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Audible Information Signals (‘Alarms’)
and Their Role in the Operating Room
Robert
K. Stoelting, M.D. Monitoring
a patient’s physiologic function during anesthesia
is intended to facilitate, but not replace, the
constant vigilance of the anesthesiologist. In this
regard, monitors may be viewed as adding an “additional
safety net” for the vigilant anesthesiologist.
Since the adoption of ASA’s Standards for
Basic Anesthetic Monitoring by the House of Delegates
on October 21, 1986, there has been an evolution
of monitoring technology and consensus among anesthesiologists,
which is reflected by the amendment of these monitoring
standards on October 21, 1998, to include pulse
oximetry and capnography.1
The existing Standards for Basic Anesthetic Monitoring
include “… an oxygen analyzer with a
low oxygen concentration limit alarm …”
and “… use of a device that is capable
of detecting disconnection of components of the
breathing system. The device must give an audible
signal when its alarm threshold is exceeded.”1
Since these standards were last amended, the development
and availability of audible information signals
as part of the physiologic monitors have continued
to evolve. Furthermore one of the 2003 Joint Commission
on Accreditation of Healthcare Organizations’
(JCAHO) National Patient Safety Goals is to “Improve
effectiveness of clinical alarm systems.”2
This JCAHO safety goal includes the statement: “Assure
that alarms are activated with appropriate settings
and are sufficiently audible with respect to distances
and competing noise within the unit.”2
JCAHO’s suggestions for meeting this goal
and its recommendations are to “develop and
implement policies that prevent turn-off capabilities
for alarms.”2
In a report of 1,000 anesthetic incidents, the fact
that an “alarm sounded” was recognized
as one of the most important factors in minimizing
the severity of the incident.3
Despite the compelling logic for utilizing audible
information signals to enhance the anesthesiologist’s
vigilance, the reality is that audible physiologic
alarms may be viewed as distractive and disruptive
by physicians, leading to the routine practice of
“silencing” the alarms.4
Audible alarms may not provide valid physiologic
information and can be associated with patient interventions
and events already known by the anesthesiologist.
Furthermore how many audible alarms (and their variety
of tones) are really needed? These questions have
led the Anesthesia Patient Safety Foundation (APSF)
to announce the following initiative:
APSF will publish, in a future edition of
the APSF Newsletter, a discussion of the use of
audible alarms on physiological monitors and the
use of audible beep tone from the pulse oximeter
during all anesthetics. In addition, APSF will
sponsor an APSF Board of Directors’ workshop
on this topic on October 22, 2004, in Las Vegas,
Nevada.
Although the announced APSF initiative is focused
on operating rooms, the intent is for the discussion
to extend beyond the operating room to include high-acuity
monitoring areas in the hospital. APSF will solicit
input from anesthesiologists and the equipment industry
to better understand the value (and flaws) of existing
audible information signals and establish how improvements
can be made to decrease the perceived disruption
and distraction that may be created by existing
audible alarms.
Ultimately any change in monitoring standards that
speaks to the use of audible alarm signals will
be based on consensus and cooperation between anesthesiologists
and those who manufacturer monitors that incorporate
audible information signals in physiologic monitors.
It is my personal bias that the audible presence
of the “beep” tone from a pulse oximeter
— plus knowing that the audible alarm on at
least one physiologic monitor of the anesthesiologist’s
choice (oxygen saturation, end-tidal carbon dioxide,
heart rate, blood pressure) is active — would
provide the desired safety net to the anesthesiologist’s
eternal vigilance without the distraction that may
be created by a “chorus” of alarms sounding
without valid physiologic reasons.
APSF intends to provide the forum for these discussions
and urges input from anesthesiologists and manufacturers
on this important anesthesia patient safety question.
References:
1. American Society of Anesthesiologists (ASA)
Standards for Basic Anesthetic Monitoring (Approved
by House of Delegates on October 21, 1986, and last
amended on October 15, 2003). ASA Standards, Guidelines
and Statements. October 2003:5-6. <www.ASAhq.org/publicationsAndServices/standards/02.pdf#2>.
2. 2003 Joint Commission on Accreditation of Healthcare
Organizations National Patient Safety Goals: Practical
Strategies and Helpful Solutions for Meeting These
Goals. <www.jcaho.org/accredited+organizations/patient+safety/npsg.htm>.
3. James RH. 1,000 anaesthetic incidents: Experience
to date. Anaesthesia. 2003; 58:856-863.
4. Block FE, Nuutinen L, Ballast B. Optimization
of alarms: A study on alarm limits, alarm sounds
and false alarms intended to reduce annoyance. J
Clin Monit Comput. 1999; 15:75-83.
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Robert K. Stoelting, M.D., Indianapolis, Indiana,
is President of the Anesthesia Patient Safety
Foundation. |
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