|
Anthony
R. Benedetto, FACHE
ABSTRACT
Six Sigma is a quality improvement methodology that was developed at
Motorola to address manufacturing quality issues. General Electric Medical
Systems Health Care Solutions (GEMS) adapted Motorola's Six Sigma approach
for use in the healthcare environment, which is a mixture of manufacturing-like
activities and service activities. GEMS was contracted to provide assistance
to the University of Texas M.D. Anderson Cancer Center Diagnostic Imaging
Film Library in the use of Six Sigma methodology to improve the film
library's performance.
This thesis
describes the application of Six Sigma methodology to our film library
improvement project. A radiology film library performs service activities
almost exclusively; thus, we hypothesized that manufacturing-based Six
Sigma methods might need significant modifications for our film library
project. Although several Six Sigma tools were found to be of little
or no value for our project, those Six Sigma tools that we found applicable
did not need any significant modification.
The most important findings were:
- Six
Sigma dramatically improves service activities,
- valid
quantitative data about services can be very difficult and expensive
to gather,
- personnel
with limited education and work experience need extensive coaching
to encourage creative and big-picture thinking, and
- change
management must be an integral component to achieve and sustain dramatic
changes.
PREFACE
Overview of Quality Improvement Methodologies
Many quality improvement (QI) methodologies have become popular during
the past few decades. Some have been formulated to provide modest, incremental
improvements; these could be categorized as "evolutionary."
A few examples of evolutionary QI methodologies are continuous quality
improvement (CQI), total quality management (TQM), and quality circles.
Another
category of QI methodologies is the "revolutionary"; these
methodologies support the idea that only drastic change with challenging
goals is truly effective. Examples of revolutionary QI methodologies
are reengineering and Six Sigma [see Kissler (1996) for a more detailed
overview].
Introduction
to Six Sigma Methodology
Six Sigma has gained popularity because of major successes achieved
by Motorola and General Electric, among other corporations. The Six
Sigma methodology will be described in much greater detail later in
this thesis. Briefly, Six Sigma involves a stringent examination of
quantitative data in conjunction with work simplification strategies
that focus on designing exceptionally high quality into the individual
steps of a process. By concentrating on high quality throughout the
process, the expense and hassle of performing extensive inspection and
rework can be avoided.
Six Sigma
was developed by Mikel Harry while he was at Motorola. At that time,
Motorola was spending almost a billion dollars per year to correct poor
manufacturing quality (Harry and Schroeder 2000). Six Sigma methodology
breaks down the manufacturing process into its component steps, measures
data on quality for each step, and focuses on improving the quality
of each step to such a high degree that the overall product quality
at the end of the manufacturing process is extraordinarily high-that
is, with minimal defects. In the first four years after adoption of
the Six Sigma methodology across its product line, Motorola had realized
$2.2 billion in savings.
Manufacturing
Versus Service Processes
By its nature, the manufacturing process is readily amenable to quantitative
analysis. The dimensions of parts can be measured with great accuracy.
The number of parts passing or failing inspection at any step can be
quantified. The amount of rework and waste material can be measured,
and reasons why each occurred can be assigned.
In the
service industries, processes dealing with customers are much more difficult
to measure, even qualitatively. As examples, the quality of an employee's
face-to-face interaction with a customer, an employee's use of good
decision-making skills, and customer satisfaction are not easy to evaluate
on a subjective high-to-low scale, much less on an objective numerical
scale. Additionally, customer interactions are rarely exactly identical
from one customer to the next. For example, a high rating for an encounter
with a difficult customer may be much more meaningful and valued than
a high rating for an encounter with an easy-to-please customer.
The
Radiology Film Library
When a patient undergoes a radiology examination, the resulting films
are placed into a film jacket and sent to the film library for storage.
The film jacket is checked out to authorized borrowers (primarily physicians)
when the patient undergoes another examination, is treated as an inpatient
in a hospital, or is seen during an outpatient clinic visit. When the
borrower is finished with the film jacket, it is returned to the film
library and reshelved.
Modern
healthcare practice in large medical centers is multidisciplinary, focused
on patient satisfaction, and attentive to cost reductions. A cancer
center, such as UT M.D. Anderson Cancer Center, exhibits these characteristics,
with special emphasis on the multidisciplinary approach to diagnosis
and treatment of cancer. The goals of increased patient satisfaction
and reduced cost are addressed, among other ways, by drastically reducing
the time between the patient's first visit and the eventual development
of a definitive plan of care. At M.D. Anderson, the goal for this initial
phase is four days, during which time the patient undergoes many tests
and has clinic visits with many physicians representing the various
oncology specialties (medical, surgical, radiation, etc). The need to
have the film jacket in multiple locations each day presents a major
challenge to a film library.
Performing
a radiology examination is quite similar to a manufacturing process
in regard to the ability to break the process into component steps and
to measure times and other quality metrics for each step. Moving the
film jacket around the campus, on the other hand, is not a rigorously
defined process in the sense of rigid standardization, inputs, outputs,
and so forth. The film jacket could be anywhere at any given moment,
and it might need to go almost anywhere on the campus. The first user
may need the film jacket long enough to delay or prevent the use of
the film jacket by the next user. A physician may take the film jacket
to a consultant without informing the film library, thereby making it
extremely difficult to track down the film jacket for a subsequent requestor.
The UT
M.D. Anderson Cancer Center contracted with General Electric Medical
Systems Health Care Solutions (GEMS) to assist us in using Six Sigma
methodology to dramatically improve the performance of our film library.
We had previously experienced great success with GEMS in improving throughput
in our computed tomography (CT) section using Six Sigma. We were concerned
that we might not be able to duplicate the success seen with the CT
section (a manufacturing-like, linear process) because most film library
processes are nonlinear, unpredictable, and difficult to quantify. Furthermore,
the CT section employs personnel with associate degree or higher education
who consider themselves healthcare professionals, whereas most of our
film library personnel have high school or General Educational Development
(GED)-level education and see their duties as a job rather than as a
calling.
Purpose
of this Thesis
The purpose of this thesis is to describe the problems we encountered
and the adaptations we made in applying Six Sigma methodology to our
film library services. Overall, the problems were related primarily
to the inherent difficulties in acquiring quantitative data about our
processes, rather than shortcomings in Six Sigma theory or practice.
We ended up choosing those elements of Six Sigma methodology that worked
for our environment and simply disregarding the remainder. Consequently,
the adaptations necessary to use Six Sigma techniques were minor, but
the challenges of developing metrics and acquiring meaningful, reliable
quantitative data were significant.
EVOLUTIONARY VERSUS REVOLUTIONARY CHANGE
Evolutionary
Change
In the beginning, there was the individual worker who was skilled in
producing baked goods, swords, baskets, and other goods. He individually
procured his raw materials, made everything with his own hands, and
sold his wares from a stall in the local town market. He gradually learned
the best way to make his products and made them the same way every day.
As our
sole proprietor became more successful, he found the need to hire helpers
to satisfy the increased demand. He realized that all of the information
he carried in his head and scribbled on scraps of parchment needed to
be conveyed to his new employees. Otherwise, his successful products
would become inconsistent in quality and he would lose customers. The
first standard operating procedure (SOP) was born.
