Sample of "Medical Meandering"
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with Medical & Transplant News.
*** Newsletter will ONLY be sent if you request it. If you have received this newsletter from another source and wish to receive it directly please send email to Kandysfl@aol.com.
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AOL Resources -
Sundays 10:00 PM ET, Kidney/Pancreas Transplant,
Keyword: People Connection, Private Room, (Keyword to: aol://2719:2-2-kidney%20pancreas%20tx)Kidney
Pancreas Tx (Keyword to: aol://2719:2-2-kidney%20pancreas%20tx)
Monday 9:00 PM ET, Liver Disease & Transplant
Keyword: Better Health, Mutual Support Room, Mutual Support Room
(Keyword to: aol://2719:3-691-Mutual%20Support%20Room)
Tuesday 9:00 PM ET, Lung Transplant
Keyword: People Connection, Private Room, Carols lung tx room
(Keyword to: aol://2719:2-2-Carols%20lung%20tx%20room)
Thursday, 7:00 PM ET, Heart Transplant
Keyword: Better Health, Health Conf. Room Health Conf (Keyword
to: aol://2719:3-193-Health%20Conference)
Friday, 9:00 PM ET All Organs/Tissues Transplant
Keyword: Better Health, IMH Conf Room, Hyperlink: IMH Chat (Keyword
to: aol://2719:3-49-IMH%20Chat)
Saturday 12:00 Midnight ET, Organ Transplant Support
Keyword: Better Health, IMH Conf Room, Hyperlink: IMH Chat (Keyword
to: aol://2719:3-49-IMH%20Chat)
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NEW CHATS --- ACCESSIBLE TO ALL ON THE WEB
Better Health and Medical Network (Keyword to: http://www.betterhealth.com/BH2/frontframe/0,1329,,00.html)
http://www.betterhealth.com is offering a dedicated transplant
chat room, as well as other medical chat rooms, which will eventually
be open 24hrs, 7days.
For Netscape 4.0 or Internet Explorer 3.0 download the i-chat
plug-in at:
ichat Download (Keyword to: http://www.ichat.com/download/index.html)
http://www.ichat.com/download/index.html
If you experiene problems loading the plugin properly, please
visit:
ichat Technical Support - Clients (Keyword to: http://www.ichat.com/help/index.html)
http://www.ichat.com/help/index.html
America Online Users: i-chat does not support AOL's browser. If
you do not have Netscape or Internet Explorer (NOT AOL's version
of IE) and do not want to download either of the browsers, you
may access the chatroom via AOL, then select HTML script, although
you may experience problems.
D/L Netscape: www.netscape.com (Keyword to: http://www.netscape.com/)
http://www.netscape.com
D/L IE: www.internetexplorer.com (Keyword to: http://www.internetexplorer.com/)
http://www.internetexplorer.com/
Tuesdays, 9:00 PM ET, Arthritis Chat
Wednesday 9:00 PM ET, Heart Transplant Support
Wednesdays, 10:00 PM ET, Transplant Support Chat
Thursdays 8:00 PM ET, Heart Smart
Many others coming soon
IF YOU'RE INTESTED IN HOSTING A CHAT PLEASE REPLY FOR INFO :).
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The International Transplant 1996 Directory, Published by "Transplant
News" (Not SacMall-Transplant News) is available at no charge, ($6.00 S&H)
from Transplant Awareness Inc. I highly recommend for anyone interested
in transplants. It includes:
*Complete listiing, by state, of every organ, tissue, eye and
bone marrow transplant
program, and patient support groups.
*All Federal government agencies and contqact person involved
in directing
transplant programs.
*Pharmaceutical/biotechnology companies.
*Insuance and managed care companies with "centers of excellence"
networks
including a list of centers by organ.
*National office of all the major transplant organizations.
*International organ, tissue, eye and bone marrow programs.
*Website internet and World Wide Web address.
Sent $6.00 for Shipping and Handling to Transplant Awareness Inc,
P. O. Box 7634 Arlington, Va. 22207. Phone 703-534-8587,
Fax 703-534-7759, Email tai01@aol.com
Thanks to Transplant News and Transplant Awareness Inc. for this
generous donation. Please contact either org. for the 1997 edition.
