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Original Research

Clinical Experience With the Use of Gauze-based Negative Pressure Wound Therapy

August 2012

Index: WOUNDS. 2012;24(8):227–233.

  Abstract: Purpose. In this preliminary study, gauze-based negative pressure wound therapy (NPWT) was used to accelerate granulation tissue formation and promote closure in a number of wound types. The authors aimed to evaluate the efficacy of gauze-based NPWT using the Chariker-Jeter technique for wounds requiring delayed closure. Methods. A retrospective review was conducted of 50 patients with wounds not suitable for immediate primary closure. After initial irrigation, debridement, and antibiotic therapy, Chariker-Jeter technique NPWT was used and dressings were changed at 24- to 48-hour intervals before secondary closure or primary closure. In addition, a 4-point category scoring system (severe, moderate, mild, and none) was used to evaluate pain. Semi-quantitative data also were obtained. Results. Wound size decreased considerably, granulation tissue formation was accelerated, and exudate was reduced and removed by the end of the treatment. The patients were followed for 12 months. Pre- and post-treatment averages of the wound surface areas were 90.21 ± 74.97 cm2 and 35.71 ± 53.63 cm2, respectively (P < 0.001). Average duration of treatment was 12.98 ± 3.18 days and average wound size reduction following the treatment was 64.61% ± 30.42%. Granulation tissue was clinically observed in all wounds by day 5. Six cases healed without any operation; the others required various reconstructive methods to cover the wounds. After surgical intervention, only 3 patients treated with gauze-based NPWT had a recurrence. No infections were observed during the follow-up period. According to the pain form, only 2 patients had severe pain. Conclusion. The gauze-based NPWT was found to be a safe and cost-effective method in temporary soft-tissue management of chronic nonhealing wounds suitable delayed closure.

Introduction

  Negative pressure wound care (NPWC) has been known to have the potential to promote wound healing, alleviate concerns such as increasing exudate and odor, and improve quality of life for patients. Various studies reported this method offers fewer dressing changes, decreased total hospitalization time, and reduced wound pain compared with conventional therapy.1   Several reports regarding polyurethane foam dressing show newly formed granulation tissue may grow into the polyurethane foam, making its removal painful during dressing changes. Foam dressing removal also can lead to damage to the wound bed.1 Various strategies by several authors have been adopted to reduce pain during dressing changes.2 However, the strategies applied did not solve the problem of pain, and the foam-based negative pressure wound therapy was not less expensive in the treatment of chronic nonhealing wounds until now.   In this study, the authors used gauze-based negative pressure wound therapy (NPWT) for the treatment of chronic nonhealing wounds suitable for delayed closure, and evaluated the efficacy of gauze-based NPWT using the Chariker-Jeter technique before delayed primary or secondary closure. The authors recorded wound dimension, patient complaints of pain, and cost at the end of the treatment period. The authors suggest that using gauze medium as a wound filler material can reduce pain during dressing changes and provide a less expensive method in the treatment of chronic wounds.

Patients and Methods

  This retrospective, non-comparative study was conducted in the department of Plastic Reconstructive Surgery (Gaziosmanpasa University, Tokat, Turkey), between 2006 and 2011. All patients gave written consent. Patients were reviewed in the following categories: pressure sores (sacral [SPS], ischial [IPS], and trochanteric [TPS]), diabetic foot ulcers (DFUs), venous ulcers (VUs), and traumas (Tr) (Table 1). First, the wounds were debrided and measured (Figures 1, 2). The application of NPWT was generally delayed for a few days to achieve postoperative homeostasis. A NPWC pump was set to continuously provide 125 mm Hg of negative pressure for the first 48 hours (Figure 3). After this period of 2 days, dressings were continued with intermittent 80 mm Hg of negative pressure, and dressing changes were consecutively performed at 24- to 48-hour intervals. The treatment was ended when sufficient accelerated granulation tissue formation, wound size reduction, and decreased exudate were observed in the wounds (Figure 4). The patients were administered antibiotics and analgesics when required. During dressing changes, most patients did not require a further dose of analgesic. After NPWT had been completed, patients underwent surgery including skin graft or flaps to cover their wounds (Figures 5-7). Data were collected on patient demographics, wound type, duration of NPWT, wound dimensions, and device-related complications.   Patients evaluated pain at dressing change and/or removal using a 4-point category scoring system form (severe, moderate, mild, and none). They marked 0 for no pain, 1 for moderate pain, 2 for mild pain, and 3 for severe pain. At the end of the treatment, the data obtained from every patient were evaluated.

