Abstract

Alongside the development and testing of new audible alarms intended to support International Electrotechnical Commission 60601-1-8, a global standard concerned with alarm safety, the categories of risk that the standard denotes require further thought and possible updating. In this article, we revisit the origins of the categories covered by the standard. These categories were based on the ways that tissue damage can be caused. We consider these categories from the varied professional perspectives of the authors: human factors, semiotics, clinical practice, and the patient or family (layperson). We conclude that while the categories possess many clinically applicable and defensible features from our range of perspectives, the advances in alarm design now available may allow a more flexible approach. We present a three-tier system with superordinate, basic, and subordinate levels that fit both within the thinking embodied in the current standard and possible new developments.

DOI

10.2345/0899-8205-51.s2.50

Publication Date

2017-02-01

Publication Title

Biomedical Instrumentation & Technology

Volume

51

Issue

s2

Publisher

Association for the Advancement of Medical Instrumentation (AAMI)

ISSN

1943-5967

Embargo Period

2024-11-22

First Page

50

Last Page

57

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