The Prevena Plus 125 is an advanced therapy unit designed for closed cyclic negative pressure wound therapy, aiding surgical incision healing with its innovative Visicheck Feature.
1.1 Overview of the Prevena Plus 125 Therapy Unit
The Prevena Plus 125 is a compact, portable therapy unit designed to deliver closed cyclic negative pressure wound therapy (CCNPWT). It is engineered to promote healing by applying controlled negative pressure to surgical incisions or wounds. The unit features an intuitive interface, a rechargeable battery, and a lightweight design, making it suitable for both clinical and home use. Its advanced Visicheck Feature ensures proper dressing application and seal integrity. The device is intended to minimize post-operative complications, such as fluid accumulation and infection, while promoting faster recovery. It is user-friendly, allowing patients to manage their therapy effectively with minimal training.
1.2 Purpose and Benefits of the Device
The Prevena Plus 125 is designed to promote healing of surgical incisions through negative pressure therapy. Its primary purpose is to hold incision edges together, reducing fluid accumulation and the risk of infection. Benefits include enhanced wound healing, minimized complications, and faster recovery. The device is portable, allowing for continuous therapy during daily activities. It also features an alert system to ensure proper functioning and patient safety. This therapy unit is ideal for post-operative care, offering a non-invasive solution to support patient recovery and improve clinical outcomes. Regular use can lead to shorter hospital stays and reduced healthcare costs, making it a valuable tool in wound management.
Components of the Prevena Plus 125
The Prevena Plus 125 includes a main therapy unit, canister, tubing, and dressing. It also features the Visicheck system for leak detection and therapy monitoring.
2.1 Main Unit Description
The Prevena Plus 125 main unit is a compact, portable device designed for closed cyclic negative pressure wound therapy. It features an intuitive interface with an ON/OFF button, an alert mute button, and LED indicators for power, alerts, and therapy status. The unit is lightweight and can be worn under clothing, making it suitable for patient mobility. It includes a carrying case for convenience. The main unit also incorporates the Visicheck Feature, which helps detect leaks and ensures proper therapy application. The device is designed for both clinical and home use, providing continuous or intermittent negative pressure to promote wound healing.
2.2 Accessories and Additional Components
The Prevena Plus 125 comes with essential accessories to ensure effective therapy. These include a flexible tubing set, a canister for fluid collection, and a dressings kit tailored for wound care. Additional components like a power adapter, carry strap, and therapy head with a foam dressing are also provided. The tubing connects the main unit to the canister, while the dressings are designed to fit various wound sizes. A carrying case is included for easy transport and discreet use. These accessories are vital for proper therapy application and patient mobility. They are designed to work seamlessly with the main unit, ensuring a comfortable and effective wound healing experience.
2.3 Understanding the Visicheck Feature
The Visicheck Feature on the Prevena Plus 125 is a critical tool for ensuring proper therapy application. It helps verify the integrity of the therapy system by checking for leaks and ensuring the dressing is securely connected. To activate Visicheck, double-press the ON/OFF button. The feature assesses the system’s seal and provides feedback on its status. If a “Marginal Leak Rate” is detected, it indicates a potential issue with the canister connection or dressing. Addressing these alerts ensures optimal therapy performance. This feature is essential for maintaining the effectiveness of the therapy and preventing complications. Regular use of Visicheck helps healthcare providers and patients achieve better wound healing outcomes.
Setting Up the Prevena Plus 125
Setting up the Prevena Plus 125 involves preparing the therapy unit, priming the tubing, locking the canister, and activating the Visicheck Feature to ensure proper therapy application.
3.1 Preparing the Therapy Unit
Preparing the Prevena Plus 125 involves ensuring the therapy unit is ready for use. Start by checking the device for any visible damage or issues. Next, ensure the canister is properly locked into the unit to prevent leaks. Activate the Visicheck Feature by double-pressing the ON/OFF button to confirm the system is functioning correctly. Review the instruction manual to familiarize yourself with the controls and settings. Ensure the tubing and dressing are prepared according to the guidelines provided. Finally, perform a quick system check to ensure all components are functioning properly before initiating therapy. Proper preparation ensures safe and effective use of the device.
3.2 Priming the Tubing and Dressing
Priming the tubing and dressing ensures proper function of the Prevena Plus 125. Begin by connecting the tubing to the canister and the dressing, ensuring a secure fit. Use the Visicheck Feature to verify the system is airtight by double-pressing the ON/OFF button. Once activated, the system will automatically check for leaks. If a “Marginal leak rate” is detected, ensure all connections are secure and repeat the process. Gently press the tubing to remove any air bubbles. Finally, inspect the dressing for proper placement and ensure it is free from wrinkles or twists. Proper priming ensures consistent therapy delivery and optimal wound healing. Always follow the manual for detailed steps.
