Outcomes of liposuction techniques for management of lipedema: a case series and narrative review
Introduction
Lipedema (lipohyperplasia dolorosa) (1) is an underdiagnosed chronic condition known as “painful fat syndrome” or “fatty deposition syndrome” due to the pain and discomfort generated by disproportional subcutaneous fat distribution (2,3). It is usually presented as a circumscribed, bilateral, symmetrical disorder that mainly affects the limbs’ fatty tissue, sparing the hands, feet, and trunk (3-5). It predominantly affects women; nonetheless, a few cases have been described in male patients (6,7).
This symmetrically disfiguring condition is associated with poor quality of life (QoL) and overall mental health afflictions (7-9). The major reasons for these issues are the lack of clear diagnosis and treatment indications, as well as related complications such as hematoma, edema, concomitant lymphedema development, and arthralgia (2,4,10,11). Additionally, patients have an increased risk of developing depression and anxiety secondary to the disappointment generated by the poor physical improvements despite diet and exercise (3,5,8).
To improve QoL, decrease morbidity, and ameliorate the psychosocial burden generated by this disease, an interdisciplinary approach is fundamental, including psychologists, physiotherapists, nutrition and obesity experts, lymphedema/lipedema nurses, and physicians for conservative and surgical treatments (4,5). Debulking surgery via liposuction has been proposed for lipedema management in the setting of no improvement with conservative treatment (12). Liposuction or suction-assisted lipectomy has been shown to improve QoL and reduce pain in this population (5,10,13,14). Wet, tumescent, and supertumescent techniques with or without vibration-assisted systems or waterjet-assisted systems have been described as potential methods with promising outcomes for the treatment of lipedema (3,5,10,15). On the other hand, dermato-fibro-lipectomy has been described mainly in highly advanced stages of lipedema or lipolymphedema, in which the tissue is very fibrotic (4).
Although most healthcare providers believe liposuction has been the most common therapeutic alternative for patients with lipedema, liposuction is chosen as a treatment option in less than 15% of patients (16). Instead, more frequently used treatments include diet and exercise (52%), compression therapy (45%), and manual lymphatic drainage (MLD) therapy (43%) (16). Despite advances in lipedema surgery, there is limited knowledge about the differences between various surgical techniques (16). This study aimed to evaluate the different surgical methods used in treating lipedema and assess their impact on clinical and patient-reported outcomes through a comprehensive review. Additionally, we share our own experience with lipedema reduction surgery. We present this article in accordance with the Narrative Review and the AME Case Series reporting checklists (available at https://atm.amegroups.com/article/view/10.21037/atm-24-165/rc).
Methods
Case series—study design and settings
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committees and with the Helsinki Declaration (as revised in 2013). A retrospective chart review of patients’ medical records was performed. All patients with lipedema who underwent liposuction from February 2018 to December 2022 were included in this study. Informed consent was obtained from all patients. All surgical procedures were performed by the same surgeon (P.C.). Surgical indications were as follows: patients aged 18 years or older, more than 5 years with the diagnosis, at least 2 months with complex decongestive therapy (CDT). Only patients with at least 12 months of follow-up were included. Patients with a history of thromboembolic disease, hypercoagulable state, and rheumatologic diseases were excluded from this study.
Case series—variables
Sociodemographic data were extracted. The stage of lipedema (Table 1) (17,18), extremity involvement, conservative therapy time, surgical indications, type of surgical technique, solution infiltration volume, average surgical time, and body mass index (BMI) variations were extracted. Patient-reported outcomes were also collected using a 5-point Likert scale and a 10-point visual analogue scale (VAS) (e.g., spontaneous pain, sensitivity to pressure, edema, bruising, restriction to movement, cosmetic reduction in QoL, and general impairment).
Table 1
Stages | Description |
---|---|
Stage 1 | The skin surface remains normal over the enlarged hypodermis, which contains palpable, pea-sized nodules within the fat. These nodules indicate enlargement and fibrosis in the extracellular matrix and the connective tissue surrounding the fat lobules |
Stage 2 | The skin appears uneven with dimples, resembling cellulite, due to the thickening and contraction of underlying connective tissue fibers over areas of increased fat, accompanied by small to larger hypodermal masses |
Stage 3† | Marked loss of elasticity in the adipo-fascia severely limits mobility. This impairs blood flow into and lymphatic drainage out of the fat lobules, leading to inflammation and subsequent fibrosis. The fibrosis becomes pronounced and easily palpable, potentially affecting the skin, which may exhibit thinning and a weakened attachment to the underlying hypodermis |
†, lymphedema can develop at any stage, but it is more commonly seen in women with stage 3 lipedema, where it is frequently referred to as lipo-lymphedema or stage 4.
The surgical techniques performed in this cohort were tumescent liposuction, vibration amplification of sound energy at resonance (VASER) liposuction, and waterjet-assisted liposuction (WAL). All solutions infiltrated were based on NaCl and adrenaline. The tumescent local anesthesia liposuction (TLAL) technique was performed by providing local anesthesia to the subcutaneous fat tissue before liposuction. VASER liposuction combines ultrasound technology’s power to disrupt the union of fat cells with liposuction. Lastly, the WAL technique employs a dual-purpose cannula that delivers pulsating, fan-shaped jets of tumescent solution, while simultaneously suctioning both the adipose tissue and the injected fluid.
Narrative review
A comprehensive search across PubMed and MEDLINE was conducted from January 1996 through August 2024. The search strategy was as follows: ((lipedema) OR (lipoedema)) OR (lipedema[MeSH Terms])) OR (lipoedema[MeSH Terms])) AND (liposuction[MeSH Terms]); and (((((lipedema) OR (lipoedema)) OR (lipedema[MeSH Terms])) OR (lipoedema[MeSH Terms])) AND ((debulking) OR (dermo-fibro-lipectomy)). From the selected studies of this search strategy, relevant citations were identified and included in the study (Table 2).
Table 2
Items | Specification |
---|---|
Date of search | August 24th, 2024 |
Databases searched | PubMed and MEDLINE |
Search terms used | ((lipedema) OR (lipoedema)) OR (lipedema[MeSH Terms])) OR (lipoedema[MeSH Terms])) AND (liposuction[MeSH Terms]); and (((((lipedema) OR (lipoedema)) OR (lipedema[MeSH Terms])) OR (lipoedema[MeSH Terms])) AND ((debulking) OR (dermo-fibro-lipectomy)) |
Timeframe | January 1996 through August 2024 |
Inclusion and exclusion criteria | Inclusion: all articles that included patients with lipedema who underwent any lipedema reduction surgery and reported their surgical technique and outcomes. Observational or interventional studies in English and Spanish were included |
Exclusion: letters to editors, animal studies, review articles, video submissions, and social media observations | |
Selection process | V.P.B. and J.M.E. performed independent search of articles throughout databases. Conflicts were solved by O.J.M. |
Study selection and inclusion criteria
Inclusion criteria were as follows: all articles that included patients with lipedema who underwent any lipedema reduction surgery and reported their surgical technique and outcomes. Observational or interventional studies in English and Spanish were included. Exclusion criteria were letters to editors, animal studies, review articles, video submissions, and social media observations. We extracted data on the reference (authors’ name), year of publication, country of origin, sample size, gender, and mean age. Surgical outcomes such as circumference, weight, and BMI were identified. Also, pre- and postoperative patient-reported outcomes were extracted (spontaneous pain, sensitivity to pressure, edema, bruising, restriction to movement, cosmetic reduction in QoL, and general impairment). The rest of the variables were the same as the case series.
Statistical analysis
A narrative synthesis of the medical literature was performed. For our case series, inference analysis was performed to assess the mean differences between two groups and three groups with the Wilcoxon matched-pairs signed-rank test and the Kruskal-Wallis rank test, respectively. If a difference was found, post-hoc analysis with Dunn’s test was performed. Statistical significance was set at P value <0.05. Stata IC-Version 16.1 was used for the analyses. Discrete variables were presented as mean and standard deviation (SD) or as median and interquartile range (IQR).
