CC BY-NC-ND 4.0 · Arch Plast Surg 2022; 49(02): 266-274
DOI: 10.1055/s-0042-1744361
Research/Experimental
Original Article

Optimizing Fat Grafting Using a Hydraulic System Technique for Fat Processing: A Time and Cost Analysis

Vincenzo Verdura*
1   Multidisciplinary Department of Medical Surgical and Dental Specialties, Plastic Surgery Unit, University of Campania “Luigi Vanvitelli,” Naples, Italy
,
Antonio Guastafierro*
1   Multidisciplinary Department of Medical Surgical and Dental Specialties, Plastic Surgery Unit, University of Campania “Luigi Vanvitelli,” Naples, Italy
,
Bruno Di Pace
2   Department of Medicine, Surgery and Dentistry “Scuola Medica Salernitana,” PhD School of Translational Medicine of Development and Active Aging, University of Salerno, Salerno, Italy
3   Department of Plastic and Reconstructive Surgery, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom
4   Anglia Ruskin University School of Medicine, Cambridge and Chelmsford, United Kingdom
,
Mario Faenza
1   Multidisciplinary Department of Medical Surgical and Dental Specialties, Plastic Surgery Unit, University of Campania “Luigi Vanvitelli,” Naples, Italy
,
Giovanni Francesco Nicoletti
1   Multidisciplinary Department of Medical Surgical and Dental Specialties, Plastic Surgery Unit, University of Campania “Luigi Vanvitelli,” Naples, Italy
,
Corrado Rubino
5   Department of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy
6   Plastic Surgery Unit, Department of Oncology and Haematology, University Hospital Trust of Sassari, Sassari, Italy
› Author Affiliations
 

Abstract

Background Many authors have researched ways to optimize fat grafting by looking for a technique that offers safe and long-term fat survival rate. To date, there is no standardized protocol. We designed a “hydraulic system technique” optimizing the relationship among the quantity of injected fat, operative time, and material cost to establish fat volume cutoffs for a single procedure.

Methods Thirty-six patients underwent fat grafting surgery and were organized into three groups according to material used: standard, “1-track,” and “2-tracks” systems. The amount of harvested and grafted fat as well as material used for each procedure was collected. Operating times were recorded and statistical analysis was performed to establish the relationship with the amount of treated fat.

Results In 15 cases the standard system was used (mean treated fat 72 [30–100] mL, mean cost 4.23 ± 0.27 euros), in 11 cases the “1-track” system (mean treated fat 183.3 [120–280] mL, mean cost 7.63 ± 0.6 euros), and in 10 cases the “2-tracks” one (mean treated fat 311[220–550] mL, mean cost 12.47 ± 1 euros). The mean time difference between the standard system and the “1-track” system is statistically significant starting from three fat syringes (90 mL) in 17.66 versus 6.87 minutes. The difference between the “1-track” system and “2-tracks” system becomes statistically significant from 240 mL of fat in 15 minutes (“1-track”) versus 9.3 minutes for the “2-tracks” system.

Conclusion Data analysis would indicate the use of the standard system, “1-track,” and “2-tracks” to treat an amount of fat < 90 mL of fat, 90 ÷ 240 mL of fat, and ≥ 240 mL of fat, respectively.


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Introduction

Autologous fat grafting is applicable to many fields of plastic surgery ranging from reconstructive to cosmetic surgery.[1] [2] Since the introduction of this technique in the 1990s[3] [4] [5] many authors have performed research into the ways in which fat grafting can be optimized by looking for a technique that offers safe and long-term fat survival rate. To date, there is no current standardized protocol or best procedure indicating how to treat aspirated fat. Indeed, the existing techniques state that it can be purified by gravity or by centrifugation,[6] [7] combined with autologous adipose-derived stem cells (ADSCs), with platelet-rich-plasma,[8] [9] or with adipose-derived mesenchymal stem cells following in vitro expansion.[10] Thirty years after its introduction, many authors continue to carry out studies looking for new systems that are able to optimize both time and expenditure while reducing fat handling and material waste. Therefore, we designed a “hydraulic system technique” specifically for fat grafting. The aim of the study is to evaluate the relationship among the quantity of injected fat, operative time, and the cost of disposable material to delineate a time and cost-effective procedure of fat processing.


#

Methods

Data were retrospectively reviewed for 36 female patients who underwent fat grafting revision surgery with our technique from March to July 2019 and who had previously undergone breast reconstruction in the 5 years prior. All patients underwent breast reconstruction following either minor or major oncological surgery, which was performed by the same surgical team. Patients were identified from the theater registers and electronic logbooks ([Table 1]).

