Replicare® Thin Hydrocolloid Dressings

REPLICARE ™ Ultra is an advanced hydrocolloid dressing which offers optimal exudate management and increased absorption capability.

Features and Benefits

REPLICARE ™ Ultra's improved design provides better evaporation through an adaptable polyurethane top film that regulates moisture vapor transmission rate. This allows excess moisture to evaporate while maintaining the proper moist wound environment.
The top film is waterproof, easy to clean and aids in the prevention of bacterial contamination.
Unique micro-thin edges and enhanced adhesive offer better adherence, reduced leakage potential and chance of edge roll.
REPLICARE ™ Ultra can remain in place for up to 7 days for convenience, fewer dressing changes and a reduction in nursing costs.
In addition, it is offered in a sacral design to conform to the difficult to dress sacral region.


Indications

For Healthcare Professional applications, REPLICARE ™ Ultra dressings may be used in Stage I through Stage IV wounds with light to moderate exudate, such as:

• Pressure Ulcers
• Leg Ulcers
• Superficial Burns
• Superficial Wounds
• Donor Sites
• Skin Abrasions
• Partial Thickness Burns

Precautions

During the body's normal healing process, unnecessary material is removed from the wound, which will make the wound appear larger after the first few dressing changes. If the wound continues to get larger after the first few dressing changes, discontinue use and consult a healthcare professional.

Should any signs of irritation (reddening, inflammation), maceration (over-hydration of the skin), hypergranulation (excess tissue) or sensitivity (allergic reactions) appear, discontinue use and consult a healthcare professional.

Do not use product if its packaging is open or damaged prior to use.

REPLICARE ™ Ultra is a single-use product. It should not be re-used.

Do not use product on (1) ulcers resulting from infection, such as tuberculosis, syphilis and deep fungal infections; (2) lesions in patients with acute vasculitis, such as periarteritis nodosa, systemic lupus erythematosus, and cryoglobulinemia; or (3) third degree burns.

REPLICARE ™ Ultra dressing must be removed prior to radiation therapy. 

Instructions for Use:

The following are designed to act as general guidelines and should only be used under the supervision of a healthcare professional.

Step 1
Cleanse the wound using sterile saline or a recommended commercial brand of wound cleanser such as Dermal Wound Cleanser. Gently pat dry the skin around the wound. SKIN-PREP ™ is recommended to protect the peri-wound skin.

Step 2
Choose a dressing that allows for ½” to 1” overlap of the wound.

Step 3
Remove the protective paper, exposing the adhesive surface. Use the clear, plastic handle to ensure aseptic application.

Step 4
Place the adhesive side to the wound and remove the handle.

Step 5
As REPLICARE ™ Ultra absorbs wound exudate, a gel is formed. When the gel reaches the upper film surface of the dressing, the dressing becomes white or opaque. Maximum absorbency is reached when the dressing becomes opaque and the exudate extends ½” from the edges of the dressing.

Changing the dressing:

Step 1
To remove the REPLICARE ™ Ultra dressing, lift one corner of the dressing and gently pull the dressing away from the wound. To aid in removal of the dressing, REMOVE ™ Adhesive Remover may be used.

Step 2
Gently cleanse the wound with tap water, sterile saline or recommended commercial brand wound cleanser such as Dermal Wound Cleanser.

Step 3
Follow instructions for applying a fresh dressing.

Replicare® Ultra Advanced Hydrocolloid Dressing

REPLICARE ™ Ultra is an advanced hydrocolloid dressing which offers optimal exudate management and increased absorption capability.

Features and Benefits

REPLICARE ™ Ultra's improved design provides better evaporation through an adaptable polyurethane top film that regulates moisture vapor transmission rate. This allows excess moisture to evaporate while maintaining the proper moist wound environment.

The top film is waterproof, easy to clean and aids in the prevention of bacterial contamination.

Unique micro-thin edges and enhanced adhesive offer better adherence, reduced leakage potential and chance of edge roll.

REPLICARE ™ Ultra can remain in place for up to 7 days for convenience, fewer dressing changes and a reduction in nursing costs.

In addition, it is offered in a sacral design to conform to the difficult to dress sacral region.

Indications

For Healthcare Professional applications, REPLICARE ™ Ultra dressings may be used in Stage I through Stage IV wounds with light to moderate exudate, such as:

• Pressure Ulcers
• Leg Ulcers
• Superficial Burns
• Superficial Wounds
• Donor Sites
• Skin Abrasions
• Partial Thickness Burns

Precautions

During the body's normal healing process, unnecessary material is removed from the wound, which will make the wound appear larger after the first few dressing changes. If the wound continues to get larger after the first few dressing changes, discontinue use and consult a healthcare professional.

Should any signs of irritation (reddening, inflammation), maceration (over-hydration of the skin), hypergranulation (excess tissue) or sensitivity (allergic reactions) appear, discontinue use and consult a healthcare professional.

Do not use product if its packaging is open or damaged prior to use.

REPLICARE ™ Ultra is a single-use product. It should not be re-used.

Do not use product on (1) ulcers resulting from infection, such as tuberculosis, syphilis and deep fungal infections; (2) lesions in patients with acute vasculitis, such as periarteritis nodosa, systemic lupus erythematosus, and cryoglobulinemia; or (3) third degree burns.

REPLICARE ™ Ultra dressing must be removed prior to radiation therapy. 

Instructions for Use:

The following are designed to act as general guidelines and should only be used under the supervision of a healthcare professional.

Step 1

Cleanse the wound using sterile saline or a recommended commercial brand of wound cleanser such as Dermal Wound Cleanser. Gently pat dry the skin around the wound. SKIN-PREP ™ is recommended to protect the peri-wound skin.