Results
Case series
Twenty-four female patients were included in this study with a median age of 37 years (IQR, 10 years). The median follow-up was 19 months (IQR, 13 months). Eleven and thirteen patients presented with stage III and stage II lipedema, respectively. All patients displayed lower extremity involvement. However, five patients had concomitant upper extremity involvement. Tumescent suction-assisted lipectomy, VASER, and WAL surgical procedures were performed in 11 (45.83%), 6 (25%), and 7 (29.17%) patients, respectively (Figure 1). In Table 3, sample characteristics are depicted based on the type of surgery. Conservative therapy with CDT was performed preoperatively in 18 patients (75%) for 2 months and for 1 month in 6 patients (25%).
Table 3
Variables | Tumescent | VASER | WAL |
---|---|---|---|
Total, n (%) | 11 (45.8) | 6 (25.0) | 7 (29.2) |
Age (years), median [IQR] | 41 [46] | 27 [49] | 35 [26] |
Follow-up (months), median [IQR] | 22 [24] | 20 [17] | 16 [12] |
Stage, n (%) | |||
Stage II | 6 (54.5) | 3 (50.0) | 4 (57.1) |
Stage III | 5 (45.5) | 3 (50.0) | 3 (42.9) |
BMI (kg/m2), mean [SD] | |||
Pre-operative | 29.3 [3.6] | 29.9 [4.4] | 31.5 [15] |
Post-operative | 26.4 [2.2] | 27.7 [3.3] | 28.2 [5.5] |
Solution infiltrated (mL), mean [SD] | 4,918 [744] | 5,400 [901] | 3,443 [571] |
Volume of total fat removed (mL), mean [SD] | 11,268 [2,296] | 10,450 [2,886] | 6,800 [847] |
Average surgical time (min), median [IQR] | 72 [38] | 63.5 [40] | 64 [94] |
Operative times, n (%) | |||
One | 3 (27.3) | 4 (66.7) | 4 (57.1) |
Two | 4 (36.4) | 2 (33.3) | 3 (42.9) |
Three | 4 (36.4) | 0 (0.0) | 0 (0.0) |
Post-operative time with CDT (months), mean [SD] | 75.9 [13.3] | 69.5 [15.4] | 66.9 [29.5] |
Complications, n (%) | |||
Infection | 1 (9.1) | 0 (0.0) | 0 (0.0) |
Epidermolysis | 1 (9.1) | 0 (0.0) | 0 (0.0) |
Seroma | 0 (0.0) | 1 (16.7) | 0 (0.0) |
VASER, vibration amplification of sound energy at resonance; WAL, waterjet-assisted liposuction; IQR, interquartile range; BMI, body mass index; SD, standard deviation; CDT, complex decongestive therapy.
Overall, the median preoperative BMI was 29.65 kg/m2 (IQR, 2.55 kg/m2), and postoperative BMI was 26.95 kg/m2 (IQR, 1.8 kg/m2). Average preoperative and postoperative BMI for different surgical procedure evaluated are shown in Figure 2. A statistically significant difference between preoperative BMI and postoperative BMI was found (P<0.05); however, no significant difference regarding the postoperative BMI between surgical techniques was determined (P=0.074). The median solution infiltrated was 4,500 mL (IQR, 1,850 mL), and the median volume of total fat removed was 9,200 mL (IQR, 4,600 mL). A statistically significant difference in the amount of total fat removal between surgical techniques was found (P=0.0015). Post-hoc analysis with Dunn’s test evidenced significant difference only between tumescent suction-assisted lipectomy and WAL (P<0.001). In Figure 3, the aforementioned variables by type of surgical technique are shown.
The median operative time was 68 min (IQR, 22 min). No significant difference in the average intraoperative time was found between the three surgical techniques (P=0.3674). Regarding the operative times, 11 (45.83%), 9 (37.50%), and 4 (16.67%) patients underwent surgery once, twice, and thrice, respectively. There was no difference regarding the surgical re-interventions between surgical techniques (P=0.0916) and requirement of post-operative CDT (P=0.2003). Lastly, a low rate of complications was evidenced. One patient (4.2%) presented seroma treated with aspiration, 1 patient (4.2%) had infection treated with antibiotics, and 1 patient (4.2%) presented epidermolysis. Preoperative and postoperative patient reported outcomes are reported in Table 4.
Table 4
Clinical effectiveness outcome† | 5-point Linkert scale† | 10-point VAS | |||||
---|---|---|---|---|---|---|---|
Pre-surgery | Post-surgery | Improvement | Pre-surgery | Post-surgery | Improvement | ||
Spontaneous pain | 2.00 | 0.75 | 1.25 | 7.10 | 2.00 | 5.1 | |
Sensitivity to pressure | 2.90 | 1.20 | 1.7 | 7.20 | 3.10 | 4.1 | |
Edema | 3.20 | 1.40 | 1.8 | 8.50 | 2.10 | 6.4 | |
Bruising | 3.10 | 1.60 | 1.5 | 7.10 | 2.10 | 5 | |
Restriction to movement | 3.20 | 0.70 | 2.5 | – | – | – | |
Cosmetic impairment | 2.80 | 0.90 | 1.9 | 8.80 | 3.50 | 5.3 | |
Reduction of QoL | 3.20 | 0.80 | 2.4 | – | – | – | |
General impairment | 2.90 | 1.20 | 1.7 | – | – | – |
†, 0, none; 1, minor; 2, medium; 3, strong; 4, very strong. VAS, visual analogue scale; QoL, quality of life.
Summary and discussion
Lipedema is usually a misdiagnosed chronic condition that afflicts female patients predominantly (7-9). Lipedema reduction surgery remains the sole technique capable of eliminating abnormal lipedema tissue, including adipocytes, nodules, fibrotic extracellular matrix, and other non-adipocyte components (6,11,19-35) (Table 5). It is also the only intervention that halts the progression of lipedema and is ideally performed before the onset of complications and disabilities associated with the condition (19,36). The indications for lipedema reduction surgery include a confirmed diagnosis of lipedema, along with evidence of patient compliance with or failure of conservative treatment approaches (36-38). In this context, the decision to proceed with surgery is primarily based on the severity of symptoms, the occurrence of lipedema-related complications, or the progression of symptoms despite conservative treatment, rather than the stage of lipedema itself (20).
Table 5
Authors, year | Country of origin | Sample size | Gender | Age (years), [range] or ± SD | Stage of lipedema | ||
---|---|---|---|---|---|---|---|
Stage I | Stage II | Stage III | |||||
Schmeller et al., 2012 (20) | Germany | 112 | F | Mean 38.8 [20–68] | 35 | 75 | 2 |
Wollina and Heinig, 2019 (21) | Germany | 111 | F | Median 44 [20–81] | 7 | 50 | 48 |
Dadras et al., 2017 (22) | Germany | 25 | F | Median 45 [23–64] | 1 | 11 | 13 |
Baumgartner et al., 2021 (23) | Germany | 60 | F | Mean 41.9 [22–68] | 18 | 42 | 0 |
Schmeller and Meier-Vollrath, 2006 (24) | Germany | 28 | F | Mean 37.7 [22–63] | 28 | 0 | |
Rapprich et al., 2011 (25) | Germany | 25 | NS | Mean 38.0/median 34.0 [22–65] | NS | NS | NS |
Wollina et al., 2014 (11) | Germany | 3 | F | Mean 68/median 72 [55–77] | 0 | 1 | 2 |
Stutz and Krahl, 2009 (26) | Germany | 30 | F | Mean 33.8 [21–63] | 0 | 5 | 25 |
Baumgartner et al., 2016 (27) | Germany | 85 | F | Mean 40.1 [22–68] | 24 | 61 | 0 |
Witte et al., 2020 (28) | Germany | 63 | NS | Median 35 | 18 | 45 | 0 |
Peled et al., 2012 (19) | USA | 1 | F | Mean 21 | 1 | 0 | 0 |
Chen et al., 2004 (6) | China | 1 | M | Mean 20 | 1 | 0 | 0 |
Current study | Peru | 24 | F | Mean 39.4 [23–73] | 0 | 13 | 11 |
Kruppa et al., 2022 (29) | Germany | 106 | NS | Mean 41 [30–51] | 11 | 61 | 34 |
Gensior et al., 2023 (30) | Germany | 504 | NS | Mean 47.81 [16–78] | NS | NS | NS |
Schlosshauer et al., 2021 (31) | Germany | 69 | F | Mean 50.6±12.8 | 0 | 0 | 69 |
Sandhofer et al., 2021 (32) | Austria | 27 | NS | Mean 41.7±12.7 | NS | NS | NS |
Kirstein et al., 2023 (33) | Germany | 34 | NS | NS | 1 | 12 | 21 |
Klöppel et al., 2024 (34) | Greece | 30 | F | Mean 32.6 [21–60] | NS | NS | NS |
Flores et al., 2024 (35) | Austria | 45 | F | Mean 38.11±3.74 [19–71] | NS | NS | NS |
SD, standard deviation; F, female; NS, not specify; M, male.
