product reference guide advanced wound care

Transcription

PRODUCT REFERENCE GUIDE
ADVANCED WOUND CARE
SYSTAGENIX
This guide has been developed to provide a useful overview of the products
available from Systagenix.
Section
Let’s Heal®
This section describes our passion and agility to drive innovation that has just one
goal: to help heal wounds, fast. This is captured by our call
to action: Let’s Heal®, which represents our unique integrated wound healing
portfolio, built of four categories:
Section
Sizes, Codes and Ordering Information
This section contains everything needed to order your Systagenix products,
including individual sizes and codes available.
Section
Product Information Guidelines
This section includes information on the Systagenix advanced wound care
portfolio. It contains details on the technical aspects of the dressings, how the
dressings work and the clinical benefits you can expect when using the dressings.
You will also find the indications and the specific wound types that the dressings
are suitable for. All in one simple, easy place for reference.
2 — Introduction
Section
4
Let’s Heal®
Section
6
Sizes, Codes and Ordering Information
Section
12 Introduction to Diagnostics
14 16 18 20 SILVERCEL® Non-Adherent Dressing
SILVERCEL® Hydro-Alginate with Silver
INADINE® Povidone Iodine Non-Adherent Dressing
ACTISORB® Activated Charcoal Dressing with Silver
22 24 26 PROMOGRAN® Matrix ORC/Collagen Dressing
PROMOGRAN PRISMA® ORC/Collagen with Silver/ORC Dressing
FIBRACOL® PLUS Collagen/Alginate Dressing
28 32 34 36 38 40 42 44 46 TIELLE® Family: Hydropolymer Adhesive Dressings
ADAPTIC TOUCH® Non-Adhering Silicone Dressing
ADAPTIC® Non-Adhering Dressing
ADAPTIC® DIGIT Non-Adhering Digit Dressing
NU-DERM® Alginate Dressing
NU-DERM® Hydrocolloid Dressing
NU-GEL® Hydrogel with Alginate
NU-GEL® Wound Dressing
BIOCLUSIVE® Transparent Dressing
Contents — 3
Let’s Test®
Let’s Protect®
4 — Section
Let’s Heal®
SILVERC
NON-AD
Let’s Promote®
PROMO
PROMO
PRISMA
Let’s Comfort®
TIELLE
ADAPTI
®
To finally provide wound
care tools which aid
a correct and timely
diagnosis.
To protect from infection,
while also managing the
secondary symptoms of
Exudate, Pain, and Odour.
SILVERCEL® NON-ADHERENT with EasyLIFT®
SILVERCEL®
INADINE®
ACTISORB® Silver 220
To promote wound healing
in ways that standard
dressings may not be able to.
PROMOGRAN®
PROMOGRAN PRISMA®
FIBRACOL® PLUS
To provide a comfortable
and effective healing
environment for all types
of wounds.
TIELLE® Family with LiquaLock®
ADAPTIC® Touch
ADAPTIC®
ADAPTIC® Digit
NU-DERM® Alginate
NU-DERM® Hydrocolloid
NU-GEL® Hydrogel
BIOCLUSIVE®
Section
— 5
SILVERCEL® NON-ADHERENT Antimicrobial Dressing
CODE
SIZE
EACHES PER
CARTON
CAD7050
5cm x 5cm
10
CAD7011
11cm x 11cm
10
CAD7020
10cm x 20cm
5
CAD7230
2.5cm x 30.5cm (rope)
5
SILVERCEL® Antimicrobial Dressing
CODE
SIZE
EACHES PER
CARTON
CAD050
5cm x 5cm
10
CAD011
11cm x 11cm
10
CAD020
10cm x 20cm
5
CAD230
5
INADINE® PVP-I Non-Adherent Antimicrobial Dressing
CODE
SIZE
EACHES PER
CARTON
P01481
5cm x 5cm
25
P01512
9.5cm x 9.5cm
25
ACTISORB® Antimicrobial dressing
CODE
6 — Section
SIZE
DRESSINGS
PER carton
CARTONs
PER box
MAS065
6.5cm x 9.5cm
10
5 (50 eaches)
MAS105
10.5cm x 10.5cm
10
5 (50 eaches)
MAS190
19cm x 10.5cm
10
5 (50 eaches)
Sizes Codes and Ordering Information
PROMOGRAN® Protease Modulating Matrix
CODE
SIZE
EACHES PER
CARTON
M772028
28cm2
10
M772123
123cm2
10
PROMOGRAN PRISMA® wound balancing matrix
CODE
SIZE
EACHES PER
CARTON
PS2028
2
28cm
10
PS2123
123cm2
10
FIBRACOL® Plus Collagen Alginate Dressing
CODE
SIZE
EACHES PER
CARTON
2981
5.1cm x 5.1cm
12
2982
10cm x 11cm
12
2983
10.2cm x 22.2cm
6
2984
1cm x 1cm 40cm (rope)
6
Section
— 7
TIELLE® Hydropolymer dressing
CODE
SIZE
EACHES PER
CARTON
TIELLE®
MTL100
7cm x 9cm
10
MTL101EN
11cm x 11cm
10
MTL102
15cm x 20cm
5
MTL103
18cm x 18cm
5
MTL105
15cm x 15cm
10
18cm x 18cm
5
10
TIELLE® SACRUM
MTL104
TIELLE® PLUS
MTP501
11cm x 11cm
MTP502
15cm x 20cm
5
MTP505
15cm x 15cm
10
20cm x 26.5cm
5
15cm x 15cm
10
10
TIELLE® PLUS HEEL
MTP508
TIELLE® PLUS SACRUM
MTP506
TIELLE® MAX
MTP701
11cm x 11cm
MTP702
15cm x 20cm
5
MTP705
15cm x 15cm
10
CODE
8 — Section
SIZE
EACHES PER
CARTON
10
TCH501
5cm x 7.6cm
TCH502
7.6cm x 11cm
10
TCH503
12.7cm x 15cm
10
TCH504
20cm x 32cm
5
ADAPTIC® Non-Adhering dressing
CODE
SIZE
EACHES PER
CARTON
2012
7.6cm x 7.6cm
50
2013
7.6cm x 20.3cm
3x36
2014
7.6cm x 40.6cm
36
2015
7.6cm x 20.3cm
24
2019
12.7cm x 22.9cm
12
CODE
SIZE
EACHES PER
CARTON
MAD003
Small 2cm Ø
10
MAD013
Medium 2.4cm Ø
10
MAD023
Large 2.8cm Ø
10
MAD042
Extra Large 3cm Ø
10
2.8cm Ø
10
ADAPTIC® Digit
ADAPTIC® Digit Toe
MAD062
Section
— 9
NU-DERM® Alginate dressing
CODE
SIZE
EACHES PER
CARTON
Cartons
Per Box
AWD112
5
5 (25 eaches)
AWD202
5cm x 5cm
10
5 (50 eaches)
AWD404
10cm x 10cm
10
5 (50 eaches)
AWD408
10cm x 20cm
5
5 (25 eaches)
CODE
SIZE
DRESSINGS
PER TRAY
TRAYS
PER CASE
10
10 (100 eaches)
NU-DERM® Hydrocolloid Border Thin
HCT101
10cm x 10cm
NU-DERM® Hydrocolloid Standard (foam backing)
HCF204
10cm x 10cm
5
10 (50 eaches)
HCF208
20cm x 20cm
5
4 (20 eaches)
NU-DERM® Hydrocolloid Border
HCB102
5cm x 5cm
20
5 (100 eaches)
HCB204
10cm x 10cm
10
16 (160 eaches)
HCB106
15cm x 15cm
5
4 (20 eaches)
10
6 (60 eaches)
5
4 (20 eaches)
NU-DERM® Hydrocolloid Border Elbow/Heel
HCH207
8cm x 12cm
NU-DERM® Hydrocolloid Border Sacrum
HCS100
10 — Section
15cm x 18cm
CODE
SIZE
TUBES
PER CARTON
CARTONS
PER BOX
MNG415
15g
10
4 (40 eaches)
MNG425
25g
6
4 (24 eaches)
CODE
SIZE
EACHES PER
CARTON
2497
9.5cm x 9.5cm
5
2498
15.2cm x 20.3cm
5
BIOCLUSIVE® Transparent dressing
CODE
SIZE
DRESSINGS
PER CARTON
Cartons
Per CASE
2460
3.8cm x 3.8cm
100
4 (400 eaches)
2461
5.1cm x 7.6cm
100
4 (400 eaches)
2463
10.2cm x 12.7cm
50
4 (200 eaches)
2465
12.7cm x 17.8cm
20
5 (100 eaches)
2467
10.2cm x 25.4cm
20
6 (120 eaches)
2469
20.3cm x 25.4cm
10
8 (80 eaches)
Section
— 11
Welcome to 21st century wound care
“The development of specific diagnostic tests for use in wounds has the potential
to revolutionize their treatment, and help improve standards of wound care
(while) aiding in the cost effective use of limited resources.”
