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Arizona Surgical Infection
Prevention (SIP) Collaborative
Summary
Problem Statement
Mission
Performance Measures
Goals
Methods
Expectations
References
Summary
The purpose of the Arizona Surgical Infection Prevention (SIP) Collaborative
is to improve the quality of care delivered to patients during surgery
in a cost-effective manner through system redesign using proven,
evidence-based practices. The goals, as reflected in process measures,
are that 100 percent of eligible patient populations receive appropriate
and timely prophylactic antibiotics. Hospitals are also strongly
encouraged to select additional prevention-related interventions
related to normothermia, glucose control, oxygenation, hair removal,
and other infection-prevention procedures to improve redesign of
their systems of care.
Problem Statement
Americans rely on their health care system for the maintenance and
improvement of health, which often involves care in the hospital
setting. Although most patients believe that the American health
care system provides the highest quality and safest care in the
world, it is estimated that four out of every one hundred hospitalized
patients in the United States suffer a serious adverse event, many
of which are avoidable. In the Institute of Medicine report, To
Err is Human, it is estimated that between 44,000 and 98,000
deaths per year result from adverse events.(1)
In comparison, there are approximately 45,000 deaths yearly from
auto accidents.
Sixty-nine percent of adverse events and deaths
in health care are due to an error in management and, thus, are
potentially preventable. Dr. Lucian Leape and colleagues have described
these types of errors, which include diagnostic failures, treatment
errors, errors in prevention, and others including communication
failure and equipment failure. (2)
Some of these errors lead to perioperative infections––a major cause
of patient injury, mortality, and health care cost. An estimated
2.6 percent of nearly 30 million operations are complicated by surgical
site infections (SSIs) each year.
Established in 1970, the Centers for Disease
Control and Prevention’s (CDC’s) National Nosocomial Infections
Surveillance (NNIS) system monitors reported trends in nosocomial
infections in U.S. acute-care hospitals. According to the NNIS system
reports, SSIs are the third most frequently reported nosocomial
infection, accounting for 14 percent to 16 percent of all nosocomial
infections among hospitalized patients.
(3) Surgical site infections are a common complication of
care, occurring in 2 percent to 5 percent of patients after clean
extra-abdominal operations (e.g., thoracic and orthopedic operations)
and in up to 20 percent of patients undergoing intra-abdominal procedures.(4–9)
Among surgical patients, SSIs were the most common nosocomial
infection, accounting for 38 percent of all such infections. When
surgical patients with nosocomial SSI died, 77 percent of the deaths
were reported as related to the infection, and the majority (93
percent) were serious infections involving organs or spaces accessed
during the operation.
(10) Cruse estimated that an SSI increased a patient’s hospital
stay by approximately ten days and cost an additional $2,000 in
1980. (11,12)
There are more recent studies, including a 1992 analysis by Martone,
which corroborate an increase in length of stay and cost (7.3 additional
postoperative hospital days and $3,152 in extra charges) in patients
with SSIs.(13–15)
If a hospital with an annual surgical volume of 10,000 operations
could reduce their 300 SSIs by half, this would result in an average
annual cost savings of approximately $450,000, based on 1992 cost
estimates. Deep SSIs involving organs or spaces are associated with
even greater increases in hospital stays and costs.
(16,17)
An estimated 40 percent to 60 percent of SSIs
are preventable with appropriate use of prophylactic antibiotics.10,18–20
Overuse, underuse, improper timing, and misuse of antibiotics occurs
in 25 percent to 50 percent of operations.21–24
A large number of hospitalized patients develop infections caused
by Clostridium difficile, and 16 percent of this type of
infection in surgical patients can be attributed to inappropriate
prophylaxis use alone.25
Inappropriate use of broad spectrum antibiotics, or prolonged courses
of prophylactic antibiotics, puts all patients at even greater health
risks due to the development of antibiotic-resistant pathogens.
In addition to the proper use of prophylactic
antibiotics and good surgical technique, other factors under the
control of the operative team have been demonstrated to significantly
affect the risk of SSI.