Technique
In our case series, three different liposuction techniques were implemented (tumescent, WAL, and VASER liposuction). In this narrative review, four surgical techniques have been used in patients with lipedema. TLAL, WAL, VASER liposuction, and modified suction-assisted lipectomy with microair. The majority of TLAL used vibration-assisted devices (Table 6).
Table 6
Authors, year | Type of surgical technique | Solution (if applicable) | Average of solution infiltrated (mL), [range] or ± SD | Average of surgical time, [range] or ± SD | Fat removed (mL), [range] or ± SD |
---|---|---|---|---|---|
Schmeller et al., 2012 (20) | TLAL with blunt vibrating + PAL | NS | Mean 7,707 [2,564–13,450] | Mean 2 h [40 min–3 h 35 min] | Mean 9,846 [1,000–25,600] per patient |
Mean 3,077 [450–7,000] per session | |||||
Wollina and Heinig, 2019 (21) | TLAL (some patients had 980 nm-diode laser-assisted liposuction) with cannulas connected to a vacuum pump developing negative pressure of 68 mmHg | LR, prilocaine, epinephrine (1:1,000,000) | NS | NS | Median 4,700 [950–14,250]† |
Dadras et al., 2017 (22) | TLAL (41 vibration-assisted device/31 waterjet-assisted device) | Saline, epinephrine (1:1,000,000) | – | Mean 1 h 56 min [58 min–4 h 11 min] | Mean 9,914 [4,000–19,850] per patient |
Mean 3,106 [1,450–6,600] per session | |||||
Baumgartner et al., 2021 (23) | NS | NS | NS | NS | NS |
Schmeller and Meier-Vollrath, 2006 (24) | TLAL with vibrating microcannulas (power-assisted liposuction) | NS | Mean 7,881 [2,740–13,500] | [1–2.5 h] | Mean 3,017 [1,060–5,500] per session |
Rapprich et al., 2011 (25) | TLAL with vibrating cannulas | Prilocaine, suprarenin, sodium bicarbonate, triamcinolone, sodium chloride‡ | Mean 5,155 [2,000–7,000] | NS | Mean 1,909±874 |
Wollina et al., 2014 (11) | TLAL microcannula 980 nm-diode laser-assisted + modified medial thigh lifts 4 months after with lower partial abdominoplasty | Prilocaine | Max 5,000 | NS | Range, 4,000–6,000† |
Stutz and Krahl, 2009 (26) | WAL | Reduced quantities of Klein’s solution | [1,000–1,500] | NS | Mean 1,115 [200–2,650]‡ |
Baumgartner et al., 2016 (27) | NS | NS | NS | NS | NS |
Witte et al., 2020 (28) | WAL with TLAL | Physiological saline solution, prilocaine, suprarenin, sodium hydrogen carbonate in combination with a remifentanil and propofol by an anesthesiologist | Lower legs: [200–400] | NS | Mean 12,922±2,922 |
Upper legs: [400–700] | |||||
Upper limb: [200–300] | |||||
Peled et al., 2012 (19) | Modified suction-assisted lipectomy with micro-air | NS | NS | NS | 1,400 each limb |
Chen et al., 2004 (6) | TLAL | LR, lidocaine, epinephrine | NS | NS | Mean 3,100 |
Current study | WAL, TLAL, and VASER liposuction | NaCl-adrenaline | Mean 4,608/median 4,500 [2,800–6,800] | Mean 1 h 12 min [11–105 min] | Mean 9,769.4 [5,000–14,650] |
Kruppa et al., 2022 (29) | PAL or WAL | Tumescent solution with saline and epinephrine (1:1,000,000) | NS | NS | Mean 6,355±2,797 |
Gensior et al., 2023 (30) | PAL | Tumescent local anesthesia | NS | NS | NS |
Schlosshauer et al., 2021 (31) | NS | NS | NS | NS | Mean 1,868±885.5 |
Sandhofer et al., 2021 (32) | PAL—MicroAire | Tumescent solution with 0.7–1.0 mg/L epinephrine | Mean 11,404±3,067 | Mean 118±17.7 min | Mean 6,111±2,029 |
Kirstein et al., 2023 (33) | NS | NS | NS | NS | Mean 3,831±1,971.08 |
Klöppel et al., 2024 (34) | PAL | NS | NS | NS | Mean 8,700±1,280 [5,900–10,600] |
Flores et al., 2024 (35) | VAL | Modified Klein’s solution with 1,000 mL LR containing 1 mL of 1:1,000 epinephrin | NS | NS | Mean 6,615.33±3,884.25 |
†, median amount of removed lipoaspirate. Does not specify if it was pure fat component. ‡, correspond to supernatant fat aspirate. SD, standard deviation; TLAL, tumescent local anesthesia liposuction; PAL, power-assisted liposuction; NS, not specify; LR, lactated Ringer’s; WAL, waterjet-assisted liposuction; VASER, vibration amplification of sound energy at resonance; VAL, vibration-assisted liposuction.
Witte et al. proposed in 2020 the use of WAL with tumescent anesthesia (3 L physiological saline solution/prilocaine 1% 50 mL/suprarenin 1:1,000 2 mL/sodium hydrogen carbonate 8.4% 40 mL) (28). A WAL device (body jet; Human Med AG, Schwerin, Germany) was used for all operations. Infiltration was performed using a 3.5-mm cannula, while liposuction was performed using a 4.8-mm cannula in all areas. Frequency and pressure were set to range 2–3 (28). Compared to other studies included in this review in which the average solution infiltration and fat removal were similar, Witte et al. [2020] reported considerably less infiltration and a large fat removal quantity (28).
Many authors preferred vibration-assisted devices as it causes less shear force and less tissue matrix trauma than traditional cannulas; therefore, non-adipose tissue is preferentially preserved. Schmeller et al. [2012] conducted liposuction on the hips and arms utilizing only TLAL with the aid of blunt, vibrating microcannulas, sized 3- and 4-mm in diameter, with a power-assisted approach (20). On average, 7,707 mL of TLAL solution was infiltrated, with a range of 2,564 to 13,450 mL. The average surgical duration was approximately 2 h, varying from 40 min to 3.3 h (20). In a separate study by Dadras et al. [2017], a total of 72 liposuction procedures were performed on 25 patients (22). The tumescent technique involved the use of saline containing epinephrine at a dilution of 1:1,000,000 (22). All procedures were carried out as inpatient surgeries under general anesthesia (22). Among these, 41 cases utilized a vibration-assisted device, while 31 employed a WAL device. The average operative time was 116 min, with a range extending from 58 to 251 min (22).
Rapprich et al. [2011] described performing liposuction using TLAL and vibrating cannulas measuring 4 mm in diameter, operated with a VibraSat® handpiece (Möller Medical, Fulda, Germany) (25). The tumescent solution employed was adapted from Sattler’s formula, consisting of 1% prilocaine (50 mL), suprarenin (1:1,000, 1 mL), sodium bicarbonate (8.4%, 6 mL), triamcinolone (10 mg/mL, 1 mL), and sodium chloride solution (0.9%, 1,000 mL) (25). The final prilocaine concentration in this mixture was approximately 0.05% (25). On average, about 6,000 mL of the tumescent solution was infiltrated per session, with a maximum volume of 7,000 mL and a minimum of 2,000 mL (25). The mean volume infiltrated was 5,155±1,304 mL. For aspiration, vibrating cannulas with three blunt openings at the tip, arranged in a Mercedes star configuration, were utilized (25).
