Wound contraction and macro-deformation during negative pressure therapy of sternotomy wounds
© Torbrand et al; licensee BioMed Central Ltd. 2010
Received: 5 August 2010
Accepted: 30 September 2010
Published: 30 September 2010
Negative pressure wound therapy (NPWT) is believed to initiate granulation tissue formation via macro-deformation of the wound edge. However, only few studies have been performed to evaluate this hypothesis. The present study was performed to investigate the effects of NPWT on wound contraction and wound edge tissue deformation.
Six pigs underwent median sternotomy followed by magnetic resonance imaging in the transverse plane through the thorax and sternotomy wound during NPWT at 0, -75, -125 and -175 mmHg. The lateral width of the wound and anterior-posterior thickness of the wound edge was measured in the images.
The sternotomy wound decreased in size following NPWT. The lateral width of the wound, at the level of the sternum bone, decreased from 39 ± 7 mm to 30 ± 6 mm at -125 mmHg (p = 0.0027). The greatest decrease in wound width occurred when switching from 0 to -75 mmHg. The level of negative pressure did not affect wound contraction (sternum bone: 32 ± 6 mm at -75 mmHg and 29 ± 6 mm at -175 mmHg, p = 0.0897). The decrease in lateral wound width during NPWT was greater in subcutaneous tissue (14 ± 2 mm) than in sternum bone (9 ± 2 mm), resulting in a ratio of 1.7 ± 0.3 (p = 0.0423), suggesting macro-deformation of the tissue. The anterior-posterior thicknesses of the soft tissue, at 0.5 and 2.5 cm laterally from the wound edge, were not affected by negative pressure.
NPWT contracts the wound and causes macro-deformation of the wound edge tissue. This shearing force in the tissue and at the wound-foam interface may be one of the mechanisms by which negative pressure delivery promotes granulation tissue formation and wound healing.
Cardiac surgery is complicated by post-sternotomy mediastinitis in 1% to 5% of all procedures  and is a life-threatening complication . The reported early mortality in post-sternotomy mediastinitis following coronary artery bypass graft surgery is between 8% and 25% [3, 4]. Conventional treatment of post-sternotomy mediastinitis includes surgical debridement, drainage, irrigation, and reconstruction using pectoral muscle flap or omentum transposition. In 1999, Obdeijn and colleagues described a new method of treatment for post-sternotomy mediastinitis using a vacuum-assisted closure technique , which is based on the principle of applying subatmospheric pressure by controlled suction through a porous dressing. The technique, also known as negative pressure wound therapy (NPWT), has resulted in reduced mortality in post-sternotomy mediastinitis .
Scientific evidence regarding the mechanisms by which NPWT promotes wound healing has started to emerge. NPWT results in the drainage of excessive fluid and debris, removal of wound edema, reduction in bacterial counts and stimulation of wound edge microvascular blood flow [7–10]. However, it is now believed that one of the major driving forces that generate granulation tissue formation is the macro-deformation of the wound edge tissue that results from the suction force created by the negative pressure. To our knowledge, there is only sparse scientific evidence for this instantaneous mechanical effect by NPWT .
The present study was performed to in detail investigate the effects of NPWT on wound contraction and wound edge tissue deformation. Magnetic resonance imaging (MRI) of the thorax was performed in a porcine sternotomy wound model. The lateral width of the wound and anterior-posterior thickness of the wound edge was measured in the images taken before and after initiation of NPWT at -75, -125 and -175 mmHg.
Materials and methods
An uninfected porcine sternotomy wound model was used in the present study. Six domestic landrace pigs of both genders, with a mean body weight of 50 kg, were fasted overnight with free access to water. The study was approved by the Ethics Committee for Animal Research, Lund University, Sweden. The investigation complied with the "Guide for the Care and Use of Laboratory Animals" as recommended by the U.S. National Institutes of Health and published by the National Academies Press (1996).