(10) These other factors include preventing hypothermia during
the procedure,
(26) maintaining high levels of inspired oxygen,
(27) controlling serum glucose within certain limits,
(28–30) and avoiding shaving the operative site.
(31–35) All of these preventive measures provide opportunities
for improvement in most hospitals.
Although the primary focus of the Collaborative
work is SSIs, infections in patients undergoing surgery are not
limited to those that involve the surgical site. Other types of
infections occurring in patients undergoing surgery include, but
are not limited to, infections of centrally inserted venous access
lines for perioperative monitoring, urinary tract infections, and
pneumonia.
Effective surgical infection prevention and harm
reduction therefore require redesigning systems with safety in mind.
(36) The fundamental law of improvement is this: every system
is perfectly designed to achieve exactly the results it gets. In
order to attain a new level of performance in safety, there must
be a new system. This applies to all forms of performance—such as
selection, timing, and duration of antimicrobial prophylaxis; thermoregulation;
oxygen tension; glucose control; hair removal; and other basic prevention
strategies. Some health care organizations have succeeded in creating
new and safer systems for SSIs.
(37) Major opportunities exist to reduce the incidence of
surgical infections, create safer care for patients requiring surgery,
create a more satisfactory work environment for health care workers,
reduce costs, and improve efficiency.
Reducing surgical infections while minimizing
antibiotic resistance remains a challenge to many health care institutions.
Health care providers are faced with the additional challenge of
trying to integrate new evidence-based infection prevention strategies,
such as perioperative glycemic control, into practice. Enlightened
management teams, regulatory agencies, health plan providers and
purchasers, and medical associations need to provide the support
required to create a culture of patient safety in our health care
systems. With this support, informed, activated hospital teams can
be empowered to make key changes to their subsystems (e.g., surgical
units). Hospital teams need to incorporate safety considerations
into their everyday work.
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Mission
The mission during this Collaborative is to achieve a breakthrough
improvement in surgical infection prevention. The primary emphasis
of this Collaborative is to create systems of care that dramatically
improve the prevention of surgical infections. The Collaborative
will take a preventive approach, which includes, but is not limited
to, preventing SSIs. Hospitals will prevent infections by implementing
a system-wide model of care, which focuses on assuring the safe
delivery of care on a day-to-day basis for patients undergoing surgery.38
The mission encourages hospitals to redesign systems within a safety
culture.
A safety culture can be defined as “the product
of individual and group values, attitudes, competencies, and patterns
of behavior that determine the commitment to, and style and proficiency
of, an organization’s health and safety programs.”
(38) Hospitals with a positive safety culture are characterized
by communications founded on mutual trust, by shared perceptions
of the importance of safety, and by confidence in the efficacy of
preventive measures.
HSAG and the Collaborative faculty will help
each hospital achieve its goal and this mission by providing support,
sharing scientific knowledge, and by teaching the application of
methods for organizational change.
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Performance Measures
Proportion
of patients who received prophylactic antibiotics within one hour
before surgical incision.
Studies indicate that antimicrobial prophylaxis
is most effective when provided prior to the initial incision. Risk
of infection increases when prophylaxis is given too early (more
than two hours prior to initial incision) or too late (after initial
incision). Many experts believe that the optimal time for administration
is 30 to 60 minutes prior to incision, or within two hours before
incision if vancomycin is required for prophylaxis.
Proportion
of patients given a prophylactic antibiotic consistent with current
recommendations.
Proportion
of patients who received prophylactic antibiotics whose antibiotics
were discontinued within 24 hours after surgery.
Studies have shown that a brief course of antimicrobial
prophylaxis, when initiated shortly before the first incision, is
as effective as longer courses. Additionally, prolonged antibiotic
use has been associated with super infection with Clostridium difficile
and may impact the development of resistant strains of bacteria.
Some experts recommend to maintain a therapeutic level only through
wound closure, and that a single dose is adequate unless the surgery
is greater than four hours, major blood loss occurs, or an antimicrobial
with a short half-life is used.
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Goals
The main goals of the Arizona SIP Collaborative
are:
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One hundred percent of patients will have antibiotic
prophylaxis initiated within one hour prior to incision.
-
One hundred percent of patients will be given
prophylactic antibiotics consistent with published guidelines.
