Future Forcast
Peering Into the Crystal Ball for 2005’s Biggest IC Issues
By Kelly M. Pyrek
The new year seems to be picking up where 2004 left off, with
the anticipated release of updated guidelines, plus continued work on issues
that persist, such as tackling ventilator-associated pneumonia, fighting
surgical site infections (SSIs) and much more. Here is a look at the most
important issues and concerns that 2005 will bring to the members of the
infection control community.
Mandatory Infection Rate Reporting
One current issue that will heat up in 2005 is the mandatory
public reporting of infection rates (see November 2004 cover story in ICT). In
early February 2005, the Association for Professionals in Infection Control and
Epidemiology (APIC) will convene a consensus conference, “Healthcare-
Associated Infections: Realizing the Benefi ts of Mandatory Public Reporting,”
to discuss the mandatory public reporting of infection data legislation that is
already underway in a handful of states. A number of stakeholders, including
legislative and regulatory offi cials, infection control professionals, hospital
administrators, risk managers, and consumer and public safety advocates, have
been invited to participate in the conference to work toward the development of
a standardized infection surveillance and reporting system that can address the
needs of consumers and healthcare institutions. The conference is sponsored by
APIC in partnership with the American Hospital Association, the Centers for
Disease Control and Prevention (CDC), Consumers Union, National Quality Forum,
and Society for Healthcare Epidemiology of America (SHEA).
“There are two primary reasons for convening this consensus
conference,” says Kathy Warye, executive director of APIC. “First and
foremost, to bring key stakeholders together to share views and approaches with
one another – this is critically important given the complexity and importance
of reporting; second, to determine a path forward that will ultimately improve
outcomes. Since infection control professionals will be central to this
activity, we feel it is important for APIC to provide a forum for the dialog and
decisions that will be made across the nation.”
“Mandatory reporting is a point of panic right now among
infection control practitioners (ICPs), says Wava Truscott, PhD, director of
scientific affairs and clinical education at Kimberly-Clark Health Care. “One
of the most important things ICPs can do is to put forth a business case for
infection reduction, including looking at what an SSI costs and how data can be
trended to show there is a reduction. The amount of data they are going to need
to collect is significant, but it’s their love in life – acquiring data and
putting it into a framework that can easily represent what’s happening with
infection rates.”
While some in the infection control community are calling for
greater political activism from ICPs in 2005, Truscott believes ICPs’ primary
responsibilities are their hospital and their community. “They are at home
with that role, but of course, there will always be people who are comfortable
in larger roles. Whatever their degree of participation, ICPs must have that
conduit of communication so they know what’s going on in their state
legislatures, are empowered to communicate that with their hospital
administration, and can comment if they disagree. Collecting the data, whether
it’s a hand-wrote system or computer based, is of paramount importance. One of
the things the Joint Commission on the Accreditation of Healthcare Organizations
(JCAHO) is really pushing is root cause analysis (RCA) and corrective actions
– showing the action, when it’s due, who’s responsible for it – but they
are also saying, ‘Make sure that you also track that it was effective once it
was in place.’ You can’t do that unless you have an effective data
collector.”
Interim influenza Vaccination Recommendations for 2004–05 influenza
Season
The CDC continues to remind healthcare professionals to
observe the interim flu vaccination recommendations in light of continued vaccination-shortage issues caused by the Chiron manufacturing plant
contamination late last year. These interim recommendations were formally
recommended on Oct. 5, 2004, and take precedence over earlier recommendations.
Additional information is available at http://www.cdc.gov/flu
or through the CDC public response hotline at (888) 246-2675.
CDC Issues 2004-05 Interim Guidance for the Use of Masks to Control influenza Transmission
On Nov. 18, 2004, the CDC issued interim guidance that was
developed in response to questions about the role of masks for controlling human
influenza when suboptimal immunization of the public could increase the
frequency of influenza infection.
The document recommends a combination of infection control
strategies to decrease transmission of influenza in healthcare settings,
including:
- Placing influenza patients in private rooms when possible
- Having healthcare personnel wear masks for close patient contact (i.e.,
within three feet) and gowns and gloves if contact with respiratory secretions
is likely
Use of surgical or procedure masks by infectious patients may help
contain their respiratory secretions and limit exposure to others. Likewise,
when a patient is not wearing a mask, as when in an isolation room, having
healthcare personnel mask for close contact with the patient may prevent nose
and mouth contact with respiratory droplets. However, no studies have definitively shown that mask use by either infectious patients or healthcare
personnel prevents influenza transmission. In the United States, disposable
surgical and procedure masks have been used widely in healthcare settings to
prevent exposure to respiratory infections, but they have not been used commonly in community settings (e.g.,
schools, businesses, public gatherings).
