Performance of the Baxter disposable patient-controlled analgesia infusor under hyperbaric conditions | Canada Hyperbarics Skip to main content
Study Anaesthesia 1994

Performance of the Baxter disposable patient-controlled analgesia infusor under hyperbaric conditions

Radcliffe J, Spencer I — Anaesthesia, 1994

Tier 2, Indexed

Automatically imported from PubMed based on relevance criteria.

Summary

What Researchers Did

Researchers tested how well a Baxter Patient-Controlled Analgesia (PCA) infusor device delivered medications under hyperbaric (increased pressure) conditions.

What They Found

They found that increased pressure, specifically at 2.3 atmospheres, caused an increase in the flow rate of the infusor devices. The flow increased by 4.27% for 5% dextrose, 1.79% for propofol, and 9.84% for 50% dextrose solutions. This suggests that the device's delivery rate changes when exposed to higher pressures.

Canadian Relevance

No direct Canadian connection identified. This study does not involve Canadian authors or a Canadian study site, nor does it focus on a specific Health Canada-recognized HBOT indication, but rather equipment used during the therapy.

Study Limitations

This study was conducted in 1994 and focused on a specific infusor model, which may not reflect the performance of newer or different drug delivery devices.

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Study Details

Study Type Study
Category Uncategorised
Source Pubmed
PubMed ID 7978139
Year Published 1994
Journal Anaesthesia
MeSH Terms Analgesia, Patient-Controlled; Disposable Equipment; Glucose; Humans; Hyperbaric Oxygenation; Pressure; Propofol; Time Factors

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Disclaimer: This study summary is provided for informational and educational purposes only. It does not constitute medical advice. The information presented reflects the findings of the original research authors and may not represent the views of Canada Hyperbarics. Always consult a qualified healthcare professional before making treatment decisions.