Step 2

Choose a dressing that allows for ½” to 1” overlap of the wound.

Step 3

Remove the protective paper, exposing the adhesive surface. Use the clear, plastic handle to ensure aseptic application.

Step 4

Place the adhesive side to the wound and remove the handle.

Step 5

As REPLICARE ™ Ultra absorbs wound exudate, a gel is formed. When the gel reaches the upper film surface of the dressing, the dressing becomes white or opaque. Maximum absorbency is reached when the dressing becomes opaque and the exudate extends ½” from the edges of the dressing.

Changing the dressing:

Step 1

To remove the REPLICARE ™ Ultra dressing, lift one corner of the dressing and gently pull the dressing away from the wound. To aid in removal of the dressing, REMOVE ™ Adhesive Remover may be used.

Step 2

Gently cleanse the wound with tap water, sterile saline or recommended commercial brand wound cleanser such as Dermal Wound Cleanser.

Step 3

Follow instructions for applying a fresh dressing.

Replicare Hydrocolloid Wound Dressings

REPLICARE ™ is a hydrocolloid dressing that contains a dense concentration of absorbent material in a thin dressing for superior absorption in the management of exuding wounds

Features

• REPLICARE's ™ cohesive properties keep the wound free of dressing residue.
• The one-handed application system will not stick to gloves.
• REPLICARE ™ has a film exterior that is waterproof and aids in prevention of bacterial contamination
• Top film can be wiped clean easily.

Benefits

• Dressing hugs curves better and stretches comfortably, with a combination of adhesion and elasticity for maximum wear time, reduced nursing time  and more cost effective use of materials.
• Bevelled edges help keep the dressing from sticking to clothing or bed linens, reducing the risk of leakage.

Indications

• REPLICARE ™ is indicated for
• Exudate absorption and the management of partial to full thickness wounds. Some typical wounds are:
• Ulcers (venous, arterial, diabetic)
• Pressure Sores
• Donor Sites
• Surgical Incisions
• Surgical Excisions
• Burns (1st and 2nd degree)
• Creation and maintenance of a moist wound environment. Moist wound environments have been established as optimal environments for the management of the wound.
• Provides physical separation between the wound and external environments to assist in preventing bacterial contamination of the wound.

Precautions
REPLICARE ™ is not indicated for the management of 3rd degree (full thickness) burns.

Instructions for Use:

Step 1

Cleanse the wound with saline solution or an appropriate wound cleanser. Cleanse and dry the periwound skin. If the periwound skin is particularly friable, it may be protected from trauma by applying SKIN-PREP ™.

Step 2

Choose a dressing large enough to cover the wound with 1” of overlap on all sides of the wound. Remove the printed backing paper exposing the adhesive surface.

Step 3

Center the dressing over the wound and press the edges firmly to the surrounding skin. Remove the small plastic application tab from the underside of the dressing and press all the sides firmly to the skin.

Renasys-G/P Gauze Dressing Kits

Description:
As part of the complete Smith & Nephew RENASYS Negative Pressure Wound Therapy System, the RENASYS gauze dressing kits help deliver customized therapy to even the most unique complexities of patients' wounds. The conformability and hydrophilic, non-adherent properties of the dressing kits make them well-suited for pain-sensitive areas, as well as irregularly shaped, tunneling and undermining wounds.

Renasys-G Wound Dressing Kits

Description:
RENASYS Drain Accessory Kits
Negative Pressure Wound Therapy Accessories

Renasys-F Foam Dressing Kits

Description:
Renasys-F Foam Dressing Kits.As a proven and familiar negative pressure wound therapy wound filler, Smith & Nephew's RENASYS foam dressings are an optimal choice for a wide variety of wound types. As the recognized industry standard, reticulated, open-cell, polyurethane foam dressings are easy to apply and the healing outcomes are proven by years of successful negative pressure use.

Renasys S-Canister

For use with the RENASYS* EZ Plus

Component List:

• Sealed, frosted canister
• With and without solidifier
• Overflow guard with tubing
• Canister tubing....See more

Renasys GO Canister

For use with the RENASYS GO

Component List:

• Sealed, frosted canister
• Solidifier
• Internal overflow guard
• Canister tubing...see more

Renasys Open Abdominal Solution & Foam Port Dressing Kits

Description:
Patients with critical open abdominal wounds require specialized treatment. When primary closure is not possible or repeat entries are necessary, you may require a comprehensive NPWT solution designed specifically for the open abdomen. The RENASYS AB supports the clinical goals of temporary abdominal closure in open abdomen patients, and works in conjunction with Smith & Nephew's RENASYS EZ Plus device, a powerful pump that is compatible with all RENASYS dressing kits.

Remove Adhesive Remover

REMOVE ™ Adhesive Remover

Features

• Aloe moisturizes and conditions the skin without greasiness.
• Gently cleans hydrocolloid, acrylic and rubber-based adhesive residues from the skin without irritation, discomfort or trauma.
• Applies easily and removes quickly with less need for reapplication.
• Non-irritating and non-sensitizing, even for ostomates and geriatric patients.
• Can be used anywhere there's a need for an adhesive dressing.
• Cost-effective and convenient single-use wipes; also available in bottles.
• Environmentally friendly and does not contain ozone-depleting chloro-fluorocarbons (CFCs).
• Laboratory and clinical safety data available.

Benefits

• Reduces adhesive trauma to the skin by thoroughly dissolving dressing, tape and appliance adhesives.
• Ideal for removing acrylic-based, rubber-based, and hydrocolloid-based residues from the skin.
• Helps maintain proper skin integrity while removing adhesive products and residues by reducing adhesive trauma.
• Gently cleans hydrocolloid, acrylic and rubber-based adhesive residues from the skin without irritation, discomfort or trauma.

