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PROFORE LITE BANDAGE KIT

Profore Lite consists of a low-adherent wound contact layer, an absorbent wool padding layer, a light conformable crepe bandage and a flexible cohesion compression bandage.  It is used in the treatment of mixed venous and arterial leg ulcers.

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PROFORE LITE BANDAGE KIT
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Profore Lite | Reduced Compression Multilayer Kit for Venous Leg Ulcer Management

CRITICAL SAFETY NOTICE: Compression bandaging systems are contraindicated in peripheral arterial disease. An ankle brachial pressure index (ABPI) assessment must be performed and documented before Profore Lite is applied. This kit must only be applied by a trained healthcare professional. It is not for patient self-application. A warning symbol is displayed on the Profore Lite packaging confirming that clinical assessment is required before use.

Not every patient with a venous leg ulcer requires or tolerates full high compression. Patients with mixed aetiology leg ulcers where some arterial impairment is present but not severe enough to contraindicate compression entirely, patients with conditions affecting their tolerance of high compression, and patients in the early stages of compression therapy may all require a lighter level of compression than the full Profore system delivers. Profore Lite is a reduced compression multilayer kit from Smith & Nephew for venous leg ulcer management where lighter compression is clinically indicated. ABPI assessment required. Applied by trained clinical staff only. No prescription required.

What Is Profore Lite?

Profore Lite is a regulated medical device from Smith & Nephew. It is a complete pre-packaged multilayer compression kit for venous leg ulcer management that delivers a lighter level of compression than the full Profore high compression system. The packaging identifies it as PROFORE LITE and displays a warning symbol confirming the requirement for clinical assessment before use.

The layer composition of Profore Lite is confirmed by the notation on the packaging: WCL + 1 + 2 + 4. This indicates that the kit contains a wound contact layer (WCL), a padding bandage (layer 1), a conforming bandage (layer 2), and an outer compression bandage (layer 4). There is no layer 3 in the Profore Lite kit. The absence of the layer 3 conforming elastic bandage that is present in the full Profore system is one of the structural differences that contributes to the lighter compression level delivered by Profore Lite.

Lighter compression is clinically indicated for patients who cannot tolerate or do not require the full high compression of the standard Profore system. This includes patients with mixed aetiology leg ulcers where ABPI falls between 0.6 and 0.8, indicating some arterial impairment that does not completely contraindicate compression but requires a reduced compression level under specialist supervision. It may also include patients with conditions that affect their tolerance of high external pressure on the lower limb.

Each Profore Lite kit contains the sterile components for a single complete application, applied in sequence by the clinical team. One kit provides all materials needed for one dressing change.

The ABPI threshold for Profore Lite differs from full high compression. ABPI of 0.8 or above supports full high compression with the standard Profore system. For Profore Lite and reduced compression systems, ABPI between 0.6 and 0.8 may be appropriate under specialist supervision. ABPI below 0.6 remains a contraindication to any compression bandaging. The decision to use reduced compression must be made by the clinical team, not independently by the patient or carer.

How Profore Lite Works

Reduced Layer System

The full Profore system applies four bandage layers plus the wound contact dressing, generating high compression at the ankle. Profore Lite uses the WCL + 1 + 2 + 4 configuration, delivering compression through fewer layers than the complete system. The total compression generated at the ankle by Profore Lite is lower than that of the full Profore system. This reduced compression is clinically appropriate for patients who require compression for venous leg ulcer management but cannot safely tolerate the higher compression levels of the full system.

Graduated Compression Principle

Like the full Profore system, Profore Lite generates graduated compression that is highest at the ankle and reduces progressively toward the knee. This pressure gradient supports venous return in the lower limb and counteracts the venous hypertension that underlies venous leg ulcer formation. The lower overall compression level of Profore Lite means the pressure gradient is delivered at a reduced magnitude compared to the full system.

Complete Kit for Each Application

Each Profore Lite kit contains all the components needed for a single complete application. At each dressing change, one kit is opened and the components are applied in the correct sequence. The kit format ensures that the appropriate components for a reduced compression application are available at each visit without the need to manage separate stocks of individual bandages.

Applied by Trained Clinical Staff

The reduced compression level of Profore Lite must still be applied consistently to be therapeutically effective. The padding must be applied evenly, the conforming layer must smooth the padded surface, and the outer compression layer must be applied at the appropriate tension for reduced compression. These technical requirements mean that Profore Lite is applied by district nurses, tissue viability nurses, and community nurses trained in compression bandaging, not by patients independently.