Over time,
he and his employees made changes that improved the products. These
changes were incorporated in the SOPs on a casual basis as they arose.
Because everything seemed to be going smoothly and business was good,
our budding entrepreneur saw no need to systematically study his processes
to see if improvements could be made that had not yet been stumbled
on. Unfortunately for him, one of his competitors had discovered that
occasionally stepping back and taking a more holistic look at her processes
yielded insights that contributed to higher quality and improved margins.
Being clever with words, she decided to give this new approach a catchy
name. However, being relatively indecisive, she could never decide between
"total quality management" or "continuous quality improvement."
This legacy remains today.
Total quality
management (TQM) and continuous quality improvement (CQI) live on today
as the most highly developed examples of evolutionary process improvement.
At their heart, TQM and CQI hold that every process contains elements
that can be improved, no matter how long the process has been in use
or how successful the end product. Rather than being content with "if
it's not broken, don't fix it," TQM and CQI proponents are more
likely to say "although it's not broken, we can make it better
if we look closely enough." Typical goals for a TQM project might
be a 10 percent reduction in accounts receivable or a 15 percent increase
in outpatient surgery cases with no staffing increase.
Evolutionary
techniques have their place in any business environment. There is no
such thing as the perfectly effective and perfectly efficient process-some
element of improvement can always be realized by a clever person or
group of people. However, highly successful processes may have been
fine-tuned so well over time that major changes simply are not needed.
In these situations, the techniques of evolutionary change work well-for
example, workers' quality circles and team meetings to discuss incremental
change.
Revolutionary
Change
Healthcare processes are far from perfect. The time from initial presentation
to cure may be long and expensive because of poorly designed diagnostic
work-up algorithms and outdated knowledge of modern drugs. Readmission
rates after surgery, or emergency admission rates for acute illnesses,
may be too high. Medical administration errors and adverse drug reactions
during inpatient stays may increase the length of stay and, consequently,
the cost of the episode. In the era of cost-based reimbursement, these
inefficiencies lingered far longer than necessary because little financial
pressure or incentive existed to improve performance. Today, in our
cost-conscious environment, we have recognized that high-quality healthcare
also tends to be low-cost healthcare, and we have become much more aggressive
about addressing quality and cost issues.
TQM and
CQI techniques are effective in producing needed change, but inherently
they are focused on incremental, piecemeal change. A team will work
on improving one segment of a process, then next year another team will
work on another segment, and so forth, until eventually the entire process
has been addressed. However, when pressure to implement broad-based
and/or major changes rapidly is placed on a process, TQM and CQI work
less well because they do not stress the importance of looking at the
entire process holistically.
When a
process is identified as being significantly flawed, tweaking and fine-tuning
bits and pieces of the process over an extended time may not be acceptable
approaches to bring the process up to the desired level of performance.
The two most popular tools for addressing revolutionary change are reengineering
and Six Sigma. They have many similarities, but they also have significant
differences.
Reengineering
is defined (Hammer and Champy 1993) as "the fundamental rethinking
and radical redesign of business processes to achieve dramatic improvements
in critical, contemporary measures of performance" [emphasis added
to reflect the four key elements of reengineering]. The personnel at
Motorola who crafted the Six Sigma philosophy "focused on making
improvements in all operations within a process, producing results far
more rapidly and effectively" (Harry and Schroeder 2000). Thus,
reengineering and Six Sigma recognize that:
- processes
are key to quality,
- most
processes are poorly designed and implemented,
- overall
success rates are very sensitive to individual subprocess success
rates, and
- rapid,
dramatic change requires looking at the entire process, not just a
few individual subprocesses.
Six
Sigma Versus Reengineering
The most important difference between reengineering and Six Sigma is
the highly structured, quantitative basis on which Six Sigma is built.
Reengineering recognizes the role of statistics and quantitative analysis,
but Six Sigma tends to place extremely heavy reliance on data to drive
decisions. "Business sense" always comes into play, but only
after the data have been used to narrow the range
Quoting
from a General Electric Six Sigma training manual (General Electric
2000), data are important because:
- "We
don't know what we don't know." [Note: our knowledge is always
incomplete.]
- "If
we can't express what we know in the form of numbers, we really don't
know much about it."
- "If
we don't know much about it, we can't control it."
- "If
we can't control it, we are at the mercy of chance."
In healthcare,
data may be especially important. Physicians are such powerful figures
within the healthcare industry that they are sometimes elevated to positions
of unchallenged authority in their specialty area. They may come to
believe that their own experience, or at least their remembrance of
their experience, is representative of the experience of all physicians
in the same specialty. They fail to realize that their memory may be
less than perfect, that some of their outcomes may have been less than
ideal, and that their patient population may be different in important
ways from the patient populations of their peers. Thus, the way they
practice their specialty is based on personal, anecdotal experience
and is rarely enriched by retrospective, quantitative study of their
career-long medical practice.
If we allow
the anecdotal experience of one or a few influential physicians to drive
our clinical pathways and other approaches to providing optimized healthcare
to all patients, we are likely to find that our real-world outcomes
fall far short of our targets. If, on the other hand, we quantitatively
analyze the results of many physicians in treating a wide variety of
patients for a carefully defined clinical condition, we are much more
likely to derive a treatment plan that will provide the best possible
outcome at the lowest cost and with the least likelihood of failing.
Data are good, but good data are better.
THE SIX SIGMA METHODOLOGY
The Six Sigma Breakthrough Strategy
Six Sigma was developed at Motorola to reduce high costs associated
with poor final product quality at the end of an assembly line (Harry
and Schroeder 2000). Motorola calculated that it was spending up to
20 percent of its total revenues (almost $1 billion per year) on correcting
poor quality discovered at the time of final inspection. The engineers
charged with reducing these costs came to the conclusion that the only
sensible way was to eliminate as many steps in each process as possible,
then to design near-perfect quality into each step. Only then would
they have a chance of low-defect final product that required essentially
zero rework to correct defects.
The eight-step Six Sigma Breakthrough Process is described by Harry
and Schroeder (2000) as:
- Recognize-realize
that a business problem exists for which Six Sigma tools may be appropriate.
- Define-clearly
express the problem and the desired final state in written form.
- Measure-use
historical or prospectively obtained data to adequately characterize
current quality, costs, and other factors.
- Analyze-apply
statistical tools and common business tools to the data to characterize
the key drivers of the problem areas identified in the Measure phase.
- Improve-develop
alternative solutions, evaluate them, and test them on a pilot basis
to determine if the desired outcome is being achieved.
- Control-determine
the best methods for ensuring that any new solution is actually working.
- Standardize-write
a new standard operating procedure and provide training to all persons
involved in the process to ensure that the process is carried out
according to the SOP.
- Integrate-implement
the new SOP and persistently use the appropriate control measures
to ensure that the process is performed in compliance with the SOP
over the long term.
Harry and
Schroeder further categorize these eight steps into four stages presented
in Table 1.