Indications

• For the removal of adhesive devices.
• For the removal of adhesive residue from skin.
• Softens adhesive on tapes, films and appliances thereby minimizing trauma caused by adhesive removal.

Precautions
Use only as directed. For external use only. Do not apply to open wounds or mucous membranes. Avoid contact with eyes. Vapor may be harmful - use with adequate ventilation. Flammable. Do not use near heat, sparks or open flame. Keep out of reach of children. Avoid contact with painted/finished surfaces.

Instructions for Use:

Step 1
Hold saturated wipe, cotton applicator or gauze at the edge of tape or appliance.

Step 2
Squeeze gently so that fluid flows between skin and adhesive.

Step 3
Slowly pull tape and keep liquid at line of adhesive.

Step 4
Cleanse skin thoroughly with water and pat dry.

WARNINGS:
Use only as directed. For external use only. Do not apply to open wounds or mucous membranes. Avoid contact with eyes. Use with adequate ventilation. Keep out of reach of children.

If swallowed, do not induce vomiting. Call physician. In case of contact with eyes, flush with water.

Proguide™ Multi-Layer High-Compression Bandage System

Description:
A multi-layer, high-compression bandage system, incorporating the patented, revolutionary "Vari-Stretch" Technology. May be used to effectively manage venous leg ulcers on mobile or immobile patients as its elastic nature provides sustained, graduated levels of compression even if patient is at rest. Available in 3 sizes to accommodate different ankle circumferences. Each system pack contains the following: 1 ProGuide wound contact layer, 1 ProGuide #1 natural padding bandage and 1 ProGuide #2 outer compression bandage.

Profore Wound Contact Layer

PROFORE ™ WCL (Wound Contact Layer) is a 14cm x 20cm (5 1/2" x 8") dressing made of knitted viscose rayon.

Features & Benefits

• Non-adherent
• Non-adhesive
• Highly porous
• Highly conformable
• Cost-effective

Non-adherent
PROFORE ™ WCL has an open knit construction, which allows exudate to pass freely, while helping to limit the adherence of the dressing to the wound.

Non-adhesive
PROFORE ™ WCL is non-adhesive and therefore recommended for wounds surrounded by sensitive skin, such as venous leg ulcers.

Highly Porous
PROFORE ™ WCL is highly porous. This helps to prevent maceration of the peri-wound by preventing exudate pooling

Highly Conformable
The knitted construction of PROFORE ™ WCL makes the dressing highly conformable, providing comfort for the patient while helping to maintain a moist environment at the wound site.

Indications

PROFORE ™ WCL is indicated to act as a non-adherent interface between the granulating wound surface and conventional absorbent dressings. It can also be used in conjunction with PROFORE ™, PROFORE ™ LF and PROFORE ™ Lite, the Multi-layer Compression Bandage Systems.

PROFORE ™ WCL provides physical separation between the wound and external environments to assist in preventing bacterial contamination of the wound.

PROFORE ™ WCL aids in the creation and maintenance of a moist wound environment. Moist wound environments have been established as optimal environments for the management of the wound.

Precautions

If reddening or sensitization occurs, discontinue use and consult a healthcare professional.

Instructions for Use:


Caution: Do not use contents if pouch is opened or damaged.

• Use a clean technique to remove the wound contact layer from the pack and apply directly to the wound.
• Either side of the WCL can be placed in contact with the wound.
• Ensure ulcerated area is covered.
• Use extra WCL as required.

Profore..Lite Multi-Layer Compression Bandage System

PROFORE ™ Lite is a multi-layer, reduced-compression bandage system. Profore Lite is best used on ankle circumferences greater than 18cm or 7¼ inches (padded).

Features

• Each PROFORE ™ Lite Multi-Layer Compression Bandage System pack contains the following:
• One PROFORE ™ WCL -- Sterile Wound Contact Layer -- helps protect the wound site and help wick away exudate into the absorbent padding.
• One PROFORE ™ #1 absorbent padding bandage -- helps absorb exudate and helps protect bony prominences.
• One PROFORE ™ #2 light conformable bandage -- helps absorb exudate and helps prepare and sculpt the leg for the application of the pressure layers.
• One PROFORE ™ #4 cohesive compression bandage -- helps maintain continuous compression and keeps the system in place for up to a full week.

Benefits

• Effective Compression
• The PROFORE  Lite system is designed to deliver effective compression to successfully manage “mixed” aetiology leg ulcers. It may also be used to manage venous ulcers in patients with ABPIs between 0.6 and 0.8 who cannot tolerate the full compression of standard PROFORE  or PROFORE  LF.

Graduated Compression

• PROFORE ™ Lite provides higher pressure at the ankle, with decreasing pressure exhibited at the calf to help improve upward blood flow.

Sustained Compression

• For up to a full week after application, the PROFORE ™ Lite system maintains effective levels of compression.

Safety

• The PROFORE ™ Lite system helps ensure that bony prominences are padded for protection. The multi-layer system means that compression is built up gradually, thus minimizing the danger of application error.

Extended Weartime

• PROFORE ™ Lite has sufficient absorptive capacity to manage exudate for up to a full week without the need for reapplication. During the initial phase of therapy you may experience increased wound drainage as the compression system actively manages the edema. If strike through happens, remove the PROFORE ™ Lite system and apply another.

Cost-Effective

• Weekly dressing changes reduce nursing time and therefore help reduce costs associated with the management of venous leg ulcers.
• Convenient
• PROFORE ™ Lite system contains everything necessary for the application of effective, sustained, graduated compression therapy. PROFORE ™ Lite reduces preparation time, simplifies stock control and ensures that the correct components are always available.

