<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JBiSE</journal-id><journal-title-group><journal-title>Journal of Biomedical Science and Engineering</journal-title></journal-title-group><issn pub-type="epub">1937-6871</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbise.2016.910B022</article-id><article-id pub-id-type="publisher-id">JBiSE-70774</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Methodologies of Biophysical Wound Healing Therapies
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jacquelyn</surname><given-names>Dawn Parente</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Margareta</surname><given-names>Müller</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Knut</surname><given-names>Möller</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Faculty of Mechanical and Medical Engineering, Furtwangen University, Villingen-Schwenningen, Germany</addr-line></aff><aff id="aff1"><addr-line>Institute of Technical Medicine, Furtwangen University, Villingen-Schwenningen, Germany</addr-line></aff><pub-date pub-type="epub"><day>23</day><month>09</month><year>2016</year></pub-date><volume>09</volume><issue>10</issue><fpage>171</fpage><lpage>179</lpage><history><date date-type="received"><day>September</day>	<month>9,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>September</month>	<year>20,</year>	</date><date date-type="accepted"><day>September</day>	<month>23,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   
   Purpose: To evaluate the effects of methodological variation of biophysical therapies on wound healing outcomes, as a prel
   iminary study to develop a composite wound healing device. Methods: A literature search was focused on the variable devices, sys-tem configurations, input parameters, and treatment durations of negative pressure wound therapy (NPWT), electrical stimulation (ES), and low-level light therapy (LLLT) from 2011 to July 2016. Results: In NPWT, lower vacuum pressures of ?50 and ?80 mmHg achieved similar tissue perfusion outcomes as earlier recommendations of ?125 mmHg, while there is no established regimen with respect to continuous, square wave, or triangular NP waveform due to inconsistent results. Use of wound filler may contribute to improved tissue granulation when compared to topical NP. An ES configuration of high-voltage pulsed current with the stimulation electrode placed in the wound bed best resembles the endogenous skin current, which guides cellular migration. However, no studies have established optimal stimulation parameters. For LLLT, laser and LED proved similarly effective. Although red light has been almost exclusively used in human pressure ulcer treatment, studies comparing blue, green, and red wavelengths more consistently show biological effects using green light. Conclu-sions: Variation in the application of mechanical, electrical, and radiant energies may be used to modulate wound healing pathways. To 2012, no studies have examined use of these biophysical modalities in combination. Further methodological studies with a systems approach would help define optimal treatment protocols for improved wound healing outcomes in clinical practice. 
   
 
</p></abstract><kwd-group><kwd>Wound Healing</kwd><kwd> Therapy</kwd><kwd> NPWT</kwd><kwd> HVPC</kwd><kwd> LLLT</kwd><kwd> Methodology</kwd><kwd> Review</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>During 2012, approximately 200,000 new patients were added to the growing number of 780,000 Germans living with unhealed wounds for three months or more [<xref ref-type="bibr" rid="scirp.70774-ref1">1</xref>]. Half of these patients received treatment, however as chronic wounds represent a disruption in normal healing pathways, additional treatment beyond standard care wound dressings may be required to complete healing. In response to this clinical need, advanced care technologies are being developed to heal refractory venous leg, diabetic foot, and pressure ulcers.</p><p>These treatments may involve application of mechanical, light, or electrical energy to the wounded skin. For example, negative pressure wound therapy (NPWT) applies vacuum pressure to a filled and sealed wound bed, while also removing tissue exudates. Electrical stimulation (ES) applies imperceptible electrical fields across the wound tissue, while low-level light therapy (LLLT) applies blue to near infrared light. Such biophysical-tissue interactions have been shown to re-stimulate the natural healing pathways.</p><p>Detailed knowledge of the pathways stimulated by these treatment modalities is growing. NWPT provides fluid removal, yet also derives efficacy from macro- and micro-deformation, the latter being transferred to single cells by the ECM and potentially the integrin-mediated interaction of the cell with the matrix [<xref ref-type="bibr" rid="scirp.70774-ref2">2</xref>]. ES seems to act by enhanced recruitment of mast cells to the wound that may be mediated by so far poorly understood pathways of electrotaxis [<xref ref-type="bibr" rid="scirp.70774-ref3">3</xref>]. Finally, LLLT seems to be acting at least in part through mitochondrial pathways and the generation of reactive oxygen species, the generation of ATP, and the stimulation of transcription factors [<xref ref-type="bibr" rid="scirp.70774-ref4">4</xref>].