-
One hundred percent of patients given prophylactic
antibiotics will have those antibiotics discontinued within
24 hours after surgery.
See “Measurement Strategy” section for exceptions,
which include patients who: are receiving vancomycin, have tourniquets,
or are undergoing C-sections.
For a list of measures related to these goals,
see the “Measurement Strategies” section. Most teams will have additional
goals related to other surgical infection prevention strategies.
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Methods
Each hospital is expected to develop a statement
on what the team expects to accomplish during the Collaborative
(an aim statement) that includes specific goals relating to preventing
surgical infections. Hospitals should begin by working initially
within a specific surgical population (pilot population), or with
one or two surgeons (clinical champions) and anesthesiologists (also
clinical champions). The ultimate goal is to spread the improvements
to other populations and throughout the entire system. Hospitals
should select initial pilot populations based on internal infection
data and/or based on the following suggested surgical procedures:
coronary artery bypass grafts (CABG), cardiac operations, colon
operations, hip and knee arthroplasty, abdominal and vaginal hysterectomy,
or selected vascular surgery procedures. To facilitate learning
during the Collaborative, hospitals should try to identify a pilot
population that is expected to result in at least 30 surgeries of
procedure-of-selected-interest per month.
Both process and outcome measurement strategies
will be used to assess organizational progress toward achieving
Collaborative goals. Hospitals will learn an improvement strategy
that includes breakthrough goals and a method to develop, test,
and implement changes in their systems. Hospitals will be expected
to collect well-defined data that relate to their aim at least monthly,
and to plot these data over time for the duration of the Collaborative.
An annotated time series or run chart will be used to assess the
impact of changes.
The Collaborative faculty will aid hospitals
in capitalizing on the learning and improvement from the focused
project by simultaneously coaching senior leaders in hospitals to
develop a system for spreading improvement to other surgical populations,
sites, units, or surgical staff.
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Expectations
HSAG and the Collaborative faculty
will:
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provide information on subject matter, application
of that subject matter, and methods for process improvement,
both during and between Learning Sessions
-
offer coaching to teams
-
provide an electronic mailing list and other
communication venues for shared learning
-
assess team progress and provide feedback to
teams monthly
-
plan and implement the four face-to-face meetings
(three Learning Sessions and an Outcomes Congress)
-
maintain and safeguard the confidentiality of
privileged data or information—whether written, photographed,
or electronically recorded, and whether generated or acquired
by the team—which can be used to identify an individual patient,
practitioner, hospital, facility, health plan, or patient population
Hospitals are expected to:
-
perform pre-work activities as outlined in Section
II of the handbook
-
connect the goals of the Collaborative work
to a strategic initiative in the hospital
-
provide a senior leader to sponsor and actively
support the team
-
provide the resources to support the team, including
resources necessary for learning sessions and staff time to
devote to this effort
-
participate in each Learning Session (participation
by all core team members is highly recommended, and participation
in the Outcomes Congress that concludes the Collaborative is
desirable)
-
identify the performance measures that the team
is going to target, including the required performance measures
related to appropriate antibiotic prophylaxis
-
plan, design, and implement plan-do-study-act
(PDSA) improvement cycles to meet the targeted performance measures
-
submit monthly reports to the team’s senior
leader and HSAG, identifying progress and PDSA cycles implemented
-
create storyboards for presentation at
each Learning Session
-
share information with the Collaborative, including
details of changes made and data to support these changes, both
during and between Learning Sessions
-
maintain and safeguard the confidentiality of
privileged data or information—whether written, photographed,
or electronically recorded, and whether generated or acquired
by the team—which can be used to identify an individual patient,
practitioner, hospital, facility, health plan, or patient population
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References
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Emori TG, Gaynes RP. (1993). An overview of
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Balthazar ER, Colt JD, Nichols RL. (1982). Preoperative
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Pomposelli JJ, Baxter JK, 3rd, Babineau TJ,
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For More information contact:
Susan Sumwalt, RN, MA, CPHQ
Clinical Quality Specialist
phone: (602) 665-6176
fax: (602) 241-0757
ssumwalt@azqio.sdps.org
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