Algorithm for the use of Drawtex® in a Tertiary Adult Burn Centre, … · 2017. 6. 19. · Hilde...
Transcript of Algorithm for the use of Drawtex® in a Tertiary Adult Burn Centre, … · 2017. 6. 19. · Hilde...
Algorithm for the use of Drawtex®
in a Tertiary Adult Burn Centre,
Tygerberg Hospital South Africa
Wayne George KleintjesMBChB (Stell), Mmed(Plast)(Stell), FCS(Plast Surg), PhD (Plast) (Stell)
Plastic & Reconstructive SurgeonHilde Du Plooy
(B.Pharm, MBA, BSc Anatomy Hons, MBChB (2022), CRA.Cape Town, South Africa
6- 9 June Addis Ababa, Ethiopia
Introduction
Retrospective Analysis
February to May 2016
Spongy / foam dressing with Leva Fibres
Allows the exudate to move away from wound
Developed in SA 1986
DRAWTEX ® POSITIONING
Need Identified
• Controversy (Couch, 2012; Ortiz et al., 2012)
• Problem: Where Drawtex® fits ?
• SOP TBH: sloughy, exudating wounds: Intrasite® gel and Bactrazene® (silver sulphadiazene)
• How does Drawtex® compare to the SOP?
Aim
1. Identify wounds for controls in the same patient that
could be used for comparison.
2. Identify the effectiveness of Drawtex® on fresh burns
3. Calculate cost-effectiveness
4. Propose an algorithm for the use of the dressing
Material & Methods
Study Subjects
Data Collection
Application Methods
Photographic Analysis
Statistical Analysis
Materials and Methods
A: Study Subjects: Criteria
Inclusion Criteria Exclusion Criteria
• Drawtex® on wounds • Skingrafted areas
• No operation in 48 hours; • Operation < 24h
• Other wounds for comparison
Materials & Methods
B: Data Collection
Parameters
• Demographic dataAge, sex
• Clinical wound analysisTBSA%, burn mechanism, area affected, treatment days
• Wound change: initial application vs later
For the wound assessment the following scale was used to measure: Slough, biofilm, exudate, epithelium, infection and wound moistness.
Other wound assessments included change in wound size, colour, odour and swab test needed.
Materials & Methods
Wound Assessment Scale Value Description
0 None
1 Mild
2 Moderate
3 Severe
Materials and Methods
C: Application Methods
DRAWTEX® GROUP CONTROL GROUP (BURN UNIT SOP)
Primary Dressing: Drawtex® Primary Dressing: Intrasite®& Bactrazine®
No secondary dressing was used, only bandages.
Secondary Dressing: Telfa®, followed by bandages.
Frequency of change: Every 48 hours Frequency of change: Every 24 hours
Cleansing and disinfection of wounds: Water, chlorhexidine and alcohol solution.MRSA: chlorhexadine soap or 1% acetic acid with pain protocol.
Materials and Methods
• Patients who had good photo records were used for comparison.
• The protocol:
iPhone camera of 10 megapixels
Photo should be taken 30 cm from the wound
A ruler must be included in the photograph
D: Photographic Analysis
Materials and Methods
• McNemar Chi square tests
• Means, standard deviation, ranges, 95 % confidence intervals
• Other statistical analysis (IBM SPSS version 23 will be used to analyse the data)
• A two-tailed p value < 0.05 = statistically significant
E: Statistical Analysis
Study Subjects
Description Number of Patients
Total number of patients admitted to burn unit of Tygerberg Hospital 100
Total number of patients available 39
Number of patients selected (N) 36
Drawtex ® patient sample (n) 36
Control patient sample (n) 8
Total number of areas to be treated in 36 patients 48
Drawtex ® areas treated out of 48 areas 40
Control areas treated out of 48 areas 8
Results
Results
Demographic data:
AGE Range Value
Minimum 17
Maximum 78
Average 33