Indications
PROFORE ™ Lite Multi-Layer Compression Bandage System is indicated for the management of "mixed" aetiology leg ulcers, where assessment has identified that the patient has some degree of arterial impairment which prevents the use of full compression (ABPI < 0.6).


Contraindications / Precautions


Contraindications
PROFORE ™ Lite should not be used on patients with an Ankle Brachial Pressure Index (ABPI) of less than 0.6, or on diabetic patients with advanced small vessel disease.


Precautions

• Should the patient develop pain or pale, cool or numb extremities distal to the dressing, the bandages should be promptly removed.
• Patients with a low ABPI and symptoms of arterial disease should be seen by a vascular specialist before application of compression.
• Care should be taken that very thin, bony, legs or legs with a prominent tibial crest should be protected with extra padding. The pressure under the bandage could bruise and harm unprotected / unpadded skin especially over bony parts of the leg.
• Compression bandaging to a leg which already has a partially blocked blood supply could completely stop the flow of blood into the leg and lead to the death of skin and muscle of the leg. Death of the muscle and skin of the leg could lead to further complications and possibly amputation of the leg.

Instructions for Use:


Step 1

• It is important to check the following
• Wash and dry the leg and apply a moisturizing cream to the unbroken skin.

Step 1a

• Apply the PROFORE ™ WCL dressing.
• Apply the PROFORE ™ WCL sterile wound contact layer directly over the wound surface. If the wound is larger than the contact dressing, PROFORE ™ WCL dressings may be purchased separately. The contact dressing will not stick to the surface of the wound, and when the wound begins draining after compression is applied, the drainage will pass through the contact dressing to be absorbed by the padding layer.

Step 2

• Apply PROFORE ™ #1 Absorbent Padding Bandage.
• With the foot flexed to 90 degrees, apply from the base of the toes to the knee using a simple spiral technique and 50% overlap. Do not apply tension. Ensure that bony prominences are padded so that the ankle measurement is greater than 18 cm or 7¼ inches. Any leftover padding may be applied directly over the wound to absorb more wound drainage.

Step 3

• Apply PROFORE ™ #2 Light Conforming Bandage
• Keeping the foot flexed to 90 degrees, apply PROFORE ™ #2 from the base of the toes to the knee using a simple spiral technique and 50% overlap. Ensure that the heel is completely covered. Secure at the top with a piece of tape or ask the patient to hold it in place.

Step 4

• Apply PROFORE ™ #4 Cohesive Compression Bandage.
• Keeping the foot flexed to 90 degrees, apply PROFORE ™ #4 from the base of the toes to the knee using a simple spiral technique with 50% overlap and 50% extension. Ensure that the heel is completely covered. PROFORE ™ #4 will adhere to itself and no tape is necessary to keep it in place. However, for added security, a piece of tape may be used for reinforcement.
• Please see Overview tab for Contraindications/Precautions
• CAUTION: Before applying the first bandage, it is important to check the following:
• Assess the patient to rule out arterial disease. The use of Doppler ultrasound is recommended.
• Measure the ankle circumference to confirm that it is greater than 18 cm or 7¼ inches (padded).
• Check if the patient's ankle circumference has changed due to a reduction in edema. Always re-measure after the initial treatment period.
• Assess the patient's limb for bony prominences or calf fibrosis. Ensure that these are well-protected using the PROFORE ™ Lite #1 padding bandage.

Profore™ Latex Free Multi-Layer Compression Bandaging System

PROFORE™ LF is a latex-free formulation, multi-layer compression bandage system. It has been developed in response to a growing concern from customers about the potential danger of latex allergy / hypersensitivity. PROFORE™ LF provides the same effective compression and sustained results as the standard PROFORE Multi-layer Compression Bandage System, but its latex-free formulation allows the healthcare provider to use it with confidence on allergy-sensitive patients. PROFORE™ LF is best used on ankle circumferences greater than 18 cm or 7¼ inches (padded).

Features

Each PROFORE™ LF system pack contains the following:

        One PROFORE™ LF wound contact layer
        One PROFORE™ LF #1 padding bandage
        One PROFORE™ LF #2 light conformable dressing
        One PROFORE™ LF #3 light compression bandage
        One PROFORE™ LF #4 flexible cohesive bandage


Benefits

Effective Compression
Proven effective in both hospital and community treatment studies, the PROFORE™ LF system is designed to deliver effective pressure.

Graduated Compression
PROFORE™ LF provides higher pressure at the ankle, with decreasing pressure exhibited at the calf.

Sustained Compression
Even a full week after application, PROFORE™ LF maintains effective levels of compression.

Safety
PROFORE™ LF pads bony prominences for protection and through the use of 2 compression layers, compression is built up gradually.

Extended Weartime
PROFORE™ LF has sufficient absorptive capacity to manage exudate for up to a full week without the need for reapplication. During the initial phase of therapy you may experience increased wound drainage as the compression system actively manages the edema. If strike through happens, remove the PROFORE™ LF system and apply another.

Cost-Effective
Weekly dressing changes reduce the nursing time required for the management of venous leg ulcers. Studies have shown that the multi-layer compression bandage system provides significant savings in cost of care.

Convenient
PROFORE™ LF system pack contains everything necessary for the application of effective graduated compression therapy. PROFORE™ LF reduces preparation time, simplifies stock control and ensures that the correct components are always available.

Indications

PROFORE™ LF Multi-Layer Compression Bandage System is indicated for the management of venous leg ulcers and associated conditions.

Contraindications

PROFORE™ LF should not be used on patients with an Ankle Brachial Pressure Index (ABPI) of less than 0.8, or on diabetic patients with advanced small vessel disease.