During periods of increased respiratory infection activity in
the community, masks should be offered as part of a respiratory hygiene/cough
etiquette strategy to patients who are coughing or have other symptoms of a
respiratory infection when they present for healthcare services (see the CDC’s
Respiratory Hygiene/Cough Etiquette in Healthcare Settings).
Masks should be worn by these patients until it is determined
that the cause of symptoms is not an infectious agent that requires isolation
precautions to prevent respiratory droplet transmission or the patient has been
appropriately isolated, either by placement in a private room or by placement in
a room with other patients with the same infection (cohorting). Once isolated,
the patient does not need to wear a mask unless transport outside the room is
necessary.
A surgical or procedure mask should be worn by healthcare
personnel who are in close contact (i.e., within three feet) with a patient who
has symptoms of a respiratory infection, particularly if fever is present, as
recommended for standard and droplet precautions. These precautions should be
maintained until the patient has been determined to be noninfectious or for the
duration recommended for the specific infectious agent.
Adults can shed influenza virus one day before symptoms
appear and up to seven days after onset of illness; thus, the selective use of
masks (e.g., in proximity to a known symptomatic person) may not effectively
limit transmission in the community. Instead, emphasis should be placed on cough
etiquette for persons with respiratory symptoms whenever they are in the
presence of another person, including at home and at school, work, and other
public settings. Important components of this strategy include encouraging
symptomatic persons to:
- Cover their nose and mouth when coughing or sneezing
- Use tissues to contain respiratory secretions and, after use, to dispose of them
in the nearest waste receptacle
- Perform hand hygiene (e.g., handwashing with
non-antimicrobial soap and water, alcohol-based hand rub, or antiseptic
handwash) after having contact with respiratory secretions and contaminated
objects/materials
The guidance document can be found at:
http://www.cdc.gov/flu/professionals/infectioncontrol/pdf/flumaskguidance.pdf.
CMS to Allow Alcohol Handrub Dispensers in Hospital Corridors
In November 2004, APIC announced that the Centers for Medicare
and Medicaid Services (CMS) would soon be lifting a regulation prohibiting the
placement of alcohol-based hand sanitizers in exit corridors in hospitals.
“You have requested that CMS take action to ensure that
alcohol-based handrubs can be conveniently accessed in healthcare facilities,”
stated CMS in a letter to APIC. “We agree that alcohol-based handrubs are a
useful and effective infection control tool, and that convenient access to
alcohol-based handrubs is an important factor in encouraging their use.”
The interim final rule was published in the Dec. 23, 2004
Federal Register, and the effective date of the rule is anticipated to be Feb.
23, 2005.
In a Sept. 22, 2004, letter to CMS, APIC had urged the agency
to revoke its policy, in light of recent studies proving that alcohol-based hand
products (formerly considered to be a fi re hazard) could indeed safely be
installed in exit corridors. “As an organization of professionals dedicated to
preventing and controlling healthcare-associated infections, we consider these
wall-mounted dispensers absolutely critical for assuring improved access and
compliance with recommended hand hygiene practices,” the APIC letter stated.
In October 2002, the CDC issued recommendations stating that
alcohol-based handrubs may be a better option than traditional handwashing with
plain soap and water. However, the outdated CMS policy made ensuring optimal
access to these products a particular challenge.
“This is an important step in the right direction and at the
right time when every opportunity to make hand hygiene easier matters,” says
APIC member Judene Bartley, MS, MPH, CIC, who played a key role in the overall
effort to demonstrate the safety of these products and to change federal policy
to ensure their ready access. “We are thrilled that CMS understands the
critical nature of this issue and that the agency is moving forward to change
this policy based on solid data.” She notes that the efforts of many brought
this about, beginning with the AHA- and CDCsponsored stakeholders meeting in
July 2003 that brought clinicians and fi re safety professionals together to
determine how they could effect this important change.
In the meantime, infection control professionals should
continue to contact their local jurisdiction if their facility is cited for
having dispensers in corridors. States vary in their approach, but CMS has been
recommending that if facilities are cited for this defi ciency, they should
request a “temporary waiver” from enforcement action in their plan of
correction.