SEX Description Number of Patients Percentage
Male 28 78%
Female 8 22%
Results
TBSA % Range Value
Minimum < 1%
Maximum 55%
Average 23%
Burn Mechanism Description Number of Patients Percentage%
Boiling Water 5 14%
Flame 29 81%
Electrical 2 6%
Paraffin 1 3%
Clinical data:
Results
Burn Area LocationNumber of Cases per
AreaPercentage %
Arms 27 56%
Legs 14 29%
Back 5 10%
Abdomen / Chest 10 21%
Head 7 15%
Treatment days Range Days
Minimum 1
Maximum 6
Average 2.6
Clinical data:
Results
GROUP DRAWTEX® n=8 CONTROL n=8
Description Initial Follow up % Change Initial Follow up % Change
Slough 17 3 -82% 16 17 6%
Biofilm 2 0 -100% 2 6 200%
Epithelium 7 16 129% 6 7 17%
Exudate 14 3 -79% 14 17 21%
Infection 2 0 -100% 2 3 50%
Moistness 15 5 -67% 15 18 20%
Wound Assessment: Parameters
ResultsTotal Wound Assessment:
Patient Number Group Initial Follow Up Difference
Patient 1 Drawtex ® 7 2 5
Control 5 6 -1
Patient 2 Drawtex ® 7 3 4
Control 7 10 -3
Patient 3 Drawtex ® 9 4 5
Control 9 10 -1
Patient 4 Drawtex ® 8 5 3
Control 8 10 -2
Patient 5 Drawtex ® 9 3 6
Control 9 7 2
Patient 6 Drawtex ® 5 3 2
Control 5 12 -7
Patient 7 Drawtex ® 7 3 4
Control 7 6 1
Patient 8 Drawtex ® 5 4 1
Control 5 7 -2
Results
Drawtex ® n=40
Variable Initial Follow up % Change
Slough 69 27 -61%
Biofilm 11 3 -73%
Epithelium 35 68 94%
Exudate 62 25 -60%
Infection 11 0 -100%
Moistness 59 28 -53%
General Results: Drawtex ® (n=40 wounds)
In general, the 40 wounds treated with Drawtex ® had:• Reduced slough with 61 %, • biofilm by 73 %, • enhanced epithelial growth with 94 %, • reduced the amount of exudate with 60 %, • reduced the rate of infection 100 % and • moisture with 53 %.
Result
Drawtex ® (n=8) Control (n=8)
Wound Colour
Initial
Assessment Follow Up Change %
Initial
Assessment
Follow
Up Change %
Green 1 0 -100% 1 0 -100%
Red 2 5 150% 0 0 0%
Yellow 3 1 -67% 4 6 50%
Yellow and Red 1 3 200% 3 2 -33%
Yellow and Green 1 0 -100% 0 0 0%
Yellow, Red and Black 1 0 -100% 0 0 0%
• When comparing the results in the follow up assessment based on the colour of the wounds:
• Those treated with Drawtex ®had an increase in red (healthy) wound tissue in five of the subjects compared to none in the control group.
• The amount of yellow (slough) tissue was significantly reduced by 67 % in the Drawtex ® group. In the control group, slough (yellow) increased with 50 %.
Results: Cost- effectiveness(C-E)
TREATMENT REGIMEN
DRESSING SKU
MEDIUM WOUND
APPLICATION 10-20 cm
TOTAL COST(24 HOURS)
TOTAL COST MEDIUM(48 HOUR
TREATMENT)
COST COMPARISON
Drawtex ® Drawtex® 20 20 x 20 x 1 N/A 102.828 102.828
Other
Intrasite® 25 g 0.5 17.91 35.82
111.35
Melolin® 10 cm x 10 cm 3 7.44 2.48
Telfa® 0 3 0 0
Bactrazine® 50 g 0.5 21.885 43.77
Bandage 0 1 0 0
Gauze Swab
0 4 14.64 29.28
Discussion: Controls & Results
• Low number of controls a.r.o. poor record keeping
• Limited – single permanent Dr/specialist
• Enquiry: clinical evidence Drawtex® more effective removing slough from wounds
• Unethical to continue doing control areas
• Drawtex®: subjectively clearly better than SOP
Patient 1: 1st Follow-up
CONTROL DRAWTEX
Patient 1: 2nd Follow-up (3 days)
CONTROL DRAWTEX
Patient 2: 1st Follow-up
CONTROL DRAWTEX
Patient 2: 2nd Follow-up (3 days)
CONTROL DRAWTEX
Patient 3: 1st Follow-up
CONTROL DRAWTEXCONTROL
Patient 3: 2nd Follow-up (3 days)
CONTROL DRAWTEX
BACTERIA TRAPPED IN DRAWTEX
A B C
A: Drawtex with E.coli.
B: Drawtex® with MRSA.
C: Drawtex® with Candida albicans.(Edwards-Jones, V., Vishnyakov, V. & Spruce, P. 2014).