Table 1

Summary collection of clinical and technical data

Number of patients

36 females

Mean age

52 (±12.5)

Comorbidities

Breast cancer (100%), hypertension (25%), smokers (25%), diabetes (12.5%), thyroiditis (12.5%)

Body mass index 30–35

11 (30.5%)

Body mass index 25–29

25 (69.5%)

Major complications

None

Minor complications

30% slight blood suffusion of the skin of the grafting area

Treated with standard system

15 (41.6%), mean of fat treated 72 mL ± 28.08, mean time 17.6 min, mean costs 4.23 ± 0.27 euros

Treated with “1-track”

11 (30.5%), mean of fat treated 183.3 mL ± 56.26, mean time 6.87 min, mean cost of 7.63 ± 0.6 euros

Treated with “2-tracks”

10 (27.7%), mean of fat treated 311 mL ± 103, mean time 9.3 min, mean cost of 12.47 ± 1 euros

Note: Data grouped according to the information of major clinical interest and their correlation with the data obtained from the use of hydraulic systems.


We obtained informed consent from the patients and conducted our study according the Declaration of Helsinki. We identified three groups in relation to the disposable materials used: the standard group, the “1-track” group, and the “2-tracks” group ([Table 2]).

Table 2

Hydraulic systems

Hydraulic systems

Disposable materials

Ref.

Cost (euro)

No.

Total cost (euro)

Standard

3-way stopcock

BD 9400198

0.46

2

0.92

60 mL Luer-Lock syringe

RAYS 6400048

0.31

2

0.62

10 mL Luer-Lock syringe

RAYS 6400128

0.09

1

0.09

50 cm Luer-Lock extension set

DELTAMED 9400185

0.53

1

0.53

500 mL Ringer's lactate solution

GALENICA SENESE 102322118

1.66

1

1.66

3.82

“1-track”

50 cm PVC extension 5-way manifold

ARIES SRL IN045915

2.64

1

2.64

60 mL Luer-Lock syringe

RAYS 6400048

0.31

5

1.55

10 mL Luer-Lock syringe

RAYS 6400128

0.09

1

0.09

3-way stopcock

BD 9400198

0.46

1

0.46

50 cm Luer-Lock extension set

DELTAMED 9400185

0.53

1

0.53

500 mL Ringer's lactate solution

GALENICA SENESE 102322118

1.66

1

1.66

6.93

“2-tracks”

50 cm PVC extension 5-way manifold

ARIES SRL IN045915

2.64

2

5.28

60 mL Luer-Lock syringe

RAYS 6400048

0.31

10

3.10

10 mL Luer-Lock syringe

RAYS 6400128

0.09

1

0.09

3-way stopcock

BD 9400198

0.46

2

0.92

50 cm Luer-Lock extension set

DELTAMED 9400185

0.53

1

0.53

500 mL Ringer's lactate solution

GALENICA SENESE 102322118

1.66

1

1.66

11.58

Abbreviation: PVC, polyvinyl chloride.


Note: Material, reference code, and costs.


The amount of harvested and grafted fat, materials used, and fat washing time data (from the start of the first syringe washing to the end of the last syringe washing for each unit of treated fat) per hydraulic system were collected ([Table 3]). The unit of treated fat corresponds to 30 mL, aspirated in one 60-mL syringe and the number of syringes needed per amount of fat were recorded and evaluated. The whole standard procedure requires the following materials: two “3-way stopcocks,” two “60-mL Luer-Lock syringes,” one “10-mL Luer-Lock syringe,” and one “extension set” ([Fig. 1]).

Table 3

Age, kind of previous breast surgery, amount of harvested and grafted fat, cost, and operating time

Age (y)

Surgery

Harvested fat (mL)

Grafted fat (mL)

Materials

Cost (euro)

Time (min)

Syringes with fat

28

r Lumpectomy

30

20

Standard

3.82

4

1

35

r Lumpectomy

30

22

Standard

3.82

5

1

51

r Lumpectomy

30

19

Standard

3.82

4

1

48

rl Lumpectomy

40

30

Standard

3.82

12

2

54

r Lumpectomy

60

47

Standard + 1 “60 mL Luer-Lock syringes”

4.13

13

2

45

r Implant contracture

60

50

Standard + 1 “60 mL Luer-Lock syringes”

4.13

10

2

53

r Mastectomy + implant

80

55

Standard + 2 “60 mL Luer-Lock syringes”

4.44

17

3

70

l Mastectomy+ expander + RT

80

65

Standard + 2 “60 mL Luer-Lock syringes”

4.44

18

3

54

rl Implant contracture

80

70

Standard + 2 “60 mL Luer-lock syringes”

4.44

18

3

53

r Mastectomy + expander

90

80

Standard + 2 “60 mL Luer-Lock syringes”

4.44

25

4

54

r Quadrantectomy + RT

100

84

Standard + 2 “60 mL Luer-Lock syringes”

4.44

23

4

57

r Mastectomy + implant

100

78

Standard + 2 “60 mL Luer-Lock syringes”

4.44

25

4

61

rl Quadrantectomy + RT

100

80

Standard + 2 “60 mL Luer-Lock syringes”

