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PROFORE 3 LITEPRESS

PROFORE 3 LITEPRESS (10cm x 8.7m) is a multi-layer, reduced-compression bandage system. Profore Lite is best used on ankle circumferences greater than 18cm or 7¼ inches. PROFORE 3 is a sustained light compression bandage and the only bandage applied in a figure-of-eight when used as a part of the PROFORE multi-layer compression bandage system. 

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PROFORE 3 LITEPRESS
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Profore 3 Litepress | Light Conforming Bandage Layer for Multilayer Compression Systems

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 any compression bandaging system is applied. Profore 3 Litepress must only be applied as part of the Profore multilayer compression system by a trained healthcare professional. It is not for patient self-application.

Each layer of a multilayer compression bandage system serves a distinct purpose. The padding layer protects bony prominences and distributes compression forces evenly. A conforming bandage layer holds the padding in position and adds a degree of elastic support before the outer compression layer is applied. Profore 3 Litepress is the third layer of the Profore multilayer compression system from Smith & Nephew. It is a light elastic conforming bandage applied over the padding layer to hold the system in place and contribute to the overall compression before the outer compression bandage is applied. 10cm x 8.7m. Clinical application only.

What Is Profore 3 Litepress?

Profore 3 Litepress is a regulated medical device from Smith & Nephew and the third-layer component of the Profore multilayer compression bandage system for venous leg ulcer management. The Profore system achieves its therapeutic compression through the cumulative effect of four layers applied sequentially from the foot to the knee. Profore 3 Litepress is the light elastic conforming bandage that forms layer three.

The four layers of the Profore system each serve a distinct purpose. Layer one is the wound contact dressing applied directly over the ulcer. Layer two is an absorbent padding bandage that protects bony prominences, absorbs wound exudate, and distributes compression forces evenly over the contours of the lower leg. Layer three, Profore 3 Litepress, is a light elastic conforming bandage applied over the padding to hold it in position, add elastic support, and create a smooth surface for the outer compression layer. Layer four is the outer compression bandage, which delivers the primary therapeutic compression.

Litepress is described as light in compression compared to the outer compression bandage. The word "lite" in the product name indicates that this bandage contributes a lighter level of compression than the outer layer. Its function is not to deliver the primary therapeutic compression alone but to work as part of the system. The total compression at the ankle is achieved by the combined contribution of all layers.

Profore 3 Litepress is 10cm wide and 8.7m in length. The long roll length reflects the amount of bandage needed to spiral from the foot to the knee with appropriate overlap.

Arterial disease must be excluded before the Profore system is applied. An ABPI of 0.8 or above is generally required for full high compression. ABPI between 0.6 and 0.8 may permit reduced compression under specialist supervision. ABPI below 0.6 is a contraindication. Any patient with symptoms of arterial insufficiency requires ABPI assessment before compression is considered.

How Profore 3 Litepress Works

The Role of Layer Three in Multilayer Compression

In a multilayer compression system, the total compression at the skin surface is the sum of the contributions from all layers applied. Layer three, Profore 3 Litepress, contributes an elastic wrapping force over the padding layer below it. This contribution holds the padding bandage in position throughout the wear period, preventing it from slipping or bunching. The light elastic nature of Litepress also smooths out any irregularities in the padded limb surface, creating a more uniform foundation for the outer compression bandage applied above it.

Conforming to Lower Limb Contour

The lower leg has a complex contour: narrow at the ankle, broader at the calf, and narrowing again below the knee. A conforming elastic bandage adapts to these changes in circumference as it is applied, maintaining consistent contact with the padded limb surface throughout the application. This conformability reduces the risk of pressure ridges forming at bandage edges that can occur with a less conforming material, and ensures the outer compression layer is applied over a smooth, even base.

Cumulative Compression in the System

Multilayer compression systems are designed so that each layer contributes to the total compression delivered. The compression from each layer adds to the compression from the layers below. Profore 3 Litepress, as layer three, adds its contribution on top of the padding. The outer compression bandage, applied over Profore 3 Litepress, then adds its larger compression contribution to produce the total therapeutic compression at the ankle. The system is validated as a whole, and the layers should not be applied in isolation.

