1/9/2024 0 Comments Hickman triple lumen catheterPercutaneous insertion of the catheter should be made into the axillary-subclavian vein at thejunction ofthe outer and mid-thirds of the clavicle lateral to the thoracic outlet.Local tissue factors will prevent proper device stabilization and/or access.Previous episodes of venous thrombosis or vascular surgical procedures at the prospective placement site.Past irradiation ofprospective insertion site.Severe chronic obstructive lung disease exists (percutaneous subclavian placement only).The patient is known or is suspected to be allergic to materials contained in this device.The patient'sbody size is insufficient to accommodate the size of the implanted device.The presence of device related infection, bacteremia, or septicemia is known or suspected.Contraindications This device is contraindicated whenever: The Hickman® TriFusion® catheter incorporates three large, equal size lumens appropriate for apheresis procedures. fluids, blood products, drugs, and parenteral nutrition solutions, as well as blood withdrawal. All Hickman® TriFusion® Catheters are designed for apheresis, and the administration of I.V. Heparin Label REPRESENTATIVE’S NAME PHYSICIAN’S SIGNATURE Hickman® TriFusion® Triple Lumen Long-Term Central Venous Catheter Indications for Use The Hickman® TriFusion® Triple Lumen Long-Term Central Venous Catheter is indicated for use in attaining short-term or long-term vascular access for intravenous infusion therapy and blood samplingviatheinternaljugularvein, external jugularvein, and subclavian vein.12 F TriFusion® Polyurethane Catheter with SureCuff® Tissue Ingrowth Cuff.ventilator associated pneumonia ( J95.Ordering Information Tip to Cuff Length French Size HickmanTriFusion Triple Lumen Long-Term Central Venous Catheter Product Code Intermediate Microintroducer Intermediate Microintroducer Intermediate Microintroducer 0.8 - White / 0.9 - Blue / 0.8 - Red 0.8 - White / 0.9 - Blue / 0.8 - Red 0.8 - White / 0.9 - Blue / 0.8 - Red 0.8 - White / 0.9 - Blue / 0.8 - Red 1.0 - White / 1.0 - Blue / 1.0 - Red 1.0 - White /1.0 - Blue / 1.0 - Red Tray Components Intermediate Microintroducer Product and Packaging Do Not Contain Natural Rubber Latex.postsurgical blind-loop syndrome ( K91.2).postmastectomy lymphedema syndrome ( I97.2).functional disturbances following cardiac surgery ( I97.0- I97.1).disorders of fluid and electrolyte imbalance ( E86- E87).cerebrospinal fluid leak from spinal puncture ( G97.0).specified complications classified elsewhere, such as:.poisoning and toxic effects of drugs and chemicals ( T36- T65 with fifth or sixth character 1-4 or 6).mechanical complication of respirator ( J95.850).complications of surgical procedures during pregnancy, childbirth and the puerperium ( O00-O9A).burns and corrosions from local applications and irradiation ( T20- T32).fitting and adjustment of external prosthetic device ( Z44.-).any encounters with medical care for postprocedural conditions in which no complications are present, such as:.
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