Anesthesia was induced with ketamine hydrochloride (Ketaminol Vet™ 100 mg/ml, Farmaceutici Gellini S.p.A, Aprilia, Italy), 15 mg/kg intramuscularly, and xylazine (Rompun Vet™ 20 mg/mL, Bayer AG, Leverkusen, Germany), 2 mg/kg intramuscularly. The pigs were intubated and mechanical ventilation was established with a Siemens-Elema 900B ventilator in the volume-controlled mode. Anesthesia was maintained by continuous intravenous infusion of propofol (Diprivan™, Astra Zeneca, Sweden), 0.1-0.2 mg/kg/min, in combination with fentanyl (Leptanal™, Lilly, France), 0.05 μg/kg/min, and atracurium besylate (Tracrium™, Glaxo, Täby, Sweden), 0.2-0.5 mg/kg/hour.
After a midline sternotomy, the pericardium was opened and a polyurethane foam dressing was placed between the sternal edges. Two non-collapsible drainage tubes were inserted into the foam. The open wound was then sealed with a transparent adhesive drape. The drainage tubes were connected to a purpose-built vacuum source (VAC® pump unit, KCI, Copenhagen, Denmark), which was set to deliver a continuous negative pressure of -75, -125 or -175 mmHg.
MRI was first performed at baseline (0 mmHg). A negative pressure was then applied and MRI was performed when the target pressure had been reached. This procedure was repeated for each negative pressure (-75, -125, and -175 mmHg). In order to eliminate time effects, the sequence of application of the three different negative pressures was varied between the animals using a 3 by 3 Latin square design.
Magnetic resonance imaging
MRI was conducted using a 1.5T system (Intera CV, Philips Medical Systems, Best, the Netherlands) with a five-element cardiac coil and the pig in the supine position. The images were acquired during ventilator-controlled end expiratory apnea at the functional residual lung capacity. Images were acquired in the transverse and sagittal planes, covering the entire thoracic cavity using a steady-state free precession sequence. Typical imaging parameters were: spatial resolution 1.1 × 1.1 mm, slice thickness 5 mm, slice gap 0 mm, repetition time 3.1 ms, echo time 1.6 ms, flip angle 60°, no ECG triggering, sensitivity-encoding factor 2.
Calculations and statistics
Statistical analysis was performed using paired Student's t-test. Significance was defined as p < 0.05. The results are presented as mean values ± the standard error of the mean (S.E.M.).
The wound edge tissue was also deformed upon application of NPWT. The decrease in lateral wound width during NPWT was greater in subcutaneous tissue (14 ± 2 mm) than in sternum bone (9 ± 2 mm), which resulted in a ratio of subcutaneous to sternal decrease in wound width of 1.7 ± 0.3 (p = 0.0423), suggesting macro-deformation of the wound edge tissue. The major decrease in lateral wound width occurred when switching from 0 to -75 mmHg and the level of negative pressure did not play a significant role for the degree of wound contraction (23 ± 4 mm at -75 mmHg and 19 ± 2 mm at -175 mmHg, for muscle tissue p = 0.0982, n = 6, Figure 3).
The present study shows wound contraction upon application of NPWT in a porcine sternotomy wound model. Furthermore, it provides detailed evidence for the deformation of the wound edge tissue. Pulling forces by the negative pressure move the subcutaneous tissue wound edges together to a greater extent than the wound edges of the sternum bone. This presumably creates shearing forces in the tissue and at the wound-foam interface. This so called macro-deformation of the tissue is believed to be one of the fundamental mechanisms by which NPWT results in wound healing . This mechanical effect of NPWT is thought to initiate a cascade of inter-related biological effects including the promotion of wound edge microvascular blood flow, removal of bacteria and stimulation of granulation tissue formation [7, 10, 13, 14].
Shearing forces at the foam-wound interface
Contraction of the wound and macro-deformation of the wound edge tissue upon NPWT, as shown in the present study, causes mechanical stress in the tissue. Mechanical stress is known to promote the expression of growth factors (e.g., vascular endothelial growth factor and fibroblast growth factor-2) and to stimulate granulation tissue formation and angiogenesis [15–17]. In a computerized model of negative pressure-induced wound deformation, most elements were stretched five to twenty percent by NPWT , which is similar to in vitro strain levels shown to promote cellular proliferation. The beneficial effects of NPWT on healing may depend on these macro-mechanical effects and the shearing forces at the foam-wound interface.
