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Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 675
INTRODUCTION
Wound has been a formidable foe for healers since
antiquity. The general principles of wound management,
entailing debridement and repeated dressings have
been established since ancient times. The key objective
of wound management is to achieve early complete
healing. Delay in healing predisposes to infection and
poses protracted morbidity. Direct closure of wound is
the most efficient way of achieving healing, however,
only clean wounds without much tissue loss are
amenable to it e.g. clean surgical wounds. In complex
wounds with tissue loss, healing can be promoted
by secondary intention or reconstruction with grafts
and flaps.1-3
VAC therapy has been reported very useful in the
treatment of both acute and chronic wounds. In 1993
Fleischmann et al. from Germany were the first to report
successful use of this technique in 15 patients with open
fractures.4 Argenta et al. from the US in 1997 pioneered
further clinical research that lead to popularity of VAC
therapy across a range of specialties.5
Since VAC therapy is a relatively novel addition to the
wound care armamentarium, its exact mechanism of
action still continues to be researched. It has been
shown to increase wound blood flow, granulation tissue
formation, and decreases edema fluid and bacteria at
the wounded site.5,6
The present study was undertaken to evaluate the effect
of VAC therapy on wound management outcomes in
patients undergoing reconstruction with STSG.
METHODOLOGY
The study was carried out at the Department of Plastic
Surgery, PIMS, Islamabad, from October 2007 to
December 2009. It included a total of 100 adult patients
of either gender aged over 13 years, having different
ABSTRACT
Objective: To evaluate the effect of vacuum-assisted closure (VAC) therapy on wound management by measuring the graft
take, wound healing time, need for any re-grafting and duration of hospitalization.
Study Design: Single blinded randomized controlled trial.
Place and Duration of Study: This study was carried out in the Department of Plastic and Reconstructive Surgery,
Pakistan Institute of Medical Sciences (PIMS), Islamabad, from October 2007 to December 2009.
Methodology: A total of 100 adult patients of either gender with acute traumatic wounds were included. Patients who
needed flap coverage as the primary intervention, and those with Diabetes, malignancy, bleeding diathesis were excluded.
Half of the patients were randomly assigned to the intervention group and the rest to the control group with lottery method.
All wounds were initially subjected to thorough excision. Wound bed preparation for STSG (split thickness skin graft) was
achieved using 10 days pre-treatment with VAC dressings in the intervention group while employing normal saline gauzes
in the control group. All patients were subsequently treated with STSG. The primary outcome measure was graft take while
the secondary outcome measures included wound healing time, need for any re-grafting and duration of hospital stay.
Results were compared in both groups using chi-square test.
Results: Marked differences were found in favour of the VAC therapy group with respect to the various wound
management outcome measures studied. i.e. graft take (greater than 95% graft take in 90% of VAC therapy group vs. 18%
of controls), wound healing time (2 weeks postgrafting in 90% of VAC therapy group vs. 18% of controls), need for re-
grafting (none among VAC therapy group vs. 8% of controls) and duration of hospital stay (less than 3 weeks in 90% of
VAC therapy group vs. 18% of controls).
Conclusion: VAC therapy should be employed in the pre-treatment of wounds planned to be reconstructed with STSG,
since it has marked advantages in the wound bed preparation compared with the traditional normal saline gauze
dressings.
Key words: Open wound. Wound bed preparation. Vacuum assisted closure therapy. Vacuum-assisted closure dressing.
Split thickness skin graft. Graft take.
Department of Plastic Surgery, Pakistan Institute of Medical
Sciences (PIMS), Islamabad.
Correspondence: Dr. Muhammad Saaiq, Room No. 20, MOs
Hostel, Pakistan Institute of Medical Sciences (PIMS),
Islamabad.
E-mail: muhammadsaaiq5@gmail.com
Received January 08, 2010; accepted August 11, 2010.
Vacuum-Assisted Closure Therapy as A Pretreatment For Split
Thickness Skin Grafts
Muhammad Saaiq, Hameed-ud-Din, Muhammad Ibrahim Khan and Saud Majid Chaudhery
ORIGINAL ARTICLE
acute traumatic wounds (of a duration of up to 06
weeks) measuring ≥ 9 cm2 surface area. Patients who
needed flap coverage as the primary intervention, and
those with either Diabetes, malignancy or bleeding
diathesis were excluded. Informed consent was taken
from all the patients for participation in the study and be
randomized to either intervention or control group
without being aware of it. Initial assessment and
diagnosis was made by history, physical examination
and necessary investigations.