World Union of Wound Healing Societies. Principles of best practice: A consensus
document: MEP Ltd. London, 2008.
Research suggests that wounds that heal well have a lower overall
protease activity than those that heal poorly. As a result, a test that readily
provides this information might be clinically useful in understanding how well a
wound is healing, and whether an intervention that modulates protease activity
may be needed.
12 — Section
Product Information
FINALLY, A TEST YOU’LL WANT TO TAKE...
coming soon.
Section
— 13
SILVERCEL NON-ADHERENT
®
SILVERCEL® Non-adherent antimicrobial dressing with silver
WHAT IS IT?
SILVERCEL® NON-ADHERENT Dressing is the next generation of Silver Antimicrobial
Dressing with the unique feature of a Non-Adherent layer that maximizes
protection of the wound bed, particularly at dressing change.
The unique composition: a mixture of alginate, carboxymethylcellulose (CMC),
and silver coated nylon fibres manages exudate effectively in infected or heavily
colonised wounds. The optimally spaced perforations on the unqiue EasyLIFT® film
layer keeps the dressing simple and convenient to use, minimizing pain and trauma
at dressing change for your patients.
HOW DOES IT WORK?
SILVERCEL® NON-ADHERENT is designed to absorb and retain high amounts of
exudate, while allowing easy, intact and atraumatic pain free removal from the
wound bed.1
The silver ions within the dressing protect the wound from bacterial contamination.1
SILVERCEL® NON-ADHERENT – designed not to stick
Maintains a sustained release of silver ions for up to 7 days in vitro 1
Stays strong for intact removal, even when wet 2
Optimally spaced perforations allow ‘free flow’ of exudate into the dressing,
and also ensure the dressing stays intact
Conforms to the wound bed for complete coverage when moist, and is
designed not to stick to the wound bed at dressing change
SILVERCEL® NON-ADHERENT has been proven to be 75% Less Adherent than
the market leading silver dressing 3
Effective against over 150 pathogens including MRSA, MRSE and VRE 2
•
•
•
•
•
•
INDICATIONS:
May help reduce infection in moderate to heavily exuding partial and full-thickness
wounds including:
Pressure ulcers Venous ulcers
Diabetic ulcers Donor sites
Traumatic and surgical wounds
Suitable for use under medical supervision, in the management of infected
wounds, or wounds which have an increased risk of infection.
•
•
•
14 — Section
•
•
Product Information
How do I use it?
Cut or fold SILVERCEL® Non-Adherent to fit the wound. Cover the dressing with a
non-occlusive secondary dressing such as one of the Tielle® Hydropolymer Dressings.
Reapply SILVERCEL® Non-Adherent when the secondary dressing has reached
its absorbent capacity or whenever good wound care practice dictates that the
dressing should be changed.
Please refer to package insert for full instructions.
CODE
SIZE
EACHES PER
CARTON
CAD7050
5cm x 5cm
10
CAD7011
11cm x 11cm
10
CAD7020
10cm x 20cm
5
CAD7230
5
References:
1. Clark, R PhD; Stephens, S-A (BSc (Hons); Del Bono, M; Abloye, O; Bayliff,
S BSc (Hons); The Evaluation of Absorbent Silver containing Dressings
In Vitro; Systagenix Wound Management. Poster Presentation CAWC
Quebec City October 2009
2.R.Clark, Michelle Del Bono, Sally-Anne Stephens, Omotayo Abioye, Simon
Bayliff: Simulated in use tests to evaluate a Non-Adherent Antimicrobial
silver alginate dressing. Presentation Quebec City October 2009.
3. Clark,Stephens,Del Bono: From Lab to Leg The importance of correlating
in-vitro and in-vivo test systems to clinical experience. Poster presented
SAWC 2010.
Section
— 15
SILVERCEL
®
SILVERCEL® Antimicrobial Dressing
WHAT IS IT?
SILVERCEL® is a sterile, non-woven pad composed of a high G (guluronic acid)
alginate, carboxymethylcellulose (CMC) and silver coated nylon fibres.
The unique composition of SILVERCEL® is designed to manage exudate and help
control infected or heavily colonised wounds.
HOW DOES IT WORK?
SILVERCEL® has a number of features that can help with controlling Infection:
SILVERCEL® minimizes the risk of maceration and leakage1, 2 and has been
proven to absorb and retain fluid even under compression
•
•In vitro studies show that the level of silver released from SILVERCEL
®
maintained beyond 7 days
Designed not to break up in the wound 1,4
SILVERCEL® maintains its strength within a moist wound environment 1,4
Effective against over 150 pathogens including MRSA and VRE 2
•
•
•
is
3
INDICATIONS:
SILVERCEL® is intended for use in the management of all moderate to heavily exuding
partial and full thickness chronic wounds including: pressure ulcers, venous ulcers,
diabetic ulcers, donor sites, traumatic and surgical wounds. As the product contains
alginate it may assist in supporting the control of minor bleeding in superficial
wounds. It is also suitable for use under medical supervision, in the management of
infected wounds, or wounds in which there is an increased risk of infection.
How do I use it?