“There might be some state fi re marshals who still have a
problem with fi re-safety issues, but the easy accessibility of alcohol handrubs
is an important thing to be doing,” Truscott says. “The most important thing
for healthcare workers to remember is to let the handrub dry before they take
off gowns that could snap and spark a static discharge that can ignite a fi re.
The handrub also must dry completely in order for it to kill the bugs.
But then again, there are certain bugs, like Candida
albicans, for example, or Clostridium and anthrax spores, that are
resistant to alcohol and always will be by nature of the organism. Alcohol
handrubs are going to make a positive impact on the reduction of infections, but
it’s going to take continued education on these aspects.”
Anticipated Release of HICPAC Isolation Guidelines
According to Michele Pearson, MD, of the CDC, ICPs likely will
now have to wait until mid-2005 for the issuance of the final “Guidelines for
Isolation Precautions: Preventing Transmission of Infectious Agents in
Healthcare Settings” from the CDC. Last summer, the CDC’s Healthcare
Infection Control Practices Advisory Committee (HICPAC) issued a draft guideline
that updates and expands the “1996 Guideline for Isolation Precautions in
Hospitals.” The period for public comment closed in mid-August 2004.
- The five-part draft guideline addresses several important
developments since 1996:
- The transition from acute-care to other healthcare
settings such as ambulatory care
- The emergence of new pathogens such as
severe acute respiratory syndrome (SARS) and the increased threat of
bioterrorism
- Evidence that environmental controls decrease the risk of lifethreatening fungal infections in the most severely immuno-compromised
individuals
- Evidence that factors such as nurse staf. ng levels and levels
of adherence by healthcare workers (HCWs) to infection control practices, has
led to new emphasis on administration’s support of infection control programs
- Continued increase in the incidence of healthcare-acquired infections (HAIs)
caused by multi-drug-resistant organisms (MDROs)
Earlier, the Society for
Healthcare Epidemiology of America issued its “SHEA Guideline for Preventing Nosocomial Transmission of Multi-drug Resistant Strains of Staphylococcus
aureus and Enterococcus,” which potentially could contradict
portions of the anticipated HICPAC document.
The SHEA recommendations are:
- Active surveillance cultures to identify the
reservoir for spread
- Use of proper hand hygiene
- Use of barrier
precautions for patients known for suspected to be colonized or infected with MRSA or VRE
- Use of good antibiotic stewardship
- Decolonization or
suppression of colonized patients
- Use of educational programs to raise
awareness
For the SHEA guidelines in depth, go to
www.shea-online.org/pdfs/SHEA_MRSA_VRE.pdf. For the draft HICPAC guidelines, go to
http://www.gpoaccess.gov/fr/index.html.
Reprocessing of Single-use Devices
In November 2004, the Food and Drug Administration (FDA)
completed a review of supplemental validation data submitted by firms that
reprocess medical devices originally intended for single use only (SUDs). The
FDA has allowed certain types of previously cleared reprocessed SUDs to be
marketed, however supplemental data for cleaning, sterility and functionality
had to be submitted to the FDA for review to determine if certain reprocessed
SUDs were safe for use. The FDA’s review determined that although many
reprocessed SUDs can continue to be legally marketed, there are a number that
can no longer be commercially distributed for use.
The lists of both legally and not legally marketed devices can
be found at http://www.fda.gov/cdrh/reuse/svs/svslist-legal.html and at
http://www.fda.gov/cdrh/reuse/svs/svslist-nolegal.html.
AIA Revised Healthcare Guidelines Open for Comment Until Jan. 31, 2005
The American Institute of Architects (AIA) and the Facility
Guidelines Institute still are accepting comments from the public on the
proposed 2006 edition of the AIA-published Guidelines for Design and
Construction of Hospital and Health Care Facilities. The Health Guidelines
Revision Committee has spent the last two years considering proposals to change
the guidelines and to clarify and add information to the document.
According to committee chairman Joseph G. Sprague, FAIA, one
of the most significant proposed changes would make single-bed private rooms a
minimum standard for new hospital construction. Healthcare professionals are
encouraged to review the draft document and submit their comments by Jan. 31,
2005. The draft document, which is marked to indicate text that has been added,
deleted or changed from the 2001 edition of the guidelines, is available through
the AIA Web site at http://www.aia.org/aah.
Senate Resolution Supports Goals of National Time Out Day
Louisiana Sen. Mary Landrieu, with Illinois Sen. Richard
Durbin and Pennsylvania Sen. Richard Santorum, has introduced Senate Resolution
469, which supports the goals and ideas of “National Time Out Day” to promote the adoption of the Joint Commission on
Accreditation of Healthcare Organizations (JCAHO)’s universal protocol for
preventing errors in the operating room. The resolution currently has been
referred to the Committee on Health, Education, Labor, and Pensions.
