Almost half of physicians report that the World Wide Web has significantly changed the way they practice medicine, according to a study released recently by the American Medical Association (AMA). Of physicians who use the Web, 78 percent say they have increased the frequency and duration of Web use. These finding are from the 2002 AMA Study on Physicians’ Use of the World Wide Web, which interviewed 977 physicians in the U.S.

In this fourth AMA survey of online physicians, 67 percent of physicians said they now go online daily–up 24 percent from 1997. Their average time spent online jumped from 4.3 hours weekly in 1997 to 7.1 hours a week in 2001. They also predicted their time online would jump to an average of 9.6 hours per week during the next six months. One constant unveiled: Only three of 10 physicians using the Internet have a Web site, the same level as two years ago.

J. Richard Gaintner, MD, FACPE, former CEO of Shands HealthCare in Gainesville, Fla., recently received the American Hospital Association’s Board of Trustees Award recognizing individuals or groups who have made substantial and noteworthy contributions to the work of AHA. “Dick has been the epitome of the skilled, caring physician executive,” said AHA President Dick Davidson. “He has demonstrated his keen insights into medical practice, physician relations, quality and patient safety.”

During his career, Gaintner served as an executive at hospitals in Boston, New York, Maryland and Connecticut. He also served AHA by participating on numerous boards and task forces, and as governing council chairman for the Section for Metropolitan Hospitals, chairman of the Committee on Hospital Medical Staffs/Medical Education and member of the Board of Directors of HealthCare Forum.

Whatever one’s sentiments are about those famous acronyms PPS and RUG–the Medicare Prospective Payment System and the Resource Utilization Groupings used to calculate those payments–on one thing almost everyone agrees: They won’t work without good software. The complexities of completing the Minimum Data Set (MDS), of tracking it with “triggers” and Resident Assessment Protocols (RAPs), and of linking all this to a RUG that defines (and defends) payment–they’re made to order for computers. And, of course, facilities are required by law to transmit these data to their government paymasters electronically. But, in practice, how well is the computerized approach working? Recently, Gary Jorgenson, RN, the technical advisor who helped Diane Carter realize her vision of an online “virtual organization” called the American Association of Nurse Assessment Coordinators (AANAC)–some 2,500 nurses specializing in PPS documentation–commented on the state of the art in an interview with Nursing Homes/Long Term Care Ma nagement Editor Richard L. Peck. He was amply qualified to do so. Although he serves both as AANAC’s Webmaster and as clinical director of information systems for NCS HealthCare, the national long-term care pharmacy firm, he has also had several years’ experience as a staff nurse and director of nursing for an Ohio nursing home. In short, he can view the vendor/nurse software relationship from both sides.

Jorgenson: Definitely. Aside from the fact that electronic transmission of data is mandatory, trying to do the MDS assessments and RUG calculations by hand would be an enormous task. In view of the challenges involved, computerization seems to be a “natural” process for this.

Peck: At AANAC meetings I’ve noticed that most of the problems NACs encounter with this system seem to be software-related, i.e., often the answer is “see your vendor about that.” Is that a correct impression?

Jorgenson: Yes, it is. And as a software developer and a nurse, I can see both sides of the situation. The nurse feels frustrated because she can’t always get the software to do everything she wants. But from the vendor’s side, these regulations change so often that it is a pure nightmare to keep up. Then, once vendors have made the change, there are questions regarding distribution of the changes and staff training to consider.

Peck: With a significant change, how long would a vendor’s response typically take?

Jorgenson: It depends on several factors. Vendors are creating software using a variety of platforms–everything from second-generation language, for which updates are a huge task, to fifth-generation language, for which changes come relatively easily. Then there is the variety of distribution methods–diskette mailers, patches posted on the company Web site, and a few application service providers (ASPs) who centralize software maintenance and eliminate distribution as a factor. Across the board, it is an amazingly broad spectrum.

Peck: In striving toward a workable software solution, what would be the ideal relationship between vendors and their NAC customers?