Statistical Analysis

  The Kolmogorov-Smirnov test was used to evaluate whether the distribution of continuous variables was normal. The t-test for 2 independent samples was used to compare the wound areas and patient characteristics between genders. The 2 paired sample t-test, or Wilcoxon rank sum test, was used to compare the wound areas between pre-treatment and post-treatment periods. Pearson’s correlation coefficients were used for determining the relation between wound areas and age of patients. The continuous variables were presented as the mean ± standard deviation. Categorical variables were presented as a count and percentage. A P value < 0.05 was considered significant. Analyses were performed using commercial software (IBM SPSS Statistics 19, SPSS Inc, IBM Co, Somers, NY).

Results

  Of the 50 participants, 31 were men and 19 were women, mean age 59.04 ± 15.07. Etiologically, the wounds were classified as pressure ulcers (31) — SPS (15), IPS (9), TPS (7), DFUs (13), VUs (4), and Tr (2) (Table 1). Reduction in wound area, accelerated granulation tissue formation, and decreased exudate were observed in all wounds. Granulation tissue was clinically noted in all wounds by day 5. Average wound size in the pre-treatment period was 90.21 ± 74.97 cm2; it was 35.71 ± 53.63 cm2 in the post-treatment period (P < 0.001) (Figure 8).   The average of total application duration was 12.98 ± 3.18 days, and average wound size reduction was 64.61% ± 30.42% (Table 1). There were statistically significant differences between 2 measurements for both men and women (P < 0.001 and P = 0.006, respectively) (Table 2, Figure 9). There was a statistically significant correlation between age and proportional changes of wound areas for all patients (r = -0.366; P = 0.009). There was a statistically significant correlation between age and proportional changes of wound areas for women (r = -0.622; P = 0.004), but no significant correlation for men (r = -0.268; P = 0.145). The wounds of 47 patients remained closed during the follow-up period, and there was no skin graft loss or flap failure. The other 3 cases, 1 SPS l and 2 IPSs, required secondary surgery to cover their wounds after 6 months. The dehisced wounds were debrided again and the gauze-based NPWT was reused in only 1 (IPS) patient before the wounds were closed to local flaps. The follow-up period was 12 months, and the wounds were free of any infection for a significant period of time, determined by clinical follow-up at 1, 3, 6, and 12 months. Six wounds did not require surgery and healed secondarily. The number of patients who had no pain on dressing removal was 38, and the number of those with severe pain was 2. The other complications of NPWC, hematoma or excessive bleeding, were not observed.

