Medication Safety Arrives Just-in-Time
Employing Toyota Production System concepts to ensure medication safety.
A woman is admitted to the hospital with a fractured femur and is gven an order for ondansetron (Zofran) for post-op nausea. Her condition worsens with vomiting, headache, diaphoresis and abdominal cramps. After examining the infusing IV bag, the nurse sees that the patient has received another patient's metronidazole (Flagyl). The patient's roommate received her ondansetron.
An assembly line worker at Yamada Electric assembles devices that have two push-buttons. For each device, a spring must be placed under each of the two buttons. The job is repetitive and if the worker is distracted she may forget to put a spring under one of the two buttons causing a defect in the finished product.
The Nature of Error
What do these two errors have in common? More than you might think.
First, neither the nurse nor the worker was cognizant of the error that
she had made. Both individuals
experienced what is known as a "slip" to human factors experts.(1) The nurse mentally transposed two tasks -
incorrectly telling herself where she wanted to hang each bag. The worker lost track of where she was in
her task, possibly due to an interruption in her work. These slips are an unavoidable fact of human
nature. Have you ever walked into a
room and forgotten why you went there?
Or put the milk away in the cupboard rather than in the refrigerator? We
all make these slips from time to time. While generally harmless, slips in the
production process cost companies millions of dollars each year. In healthcare,
slips in patient care can cost lives.
The good news is that slips are easily managed. In either case, a simple check would have
alerted the individual to her slip and avoided the error. For the worker, the solution could be as
easy as employing a small dish.(2,3) Preceding each
assembly, she would count out two springs from a bin and place them in the
small dish. After assembly is complete, but before she passes the device on
down the line, she could look at the dish. If a spring remains, an error has
occurred. The worker knows a spring has been omitted and she can correct the
omission immediately. Likewise, if
barcoded patient identification tags had been scanned and matched to each
patientís medication order before the nurse hung either i.v. bag, the nurseís
slip would have been caught prior to administration. A barcode-enabled point of
care (BPOC) system would alert the nurse with a visual or audible message
relaying the patient/medication mismatch. The cost of inspection (looking at
the dish or running the barcode scanner) is minimal yet effective. Employing
failsafe mechanisms such as these is at the core of the world renowned Toyota
Production System (TPS) and a driving force in Japan's remarkable quality
improvement success.
This comparison of two quality improvement processes - increased patient
safety through medication error reduction and Toyota's quest for lower costs
through zero-defect production - evaluates some of the similarities, boundaries
and practical applications of TPS' core principles within the medication use
process. The intent in highlighting the
correlation is to illustrate the potential of BPOC technology in the context of
a success story that in many ways has followed a parallel course.
TPS and The Medication Use Process
It is interesting to note that an environmental correlation can be drawn
between the climate that gave birth to the TPS after World War II and the
current challenges facing inpatient healthcare. The concept of TPS was established in recognition of Japan's lack
of natural resources, making the cost of raw materials disadvantageous when
compared to European and American countries.(4) To overcome this handicap, it was essential
for Japanese industries to produce better quality goods at a lower production
cost than those of the other countries.
Likewise, the contemporary issue of patient safety is more than a risk
management or public relations problem. The U.S. Attorney General's office has
estimated that more than $.30 on every healthcare dollar is wasted. Just as it
did in the auto industry in the 1980s, improving quality through error
reduction can drive down healthcare costs. Reducing error may be the key to
resurrecting the financial health of more than 50 percent of US hospitals that
operate with less than a 3 percent profit margin.(5)
Another defining factor of the TPS was the need to reduce labor costs in
order to be competitive. Toyota employed teams of multi-skilled workers
operating highly flexible and increasingly automated machines to produce
volumes of products in enormous variety.(4) While we rarely regard our nation's healthcare labor force
shortage as advantageous, tight resources may, in part, be credited with
creating a highly skilled and flexible nursing profession. Nurses epitomize an ideal multi-tasking
workforce able to perform numerous activities and take responsibility for their
own process improvement.
One further similarity exists between the TPS ideal and the state of our
medication use process today. TPS was
designed to forecast based on actual demand(6), that is the number of goods already requested by
customers. To determine actual demand,
car dealers around Japan send daily reports to Toyota - the resulting data
serves as the production requirements for the plants. The ultimate goal of the TPS is to create a production
environment capable of delivering a single unit as it is ordered.(7)
The philosophy behind "just-in-time" (JIT) production is not to sell
products produced, but to produce products to replenish those that have been
sold. To do this, JIT production supplies the right parts at exactly the right
time and in exactly the right amount at every step in the process. Sound
familiar? These are the very principles that shape modern pharmaceutical care.
Demand for medications is not forecasted but rather met by a supply based on
dynamic orders, patient reactions, lab results and a myriad of other
factors. Enormous effort made in the
past 20 years has resulted in a pharmaceutical standard of the "unit dose."(8)
This factor uniquely positions hospitals to implement many of the
quality improvement concepts that have served Toyota so well.
TPS Forces at Play in Medication Administration
The Japanese are good at manufacturing. Just ask any global producer
with whom they competed in the 1980s. The competitors will probably tell you
how the Japanese captured a large share of the global-market by creating
world-class standards in design, materials, and management. How did they do
it? They created a comprehensive system
built on three core concepts and then honed that system over several decades.
These same concepts, illustrated in detail below, may serve healthcare leaders
well in improving medication use for optimal patient outcomes.
First, kanban is a simple parts-movement system that enables JIT
production of goods by moving parts from one workstation to another on a
production line. The essence of the kanban concept is that a supplier should
only deliver components to the production line when they are needed, so that
there is no storage in the production area.(9) Within this system,
workstations only produce/deliver desired components when they receive a card
and an empty container, indicating that more parts will be needed in
production. This concept is fundamental
to American hospitals as evidenced by the effort to remove dangerous and often
misused floorstock drugs from patient care areas. Today, round-the-clock pharmacies may be automatically prompted
to provide the medications necessary to replenish empty dispensing drawers as
needed to fulfill the physicians order.
