journal article·2022-08-21Open access

Activation of Tissue Reparative Processes by Glow-Type Plasma Discharges as an Integral Part of the Therapy of Decubital Ulcers

Sergej V. Belov, Yurij K. Danilejko, Sergey V. Gudkov, Aleksej B. Egorov, Vladimir I. Lukanin, Vladimir B. Tsvetkov, Evgeny L. Altukhov, Marina V. Petrova, Alexey A. Yakovlev, Elkhan G. Osmanov, Mikhail V. Dubinin, Evgenia A. Kogan, Viktor P. Seredin, Aleksandr M. Shulutko

Applied Sciences· Volume 12· Issue 16

Abstract

The results of a clinical study of the complex treatment of pressure ulcers using the method of activation of reparative processes in tissues by cold plasma discharges initiated by high-frequency current are presented. Activation was carried out with a specialized device generating cold plasma discharges at frequencies of 0.11, 2.64, and 6.78 MHz. It was shown that the process of activation in the skin and muscle tissues of the bedsore zone proceeds most efficiently when using a current with a frequency of 6.78 MHz as compared to currents with a frequency of 2.64 and 0.11 MHz. For a needle electrode with a diameter of 0.3 mm, the optimal exposure parameters were power—(5.0 ± 1.5) W and time—(2.0–3.0) s. The results of the analysis of histological samples, histochemical, and bacteriological analysis confirmed the effect and showed the dynamics of the process of activation of reparative processes in the tissues of the bedsore wound under the influence of cold plasma discharges and a decrease in microbial contamination. The most pronounced effect of activation was formed during the period from 14 to 21 days. The effectiveness of therapy by the method of activation of reparative processes with cold plasma discharges, according to the criterion of the rate of wound healing, ranged from 14 to 16%, depending on the etiology of the decubitus wound. It is concluded that the activation of tissue reparative processes by glow-type plasma discharges as an integral part of the treatment of decubital ulcers is an effective link in the complex treatment of pressure sores.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Wound Healing and Treatments · Burn Injury Management and Outcomes · Dermatologic Treatments and Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Prokhorov General Physics Institute of the Russian Academy of Sciences, Vavilov St. 38, 119991 Moscow, Russia

Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, St. Petrovka 25, bld. 2, 107031 Moscow, Russia

I. M. Sechenov First Moscow State Medical University, Ministry of Health of the Russian Federation, Trubetskaya Str. 8-2, 119991 Moscow, Russia

Department of Biochemistry, Cell Biology and Microbiology, Mari State University, pl. Lenina 1, 424001 Yoshkar-Ola, Russia

Funding

Ministry of Science and Higher Education of the Russian Federation

References (50)