Application

Who Applies Profore Lite

  • Trained healthcare professionals only: district nurses, tissue viability nurses, community nurses trained in compression bandaging.
  • ABPI must be performed and documented before the first application.
  • The decision to use reduced compression rather than full high compression must be made by the clinical team.

Application Sequence

  • Open one Profore Lite kit per application.
  • Apply the ankle shaping component before all other layers.
  • Apply the wound contact layer over the ulcer.
  • Apply the padding bandage from the foot to below the knee.
  • Apply the conforming bandage over the padding.
  • Apply the outer compression bandage to complete the system.

After Application

  • Check patient comfort after all layers are applied.
  • Confirm no signs of arterial compromise.
  • If pain, cold toes, numbness, or colour change develops, remove all layers immediately.

If the patient reports pain, tightness, cold feet, numbness, tingling, or colour change after the system is applied, remove all bandage layers immediately and seek clinical assessment. Do not reapply compression until the cause has been assessed. This applies to all compression systems including Profore Lite.

Kit Contents

Ankle Shaping Component

Applied before all bandage layers. Fills the anatomical hollows around the malleoli to create a more even ankle profile for the overlying compression layers.

Wound Contact Layer

Applied directly over the ulcer surface before the bandage layers. Provides a suitable wound interface as the first layer of the system.

Padding Bandage

The main padding layer applied from the foot to below the knee. Protects bony prominences, absorbs wound exudate, and distributes compression forces evenly over the lower limb.

Conforming Bandage

Applied over the padding layer to hold it in position and smooth the padded limb surface before the outer compression layer is applied.

Outer Compression Bandage

The outermost layer that completes the Profore Lite reduced compression system. Applied in a spiral technique to deliver the outer compression contribution of the WCL + 1 + 2 + 4 system.

All components are included in a single pre-packaged sterile kit. One kit provides the materials for a single complete system application.

Safety Information and Precautions

Contraindications

  • Peripheral arterial disease with ABPI below 0.6.
  • Confirmed limb ischaemia.
  • Severe uncontrolled cardiac failure.

Cautions Specific to Reduced Compression

  • ABPI between 0.6 and 0.8: reduced compression under specialist supervision is potentially appropriate but must be a supervised clinical decision.
  • Peripheral neuropathy: reduced sensation impairs the patient's ability to report compression pain even at reduced compression levels.
  • Diabetes with vascular complications.

Warning Signs After Application

  • Pain or increasing discomfort in the bandaged limb.
  • Cold toes or pallor of the digits.
  • Numbness or tingling in the foot.
  • Any of these requires immediate removal of all layers and clinical reassessment.

Suitability

Patients for Whom Profore Lite Is Appropriate

  • Patients with mixed aetiology leg ulcers where ABPI falls between 0.6 and 0.8 and the clinical team has determined that reduced compression under supervision is appropriate
  • Patients who cannot tolerate full high compression due to conditions affecting their tolerance of external pressure
  • Patients for whom the clinical team has prescribed reduced rather than high compression based on ABPI, clinical assessment, and specialist guidance

Profore Lite vs Full Profore System

Profore Lite and the full Profore system are both multilayer compression kits from Smith & Nephew for venous leg ulcer management. The full Profore system delivers high compression using four bandage layers and is appropriate for patients with ABPI of 0.8 or above and no other contraindications. Profore Lite delivers reduced compression using the WCL + 1 + 2 + 4 layer configuration and is suited to patients who require lighter compression. The choice between the two systems is a clinical decision based on ABPI measurement and the overall clinical assessment of the patient.

Purchasing Profore Lite

Profore Lite is a regulated medical device and does not require a prescription. The complete kit is available from Pharmacy Planet for clinical purchasers.

Our pharmacists can advise on Profore Lite and on other compression system options from the Smith & Nephew range.

This is a clinical product for use by trained healthcare professionals. ABPI assessment and clinical decision-making regarding the appropriate compression level must precede use. It is not for patient self-application.

Storage

  • Store in a cool, dry place away from direct heat and sunlight.
  • Do not store above 25 degrees C.
  • Keep in original sealed packaging until use.
  • Check expiry date before use.
  • Keep out of reach of children.

Why Choose Pharmacy Planet?

Pharmacy Planet is a GPhC registered online pharmacy. Profore Lite is a genuine Smith & Nephew product stocked through regulated UK supply chains.

Our pharmacists can advise on Profore Lite and on the full range of Profore compression system products for different compression levels and patient needs.

