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  • 7/25/2019 Implementing Aorn Recommended Practices for Electrosurgery

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    Implementing AORN

    Recommended Practicesfor ElectrosurgeryLISA SPRUCE, DNP, RN, ACNP-BC, ANP-BC, ACNS-BC, CNOR;

    MELANIE L. BRASWELL, DNP, RN, CNS, CNOR

    www.aorn.org/CE

    2.8

    ABSTRACT

    Technology is constantly changing, and it is important for perioperative nurses to stay

    current on new products and technologies in the perioperative setting. AORNs Rec-

    ommended practices for electrosurgery addresses safety standards that all periop-

    erative personnel should follow to minimize risks to both patients and staff members

    during the use of electrosurgical devices. Recommendations include how to select

    electrosurgical units and accessories for purchase, how to minimize the potential for

    patient and staff member injuries, what precautions to take during minimally inva-

    sive surgery, and how to avoid surgical smoke hazards. The recommendations also

    address education/competency, documentation, policies and procedures, and quality

    assurance/performance improvement. Perioperative nurses should consider the use of

    checklists and safety posters to remind staff members of the dangers of electrosurgery

    and the steps to take to minimize the risks for injury. AORN J95 (March 2012) 373-384.

    AORN, Inc, 2012. doi: 10.1016/j.aorn.2011.12.018

    Key words: electrosurgery, electrosurgical unit, ESU, active electrode, bipolar

    active electrode, dispersive electrode, monopolar electrosurgery, ultrasonic de-

    vice, argon enhanced coagulation technology, surgical smoke, minimally invasive

    surgery, MIS.

    The AORN Recommended practices for

    electrosurgery was published in July 2009

    online in Perioperative Standards and

    Recommended Practices. The purpose of the re-

    vised recommended practices (RP) document is toprovide guidance to perioperative nurses in the

    use and care of electrosurgical equipment, includ-

    ing high frequency, ultrasound, and argon beam

    modalities.1(p99) There are 14 practice recom-

    mendations that represent what is believed to be

    an optimal level of practice. Hospital and ambula-

    tory patient scenarios representing possible patient

    safety situations are provided here to exemplify

    indicates that continuing education contact hours

    are available for this activity. Earn the contact hours

    by reading this article, reviewing the purpose/goal and

    objectives, and completing the online Learner Evalua-

    tion athttp://www.aorn.org/CE.The contact hours

    for this article expire March 31, 2015.

    RECOMMENDED PRACTICES

    doi: 10.1016/j.aorn.2011.12.018

    AORN, Inc, 2012 March 2012 Vol 95 No 3 AORN Journal 373

    http://www.aorn.org/CEhttp://www.aorn.org/CEhttp://www.aorn.org/CEhttp://www.aorn.org/CEhttp://www.aorn.org/CE
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    ways that practice recommendations for electro-

    surgery might be implemented.

    WHATS NEW?

    Electrosurgery was introduced in the 1920s and is

    commonly used today. However, new safety fea-

    tures have been incorporated into current electro-

    surgical unit (ESU) and active and dispersive

    electrode designs. Electrosurgical unit devices

    present risks for patient injury; the most common

    form of patient injury is a burn at the dispersive

    electrode site.2 In addition to presenting a risk

    for patient injury, these devices can cause fires,

    electrical shock, or explosions and may inter-

    fere with other critical implanted electronic

    medical devices such as pacemakers. This RP

    document updates perioperative nurses on safe

    practices in electrosurgery.

    RATIONALE

    Patient safety is the number-one priority for

    perioperative nurses, and keeping patients and

    staff members safe during the use of ESUs is

    essential. Electrosurgical technology poses a

    very high risk to the patient and can cause

    permanent disfiguring injuries or death.3 In

    addition, there is a high degree of risk to

    personnel, such as shocks and burns, in the

    presence of this device.

    The generator of the ESU is the electricity

    source. The monopolar electrosurgery circuit is

    composed of the generator, the active electrode,

    the patient, and the patient dispersive electrode

    (ie, return electrode) (Figure 1). The patients

    tissue provides impedance, and heat is produced

    as the electrodes overcome the impedance. In

    ground-referenced generators, alternative path-

    ways to the ground may include the OR bed,

    stirrups, staff members, and equipment, provid-

    ing a potential risk of alternate site injury.

    Isololated generators minimize this risk for in-

    jury because the preferred pathway return to the

    ground is through the generator.

    This RP document addresses the safety mea-

    sures that all perioperative personnel should use

    to minimize risk to both patients and staff

    members. The Association for the Advancement

    of Medical Instrumentation has established min-

    imum safety and performance standards for us-

    ing ESU systems, which have been approved by

    the American National Standards Institute and

    the International Electrotechnical Commission.4

    Figure 1. The monopolar electrosurgical circuit is composed of the generator, the active electrode, the

    patient, and the patient dispersive electrode.

    March 2012 Vol 95 No 3 SPRUCEBRASWELL

    374 AORN Journal

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    DISCUSSION

    Most perioperative nursing strategies for ensuring

    patient safety while electrosurgery is being used

    are task oriented. Working as a team and follow-

    ing patient safety protocols and checklists will

    help remind staff members of the key steps for

    electrosurgical safety. At times, nurses take for

    granted that patients are going to be safe. Electro-

    surgery is used every day in the OR, and it is easy

    to let ones guard down. The use of tools such as a

    patient safety poster (Figure 2)can help periopera-

    tive personnel remember the key components of

    electrosurgery. Developing tools such as this one in

    individual practice settings reminds staff members

    that patient safety is a team responsibility.