Some researchers advocate for the use of WAL due to its effectiveness in targeting adipose tissue. This technique involves directing a jet of tumescent solution to dislodge fat lobules while maintaining the structural integrity of blood vessels, lymphatic vessels, nerves, and septa retinaculi cutis. Stutz and Krahl [2009] utilized WAL on both legs to treat lipedema, employing a body jet system (Human Med AG) (26). The procedure involved a reduced volume of Klein’s solution (39) (1.0–1.5 L) to avoid significant tissue distension. A 3.5-mm body jet infiltration cannula was used and at range of 2. Sufficient anesthesia was achieved before moving immediately to the aspiration phase (no delay after infiltration) (26). A 3.5-mm irrigation-aspiration cannula was carefully directed along the lymphatic collectors, with a vacuum pressure maintained between 0.6–0.8 bar during the entire process (26). The volume of aspirated fluid ranged from 250 to 2,350 mL (26). The authors noted that WAL mobilized adipose cells in a similar fashion to vibration-assisted liposuction, but with less damage to blood vessels (26). Additionally, they demonstrated that WAL caused minimal disruption of lymphatic tissue, confirmed using the D2-40 immunohistochemical marker (from Zytomed, Berlin, Germany) (26). This method also preserved the collagen-fibrous septal connective tissue framework, which increases postoperative recovery and aids fibrous tissue retraction (26).
Most authors have encouraged the use of epinephrine in the infiltration to avoid toxicity with local anesthetics and to offer a better safety profile. Sandhofer et al. [2021] examined the serum levels of lidocaine and epinephrine following large-volume liposuction in 27 patients with lipedema (32). The procedure involved administering an average of 11,404 mL of tumescent anesthetic solution (32). The total amount of lidocaine administered averaged 3,061.9 mg, corresponding to 34.23 mg/kg of body weight. The mean dose of epinephrine was 9.7 mg, equating to 0.11 mg/kg of body weight (32). Lidocaine levels in the blood showed a biphasic pattern, peaking first at 4 h post-surgery with an average concentration of 1.65 µg/mL, and then again at 16 h post-operation with a mean concentration of 1.55 µg/mL (32). When patients were categorized by epinephrine concentration in the tumescent fluid, those receiving a lower epinephrine dose (0.7 mg/L) exhibited prolonged elevated lidocaine levels for up to 28 h postoperatively, compared to those who received a higher concentration of epinephrine (1.0 mg/L) (32).
Lipoaspirate and procedure
Currently, there is no clear scientific evidence indicating a specific maximum volume for liposuction that could jeopardize patient safety. Patients might be better served by treating large-volume liposuction as a staged procedure rather than attempting it all at once (40). In the context of lipoedema, large-volume liposuction exhibits notable differences from cosmetic liposuction, primarily because the risks and complications associated with limb surgeries are significantly greater compared to those in the central body regions (40). As a result, stringent selection criteria have been proposed, including the presence of persistent symptoms for over a year, considerable functional limitations, a stable body weight maintained for at least 12 months, and a BMI of less than 35 kg/m2 (40-42).
Debulking lipedema tissue often necessitates larger suction aspirate volumes than traditional liposuction, as well as multiple surgeries spaced at appropriate intervals (36). Unlike cosmetic liposuction, this procedure provides significant benefits in terms of mobility, pain relief, and overall health by removing lipedema tissue (36). Schmeller et al. [2012] documented a series of 112 patients undergoing suction-assisted lipectomy (20). Of 112 patients, 12 patients were operated on once, 29 patients twice, 28 patients three times, 23 patients four times, 12 patients five times, four patients six times, and four patients seven times (20). The minimum time between the operations was 1 month (20). The average amount of fat removed was 9,846 mL per person (range, 1,000–25,600 mL per person) or 3,077 mL per session (range, 450–7,000 mL per person), depending on the size and number of operated areas (20). Wollina and Heinig [2019] reported on 111 patients who underwent a total of 334 liposuction procedures at their department, averaging 3.01 sessions per patient (21). The median volume of lipoaspirate was 4,700±7,579 mL, with a range from 950 to 14,250 mL (21).
In our series, we found that the volume of fat removed differed significantly between surgical techniques, particularly when comparing tumescent liposuction with the WAL technique. This disparity may be attributed to WAL’s mechanism, which involves the use of a controlled, high-pressure water spray to gently dislodge fat cells while simultaneously performing suction. Using a WAL device (body jet; Human Med AG), Witte et al. [2020] noted that 6 patients (10%) underwent a single procedure, 21 patients (33%) had two procedures, 24 patients (38%) had three, and 12 patients (19%) underwent four procedures. On average, 12,922±2,922 mL of fat was removed per patient across all surgeries (28).
Dadras et al. [2017] performed on average 3 suction-assisted lipectomy procedures per patient, with a range of 1 to 7 procedures (22). The mean volume of removed fat per liposuction procedure was 3,106 mL (range, 1,450–6,600 mL) and the mean volume of total removed fat per patient was 9,914 mL (range, 4,000–19,850 mL) (22). Likewise, Rapprich et al. [2011] indicated that patients were treated in 1 to 5 sessions (mean, 2.5±1.1 sessions; median, 2 sessions) usually at 4-week intervals (25). For each session, the aspiration volume was an average of 2,482±968 mL and the pure fat component was on average 1,909±874 mL or 77% (25).
Kruppa et al. [2022] recently evaluated 106 patients who underwent a total of 298 liposuction procedures. A tumescent solution composed of saline and epinephrine (1:1,000,000) was used for tissue infiltration, with a maximum of 6,000 mL administered per session (29). The primary surgical goal was to remove an amount of fat corresponding to approximately 6% of the patient’s body weight (29). This often required mega-liposuction, defined as the removal of at least 4 L of pure fat or 5 L of total aspirate (29). On average, patients completed a three-stage surgical regimen, with a mean lipoaspirate volume of 6,355±2,797 mL per procedure. The total cumulative lipoaspirate per patient across the stages averaged 17,887±10,341 mL, with the highest recorded volume reaching 66,200 mL (29). For patients undergoing multistage treatments, the median time span of the surgical process was 8 months (IQR, 4–14 months) (29). Kruppa et al. [2022] indicated that they did not find a significant correlation between the primary endpoint (reduction in CDT score) or secondary endpoints (improvement in lipedema-associated complaints) and the amount of total lipoaspirate or aspirate per liposuction, which indicated that the amount of volume aspirated should be individualized and tailored to each patient (29).
Anthropometric outcomes
Suction-assisted lipectomy for lipedema reduction surgery results in a significant decrease in limb circumference measurements (Table 7). Schmeller et al. [2012] reported that the removal of subcutaneous fatty tissue led to a reduction in the circumference of the hips, legs, and/or arms, ultimately producing a more proportionate body after surgery. Average reductions were 8 cm (range, 1–23 cm) in the thighs (inguinal region) and 4 cm (range, 1–11 cm) in the mid-calves (20). Likewise, Wollina and Heinig [2019] reported a median 6±1.6 cm-limb circumference reduction at the level of the thighs in 111 patients (21). Similarly, using Image-3D-system (Fa. Bauerfeind, Zeulenroda-Triebes, Germany) and a digital camera to take photos of the leg at different angles, Rapprich et al. [2011] achieved an average reduction of leg volume of 6.9 % after liposuction (range from 0.9% to 19.8%) (25).