4.44

23

4

52

r Mastectomy + expander

100

70

Standard + 2 “60 mL Luer-Lock syringes”

4.44

23

4

52

r Mastectomy + implant

100

70

Standard + 2 “60 mL Luer-Lock syringes”

4.44

24

4

63

l Implant contracture

120

91

“1-track”

6.93

7

4

48

l Latissimus dorsi flap + implant

120

100

“1-track”

6.93

7

4

55

r Mastectomy + implant

120

100

“1-track”

6.93

7

4

48

r Latissimus dorsi flap + implant

150

130

“1-track” + 1 “60 mL Luer-Lock syringes”

7.24

13

5

46

rl Quadrantectomy + RT

150

132

“1-track” + 1 “60 mL Luer-Lock syringes”

7.24

14

5

49

l Mastectomy + implant

200

170

“1-track” + 3 “60 mL Luer-Lock syringes”

7.86

14

7

50

rl Mastectomy + implants

200

170

“1-track” + 3 “60 mL Luer-Lock syringes”

7.86

12

7

62

r Mastectomy

200

160

“1-track” + 3 “60 mL Luer-Lock syringes”

7.86

14

7

45

rl Mastectomy + implant

220

192

“1-track” + 3 “60 mL Luer-Lock syringes”

7.86

15

8

45

rl Mastectomy + implant

260

210

“1-track” + 5 “60 mL Luer-Lock syringes”

8.48

22

9

52

rl Mastectomy + implant

280

235

“1-track” + 6 “60 mL Luer-Lock syringes”

8.79

23

10

44

rl Mastectomy

220

185

“2-tracks”

11.58

8

8

55

rl Mastectomy

230

190

“2-tracks”

11.58

10

8

51

rl Mastectomy

230

185

“2-tracks”

11.58

10

8

60

l Mastectomy

250

200

“2-tracks” + 1 “60 mL Luer-Lock syringes”

11.89

13

9

69

l Mastectomy

250

215

“2-tracks” + 1 “60 mL Luer-Lock syringes”

11.89

14

9

59

r Quadrantectomy + l mastectomy and implant

310

280

“2-tracks” + 3 “60 mL Luer-Lock syringes”

12.51

13

11

54

r Mastectomy + l quadrantectomy and RT

320

280

“2-tracks” + 3 “60 mL Luer-Lock syringes”

12.51

14

11

57

r Quadrantectomy + l mastectomy and implant

350

295

“2-tracks” + 4 “60 mL Luer-Lock syringes”

12.82

15

12

62

l Mastectomy + implant

400

350

“2-tracks” + 6 “60 mL Luer-Lock syringes”

13.44

15

14

44

rl Prophylactic mastectomy

550

460

“2-tracks” + 11 “60 mL Luer-Lock syringes”

14.99

22

19

Abbreviations: l, left; r, right; RT, radiotherapy.


Note: Data grouped for each patient, according to the type of hydraulic system materials (respectively the standard system, “1-track,” and “2-tracks” ones).


Zoom Image
Fig. 1 The standard system. (A) Module A is joined to Module B through a “3-way stopcock.” Ringer solution is introduced into the system drawn from syringe A and then transferred to syringe B. After fat-washing in syringe B, the liquids are expelled through the extension set. (B) Module B is reused to set up the fat injection.

A tumescent solution is set up and a “3-way stopcock” (stopcock A) is joined to an infusion set as well as to a 60-mL Luer-Lock syringe (syringe A), making up Module A ([Fig. 1A]), and then to an extension set connected to a blunt infiltration cannula. The infusion set is connected to the tumescent solution bag and the solution is aspirated from the bag to fill syringe A. The following step consists in making a small cutaneous incision to insert the cannula for infiltration while turning the valve and the solution is then gradually released by the surgeon.

Lipoaspiration is performed after approximately 10 minutes with a 3-mm blunt aspiration cannula connected to a 60-mL Luer-Lock syringe: approximately 30 mL of fat (syringe B) is collected. The tumescent solution bag is replaced with a lactate Ringer 500 mL bag. A second “3-way stopcock” (stopcock B), joined to syringe B, is then added between the first stopcock (A) and the extension set. The latter serves to drive away the fluids directly into a special waste container. At this stage, Module B ([Fig. 1A]) is considered as functional.

Thirty milliliters of Ringer solution are aspirated from the bag with syringe A, changing the stopcock position by turning it. The solution is then pumped from syringe A into syringe B by a simple valve regulation (we open the connection between the first and the second stopcock and close the second stopcock's third valve). Fat washing is performed by the “lulling” of the system until a yellow and heterogeneous lipoaspirate is obtained. The fluid component derived from washing is now drained out through the extension set. For large amounts of fat, instead, one (“1-track”) ([Fig. 2]) or two (“2-tracks”) ([Fig. 3]) “50 cm polyvinyl chloride (PVC) extension line with a 5-way manifold” could be used, replacing the 3-way stopcocks, so that up to 120 or 240 mL of lipoaspirate can be treated at the same time.