Table
1. Six Sigma, as Described by Harry and Schroeder (2000)
|
Stage
|
Breakthrough
Strategy Phase
|
Objective
|
|
Identification
|
Recognize
Define
|
Identify
key
business issues
|
|
Characterization
|
|
Understand
current performance levels
|
|
Optimization
|
|
Achieve
breakthrough improvement
|
|
Institutionalization
|
|
Transform
how day-to-day business is conducted
|
The
GE Twist on Six Sigma
The General Electric Company (GE) has been one of the highly visible
success stories for Six Sigma (Harry and Schroeder 2000). GE recognizes
the same elements as given in Table 1, but they label the stages somewhat
differently (General Electric 2000). My understanding of the GE philosophy
is presented in Table 2.
|
Stage
|
Breakthrough
Strategy Phase
|
Objective
|
|
Define
|
|
Identify key business issues
|
|
Measure
|
Measure
|
Understand
current performance levels
|
|
Analyze
|
Analyze
|
|
|
Improve
|
|
Achieve
breakthrough improvement
|
|
Control
|
|
Transform
how day-to-day business is conducted
|
GEMS uses the acronym DMAIC (de-may'-ik) to encapsulate the philosophy
for its own employees and for clients.
Six Sigma as a Solution to Manufacturing Problems
Six Sigma was developed at Motorola to address a manufacturing problem.
For the purpose of this thesis, a manufacturing process need not be
the assembly of a widget on a traditional factory assembly line. Rather,
a manufacturing process can be thought of as any process whereby resources
are applied in a sequential manner to produce a single product or service,
with relatively high predictability in any individual step of the process.
Our CT throughput project is described later in this article to further
demonstrate how healthcare processes fit this manufacturing process
model.
- The
weakest link in the chain: In a manufacturing process, when the first
step is completed, the second step is always the same; when the second
step is completed, the third step is always the same; and so on. At
the end of the day, all full cycles of the process have gone through
all of the steps in the same order. If the process is well designed,
each step will have been performed with predictable expenditure of
resources and with predictable quality.
In a manufacturing process, the quality of the final service or product
can be calculated from the quality at the end of each step. For example,
if the "success rate" of Step 1 is 90 percent and the success
rates of Steps 2 and 3 are 95 percent and 90 percent, respectively,
the overall success rate of the process will be 0.90 x 0.95 x 0.90
= 0.77, or 77 percent (see Table 3). In Six Sigma terminology, this
is called "rolled throughput yield."
Table 3. Rolled Throughput Yield
| Example |
Step
1 |
Step
2 |
Step
3 |
Overall
Success Rate |
| 1 |
0.900 |
0.950 |
0.900 |
0.77
(77%) |
| 2 |
0.983
|
0.983 |
0.983
|
0.95
(95%) |
| 3 |
0.950 |
1.000
|
1.000
|
0.95
(95%) |
If the goal is to have an overall success rate of 95 percent (Example
2 in Table 3), the success rates of each individual step will need
to be higher than 95 percent, because the overall success rate is
the product of the individual rates. Note also that the success rate
of each individual step must be no lower than the overall desired
success rate; that is, the overall success rate cannot be higher than
the success rate of the least successful intermediate step. If each
of the individual success rates were equal, each would need to be
98.3 percent to achieve an overall success rate of 95 percent. In
the Example 3 in Table 3, if we want the overall success rate to be
95 percent and if Step 1 has a success rate of 0.95, Steps 2 and 3
must be perfect (success rates of 1.0). As will be mentioned later,
rolled throughput yield does not fit the film library because almost
every interaction is different. However, the concept that the worst-performing
step limits performance is still valid and important.
- Introduction
to Six Sigma statistical foundation: The "six sigma"
in Six Sigma is derived from the statistics of a Gaussian distribution.
The Gaussian (also called "normal") distribution is the
familiar bell-shaped curve that describes many biological and nonbiological
processes.
The Gaussian distribution is characterized by the mean and the standard
deviation. The mean, , is the average value of all of the individual
values making up the data set. The standard deviation, (Greek
symbol for sigma), is a measure of how widely spread the data are
around the mean; for example, a large value of represents a
large spread of the data. The data are divided equally on both sides
of the mean, so that half of the data are above the mean and half
are below the mean. Mathematically, the area under the Gaussian curve
between any two points on the x-axis represents the total number of
data points whose x-values lie in that range (see Figure 1). (Call
(312) 424-9473 to obtain a copy of Figure 1.).
For example, suppose we wish to analyze the radiology report turnaround
time (TAT), which can be defined as the time from the end of the patient's
examination to the time the radiologist signs the final edited report.
We would measure the TAT for each report and arrange the data in a
table that lists each TAT range of interest (say, 30-minute increments)
and gives the number of TATs that fall in that time range. The resulting
distribution could be plotted on rectangular graph paper, with the
y-axis being the number of reports in each TAT range and the x-axis
being the report turnaround times. The Gaussian distribution would
predict that 68.3 percent of all of the reports would have TATs that
fall in the range µ ±1, 95.4 percent would fall
in the range µ ± 2, 99.7 percent in the range µ±
+ 3, and so on.
Another way of using the ranges described in the previous paragraph
is to predict how many data points would not fall within any
given range. In the case of µ ± 2 for example,
4.6 percent of the reports would have turnaround times that were either
shorter than the bottom of the range or longer than the top of the
range. Because we are only interested in the long TATs, and because
the Gaussian distribution predicts an equal number above the range
and below the range, we would expect 2.3 percent to be longer than
µ± 2. If we now set µ± 2 as
our target, that is, we do not want TATs to be longer than this value,
we see that 2.3 percent of all reports would have TATs longer than
our target. In Six Sigma terminology, these reports would be called
"defects."
Six Sigma proposes that each step in a multistep process should have
fewer than µ± 6 defects, which corresponds to 0.0000002
percent defects, or two defects in every one billion opportunities.
When reading the Six Sigma literature, however, the figure cited most
frequently is 3.4 defects per one million opportunities. This less
stringent figure is based on the observation that processes inherently
vary slightly from day to day and that this variation is unavoidable
and acceptable statistically. [Note for the statistically sophisticated
reader: Long-term drift in processes is accounted for by introducing
a ±1.5 shift. Thus, when looking up 3.4 defects per million
in a Z table, you will find that this value falls at ±4.5,
not ± 6. See Chapter 8 of Harry and Schroeder (2000)
for a more complete discussion. Also, sample sizes are always chosen
to be large enough to minimize the differences between population
and sample descriptors.]
For
a concrete example, suppose the average number of patient bills processed
per day by a single clerk is ten, with a standard deviation of three.
If we look at an individual clerk's performance over the next 100
days, we would expect the daily output during 95 of those 100 days
(95% of the data) to be 10± 2s± (2)(3) =
10 ± 6, or as few as 4 bills and as many as 16 bills. (Statistically,
the µ± 2 range is called the 95% confidence interval.)
During the other five days, the clerk is likely to process fewer than
4 bills or more than 16 bills.
A major element of Six Sigma philosophy is to first reduce variability
in a process before trying to shift the average performance. (Statistically,
the standard deviation is reduced first, then the mean is shifted.)
The rationale is that a process showing a great deal of variability
is likely to have multiple major and minor factors driving the variability,
making it difficult to focus on the "vital few" truly important
factors. For example, failure to have an SOP and to have properly
trained the personnel on the SOP are likely to be the primary causes
of high variability in the beginning stages of a quality improvement
project. Once these remedies have been put into place, any residual
variability and any variation from average targeted performance is
likely to be due to important factors in the process itself.