Table 7
Authors, year | Reduction of limb circumference (cm), [range] or ± SD | Weight change (kg)† | BMI change (kg/m2)† | Complications |
---|---|---|---|---|
Schmeller et al., 2012 (20) | Mean T: 8 [1–23]/LL: 4 [1–11] | Mean (−) 0.4 | NS | 1.4% wound infections (4 erysipelas and 1 abscess) |
0.3% bleeding | ||||
Wollina and Heinig, 2019 (21) | Median 6±1.6 | NS | NS | 100% temporary met-hemoglobinemia |
98% bruising | ||||
82% temporary burning sensation | ||||
0.6% mild arm-vein phlebitis | ||||
0.3% seizure during meta-hemoglobinemia | ||||
0.3% postoperative anemia requiring blood transfusion | ||||
0.3% pulmonary fat embolism | ||||
0.3% pneumonia | ||||
Dadras et al., 2017 (22) | NS | NS | Mean (−) 1.4 | 1.39% erysipelas |
Baumgartner et al., 2021 (23) | NS | Mean (+) 0.5 | NS | NS |
Rapprich et al., 2011 (25) | NS | NS | NS | 4% DVT |
Wollina et al., 2014 (11) | NS | Mean (−) 1.8/median 0 | NS | None |
Witte et al., 2020 (28) | NS | Mean (−) 5.6 | Mean (−) 2.3 | NS |
Peled et al., 2012 (19) | NS | Mean (+) 9 | NS | NS |
Chen et al., 2004 (6) | Mean T: 9/RC: 5/LC: 6 | NS | NS | NS |
Current study | NS | NS | Mean (−) 2.8 | 4.2% seroma |
4.2% infection | ||||
4.2% epidermolysis | ||||
Kruppa et al., 2022 (29) | NS | NS | Mean 2.7 (IQR, 1.1–5.2) | 1.3% wound infections |
0.7% seroma | ||||
0.3% postoperative bleeding | ||||
Gensior et al., 2023 (30) | NS | NS | NS | 1.79% infection |
0.79% seroma | ||||
0.28% erysipelas | ||||
0.14% dry necrosis | ||||
0.07% DVT | ||||
Kirstein et al., 2023 (33) | NS | NS | Mean 2.47±3.2 | 75% had complications |
Klöppel et al., 2024 (34) | NS | NS | NS | 53% swelling |
43% hardening or loosening of skin | ||||
40% sensory disturbances | ||||
20% dents |
†, before and after surgery. SD, standard deviation; BMI, body mass index; T, tights; LL, lower legs; NS, not specific; DVT, deep venous thrombosis; RC, right calf; LC, left calf; IQR, interquartile range.
In our case series, a significant reduction in BMI was observed between the pre- and post-operative periods, highlighting that liposuction not only enhances patient-reported outcomes but also contributes to a measurable decrease in BMI. Comparably, Witte et al. [2020] also documented significant reductions in both BMI and weight following liposuction (28). Kruppa et al. [2022], after a median follow-up of 20 months, noted a significant decrease in BMI (by 2.7 kg/m2; IQR, 1.1–5.2 kg/m2) and a reduction in the size of the affected areas by two European clothing sizes (IQR, 2–4) after liposuction (P<0.001) (29). Similarly, Kirstein et al. [2023] used a mixed regression model to analyze 56 patients and found a notable reduction in BMI after surgery, with BMI being 1.65 times higher prior to liposuction [95% confidence interval (CI): 0.67–2.64, P=0.002] (33).
Interestingly, several studies have found no significant reduction in BMI following suction lipectomy. For instance, Flores et al. [2024] analyzed 45 liposuction procedures performed on 36 patients, including 35 procedures targeting the lower extremities and 10 on the upper extremities. The average volume of fat removed was 6,615.33±3,884.25 mL, and the mean preoperative BMI was 32.18±7.26 kg/m2 (35). Despite the large volumes of fat aspirated, no significant changes in BMI were observed postoperatively (35). Notably, a larger proportion of patients underwent suction lipectomy exclusively on the upper limbs, which may have less impact on BMI compared to liposuction of the lower limbs. Other studies have demonstrated that not all patients achieve a sustained weight reduction. Baumgartner et al. [2021] reported post-surgical weight gain in 43.3% of their patients, 7.9 kg on average (range, 0.5–39.5 kg) (23).
Symptom control
Pain reduction is a primary goal of liposuction, while body contouring and weight modification are secondary objectives. Suction-assisted lipectomy for lipedema reduction surgery results in a significant improvement of symptoms associated with lipedema. Using a Likert scale from 0 to 5, Schmeller et al. [2012] reported that the removal of subcutaneous fatty tissue led to improvement or amelioration of spontaneous pain (P<0.001), pain because of pressure (P<0.001), edema (P<0.001), bruising (P<0.001), and restriction of movement (P<0.001) following liposuction (20). Likewise, Wollina and Heinig [2019] reported that suction-assisted lipectomy resulted in a significant reduction in pain scores, as measured on the 10-point VAS, decreasing from a preoperative value of 7.8±2.1 to 2.2±1.3 postoperatively in 111 patients (21). Also, they noted that 20.9% and 29.1% of patients felt that bruising after minor trauma improved somewhat or completely resolved following liposuction, respectively (P<0.5) (21). Large-scale studies have not established a clear association between pain reduction and volume loss (14). In other series using a WAL device (body jet; Human Med AG), Witte et al. [2020] indicated a significant reduction in pain, sensitivity to touch, bruising, feeling of tension, feeling of “heavy” legs, swelling, itching, running impairment, occupational impairment, general impairment, and aesthetic impairment after surgery (P<0.001) (28).
Suction-assisted lipectomy for lipedema significantly improves patients’ subjective perception of mobility. Wollina and Heinig [2019] reported that all patients (100%) experienced some degree of improvement in mobility after liposuction. Notably, 86% of patients reported marked improvement or complete resolution of impairment, while 14% experienced minor to moderate improvements (21). In a recent study by Kirstein et al. [2023], involving 56 patients, the authors assessed symptoms both before and after surgery (33). The mixed-model analysis revealed that preoperative pain was 2.67 times higher compared to postoperative levels (95% CI: 2.09–3.25, P<0.001) (33). Similarly, preoperative pressure sensitivity was 1.97 times greater than after surgery (95% CI: 1.21–2.71, P<0.001). Additionally, walking limitations were found to be 2.26 times higher before surgery than postoperatively (95% CI: 1.49–3.03, P<0.001) (33).
While the cosmetic improvements from liposuction may not be permanent, the functional benefits often persist over time, especially when the procedure is performed for lipedema. Dadras et al. [2017] evaluated symptom improvement following liposuction at two different time points during the postoperative period [first postoperative value (postOp-T1) and second postoperative value (postOp-T2)] (22). Bonferroni-corrected P values showed significantly improved values comparing preoperative values and postoperative values at the two different time points for spontaneous pain, bruising, sensitivity to pressure, feeling of tension, cosmetic impairment, and general impairment (P<0.001) (22). Remarkably, cosmetic impairment scores aggravated comparing the postOp-T2 to the postOp-T1 (22).
The amount of volume aspirated at the time of surgery may not strongly correlate with the degree of symptom improvement. Evaluating 15 symptoms like muscle cramps, lower limb heaviness, itching, and pain, Rapprich et al. [2011] were able to reduce 58% symptomatologic burden at 6 months after surgery with suction-assisted lipectomy (P<0.001) (25). In a scale from 0 to 150, the average score before liposuction was 92.0±21.3, and 6 months after surgery was 39.0±23.2 (25). The authors found that the reduction in measured volume did not statistically correlate with the degree of improvement of symptoms (25).
Reduction in conservative
The European Lipedema Forum Consensus in 2020 highlighted significant changes in the understanding, diagnosis, and treatment of lipedema due to advancements in the comprehension of the disease (43). Previously, lipedema was believed to involve “fluid in fat”, a concept that gave rise to its name (43). However, there is no scientific evidence to support this hypothesis. Consequently, it is inaccurate to attribute the benefits of MLD to “drainage effects”. In fact, improvements in pain following MLD therapy are mainly observed in the initial stages of treatment (43). Compression therapy remains a critical component in lipedema management, although its therapeutic effects are due to its anti-inflammatory properties rather than drainage (43). Additionally, it is incorrect to assert that lipedema is a progressive condition, that weight loss is ineffective, or that lipedema leads to lymphedema, as no scientific evidence currently supports these claims (43).
Recent and most contemporary studies have indicated liposuction for lipedema management only generates minimal reduction in the need for non-surgical treatments or conservative therapies. Schmeller et al. [2012] reported that among patients who had undergone lymphatic drainage and compression therapy prior to surgery, 20% required less post-surgery, 13% needed only compression, 6% required only lymphatic drainage, and only 15% no longer required either treatment (20). Thirteen percent of patients still required both lymphatic drainage and compression therapy following surgery (20). In a similar series of 111 patients documented by Wollina and Heinig [2019], only 16.4% were able to completely abandon CDT at a median follow-up of 2.0±2.1 years (21).