Application
Fold or cut to the size of the wound and apply directly to the wound. Loosely pack
deep wounds ensuring that the dressing does not overlap the edges of the wound.
Secure in position with a non-occlusive secondary dressing like TIELLE®
Hydropolymer dressing.
16 — Section
Product Information
CODE
SIZE
EACHES PER
CARTON
CAD050
5cm x 5cm
10
CAD011
11cm x 11cm
10
CAD020
10cm x 20cm
5
CAD230
5
References:
1. Teot L et al. The management of wounds using SILVERCEL™ Hydro-Alginate.
Wounds UK Supplement. 2005.1(2)
2. Addison D et al. An Antimicrobial Dressing for moderate to heavily exuding
infected and critically colonised wounds. Systagenix Wound Management
Gargrave U.K. Poster presented at EWMA Pisa May 2003
3.Rennison T et al. Evaluations of a silver Hydro-Alginate dressing to Determine
suitability for use on chronic wounds. Systagenix Wound Management
Gargrave U.K. Poster presented at EWMA Prague May 2006.
4. Clark R, PhD; Stephens S-A, BSc (Hons); Del Bono, M; Abioye, O; Bayliff S, BSc (Hons).
Simulated in-use tests to evaluate a non-adherent antimicrobial silver alginate
wound dressing. SAWC, Texas, Dallas 2009
Section
— 17
INADINE
®
INADINE® PVP-I Non-Adherent Dressing
WHAT IS IT?
INADINE® PVP-I Non-Adherent Dressing consists of a low adherent knitted viscose
fabric impregnated with a polyethylene glycol (PEG) base containing 10% Povidone
Iodine; equivalent to 1.0% available iodine.
INADINE® Dressings are designed to protect the wound, even if infected.
HOW DOES IT WORK?
The Povidone molecule provides an effective, and controlled release of iodine. The
polyethylene glycol provides a water-soluble environment, which allows the Iodine
to reach the bacteria in the wound.
INADINE® Dressing has long been established for use in wound care, its
features include:
•Povidone Iodine controls bacteria by reducing bacterial load and inhibits
infection 1-3
Povidone Iodine is a broad spectrum antimicrobial 1-3
Safe for use on adults and children and in combination with systemic
antibiotics 1-3
•
•
INDICATIONS:
INADINE® Dressing is designed to protect the wound, even if infected. INADINE®
Dressing is indicated for the management of ulcerative wounds and may also be
used for the prevention of infection in minor burns and traumatic skin loss injuries.
How do I use it?
Application
Apply directly to the wound or burn site. To ensure INADINE® dressing stays in situ,
use with a secondary dressing like TIELLE® Hydropolymer dressing.
Changing the dressing
When the colour of the dressing turns to white, this indicates the loss of antiseptic
efficacy and this is when the INADINE® dressing should be changed.
18 — Section
Product Information
CODE
SIZE
EACHES PER
CARTON
P01481
5cm x 5cm
25
P01512
9.5cm x 9.5cm
25
References:
1. Mclure A.R et al Journal of Hospital Infection. 1992 Aug;21(4):291-9.
2. Goldenheim P.D Postgrad. Med.Jnl.,1993;69 (suppl.3):S97-S105.
3. Adams l. Wound healing altered with the use of povidone iodine. 1985.
4. A. Langely. INADINE wound dressings speed healing, reduce patient
discomfort and cut costs by almost 40%. Burns 1989. Vol. 15.
Section
— 19
ACTISORB SILVER 220
®
ACTISORB® ACTIVATED CHARCOAL DRESSING WITH SILVER
WHAT IS IT?
ACTISORB® Silver 220 Dressing consists of activated charcoal impregnated with
silver and encased in a nylon sleeve. ACTISORB® Silver 220 Dressing is designed to
trap wound malodour while protecting the wound from infection. By removing
harmful elements from the wound, a more stable wound healing environment
can be achieved.
HOW DOES IT WORK?
Activated charcoal traps odour and bacterial toxins
•Binds toxins which are known to impair healing
•Reduces wound odour and improves patient’s quality of life
5,6
2
Silver kills bacteria
Reduces infection and exudate 3, 4
Effective wet or dry
Consistent adsorption of bacteria
•
1
•
INDICATIONS:
ACTISORB® Silver 220 Dressing is suitable as the first therapeutic step in the
management of all chronic wounds. It is indicated for fungating carcinomas,
ulcerative, traumatic and surgical wounds where bacterial contamination,
infection or odour occurs.
How do I use it?
Application
Apply directly to the wound or malodourous site. Where absorption is required
support use with a secondary dressing like TIELLE® Hydropolymer dressing.
ACTISORB® Silver 220 can be easily packed into deep wounds, and is effective
wet or dry.
ACTISORB® Silver 220 dressing should not be cut, otherwise particles of activated
carbon may get into the wound and cause discoloration.
20 — Section
Product Information
CODE
SIZE
Dressings
per carton
cartons
per box
MAS065
6.5cm x 9.5cm
10
5 (50 eaches)
MAS105
10.5cm x 10.5cm
10
5 (50 eaches)
MAS190
19cm x 10.5cm
10
5 (50 eaches)
References:
1.Russel AD et al. Antimicrobial activity and action of silver. Progress in
Medicinal Chemistry. 31, 351-370, Elsevier Service 1994
2. Price PE et al. J Wound Care; 9(2):93-95
3. Milward PA. Nursing Times 1991; 87(13):70-72.
4. Leak, K. PEG site infections: a novel use for ACTISORB* Silver 220.Br J
Community Nurs. 2002; 7 (6)
5. Kramer A et al Antibacterial activity and endotoxin-binding capacity of
ACTISORB* Silver 220. J Hospital Infect. 2003; 53: 511-4.
6.Robson MC et al. Wound healing alterations caused by infection. Clinics in
Plastic Surgery 1990; 17: 485-492.
Section
— 21
PROMOGRAN
®
PROMOGRAN® Protease Modulating Matrix
WHAT IS IT?
PROMOGRAN® matrix is sterile, freeze-dried composite of 55% collagen and 45%
oxidised regenerated cellulose (ORC).
PROMOGRAN® matrix is designed to promote an optimal healing environment. 1
With PROMOGRAN® matrix stalled wounds close: faster,1,2 cost effectively. 1,3,4
In the presence of exudate the PROMOGRAN® matrix transforms into a soft and
conformable, biodegradable gel: this allows contact with all areas of the wound.
HOW DOES IT WORK?
PROMOGRAN® matrix has been proven to reduce levels of proteases such as MMPs
and Elastase. This may restore the balance of the wound microenvironment,
promoting granulation tissue and helping the wound close.5
Reducing MMP and Elastase activity has been shown to reduce wound surface
area.
Collagen/ORC is more effective than collagen alone:
Binds and inactivates 3 times more proteases 5,6,7
Enhances granulation tissue formation 8
Reduces bacterial growth 5-7, 9
Protects growth factors 10
•
•
•
•
INDICATIONS:
PROMOGRAN® matrix is indicated for the management of all wounds
healing by secondary intent which are clear of necrotic tissue, including:
Diabetic ulcers
Venous ulcers
Pressure ulcers
Ulcers caused by mixed vascular aetiologies
PROMOGRAN® matrix has demonstrated haemostatic properties.