Precautions

Should the patient develop pain or pale, cool or numb extremities distal to the dressing, the bandages should be promptly removed. If the patient has a very thin ankle or very prominent tibial crest, extra padding should be applied to these areas to prevent pressure necrosis.

Failure to detect significantly reduced arterial flow can result in pressure necrosis, amputation or even death.

The risk of arterial as well as venous disease rises with age.

Insctructions for Use:


Caution: Before applying the first bandace, it is important to check the following:

    Assess the patient to rule out arterial disease. The use of Doppler ultrasound is recommended.
    Measure the ankle circumference to confirm that it is greater than 18 cm or 7¼ inches (padded).
    Check if the patient's ankle circumference has changed due to a reduction in edema. Always re-measure after the initial treatment period.
    Assess the patient's limb for bony prominences or calf fibrosis. Ensure that these are well protected using the PROFORE ™ LF #1 padding bandage.

    Apply PROFORE ™ LF in the following sequence:


Step 1

Wash and dry the leg and apply a moisturizing cream to the unbroken skin

Step 2

Apply the PROFORE ™ LF WCL sterile wound contact layer. Remove from the pack with sterile forceps and apply to the wound. Hold in place until covered by by PROFORE ™ LF #1

Step 3

PROFORE ™ LF #1 padding bandage
Apply from the base of the toes to the knee using a simple spiral technique and 50% overlap. Do not apply tension.

Step 4

PROFORE ™ LF #2 light conformable bandage
Apply from the base of the toes to the knee, over PROFORE ™ LF #1, using a simple spiral technique and 50% overlap. Use tape to secure.

Step 5

PROFORE ™ LF #3 ight compression bandage
Apply from the base of the toes to the knee, using a figure of eight technique at 50% extension. Use the central yellow line as guidance for 50% overlap. Use tape to secure.

Step 6

PROFORE ™ LF #4 flexible cohesive bandage
Apply from toe to knee using a spiral technique with 50% extension and 50% overlap. Press lightly on the bandage to ensure that the bandage adheres to itself. Apply the bandage steeply across the foot to reduce build-up of material over the front of the ankle.

Profore Four Layer High Compression Bandaging System

PROFORE ™ is a multi layer compression bandage system.

Features


Each system pack contains the following:

• One PROFORE ™ wound contact layer
• One PROFORE ™ #1 natural padding bandage
• One PROFORE ™ #2 light conformable dressing
• One PROFORE ™ #3 light compression bandage
• One PROFORE ™ #4 flexible cohesive bandage

Benefits

• Effective Compression
• Proven effective in both hospital and community treatment studies, the PROFORE ™ system is designed to deliver effective pressure.
• Graduated Compression
• PROFORE ™ provides higher pressure at the ankle, with decreasing pressure exhibited at the calf.
• Sustained Compression
• Even a full week after application, PROFORE ™ maintains effective levels of compression.
• Safety
• PROFORE ™ pads bony prominences for protection and through the use of 2 compression layers, compression is built up gradually.
• Extended Weartime
• Profore has sufficient absorptive capacity to manage exudate for up to a full week without needing re-application. The initial applications of PROFORE ™ may have to be changed every 3 to 4 days, when drainage is high.
• Cost-Effective
• Weekly dressing changes reduce the nursing time required for the management of venous leg ulcers. Studies have shown that the multi-layer compression bandage system provides significant savings in cost of care.
• Convenient
• PROFORE ™ system pack contains everything necessary for the application of effective graduated compression therapy. PROFORE ™ reduces preparation time, simplifies stock control and ensures that the correct components are always available.

Indications

The multi-layer compression bandage system has been specifically designed for the management of venous leg ulcers and associated conditions. The system pack can be used on patients with ankle circumferences of greater than 18cm or 7¼ inches (padded).

Precautions

• Do not use on patients with an ankle brachial pressure index (ABPI) of less than 0.8, or on diabetic patients with advanced small vessel disease.
• Should the patient develop pain or pale, cool or numb extremities distal to the dressing, the bandages should be promptly removed. If the patient has a very thin ankle or very prominent tibial crest, extra padding should be applied to these areas to prevent pressure necrosis.
• Failure to detect significantly reduced arterial flow can result in pressure necrosis, amputation or even death.
• This product has components that contain natural rubber latex which may cause allergic reactions in some individuals.
• The risk of arterial as well as venous disease rises with age.

Insctructions for Use:

Step 1

• Wash and dry leg and apply a moisturizing cream to the unbroken skin.

Step 2

• PROFORE ™ WCL sterile wound contact layer
• Remove from the pack with sterile forceps and apply to the wound. Hold in place until covered by PROFORE ™ #1.

Step 3

• PROFORE ™ #1 natural padding bandage
• Apply from the base of the toes to the knee using a simple spiral technique and 50% overlap. Do not apply tension.

Step 4

• PROFORE ™ #2 light conformable bandage
• Apply from the base of the toes to the knee, over PROFORE ™ #1, using a simple spiral technique and 50% overlap. Use tape to secure.

Step 5

• PROFORE ™ #3 light compression bandage
• Apply from the base of the toes to the knee, using a figure of eight technique at 50% extension. Use the central yellow line as guidance for 50% overlap. Use tape to secure.

Step 6

• PROFORE ™ #4 flexible cohesive bandage
• Apply from toe to knee using a spiral technique with 50% extension and 50% overlap. Press lightly on the bandage to ensure that the bandage adheres to itself. Apply the bandage steeply across the foot to reduce build-up of material over the front of the ankle.

