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T. Koller
2. In the inammatory and proliferation phase, the cortical mapping of the primary wound area receives hardly any signals in patients with deep dermal defects. The cortical arrangement of the primary wound area is therefore dependent on indirect information from the secondary wound area. This results in a more difcult differentiated perception with an additional slowed motor and/or ver­bal protective response. These two disadvan­tages present therapists with a major challenge.
Thus, pain statements from patients with deep dermal defects are not sufcient to ensure an ade­quate dosage of the therapeutic intervention. Based on tissue and pain physiology as well as the phases of wound healing, an appropriate functional stimulus can be set using the tactile diagnosis of the rst and second connective tis­sue resistance. This has been empirically well proven [1, 5, 6, 10, 11].
It is the task of the therapist to discuss this pain processing problem in detail with the patient to develop a strategy together. Fear of pain can cause patients to avoid movement. However, it is important that they are again able to distinguish “pulling” (Aδ-ber) from “hurt­ing” (C-ber).
Caution!
• Subjective pain statements by the patient should never be the only criterion for the adequate dosage of therapeutic inter­ventions for deep dermal defects or hypertrophic scars.
• In addition to the high pain medication in the acute phase and different (emo­tionally colored) pain perception, the direct or indirect pain conduction is altered.
• Therefore, objective indicators are required, for example the rst and sec­ond increases in connective tissue resistance.
Connective Tissue Resistance (R1 andR2)
Basically, it is important to distinguish between the quantity and quality of movement. The quan­tity of movement is the physically objectively measurable extent of movement. In contrast, the quality of movement includes the ow, dynamics as well as rhythm, and harmony of movement. These are qualities that are subjectively palpable during movement. To be able to assess the quan­tity and quality of a movement correctly, the ther­apist rst needs theoretical knowledge: What quantity and quality can be expected of a joint or tissue in an uninjured state? In addition, however, extensive practical experience and tactile skills are also required.
As a rule, a healthy joint or tissue always behaves in the same way: within its range of motion, it has a smaller or larger “neutral zone.” At the end of the range of motion there is a “physiological space,” followed by a “paraphysi­ological space” (Fig.2).
The “neutral zone” is usually located in the middle of the range of motion and is character­ized by a very small increase in resistance (R1 at the end of “neutral zone”). The “physiological space” begins with the second signicant resis­tance of the connective tissue (R2). The thera­pist passively mobilizes the tissue to a greater or lesser extent in this area—depending on the intensity of the manual gradation (dosage) and the currently prevailing wound-healing phase. The “paraphysiological space” can only be reached by an impulse mobilization (manipula­tion). Post-traumatically or postoperatively the anatomical barrier has moved forward. The rea­son for this is collagen type III, which predomi­nates in the proliferation phase. It is responsible for the integrity of the injured structure and causes the rapid formation of water-soluble crosslinks. Temporary collagen type III does not withstand mechanical shear and acceleration forces very well. Overdosage is therefore quickly possible, especially in the proliferation phase. Microtraumatic injuries trigger new inammatory phases, which can lead to
Range of movement
Neutral point
al
Anatomical
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Activemovementlimit
resistance
neutral zone
R1
Fig. 2 Behavior of resistance depending on the extent of movement in joints and connective tissue. R1 represents the rst and R2 represents the second signicant increase in connective tissue resistance. Depending on the intensity of the manual gradation (dosage), therapists treat passively more or less into the physiological space. The paraphysio­logical space is only achieved by impulse mobilization. If the anatomical barrier is exceeded, cell damage occurs
Barrier (potential cell damage)
Paraphysiologic
space
R2
(manipulation)
Physiological
space
(mobilisation)
(lesion) which results in an inammatory reaction. This ana­tomical barrier is important in posttraumatic and postopera­tive conditions due to adhesions and water-soluble crosslinks that are moved to the front. Especially in the proliferation phase, this can quickly lead to overdosing. Microtraumatic injuries trigger new inammatory phases, which result in increased tissue and movement restriction [12] (Courtesy of Own illustration)
increased tissue restriction, and thus restricting movement.
Clinical Tip
• In comparison to healthy skin, the rst marked increase in connective tissue resistance usually occurs much faster around a spontaneously healed scar or in an area with surgical coverage.
• The distance between the rst and sec­ond marked increase in connective tissue resistance is also usually considerably shorter than in healthy skin.