PROMOGRAN® matrix can be used under compression therapy.
•
•
•
•
•
How do I use it?
Preparation
1.Prepare the wound per standard wound care protocol and debride when necessary.
2.PROMOGRAN® matrix may be used when visible signs of infection are present in the
wound area only when proper medical treatment addresses the underlying cause.
22 — Section
Product Information
3.Hydrate with saline for wounds with low or no exudate.
Application
1.Apply directly to wound, covering the entire wound bed. PROMOGRAN® matrix
forms a gel on contact with exudate or through saline hydration.
2.Cover PROMOGRAN® matrix with a secondary dressing to maintain a moist
wound healing environment.
3.Choose a suitable secondary dressing depending on level of exudate.
4. The biodegradable gel is naturally absorbed over time.
CODE
SIZE
EACHES PER
CARTON
M772028
28cm2
10
M772123
123cm2
10
References:
1. Lazaro-Martinez et al. Randomized comparative trial of a collagen/oxidized
regenerated cellulose dressing in the treatment of neuropathic diabetic
foot ulcers. F.R. Circ. Esp.2007, 82(1), 27-31
2. Veves A et al. A randomized, controlled trial of Collagen/ORC vs. standard
treatments in the management of diabetic foot ulcers. Arch Surg
2002;137:822-827
3. Snyder. Sequential therapies and advanced wound care products as a
standard practice in the home care setting. Home health abstract for SAWC,
San Diego, April 2008 (presentation at the J&J satellite symposium)
4. Ghatenekar O. Willis. M. Persson U. Health Economics. ‘Cost effectiveness
of treating deep diabetic foot ulcers with collagen/ORC in four European
countries’. J Wound Care, Vol 11, No2. Feb 2002
5. Cullen B, Smith R, McCulloch E, Silcock D, Morrison L. Mechanism of action of
Collagen/ORC, a protease modulating matrix for treatment of diabetic foot
ulcers. Wound Rep Regen 2002;10:16-25.
6. Cullen B. The role of oxidized regenerated cellulose/collagen in chronic
wound repair. Part 2. Ostomy Wound Manage.2002 Jun;48(6 suppl):8-13
7.Smeets R, Ulrich D, Unglaub F, Woltje M, Pallua N. Effect of oxidized
regenerated cellulose/collagen matrix on proteases in wound exudate of
patients with chronic venous ulceration. Int Wound J 2008;5:195-203.
8.Hart J, Silcock D, Gunnigle S, Cullen B, Light ND, Watt PW. The role of
oxidized regenerated cellulose / collagen in wound repair: effects in vitro
on fibroblast biology and in vivo in a model of compromised healing. Int J
Biochem Cell Biol 2002;34:1557-1570.
9. Cullen, B., Jenkins, E., Gibson, M., McInroy, L., Clark R. The effect of collagen
based wound dressings on bacterial growth. SAWC, Dallas, 2009.
10.Cullen et al. Use of oxidized regenerated cellulose in facilitating wound
healing. Presented at EWMA 2010
Section
— 23
PROMOGRAN PRISMA
®
PROMOGRAN PRISMA® Matrix Wound Dressing
WHAT IS IT?
PROMOGRAN PRISMA® matrix is a freeze-dried composite of collagen, oxidised
regenerated cellulose (ORC) and silver.
Made from a matrix of 55% collagen, 44% ORC and 1% ORC/Silver
•
PROMOGRAN PRISMA® matrix is designed to ‘kick start’ the healing process while
providing protection from infection.1-2
In the presence of exudate PROMOGRAN PRISMA® matrix transforms into a soft
and conformable, biodegradable gel; this allows contact with all areas of the
wound.
With PROMOGRAN PRISMA® matrix see stalled wounds close: faster,3-5 cost
effectively,3,6 while providing protection from infection. 7-8
HOW DOES IT WORK?
PROMOGRAN PRISMA® matrix binds and inactivates proteases such as MMPs
and Elastase to help rebalance the wound microenvironment, while providing
low level silver to help prevent infection.1-2
By reducing activity of both MMPs and Elastase, wound surface area can be reduced.
INDICATIONS:
PROMOGRAN PRISMA® matrix is indicated for the management of all wounds
healing by secondary intent which are clear of necrotic tissue including:
Diabetic ulcers
Venous ulcers
Pressure ulcers
Ulcers caused by mixed vascular aetiologies
PROMOGRAN PRISMA® matrix has known haemostatic properties.
PROMOGRAN PRISMA® matrix can be used under compression therapy.
•
•
•
•
•
How do I use it?
Preparation
1.Prepare the wound per standard wound care protocol and debride when necessary.
2.PROMOGRAN PRISMA® matrix may be used when visible signs of infection are
present in the wound area only when proper medical treatment addresses the
underlying cause.
24 — Section
Product Information
3.Hydrate with saline for wounds with low or no exudate.
Application
1.Apply directly to wound, covering the entire wound bed. PROMOGRAN PRISMA®
matrix forms a gel on contact with exudate or through saline hydration.
2.Cover PROMOGRAN PRISMA® matrix with a secondary dressing to maintain a
moist wound healing environment.
3.Choose a suitable secondary dressing depending on level of exudate.
4. The biodegradable gel is naturally absorbed over time.
CODE
SIZE
EACHES PER
CARTON
PS2028
28cm2
10
PS2123
123cm2
10
References:
1. Cullen B et al. ORC/Collagen Matrix Containing Silver Controls Bacterial
Bioburden while Retaining Dermal Cell viability. Poster presented at EWMA
Prague, May 2006
2. Gregory S et al. The Ability of ORC/Collagen containing silver to reduce
Bioburden and retain dermail Cell Viability. Johnson & Johnson Wound
Management, Gargrave, UK. Poster presented at ETRS Stuttgart, September
2005
3. Nisi G et al. Use of protease-modulating matrix in the treatment of pressure
sores. Chir Ital 2005;57:465-8
4. Lazaro-Martinez et al. Randomized comparative trial of a collagen/oxidized
regenerated cellulose dressing in the treatment of neuropathic diabetic foot
ulcers. F.R. Circ. Esp.2007, 82(1), 27-31
5. Veves A et al. A randomized, controlled trial of PROMOGRAN® (a collagen/
oxidised regenerated cellulose dressing) vs. standard treatments in the
management of diabetic foot ulcers. Arch Surg 2002;137:822-827
6. Cullen, B., Domnelly, T., Rennison, T. Can excessive levels of silver be
detrimental to healing? SAWC, San Diego, 2008
7. Gregory S et al. The Ability of ORC/Collagen containing silver to reduce
Bioburden and retain dermail Cell Viability. Johnson & Johnson Wound
Management, Gargrave, UK. Poster presented at ETRS Stuttgart, September
2005
8. Cullen, B., Nisbet, L., Gibson, M., Lanzara, S., Zamboni, P. A clinical study
examining the effect of ORC/Collagen/Silver-ORC on healing and wound
biochemistry. SAWC, Dallas, 2009
Section
— 25
FIBRACOL PLUS
®
FIBRACOL® Plus Collagen Alginate Dressing
WHAT IS IT?