The mechanical effect of NPWT on the wound edge tissue is also believed to alter microvascular blood flow. Close to the wound edge there is contraction of the tissue resulting in hypoperfusion [18–20]. Factors released in response to hypoperfusion are strong stimulators of angiogenesis and granulation tissue formation, which may be one of the mechanisms governing the positive effects of NPWT. Pressure against the wound wall may also be beneficial since it has been shown to tamponade superficial bleedings during surgical procedures  and reduce wound edge edema. Further away from the wound edge, microvascular blood flow is increased upon negative pressure application. It may be speculated that the pulling forces on the wound edge tissue opens up capillary beds and surges blood to the area. The present study shows differences in the wound edge tissue deformation when comparing subcutaneous and muscle tissue. Similarly, blood flow effects by NPWT are different in subcutaneous and muscle tissue [19, 20]. It may be speculated that the mechanical effects that NPWT result in depend on the density of the tissue and the tissue composition of the treated wound.
In sternotomy wounds, there are underlying vital structures and an important aspect during treatment of these wounds is the heart and lung function and the reconstruction of a stable thorax. The present study shows that the sternotomy wound contracts during NPWT. This is in concordance with one of our previous studies showing that the sternum is stabilised and can withstand external forces during NPWT . Stabilization of the sternum enables early mobilization which is crucial for the clinical outcome [22, 23].
Heart and lung function
As shown by the present study, NPWT contracts the wound and draws the two sternal edges together, thereby resealing the thoracic cavity. NPWT thus largely restores the macroscopic anatomical conditions in the thorax, which may explain the clinical benefits of NPWT over open-chest care, including reduced need for mechanical ventilation [24, 25]. Sternotomy wound contraction and resealing of the sternum also has effects on the heart pumping function. The findings that cardiac output decreases during NPWT [26, 27] have been a reason for concern. However, we now believe that cardiac output increases and the energy efficiency of cardiac pumping decreases upon sternotomy and both these measures return to pre-sternotomy levels when the thorax is resealed by NPWT. It is reassuring to know that the effects on cardiac pumping function upon resealing of the thorax is physiological since many patients with deep sternal wound infections suffer impaired cardiac function and heart failure and may thereby be especially vulnerable to increased cardiac load.
Different levels of negative pressure
In the present study, the greatest change in wound diameter was observed between 0 and -75 mmHg, and the level of negative pressure did not play a significant role for the degree of wound contraction. Similar findings were shown in a study by Isago et al , carried out in peripheral rat wounds and using polyurethane foam. Negative pressures of -50, -75 and -125 mmHg caused similar reduction in wound area. Furthermore, in a pig sternotomy wound model , the wound contraction upon NPWT application was similar in wounds treated with low (-50 to -100 mmHg) and high (-150 to -200 mmHg) negative pressures. Thus, both low and high levels of negative pressure will induce macro-mechanical deformation during NPWT.
In conclusion, NPWT contracts the wound and causes macro-deformation of the wound edge tissue. This mechanical stress in the tissue and at the wound-foam interface creates shearing forces that is known to promote granulation tissue formation and facilitate healing.
We thank Einar Heiberg, PhD, for valuable help and advice regarding image analysis. This study was supported by the Swedish Medical Research Council, Lund University Faculty of Medicine, the Swedish Government Grant for Clinical Research, Lund University Hospital Research Grants, the Swedish Medical Association, the Royal Physiographic Society in Lund, the Åke Wiberg Foundation, the Anders Otto Swärd Foundation/Ulrika Eklund Foundation, the Magnus Bergvall Foundation, the Crafoord Foundation, the Anna-Lisa and Sven-Erik Nilsson Foundation, the Jeansson Foundation, the Swedish Heart-Lung Foundation, Anna and Edvin Berger's Foundation, the Märta Lundqvist Foundation, and the Lars Hierta Memorial Foundation.
