A syringe plunger loses lubrication as it ages and as a result, the amount of underdelivery increases, which could on occasion, be significant. Syringe function can be adversely affected by variations in plunger dimension and lubricity, which can result in greater force required to move the syringe plunger. Use of a syringe with the CADD® administration set may result in UNDERDELIVERY of medication. Pump failure suspends medication delivery. If the pump is used to deliver life-sustaining medication, and additional pump must be available. To avoid explosion hazard, do not use the pump in the presence of flammable anesthetics or explosive gases. It is important that you understand and follow these warnings and cautions.įailure to properly follow warnings, cautions, and instructions could result in death, serious injury, or damage to the pump. Perform only those procedures for which you have received training.īefore operating the pump, you should read the following list of warnings and cautions. This guide is intended to supplement those instructions. Your health care provider will instruct you on the proper use of this pump. There is also an option to have a KVO (keep vein open) infusion rate at the end of the infusion. Your pump is programmed for Taper delivery and is used for therapies that require a plateau rate of infusion with the option of tapering at the beginning and/or end of the infusion. This pump can be reprogrammed by your health care provider as your medication needs change. Your prescription is programmed into your pump by your health care provider according to your physician’s specific orders. Your physician has prescribed a therapy specifically for you. The CADD®-Solis VIP pump can be carried with you and is designed to deliver medication into your body. Your doctor recommends the CADD®-Solis VIP ambulatory infusion pump as part of your treatment. What if I Drop or Hit the Pump?.36Īlarms and Messages.37Īlarm Help Screens.39 Priming the Tubing without Changing the Cassette. Priming the Tubing and Connecting to Your Catheter. Removing a Cassette.19Īttaching a New Cassette. Using the Rechargeable Battery Pack or AC Adapter. The wireless bi-directional communication sets the foundation for integrating pain management data delivery directly into the patient records in a hospital’s Electronic Health Records (EHR auto-documentation), saving clinicians time charting and increasing documentation accuracy.”įor more information about the CADD ®-Solis PCA and epidural pump, or for a copy of the report, contact Glen Johnson, NordUK Senior Marketing Manager at Smiths Medical, on 01233 722 100, email or visit. Glen Johnson, NordUK Senior Marketing Manager at Smiths Medical, says: “Smiths Medical is committed to patient safety and adoption of smart infusion pumps. For the hospital, the CADD ®-Solis system is designed to enhance patient safety through ‘smart programming’ (use of medication safety software) and reduce the risk of tubing misconnections, while providing a comprehensive and intuitive user experience for the healthcare provider. The CADD ®-Solis pump maintains the advantages of an ambulatory pump for patient mobility and provides a single system that effectively delivers IV PCA, epidural, peripheral nerve blocks and subcutaneous from pump to patient. The CADD ®-Solis v4 system is a continuation of Smiths Medical’s commitment to advance patient care and help improve patient outcomes through leading-edge technology. ECRI is an independent non-profit organisation improving the safety, quality and cost-effectiveness of care across all healthcare settings worldwide ( The report highlights ECRI’s evaluation ratings, test results and purchasing recommendations for the CADD ®-Solis pump. Smiths Medical, a leading medical device manufacturer, announces the release of the ECRI evaluation report for CADD ®-Solis v4 with wireless communication Patient-Controlled Analgesic (PCA) and epidural infusion pump.

Cadd solis pca pump