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Education & Training

Clipping, Prepping and Draping


for Surgical Procedures
by Ellen Anderson Manz, RN, BSN; Debbie Gardner, LPN, OPAC; and Maret
Millard, NREMT-B

84 MANAGING INFECTION CONTROL August 2006


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Objectives Introduction
After completion of this self-study activity, the learner Because of the number of factors that can contribute
will be able to: to surgical site infections (SSI), experts generally talk in
1. D i fferentiate the clinical benefits of hair removal by terms of reducing the risk rather than the rate of SSI. It is well
means of clipping versus shaving. recognized that the major microorganisms responsible for
2. Identify the properties of effective surgical skin prepara- SSIs reside on the patient’s skin, making preoperative skin
tion agents. preparation and creation of a sterile field/surface a logical
3. Describe the principles of draping as they relate to approach to risk reduction.
prevention of infection. The early 19th century surgeon “operated in a Prince
Albert coat and used the same sponges for every patient he
Test Questions treated.” It wasn’t until mid-19th century that the idea of
True or False protecting the surgical wound from contamination became a
1. Nowhere in the CDC Guideline for Prevention of Surgical subject of great interest and concern in the operating room.1
Site Infection Recommendations does it state that one Prior to this time, all emphasis was on cleaning of the room
antiseptic agent is preferred over other antiseptics. and the instruments used.
2. If hair at or around the incision site needs to be removed, As members of the healthcare team, surgeons, nurses
the method that best preserves the patient’s skin integrity and other healthcare professionals are entrusted with
is a clippers. the safety and welfare of those who undergo surgical
3. Aseptic technique and sterile technique are synonymous intervention. As a patient advocate, the perioperative nurse
terms. has, as one of his or her most important functions, the
4. Alcohol, Iodophors and CHG are the most common responsibility for monitoring and maintaining best practices
antimicrobials used for patient skin preps. during the perioperative period.
5. Most commonly used patient skin preps meet the FDA A surgical conscience (that concept which allows for no
criteria for immediate kill and persistent activity. compromise in the principles of aseptic technique) builds on
6. Fluid strike-through associated with drape materials is the principles of asepsis and is an act of mental discipline.
always visible to the surgical team. It involves inspection and regulation of one’s own practice,
7. The longer the time between hair removal and the operation, with particular attention to deviations from acceptable, safe
the lower the infection rates. practices, especially during the intraoperative phase of the
8. An ideal preoperative skin prep agent should be broad surgical experience. 2
spectrum, safe, fast-acting and persistent. As the surgical conscience is fully developed, the
9. Prior to the draping process, it is critical to plan ahead perioperative nurse is always asking himself or herself:
and anticipate what drapes will be used for the procedure. 1. Is this the best practice?
10. Preoperative skin preparation sterilizes the patient’s skin. 2. Do I have everything necessary for this procedure?
3. Have I done all I can do to provide a safe, therapeutic
environment for my patient?

Every attempt must be made toward preventing the invasion


Many thanks to the team at 3M Health Care of microorganisms into the surgical wound. Two methods are
for working with Managing Infection Control utilized that, if practiced with precision, can prevent serious
to provide the following accredited course. This complications to the already compromised surgical patient:
inservice is 3M Health Care Provider approved  Aseptic Technique—The methods by which microbial
by the California Board of Registered Nurses, contamination is prevented in the environment.3
CEP 5770 for one (1) contact hour. This form  Sterile Technique—Refers to creating and working
is valid up to five (5) years from the date of within the sterile field. To protect the patient during
publication. Instructions for submitting results invasive procedures, microorganisms in the sterile field
are on page 97. are kept to an irreducible minimum.3
Managing Infection Control and 3M Health
Care will be working collaboratively to provide By using the best theoretical knowledge available today
continuing education courses in monthly editions to prepare the patient, and create and maintain the sterile field,
of Managing Infection Control. perioperative nurses play a vital and significant role in
protecting the patient from infection.

