The Prevena Plus 125 System is an innovative solution designed to manage closed surgical incisions, aiding in recovery and preventing post-operative complications effectively․
Overview of the Prevena Plus 125
The Prevena Plus 125 System is a specialized medical device designed to manage closed surgical incisions, particularly those that continue to drain after sutured or stapled closure․ It is intended to promote healing, reduce the risk of complications, and improve patient outcomes․ The system utilizes negative pressure therapy to create a controlled environment around the incision site, facilitating the removal of fluid and promoting tissue repair․
Its compact and portable design makes it suitable for use in various clinical settings, including hospitals and outpatient facilities․ The Prevena Plus 125 is commonly used in surgeries where post-operative drainage is a concern, such as cardiovascular, general, or orthopedic procedures․ The system is user-friendly, allowing healthcare professionals to easily apply and monitor therapy, ensuring optimal results and minimizing the risk of infection or dehiscence․
Key Features and Benefits
The Prevena Plus 125 System offers advanced features that enhance surgical incision management․ Its compact, lightweight design ensures portability, making it ideal for use in various clinical settings․ The system incorporates a user-friendly interface with intuitive controls, allowing healthcare professionals to easily operate and monitor therapy․ The Prevena Plus 125 provides adjustable negative pressure settings, enabling personalized treatment for different patient needs and wound types․
Key benefits include reduced risk of post-operative complications, such as infection or dehiscence, and faster healing times․ The system’s ability to manage fluid effectively minimizes the need for frequent dressing changes, improving patient comfort and reducing healthcare resource utilization․ Its real-time monitoring capabilities ensure continuous therapy delivery, promoting optimal wound healing outcomes․ These features make the Prevena Plus 125 a valuable tool in post-surgical care․
Components of the Prevena Plus 125
The Prevena Plus 125 includes a control unit, fluid canisters, dressings, tubing sets, and sensors․ Accessories like power sources and carrying cases are also provided․
Hardware Components
The Prevena Plus 125 System includes a compact control unit designed for portability and ease of use․ The control unit houses the electronic components responsible for managing therapy settings and monitoring the system’s operation․ It is equipped with a user-friendly interface, including a display screen and control buttons, allowing healthcare professionals to set and adjust parameters according to patient needs․ Additional hardware components include the fluid canisters, which collect excess drainage from the surgical site, and the pressure regulation module, ensuring consistent negative pressure therapy․ The system also features sensors that monitor pressure levels and alert the user to any deviations from set parameters․ These components work together to provide a reliable and efficient solution for managing surgical incisions․
Accessories and Consumables
The Prevena Plus 125 System requires specific accessories and consumables to ensure optimal performance․ These include a range of sterile dressings designed for use with negative pressure therapy, such as foam dressings and transparent films․ The dressings are tailored to fit various wound sizes and shapes, promoting effective drainage and tissue healing․ Additional consumables include tubing sets, which connect the dressings to the control unit, and fluid collection canisters that store drainage from the surgical site․ These components are essential for maintaining a closed, sterile environment and ensuring the system functions as intended․
Other accessories may include power cords, patient adapters, and protective covers for the control unit․ Regular replacement of consumables is necessary to maintain hygiene and system efficiency, as outlined in the user manual․
Indications for Use
The Prevena Plus 125 System is indicated for the management of closed surgical incisions, particularly those with persistent drainage after sutured or stapled closure․
Approved Surgical Applications
The Prevena Plus 125 System is designed for use in various surgical procedures, including cardiovascular, orthopedic, and abdominal surgeries․ It is particularly effective in managing closed surgical incisions that continue to drain following sutured or stapled closure․ The system is approved for use in post-operative care to promote healing, reduce the risk of complications, and improve patient outcomes․ It is suitable for surgeries where fluid accumulation at the incision site is a concern․ The device is not intended for use on open or infected wounds․ Its application is supported by clinical evidence demonstrating its ability to minimize post-surgical complications and enhance recovery․ Always refer to the user manual for specific guidelines on approved applications and contraindications․
