DOI QR코드

DOI QR Code

Negative Pressure Wound Therapy of Chronically Infected Wounds Using 1% Acetic Acid Irrigation

  • Jeong, Hii Sun (Department of Plastic and Reconstructive Surgery, Kangnam Sacred Heart Hospital, Hallym University College of Medicine) ;
  • Lee, Byeong Ho (Department of Plastic and Reconstructive Surgery, Kangnam Sacred Heart Hospital, Hallym University College of Medicine) ;
  • Lee, Hye Kyung (Department of Plastic and Reconstructive Surgery, Eulji General Hospital, Eulji University College of Medicine) ;
  • Kim, Hyoung Suk (Department of Plastic and Reconstructive Surgery, Myongji Hospital, Kwandong University College of Medicine) ;
  • Moon, Min Seon (Department of Plastic and Reconstructive Surgery, Myongji Hospital, Kwandong University College of Medicine) ;
  • Suh, In Suck (Department of Plastic and Reconstructive Surgery, Kangnam Sacred Heart Hospital, Hallym University College of Medicine)
  • Received : 2014.10.21
  • Accepted : 2014.12.15
  • Published : 2015.01.15

Abstract

Background Negative-pressure wound therapy (NPWT) induces angiogenesis and collagen synthesis to promote tissue healing. Although acetic acid soaks normalize alkali wound conditions to raise tissue oxygen saturation and deconstruct the biofilms of chronic wounds, frequent dressing changes are required. Methods Combined use of NPWT and acetic acid irrigation was assessed in the treatment of chronic wounds, instilling acetic acid solution (1%) beneath polyurethane membranes twice daily for three weeks under continuous pressure (125 mm Hg). Clinical photographs, pH levels, cultures, and debrided fragments of wounds were obtained pre- and posttreatment. Tissue immunostaining (CD31, Ki-67, and CD45) and reverse transcription-polymerase chain reaction (vascular endothelial growth factor [VEGF], vascular endothelial growth factor receptor [VEGFR]; procollagen; hypoxia-inducible factor 1 alpha [HIF-1-alpha]; matrix metalloproteinase [MMP]-1,-3,-9; and tissue inhibitor of metalloproteinase [TIMP]) were also performed. Results Wound sizes tended to diminish with the combined therapy, accompanied by drops in wound pH (weakly acidic or neutral) and less evidence of infection. CD31 and Ki-67 immunostaining increased (P<0.05) post-treatment, as did the levels of VEGFR, procollagen, and MMP-1 (P<0.05), whereas the VEGF, HIF-1-alpha, and MMP-9/TIMP levels declined (P<0.05). Conclusions By combining acetic acid irrigation with negative-pressure dressings, both the pH and the size of chronic wounds can be reduced and infections be controlled. This approach may enhance angiogenesis and collagen synthesis in wounds, restoring the extracellular matrix.

