Prevena Plus 125 Instruction Manual: A Comprehensive Guide
This manual details the PREVENA PLUS 125 Therapy Unit’s use for infection reduction and wound healing. It’s a single-use, disposable system; consult the included manual and a clinician before use.
The PREVENA PLUS 125 Therapy Unit represents an advanced approach to closed wound management, designed to facilitate healing and minimize the risk of complications following surgical procedures. This innovative system employs controlled negative pressure wound therapy (NPWT) to gently draw excess fluids from the wound site, promoting a healthier environment for tissue regeneration.
As a single-use, disposable device, the Prevena Plus 125 prioritizes patient safety and convenience. It’s intended for use on closed or partially closed incisions, offering a proactive solution to reduce the incidence of surgical site infections (SSIs). The system comprises a therapy unit, a specialized dressing, and connecting tubing, all working in synergy to deliver consistent and reliable negative pressure.
Understanding the capabilities and proper operation of the Prevena Plus 125 is crucial for healthcare professionals and patients alike. This manual provides comprehensive instructions, covering everything from pre-treatment assessment to troubleshooting common alarms. Always refer to the complete Instructions For Use and consult with a clinician prior to initiating therapy.
Intended Use and Indications for Use
The PREVENA PLUS 125 Therapy Unit is specifically indicated for use on closed or partially closed surgical incisions, traumatic wounds, and ulcers. Its primary intended use is to reduce the incidence of surgical site infections (SSIs) and promote optimal wound healing through the application of controlled negative pressure. This therapy is particularly beneficial for patients at higher risk of developing complications, such as those with compromised immune systems or underlying health conditions.
The system is designed for use in various clinical settings, including hospitals, surgical centers, and extended care facilities. It’s appropriate for a wide range of incision types and locations, though individual patient assessment is vital. The Prevena Plus 125 is not intended for use on deep, open wounds, or those with exposed bone or tendon.
Prior to initiating therapy, clinicians should carefully evaluate the patient’s wound and overall health status to determine if the Prevena Plus 125 is the appropriate treatment option. Always adhere to the detailed Instructions For Use and consult with a qualified healthcare professional.
Product Components and Description
The PREVENA PLUS 125 Therapy Unit is a complete, self-contained system designed for single-patient use. Key components include the therapy unit itself – a compact, portable device delivering controlled negative pressure – and a specialized dressing kit. This kit contains a unique, multi-layered dressing designed to interface with the unit and the wound bed.
The dressing typically consists of a soft absorbent layer, a semi-permeable membrane, and an adhesive layer for secure application. A connecting tube facilitates the transfer of negative pressure from the unit to the dressing. The Prevena Carrying Case is also included, providing a convenient and protective means for transportation.
The therapy unit features intuitive controls and visual indicators to monitor performance. It’s a disposable system, eliminating the need for cleaning and sterilization. Each unit is individually packaged to ensure sterility and prevent contamination. Refer to the detailed component list within the manual for a comprehensive overview.
Understanding the Therapy Unit Indicators and Alerts
The PREVENA PLUS 125 Therapy Unit utilizes several indicators and alerts to communicate its operational status and potential issues. Visual indicators, such as LED lights, display power status, pressure level, and alarm conditions. A consistent green light typically signifies normal operation, while flashing or colored lights indicate a problem.
Audible alarms alert the user to critical events, including low battery, occlusion (blockage in the tubing), or loss of negative pressure. The manual provides a detailed explanation of each alarm’s meaning and the appropriate corrective action. It’s crucial to familiarize yourself with these alerts before initiating therapy.
Understanding these signals is vital for ensuring effective and safe wound care. Always consult the manual for specific alarm resolutions and troubleshooting steps. Ignoring alerts could compromise therapy effectiveness or potentially harm the patient. Refer to the “Alarm Resolutions” section for detailed guidance.
Pre-Treatment Assessment and Patient Preparation
Prior to initiating PREVENA PLUS 125 therapy, a thorough patient assessment is essential. This includes evaluating the wound characteristics – size, depth, location, and presence of infection – as well as the patient’s overall health status and any contraindications. A clinician should determine if the patient is a suitable candidate for negative pressure wound therapy.