Contraindications
The Prevena Plus 125 System is contraindicated for use on open or infected wounds, as it is specifically designed for closed surgical incisions․ It should not be applied to incisions with active drainage that exceeds the device’s capacity․ Additionally, the system is not intended for use on patients with known hypersensitivity to any of its components․ It is also contraindicated for use on incisions where the skin and underlying tissues are not adequately closed or are necrotic; The device should not be used in the presence of active infection or where an infection is suspected․ Always consult the user manual for a comprehensive list of contraindications and ensure proper patient selection to avoid adverse outcomes․ Proper assessment of the surgical site is critical before applying the Prevena Plus 125 System․
Preparation and Setup
Thoroughly unpack and inspect all components․ Sterilize reusable parts as per instructions․ Connect the therapy unit to the Dressing Set․ Power on and perform a system check․
Unpacking and Sterilization
Start by carefully unpacking the Prevena Plus 125 System from its sealed packaging․ Inspect all components for any visible damage or defects․ The system includes the therapy unit, Dressing Set, and accessories․ Reusable components, such as the therapy unit, must be cleaned with a soft, dry cloth and mild detergent before sterilization․ Avoid using abrasive materials or chemical disinfectants, as they may damage the device․ Disposable components, like the Dressing Set, should not be resterilized or reused․ Once cleaned, reusable parts can be sterilized using standard medical sterilization methods, ensuring all surfaces are dry before use․ Always follow the manufacturer’s guidelines for proper sterilization to maintain system performance and patient safety․ Proper preparation ensures optimal functionality and minimizes risks during therapy․ Adhere strictly to the manual instructions for unpacking and sterilization procedures․
Powering the Device
To power the Prevena Plus 125 System, connect the provided AC/DC adapter to the therapy unit and plug it into a compatible electrical outlet․ Ensure the outlet meets the specified voltage requirements․ The device also features a rechargeable battery, which provides up to 12 hours of continuous operation․ Charge the battery fully before use, allowing approximately 4 hours for a complete charge․ The power button, located on the front panel, illuminates when the device is turned on․ A green light indicates normal operation, while a red light signals low battery or an error․ Always verify proper power connection before initiating therapy․ For portable use, ensure the battery is fully charged or keep the device plugged in during operation․ Follow the manual for specific power management instructions to ensure uninterrupted therapy delivery․
Operating the Prevena Plus 125
The Prevena Plus 125 is designed for managing closed surgical incisions․ Operation involves initializing therapy via the user-friendly interface, following manual guidelines for effective therapy delivery and minimizing post-operative complications․
Starting the Therapy
Starting therapy with the Prevena Plus 125 involves a straightforward process․ Begin by ensuring the device is properly prepared and the patient is ready․ Follow the manual guidelines to place the device correctly on the closed surgical incision․ Connect the therapy unit to the dressing, ensuring a secure and airtight seal․ Power on the device and select the appropriate therapy settings based on the surgeon’s instructions or the manual․ Once activated, the system will begin operating, providing continuous negative pressure to promote wound healing and reduce fluid accumulation․ Always ensure proper placement and connection to avoid complications․ The system is designed for ease of use, with clear indicators and alarms to notify if adjustments are needed․ Proper initiation of therapy is crucial for optimal results and patient safety․
Adjusting Settings
Adjusting settings on the Prevena Plus 125 is a user-friendly process designed to optimize therapy for individual patient needs․ Using the control panel, healthcare professionals can modify parameters such as negative pressure levels and therapy duration․ The system allows for precise adjustments to ensure effective wound management while minimizing discomfort․ Pressure settings can be customized within predefined ranges, guided by the device’s intuitive interface․ Additionally, therapy modes can be switched to accommodate different stages of healing․ Always refer to the manual for specific guidelines on adjusting settings to ensure safety and efficacy․ The device provides real-time feedback, enabling immediate adjustments if necessary․ Proper setting customization is essential for achieving desired clinical outcomes and patient comfort during therapy․ Follow the manual’s instructions to avoid errors and ensure optimal performance of the Prevena Plus 125 System․