August 2006 MANAGING INFECTION CONTROL 85


Education & Training

Hair Removal
Disruption of the skin surface
compromises the line of defense by

SURGICAL SITE creating an entry for microorganisms.


As part of your patient preoperative

INFECTIONS (SSI)
skin-prepping regimen, hair removal
may be necessary. Shaving the
surgical site began in the late 1800s
and until recently has been accepted.
are the second most common We now have clear and convincing

healthcare associated infection


research that shows shaving can create
nicks and microscopic epidermal cuts

(HAI) among hospitalized patients. that permit bacterial contamination.


Use of a clipper rather than razors
has been shown to decrease infection
rates. Studies such as those conducted
Skin is the patient’s first line of defense against infection. Because the skin cannot by Jepsen et al5, Alexander et al6, and
be sterilized, it must be properly prepared in order to reduce the microbial count to the Sellick et al 7 present comparative
lowest possible, thereby reducing the risk of infection. According to the Centers for data on infection rates in surgical
Disease Control and Prevention (CDC) Guideline for Prevention of Surgical Site patients whose incision sites were
Infections (SSI), for most SSIs, the source of pathogens is the endogenous flora of the clipped rather than shaved. In all
patient’s skin, mucous membranes or hollow viscera. When mucous membranes or articles the authors concluded that
skin are incised, the exposed tissues are at risk for contamination with endogenous hair removal using an electrical
flora.4 Two methods are used to prepare the surgical site prior to draping: clipper appeared to decrease the
1. Hair removal (only when it compromises the incisional area); infection rates postoperatively (see
2. The surgical skin prep during the intraoperative phase. Figure 1 on page 86).

Recommended Practices
Figure 1. Infection Rates: Clipping vs. Shaving and Guidelines
The research results have been so
overwhelmingly in favor of clipping
that several healthcare organizations
recommend a procedural change from
shaving to clipping. The Association
of periOperative Registered Nurses
(AORN) Recommended Practices for
Skin Preparation of Patients states,
“When hair removal is necessary, an
electric or battery powered clipper
with a disposable or reusable head
that can be disinfected between
patients should be used, if possible.8”
The CDC states, “If hair is removed,
remove immediately before the
operation, preferably with electric
clippers.4” The CDC has rated this
category IA, meaning it is supported by
well-designed experimental, clinical
or epidemiological studies. In the
July 2000 Bulletin of the American
College of Surgeons (ACS), the

86 MANAGING INFECTION CONTROL August 2006


Education & Training

CDC Guideline was summarized and endorsed. The Association 1982 recommended clipping the hair, leaving 1 to 2 mm on
of Practitioners in Infection Control (APIC) also recommends the skin. It was noted, “When properly used this way, the
clipping, stating, “A depilatory or clipping in preference electrical clippers do not damage or abrade the skin.” 11
to shaving for hair removal is an intervention that reduces As long as clippers are used according to the manufacturer’s
microbial contamination of the wound and lowers the directions, stubble length will be 1 to 2 mm in length, which
infection risk.”9 is desirable. If your staff is concerned about stubble length,
Hair should only be removed when it interferes with the make sure the correct angle of clipping is performed when
incision site. But if hair is to be removed, it should take place using clippers.
immediately prior to surgery, in a preoperative environment
and with an electrical clipper in order to minimize the risk of Patient Skin Preparation
infection.4,8 Concerns about stubble length have existed since After the patient has been anesthetized and positioned
clippers first entered the hair removal market in 1986. Studies on the operating table, the incision site, as well as an extensive
show that remaining stubble demonstrates preserved skin area surrounding it, must be disinfected using a topical
integrity. Razors cause microscopic cuts and nicks, some of antimicrobial agent immediately prior to draping.
which are not visible to the naked eye. “In fact, the stubble
should be reassuring,” commented William C. Beck, MD, Recommended Practices and Guidelines
FACS, in a 1986 editorial in Su rg e ry, Gynecology & The 1999 CDC Guideline for Prevention of Surgical Site
Obstetrics. “It gives assurance that the superficial skin Infection states: “Use an appropriate antiseptic agent for skin
squames have not been disturbed.” 10 Comments made preparation.” Nowhere in the recommendations does it state
by panelists at an AORN question-and-answer session in that one antiseptic agent is preferred over other antiseptics. The