</p><p>Although increasing evidence supports the clinical usage of these therapies, routine treatment protocols have not yet been established. Importantly, variations of equipment and technique may introduce variations at the wound surface that influence healing. Therefore, this review evaluates the effect of variations in methodological approaches of NPWT, ES, and LLLT on healing pathways. Such developments would help define the wound system, establish primary biophysical-tissue interactions, and develop optimized protocols for specific wound healing needs leading towards broader adoption into clinical practice for improved care of chronic wounds.</p></sec><sec id="s2"><title>2. Literature Search</title><p>This work is a preliminary study towards the design of a composite biophysical wound healing device. Thus, a PubMed database search from 2011 to July 2016 was conducted for reviews in English of NPWT (243 results), ES and wound (200 results), and LLLT and wound (51 results). Notably, selection criterion was for reviews focusing on studies of the effect of variable methodologies on outcomes, rather than efficacy. Therefore, 1 paper was selected for NPWT [<xref ref-type="bibr" rid="scirp.70774-ref5">5</xref>], 0 for ES, and 1 for LLLT [<xref ref-type="bibr" rid="scirp.70774-ref6">6</xref>]. Finally, the search criteria were relaxed to include reviews of the efficacy of ES, while also including a recommendation for selecting stimulation parameters; thus, 2 relevant LLLT review papers were selected. In total, these reviews provided 130 studies of variable methodology which were previously reviewed through July 2016. Therefore, this work provides a summary through 2010 (NPWT), 2013 (ES), and 2012 (LLLT) of the effect of methodological variation on wound healing outcomes.</p><p>All 43 NPWT studies were in in vitro cell systems or in in vivo animal models; no clinical data were available. Most studies were in porcine models, while tissue perfusion was a commonly reported outcome. Laser and LED were compared in in vitro and in vivo mouse and rat animal models. Additional methodological studies in the LLLT review were selected, which used a range of either wavelength or dosage, and reviewed independently. For ES, 1 paper reviewed randomized controlled trials (RCTs) and observational studies for pressure wounds [<xref ref-type="bibr" rid="scirp.70774-ref7">7</xref>] and the other reviewed 10 RCTs on pressure ulcer, chronic leg ulcers, and diabetic foot ulcers [<xref ref-type="bibr" rid="scirp.70774-ref8">8</xref>].</p></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Mechanical</title><p>Study results are summarized in <xref ref-type="table" rid="table1">Table 1</xref>. Amongst the 14 available NPWT systems, no studies have statistically compared device performances or wound interface materials. Transmission of NP is more efficient through perforated drainage conduits inserted into various wound fillers than through a non-perforated drain [<xref ref-type="bibr" rid="scirp.70774-ref9">9</xref>].</p><p>As compared to the Redon drain (topical NP), NPWT transmitted through wound fillers results in significantly greater tissue granulation in human sacral pressure ulcers [<xref ref-type="bibr" rid="scirp.70774-ref10">10</xref>]. Both gauze and foam transmitted NP efficiently [<xref ref-type="bibr" rid="scirp.70774-ref11">11</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref13">13</xref>]; there is no evidence to favor a particular wound filler [<xref ref-type="bibr" rid="scirp.70774-ref5">5</xref>]. However, some preclinical evidence suggests the use of foam may preferentially promote cell proliferation as compared to gauze [<xref ref-type="bibr" rid="scirp.70774-ref14">14</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref17">17</xref>].</p><p>Across a range of NP magnitudes, maximum peak tissue perfusion was initially achieved at −125 mmHg [<xref ref-type="bibr" rid="scirp.70774-ref23">23</xref>]. Yet, subsequent studies of NP magnitude have achieved similar tissue perfusion, granulation tissue formation, and wound closure outcomes to −125 mmHg at −80 mmHg [<xref ref-type="bibr" rid="scirp.70774-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref22">22</xref>] and at −50 [<xref ref-type="bibr" rid="scirp.70774-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref18">18</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref20">20</xref>]. Studies of NP continuous, square wave, and triangular waveforms have resulted in inconsistent granulation tissue formation outcomes [<xref