Discussion

  Topical NPWT involves active drainage of chronic over-exudative wounds. In this technique, a porous material (antimicrobial gauze or foam) is placed in the wound bed and enclosed using polyurethane films to form an airtight seal.3,4 This kind of dressing has been shown to be beneficial in a wide variety of wounds, including pressure ulcers, leg ulcers, skin grafts, sternal and abdominal wounds, traumatic injuries, postfasciotomy closures, and lymphorrhea.4,5 Although the bulk of the literature regarding NPWT describes one vacuum-assisted closure system (V.A.C. Therapy®, KCI, San Antonio, TX), the use of alternative dressing interfaces and vacuum sources also has been presented. The first use of gauze as a medium was reported by Chariker et al6 in 1989. They reported that negative pressure enhanced the closure of incisional fistulae by improving drainage control, reducing skin damage, improving wound granulation and contraction, and reducing nursing costs. The technique uses moistened gauze as a wound interface and 80 mm Hg of negative pressure.7 Campbell et al8 published a retrospective analysis in 2008, which proved the effectiveness of gauze as a wound filler material and applied the pressure at -80 mm Hg for the duration of therapy. Generally, pressures are targeted at -125 mm Hg, although no clinical data identify an optimum pressure. However, in a recent report, reduction in wound volume was suggested to be unrelated to pressures between -50 mm Hg and -125 mm Hg.8 In this study, the authors used continuous 125 mm Hg of negative pressure in wounds for the first 48 hours. After the wounds were properly cleaned by continuous and high pressure, the authors continued dressings with intermittent 80 mm Hg of negative pressure at 24- to 48-hour intervals. The pressure delivered to the wound bed by a suction tube and a wound filler—gauze, or foam—creates the mechanical stress on the surface of the wound. In the cells exposed to negative pressure, integrin bridges in their cytoskeletons are disrupted; thus, cell proliferation is stimulated. The other effect of negative pressure is elimination of proteases that inhibit healing of the lesion.9,10 The most important effect of negative pressure is provided by the mechanical pump. Therefore, a useful wound filler material should transduce the negative pressure to the wound bed equally.   As evidence of granulation tissue appears, wound management guidelines can be divided in terms of 3 groups of patients7: Group A wounds must be closed with either local flaps or free tissue transfer.; these include wounds with exposed joints, tendons, and fractures. Group B wounds are amenable to closure with a skin graft; these wounds are typically larger than 5 cm2 and require 2 to 4 weeks to close by secondary intention. Group C wounds are amenable to closure by secondary intention; these are smaller wounds that can be managed with other moist, nonadherent dressings. In the present series, only 5 cases were in Group C, and they healed secondarily. The duration of vacuum therapy averaged 12.98 days to secondary closure. Granulation was clinically noted in all patients by day 5, illustrating the short time needed to produce a healthy, granulating tissue bed. In a similar study of 75 patients with open wounds of the lower extremity (of which 49 were the result of trauma), granulation tissue was present by day 4 of vacuum therapy, with decreased edema and bacterial counts.11 Another study reported results of 21 consecutive patients with high-energy, soft-tissue wounds who underwent vacuum therapy for an average of 19.3 days.12 Bollero et al13 likewise reported rapid granulation tissue formation in 35 patients with lower limb traumatic wounds who underwent vacuum therapy. In another study by Chariker et al7, this method was used in 24 pediatric patients with upper and lower extremity injuries. The duration of vacuum therapy averaged 10 days to primary closure and 17 days for secondary closure. Granulation was noted in all patients by day 4, illustrating the short time needed to produce a healthy, granulating tissue bed.   Clare et al14 used NPWT with growth factors in 17 cases of persons with diabetes and vascular insufficiency in their extremities. They accomplished treatment without any need for surgery in 6 cases. De Franzo et al15 needed surgery for only 12 of 75 patients with wounds on a lower extremity treated with the same procedure. Also, De Lange et al16 did not need any surgical procedure to cover the wounds in 29 of 100 cases. In that study, the defect was left for secondary healing in only 1 case because of its decreased dimensions. In the present study, 6 cases did not undergo an operation, and these wounds were left to secondary healing; however, these wounds were relatively smaller in dimension than that of others at the beginning of treatment. Other wounds required various reconstructive surgery procedures.   