Applied by Trained Clinical Staff

The therapeutic compression delivered by the Profore system depends on the technique used to apply each layer. Profore 3 Litepress is applied in a spiral technique with a consistent overlap and tension. The compression contribution of the layer depends on the tension at which it is applied. Application that is too tight or too loose alters the total compression delivered and may move it outside the therapeutic range. Consistent application technique requires training and clinical experience.

Application

Who Applies Profore 3 Litepress

  • Profore 3 Litepress is applied by trained healthcare professionals only.
  • Appropriate applicators include district nurses, tissue viability nurses, and community nurses trained in multilayer compression bandaging.
  • ABPI must be completed and documented before the first application of the system.

Application within the Profore System

  • Apply the wound contact layer and padding layer (layers one and two) before Profore 3 Litepress.
  • Apply Profore 3 Litepress over the padding layer in a spiral technique from the base of the toes upward.
  • Apply with consistent tension and overlap throughout.
  • Apply the outer compression bandage (layer four) over Profore 3 Litepress to complete the system.

Assessment After Application

  • Check patient comfort after the system has been completed.
  • Check limb perfusion and ensure no signs of arterial compromise are present.
  • If the patient reports pain, cold toes, numbness, or colour change, remove the system immediately.

If pain, cold toes, numbness, tingling, or colour change develops after the compression system is applied, remove all bandage layers immediately and reassess arterial status. Do not reapply compression until the cause has been investigated.

Product Specification

Profore 3 Litepress 10cm x 8.7m

Profore 3 Litepress is supplied as a single 10cm wide, 8.7m length roll. The 8.7m length provides sufficient bandage to spiral from the foot to the knee with consistent overlap in a standard adult lower limb application. Width and length are fixed for this component.

Safety Information and Precautions

Contraindications

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

Cautions

  • ABPI between 0.6 and 0.8: reduced compression may be applied under specialist supervision only.
  • Peripheral neuropathy: impaired sensation reduces the patient's ability to report compression pain.
  • Diabetes with vascular complications.

Warning Signs After Application

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

Suitability

Clinical Use as Part of the Profore System

Profore 3 Litepress is used as layer three within the complete Profore four-layer compression system for venous leg ulcer management. It is not intended for use as a standalone bandage outside the Profore system context. The compression and clinical outcomes associated with multilayer compression systems are based on the validated four-layer system applied as a whole. Substituting individual components or using layers out of sequence may alter the compression delivered and the clinical outcome.

Purchasing Profore 3 Litepress

Profore 3 Litepress is a regulated medical device and does not require a prescription. The 10cm x 8.7m roll is available from Pharmacy Planet for clinical purchasers.

Our pharmacists can advise on Profore system components and on ordering for clinical settings.

Profore 3 Litepress is a clinical product for use as part of the Profore multilayer compression system by trained healthcare professionals. ABPI assessment must precede use of the system.

Storage

  • Store in a cool, dry place away from direct heat and sunlight.
  • Do not store above 25 degrees C.
  • Keep in original 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 3 Litepress is a genuine Smith & Nephew product stocked through regulated UK supply chains.

Our pharmacists can advise on Profore system components and on the full range of compression therapy products from Smith & Nephew.

References

  1. Smith & Nephew. Profore Multilayer Compression Bandaging System — Product Information. 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 3 LITEPRESS

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 any compression bandaging system is applied. Profore 3 Litepress must only be applied as part of the Profore multilayer compression system by a trained healthcare professional. It is not for patient self-application.

Each layer of a multilayer compression bandage system serves a distinct purpose. The padding layer protects bony prominences and distributes compression forces evenly. A conforming bandage layer holds the padding in position and adds a degree of elastic support before the outer compression layer is applied. Profore 3 Litepress is the third layer of the Profore multilayer compression system from Smith & Nephew. It is a light elastic conforming bandage applied over the padding layer to hold the system in place and contribute to the overall compression before the outer compression bandage is applied. 10cm x 8.7m. Clinical application only.

Profore 3 Litepress is a regulated medical device from Smith & Nephew and the third-layer component of the Profore multilayer compression bandage system for venous leg ulcer management. The Profore system achieves its therapeutic compression through the cumulative effect of four layers applied sequentially from the foot to the knee. Profore 3 Litepress is the light elastic conforming bandage that forms layer three.

