18 years that consulted the aesthetic medicine office voluntarily for localized adiposity reduction using microwaves for a minimum of three sessions were included consecutively. Patients with pregnancy less than four months postpartum, incomplete medical record, no follow-up after the third session, any medical contraindications to the procedure, and a lack of desire to participate in the study were excluded.
2.3. Instrument and Data Recollection
For data recollection, an instrument validated by the aesthetic medical center was used, and it included all the evaluated variables. Patient personal data were collected by trained nurses, and the clinical evaluation and anthropometric data were collected by the treating physician (the same in all cases).
2.4. Variables
The variables of interest were classified as sociodemographic, clinical, and device-specific. Sociodemographic variables were age (years), occupation, socioeconomic stratum, and educational level; clinical variables included past medical history of aesthetic surgery in the body, area of interest, gynecological history such as menopause or use of contraception, and anthropometric measurements were taken before and after treatment and included BMI (weight (kg)/height (m2) taken with the patient in underwear with a weight and height meter; abdominal perimeter (cm) taken standing with a flexible measuring tape midpoint between the inferior costal margin (inferior border of the 10th rib) and the iliac crest (anterosuperior iliac spine) between the end of expiration and the beginning of the inspiration of the respiratory cycle in accordance to the international directives [10]; skinfold measurement with a body fat caliper (mm) was taken by holding it firmly between the thumb and index fingers; evaluated skinfolds included tricipital, subscapular, abdominal, and iliac crest, measured using the recommendations in the protocol proposed by Norton et al. [11]; superior abdominal skinfold was taken along the midline between the inferior costal margin and the umbilicus; the posterior waist skinfold was taken along the posterior costal margin and demargin of the posterior axillary line; the trochanteric skinfold was measured 1 cm inferior to the gluteal fold in the lateral thigh area; the thigh skinfold was taken at 1 cm of the gluteal fold along the anterior midline on the inner thigh of the abductors area. Among the variables associated with the device, the type of handpiece used, the power, and the measured/indicated dose of the device were evaluated.
2.5. Procedure
Initially, a general analysis of the physical condition of each patient was made to identify the treatment areas and evaluate the type and state of the imperfection or pathology (localized adiposity, EFP, skin laxity) to define the suitability of the microwave treatment and the most adequate protocol. All patients were advised nutritionist support, and none exercised. Once the procedure was explained, a consent form was signed, and the previously described anthropometric parameters were measured in the treatment areas. These areas were delimited and then divided into secondary areas of 15 × 15 cm2. Skinfold test results by area were introduced in the microwave device that automatically selects the appropriate handpiece, which could be “Deep,” ideal for deep adiposity, or “Shallow” for cellulite, flaccidity, or adiposity with a fibrotic component, according to the degree given by the body caliper. The parameters of power and dosing pre-established by the device were used, adding 30% in each session with a 5°C cooling.
Skinfold areas with a thickness >2 cm (subdermal fat should be at least 1 cm thick) but <5.5 cm were identified. After cleaning with a normal saline solution, a vaseline layer was applied in the treatment area to obtain adequate contact between the handpiece and the skin, a better coupling, and greater fluidity of movement. The handpiece indicated by the device was used, keeping it perpendicular and in permanent contact with the skin, making soft continuous movements on the secondary zones for at least 7–10 minutes to cover the zone completely and homogeneously. The handpiece can be accessorised with contact and temperature sensors in order to assure a safe treatment. In order to carry out a lymphatic drainage, circular movements were performed within each demarcated treatment area, privileging a gradual ascending advancement along the lower limb and arm in the direction of the lymph node stations, repeating several steps until the exhaustion of the dose set for that area. The interval between sessions was 20–45 days following the previously described procedure.
2.6. Data Analysis
The participant’s general characteristics description was made using absolute and relative frequencies for the qualitative variables. For quantitative variables, measures of central tendency and dispersion were used according to the data distribution determined by the Shapiro–Wilk test: for normal distribution, variables mean and SD (standard deviation), in non-normal median and interquartile range (IQR), were used. The data were summarized in tables. To establish localized adiposity improvement, a mean difference was proposed, using a repeated measures t-test for variables with normal distribution and the Wilcoxon signed-rank test for non-normal distributions, assuming a null hypothesis of a mean difference equal to 0. Results were verified with its respective confidence interval (CI) and
2.7. Biases
The presence of selection and measurement biases that could alter the results was considered. Selection bias could not be controlled, as for measurement bias, a single previously calibrated measuring instrument was used, and participants’ physical evaluation was made by a sole investigator.