Zoom Image
Fig. 2 “1-track” system. “50 cm polyvinyl chloride (PVC) extension line with a 5-way manifold” replacing the “3-way stopcock.” Here, up to 5 syringes of fat can be simultaneously processed.
Zoom Image
Fig. 3 “2-tracks” system. Intraoperative photo of two “50 cm polyvinyl chloride (PVC) extension lines with 5-way manifolds” working in parallel.

The subsequent fat injection is performed as follows: stopcock B with the loaded syringe B is disconnected and joined both to a 10-mL syringe and to the blunt infiltration cannula ([Fig. 1B]). In one step, using a simple valve rotation, the operator can first switch the fat from syringe B to the 10-mL syringe and then to the blunt cannula for injection.

The average of the time data was calculated and a statistical linear interpolation of nonmeasurable data (Microsoft Excel Linear Prevision) according to available samples per each system was performed. The relative 95% confidence intervals (CIs) of the mean values were then calculated and recorded. The time data (and relative CIs) between the various systems for each unit of volume were compared. Whenever there was a statistically significant difference for the average time values according to the relative CIs, the lowest time value for the system selection was chosen as the cutoff.


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Results

A total of 36 patients, with an average age of 52 (28–70) years, were included in this study and recorded in [Table 1] according to their main pathologies, comorbidities, body mass index, and surgical complications. Each patient underwent lipofilling as the final or intermediate step of their reconstructive procedure following breast cancer surgery ([Table 3]).

In 15 cases, with a mean age of 51 (28–70) years, the standard materials were used ([Fig. 1]; [Table 3]], in some cases with the addition of “60 mL Luer-Lock syringes” ([Table 2]): the average amount of 72 (30–100) mL of fat was treated to obtain 56 (19–84) mL of fat to graft, with a mean cost of 4.23 ± 0.27 euros.

In 11 cases, with a mean age of 51 (45–63) years, the “1-track” materials were utilized ([Fig. 2]; [Table 3]), in some cases with the addition of “60 mL Luer-Lock syringes”: a mean of 183.3 (120–280) mL of fat was harvested and treated, obtaining 153.3 (91–235) mL of fat to graft, with a mean cost of 7.63 ± 0.6 euros.

In 10 cases, the “2-tracks” materials were used ([Fig. 3]; [Table 3]), in some cases with the addition of “60-mL Luer-Lock syringes” ([Table 2]): an average of 311 (220–550) mL of fat was treated, obtaining a mean of 264 (185–460) mL of fat, with a cost of 12.47 ± 1 euros.

Time data analysis ([Table 4]; [Fig. 4]) shows that at three fat syringes (90 mL), the mean value by the standard system is 17.66 minutes (95% CI = 16.23, 19.10); while for the “1-track” system it is 6.87 minutes (95% CI = 3.15, 10.58), hence the difference is statistically significant. The mean time difference between the “1-track” system and the “2-tracks” system becomes significant from 240 mL of fat onwards: 15 minutes for the“1-track” system versus 9.3 minutes (95% CI = 6.99, 11.67) for the “2-tracks” system.

Table 4

Values of the treated fat with relative average times per procedure, 95% confidence intervals (CI) and related costs

Standard system

“1-track” system

“2-tracks” system

No. of syringes

Fat (mL)

Mean time (min)

CI

Cost (euro)

Mean time (min)

CI

Cost (euro)

Mean time (min)

CI

Cost (euro)