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Education & Training

recommendations continue to state that the skin prep should be FDA testing for patient skin preparation measures
applied in concentric circles moving toward the periphery, and the effectiveness and persistence of a product against normal
that the prep area should be large enough to extend the incision, skin flora. Two prep sites are tested: the abdomen, which is
or create new incisions or drain sites.4 The AORN Recommended considered a dry site, and the groin, which is considered a
Practices for Skin Preparation of Patients state:8 moist site and will thus have more resident flora. The skin sites
1. Remove soil and transient organisms: are prepped following manufacturer’s directions for use,
a. Patient showers; allowed to dry, and then covered with a sterile gauze and tape
b. Special cleansing of the surgical site; dressing. The scrub cup test is followed to sample the sites
c. Washing the site immediately before prepping. at 10 minutes and six hours post-prep. The FDA pass criteria
2. Reduce resident microbial counts to subpathogenic amounts: for a patient prep at the 10-minute time point is a two-log
Use antimicrobial preoperative skin prep. reduction on the abdomen and a three-log reduction on the
3. Inhibit rapid rebound growth of microorganisms: groin, with both sites maintaining counts below baseline out to
Use persistent antimicrobial preoperative skin prep agent. six hours post-prep.12
Table 1 on page 90 shows a comparison of the most
Food and Drug Administration (FDA) common types of patient skin preparations and their ability to
The Food and Drug Administration (FDA) regulates meet the FDA criteria. As you can see, both the aqueous-based
antimicrobial products used in the healthcare setting, including preps as well as the alcohol-based preps meet the FDA criteria,
patient preoperative skin preps. It regulates active ingredients although application time and method will vary by product.
allowed in the formulation of these products, the labeling of Because the most commonly used patient skin preps meet
products, and the claims that manufacturers can make. the FDA criteria for immediate kill and persistent activity, and

88 MANAGING INFECTION CONTROL August 2006


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Table 1. Preoperative Skin Preparations Meeting FDA Criteria13,14,15,16,17

Meets FDA Meets FDA


Criteria Abdomen Criteria Groin

10 min 6 hour 10 min 6 hour

Aqueous Iodophor scrub and paint Yes Yes Yes Yes


(i.e., Cardinal® Scrub Care® brand)

Aqueous CHG skin prep Yes Yes Yes Yes


(i.e., Hibiclens® brand)

Aqueous Iodophor one-step prep Yes Yes Yes Yes


with polymer (i.e., One-Step Prep by 3M™)

Alcohol-Iodophor with water-insoluble polymer Yes Yes Yes Yes


(i.e., DuraPrep™ brand)

Alcohol-CHG skin prep Yes Yes Yes Yes


(i.e., ChloraPrep® brand)

90 MANAGING INFECTION CONTROL August 2006


Education & Training

because most patients only get prepped once so that cumulative that blood and saline irrigation can significantly reduce
activity is not a factor, let’s consider what other factors are the microbial effectiveness of some surgical patient preps.
important in surgery. When iodophor-based preps have a polymer that keeps
them from being removed by blood and saline, they
 Drape adhesion: Incise drapes are commonly used in remain bactericidal. 13,14
surgery, particularly for high-risk procedures like open
heart surg e r y, joint replacement and other implant  Application Instructions: The efficacy of an antimicrobial
s u rgeries, neurosurg e r y, and trauma. Because preps do product is based on its proper application. Failure to follow
not sterilize but only disinfect the skin, incise drapes manufacturers’ directions for use could significantly
provide a sterile surface at the start of surgery. When the impact the product’s ability to kill microorganisms. It is
drape lifts at the wound edge, the exposed skin allows for well documented that bacteria from the skin are the
the potential of bacteria being transferred into the wound. leading causes of surgical site infections.
In one study, drape lift was associated with a six-fold
increase in surgical site infections.18 Even among one-step preps, there is a wide range of
instructions for use, and some preps actually have diff e r e n t
 Blood and Saline Challenge: Another critical factor to instructions depending on whether the area is considered
consider for a surgical patient prep is the challenge by to be a dry site, like the abdomen, or a moist site, like the
blood and saline during the surgical procedure. In the groin or axilla. Compliance to protocol is much easier to
FDA-required testing, once the prep is dry, it remains dry attain when direction are the same, regardless of the area
and covered without any fluid challenges. Studies show being prepped.