3.3 Locking the Canister
To lock the canister in the Prevena Plus 125, align it with the main unit and gently slide it into place until it clicks securely. Ensure the canister is fully seated and the locking mechanism is engaged. After locking, perform a system check by double-pressing the ON/OFF button to activate the Visicheck Feature. This will verify the integrity of the seal. If a “Marginal leak rate” is detected, recheck the canister alignment and connections. Once locked and verified, the device is ready for therapy. Properly securing the canister ensures consistent negative pressure delivery and prevents leaks during operation. Always verify the system after locking to ensure optimal functionality.
3.4 Activating the Visicheck Feature
To activate the Visicheck Feature on the Prevena Plus 125, press the ON/OFF button twice in quick succession. This initiates a system check to ensure proper sealing. After activation, the device will display the status. If a “Marginal leak rate” is indicated, recheck the canister alignment and tubing connections. The Visicheck Feature ensures therapy effectiveness by confirming system integrity. Perform this step after locking the canister and before starting therapy to guarantee accurate negative pressure delivery. Proper activation confirms the system is ready for operation, ensuring optimal therapy performance.
Operating the Prevena Plus 125
Operating the Prevena Plus 125 involves turning the device on/off, adjusting settings, and monitoring sessions. Use the ON/OFF button to start therapy and handle alarms as needed.
4.1 Turning the Device On and Off
To turn the Prevena Plus 125 on, locate the ON/OFF button on the main unit and press it firmly until you hear a beep. Ensure the canister is locked and the dressing is properly applied before starting therapy. The device will not activate unless these conditions are met. Once activated, the unit will begin operating, providing cyclic negative pressure to the surgical site. To turn the device off, press and hold the same ON/OFF button until the beep sounds again, indicating the unit has powered down. Always follow proper shutdown procedures to ensure patient safety and maintain device functionality.
4.2 Adjusting Therapy Settings
To adjust therapy settings on the Prevena Plus 125, use the control panel buttons to navigate through the menu. Press the SELECT button to choose the desired setting, such as pressure level or cycle duration. Use the UP and DOWN arrows to modify the value. Once adjustments are made, press SELECT again to save and return to the main screen. Settings should only be changed based on clinical requirements and under professional guidance. Ensure the device confirms the changes with a beep or message. Always refer to the instruction manual for specific guidance on therapy parameters. The device will revert to default settings if not saved properly, so confirmation is essential before proceeding.
4.3 Monitoring the Therapy Session
During therapy, monitor the Prevena Plus 125 by checking the LCD display for pressure levels, cycle status, and alerts. Ensure the dressings remain secure and the canister is properly locked. If an alert occurs, refer to the alarm conditions section to resolve the issue. The device provides audible and visual feedback to indicate normal operation or potential issues. Regularly inspect the tubing and connections for leaks or blockages. Press the ALERT MUTE button to temporarily silence alarms if needed. Always ensure the therapy unit is functioning correctly to maintain effective wound healing. Follow the instruction manual for guidance on interpreting display messages and addressing any concerns promptly. Proper monitoring ensures optimal therapy outcomes and patient safety.
4.4 Understanding Alarm Conditions
The Prevena Plus 125 alerts users through visual and audible alarms to indicate potential issues during therapy. Common alarm conditions include low battery, system errors, or therapy interruptions. When an alarm occurs, the device displays an error message on the LCD screen. To address the issue, press and hold the center of the ALERT MUTE button for three seconds to silence the audible alert temporarily. Refer to the instruction manual for specific trouble codes and solutions. If the alarm persists, check the tubing, canister, and dressings for leaks or disconnections. Ensure all components are properly secured and functioning. Addressing alarm conditions promptly ensures continuous therapy and optimal healing outcomes. Always consult the manual or contact a healthcare professional if unresolved issues arise. Proper handling of alarms is crucial for maintaining therapy effectiveness and patient safety.
Maintenance and Troubleshooting
Regular maintenance ensures optimal performance. Clean the device, check for wear, and ensure all components function correctly. Address issues promptly to maintain therapy effectiveness and safety.
5.1 Daily Maintenance Tips
Daily maintenance is crucial for the Prevena Plus 125 to function effectively. Start by cleaning the exterior with a soft cloth and mild detergent, avoiding harsh chemicals. Regularly inspect tubing and connectors for signs of wear or damage, replacing them if necessary. Ensure the canister is properly locked after use to prevent leaks. Check the alert mute button for functionality and clean it gently to avoid dust buildup. Always store the device in a dry, cool place when not in use. Following these steps ensures the device remains in optimal condition and ready for therapy sessions.