The four layers of the Profore system each serve a distinct purpose. Layer one is the wound contact dressing applied directly over the ulcer. Layer two is an absorbent padding bandage that protects bony prominences, absorbs wound exudate, and distributes compression forces evenly over the contours of the lower leg. Layer three, Profore 3 Litepress, is a light elastic conforming bandage applied over the padding to hold it in position, add elastic support, and create a smooth surface for the outer compression layer. Layer four is the outer compression bandage, which delivers the primary therapeutic compression.

Litepress is described as light in compression compared to the outer compression bandage. The word "lite" in the product name indicates that this bandage contributes a lighter level of compression than the outer layer. Its function is not to deliver the primary therapeutic compression alone but to work as part of the system. The total compression at the ankle is achieved by the combined contribution of all layers.

Profore 3 Litepress is 10cm wide and 8.7m in length. The long roll length reflects the amount of bandage needed to spiral from the foot to the knee with appropriate overlap.

Arterial disease must be excluded before the Profore system is applied. An ABPI of 0.8 or above is generally required for full high compression. ABPI between 0.6 and 0.8 may permit reduced compression under specialist supervision. ABPI below 0.6 is a contraindication. Any patient with symptoms of arterial insufficiency requires ABPI assessment before compression is considered.

The Role of Layer Three in Multilayer Compression

In a multilayer compression system, the total compression at the skin surface is the sum of the contributions from all layers applied. Layer three, Profore 3 Litepress, contributes an elastic wrapping force over the padding layer below it. This contribution holds the padding bandage in position throughout the wear period, preventing it from slipping or bunching. The light elastic nature of Litepress also smooths out any irregularities in the padded limb surface, creating a more uniform foundation for the outer compression bandage applied above it.

Conforming to Lower Limb Contour

The lower leg has a complex contour: narrow at the ankle, broader at the calf, and narrowing again below the knee. A conforming elastic bandage adapts to these changes in circumference as it is applied, maintaining consistent contact with the padded limb surface throughout the application. This conformability reduces the risk of pressure ridges forming at bandage edges that can occur with a less conforming material, and ensures the outer compression layer is applied over a smooth, even base.

Cumulative Compression in the System

Multilayer compression systems are designed so that each layer contributes to the total compression delivered. The compression from each layer adds to the compression from the layers below. Profore 3 Litepress, as layer three, adds its contribution on top of the padding. The outer compression bandage, applied over Profore 3 Litepress, then adds its larger compression contribution to produce the total therapeutic compression at the ankle. The system is validated as a whole, and the layers should not be applied in isolation.

Applied by Trained Clinical Staff

The therapeutic compression delivered by the Profore system depends on the technique used to apply each layer. Profore 3 Litepress is applied in a spiral technique with a consistent overlap and tension. The compression contribution of the layer depends on the tension at which it is applied. Application that is too tight or too loose alters the total compression delivered and may move it outside the therapeutic range. Consistent application technique requires training and clinical experience.

Who Applies Profore 3 Litepress

  • Profore 3 Litepress is applied by trained healthcare professionals only.
  • Appropriate applicators include district nurses, tissue viability nurses, and community nurses trained in multilayer compression bandaging.
  • ABPI must be completed and documented before the first application of the system.

Application within the Profore System

  • Apply the wound contact layer and padding layer (layers one and two) before Profore 3 Litepress.
  • Apply Profore 3 Litepress over the padding layer in a spiral technique from the base of the toes upward.
  • Apply with consistent tension and overlap throughout.
  • Apply the outer compression bandage (layer four) over Profore 3 Litepress to complete the system.

Assessment After Application

  • Check patient comfort after the system has been completed.
  • Check limb perfusion and ensure no signs of arterial compromise are present.
  • If the patient reports pain, cold toes, numbness, or colour change, remove the system immediately.

If pain, cold toes, numbness, tingling, or colour change develops after the compression system is applied, remove all bandage layers immediately and reassess arterial status. Do not reapply compression until the cause has been investigated.

Profore 3 Litepress 10cm x 8.7m

Profore 3 Litepress is supplied as a single 10cm wide, 8.7m length roll. The 8.7m length provides sufficient bandage to spiral from the foot to the knee with consistent overlap in a standard adult lower limb application. Width and length are fixed for this component.