References

  1. Smith & Nephew. Profore Lite — Product Information. REF #66000415. Smith & Nephew. https://www.smith-nephew.com. Accessed June 2026.
  2. National Institute for Health and Care Excellence. Chronic wounds: advanced wound dressings and antimicrobial dressings. NICE Evidence Review. https://www.nice.org.uk. Accessed June 2026.
  3. NHS. Venous leg ulcer: treatment and compression therapy. https://www.nhs.uk/conditions/leg-ulcer. Accessed June 2026.
  4. Wounds UK. Best Practice Statement: Compression hosiery. https://www.wounds-uk.com. Accessed June 2026.
PROFORE LITE BANDAGE KIT

CRITICAL SAFETY NOTICE: Compression bandaging systems are contraindicated in peripheral arterial disease. An ankle brachial pressure index (ABPI) assessment must be performed and documented before Profore Lite is applied. This kit must only be applied by a trained healthcare professional. It is not for patient self-application. A warning symbol is displayed on the Profore Lite packaging confirming that clinical assessment is required before use.

Not every patient with a venous leg ulcer requires or tolerates full high compression. Patients with mixed aetiology leg ulcers where some arterial impairment is present but not severe enough to contraindicate compression entirely, patients with conditions affecting their tolerance of high compression, and patients in the early stages of compression therapy may all require a lighter level of compression than the full Profore system delivers. Profore Lite is a reduced compression multilayer kit from Smith & Nephew for venous leg ulcer management where lighter compression is clinically indicated. ABPI assessment required. Applied by trained clinical staff only. No prescription required.

Profore Lite is a regulated medical device from Smith & Nephew. It is a complete pre-packaged multilayer compression kit for venous leg ulcer management that delivers a lighter level of compression than the full Profore high compression system. The packaging identifies it as PROFORE LITE and displays a warning symbol confirming the requirement for clinical assessment before use.

The layer composition of Profore Lite is confirmed by the notation on the packaging: WCL + 1 + 2 + 4. This indicates that the kit contains a wound contact layer (WCL), a padding bandage (layer 1), a conforming bandage (layer 2), and an outer compression bandage (layer 4). There is no layer 3 in the Profore Lite kit. The absence of the layer 3 conforming elastic bandage that is present in the full Profore system is one of the structural differences that contributes to the lighter compression level delivered by Profore Lite.

Lighter compression is clinically indicated for patients who cannot tolerate or do not require the full high compression of the standard Profore system. This includes patients with mixed aetiology leg ulcers where ABPI falls between 0.6 and 0.8, indicating some arterial impairment that does not completely contraindicate compression but requires a reduced compression level under specialist supervision. It may also include patients with conditions that affect their tolerance of high external pressure on the lower limb.

Each Profore Lite kit contains the sterile components for a single complete application, applied in sequence by the clinical team. One kit provides all materials needed for one dressing change.

The ABPI threshold for Profore Lite differs from full high compression. ABPI of 0.8 or above supports full high compression with the standard Profore system. For Profore Lite and reduced compression systems, ABPI between 0.6 and 0.8 may be appropriate under specialist supervision. ABPI below 0.6 remains a contraindication to any compression bandaging. The decision to use reduced compression must be made by the clinical team, not independently by the patient or carer.

Reduced Layer System

The full Profore system applies four bandage layers plus the wound contact dressing, generating high compression at the ankle. Profore Lite uses the WCL + 1 + 2 + 4 configuration, delivering compression through fewer layers than the complete system. The total compression generated at the ankle by Profore Lite is lower than that of the full Profore system. This reduced compression is clinically appropriate for patients who require compression for venous leg ulcer management but cannot safely tolerate the higher compression levels of the full system.

Graduated Compression Principle

Like the full Profore system, Profore Lite generates graduated compression that is highest at the ankle and reduces progressively toward the knee. This pressure gradient supports venous return in the lower limb and counteracts the venous hypertension that underlies venous leg ulcer formation. The lower overall compression level of Profore Lite means the pressure gradient is delivered at a reduced magnitude compared to the full system.

Complete Kit for Each Application

Each Profore Lite kit contains all the components needed for a single complete application. At each dressing change, one kit is opened and the components are applied in the correct sequence. The kit format ensures that the appropriate components for a reduced compression application are available at each visit without the need to manage separate stocks of individual bandages.

Applied by Trained Clinical Staff

The reduced compression level of Profore Lite must still be applied consistently to be therapeutically effective. The padding must be applied evenly, the conforming layer must smooth the padded surface, and the outer compression layer must be applied at the appropriate tension for reduced compression. These technical requirements mean that Profore Lite is applied by district nurses, tissue viability nurses, and community nurses trained in compression bandaging, not by patients independently.