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Education & Training

 Product Warnings: Product warnings are part of the In order to provide the best protection for each procedure, the
FDA-required labeling and are present to protect the perioperative nurse needs to think through the basic principles
patient from misuse of the product. Healthcare facilities of draping.
that choose to disregard specific warnings may increase
their facility’s liability. Principles of Draping
1. Isolate
Product warnings will vary significantly between patient Dirty from clean (e.g., groin, colostomy and equipment
skin preps based on the active ingredients. It is important that from the area to be prepped). Isolation is accomplished by
the end user carefully reads all directions for use, warnings and using an impervious drape, usually fabricated from a
all other label information before using any product to provide plastic material. Any impervious material can be used.
safe and effective patient prepping.
The challenges that face surgical preps are very different 2. Barrier
from those for surgical hand antisepsis and even intravascular Provides an impervious layer; must have a plastic film to
catheter site preps. Choosing the right antimicrobial for the prevent strike-through.
right indication is critical in helping reduce the risk of surgical
site infection for your patients. 3. Sterile Field
Creation of a sterile field is through sterile presentation of
Draping the drape and aseptic application technique. If the drape
Part of the role of the perioperative nurse is to “pull” the used is not impervious, an additional impervious layer
correct drapes as well as instruments prior to each procedure. needs to be added.

92 MANAGING INFECTION CONTROL August 2006


Education & Training

4. Sterile Surface
Because skin cannot be sterilized, it is necessary to apply an incise drape to
create a sterile surface. Only an incise drape can create a sterile surface.

5. Equipment Cover
Sterile drapes cover nonsterile equipment or organize equipment used on
the sterile field. This helps to protect the patient from the equipment as well
as to protect and prolong the life of the equipment.

6. Fluid Control
Collection of fluid keeps the patient dry, decreases healthcare worker
exposure and decreases clean up. A fluid control system should be used
any time the procedure is known to include large amounts of body fluids
or irrigating solution.

Everyone has his or her opinion with regard to what constitutes an acceptable
drape material. It is important to recognize there is no one material that meets all
the needs of the clinician. Rather, each material has characteristics that make it
either more or less suited for draping specific surgical procedures. In other
words, a material characteristic that makes a material an excellent choice for an
ophthalmic drape might make it a poor choice for an orthopedic drape.

Surgical Drape Characteristics


Regardless of which materials are used, all surgical drape materials should
possess the following traits:
 Abrasion resistance—The material surface should not abrade during normal
use, under wet and dry conditions.
 Barrier properties—The ability of a material to resist the penetration of
liquids and/or micro organisms.
 Biocompatibility—A material free of toxic ingredients.
 D r a p e a b i l i t y—The ability of a material to conform to the shape of the
object over which it is placed.
 Electrostatic properties—In the context of a surgical drape, the ability of
the material to accept or dissipate an electrical charge is desirable.
 Nonflammability—The materials should not support open combustion.
 Nonlinting—Drape materials should not contain, or generate with normal
use, free fiber particles.
 Tensile strength—Drape materials should be strong enough to withstand the
stresses encountered during typical use when wet or dry.

In addition to the required traits referenced above, some applications call


for the drape materials to be:
 Breathable—Capable of allowing gas and moisture vapor to pass through
the material while maintaining a barrier to fluids and microorganisms.
 Absorbent—The ability to absorb and hold fluid while maintaining a barrier
to penetration of fluid and microorganism through the drape.