Contraindications

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

Cautions

  • ABPI between 0.6 and 0.8: reduced compression may be applied under specialist supervision only.
  • Peripheral neuropathy: impaired sensation reduces the patient's ability to report compression pain.
  • Diabetes with vascular complications.

Warning Signs After Application

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

Clinical Use as Part of the Profore System

Profore 3 Litepress is used as layer three within the complete Profore four-layer compression system for venous leg ulcer management. It is not intended for use as a standalone bandage outside the Profore system context. The compression and clinical outcomes associated with multilayer compression systems are based on the validated four-layer system applied as a whole. Substituting individual components or using layers out of sequence may alter the compression delivered and the clinical outcome.

Profore 3 Litepress is a regulated medical device and does not require a prescription. The 10cm x 8.7m roll is available from Pharmacy Planet for clinical purchasers.

Our pharmacists can advise on Profore system components and on ordering for clinical settings.

Profore 3 Litepress is a clinical product for use as part of the Profore multilayer compression system by trained healthcare professionals. ABPI assessment must precede use of the system.

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

Pharmacy Planet is a GPhC registered online pharmacy. Profore 3 Litepress is a genuine Smith & Nephew product stocked through regulated UK supply chains.

Our pharmacists can advise on Profore system components and on the full range of compression therapy products from Smith & Nephew.

References

  1. Smith & Nephew. Profore Multilayer Compression Bandaging System — Product Information. 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 3 Litepress is the third layer of the Profore multilayer compression system from Smith & Nephew for venous leg ulcer management. It is a light elastic conforming bandage applied over the padding layer to hold it in position, add elastic support, and create a smooth surface for the outer compression bandage. 10cm x 8.7m. Applied by trained clinical staff as part of the complete four-layer system. ABPI assessment required. No prescription required.

Layer three in the Profore system is the conforming elastic bandage applied over the padding layer. Its role is to hold the padding in position, smooth out the contoured surface of the padded limb, add a light elastic compression contribution, and create an even base for the outer compression bandage applied above it. It is not the primary compression layer. That function belongs to the outer compression bandage. The total compression is achieved by the combined effect of all four layers.

No. Profore 3 Litepress is designed for use as layer three within the complete Profore multilayer compression system. It is not validated or intended for use as a standalone compression bandage. The clinical outcomes associated with the Profore system are based on the validated four-layer system applied in the correct sequence. Using a single layer without the rest of the system will not deliver the therapeutic compression needed for venous leg ulcer management.

Profore 3 Litepress is layer three of the Profore system: a light elastic conforming bandage that holds the padding in place and creates a smooth surface for the outer layer. Profore+ is layer four: the outer compression bandage that delivers the primary therapeutic compression. Both are components of the same system, applied in sequence. Litepress is applied before Profore+, not instead of it.

Compression bandaging should feel firm but not painful when applied correctly and to a patient with adequate arterial circulation. Some initial tightness and a sensation of pressure are normal. Significant pain, increasing discomfort, cold toes, numbness, or tingling are not normal and indicate the compression may be too tight or that arterial blood flow is being compromised. Any of these symptoms should prompt immediate removal of all bandage layers and contact with the clinical team.

The Profore system is typically changed weekly under normal circumstances. Changes may be needed more frequently if wound status requires inspection, if exudate levels are high, or if limb dimensions change significantly as oedema resolves. The district or community nurse determines the change interval based on clinical assessment at each visit. Early in treatment, as oedema reduces and limb shape changes, more frequent changes may be needed to maintain effective compression.

ABPI stands for ankle brachial pressure index. It compares blood pressure at the ankle with blood pressure in the arm to assess whether arterial blood supply to the lower limb is adequate. Compression bandaging reduces blood flow in the leg. In a patient with arterial disease, compression can further reduce arterial flow and cause limb ischaemia. An ABPI of 0.8 or above generally confirms safe arterial circulation for high compression. ABPI below 0.6 is a contraindication. This test must be performed before compression is started.

No. Profore 3 Litepress is a regulated medical device and does not require a prescription. It is available from Pharmacy Planet for clinical purchasers. It is a clinical product for use as part of the Profore multilayer compression system by trained healthcare professionals. ABPI assessment must precede use.

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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