Conversely, other reports have indicated that liposuction significantly reduces the need for conservative therapy in the majority of patients. According to Rapprich et al. [2011] approximately two-thirds of the patients received MLD and compression therapy prior to undergoing liposuction (25). Six months after the final liposuction session, only 8% of patients reported that they still required MLD, though less frequently (25). Also, only 16% of patients indicated that they occasionally or regularly wore compression stockings post-procedure (25). Witte et al. [2020] using WAL, indicated a significant reduction of MLD and compression garments after surgery (28). The percentage of patients requiring MLD after surgery was reduced from 88.9% to 39.7% (P<0.001) while compression garments use was reduced from 95.2% to 31.7% (P<0.001) (28).
Lipedema stage & outcomes
The stage of lipedema influences the clinical outcomes of liposuction. Patients with earlier stages of lipedema tend to have better responses to suction-assisted lipectomy than those with more advanced stages. Kruppa et al. [2022] determined that patients with stages I and II lipedema exhibited a more significant reduction in their composite VAS scores for QoL (median reduction of 46%; IQR, 24.6% to 60.9%) compared to those with stage III lipedema (20%; IQR, 12.7% to 51.3%; P=0.0107) (29). Additionally, patients with stage I and II lipedema showed a more pronounced decrease in the requirement of CDT scores (50%; IQR, 8.3% to 100%) compared to those in stage III (16.7%; IQR, 0 to 50%; P=0.0019), indicating a better response to liposuction at early stages (29).
Kruppa et al. [2022] also showed a reduction in the CDT score with a median of 37.5% (IQR, 0 to 88.8%) following large-volume liposuction in all stages of lipedema (P<0.001) (29). The percentage of patients that were able to stop compression garments postoperatively was higher in stage I and II patients (41.7%) compared to stage III patients (20.6%; P=0.0487) (29). Likewise, a higher proportion of patients with stage I and II (33.3%) did not need any conservative treatment postoperatively compared to stage III patients (8.8%; P<0.008) (29).
Similarly, Dadras et al. [2017] assessed the overall impairment in patients with stage II and stage III lipedema both preoperatively and at two postoperative time points (22). Although the general impairment values were significantly improved at postoperative point 1 (mean, 16 months) and point 2 (mean, 37 months) compared to preoperative levels, stage III patients experienced a notable increase in the severity of their symptoms between the first and second postoperative follow-ups (22).
Duration of results
Baumgartner et al. [2021] conducted a longitudinal study following 60 patients with stage I and II lipoedema over an extended period (23). Their findings revealed that the improvements in spontaneous pain, pressure sensitivity, swelling, bruising, and restricted movement observed at 4 and 8 years post-lower limb liposuction were maintained even 12 years after the procedure (23). Self-reported measures of cosmetic dissatisfaction, QoL, and overall functional impairment also remained stable 12 years postoperatively (23). Furthermore, the reduction in reliance on conservative treatments, such as decongestive therapy and compression garments, paralleled those seen at the earlier follow-up intervals (23). In this setting, long-term outcomes for patients with stage III lipoedema must be evaluated in future studies (23).
Complications
Patients who undergo suction-assisted lipectomy for the management of lipedema experience minimal complications after surgery and therefore, benefits outweigh risks in most cases (Table 7). Schmeller et al. [2012] reported a 1.4% rate of infection in which three cases were simple erysipelas and one case had an abscess. The authors also reported a 0.3% rate of postoperative bleeding with significant hemoglobin drop (5.2 g/dL drop) (20). In a series using vibration-assisted device for liposuctions in 57% of the cases and a WAL device for the remaining 43% of the cases, the complication rate was 1.39% (22). Witte et al. [2020] using WAL, indicated that they did not encounter significant complications in any of the patients (28). Postoperative swelling was present for a mean of 4.3 weeks; patients were absent from work for a mean of 2.7 weeks postoperatively (28).
Liposuction for lipedema can be safely performed in patients with varying stages of lipedema even in the presence of different comorbidities. In a recent investigation by Kruppa et al. [2022], 106 patients were evaluated after undergoing a total of 298 liposuction procedures (29). The study population included patients with varying stages of lipedema: 11 patients (10.4%) with stage I, 61 patients (57.6%) with stage II, and 34 patients (32.1%) with stage III (29). The cohort exhibited a high prevalence of comorbidities, with 37.6% classified as obese (BMI >35 kg/m2), 36.8% having allergies, 31.1% diagnosed with hypothyroidism, 25.5% experiencing depression, 25.5% suffering from sleep disorders, 24.5% with hypertension, 22.6% with migraines, and 18.9% with skin disorders (29). Despite the fact that 69.1% of the liposuction procedures were categorized as mega-liposuction, the study reported a low incidence of complications (29). The observed complications were minor and included wound infections in 1.3% of cases, seroma formation in 0.7%, and postoperative bleeding in 0.3% (29). Although a subset of patients developed excess skin following multiple liposuction treatments, only 2 patients (1.9%) pursued corrective surgery (29).
In other series, the rate of complications has been higher with some major complications significantly affecting the postoperative course of patients. For instance, the use of local anesthetics in tumescent anesthesia can lead to a marked production of methemoglobin (21). Certainly, in one of the largest series, the authors indicated that the most common complication they encountered was temporary methemoglobinemia (100%) (21). This was treated by intravenous injection of toluidine blue (21). In a number of initial liposuctions, 1 g intravenous vitamin C was administered (21). Also, temporary burning sensations and bruising were noted in 82% and 98% of cases (21). A generalized seizure episode was evident during methemoglobinemia in a 34-year-old female without known comorbidities (0.3%) (21). Significant anemia requiring a blood transfusion was seen in 1 patient (0.3%), two patients presented with mild arm-vein phlebitis (0.6%), microscopic pulmonary fat embolism was seen in one patient (0.3%), and one patient required intensive care unit (ICU) admission for management of pulmonary issues (0.3%) (21). In another series, Rapprich et al. [2011] had a patient with lower limb deep vein thrombosis 1 week after surgery (4%) (25).
In another series, the authors conducted 1,400 lymphological liposculpture procedures across 504 patients with lipedema, with 504 procedures targeting the inner half of the limbs, 504 targeting the outer half, and 392 performed on the upper arms (30). Within 30 days after surgery, 43 patients (3.07%) experienced adverse effects (30). Surgical site infections were observed in 25 patients (1.79%), while seroma formation occurred in eleven patients (0.79%) (30). Additionally, erysipelas developed in 4 patients (0.28%), dry necrosis in 2 patients (0.14%), and deep vein thrombosis in 1 patient (0.07%) (30).
QoL
Suction-assisted lipectomy for lipedema reduction surgery results in a significant improvement of QoL (Table 8). Multiple authors have reported a statistically significant improvement of QoL using different instruments following liposuction. Using a Likert scale from 0 to 5, Schmeller et al. [2012] reported that the removal of subcutaneous fatty tissue led to improvement of QoL from a preoperative score of 3.36±0.86 to 0.76±0.91 postoperatively (P<0.001) (20).
Table 8
Patient-reported outcomes† | 5-point Likert scale‡ (20,23) | 10-point VAS | |||||
---|---|---|---|---|---|---|---|
Pre-surgery | Post-surgery | Improvement | Pre-surgery | Post-surgery | Improvement | ||
Spontaneous pain | 1.86 | 0.42 | 1.44 | 6.86 (22,25,28) | 2.16 (22,25,28) | 4.7 | |
Sensitivity to pressure | 2.90 | 0.97 | 1.93 | 6.99 (22,25) | 3.14 (22,25) | 3.85 | |
Edema | 3.07 | 1.31 | 1.76 | 7.68 (25) | 2.71 (25) | 4.97 | |
Bruising | 3.03 | 1.34 | 1.69 | 7.32 (22,25) | 3.5 (22,25) | 3.75 | |
Restriction to movement | 2.04 | 0.40 | 1.80 | 4.6 (25) | 1.6 (25) | 3 | |
Cosmetic Impairment | 3.30 | 1.18 | 2.12 | 9.05 (22,25,28) | 3.26 (22,25,28) | 5.80 | |
Reduction of QoL/impairment of QoL | 3.38 | 0.83 | 2.55 | 8.7 (25) | 3.6 (25) | 5.10 | |
General impairment | 2.82 | 0.94 | 1.88 | – | – | – |
†, current case series is included in this calculation, except for restriction to movement, reduction of QoL, and general impairment in VAS. ‡, 0, none; 1, minor; 2, medium; 3, strong; 4, very strong. VAS, visual analogue scale; QoL, quality of life.