    Developing standardized protocols and check-

    lists for each operating arena is another way to

    reinforce all of the key safety strategies. Protocols

    and checklists should be based on AORNs rec-

    ommended practices. An example of different

    protocols might be for patients who are undergo-

    ing general surgery versus those who are under-

    going minimally invasive surgery. Protocols for

    patients undergoing minimally invasive surgery

    would have additional safety steps because of the

    risks involved with using distention media.

    Recommendation I

    Personnel selecting new

    and refurbished [ESUs] and

    accessories for purchase or

    use should make decisions

    based on safety features to

    minimize risks to patients and

    personnel.1(p99) Personnel

    involved in purchasing deci-sions should consider

    the following:

    The most frequently re-

    ported injury to patients

    is a burn at the site of

    the dispersive electrode.2

    Look for a dispersive

    electrode that will

    minimize this risk, such as through the use of

    return electrode contact quality monitoring.2,5

    Speak to vendors and get a detailed explana-

    tion of the safety features of the equipment

    being considered for purchase.

    Form an interdisciplinary group to ask ques-

    tions and discuss the risks and benefits to pa-

    tients of this type of equipment.

    Standardize equipment across the facility so

    there is no variation in practice, which helps

    ensure that all patients are treated with the

    same safety standards related to ESU use.

    Recommendation II

    The ESU should be used in a manner that mini-

    mizes the potential for injuries.1(p100) Patientinjuries, user injuries, and fires do occur. Periop-

    erative nurses should be knowledgeable of and

    diligent in adhering to the basic principles of ESU

    safety. Perioperative nurses should speak up and

    challenge other team members if patient safety

    issues arise or strategies are not consistently fol-

    lowed. Perioperative nurses should consider the

    following steps for creating a safe electrosurgical

    environment:

    Read and attach the manufacturers manual tothe unit or cart on which the ESU sits.

    Educational Resources

    Periop Modules: Electrosurgery. http://www.aorn.org/

    Education/Specialty_Education/Periop_Modules.aspx.

    AORN Video Library:Electrosurgery: Function, Practice &

    Safety. http://cine-med.com/index.php?navnursing&subnav

    aorn&id

    1937. Perioperative Management Resources: Evaluation of New Tech-

    nology. http://www.aornbookstore.org/.

    Surgical Smoke Evacuation Tool Kit.http://www.aorn.org/

    Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_

    ToolKit/Download_the_Surgical_Smoke_Evacuation_

    Tool_Kit.aspx.

    Web site access verified December 12, 2011.

    RP IMPLEMENTATION GUIDE: ELECTROSURGERY www.aornjournal.org

    AORN Journal 375

    http://www.aorn.org/Education/Specialty_Education/Periop_Modules.aspxhttp://www.aorn.org/Education/Specialty_Education/Periop_Modules.aspxhttp://www.aorn.org/Education/Specialty_Education/Periop_Modules.aspxhttp://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://www.aornbookstore.org/http://www.aornbookstore.org/http://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aorn.org/Clinical_Practice/ToolKits/Surgical_Smoke_Evacuation_ToolKit/Download_the_Surgical_Smoke_Evacuation_Tool_Kit.aspxhttp://www.aornbookstore.org/http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://cine-med.com/index.php?nav=nursing%26subnav=aorn%26id=1937http://www.aorn.org/Education/Specialty_Education/Periop_Modules.aspxhttp://www.aorn.org/Education/Specialty_Education/Periop_Modules.aspx
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    Electrosurgical Safety

    It Takes a TEAM to:

    Know how to:

    Check the machine and accessories before use.

    Avoid risks to patient and staff.

    Solve simple problems.

    Prepare the patient safely.

    Assess the patients skin before and after elec-

    trosurgery use.

    Understand:

    What equipment you are using.

    How to minimize risk.

    Electrosurgery principles

    Importance of letting the prep dry!

    Why the active electrode is stored in a holster when

    not in use.

    Every year patients and members of the surgery team are injured during cases where electrosurgical

    technology is used. Often times injuries occur due to operator error and not from the equipment it-

    self. It takes a team to assure patients and staff are safe from injury! Everyone should understand

    the risks and take action to prevent a mishap from occurring.

    We want to make surgical procedures around the world something that patients

    and surgeons quickly forget because they have gone right rather than wrong.

    ~Sir Liam Donaldson

    Consider:

    The patients weight, fat distribution,

    and age.

    Active implants such as a pacemaker

    or ICD-patient cleared by cardiology.

    Allergies.

    The position of the return electrode

    and metal implants, patient position,

    operating site, scars and tattoos.

    Be aware of:

    The ESU has had proper maintenance, is in good working order with proper ac-

    cessories.

    The lowest power setting is being used.

    The alarms, never silence them!

    The potential for injury due to direct or capacitive coupling.

    The correct accessories go with the correct machine.

    How to report events and near misses.

    The danger of activating the ESU while staff are in direct contact with the pa-

    tient.

    Special precautions with argon enhanced coagulation.

    Safety doesnt happen by accident!

    Figure 2. A patient safety poster can remind staff members of precautions to take during electrosurgery.

    March 2012 Vol 95 No 3 SPRUCEBRASWELL

    376 AORN Journal

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    Ensure that the ESU is mounted on a tip-

    resistant cart or shelf and is protected from

    liquids.