The second feature of the TPS that can bring immeasurable value to the
medication use process is the aforementioned use of failsafe devices known in
Japan as poka-yoke. A poka-yoke device is any mechanism that either
prevents a mistake from being made or makes the mistake obvious at a glance.(10)
The ability to detect a mistake at a glance prior to production means
that the error does not reach the customer and the source of error is limited
to prior steps in the process. Poka-yoke devices fall into two major
categories: prevention and detection.(11) A prevention device
engineers the process so that it is impossible to make a mistake at all. In
healthcare, we commonly refer to similar conventions as "forcing functions".(12,2)
Consider the method employed in anesthesia to eliminate the confusion of
oxygen tanks with other gases. Hoses that fit oxygen tanks will not connect to
other sorts of tanks, virtually eliminating accidental administration of the
wrong gas. A detection device typically warns the user of a problem, but it
does not enforce the correction. We are surrounded every day by both detection
and prevention poka-yoke devices. A microwave will not work if the door is open
(a prevention device). A car beeps if the key is left in the ignition (a
detection device). A few years ago, some cars were designed not to start until
the passengers had buckled their seat belts (a prevention device); but this
mechanism was too intrusive and was replaced by a warning beep (a detection
device).(11)
In healthcare as in manufacturing, quality assurance is largely reliant
on inspection. Self-inspection relies on the worker to inspect the
product he/she processes. Often, the worker may compromise judgments and accept
items that ought to be rejected or make inspection errors unintentionally due
to fatigue, stress, or other pressures.(2) This is similar to the current expectation placed on nurses
to intercept all errors in the medication use process at the tail end of the
production chain - during administration. A better technique, successive
inspection, provides objectivity.(2) Workers inspect
products passed along from the previous operation before processing them on
themselves. On average an 80-90%(7) reduction in the number of manufacturing defects can be achieved by
adopting successive inspection. Successive inspection techniques have long been
used by pharmacists and nurses to intercept as many as 70% of the errors made
in the medication use process prior to administration.(13)
However, successive checks rely on human factors to detect error and
fail to provide rapid feedback when errors occur. When enhanced with a poka-yoke device, the nurse can consistently
ensure that proper conditions exist prior to administration.
Finally, the concept of kaizen, meaning continuous improvement,
is central to all TPS success and imperative for healthcare organizations to
achieve patient safety. Toyota team members are responsible for their own
improvement - taught to kaizen their jobs to achieve higher efficiency, better
quality and lower costs.(10) This is challenging in the medical environment where inter-disciplinary
dependencies are great and errors are passed along through many hands.
Politics, power dynamics and ownership issues quickly surface in this
environment. However, until quality can
be assured at the intermediate steps, mutli-disciplinary teams are necessary to
resolve quality issues. When a comprehensive medication management solution is
realized, it will address all the components of the process: ordering, clinical
checking, transcription, drug distribution, automated drug-dispensing-device
interfaces, positive patient/drug identification via barcodes, documentation of
medication administration, patient monitoring, charge capture based on
administration, supply chain management and error and outcomes analysis.(6)
Each step in the process will then be subject to enhanced checks and
each discrete team can take responsibility for kaizen related to their daily
work.
BPOC Measures Up
Nursing activities such as medication administration are highly
responsive to the implementation of poka-yoke devices because most errors made
in nursing practice are slips (errors in execution) rather than errors in
planning.(1) BPOC systems exemplify technology designed to manage slips
in that they do not merely examine administrations after the fact (for example
through retrospective chart review). Instead, they provide for before-the-fact,
enhanced self inspection whereby errors are intercepted prior to administering
the medication. The systems safeguard the bedside, enabling immediate feedback
to the nurse. Also, BPOC is designed to
stop predefined errors. The dish in the
manufacturing example kept the worker from forgetting to insert a spring. It would
not detect, for instance, a situation where the worker accidentally dropped a
spring on the ground without noticing.(13) What's more, a
worker wishing to ignore a spring remaining in the dish could do so. Likewise,
a BPOC system is focused on preventing specific errors rather than detecting
all possible errors in the medication use process. While the system can provide a "do not crush" warning for certain
medications, it cannot ensure that the nurse heeds this warning.
Another parallel between the conventions of the TPS and
the design of BPOC technology is the real-time nature of the supplier
(pharmacy) to production (nursing) relationship. Just as uninterrupted flow is critical to JIT production, the
immediate and accurate response of the pharmacist underlies the quality of
every administration. By communicating
with the pharmacy information system via a real-time connection, nurses are
able to act upon new and modified orders as they enter the system. Future developments in BPOC technology will
extend the system's communication abilities to yet another supplier, the
laboratory. The result is a
computerized version of the kanban system providing clinical information to
each caregiver necessary to effectively deliver medication therapies to the patient.
As a detection device, BPOC systems impact nursing
behavior by providing visual and/or audible alerts when a potential error is
detected. For example, a warning appears on the computer screen when a
medication is scanned that, if administered, would put the patient over the
safe maximum daily dose limit. Systems
may also be configured to provide messages based on, but not central to the
medication administration. Much like a
car will warn the driver of low oil levels while the car is still operable, a
BPOC system may offer a comment that the medication scanned has a sound-alike
drug and remind the nurse of the appropriate indication for each therapy. In addition, a well-designed BPOC system
will proactively guard against common slips by providing worklists and by
clearly indicating one's position in the process flow.
There is one final comparison worthy of comment. BPOC technology is the medical equivalent to
aviation's "black-box" recording device.
One of the great challenges in the analysis of human error is obtaining
enough data to understand how an accident occurred. Computers have the ability
to record user actions automatically much the way "black boxes" in airplanes
record all vital flight information.(1) BPOC incorporates
such tracking features in order to analyze problems when they do occur. This
information is critical to carrying out the steps of effective kaizen. When error trends are detected, a plan is
established to improve the process.