1

30

4.333333

2.90–5.77

3.82

6.93

2

60

11.66667

7.87–15.46

4.13

5.17

1.44–8.9

6.93

3

90

17.66667

16.23–19.10

4.44

6.87

3.15–10.58

6.93

4

120

23.83333

22.80–24.87

4.44

7

6.93

5

150

30.336391

29.42–31.25

4.44

13.5

7.15–19.85

7.24

8.7

6.11–11.33

11.58

6

180

36.771962

35.83–37.72

4.44

13.3

/

7.86

9.5

6.96–12.03

11.58

7

210

43.207533

42.24–44.18

4.44

13.33333

10.46–16.20

7.86

10.2

7.8–12.7

11.58

8

240

49.643105

48.64–50.64

4.44

15

-

7.86

9.3

6.99–11.67

11.58

9

270

56.078676

55.05–57.10

4.44

23

-

8.48

13.5

7.1519.85

11.89

10

300

62.514247

61.46–63.57

4.44

22

-

8.79

13.5

-

11.89

11

330

68.949819

67.87–70.03

4.44

24.176071

19.48–28.87

8.79

13.5

7.15–19.85

12.51

12

360

75.38539

74.28–76.49

4.44

26.525058

21.81–31.24

8.79

15

-

12.82

13

390

81.820961

80.69–82.95

4.44

28.952345

24.21–33.70

8.79

15

-

13.13

14

420

88.256532

87.10–89.41

4.44

31.379631

26.61–36.15

8.79

15

-

13.44

15

450

94.692104

93.51–95.87

4.44

33.572019

28.78–38.36

8.79

16

-

13.75

16

480

101.12768

99.93–102.33

4.44

35.999306

31.18–40.82

8.79

18

-

14.06

17

510

107.56325

106.34–108.79

4.44

38.348293

33.50–43.19

8.79

20

-

14.37

18

540

113.99882

112.75–115.25

4.44

40.775579

35.90–45.65

8.79

21

-

14.68

19

570

119.14727

117.88–120.41

4.44

42.889667

37.99–47.78

8.79

22

-

14.99

Note: Values of the treated fat with relative average times per procedure and 95% confidence intervals. All values obtained by linear interpolation are highlighted in gray. The time cutoffs which are useful for defining the hydraulic system of choice are highlighted in green. For each quantity of fat to be purified, both the average time and the planned expenditure for each of the three systems is reported.


Zoom Image
Fig. 4 Time data analysis diagram and related systems. On the x-axis, the amount of fat contained in a progressive number of syringes is reported (30 mL = 1 syringe; 60 mL = 2 syringes; etc.), while on the y-axis, the time in minutes is reported. The blue lines represent the trend of the average times of the procedures for number of syringes needed, in green the relative 95% confidence interval (CI). The red lines, instead, represent the calculated predictions, with relative CI. For fat values treated with 2 syringes (up to 90 mL), the CI of the standard system and “1-track” are not overlapped. For fat values treated with 8 syringes (> 210 mL), the average time with the “1-track” is outside the CI of the “2-tracks” system.

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Discussion

Studies into fat grafting infection[11] [12] and antibiotic resistance mean that surgeons perform lipofilling according to strict sterile regulations. To reduce fat contamination, fat should be manipulated as little as possible, and treated in a closed system without enzymatic elements, thus increasing the technique's costs.[13] Our initial purpose was to use systems already present in clinical practice making it possible to construct a simple module.

Indeed, we used material available in every operating room guaranteeing the closed circuit in each phase of the procedure. Tedde's system, described by Rubino et al[14] in 2014, was used as the first step of our technique (tumescent solution's infiltration) and then for fat washing. The Lull System by Morselli et al,[15] represented the main principle for our fat washing, the second step of the standard system ([Fig. 1A]) and our Module B. Finally, the “stopcock technique” described by Paolini et al[16] was used to perform fat infiltration through a closed and manageable circuit. Our new contribution is of most relevance when higher quantities of fat are needed.

Time analysis reveals at which amount of fat processing the use of the hydraulic system results in significantly shorter mean time. Data from [Table 4] show that for 1 or 2 fat syringes (30–60 mL of fat) there is not any significant difference between the standard and the “1-track” system, whereas from three syringes onwards (treated fat from 90 mL and above), the difference is statistically significant and, therefore, the use of the “1-track” system is more time efficient than the standard system (standard system, 17.66 minutes [95% CI = 16.23, 19.10]; “1-track” system, 6.87 minutes [95% CI = 3.15, 10.58]). The first cutoff was established at 90 mL for the use of the “1-track” system. For this amount of treated fat there is a cost difference of 2.49 euros between the two systems ([Table 4]), which we believe to be suitable when considering the 10 minutes saved.

From 90 to 210 mL of treated fat there is no statistically significant difference between the “1-track” and “2-tracks” systems. The difference between the “1-track” and “2-tracks” systems became significant from 240 mL (8 syringes) upwards, meaning that from that point the “2-tracks” system is more time efficient than the “1-track” system, on the basis of our data. Hence, we set the second cutoff for the choice of the “2-tracks” system (“1-track,” 15 minutes; “2-tracks,” 9.3 minutes [95% CI = 6.99, 11.67]) ([Fig. 4]). For this amount of treated fat there is a cost difference of only 7.14 euros which saves around 6 minutes ([Table 4]). The increase in treated fat leads to further savings with the “2-tracks” system. Indeed, these systems make it possible for us to adapt materials and costs to clinical necessity ([Table 4]).

The staminality and the reabsorption of grafted fat have been widely debated for years.[7] [8] [9] [10] [17] Gupta et al[18] in a noteworthy review in 2015, stated that literature was insufficient to clearly establish any fat graft processing method as superior to another one in long-term retention of transplanted graft volume. He stated that decanted fat graft contains the highest number of contaminants and the highest number of viable adipocytes while centrifugated fat graft contains the lowest amounts of the former. Rigotti et al[10] demonstrated that the addition of platelets-rich plasma did not have significant advantages for regeneration over the use of expanded ADSCs or stromal vascular fraction (SVF)-enriched fat in skin rejuvenation. Therefore, the graft should be gently washed and/or contaminates should be further removed through centrifugation. Recently Morselli et al[15] [19] and Zhu et al[20] reported two closed systems for fat washing with decantation and centrifugation, showing that their procedures achieved the best balance between purification and amount of stem cells.