• The second marked increase in connec­tive tissue resistance feels hard, stiff, and wooden. The aim is to use therapeu­tic measures to gradually extend the dis­tance between the rst and second marked increase in connective tissue resistance and thus restore the function of the connective tissue.
Mechanical Stimulation
Mechanotransduction
It is known from the literature that the absence of mechanical stimulus is associated with a loss of functional alignment of the bers. It has also been shown that too much mechanical stress quickly leads to an overdosing (cell damage, renewed inammatory reaction) [1, 4,
5, 13, 14].
The transmission of mechanical stimuli in the body, for example, by manual techniques, seems to take place in two signaling pathways. Empirically, a “release” in the tissue can often be perceived after only a few minutes. The mechani­cal stimulus must, therefore, have an effect directly on the tissue, for example, the release of possible pathological crosslinks (water-soluble type) or reactive tonus changes in the connective tissue. The second signaling pathway has been scientically researched under the term “mecha­notransduction.” This is the reaction inside the cell to a mechanically applied external stimulus.
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If the stimulus is adequate, the cell reacts with a gene transcription and thus inuences the cyto­skeleton and the ECM and thus the quality of the affected cell [7, 13, 1519]. The aim of the thera­peutically applied manual techniques is therefore not (as previously assumed) to lengthen collagen bers by stretching but to directly inuence cell biological processes by means of adequate stimulation.
What dosage is adequate during the wound­healing phases in relation to functional stimula­tion at the cellular level? Various aspects are described below:
Bouffard etal. (2008) observed a decrease in TGF-beta 1 concentration and collagen synthesis after tissue injury by 20–30% static tissue stretch­ing for 10min daily [15].
TGF-beta 1 is a local cytokine that is associ­ated with wound healing and tissue brosis. The results of this study suggest that tissue stretching during wound healing leads to a reduction in TGF-beta 1 levels and thus to altered collagen synthesis. This could be an important natural mechanism in limiting excessive scarring [3].
Balestrini and Biliar (2009) were able to demonstrate a positive effect on the extensibil­ity of the extracellular matrix with daily 5% tis­sue stretching for 24h. The authors found that a stretching stimulus that was too strong and lasted too long led to increased collagen syn­thesis and thus to increased tissue restriction. This could only be achieved therapeutically with the help of a splint and well-dosed stimu­lation [13].
In a review, Andalib etal. (2016) summarized selected studies on mechanotransduction. They also addressed the question of mechanical forces acting on cells. These are given in the former force unit “Dyne” (replaced by the SI unit “Newton” [N] since 1978). The converted data shows that all cells were mechanically stimulated with a force between 0.00002N and 0.00058N.In all included studies, a mechanotransduction effect was found [16]. These ndings indicate that cells are highly mechanosensitive. Only min­imal forces are required for a cell to respond to a mechanical stimulus.
The mechanotransduction process is shown schematically in Fig.3. The mechanosensors are stimulated by an external mechanical stimulus (here using the example of a broblast). These in turn activate “adapter proteins,” which are located on the cell nucleus membrane (nuclear mem­brane). These “adapter proteins” transmit the mechanical stimulus to the cytoskeleton. In this way, they stimulate the skeletal structure. The cell reacts with a gene transcription and passes on correspondingly altered (adapted) processes and products to the extracellular matrix. Thus, a cell response to an external mechanical stimulus takes place [8, 15].
The cytoskeleton of every cell is normally under physiological tension. This tension is in balance with the texture of the ECM and the functional mechanical stimuli in daily life.
In the case of pathological scarring, however, this physiological tension of the cytoskeleton is already increased. This leads to higher sensitivity to mechanical stimuli. Due to the increased col­lagen deposits and myobroblast activity, the ECM has a higher tension and stiffness than physiological skin (tissue). This imbalance is responsible for the fact that mechanical stimuli occurring in daily life can already be perceived as overload at the cellular level and lead to an over­reaction in the cell. This can end in a pathological brosis process.
Important to Know
• In manual scar therapy, the dosage approach should be selected in such a way that a physiological balance can be restored regarding intra- and extracellu­lar mechanical tension.
Unfortunately, the facts explained so far do not allow a clear conclusion regarding the correct dosage. However, by putting the individual pieces of the puzzle together, it is possible to approach the area of adequate and functional dosage.
