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Is Hunting Good Or Bad

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NSAIDs possess a certain risk for kidney toxicity which contributes to fluid retention and edema while also promoting the aggravation of hypertension.



However, often underappreciated are the blood pressure and kidney effects of NSAIDs. It has long been noted that a potential risk of NSAIDs is a destabilization of blood pressure control in hypertensive patients, particularly if they are treated with ACE inhibitors.

Direct kidney toxicity, deleterious changes in kidney blood flow, and decline in kidney function are seen as a consequence in patients treated with NSAIDs. Edema and worsening of congestive heart failure (CHF) are also potential known consequences of NSAIDs. NSAIDs may also interfere with the cardioprotective effects of aspirin.

However... all is not doom and gloom for NSAIDS.

A study of Medicare patients with osteoarthritis provides additional evidence that non-steroidal anti-inflammatory drugs (NSAIDs) such as aspirin reduce the risk of colorectal cancer. Earlier investigations of the drugs' impact on tumor development could not rule out the possibility that an observed protective effect was caused by other preventive health care measures. Researchers note, however, that safer drugs are probably needed before regular preventive therapy can be recommended.

Elizabeth Lamont, MD, MS, of the Massachusetts General Hospital Cancer Center, the study's lead author, states, "Although patients face risks such as bleeding or kidney damage from NSAIDS, they probably are at a lower risk of developing colorectal cancer." Because of the risks posed by the dosage used to treat osteoarthritis, she stresses that currently available NSAIDs should not be used solely to prevent cancer.

Earlier randomized trials indicated that NSAID treatment could possibly prevent the development of precancerous colorectal polyps, but whether or not such therapy also reduces the risk of invasive colorectal cancer has not yet been confirmed. Those trials used relatively low doses of aspirin and showed no significant differences in colorectal cancer rates between the aspirin and placebo groups. While many observational studies have shown a protective effect of NSAIDs against colorectal cancer, interpretation of some of those results may have been clouded by other healthy behaviors of the participants.

First, the researchers reviewed data from the 1993-94 National Ambulatory Medical Care Survey, in which physicians report on the diagnoses of and treatments prescribed to patients seen during a randomly selected week. Those results verified that older patients with osteoarthritis were more than four times as likely to take NSAIDs as were those without osteoarthritis. They then analyzed information from the Survival Epidemiology and End-Results (SEER)-Medicare program, studying groups of elderly Medicare patients with and without colorectal cancer, to search for associations with NSAID use.

Comparing information on 4,600 individuals with colorectal cancer to data from 100,000 controls, they found that a history of osteoarthritis was associated with a 15 percent reduction in the likelihood of a colorectal cancer diagnosis.

"The magnitude of colorectal cancer risk reduction between patients with and without osteoarthritis is completely consistent with the risk reduction for pre-cancerous polyps reported in clinical trials of NSAIDs," Lamont says.

The study appears in the August 2007 Journal of General Internal Medicine.

The study also raises the 64 dollar question which is “What is the risk/benefit of taking an NSAID for cancer prevention versus the risk of cardiovascular side-effects?

As a practicing rheumatologist, I am in a constant battle with cardiologists who want to stop NSAID therapy. In addition to quality of life issues, this most recent study also raises another issue- that of possible colon cancer prevention.
Is Hunting Good Or Bad
Medical experts say that they want their patients' treatment to be “evidence-based” – that is, chosen on the basis of good research studies. They are often critical of complementary and alternative medicine (CAM) because of the limited research available by mainstream Western medical standards for any particular treatment.

The trouble is that it is hard even for doctors, let alone consumers, to figure out whether a treatment is good or bad in a particular case. This problem affects not only treatments with mainstream drugs, but also with the many different types of CAM. Especially in CAM, practitioners usually try to individualize the treatment for the unique physical and psychosocial situation of the person as a whole. What makes it so hard to tell if a treatment might be “good” or “bad” for you?

First, research studies are not individualized; rather, scientists typically do their studies on large groups of people – and then scientists average the results over everyone who participated. So, group averages do not tell doctors very much about what will work for you as the individual in front of them in the office. And the formal research testing doesn't always tell them the possible interactions between the treatment and other factors – other medications, natural products, other conditions you may have that the research study participants didn't have, genetics, environmental exposures – that can each increase or decrease the effectiveness and/or the safety of the treatment for you.

In short, research evidence often doesn't give your doctor - or you - the information he or she needs to decide whether or not a treatment will be good or bad for you in your particular and unique situation. Advice of friends and family, as well as health food store clerks, can sometimes be helpful, but they usually only know what worked for them. You can't know if you will have the same or different result.

Second, the results of any research study are most relevant to the precise conditions under which the scientists tested a particular treatment. For example, most “good” research studies recruit patients who have fewer health problems and use fewer drugs than the average patient in a doctor's office. Studies also focus on a specific outcome for a short period of time, usually an outcome that is relevant to the patients' disease, not to the patient. And they observe for 8-12 weeks or so.

If scientists test a treatment's effects on persons with headaches for 12 weeks, but the CAM treatment helps other symptoms (not headache) get better, improves overall energy, and gives them a greater sense of well-being in 12 weeks (but has little effect on the headaches until week 20 or later), the conclusion will be that the treatment “doesn't work.”

Meanwhile, CAM practitioners and patients are puzzled and even outraged to hear the results - because of the contradictions between the research conclusions and their own experience in the real world. But in the real world outside of a research study, the practitioners and patients were able to look at more than the headaches, and they were able to allow the treatment more than 12 weeks to work.

Third, people who do and don't use CAM differ in their personality type. People who choose to try CAM treatments score higher than CAM non-users on the trait of openness to experience. Openness is one of the five major dimensions of personality, along with extraversion, conscientiousness, agreeableness, and neuroticism. Other research has shown that people high in trait openness may have not only a different psychology, but also a different biology and genetics, than people low in that trait.

If a research study happens to recruit a lot of people who are low in trait openness and a CAM treatment doesn't work during the study, the results could be valid – but not relevant to the majority of people who actually use the treatment in the real world, outside the research study.

For now, the bottom line is to use common sense. If doctors and other experts haven't found any serious side-effects of a CAM treatment and your own health care providers don't see any significant risks for you with your unique health issues - and some people find the treatment helpful for problems like yours - consider trying it. Continue it if it helps; stop it if you get worse or develop a new problem.

And keep educating yourself about your health care treatment options – empower yourself with information. Don't expect your doctor or other health care providers to have all of the answers or for any one research study to give them or you the final word.
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About Author
Both Nathan Wei & Iris Bell are contributors for EditorialToday. The above articles have been edited for relevancy and timeliness. All write-ups, reviews, tips and guides published by EditorialToday.com and its partners or affiliates are for informational purposes only. They should not be used for any legal or any other type of advice. We do not endorse any author, contributor, writer or article posted by our team.

Nathan Wei has sinced written about articles on various topics from Arthritis Pain, Health and Arthritis Signs. athan Wei, MD FACP FACR is a rheumatologist and Director of the Arthritis and Osteoporosis Center of Maryland. He is a Clinical Assistant Professor of Medicine at the University of Maryland School of Medicine. For more info:. Nathan Wei's top article generates over 550000 views. to your Favourites.

Iris Bell has sinced written about articles on various topics from Arthritis Signs. . Iris Bell's top article generates over 1900 views. to your Favourites.
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