| Miscommunication
Important Cause of Treatment Errors
ACE
Inhibitor Drugs Underused, Study Finds
NEJM
Study Finds Disparities in Treatment for Black Medicare Patients
NCQA
Releases Draft Program for Comment
Provider
Tracking May Help Disparities in Care, AHRQ Study Says
AcademyHealth
Outcomes Resources Now Online
Miscommunication
Important Cause of Treatment Errors
A study published
in the July-August issue of the Annals of Family Medicine found that miscommunication
appears to play an important role in propagating diagnostic and treatment
mistakes.
In “A
String of Mistakes: The Importance of Cascade Analysis in Describing,
Counting, and Preventing Medical Errors,” researchers examined 18
US family physicians participating in a six-country international study,
who filed 75 anonymous error reports.
The narratives
were examined to identify the chain of events and the predominant proximal
errors. We tabulated the consequences to patients, both reported by physicians
and inferred by investigators. Although 83% of the errors that ultimately
occurred were mistakes in treatment or diagnosis, two of three were set
in motion by errors in communication. Fully 80% of the errors that initiated
cascades involved informational or personal miscommunication. Examples
of informational miscommunication included communication breakdowns among
colleagues and with patients (44%), misinformation in the medical record
(21%), mishandling of patients’ requests and messages (18%), inaccessible
medical records (12%), and inadequate reminder systems (5%).
When asked
whether the patient was harmed, physicians answered affirmatively in 43%
of cases in which their narratives described harms. Psychological and
emotional effects accounted for 17% of physician-reported consequences
but 69% of investigator-inferred consequences.
Cascade analysis
of physicians’ error reports is helpful in understanding the precipitant
chain of events, but physicians provide incomplete information about how
patients are affected, researchers concluded.
For more
info, www.annfammed.org
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ACE
Inhibitor Drugs Underused, Study Finds
Almost a
third of heart failure patients face an increased risk of death because
they do not receive an angiotensin-converting enzyme (ACE) inhibitor,
according to a report in the Aug. 3 rapid access issue of Circulation:
Journal of the American Heart Association.
A review
of data from the Centers from Medicare & Medicaid Services’
National Heart Care Project showed that 32% of elderly heart failure patients
were discharged from hospitals without prescriptions for ACE inhibitors.
Patients discharged without anti-angiotensin therapy had a 14% greater
risk of dying within a year compared to patients treated with ACE inhibitors.
The use of angiotensin receptor blockers (ARBs), an alternative to ACE-inhibitors
in some patients with heart failure, did not explain the low rates of
appropriate therapy.
The study
adds to previous evidence that ACE inhibitors are widely underused in
patients who are eligible to receive the drugs. In particular, prescription
rates for ACE inhibitors have not increased for hospitalized Medicare
patients who should be receiving the drugs to treat heart failure, researchers
reported
Overall,
68% of the patients had prescriptions for ACE inhibitors upon hospital
discharge. The proportion of patients treated with ACE inhibitors was
69% during 1998–1999 and 67 percent between 2000 and 2001. When
ACE inhibitors and ARBs were considered together, 78 percent of patients
had prescriptions at hospital discharge.
http://circ.ahajournals.org.
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NEJM
Study Finds Disparities in Treatment for Black Medicare Patients
To a large
extent, different groups of physicians treat elderly black and white Medicare
patients, providing insights into possible explanations for the pervasive
health disparities between blacks and whites, according to a study by
researchers at Memorial Sloan-Kettering Cancer Center and the Center for
Studying Health System Change in the Aug. 5 New England Journal of
Medicine.
Eighty percent
of the primary care visits by elderly black Medicare patients were to
22% of physicians, and those physicians treating black patients were more
likely to report difficulty getting hospital admissions, specialty referrals
and other care for their patients, the study found.
Physicians
treating black patients provided more charity care; derived a higher percentage
of their practice revenue from Medicaid, the state-federal health care
program for the poor; were less likely to be board certified in their
primary specialty; and more often practiced in low-income neighborhoods
than physicians treating white patients, the study found.