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Reader Requested Info...A Randomized Controlled Trial of Epoprostenol
Therapy for Severe Congestive Heart Failure: The Flolan International
Randomized Survival Trial (FIRST) Summary: This trial evaluated
the effects of epoprostenol on patients with severe left ventricular
failure. Patients with class IIIB/IV congestive heart failure
and decreased left ventricular ejection fraction were eligible
for enrollment if angiography documented severely compromised
hemody namics while the patient was receiving a regimen of digoxin,
diuretics, and an angiotensin-converting enzyme inhibitor. We
randomly assigned 471 patients to epoprostenol infusion or standard
care. The primary end point was survival; secondary end points
were clinical events, congestive heart failure symptoms, distance
walked in 6 minutes, and quality-of-life measures. The median
dose of epoprostenol was 4.0 ng/kg/min, resulting in a significant
increase in cardiac index (1.81 to 2.61 L/min/m2), a decrease
in pulmonary capillary wedge pressure (24.5 to 20.0 mm Hg), and
a decrease in systemic vascular resistance (20.76 to 12.33 units).
The trial was terminated early because of a strong trend toward
decreased survival in the patients treated with epoprostenol.
Chronic intravenous epoprostenol therapy is not associated with
improvement in distance walked, quality of life, or morbid events
and is associated with an increased risk of death.
[Am Heart J 134(1): 44-55, 1997. © 1997 Mosby-Year Book, Inc.]
In summary, despite both conceptual and preliminary clinical evidence
of benefit, chronic epoprostenol infusion in severe left ventricular
failure resulted in increased mortality rates and no evidence
of improved quality of life. Efforts to improve the plight of
severely symptomatic patients caused by left ventricular failure
should focus on other avenues. This trial points out the critical
importance of controlled trials that are
adequately sized and have objective measurements to assess the
clinical impact of therapeutic interventions. The poor outcome
of both the control group and the experimental group in this trial
despite treatment with standard regimens for heart failure emphasizes
the need to continue efforts in this field. The Flolan International
Randomized Survival ... (Keyword to: http://www.medscape.com/mosby/AmHeartJ/1997/v134.n01/ahj1341.califf/ahj1341.califf.html)
http://www.medscape.com/mosby/ AmHeartJ/ 1997/v134. n01/ahj1341.califf/ahj1341.califf.html
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A Preliminary Study of Ribavirin Plus Interferon in the Treatment
for Chronic Hepatitis C Robert J. Bailey, MD, University of Alberta
Edmonton, Alberta and Daphne L. Meyer, RN GI Research Capital
Health Region Edmonton, Alberta
Learning Objectives:
* To review preliminary data from a Canadian trial of interferon
plus ribavirin therapy for
chronic hepatitis C * Interferon and ribavirin have a role to
play in patients not responding and/or relapsing after previous
treatment with interferon
* It remains to be seen how effective the role is in patients
not responding to past
interferon
* Ribavirin is a safe medication in combination with interferon
Abstract:
Interferon alpha (IFN) monotherapy has resuslted in sustained
response rates for approximately 20% of patients with hepatitis
C. Ribavirin, a guanosine analogue, when used alone in patients
with hepatitis C alters transaminase values but fails to influence
the course of the disease. Preliminary studies with the two drugs,
IFN and ribavirin, in combination appear promising. The present
study was designed to assess the combination of the two drugs
in patients who had not responded to IFN or who
had relapsed when a trial of IFN had been completed.
41 patients with aminotransferases at least 1.5 times above normal
and a positive test for hepatitis C RNA by polymerase chain reaction
are undergoing treatment. Of these 41, ten relapsed after an initial
course of IFN and 31 patients were nonre-sponders to IFN. Both
groups are being treated with a combination of IFN 3 million units
three times per week and ribavirin 1000 mg per day for wt. 75
kg. The treatment period is 12 months for the relapse group, six
months for the non-responders.
At three months, ten of ten patients in the relapse group have
a normal ALT (mean 19.25). Hepatitis C RNA levels are Of the 12
patients who responded at three months, 11 have received treatment
for six months. Nine remain with a biochemical response (normal
ALT's). Hepatitis C RNA levels remain to be reported in this group.
The combination of IFN and ribavirin has few side effects, most
attributed to IFN. Ribavirin led to a drop (mean 26 g/L) in hemoglobin
and a rise (mean 9 mmol/L) in total bilirubin in five patients.
These preliminary results indicate that IFN and ribavirin appear
to be encouraging as a combination to treat patients with hepatitis
C.
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Drug May Offer New Way to Beat Colds NEW YORK (Reuters) -- It's
not a cure, but researchers say a new drug can cut the misery
of the common cold by blocking uptake of the virus itself. The
drug "reduces the illness associated with (laboratory-introduced)
rhinovirus colds in humans," reports Dr. Ronald Turner, an expert
on the common cold at the University of South Carolina in Charleston.