Primapore™ IV Adhesive Non-Woven Wound Dressing

PRIMAPORE ™ dressings combine an absorbent pad with a soft and conformable fixative layer for the simple and effective management of sutured wounds.                                                                                                                                                                                                                                                                     

Features

• Soft breathable cover
• Highly absorbent pad
• Low allergy adhesive
• Conformable pad and cover

Benefits

• Highly absorbent and low-adherent pad
• The polyester wound contact layer enables the passage of blood or exudate into the highly absorbent pad while maintaining a good healing environment and minimal pain on dressing removal.
• Safe and secure fixation
• The low allergy acrylic adhesive is evenly spread onto the non-woven backing surface providing a safe and secure dressing fixation over the wound site.
• Soft and conformable
• Ensures patient comfort and conformability to all wound sites (even the more difficult areas like shoulders and axillae).
• Ease of use
• The protector paper, which is slit across the width of the dressing, enables quick application without the risk of touching the absorbent pad or adhesive area with fingers or forceps. The easily opened packaging facilitates aseptic dressing technique.
• Patient comfort
• The thick pad minimizes fluid strike-through and helps to protect the wound from trauma.

Indications

To dress post-operative wounds, minor cuts, abrasions, lacerations and puncture sites where a water-resistant dressing, which aids in the prevention of bacterial contamination, is required.
May be used as a secondary dressing over gels, ointments and other primary dressings.

Pico Single Use Negative Pressure Wound Therapy System

PICO is intended for use in wound sizes (surface area x depth) up to 400 cm3 which are considered to be low to moderately exuding.
The kit is intended to be used for a maximum of 7 days on low exuding wounds and 6 days on moderately exuding wounds. Therapy duration of the kit may be less than indicated if clinical practice or other factors such as wound type, wound size, rate or volume of exudate, orientation of the dressing or environmental conditions, result in more frequent dressing changes.

Instructions for Use:
PICO is indicated for patients who would benefit from a suction device (negative pressure wound therapy) as it may promote wound healing via removal of low to moderate levels of exudate and infectious materials.


Examples of appropriate wound types include:

• Chronic
• Acute
• Traumatic
• Subacute and dehisced wounds
• Partial-thickness burns
• Ulcers (such as diabetic or pressure)
• Flaps and grafts
• Closed surgical incisions

Opsite™ Transparent Adhesive Waterproof Film Dressings

 
OPSITE ™ is a transparent, adhesive film. The film is moisture vapor permeable, conformable and extensible. It is widely used to provide a moist wound environment for superficial wounds; it is also ideal for use as a secondary dressing.

Features

• Superior film with acrylic adhesive
• Waterproof film
• Simple, effective application technique
• Adaptable to awkward areas

Benefits

• OPSITE ™ has set the standard in moist wound care by retaining the natural wound exudate. OPSITE ™ provides moisture vapor permeability allowing excess exudate to evaporate, helping prevent skin maceration.
• Superior film with acrylic adhesive
• The OPSITE ™ film is highly extensible and conformable, which combined with its moisture vapor permeability, means the dressing can be left in place for up to 7 days. This minimizes interference at the wound site and reduces the amount of nursing time required.
• Waterproof
• OPSITE ™ is resistant to water and body fluids, allowing the patient to bathe without changing dressings. It also aids in the prevention of bacterial contamination.
• Adaptable to Awkward Areas
• OPSITE ™ has been designed to be adaptable for use on all areas of the body. It can be easily cut into strips or shapes for application to awkward areas such as heels, elbows and knees.

Indications

• Superficial wounds, such as shallow pressure sores, minor burns, cuts and abrasions.
• Use as a secondary dressing, for example over INTRASITE ™ Gel Amorphous Hydrogel Dressing or ALLEVYN ™ Cavity Wound Dressing.
• To provide catheter fixation.

Precautions

• OPSITE ™ may be used on clinically infected wounds if the following precautions are followed:
• The patient should be under medical/clinical supervision
• The dressing should be changed daily
• The patient should be receiving suitable systemic treatment.
• Immuno-compromised patients and diabetic patients may require extra supervision. Care should be taken to avoid skin damage by repeated applications on patients with thin or fragile skin.
• In common with all adhesive products, some cases of irritation and/or maceration of the skin surrounding the wound have been reported. It should be noted that inappropriate use or too frequent dressing changes, particularly in patients with fragile skin, can result in skin stripping.

Opsite™ Post-Op Composite Dressings

Features & Benefits

• High MVTR - The patented REACTIC ™ film has a unique molecular structure making it significantly more permeable to water vapor than ordinary films in the presence of moisture.
• Waterproof Film - Patient can shower with the dressing in place.
• Bacterial Barrier - Helps protect the site against extrinsic contamination, reducing the risk of infection by bacteria.
• Latex-Free Formula - A unique grid pattern adhesive.
• Highly-Absorbent Pad - Rapidly absorbs exudate. Allows lateral spread across the pad to maximize absorbency and help reduce the risk of skin maceration.
• Low Adherence - The wound contact layer enables exudate to pass through to allow minimal trauma on removal.
• Conformable - Comfortable and non-restrictive for the patient.
• Round Corners / Thin Film - Reduces occurences of lifting or snag, helping the dressing stay in place longer.

Benefits

• Waterproof
• The OPSITE ™ Post-Op film is impermeable to water and body fluids, allowing the patient to shower without changing dressings.
• Bacterial Barrier
• The OPSITE ™ Post-Op film provides a bacterial barrier, helping to reduce the risk of secondary infection.
• High MVTR
• OPSITE ™ Post-Op has a unique molecular structure that ‘switches on' in the presence of moisture, preventing accumulation of moisture underneath the dressing, which reduces bacterial growth and the risk of maceration.
• Transparent Film
• The clear film allows the user to monitor the level of fluid and check for infection without removing the dressing, thus increasing wear time.
• Absorbent, Low-adherent Pad
• The thick pad is highly absorbent, minimising the number of dressing changes whilst protecting the wound from further injury. The low-adherent wound contact layer leaves the wound site clean and comfortable, reducing pain when changing the dressing.
• Conformable
• OPSITE ™ Post-Op is highly conformable, even over the most awkward body contours. Its extensibility does not restrict movement, ensuring that it is comfortable for the patient. The unique dressing carrier keeps the film firm, allowing easy application.