“The
findings paint a picture of two health systems, where physicians treating
black patients appear to have less access to important clinical resources
and be less well trained clinically than physicians treating white patients,”
said Peter B. Bach, MD, the study’s lead author and a researcher
in the Department of Epidemiology and Biostatistics at Memorial Sloan-Kettering
Cancer Center in New York City. Bach’s earlier studies of racial
disparity in cancer outcomes demonstrated that the poor quality health
care received prior to a black patient’s cancer diagnosis contributed,
in part, to their lower rates of cancer survival.
On average,
a higher proportion of physicians practicing in communities where visits
by white patients occurred reported they could access important health
services for their patients than physicians who practice in communities
where black patients receive care, the study found.
The study
is based on information from HSC’s nationally representative Community
Tracking Study Physician Survey, which collects information from 12,000
practicing physicians, and Medicare claims information from a representative
sample of 5 percent of Medicare beneficiaries. Data on physicians and
patient visits were linked with the use of the physicians’ unique
provider identification number, and a total of 4,355 primary care physicians,
43,032 elderly Medicare patients and 150,391 patient visits were included
in the study.
The study
was coauthored by Deborah Schrag, MD, MPH., and Ramsey C. Tate, Memorial
Sloan-Kettering Cancer Center, and J. Lee Hargraves, PhD, Center for Studying
Health System Change, and was supported by grants from the National Cancer
Institute, The Robert Wood Johnson Foundation, the American Cancer Society,
and the American Lung Association of New York City.
For more
info, www.hschange.org.
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NCQA
Releases Draft Program for Comment
The National
Committee for Quality Assurance (NCQA) has released for public comment
draft standards for “Quality Plus,” a supplemental accreditation
program that is designed to highlight health plans whose innovative approaches
to member communications, care management, physician compensation and
other activities are models for the industry.
The voluntary
program also seeks to engage newer health plan types such as consumer-directed
health plans that represent a growing sector of the health care. The initial
set of draft standards focus on how well a plan uses technology to provide
members with interactive health tools and information about pharmacy benefits,
claims and health improvement.
The Quality
Plus program is part of NCQA’s multi-year effort to transition to
a more flexible generation of measurement and accreditation programs aimed
at a wider range of organizations. Through Quality Plus, NCQA will introduce
new standards that will give employers insight into whether or not a plan
represents a good value, as well as standards designed to encourage more
focused care management.
Quality Plus
standards fall broadly into three areas. They are: member connections,
physician and hospital quality and health improvement.
Comments
on the draft Member Connections standards are due by Sept. 15. Relevant
sections of the draft standards can be downloaded from NCQA’s Web
site at www.ncqa.org/Programs/Accreditation/MCO2005PubComment.htm.
Comments should be submitted online to ME2005@ncqa.org.
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Provider
Tracking May Help Disparities in Care, AHRQ Study Says
An AHRQ report,
“Strategies for Improving Minority Healthcare Quality,” shows
that there is excellent evidence that suggests provider tracking and reminder
systems are effective in improving the quality of care for racial and
ethnic minority patients.
The study
also suggests that cultural competence training can increase the knowledge
and improve the attitudes and skills of health care providers. However,
the researchers found it difficult to conclude which specific types of
training interventions are effective in improving particular outcomes.
Even within an outcome category, there is no uniformity in outcome measurement,
making it difficult to determine which specific types of knowledge, attitudes,
or skills are affected by cultural competence training. For more info,
www.ahrq.gov/clinic/epcsums/minqusum.htm.
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AcademyHealth
Outcomes Resources Now Online
AcademyHealth,
a health services research group, has developed a core list of books,
journals, Web sites, and bibliographic databases in the field of health
outcomes. Developed under contract with the National Library of Medicine
Health Outcomes Core Library.
This project
serves as a guide for individuals new to the field or those interested
in developing a collection of resources in health outcomes.
For more
info, www.academyhealth.org/publications/healthoutcomes.htm.
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