Jorgenson: If I were to advise a nurse about anything regarding this, I would say look for support, support, support. But here, too, one encounters unusual situations. A vendor might be marketing 15-year-old software that is all but obsolete, but the company provides excellent support and has a strong user base. Another vendor might offer new, state-of-the-art software but have no support mechanism in place. The best thing for the nurse to do is to contact some of the customers of the vendors in which she’s interested. In fact, with the AANAC Web site, NACs have a national forum available to talk with customers nationwide.

Peck: When it comes to improving the relationship, what should nurses consider?

Jorgenson: They really need to try for a greater level of computer literacy. It’s not that nurses are computer-illiterate. It’s that they’re computer-uninterested. They went into nursing to care for patients, not to manipulate computer keyboards. But they should still try to expand their knowledge base to some extent though books, magazines, seminars or college courses. In fact, that seems to be happening–in my contacts with facilities throughout the country, I see more and more nurses taking on the role of the “information system (IS) nurse.” That’s becoming an actual job title.

Peck: How about vendors; what should they do to improve matters?

Jorgenson: I would urge them to have a greater Web presence, to use the Internet not only for marketing purposes, but for interactive customer support. There is some of this going on, but not much as yet.

Peck: What would you say is the major future issue that they should all be addressing?

Jorgenson: Nurses should take care to ask vendors about security issues–about patient confidentiality protections, and such terms as firewalls and encryption. These are about to become major issues for all healthcare organizations that transmit data electronically, because of the issuance of regulations pertaining to the Health Insurance Portability and Accountability Act of 1996 (HIPAA). The Act hasn’t had much direct impact yet, but regulations continue to emerge, and some are going to require compliance by late next year. That’s a responsibility both for vendors and for users.

NEW YORK — An article in the Aug. 22 Journal of the American Medical Association reported patients taking Celebrex (celecoxib) and Vioxx (rofecoxib) may run a higher risk of getting cardiovascular disease, a charge each drug maker vehemently denies.

The contents of the JAMA article were picked up by many news organizations.

“Pharmacia and Pfizer believe the conclusions drawn by the analysis in the JAMA article were flawed and unsound,” Pfizer, a co-marketer of Celebrex (celecoxib), reported in a statement issued the same day the study was published. “It contains no new clinical information and is based on an inappropriate re-analysis of several older clinical studies containing data that were not suitable for combination and comparison.”

Merck reportedly agreed with some of the study’s conclusions, but maintained that data exists that shows no increase in cardiovascular risk in patients taking its drug, Vioxx (rofecoxib). Celebrex and Vioxx, both used to treat arthritis, account for a combined $6 billion in annual prescription sales.

Dr. Eric J. Topol, chairman of cardiovascular medicine at the Cleveland Clinic Foundation, used data from two major clinical trials each company had run previously in an attempt to demonstrate their respective stomach-safety profiles. In Topol’s cardiac study, Merck’s Vioxx fared slightly worse and had more cardiac problems associated with it than Pfizer/Pharmacia’s Celebrex. Both Celebrex and Vioxx are cox-2 inhibitors.

“Our findings suggest a potential increase in cardiovascular event rates for the presently available cox-2 inhibitors,” Topol wrote. “It is possible that concomitant use of aspirin may not fully offset the risk of selective cox-2 inhibitors. However, definitive evidence of such an adverse effect will require a prospective randomized clinical trial.”

Topol acknowledged the limits of his study and even suggested cox-2s might alleviate atherosclerosis. “On the other hand, the inflammatory component of atherosclerosis has recently been emphasized and may be suppressible by cox-2 inhibitors,” Topol said. Still, Topol said the “remarkable exposure and popularity” of cox-2 inhibitors should compel researchers to conduct a randomized trial of their long-term effect on cardiovascular health. “Until then,” he said, “we urge caution in prescribing these agents to patients at risk for cardiovascular morbidity.”

The American Medical Association (AMA) has reached a settlement with Dr George Lundberg, avoiding a possible lawsuit by him.

