Welcome to the Prevena Plus 125 Instruction Manual. This guide provides essential information for the safe and effective use of the Prevena Plus 125 Therapy Unit, designed to manage closed surgical incisions through continuous negative pressure. Intended for patients and caregivers, this manual outlines proper setup, operation, and maintenance to ensure optimal therapy outcomes and minimize complications. Adhering to these instructions is crucial for achieving desired results and preventing potential issues during treatment.

1.1 Overview of the Prevena Plus 125 Therapy Unit

The Prevena Plus 125 Therapy Unit is a portable, single-use medical device designed to manage closed surgical incisions. It applies continuous negative pressure of -125mmHg to remove fluid and promote healing. The unit is intended for home use, offering a discreet and lightweight solution for post-surgical recovery. It works in conjunction with specialized dressings to create a controlled environment, reducing the risk of complications and supporting faster recovery. This therapy is prescribed for patients requiring advanced incision care.

1.2 Importance of Following the Instruction Manual

Following the Prevena Plus 125 Instruction Manual is essential for safe and effective therapy. Proper adherence ensures the device operates correctly, minimizing risks of complications. Failure to follow instructions may lead to leaks, improper pressure application, or device malfunction, potentially harming the patient or delaying recovery. The manual provides critical guidance for patients and caregivers, outlining setup, operation, and troubleshooting steps. Adhering to these guidelines is crucial for achieving optimal therapeutic outcomes and maintaining patient safety throughout the treatment period.

Components of the Prevena Plus 125 System

The Prevena Plus 125 System includes the therapy unit, Prevena Restor dressings, connectors, tubing, and a canister. These components work together to apply negative pressure, promoting wound healing. Proper assembly ensures effective therapy. Detailed descriptions and usage instructions are provided in the following sections.

2.1 Description of the Therapy Unit

The Prevena Plus 125 Therapy Unit is a portable, user-friendly device designed to apply continuous negative pressure (-125mmHg) to closed surgical incisions. It consists of a control panel, canister for fluid collection, and tubing connecting to the dressing. The unit is lightweight, allowing for mobility, and includes indicators for alerts such as low battery or blockages. It also features a Visicheck system to monitor leaks, ensuring proper therapy function. This system is essential for promoting wound healing and reducing post-surgical complications in a home or clinical setting.

2.2 Accessories and Dressings

The Prevena Plus 125 system includes specialized dressings and accessories designed for optimal therapy performance. Prevena Restor dressings feature Sensat.R.A.C. technology, ensuring customized fit and pressure distribution. Accessories like patch strips and excess drape help seal leaks, while the tubing connects the dressing to the therapy unit. These components work together to maintain negative pressure, promote healing, and protect the surgical site. Proper use of dressings and accessories is critical for effective therapy and minimizing complications. Always follow the instructions for application and maintenance.

Setting Up the Prevena Plus 125 Therapy Unit

Setting up the Prevena Plus 125 involves preparing the device, connecting the dressing, and ensuring proper seals. Follow the instructions carefully to ensure therapy effectiveness and safety.

3.1 Preparing the Device for Use

Before using the Prevena Plus 125 Therapy Unit, ensure all components are included and the device is fully charged. Check for any visible damage or tampering.
– Turn on the unit and allow it to power up completely.
– Ensure the canister is properly locked into place and the tubing is not kinked.
– Verify the negative pressure setting matches your clinician’s instructions.
– Conduct a system check to ensure all alarms and indicators function correctly.
– Place the unit on a stable, flat surface, away from direct sunlight and moisture.
– Always follow the manufacturer’s guidelines for preparation and safety.

3.2 Connecting the Dressing to the Therapy Unit

To connect the dressing to the Prevena Plus 125 Therapy Unit:
– Remove the dressing from its packaging, ensuring the tubing is intact and not kinked.
– Align the dressing’s connector with the unit’s port and securely attach it.
– Ensure the dressing is properly sealed to the skin, using additional drape strips if necessary to prevent leaks.
– Check for any obstructions in the tubing and confirm the canister is locked into place.
– Once connected, turn on the unit and allow it to initiate therapy.
– Always follow the manufacturer’s instructions for a secure and proper connection.

Operating the Prevena Plus 125 Therapy Unit

Turn on the unit, ensure the canister is locked, and confirm the tubing is securely connected. Monitor the therapy settings and check for any leaks or blockages regularly.