Table 4. Reduce Variability First (example of patient bill generation)
|
Mean
|
S.D.
|
Mean
± 2 SD
|
95%
Confidence Interval
|
|
10
|
7
|
10
± 14
|
0-24
|
|
10
|
4
|
10
± 8
|
2-18
|
|
10
|
1
|
10
± 2
|
8-12
|
In the billing clerk example, we might want the clerk to eventually
process a mean of 15 bills per day. Suppose that the clerk's standard
deviation is 7 bills per day, yielding a 95 percent confidence interval
of 0 to 24 bills per day (negative output is not possible, so the
lower end of the interval is 0). Before we try to edge the mean output
up to 15, we would want to get the clerk working predictably with
very few days at the lower daily output levels, which translates into
a need to reduce the standard deviation to a much smaller number.
Note in Table 4 that increasingly smaller standard deviations result
in fewer low-output days.
- CT throughput
example: Due to growth in our CT workload, our institution found that
we were not able to meet the demands of our referring physicians.
The usual reaction to such a dilemma is to consider adding shifts
or purchasing additional CT scanners. Although initially plausible,
such solutions can be quite expensive, with no guarantee of success.
For example, running the scanners 24 hours per day will not increase
throughput if patients are not willing to come to the scanner at 4:00
in the morning! We decided that an opportunity to increase throughput
might be available without such drastic measures.
The multistep process of performing an outpatient CT exam is an example
of a healthcare process that fits the manufacturing model for which
Six Sigma was originally developed. The following steps are performed
exactly in this sequence for every patient:
- The
patient arrives.
- The
patient receives any necessary preparation.
- The
examination is performed.
- The
films are printed.
- The
radiologist interprets the images and dictates a report.
- The
transcriptionist prepares the preliminary report.
- The
radiologist edits and signs the report.
- The
report is sent to the requesting physician and to the patient's
chart.
If operations are standardized, the length of time for each step
can be calculated from historical data, including an estimate of
each step's variability (its standard deviation). Based on these
calculated times, the number of patients per eight-hour shift can
readily be calculated.
When we employed Six Sigma techniques to increase our CT throughput,
we quickly found that each step had not been optimized. For example,
patient preparation times that initially were 45 minutes have been
reduced to less than 5 minutes in many cases. We also found that
we needed to design our CT processes to take advantage of the fact
that we had nine essentially identical CT scanners, which cushions
us against cascading delays when one patient experiences a delay
in his or her examination process. For example, if a patient develops
a contrast reaction during an examination, that patient's examination
would be protracted, and the next patient scheduled for that scanner
would be delayed. With multiple identical scanners, we were able
to redesign the process to make sure that patients were reassigned
to the next available scanner. Although this seems obvious when
seen on this page, it is not straightforward or easy to accomplish
when the scanners are spread out geographically across a large institution.
Our Six Sigma CT throughput project ran formally for about two years.
The initial improvement in throughput, with no additional machines
or shifts, was a 45 percent increase in examinations (Elsberry 2000).
The project is still ongoing, although less formally, since that
time, because CT scanner technology continually changes and because
the geographical distribution of our scanners frequently changes.
Every change presents an opportunity for conditions to worsen; fortunately,
every change also represents a potential opportunity for conditions
to improve nonlinearly.
Radiology
Film Library Does Not Fit the Manufacturing Model
- Film
library overview: The UT M.D. Anderson Cancer Center Film Library
performs four important major functions: storing films, receiving
and in processing films from other institutions, lending films to
on-campus users, and lending films to off-campus users. Some film
libraries have responsibility for report distribution and other clerical
functions. However, all film libraries perform the four core functions
mentioned above. Figure 2 is a schematic representation of these functions
at M.D. Anderson. (Call (312) 424-9473 to obtain a copy of Figure
2.)
- Film
library compared to CT: Key criteria mentioned earlier for the manufacturing
model were that the individual steps are predictable and that they
are rigidly sequential. The handling of film jackets is the antithesis
of these criteria. A film jacket already could be checked out to any
one of 1,000 or more borrowers (physicians, clinics, radiology sections,
etc) when a requestor asks for it. Patients go to clinic visits and
radiology exams in patterns that vary from clinic to clinic, and sometimes
even among physicians within a given clinic. Something unexpected
that shows up on a CT scan may trigger an immediate add-on magnetic
resonance imaging (MRI) scan, with the film jacket needed in both
locations when the radiologists interpret the two exams.
When a film library comes under criticism, the criticism tends to
be global: "fix the film library!" After only superficial
scrutiny, it becomes quite clear that "the film library"
is not a clear-cut single process that follows the manufacturing model,
such as a CT scan does. Rather, the film library is actually a large
suite of processes that are related and interdependent, but not describable
as a collection of steps that are predictable and easy to quantify.
Clearly, the concept of rolled throughput yield makes no sense for
"the film library." Does this make the concept wrong? No.
Rolled throughput yield simply is a tool that is inapplicable and
remains in the toolbox unused. This was one of the important lessons
learned in our film library project.
DIFFICULTIES
ENCOUNTERED USING SIX SIGMA IN FILM LIBRARY PROCESSES
Data: Generation, Validity, and Feedback
- Information
systems: As was shown in Figure 2, the radiology information system
(RIS) is at the center of a film library's operations. The RIS is
a computer system that tracks patients and films, generates bills,
captures reports, and so forth. Each patient's film jacket is bar-coded
for easy, reliable check-in and check-out. Every new exam is entered
automatically into the RIS. At our institution, movement of the patient
through the radiology department is also tracked in the RIS, which
is of value to the film library when a requestor asks to see films
before the radiologist has rendered the interpretation of an exam.
The selection of a radiology information system is always a compromise
among less-than-optimal options. No vendor provides a product that
exactly fits an institution. In some cases, the fit is not very good
at all, but an RIS must be purchased anyway, because a large radiology
department cannot be run manually. If the persons evaluating the fit
are biased toward patient tracking and billing, it is possible for
an RIS to have good performance for these functions but less than
adequate performance for film library functions. Rarely can an RIS
be customized by the purchaser to optimally handle local peculiarities.
Even with the best RIS, problems arise because of the usual lack of
full integration of the RIS with other institutional systems. For
example, we retrieve roughly 1,500 to 1,800 film jackets every weekday
night and deliver them to a clinic or radiology section for the next
day's appointments. Our RIS does not provide for importing of appointment
information from the scheduling module of the institution's healthcare
information system (HIS) to the RIS. Although the HIS can produce
a listing of all appointments, it does not know which patients have
film jackets. Thus, in the past the film librarians spent many hours
looking for film jackets that did not exist. Fortunately, our radiology
informatics group wrote an interface program that takes a nightly
dump of information from the HIS scheduling module and compares it
against the film jacket listings in the RIS, then prints a pull list
for our film librarians. Unfortunately, this program has been less
reliable than we would prefer, so the film librarians too frequently
end up devising impromptu workarounds when the program misbehaves.
Also, because of limited availability of programming support, changes
to the program are practically impossible to obtain when clinical
operations change.
An example of a film library metric whose data can be readily gathered
from an information system with minimal manual data collection is
the percentage of film jackets requested by potential borrowers that
are delivered each morning. The program mentioned above provides a
count of all of the appointment labels printed (denominator). The
number of appointment labels remaining after all of the jackets have
been placed on the delivery carts is hand counted (numerator). This
percentage can be calculated daily with little effort.
