Report
Finds a Heavy Toll From Medication Errors
By GARDINER
HARRIS
WASHINGTON, July 20 — Medication errors harm 1.5 million people
and kill several thousand each year in the United States, costing the nation at
least $3.5 billion annually, the Institute
of Medicine concluded in a report released on Thursday.
Drug errors
are so widespread that hospital patients should expect to suffer one every day
they remain hospitalized, although error rates vary by hospital and most do not
lead to injury, the report concluded.
The report, “Preventing Medication
Errors,” cited the death of Betsy Lehman, a 39-year-old mother of two and a
health reporter for The Boston Globe, as a classic fatal drug mix-up. Ms. Lehman
died in 1993 after a doctor mistakenly gave her four times the appropriate dose
of a toxic drug to treat her breast
cancer.
Recommendations to correct these problems include systemic
changes like electronic prescribing and tips for consumers like advising
patients to carry complete listings of their prescriptions to every doctor’s
visit, the report said.
“The incidence of medication errors was
surprising even to us,” said J. Lyle Bootman, dean of the University
of Arizona College of Pharmacy. “The solutions are complex and far-reaching
and will present challenges.”
The report is the fourth in a series done
by the institute, the nation’s most prestigious medical advisory organization,
that has called attention to the enormous health and financial burdens brought
about by medical errors.
The first report, “To Err Is Human,” was
released in 1999 and caused a sensation when it estimated that medical errors of
all sorts led to as many as 98,000 deaths each year — more than was caused by
highway accidents and breast cancer combined.
After the first report,
health officials and hospital groups pledged reforms, but many of the most
important efforts have been slow to take hold.
Drug computer-entry
systems, which are supposed to ensure that hospital patients get the right drugs
at the right dose, are used in just 6 percent of the nation’s hospitals, said
Charles B. Inlander, president of the People’s Medical Society, a consumer
advocacy group, and an author of the report released Thursday.
Electronic
medical records can help ensure that patients do not receive toxic drug
combinations. The 1999 report urged widespread adoption of these systems.
Thursday’s report called for all prescriptions to be written electronically by
2010.
Just 3 percent of hospitals have electronic patient records, said
Henri Manasse, chief executive of the American Society of Health-System
Pharmacists. Few doctors prescribe drugs electronically.
Even simple
medication safety recommendations — block printing on hand-written prescription
forms — are widely ignored.
Arthur Levin, director of the Center for
Medical Consumers and an author of the 1999 report, said that just about
everyone in the health system was to blame. “This country has not taken
seriously the alarms we sounded in 1999,” Mr. Levin said. “Why?”
Health
organizations defended their efforts.
Alicia Mitchell, a spokeswoman for
the American Hospital Association, said that since 1999 hospitals had “actively
engaged in looking at using information technology to improve patient
safety.”
A recent poll by the association of its members found that 92
percent intended to adopt electronic patient records, Ms. Mitchell said. But
such systems are complicated and need to be built gradually, she
said.
Thursday’s report urged the Food
and Drug Administration to improve and standardize the drug information
leaflets given consumers. It noted that confusing information on drug labels was
an important cause of medication errors.
On Tuesday, the drug agency
finished a years-long process by issuing voluntary guidelines to reform consumer
drug information leaflets, said Dr. Scott Gottlieb, the agency’s deputy
commissioner. Many of these leaflets are not regulated by the F.D.A.
And
on June 30, the agency completed a lengthy effort to clarify and standardize
information on drug labels. The new labels could prevent nearly 300,000
medication errors each year and will make electronic prescribing efforts far
easier to carry out, Dr. Gottlieb said.
Thursday’s report said that the
common practice whereby drug companies provided free drug samples to doctors
should be discouraged because such samples were poorly controlled. It urged drug
makers to package more pills in individual packages. And it criticized drug
makers as failing to disclose the results of all clinical trials involving their
drugs.
Alan Goldhammer, a spokesman for the Pharmaceutical Research and
Manufacturers of America, a drug industry trade group, said he differed with
some of the report’s conclusions but concurred with the broad goals of
increasing the use of information technology to reduce medication errors.
“Everybody is working on that right now,” he said.
Thursday’s
report said that in any given week, four out of five adults in the United States
took at least one medication. A third take at least five different medications.
As the use of medications has soared, so, too have medication errors, Dr.
Manasse said.
Effective strategies to prevent such errors have, however,
been known for years, Mr. Inlander said.
“This is not rocket science,”
Mr. Inlander said. “It’s simple. The key is having the will to make these
changes in an organized and uniform way. And it’s not that expensive.”