5.2 Handling Common Alerts and Alarms
The Prevena Plus 125 features an alert system to notify users of potential issues. Common alerts include low battery, leak detection, or a full canister. When an alert occurs, the device will emit an audible signal and display a message on the screen. To address these, first identify the cause by referring to the manual or the device’s display. For example, a leak alert may require checking the canister lock or tubing connections. The alert mute button can silence the audible alert temporarily, but the underlying issue must be resolved to ensure proper function. Always follow the recommended troubleshooting steps to restore normal operation and maintain therapy effectiveness.
5.3 Troubleshooting Common Issues
Common issues with the Prevena Plus 125 include the Visicheck Feature indicating a marginal leak or the device not turning on. If a leak is detected, ensure the canister is securely locked and tubing connections are tight. For power issues, check the battery level or ensure the unit is properly charged. If the canister appears full but isn’t emptying, verify the tubing for kinks or blockages. Reset the system by turning it off and on again. If issues persist, consult the manual or contact a healthcare professional. Regular maintenance and proper usage can prevent many of these problems, ensuring effective therapy and patient comfort.
Safety Precautions
Always follow safety guidelines to avoid accidents; Ensure proper handling of the device, and keep it out of reach of children. Use as directed.
6.1 General Safety Information
The Prevena Plus 125 is designed for safe operation, but proper handling is essential. Ensure the device is used in an electromagnetic environment with controlled disturbances. Avoid exposing the unit to extreme temperatures or moisture. Always follow the manufacturer’s instructions for setup and maintenance. Patients should be monitored regularly during therapy to prevent complications. Ensure the device is kept out of reach of children and unauthorized users. In case of emergencies, refer to the user manual for guidance. Proper training and adherence to safety protocols are crucial for effective and secure use of the therapy unit. Regular checks and maintenance can prevent potential hazards.
6.2 Contraindications for Use
The Prevena Plus 125 is not suitable for all patients. It should not be used in cases of active bleeding, untreated osteomyelitis, or in the presence of malignancy in the wound. Patients with sensitivity to the device components or dressings should avoid its use. Additionally, the device is contraindicated for non-enteric fistulas, exposed blood vessels, or organs. Use with caution in patients with compromised wound healing or those requiring anticoagulant therapy. The device is not intended for pediatric use without medical supervision. Always consult the manufacturer’s guidelines and medical professionals before applying the therapy to ensure patient safety and suitability.
6.3 Warnings and Cautions
Adherence to guidelines is crucial for safe use of the Prevena Plus 125. Ensure proper application to avoid leaks or improper sealing. Use in environments with high oxygen levels or flammable gases requires caution due to explosion risks. Patients should avoid submerging the device in water and handle tubing carefully to prevent damage. The device may not be suitable for patients with certain medical conditions or sensitivities. Regular monitoring is essential to prevent complications. Follow the manual instructions carefully and consult healthcare professionals for personalized advice to ensure safe and effective therapy.
Clinical Considerations
The Prevena Plus 125 is designed for closed cyclic negative pressure wound therapy, promoting healing in surgical incisions. It’s essential to consider patient-specific criteria and therapy limitations.
7.1 Indications for Use
The Prevena Plus 125 is primarily indicated for use in closed cyclic negative pressure wound therapy, particularly for managing surgical incisions. It is designed to promote healing by applying negative pressure, which helps to close incision edges and reduce the risk of complications. The device is suitable for post-surgical patients requiring continuous or intermittent negative pressure therapy. It is commonly used for wounds resulting from cardiovascular, orthopedic, or general surgeries. The therapy is beneficial for patients at risk of wound dehiscence or those with delayed healing. However, it is contraindicated for open wounds, active bleeding, or infected sites. Proper patient selection is critical for effective therapy outcomes.
7.2 Limitations of Therapy
The Prevena Plus 125 is not suitable for all patients or conditions. It is ineffective for open or necrotic wounds, and its use is contraindicated in cases of active bleeding or infection. The device requires precise application and maintenance to function optimally, and improper use may lead to reduced efficacy. Additionally, the therapy may not be appropriate for patients with certain medical conditions or those unable to adhere to prescribed protocols. While it aids in wound healing, it does not address underlying tissue damage or infections. Patient compliance and proper training are essential for achieving desired outcomes. The device’s effectiveness may also be limited by factors such as wound depth or location, requiring careful assessment before use.