Our RIS focuses on the end points of processes and provides little
information about intermediate steps. For example, suppose we wish
to assess how promptly we retrieve film jackets when a requestor is
at our loan window or places a request telephonically. When a requestor
asks about the availability of a film jacket, it would be helpful
if the time of the initial RIS inquiry were logged, because this is
usually within a few seconds after the arrival of the requestor at
the loan window or after making the request telephonically. Our RIS
captures the final checkout time, but not the time of the initial
inquiry. To assess our performance in delivering film jackets rapidly
to requestors, we must capture the time of the initial inquiry manually.
- The
challenges of manual data collection: Because of the paucity of
managerially useful data available from most information systems,
much of the data needed for a Six Sigma analysis must be collected
manually. Manual data collection is time consuming and is a hassle
for the person(s) who collect the data. When the frontline employee
is the one who must collect the data, the employee must be educated
about the importance of the data and about the exact data that are
needed. Then, the employee must actually collect the data as prescribed.
For some employees, a supervisor must closely monitor the data collection
to ensure that the data are collected accurately and completely.
A film library example is the metric for the timeliness of fulfilling
a customer's request. Our metric specifies target fulfillment times
for film jackets requested in person at the loan window and for telephone/fax/e-mail
requests. To calculate these times, the request submittal time and
the check-out time must be captured. Determining one or both of these
times may also require the patient's medical record number so that
the time can be retrieved from the radiology information system. Each
e-mail and fax request automatically receives a time stamp, provided
that the internal clocks are set accurately. However, the request
submitted in person at the loan window and the telephone request require
the film librarian to note the submittal time on a log sheet. The
first step that the film librarian takes upon receiving an in-person
or telephone request is to look up the films in the RIS; then he or
she pulls the jacket from the shelves if it is available in the film
library. For an in-person request, the jacket is quickly checked out
to the requestor, and the film librarian prepares to work with the
next customer. Thus, for both the in-person request and the telephone
request, recording the original submittal time is not part of the
normal workflow. The film librarian is likely to guess at the submittal
time in retrospect. The longer the lapse in time between the transaction
and the film librarian remembering that they need to enter the submittal
time, the less accurate the guess. As the target fulfillment time
for a loan window transaction is about five minutes, even small inaccuracies
in the submittal time can seriously distort the data.
- Data
that are impossible to obtain: The fundamental metric of Six Sigma
is defects per million opportunities, which translates in common language
as the percentage error rate. Error rates require knowledge of the
number of errors associated with a population of transactions (the
numerator) and the total number of transactions (the denominator).
Techniques can be devised to measure the number of errors, although
some errors can be very difficult to identify. The bigger challenge
can be the denominator, that is, the total number of transactions.
Some important performance measures are impossible to obtain, so substitute
(usually inferior) measures must be used.
A film library example of an impossible-to-obtain metric is the number
of outside films that arrive in the institution that are not reported
to the film library for entry into the RIS. Outside films are films
that were generated at other institutions and that are brought or
sent to our institution for review by the patient's physicians and
for comparison to radiology exams performed here. A high reporting
rate helps when other potential borrowers request these outside films.
In this example, both the numerator and the denominator are essentially
impossible to obtain. Some clinics may fail to notify the film library
that outside films have arrived. If clinic personnel do not send the
films to the film library for filing in the patient's M.D. Anderson
film jacket, but instead hold the films in the clinic or send the
films back themselves, the film library never knows that the films
are on the campus. Thus, we cannot know about their failure to report
the films (numerator), and we cannot know that the films were on the
campus (denominator). With 20,000+ new patients per year, each of
whom is likely to bring or send outside films, it is logistically
impossible to design a system for ensuring that the arrival of every
outside film is captured.
- Tracking
film librarian errors: Film librarians undergo training in basic
customer service skills, such as telephone etiquette, and in specialized
film library procedures. As they go about their duties, they interact
with colleagues and customers face to face. They interact with the
RIS, the computer for the off-site warehouse, and other information
systems. Finally, they perform repetitive manual tasks, such as filing
film jackets in the shelves, which are not observable by the supervisor
on a continual basis and are not captured in an information system.
No enduring record exists of face-to-face interactions. Unless a supervisor
happened to personally witness the interaction, no independent evaluation
is made of the quality of the interaction. Even when the supervisor
witnesses an interaction, the evaluation is inherently subjective
and difficult to quantify. Finally, during a face-to-face interaction,
there are many factors to evaluate, so making a judgment about the
quality of the interaction requires assessment of multiple factors
in a very short time, then making a record of that assessment in a
quick, reliable, and retrievable manner.
For a machine interaction, there are two types of error. The first
type is an error of commission; that is, the film librarian performs
an improper action. In many cases, these errors will be noticed and
can be tracked back to the person who committed them. However, this
tracking ability relies on the information system's built-in error
capture mechanisms. If the RIS does not capture errors, does not capture
the identity of an operator, or does not readily allow reports tailored
to the investigation of errors, the RIS is of no help in identifying
errors of commission. RIS vendors seem to have the misperception that
all users will always comply with all published policies and procedures.
The second type of machine interaction error is an error of omission;
that is, the film librarian fails to perform a required action. When
and if these errors are detected, they can be extremely difficult
to track, because there is no machine record of the action. Sometimes
an action could have been performed only by a particular individual,
but such occurrences are uncommon in a large, busy film library where
similar duties are performed by multiple people on all three shifts
and during the weekend.
Irrespective of whether interactions are face to face or with the
RIS, quantifying these interactions is surprisingly difficult. A fundamental
metric of Six Sigma is the ratio of defects to opportunities, that
is, the number of defects observed divided by the total number of
opportunities for those defects to occur. Even though every check-out
and check-in of a jacket may be tracked using the RIS, the total number
of opportunities, that is, the total number of handlings, is rarely
available.
As a more concrete example, suppose that 300 film jackets were sent
to the CT section today. When we check the RIS, however, we find that
ten film jackets still show that they are in the file room, meaning
they are physically in the CT section but had not been properly checked
out in the RIS. This is a defect rate of 3 percent (10 defects out
of 300 opportunities). While each of the ten improper check-outs could
be detected by querying the RIS, all of the data necessary to calculate
this error rate cannot be extracted from the RIS. For example, can
we ask the RIS to give us a report of all jackets checked out to the
CT section on this date? Can we ask the RIS to compare a list of the
patients whose film jackets were requested against a list of the jackets
checked out to the CT section? Very few commercial RIS products offer
this level of functionality.
In our case, we must walk to the CT section, write down the medical
record numbers on all of the film jackets that we find there, then
promptly look up the film jackets manually in the RIS to determine
if they were properly checked out. Although doable, this certainly
makes the acquisition and analysis of data unattractive and expensive.
If we let the obstacles discourage us from collecting the data, the
resulting lack of data means that the process can be out of control
without our knowledge.