OR staff separate draping materials into two general categories:


1. Reusable or multiple use products, which are usually constructed of textiles.
2. Disposable or single use products, which are usually constructed of
nonwoven materials.

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Education & Training

STRIKE THROUGH is a serious problem and


the reason surgeons and nurses believe multiple layers
of drapes are necessary.

Sterile surgical drapes protect the patient from infection by preventing materials is the introduction of free fiber
m i c r o o rganisms from making their way into the skin opening created particles (lint) into the operating room
during surg e r y. Surgical drapes are effective because microorg a n i s m s environment. Once airborne, lint can settle on
cannot move by themselves and rely on dust, fluids or contact to move contaminated surfaces and then become
them. If a drape material allows fluid to penetrate, it creates a pathway airborne again, settling on the sterile field
and a mode of transportation for organisms to invade the sterile field. and in the surgical incision, contaminating
The penetration of a drape, gown or mask by fluids is known as “strike other material or tissue on which it settles.
through.” Strike through is a serious problem and the reason surgeons and Lint also clogs OR ventilation filters,
nurses believe multiple layers of drapes are necessary. decreasing their eff e c t i v e n e s s .
The second common material failure that can lead to infection Standards only apply to these materials
is failure of the adhesive interface. Everything under the sterile surgical when they are converted into drapes, gowns
drape is a source of contamination. If the drape gapes or moves, or masks intended for sale. The FDA then
contamination can be introduced into the sterile field and an infection regulates these products as Class 1 sterile
arise. Another source of potential infection associated with drape medical devices, per Rule 1 for noninvasive
devices, meeting all standards for basic safety
and eff i c a c y. Every surgical drape on the
market has met these basic standards to gain
approval for sale. Drape manufacturers also
receive guidance from industrial associations
such as the Association of the Nonwoven
Fabric Industry (INDA) and the Association
for the Advancement of Medical Instrumentation
(AAMI). These organizations are comprised
of representatives from interested companies
such as 3M, Kimberly Clark, Johnson &
Johnson, and others. The purpose of these
industrial associations is to create standardized
terms and test methods that will protect
the interests of the industry at large and
member companies specifically. Standards
and test methods developed under these
o rganizations are voluntary and enforced by
the member manufacturers.

AORN Recommended Practices


The most followed recommendations
are the AORN Recommended Practices for
Selection and Use of Gowns and Drapes. These
recommended practices state that surg i c a l
drapes should:19

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 Provide appropriate barriers to microorganisms, particulate matter


and fluids;
 Be appropriate to methods of sterilization;
 Maintain adequate integrity and durability;
 Withstand physical conditions;
 Resist tears, punctures, fiber strains and abrasions;
 Be free of toxic ingredients;
 Be low linting;
 Have positive cost:benefit ratios;
 Have an acceptable quality level;
 Be used and processed according to manufacturers’ written instructions.

Contamination of equipment and personnel is prevented by the


placement of a bacterial barrier or sterile drape over an item located within
the boundary of the sterile field. During surgery, the patient, once covered
with the sterile drape, becomes the center of the sterile field. Should the
drapes become permeated or moist, they must be considered contaminated.
Corrective action must be initiated to cover the area in question, or the
drapes must be changed.

Summary
When preparing for each procedure, always walk through each step to
assure the best practice for that procedure. Surgical site infections (SSI)
are the second most common healthcare associated infection (HAI) among
hospitalized patients. These infections number approximately 500,000 per
year, among an estimated 27 million surgical procedures, and account for
approximately one quarter of the estimated two million HAIs in the United
States each year.20 Infections result in longer hospitalizations and higher
costs. It is everyone’s duty to always know your procedure in order to reduce
the risk to yourself as well as to your patient. By knowing your procedure
and developing your surgical conscience, you decrease the risk to your
patients. (See Table 2 on page 96.) ✛