Half of the patients were randomized to the intervention
group (those whose wounds were pre-treated with VAC
therapy before STSG) and half to the control group
(whose wounds were pre-treated with daily normal
saline gauze dressings before STSG). Simple random
sampling was done with lottery method. The two groups
were matched for age, gender, and wound
characteristics including size and site of the wound.
Initially all wounds were debrided with thorough surgical
excision of devitalized tissues, and tissue sent for
bacterial culture and sensitivity tests. Before proceeding
to STSG reconstruction, the wounds were optimized
with 10 days pre-treatment, using VAC dressings in the
intervention group (two VAC dressings each maintained
for 5 days) while employing daily normal saline gauze
dressings in the control group. This pre-treatment was
continued for 10 days when STSG reconstruction was
undertaken in all culture-negative patients.
For VAC dressing, two synthetic foam sheets were
fashioned to the size and shape of the wound and
applied to cover the wound with a Redivac suction drain
(with multiple side ports) sandwiched between the two
layers. A transparent sealing plastic membrane sheet
(OpsiteTM in small wounds and plastic food wrap for
large wounds) was then applied to the foam layers,
making the system water tight and air tight. Thus the
open wound was converted into a close controlled one.
The suction drain was connected to suction machine or
wall vacuum suction maintained at 50-120 mmHg
intermittently. At the end of 5 days, VAC dressing was
removed and a fresh VAC dressing applied after
washing the wound with normal saline and undertaking
wound debridement if needed. After 10 days of VAC
therapy, STSG reconstruction was undertaken in all
culture-negative patients.
All patients underwent reconstruction with intermediate
thickness STSG (0.012–0.015 inch). All skin grafts were
meshed 1.5:1 ratio. The skin grafts were applied on the
granulating wound bed and secured in place with
staples. Non adherent sofratulle gauzes were placed
onto the skin graft prior to the application of tie over and
absorbent dressings. The dressings were left in place
until 5th postoperative. During this time, the patients
were kept on bed rest to avoid any shearing forces on
the grafted wounds. On the 5th postoperative day, the
dressings were removed and wounds assessed by
gross inspection for graft take which was measured as
the percentage of the grafted surface area where graft
was taken by wound bed. The patients were stratified
into three groups with regard to graft take: good take
where ≥ 95% graft was taken, fair take where 80-95%
wound surface had taken graft and poor take where less
than < 80% wound surface had taken graft.
Following discharge, the wound dressings were changed
every 3rd day for 10 days. Wounds were examined on
14th postoperative day of grafting for evidence of
healing with stable skin coverage and/or need for re-
grafting. Figures 1 through 4 are representative pictures
of one of the VAC treated patients.
The data were analysed through SPSS version 10 and
various descriptive statistics were used to calculate
frequencies, percentages, means and standard deviation.
The numerical data such as age, wound size and
duration of hospital stay were expressed as mean ±
standard deviation while the categorical data such as
the site of wounds, causes of wounds, and organisms
cultured were expressed as frequency and percentages.
The percentages of various outcome variables were
compared by employing chi-square test and a p-value of
less than 0.05 was regarded as statistically significant.
RESULTS
Out of a total of 100 patients, 86% (n=86) were males.
The age ranged from 13-65 years, with a mean of 33.07
± 13.60 years. Majority of the patients were in their 3rd
and 4th decades of life.
Most frequent location of the wounds was lower limb
(n=56), followed by upper limb (n=24), trunk (n= 14), and
scalp (n=6). The causes of wounds included road traffic
accidents in 72%, machine injuries in 12%, falls in 6%,
676 Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679
Muhammad Saaiq, Hameed-ud-Din, Muhammad Ibrahim Khan and Saud Majid Chaudhery
Figure 1: Road traffic accident victim
with degloving injury right thigh.
Figure 2: VAC dressing in place after
radical debridement.
Figure 3: Wound rendered graftable
by two VAC dressings.
Figure 4: Good graft take on 5th
postoperative day.
firearm injuries in 4%, blast injuries in 4% and fire
crackers in 2%. Wound surface area ranged from 9 cm2
to 500 cm2. The overall mean wound surface area was
64. 58± 90.88 cm2.