It can be assumed that there is a signicant difference between the application of a high and
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1
Mechanical stimulus
2
3
Fig. 3 Schematically depicted mechanotransduction pro­cess of the reaction of a broblast cell to an external mechanical stimulus [7, 13, 1519] (Courtesy of T.Koller). (1) A mechanical stimulus is applied by a phys­iological movement or manual input by hand. (2) Mechanosensors on the cell membrane register the uid displacement and transmit this signal into the cell. (3) The
5
Gene
Transcription
4
mechanosensors activate “adapter proteins” which trans­mit the mechanical stimulus to the cytoskeleton. (4) The cell reacts with a gene transcription and passes on corre­spondingly altered (adapted) products to the extracellular matrix. (5) Newly functionally aligned collagen networks after an injury or through “new use” due to a new activity
a low dosage. This consideration refers to the active phase of a scar and it is not yet mature state. Therefore, amplitude, duration, and fre­quency are important parameters that should be considered in connection with the wound-healing phases [15].
Amplitude
Amplitude is dened as the largest excursion of an oscillation or a pendulum from the center position or as the oscillation range. If the mechan­ical stimulus (the amplitude) is too strong, the reaction of the cell nucleus becomes much less controllable. This can quickly lead to an overre­action of the cell. Due to the persistent inamma­tory state, the cell is more sensitive. This leads to the hypothesis that stimuli that are harmless to the physiological skin may already represent an overdose in scars [20].
Since mechanotransductive cell responses are initiated by minimal forces (up to 0.00058 N), functional alignment is already achieved with very gentle manual therapeutic interventions. In the back region, the empirically known marked increases in connective tissue resistance R1 and R2 are 1–2N for R1 and 2–4N for R2 [10, 11]. Thus, it can be assumed that manual interven­tions in the area of R1 probably already provide a sufciently adequate stimulus for the scar tissue to induce a mechanotransductive response of the cell and thus a functional alignment of the extra­cellular matrix.
In the proliferation phase, R1 appears to be an important indication for a wound-healing­adapted dosage. In the remodulation phase, a dosage up to R2 is acceptable.
Several years of clinical experience with severely burned patients show that in the prolif-
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eration phase manual scar techniques should only be used until the rst increase in connective tis­sue resistance is reached. This is because the tis­sue is signicantly less resilient than comparable connective tissue in the same wound-healing phase [5]. Due to the delayed wound healing, burn scars often have a considerably prolonged proliferation phase. As a result, the transition from R1 to R2 is empirically experienced as smooth (Fig.4).
In the case of linear (surgical) scars, the clini­cal situation is more stable. There is no mechani­cal overdosage if the dosage is increased up to the second connective tissue resistance in the prolif­eration phase and if it is increased into the second connective tissue resistance in the remodulation phase (Fig.5).
Koller (2018, 2019) conducted a pilot study on interrater reliability to determine R1 and R2.
Stretching tissue / scar
The results were promising. Therapists appear to be able to detect the rst signicant increase in connective tissue resistance with moderate (ICC2=0.67) and the second signicant increase in connective tissue resistance with good interra­ter reliability (ICC2 = 0.80). Regarding direct and indirect pain conduction, it can be assumed that C-ber activity progressively sets in with the second marked increase in connective tissue resistance (R2) and that until R2 mainly the Aδ bers are active as a “warning signal” of cell damage [10, 11].
Frequency
The frequency describes how fast repetitions within a periodic process follow each other per second. The unit of frequency is Hertz (Hz).
