prevena plus 125 instruction manual

Safety Information and Warnings

The Prevena Plus 125 Therapy Unit requires adherence to specific safety guidelines to prevent adverse effects․ Always consult a clinician before use and follow instructions carefully․ The device is contraindicated for certain conditions, such as open wounds with necrosis or active bleeding․ Ensure proper handling to avoid electromagnetic interference and maintain sterility․ Regular monitoring is essential to prevent complications and ensure therapy effectiveness․ Patient safety is paramount, and any deviations from guidelines may lead to serious health risks․

3․1 Contraindications for Use

The Prevena Plus 125 Therapy Unit is not suitable for all patients․ Contraindications include open wounds with necrosis, active bleeding, or exposed organs․ It should not be used on patients with allergies to the dressings or components of the system․ Additionally, the device is contraindicated for wounds with unresolved undermining or tunneling, as well as in cases where negative pressure therapy is not medically advised․ Always consult a clinician to ensure safe and appropriate use of the device․

3․2 Precautions and Safety Measures

Regularly inspect the therapy unit and dressings for leaks or damage․ Ensure the canister is securely locked to prevent fluid spills․ Avoid kinking the tubing, as this may disrupt therapy․ Handle the device with care to prevent drops or damage․ Always monitor for alarms and address them promptly․ Follow proper hygiene practices when handling dressings and the unit․ Use only compatible dressings and accessories to maintain safety and effectiveness․ Adhere to all warnings and guidelines provided in the manual to ensure safe operation and optimal therapy outcomes․

Installation and Setup

Unpack the Prevena Plus 125 Therapy Unit and ensure all components are included․ Connect the dressing to the unit, ensuring a secure seal․ Set the pressure to -125mmHg and confirm proper function before use․

4․1 Unpacking and Preparing the Device

Begin by carefully unpacking the Prevena Plus 125 Therapy Unit and its accessories․ Ensure all components, including the therapy unit, dressings, and tubing, are included and undamaged․ Place the device on a flat, stable surface and connect the power source․ If using the battery, charge it fully before first use․ Familiarize yourself with the controls and ensure the device is free from any visible damage․ Always refer to the manual for specific preparation steps to ensure safe and effective use․

4․2 Connecting the Dressing to the Therapy Unit

To connect the dressing to the Prevena Plus 125 Therapy Unit, ensure the dressing is properly sealed over the surgical site․ Attach the tubing from the dressing to the unit’s port, ensuring a secure connection․ Verify that the canister is correctly locked into place and the tubing is free from kinks or blockages․ Turn on the unit and check for proper suction․ Use 3M Prevena Patch Strips or excess drape to seal any leaks․ Follow the manual’s guidance for a secure and effective connection․

Operating the Prevena Plus 125

Turn on the therapy unit and set the pressure to -125mmHg․ Monitor the therapy status through indicator lights and alarms․ Ensure continuous operation as prescribed․

5․1 Turning On the Therapy Unit

To activate the Prevena Plus 125, press and hold the power button until the indicator lights illuminate․ Ensure the device is placed on a stable, flat surface in a well-ventilated area․ The therapy unit will perform a self-test, and the green Therapy Life Indicator lights will display the remaining therapy days․ Once initialized, the unit will begin operating at the preset -125mmHg pressure․ Always follow the instructions provided in the manual for proper startup and usage․ If unsure, consult a healthcare professional․

5․2 Setting the Pressure (-125mmHg)

The Prevena Plus 125 Therapy Unit is preset to deliver continuous negative pressure at -125mmHg․ To ensure proper operation, verify the pressure setting matches your clinician’s prescription․ Once the therapy unit is turned on, the pressure will automatically adjust to the preset level․ Always confirm the pressure reading on the display before starting therapy․ If adjustments are needed, consult the manual or contact a healthcare professional․ Proper pressure setting is crucial for effective therapy and patient safety․

5․3 Monitoring the Therapy Status

Monitor the therapy status by checking the display for active therapy indicators․ The green Therapy Life Indicator lights show the remaining therapy days․ Ensure the unit is functioning correctly by verifying the pressure reading matches the prescribed -125mmHg․ If an alarm sounds, refer to the troubleshooting guide to address issues like blockages or full canisters․ Regularly inspect the dressing and tubing for leaks or kinks․ Proper monitoring ensures effective therapy and patient safety․ Always follow the manual’s guidance for resolving alarms and maintaining therapy continuity․

Maintenance and Troubleshooting

Regularly clean the therapy unit with a soft cloth and mild detergent․ Check tubing and dressings for leaks or kinks․ Resolve alarms promptly by addressing blockages or full canisters․ Ensure proper function and patient safety through consistent maintenance and troubleshooting․

6․1 Cleaning and Caring for the Device

Regular cleaning and proper care are essential for maintaining the Prevena Plus 125 Therapy Unit․ Use a soft, dry cloth to wipe the exterior, avoiding harsh chemicals or submerging the device in water․ Ensure the unit is dry before storing or using it again․ Clean the canister and tubing as instructed, and replace disposable parts as needed․ Proper maintenance ensures optimal performance, patient safety, and hygiene․ Always refer to the manual for detailed cleaning procedures and guidelines․