7.3 Patient Selection Criteria
Appropriate candidates for Prevena Plus 125 therapy are those with closed surgical incisions at risk of complications. Patients must have intact, viable tissue surrounding the incision and no active infection. They should have no known allergies to the materials used in the device. Additionally, patients must be able to comply with therapy protocols, including wearing the device continuously and attending follow-up appointments. Those with significant medical conditions, such as uncontrolled diabetes or poor circulation, may require further evaluation. Pregnant or breastfeeding patients should consult their healthcare provider before use. Proper patient selection ensures optimal outcomes and minimizes potential risks associated with therapy.
Patient Care and Management
Patient care involves preparing the patient for therapy, monitoring progress, addressing comfort, and providing education to ensure safe and effective use of the Prevena Plus 125.
8.1 Preparing the Patient for Therapy
Preparing the patient for therapy involves educating them on the device’s purpose and proper use. Ensure the patient’s skin is clean and dry before applying the dressing. Fit the Prevena Plus 125 securely, ensuring comfort and proper alignment. Patients should be instructed on how to wear the unit under clothing and use the carrying case for portability. Emphasize the importance of following instructions for sleeping and showering to maintain therapy continuity. Provide clear guidance on monitoring the device and addressing any concerns promptly to ensure a smooth therapy experience.
8.2 Monitoring Patient Progress
Regularly monitor the patient’s progress to ensure effective therapy. Check the therapy unit’s settings and confirm proper operation. Assess the surgical site for healing signs, such as closed incision edges. Review the canister’s fluid level and ensure it’s within acceptable limits. Address any issues promptly, like alarms or leaks, to maintain therapy continuity. Educate the patient to report changes or discomfort. Document progress for follow-up care. Proper monitoring helps achieve optimal healing outcomes and minimizes complications. Always follow the Prevena Plus 125 instruction manual for specific guidance on patient monitoring.
8.3 Addressing Patient Comfort
Patient comfort is crucial during therapy with the Prevena Plus 125. Ensure the therapy unit is worn securely under clothing using the provided carrying case, allowing for discreet mobility. Regularly inspect the dressing and tubing for proper fit to avoid irritation. Address any discomfort by adjusting the unit’s position or repositioning the canister. If alarms occur, resolve the issue promptly to minimize patient anxiety. Encourage patients to report any pain or tightness for timely intervention. Proper patient education on wearing and managing the device can enhance comfort and adherence to therapy. Always prioritize patient well-being to ensure a positive experience with the Prevena Plus 125.
8.4 Patient Education
Patient education is essential for successful therapy with the Prevena Plus 125. Ensure patients understand the purpose of the device, its operation, and the importance of adhering to therapy schedules. Demonstrate how to wear the unit, including proper placement in the carrying case, and explain how to manage the tubing and dressing. Teach patients to recognize and respond to alarms, such as muted alerts or system notifications. Emphasize the significance of the Visicheck Feature in ensuring therapy effectiveness. Provide guidance on daily activities, such as showering and sleeping with the device, and advise on when to seek assistance. Clear communication and thorough education empower patients to manage their therapy confidently and safely.
The Prevena Plus 125 is an effective solution for surgical wound healing, utilizing negative pressure therapy and the Visicheck Feature to ensure proper dressing sealing and therapy effectiveness, promoting optimal recovery and patient comfort.
9.1 Summary of Key Points
The Prevena Plus 125 is a closed cyclic negative pressure therapy unit designed to promote surgical incision healing. It features the Visicheck system to ensure proper dressing sealing and therapy effectiveness. The device aids in holding incision edges together, reducing fluid accumulation, and minimizing the risk of complications. It is portable, easy to use, and can be worn under clothing, making it suitable for both clinical and home care settings. Proper preparation, priming, and activation of the Visicheck Feature are essential for optimal performance. Regular maintenance and adherence to safety guidelines ensure patient comfort and effective therapy outcomes. Following the instruction manual is crucial for proper device operation and patient care.
9.2 Final Tips for Effective Use
For optimal results with the Prevena Plus 125, ensure proper preparation and priming of the device before use. Regularly check for leaks and confirm the canister is securely locked to maintain therapy consistency. Keep the unit clean and store it in a dry environment when not in use. Always follow the instruction manual for troubleshooting and maintenance to prevent device malfunctions. Patients should wear the device as directed, even during sleep, and shower according to the provided guidelines. Monitor therapy progress and address any discomfort promptly. Adhere to healthcare provider recommendations for therapy duration and settings. By following these tips, users can maximize the effectiveness of the Prevena Plus 125 and achieve the best possible outcomes.