Small-scale changes are carried out and the results are observed and
tracked. With these data, hospitals can
evaluate the result and determine whether an improvement has been
achieved. Without this analysis, little
can be known about the impact of error reduction measures. Despite significant hospital investments in
information technology, quality management experts cite an "analytical gap" as
a major reason that clinical care is not better managed and patterns of medical
errors are missed.(6)
Additional sources of capital will not become available for information
technology investment until more healthcare executives can be persuaded that
the business case for care management has real payoff in the form of eliminated
"rework" due to sub-optimal patient outcomes and reduced costs of malpractice
risks.(6) In response to the
medication error problem, the analytical gap is bridged by the implementation
of BPOC technology.
Why now?
Today there is a resurgence of interest among automakers in cost
reduction through quality improvement.
However, unlike the legendary efforts of Toyota, the current effort is
firmly rooted in the American automotive industry and the focus is on tackling
the rising cost of employee healthcare. Healthcare benefits saddle US
automakers with an exorbitant expense, about $800 to $1,200 per vehicle(14), that foreign
competitors often do not carry. From 1999 to 2000, healthcare expenses at
General Motors jumped $300 million, to $3.9 billion for coverage of its 1.2
million beneficiaries(17). The situation is escalating as a large
number of GM employees are aged 40-54, a life stage when healthcare costs
usually peak. That means on top of already high rates of health-care inflation,
GM is expecting a surge in healthcare costs that could last for two decades. In
response to this situation, GM, the largest private purchaser of healthcare in
the nation, has spearheaded an effort to advocate widespread adoption of error
reduction practices including the computerization of the medication use
process. Where healthcare professionals and government regulators have
struggled to do so, automotive employers have offered up viable best practices
for improving the quality of care from a most unlikely source -
manufacturing.
Association
for Manufacturing Excellence: www.ame.org.
Associate
Press. The Arizona Republic, Monday, June 11, 2001.
Balakrishnan,
R. The Toyota Production System: A Case study of Creativity and Innovation in
Automotive Engineering.
Bernstein,
Jack. (1984) "GM exec discusses commitment to kanban; system has
'tremendous potential,' he says. (Leonard J. Ricard)" Automotive News, Nov
19, p48(1).
Coile,
Russel C. Quality Pays: A Case for Improving Clinical Care and Reducing Medical
Errors. Journal of Healthcare Management, Vol. 46, Num 3, May/June 2001.
Felciano,
Ramon M. "Human Error as a Toll in Designing Health care Information Systems."
Journal Club Talk, February 7, 1995.
Grout, John
R. and Brian T. Downs. A Brief Tutorial on Mistake-proofing, Poka-yoke and ZQC.
Available at: www.campbell.berry.edu/ faculty/jgrout/ tutorial.html
Jacobs,
Raymond A. Just-In-Time (JIT) Production, Ashland University web page.
Leape,
Lucian. Systems Analysis of Adverse Drug Events. Journal of the American
Medical Association, Vol. 274, No. 1, 1995
Norman,
D.A. The design of everyday things. New York Doubleday,1989.
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Toyota Production System. Available at:
Ohno,
Taichi. Toyota Production System: Beyond Large Scale Production. 1978.
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Ashok. Japanese Management Systems. De Montfort University Web Page
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Harry. Paper presented at the Sixth International Conference on Software
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Shingo, A Study of the Toyota Production System Form an Industrial Engineering
Viewpoint, 1989.
Shingo, Shigeo. Zero quality
control: source inspection and the poka-yoke system. A.P. Dillion. Portland,
Oregon: Productivity Press. 1986.trans.
LEGISLATIVE & REGULATORY
State Legislation
New York
The New York Public Interest Research Group estimates that New York's
pharmacists, physicians and hospitals make more than 3 million medication
errors each year, and that 500 deaths are a direct result. Because health care
personnel are not required to report prescription errors, the actual totals are
unknown. Richard Gottfried (D-Manhattan), chairman of the Assembly Health
Committee, said he expects his bill requiring all medical personnel to report
errors to pass the Assembly this summer.
New York Sen. Chuck Schumer's bill, the Health
Information Technology and Quality Improvement Act of 2001, would allocate $355
million to hospitals nationwide to use toward implementing computerized
prescription systems in hospitals. Unlike the Medication Errors Reduction Act
of 2001, however, the Schumer bill has no Republican co-sponsors.
Massachusetts
Massachusetts State senators Richard T. Moore, Dianne Wilkerson, and
Bruce E. Tarr introduced SB571. The
legislation would provide payment of a one-time bonus to healthcare providers
for the implementation of medical error reduction technology. Funding would go to facilities that certify
to the commissioner that they have implemented a comprehensive computerized
medication order entry system or other computerized system designed to
identify, track and prevent medical errors.
Missouri
Missouri bill HB620 put forth by Republican Rep. James V. Froelker,
requires the Department of Health to develop recommendations on methods of
reducing medication errors. "The methods include increasing prescription legibility,
developing medication error reporting plans, minimizing the confusion in
prescription drug labeling and packaging, and increasing patient education
concerning prescribed medications."
The department is required to submit the
recommendations to the General Assembly by January 1, 2002.
Connecticut
Bill 6941, introduced before the General Assembly, requires the adoption
of a plan to substantially reduce or eliminate medical errors by hospitals,
outpatient surgical facilities and outpatient clinics and the establishment of
a related reporting system. All healthcare providers must submit a plan to the
commissioner for approval.
Nevada
The Nevada legislature is considering a resolution that directs the
Legislative Committee on Health Care to conduct an interim study concerning
development of systems for reporting medical errors.
Oklahoma
Oklahoma is the first state to provide legal protection to the MedMARx
database, which is administered by U.S. Pharmacopeia (USP). Through the
database, health care professionals can report anonymously on drug errors and
compare anonymously their hospital to others to follow trends and pinpoint
problem areas. The new legal protection also applies to USP's Medication Errors
Reporting Program, which it runs in cooperation with the Institute for Safe
Medication Practices.
Minnesota
Minnesota Gov. Jesse Ventura signed a groundbreaking new law, Senate
File 560. The law changes the Minnesota Peer Review Statute, which previously
inhibited the exchange of information from one hospital to the next for fear of
litigation. In essence, the law will
help improve communication between health care organizations and help hospitals
learn from adverse events and near misses by allowing hospitals, doctors and
medical staff to anonymously report medical errors in a web-based registry that
can be aggregated and accessed by other health care professionals and the
public.