4.1 Starting the Therapy

Turn on the Prevena Plus 125 Therapy Unit by pressing the power button. Ensure the canister is securely locked and the tubing is properly connected to both the unit and the dressing. Confirm the therapy settings match your clinician’s prescription. Once activated, the unit will begin applying continuous negative pressure. You may hear a brief beep indicating the therapy has started. Allow the unit to run uninterrupted to ensure proper wound management and fluid removal.

4.2 Monitoring the Device

Regularly monitor the Prevena Plus 125 Therapy Unit for alerts, indicators, and proper function. Check for audible alarms or visual alerts, which signal issues like blockages or low battery. Ensure the canister is not full and that there are no leaks or kinks in the tubing. Use the Visicheck feature to assess leak levels and follow troubleshooting steps if necessary. Maintain the device in a controlled environment and ensure it remains charged for continuous therapy. Proper monitoring ensures effective wound management and patient safety.

Troubleshooting Common Issues

Address common issues like leaks, blockages, or alerts by checking connections, ensuring the canister is secure, and consulting the manual for guidance. Proper troubleshooting ensures therapy continuity and effectiveness.

5.1 Identifying and Correcting Leaks

Identify leaks by checking the Visicheck feature or audible alerts. Ensure the canister is securely locked and tubing is not kinked. Seal leaks using 3M Prevena Patch Strips or excess drape around the dressing edges. If issues persist, consult the manual or contact a clinician. Promptly addressing leaks ensures consistent negative pressure, maintaining therapy effectiveness and preventing complications. Regular checks help minimize interruptions and promote optimal wound healing throughout the treatment duration.

5.2 Addressing Alerts and Indicators

The Prevena Plus 125 Therapy Unit features alerts and indicators to ensure proper functionality. Audible alerts, such as two repeating beeps, may indicate blockages or low battery. Check the canister for a full status or kinked tubing. Use the Visicheck feature to assess leak levels. Addressing these alerts promptly prevents therapy interruptions. Refer to the manual or consult a clinician if issues persist. Monitoring these indicators ensures continuous therapy and supports effective wound management throughout the treatment process.

Patient Guidance for Using the Prevena Plus 125

Patient guidance focuses on daily care, monitoring, and troubleshooting. Proper wound management, dressing changes, and device maintenance are emphasized to ensure safe and effective therapy outcomes. Refer to the manual for detailed instructions.

6.1 Daily Maintenance and Care

Daily maintenance is crucial for optimal therapy performance. Patients should check for leaks, ensure the canister is securely locked, and monitor battery levels. Regularly inspect the dressing and tubing for kinks or blockages. Keep the therapy unit clean and dry, avoiding submersion in water. Follow proper hand hygiene when handling the device or dressings. Refer to the manual for detailed care instructions to maintain device functionality and ensure therapeutic effectiveness throughout the treatment period.

• Check for leaks daily.
• Ensure the canister is locked.
• Monitor indicators and alerts.
• Keep the device clean and dry.
• Follow hygiene practices during dressing changes.

6.2 Bathing and Dressing Changes

Bathing requires careful handling of the Prevena Plus 125 system. Keep the therapy unit dry; avoid submerging it in water. Use a waterproof cover if necessary. For dressing changes, follow the manual’s instructions and your clinician’s guidance. Ensure the incision site is clean and dry before applying a new dressing. Use Prevena Restor dressings for compatibility. If leaks occur, seal them with drape strips or additional adhesive. Refer to the troubleshooting section for leak correction.

• Keep the therapy unit dry during baths.
• Use waterproof protection if needed.
• Follow proper dressing change procedures.
• Seal leaks promptly to maintain therapy effectiveness.

Disposal and End of Therapy

At the end of therapy, return the Prevena Plus 125 Therapy Unit to your physician for proper disposal. Dispose of all waste according to local regulations.

• Return the unit to your physician.
• Dispose of waste locally.

7.1 Proper Disposal of the Therapy Unit

The Prevena Plus 125 Therapy Unit must be returned to your physician at the end of therapy for appropriate disposal. Ensure all components, including dressings and accessories, are securely packaged. Follow local regulations for medical device disposal to prevent environmental harm. Improper disposal may lead to regulatory non-compliance. Always consult your healthcare provider for specific guidance on disposal procedures.