The initial culture of the wounds sent at the first wound
debridement showed growth of organisms in 17
patients. The most commonly found organisms were
Staphylococcus aureus (n = 11), followed by coagulase
negative Staphylococcus (n = 2), Enterococcus faecalis (n = 2),
Pseudomonas aeruginosa (n = 1), and Escherichia coli (n = 1).
The repeat culture of these patients after 5 days
treatment with intravenous antibiotics were negative for
growth of organisms. The most frequently instituted
antibiotic was co-amoxiclave.
Greater than 95% graft take was seen in 45 (90%)
patients of the VAC group compared to only 9 (18 %) of
the control group. Table I shows the graft take as
percentage of the grafted surface area.
None of the patients in VAC group needed re-grafting,
however, 4 (8%) patients among the control group were
re-grafted for residual areas of graft failure. The
remaining patients with partial skin graft failure healed
successfully with repeated dressings, alginate dressings
and healing by secondary intention.
Duration of hospital stay was significantly shorter among
the VAC group patients (Table II). Table III depicts the
healing time observed among the patients of the two
groups.
The hospital stay was 18-35 days with a mean of 21.58
± 3.58 days. There was no in-hospital mortality.
DISCUSSION
In this study, as the inclusion criteria was open wounds
of traumatic origin, majority of the patients were young
males. Males are more frequently involved in outdoor
activities and hence more prone to sustain different
traumatic insults because of road traffic accidents, falls,
firearm injuries and blasts etc. Predominant involvement
of young males further amplifies the grave implications
of such disabling injuries. Male predominance and more
frequent involvement of younger population is well
documented in the context of trauma in general.7 With
increasing civil violence, there is an increasing number
of patients with blast injuries as well.
In this study the use of VAC therapy as pre-treatment for
skin grafts, favourably influenced the management of
open wounds. In the past, a number of adjuvant
therapies such as use of skin substitutes, growth factors
and hyperbaric oxygen etc. have been employed to
expedite wound healing. VAC therapy was found a better
alternative in this regard as it is more economical and
safer. The present findings are in conformity with those
of other published studies.8-10
In this study, VAC therapy was employed only in the
preparatory phase before skin grafting of the wounds.
Several published studies have successfully used VAC
dressings for securing skin grafts postoperatively,
especially in wounds with exudative, irregular, or mobile
recipient beds and in difficult anatomic locations. It has
been reported to stabilize the skin graft and conform it
well to the shape of recipient bed, remove edema fluid,
decrease bacterial counts, and provide a secured
dressing. All these factors further improve the graft
survival and reduce the need for repeat skin grafting.11-14
In this study healing time and hospital stay were
significantly reduced in the patients treated with VAC
therapy. Other published studies have also shown fast
healing with VAC therapy.15-17 A variety of factors have
been described to account for the accelerated healing.
VAC therapy continually decontaminates the wound and
drains the wound surface of exudates, which contain
large amounts of proteases. Those would normally
inhibit fibroblastic division, collagen production, and cell
growth. Fluid removal helps with localized edema that
otherwise causes an increase in interstitial pressure with
consequent occlusion of microvasculature and
lymphatics, decreased nutrient, and oxygen delivery.
Protein degradation enzyme is released with metabolic
waste accumulation and increased bacterial
colonization, which causes capillary damage and
hypoxia. VAC therapy also provides a moist environment
to promote granulation tissue formation and prevents
eschar formation, which allows for a smoother pathway
to re-epithelialize the wound surface. Angiogenesis is
stimulated, which improves tissue oxygenation and
tissue reconstruction. This enhanced angiogenesis
occurs even in patients with diabetic microangiopathy,
and promotes healing of distal lesions.18,19 Micro-
mechanical forces exerted on wound surface by low
Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 677
Vacuum-assisted closure therapy as a pretreatment for split thickness skin grafts
Table I: The take of split thichness skin graft among the patients
(n=50 each group).
S. No. Graft take % Number of patients Nnumber of patients p-value
(VAC group) (control group) (%)
1 ≥ 95% 45 (90%) 9 (18%) p < 0.001*
2 80-94% 4 (8%) 32 (64%) p < 0.001*
3 < 80% 1 (2 %) 9 (18%) 0.03*
* p-value significant = < 0.05.
Table II: The duration of hospital stay (n=50 each group).