Florida
The state would be able to post accounts of medical mistakes on the
Internet under a patient safety bill HB 1895.
Hospitals and surgical centers would be required to summarize and post
"adverse incident reports" quarterly on a state website, so that health
professionals could watch for trends and learn from one another's failures.
FEDERAL ACTIONS
Senate Bill Takes on Medication Error Reduction
Sens. Bob Graham and Olympia Snowe introduced the Medication Errors
Reduction Act of 2001 (S.824) that would give hospitals and skilled nursing
homes $97.5 million in grants from 2002-2011 to offset the costs of
error-reducing technology. Health care facilities would have the option of
choosing between a myriad of available error-reducing technologies, including
computer physician order entry, bedside verification through the use of bar
codes and use of a hand-held computerized scanner, electronic medical record
systems, and automated pharmacy dispensing systems.
HHS Task Force to Improve Patient Safety Standards
HHS Secretary Tommy Thompson announced the establishment of a new
Patient Safety Task Force within HHS that will coordinate a joint effort among
several agencies to improve existing systems to collect data on patient safety.
To fund this effort, HHS' fiscal 2002 budget proposal includes up to $72
million, an increase of $15 million over FY 2001.
Website on Medical Mistakes
The Patient Safety Task Force introduced by HHS Secretary Tommy Thompson
will spearhead the implementation of an Internet-based reporting system to
minimize the burden of reporting adverse events and errors. The Centers for
Disease Control and Prevention and the Food and Drug Administration will
provide data on medical errors while the Agency for Healthcare Research and
Quality will analyze the causes of medical errors. President Bush is asking
Congress for $12 million in start-up money for the medical-error reporting
system, which, officials say, is part of a larger effort to reduce medical
mistakes. n The Washington Post
TalkingQuality.gov
Non-governmental initiatives to disseminate health care quality
comparative data and develop medical error reduction strategies are being
encouraged by state agencies as well as Congress and the federal government.
HHS' Agency for Health Care Research and Quality is developing a website -
"talkingquality.gov" - that will publish a workbook for entities interested in
developing health plan comparative information websites and publications. The
site is expected to be operational soon.
Testimony on New Technology
Some senators are calling for nearly $1 billion to help hospitals and
technology companies invest in devices to avoid more deaths and injuries.
Products demonstrated during a hearing for the Senate Special Committee on
Aging included Pharmacy dispensing robotics, barcode enabled point of care
systems, computerized documentation, talking pill bottles, and others. n Health News Daily,
Volume 13, Issue 112
Secretary
Thompson Testifies Before Senate Committee
In his testimony to the Senate HELP committee, Sec. Thompson pointed to
the inadequate systems of care that result in approximately $29 billion in
excess healthcare expenditures and lost productivity each year. He then offered up what he calls a "very
promising way to improve healthcare safety."
"First there's great potential for using the bar-coding
technology, so prevalent in our society today, as an effective safeguard
against medical mistakes. Doctors and nurses would be able to scan the barcode
on a bracelet worn by a patient to monitor what medications they are [giving]
and effectively administer those medicines to those patients. Grocers and
everybody [who has] been in a checkout line has watched this technology record
our purchase of over the counter drugs. And this simple technology could be
used to track the dispensing and the usage of pharmaceuticals to prevent
mistakes. Simple human errors would be curtailed significantly. Bar coding
would also reduce stress on overworked nurses and provide real cost savings."
Cohen Testifies Before house
Michael R. Cohen, president of the Institute for Safe Medication
Practices (ISMP) testified before the Subcommittee on Health of the House
Committee on Ways and Means Hearing on Medicare Reform. Mr. Cohen said that
purchasers of pharmacy services payers - including Medicare - should require
providers to comply with standards most likely to enhance medication safety
including the effective use of technologies such as robotics, bar coding of
pharmaceuticals and computerized prescriptions. He encouraged the creation of
incentives to reward healthcare organizations that adopt technology known to
reduce medication errors.
JCAHO
Similar-Sounding Drug Names Contribute to Medical Mistakes
The Joint Commission on
Accreditation of Healthcare Organizations last week alerted nearly 19,000
hospitals, clinics and nursing homes to the potentially life-threatening consequences
of mixing up similar-sounding brand and generic drug names. To help reduce the
number of incorrect prescriptions, the commission advised health-care
organizations to make sure that prescriptions include the purpose of the
medication; that all drug labels include both the generic and brand name and
that patients receive written information about their medications that includes
the brand name and generic name.
n Los Angeles
Times, Monday, June 4, 2001
Put JCAHO and ISMP Newsletters To Work
Since February 1998 JCAHO has published the Sentinel Event Alert to
provide important information about the occurrence and management of sentinel
events in accredited organizations. Since January 1, 2001, JCAHO has required
organizations that seek accreditation to proactively address all issues covered
in the Sentinel Event Alert in an effort to prevent similar occurrences in
their own organizations. JCAHO expects healthcare organizations to address
suggestions made in future issues of Sentinel Event Alert within 45 days of the
publication's release. So far, there have been five Sentinel Event Alert
publications that deal with medication error reduction and ISMP has contributed
to the content of each:
May 2001:
Look-alike, Sound-alike Drug Names
February 2001:
Mix-up Leads to a Medication Error
November 2000:
Infusion Pumps: Preventing Future Adverse Events
November 1999:
High-Alert Medications and Patient Safety
February 1998: Medication Error
Prevention - Potassium Chloride
A future issue is expected to deal with dangerous abbreviations. n ISMP Medication Safety Alert!
Volume 6, Issue 13
Hospitals Must Tell Patients of Mistakes
Beginning July 1st,
hospitals will be required to tell patients when they've been victims of
medical errors under new safety standards put forth by the Joint Commission on
Accreditation of Healthcare Organizations, a nonprofit group that monitors
nearly 5,000 hospitals nationwide. Under the guidelines, hospitals that don't
discuss harmful mistakes with patients and fail to prove to commission
investigators that they're doing so will risk losing their accreditation. To
aid in meeting this standard, Congress is calling for nearly $1 billion to help
hospitals and technology companies invest in devices to avoid medical errors. n Detroit News
RESEARCH
AHRQ Paper on Reducing and Preventing ADEs
In a recent paper The Agency for Healthcare Research and Quality (AHRQ)
describes various ways to reduce and prevent Adverse Drug Events (ADEs). This paper summarizes research funded by
AHRQ, and outlines topics for new research.