Discussion: Effectiveness on fresh burns:
• There was a clear decrease in moisture on the wounds.
• The question then arises: On which fresh burns will this moisture reduction be most beneficial.
• From the wound assessment data it seems that fresh burns with slough will have the best benefit from the use of Drawtex ®
Discussion: Effectiveness
• The clean fresh burn, superficial to mid-partial thickness has the most benefit from a skin substitute of which there are many available.
• Even though the SOP also removed slough it took much longer than Drawtex ®.
• One could make an argument for the presence of more pseudo-slough with the Intrasite® and Bactrazene®, but the clinical evidence in the photos were very convincing.
Discussion: Mechanism of Action
The question remains as to the mechanisms responsible for the actions seen with Drawtex in wound treatment.
The three mechanisms: Capillary, Hydroconductive and Electrostatic actions.
These proposed mechanisms may not totally explain the actions of Drawtex due to the difficulty of applying
physicochemical theory to biological systems.
A B
A: Scanning electron micrograph (SEM) of Drawtex® at 1000 times magnification. B: Drawtex hydrated under SEM at 1000 times magnification
(Edwards-Jones, V., Vishnyakov, V. & Spruce, P. 2014).
Discussion: Mechanism of Action
1. ABSORPTION WITHIN THE FIBRES
Capillary/Tubular Arrangements
Discussion: Mechanism of Action
2. NEGATIVE SUCTION EFFECT WITHIN FIBRE GAPS
Venturi Effect: Fluid between Tubules
Discussion: Mechanism of Action
2. NEGATIVE SUCTION EFFECT WITHIN FIBRE GAPS
Discussion: Mechanism of Action
3. DIFFUSION GRADIENT
Discussion: Mechanism of Action
3. DIFFUSION GRADIENT
Transectional View Fluid Absorbtion
Discussion: Mechanism of Action
4. ELECTRICAL CHARGE AND GRADIENT
Discussion: Mechanism of Action
5. STEPLADDER (ZIG ZAG) MOVEMENT OF WATER
LM, 4x magnification; Trypan Blue
LM, Trypan Blue, 4x magn
Discussion: Mechanism of Action
6. HYDROPHYLLIC PROPERTIES
Discussion: Mechanism of Action
7. MECHANICAL REMOVAL OF SLOUGH
Discussion: Mechanism of Action
7. MECHANICAL REMOVAL OF SLOUGH
Mechanical Removal: Adherence
Discussion: Cost-effectiveness
• The Drawtex® was mostly changed every two days (average data analysed was 2.6 days –without error correction)
• The cost of physical labour we did not include in the calculation, but it is a significant factor
• In a nursing staff shortage climate that must also be considered.
• Therefore the overall benefit of having effective slough removal every 2nd day with Drawtex ® was a huge benefit in the Burn Centre.
Proposed Algorithm
Burn Injury
Exudate
Colour
Wound Swab High (Old Wound) Low (New Wound)
Red or PinkYellow
Drawtex ® Skin Substitute
Proposed Acronym: Wound parameter assessment
BE ME SIC SOS B: Biofilm;
E: Epithelium;
M: Moistness;
E: Exudate;
S: Slough;
I: Infection;
C: Colour;
S: Swab;
O: Odour;
S: Size.
Conclusion
• Based on the current literature, the efficacy of Drawtex ®hydro-conductive dressings has not been described in a tertiary burn unit, specializing in adult burn care, such as Tygerberg Hospital.
• The study found that Drawtex ® delivers better results compared to the control group and therefore Drawtex ® is recommended for moderate to highly exuding wounds with slough.
• The proposed algorithm can be applied in burn wound assessments in both public and private tertiary institutes.
• Knowledge regarding the understanding of the efficacy thereof will contribute to the effective treatment management and protocol development for tertiary burns.
Limitations and Future Research
LIMITATIONS:• The sample size might be too small to derive meaningful conclusions,
however the limitation thereof will be determined based on the results
obtained from the data collected.
• Some data from the patient files may be inconclusive or not meet the
selection criteria.
• The selection was based on the quality, positioning, lighting, measurement
ruler as well as the similarity between compared areas.
AREAS OF FUTURE RESEARCH: • Application to skin graft procedures, to determine the efficacy thereof
when covering meshed skin grafts.
• Odour: improvement by selecting appropriate patients.