Show source-provided references
1. Assessment and management of pressure ulcers in the elderly: Current strategies10.2165/11318340-000000000-00000 ↗
2. Pressure ulcers: Current understanding and newer modalities of treatment10.4103/0970-0358.155260 ↗
3. Patient risk factors for pressure ulcer development: Systematic review10.1016/j.ijnurstu.2012.11.019 ↗
4. Risk factors for mortality after spinal cord injury in the USA10.1038/sc.2013.2 ↗
5. Decubitus: Prevention and treatment
6. From Decubitus and Pressure Ulcers to Pressure Injuries10.1097/01.ASW.0000553114.57290.be ↗
7. Pressure ulcers: The core, care and cure approach10.12968/bjcn.2019.24.Sup12.S38 ↗
8. Review of the Current Management of Pressure Ulcers10.1089/wound.2016.0697 ↗
9. Therapeutic options for pressure ulcers
10. Morphological and physiological aspects of the course of the wound process (literature review)
11. Dressings and topical agents for treating pressure ulcers
12. International Consensus on drug allergy10.1111/all.12350 ↗
13. 2015 update of the evidence base: World Allergy Organization anaphylaxis guidelines10.1186/s40413-015-0080-1 ↗
14. Immediate-type hypersensitivity drug reactions10.1111/bcp.12297 ↗
15. Immunologic evaluation of drug allergy10.4168/aair.2012.4.5.251 ↗
16. Adverse drug reactions and organ damage: The skin10.1016/j.ejim.2015.11.017 ↗
17. Drugs as important factors causing allergies
18. Idiosyncratic adverse drug reactions: Current concepts10.1124/pr.113.007450 ↗
19. Arndt, S., Unger, P., Wacker, E., Shimizu, T., Heinlin, J., Li, Y.-F., Thomas, H.M., Morfill, G.E., Zimmermann, J.L., and Bosserhoff, A.K. (2013). Cold atmospheric plasma (CAP) changes gene expression of key molecules of the wound healing machinery and improves wound healing in vitro and in vivo. PLoS ONE, 8.10.1371/journal.pone.0079325 ↗
20. Cui, H.S., Joo, S.Y., Cho, Y.S., Park, J.H., Kim, J.-B., and Seo, C.H. (2020). Effect of Combining Low Temperature Plasma, Negative Pressure Wound Therapy, and Bone Marrow Mesenchymal Stem Cells on an Acute Skin Wound Healing Mouse Model. Int. J. Mol. Sci., 21.10.3390/ijms21103675 ↗
21. Trends in surface engineering of biomaterials: Atmospheric pressure plasma deposition of coatings for biomedical applications10.1051/epjap/2011110192 ↗
22. Regulating the antibiotic drug release from β-tricalcium phosphate ceramics by atmospheric plasma surface engineering10.1039/C6BM00411C ↗
23. The effects of non-thermal atmospheric pressure plasma jet on attachment of osteoblast10.1016/j.cap.2012.12.022 ↗
24. The effects of cold atmospheric plasma on cell adhesion, differentiation, migration, apoptosis and drug sensitivity of multiple myeloma10.1016/j.bbrc.2016.04.027 ↗
25. Low temperature plasma promoting fibroblast proliferation by activating the NF-κB pathway and increasing cyclinD1 expression10.1038/s41598-017-12043-w ↗
26. Tominami, K., Kanetaka, H., Sasaki, S., Mokudai, T., Kaneko, T., and Niwano, Y. (2017). Cold atmospheric plasma enhances osteoblast differentiation. PLoS ONE, 12.10.1371/journal.pone.0180507 ↗
27. Activation of Repair Processes in Patients with Bedsores Using Pulsed Radio Frequency Currents10.1007/s10527-021-10095-x ↗
28. Device for activating reparative processes by low-temperature plasma discharges in patients with decubitus ulcers: Parameter optimization and efficiency assessment
29. On the dose of plasma medicine: Equivalent total oxidation potential (ETOP)10.1063/5.0008881 ↗
30. On the dose of plasma medicine: Plasma-activated medium (PAM) and its effect on cell viability10.1063/5.0089357 ↗
31. High-frequency electrical stimulation of the wound process in patients after surgical treatment of rectal fistulas and epithelial coccygeal tract
32. Specific Features of Generation of Low-Temperature Plasma in High-Frequency Plasma Electrosurgical Apparatuses10.1007/s10527-011-9210-4 ↗
33. Validity and reliability of the Pressure Sore Status Tool
34. Effects of Low Temperature Plasma Glow Discharge on the Proliferative Activity of Cells and the Repair Functions of Tissues in Animals and Plants10.1007/s10527-020-09953-x ↗
35. Modern methods of stimulating process of postoperative wounds regeneration10.20333/2500136-2020-3-54-60 ↗
36. Histological and ultrastructural evaluation of the effects of a radiofrequency based nonablative dermal remodeling device: A pilot study10.1001/archderm.140.2.204 ↗
37. Mitochondria, calcium homeostasis and calcium signaling
38. Modulation of calciumactivated potassium channels10.1007/s00359-002-0281-2 ↗
39. Atmospheric-pressure plasma sources: Prospective tools for plasma medicine10.1351/PAC-CON-09-10-35 ↗
40. Low-temperature plasmas at atmospheric pressure: Towards new pharmaceutical treatments in medicine. fundam
41. Formation of ROS and RNS in water electro-sprayed through transient spark discharge in air and their bactericidal effects10.1002/ppap.201200113 ↗
42. Correlations between gaseous and liquid phase chemistries induced by cold atmospheric plasmas in a physiological buffer10.1039/C8CP00264A ↗
43. Belov, S.V., Lobachevsky, Y.P., Danilejko, Y.K., Egorov, A.B., Simakin, A.V., Maleki, A., Temnov, A.A., Dubinin, M.V., and Gudkov, S.V. (2020). The Role of Mitochondria in the Dual Effect of Low-Temperature Plasma on Human Bone Marrow Stem Cells: From Apoptosis to Activation of Cell Proliferation. Appl. Sci., 10.10.3390/app10248971 ↗
44. Reactive oxygen species-induced lipid peroxidation in apoptosis, autophagy, and ferroptosis10.1155/2019/5080843 ↗
45. High levels of Fis1, a pro-fission mitochondrial protein, trigger autophagy10.1016/j.bbabio.2008.05.442 ↗
46. Electroporation and its Relevance for Cardiac Catheter Ablation10.1016/j.jacep.2018.06.005 ↗
47. Textbook: Electroporation of cells in complex materials and tissues10.1063/1.4949264 ↗
48. Changes in membrane structure induced by electroporation as revealed by rapid-freezing electron microscopy10.1016/S0006-3495(90)82348-1 ↗
49. Danilejko, Y.K., Belov, S.V., Egorov, A.B., Lukanin, V.I., Sidorov, V.A., Apasheva, L.M., Dushkov, V.Y., Budnik, M.I., Belyakov, A.M., and Kulik, K.N. (2021). Increase of Productivity and Neutralization of Pathological Processes in Plants of Grain and Fruit Crops with the Help of Aqueous Solutions Activated by Plasma of High-Frequency Glow Discharge. Plants, 10.10.3390/plants10102161 ↗
50. An Activated Potassium Phosphate Fertilizer Solution for Stimulating the Growth of Agricultural Plants10.3389/fphy.2020.618320 ↗