Some interesting findings include:
Patients who experienced adverse drug events
(ADEs) were hospitalized an average of 8 to 12 days longer than patients who
did not suffer ADEs, and their hospitalization cost $16,000 to $24,000 more.
28% to 95% of ADEs can be prevented by
reducing medication errors through computerized monitoring systems.
Computerized order entry has the potential
to prevent an estimated 84 percent of dose, frequency, and route errors.
Hospitals
can save as much as $500,000 annually in direct costs by using computerized
systems.
Costs of Drug Related Problems on the Rise
A recent study published in the "Journal of the American Pharmaceutical
Association" updates a 1995 estimate of $76.6 billion for the annual cost of
drug-related morbidity and mortality resulting from drug-related problems
(DRPs) in the ambulatory setting. This
study updated Johnson and Bootman's 1995 cost-of-illness model assessing the
morbidity and mortality associated with DRPs. Since 1995, the costs associated
with DRPs have more than doubled to an estimated annual average of $177.4
billion.
NCCMERP Revises Medication Error Index
The National Coordinating Council for Medication Error Reporting and
Prevention (NCCMERP) has revised the Index for Categorizing Medication Errors.
This update of the 1996 Index considers factors such as whether the error
reached the patient and the severity of harm to the patient. Its primary
purpose is to help track medication errors in a consistent, systematic manner.
Nurses Cite Errors in Medications
One-third of 800 nurses surveyed said patients in their units missed
medications or had them delivered late at least once a week. Eight percent said
wrong dosages or drugs were given to patients each week. The survey was
conducted by a polling company for the Service Employees International Union,
amid a push for federal action to combat the nursing shortage. n The Atlanta Constitution
Health care workers in poll see need for change
In a new survey sponsored by the Robert Wood Johnson Foundation of 1,000
medical workers, 95 percent of doctors said they had witnessed serious medical
errors. The physicians and a sampling
of nurses and executives gave the nation's Medicare system mediocre ratings
overall. 61 percent of health care providers surveyed said they accept common
errors as routine practice. Just 42 percent said the care is "very good" or
"excellent." One in five rated it poor to fair. Four of five agreed that
fundamental change was needed and one in 10 favored a complete overhaul of the
health care system. To jump-start a
solution, the RWJF will spend $20.9 million over three years to fund projects
by hospitals and doctor groups to improve health care.
IOM Report #3
The Institute of Medicine issued a new publication "Envisioning the
National Health Care Quality Report,"outlining its vision for the first annual
report on the quality of healthcare in the United States. The report, to be
issued sometime in the next three years by the Agency for Healthcare Research
and Quality, should be tailored to specific audiences, highlighting health care
quality achievements as well as shortcomings, and serving as a barometer to
gauge progress toward improving the health care delivery system's performance.
Children at Risk for Drug Errors
According to a study in the Journal
of the American Medical Association, potentially harmful medication errors are
three times more common among hospitalized children than adults. In a six-week
study at Children's Hospital in Boston and Massachusetts General Hospital for
Children, 616, or 5.7%, of 10,778 medication orders contained errors, the
majority of which occurred when physicians wrote the orders. The overall error
rate was similar to those found in previous studies of adult hospitals, but the
number of potentially harmful errors was three times greater. The study authors
say the results underscore the value of developing technology-based strategies
to help prevent medical mistakes. The researchers noted "Despite a
comprehensive multidisciplinary approach to data collection, we probably failed
to detect some errors, particularly administration errors detected by trained
observers following nurses during routine patient care."
n Modern
Healthcare
Principles of Pediatric Safety
The American Academy of Pediatrics
(AAP) now has new recommendations on how to protect children from medical
errors in a new policy statement entitled, "Principles of Patient Safety in
Pediatrics". The AAP urges health care organizations to take into account the
issues unique to pediatric patient safety. To lessen errors, the nation's
pediatricians call for more research into how information technology can
improve patient safety, since computerized ordering of medications has been
shown to decrease errors.
n June issue of Pediatrics
TAKING ACTION
PENNSYLVANIA PATIENT SAFETY COLLABORATIVE
The Pennsylvania Patient Safety Collaborative (PPSC) was officially
launched in May. The collaborative is a network of 24 organizations representing
health care providers, insurers, organized labor, private industry, and
consumers whose goal is to address the systematic issues that lead to medical
errors and to work to reduce patient injury from errors through identification
and correction of the causes of medical errors. Last month, the PPSC released a
monograph -- "Elements of a Culture of Safety."
Wisconsin Patient Safety Work Group
Representatives from a number of diverse organizations and health care
professionals have been meeting since May 2000 to consider methods to improve
patient safety and reduce medical errors in Wisconsin. Initial discussions focused on patient
safety initiatives in hospitals, extended care facilities, nursing homes and other
health care facilities.
Illinois appoints task force on Patient Safety
A 13-member task force appointed by Governor George H. Ryan to examine
issues related to patient safety in Illinois reported its findings and
recommendations for improving the Illinois health care system. According to the
report, one area that requires further review is the consideration of the
issues surrounding the automation or computerization of systems to increase
patient safety. Specifically, the task force identified a need for the state to
take steps to demonstrate a commitment to build an information infrastructure
that supports health care delivery with the "goal of eliminating most
handwritten clinical data by the end of the decade."