S. No. Duration of Number of patients Number of patients p-value
hospital stay (VAC group) (control group) (%)
1 Upto 20 days 45 (90%) 9 (18%) p < 0.001*
2 21-28 days 5 (10%) 37 (74%) p < 0.001*
3 > 28 days - 4 (8%) 0.349 **
* p-value significant = < 0.05; ** = not significant.
Table III: Time to complete healing observed among the patients
(n=50 each group).
S. No Time to complete No. of patients No. of patients p-value
healing (VAC group) (control group) (%)
1 2 weeks postgrafting 45 (90%) 9 (18%) p < 0.001*
2 3-4 weeks postgrafting 3 (6%) 36 (72%) p < 0.001*
3 > 4 weeks postgrafting 2 (4 %) 5 (10%) 0.111 **
* p-value significant = < 0.05; ** = not significant.
pressure suction are also important. This mechanism
mimics the stretch-induced cell proliferation typically
operative in tissue expansion phenomenon seen else-
where in the body. 20,21
Owing to its low cost, VAC therapy can provide an
economical alternative to the other available costly local
wound management measures. Such economic
implications of wound management are particularly
important in the context of our poor patients. Cost
effectiveness has also been reported in terms of
shortened hospital stays, and decreased overall medical
cost in the published literature. 22,23
In this study VAC therapy was additionally found to be
more comfortable for patients as well as the surgical
staff. It obviated the need for daily dressing changes.
Similar findings have been reported by other studies as
well.22,23
This study has some limitations. It is a single centred
study. Blinding of the treating doctors was not possible
and so observer bias could not be eliminated
completely.
This study should prompt other local studies and hence
allow more meaningful comparison of results in our own
population. We recommend the conduct of a multicentre
local study to confirm and improve upon our results.
Additionally a local study may be conducted to compare
the cost of VAC therapy versus other wound preparatory
methods such as use of skin substitutes or growth
factors, and hence evolve an evidence base to confirm
VAC therapy as an economical alternative to the other
costly local wound management measures.
CONCLUSION
VAC therapy should be employed in the pre-treatment of
wounds planned to be reconstructed with STSG, given
its significant advantages in the wound bed preparation
compared with traditional normal saline gauze
dressings.
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discussion 933-4..
12. Weinfeld AB, Kelley P, Yuksel E, Tiwari P, Hsu P, Choo J, et al.
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678 Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679
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Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 679
Vacuum-assisted closure therapy as a pretreatment for split thickness skin grafts
G G G G G *G G G G G

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Vacuum-assisted closure therapy

  • 1. Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 675 INTRODUCTION Wound has been a formidable foe for healers since antiquity. The general principles of wound management, entailing debridement and repeated dressings have been established since ancient times. The key objective of wound management is to achieve early complete healing. Delay in healing predisposes to infection and poses protracted morbidity. Direct closure of wound is the most efficient way of achieving healing, however, only clean wounds without much tissue loss are amenable to it e.g. clean surgical wounds. In complex wounds with tissue loss, healing can be promoted by secondary intention or reconstruction with grafts and flaps.1-3 VAC therapy has been reported very useful in the treatment of both acute and chronic wounds. In 1993 Fleischmann et al. from Germany were the first to report successful use of this technique in 15 patients with open fractures.4 Argenta et al. from the US in 1997 pioneered further clinical research that lead to popularity of VAC therapy across a range of specialties.5 Since VAC therapy is a relatively novel addition to the wound care armamentarium, its exact mechanism of action still continues to be researched. It has been shown to increase wound blood flow, granulation tissue formation, and decreases edema fluid and bacteria at the wounded site.5,6 The present study was undertaken to evaluate the effect of VAC therapy on wound management outcomes in patients undergoing reconstruction with STSG. METHODOLOGY The study was carried out at the Department of Plastic Surgery, PIMS, Islamabad, from October 2007 to December 2009. It included a total of 100 adult patients of either gender aged over 13 years, having different ABSTRACT Objective: To evaluate the effect