Who Applies Profore Lite

  • Trained healthcare professionals only: district nurses, tissue viability nurses, community nurses trained in compression bandaging.
  • ABPI must be performed and documented before the first application.
  • The decision to use reduced compression rather than full high compression must be made by the clinical team.

Application Sequence

  • Open one Profore Lite kit per application.
  • Apply the ankle shaping component before all other layers.
  • Apply the wound contact layer over the ulcer.
  • Apply the padding bandage from the foot to below the knee.
  • Apply the conforming bandage over the padding.
  • Apply the outer compression bandage to complete the system.

After Application

  • Check patient comfort after all layers are applied.
  • Confirm no signs of arterial compromise.
  • If pain, cold toes, numbness, or colour change develops, remove all layers immediately.

If the patient reports pain, tightness, cold feet, numbness, tingling, or colour change after the system is applied, remove all bandage layers immediately and seek clinical assessment. Do not reapply compression until the cause has been assessed. This applies to all compression systems including Profore Lite.

Ankle Shaping Component

Applied before all bandage layers. Fills the anatomical hollows around the malleoli to create a more even ankle profile for the overlying compression layers.

Wound Contact Layer

Applied directly over the ulcer surface before the bandage layers. Provides a suitable wound interface as the first layer of the system.

Padding Bandage

The main padding layer applied from the foot to below the knee. Protects bony prominences, absorbs wound exudate, and distributes compression forces evenly over the lower limb.

Conforming Bandage

Applied over the padding layer to hold it in position and smooth the padded limb surface before the outer compression layer is applied.

Outer Compression Bandage

The outermost layer that completes the Profore Lite reduced compression system. Applied in a spiral technique to deliver the outer compression contribution of the WCL + 1 + 2 + 4 system.

All components are included in a single pre-packaged sterile kit. One kit provides the materials for a single complete system application.

Contraindications

  • Peripheral arterial disease with ABPI below 0.6.
  • Confirmed limb ischaemia.
  • Severe uncontrolled cardiac failure.

Cautions Specific to Reduced Compression

  • ABPI between 0.6 and 0.8: reduced compression under specialist supervision is potentially appropriate but must be a supervised clinical decision.
  • Peripheral neuropathy: reduced sensation impairs the patient's ability to report compression pain even at reduced compression levels.
  • Diabetes with vascular complications.

Warning Signs After Application

  • Pain or increasing discomfort in the bandaged limb.
  • Cold toes or pallor of the digits.
  • Numbness or tingling in the foot.
  • Any of these requires immediate removal of all layers and clinical reassessment.

Patients for Whom Profore Lite Is Appropriate

  • Patients with mixed aetiology leg ulcers where ABPI falls between 0.6 and 0.8 and the clinical team has determined that reduced compression under supervision is appropriate
  • Patients who cannot tolerate full high compression due to conditions affecting their tolerance of external pressure
  • Patients for whom the clinical team has prescribed reduced rather than high compression based on ABPI, clinical assessment, and specialist guidance

Profore Lite vs Full Profore System

Profore Lite and the full Profore system are both multilayer compression kits from Smith & Nephew for venous leg ulcer management. The full Profore system delivers high compression using four bandage layers and is appropriate for patients with ABPI of 0.8 or above and no other contraindications. Profore Lite delivers reduced compression using the WCL + 1 + 2 + 4 layer configuration and is suited to patients who require lighter compression. The choice between the two systems is a clinical decision based on ABPI measurement and the overall clinical assessment of the patient.

Profore Lite is a regulated medical device and does not require a prescription. The complete kit is available from Pharmacy Planet for clinical purchasers.

Our pharmacists can advise on Profore Lite and on other compression system options from the Smith & Nephew range.

This is a clinical product for use by trained healthcare professionals. ABPI assessment and clinical decision-making regarding the appropriate compression level must precede use. It is not for patient self-application.

  • Store in a cool, dry place away from direct heat and sunlight.
  • Do not store above 25 degrees C.
  • Keep in original sealed packaging until use.
  • Check expiry date before use.
  • Keep out of reach of children.

Pharmacy Planet is a GPhC registered online pharmacy. Profore Lite is a genuine Smith & Nephew product stocked through regulated UK supply chains.

Our pharmacists can advise on Profore Lite and on the full range of Profore compression system products for different compression levels and patient needs.