Indications
To dress post-operative wounds, minor cuts, abrasions, lacerations and puncture sites where a waterproof dressing, which aids in the prevention of bacterial contamination, is required.

Instructions for Use:


Step 1

• Remove one part of the silicone backing paper (marked "1") prior to application.

Step 2

• Position dressing onto the skin and remove the second part of the silicone backing paper. Smooth the dressing down into place, applying light pressure.

Step 3

• Finally, peel off the dressing carrier (marked "2").

Step 4

• Dressing in place.

Composite Dressings

Features & Benefits

• High MVTR - The patented REACTIC ™ film has a unique molecular structure making it significantly more permeable to water vapor than ordinary films in the presence of moisture.
• Waterproof Film - Patient can shower with the dressing in place.
• Bacterial Barrier - Helps protect the site against extrinsic contamination, reducing the risk of infection by bacteria.
• Latex-Free Formula - A unique grid pattern adhesive.
• Highly-Absorbent Pad - Rapidly absorbs exudate. Allows lateral spread across the pad to maximize absorbency and help reduce the risk of skin maceration.
• Low Adherence - The wound contact layer enables exudate to pass through to allow minimal trauma on removal.
• Conformable - Comfortable and non-restrictive for the patient.
• Round Corners / Thin Film - Reduces occurences of lifting or snag, helping the dressing stay in place longer.

Benefits

• Waterproof
• The OPSITE ™ Post-Op film is impermeable to water and body fluids, allowing the patient to shower without changing dressings.
• Bacterial Barrier
• The OPSITE ™ Post-Op film provides a bacterial barrier, helping to reduce the risk of secondary infection.
• High MVTR
• OPSITE ™ Post-Op has a unique molecular structure that ‘switches on' in the presence of moisture, preventing accumulation of moisture underneath the dressing, which reduces bacterial growth and the risk of maceration.
• Transparent Film
• The clear film allows the user to monitor the level of fluid and check for infection without removing the dressing, thus increasing wear time.
• Absorbent, Low-adherent Pad
• The thick pad is highly absorbent, minimising the number of dressing changes whilst protecting the wound from further injury. The low-adherent wound contact layer leaves the wound site clean and comfortable, reducing pain when changing the dressing.
• Conformable
• OPSITE ™ Post-Op is highly conformable, even over the most awkward body contours. Its extensibility does not restrict movement, ensuring that it is comfortable for the patient. The unique dressing carrier keeps the film firm, allowing easy application.

Indications
To dress post-operative wounds, minor cuts, abrasions, lacerations and puncture sites where a waterproof dressing, which aids in the prevention of bacterial contamination, is required.

Instructions for Use:


Step 1

• Remove one part of the silicone backing paper (marked "1") prior to application.

Step 2

• Position dressing onto the skin and remove the second part of the silicone backing paper. Smooth the dressing down into place, applying light pressure.

Step 3

• Finally, peel off the dressing carrier (marked "2").

Step 4

• Dressing in place.

Transparent Adhesive Film Dressings

  IV3000 ™ Transparent Adhesive Film Dressing Features

• Moisture responsive High Moisture Vapor Transmission Rate film
• Grid pattern adhesive
• Transparent and conformable
• Wide range of sizes and delivery systems to suit peripheral central line and epidural catheters
• Film acts as a barrier to bacteria including MSRA

Benefits

• Reduces risk of infection by preventing moisture accumulation - The patented Reactic* film in IV3000 ™ has a unique molecular structure which is significantly more permeable to water vapor than ordinary films. This helps prevent the accumulation of moisture underneath the dressing and assists in the reduction of bacterial growth and the risk of catheter-related infection.
• Minimizes unscheduled dressing changes - The higher permeability of IV3000 ™ keeps the skin drier so improving dressing adherence and reducing the number of unscheduled dressing changes.
• Greater patient comfort - IV3000 ™ is kind to the patient's skin. It's low allergy adhesive and highly permeable Reactic film may help prevent skin maceration or irritation and result in improved patient comfort.
• Excellent catheter stability - The highly conformable IV3000 ™ film allows the patient to move freely and yet will remain firmly adhered around the catheter hub so ensuring excellent fixation.
• Convenient visual inspection - IV3000 ™ is transparent and so allows regular inspection of the catheter insertion site for signs of infection or phlebitis without the need for dressing removal.
• Easy application and removal - IV3000 ™ is designed to provide easy aseptic application and removal. Its unique grid pattern adhesive reduces pain on removal due to grid adhesive spread and so minimizes patient discomfort on removal. It also leaves less adhesive residue on the patient's skin.

Indications

• IV3000 ™ is indicated for peripheral and central venous catheter fixation.
• Provides physical separation between the catheter site and external environments to assist in preventing contamination of the catheter site.
• Creates an environment for managing moisture at the catheter site through increased Moisture Vapor Transmission Rates.
• Precautions
• IV3000 ™ should be used on IV sites only. If a film dressing is required for open wounds such as pressure sores, burns or donor sites, OPSITE ™ FLEXIGRID ™ Adhesive Film Dressings should be used.
• Use on prepared dry skin only.
• Do not stack dressings or allow dressings to overlap. Periodically monitor the dressing and catheter site to confirm secure attachment and continued proper infusion, especially after bathing, showering, or if the dressing and catheter site becomes wet. If the dressing comes off, evaluate to ensure proper catheter placement, and then apply a new dressing. As with all adhesive products, apply and remove carefully from sensitive or fragile skin.