He presented his
findings Tuesday during a meeting of the American Society for
Microbiology (ASM) in Toronto. Rhinoviruses are viruses that infect
the nose, causing about 40% of colds in adults. They bind to human
cells via a receptor called 'intracellular adhesion molecule-1,'
or ICAM-1. When this binding is complete, infection can occur.
Turner led a team of genetic engineers to create a molecule called
BIRR 4, which closely mimics the structure of ICAM-1. When BIRR
4 is introduced into the nose via a nasal spray, it acts as a
'decoy' -- luring rhinoviruses away from ICAM-1 receptors. An
ASM statement explains that fewer rhinoviruses are then left to
bind with 'real' receptors -- "preventing attachment of the virus
to nasal cells." At present, drugs used to combat colds merely
limit the body's immune response to the virus. Previously developed
antiviral drugs have proven ineffective, with the added drawback
of unwanted side
effects. Two major drug companies -- Bayer and Boehringer Ingelheim
-- are currently developing these types of drugs. The cost to
the consumer of such a medication, if and when one became commercially
available, is unknown.
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An important quotation about Alpha1 Antitrypsin Deficiency In
the relatively short span of 30 years since its discovery, the
growing understanding of alpha1-AT [alpha1-antitrypsin] deficiency
and its therapy has revolutionized pulmonary medicine. Research
linking smoking to the development of emphysema in non-alpha1-AT-deficient
individuals has added a scientific basis to the recommendations
against
smoking for all individuals with early emphysema....While understanding
of the pathophysiology and the development of a therapy for alpha1-AT-associated
emphysema document a dramatic success story, a number of unresolved
questions remain. Still not understood are those additional factors,
other than genotype and environmental exposure, that determine
the broad clinical variability observed in individuals with alpha1-AT
deficiency. How the medical community will meet the
challenge of disseminating genetic advances made in the laboratory
to the practicing clinician and society is also highlighted by
the slow spread of information about alpha1-AT deficiency. One
recent study showed that patients with alpha1-AT deficiency were
not diagnosed until a mean age of 41, after 5.7 years of dyspnea
and/or othe respiratory symptoms. Additionally, 42% of the patients
saw an average of three physicians before their condition was
correctly diagnosed. -Wulfsberg EA, Hoffman DE, Cohen MM, Alpha1-Anyitrypsin
deficiency: impact of genetic discovery
on medicine and society. JAMA. 1994; 271:217-22.
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Porcine neural cell product for transplantation into people with
advanced Parkinson's disease was well tolerated in patients treated
with the therapy in a phase I study. The study results, presented
Sunday at a medical symposium in San Diego, also showed evidence
of clinical improvement in patients who were treated with NeuroCell-PD.
In the study's 10 evaluable patients who were measured at a time
when their L-dopa medication was wearing off, preliminary data
indicated an average improvement of 13.2 points at six months
after surgery on a standardized scale that measures a patient's
ability to perform a variety of movements. This result was statistically
significant, compared to an evaluation that was taken prior to
surgery (p<0.05).
Although there have not been any absolute epidemiologic studies
on Parkinson's disease, medical experts believe that approximately
500,000 Americans have Parkinson's disease, and another 50,000
cases are diagnosed each year. The resulting medical expenses,
early retirement, and nursing home care cost $5.6 billion a year.
http://www.genzyme.com
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St. John's Wort Study Launched Bethesda, MD--The National Institutes
of Health (NIH) is launching the first U.S. clinical trial of
St. John's wort, an herb widely used in Europe to treat depression.
The three-year study, sponsored by NIH's Office of Alternative
Medicine (OAM), the National Institute of Mental Health (NIMH)
and
the Office of Dietary Supplements (ODS), will include 336 patients
with major depression who will be randomly assigned to one of
three treatment arms for an eight-week trial. One-third of the
patients will receive a uniform dose of St. John's wort, another
third will be given placebo, and the final third will take a selective
serotonin reuptake inhibitor (SSRI), a type of antidepressant
commonly prescribed for
depression. "This study will give us definitive answers about
whether St. John's wort works for clinical depression," said NIMH
Director Steven E. Hyman, M.D. "The study will be the first rigorous
clinical trial of the herb that will be large enough and long
enough to fully assess whether it produces a therapeutic effect."