2.8. Ethical Aspects
The participant centers oversaw data confidentiality and informed consent by Colombian law (Ley 1581 de 2012). The procedures followed were in accordance with the Declaration of Helsinki. The authority provided approval and the corresponding ethical approval code.
3. Results
35 participants were included, 32 women (91.43%) and 3 men (8.57%); the mean age was 47.5 years (SD 9.00); 51.42% (n = 18) were married; the distribution among socioeconomic strata 3, 4, and 5 was similar; the highest educational level was a university in 91.43% (n = 32) of participants; 45.71% (n = 16) had a body mass index (BMI) of the overweight/obesity range previous to treatment; 85.71% (n = 30) had no past medical history of aesthetic surgery on the areas of interest; meanwhile, 14.49% (n = 5) have had liposuction, liposculpture, or abdominoplasty. Table 1 describes the initial characteristics of the participants. All participants received three sessions of body remodeling using microwaves in the following areas: thigh 14.29% (n = 5), abdomen and back 34.29% (n = 12), in these three areas 40% (n = 14) and in the four areas (abdomen, back, thigh, and triceps) 11.43% (n = 4). Lower limbs were treated with a power range of 130–160 Watts and an energy dose range of 90–140 Jules using the “Shallow” handpiece in 63.2% of cases, and the trunk area was treated with a power range of 120–160 Watts and an Energy dose range of 80–150 Jules using the “Deep” handpiece in 61.4% of cases. Weight was F(1, 34) = 29.07 (
Table 1
Sociodemographic characteristics and medical history.
Sociodemographic characteristics and medical history | n = 35 (%) |
Sex | |
Women | 32 (91.43) |
Men | 3 (8.57) |
Marital status | |
Married | 18 (51.42) |
Single | 13 (37.14) |
Divorced | 2 (5.72) |
Cohabitants | 1 (2.86) |
No data | 1 (2.86) |
Socioeconomic levels | |
3 | 10 (28.57) |
4 | 12 (34.29) |
5 | 11 (31.43) |
6 | 2 (5.71) |
Educational level | |
Secondary school | 2 (5.71) |
Bachelor’s degree | 32 (91.34) |
Postgraduate | 1 (2.86) |
Labor | |
Health | 6 (17.14) |
Lawyer | 3 (8.57) |
Finance/economics | 4 (11.43) |
Commerce | 7 (20) |
Arts | 2 (5.71) |
Engineering | 2 (5.71) |
Others | 11 (31.43) |
Body mass index (BMI) | |
Normal | 19 (54.29) |
Overweight | 12 (34.28) |
Obese | 4 (11.43) |
Previous aesthetic surgery | |
Yes | 5 (14.29) |
No | 30 (85.71) |
Menopause (n = 32) | |
Yes | 8 (25) |
No | 24 (75) |
Current use of contraceptives (n = 32) | |
Yes | 3 (9.38) |
No | 29 (90.63) |
Table 2
Pre and post-treatment measurements.
Variables | Pretreatment | Post-treatment | F (df) | p |
Mean (SD) | Mean (SD) | |||
Weight | 66.58 (8.26) | 63.69 (6.99) | 29.07 (1, 34) | 0.001 |
BMI | 25.24 (3.42) | 24.14 (2.67) | 27.42 (1, 34) | 0.001 |
Waist perimeter | 92.15 (9.15) | 82.98 (6.79) | 49.59 (1, 26) | 0.001 |
Superior abdomen skinfold | 27.18 (10.09) | 19.89 (7.63) | 63.13 (1, 27) | 0.001 |
Abdominal skinfold | 31.19 (9.92) | 21.63 (7.87) | 82.32 (1, 26) | 0.001 |
Iliac crest skinfold | 37.38 (8.20) | 26.81 (7.12) | 114.33 (1, 23) | 0.001 |
Subscapular skinfold | 29.57 (8.63) | 21.74 (5.53) | 67.47 (1, 22) | 0.001 |
Posterior waist skinfold | 34.05 (8.22) | 26.10 (7.74) | 27.36 (1, 20) | 0.001 |
Trochanteric skinfold | 46.08 (12.52) | 35.58 (12.21) | 26.94 (1, 17) | 0.001 |
Inner thigh skinfold | 38.8 (9.64) | 29.07 (8.10) | 50.18 (1, 14) | 0.001 |
Tricipital skinfold | 26.38 (3.45) | 18.25 (2.06) | 96.76 (1, 3) | 0.002 |
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3.1. Subgroup Analysis
Subgroup analysis was made for the BMI variable. Due to the low patient number with obesity, two groups were created, one group included those with a pretreatment BMI between 18.5 and 24.9 considered “normal” and another group with those who had a BMI equal or greater than 25 categorized as “overweight/obese”, and this was made to have similar sample sizes in each group. The mixed type variance analysis showed statistically significant differences between the category “BMI overweight/obese” compared with “normal” BMI in pretreatment weight (10.28; CI 95% 6.07–14.4 8), as well as post-treatment (7.77; CI 95% 3.57–11.97); in pre- and post-treatment abdominal perimeter (11.21; IC 95% 6.37–16.45 and 7.46; CI 95% 2.41–12.5), respectively; superior abdomen (12.97; CI 95% 