Instructions for Use:
Clean and thoroughly dry application area.


Step 1

• Remove approximately half of the protector paper and centre the dressing over the insertion site.

Step 2

• Smooth the dressing down on to the patient's skin working from the catheter outwards and remove the remaining protector paper. Be careful not to apply the dressing under tension.

Step 3

• The protector paper may be removed from the orange tape handles and the entire handle adhered to the patient's skin.

Step 4

• Alternatively a portion of the tape handles can be torn off with the protector paper still in place. This can then be removed and the tape handles used to help secure the catheter hub or tubing. They may also be used for documentation.

Step 5

• Remove dressing by loosening the orange handles and stretching the dressing parallel to the patient's skin while stabilising the patient's skin and catheter with the other hand. Alternatively, use an alcohol wipe to break the adhesive seal. If the skin is particularly fragile, then warm soap and water may be used to break the adhesive bond and to ease the dressing off.

1-Hand Delivery Transparent Adhesive Moisture Responsive Catheter Film Dressings

IV3000 ™ 1-Hand Moisture Responsive Cannula Fixation Dressing

IV3000 ™ 1-Hand is a moisture responsive transparent film dressing specifically designed to meet the needs of catheter fixation and to keep the catheter site dry. Independent clinical experts have proven IV3000 to offer safe, secure and cost effective catheter fixation and believe it to be ‘a technological advance for IV site care'. The 1-Hand delivery system provides quick and easy aseptic application to all major catheter types.

Indications

• IV3000 ™ 1-Hand is indicated for peripheral and central venous catheter fixation.
• Provides physical separation between the catheter site and external environments to assist in preventing contamination of the catheter site.
• Creates an environment for managing moisture at the catheter site through increased Moisture Vapor Transmission Rates.

Precautions

• Use on prepared dry skin only. Do not stack dressings, or allow dressings to overlap. Periodically monitor the dressing and catheter site to confirm secure attachment and continued proper infusion, especially after bathing, showering, or if the dressing and catheter site becomes wet. If the dressing comes off, evaluate to ensure proper catheter placement, and then apply a new dressing. As with all adhesive products, apply and remove carefully from sensitive or fragile skin. When using IV3000 ™ 1-Hand to secure tubing sets of portable infusion pumps, including insulin pumps for diabetics, extra care should be exercised during periods of vigorous activity or when exposed to wet conditions. Check dressing frequently to assure adhesion of dressing, as a loss of adhesion can occur, potentially resulting in catheter dislodgement and loss of medication flow.
• Users of IV3000 ™ 1-Hand (product code 4007) may consider using the larger IV3000 ™ 1-Hand (product code 4008) dressing, with a greater adherent surface area, as a replacement dressing where additional adhesion is needed.

Features

• Moisture responsive high moisture vapor transmission rate film
• Grid pattern adhesive
• Transparent and conformable
• 1-Hand delivery system
• Film acts as a barrier to bacteria including MSRA

Benefits

• May help reduce risk of infection by preventing moisture accumulation - The patented REACTIC ™ film in IV3000 ™ has a unique molecular structure which is significantly more permeable to water vapor than ordinary films. This may help prevent the accumulation of moisture underneath the dressing and assists in the reduction of bacterial growth and the risk of catheter-related infection.
• Minimizes unscheduled dressing changes - The higher permeability of IV3000 ™ keeps the skin drier so improving dressing adherence and reducing the number of unscheduled dressing changes.
• Greater patient comfort - IV3000 ™ is kind to the patient's skin. Its low allergy adhesive and highly permeable Reactic film may help prevent skin maceration or irritation and result in improved patient comfort.
• Excellent catheter stability - The highly conformable IV3000 ™ film allows the patient to move freely and yet will remain firmly adhered around the catheter hub so ensuring excellent fixation.
• Convenient visual inspection - IV3000 ™ is transparent and so allows regular inspection of the catheter insertion site for signs of infection or phlebitis without the need for dressing removal.
• Easy application and removal - The 1-Hand delivery system is designed to provide quick and easy aseptic application. It also allows the dressing to be applied with 1-Hand if required leaving the other hand free to stabilize the catheter or patient. The unique grid pattern adhesive makes dressing removal easier than with ordinary films and leaves less adhesive residue on the patient's skin.

Reimbursement Information

• Usual Allowable Amount: Same as transparent film -- up to 3 per week.
• Specific Coverage Criteria: Surgical dressing: Qualifies if used on a catheter entry point (except for infusion pumps) where the catheter is inserted into a blood vessel.
• Documentation as surgical dressing: Must include 1) date of surgical procedure; 2) length, width, and depth of the surgical wound (depth should be based on the wound prior to suturing).

Instructions for Use:
Clean and thoroughly dry application area.

Step1

• Remove the protector paper (1) and center the dressing over the catheter insertion site.

Step 2

• Place the dressing on the catheter hub and adhere the dressing to the patient's skin. Remove the remaining protector paper (2)

Step 3

• Remove the printed carrier (3) by lifting the non-adhesive edge and pulling diagonally until the carrier is removed.

Step 4

• Mold the film around the catheter to complete the dressing application.

Step 5

• Remove dressing by loosening the film and stretching the dressing parallel to the patient's skin while stabilizing the patient's skin and catheterwith the other hand. If the skin is particularly fragile then warm soap and water may be used to break the adhesive bond and to ease the dressing off.