    Do not silence alarmsall alarms and acti-

    vation indicators should be operational, au-

    dible, and visible at all times. It is easy to

    become distracted and to experience nor-

    malization of deviation (eg, the acceptance

    of activities that would normally be deemed

    unacceptable). There is a natural human

    tendency to ignore safety standards and

    alarms over time when no event has occurred.

    Nurses should be aware of this phenomenon

    and always be diligent in ensuring patient

    safety.

    Confirm the power settings with the operator

    before the ESU is activated and use the low-

    est setting to achieve the desired tissue

    effect.2,6-9 If the operator requests a contin-

    ued increase in power, the nurse should

    check the entire ESU and accessories for

    cord connections and adequate placement of

    the dispersive electrode.6,10,11 If there is a

    continued request to increase power, this

    could indicate that there is a problem with

    the unit, the connections, or the placement

    of the grounding pad. Nurses should not as-

    sume that it is okay to

    increase power without

    stopping the procedure

    and checking the ma-

    chine and the patient.

    Surgery should not con-

    tinue if there is a con-

    cern that the machine is

    not working properly.

    Recommendation III

    The electrical cords and

    plugs of the ESU should be

    handled in a manner that

    minimizes the potential for

    injury and subsequent patient

    and user injuries.1(p101)

    When cords and plugs are handled improperly,

    the insulation can become frayed or broken,

    which presents an electrical hazard. A survey of

    the ESU physical environment only takes a min-

    ute and should be a part of routine preparation for

    every procedure. The perioperative nurse should

    take the time to perform this critical survey and

    consider the following actions to protect patients

    and staff members:

    Do not place tension on the cord and make

    sure the length is adequate; do not use exten-

    sion cords.10

    Place the ESU near the sterile field; the cord

    should reach the wall or outlet without

    stress and without blocking a traffic path.10

    Do not allow kinks, knots, or bends in the cord.

    Hold the plug, not the cord, when removing

    the ESU from the outlet.

    Keep the cord dry.10

    Check the cord for breaks, nicks, or cracks

    and remove it from use for repair or replace-

    ment if needed.10

    Recommendation IV

    The active electrode should be used in a manner

    that minimizes the potential for injuries1(p101)

    (Figure 3). Incompatibility of the active electrode

    Resources for Implementation

    AORN Clinical Answers. http://www.aorn.org/Clinical_

    Practice/Clinical_Answers/Clinical_Answers.aspx.

    AORN Nurse Consult Line. 800-755-2676 or 303-755-6300,

    option 1.

    EHR Perioperative Framework.http://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_

    Framework.aspx.

    ORNurseLink. http://www.aorn.org/ORNurseLink/.

    Perioperative Job Descriptions and Evaluation Tools.http://

    www.aorn.org/Secondary.aspx?id20740&terms

    perioperative%20competencies.

    Web site access verified December 12, 2011.

    RP IMPLEMENTATION GUIDE: ELECTROSURGERY www.aornjournal.org

    AORN Journal 377

    http://www.aorn.org/Clinical_Practice/Clinical_Answers/Clinical_Answers.aspxhttp://www.aorn.org/Clinical_Practice/Clinical_Answers/Clinical_Answers.aspxhttp://www.aorn.org/Clinical_Practice/Clinical_Answers/Clinical_Answers.aspxhttp://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_Framework.aspxhttp://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_Framework.aspxhttp://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_Framework.aspxhttp://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_Framework.aspxhttp://www.aorn.org/ORNurseLink/http://www.aorn.org/ORNurseLink/http://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/Secondary.aspx?id=20740%26terms=perioperative%20competencieshttp://www.aorn.org/ORNurseLink/http://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_Framework.aspxhttp://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_Framework.aspxhttp://www.aorn.org/Clinical_Practice/EHR_Periop_Framework/EHR_Perioperative_Framework.aspxhttp://www.aorn.org/Clinical_Practice/Clinical_Answers/Clinical_Answers.aspxhttp://www.aorn.org/Clinical_Practice/Clinical_Answers/Clinical_Answers.aspx
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    with the ESU as well as unintentional activation

    and incomplete circuitry pose safety hazards to

    patients and staff members.12,13 Perioperative

    nurses should be diligent in monitoring for unin-

    tentional activation, problems arising with the

    ESU, or unsafe practices, and they should speak

    up when patient safety is threatened. It is impor-

    tant to ensure that electrosurgery not be used in

    the presence of gastrointestinal gases12,14-17 or in

    an oxygen-enriched environment.14,18-21 Caution

    should be used when activating the active

    electrode near the head and neck region or in

    the presence of combustible anesthetic gases.

    The active electrode should be used as far away

    as possible from the oxygen source. Periopera-

    tive nurses can take the following actions to

    lessen risks:

    Coordinate with the anesthesia professional to

    minimize the oxygen concentration.

    Always visually inspect the active electrode

    at the field before use. Look for cord or

    handpiece damage and incompatibility of the

    accessories with the ESU.

    Observe the sterile field when the ESU is in

    use and, when necessary, remind the surgeon,

    technician, or assistant that the active elec-

    trode should be placed in a nonconductive

    safety holster when it is not in use.2,9,14,22

    Place the foot pedal near the user of the active

    electrode to reduce the risk of unintentional

    activation by other team members.8,14

    Remove accumulated eschar from the active

    electrode tip away from the incision.12,18

    Follow fire safety measures,23 and consider

    using a checklist to make sure none of the

    following steps are accidentally missed:

    Do not activate the active electrode in the

    presence of flammable agents.