Since our study is an evolution of the fat washing technique proposed by Morselli et al, it was deemed unnecessary to demonstrate the quality and survival rate of the transferred fat. Indeed, Morselli et al[15] [19] has already outlined that his technique rendered good fat survival rates. Decantation caused no harm to mature adipocytes and preserved an elevated amount of ADSCs among all the SVF. The endpoints on which he focused were chosen to assess the in vitro regenerative potential of the processed tissue. He showed the highest amount of SVF cells isolated with his technique in terms of decantation and centrifugation samples, with a difference of around four and sixfold higher, respectively.

Furthermore, automated closed-system isolation devices allow clinicians to isolate a patient's cells and readminister the cells back to the patient within the same surgery.[21] Ambient air exposure and transfer between syringes significantly decreased viability.[22] New methods for fat washing in a closed system have been proposed by different companies.[20] [23] However, some of these are expensive and time consuming, in fact, Rodriguez et al[24] showed the possibility of treating 250 mL of fat in 110 minutes with a cost of 250 dollars with their technique.

Despite its simplicity, in our experience, it is important to note that our technique needs a certain level of practical training during its first uses. Moreover, we do not recommend fat transfer through the stopcocks before washing as this operation could result in the pressure being too high and an obstruction of the system. Disposable materials are commonly available in any operating room but, should “a 50-cm PVC extension 5-way manifold” be unavailable, several “3-way stopcocks” in a series can be used, despite system stability possibly being reduced. Another limitation of our study consists in having obtained some data through linear interpolation. However, in this case, the use of CIs allowed us to simulate the forecast more efficiently.

The costs of the hydraulic systems in our study range from 3.82 to 14.99 euros and we treated up to 550 mL of fat in less than 30 minutes.


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Conclusion

Data analysis would indicate the use of the standard system, “1-track,” and “2-tracks” to treat an amount of fat < 90 mL of fat, 90 ÷ 240 mL of fat, and ≥ 240 mL of fat, respectively. Our technique is straightforward and requires a very low-cost device, particularly since expensive lipofilling machines may not be available in many countries. The hydraulic systems guarantee time saving and contribute to saving resources in a time of international spending reviews.


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Conflict of Interest

None declared.

Ethical Approval

The study was approved by the University of Salerno (IRB No. ORSA185920) and performed in accordance with the principles of the Declaration of Helsinki. Written informed consent was obtained.


Ethical Approval

* Joint first authors.