- Raudat CW, Pagel J, Woodhall D: Early intervention and aggressive management of infected median sternotomy incision: a review of 2242 open-heart procedures. Am Surg. 1997, 63 (3): 238-41. discussion 241-2PubMedGoogle Scholar
- El Oakley RM, Wright JE: Postoperative mediastinitis: classification and management. Ann Thorac Surg. 1996, 61 (3): 1030-6. 10.1016/0003-4975(95)01035-1.View ArticlePubMedGoogle Scholar
- Crabtree TD, Codd JE, Fraser VJ: Multivariate analysis of risk factors for deep and superficial sternal infection after coronary artery bypass grafting at a tertiary care medical center. Semin Thorac Cardiovasc Surg. 2004, 16 (1): 53-61. 10.1053/j.semtcvs.2004.01.009.View ArticlePubMedGoogle Scholar
- Lu JC, Grayson AD, Jha P: Risk factors for sternal wound infection and mid-term survival following coronary artery bypass surgery. Eur J Cardiothorac Surg. 2003, 23 (6): 943-9. 10.1016/S1010-7940(03)00137-4.View ArticlePubMedGoogle Scholar
- Obdeijn MC, de Lange MY, Lichtendahl DH: Vacuum-assisted closure in the treatment of poststernotomy mediastinitis. Ann Thorac Surg. 1999, 68 (6): 2358-60. 10.1016/S0003-4975(99)01159-5.View ArticlePubMedGoogle Scholar
- Sjogren J, Gustafsson R, Nilsson J: Clinical outcome after poststernotomy mediastinitis: vacuum-assisted closure versus conventional treatment. Ann Thorac Surg. 2005, 79 (6): 2049-55. 10.1016/j.athoracsur.2004.12.048.View ArticlePubMedGoogle Scholar
- Argenta LC, Morykwas MJ: Vacuum-assisted closure: a new method for wound control and treatment: clinical experience. Ann Plast Surg. 1997, 38 (6): 563-76. 10.1097/00000637-199706000-00002. discussion 577View ArticlePubMedGoogle Scholar
- Clare MP, Fitzgibbons TC, McMullen ST: 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.View ArticlePubMedGoogle Scholar
- Domkowski PW, Smith ML, Gonyon DL: Evaluation of vacuum-assisted closure in the treatment of poststernotomy mediastinitis. J Thorac Cardiovasc Surg. 2003, 126 (2): 386-90. 10.1016/S0022-5223(03)00352-0.View ArticlePubMedGoogle Scholar
- Morykwas MJ, Argenta LC, Shelton-Brown EI: Vacuum-assisted closure: a new method for wound control and treatment: animal studies and basic foundation. Ann Plast Surg. 1997, 38 (6): 553-62. 10.1097/00000637-199706000-00001.View ArticlePubMedGoogle Scholar
- Saxena V, Hwang CW, Huang S: Vacuum-assisted closure: microdeformations of wounds and cell proliferation. Plast Reconstr Surg. 2004, 114 (5): 1086-96. 10.1097/01.PRS.0000135330.51408.97. discussion 1097-8View ArticlePubMedGoogle Scholar
- Heiberg E, Sjögren J, Ugander M: Design and Validation of Segment - freely available software for cardiovascular image analyses. BMC Med Imaging. 2010, 10: 1-10.1186/1471-2342-10-1.View ArticlePubMedPubMed CentralGoogle Scholar
- Morykwas MJ, Simpson J, Punger K: Vacuum-assisted closure: state of basic research and physiologic foundation. Plast Reconstr Surg. 2006, 117 (7 Suppl): 121S-126S. 10.1097/01.prs.0000225450.12593.12.View ArticlePubMedGoogle Scholar
- Malmsjo M, Ingemansson R, Sjogren J: Mechanisms governing the effects of vacuum-assisted closure in cardiac surgery. Plast Reconstr Surg. 2007, 120 (5): 1266-75. 10.1097/01.prs.0000279326.84535.2d.View ArticlePubMedGoogle Scholar
- Quinn TP, Schlueter M, Soifer SJ: Cyclic mechanical stretch induces VEGF and FGF-2 expression in pulmonary vascular smooth muscle cells. Am J Physiol Lung Cell Mol Physiol. 2002, 282 (5): L897-903.View ArticlePubMedGoogle Scholar