References
1. Manley YB. Surgical scrubbing, then and now. JORRI. 1980:1(1):28-31.
2. Fairchild SS. Perioperative Nursing Principles and Practice. 2nd ed. Boston, Mass:
Little, Brown, and Company. 1996.
3. Phillips N. Berry & Kohn’s Operating Room Technique. 10th ed. St. Louis, Mo:
Mosby. 2004:247.
4. CDC .Guideline for Prevention of Surgical Site Infection. 1999. Available at:
http://www.cdc.gov/ncidod/dhqp/gl_surgicalsite.html.
5. Jepsen OB, Bruttomesso KA. The effectiveness of preoperative skin preparations: an
integrative review of the literature. AORN J. 1993:58:477-484.
6. Alexander JW, Fischer JE, Boyajian M, Palmquist J, Morris MJ. The influence of
hair-removal methods on wound infections. Arch Surg. 1983:118:347-352.
7. Sellick JA, Stelmach M, Mylotte JM. Surveillance of surgical wound infections
following open-heart surgery. Infect Control Hosp Epidemiol. 1991:12(10):591-596.
8. AORN. Recommended practices for skin preparation of patients. Standards,
Recommended Practices, and Guidelines. Denver, Colo: AORN, Inc. 2005:443-446.
9. S u rgical site infections. APIC Infection Control and Applied Epidemiology
Principles and Practice. St. Louis, Mo: Mosby Year Book; 1996:11-1.
10. Sacred Cows: Hair Clipping Superior to Preoperative Shave. OR Manager.
1990:6(2):2.
11. The Experts Research Q:A. AORN J. 1982:35(6):3.
12. Food and Drug Administration. Topical antimicrobial drug products for over-the-
counter human use: tentative final monograph for healthcare antiseptic drug
products- proposed rule. Federal Register. 1994:59:31441-31452.

August 2006 MANAGING INFECTION CONTROL MANAGING INFECTION CONTROL 95


Education & Training

Table 2. Glossary

Antiseptic Any substance that inhibits the growth of bacteria; they may be physical
or chemical.

Aseptic Technique The methods by which microbial contamination is prevented in


the environment.

Barrier Material used to reduce or inhibit the migration or transmission of


microorganisms in the environment.

The presence of pathogenic microorganisms, organic debris and dirt;


Contamination generally refers to a specific object, substance, or tissue that contains
microorganisms, especially disease-producing microorganisms.

Depilatory Topical chemical agent used to remove hair from the patient’s skin.

Healthcare Associated Infection An infection that originates during the patient’s hospitalization.

Infection The invasion and multiplication of microorganisms in body tissues that


cause cellular injury and clinical symptoms.

An organism that is too small to be seen with the naked eye and
Microorganism requires a microscope. Bacteria, viruses, fungi and protozoa are generally
called microorganisms.

Antiseptic product category of the FDA’s Tentative Final Preparation


Preoperative Skin Preparation Agent Monograph for Antiseptic Drug Products used to describe an agent used
for the preparation of the skin prior to surgery or an injection that helps
reduce bacteria that potentially can cause skin infection.

Microorganisms persistently isolated from most people’s skin. These


Resident Microorganisms microorganisms are considered to be permanent residents of the skin and
are not readily removed by mechanical friction.

Skin Preparation The process of chemical and mechanical cleansing of the skin.

The area around the site of incision into tissue or introduction of an


Sterile Field instrument into a body orifice that has been prepared for the use of sterile
supplies and equipment. This area includes all furniture covered with
sterile drapes and all personnel who are properly attired.

Refers to creating and working within the sterile field. To protect the
Sterile Technique patient during invasive procedures, microorganisms in the sterile field are
kept to an irreducible minimum.

Surgical Site Infections Infections that occur 30 days after an operation; classified as superficial
incisional, deep incisional, or organ/space.

Transient Microorganisms Microorganisms isolated from the skin, but not demonstrated to be
consistently present in the majority of people. They are considered
transient because they can be readily transmitted on hands unless removed
by mechanical friction, and soap and water washing.