FIBRACOL® Plus Dressing combines the structural support of collagen with the
exudate management of alginate. FIBRACOL® Plus Dressing is composed of 90%
collagen and 10% alginate.
HOW DOES IT WORK?
The combination of collagen and alginate provides the versatility needed when
addressing a variety of wound types and a wide range of exudate levels (from
low to high).
FIBRACOL® Plus Dressing maintains a moist wound environment which is
conducive to granulation tissue formation and epithelialisation that enables
healing to proceed optimally.
INDICATIONS:
FIBRACOL® Plus Dressing is indicated for the management of exuding wounds
including:
Full-thickness and partial-thickness wounds
Pressure ulcers
Venous ulcers
Ulcers caused by mixed vascular etiologies
Diabetic ulcers
Second-degree burns
Donor sites and other bleeding surface wounds
Abrasions
Traumatic wounds healing by secondary intention
Dehisced surgical incisions
•
•
•
•
•
•
•
•
•
•
How do I use it?
Application
Cut FIBRACOL® Plus Dressing to the size of the wound with sterile scissors
Apply directly to the wound, covering the entire wound bed. FIBRACOL® Plus
Dressing forms a gel on contact with exudate or through saline hydration
Pack deep wounds loosely
•
•
•
26 — Section
Product Information
•For minimally exudating wounds, apply to a moistened wound bed to initiate
gel-forming process
•Cover with an appropriate secondary dressing to maintain a moist woundhealing environment
CODE
SIZE
EACHES PER
CARTON
2981
5.1cm x 5.1cm
12
2982
10cm x 11cm
12
2983
10.2cm x 22.2cm
6
2984
1cm x 1cm x 40cm (rope)
6
Section
— 27
TIELLE
®
TIELLE® Hydropolymer FOAM dressings
WHAT IS IT?
The TIELLE® Family has a unique design compared to ordinary foams; it
contains LiquaLock® technology, which cleverly retains exudate while also
letting moisture vapour pass through the dressing, helping to provide an
optimal moist wound healing environment.
Managing exudate better helps wounds heal faster and increases patient
comfort. For instance, in a clinical evaluation of 6993 patients TIELLE®
dressings were proven to be clinically efficacious in all wound types studied,
with 95% healing or improvement after 4 weeks of treatment, and improved
the patients’ quality of life.1
The TIELLE® Family comes in a wide range of sizes, shapes and absorbencies,
allowing you to find a dressing that suits your patients’ needs.
HOW DOES IT WORK?
Comfort for the wound
As exudate is absorbed by the dressing, it is designed to expand and
conform to the contours of the wound bed, which helps minimize exudate
build-up and the chance of maceration. The super absorbent layer of
TIELLE® Plus and TIELLE® Max absorbs up to 30x its own weight.5
Under normal use, the LiquaLock® technology locks fluid into the cell walls,
which means reduced potential for it to be released back into the wound2-4
The vapour-permeable backing allows moisture vapour to transfer through
the back of the dressing, allowing for absorption of additional exudate
TIELLE dressings do not gel or disintegrate- for easy removal and less pain
•
•
•
•
Comfort for you
•The adhesive dressings allow repositioning as needed on initial application,
yet stays were it is placed
•The non-adhesive dressings are cut-able and can be used for all levels of
exudate
Comfort for the patient
TIELLE® and TIELLE® Plus control leakage and odour for better patient
quality of life1,5
•
28 — Section
Product Information
–The adhesive variants require no secondary dressing or tape but still
allow for skin-friendly removal , due to the unique water-deactivated
adhesive
–The polyurethane adhesive and backing provide a bacterial and
contaminant barrier6
–Adhesive dressings can be worn in the shower
Comfort for the budget
Cost-effective wound care relies on reducing the time to healing, but also
on reducing the number of dressing changes needed
The superior fluid handling7 of TIELLE® Plus and TIELLE® Max means fewer
dressing changes
All TIELLE® Family dressings provide a wear time of up to seven days
depending on wound condition and exudate level
•
•
•
INDICATIONS:
TIELLE® Family dressings are indicated for:
pressure ulcers, diabetic ulcers, lower extremity ulcers, donor sites, post-surgical
or traumatic wounds.
TIELLE® dressings are suitable for use under compression bandaging.
TIELLE® range of dressings are indicated for the management of different levels
of exuding wounds.
TM
TM
TM
TIELLE® Family
TM
Exudate level
Adhesive
Cut-able
✔
—
✔
—
✔
—
✔
—
✔
—
—

TM
TIELLE®
TM
TM
TM
TIELLE® Sacrum
TM
TM
TM
TIELLE® Plus
TM
TM
TM
TIELLE Plus Sacrum
®
TM
TM
TIELLE Plus Heel
®
TIELLE® Max
TM
TM
Section
— 29
TIELLE
®
How do I use it?
Application
Dressing Change
TIELLE® / TIELLE® PLUS
Prepare the wound
according to wound
management protocol.
Ensure surrounding
skin is dry.
For fragile or friable
skin just apply sterile
water or saline to a
swab.
TIELLE® MAX
Prepare the wound
according to wound
management protocol.
If required, cut TIELLE®
MAX to the desired
size before removing
the backing paper.
TIELLE® MAX
Change dressing when
fluid is present at the
edges of the dressing.
Select the appropriate
TIELLE® dressing,
allowing hydropolymer
center to overlap the
wound edge by 1cm.
Lift one corner and
apply the swab to
the underside of the
dressing as it is gently
peeled back, breaking
the adhesive seal.
Assure all edges are completely
sealed
TIELLE® MAX
Leave at least 1cm
border overlapping the
wound edge.
TIELLE® MAX
On removal, pinch one
corner of the dressing
and carefully peel back.
Once applied,
petroleum jelly
smoothed over
the edges of the
adhesive dressing
gives additional water
repellency if required.
Dressings may be left
in place for up to 7 days.
TIELLE® MAX
Remove backing paper
and position this side
of the dressing over
the wound site.
TIELLE® MAX
Dressings may be left
in place for up to 7 days.
30 — Section
Product Information
Please note: TIELLE® can be
used in conjunction with
dressings such as SILVERCEL®
or PROMOGRAN PRISMA®
Matrix.