ref-type="bibr" rid="scirp.70774-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref24">24</xref>]. Thus, new evidence supports the use of a</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> The variable equipment and techniques studied in negative pressure wound therapy (NPWT)</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Mechanical</th><th align="center" valign="middle"  colspan="3"  >In vitro and in vivo porcine model results [<xref ref-type="bibr" rid="scirp.70774-ref2">2</xref>]</th></tr></thead><tr><td align="center" valign="middle" >Options</td><td align="center" valign="middle" >Notes</td><td align="center" valign="middle" >Selection</td></tr><tr><td align="center" valign="middle" >Devices</td><td align="center" valign="middle" >14 NPWT systems or Redon drain</td><td align="center" valign="middle" >Wound filler or topical NP only</td><td align="center" valign="middle" >NPWT [<xref ref-type="bibr" rid="scirp.70774-ref10">10</xref>]</td></tr><tr><td align="center" valign="middle" >Wound filler</td><td align="center" valign="middle" >Foam or gauze</td><td align="center" valign="middle" >Foam and tissue Granulation [<xref ref-type="bibr" rid="scirp.70774-ref14">14</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref17">17</xref>]</td><td align="center" valign="middle" >Either [<xref ref-type="bibr" rid="scirp.70774-ref5">5</xref>]</td></tr><tr><td align="center" valign="middle" >Interface material</td><td align="center" valign="middle" >Impregnated gauze</td><td align="center" valign="middle" >No statistical studies</td><td align="center" valign="middle" >Inconclusive</td></tr><tr><td align="center" valign="middle" >Drainage conduit</td><td align="center" valign="middle" >Preforated or non-perforated</td><td align="center" valign="middle" >Within or on top of wound filler</td><td align="center" valign="middle" >Perforated [<xref ref-type="bibr" rid="scirp.70774-ref9">9</xref>]</td></tr><tr><td align="center" valign="middle" >NP magnitude</td><td align="center" valign="middle" >−25 mmHg to −400 mmHg</td><td align="center" valign="middle" >Tissue perfusion modulation</td><td align="center" valign="middle" >−50 [<xref ref-type="bibr" rid="scirp.70774-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref18">18</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref20">20</xref>] to −80 mmHg [<xref ref-type="bibr" rid="scirp.70774-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref22">22</xref>]</td></tr><tr><td align="center" valign="middle" >NP waveforms</td><td align="center" valign="middle" >Continuous, square, or triangular wave</td><td align="center" valign="middle" >Inconsistent results [<xref ref-type="bibr" rid="scirp.70774-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref24">24</xref>]</td><td align="center" valign="middle" >Inconclusive</td></tr><tr><td align="center" valign="middle" >Treatment duration</td><td align="center" valign="middle" >Study duration only</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >Inconclusive</td></tr></tbody></table></table-wrap><p>lower NP magnitude, while there is insufficient evidence to define a NP waveform regimen.</p></sec><sec id="s3_2"><title>3.2. Electrical</title><p>Electrode placement in the wound most resembles the skin endogenous electrical field to improve healing rates [<xref ref-type="bibr" rid="scirp.70774-ref25">25</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref27">27</xref>]. AC stimulation [<xref ref-type="bibr" rid="scirp.70774-ref28">28</xref>] and asymmetric AC pulses [<xref ref-type="bibr" rid="scirp.70774-ref29">29</xref>], resulted in faster healing rates than DC waveforms. Variations in applied voltages [<xref ref-type="bibr" rid="scirp.70774-ref30">30</xref>] and stimulation duration [<xref ref-type="bibr" rid="scirp.70774-ref31">31</xref>] demonstrated a dose-dependent induced cell migration of keratinocytes and fibroblasts [<xref ref-type="bibr" rid="scirp.70774-ref32">32</xref>], respectively. Thus, high-voltage pulsed current (HVPC) stimulation has emerged as a treatment modality with the most clinical potential for use in chronic wound healing, while also minimizing the risk of burns and having a greater depth of current penetration [<xref ref-type="bibr" rid="scirp.70774-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref34">34</xref>].</p><p>No studies have compared the methodological parameters of HVPC on wound healing outcomes. Thus, only HVPC parameter ranges can be reported. The commonly used HVPC parameters are summarized in <xref ref-type="table" rid="table2">Table 2</xref>.</p></sec><sec id="s3_3"><title>3.3. Radiant</title><p>Study results are summarized in <xref ref-type="table" rid="table3">Table 3</xref>. Laser or LED devices differ by their emission mechanisms, however any differences in their light properties are lost during photo-tissue interactions [<xref ref-type="bibr" rid="scirp.70774-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref36">36</xref>]. Accordingly, studies comparing laser and LED for LLLT application have resulted in similar biological effects [<xref ref-type="bibr" rid="scirp.70774-ref6">6</xref>].