Rx Urged for Drug Errors in New York Hospitals
New York Public Interest Research
Group (NYPIRG), the Center for Medical Consumers and the Statewide Senior
Action Council of New York State have teamed up to call for statewide
legislation that would help eliminate pharmacists' dosage mix-ups and confusion
over similarly named drugs by mandating computerized prescription ordering and
dispensing systems in all hospitals, doctors offices and clinics.
n Times Union
Albany, NY
Bar Coding Injectables
American Pharmaceutical Partners, Inc. (APP), a supplier of specialty
injectables in the U.S. is taking a leadership role in the efforts to reduce
medication errors with plans to introduce bar codes for all sizes of
products. Currently, all of APP's
products packaged in 50 mL or larger vials incorporate a bar code on the
individual vial. Going forward, APP's plan is to bar code new products, even
individual vials as small as 2 mL. These products can be easily read by most
scanning systems currently available.
"Since it appears that bar code technology may eventually be universally
required in most healthcare facilities, our bar coded injectables will
facilitate the adoption of this important technology," said Jeffrey Yordon,
Chief Operating Officer of APP.
n PRNewswire
HMOs To Monitor Patient Safety
Joining a growing number of health plans nationwide, Blue Cross and Blue
Shield of Massachusetts and Tufts Health Plan have hired companies with
sophisticated computer software to search patients' insurance claims and
pharmacy records to identify those who are not receiving, or may not be
obeying, the best medical treatment for their condition. Armed with lists of
potential medical errors, medication conflicts, and cases of noncompliance,
company or HMO nurses will call these patients or their doctors and try to
persuade them to change. n The Boston Globe
ASHP Adopts Barcoding Policy
The American Society of Health-System Pharmacists House of Delegates met
this past June to discuss the use of machine-readable coding. As a result of this discussion, the Council
issued a declaration of the following:
The identity of all medications should be verifiable
through machine-readable coding technology;
ASHP will support the goal that all medications be
verified before they are administered to patients in the inpatient setting;
ASHP will urge the Food and Drug Administration to
mandate that standardized machine-readable coding be placed on all
manufacturers' single-unit drug packaging to (1) ensure the accuracy of
medication administration, (2) improve efficiencies within the medication-use
process, and (3) improve overall public health and patient safety.
The Council members expressed skepticism that the
pharmaceutical industry would act without a mandate from FDA. Still, it is believed that the profound
improvements in patient safety that machine-readable coding can offer
necessitate the creation of a stronger policy statement promoting the adoption
of this technology.
CHIM Launches Patient Safety Initiative
As part of the Patient Safety Initiative launched last February, CHIM
and its corporate partners (3M Health Information Systems, Eclipsys Corp.,
ePhysician and Per-Se Technologies) will gather data from technology vendors
and healthcare institutions to build an impartial picture of how information
technology can help reduce medical errors in both ambulatory and inpatient
settings. A CHIM task force is forming
an Advisory Board that will evaluate performance data submitted in case study
format. n Managed Healthcare Executive, Vol. 11, Issue 3
Positioned for Safety
In order to expand and share its knowledge of safety practices, the
Institute for Safe Medication Practices sponsored a medication safety contest.
The winning entry in the category Job Description for a Medication Safety
Practitioner went to Covenant Health Systems in Lubbock, TX, for its position,
"nurse specialist, medication administration." n Nursing
IHI Announces New Collaborative
In June, a select group of organizations from around the world began to
work intensely with expert faculty to rapidly implement the world's best ideas
for improving patient safety. The goal of the "Quantum Leaps in Patient Safety:
Redesigning Culture and Processes of the Medication System" project is to
deploy a medication system that is safer by a factor of ten. Through this
collaborative, participating organizations will redesign core processes of
their medication delivery system.
"Never Events" Project
The National Quality Forum's project to develop a list of "never events"
is nearing completion for external review. Never events are adverse events that
are so apparently preventable that it can be legitimately presumed that they
are the result of an error or mishap. The project seeks to identify measures
that can be adopted by states as they develop patient safety reporting systems.
The "Never Events" project is funded by the Agency for Healthcare Research and
Quality and the Health Care Financing Administration.
Cause For Concern
Overdose Kills Girl at Children's Hospital
A 9-month-old girl died after a misplaced decimal point caused a
Children's Hospital nurse to administer a massive overdose of morphine,
illustrating a problem that plagues hospitals nationwide. Children's Hospital officials said that,
instead of two 0.5 milligram doses of morphine, a narcotic prescribed to
control postoperative pain, the child was given two doses of 5 milligrams each
-- 10 times the amount the surgeon intended. The doses were given two hours
apart as the girl recovered from successful surgery that day. Officials said
the girl did not exhibit a reaction until hours later. The medication error
consisted of three consecutive mistakes by a physician, a transcriber and a
nurse.
A surgeon wrote a postoperative order for 0.5
milligrams of morphine if needed in the judgment of the nurse. The dosage was
correct but the order did not follow a protocol requiring a zero to precede the
decimal point, so that it would have read "0.5 milligrams." The order was
transcribed by a unit clerk whose handwritten notation on a temporary
medication administration record failed to include a zero or decimal point, so
that it read "5 milligrams." The nurse tending the child on a medical-surgical
floor followed the order without question and injected the morphine into the
girl's intravenous line. n
The Washington Post
Cook County Hospital To Pay $12 million For Error
In what is the highest malpractice payout in Cook County Hospital
history, county officials have approved a $12 million medical malpractice
settlement stemming from an error that has left a 42-year-old woman with severe
brain damage.
When the woman was admitted to County Hospital
suffering from burns, a nurse administered a dose of potassium phosphate that
was five times stronger than the attending physician had prescribed. The
medication stopped the woman's heart for 35 minutes before doctors revived her.
According to records, the nurse calculated the
medication dose as ordered by the doctor. She then checked her calculations
with a colleague and was advised, incorrectly, to add more potassium phosphate.
After preparing a solution that was almost five times more concentrated than
ordered by the physician, she administered the medication through an
intravenous drip. And instead of dispensing the dosage over the usual four- to
six-hour period, the IV was incorrectly calibrated to deliver the concentrated
dosage in about one hour. n Chicago Tribune
California Jury Awards $1.5 million For Undertreatment of Pain
An Alameda County California jury issued a $1.5 million ruling that will
forever change the way healthcare providers view the legal significance of
effective pain care for the terminally ill. The case called Bergman v. Eden
involved care provided to William Bergman, an 85-year-old Californian dying of
lung cancer. Mr. Bergman was admitted
to Eden Medical Center in Northern California complaining of intolerable pain.