Patient preparation involves explaining the therapy process, potential benefits, and possible discomforts. Ensure the patient understands the importance of keeping the therapy unit and dressing system intact. Skin surrounding the wound should be assessed for integrity and prepped according to established clinical protocols.
Proper positioning of the patient is also crucial for optimal therapy delivery. The chosen position should minimize tension on the dressing and allow for consistent negative pressure application. Consult the manual for specific guidance on patient positioning and preparation techniques.
Dressing Application Instructions
Dressing application is a critical step for successful PREVENA PLUS 125 therapy. Begin by ensuring the wound bed is clean and dry, following established wound care protocols. Select an appropriate dressing that conforms to the wound shape and size, ensuring complete contact with the wound bed.
Apply the dressing carefully, avoiding air pockets or wrinkles that could compromise negative pressure distribution. Secure the dressing with appropriate tape or securing devices, ensuring a tight seal to prevent leakage. The dressing should extend beyond the wound edges to facilitate adhesion of the PREVENA film.
Follow the detailed dressing application instructions on page 7 of the provided documentation. Remember that incision size and location may vary; adapt the dressing accordingly. Proper application is vital for optimal wound healing and minimizing complications.
Connecting the Therapy Unit to the Dressing
Connecting the PREVENA PLUS 125 Therapy Unit to the applied dressing requires careful attention to ensure a secure and leak-free connection. Locate the therapy unit’s connector port and the corresponding port on the dressing film. Gently align the two ports, ensuring they are free from debris or obstructions.
Firmly push the therapy unit connector into the dressing port until a secure “click” is heard or felt, indicating a proper seal. Visually inspect the connection to confirm it is fully engaged and that no gaps are present. A compromised connection can lead to ineffective therapy and potential wound complications.
Ensure the tubing is not kinked or twisted, as this can impede airflow. Regularly check the connection throughout therapy to maintain optimal negative pressure. Refer to the user manual for detailed diagrams and troubleshooting tips regarding connection issues.
Setting Negative Pressure Levels
Setting the appropriate negative pressure level on the PREVENA PLUS 125 Therapy Unit is crucial for effective wound healing. The prescribed pressure, determined by a clinician, will vary based on wound characteristics, patient condition, and treatment goals. Consult the physician’s orders before adjusting any settings.
The therapy unit features intuitive controls for adjusting the negative pressure. Typically, this involves using the “increase” and “decrease” buttons to select the desired mmHg level. The current pressure setting is displayed on the unit’s screen. Start with the lowest recommended pressure and gradually increase as directed by the healthcare provider.
Monitor the wound site closely after each adjustment to assess the patient’s tolerance and the therapy’s effectiveness. Avoid setting excessively high pressures, as this can cause pain or tissue damage. Refer to the user manual for detailed instructions and safety precautions regarding pressure adjustments.
Operating the Prevena Plus 125 Therapy Unit
Operating the PREVENA PLUS 125 Therapy Unit is designed to be straightforward, but careful attention to the instructions is essential. Once the dressing is connected and the negative pressure level is set, press the “start” button to initiate therapy. The unit will begin applying continuous negative pressure to the wound site.
Regularly monitor the unit’s display for any alerts or alarms. The screen provides information on battery life, pressure level, and system status. Ensure the unit remains securely connected to the power source during operation. Avoid interrupting the therapy unless absolutely necessary, and always follow the clinician’s instructions.
The PREVENA unit is designed for continuous operation. Patients should be educated on the importance of maintaining the unit’s functionality and reporting any issues immediately. Consult the user manual for detailed troubleshooting guidance and safety information. Proper operation ensures optimal wound healing outcomes.
Alarm Resolutions and Troubleshooting
Alarm resolution with the PREVENA PLUS 125 Therapy Unit requires a systematic approach. Common alarms include low battery, occlusion (blockage in the tubing), and system malfunction. For a low battery alarm, replace or recharge the unit immediately. An occlusion alarm indicates a kink or blockage; carefully inspect the tubing and dressing for obstructions.
If an occlusion is identified, gently reposition the tubing or dressing to restore flow. System malfunction alarms require contacting a healthcare professional. Consult the user manual for specific error codes and corresponding solutions. Do not attempt to repair the unit yourself.