Dr Lundberg was fired last month as editor of JAMA (the journal of the American Medical Association) because he “fast tracked” the publication of a paper–which indicated that university students in the United States did not think that oral sex was “real sex”–in the midst of the impeachment trial of President Clinton.

In a bland and uninformative statement both parties said that they had resolved “substantive differences” and “wish to underscore their absolute commitment to JAMA’s editorial integrity, independence, and excellence.” Terms of the agreement and whether there was a monetary settlement were “private and confidential,” said an AMA spokesperson. Dr Lundberg’s lawyer did not return telephone calls.

The joint statement indicated that Dr Lundberg would continue “contributing to scientific medical research and medical journalism, including JAMA, subject to editorial discretion.”

The AMA spokesperson said, “Dr Lundberg will not be hired again. He can submit papers and will be treated as other contributors. It’s up to the JAMA editors.”

Dismissal of Dr Lundberg after 17 years as editor, brought a flood of protest. An editorial supporting Dr Lundberg was signed by 26 JAMA editors (including the two interim editors of the journal), 10 editors of affiliated AMA journals, and 16 members of the editorial board (JAMA 1999: 281;460). Dr Donald Lindberg, director of the National Library of Medicine, part of the National Institutes of Health, resigned from JAMA’s editorial board.

Meanwhile, the AMA appointed a committee to be headed by one of the protesters, Dr Roger Rosenberg, professor of neurology at the University of Texas Southwestern Medical Center in Dallas, to Conduct an international search for a new editor.

The AMA officer who fired Dr Lundberg, executive vice president Dr E Ratcliffe Anderson, said, “The AMA will go to whatever lengths are necessary to demonstrate its absolute commitment to editorial independence … The committee also will be charged with determining how the editor’s performance can best be measured.”

Clinical Quiz questions are based on selected articles in this issue. Answers appear in this issue.

American Family Physician has been approved by the American Academy of Family Physicians as having educational content acceptable for Prescribed credit hours. Term of approval covers issues published within one year from the beginning distribution date of August 2001. This issue has been approved for up to 3 Prescribed credit hours. Credit may be claimed for one year from the date of this issue.

The American Academy of Family Physicians is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

The AAFP designates this educational activity for a maximum of 3 hours in Category 1 credit toward the American Medical Association Physician’s Recognition Award. Each physician should claim only those hours of credit that he or she actually spent in the educational activity.

AAFP Credit

Each copy of AFP contains a Clinical Quiz answer card. AAFP members may use this card to obtain the designated number of Prescribed credit hours for the year in which the card is postmarked.

AMA/PRA Category 1 Credit

AAFP members who satisfy the Academy’s continuing medical education requirements are automatically eligible for the AMA/PRA.

Physicians who are not members of the AAFP are eligible to receive the designated number of credit hours in Category 1 of the AMA/PRA on completion and return of the Clinical Quiz answer card. AFP keeps a record of AMA/PRA Category 1 credit hours for nonmember physicians. This record will be provided on request; however, nonmembers are responsible for reporting their own Category 1 CME credits when applying for the AMA/PRA or other certificates or credentials.

For health care professionals who are not physicians and are AFP subscribers, a record of CME credit is kept by AAFP and will be provided to you on written request. You are responsible for reporting CME hours to your professional organization.

NOTE: The full text of AFP is available online (http://www.aafp.org/afp), including each issue’s Clinical Quiz. The table of contents for each online issue will link you to the Clinical Quiz. Just follow the online directions to take the quiz and, if you’re an AAFP member, you can submit your answers for CME credit.

Instructions

(1) Read each article, answer all questions on the quiz pages and transfer your answers to the Clinical Quiz answer card (bound into your copy of AFP). This will help you avoid errors and permit you to check your answers against the correct answers.

(2) Mail the Clinical Quiz answer card within one year (by August 31, 2002). The bar code on the answer card contains your identification for CME credit hours.

Before beginning the test, please note:

Each Clinical Quiz includes two types of questions: Type A and Type X.