After five days in the hospital, where nurses charted pain levels ranging from
7-10, Mr. Bergman was discharged to die at home, still in agony. His family ultimately consulted another
physician who prescribed proper pain medication and Mr. Bergman finally
obtained relief before he died in hospice care. "This is an important victory for advocates of pain care. Physicians have under treated pain for a
very long time with no accountability," said Kathryn Tucker, Director of Legal
Affairs for Compassion in Dying Federation.
n AP/Seattle Post-Intelligencer
Inmates at High Risk for Medication Errors
According to a legislative audit, the Wisconsin Department of
Corrections complies with fewer than half of the national prison health care standards.
Among the audit findings an interesting fact surfaced. At most prisons, prescriptions are
distributed by corrections officers who receive only four hours of training on
what they are handling and what the effects of the drugs could be.
n The Milwaukee Journal Sentinel
Medication Errors In Schools
A recent survey of over 600 school nurses found that during the previous
year nearly half reported errors in giving the students their medications.
Eighty percent reported missing a dose. Other errors included double dose
(23%), giving a drug without permission (21%), and giving the wrong medicine
(20%). Only a quarter of the nurses
said they always gave the medicine to the students. The rest delegate this
responsibility at least some of the time to unlicensed personnel -- most of the
time the school secretary.
n Pediatrics for Parents, ISSN: 0730-6725; Volume 19; Issue
3
Grants
HHS Plan To Streamline Grants Process
HHS Secretary Tommy Thompson issued a government-wide plan to streamline
grants programs to make it easier and less costly for grant recipients to work
with the federal government. Elements of the plan would reduce the amount of
data required for grant applications and reports, reduce the number of required
forms, and incorporate new technology and electronic processes into the grants
process to reduce paperwork. HHS awards roughly half of the $325 billion in
grants issued each year under more than 600 federal programs.
$20.9 million for Error-Free System Development
The Institute for Healthcare Improvement and the Robert Wood Johnson
Foundation launched a $20.9 million initiative aimed at reducing medical
errors. The "Pursuit of Perfection" program will provide grants to 12
institutions to design error-free systems. The funding was announced on the
heels of a survey released by IHI and sponsored by RWJF showing that some 61%
of health care providers accept common medical errors as routine practice.
AHRQ to Fund Research Dissemination & Education
Up to $1.5 million will be awarded by the Agency for Healthcare Research
and Quality to fund the first-year costs of four to seven projects that
demonstrate and evaluate innovative approaches to educating health care
providers, disseminating the results of patient safety research, and promoting
awareness of the need to improve safety.
AHRQ Grant to Study effect of working conditions on quality OF care
The Agency for Healthcare Research and Quality (AHRQ) has announced
plans for $7.5 million in research grants that will examine the effect of
working conditions on healthcare workers' ability to provide safe, high-quality
care. AHRQ is seeking applications that will explore the relationship between
working conditions that affect healthcare workers and the safety and quality of
care they provide, and test innovative approaches to working conditions that
have been effective in improving the quality of a product or service other than
healthcare.
Events
Premier Partnership Symposium
2001: Patient Safety
October 10-12, 2001 - Dallas, Texas
Hosted by the Partnership for Patient Safety (p4ps) and co-sponsored by
Premier, Inc. and VHA Inc., this conference is a collaboration among
organizations that are working to design and support the safest possible
healthcare systems.
Health Forum's Summit 2001 - The
Leader's Edge
July 29 -August 1 - San Diego, CA
Health Forum's Summit 2001 offers knowledge and ideas to help hospital
executives meet organizational challenges and opportunities head-on.
Melior Conference on Error
Reporting
July 27 - Needham, MA
"Medical Error Reporting: Saving
Patients, Saving Money by Discussing the Undiscussable," is a conference on
ways to stimulate, use, and benefit from increased reporting. For more
information, contact: Ken Farbstein at
781-444-5525.
New Frontiers in Patient Safety
August 2-3 - Tampa, FL
The Florida Society for Healthcare Risk Management (FSHRM) will present
"New Frontiers in Patient Safety." For more on the program, call the Florida
Hospital Association (FHA) at (407) 841-6230.
Patient Safety: Disclosure and
Defense
September 13 - Fort Worth, TX
The North Texas Society for Healthcare Risk Management (NTSHRM) will
present "Patient Safety: Disclosure and Defense." Contact Teresa Giles, at
(214) 989-2179.
Patient Safety through six sigma
September 24-25 - San Francisco, CA
This conference has been developed for senior executives and quality
professionals who are in the process of implementing statistical tools and
methods for quality improvement in their healthcare organizations.
Bridge News
Study Finds Reduction in Medication Errors Through Use of Innovative Technology
A recent study of barcode-enabled point of care (BPOC) technology used
in the healthcare industry shows that the use of BPOC systems has resulted in a
65 percent to 74 percent documented decrease in medication errors.
Published in April 2001 by Bridge Medical, the study is the first
comprehensive literature review dedicated to BPOC systems, and shows that use
of the technology in medication administration has been demonstrated to be an
effective tool in decreasing medication errors and enhancing patient safety. n Business Wire , Publication
date: 2001-05-29
Bridge Medical Partners with Healthcare-ID
Bridge Medical formalized a partnership with Healthcare-ID Inc. to
expand the capabilities of the Bridge MedPoint system to include verification
of blood transfusions and laboratory specimens. Now, through the integration
with Healthcare-ID's proprietary software, the MedPoint system offers
transfusion verification and specimen tracking to health care providers.
Healthcare-ID's transfusion verification system works
to assure that the patient receives the correct typed and cross-matched unit of
blood. Prior to beginning a transfusion, the bar code ID on the patient
bracelet is scanned by the health care professional to assure the match between
patient and blood product, verify the unit number and compare patient/unit
compatibility. Additionally, the software captures the patient's vital signs
before, during and at the completion of the transfusion, and documents patient
reactions to the transfusion. Data also is provided for the transfusion
management reporting system and patient charting. The specimen tracking program
from Healthcare-ID assures a permanent link between the patient and the
laboratory specimen to prevent identification errors on lab samples. At the
time of specimen collection, the health care professional scans the patient's
bracelet and prints out the appropriate specimen container labels at the
bedside. The increased accuracy results in fewer redraws for patients and
speeds processing once the specimen is received in the lab.
