cadd solis pump manual
The CADD-Solis Pump is a state-of-the-art ambulatory infusion pump designed for safe and efficient medication delivery. It supports various therapies, including IV, epidural, and PCA, ensuring precise dosing. Portable and user-friendly, it features advanced programming options and safety mechanisms to enhance patient care. This manual provides comprehensive guidance on setup, operation, and troubleshooting;
1.1 Overview of the CADD-Solis Pump
The CADD-Solis Pump is a portable, ambulatory infusion pump designed for precise medication delivery. It supports continuous, intermittent, and PCA (Patient-Controlled Analgesia) modes, making it versatile for various therapies. The pump is lightweight, user-friendly, and equipped with advanced safety features to ensure accurate dosing and minimize errors. Its intuitive interface allows healthcare professionals to program and monitor infusions efficiently. The system is ideal for IV, epidural, and subcutaneous deliveries, offering a reliable solution for patient care in clinical and home settings.
1.2 Purpose of the Manual
This manual serves as a comprehensive guide for the CADD-Solis Pump, providing detailed instructions for its safe and effective use. It covers setup, operation, programming, and maintenance to ensure optimal functionality. Intended for healthcare professionals and patients, the manual emphasizes safety, proper usage, and troubleshooting. By following the guidelines, users can maximize the pump’s capabilities while minimizing risks, ensuring accurate medication delivery and enhanced patient care.
1.3 Structure of the Manual
This manual is organized into nine main sections for easy navigation. It begins with an introduction to the CADD-Solis Pump, followed by detailed features and specifications. Subsequent sections cover setup, operation, programming, maintenance, and troubleshooting. Safety guidelines and regulatory information are also included to ensure compliance and safe use. Each section is designed to provide clear, step-by-step instructions, making it a valuable resource for both healthcare professionals and patients using the pump.
Features and Specifications
The CADD-Solis Pump features a rechargeable lithium-ion battery, supporting continuous, intermittent, and TPN delivery modes. It includes medication safety software and is FDA-compliant, ensuring portable and precise infusion therapy.
2.1 Key Features of the CADD-Solis Pump
The CADD-Solis Pump is a portable ambulatory infusion pump designed for precision and safety. It supports continuous, intermittent, and TPN delivery modes, with a rechargeable lithium-ion battery for extended use. The pump features medication safety software, user-friendly controls, and PCA mode for patient-controlled analgesia. Its durable, lightweight design ensures portability, while advanced safety mechanisms prevent errors. Customizable programming and integration with medication cassettes enhance versatility, making it ideal for various infusion therapies in clinical and home settings.
2.2 Technical Specifications
The CADD-Solis Pump operates with precise flow rates of 0.1 to 1000 mL/hour, ensuring accurate medication delivery. It uses lithium-ion batteries or 4 AA alkaline batteries, providing up to 48 hours of continuous operation. The pump weighs approximately 1.3 lbs and measures 4.5 x 3.5 x 1.5 inches. It supports pressures up to 39 psi and is compatible with a wide range of IV solutions. The device includes audible alarms for errors, low battery, and occlusions, ensuring patient safety and reliable performance.
Setting Up the Pump
Setting up the CADD-Solis Pump involves cleaning the work area, washing hands, opening the battery compartment, inserting 4 new AA batteries, and performing initial checks to ensure proper functionality.
3.1 Preparing the Pump for Use
To prepare the CADD-Solis Pump, first clean the work area and wash your hands. Open the battery compartment and insert 4 new AA batteries, ensuring correct polarity. Close the compartment securely. Perform initial checks to verify proper functionality, such as ensuring no alarms are active and the display is clear. This step ensures the pump is ready for safe and accurate medication delivery.
3.2 Inserting Batteries and Initial Checks
Open the battery compartment and insert 4 new AA batteries, ensuring correct polarity. Close the compartment securely. Perform initial checks: turn on the pump, verify the display is clear, and ensure no alarms are active. Check for any error messages or unusual sounds. If the pump powers on successfully, proceed with programming or priming. Proper battery installation and initial checks are crucial for safe and reliable operation of the CADD-Solis Pump.
