Anesthesia Machine Checkout
Ramon Larios
Esther Sung
▪ INTRODUCTION
The delivery of a safe anesthetic in modern-day practice begins with a checkout of the anesthesia machine. Improper or lack of inspection of anesthetic equipment prior to use has been associated with several significant incidents. Failure to check equipment clearly results in an increased risk of operative morbidity and mortality. With the large variety of anesthetic delivery systems available today, it is critical to understand the basic components of the system so that malfunctions can be detected prior to use or when failure occurs during use. Moreover, regular testing may lead to improved preventive maintenance and enhanced familiarity with the equipment. This chapter focuses on the fundamental components of the anesthesia machine checkout. Specific issues related to unique anesthesia delivery systems should be resolved by referring to the appropriate manufacturers’ operator manuals.
▪ HISTORY OF MACHINE CHECKOUT RECOMMENDATIONS
In 1993, a joint effort between the American Society of Anesthesiologists (ASA) and the U.S. Food and Drug Administration (FDA) resulted in the 1993 FDA Anesthesia Apparatus Checkout Recommendations. This simplified the initial 1986 preuse checkout and made it more userfriendly. At the time, the 1993 checklist focused on components that were immediately dangerous for patients and mechanisms that failed more regularly. This checklist was applicable to most commonly available anesthesia machines. Nevertheless, despite the recognized importance of an anesthesia machine checkout, available evidence suggests that the 1993 recommendations were neither well understood nor reliably used by anesthesia providers.
Moreover, because of recent and ongoing fundamental changes to the various anesthesia machine designs, the 1993 FDA preuse checklist may no longer be universally applicable to all anesthesia delivery systems. As more machines incorporate electronic checkouts, the user must determine which portions are automatically checked and which portions require manual checks. In such cases, the anesthesia care provider must be aware that the electronic machine check may not be a comprehensive preanesthesia checkout, and the user should follow the original equipment manufacturers’ recommended preuse checklist.
As a result, in 2005, the ASA‘s Committee on Equipment and Facilities, in conjunction with the American Association of Nurse Anesthetists (AANA) and the American Society of Anesthesia Technologists and Technicians (ASATT), began to develop a revised preuse checklist that was designed to be more workstation specific. These recommendations were published in 2008 and were intended to eventually replace the 1993 FDA Anesthesia Apparatus Checkout Recommendations. Rather than a checklist with specific instructions on how to perform each test, these new guidelines elaborate on specific systems and subsystems that must be evaluated. It is ultimately up to the user, along with the anesthesia machine manufacturer, to determine the actual mechanisms and/or specific checks that should be used to accomplish these subsystem evaluations. Appropriate personalized checkout procedures may need to be developed for individual machines and practices.
The 1993 Anesthesia Apparatus Checkout Recommendations placed all of the responsibility for the preuse checkout on the anesthesia provider. The new 2008 recommendations identify certain aspects of the preanesthesia checkout that may be performed by a qualified anesthesia
technician or a biomedical technician (http://www.apsf.org/newsletters/html/2008/spring/05_new_guidelines.htm).
technician or a biomedical technician (http://www.apsf.org/newsletters/html/2008/spring/05_new_guidelines.htm).
Redundancy in the critical aspects of the checkout process makes it more likely that problems will be identified prior to use for a patient. Nevertheless, regardless of the additional support of technicians, the anesthesia care provider is ultimately responsible for the proper function of all equipment used to deliver anesthesia care.
▪ ANESTHESIA MACHINE CHECKOUT PROCEDURE
As stated earlier, the goal of the preanesthesia checkout is to allow for the safe delivery of anesthesia care. Requirements for safe delivery of anesthetic care include the following:
Reliable delivery of oxygen at any appropriate concentration up to 100%
Reliable means of positive pressure ventilation
Availability of functional backup ventilation equipment
Controlled release of positive pressure from the breathing circuit
Anesthesia vapor delivery (if intended as part of the anesthetic plan)
Adequate suction
Means to conform to standards for patient monitoring
The new guidelines for the preanesthesia checkout procedures consist of 15 items. These items must be performed as part of a complete preanesthesia checkout on a daily basis. (Items that must be completed prior to each procedure are in bold). The 15 items are as follows:
Verify auxiliary oxygen cylinder and self-inflating manual ventilation device are available and functioning.