As difficult as it can be to dig data out of the bowels of the RIS,
it is even more difficult to obtain quantitative data on face-to-face
interactions that do not involve an entry in the RIS. For example,
a physician will come to the loan window and ask to see a patient's
films. The film librarian retrieves the film jacket and hands it to
the physician, who reviews the films briefly in a nearby viewing area
and promptly returns them. In this transaction, the film librarian
should come to the loan window promptly and should greet the physician
courteously. The film librarian must obtain the necessary information,
search the RIS, and retrieve the film jacket. Upon the return of the
films, the film librarian must reshelve the films in their original
location. If the physician walks off with the films without properly
signing them out, the film librarian must try to remember the physician's
name and check out the films to the physician in the RIS. In a busy
environment, the physician's name may be lost forever.
All of these important pieces of the transaction occur with no RIS
record of the transaction. When attempting to assess the quality of
this service, essentially no historical data are available. Is the
physician having to wait too long for an initial greeting? Are the
films available a high enough percentage of the time? Is the physician
having to wait too long for the films to be retrieved? Are "borrowers"
walking off with films too frequently? All of these important operational
questions, the answers to which have an impact on many other film
library operations, are impossible to retrieve from the RIS or from
any other information system. Obtaining them requires manual observation
of multiple transactions by a trained observer over an extended period
of time. Once again, this can be done, but it is so time consuming
and tedious that it is likely to be sampled infrequently, perhaps
too infrequently to rapidly alert us to unsatisfactory levels of performance.
Another example of a manual task that is neither observable on a continual
basis nor tracked in the RIS is the accuracy with which film jackets
are filed in the shelves. Inaccurately filed film jackets lead to
extended search times, overlooked film jackets, and frustrated film
librarians and requestors. Figure 3 is a data collection sheet used
by a supervisor or other designated auditor. (Call (312) 424-9473
to obtain a copy of Figure 3.) To collect these data, the auditor
must manually inspect 100 percent of the film jackets in a shelving
section, checking for each of the listed errors. In a large film library,
this is a tedious, mind-numbing, and time-consuming task. Fortunately,
the data are powerful. Figure 4 is a summary of three data collection
sessions, showing highly variable performance between different film
librarians. (Call (312) 424-9473 to obtain a copy of Figure 4.) We
were able to use these data to focus on those film librarians whose
performance was substandard by providing remedial education or closer
supervision, as appropriate.
- Six
Sigma reporting tools are difficult for frontline employees to grasp:
Film library employees tend to have little education beyond high school.
Even supervisory personnel may have joined the film library soon after
high school and may not have pursued additional college-level education.
Their foundation for understanding percentages, statistics, and important
Six Sigma concepts is weak. Data that Six Sigma leaders find compelling
may be lost on the frontline employee, making it difficult to rouse
the employee to corrective action.
Percentage error rates are fairly well understood by most frontline
employees, because they have been exposed to such calculations in
high school grade calculations, as what constitutes an A, a B, or
an F. To most of us, a grade of A represents superior performance.
A grade of A might be awarded for a 90 percent success rate. When
we measure film library performance and find that a particular metric
is 94 percent, the reaction of most frontline employees is that they
have done well. However, in Six Sigma, we are aiming for a 99.9999
percent success rate. Explaining why 94 percent is good enough for
an A in school, but not nearly good enough at work, is a leadership
challenge.
Developing
Solutions
- Baseline
data require that a decent process already exist: During the Measure
and Analyze phases, baseline data are gathered to help pinpoint factors
that are driving substandard performance. A performance standard may
need to be established de novo during the Define phase, because of
the discovery of an important area of substandard performance or due
to lack of an existing performance standard. During the Measure phase,
baseline data would be collected to define the degree of substandard
performance. The most likely explanation of substandard performance
in some cases may be that a formal process addressing this area has
never been in place. The Analyze phase is predictably going to demonstrate
very poor performance.
A film library example is the timeliness of return of films that we
lend to other institutions. Although we had always specified a loan
period when we lend the films, we rarely monitored the return of the
films on a systematic basis. Rather, we chased down the films when
a new requestor asked for them. As we cannot promptly fulfill the
new request if the films are not under our control, it became clear
that we needed to implement a formal method of systematically following
up on delinquent films. Our RIS has not been helpful to date, because
its dunning functionality cannot distinguish between on-campus and
off-campus delinquencies. When we measured the return rate, we found
it (unsurprisingly) to be dismal. The major factor driving the poor
return rate was determined to be failure to have a process for following
up with borrowers to get the films returned promptly. We did not need
data to tell us this, but we had to establish a baseline so that we
could observe improvements as we implement the new process. The baseline
also helped us narrow the list of factors likely to cause problems
so that we could address them in the new SOP.
- Frontline
employees have difficulty dealing with multistep processes:
Most high school graduates have not been exposed to problems that
have dozens of steps and multiple conditional branches. Film library
problems are of this type, frequently generating process maps several
pages long. Following a complicated process from start to finish,
especially when one conditional branch leads immediately to another
(or two, three, or more), is a skill that is difficult to acquire
in the short time span of a Six Sigma project team. The Six Sigma
leader is faced with the challenge of getting the team members to
understand the existing complicated multistep process. Then the team
must cope with the even more difficult task of considering alternative
subprocesses and their effects on the process. These challenges are
surmountable, but upper management must understand that project times
will be lengthened when working with employees whose educational and
work experience backgrounds are limited.
- Involving
the evening, night, and weekend shifts:
A fundamental tenet of Six Sigma, indeed any process improvement effort,
is that all stakeholders must be included, especially those at the
front line who deal with the customers every day and who know the
problems most intimately. A film library in a large institution operates
365 days per year, 24 hours per day. The weekend shifts may be staffed
with personnel who work only during the weekend. In contrast, weekday
day shift is the usual schedule for film library leaders, information
systems representatives, clinic personnel, and other persons who are
included as project team members. Scheduling meetings to accommodate
day-shift personnel is already a challenge; scheduling meetings that
require the attendance of people from all three weekday shifts, plus
the weekend shift, is extremely challenging. The usual compromise
is to have a series of meetings: Monday morning meetings (for weekend
night-shift employees and weekday day-shift employees), Friday afternoon
meetings (for weekend evening-shift employees and weekday day-shift
employees), midweek morning meetings (for weekday night shift and
day-shift employees), and midweek afternoon meetings (for weekday
evening-shift and day-shift employees). While this gets everybody
into a meeting (except weekend day-shift employees), it leads to an
inefficient extended series of meetings because each team must spend
time at each meeting catching up with what was done at the other teams'
meetings. The meetings must reiterate problems, rather than homing
in quickly on a potential one-meeting solution if everyone were in
the same room at the same time. These challenges are surmountable,
but upper management must understand that project times will be lengthened
because of the need for multiple iterative meetings.
Change
Management Must Be Integral and Intensive
An evolutionary process improvement project requires attention to change
management, as very few people welcome change. A Six Sigma project requires
exceptional attention to change management, because the desired change
is revolutionary, not just evolutionary. The way a person performs his
or her job is likely to change in many respects, which is uncomfortable
and, sometimes, threatening. Involving all stakeholders from the very
beginning of the Six Sigma project is necessary, because they repeatedly
see and hear the reasons why change is needed, but stakeholder involvement
alone is not sufficient.
Implementation of major changes can be very threatening, especially
for employees in the lower pay grades typical of film library positions.