7.69–18.25 and 9.56; CI 95% 4.28–14.85); subscapular skinfold (12.76; CI 95% 8.46–17.06 and 6.99; CI 95% 2.69–11.29); unlike what was found in abdominal (4.69; CI 95% −2.09–11.47 and 5.16; CI 95% −1.61–11.94), iliac crest (3.71; CI 95% −2.44–9.87 and 5.61; CI 95% −0.54–11.76), and trochanteric (3.62; CI 95% −9.97–17.22 and 1.13; CI 95% −12.46–14.73) skinfolds, where no differences were found. Posterior waist skinfold showed differences in pretreatment BMI but not in post-treatment between the two groups (7.53; CI 95% 0.94–14.13 and 5.15; CI 95% −1.45–11.74). In the intragroup analysis, when comparing both moments, no statistically significant differences were found in weight, both in the normal BMI group and the overweight/obese group (−1.74; CI 95% −5.76–2.28 and −4.24; IC 95% −8.62–0.14), nor in the trochanteric fold (−9.81; CI 95% −19.94–0.33 and −12.3; CI 95% −28.64–4.04). Differences were found in the abdominal perimeter (−7.12; CI 95% −12.25–−1.98 and −11.07; CI 95% −16.02–−6.12), in the normal BMI group, and in the overweight/obese group, respectively, as well as in the abdominal skinfold (−9.79; CI 95% −16.44–−3.13 and −9.31; CI 95% −16.21–−2.40), iliac crest (−11.59; CI 95% −17.99–−5.19 and −9.69; CI 95% −15.58–−3.80), subscapular (−4.82; CI 95% −9.12–−0.42 and −10.58; CI 95% −14.79–−6.38); meanwhile, in the superior abdominal skinfold, differences were found in the overweight/obese group but not in the normal BMI (−8.87; CI 95% −13.96–−3.78 and −5.46; CI 95% −10.93–0.01), respectively, as well as in the posterior waist (−9.09; CI 95% −15.53–−2.65 and −6.7; CI95% −13.45–0.05).
4. Discussion
Because 80% of the microwave energy is focused on the adipocytes and the remaining 20% is absorbed by the epidermal and dermal layers, hence, there is no risk of causing overheating points on the skin and the energy achieves a greater depth [12]. Differences are found in studies concerning the effectiveness of the microwave system in the treatment of localized adiposity [1–4, 13]; this study is the first in a Latin-American population, in which a reduction in the skinfold test measurements of different body zones is achieved using this system (2.45 GHz). All patients were Colombian, with a strong female predominance as reported in the literature [1, 14] that could be associated with the anatomical, genetic, and hormonal predisposition for developing alterations in the adipose tissue when comparing them with men [6], as well as the greater propensity for aesthetics in females. The average age was 47 years, and most patients had a university education (91.34%), which could indicate that a higher educational level has a greater tendency for self-care and a better economic income, allowing access to this service and a greater disposition to improve their quality of life. The 14.49% of patients had a past medical history of an aesthetic surgical intervention, and despite this being the gold standard for treating localized fat, it does not act on skin laxity or cellulite; additionally, the current tendency is toward nonsurgical procedures, more conservative and with less adverse effects. Different parameters were applied according to the skinfold test results and the visual physical exam, with individualized treatment for each patient. Although the device has predetermined parameters for the handpiece selection, a standardized parameter cannot be given without proper measuring and evaluation of each patient. The “Shallow” handpiece was used for the treatment of EFP, improving and dissolving fibrosis as well as enhancing skin tension, while, in the abdomen, the “Deep” handpiece was used to favor adipolysis of localized fat. Both handpieces were used in different treatment sessions. The predominant fat distribution was abdominal and in the trochanteric area. In abdominal fat, one of the most important measurements when treating weight loss is the abdominal perimeter is a cardiovascular and metabolic syndrome predictive factor, independent of the patient’s BMI [10]. After three sessions of microwave, differences were found in pre and post-treatment abdominal perimeter with a median of 7 cm (z = 4.545,
The Shapiro–Wilk test is a statistical hypothesis test that is used to determine whether or not a given data set is normally distributed [15].