"The compilation of research done thus far, although encouraging,
still leaves some unanswered questions about exactly how the herb
works," said Wayne B. Jonas, M.D., director of OAM, which is funding
the study. "The interest and collaboration among these three NIH
components in this clinical trial will provide the scientific
expertise and clinical guidance to rigorously investigate this
herb's benefit or risk in the treatment of depression." In Germany,
where physicians routinely prescribe herbs for a variety of medical
illnesses, millions of doses of St. John's wort, known also by
its botanical name, Hypericum perforatum, are used daily. However,
no studies of long-term use have been conducted and published
studies have used several different doses. This study will use
a standardized preparation containing a 900 mg daily dose of the
herb. In addition, study participants who respond positively will
be followed for another 18 weeks. The goal of the followup is
to determine if patients given St. John's wort have fewer relapses
than patients given placebo.
An overview of 23 clinical studies in Europe, published August
3, 1996, in the British Medical Journal, found that the herb may
be useful in cases of mild to moderate depression. The NIH study
will examine patients with the moderate form of the disorder.
NIH officials said the clinical trial will be coordinated by Jonathan
Davidson, M.D., at Duke University Medical Center, which has received
a three-year contract to conduct the $4.3 million study. Patient
enrollment is expected to start next spring. For information,
call NIMH (301) 443-4536 or visit the NIMH Website at http://www.nimh.nih.gov.
Or: OAM Clearinghouse 1-888-644-6226 or visit the OAM website
at http://altmed.od.nih.gov. Watch for the new ODS website in
late Fall at
http://dietary-supplements.info.nih.gov. For info call ODS: 301-435-2920.
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Treatment for Incontinence MINNEAPOLIS, Sept. 29 /PRNewswire/Medtronic,
Inc. (NYSE: MDT) today announced clearance by the U.S. Food and
Drug Administration to market Interstim(R) Continence Control
Therapy, the first implantable treatment ever to use electrical
stimulation of the sacral nerves to manage urinary urge incontinence.
It is estimated by the Agency for Health Care Policy and Research
that approximately 13 million Americans suffer from urinary incontinence,
costing the nation's health care system an estimated $11.2 billion
annually. Of incontinence
sufferers, approximately five million people suffer from urge
incontinence -- strong, sudden urges to urinate followed by the
involuntary losses of urine. This form of incontinence is particularly
distressing for people because of the unpredictability of the
frequency and severity of these leaking episodes. While it affects
both men and women, more than 85% of sufferers in this country
are women between the ages of 30 and 59. Similar to the way a
pacemaker delivers electrical stimulation to the heart, the Interstim
Continence Control Therapy uses electrical pulses to help control
ladder function -- avoiding or at least reducing accidental urination
or leakage. It currently is being used by physicians and patients
in Europe, Canada, Australia, Africa and the Middle East. Patients
interested in the Interstim Continence Control Therapy
should consult their physician or a urologist to discuss risks
and benefits and to assess whether this therapy is appropriate
for them. Patients and physicians can
call 800-664-5111, extension 3000.
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Significant Purchasing Power on Rx Medications AKRON, Ohio, Sept.
29 /PRNewswire/ -- As a result of soaring enrollment in femScript(R)
and aVida Rx(TM) over 200,000 men and women nationwide -- people
without insurance coverage for medications or those whose plans
do not cover the cost of certain drugs are collectively saving
millions of dollars on brand name prescriptions for a wide variety
of medical conditions. Since health plans may limit or do not
offer coverage for certain prescriptions -- including Medicare
-- the opportunity to save on brand name drugs
has wide appeal. Consumers enroll via the Internet, www.femscript.com,or
a toll-free call to 800-511-1314 for an annual membership fee
of $9.95. Presentation of a membership card along with a prescription
for one of the eligible brand products entitles an individual
to the program savings at more than 25,000 participating pharmacies.
femScript(R) and aVida Rx(TM) formulary products are equal or
similar to drugs that an individual may now be taking, and Mindala
says most physicians are willing to accommodate patients with
a revised prescription when medically appropriate to save their
patients money. For more information contact Jim Mindala of FFI
Health Services, Inc. at 800-290-2007 ext. 16 or Laura Carabello
of CPR Communications, Inc., 201-641-1911.
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Reader Requested Info...Diabetes and Depression By Laura Helmuth,
DIABETES.COM One of the most common and potentially dangerous
side effects of diabetes is rarely included in the standard list
of possible complications. This condition, depression, is common
in the non-diabetic population as well, but coupled with diabetes,
it can interfere with disease management and lead to a web of
physical, mental, and emotional complications. Fortunately, depression
is treatable.
If you learn to recognize its danger signs, and know how to seek
treatment, depression can be controlled. One unexpected benefit
may be that, once depression has lifted, your diabetes should
become much easier to manage.
