Understanding IV antimicrobial drug losses: the importance of flushing infusion administration sets

Balwinder Bolla1, Yeshmita Buxani1, Rebecca Wong1

  • 1United Lincolnshire Hospitals NHS Trust, Lincoln County Hospital, Greetwell Road, Lincoln LN2 5QY, UK.

Abstract

Insights

Flushing intravenous (IV) lines after administering antimicrobial drugs prevents significant drug loss, ranging from 2% to over 20%. This practice is crucial for effective treatment and patient safety.

Area of Science:

  • Pharmacology
  • Patient Safety
  • Healthcare Administration

Background:

  • Intravenous (IV) drugs are standard inpatient treatments.
  • Failure to flush IV lines post-administration leads to drug dose loss.
  • Underdosing of IV antimicrobials can reduce treatment efficacy, risking patient deterioration and antimicrobial resistance.

Purpose of the Study:

  • Quantify antimicrobial drug loss from non-flushed IV infusion lines.
  • Increase awareness of this potential patient safety risk.
  • Provide recommendations for effective risk mitigation.

Main Methods:

  • Calculated percentage drug loss for 39 IV antimicrobials.
  • Utilized residual volumes from IV infusion lines in an acute healthcare setting.
  • Assumed a theoretical adult male patient (70kg) with normal renal function for dosing calculations.

Main Results:

  • Drug losses ranged from 2% to 33% for assessed antimicrobials when infusion lines were not flushed.
  • Over 10% drug loss occurred for 26 of 39 antimicrobials.
  • Five antimicrobials experienced over 20% drug loss.

Conclusions:

  • Unintentional antimicrobial underdosing may be prevalent in clinical practice.
  • Flushing IV lines is strongly recommended to ensure complete drug administration.
  • National initiatives are needed to review IV administration protocols for enhanced patient safety.

Related Concept Videos

Drug Accumulation During Multiple Dosing: Intermittent IV Infusions01:24

Drug Accumulation During Multiple Dosing: Intermittent IV Infusions

Intermittent intravenous (IV) infusion is a method of drug administration where medications are delivered over short infusion periods followed by intervals of no drug delivery. This approach helps to prevent sustained high drug concentrations in the bloodstream, reducing the risk of adverse effects associated with prolonged exposure. Unlike continuous infusion, steady-state concentrations may not be achieved during a single dosing cycle but can be reached through repeated...
61
Dosage Interval and Administration Route: Determination Methods01:19

Dosage Interval and Administration Route: Determination Methods

A medication’s effectiveness largely depends on its appropriate dosage and the route of administration. Dosage ensures that a sufficient drug concentration is maintained in the bloodstream to elicit the desired therapeutic effect without causing toxicity. The route of administration affects the drug's bioavailability, rate of absorption, and onset of action, which are crucial for achieving optimal therapeutic outcomes. Drug dosage calculations are critical to tailoring therapy to...
53
One-Compartment Model: IV Infusion01:09

One-Compartment Model: IV Infusion

Intravenous (IV) infusion is often utilized when continuous and controlled drug delivery is necessary, such as during surgery or in the treatment of chronic diseases. This method offers numerous advantages, including immediate drug action, precise control over dosage, and bypassing the first-pass metabolism.
The one-compartment model for IV infusion uses mathematical equations to describe the rate of change in drug quantity in the body. At steady-state or infusion equilibrium, the drug input...
332
Drug Dosing in Renal Diseases: Dose Adjustments Based on Drug Clearance and Elimination Rate Constant01:25

Drug Dosing in Renal Diseases: Dose Adjustments Based on Drug Clearance and Elimination Rate Constant

In patients with renal disease, dosage adjustments are necessary to maintain therapeutic plasma drug concentrations and prevent toxicity or subtherapeutic exposure. Renal impairment alters drug pharmacokinetics, especially in conditions like uremia, where changes such as prolonged elimination half-life and altered apparent volume of distribution can significantly affect drug disposition. These changes require careful modification of the dosing regimen to achieve the desired clinical...
36
Two-Compartment Open Model: IV Infusion01:15

Two-Compartment Open Model: IV Infusion

A two-compartment model is a vital tool in pharmacokinetics, providing an essential understanding of drug behavior, especially for those administered via zero-order intravenous infusion. This model outlines two compartments: the central compartment, where elimination occurs, and the peripheral compartment.
The model illustrates the decrease in plasma drug concentration from the central compartment with a specific equation. It shows that under steady-state conditions, the drug's input rate...
381
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations01:15

Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations

Gentamicin, an aminoglycoside antibiotic, is commonly administered via intermittent intravenous infusion to treat severe infections. An intermittent one-hour infusion of gentamicin, administered at eight-hour intervals, allows for precise control of plasma drug concentrations, minimizing toxicity while ensuring therapeutic efficacy. Pharmacokinetic principles govern the dynamics of plasma concentrations and can be mathematically described using specific equations.The plasma drug concentration...
41