Balestrini and Biliar (2006) found that a cycli-
cal stretch stimulus with 0.2 Hz and moderate
Fig. 4 Summarizing presentation of wound-healing­phase-adapted and tissue-specic dosages in the manual therapy of burn scars (Courtesy of Own presentation). (1) In the proliferation phase, around the rst signicant increase in connective tissue resistance (amplitude). (2) In the remodulation phase, progressing up to the second
2-58 Dynes corresponds to
0.00002-
0.00058N
Dosage during
the proliferation
phase
Tissue specific
(collagen type III)
n
3
Dosage during the
remodeling phase (tissue-
specific) and later
(collagen type I)
1
1.CTR* (R1)
*Connective tissue
resistance increase (CTR)
Stretching tissue / scar
2
Paraphysio-
logical
2.CTR*
(R2)
remarkable increase in connective tissue resistance (amplitude). (3) R1 and R2 are exemplary. Connective tis­sue displaceability in the back is within a range of 1–4N [11] (much higher than the broblast needs for mechano­transductive cell response)
potential cell damage
space
mechanotransduction
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Stretching tissue/ scar
Dosage during the proliferation phase
Tissue specific (collagen
*Connective tissue
resistance increase (CTR)
2-58 Dynes corresponds to
0.00002-
0.00058N
1.CTR* (R1)
3
Stretching tissue / scar
Fig. 5 Summarizing presentation of wound-healing phase adapted and tissue-specic dosages in manual ther­apy of injured tissue (post-traumatic/postoperative) (Courtesy of Own presentation). (1) In the proliferation phase, progressing up to the second remarkable increase in connective tissue resistance (amplitude). (2) In the
Dosage during the
remodeling phase (tissue-
specific) and later
2
1
type III)
Paraphysio-
logical
2.CTR*
(R2)
remodulation phase, into the second remarkable increase in connective tissue resistance (amplitude). (3) R1 and R2 are exemplary. Connective tissue displaceability on the back is within a range of 1–4N [11] (much higher than the broblast needs for a mechanotransductive cell response)
potential cell damage
space
amplitude stimulates the broblasts to produce a more resistant matrix. The tissue density increases, and the bers are reorganized. Histologically, a signicant decrease in thickness was observed. After this stimulus, the tissue was thinner, denser, and better organized [14].
increase in collagenase production with cyclic stretching on broblasts compared to static stretching [21].
a slight stretching, tailored to the respective wound-healing phase with intermittent oscilla­tion (0.2Hz) at the end of the respective ampli­tude. These assumptions correlate with empirical and clinical experience but have not yet been proven in human research.
Carano et al. (1996) demonstrated a 200%
Clinically recommendable would therefore be
Duration
How long should a stimulus be applied? This is another fundamental question regarding dos­age. Although splints and other stretching techniques are widely used, there are no research results on humans available in the lit­erature. Only effects from animal studies can serve as a basis for clinical considerations and empirical experience.
Bouffard etal. were able to demonstrate good results (reduced TFG-beta 1) with daily 10min stretching and moderate amplitude (20% stretch­ing) [15]. However, practical experience shows that splint applications over several hours also produce positive effects.
Carano et al. (1996) conducted research on cell cultures of articial ligaments. They found
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that a ve-minute application time was most effective in terms of wound healing for a previ­ously placed lesion [21].
Empirically, good results are achieved with application times of 1min per location, three to ve times per therapy unit. Usually, one to two therapy units per day are realistic in the clinical setting.
Clinical Tip
• Recommended dosage for large-area and deep dermal scars:
– In the proliferation phase: around the
rst marked increase in connective tissue resistance (amplitude)
– In the remodulation phase: progres-
sively up to the second marked increase in connective tissue resis­tance (amplitude)
• Dosage recommendations for linear
scars:
– In the proliferation phase: up to the
second marked increase in connec­tive tissue resistance (amplitude)
– In the remodulation phase: progres-
sively into the second marked increase in connective tissue resis­tance (amplitude)
• Application duration: In general 1min per location, three to ve times per ther­apy unit in addition to an oscillating fre­quency of 0.2 Hz at the end of the respective amplitude
effective and purposeful in terms of regaining function:
– Manual scar therapy – Compression – Silicone – Splints – Tape (Kinesio®) – Vacuum massage – Scar care (with ointments)
Important to Know
In order to counteract pathological scar­ring, the following factors must always be considered:
• Avoid increase of blood ow
• Mechanical forces in adjusted dosage
• General tension reduction of the tissue
• Prevent overstrain from daily activities
Caution!
Sliding on the skin leads to increased shear forces and hyperemia. Excessive external mechanical forces can result in pathologi­cal wound healing [8]. The tension can be positively inuenced by manual tech­niques, compression and silicone, splints, tape, and vacuum massage. Behavior that is in line with wound healing is also essential for daily life.