    Time alcohol-based prep agents so the

    minimum dry time recommended by the

    manufacturer is allowed to pass, and do

    not allow the surgical technologist or

    Figure 3. The active electrode should be used in a manner that minimizes the potential for injuries.

    March 2012 Vol 95 No 3 SPRUCEBRASWELL

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    surgeon to drape the patient until the

    prep agent has dried.

    Remove suture packets containing alcohol

    from the sterile field as soon as possible.

    Moisten sponges that are used near the ac-

    tive electrode tip.18,24,25

    Arrange surgical drapes to minimize the

    buildup of oxidizers (eg, oxygen, nitrous

    oxide).

    Always have a wet towel, saline, or wa-

    ter available on the sterile field to extin-

    guish a fire.

    Be prepared to immediately extinguish

    flames should they occur.

    Recommendation V

    When monopolar electrosurgery is used, a dis-

    persive electrode should be used in a manner

    that minimizes the potential for injuries.1(p104)

    It is extremely important to make sure the dis-

    persive electrode has uniform contact with the

    patients skin. The perioperative RN should

    verify this before surgery begins. If the nurse

    notes that there is poor contact, he or she

    should institute corrective actions, such as re-moving any oil, lotion, moisture, prep solution,

    or excessive hair that may be interfering with

    contact; moving the dispersive electrode to an-

    other site; or applying a new pad. The nurse

    should not use tape to hold the dispersive elec-

    trode in place.

    The nurse should ensure that the patient does

    not contact any metal devices such as the bed,

    stirrups, positioning devices, or safety strap

    buckles to prevent a possible burn from di-rected current. Patient jewelry that is between

    the active and dispersive electrodes should be

    removed. Electrocardiogram electrodes should

    be placed as far away from the surgical site as

    possible. When removing the electrode, the

    nurse should hold the adjacent skin in place

    and peel the electrode back slowly to prevent

    denuding the skin.

    The nurse also should implement the following

    as part of routine patient care:

    Assess the patients skin before and after ESU

    use to assess for any injuries.

    Use dual-foil electrodes to make sure there isno impedance through the patients tissue.6 If

    the impedance is too high, the ESU alarm will

    sound and the ESU will stop functioning, thus

    protecting the patient from harm.2

    A single-use dispersive electrode should be

    compatible with the ESU. Discard the elec-

    trode after it has been used. If repositioning is

    needed, discard the electrode and use a new

    single-use product.11,26 Never reposition a

    used electrode. Make sure to use the correct size of dispersive

    electrode for individual patients. There are

    different sizes, and they should not be folded,

    cut, or altered in any way.

    Identify the expiration date on a single-use dis-

    persive electrode package before opening it and

    do not use it if it is past the manufacturers expi-

    ration date. Check the integrity of the product

    and do not use it if there are flaws, damage, dis-

    coloration, poor adhesive, or dryness, becausethese could prevent adequate contact.6,8,11,27

    Place the dispersive electrode on well-perfused

    muscle, which is a better conductor of elec-

    tricity than adipose tissue.11 Also, place the

    electrode on clean, dry, and intact skin on the

    same side as the surgery and as close as possi-

    ble to the site.

    Do not place the electrodes over bony promi-

    nences, scar tissue, hair, weight-bearing sur-

    faces, potential pressure points, tattoos, or ametal prosthesis; distal to a tourniquet; or near

    a warming device.

    Place the dispersive electrode on the patient

    after final positioning. If the patient is reposi-

    tioned during surgery, verify that the electrode

    is still in contact with the patients skin.

    A capacitive coupled return electrode is a non-

    adhesive return electrode that is placed close to

    RP IMPLEMENTATION GUIDE: ELECTROSURGERY www.aornjournal.org

    AORN Journal 379

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    the patient and forms a capacitor with the patient,

    returning electrical current from the patient back

    to the ESU. If a capacitive coupled pad is used,

    the nurse should ensure that the pad is the appro-

    priate size for the patient and that there is ade-

    quate contact by confirming there are no materi-

    als, such as foam, gel pads, or extra linen,

    between the patient and the pad.

    Recommendation VI

    Personnel should take additional precautions

    when using electrosurgery during minimally inva-

    sive surgery (MIS).1(p107) Specific patient injury

    can occur from direct coupling, insulation failure,

    and capacitive coupling.6 Perioperative RNs

    should understand these concepts and implementprecautions to prevent patient injury.

    Direct coupling is the contact of an energized

    active electrode tip with another metal instrument

    or object in the surgical field. This can occur

    when the surgeon or other user accidentally acti-

    vates the ESU when the active electrode is touch-

    ing another metal instrument, thus energizing that

    instrument. This energy will seek a pathway to

    the ground and can cause a significant patient

    injury. Capacitive coupling is the transfer of elec-trical current from the active electrode through

    intact insulation to adjacent conductive items (eg,

    tissue, trocars). This occurs when combination

    plastic and metal trocar systems are used.28-30 A

    current can be generated from the conductor to

    the nonconductor and the current can seek a path-

    way through the patients tissues on its way to the

    return electrode.

    The following safety measures are important to

    incorporate into nursing practice for MIS:

    Make sure the gas used for insufflation is non-

    flammable (eg, carbon dioxide).

    Make sure that conductive trocar systems

    are being used. This allows the current to

    flow safely between the cannula and the ab-

    dominal wall.

    Do not use hybrid trocar systems (ie, combi-

    nation plastic and metal).