Please note: TIELLE® can be
used in conjunction with
dressings such as SILVERCEL®
or PROMOGRAN®
CODE
SIZE
EACHES PER
CARTON
TIELLE®
MTL100
7cm x 9cm
10
MTL101EN
11cm x 11cm
10
MTL102
15cm x 20cm
5
MTL103
18cm x 18cm
5
MTL105
15cm x 15cm
10
18cm x 18cm
5
10
TIELLE® SACRUM
MTL104
TIELLE PLUS
®
MTP501
11cm x 11cm
MTP502
15cm x 20cm
5
MTP505
15cm x 15cm
10
20cm x 26.5cm
5
15cm x 15cm
10
10
TIELLE® PLUS HEEL
MTP508
TIELLE® PLUS SACRUM
MTP506
TIELLE® MAX
MTP701
11cm x 11cm
MTP702
15cm x 20cm
5
MTP705
15cm x 15cm
10
References:
1.Evaluation of TIELLE® hydropolymer dressings in the management of chronic
exudating wounds in primary care. Diehm C., Lawall, H. Int. Wound J. 2005,
2(1):26-35.
2. A non-comparative multicentre clinical evaluation of a new hydropolymer
adhesive dressing. Taylor, A., Lane, C., Walsh, J., Whittaker, S., Ballard, K., Young,
S.R. J Wound Care 1999, 8(10):489-492.
3.Hydropolymer dressings in the management of wound exudate. Carter, K. Br.
J. Comm. Nursing 2003, 8(9) Suppl: 10-16.
4. The Evaluation of Fluid Retention in Foam Dressings, Foster S. and Mistry, P.,
Wounds UK 2010.
5. Clinical evaluation of TIELLE® Plus dressing in the management of exudating
chronic wounds. Schulze, H.J. Br. J. Comm. Nursing 2003, 8(11):18-22.
6. Boothman S. et al, Bacterial Barrier characteristics of TIELLE® to the proposed
CEN Test Method, Poster 2002.
7. An evaluation of wound dressings to manage wound exudate and conform
to the wound bed, Cullen B. et al, poster SAWC 2010.
Section
— 31
ADAPTIC TOUCH
®
WHAT IS IT?
ADAPTIC TOUCH® Non-Adhering Silicone Dressing is non-adherent and flexible
with an open mesh comprised of cellulose acetate coated with soft tack silicone.
It is designed to stay in place and to be atraumatic during dressing change.1,2
HOW DOES IT WORK?
Soft tack silicone assists dressing application, conformability and
atraumatic removal 1,2
Advanced mesh design means minimized risk of exudate pooling and
secondary dressing adherence to the wound 1,2
•
•
•Ask us about overall cost savings compared to top silicone primary contact
layer brands
INDICATIONS:
ADAPTIC TOUCH® Non-Adhering Silicone Dressing is indicated for use in the
management of dry to heavily exuding, partial and full-thickness chronic wounds
including:
Venous ulcers
Decubitus (pressure) ulcers
Diabetic ulcers
Donor sites
First and second degree burns
It is also suitable for use, under medical supervision, with negative pressure wound
therapy (NPWT).1
•
•
•
•
•
•
How do I use it?
Dressing selection
Select a size of ADAPTIC TOUCH® that is larger than the wound to ensure
dressing can be applied to intact skin surrounding the wound margins
ADAPTIC TOUCH® can be cut to size and the dressing will not unravel or
shed fibres
If more than one piece of ADAPTIC TOUCH® is required, ensure dressings
overlap to avoid secondary dressing adherence to the wound; however
overlap should be minimized to prevent occlusion of holes
Dressing application
Prepare the wound according to wound management protocol
•
•
•
•
32 — Section
Product Information
•Ensure skin surrounding the wound is dry
•Remove protective films from dressing
•Place ADAPTIC TOUCH dressing directly over the wound and smooth in
®
place around the wound
•Cover with an appropriate semi-occlusive secondary dressing, e.g. TIELLE
®
Hydropolymer Dressing
CODE
SIZE
EACHES PER
CARTON
10
TCH501
5cm x 7.6cm
TCH502
7.6cm x 11cm
10
TCH503
12.7cm x 15cm
10
TCH504
20cm x 32cm
5
References:
1. Stephens S. et al., Evaluation of a non-adhering silicone wound contact
dressing with optimised design for the management of dry to heavily
exuding wounds (in vitro/vivo). Poster, Wounds UK 2010
2. Stephens S. et al., Evaluation of the properties of a non-adhering silicone
primary wound contact layer (in vitro). Poster, Wounds UK 2010
Section
— 33
ADAPTIC
®
ADAPTIC® Non-Adhering dressing
WHAT IS IT?
ADAPTIC® Non-Adhering Dressing is a primary dressing made of knitted cellulose
acetate fabric, impregnated with a specially formulated petrolatum emulsion.
It is designed to help protect the wound while preventing the dressing from
adhering to the wound1 and to minimize pain and trauma upon removal.2,3
HOW DOES IT WORK?
ADAPTIC® Non-Adhering Dressing protects the fragile tissue in wounds by its
unique structure with small mesh size, preventing tissue adherence to either
the ADAPTIC® dressing or the secondary dressing on top of it
•
•The mesh allows for exudate to easily pass through to the secondary dressing
used, preventing maceration of the wound surface
®
Non-Adhering Dressing to be
cut to wound size without unravelling or shredding
ADAPTIC® Non-Adhering Dressing removes cleanly from the wound,
minimizing trauma and pain 2,3
•Knitted cellulose acetate fabric allows ADAPTIC
•
INDICATIONS:
ADAPTIC® Non-Adhering Dressing is indicated for dry to highly exuding wounds
where adherence of dressing and exudate is to be prevented, including:
First and second degree burns
Abrasions, grafts
Venous ulcers
Pressure ulcers
Nail extractions
Eczema, staples
Surgical incisions
Lacerations
Reconstructive procedures
Suture lines
•
•
•
•
•
•
•
•
•
•
How do I use it?
Prepare the wound according to wound management protocol
Ensure skin surrounding the wound is dry
Cut ADAPTIC® Non-Adhering Dressing to size if required and place directly on
the wound
Cover with a sterile secondary dressing of your choice depending on the
amount of wound exudate
ADAPTIC® Non-Adhering Dressing may be left in place for several days
depending upon amount of exudate
•
•
•
•
•
34 — Section
Product Information
CODE
SIZE
EACHES PER
CARTON
2012
7.6cm x 7.6cm
50
2013
7.6cm x 20.3cm
3x36
2014
7.6cm x 40.6cm
36
2015
7.6cm x 20.3cm
24
2019
12.7cm x 22.9cm
12
References:
1.Hollinworth H and Collier M. Nurses’ view about pain and trauma at dressing
changes: results of a national survey. J Wound Care 2000 : 9 : 369-73
2.EWMA Position Document: Pain at wound dressing changes. European
Wound Management Association, 2002
3. Terrill PJ and Varughese G. A comparison of three primary non-adherent
dressings applied to hand surgery wounds. J Wound Care 2000 : 9 : 359-63
Section
— 35
ADAPTIC DIGIT
®
WHAT IS IT?
ADAPTIC® DIGIT Non-Adhering Digit Dressing is made of a unique tacky
silicone coated open-knit cellulose fabric with a double-coiled tubular
bandage that is specifically designed for dressing fingers and toes
ADAPTIC® DIGIT is comfortable, convenient to apply and easy to remove for
mild to severe digit injuries
•
•
HOW DOES IT WORK?
