There is currently a study being conducted to determine which ambulatory infusion pump is the most effective for 5-fluor

In most cases, 5-fluorouracil (5-FU) is administered as an outpatient treatment using an ambulatory infusion pump because of the lengthy infusion time of 46–48 hours required

In most cases, 5-fluorouracil (5-FU) is administered as an outpatient treatment using an ambulatory infusion pump because of the lengthy infusion time of 4648 hours required. However, pumps can be divided into two types. The first is the standard pump. a. a. a. a. a. a. a. a. a. a. a. a. a. Figure 1 depicts an example of a small and compact elastomeric pump Syringe Pump is capable of performing its function while remaining small and compact. The electronic pump, on the other hand, is larger, more flamboyant, and comes with a slew of bells and whistles (both literally and metaphorically) to complement its appearance. The following section lists the advantages and disadvantages of each of the alternatives.

Many people believe electronic pumps are more prone to malfunctioning as a result of an accidental fatal overdose of 5-FU administered via an electronic pump. The use of both electronic and elastomeric pumps has been associated with accidental 5-FU overdoses in more recent reports, demonstrating Injection Pump neither is completely risk-free. When making a decision, it is important to consider a patient's ability to troubleshoot the pump, the weight and availability of the pump, the cost and insurance coverage, and a variety of other factors.

Streamline the efficiency with which independent double checks (for example, on infusion volume and pump programming) are completed and documented by developing a structured process for doing so (for example, using checklists); develop a process for how this step is accomplished when the medication is administered in a setting where only one clinician is present (for example, in the patient's home), and document the process.

Any problems should be reported in accordance with institutional procedures, and a voluntary report to the Food and Drug Administration (FDA) should be filed.



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