FEATURES INTENDED TO PREVENT HUMAN ERROR
·
The
medical gas pin index and diameter index safety systems
ensure that medical gas connections are made correctly.
·
Therefore,
one cannot hang a nitrous oxide cylinder in an oxygen
hanger yoke or connect a nitrous oxide hose to the oxygen pipeline inlet
of the machine.
·
The
“fail-safe” valve is a pressure-sensitive device
that interrupts flow of all hypoxic gases on the machine to their flow control
valves if the supply pressure of oxygen in the intermediate-pressure system
(i.e., components downstream of the first stage oxygen regulator that reduces
the high pressure in the tank to 45 pounds per square inch gauge [psig] and upstream
of the oxygen flow control needle valve) falls below a
threshold (˜20 psig in GE machines; 12 psig in
Dräger machines).
·
When
the pressure of oxygen in the intermediate-pressure system falls below 30 psig,
an oxygen supply pressure failure alarm is
annunciated.
·
The
oxygen flow control knob is “touch coded”; that
is, it is fluted and larger
in diameter than the other gas flow control knobs and is normally located on the right of all other gas flow control
valves.
·
In
the Dräger Fabius GS workstation, the gas flow controls
are arranged vertically, with the oxygen flow control knob as the
lowest.
·
Key-fill systems for anesthesia vaporizers are safety features that also decrease
the likelihood of atmospheric contamination during vaporizer filling.
·
The most
important of such systems is the Safe-T-Fill system
used on desflurane bottles and desflurane vaporizers because filling a
vaporizer specific for another agent with desflurane could result in a lethal
overdose of desflurane.
·
A pressure relief valve built into the machine common
gas outlet, breathing system, or ventilator provides some protection against
positive pressure barotrauma.
FEATURES TO CORRECT FOR USE ERROR
·
Gas flow proportioning systems
ensure a minimum oxygen concentration of 25% when nitrous oxide and oxygen are
being used.
·
Therefore,
if the anesthesiologist were to accidentally attempt to increase the flow of
nitrous oxide, either the oxygen flow would be
increased automatically or the flow of nitrous
oxide would be limited according to the flow of oxygen that was set.
·
On older machines,
during use of the anesthesia ventilator, changes in fresh gas flow,
inspiratory-expiratory (I:E) ratio, or respiratory rate cause changes in
delivered tidal volume that might result in overventilation,
underventilation, or even barotrauma.
·
On modern systems (e.g., GE workstations that incorporate
a ventilator with the Smart Vent feature, Dräger Fabius GS, and Apollo
workstations), once the ventilation parameters have been set, they are
maintained because the ventilator or circuit automatically
compensates for changes in gas flow settings.
·
In the GE workstations with Smart Vent, tidal volume is
monitored continually by a computer.
·
If
measured tidal volume changes from that set to be
delivered, the computer adjusts the volume delivered by the ventilator
bellows.
·
Dräger and Datascope Anestar
workstations use fresh gas decoupling to maintain a constant tidal volume.
·
In
this system, during the inspiratory phase, a decoupling
valve closes so that fresh gas entering the breathing system is directed into the reservoir bag and only gas from the ventilator is delivered to the patient.
·
During exhalation,
the ventilator chamber refills from the fresh gas flow
and the fresh gas that was collected in the reservoir bag during the previous
inspiration.
·
A vaporizer interlock system prevents the unintentional
simultaneous use of more than one vaporizer.
MONITORING SYSTEMS
·
A
monitor of oxygen in the gas delivered to the patient is mandatorily enabled, and the low
oxygen concentration alarm is
activated whenever the anesthesia
workstation is capable of delivering an anesthetic gas mixture from the common
gas
outlet.
Other monitors in the anesthesia
workstation include pressure, volume, flow, and
gas composition. Some also incorporate
airway gas flow monitoring. The breathing system lowpressure
monitor alarm is automatically enabled when the
ventilator
is turned on.
ALARM SYSTEMS
Contemporary workstations incorporate an
integrated prioritized alarm system with visible and
audible alerts when set
parameter limits are exceeded.
An important safety feature of all modern
machines/workstations is the preuse checkout. In
1993, the U.S. Food and Drug
Administration (FDA) published anesthesia apparatus checkout recommendations. The
machine should be checked by
an educated user. Item no. 1 on the FDA checklist is that
an alternative means to ventilate the patient's
lungs should be
present and functioning. Therefore, if a
problem arises with the machine, the patient's lungs can be ventilated using a selfinflating
resuscitation bag (e.g., Ambu
bag). If a machine problem
arises and the cause/remedy is not immediately obvious, one should
instinctively reach for the resuscitation bag and call
for help. A recent analysis of the American
Society of Anesthesiologists Closed
Claims Project data found that 35% of adverse outcomes were likely preventable
if a
proper preuse checkout had been
performed.
Recognizing that not all of the FDA 1993
checkout recommendations can be applied to many of the contemporary
workstations, in 2008, the American
Society of Anesthesiologists published guidelines applicable to all anesthesia
delivery systems so that individual departments can develop their own workstation-specific
preuse checkout that can be
performed consistently and expeditiously.
The 2008 guidelines are intended to provide a template for developing checkout
procedures that are appropriate for each
individual anesthesia machine design and practice setting. They discuss which
systems and components should be checked,
the checkout interval (e.g., before first case
vs. before every case), and who
may be responsible for performing each
checkout procedure—the anesthesiologist or technician (Table 59.1). Examples
of user-developed workstation-specific
checkouts are available on the American Society of Anesthesiologists'