Troubleshooting often involves verifying all connections are secure and the dressing is properly sealed. If alarms persist, discontinue therapy and seek guidance from a clinician. Maintaining a log of alarms and resolutions can aid in identifying recurring issues. Always prioritize patient safety and follow established protocols.
Monitoring Therapy and Assessing Wound Progress
Monitoring the PREVENA PLUS 125 Therapy Unit involves regular observation of the unit’s indicators and the wound site. Assess the dressing for proper seal and ensure consistent negative pressure is being delivered. Document the pressure level and any alarms encountered during therapy.
Wound assessment should be performed at scheduled intervals, as directed by a healthcare professional. Evaluate the wound for signs of healing, such as decreased size, reduced drainage, and improved tissue granulation. Note any changes in wound appearance, including increased redness, swelling, or odor, which may indicate infection.
Patient comfort and skin integrity around the wound edges are crucial. Regularly inspect the peristomal skin for irritation or breakdown. Adjust the therapy settings or dressing as needed, based on the wound assessment and patient feedback. Consistent documentation of wound progress is essential for optimizing therapy outcomes.
Carrying Case Usage and Transportation
The Prevena Carrying Case is designed for convenient and safe transportation of the Prevena Plus 125 Therapy Unit. Ensure the unit is securely placed within the case before moving it, protecting it from potential damage during transit. The case facilitates maintaining a sterile environment for the therapy unit.
When transporting the unit, avoid exposing it to extreme temperatures or moisture. Do not stack heavy objects on top of the carrying case, as this could compromise the unit’s functionality. The case is intended for single-patient use and should not be used to transport other medical devices.
The exterior of the Prevena Carrying Case can be wiped clean with a disinfectant solution, as advised on page 10 of related documentation. This helps maintain hygiene during transportation and storage. Always verify the unit’s integrity after transport before initiating therapy.
Cleaning and Disinfection Procedures
Maintaining cleanliness is crucial when using the Prevena Plus 125 Therapy Unit. The Prevena 125 Therapy Unit and its Carrying Case can be wiped down for external cleaning. Use a compatible disinfectant solution, ensuring it doesn’t penetrate the unit’s internal components.
Prior to disinfection, disconnect the therapy unit from the power source. Avoid immersing the unit in liquids or using abrasive cleaners, as these can cause damage. Focus cleaning efforts on the exterior surfaces of both the unit and the carrying case.
Follow the disinfectant manufacturer’s instructions regarding contact time and safety precautions. Ensure the unit is completely dry before reconnecting it to the power source or resuming therapy. Proper cleaning and disinfection contribute to patient safety and prevent potential infections. Refer to the full instruction manual for detailed guidance and approved cleaning agents.
Disposal of the Prevena Plus 125 Unit
The PREVENA PLUS 125 Therapy Unit is designed for single-use only and should be disposed of properly after the completion of therapy. Do not attempt to reuse any component of the unit, as this could compromise its effectiveness and potentially introduce infection risks.
Dispose of the unit in accordance with all applicable federal, state, and local regulations regarding medical waste. This may involve placing the unit in a designated biohazard container or following specific guidelines for disposable medical devices.
Consult your healthcare provider or facility’s waste management protocols for detailed instructions on proper disposal procedures. Ensure the unit is completely disconnected from any power source before disposal. Proper disposal safeguards both environmental health and public safety; Refer to the complete Instructions for Use for further clarification and compliance information.
Important Safety Information and Precautions
Important: The Prevena Plus 125 Therapy Unit is a medical device and should only be used under the supervision of a qualified healthcare professional. Always consult with your clinician before initiating therapy and throughout the treatment process.
Ensure the therapy unit and dressing are appropriate for your specific wound type and condition. Do not use the device on uncontrolled bleeding, exposed organs, or in situations where negative pressure therapy is contraindicated.
Regularly monitor the wound site for signs of infection, such as increased pain, redness, swelling, or discharge. If any of these symptoms occur, immediately contact your healthcare provider. The Prevena Carrying Case can be wiped clean for transport, but avoid submerging the unit in liquids.
Review the complete Instructions for Use for a comprehensive list of safety precautions and potential risks associated with the Prevena Plus 125 system.