96 MANAGING INFECTION CONTROL August 2006


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13. 3M™ DuraPrep Surgical Solution Safety


and Efficacy Data; Evaluating Antimicrobial
Effectiveness of DuraPrep™ Surgical Solution Nursing CEU Application Form
Against Resident Human Skin Flora on Abdomen This inservice is 3M Health Care Provider approved by the
and Groin Sites. [St. Paul, Minnesota]: [3M California Board of Registered Nurses, CEP 5770 for (1) contact
Medical Division]. 2006:19.
14. 3M™ One-Step Patient Prep Safety and Efficacy hour. This form is valid up to five years from the date of publication.
Data. [St. Paul, Minnesota]: [3M Medical 1. Make a photocopy of this form.
Division].2006:4-5. 2. Print your name, address and daytime phone number and
15. ChloraPrep® Clinical Compendium. [Leawood,
position/title.
Kansas]: [Medi-Flex®, Inc]. 2005:25.
16. Dyna-hex® Chlorhexidine Gluconate [Technical 3. Add your social security number or your nursing license number.
Information Packet]. [Chicago, IL], Xttrium 4. Date the application and sign.
Laboratories Inc. 1986. 5. Answer the CE questions.
17. S c rub Care ® Povidone Iodine Antimicrobial
Solutions, In Vivo Efficacy Study. [McGaw Park, 6. Submit this form and the answer sheet to:
Illinois]: [Cardinal Health]. 2004:8. Workhorse Publishing
18. Alexander JW, Aerni S, Plettner JP. Development Managing Infection Control
of a safe and effective one-minute preoperative
PO Box 25310, Scottsdale, AZ 85255-9998
skin preparation. Arch Surg. 1985;120:1357-
1361. 7. Participants who score at least 70% will receive a certificate of
19. AORN. Recommended practices for selection completion within 30 days of Managing Infection Control’s
and use of gowns and drapes. S t a n d a rd s , receipt of the application.
Recommended Practices, and Guidelines.
Denver, Colo: AORN, Inc. 2005:371-376.
20. Graves EJ, Gillum BS. Detailed diagnoses and
procedures, National Hospital Discharge Survey, Application
1994. Vital Health Stat 13. 1997;(127):1-145.
Please print or type.
Name: _______ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __ _ _ _ _ _ _ ____________ _ ___
Ellen Anderson Manz is currently the 3M
Technical Service Specialist for topical
antimicrobial products in St. Paul, Minn. She Mailing Address: ____________________ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __
lectures extensively on antimicrobials, hand
hygiene and patient prepping. Ellen has 13 City, State, Country, Zip: ________________________________
years experience in the operating room. She
was the OR Clinical Educator for the
HealthEast Health Care System in St. Paul. Daytime phone: ( )___________________ _ _ _ _ _ __ _ _ __
She is a member of AORN and AORN
Assembly, Industry and Consulting. Position/Title: _________________ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __
Deborah Gardner, LPN, OPAC, CIC, is
a technical service specialist for 3M Health
Care, St. Paul, Minn. She has more than 30 Social Security or Nursing License Number :
years experience in the medical field, including
operating room nursing and clinical assessment. _________________________________________ _ _ _ _ _ _ _ _ _ _ _
She has written several publications dealing
with infection prevention and has spoken to
local AORN groups. Date application submitted: _________________________ _ _ _ _ _
Maret Millard is currently the 3M
Technical Service Specialist for surgical
Signature: ____________________________________________
clippers, masks and respirators in St. Paul,
Minn. Maret also works in the emerg e n c y Offer expires August 2011
room of Regions Hospital, a level I trauma
center, as an Emergency Medical Technician;
and is a member of the National Association
ANSWERS
of Emergency Medical Technicians (NAEMT).
Maret is a speaker and instructor for the 1. T 2. T 3. F 4. T 5. T
Infection Prevention Interactive Education 6. F 7. F 8. T 9. T 10. F
CD Rom program.
70-2009-7475-9 Reprint with permission from Workhorse Publishing L.L.C.
Copyright©2006/Workhorse Publishing L.L.C./All Rights Reseved.

August 2006 MANAGING INFECTION CONTROL 97

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