7.2 Returning the Device to the Physician

After completing therapy, return the Prevena Plus 125 Therapy Unit to your physician. Ensure the device is turned off and all components, including tubing and dressings, are securely packaged. Follow your physician’s specific instructions for return procedures. This ensures proper handling and disposal, adhering to medical regulations. Contact your healthcare provider to schedule a follow-up appointment for device return and further guidance. This step is crucial for maintaining compliance and safety standards.

Electromagnetic Compatibility

The Prevena Plus 125 Therapy Unit is designed for use in controlled electromagnetic environments. Ensure it operates in areas with minimal radiated RF disturbances to avoid interference.

8.1 Operating in Controlled Environments

The Prevena Plus 125 Therapy Unit is intended for use in environments with controlled electromagnetic interference. Ensure the device operates in areas with minimal radiated RF disturbances to prevent malfunction. Users must adhere to the guidelines provided in the manual to maintain electromagnetic compatibility. Failure to do so may result in inaccurate therapy delivery or device failure. Always consult the manual for specific instructions on operating in controlled environments to ensure safe and effective therapy outcomes.

Customization and Dressing Options

The Prevena Plus 125 system offers customizable dressing solutions, including Prevena Restor Dressings with SENSAT;R.A.C.™ technology, designed to provide tailored therapy for various wound sizes and locations. This section explains how to select and apply the appropriate dressings to optimize therapy outcomes, ensuring a secure fit and effective negative pressure delivery. Proper customization enhances patient comfort and promotes healing efficiency, making it a key aspect of the therapy process.

9.1 Using Prevena Restor Dressings

The Prevena Restor Dressings are designed for use with the Prevena Plus 125 Therapy Unit, offering customizable solutions for surgical incision management. Featuring SENSAT.R.A.C.™ technology, these dressings ensure precise negative pressure delivery. They are tailored to fit various wound sizes and locations, promoting optimal healing environments. Proper application involves aligning the dressing with the incision and securing it with the provided strips. Always follow the instructions for use to ensure correct placement and function. This customization enhances therapy effectiveness and patient comfort during recovery.

Safety Information

The Prevena Plus 125 Therapy Unit is intended for closed surgical incisions under -125mmHg continuous negative pressure. Contraindications include open wounds, exposed organs, or hyperbaric oxygen therapy. Use in uncontrolled electromagnetic environments may affect performance. Always consult a clinician before application and follow instructions for use carefully to minimize risks and ensure safe therapy.

10.1 Contraindications and Warnings

The Prevena Plus 125 Therapy Unit is contraindicated for use on open wounds, exposed organs, or in the presence of necrotic tissue. It should not be used during hyperbaric oxygen therapy or in uncontrolled electromagnetic environments. The device is not intended for use on staples, sutures, or clips. Active bleeding, cancer, or sensitivity to components are additional contraindications. Always consult a clinician before use to ensure safe application and avoid potential complications. Proper adherence to warnings and contraindications is essential for effective therapy.

Frequently Asked Questions

This section addresses common inquiries about the Prevena Plus 125, helping users understand its operation, troubleshooting, and maintenance for optimal therapy outcomes.

11.1 Common Questions About the Prevena Plus 125

How long does the Prevena Plus 125 battery last? Typically up to 7 days. Can I shower with the device? Yes, but follow sealing instructions. What causes leaks? Poor drape adhesion or kinked tubing. Why does the unit beep? Alerts for blockages, low battery, or leaks. How do I address a marginal leak? Ensure the canister is locked and check for kinks. For more details, refer to the troubleshooting section or consult a clinician. Always follow the manual for safe operation.

The Prevena Plus 125 Instruction Manual provides comprehensive guidance for safe and effective use. Proper adherence ensures successful therapy, while disposal and clinician consultation are emphasized for optimal outcomes.

12.1 Summary of Key Points

The Prevena Plus 125 Instruction Manual is a comprehensive guide for patients and caregivers. It covers setup, operation, and maintenance of the therapy unit, emphasizing safety and effectiveness. Key topics include proper use of dressings, troubleshooting leaks, and addressing alerts. Patient guidance on daily care, bathing, and dressing changes is provided to ensure optimal recovery. Importantly, the manual stresses the need for clinician consultation and adherence to instructions for successful therapy outcomes and proper disposal of the device.