No applicator or scissors are needed making it easy and simple to use:
•ADAPTIC
DIGIT is conformable and non-bulky, therefore allowing maximum
digit flexibility
ADAPTIC® DIGIT removes cleanly from the wound, minimizing trauma and
pain1
®
•
INDICATIONS:
ADAPTIC® DIGIT Dressing is indicated to manage a range of mild to severe
digit injuries.
How do I use it?
1.Remove shiny backing strip.
2.Place primary non-adhering layer over digit tip and gently smooth to cover any
broken skin.
3.Roll down lower ring of tube bandage over primary strip (and secondary dressing if
required). Follow this with the top ring to form a double layered tube for protection.
36 — Section
Product Information
CODE
SIZE
EACHES PER
CARTON
MAD003
Small 2cm Ø
10
MAD013
Medium 2.4cm Ø
10
MAD023
Large 2.8cm Ø
10
MAD042
Extra Large 3cm Ø
10
2.8cm Ø
10
ADAPTIC® Digit
ADAPTIC® Digit Toe
MAD062
Reference:
1. Whittaker S. A dressing for the occasion? A comparative trial of two dressings for digit injuries. Professional Nurse Magazine, 1994 Aug. 729-732
Section
— 37
NU-DERM ALGINATE
®
NU-DERM® Alginate WOUND dressing
WHAT IS IT?
NU-DERM® Alginate Wound Dressing is a sterile, non-woven pad consisting of
high G (guluronic acid) alginate and carboxymethylcellulose (CMC) fibre.
NU-DERM® Alginate Wound Dressing is designed to be fast gelling and to allow
intact removal.
HOW DOES IT WORK?
High absorbent capacity1, for fewer dressing changes
Absorbs 20x its weight in exudate
•
•
•Quickly forms a hydrophilic gel at the wound surface to help create a moist
wound healing environment
•Conformable when moist; less disruptive to new tissue
•Maintains tensile strength when wet for intact dressing removal; minimizes
1
the need the need for wound irrigation
•Can be cut or folded to accommodate wound bed
INDICATIONS:
NU-DERM® Alginate Wound Dressing is indicated for the management of
moderate to heavily exuding chronic wounds and to control minor bleeding in
superficial acute wounds.
Chronic wounds: Pressure ulcers, leg ulcers, venous stasis ulcers, diabetic ulcers
and arterial ulcers.
Superficial acute wounds: Abrasions, lacerations, donor sites and postoperative wounds.
How do I use it?
Application
Select a size of NU-DERM® Alginate Wound dressing that is slightly larger than
the wound.
1.Cut (using clean scissors), or fold the dressing to fit the wound. Loosely pack deep
wounds, ensuring the dressing does not overlap the wound margins.
2.For heavily exuding wounds, apply to wound bed directly. For wounds with
minimal exudate, apply to moistened wound bed.
3.Cover and secure NU-DERM® Alginate wound dressing with a non-occlusive or
semi-occlusive secondary dressing.
38 — Section
Product Information
CODE
SIZE
EACHES PER
CARTON
Cartons
Per Box
AWD112
2.5cm x 30.5cm Rope
5
5 (25 eaches)
AWD202
5cm x 5cm
10
5 (50 eaches)
AWD404
10cm x 10cm
10
5 (50 eaches)
AWD408
10cm x 20cm
5
5 (25 eaches)
Reference:
1. Data on file
Section
— 39
NU-DERM HYDROCOLLOID
®
WHAT IS IT?
NU-DERM® Hydrocolloid Dressing is a sterile hydrocolloid wound dressing designed
to maintain a moist wound environment. The NU-DERM® Hydrocolloid Wound
Dressings consist of a wound contact layer of hydrocolloid and come in a variety of
shapes and sizes. The top layer is either a semi-permeable polyurethane film (Border
and Thin), or a film-coated polyurethane foam (Standard).
The Border product is conformable, has a top layer of low-friction film, and has
bevelled edges all around the product - the border itself is a continuation of the
skin-friendly hydrocolloid adhesive material
•
•The Standard product has a top layer of foam, rounded corners, and is uniform
in thickness
•The semi-transparent Thin product, which is conformable and has a top layer of
low-friction film, allows close and easy monitoring of the wound bed without
dressing removal
HOW DOES IT WORK?
Helps maintain a moist wound healing environment and encourages autolytic
debridement, thus enabling granulation to proceed under optimum conditions
Designed to protect low risk wounds against bacterial contamination*
The dressing material interacts with wound exudate to form a soft gel - due
to the matrix formulation of the hydrocolloid material, most of the gel is
removed together with the dressing, resulting in little or no damage to the
newly formed tissue
The dressings are waterproof and remain in place during showering
•
•
•
•
INDICATIONS:
NU-DERM® Border and NU-DERM® Standard are primarily indicated for the
management of light to moderately exuding pressure sores and leg ulcers
NU-DERM® Thin is primarily indicated for the management of superficial dry/
lightly exuding wounds, post-operative wounds, and superficial wounds and
abrasions; however it is also useful on small wounds towards the end of the
healing phase
•
•
How do I use it?
Application
1.Remove the large part of the protective backing paper from the dressing.
40 — Section
Product Information
2. Apply the exposed part of the dressing, centering it over the wound bed.
3. Remove the small part of the protective backing paper from the dressing and apply.
4.Ensure all edges are smooth and firmly secured.
CODE
SIZE
DRESSINGS
PER TRAY
TRAYS
PER CASE
10
10 (100 eaches)
NU-DERM® Hydrocolloid Border Thin
HCT101
10cm x 10cm
NU-DERM® Hydrocolloid Standard (foam backing)
HCF204
10cm x 10cm
5
10 (50 eaches)
HCF208
20cm x 20cm
5
4 (20 eaches)
NU-DERM® Hydrocolloid Border
HCB102
5cm x 5cm
20
5 (100 eaches)
HCB204
10cm x 10cm
10
16 (160 eaches)
HCB106
15cm x 15cm
5
4 (20 eaches)
10
6 (60 eaches)
5
4 (20 eaches)
NU-DERM® Hydrocolloid Border Elbow/Heel
HCH207
8cm x 12cm
NU-DERM® Hydrocolloid Border Sacrum
HCS100
15cm x 18cm
* Consult a physician prior to using NU-DERM® Hydrocolloid Dressings on lesions caused by tuberculosis, syphilis or deep fungal infections, cancer and wounds at
high risk of infection
Section
— 41
NU-GEL
®
HYDROGEL WITH ALGINATE
WHAT IS IT?
NU-GEL® Hydrogel is a transparent hydro-active amorphous gel containing sodium
alginate that gently and effectively rehydrates necrotic tissue and fibrinous
slough, and is designed to create an ideal moist wound healing environment for
granulating and epithelising wounds.1
HOW DOES IT WORK?