    Examine the electrodes used in MIS for insu-

    lation failure. If the insulation is not intact, an

    alternative pathway can be formed and can

    cause serious patient injuries.28,31-36 There are

    multiple methods used to detect insulation

    failure. One is the use of two different colors

    on the active electrode. The insulation is a

    different color than the material of which the

    active electrode is made, so it is visible if the

    insulation fails, indicating the active electrode

    should not be used. Active continuous moni-

    toring systems are another detection method

    that continuously monitor for insulation failure

    or capacitive coupling and automatically shut

    down when a breach is detected.

    Instruct patients to report symptoms of elec-

    trosurgical injury (eg, fever, abdominal pain,

    vomiting) after MIS, and remind them that

    symptoms can occur after discharge from the

    postanesthesia care unit.

    Recommendation VII

    Bipolar active electrodes, including vessel oc-

    cluding devices, should be used in a manner

    that minimizes the potential for injuries.1(p108)

    Unlike monopolar electrodes, bipolar electrodeshave two poles. The current flows between the

    two poles and back to the ESU, so there is no

    need for a dispersive electrode (Figure 4). Only

    the tissue grasped is included in the electrical

    current and there is no chance of stray current or

    alternative pathways. The perioperative nurse

    should make sure that the monopolar and bipolar

    plugs on the ESU are differentiated, that proper

    accessories are used, and that the correct cord is

    plugged in to the correct bipolar plug. Bipolaractive electrodes provide precise hemostasis be-

    cause the current runs between the two tines of

    the electrode and not through the patient.

    Recommendation VIII

    Ultrasonic devices should be used in a manner

    that minimizes potential injuries.1(p109) Ultra-

    sonic devices do not create electrical energy. A

    generator is used to produce ultrasonic energy

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    and mechanical vibrations that cut and coagu-

    late, causing denaturation of protein and the

    formation of a coagulum. There is no need for

    a dispersive electrode. The biggest risk with

    ultrasonic devices is the risk to personnel who

    are operating the device. Inhalation of aerosols

    generated by the ultrasonic ESU should be min-

    imized by using measures such as smoke evac-

    uation systems and wall suction with an in-line

    ultra-low penetration air (ULPA) filter.

    Recommendation IX

    Argon enhanced coagulation technology (AEC)

    poses unique risks to patient and personnel safety

    and should be used in a manner that minimizes

    the potential for injury.1(p109) This type of

    technology is a form of electrosurgery that uses

    radio-frequency coagulation from an ESU that is

    capable of delivering monopolar current through a

    flow of ionized argon gas. The argon gas carries

    the current from the active electrode to the tissue

    so the active electrode never has to actually come

    into contact with the tissue. This is useful for

    hard-to-reach places.

    During the use of AEC, all manufacturers

    written instructions should be followed in addition

    to all of the safety measures for monopolar sur-

    gery. The perioperative nurse should implement

    the following actions to promote patient safety:

    Purge the air from the argon gas line by acti-

    vating the system before use and after moder-

    ate delays between activations and between

    uses. Purging the gas line minimizes the riskof gas embolism. The gas flow should be lim-

    ited to the lowest level possible that achieves

    the desired effect.

    Do not place the active electrode in direct

    contact with tissue and remove it from patient

    tissue after each activation. If there is direct

    contact with tissue, the gas can be forced into

    a vessel and cause gas emboli, which could be

    fatal to the patient.

    To prevent potential patient injury or death asa complication of argon gas technology, the

    perioperative RN should take the following

    steps as part of care:

    Make sure that endoscopic insufflators have

    audible and visual over-pressurization

    alarms that cannot be deactivated. The

    AEC is a secondary source of gas inside

    the patient and can cause a rapid rise in

    Figure 4. In bipolar electrosurgery, current flows between the two poles and back to the electrosurgery unit

    without the need for a dispersive electrode.

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    intra-abdominal pressure, possibly causing

    gas emboli to form.

    Monitor patients for gas emboli, specifi-

    cally end-tidal carbon dioxide, during the

    procedure.

    Recommendation X

    Potential hazards associated with surgical smoke

    generated in the practice setting should be identified,

    and safe practices established.1(p110) The National

    Institute of Occupational Safety and Health recom-

    mends that smoke evacuators be used to reduce the

    potential adverse effects of surgical smoke to per-

    sonnel and patients. Local exhaust ventilation (LEV)

    (eg, smoke evacuator, wall suction with in-line

    ULPA filter) should be used as the primary methodof smoke evacuation. The suction wand of the

    smoke evacuation should not be farther than two

    inches from the source of the smoke. Nurses should

    evaluate the type of LEV needed in their practice

    settings for surgical procedures. The type of

    LEV is based on adequacy to ensure safe re-

    moval of the anticipated amount of surgical

    smoke. Perioperative nurses should use respira-

    tory protection (ie, a fit-tested surgical N95 fil-

    tering facepiece respirator or high-filtrationmask) as secondary protection.

    The Final Four

    The final four recommendations in each AORN

    RP document discuss education/competency, doc-

    umentation, policies and procedures, and quality

    assurance/performance improvement. These four

    topics are integral to the implementation of

    AORN practice recommendations. Personnel

    should receive initial and ongoing education and

    competency validation as applicable to their roles.

    Implementing new and updated RPs affords an

    excellent opportunity to create or update compe-

    tency materials and validation tools. AORNs

    perioperative competencies team has developed

    the AORN Perioperative Job Descriptions and

    Competency Evaluation Tools37 to assist perioper-

    ative personnel in developing competency evalua-

    tion tools and job descriptions.