Noninvasive Treatment Options
Scar maturation can have a negative effect on function. Physiological wound contracture leads to increased tension in the tissue and mobility decreases. Therapists try to counteract these neg­ative effects as much as possible to achieve an optimal functional result. The following thera­peutic options are based on the mechanotrans­ductor mode of action. They are considered to be
Compression
In everyday clinical practice, textile compression therapy is standard for the prevention and treat­ment of hypertrophic scars. However, it has not yet been conclusively claried on which humoral, cellular, or mechanical processes the effect of compression therapy is based [22]. The results of the systematic review and meta-analysis of Ai
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etal. (2017) show that patients with hypertrophic scarring receiving compression therapy showed signicant improvements regarding redness, pig­mentation, thickness, and hardness of the scar. In addition, it is known that the application of pres­sure relieves itching and pain in active hypertro­phic scars [23]. Continuous pressure on an active scar causes numerous small vessels to close isch­emically. Ischemia leads to increased apoptosis of myobroblasts during scar maturation causing a reorganization of the extracellular matrix [3]. Compression-induced hypoxia shifts the colla­gen synthesis toward catabolism [24]. This may lead to the destruction of existing collagen bers and thus to a lower density of the scar structure. At the same time, the new stimulation (mechani­cal compression) allows a more functional re­synthesis of collagen. This results in a qualitatively better and functionally more resil­ient scar tissue [22].
Patients with deep second-degree and third­degree burns as well as with other scars prone to hypertrophy receive customized compression garments [25]. It is recommended to wear com­pression garments consistently day and night until the end of scar maturation to achieve the most aesthetic scar maturation possible with min­imal functional restrictions. A short interruption of the compression therapy is needed to change the compression garment, perform personal hygiene, and care for the scar [22].
The duration of the compression therapy depends on several factors:
are used. The terms “comfort” and “strong” refer to the product descriptions by this company.
Phase 1: Early Phase
Patients receive surgical interventions in the acute hospital. As a result, the wound volumes often uctuate greatly and sometimes the wound areas are still oozing.
Expensive custom-made compression prod­ucts would not be appropriate in this phase. With tubular bandages (e.g., Eesiban®) and self­adhesive dressings (e.g., CobanTM®), however, a transition from classic wound dressing to com­pression (10–14mmHg) can take place early in the healing process. At the same time, early com­pression can be supplemented by ready-to-wear products. This also improves treatment adherence.
Phase 2: Customized Compression (“Comfort”; Viscose/Elastane)
In this phase, wound healing is largely com­pleted. Patients with extensive wounds are usu­ally transferred to a rehabilitation clinic. People with minor injuries usually receive outpatient follow-up treatment. Now the compression treat­ment begins with custom-made, soft, comfort­able material of compression class II.
Depending on wound healing, a gradual start is also possible. In areas with wounds that are still oozing, materials from the early phase are still used. The custom-made products are used in healed regions.
– Severity of scars (depth of burn) – Localization and extension of scars – Individually different healing reactions – Acceptance to therapy, patience of the patient
and relatives
Empirical values show a period of at least
8–24months [22].
The following literature-based “three-phase model” of compression has established itself in recent years at the University Hospital Zurich and the Bellikon Rehabilitation Clinic. Flat- knitted products of the Swiss company TTK
Phase 3: Customized Compression (“Strong”; Polyamide/Elastane)
Once wound healing is complete, the scar tissue becomes more resilient and pressure sensitivity decreases. The patient is active again and largely independent in daily life. A further individual treatment with more robust material should be aimed for.
They are then more able to tolerate the com­pression 23h/24h. This is a decisive factor for the success of compression therapy [26]. Physiologically healed scars do not necessarily require compression. If patients are involved in
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therapy decisions, this improves their adherence. If, in addition to the scar problem, lymphatic insufciency exists, a treatment with compres­sion class III products should be considered.
Custom-made articles should be made of materials that are comfortable to wear and have good haptics. Compression materials that are hard, stiff, or even scratchy are not very well accepted.
Experience shows that compression garments should meet the following requirements [22]:
– Exact reproduction of the skin prole without
incisive wrinkling (risk of pressure points)
– Uniform compression with the least possible
functional interference
– Few, at, and exible seams – Seams should not be directly on the joints – Good skin tolerance – Durable, breathable, and easy to clean.
Colored material can promote acceptance. However, it should be noted that colored materi­als often have a harder feel due to the higher pig­mentation of the material.
The various compression classes (RAL stan­dard) have the following pressure characteristics [27]:
methods of scar treatment, although so far there is only weak evidence for this form of therapy to treat existing scars or for prophylaxis. The effect is based on increased hydration of the scar tissue, caused by silicone gel as a water-impermeable membrane. This mode of action corresponds to an occlusion. In addition, this probably leads to reduced blood circulation or angiogenesis and thus to reduced collagen synthesis [28].