  • References

  • 1 Condé-Green A, Marano AA, Lee ES. et al. Fat grafting and adipose-derived regenerative cells in burn wound healing and scarring: a systematic review of the literature. Plast Reconstr Surg 2016; 137 (01) 302-312
  • 2 Guisantes E, Fontdevila J, Rodríguez G. Autologous fat grafting for correction of unaesthetic scars. Ann Plast Surg 2012; 69 (05) 550-554
  • 3 Fournier PF. Liposculpture: My Technique. Paris: Arnette-Blackwell Editors; 1996
  • 4 Flynn TC, Coleman II WP, Field LM, Klein JA, Hanke CW. History of liposuction. Dermatol Surg 2000; 26 (06) 515-520
  • 5 Illouz YG. History and current concepts of lipoplasty. Clin Plast Surg 1996; 23 (04) 721-730
  • 6 Girard AC, Mirbeau S, Gence L. et al. Effect of washes and centrifugation on the efficacy of lipofilling with or without local anesthetic. Plast Reconstr Surg Glob Open 2015; 3 (08) e496
  • 7 Botti G, Pascali M, Botti C, Bodog F, Cervelli V. A clinical trial in facial fat grafting: filtered and washed versus centrifuged fat. Plast Reconstr Surg 2011; 127 (06) 2464-2473
  • 8 Modarressi A. Platelet rich plasma (PRP) improves fat grafting outcomes. World J Plast Surg 2013; 2 (01) 6-13
  • 9 Wu LW, Chen WL, Huang SM, Chan JY. Platelet-derived growth factor-AA is a substantial factor in the ability of adipose-derived stem cells and endothelial progenitor cells to enhance wound healing. FASEB J 2019; 33 (02) 2388-2395
  • 10 Rigotti G, Charles-de-Sá L, Gontijo-de-Amorim NF. et al. Expanded stem cells, Stromal-vascular fraction, and platelet-rich plasma enriched fat: comparing results of different facial rejuvenation approaches in a clinical trial. Aesthet Surg J 2016; 36 (03) 261-270
  • 11 Maamari RN, Massry GG, Holds JB. Complications associated with fat grafting to the lower eyelid. Facial Plast Surg Clin North Am 2019; 27 (04) 435-441
  • 12 Seo DH, Shin JY, Roh SG, Chang SC, Lee NH. Non-tuberculous Mycobacterium infection after transfer of autologous fat to the face: a rare case. Br J Oral Maxillofac Surg 2019; 57 (02) 185-187
  • 13 Bianchi F, Maioli M, Leonardi E. et al. A new nonenzymatic method and device to obtain a fat tissue derivative highly enriched in pericyte-like elements by mild mechanical forces from human lipoaspirates. Cell Transplant 2013; 22 (11) 2063-2077
  • 14 Rubino C, Marongiu F, Manzo MJ. et al. A simple and cheap system to speed up and to control the tumescent technique procedure: the Tedde's system. Eur Rev Med Pharmacol Sci 2014; 18 (11) 1647-1648
  • 15 Morselli PG, Giorgini FA, Pazzini C, Muscari C. Lull pgm system: a suitable technique to improve the regenerative potential of autologous fat grafting. Wound Repair Regen 2017; 25 (04) 722-729
  • 16 Paolini G, Amoroso M, Longo B, Sorotos M, Karypidis D, Santanelli di Pompeo F. Simplified lipostructure: a technical note. Aesthetic Plast Surg 2014; 38 (01) 78-82
  • 17 De Francesco F, Guastafierro A, Nicoletti G, Razzano S, Riccio M, Ferraro GA. The selective centrifugation ensures a better in vitro isolation of ASCs and restores a soft tissue regeneration in vivo. Int J Mol Sci 2017; 18 (05) E1038
  • 18 Gupta R, Brace M, Taylor SM, Bezuhly M, Hong P. In search of the optimal processing technique for fat grafting. J Craniofac Surg 2015; 26 (01) 94-99
  • 19 Morselli PG, Micai A, Giorgini FA. “Lull pgm system” for autologous fat grafting: a simple closed system with minimal equipment and no extra cost. Plast Reconstr Surg Glob Open 2016; 4 (08) e851
  • 20 Zhu M, Cohen SR, Hicok KC. et al. Comparison of three different fat graft preparation methods: gravity separation, centrifugation, and simultaneous washing with filtration in a closed system. Plast Reconstr Surg 2013; 131 (04) 873-880
  • 21 Nordberg RC, Loboa EG. Our fat future: translating adipose stem cell therapy. Stem Cells Transl Med 2015; 4 (09) 974-979
  • 22 Cucchiani R, Corrales L. The effects of fat harvesting and preparation, air exposure, obesity, and stem cell enrichment on adipocyte viability prior to graft transplantation. Aesthet Surg J 2016; 36 (10) 1164-1173
  • 23 Tremolada C, Colombo V, Ventura C. Adipose tissue and mesenchymal stem cells: state of the art and Lipogems® technology development. Curr Stem Cell Rep 2016; 2: 304-312
  • 24 Rodriguez J, Pratta AS, Abbassi N. et al. Evaluation of three devices for the isolation of the stromal vascular fraction from adipose tissue and for ASC culture: a comparative study. Stem Cells Int 2017; 2017: 9289213