of vacuum-assisted closure (VAC) therapy on wound management by measuring the graft take, wound healing time, need for any re-grafting and duration of hospitalization. Study Design: Single blinded randomized controlled trial. Place and Duration of Study: This study was carried out in the Department of Plastic and Reconstructive Surgery, Pakistan Institute of Medical Sciences (PIMS), Islamabad, from October 2007 to December 2009. Methodology: A total of 100 adult patients of either gender with acute traumatic wounds were included. Patients who needed flap coverage as the primary intervention, and those with Diabetes, malignancy, bleeding diathesis were excluded. Half of the patients were randomly assigned to the intervention group and the rest to the control group with lottery method. All wounds were initially subjected to thorough excision. Wound bed preparation for STSG (split thickness skin graft) was achieved using 10 days pre-treatment with VAC dressings in the intervention group while employing normal saline gauzes in the control group. All patients were subsequently treated with STSG. The primary outcome measure was graft take while the secondary outcome measures included wound healing time, need for any re-grafting and duration of hospital stay. Results were compared in both groups using chi-square test. Results: Marked differences were found in favour of the VAC therapy group with respect to the various wound management outcome measures studied. i.e. graft take (greater than 95% graft take in 90% of VAC therapy group vs. 18% of controls), wound healing time (2 weeks postgrafting in 90% of VAC therapy group vs. 18% of controls), need for re- grafting (none among VAC therapy group vs. 8% of controls) and duration of hospital stay (less than 3 weeks in 90% of VAC therapy group vs. 18% of controls). Conclusion: VAC therapy should be employed in the pre-treatment of wounds planned to be reconstructed with STSG, since it has marked advantages in the wound bed preparation compared with the traditional normal saline gauze dressings. Key words: Open wound. Wound bed preparation. Vacuum assisted closure therapy. Vacuum-assisted closure dressing. Split thickness skin graft. Graft take. Department of Plastic Surgery, Pakistan Institute of Medical Sciences (PIMS), Islamabad. Correspondence: Dr. Muhammad Saaiq, Room No. 20, MOs Hostel, Pakistan Institute of Medical Sciences (PIMS), Islamabad. E-mail: muhammadsaaiq5@gmail.com Received January 08, 2010; accepted August 11, 2010. Vacuum-Assisted Closure Therapy as A Pretreatment For Split Thickness Skin Grafts Muhammad Saaiq, Hameed-ud-Din, Muhammad Ibrahim Khan and Saud Majid Chaudhery ORIGINAL ARTICLE
  • 2. acute traumatic wounds (of a duration of up to 06 weeks) measuring ≥ 9 cm2 surface area. Patients who needed flap coverage as the primary intervention, and those with either Diabetes, malignancy or bleeding diathesis were excluded. Informed consent was taken from all the patients for participation in the study and be randomized to either intervention or control group without being aware of it. Initial assessment and diagnosis was made by history, physical examination and necessary investigations. Half of the patients were randomized to the intervention group (those whose wounds were pre-treated with VAC therapy before STSG) and half to the control group (whose wounds were pre-treated with daily normal saline gauze dressings before STSG). Simple random sampling was done with lottery method. The two groups were matched for age, gender, and wound characteristics including size and site of the wound. Initially all wounds were debrided with thorough surgical excision of devitalized tissues, and tissue sent for bacterial culture and sensitivity tests. Before proceeding to STSG reconstruction, the wounds were optimized with 10 days pre-treatment, using VAC dressings in the intervention group (two VAC dressings each maintained for 5 days) while employing daily normal saline gauze dressings in the control group. This pre-treatment was continued for 10 days when STSG reconstruction was undertaken in all culture-negative patients. For VAC dressing, two synthetic foam sheets were fashioned to the size and shape of the wound and applied to cover the wound with a Redivac suction drain (with multiple side ports) sandwiched between the two layers. A transparent sealing plastic membrane sheet (OpsiteTM in small wounds and plastic food wrap for large wounds) was then applied to the foam layers, making the system water tight and air tight. Thus the open wound was converted into a close controlled one. The suction drain was connected to suction machine or wall vacuum suction maintained at 50-120 mmHg intermittently. At the end of 5 days, VAC