6․2 Resolving Common Issues and Alarms

Addressing alarms and issues promptly ensures uninterrupted therapy․ Common alarms include low battery, blockages, or leaks․ For blockages, check tubing for kinks and ensure the canister is securely locked․ Low battery alerts require charging or replacing the battery․ If a leak is detected, inspect dressings and connections, sealing any gaps with 3M Prevena Patch Strips․ For persistent issues, press and hold the mute button to silence alarms temporarily․ Always consult the manual for detailed troubleshooting steps and solutions to maintain optimal device function and patient comfort․

Patient Mobility and Portability

The Prevena Plus 125 Therapy Unit is lightweight and portable, designed for patient mobility․ The carrying case allows easy transport, enabling continued therapy during daily activities and travel․

7․1 Using the Carrying Case

The Prevena Plus 125 Therapy Unit comes with a non-sterile carrying case designed for patient mobility․ This case allows easy transport of the therapy unit, dressings, and accessories․ Its lightweight and durable design ensures secure transport, enabling patients to move freely while continuing therapy․ The carrying case is ideal for travel and daily activities, providing convenience and ensuring uninterrupted therapy as prescribed by healthcare professionals․

7․2 Guidelines for Travel and Daily Activities

The Prevena Plus 125 Therapy Unit is designed for portability, allowing patients to maintain therapy during daily activities and travel․ Always keep the device on as prescribed, even during sleep or showering․ Use the carrying case to secure the unit and accessories while moving․ Ensure the therapy unit is properly sealed and the dressings are intact to avoid interruptions․ For extended travel, pack extra batteries and follow the provided guidelines for safe transport․ Always consult the user manual or healthcare provider for specific instructions․

Technical Specifications

The Prevena Plus 125 Therapy Unit weighs 0․29 kg, measures 16․3 cm (L) x 5․5 cm (H), and operates on battery or electric power for portability and convenience․

8․1 Dimensions and Weight

The Prevena Plus 125 Therapy Unit is designed for portability, weighing 0․29 kg and measuring 16․3 cm (length) x 5․5 cm (height)․ Its compact design ensures easy handling and patient mobility, making it ideal for use at home or while traveling․ The lightweight construction minimizes strain, while the dimensions allow for discreet placement․ This ergonomic design supports patient comfort and adherence to therapy regimens without compromising performance or functionality․ These specifications ensure the device remains user-friendly and accessible for extended periods of use․

8․2 Battery and Power Options

The Prevena Plus 125 Therapy Unit operates efficiently using both battery and electrical power, offering flexibility for home and portable use․ The rechargeable battery provides reliable performance, with clear indicators for low charge status․ A Therapy Life Indicator displays the remaining therapy days, counting down from activation․ The unit continues to count down even when turned off, ensuring accurate tracking․ A low-charge alert notifies users when power is running low, while the included carrying case enhances portability and accessibility during daily activities or travel․

Clinical Benefits and Indications

The Prevena Plus 125 Therapy Unit offers clinical benefits by reducing surgical site infections and managing seroma and fluid accumulation, promoting improved wound healing and patient outcomes․

9․1 Reducing Surgical Site Infections

The Prevena Plus 125 Therapy Unit is designed to reduce the risk of surgical site infections by applying continuous negative pressure (-125mmHg)․ This therapy helps remove fluid from the surgical site, promoting a clean environment and reducing the chance of infection․ The system is FDA-cleared for use in closed surgical incisions, making it a trusted solution for post-operative care․ By minimizing fluid accumulation and seroma formation, it supports faster healing and reduces complications, ensuring better patient outcomes․

9․2 Managing Seroma and Fluid Accumulation

The Prevena Plus 125 Therapy Unit effectively manages seroma and fluid accumulation at surgical sites by applying continuous negative pressure (-125mmHg)․ This promotes a dry environment, reducing the risk of fluid buildup that can lead to complications․ The system is designed for closed surgical incisions, making it an ideal solution for post-operative care․ By removing excess fluid, it helps prevent seroma formation, supports tissue healing, and minimizes the need for additional interventions, ensuring a smoother recovery process for patients․

10․1 Summary of Key Points

The Prevena Plus 125 Instruction Manual provides essential guidance for safe and effective use of the therapy unit․ It covers installation, operation, and maintenance, ensuring optimal therapy outcomes․ Proper setup, pressure settings, and monitoring are crucial for patient safety․ Adherence to safety precautions and troubleshooting tips helps minimize risks․ Regular maintenance extends device longevity․ By following the manual, users can maximize the benefits of negative pressure therapy for managing surgical wounds and reducing complications․ Always consult a clinician for personalized advice․

10․2 Importance of Adherence to Instructions

Adhering to the Prevena Plus 125 Instruction Manual is critical for ensuring patient safety, effective therapy, and proper device function․ Failure to follow guidelines may lead to complications, reduced efficacy, or device malfunction; Strict compliance minimizes risks, such as infections or fluid management issues, and ensures optimal negative pressure application․ Always consult a clinician for personalized advice and refer to the manual for troubleshooting and maintenance․ Proper use enhances therapy outcomes and protects both the patient and the device․