Additionally, a dramatic change in a process may be overwhelming to
those who have had little experience with making sudden changes, either
at work or in their private life. Even if they are motivated to change,
the extent and rapidity of change may be more than they can handle.
Thus, not only must employees be educated about the need for change,
but their ability to cope with change must be assessed and implementation
plans must be tailored to introduce change at an acceptable rate.
For any one project, this tailoring is fairly straightforward. However,
when multiple Six Sigma projects make recommendations for process changes
(we had nine mini-project teams within our overall Six Sigma project),
the film library leadership team must consider the entire film library's
ability to absorb change. The film library leadership must also balance
upper management's desire for rapid change against the ability of the
film library staff to cope with it. An individual project team's recommendations
may be easy to implement quickly, but implementing multiple teams' recommendations
may require an extended implementation period to ensure success, especially
if any other recommendations require coordination or are in conflict
with each other.
We commissioned a Six Sigma project team to improve the cycle time for
mailing out M.D. Anderson films on loan. When we began, two mail-out
film librarians were functioning virtually unsupervised and with no
written SOP. Requests were not logged in to ensure that all requests
were processed, so some requests had cycle times of weeks, because the
paperwork was misplaced and not discovered until someone called to complain.
Additionally, there was no in-process documentation of what work had
been accomplished, so that an unexpected absence of one film librarian
meant that the other film librarian could not easily tell what requests
were extant and what remained to be done on each request. The top graph
in Figure 5 shows the baseline data. (Call (312) 424-9473 to obtain
a copy of Figure 5.)
The project team recommended a new SOP, the most important feature of
which was the creation of a tracking form so that each step of the process
was documented. The second graph in Figure 5 shows that the new SOP
was quite effective in eliminating outliers and in reducing the average
cycle time. During this period of time, our GEMS consultant was working
very closely with the mail-out film librarians to answer questions and
guide them through use of the new tools.
The third graph in Figure 5 demonstrates a return to the baseline state
after the consultant moved on to other mini-project teams and the mail-out
film librarians failed to comply with the new SOP. In response to this
regression to the old performance, a log-in sheet was created, a change
to strict first in, first out (FIFO) processing was implemented, a new
mail-out film librarian has joined the team, and a new supervisor has
begun monitoring the mail-out team's performance more closely. The fourth
graph in Figure 5 shows that this refocused attention to the SOP has
reduced the mean and median cycle times, but unfortunately has not yet
reduced the long-cycle-time outliers to an acceptable level. We are
gathering detailed data about the outliers to better understand the
reason for their existence and to develop methods to minimize their
occurrence. (See Kotter [1996] for an excellent discussion of change
management.)
CULTURE,
POWER DIFFERENTIALS, AND OTHER FACTORS THAT CAN COMPROMISE THE SUCCESS
OF A SIX SIGMA PROJECT IN A MEDICAL ENVIRONMENT
The factors discussed in this section can make or break a Six Sigma
performance improvement effort. None of them is specifically a Six Sigma
issue, but, rather, each is an issue that any performance improvement
project may face. They rise to a higher level of importance in a Six
Sigma project, because Six Sigma projects have high expectations and
require heavy investment of institutional resources. Failure of a Six
Sigma project can be significantly more painful than failure of a CQI
project.
The
STAT Trump Card
Processes and staffing levels in a film library always address the various
levels of urgency expected. When a single STAT request arrives in isolation,
it is usually handled well. When multiple STAT requests arrive within
a short time period, the film librarians triage the requests to the
best of their ability and make sure that all such requests are completed
as quickly as possible. Some requestors inevitably will feel that their
requests routinely take too long, so they will begin labeling all of
their requests as STAT. If too many requestors adopt this approach,
the SOP that was so carefully crafted to handle STAT and routine requests
in a timely, orderly manner begins to unravel.
Most
Customers "Outrank" Film Librarians
The customers of a film library include patients, physicians (including
radiologists), nurses, and clinic managers and their representatives.
Each of these types of customers "outranks" the frontline
film librarian. The institutional customers are usually in a higher
pay grade position. Even many patients have higher educational levels
than the film librarians. When conflicts arise, the film librarian is
in an inferior position to defend and enforce film library policies.
For many film librarians, the response is to accede to the insistent
or irate customer. The result is a violated SOP and the occurrence of
the downstream negative consequences the SOP was developed to avoid
in the first place.
A more insidious result is that the film librarians begin to feel that
their skills are undervalued and that no one respects them. By this
point, SOPs are either routinely ignored or the enforcement of SOPs
has led to ugly confrontations. A major task of the film library leadership
team is to educate institutional leaders about the importance of compliance
with film library SOPs. Institutional leaders, in turn, must demonstrate
a firm, public commitment to enforcement of film library SOPs. If certain
physicians or clinics are permitted to thumb their noses at the SOPs,
word will get around to the entire institution and all of the hard work
invested in the Six Sigma project will be wasted. Additionally, turnover
of the truly excellent film librarians is likely to be high, because
good workers will not endure such unsatisfactory working conditions.
Changes
Are Difficult to Communicate and Sustain in a 24/7 Operation
As mentioned earlier, around-the-clock operation presents the challenge
of establishing a two-way dialogue with workers on the shifts other
than the weekday day-shift. During the early phases of a Six Sigma project,
it was seen to be difficult to include all shifts in project team meetings.
During the Implement and Control phases, it is equally difficult to
ensure that new processes are implemented properly, then sustained,
on all shifts. Special efforts must be devoted to monitoring off-shift
performance and following up quickly when the data indicate that performance
is not up to expectations.
Non-Film
Library Stakeholders can Refuse to Change Behaviors
The film library affects and is affected by many elements of the institution
outside of the radiology department, yet the film library leadership
team has no control, and very little influence, over them. Upper management
must recognize the important role of film library SOP compliance in
accomplishing the objectives of the institution and must be prepared
to be firm with physicians, nurses, and clinic personnel who fail to
comply. For example, a film jacket loan period of 24 hours is established
for on-campus borrowers. A physician may check out a film jacket and
fail to return it promptly. When the film library receives another request
for that film jacket, the physician may refuse to release it, thereby
jeopardizing the patient's care by delaying access of the second requestor.
A very clear message must be sent from the medical staff office that
such behavior is unacceptable. If the physician happens to be the chief
of surgery or the biggest revenue generator in the institution, the
situation can become quite uncomfortable. Nevertheless, favored treatment
of any person eventually leads to everyone expecting the same favored
treatment.
A related aspect is the belief by some radiologists that, because the
film library is part of radiology, radiologists should have higher priority
when competing requests occur. For example, a patient may be scheduled
for a clinic visit in the morning and a radiology procedure in the afternoon.
Because the radiologist fears that the clinic will not return the films
in time for the afternoon procedure, causing the radiology department
to have a protracted cycle time, the radiologist may instruct the film
library to never send films to a clinic when there is a radiology procedure
the same day. If this is allowed to continue, the underlying issue of
getting the films from the clinic to the radiology department in a timely
manner is ignored, whereas it may be solvable with little effort. In
the meantime, however, the physician who did not have the films available
for clinic visits is going to bad-mouth the film library. Thus, the
film library will get the rap for something that is turf-related and
outside of the influence of the film library leadership team.