</p><p>All studies comparing the biological effects of blue, green, and red wavelengths for LLLT application showed the effectiveness of green light, while results are inconsistent for blue and red light. In particular, green and red light but not blue light were effective, on increasing fibroblast numbers [<xref ref-type="bibr" rid="scirp.70774-ref37">37</xref>], migratory or proliferative effects [<xref ref-type="bibr" rid="scirp.70774-ref38">38</xref>], or increased angiogenesis [<xref ref-type="bibr" rid="scirp.70774-ref39">39</xref>]. In contrast, green and blue light were effective, but not red</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> The variable equipment and techniques studied in electrical stimulation (ES)</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Electrical</th><th align="center" valign="middle"  colspan="3"  >Human pressure ulcer results [<xref ref-type="bibr" rid="scirp.70774-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref5">5</xref>]</th></tr></thead><tr><td align="center" valign="middle" >Options</td><td align="center" valign="middle" >Notes</td><td align="center" valign="middle" >Selection</td></tr><tr><td align="center" valign="middle" >Electrode configuration</td><td align="center" valign="middle" >Treatment electrode in wound or all electrodes surrounding wound</td><td align="center" valign="middle" >Resembles skin electrical current</td><td align="center" valign="middle" >Electrode in wound [<xref ref-type="bibr" rid="scirp.70774-ref25">25</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref27">27</xref>]</td></tr><tr><td align="center" valign="middle" >Waveform</td><td align="center" valign="middle" >DC, DC pulse, Symmetric AC pulse, Asymmetric AC pulse, High-voltage pulsed current (HVPC)</td><td align="center" valign="middle" >Faster healing rates</td><td align="center" valign="middle" >HVPC [<xref ref-type="bibr" rid="scirp.70774-ref28">28</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref33">33</xref>]</td></tr><tr><td align="center" valign="middle" >Stimulation electrode</td><td align="center" valign="middle" >Anode or cathode</td><td align="center" valign="middle" >Alternative healing pathways</td><td align="center" valign="middle" >Inconclusive</td></tr><tr><td align="center" valign="middle" >Stimulation parameters</td><td align="center" valign="middle" >50 - 100 μs double-peaked impulses 80 - 105 pulse per second frequency 50 - 200 V voltage 2 - 2.5 A peak-current amplitude</td><td align="center" valign="middle" >No optimization studies</td><td align="center" valign="middle" >Inconclusive</td></tr><tr><td align="center" valign="middle" >Treatment duration</td><td align="center" valign="middle" >45, 60, 120 minutes</td><td align="center" valign="middle" >Wound closure</td><td align="center" valign="middle" >60+ minutes [<xref ref-type="bibr" rid="scirp.70774-ref31">31</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> The variable equipment and techniques studied in low-level light therapy (LLLT)</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Radiant</th><th align="center" valign="middle"  colspan="3"  >In vitro and in vivo mouse and rat model results [<xref ref-type="bibr" rid="scirp.70774-ref3">3</xref>]</th></tr></thead><tr><td align="center" valign="middle" >Options</td><td align="center" valign="middle" >Notes</td><td align="center" valign="middle" >Selection</td></tr><tr><td align="center" valign="middle" >Device</td><td align="center" valign="middle" >Laser or light-emitting diode (LED)</td><td align="center" valign="middle" >Similar effects at similar settings</td><td align="center" valign="middle" >Either [<xref ref-type="bibr" rid="scirp.70774-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref36">36</xref>]</td></tr><tr><td align="center" valign="middle" >Wavelength</td><td align="center" valign="middle" >Blue, green, red, near infrared (456 - 1064 nm)</td><td align="center" valign="middle" >Wavelength-dependent tissue chromophores</td><td align="center" valign="middle" >Green [<xref ref-type="bibr" rid="scirp.70774-ref37">37</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" >Dose</td><td align="center" valign="middle" >0.09 - 90 J/cm<sup>2</sup></td><td align="center" valign="middle" >Dose-dependent activation and inhibitory effects</td><td align="center" valign="middle" >Up to 5 J/cm<sup>2</sup> [<xref ref-type="bibr" rid="scirp.70774-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.70774-ref42">42</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref46">46</xref>]</td></tr><tr><td align="center" valign="middle" >Treatment duration</td><td align="center" valign="middle" >1 - 2, 5 - 10, 60 - 120 minutes</td><td align="center" valign="middle" >Varying irradiance, constant energy density</td><td align="center" valign="middle" >10 