Monitoring the System
Monitoring the Prevena Plus 125 System is essential to ensure optimal performance and patient safety during therapy․ The device features a user-friendly interface with real-time feedback, allowing healthcare professionals to track key parameters such as pressure levels, therapy duration, and system status․ Regular checks should be performed to verify that the system is functioning correctly and that all connections are secure․ Visual and audible alarms will alert users to any deviations from set parameters or potential issues, such as blockages or low battery levels․ Monitoring also involves observing the patient’s response to therapy and adjusting settings as needed to ensure comfort and efficacy․ Proper monitoring helps identify and address issues early, promoting better outcomes and minimizing complications․ Always consult the manual for detailed guidance on monitoring procedures and alarm responses․
Troubleshooting Common Issues
Troubleshooting the Prevena Plus 125 involves identifying and resolving issues like error codes or system malfunctions․ Refer to the manual for solutions to ensure proper function and minimize downtime․
Alarm Codes and Solutions
The Prevena Plus 125 System features a comprehensive alarm system to notify users of potential issues․ Common alarm codes include low suction pressure, high fluid levels, or system malfunctions․ Each code is accompanied by a specific solution, such as checking tubing connections, emptying the fluid canister, or restarting the device․ The manual provides detailed explanations for each alarm code, ensuring quick troubleshooting and minimal disruption to therapy․ Regular maintenance and adherence to guidelines can help prevent alarms from occurring․ Always refer to the user manual for a full list of codes and step-by-step solutions to address issues effectively and maintain optimal system performance․
System Malfunction and Repair
In the event of a system malfunction, the Prevena Plus 125 may exhibit issues such as failure to initiate therapy, unusual noise, or inability to maintain suction․ Users should first power cycle the device by turning it off and on again․ If the issue persists, check for blockages in tubing or connections․ For internal malfunctions, refer to the troubleshooting guide in the manual․ If problems cannot be resolved, contact authorized service personnel for repair․ Always ensure repairs are performed by qualified individuals to maintain system integrity and safety․ Regular maintenance, such as cleaning and updating software, can help prevent malfunctions․ Detailed repair procedures and guidelines are outlined in the manual to ensure optimal performance and patient safety․
Maintenance and Storage
Regular maintenance, including cleaning and inspecting for damage, is essential․ Store the device in a dry, cool place, following manufacturer guidelines to ensure functionality and safety․
Cleaning and Disinfection
Cleaning and disinfection of the Prevena Plus 125 System are critical to maintain its functionality and prevent infection risks․ Use a soft, lint-free cloth and mild detergent to wipe down external surfaces, avoiding abrasive materials that could damage the device․ Ensure all visible soil or debris is removed thoroughly․ For disinfection, apply a solution of 70% isopropyl alcohol or a compatible disinfectant recommended by the manufacturer․ Allow the solution to sit for the recommended contact time before rinsing with sterile water and drying completely․ Avoid submerging the device in liquid, as this may cause damage․ Always follow the manufacturer’s guidelines to ensure proper cleaning and disinfection procedures are performed safely and effectively․
Storage Conditions
The Prevena Plus 125 System should be stored in a clean, dry environment, away from direct sunlight and moisture․ The ideal storage temperature is between 15°C and 30°C (59°F to 86°F), with relative humidity below 60%․ Avoid exposing the device to extreme temperatures, such as those below 0°C (32°F) or above 35°C (95°F)․ Store the system in its original packaging to protect it from dust and physical damage․ Do not store the device in areas prone to flooding or high humidity․ Ensure all components are securely packed and labeled for easy identification․ Always follow the manufacturer’s storage guidelines to maintain the system’s performance and longevity․ Proper storage conditions are essential to ensure the device remains functional and ready for use when needed․