Silicone offers a decisive advantage, espe­cially in burn scars: it reduces the mechanical shearing forces in relation to the “external envi­ronment” and thus prevents direct friction on the scar surface. However, there is still no denitive evidence of this.
When should silicone be used in scar therapy? The following methods of application have proven themselves in practice:
Silicone patches:
– In case of excessive mechanical tension on the
tissue or scar surface
– In case of hypertrophy and excessive keloid
formation
– In case of severe itching (mainly because of
the hydration properties)
Customized silicone pads:
– Compression class I: moderate compression
(18.0–21.0mmHg)
– Compression class II: medium compression
(23.0–32.0mmHg)
– Compression class III: strong compression
(34.0–46.0mmHg)
The unit of measurement [mmHg; millimeters of mercury] is used to specify the static pressure. Measuring instruments for compression therapy are offered by TT Meditrade (Denmark), for example, Kikuhime®.
Silicone
Since 1981, silicone has been used in the treat­ment of deep dermal defects and hypertrophic scars. Today, it is one of the most common
– In case of undercuts (recesses/indentations in
the tissue) – In case of anatomically complex shapes – In case of extensive depressions and
unevenness
Silicone in the facial area:
– Always in combination with hard shell masks
or partial masks. – Silicone gel is used for small areas.
To clean or aerate the skin/scar and the sili-
cone pad, daily application breaks of no more than 1h must be adhered to. The silicone gel is applied twice a day to the lesions being treated.
The advantage of this therapy option is its
ease of application. Only rarely do side effects such as folliculitis, erosion, or itching occur.
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Silicone gel is often used in combination with other procedures or in postoperative scar pro­phylaxis. Compared to silicone gel patches, it has the additional advantage that it can also be used on highly visible body parts and over joints. The gel can also be used to apply sun protection products or cosmetics. The side effect of macer­ation, which is often observed when the patches are worn for a longer period, can also be avoided with silicone gel. Silicone of any kind must not be used on open wounds. Experience has shown that failure to observe daily hygiene measures (during the break in application) can lead to skin irritation.
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Fig. 6 Tape for mechanical relief of a scar (Figure: Rehabilitation Clinic Bellikon)
Splints
A great advantage of specic, custom-made splints is the duration of application. Splint appli­cations (several times a day in addition to the therapy) make it possible to set a functionally adequate stimulus. Optimal tting of a splint is often a major challenge at the beginning of reha­bilitation and is resource intensive. Due to vol­ume uctuations resulting from different application techniques of the bandages, potential pressure points are a constant risk, which is why splints must be checked and adjusted regularly. Splints are ideal for the hand, wrists, elbow, ankle, and mouth. The dosage (wearing time, angle, and extent of movement for dynamic splints) must be adapted to the respective wound­healing phase (see Figs.4 and 5).
Tape
A standard kinesiotape® can be used to relieve scars, wounds, or areas that are subject to exces­sive mechanical tension. This requires the possi­bility to apply the tape on physiological skin or already very stable scarred skin. For sensitive skin, skin protection or removal sprays are recommended.
The length of the tape should correspond to the area to be relieved. The therapist cuts the tape lengthwise, and in the middle, xes the rst
“anchor” on the tissue and xes the two branches of the tape “surrounding the scar” (Fig.6). There should be as much scar tissue as possible between the two legs of the tape. This leads to a visible and noticeable mechanical stress relief.
The tape may remain on the skin for a maxi­mum of 5days. Further application should only take place after a day’s rest. In patients with burn scars, a wearing period of 3 days seems to be optimal [29].
Vacuum Massage
Vacuum massage is a noninvasive mechanical massage technique invented to treat burns and scars. To date, no effects of vacuum massage on thickness and density of human scar tissue have been reported. In the skin endothelial cells, bro­blasts and myobroblasts embedded in the ECM sense mechanical stimuli (created by vacuum massage) and may promote intracellular pro­cesses leading to matrix remodeling. Preliminary results show that the disruption of the epidermis may indicate that vacuum massage could be able to actually breach the skin barrier. The statisti­cally signicant changes in the dermal layers could suggest an increased ECM production after vacuum massage [30]. The use of vacuum mas­sage is recommended toward the end of the remodulation phase or outside the classic wound­healing phases.