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Aerosol Guide - AARC.org

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Small-volume Nebulizers<br />

Small-volume nebulizers (SVNs) are popular aerosol generators with clinicians and<br />

patients as they convert drug solutions or suspensions into aerosols that deposit into the<br />

patient’s lower respiratory tract with minimal patient cooperation.<br />

Advantages and Disadvantages of SVNs<br />

Nebulizers have long been the cornerstone of medical aerosol therapy in the acute and<br />

critical care setting. Also, they are frequently the device selected for patients such as infants,<br />

small children, and the elderly who are unable to operate, coordinate, or cooperate with the<br />

use of various inhalers. This functionality offsets the issues of portability, weight, noise, cost,<br />

and time of administration associated with nebulizers. Table 4 lists the advantages and disadvantages<br />

of small-volume nebulizers.<br />

Table 4. Advantages and disadvantages of SVNs<br />

(Modified, with permission, from Reference 1)<br />

Advantages<br />

Disadvantages<br />

Ability to aerosolize many drug solutions Treatment times may range from 5–25<br />

minutes.<br />

Ability to aerosolize drug mixtures (>1 drug), Equipment required may be large and<br />

if drugs are compatible<br />

cumbersome.<br />

Minimal patient cooperation or coordination Need for power source (electricity, battery,<br />

is needed.<br />

or compressed gas)<br />

Useful in very young, very old, debilitated Potential for drug delivery into the eyes<br />

or distressed patients<br />

with face mask delivery<br />

Drug concentrations and dose can be<br />

Variability in performance characteristics<br />

modified.<br />

among different types, brands, and models<br />

Normal breathing pattern can be used, Assembly and cleaning are required.<br />

and an inspiratory pause (breath-hold) is Contamination is possible with improper<br />

not required for efficacy.<br />

handling of drug and inadequate cleaning.<br />

Nebulizers are regulated as medical devices by the U.S. Food and Drug Administration<br />

(FDA) Center for Devices and Radiological Health (CDRH). They are tested in accordance<br />

with applicable standards for medical device electrical safety, electromagnetic compatibility,<br />

environmental temperature and humidity, shock and vibration as well as for their biocompatibility<br />

of materials.<br />

Nebulizers are designed to be used with a broad range of liquid formulations. Drugs for<br />

use with nebulizers are approved by the FDA and the Center for Drug Evaluation and<br />

Research (CDER). Historically, drug solutions for inhalation were approved based on studies<br />

using standard jet nebulizers (the first type of SVN) ranging in efficiency from 6–12%. The<br />

use of more efficient nebulizers created the risk of delivering inhaled dose above the upper<br />

threshold of the therapeutic window, increasing the risk of side effects and toxicity.<br />

Consequently, the FDA requires that the drug label of new liquid formulations identify the<br />

nebulizers used in the clinical studies (Table 5). Because drug delivery varies with different<br />

nebulizer types, it is important to use the nebulizer cited on the drug “label” when possible.<br />

At the very least, clinicians should be aware of the relative performance of the “label”<br />

nebulizer.<br />

10 American Association for Respiratory Care A <strong>Guide</strong> to <strong>Aerosol</strong> Delivery Devices for Respiratory Therapists, 3rd Edition © 2013

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