Bridge Helps Hospitals Meet New Safety Standards
Bridge Medical, Inc., announced that the Bridge MedPoint system can help
hospitals meet the new industry safety standards enacted by the Joint
Commission on Accreditation of Healthcare Organization (JCAHO), as well as
reduce medication errors. MedPoint is
an easy-to-use, integrated and comprehensive system designed to address a broad
spectrum of patient-safety concerns.
"The Bridge MedPoint system can be a valuable solution
to hospitals as they work to meet the new JCAHO patient-safety standards," said
John Grotting, president and CEO, Bridge Medical. "The Bridge MedPoint system takes the blame out of medication
management by providing hospitals with the tools they need to intercept errors
and eliminate the system flaws that are the root causes of errors."
According to the 1999 Institute of Medicine Report, medical
errors kill as many as 98,000 Americans each year. Studies indicate that seven percent or more of these deaths are
caused by medication errors.
"The sad and simple truth is that many of these deaths
are preventable with affordable health information technology," continued
Grotting. "Bridge was founded to help
healthcare providers eliminate medication errors, prevent adverse drug events
and improve the outcome of medication therapies."
The MedPoint system provides a safety net at the point
of care by checking the "five rights" (right patient, right drug, right dose,
right route of administration, right time), by alerting nurses to high-risk
medications (look-alike, sound-alike, maximum daily doses, etc.), and by
verifying laboratory specimen and blood transfusion identification. Before a medication or blood component is
administered or a lab specimen is drawn, the nurse scans his or her ID, the
patient's ID and the medication or blood product. MedPoint automatically creates the Medication Administration
Record or Blood Transfusion Record, eliminating repetitive and time-consuming
tasks for nurses, and generates reports that allow hospitals to identify and
eliminate system flaws.
Bridge & Northern Michigan Hospital Featured on Eye on Info Magazine
Reporters for Eye on Info, a special supplement of Modern Healthcare,
spent three months researching the medical-error problem and interviewing key
managers at 14 healthcare organizations that have begun addressing the problem.
They found that quality-focused hospitals were able to streamline clunky
processes and better direct the action within the hospital, saving time and
money while operating more safely.
In an article entitled "Drug delivery fraught with
risks" by Jeff Tieman, Eye on Info features the success of Northern Michigan
Hospital and the Bridge MedPoint system.
Efforts at Sacred Health Medical Center cited in Health Trends
In an article called "Quality is a Business Strategy", HealthTrends
editor, Russ Coile, cites the outstanding work of Sacred Heart Medical Center
in Spokane, WA. The article reads:
"Working with Bridge Medical, a San Diego-based firm that provides error
reporting software, the hospital believes that 10-15 percent of its operating
costs involve duplicative rework and complications caused by adverse events, as
much as $40 million to $50 million at Sacred Heart. Bridge Medical estimates a
savings of over $1.6 million at the hospital annually by addressing the problem
of medication errors."
Terance Kinninger Joins Bridge Medical As Chief Financial Officer
Bridge Medical, Inc. welcomed Terance Kinninger as Chief Financial
Officer, Senior Vice President of Business Development. Mr. Kinninger comes to
Bridge with over 17 years of executive financial and operational management
experience in high growth technology companies. He has worked with both
publicly held and venture capital backed software companies. Most recently he
was Senior Vice President and Chief Financial Officer of WebSideStory Inc., an
applications service provider.
Gordon Sprenger Joins Bridge Medical Board
Bridge Medical Inc. announced that Gordon Sprenger, president and chief
executive officer of Allina Health System, has been elected to Bridge's board
of directors. Mr. Sprenger is past-chairman of the American Hospital
Association board of trustees and past board chair of Voluntary Hospitals of
America.
"Bridge's technologies and services will be a tremendously valuable
resources for health care providers," Sprenger stated. "If we're serious about
eliminating error, we have to provide the support the people delivering care
need to prevent error. Bridge's bar-code and networking technology brings
powerful new resources to the bedside."n
Business Wire
Literature Review of Barcode-enabled Point of Care Systems
Get your copy today!
In an effort to carry a message to healthcare executives, payers,
regulators and other healthcare decision makers Bridge Medical published a
20-page literature review, "The Effect of Barcode-Enabled Point of Care
Technology on Medication Administration Errors". The industry has embraced
this paper as a practical guide to BPOC technology. The review describes the features, implementation barriers and
documented success of BPOC systems as reported by numerous researchers and
hospitals.
To receive a copy, please contact
Bridge Medical at (858) 350-0100 or access the paper online at
www.MedErrors.com.
It's the 21st Century Go Digital!
Join The Point of Care Listserv Today
The topic of medication safety is at the center of medical, congressional
and consumer discourse today. As a
result, there is a wealth of information available to you with just the click
of a mouse key. In our e-mail version
of The Point of Care, we have taken the time to locate the resources for
you and will provide web links to all relevant materials and sites whenever
possible. A hardcopy newsletter simply
cannot deliver such convenience to your fingertips.
Bridge Medical is pleased to provide the medication error community with
The Point of Care at no charge.
To streamline our quarterly publication and to offer you the most
complete resource possible, we have established an online subscription service
for our e-mail version of the newsletter.
Please take a moment to sign up for this service. Hardcopy distribution of The Point of
Care will be limited going forward so reserve your e-copy now ñ subscribe
online!
Subscribing is simple. Visit
www.MedErrors.com and follow the instructions.
We require only your name and e-mail address, both of which are kept
confidential and used solely to distribute The Point of Care.
There are plenty of reasons to trade the familiar pulp-based medium for
the electronic word. It's environmentally friendly, financially responsible,
and an administrative convenience. Most
importantly, an e-newsletter can deliver far more value to you, the
reader. Subscribe today.
If you prefer, call us at 1-800-350-0100 or email us at
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