In the present study, average pre-treatment wound size was 90.21 cm2, while the post-treatment period averaged a wound size of 35.71 cm2, a statistically significant difference (P < 0.001). The authors observed that the wound areas decreased at a rate of 64.61%, and in all wounds granulation tissue formation and increased contraction were observed.   Gauze-based NPWT may be more practical and useful in smaller undermined wounds, such as DFUs. Following surgical debridement, patients were effectively treated and prepared for surgery by topical NPWT with antimicrobial gauze dressings. Although the foam-based system is preferred in large and deep wounds in many centers, gauze as a wound filler seems to be easier to apply and conform to complicated geometries of the wounds. In a study by Dunn et al,17 the gauze-based system was used during the pre-and post-grafting period at a continuous negative pressure of -80 mm Hg. The authors suggested that split-thickness skin grafts might provide the ideal indication for the adoption of gauze-based NPWT. According to the author’s experiences, the gauze-based system seems to be more useful and feasible for group B or grade 1 and 2 wounds. The gauze medium may require using more material to fill in a large and deep wound compared to foam. This can raise cost of treatment. However, recent reports indicated that the type of interface material does not affect the pressure transduction to the wound.18,19   Comparative and prospective studies are needed to assess the efficacy of a gauze-based system on large and deep wounds. The aim of NPWT is to prepare the wounds for surgery. The excessive use of this method can lead to extended duration of hospitalization and increased cost of treatment. NPWT should be considered a temporary or bridge technique for management of wounds, meaning it is used to promote wound healing before closure, either by secondary intention or by grafting or flap placement.7   In the postoperative period, sufficient and proper wound care, as well as passive and active exercises, are essential for providing long-lasting positive results and reducing recurrence rate. The patients should not lie down or sit down on their flaps for 3 weeks. At the end of the 3-week period, patients can sit down on the flap for only 15 minutes a day. In the authors’ study, 3 patients required secondary surgery in postoperative 6 months. These patients had SPS (1 case) and IPS (2 cases) pressure ulcers. The gauze-based NPWT was reused in only 1 patient with an IPS because of total dehiscense.   IPSs have a high incidence of recurrence despite successful reconstructive treatments. In the literature, it is reported that the reoccurrence rate ranges from 27.8% to 63%. In IPSs, myocutaneous flaps can be used to reduce recurrence rate and the wounds should be protected from long-lasting pressure and shearing forces as an important factor in decubitis ulcers, especially in paraplegics.   In their study of 51 pediatric patients, Caniano et al20 reported the cost-effectiveness of NPWT with foam therapy on nonhealing wounds. Although cost-effectiveness was not the focus of the current report, NPWT was shown to be an economical treatment for adult patients, especially those with pressure ulcers. According to Vidrine,21 cost is a major disadvantage in foam-based NPWT. Even in developed countries, the cost of wound care has exorbitant rates. Therefore, when deciding on the method of treatment, the efficiency as well as the cost of treatment should be considered.   The current study suggests use of gauze-based dressings is an effective method of NPWT. In the authors’ study, polyurethane foam dressing was found to be insufficient for cost-effectiveness compared to the gauze-based dressing. The cost of the polyurethane foam dressing in total is $75,500 for 50 patients, while the gauze-based dressing is $30,000 for 50 patients. From the patient perspective, NPWT may be associated with reduced discomfort due to pain, medication usage, and costs.3 Most NPWT dressings need only to be changed every 2 to 5 days, sometimes less. Therefore, the method reduces material resources, staff time, and patient discomfort during painful dressing changes.4 Pain depends on many clinical variables, including the presence of analgesic, neuropathy, and paraplegia.3 In the present study, the number of the patients who complained of pain was very low.   In this study, the authors found a statistically significant correlation between age and proportional change in wound areas for women, but no significant correlation for men. An area for future exploration is that one of the most important results of hormonal changes is the age-related delay in cutaneous wound healing. Reduced estrogen levels play a negative role on cellular and tissue response to injury. This effect includes impaired cytokine signal transduction, unchecked inflammation, and altered protein balance, and can have a major impact on the rate of wound healing.22,23