The Shapiro–Wilk test and the Kolmogorov–Smirnov test are two well-known and historically commonly employed quantitative methods for determining data normality [16].
Both tests compare the study sample’s scores to a normally distributed set of scores with the same mean and standard deviation; their null hypothesis is that the sample distribution is normal.
The Shapiro–Wilk test was selected for this study since it is more appropriate for small sample sizes (N ≤ 50), but it can also be validly applied to large sample sizes. Furthermore, the Shapiro–Wilk test provides greater power than the Kolmogorov–Smirnov test. For these reasons, the Shapiro–Wilk test has been recommended as the numerical means for assessing data normality [17, 18]. In addition, Wilcoxon signed-rank test (WSR) was used in this research for non-normal distributions, assuming a null hypothesis of a mean difference equal to 0.
The WSR was more often the more powerful test, and the magnitude of the WSR’s power advantage often increased with sample size [19]; it has salient advantages over the one-sample t-test for testing the null hypothesis [20]. The main benefit of the Wilcoxon signed-rank test is that it does not depend on the parameters or the form of the parent distribution. No assumptions regarding the distribution’s shape are necessary. For this reason, this test is often used as an alternative to t-tests whenever the population cannot be assumed to be normally distributed [21].
Study limitations included a lack of a control group, a small sample size, similar to that found in the literature, a small number of men included, which is not enough to establish comparisons, and given the differences between android and gynoid morphology, it is not possible to extrapolate female results to males. Despite this, male subjects had a successful fat decrease in localized fat. Future studies should delve into this to establish sex differences.
5. Conclusions
This is the first study using the microwave system in a Latin-American population for body contour treatment. The positive results particularly achieved by the skinfold test in all treatment areas, which showed a statistically significant reduction of localized adiposity, and the lack of major adverse effects makes this technique an excellent option for the treatment of patients seeking body remodeling. Continued research in this area with methods that allow a more objective measurement of body fat, studies with a larger sample, inclusion of a male population, and evaluation of long-term outcomes (> six months) are strongly encouraged to improve the current evidence.
Ethical Approval
This study was conducted in accordance with the Declaration of Helsinki.
Consent
Informed consent was obtained from all subjects involved in the study.
Authors’ Contributions
AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, and P. A-B conceptualized the study; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, and P. A-B developed methodology; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, I.F, and P.A-B provided software; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, I.F, and P. A-B validated the study; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, and P. A-B performed formal analysis; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, and P. A-B investigated the study; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, and P. A-B collected resources; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, I.F, and P. A-B curated the data; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, and P. A-B prepared the original draft; AIRR, N.PM-V, D.S-B, and I.F reviewed and edited the study; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, and P. A-B visualized the study; AIRR, N.P.M-V, D.S-B, T.C-V, P.L-B, I.F, and P. A-B supervised the study; AIRR performed project administration; AIRR and P. A-B performed funding acquisition. All authors have read and agreed to the published version of the manuscript.
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Abstract
Background. The microwave body remodeling system is indicated for people who want to improve their physical appearance as it can penetrate deep tissues, causing thermic stress on adipocytes to produce adipolysis while in superficial tissues, it dissolves fibrous tracts and stimulates new collagen. Objectives. The aim of this study was to assess the localized adiposity reduction in Latin American patients using a microwave system. Methods. A total of 35 patients with a mean age of 47.5 (±9.0) years received body remodeling treatment, using the microwave system between the years 2019–2022 in a Bogota, Colombia reference center. Data descriptive analysis was made as well as single-factor repeated measures ANOVA to show pre- and post-treatment difference, and mixed ANOVA for body mass index (BMI) subgroup analysis was performed. Results. In all patients examined, statistical significant differences were found in pre- and post-treatment skinfold test for each body area: superior abdomen (F(1,27) = 63.13;
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Details

1 Aesthetic Physician, Aesthetic Dermatology Service, Laser Medical Care Clinic, Bogotá, Colombia; Professor of Dermatology, National University of Colombia, Bogotá, Colombia
2 Dermatology Resident, National University of Colombia, Bogotá, Colombia
3 Specialist and Master in Clinical Epidemiology, University Foundation of Health Sciences, Bogotá, Colombia
4 El.En. Group, 50041 Calenzano, Florence, Italy
5 Master in Clinical Epidemiology, Resident Dermatology, National University of Colombia, Bogotá, Colombia