dressing was removed and a fresh VAC dressing applied after washing the wound with normal saline and undertaking wound debridement if needed. After 10 days of VAC therapy, STSG reconstruction was undertaken in all culture-negative patients. All patients underwent reconstruction with intermediate thickness STSG (0.012–0.015 inch). All skin grafts were meshed 1.5:1 ratio. The skin grafts were applied on the granulating wound bed and secured in place with staples. Non adherent sofratulle gauzes were placed onto the skin graft prior to the application of tie over and absorbent dressings. The dressings were left in place until 5th postoperative. During this time, the patients were kept on bed rest to avoid any shearing forces on the grafted wounds. On the 5th postoperative day, the dressings were removed and wounds assessed by gross inspection for graft take which was measured as the percentage of the grafted surface area where graft was taken by wound bed. The patients were stratified into three groups with regard to graft take: good take where ≥ 95% graft was taken, fair take where 80-95% wound surface had taken graft and poor take where less than < 80% wound surface had taken graft. Following discharge, the wound dressings were changed every 3rd day for 10 days. Wounds were examined on 14th postoperative day of grafting for evidence of healing with stable skin coverage and/or need for re- grafting. Figures 1 through 4 are representative pictures of one of the VAC treated patients. The data were analysed through SPSS version 10 and various descriptive statistics were used to calculate frequencies, percentages, means and standard deviation. The numerical data such as age, wound size and duration of hospital stay were expressed as mean ± standard deviation while the categorical data such as the site of wounds, causes of wounds, and organisms cultured were expressed as frequency and percentages. The percentages of various outcome variables were compared by employing chi-square test and a p-value of less than 0.05 was regarded as statistically significant. RESULTS Out of a total of 100 patients, 86% (n=86) were males. The age ranged from 13-65 years, with a mean of 33.07 ± 13.60 years. Majority of the patients were in their 3rd and 4th decades of life. Most frequent location of the wounds was lower limb (n=56), followed by upper limb (n=24), trunk (n= 14), and scalp (n=6). The causes of wounds included road traffic accidents in 72%, machine injuries in 12%, falls in 6%, 676 Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 Muhammad Saaiq, Hameed-ud-Din, Muhammad Ibrahim Khan and Saud Majid Chaudhery Figure 1: Road traffic accident victim with degloving injury right thigh. Figure 2: VAC dressing in place after radical debridement. Figure 3: Wound rendered graftable by two VAC dressings. Figure 4: Good graft take on 5th postoperative day.
  • 3. firearm injuries in 4%, blast injuries in 4% and fire crackers in 2%. Wound surface area ranged from 9 cm2 to 500 cm2. The overall mean wound surface area was 64. 58± 90.88 cm2. The initial culture of the wounds sent at the first wound debridement showed growth of organisms in 17 patients. The most commonly found organisms were Staphylococcus aureus (n = 11), followed by coagulase negative Staphylococcus (n = 2), Enterococcus faecalis (n = 2), Pseudomonas aeruginosa (n = 1), and Escherichia coli (n = 1). The repeat culture of these patients after 5 days treatment with intravenous antibiotics were negative for growth of organisms. The most frequently instituted antibiotic was co-amoxiclave. Greater than 95% graft take was seen in 45 (90%) patients of the VAC group compared to only 9 (18 %) of the control group. Table I shows the graft take as percentage of the grafted surface area. None of the patients in VAC group needed re-grafting, however, 4 (8%) patients among the control group were re-grafted for residual areas of graft failure. The remaining patients with partial skin graft failure healed successfully with repeated dressings, alginate dressings and healing by secondary intention. Duration of hospital stay was significantly shorter among the VAC group patients (Table II). Table III depicts the healing time observed among the patients of the two groups. The hospital stay was 18-35 days with a mean of 21.58 ± 3.58 days. There was no in-hospital mortality. DISCUSSION In this study, as the inclusion criteria was open wounds of traumatic origin, majority of the patients were young males. Males are more frequently involved in outdoor activities and hence more prone to sustain different traumatic insults because of road traffic accidents, falls, firearm injuries and blasts etc. Predominant involvement of young males further amplifies the