Type A questions have only one correct answer and may have four or five choices. Here is a typical Type A question:

Q1. Most allergic reactions to foods are:

[ ] A. Due to IgA deficiency.
[ ] B. Due to IgG and IgM antibodies.
[check] C. IgE-mediated.
[ ] D. Due to enzyme deficiencies.
[ ] E. Due to toxins.

Type X questions may have one or more correct answers. They are multiple true-false questions with four options. Here is a typical Type X question:

Q2.  Causes of varicosities in pregnancy
include:

[check] A. Hormonal changes.
[check] B. Venous compression.
[check] C.  Familial tendency.
[check] D. Prolonged sitting and standing.

Clinical Quiz questions are written by the associate and assistant editors of AFP.

Recent headlines proclaiming that one of five Ayurvedic herbal medicine products contains toxic levels of lead, mercury and arsenic were wildly misleading. The study on which the news stories were based, published in the December 15, 2004 issue of The Journal of the American Medical Association, involved a small sample of products manufactured in India or Pakistan and sold in South Asian groceries in Boston.

The American Herbal Products Association points out that the ingredients found in the sample have been illegal in American-made dietary supplements since 1906.

BOSTON — Shared Decision-Making(R) Videos Help Individuals Understand Their Conditions

Health Dialog Services Corporation today announced that two of the company’s educational videos were recognized by the American Medical Writers Association (AMWA) at the 9th New England Chapter Awards Banquet, held Thursday, June 15 in Waltham, Massachusetts. “Early Breast Cancer - Hormone Therapy and Chemotherapy: Are They Right for You?” and “Living with Metastatic Breast Cancer: Making the Journey Your Own” were recognized with Will Solimene Awards for Excellence in Medical Communication.

The Will Solimene Awards are presented by the New England Chapter of the AMWA to chapter members in recognition of outstanding work in medical, biomedical, and health communication. The independent, regional, writing recognition program was initiated in 1990. Entries are judged on accuracy of content, quality, and style of writing, as well as originality, achievement of purpose, and overall impact.

The two recognized videos are part of Health Dialog’s broader library of member support tools and are based on the research of the Foundation for Informed Medical Decision Making (FIMDM). Health Dialog’s Shared Decision-Making(R) videos provide evidence-based, unbiased information on treatment options and disease management and are just one of the resources offered to members through Health Dialog’s whole person care management program, which encourages individuals to take a proactive role in their healthcare with their physicians.
“These two videos were selected from among many outstanding entries submitted to this year’s competition,” said Jill Shuman, Awards Director for the New England Chapter of AMWA. “The Will Solimene Awards are presented for print and electronic entries that demonstrate excellence in medical communication, as judged by a panel of experienced and award-winning writers and editors.”

“Health Dialog is honored to have won these Will Solimene Awards,” said Bill Brennan, Senior Vice President, Content Services, Health Dialog. “This recognition reflects Health Dialog’s commitment to producing accurate, easy-to-understand videos that inform and support the needs of our members facing complex or confusing medical decisions and conditions.”

> On Nov. 29, the Centers for Disease Control and Prevention issued a safety alert calling on all health care facilities to use safer needles. The alert noted that using safer products could lead to an 80% reduction in injuries. Fifty types of protected needles and syringes have been approved by the Food and Drug Administration for sale; however, the American Nurses Association reports that only about 15% of hospitals use safer needles, largely because they are more expensive.

On November 22, HFMA, the American Hospital Association, and eight other healthcare groups addressed a letter to HCFA Administrator Nancy-Ann DeParle requesting an increase in the agency’s reimbursement to hospitals for photocopying expenses. The letter stated that the rate of $0.07 per page set in 1992 “was significantly below the market rate when set and ignored the cost of search and retrieval.” Because hospitals must provide documentation upon request by a peer review organization (PRO), photocopying expense associated with a PRO review can be substantial.

The letter did not specify what the per-page increase should be, but noted that HCFA charges “$0.10 per page with a search-and-retrieval fee averaging between $25-$50 per search” when fulfilling a Freedom of Information Act request.

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