Film
Librarian Job Is Rarely a Career Choice
In too many institutions, the film librarian position is barely above
the housekeeping and dietary aide positions. The film library is viewed
by employees as a stepping stone from the minimum wage jobs up to the
"good" jobs. Their motivation is acquiring work experience
and finding a better job, not becoming an excellent film librarian.
When faced with the necessity to be self-starting or to go out of their
way to satisfy an urgent or unusual request, it is unwise to expect
them to rise to the occasion.
Tight
Labor Markets
At the time this thesis was written, unemployment was at very low levels.
A good film librarian quickly learns that he or she has acquired computer,
time management, and customer service skills that may be much more richly
rewarded in higher paying positions. Turnover will be high unless film
librarian pay rates are upgraded to remain competitive.
Tight labor markets make it more difficult to attract good candidates
for film library positions. Film libraries "offer" a high
pressure, high volume, physically taxing, low pay environment. Even
when candidates are relatively plentiful, it is difficult to attract
and retain good people. When job candidates have lots of options, film
libraries have a tough time winning them over.
A less obvious concern about tight labor markets is that managers are
more likely to tolerate an employee who exhibits substandard performance,
reasoning that substandard performance is better than having a vacancy.
The reader of this thesis readily sees the fallacy of this argument,
but the manager who is in the thick of the battle and who will feel
the pain of the vacancy has a more difficult time coming to terms with
it.
Job
Security Issues as Radiology Moves to Filmless Operation
Radiology is making a transition to filmless operation. In some large
institutions, the transition is well underway, even to the point where
no films are being generated for routine clinical exams. As the film
librarians (and candidates for vacant positions) begin to notice this
transition, they quickly realize that the need for their jobs is going
to disappear within a few years. This realization does not necessarily
cause employee motivation to rise (Johnson 1998), and it certainly contributes
to turnover among the good employees, who are able to find employment
elsewhere.
A Six
Sigma Project Will Be Expensive
A Six Sigma project is commissioned to solve a major problem, so the
stakes on the outcome side are high. It should not be a surprise that
a major payoff requires a major investment of institutional resources.
A major Six Sigma project will require participation of key people from
multiple components of the institution, all of whose time will represent
a loss from their usual duties. Upper management must understand that
performance in these usual duties will suffer, and the leaders of these
areas must be shown tolerance for any reduced performance.
Not only must all stakeholders be involved, but only the best of the
stakeholders should be involved. The project leader must be an experienced,
accomplished employee. When this person is diverted from his or her
normal duties for an extended time, the employee's supervisor is likely
to feel considerable pain due to the employee's absence. Likewise, the
best technologists, the best nurses, and the best clerks will be selected,
again causing pain during their team meeting absences.
A Six Sigma project is data driven. Most institutional information systems
are not set up to allow non-IS personnel to extract data that are meaningful
to the project team. Thus, one or more IS personnel will need to be
assigned in support of the team, because a Six Sigma project without
data may be worse than doing nothing.
Obtaining
Cooperation from Borrowers
A film library has many stakeholders. A partial list includes referring
physicians, radiologists, patients, film librarians, clinics, radiology
sections, and outside institutions. The film library manager has operational
authority over only one of these groups. The other groups are not only
not under the control of the film library manager, but they "outrank"
the film library manager when disputes arise. If a clinic using a film
jacket transfers the jacket to another clinic for a consultation but
fails to tell the film library, the RIS will show the film jacket to
be in the original clinic. A subsequent requestor will have to wait
while the film library calls the original clinic and eventually tracks
down the film jacket.
What impact does this lack of cooperation from borrowers have on the
film library's Six Sigma performance? If one of the Six Sigma metrics
is "time from request of a film jacket until film jacket delivered
to requestor," any failure to release a film jacket, or any undocumented
transfer of a film jacket, is going to show up as a higher-than-specification
transaction. If one of the Six Sigma metrics is a question on a satisfaction
survey that asks the physicians' agreement with the statement, "The
film library always retrieves film jackets promptly for me," the
metric will suffer.
Another way that lack of cooperation appears is what Harry and Schroeder
(2000) call "the hidden factory." The hidden factory is the
many actions performed by film librarians to compensate for failures
in earlier handling of a film jacket. In the improper jacket transfer
described in the preceding paragraphs, the film jacket may have been
checked out to Clinic A. A physician in Clinic A took the film jacket
to Clinic B and gave it to another physician for an informal consultation.
In all likelihood, the Clinic A physician did not tell anyone else in
Clinic A what he was doing, and the physician in Clinic B did not tell
anyone in Clinic B that she had the film jacket. When a third physician
comes to the film library loan window looking for the film jacket, the
film librarian will look up the jacket in the RIS. Seeing that the jacket
is checked out to Clinic A, the film librarian will call Clinic A and
talk to the front desk receptionist. The receptionist will ask if anyone
knows anything about the film jacket. After an extended hold on the
telephone, the receptionist will deny that Clinic A has the film jacket.
The film librarian will then look up the patient's appointment schedule
in the HIS, figure out the name of the physician who actually saw the
patient, and call the clinic asking to speak with the physician. With
luck, the physician's nurse will tell the film librarian that the physician
mentioned taking the film jacket to Clinic B for a consultation; the
nurse will not remember that a physician's name was mentioned. The film
librarian will call Clinic B and talk to the front desk receptionist.
The receptionist will look on their film jacket cart and will not see
the patient's film jacket, and he will not see the patient on their
appointment list, so he will deny any knowledge of the film jacket.
If the film librarian is persistent enough, more phone calls and/or
visits to Clinic A and Clinic B searching for the film jacket will occur,
and the film jacket will eventually be found and checked out to the
new borrower.
If the Clinic A physician or the Clinic B physician had made a 30-second
call to the film library to report the transfer, this entire saga could
have been avoided. As it was, the new requestor was frustrated, the
film librarian was frustrated, the personnel in the clinics were frustrated,
and valuable time was lost by a lot of highly paid people. But all of
this frustration and waste is undocumented and not visible-it is the
hidden factory that eventually turns a poor-quality situation into an
acceptable situation, but at great cost.
CONCLUSIONS
When we set out to "fix the film library," we knew that Six
Sigma tools had worked very well for our CT throughput problem. We also
felt that the fundamental Six Sigma philosophy could be used in a film
library environment. But we were less sure about the degree of adaptation
we would need to make, because many of the Six Sigma tools are best
suited for a manufacturing model.
The basic concept that any process could be subjected to the Define-Measure-Analyze-Improve-Control
(DMAIC) analysis proved to be true. The DMAIC technique appears to be
equally applicable to the manufacturing model and to the services model.
Having said that, however, it is much more difficult to acquire data
for a service-model process than for a manufacturing-model process.
The Measure and Control phases are a much bigger challenge for the service-model
process, because the subprocesses themselves may be harder to quantify
and the data may be difficult to gather once a metric is determined.
A Six Sigma project requires a sizable investment of institutional resources,
primarily in terms of the time spent away from their regular jobs by
the best people in each stakeholder category while participating in
Six Sigma project team meetings and in doing any project "homework."
Also, most Six Sigma projects would benefit from having a full-time
leader assigned to the project, rather than asking someone to try to
fulfill Six Sigma responsibilities in addition to his or her regular
duties. Insti |