    Documentation of nursing care should include

    patient assessment, plan of care, nursing diagnosis,

    and identification of desired outcomes and interven-

    tions, as well as an evaluation of the patients re-

    sponse to care. Implementing new or updated RPs

    may warrant a review or revision of the relevant

    documentation being used in the facility.

    Policies and procedures should be developed,

    reviewed periodically, revised as necessary, and

    readily available in the practice setting. New or

    updated RPs may present an opportunity for col-

    laborative efforts with nurses and personnel from

    other departments in the facility to develop

    organization-wide policies and procedures that

    support the RPs. The AORN Policy and Proce-

    dure Templates, 2nd edition,38 provides a collec-

    tion of 15 sample policies and customizable tem-

    plates based on AORNs Perioperative Standards

    and Recommended Practices. Regular quality im-

    provement projects are necessary to improve patient

    safety and to ensure safe, quality care. For details on

    the final four practice recommendations that are spe-

    cific to the RP document discussed in this article,

    please refer to the full text of the RP document.

    AMBULATORY PATIENT SCENARIOMs P, a 20-year-old female patient, underwent a

    routine excision of a large mass under her left

    arm. The procedure took approximately 40 min-

    utes. The ESU was in use and initial settings

    were cut/coagulate at 30 watts. The dispersive

    electrode was placed on the patients left lateral

    thigh. During the procedure, the surgeon requested

    that the settings be increased because of an inade-

    quate desired effect. The physician repeatedly

    requested that the settings be increased, and the

    last setting recorded was 70 watts. After the pro-

    cedure, the circulating nurse noticed that the dis-

    persive electrode was not in good contact with the

    patients skin but the skin appeared to be intact

    and free of injury.

    During a routine postoperative skin check, the

    postanesthesia care nurse noted a ring in the pa-

    tients navel that had not been removed before

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    surgery and a bright red area of skin injury

    around the ring. Further investigation revealed

    that the preoperative nurse had failed to discover

    the navel ring even though it was documented

    that all jewelry had been removed.

    Preoperative care in the ambulatory setting can

    become a familiar routine, with the readying of pa-

    tients, use of checklists, and use of common equip-

    ment such as the ESU. Often, simple steps and in-

    quiries are overlooked because they are such a part

    of the routine care of patients. In this case, because

    the dispersive electrode did not adhere appropriately

    to the patients skin, the electric current sought an

    alternate pathway through the patient and through

    the metal on her skin, thus causing a burn.

    When a surgeon repeatedly asks for an increase

    in settings, the procedure should be halted while

    the circulating nurse inspects the connections and

    electrodes. If all are intact and the problem con-

    tinues, the unit should be removed from the room

    and tagged for inspection, and a new unit should

    be brought in for use. It is imperative to remem-

    ber that nurses are advocates for patients who are

    unable to speak for themselves.

    HOSPITAL PATIENT SCENARIOMr D, a 74-year-old married man, father of four,

    and grandfather of 11, underwent a digital rectal

    exam during a routine physical and had an elevated

    prostate-specific antigen (PSA) screening and a posi-

    tive needle biopsy that indicated prostate cancer. He

    subsequently underwent a video-assisted laparo-

    scopic prostatectomy with pelvic lymph node dis-

    section. His surgery was completed in less than four

    hours. His estimated blood loss was minimal. Post-

    operatively, he was admitted to the urology unit

    floor to advance to discharge. On postoperative day

    one, Mr D reported pain at one of the single trocar

    incision sites. This incision did not show signs of

    erythematic or purulent drainage. His abdomen was

    distended. He had persistent bowel sounds. He re-

    ported nausea and had vomiting and diarrhea. How-

    ever, he did not experience abdominal pain, his

    white blood count was within normal limits, and he

    did not have a fever. Overall, Mr D had an atypical

    presentation for an intra-abdominal abscess.

    However, Mr D experienced a cardiovascular col-

    lapse from sepsis and died four days after surgery.

    After an autopsy was performed, it was deter-

    mined that during Mr Ds surgery, a laparoscopic

    instrument for which the protective insulated cov-

    ering had worn off was used. This created a ther-

    mal injury to a portion of his bowel that was un-

    detected during the surgery.

    A laparoscopic thermal injury may occur in as

    little as two seconds.28,39,40 A laparoscopic thermal

    injury is the result of tissue death, which can occur

    if a temperature differential of 30 C is reached.40 A

    laparoscopic thermal injury is the result of this tis-

    sue death. Thermal injuries also may occur if the

    insulated covering on an instrument is relatively

    thin. All perioperative personnel, including central

    sterile supply department staff members, surgical

    technologists, surgeons, and nurses, are responsible

    for maintaining the integrity of surgical instruments.

    If an instrument is suspected of having a defect, it

    must be removed from circulation until it can be

    repaired or replaced to prevent injuries.

    CONCLUSION

    Patients in the perioperative setting are in a

    highly technical, high-risk area. As the technology

    evolves, it is imperative that perioperative RNs

    understand not only the components of electrosur-

    gery but also the potential risks to patients and

    personnel. Understanding these risks and imple-

    menting safety practices can significantly reduce

    the chance of injury. Nurses must be diligent

    about patient safety and make sure that safety

    precautions and practices are implemented in ev-

    ery case, for every patient, every time.

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    ing surgery. J Burn Care Res. 2006;27(6):895-900.