minutes or less [<xref ref-type="bibr" rid="scirp.70774-ref47">47</xref>]</td></tr></tbody></table></table-wrap><p>light, in decreasing wound size [<xref ref-type="bibr" rid="scirp.70774-ref40">40</xref>] or increasing healing rate [<xref ref-type="bibr" rid="scirp.70774-ref41">41</xref>]. Dose values up to 5 J/cm<sup>2</sup> produced the most significant biological effects [<xref ref-type="bibr" rid="scirp.70774-ref6">6</xref>]. In particular, doses of 4 J/cm<sup>2</sup> are more effective than 8 J/cm<sup>2</sup> [<xref ref-type="bibr" rid="scirp.70774-ref42">42</xref>], while doses of 10 and 16 J/cm<sup>2</sup> promoted inhibitory effects [<xref ref-type="bibr" rid="scirp.70774-ref43">43</xref>]-[<xref ref-type="bibr" rid="scirp.70774-ref46">46</xref>]. Finally, variance in output power and exposure time can be modulated to achieve a specified energy density and as a result influence outcomes [<xref ref-type="bibr" rid="scirp.70774-ref47">47</xref>].</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>The influence of varying negative pressure and strain on tissue perfusion outcomes has been well explored in animal models. Data collected to date suggest the use of wound filler may promote tissue growth. Application of lower NP magnitudes achieved results similar to those at higher NPs; however, a NP waveform regimen has not been optimized. Interestingly, the use of wound filler in NPWT may be associated with promotion of tissue growth. Therefore, more understanding of the physical effect of foam and negative pressure on the internal tissue and vessel pressures, as well as at the cellular level would help in tailoring wound healing needs, in particular, through the modulation of tissue growth and perfusion.</p><p>With an appropriately selected electrode configuration and waveform type, application of electrical energy resembles the endogenous skin current. Thus, HPVC has emerged as the leading ES type for healing in human pressure ulcers. However, the lack of methodological studies on the input parameters of HVPC indicates an opportunity for further development. Ongoing debates in this field involve the selection of the anode or cathode electrode for activation, where effects broadly diverge between immune or remodeling healing pathways [<xref ref-type="bibr" rid="scirp.70774-ref48">48</xref>].</p><p>In LLLT the use of both laser and LED promote healing and the primary photo-tissue reactions of wavelength-specific light absorption by skin chromophores are well studied. Yet, the exact biological mechanisms resulting in enhanced proliferation are still only partly understood. Interestingly, although red light has almost exclusively been used in human applications, studies using blue, green, and red wavelengths have more consistently resulted in biological effects with green light.</p><p>More recent methodological studies, which have not yet been reviewed in the literature, will be more extensively searched and reviewed in the future. While there is an abundance of literature analyzing the effect of each of the above treatment modalities, through 2012, a combination of biophysical modalities for wound healing was not studied. Specification of such a device should include consideration of the results of these comparative modes, devices, and parameters. Perhaps due to the particular advantages of each biophysical modality―tissue perfusion and edema reduction, immune and cellular stimulation, and reactivation of healing processes―a wisely selected combination of modalities may hold great potential for a significant improvement in the treatment of chronic wounds. Finally, unified reporting of methodological inputs, specifically as biophysical energies, dosages, and treatment durations would greatly contribute to the development of a wound model for control and modulation of wound healing outcomes, as well as a system for studying fundamental biophysical-tissue interactions.</p></sec><sec id="s5"><title>5. Conclusions</title><p>Mechanical, electrical, and radiant biophysical energies have been used to successfully re-activate wound healing pathways. Variations in their input parameters produce variations in cellular responses, which can be modulated and possibly combined to achieve wound-specific healing outcomes. Further methodological studies with a systems approach would help define treatment protocols and facilitate the adoption of biophysical wound healing treatments into clinical practice for improved wound healing outcomes.</p></sec><sec id="s6"><title>Cite this paper</title><p>Parente, J.D., M&#252;ller, M. and M&#246;ller, K. (2016) Methodologies of Biophysical Wound Healing Therapies. J. Biomedical Science and Engineering, 9, 171-179. http://dx.doi.org/10.4236/jbise.2016.910B022</p></sec></body><back><ref-list><title>References</title><ref id="scirp.70774-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Heyer, K., et al. 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