Operating the Pump
The CADD-Solis Pump operates in continuous, intermittent, or PCA modes, offering precise medication delivery. Key functions include starting/stop and real-time monitoring for safe therapy administration.
4.1 Starting and Stopping the Pump
To start the pump, press “T” to begin a new patient session. The pump will prompt confirmation to stop. Press “Yes,” then clamp the tubing and disconnect from the patient. Unlock and remove the medication cassette if necessary. To stop the pump, follow similar steps, ensuring all lines are clamped and the pump is powered off when not in use. Always refer to the manual for detailed instructions to ensure safe operation and maintain patient safety.
4.2 Delivery Modes (Continuous, Intermittent, TPN)
The CADD-Solis Pump offers versatile delivery modes to meet diverse clinical needs. Continuous mode provides a steady infusion rate, while Intermittent mode delivers medication at predetermined intervals. TPN (Total Parenteral Nutrition) mode ensures precise delivery for nutritional support. Each mode can be programmed to accommodate varying therapy requirements, offering flexibility for patient-specific treatments. The pump also supports PCA (Patient-Controlled Analgesia) for pain management. Always refer to the manual for specific programming instructions to ensure accurate and safe delivery of medication.
4.3 Monitoring the Pump
Regular monitoring of the CADD-Solis Pump is essential for safe and accurate therapy delivery. The pump features alarms and error messages to alert users of issues such as air in the tubing, low battery, or occlusions. The display shows real-time status, including infusion rate, volume delivered, and remaining volume. Users should periodically inspect the tubing and cassette for kinks or air bubbles. Proper monitoring ensures optimal performance and patient safety, allowing for timely interventions if issues arise during infusion. Always follow the manual’s guidance for troubleshooting and maintenance.
Programming the Pump
Programming the CADD-Solis Pump involves setting infusion parameters like rate, volume, and mode. It can be done manually or via protocol-based options for consistent therapy delivery. The pump supports multiple programmable profiles, ensuring flexibility for various patient needs and therapies.
5.1 Manual Programming Options
The CADD-Solis Pump offers manual programming for precise control over infusion settings. Users can set parameters such as infusion rate, volume, and delivery mode directly on the pump. This feature is useful when a specific protocol isn’t available in the library or when immediate adjustments are needed. Manual programming ensures flexibility and customization for individual patient needs, allowing healthcare providers to tailor therapy accurately. The pump’s intuitive interface simplifies the process, reducing the risk of errors during setup.
5.2 Protocol-Based Programming
Protocol-based programming on the CADD-Solis Pump streamlines infusion setup by using predefined therapy protocols. Users can select from a library of established protocols, each defined by therapy, qualifier, and drug parameters. This mode ensures consistency and reduces programming errors. Protocols are easily customizable to meet specific patient needs. The pump also supports medication safety software, enhancing accuracy and compliance with institutional guidelines. This feature is ideal for standardizing care while maintaining flexibility for individualized treatment plans, ensuring safe and efficient medication delivery.
5.3 Patient-Controlled Analgesia (PCA) Mode
The PCA mode allows patients to self-administer bolus doses of pain medication, enhancing comfort and satisfaction. Patients must understand the relationship between pain and pump activation and be physically capable of triggering the pump. Clinicians program parameters such as bolus dose, lockout interval, and maximum doses. The pump delivers medication as programmed, with a lockout period to prevent overdosing. This mode is ideal for post-operative or chronic pain management, offering patients control while ensuring safe, monitoring of medication delivery.
Maintenance and Care
Regular cleaning and disinfecting of the pump ensure optimal performance. Replace parts and accessories as needed, following the manual’s guidelines to maintain safety and functionality.
6.1 Cleaning and Disinfecting the Pump
Clean and disinfect the CADD-Solis Pump regularly to maintain hygiene and functionality. Use a soft cloth dampened with 70% isopropyl alcohol to wipe external surfaces. Avoid harsh chemicals or abrasive materials. Ensure all visible debris is removed. For internal components, follow the manual’s specific cleaning procedures. Regular disinfection helps prevent contamination and ensures accurate medication delivery. Always refer to the manual for detailed instructions on proper cleaning and disinfecting techniques to maintain patient safety and pump performance.