For centuries, physicians have noticed that chronic disease and
depression are frequent companions. As early as 1684, Dr. Thomas
Willis wrote of the "Sadness, or long sorrow" that accompanies
many chronic illnesses. If it had been 1984, he might have written
that depression seems to exacer bate diabetes, and possibly even
trigger it. Although it is not true of all diabetes cases, many
people report that the onset of their type II diabetes occurred
during a time of severe stress or depression.
Even if stress or depression did not precipitate your diabetes,
one thing is clear: Diabetes can be very depressing. In the general
population, the lifetime risk of depression is 10 to 25 percent
for women and 5 to 12 percent for men. However, the prevalence
of depression in the diabetic community is much higher--25 to
33 percent. Anyone with a chronic medical condition suffers an
increased risk of depression, but the relationship between diabetes
and depression is particularly strong because the
disease has so many possible complications, and makes relentless
demands on people who have it. Laura Helmuth is a Berkeley, California,
psychologist and writer.
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Got Allergies? Try Washing Your Cat October 3, 1997 NEW YORK (Reuters)
- If you love your cat - but your allergies are driving you crazy
- there may be a ray of hope. A new study suggests that frequently
washing your feline could reduce shedding of allergy-irritating
proteins. But getting the little kitty into the bathtub every
two to four weeks without some serious bites and scratches can
be another matter entirely, notes senior investigator Dr. Judith
Woodfolk, a research associate at the
University of Virginia Asthma and Allergic Diseases Center in
Charlottesville. And the technique may or may not be successful
at reducing sniffling and sneezing, depending on how much allergen
your cat produces.
"The major findings of the paper are that even though the (allergen)
levels are reduced, they are not maintained at low levels for
long periods of time so you would have to repeatedly wash the
cat - which may not that feasible for the patient," she said.
"It works to a degree, but its unfortunately not a very satisfactory
method."
Of the 6 million people in the U.S. that are allergic to cats,
one out of three live with at least one cat in the house, according
to the report in a recent issue of the Journal of Allergy and
Clinical Immunology. Contrary to common belief, cat hair is not
the cause of an allergic reaction. Rather proteins secreted by
the sebaceous glands in the skin accumulate on cats' hair and
can become airborne, lingering long after the cat is gone - and
causing an allergic reaction. Success may also depend on the amount
of allergen made by the cat. In the study, the cats had roughly
67 milligrams of the most allergenic protein, but varied from
3 to 142 milligrams. Total immersion reduced cat allergens by
anywhere from 19% to 92%. While removing carpets and sofas that
retain cat allergens and filtering the air are largely ineffective
at making a dent in allergen load on their own, more study is
needed to determine if adding a third step - regular cat washings
- could help reduce symptoms, the
authors concluded. SOURCE: Journal of Allergy and Clinical Immunology
(1997;100:307-312)
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Thanks to novijo@chesco.com ...
This 85 year old couple, having been married almost 60 years,
had died in a car crash. They had been in good health the last
ten years mainly due to her interest in health food, and exercise.
When they reached the pearly gates, St. Peter took them to their
mansion which was decked out with a beautiful kitchen and master
bath suite and Jacuzzi. As they "oohed and aahed" the old man
asked Peter how much all this was going to cost. "It's free,"
Peter replied, "this is Heaven."
Next they went out back to survey the championship golf course
that the home backed up to. They would have golfing privileges
everyday and each week the course changed to a new one representing
the great golf courses on earth. The old man asked, "what are
the green fees?".Peter's reply, "This is heaven, you play for
free."
Next they went to the club house and saw the lavish buffet lunch
with the cuisines of the world laid out. "How much to eat?" asked
the old man. "Don't you understand yet? This is heaven, it is
free!" Peter replied with some exasperation. "Well, where are
the low fat and low cholesterol tables?" the old man asked timidly.
Peter lectured, "That's the best part...you can eat as much as
you like of whatever you like and you never get fat and you never
get sick. This is Heaven."
With that the old man went into a fit of anger, throwing down
his hat and stomping on it, and shrieking wildly. Peter and his
wife both tried to calm him down, asking him what was wrong. The
old man looked at his wife and said, "This is all your fault.
If it weren't for your blasted bran muffins, I could have been
here ten years ago!
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Chat hosts are welcome to list their scheduled chats.
All readers are invited to submit items of interest.
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Please note* If the news article is a press release it may in
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Copyright (c) 1997 Kandysfl@aol.com. All rights reserved. You
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