In a recent prospective study assessing QoL following liposuction for lipoedema, 30 female patients with a mean BMI of 27.2±3.7 kg/m2 were examined (34). The classification of disease severity among these patients was as follows: 7% were categorized as having mild lipoedema, 47% as moderate, 43% as severe, and 3% as very severe (34). Notably, 83% of the participants reported having previously received MLD and/or used compression therapy as part of their treatment regimen (34). During the liposuction procedure, an average of 8.7±1.28 L (ranging from 5.9 to 10.6 L) of adipose tissue was aspirated from the thighs, knees, and calves. The study found no serious postoperative complications (34). Overall satisfaction with the surgical outcomes at 6 months postoperatively was notably high, averaging 7.9±1.82 on a 0 to 10 scale (34), Regarding satisfaction with the treated area, 23% of patients reported being very satisfied, while 63% were fairly satisfied. Furthermore, 93% of patients experienced an improvement in personal well-being following the surgery (34). The Questions on Life Satisfaction Modules (FLZM) (44) results indicated significant enhancements in all three evaluated domains: general life satisfaction, health status, and body image (34). The Patient Health Questionnaire-4 (PHQ-4) (45) assessment revealed notable reductions in both anxiety and depression levels, as well as overall mental stress. Additionally, the Rosenberg Self-Esteem Scale (RSES) (46) demonstrated a significant increase in self-esteem postoperatively (34).
Suction-assisted lipectomy appears to have a beneficial effect on mood in patients with lipoedema. According to the PHQ-9 scale, patients who underwent liposuction for treatment of lipedema improved from experiencing moderate to severe depression preoperatively (mean score of 10.84±6.38) to a mild depressive state after surgery (mean score of 8.27±6.45) (33). The World Health Organization Quality of Life-BREF (WHOQOL-BREF) assessment revealed a significant positive correlation between liposuction and improvements in the physical domain scores (95% CI: 12.84–4.86, P<0.001). However, no significant correlations were observed between the surgery and the psychological, social, or environmental domains (33).
Liposuction improves QoL in patients with lipedema, even in patients with severe stage III lipedema. In a retrospective study involving 69 female patients with stage III lipoedema, liposuction was performed as a therapeutic intervention (31). On average, each patient underwent 2.9±1.9 liposuction sessions, with the number of sessions varying between 1 and 12. Of these patients, 20 completed the Freiburg Quality of Life Assessment for lymphatic disorders, Short Version (FLQA-lk) questionnaires (47) both prior to the procedure and 6 months postoperatively (31). The findings indicated a notable enhancement in disease-specific QoL following liposuction treatment, with significant improvements observed across all subscales and the overall score (31).
Kruppa et al. [2022] conducted an evaluation of QoL—including spontaneous pain, pressure sensitivity, feelings of tension, bruising, body image perception, and overall impairment—and found substantial improvements across all measured parameters following liposuction as indicated by significant reductions in VAS scores (P<0.001) (29). This study demonstrated high overall patient satisfaction with the multistage surgical treatment, with a median VAS score of 9 (IQR, 7–10). Furthermore, notable enhancements were observed in sexual QoL, demonstrated by a reduction in impairment scores from a preoperative VAS score of 7.5 (IQR, 4.0–8.25) to a postoperative VAS score of 3.0 (IQR, 1–5) (P<0.001) (29).
Malcolm et al. [2024] reported a series of forty-seven patients that received tumescent liposuction over 5 years (48). Most patients (77%) were diagnosed with stage 2 (n=16) and 3 (n=20) lower limb lipedema. After liposuction, they evidence a significant reduction of depression and anxiety (P<0.05) using Hospital Anxiety and Depression Scale (48). Using the QoL scores from the LYMQoL questionnaire, the authors demonstrated a significant improvement of QoL overall in patients with lipedema following liposuction, with stage 3 patients achieving the most notable improvement (P<0.001) (48). After surgery, patients also demonstrated a significant improvement in functional ability using the Lower Extremity Functional Scale (LEFS) (P<0.005) (48).
Limitations
Significant limitations arise due to the substantial heterogeneity among studies and the various instruments used to assess patient-reported outcomes. Additionally, all studies included in this review are either case reports or case series, which are observational and inherently lack randomization. As a result, they are more susceptible to confounding bias. Furthermore, the case series in this study are limited by their small sample sizes, reducing the statistical power of the findings. We did not include waist-to-height-ratio in order to evaluate co-incidence of obesity. Only using BMI leads to inaccurate diagnoses overestimating overweight and obesity (1,43).
Conclusions
Liposuction has been shown to be a safe and effective alternative when conservative therapy fails to treat lipoedema. All liposuction techniques used to date have had a positive impact on both clinical and patient-reported outcomes, with these benefits being sustained over time. However, further studies with stronger levels of evidence are needed to support these findings and to evaluate differences between surgical techniques, ideally using standardized assessment tools such as the VAS.
Acknowledgments
Funding: None.
Footnote
Reporting Checklist: The authors have completed the AME Case Series and the Narrative Review reporting checklists. Available at https://atm.amegroups.com/article/view/10.21037/atm-24-165/rc
Peer Review File: Available at https://atm.amegroups.com/article/view/10.21037/atm-24-165/prf
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://atm.amegroups.com/article/view/10.21037/atm-24-165/coif). O.J.M. serves as an unpaid editorial board member of Annals of Translational Medicine from July 2024 to June 2026. The other authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committees and with the Helsinki Declaration (as revised in 2013). Informed consent was obtained from all patients.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
References
- Brenner E, Forner-Cordero I, Faerber G, et al. Body mass index vs. waist-to-height-ratio in patients with lipohyperplasia dolorosa (vulgo lipedema). J Dtsch Dermatol Ges 2023;21:1179-85. [Crossref] [PubMed]
- Fife CE, Maus EA, Carter MJ. Lipedema: a frequently misdiagnosed and misunderstood fatty deposition syndrome. Adv Skin Wound Care 2010;23:81-92; quiz 93-4. [Crossref] [PubMed]
- Langendoen SI, Habbema L, Nijsten TE, et al. Lipoedema: from clinical presentation to therapy. A review of the literature. Br J Dermatol 2009;161:980-6. [Crossref] [PubMed]
- Kruppa P, Georgiou I, Biermann N, et al. Lipedema-Pathogenesis, Diagnosis, and Treatment Options. Dtsch Arztebl Int 2020;117:396-403. [Crossref] [PubMed]
- Torre YS, Wadeea R, Rosas V, et al. Lipedema: friend and foe. Horm Mol Biol Clin Investig 2018;33:/j/hmbci.2018.33.issue-1/hmbci-2017-0076/hmbci-2017-0076.xml
- Chen SG, Hsu SD, Chen TM, et al. Painful fat syndrome in a male patient. Br J Plast Surg 2004;57:282-6. [Crossref] [PubMed]
- Wold LE, Hines EA Jr, Allen EV. Lipedema of the legs; a syndrome characterized by fat legs and edema. Ann Intern Med 1951;34:1243-50. [Crossref] [PubMed]
- Alwardat N, Di Renzo L, Alwardat M, et al. The effect of lipedema on health-related quality of life and psychological status: a narrative review of the literature. Eat Weight Disord 2020;25:851-6. [Crossref] [PubMed]
- Dudek JE, Białaszek W, Ostaszewski P, et al. Depression and appearance-related distress in functioning with lipedema. Psychol Health Med 2018;23:846-53. [Crossref] [PubMed]
- Forner-Cordero I, Szolnoky G, Forner-Cordero A, et al. Lipedema: an overview of its clinical manifestations, diagnosis and treatment of the disproportional fatty deposition syndrome - systematic review. Clin Obes 2012;2:86-95. [Crossref] [PubMed]
- Wollina U, Heinig B, Nowak A. Treatment of elderly patients with advanced lipedema: a combination of laser-assisted liposuction, medial thigh lift, and lower partial abdominoplasty. Clin Cosmet Investig Dermatol 2014;7:35-42. [Crossref] [PubMed]
- Wollina U, Heinig B, Schönlebe J, et al. Debulking surgery for elephantiasis nostras with large ectatic podoplanin-negative lymphatic vessels in patients with lipo-lymphedema. Eplasty 2014;14:e11.