- Rivilis I, Milkiewicz M, Boyd P: Differential involvement of MMP-2 and VEGF during muscle stretch- versus shear stress-induced angiogenesis. Am J Physiol Heart Circ Physiol. 2002, 283 (4): H1430-8.View ArticlePubMedGoogle Scholar
- Urschel JD, Scott PG, Williams HT: The effect of mechanical stress on soft and hard tissue repair; a review. Br J Plast Surg. 1988, 41 (2): 182-6. 10.1016/0007-1226(88)90049-5.View ArticlePubMedGoogle Scholar
- Sjögren J, Gustafsson R, Koul B: Selective mediastinal tamponade to control coagulopathic bleeding. Ann Thorac Surg. 2003, 75 (4): 1311-3. 10.1016/S0003-4975(02)04570-8.View ArticlePubMedGoogle Scholar
- Wackenfors A, Gustafsson R, Sjogren J: Blood flow responses in the peristernal thoracic wall during vacuum-assisted closure therapy. Ann Thorac Surg. 2005, 79 (5): 1724-30. 10.1016/j.athoracsur.2004.10.053. discussion 1730-1View ArticlePubMedGoogle Scholar
- Wackenfors A, Sjogren J, Gustafsson R: Effects of vacuum-assisted closure therapy on inguinal wound edge microvascular blood flow. Wound Repair Regen. 2004, 12 (6): 600-6. 10.1111/j.1067-1927.2004.12602.x.View ArticlePubMedGoogle Scholar
- Mokhtari A, Petzina R, Gustafsson L: Sternal stability at different negative pressures during vacuum-assisted closure therapy. Ann Thorac Surg. 2006, 82 (3): 1063-7. 10.1016/j.athoracsur.2006.04.085.View ArticlePubMedGoogle Scholar
- Gustafsson RI, Sjogren J, Ingemansson R: Deep sternal wound infection: a sternal-sparing technique with vacuum-assisted closure therapy. Ann Thorac Surg. 2003, 76 (6): 2048-53. 10.1016/S0003-4975(03)01337-7. discussion 2053View ArticlePubMedGoogle Scholar
- Hersh RE, Jack JM, Dahman MI: The vacuum-assisted closure device as a bridge to sternal wound closure. Ann Plast Surg. 2001, 46 (3): 250-4. 10.1097/00000637-200103000-00008.View ArticlePubMedGoogle Scholar
- Kutschka I, Frauendorfer P, Harringer W: [Vacuum assisted closure therapy improves early postoperative lung function in patients with large sternal wounds]. Zentralbl Chir. 2004, 129 (Suppl 1): S33-4.PubMedGoogle Scholar
- Ramnarine IR, McLean A, Pollock JC: Vacuum-assisted closure in the paediatric patient with post-cardiotomy mediastinitis. Eur J Cardiothorac Surg. 2002, 22 (6): 1029-31. 10.1016/S1010-7940(02)00562-6.View ArticlePubMedGoogle Scholar
- Conquest AM, Garofalo JH, Maziarz DM: Hemodynamic effects of the vacuum-assisted closure device on open mediastinal wounds. J Surg Res. 2003, 115 (2): 209-13. 10.1016/S0022-4804(03)00331-7.View ArticlePubMedGoogle Scholar
- Petzina R, Ugander M, Gustafsson L: Hemodynamic effects of vacuum-assisted closure therapy in cardiac surgery: assessment using magnetic resonance imaging. J Thorac Cardiovasc Surg. 2007, 133 (5): 1154-62. 10.1016/j.jtcvs.2007.01.011.View ArticlePubMedGoogle Scholar
- Torbrand C, Ugander M, Engblom H: Changes in cardiac pumping efficiency and intra-thoracic organ volume during negative pressure wound therapy of sternotomy wounds, assessment using magnetic resonance imaging. Int Wound J. 7 (4): 305-11.Google Scholar
- Isago T, Nozaki M, Kikuchi Y: Effects of different negative pressures on reduction of wounds in negative pressure dressings. J Dermatol. 2003, 30 (8): 596-601.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.