Anesthesia ventilator failure resulting in the inability to provide patient ventilation is rare but can occur at anytime. For those situations where the problem cannot be immediately identified or corrected, a manual ventilation device (e.g., bag valve mask) may be necessary to provide positive pressure ventilation until the problem is resolved. As a result, a self-inflating manual ventilation device and an auxiliary oxygen cylinder should be available and checked for proper function at each anesthesia setting.
In addition, the oxygen cylinder should have a regulator and a device to open the cylinder valve should be present. A full E cylinder of oxygen has a pressure of about 2,000 pound-force per square inch gauge (psig), which is equivalent to around 625 L of oxygen. After checking the oxygen cylinder pressure to ensure adequate supply, the cylinder should be stored with the valve closed in order to prevent unintended leakage or drainage of oxygen.
Verify patient suction is adequate to clear the airway.
The immediate ability to clear airway secretions or gastric contents is essential for safe anesthetic care. Inability to visualize the glottic opening and therefore delay in timely acquisition of a secure airway can be dangerous and possibly fatal. Aspiration of gastric contents can cause prolonged intubation and airway complications. Adequate strength of the suction can be tested by occluding the suction tubing orifice with the underside of a thumb and determining if the weight of the suction tubing can be supported at waist height. Prior to anesthesia, adequate suction should be checked and a rigid suction catheter (e.g., Yankauer) should be available on the machine.
Turn on the anesthesia delivery system and confirm that AC power is available.
AC power and the availability of backup battery power should be confirmed prior to the delivery of anesthesia. Visual indicators of the power systems exist on most anesthesia delivery systems. These should be confirmed as should appropriate connection of the power cord to a working AC power source. If the AC power is not confirmed, complete system shutdown is at risk when battery power is unknowingly depleted. Desflurane vaporizers, if used, should be checked for adequate electrical power source as well.
Verify availability of required monitors and check alarms.
The patient’s oxygenation, ventilation, circulation, and temperature should be continually evaluated according to the ASA‘s Standards for Basic Anesthetic Monitoring. Verification of the availability and proper function of the appropriate monitoring supplies should be performed prior to each anesthetic. Examples of necessary equipment include, but are not
limited to, blood pressure cuffs, pulse oximetry probes, electrocardiogram (ECG) leads, and capnography. Moreover, the appropriate audible or visual alarms that would indicate problems with, or disruption of, patient oxygenation, ventilation, circulation, and temperature should be intact. It is prudent for the anesthesiology technician to turn off the monitors and then turn them back on between cases to be sure that alarms are reset to default values as designed by each individual institution.
Verify that pressure is adequate on the spare oxygen cylinder mounted on the anesthesia machine.
Spare oxygen cylinders are mounted on anesthesia machines in the event that central oxygen supply is lost. Anesthesia machines require oxygen not only to provide oxygen to the patient but often to power pneumatically driven ventilators. The pressure of the oxygen cylinders should be checked to ensure an acceptable amount of backup oxygen is available. The oxygen cylinder valves should be closed after verification in order to prevent unrecognized depletion of the cylinder due to pressure fluctuations in the machine during mechanical ventilation or in the event of actual pipeline supply failure.
Rarely, the cylinder is intended to be the primary oxygen source. In these cases, if the ventilator is pneumatically driven, then the oxygen cylinder supply may be depleted quickly. As a result, manual or spontaneous ventilation may be more appropriate in order to maximize the duration of oxygen supply. On the other hand, the duration of oxygen supply for electrically powered or piston-driven ventilators depends only on total fresh oxygen gas flow.
Verify that the piped gas pressures are ≥50 psig.Full access? Get Clinical Tree