grave implications of such disabling injuries. Male predominance and more frequent involvement of younger population is well documented in the context of trauma in general.7 With increasing civil violence, there is an increasing number of patients with blast injuries as well. In this study the use of VAC therapy as pre-treatment for skin grafts, favourably influenced the management of open wounds. In the past, a number of adjuvant therapies such as use of skin substitutes, growth factors and hyperbaric oxygen etc. have been employed to expedite wound healing. VAC therapy was found a better alternative in this regard as it is more economical and safer. The present findings are in conformity with those of other published studies.8-10 In this study, VAC therapy was employed only in the preparatory phase before skin grafting of the wounds. Several published studies have successfully used VAC dressings for securing skin grafts postoperatively, especially in wounds with exudative, irregular, or mobile recipient beds and in difficult anatomic locations. It has been reported to stabilize the skin graft and conform it well to the shape of recipient bed, remove edema fluid, decrease bacterial counts, and provide a secured dressing. All these factors further improve the graft survival and reduce the need for repeat skin grafting.11-14 In this study healing time and hospital stay were significantly reduced in the patients treated with VAC therapy. Other published studies have also shown fast healing with VAC therapy.15-17 A variety of factors have been described to account for the accelerated healing. VAC therapy continually decontaminates the wound and drains the wound surface of exudates, which contain large amounts of proteases. Those would normally inhibit fibroblastic division, collagen production, and cell growth. Fluid removal helps with localized edema that otherwise causes an increase in interstitial pressure with consequent occlusion of microvasculature and lymphatics, decreased nutrient, and oxygen delivery. Protein degradation enzyme is released with metabolic waste accumulation and increased bacterial colonization, which causes capillary damage and hypoxia. VAC therapy also provides a moist environment to promote granulation tissue formation and prevents eschar formation, which allows for a smoother pathway to re-epithelialize the wound surface. Angiogenesis is stimulated, which improves tissue oxygenation and tissue reconstruction. This enhanced angiogenesis occurs even in patients with diabetic microangiopathy, and promotes healing of distal lesions.18,19 Micro- mechanical forces exerted on wound surface by low Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 677 Vacuum-assisted closure therapy as a pretreatment for split thickness skin grafts Table I: The take of split thichness skin graft among the patients (n=50 each group). S. No. Graft take % Number of patients Nnumber of patients p-value (VAC group) (control group) (%) 1 ≥ 95% 45 (90%) 9 (18%) p < 0.001* 2 80-94% 4 (8%) 32 (64%) p < 0.001* 3 < 80% 1 (2 %) 9 (18%) 0.03* * p-value significant = < 0.05. Table II: The duration of hospital stay (n=50 each group). S. No. Duration of Number of patients Number of patients p-value hospital stay (VAC group) (control group) (%) 1 Upto 20 days 45 (90%) 9 (18%) p < 0.001* 2 21-28 days 5 (10%) 37 (74%) p < 0.001* 3 > 28 days - 4 (8%) 0.349 ** * p-value significant = < 0.05; ** = not significant. Table III: Time to complete healing observed among the patients (n=50 each group). S. No Time to complete No. of patients No. of patients p-value healing (VAC group) (control group) (%) 1 2 weeks postgrafting 45 (90%) 9 (18%) p < 0.001* 2 3-4 weeks postgrafting 3 (6%) 36 (72%) p < 0.001* 3 > 4 weeks postgrafting 2 (4 %) 5 (10%) 0.111 ** * p-value significant = < 0.05; ** = not significant.
  • 4. pressure suction are also important. This mechanism mimics the stretch-induced cell proliferation typically operative in tissue expansion phenomenon seen else- where in the body. 20,21 Owing to its low cost, VAC therapy can provide an economical alternative to the other available costly local wound management measures. Such economic implications of wound management are particularly important in the context of our poor patients. Cost effectiveness has also been reported in terms of shortened hospital stays, and decreased overall medical cost in the published literature. 