Address for correspondence

Vincenzo Verdura, MD
Via Michele Pellicani n.16/M Ruvo di Puglia, BA 70037
Italy   

Publication History

Article published online:
06 April 2022

© 2022. The Korean Society of Plastic and Reconstructive Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Condé-Green A, Marano AA, Lee ES. et al. Fat grafting and adipose-derived regenerative cells in burn wound healing and scarring: a systematic review of the literature. Plast Reconstr Surg 2016; 137 (01) 302-312
  • 2 Guisantes E, Fontdevila J, Rodríguez G. Autologous fat grafting for correction of unaesthetic scars. Ann Plast Surg 2012; 69 (05) 550-554
  • 3 Fournier PF. Liposculpture: My Technique. Paris: Arnette-Blackwell Editors; 1996
  • 4 Flynn TC, Coleman II WP, Field LM, Klein JA, Hanke CW. History of liposuction. Dermatol Surg 2000; 26 (06) 515-520
  • 5 Illouz YG. History and current concepts of lipoplasty. Clin Plast Surg 1996; 23 (04) 721-730
  • 6 Girard AC, Mirbeau S, Gence L. et al. Effect of washes and centrifugation on the efficacy of lipofilling with or without local anesthetic. Plast Reconstr Surg Glob Open 2015; 3 (08) e496
  • 7 Botti G, Pascali M, Botti C, Bodog F, Cervelli V. A clinical trial in facial fat grafting: filtered and washed versus centrifuged fat. Plast Reconstr Surg 2011; 127 (06) 2464-2473
  • 8 Modarressi A. Platelet rich plasma (PRP) improves fat grafting outcomes. World J Plast Surg 2013; 2 (01) 6-13
  • 9 Wu LW, Chen WL, Huang SM, Chan JY. Platelet-derived growth factor-AA is a substantial factor in the ability of adipose-derived stem cells and endothelial progenitor cells to enhance wound healing. FASEB J 2019; 33 (02) 2388-2395
  • 10 Rigotti G, Charles-de-Sá L, Gontijo-de-Amorim NF. et al. Expanded stem cells, Stromal-vascular fraction, and platelet-rich plasma enriched fat: comparing results of different facial rejuvenation approaches in a clinical trial. Aesthet Surg J 2016; 36 (03) 261-270
  • 11 Maamari RN, Massry GG, Holds JB. Complications associated with fat grafting to the lower eyelid. Facial Plast Surg Clin North Am 2019; 27 (04) 435-441
  • 12 Seo DH, Shin JY, Roh SG, Chang SC, Lee NH. Non-tuberculous Mycobacterium infection after transfer of autologous fat to the face: a rare case. Br J Oral Maxillofac Surg 2019; 57 (02) 185-187
  • 13 Bianchi F, Maioli M, Leonardi E. et al. A new nonenzymatic method and device to obtain a fat tissue derivative highly enriched in pericyte-like elements by mild mechanical forces from human lipoaspirates. Cell Transplant 2013; 22 (11) 2063-2077
  • 14 Rubino C, Marongiu F, Manzo MJ. et al. A simple and cheap system to speed up and to control the tumescent technique procedure: the Tedde's system. Eur Rev Med Pharmacol Sci 2014; 18 (11) 1647-1648
  • 15 Morselli PG, Giorgini FA, Pazzini C, Muscari C. Lull pgm system: a suitable technique to improve the regenerative potential of autologous fat grafting. Wound Repair Regen 2017; 25 (04) 722-729
  • 16 Paolini G, Amoroso M, Longo B, Sorotos M, Karypidis D, Santanelli di Pompeo F. Simplified lipostructure: a technical note. Aesthetic Plast Surg 2014; 38 (01) 78-82
  • 17 De Francesco F, Guastafierro A, Nicoletti G, Razzano S, Riccio M, Ferraro GA. The selective centrifugation ensures a better in vitro isolation of ASCs and restores a soft tissue regeneration in vivo. Int J Mol Sci 2017; 18 (05) E1038
  • 18 Gupta R, Brace M, Taylor SM, Bezuhly M, Hong P. In search of the optimal processing technique for fat grafting. J Craniofac Surg 2015; 26 (01) 94-99
  • 19 Morselli PG, Micai A, Giorgini FA. “Lull pgm system” for autologous fat grafting: a simple closed system with minimal equipment and no extra cost. Plast Reconstr Surg Glob Open 2016; 4 (08) e851
  • 20 Zhu M, Cohen SR, Hicok KC. et al. Comparison of three different fat graft preparation methods: gravity separation, centrifugation, and simultaneous washing with filtration in a closed system. Plast Reconstr Surg 2013; 131 (04) 873-880
  • 21 Nordberg RC, Loboa EG. Our fat future: translating adipose stem cell therapy. Stem Cells Transl Med 2015; 4 (09) 974-979
  • 22 Cucchiani R, Corrales L. The effects of fat harvesting and preparation, air exposure, obesity, and stem cell enrichment on adipocyte viability prior to graft transplantation. Aesthet Surg J 2016; 36 (10) 1164-1173
  • 23 Tremolada C, Colombo V, Ventura C. Adipose tissue and mesenchymal stem cells: state of the art and Lipogems® technology development. Curr Stem Cell Rep 2016; 2: 304-312
  • 24 Rodriguez J, Pratta AS, Abbassi N. et al. Evaluation of three devices for the isolation of the stromal vascular fraction from adipose tissue and for ASC culture: a comparative study. Stem Cells Int 2017; 2017: 9289213

Zoom Image
Fig. 1 The standard system. (A) Module A is joined to Module B through a “3-way stopcock.” Ringer solution is introduced into the system drawn from syringe A and then transferred to syringe B. After fat-washing in syringe B, the liquids are expelled through the extension set. (B) Module B is reused to set up the fat injection.
Zoom Image
Fig. 2 “1-track” system. “50 cm polyvinyl chloride (PVC) extension line with a 5-way manifold” replacing the “3-way stopcock.” Here, up to 5 syringes of fat can be simultaneously processed.
Zoom Image
Fig. 3 “2-tracks” system. Intraoperative photo of two “50 cm polyvinyl chloride (PVC) extension lines with 5-way manifolds” working in parallel.
Zoom Image
Fig. 4 Time data analysis diagram and related systems. On the x-axis, the amount of fat contained in a progressive number of syringes is reported (30 mL = 1 syringe; 60 mL = 2 syringes; etc.), while on the y-axis, the time in minutes is reported. The blue lines represent the trend of the average times of the procedures for number of syringes needed, in green the relative 95% confidence interval (CI). The red lines, instead, represent the calculated predictions, with relative CI. For fat values treated with 2 syringes (up to 90 mL), the CI of the standard system and “1-track” are not overlapped. For fat values treated with 8 syringes (> 210 mL), the average time with the “1-track” is outside the CI of the “2-tracks” system.