    28. Wu MP, Ou CS, Chen SL, Yen EYT, Rowbotham R.

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    gery in laparoscopy. Am J Surg. 2000;179(1):67-73.29. Tucker RD, Voyles CR, Silvis SE. Capacitive coupled

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    30. Wang K, Advincula AP. Current thoughts in electrosur-

    gery.Int J Gynaecol Obstet. 2007;97(3):245-250.

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    Problems Gen Surg. 2002;19(2):5-17.

    32. Guidance section: ensuring monopolar electrosurgical

    safety during laparoscopy. Health Devices. 1995;24(1):

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    33. ECRI. Safety technologies for laparoscopic monopolar

    electrosurgery; devices for managing burn risks. HealthDevices. 2005;34(8):259-272.

    34. Evaluation of electroscope electroshield system.Health

    Devices. 1995;24(1):11-19.

    35. Dennis V. Implementing active electrode monitoring: a

    perioperative call. SSM. 2001;7(2):32-38.

    36. Yazdani A, Krause H. Laparoscopic instrument insula-

    tion failure: the hidden hazard. J Minim Invasive Gyne-

    col. 2007;14(2):228-232.

    37. Perioperative Job Descriptions and Competency Evalua-

    tion Tools [CD-ROM]. Denver, CO: AORN, Inc. In press.

    38. Policy and Procedure Templates, 2nd ed [CD-ROM].

    Denver, CO: AORN, Inc; 2010.

    39. Shirk GJ, Johns A, Redwine DB. Complications of laparo-

    scopic surgery: how to avoid them and how to repair

    them.J Minim Invasive Gynecol. 2006;13(4):352-359.

    40. Saye WB, Miller W, Hertzmann P. Electrosurgery ther-

    mal injury. Myth or misconception? Surg Laparosc

    Endosc. 1991;1(4):223-228.

    Lisa Spruce, DNP, RN, ACNP-BC, ANP-BC,

    ACNS-BC, CNOR, was the corporate clinical

    manager of surgical services, UHS of Delaware,

    Inc, King of Prussia, PA, at the time this article

    was written.Dr Spruce has no declared affiliation

    that could be perceived as posing a potential

    conflict of interest in the publication of this article.

    Melanie L. Braswell,DNP, RN, CNS, CNOR, is

    an advanced practice nurse, Sinai Hospital of

    Baltimore, MD.Dr Braswell has no declared

    affiliation that could be perceived as posing a

    potential conflict of interest in the publication of

    this article.

    March 2012 Vol 95 No 3 SPRUCEBRASWELL

    384 AORN Journal

    http://www.mdsr.ecri.org/summary/detail.aspx?doc_id=8197http://www.mdsr.ecri.org/summary/detail.aspx?doc_id=8197http://www.mdsr.ecri.org/summary/detail.aspx?doc_id=8197http://www.mdsr.ecri.org/summary/detail.aspx?doc_id=8197http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=767284http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=837984http://www.mdsr.ecri.org/summary/detail.aspx?doc_id=8197http://www.mdsr.ecri.org/summary/detail.aspx?doc_id=8197
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    CONTINUING EDUCATION PROGRAM

    2.8

    www.aorn.org/CEImplementing AORN RecommendedPractices for Electrosurgery

    PURPOSE/GOAL

    To educate perioperative nurses about how to implement the AORN Recommended

    practices for electrosurgery in inpatient and ambulatory settings.

    OBJECTIVES

    1. Identify potential risks involved with the use of electrosurgery.

    2. Discuss AORNs practice recommendations for the use and care of electrosurgi-

    cal equipment.

    3. Discuss methods for implementing AORNs practice recommendations for

    electrosurgery.

    The Examination and Learner Evaluation are printed here for your conve-

    nience. To receive continuing education credit, you must complete the Exami-

    nation and Learner Evaluation online at http://www.aorn.org/CE.

    QUESTIONS

    1. The most common form of patient injury during

    the use of electrosurgery is

    a. a burn at the dispersive electrode site.

    b. a positioning injury.

    c. a capacitive-coupling injury.

    d. an injury related to an electrosurgical fire.

    2. In addition to the risk of patient injury, risks in-

    volved with using electrosurgery include

    1. electrical shock.

    2. explosion.

    3. fire.

    4. interference with a patients pacemaker.

    a. 1 and 2 b. 3 and 4

    c. 1, 2, and 3 d. 1, 2, 3, and 4

    3. Activities that can help remind staff members of

    the key steps for electrosurgical safety include

    1. posting an electrosurgery-related patient safety

    poster.

    2. developing standardized patient safety protocols.

    3. using checklists.

    4. working as a team.

    a. 1 and 3 b. 2 and 4

    c. 2, 3, and 4 d. 1, 2, 3, and 4

    4. In considering the purchase of new or refurbished

    electrosurgical units or accessories, perioperative

    nurses should

    1. speak to vendors about safety features.

    2. avoid products with return electrode contact

    quality monitoring.

    EXAMINATION

    AORN, Inc, 2012 March 2012 Vol 95 No 3 AORN Journal 385

    http://www.aorn.org/CEhttp://www.aorn.org/CEhttp://www.aorn.org/CEhttp://www.aorn.org/CEhttp://www.aorn.org/CE
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    3. form an interdisciplinary group to discuss the

    risks and benefits of the equipment.

