Bacterial contamination of multiple-dose vials: a prevalence study

Frauke Mattner1, Petra Gastmeier

  • 1Institute for Medical Microbiology and Hospital Epidemiology, Medical School Hannover, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany.

Abstract

Insights

Multiple-dose vials (MDVs) pose infection risks. A study found risky handling and contamination of MDVs in a hospital, highlighting the need for strict infection control measures to prevent outbreaks.

Area of Science:

  • Infection Control
  • Hospital Epidemiology
  • Microbiology

Background:

  • Two fatal meningitis cases caused by Pseudomonas aeruginosa were linked to contaminated multi-dose vials (MDVs) of contrast media in Germany, 2001.
  • This incident prompted an investigation into the prevalence of MDV use and contamination in a tertiary hospital.

Purpose of the Study:

  • To assess the usage patterns and contamination rates of multiple-dose vials (MDVs) in a large tertiary hospital.
  • To identify potential risks associated with MDV handling and storage practices.

Main Methods:

  • A prevalence study was conducted on a single day in November 2001 at a 1300-bed hospital.
  • All used MDVs were collected, and data on medication, labeling, storage temperature, ward, and opening dates were recorded.
  • Sterility testing was performed on each collected vial.

Main Results:

  • Opened MDVs were present in all hospital wards.
  • A contamination rate of 0.9% was observed, with one vial and one spike contaminated by Staphylococcus epidermidis.
  • Significant issues included poor labeling of opening dates (50% marked), expired vials (13%), improper storage (only 19% refrigerated), and use of non-preserved medications in 109 MDVs.

Conclusions:

  • Handling of MDVs in the hospital was found to be suboptimal, posing a significant infection risk.
  • Recommended infection control measures include strict adherence to manufacturer guidelines, proper storage temperatures, clear labeling of opening dates, and avoiding multi-use of non-preserved medications.

Related Concept Videos

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...
240
Bioavailability Study Design: Single Versus Multiple Dose Studies01:11

Bioavailability Study Design: Single Versus Multiple Dose Studies

Bioavailability studies are essential for understanding how a drug is absorbed, distributed, metabolized, and excreted in the body. These studies assess the extent and rate at which the active pharmaceutical agent becomes available at the site of action. The design of bioavailability studies can involve single-dose or multiple-dose regimens, each with distinct advantages and limitations.Single-dose studies are the preferred approach due to their simplicity and reduced drug exposure for...
223
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...
240
Determination of Multiple Dosing Parameters: Loading and Maintenance Doses01:25

Determination of Multiple Dosing Parameters: Loading and Maintenance Doses

A loading dose is an essential pharmacological strategy to rapidly achieve the target plasma drug concentration necessary for an immediate therapeutic effect. This approach is especially critical for drugs characterized by slow absorption or extended half-lives, where delaying therapeutic plasma levels could compromise treatment outcomes. By administering a loading dose, clinicians ensure a prompt onset of drug action, even for agents with complex pharmacokinetic profiles.Achieving steady-state...
230
Drug Accumulation During Multiple Dosing: Repetitive IV Injections01:21

Drug Accumulation During Multiple Dosing: Repetitive IV Injections

Calculating drug dosage and accumulation in multiple-dose regimens is crucial for achieving therapeutic efficacy while avoiding toxicity. This involves determining the plasma drug concentrations over time to optimize dosing schedules. The principle of superposition is fundamental in this process, allowing for the prediction of drug concentration in plasma following multiple doses based on single-dose data.The principle of superposition asserts that the plasma concentration-time curves from...
265
Prevalence and Incidence01:08

Prevalence and Incidence

In statistical epidemiology and health sciences, two essential metrics—prevalence and incidence—are fundamental for understanding disease dynamics within a population. These measures enable public health officials, epidemiologists, and researchers to assess the burden of diseases, allocate resources effectively, and design impactful public health policies and interventions.
Prevalence indicates the proportion of individuals in a population who have a specific disease or health...
1.7K