For the first time, nurses, surgeons, and hospitals
throughout the country are being required by JCAHO to adopt a common set of
operating room procedures in order to help curb the alarming number of deaths
and injuries due to medical errors. The universal protocol, endorsed by more
than 50 national healthcare organizations, calls for surgical teams to call a
“time out” before surgeries begin in order to verify the patient’s
identity, the procedure to be performed, and the site of the procedure. JCAHO’s 4,579 accredited hospitals, 1,261 ambulatory care
facilities, and 131 accredited offi ce-based surgery centers were required to
adopt the universal protocol beginning July 1, 2004.
For the language of SR 469, go to
http://www.aorn.org/policy/sr469.htm.
Issues of Continuing Importance in 2005
Truscott is joined by thousands of ICPs who express concern
over issues that will continue to plague them in 2005.
“Ventilator-associated pneumonia (VAP) is a huge issue; it
will take continued education and teaching the things we already know that can
make a big difference. We also need to remain vigilant on bioterrorism-related
issues, continuing our drills and preparation. We should remember that treating
plague is not a lot different than treating another droplet-borne disease; if we
are treating normal diseases the way we should and just connecting the two, we
wouldn’t panic – we would already know what to do. Related to biological
protection, one of the areas in which we are seeing tremendous weakness is eye
protection – I think it is being neglected. Healthcare workers must realize
that if they are wearing a mask to stop droplets, those same droplets can get
into the eye and the mucousal inlet. This year, the CDC and APIC are trying to
emphasize proper removal of used personal protective garments. Experts are
fairly certain that SARS was transferred via touching the exterior of masks and
other personal protective equipment (PPE) and then touching the nose or the eyes
– it’s an action we don’t think about enough.”
Truscott says that another hot topic for 2005 could be the
increased emphasis on supplemental oxygen for reducing infections. “Recently
there was a large colorectal surgery study wherein half the group was given 30
percent supplemental oxygen and the other group was given 80 percent
supplemental oxygen; the difference in infection rate was 50 percent. This could
be a significant finding for the infection control community.”
Truscott adds that the implementation of the fi t testing of
respirators, as mandated by the Occupational Safety and Health Administration
(OSHA) last year, will be an important issue. “Many respirator manufacturers
are working on methods that might be much more user-friendly, faster and easier
to do,” she says.
“For 2005 I’d like to see continued work to decrease the
amount of fl ash sterilization,” Truscott continues. “I have been in some
ORs lately that are getting farther and farther away from the old red line; I
know all about killing the sacred cows, but even so, we are getting lax in the
OR. I have seen long earrings; a stylish use of headwear about
three inches back behind the hairline; doors propped open while ORs were being
prepped; I have seen eggcrate foam rubber on surgery tables with merely a sheet
over it, and it is only changed out when it looks dirty … these things scare
me.” Truscott says she has witnessed these infractions in large teaching
facilities, and quips, “They are also teaching people to do things the wrong
way!”
Truscott also believes 2005 will see even more of a shift from
latex gloves to synthetic gloves. “This will be driven by not only the expense
of latex, but so that people don’t have to worry about latex allergies,” she says. “There is a constant argument about what type of
synthetics to use, as far as barrier properties go; I am anti-vinyl for the
wrong places; vinyl always has a place in maybe 30 percent of the hospital,
but just not in the other 70 percent. And then there is the argument about
powder. All of the emphasis on the reduction of powder has been
focused around decreasing latex allergy, and the inhalation route; well, it
absorbs protein, but it also absorbs endotoxins, chemicals, and organisms. There
are several studies that show if you use powder gloves, whether they are exam or
surgical, there are more bugs in the air that can get into your patient. I think
that issue will be a push, especially in the OR; we’re doing so much better on
exam gloves, but in the OR, it’s about 55 percent powder. If you bring one
powder glove into the OR, you might as well discount the rest of the powder-free
gloves because you are contaminating the area.
The injurious effects of micro foreign bodies and debris – a
combination of powder, lint, not cleaning up after suture trims, and hair that
is falling into the wound, are documented. There also are particles that are not
cleaned properly in CS or SPD that are sterile but nonetheless they are
foreign-body particles that are introduced into the wound, thus affecting
granulomas, adhesions, wound healing, and infection rates.”
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