- Shavit E, Wollina U, Alavi A. Lipoedema is not lymphoedema: A review of current literature. Int Wound J 2018;15:921-8. [Crossref] [PubMed]
- Kodim A, Wollina U. Microcannular liposuction in tumescent anesthesia in lipedema patients: an analysis of 519 liposuctions. Wien Med Wochenschr 2023;173:290-8. [Crossref] [PubMed]
- Warren Peled A, Kappos EA. Lipedema: diagnostic and management challenges. Int J Womens Health 2016;8:389-95. [Crossref] [PubMed]
- Aday AW, Donahue PM, Garza M, et al. National survey of patient symptoms and therapies among 707 women with a lipedema phenotype in the United States. Vasc Med 2024;29:36-41. [Crossref] [PubMed]
- Strößenreuther R, Baumeister RGH. Lipödem und Cellulitis: sowie andere Erkrankungen des Fettgewebes. Köln: Viavital-Verlag; 2001.
- Meier-Vollrath I, Schmeller W. Lipoedema--current status, new perspectives. J Dtsch Dermatol Ges 2004;2:181-6. [Crossref] [PubMed]
- Peled AW, Slavin SA, Brorson H. Long-term Outcome After Surgical Treatment of Lipedema. Ann Plast Surg 2012;68:303-7. [Crossref] [PubMed]
- Schmeller W, Hueppe M, Meier-Vollrath I. Tumescent liposuction in lipoedema yields good long-term results. Br J Dermatol 2012;166:161-8. [Crossref] [PubMed]
- Wollina U, Heinig B. Treatment of lipedema by low-volume micro-cannular liposuction in tumescent anesthesia: Results in 111 patients. Dermatol Ther 2019;32:e12820. [Crossref] [PubMed]
- Dadras M, Mallinger PJ, Corterier CC, et al. Liposuction in the Treatment of Lipedema: A Longitudinal Study. Arch Plast Surg 2017;44:324-31. [Crossref] [PubMed]
- Baumgartner A, Hueppe M, Meier-Vollrath I, et al. Improvements in patients with lipedema 4, 8 and 12 years after liposuction. Phlebology 2021;36:152-9. [Crossref] [PubMed]
- Schmeller W, Meier-Vollrath I. Tumescent liposuction: a new and successful therapy for lipedema. J Cutan Med Surg 2006;10:7-10. [Crossref] [PubMed]
- Rapprich S, Dingler A, Podda M. Liposuction is an effective treatment for lipedema-results of a study with 25 patients. J Dtsch Dermatol Ges 2011;9:33-40. [Crossref] [PubMed]
- Stutz JJ, Krahl D. Water jet-assisted liposuction for patients with lipoedema: histologic and immunohistologic analysis of the aspirates of 30 lipoedema patients. Aesthetic Plast Surg 2009;33:153-62. [Crossref] [PubMed]
- Baumgartner A, Hueppe M, Schmeller W. Long-term benefit of liposuction in patients with lipoedema: a follow-up study after an average of 4 and 8 years. Br J Dermatol 2016;174:1061-7. [Crossref] [PubMed]
- Witte T, Dadras M, Heck FC, et al. Water-jet-assisted liposuction for the treatment of lipedema: Standardized treatment protocol and results of 63 patients. J Plast Reconstr Aesthet Surg 2020;73:1637-44. [Crossref] [PubMed]
- Kruppa P, Georgiou I, Schmidt J, et al. A 10-Year Retrospective before-and-after Study of Lipedema Surgery: Patient-Reported Lipedema-Associated Symptom Improvement after Multistage Liposuction. Plast Reconstr Surg 2022;149:529e-41e. [Crossref] [PubMed]
- Gensior M, Cornely M. Complications and their management in the surgical treatment of lipohyperplasia dolorosa. Dermatologie (Heidelb) 2023;74:114-20. [Crossref] [PubMed]
- Schlosshauer T, Heiss C, von Hollen AK, et al. Liposuction treatment improves disease-specific quality of life in lipoedema patients. Int Wound J 2021;18:923-31. [Crossref] [PubMed]
- Sandhofer M, Hofer V, Sandhofer M, et al. High Volume Liposuction in Tumescence Anesthesia in Lipedema Patients: A Retrospective Analysis. J Drugs Dermatol 2021;20:326-34. [Crossref] [PubMed]
- Kirstein F, Hamatschek M, Knors H, et al. Patient-Reported Outcomes of Liposuction for Lipedema Treatment. Healthcare (Basel) 2023;11:2020. [Crossref] [PubMed]
- Klöppel M, Römich D, Machens HG, et al. Quality of life following liposuction for lipoedema: a prospective outcome study. J Plast Reconstr Aesthet Surg 2024;91:70-8. [Crossref] [PubMed]
- Flores T, Kerschbaumer C, Jaklin FJ, et al. High-Volume Liposuction in Lipedema Patients: Effects on Serum Vitamin D. J Clin Med 2024;13:2846. [Crossref] [PubMed]
- Reich-Schupke S, Schmeller W, Brauer WJ, et al. S1 guidelines: Lipedema. J Dtsch Dermatol Ges 2017;15:758-67. [Crossref] [PubMed]
- Hardy D, Williams A. Best practice guidelines for the management of lipoedema. Br J Community Nurs 2017;22:S44-8. [Crossref] [PubMed]
- Peprah K, MacDougall D. Liposuction for the Treatment of Lipedema: A Review of Clinical Effectiveness and Guidelines. Ottawa: Canadian Agency for Drugs and Technologies in Health; 2019.
- Klein JA. The tumescent technique for lipo-suction surgery. Am J Cosmet Surg 1987;4:263-7.
- Dancey A, Pacifico M, Kanapathy M, et al. Summary document on safety and recommendations on liposuction for lipoedema: Joint British association of aesthetic plastic surgeons (BAAPS)/British association of plastic reconstructive and aesthetic surgeons (BAPRAS) expert liposuction group. J Plast Reconstr Aesthet Surg 2023;77:400-7. [Crossref] [PubMed]
- Buck DW 2nd, Herbst KL. Lipedema: A Relatively Common Disease with Extremely Common Misconceptions. Plast Reconstr Surg Glob Open 2016;4:e1043. [Crossref] [PubMed]
- Bertsch T, Erbacher G, Elwell R. Lipoedema: a paradigm shift and consensus. J Wound Care 2020;29:1-51. [Crossref] [PubMed]
- Bertsch T, Erbacher G, Corda D, et al. Lipödem–Mythen und Fakten Teil 5. Phlebologie 2020;49:31-50.
- Henrich G, Herschbach P. Questions on Life Satisfaction (FLZM): a short questionnaire for assessing subjective quality of life. Eur J Psychol Assess 2000;16:150-9.
- Löwe B, Wahl I, Rose M, et al. A 4-item measure of depression and anxiety: validation and standardization of the Patient Health Questionnaire-4 (PHQ-4) in the general population. J Affect Disord 2010;122:86-95. [Crossref] [PubMed]
- Schmitt DP, Allik J. Simultaneous administration of the Rosenberg Self-Esteem Scale in 53 nations: exploring the universal and culture-specific features of global self-esteem. J Pers Soc Psychol 2005;89:623-42. [Crossref] [PubMed]
- Augustin M, Bross F, Földi E, et al. Development, validation and clinical use of the FLQA-I, a disease-specific quality of life questionnaire for patients with lymphedema. Vasa 2005;34:31-5. [Crossref] [PubMed]
- Malcolm L. A retrospective comparative study of patient-reported outcome measures, pre-treatment and twelve months post-treatment using tumescent liposuction for the management of lower limb lipoedema. JPRAS Open 2024;41:285-94. [Crossref] [PubMed]