References

  1. Smith & Nephew. Profore Lite — Product Information. REF #66000415. Smith & Nephew. https://www.smith-nephew.com. Accessed June 2026.
  2. National Institute for Health and Care Excellence. Chronic wounds: advanced wound dressings and antimicrobial dressings. NICE Evidence Review. https://www.nice.org.uk. Accessed June 2026.
  3. NHS. Venous leg ulcer: treatment and compression therapy. https://www.nhs.uk/conditions/leg-ulcer. Accessed June 2026.
  4. Wounds UK. Best Practice Statement: Compression hosiery. https://www.wounds-uk.com. Accessed June 2026.
Frequently Asked Questions

Profore Lite is a reduced compression multilayer kit from Smith & Nephew for venous leg ulcer management where lighter compression is clinically indicated. Using the WCL + 1 + 2 + 4 layer configuration, it delivers lower compression than the full Profore system. Suited to patients where full high compression is not appropriate, including those with ABPI between 0.6 and 0.8 under specialist supervision. Clinical application only. ABPI required. No prescription required.

Profore Lite delivers reduced compression and uses fewer bandage layers than the full Profore system. The full Profore system applies four bandage layers and delivers high compression, appropriate for patients with ABPI of 0.8 or above. Profore Lite uses the WCL + 1 + 2 + 4 configuration, providing lighter compression for patients who cannot tolerate or do not require high compression. The choice between them is a clinical decision based on ABPI and overall patient assessment.

Profore Lite is suited to patients for whom the clinical team has determined that reduced compression is appropriate rather than full high compression. This includes patients with ABPI between 0.6 and 0.8, where reduced compression under specialist supervision may be clinically appropriate, and patients with conditions that limit their tolerance of high external pressure. The decision is made by the clinical team, not the patient independently. ABPI assessment must be performed before any compression system is chosen.

Yes. ABPI assessment is required before Profore Lite is applied, just as it is for any compression system. ABPI below 0.6 remains a contraindication even for reduced compression systems. For Profore Lite, ABPI between 0.6 and 0.8 may support the use of reduced compression under specialist supervision. ABPI of 0.8 or above would typically support the use of the full Profore high compression system rather than Profore Lite, unless there are other clinical reasons to use reduced compression.

This notation describes the layer composition of the Profore Lite kit. WCL stands for Wound Contact Layer, the dressing applied directly to the ulcer surface. 1 is the padding bandage layer. 2 is the conforming bandage layer. 4 is the outer compression bandage layer. There is no layer 3 in Profore Lite, which distinguishes it from the full Profore system and contributes to its lower total compression level.

The Profore Lite kit contains wound contact layer, ankle shaping, padding, conforming, and outer compression components, all pre-packaged in a single sterile kit. One kit is used per dressing change. Each component is applied in the correct sequence by the district or community nurse.

Contact your district or community nurse immediately if you experience pain, tightness, numbness, tingling, or cold toes after the compression system has been applied. Do not wait for the next scheduled visit. If symptoms are severe and you cannot reach your nurse promptly, attend your nearest urgent care setting. Even at reduced compression levels, any compression system can cause problems if the limb circulation is compromised. Removal of all bandage layers relieves the pressure while you seek help.

No. Profore Lite is a regulated medical device and does not require a prescription. The complete kit is available from Pharmacy Planet for clinical purchasers. It is a clinical product for use by trained healthcare professionals managing venous leg ulcers with compression therapy. ABPI assessment and a clinical decision about the appropriate compression level must precede use.

No. Profore Lite must only be applied by a trained healthcare professional, such as a district nurse, tissue viability nurse, or community nurse trained in compression bandaging. It is not designed or licensed for patient self-application. Correct tension and layer sequencing are essential for the system to be both safe and clinically effective, and these require professional training and assessment at each application.

Profore Lite can only be used after ABPI assessment confirms it is safe to do so. Any degree of significant peripheral arterial disease, particularly ABPI below 0.6, is a contraindication to compression bandaging, including reduced compression systems like Profore Lite. Where ABPI falls between 0.6 and 0.8, reduced compression may be considered appropriate, but only under specialist supervision and as part of a documented clinical decision. Confirmed limb ischaemia is an absolute contraindication regardless of ABPI.

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Review By

HARMINDER ‘HARMY’ KAUR

Last Updated On : Mar 13 2026

BSc(hons) Pharmacy

GPhC Number: 2061107

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Last Reviewed On : Mar 23 2026

BSc Pharm, MRPharmS, Independent Prescriber, Superintendent Pharmacist, Clinical Lead

GPhC Number: 2050925