22,23 In this study VAC therapy was additionally found to be more comfortable for patients as well as the surgical staff. It obviated the need for daily dressing changes. Similar findings have been reported by other studies as well.22,23 This study has some limitations. It is a single centred study. Blinding of the treating doctors was not possible and so observer bias could not be eliminated completely. This study should prompt other local studies and hence allow more meaningful comparison of results in our own population. We recommend the conduct of a multicentre local study to confirm and improve upon our results. Additionally a local study may be conducted to compare the cost of VAC therapy versus other wound preparatory methods such as use of skin substitutes or growth factors, and hence evolve an evidence base to confirm VAC therapy as an economical alternative to the other costly local wound management measures. CONCLUSION VAC therapy should be employed in the pre-treatment of wounds planned to be reconstructed with STSG, given its significant advantages in the wound bed preparation compared with traditional normal saline gauze dressings. REFERENCES 1. Galiano RD, Mustore TA. Wound care. In: Thorne CH, Beasley RW, Aston SJ, Bartlett SP, Gurtner GC, Spear SL, editors. Grabb and Smith's plastic surgery. 6th ed. Philadelphia: Lippincott Williams & Wilkins; 2007. p. 23-32. 2. Robson MC, Steed DL, Franz MG. Wound healing: biologic features and approaches to maximize healing trajectories. Curr Probl Surg 2001; 38:72-140. 3. Breasted D. The Edwin Smith surgical papyrus. Chicago: University of Chicago Press; 1930. 4. Fleischmann W, Strecker W, Bombelli M, Kinzl L. [Vacuum sealing as treatment of soft tissue damage in open fractures]. Unfallchirurg 1993; 96:488-92. German. 5. Argenta LC, Morykwas MJ. Vacuum-assisted closure: a new method for wound control and treatment: clinical experience. Ann Plast Surg 1997; 38:563-76; discussion 577. Comment in: Ann Plast Surg 2000; 45:332-4; discussion 335-6. 6. Morykwas MJ, Argenta LC, Shelton-Brown EI, McGuirt W. Vacuum-assisted closure: a new method for wound control and treatment: animal studies and basic foundation. Ann Plast Surg 1997; 38:553-62. Comment in: Ann Plast Surg 2000; 45:332-4; discussion 335-6. 7. Saaiq M, Shah SA. Thoracic trauma: presentation and management outcome. 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Circumferential negative-pressure dressing (VAC) to bolster skin grafts in the reconstruction of the penile shaft and scrotum. Ann Plast Surg 2005; 54:178-83. 13. Hallberg H, Holmstrom H. Vaginal construction with skin grafts and vacuum-assisted closure. Scand J Plast Reconstr Surg Hand Surg 2003; 37:97-101. 14. Molnar JA, De Franzo AJ, Marks MW. Single-stage approach to skin grafting the exposed skull. Plast Reconstr Surg 2000; 105: 174-7. 15. Braakenburg A, Obdeijin MC, Feitz R, van Rooij IA, van Griethuysen AJ, Klinkenbijl JH, et al. The clinical efficacy and cost effectiveness of the vacuum-assisted closure technique in the management of acute and chronic wounds: a randomized controlled trial. Plast Reconstr Surg 2006; 118:390-7. 16. Vuerstaek JD, Vainas T, Wuite J, Nelemans P, Neumann MH, Veraart JC. State-of-the-art treatment of chronic leg ulcers: a randomized controlled trial comparing vacuum-assisted closure (VAC) with modern wound dressings. J Vasc Surg 2006; 44: 1029-37; discussion 1083. Epub 2006 Sep 206. Comment in: J Vasc Surg 2007; 46:614-5; author reply 615-6. 17. Timmers MS, Le Cessie S, Banwell P, Jukema GN. The effects of varying degrees of pressure delivered by negative-pressure wound therapy on skin perfusion. Ann Plast Surg 2005; 55:665-71. 18. Morris GS, Brueilly KE, Hanzelka H. Negative pressure wound therapy achieved by vacuum-assisted closure: evaluating the assumptions. Ostomy Wound Manage 2007; 53:52-7. 19. Demaria RG, Giovannini UM, Téot L, Frapier JM, Albat B. Topical negative pressure therapy. A very useful new method to treat severe infected vascular approaches in the groin. J Cardiovasc Surg (Torino) 2003; 44:757-61. 678 Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 Muhammad Saaiq, Hameed-ud-Din, Muhammad Ibrahim Khan and Saud Majid Chaudhery
  • 5. 20. Saxena V, Hwang CW, Huang S, Eichbaum Q, Ingber D, Orgill DP. Vacuum-assisted closure: microdeformations of wounds and cell proliferation. Plast Reconstr Surg 2004; 114:1086-96; discussion 1097-8. 21. De Filippo RE, Atala A. Stretch and growth: the molecular and physiologic influences of tissue expansion. Plast Reconstr Surg 2002; 109:2450-62. 22. Trueman P. Health economics and topical negative pressure therapy. In: Calne S, editor. Position document. Denmark: European Wound Management Association; 2007. p. 5-9. 23. Jones SM, Banwell PE, Shakespeare PG. Advances in wound healing: topical negative pressure therapy. Postgrad Med J 2005; 81:353-7. Journal of the College of Physicians and Surgeons Pakistan 2010, Vol. 20 (10): 675-679 679 Vacuum-assisted closure therapy as a pretreatment for split thickness skin grafts G G G G G *G G G G G