Keywords

References

  1. Arias CA, Murray BE. Antibiotic-resistant bugs in the 21st century: a clinical super-challenge. N Engl J Med 2009;360: 439-43. https://doi.org/10.1056/NEJMp0804651
  2. Merckoll P, Jonassen TO, Vad ME, et al. Bacteria, biofilm and honey: a study of the effects of honey on 'planktonic' and biofilm-embedded chronic wound bacteria. Scand J Infect Dis 2009;41:341-7. https://doi.org/10.1080/00365540902849383
  3. de Laat EH, van den Boogaard MH, Spauwen PH, et al. Faster wound healing with topical negative pressure therapy in difficult-to-heal wounds: a prospective randomized controlled trial. Ann Plast Surg 2011;67:626-31. https://doi.org/10.1097/SAP.0b013e31820b3ac1
  4. Kim BS, Choi WJ, Baek MK, et al. Limb salvage in severe diabetic foot infection. Foot Ankle Int 2011;32:31-7. https://doi.org/10.3113/FAI.2011.0031
  5. Scherer SS, Pietramaggiori G, Mathews JC, et al. The mechanism of action of the vacuum-assisted closure device. Plast Reconstr Surg 2008;122:786-97. https://doi.org/10.1097/PRS.0b013e31818237ac
  6. Milner SM. Acetic acid to treat Pseudomonas aeruginosa in superficial wounds and burns. Lancet 1992;340:61.
  7. Ryssel H, Kloeters O, Germann G, et al. The antimicrobial effect of acetic acid: an alternative to common local antiseptics? Burns 2009;35:695-700. https://doi.org/10.1016/j.burns.2008.11.009
  8. Ryssel H, Gazyakan E, Germann G, et al. Antiseptic therapy with a polylacticacid-acetic acid matrix in burns. Wound Repair Regen 2010;18:439-44. https://doi.org/10.1111/j.1524-475X.2010.00610.x
  9. Ryssel H, Germann G, Riedel K, et al. Suprathel-acetic acid matrix versus acticoat and aquacel as an antiseptic dressing: an in vitro study. Ann Plast Surg 2010;65:391-5. https://doi.org/10.1097/SAP.0b013e3181d6e2f2
  10. Wedam SB, Low JA, Yang SX, et al. Antiangiogenic and antitumor effects of bevacizumab in patients with inflammatory and locally advanced breast cancer. J Clin Oncol 2006;24: 769-77. https://doi.org/10.1200/JCO.2005.03.4645
  11. Gill SE, Parks WC. Metalloproteinases and their inhibitors: regulators of wound healing. Int J Biochem Cell Biol 2008; 40:1334-47. https://doi.org/10.1016/j.biocel.2007.10.024
  12. Beidler SK, Douillet CD, Berndt DF, et al. Multiplexed analysis of matrix metalloproteinases in leg ulcer tissue of patients with chronic venous insufficiency before and after compression therapy. Wound Repair Regen 2008;16:642-8. https://doi.org/10.1111/j.1524-475X.2008.00415.x
  13. Leonardi A, Cortivo R, Fregona I, et al. Effects of Th2 cytokines on expression of collagen, MMP-1, and TIMP-1 in conjunctival fibroblasts. Invest Ophthalmol Vis Sci 2003;44:183-9. https://doi.org/10.1167/iovs.02-0420
  14. Ladwig GP, Robson MC, Liu R, et al. Ratios of activated matrix metalloproteinase-9 to tissue inhibitor of matrix metalloproteinase-1 in wound fluids are inversely correlated with healing of pressure ulcers. Wound Repair Regen 2002;10: 26-37. https://doi.org/10.1046/j.1524-475X.2002.10903.x
  15. Bosanquet DC, Harding KG. Wound duration and healing rates: cause or effect? Wound Repair Regen 2014;22:143-50. https://doi.org/10.1111/wrr.12149
  16. Rippke F, Schreiner V, Schwanitz HJ. The acidic milieu of the horny layer: new findings on the physiology and pathophysiology of skin pH. Am J Clin Dermatol 2002;3:261-72. https://doi.org/10.2165/00128071-200203040-00004
  17. Leveen HH, Falk G, Borek B, et al. Chemical acidification of wounds. An adjuvant to healing and the unfavorable action of alkalinity and ammonia. Ann Surg 1973;178:745-53. https://doi.org/10.1097/00000658-197312000-00011
  18. Percival SL, McCarty S, Hunt JA, et al. The effects of pH on wound healing, biofilms, and antim icrobial efficacy. Wound Repair Regen 2014;22:174-86. https://doi.org/10.1111/wrr.12125
  19. Mah TF, O’Toole GA. Mechanisms of biofilm resistance to antimicrobial agents. Trends Microbiol 2001;9:34-9. https://doi.org/10.1016/S0966-842X(00)01913-2
  20. Kim PJ, Attinger CE, Steinberg JS, et al. Negative-pressure wound therapy with instillation: international consensus guidelines. Plast Reconstr Surg 2013;132:1569-79.
  21. Schneider LA, Korber A, Grabbe S, et al. Influence of pH on wound-healing: a new perspective for wound-therapy? Arch Dermatol Res 2007;298:413-20. https://doi.org/10.1007/s00403-006-0713-x
  22. Kiyokawa K, Takahashi N, Rikimaru H, et al. New continuous negative-pressure and irrigation treatment for infected wounds and intractable ulcers. Plast Reconstr Surg 2007; 120:1257-65. https://doi.org/10.1097/01.prs.0000279332.27374.69
  23. Ugaki S, Kasahara S, Arai S, et al. Combination of continuous irrigation and vacuum-assisted closure is effective for mediastinitis after cardiac surgery in small children. Interact Cardiovasc Thorac Surg 2010;11:247-51. https://doi.org/10.1510/icvts.2010.235903
  24. Greener B, Hughes AA, Bannister NP, et al. Proteases and pH in chronic wounds. J Wound Care 2005;14:59-61. https://doi.org/10.12968/jowc.2005.14.2.26739
  25. Leonardi A, Cortivo R, Fregona I, et al. Effects of Th2 cytokines on expression of collagen, MMP-1, and TIMP-1 in conjunctival fibroblasts. Invest Ophthalmol Vis Sci 2003; 44:183-9. https://doi.org/10.1167/iovs.02-0420

Cited by

  1. Use of negative pressure wound therapy as an adjunct to the treatment of extremity soft-tissue sarcoma with ulceration or impending ulceration vol.12, pp.1, 2015, https://doi.org/10.3892/ol.2016.4654
  2. EWMA Document: Negative Pressure Wound Therapy : Overview, Challenges and Perspectives vol.26, pp.suppl3, 2017, https://doi.org/10.12968/jowc.2017.26.sup3.s1
  3. EWMA Document: Negative Pressure Wound Therapy : Overview, Challenges and Perspectives vol.26, pp.suppl3, 2017, https://doi.org/10.12968/jowc.2017.26.sup3.s1
  4. Is NS-EDTA Effective in Clearing Bacteria From Infected Wounds in a Rat Model? vol.476, pp.5, 2015, https://doi.org/10.1007/s11999.0000000000000232
  5. Non-antibiotic antimicrobial interventions and antimicrobial stewardship in wound care vol.27, pp.6, 2015, https://doi.org/10.12968/jowc.2018.27.6.355
  6. Gold nanoparticles for tracking bacteria clearance by regulated irrigation and negative pressure-assisted wound therapy vol.13, pp.15, 2015, https://doi.org/10.2217/nnm-2018-0053
  7. Non-invasive nanosecond electroporation for biocontrol of surface infections: an in vivo study vol.8, pp.None, 2018, https://doi.org/10.1038/s41598-018-32783-7
  8. Recent Advances in Non-Conventional Antimicrobial Approaches for Chronic Wound Biofilms: Have We Found the ‘Chink in the Armor’? vol.7, pp.2, 2019, https://doi.org/10.3390/biomedicines7020035
  9. Efficacy of locally-available cleaning methods in removing biofilms from taps and surfaces of household water storage containers vol.3, pp.1, 2020, https://doi.org/10.1038/s41545-020-0061-y
  10. Negative pressure wound therapy with instillation: International consensus guidelines update vol.17, pp.1, 2015, https://doi.org/10.1111/iwj.13254
  11. Socioeconomic effects of pressure ulcer vol.64, pp.1, 2021, https://doi.org/10.5124/jkma.2021.64.1.11
  12. Non-surgical treatment for pressure ulcer vol.64, pp.1, 2021, https://doi.org/10.5124/jkma.2021.64.1.26