6.2 Replacing Parts and Accessories
Regularly replace parts and accessories to ensure optimal pump performance. Use only genuine CADD-Solis components for safety and compatibility. Replace batteries every time you start a new IV bag, using 4 new AA batteries. Tubing and medication cassettes should be replaced as indicated by the manual or when visibly worn. Inspect the battery compartment for damage and replace if necessary. Always follow proper disposal methods for used parts. Replace protective covers on screens or displays to prevent scratches. After replacing any part, test the pump to ensure proper function and safety.
Troubleshooting Common Issues
Identify and address common issues promptly. Check for air in tubing, alarms, or unresponsive keys. Restart the pump if it fails to activate. Refer to the manual for specific error resolutions and maintenance tips to ensure smooth operation.
7.1 Alarms and Error Messages
The CADD-Solis Pump alerts users with specific alarms for issues like low battery, occlusion, or air in the tubing. Error messages provide clear guidance for resolution. Address alarms promptly by checking tubing connections, priming, or restarting the pump if necessary. Refer to the manual for detailed troubleshooting steps and error code explanations to ensure optimal functionality and patient safety. Properly acknowledging and resolving alarms is crucial for maintaining accurate medication delivery.
7.2 Resolving Common Operational Problems
Common issues with the CADD-Solis Pump include unresponsive keys, air in the tubing, or battery depletion. To resolve these, restart the pump, check for blockages, and ensure proper battery installation. If the pump fails to start, verify programming settings and connections. For air detection issues, prime the tubing and restart. Always refer to the manual for specific troubleshooting steps to address errors effectively and maintain seamless operation. Regular maintenance and checks can prevent many operational problems.
Safety Guidelines
Always follow safety protocols when using the CADD-Solis Pump. Ensure proper training, handle alarms promptly, and avoid unauthorized modifications. Regular maintenance and updates are essential for safe operation.
8.1 General Safety Precautions
Always ensure proper training before operating the CADD-Solis Pump. Monitor patients closely during infusion therapy. Avoid exposing the pump to extreme temperatures or moisture. Use only approved accessories and batteries. Regularly inspect tubing and connectors for damage. Follow proper cleaning and disinfection procedures. Keep emergency procedures handy. Adhere to FDA guidelines and manufacturer recommendations. Report any malfunctions immediately. Ensure the pump is used only for its intended purposes. Always follow the manual instructions for safe operation.
8.2 Handling Alarms and Emergencies
When an alarm sounds, acknowledge it by pressing ‘Acknowledge’ and investigate causes like air in tubing or low battery. Clamp and replace tubing if necessary. Check the cassette for proper placement and ensure it’s securely connected. If the pump stops, restart it or use backup power. Always prioritize patient safety. For unresolved issues, refer to the troubleshooting section for detailed solutions and follow all manufacturer guidelines.
Regulatory and Compliance Information
The CADD-Solis Pump complies with FDA regulations and medical standards, ensuring safe and reliable operation. Adherence to these guidelines guarantees optimal performance and patient safety.
9.1 FDA Classification and Recalls
The FDA classifies the CADD-Solis Pump as a Class II medical device, requiring special controls to ensure safety and effectiveness. Recent recalls, such as the Class I recall issued for air detector failures in manual mode, highlight the importance of adhering to FDA guidelines. Smiths Medical has addressed these issues through software updates and user notifications, ensuring compliance and maintaining patient safety standards.
9.2 Compliance with Medical Standards
The CADD-Solis Pump adheres to stringent international medical standards, including ISO and IEC requirements, ensuring reliability and safety. It is designed to meet the needs of various infusion therapies, such as IV, epidural, and PCA, while complying with regulatory guidelines. Regular updates and certifications demonstrate its alignment with global medical device standards, ensuring it remains a trusted tool for healthcare professionals.