Conclusion

  In conclusion, the wounds showed significant and consistent reduction using the Chariker-Jeter method of NPWT. The cost of treatment and hospitalization time of the patients were decreased. Further and comparative studies should be performed to understand the advantages or disadvantages of dressing materials such as antibacterial gauze-based or polyurethane foam. The authors suggest gauze-based NPWT in the management of chronic nonhealing wounds suitable for delayed closure can be an inexpensive and effective method.

References

1. Krasner DL. Managing wound pain in patients with vacuum-assisted closure devices. Ostomy Wound Manage. 2002;48(5):38-43. 2. Franczyk M, Lohman RF, Agarwal JP, et al. The impact of topical lidocaine on pain level assessment during and after vacuum-assisted closure dressing changes: a double-blind, prospective, randomized study. Plast Reconstr Surg. 2009;124(3):854-861. 3. Hurd T, Chadwick P, Cote J, et al. Impact of gauze-based NPWT on the patient and nursing experience in the treatment of challenging wounds. Int Wound J. 2010;7(6):448-455. 4. Psoinos CM, Ignotz RA, Lalikos JF, et al. Use of gauze-based negative pressure wound therapy in a pediatric burn patient. J Pediatr Surg. 2009;44(12):e23-26. 5. Abai B, Zickler RW, Pappas PJ, et al. Lymphorrea responds to negative pressure wound therapy. J Vasc Surg. 2007;45(3):610-613. 6. Chariker ME, Jeter KF, Tintle TE, Bottsford JE. Effective management of incisional and cutaneous fistulae with closed suction wound drainage. Contemp Surg. 1989;34:59-63. 7. Chariker ME, Gerstle TL, Morrison CS. An algorithmic approach to the use of gauze-based negative-pressure wound therapy as a bridge to closure in pediatric extremity trauma. Plast Reconstr Surg. 2009;123(5):1510-1520. 8. Campbell PE, Smith GS, Smith JM. Retrospective clinical evaluation of gauze-based negative pressure wound therapy. Int Wound J. 2008;5(2):280-286. 9. Banwell PE, Musgrave B. Topical negative pressure therapy: mechanisms and indications. Int Wound J. 2004;1(2):95-106. 10. Scherer SS, Pietramaggiori G, Mathews JC, et al. The mechanism of action of the vacuum-assisted closure device. Plast Reconstr Surg. 2008;122(3):786-797. 11. DeFranzo AJ, Argenta LC, Marks MW, et al. The use of vacuum-assisted closure therapy for the treatment of lower extremity wounds with exposed bone. Plast Reconstr Surg. 2001;108(5):1184-1191. 12. Herscovici D Jr, Sanders RW, Scaduto JM, Infante A, DiPasquale T. Vacuum-assisted wound closure (VAC therapy) for the management of patients with high-energy soft tissue injuries. J Orthop Trauma. 2003;17(10):683-688. 13. Bollero D, Carnino R, Risso D, Gangemi EN, Stella M. Acute complex traumas of the lower limbs: a modern reconstructive approach with negative pressure therapy. Wound Repair Regen. 2007;15(4):589-594. 14. Clare MP, Fitzgibbons TC, McMullen ST, et al. Experience with the vacuum assisted closure negative pressure technique in the treatment of non-healing diabetic and dysvascular wounds. Foot Ankle Int. 2002;23(10):896-901. 15. DeFranzo AJ, Marks MW, Argenta LC, Genecov DG. Vacuum assisted closure for the treatment of degloving injuries. Plast Reconstr Surg. 1999;104(7):2145-2148. 16. De Lange MY, Schasfoort RA, Obdeijn MC, Van Der Werff JFA, Nicolai JPA. Vacuum assisted closure: indications and clinical experience. Eur J Plast Surg. 2000;23(4):178-181. 17. Dunn RM, Ignotz R, Mole T, Cockwill J, Smith JM. Assessment of gauze-based negative pressure wound therapy in the split-thickness skin graft clinical pathway-an observational study. Eplasty. 2011;16: 11:e14. 18. Malmsjö M, Lindstedt S, Ingemansson R. Influence on pressure transduction when using different drainage techniques and wound fillers (foam and gauze) for negative pressure wound therapy. Int Wound J. 2010;7(5):406-412. 19. Malmsjö M, Ingemansson R, Martin R, Huddleston E. Negative pressure wound therapy using gauze or open-cell polyurethane foam: similar early effects on pressure transduction and tissue contraction in an experimental porcine wound model. Wound Repair Regen. 2009;17(2):200-205. 20. Caniano DA, Ruth B, Teich S. Wound management with vacuum assisted closure: experience in 51 pediatric patients. J Pediatr Surg. 2005;40(1):128-132. 21. Vidrine DM, Kaler S, Rosenthal EL. A comparison of negative-pressure dressing versus bolster and splitting of the radial forearm donor site. Otolaryngol Head Neck Surg. 2005;133(3):403-406. 22. Ashcroft GS, Ashworth JJ. Potential role of estrogens in wound healing. Am J Clin Dermatol. 2003;4(11):737-743. 23. Gilliver SC, Ashworth JJ, Ashcroft GS. The hormonal regulation of cutaneous wound healing. Clin Dermatol. 2007;25(1):56-62. Umut Tuncel, MD; and Aydin Turan, MD are from the the Department of Plastic Reconstructive and Aesthetic Surgery, Gaziosmanpasa University, Tokat, Turkey. M. Alper Bayraktar, MD is from the Department of Plastic Reconstructive and Aesthetic Surgery, Çekirge State Hospital, Bursa, Turkey. Ufuk Aydin, MD is from the Department of Plastic Reconstructive and Aesthetic Surgery, Edirne State Hospital, Edirne, Turkey. Unal Erkorkmaz, PhD is from the Department of Biostatistics, Gaziosmanpasa University, Tokat, Turkey. Address correspondence to: Umut Tuncel, MD Gaziosmanpasa University, Faculty of Medicine Department of Plastic Reconstructive and Aesthetic Surgery 60100, Tokat, Turkey drumuttuncel@gmail.com

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