NU-GEL® Hydrogel gently and effectively provides rehydration of the wound for
autolytic debridement, significantly decreasing the amount of necrotic tissue
and slough2
•
•The
alginate increases the absorptive capacity of NU-GEL® Hydrogel and
improves the ability to control wound exudate1 for longer wear time1
NU-GEL® Hydrogel can be applied to the wound with a simple one-handed
technique
•
INDICATIONS:
NU-GEL® Hydrogel is indicated for debridement and desloughing of wounds
together with the management of chronic wounds throughout all stages of the
healing process including:
dry necrotic wounds
soft, sloughy wounds
granulating/epithelialising wounds
•
•
•
Precaution
NU-GEL® Hydrogel contains propylene glycol which might cause irritation or
sensitisation in a small number of patients.
If such reactions are noted, use of NU-GEL® Hydrogel should be discontinued.
If wound infection is present, appropriate antimicrobial therapy should be initiated
- the use of NU-GEL® Hydrogel may be continued under medical supervision.
How do I use it?
Application
NU-GEL® Hydrogel can be applied to the wound with a simple one-handed
technique.
42 — Section
Product Information
•Hold the concertina pack in one hand and direct NU-GEL
Hydrogel into the
wound site by applying and even pressure to the base of the concertina pack with
thumb or heel of hand. The nozzle tip should be held clear of the wound surface
Apply NU-GEL® Hydrogel to the whole wound to a depth of at least 5mm
Cover with a suitable secondary dressing appropriate to the level of exudate
Any unused gel should be discarded
®
•
•
•
CODE
SIZE
tubes per
carton
cartons
per box
MNG415
15g
10
4 (40 eaches)
MNG425
25g
6
4 (24 eaches)
References:
1. A study of two hydrogels used in the management of pressure sores, T.
Young et al. Published in the Proceedings of the 6th European Conference
on Advances in Wound Management. Conference held in Amsterdam, 1-4th
October 1996
2. Autolytic debridement of chronic wounds using a Hydrogel (NU-GEL®).
Vanscheidt V, Hasse G & Wunsch N. Vasomed: 9, Jan. 1997; 26-34
Section
— 43
NU-GEL WOUND DRESSING
®
WHAT IS IT?
NU-GEL® Wound Dressing is a hydrogel dressing consisting of polyvinyl pyrrolidone
in water.
The gel is supported by a fusible fibre scrim and protected on both sides by
polyethylene film.
HOW DOES IT WORK?
NU-GEL® Wound Dressing provides a moist environment conductive for optimal
wound healing. It protects against dehydration, bacterial contamination and
absorbs exudate from the wound.
•Helps
maintain moist wound environment which encourages autolytic
debridement
Designed to protect against dehydration and provide a physical barrier against
bacterial contamination
Naturally cooling & soothing to help reduce patient pain and discomfort
Absorbs exudate which helps reduce pooling of fluid
Remains intact; does not break down
Translucent - allows monitoring of wound without disturbing the dressing
Versatile - can be cut to size of the wound
•
•
•
•
•
•
INDICATIONS:
NU-GEL® Wound Dressing is indicated for first and second degree burns, partial
thickness wounds, decubitus ulcers, donor sites, severe sunburn, superficial injuries
or secreting dermal lesions, superficial lacerations, cuts and abrasions, incisions,
skin reactions to oncology procedures, dermabrasions and other dermatologic
procedures such as facelifts and other plastic surgery procedures.
How do I use it?
Application
1.Cleanse the wound of excess exudate.
2.Cut the dressing to size with sterile scissors if necessary.
3.Remove the thicker protective plastic film from the dressing and apply the
exposed side of the dressing to the wound.
4.Secure the dressing with tape or cover with gauze and tape down.
5.The dressing may be refrigerated (minimum 1 hour) to enhance the cooling effect.
44 — Section
Product Information
6.The dressing may be left in place up to 72 hours depending upon the amount of
exudate.
Allowing the top plastic film to remain in place retards drying of the dressing.
However, if it is desired to apply multiple dressings or to use the dressing to fill a
wound cavity, then the top plastic film may be removed. Then a secondary semiocclusive dressing such as BIOCLUSIVE® Transparent Dressing may be applied.
CODE
SIZE
EACHES PER
CARTON
2497
9.5cm x 9.5cm
5
2498
15.2cm x 20.3cm
5
Reference:
1.Multicentre evaluation of NU-GEL® dressing in full-thickness chronic wounds of the lower extremities Morton I. Altman and Gerit TI. Mulder, California College of
Podiatric Medicine, San Francisco, California, USA; and Wound Healing Institute, Aurora, Colorado, USA
Section
— 45
BIOCLUSIVE
®
BIOCLUSIVE® Transparent dressing
WHAT IS IT?
BIOCLUSIVE® Transparent Dressings are made from thin, transparent
polyurethane film and can be used on Wound Care and Access Devices.
BIOCLUSIVE® Dressings may also be used as secondary dressings with
PROMOGRAN®, PROMOGRAN PRISMA®, NU-GEL® Hydrogel with Alginate and
NU-GEL® Wound Dressing for wounds with low levels of exudate.
HOW DOES IT WORK?
•Allows oxygen vapour transfer and helps maintain a moist wound-healing
environment1
Permits continuous observation
Works as a physical bacterial/viral barrier and protects site from external
contamination1
Helps secure catheters, reducing mechanical irritation
Minimizes skin irritation1 and helps protect fragile tissue1
Three-step application, forgiving adhesive for a controlled and waste-free
application
•
•
•
•
•
INDICATIONS:
BIOCLUSIVE® Transparent Dressings should be used under Health Care
Professional direction for the following indications; low exuding wounds where
observation and protection are desired e.g. General Wound Care, skin biopsies,
donor sites, superficial partial thickness burns and surgical incisions. They are
also indicated to aid in securing peripheral IVs and Central Venous Catheters.
How do I use it?
Application
1.Ensure site is clean and dry.
2.Remove center backing liner.
3.Apply dressing over site. One at a time, peel away side backing papers while
smoothing film onto skin.
46 — Section
Product Information
CODE
SIZE
DRESSINGS
PER CARTON
CARTONS
PER CASE
2460
3.8cm x 3.8cm
100
4 (400 eaches)
2461
5.1cm x 7.6cm
100
4 (400 eaches)
2463
10.2cm x 12.7cm
50
4 (200 eaches)
2465
12.7cm x 17.8cm
20
5 (100 eaches)
2467
10.2cm x 25.4cm
20
6 (120 eaches)
2469
20.3cm x 25.4cm
10
8 (80 eaches)
Reference:
1. Thomas S (1990) Semipermeable Film Dressings. In: Wound Management and Dressings. London. The Pharmaceutical Press. Pages 25-34
Section
— 47
48
49
50
51
Customer Care / Service à la cilentèle
Telephone (english) 1-877-216-0187
Téléphone (français) 1-877-280-4468
Fax
1-866-523-5157
Email: customercareca@systagenix.com
SYS/CAN/561/0611
Head Office / Siège social
Telephone
1-866-462-1488
© Systagenix Wound Management 2011. Brands marked with ® or ™
are trademarks of Systagenix. All other products referenced herein are
acknowledged to be trademarks of their respective owners.
www.systagenix.ca

product reference guide advanced wound care

Transcription

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