    4. help ensure equipment is standardized across

    the facility.

    a. 1 and 2 b. 3 and 4

    c. 1, 3, and 4 d. 1, 2, 3, and 4

    5. It is permissible to disengage the activation indi-

    cator on the electrosurgical unit if it is interfering

    with the ability to hear the surgeons directions

    during surgery.

    a. true b. false

    6. In handling the electrosurgical unit (ESU) to min-

    imize the potential for injury, the perioperative

    nurse should

    a. place the ESU near enough to the sterile fieldthat the cord reaches the wall outlet without

    stress.

    b. tape down any kinks or knots in the cord to

    prevent trips and falls.

    c. use an extension cord if the ESU cord is not

    long enough.

    d. hold the cord when removing the ESU from

    the outlet.

    7. To minimize injuries during use of the active

    electrode, the perioperative nurse can1. visually inspect the active electrode at the field

    before it is used.

    2. coordinate with the anesthesia professional to

    minimize the oxygen concentration.

    3. remind the surgeon, technician, or assistant to

    place the active electrode in a conductive

    safety holster when it is not in use.

    4. place the foot pedal between the surgeon and

    assistant so that either may activate the device

    as needed.

    5. moisten sponges that are used near the active

    electrode tip.

    a. 1 and 2 b. 1, 2, and 5

    c. 3, 4, and 5 d. 1, 2, 3, 4, and 5

    8. During the use of monopolar electrosurgery, if

    there is not uniform contact between the patients

    skin and the dispersive electrode, the periopera-

    tive nurse should consider

    1. applying a new pad.

    2. repositioning the used dispersive electrode to

    another site.

    3. removing any oil, lotion, moisture, or prep

    solution that may be interfering with contact.

    4. removing excessive hair that may be interfer-ing with contact.

    5. using tape to hold the dispersive electrode in

    place.

    a. 3 and 5 b. 1, 3, and 4

    c. 1, 2, 3, and 4 d. 1, 2, 3, 4, and 5

    9. Conductive trocar systems and hybrid trocar sys-

    tems are equally safe for use during minimally

    invasive surgery.

    a. true b. false

    10. To reduce the potential adverse effects of surgicalsmoke to personnel and patients, ___________

    should be used as the primary method of

    protection.

    a. local exhaust ventilation

    b. fit-tested surgical N95 filtering facepiece

    respirators

    c. high-filtration masks

    The behavioral objectives and examination for this program were prepared by Kimberly Retzlaff, editor/team lead, with consulta-

    tion from Rebecca Holm, MSN, RN, CNOR, clinical editor, and Susan Bakewell, MS, RN-BC, director, Perioperative Education.

    Ms Retzlaff, Ms Holm, and Ms Bakewell have no declared affiliations that could be perceived as potential conflicts of interest inthe publication of this article.

    March 2012 Vol 95 No 3 CE EXAMINATION

    386 AORN Journal

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    CONTINUING EDUCATION PROGRAM

    2.8

    www.aorn.org/CEImplementing AORN RecommendedPractices for Electrosurgery

    This evaluation is used to determine the extent

    to which this continuing education program

    met your learning needs. Rate the items as

    described below.

    OBJECTIVES

    To what extent were the following objectives of this

    continuing education program achieved?

    1. Identify potential risks involved with the use of

    electrosurgery. Low 1. 2. 3. 4. 5. High

    2. Discuss AORNs practice recommendations for

    the use and care of electrosurgi-

    cal equipment. Low 1. 2. 3. 4. 5. High

    3. Discuss methods for implementing AORNs prac-

    tice recommendations for electrosurgery.

    Low 1. 2. 3. 4. 5. High

    CONTENT

    4. To what extent did this article increase your

    knowledge of the subject matter?

    Low 1. 2. 3. 4. 5. High

    5. To what extent were your individual objectives

    met? Low 1. 2. 3. 4. 5. High

    6. Will you be able to use the information from this

    article in your work setting? 1. Yes 2. No

    7. Will you change your practice as a result of read-

    ing this article? (If yes, answer question #7A. If

    no, answer question #7B.)

    7A. How will you change your practice? (Select all

    that apply)

    1. I will provide education to my team regard-

    ing why change is needed.

    2. I will work with management to change/

    implement a policy and procedure.

    3. I will plan an informational meeting with

    physicians to seek their input and acceptanceof the need for change.

    4. I will implement change and evaluate the

    effect of the change at regular intervals

    until the change is incorporated as best

    practice.

    5. Other:

    7B. If you will not change your practice as a result

    of reading this article, why? (Select all that

    apply)

    1. The content of the article is not relevant to

    my practice.

    2. I do not have enough time to teach others

    about the purpose of the needed change.

    3. I do not have management support to make

    a change.

    4. Other:

    8. Our accrediting body requires that we verify

    the time you needed to complete the 2.8 con-

    tinuing education contact hour (168-minute)

    program:

    This program meets criteria for CNOR and CRNFA recertification, as well as other continuing education requirements.

    AORN is accredited as a provider of continuing nursing education by the American Nurses Credentialing Centers Commission on Accreditation.

    AORN recognizes these activities as continuing education for registered nurses. This recognition does not imply that AORN or the American Nurses Credentialing Center

    approves or endorses products mentioned in the activity.

    AORN is provider-approved by the California Board of Registered Nursing, Provider Number CEP 13019. Check with your state board of nursing for acceptance of this

    activity for relicensure.

    Event:#12507; Session:#0001; Fee: Members $14, Nonmembers $28

    The deadline for this program is March 31, 2015.

    A score of 70% correct on the examination is required for credit. Participants receive feedback on incorrect answers. Eachapplicant who successfully completes this program can immediately print a certificate of completion.

    LEARNER EVALUATION

    http://www.aorn.org/CEhttp://www.aorn.org/CE