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lördag, mars 31, 2012




What Your Doctor Is Reading

Update From the Medical Journals: March 2012

March 30, 2012


By Mary Pickett, M.D.
Harvard Medical School



What's the latest news in the medical journals this month? Find out what your doctor is reading.

-Women Need Fewer Pap Tests, Says New Recommendations
-Transplant Technique Ends Need For Anti-Rejection Drugs
-More News in Brief: Statins Are Linked to Forgetfulness and Diabetes; Drug Speeds Recovery of Brain Function After Head Trauma; Deaths Due to Infection Doubled in a Decade

Women Need Fewer Pap Test, Says New Recommendations

With new recommendations, many women can now stretch the time between Pap tests to every five years. In an incredible show of unity, the American Cancer Society (ACS), the U.S. Preventative Services Task Force (USPSTF), the American Society for Colposcopy and Cervical Pathology (ACCP) and the American Society for Clinical Pathology (ASCP) have all agreed on new screening recommendations. Each group published the guidelines separately (with minor differences in wording or emphasis) but they generally agree.

These groups represent four out of five of the expert groups that advise women about Pap tests. (The other expert group, the American College of Obstetrics and Gynecology (ACOG), is reviewing this new guideline. It is likely that the ACOG will accept the same recommendations. Members of ACOG were present at the committee meetings, and ACOG has made a statement about how helpful it can be for patients if expert groups all agree.)

The best timing and frequency for cancer screening tests balances the benefits, hassles and risks of testing. Our goal should be to use screening tests often enough to catch every — or almost every — cancer, but not so often that we put women through false alarms, extra exams, biopsies that are not necessary and unnecessary treatments. Treatments for abnormalities that are found on a Pap test can result in a slightly higher risk for pregnancy complications, such as pre-term labor and early (premature) delivery.

In the case of Pap tests, we can safely change to less frequent testing. We have more than a half century of data on the use of the test. We also have modernized techniques that improve the ability of the Pap test to screen for cancer. Now we can check for HPV particles in a Pap test. Changes on the cervix usually occur after infection with the human papillomavirus (HPV).

The new recommendations tell doctors when they should only check your Pap for abnormal cells (a microscope test called "cytology") and when they should also check for virus particles (a chemical test called "HPV testing"). When Pap tests are checked for both cytology and HPV, this is called "co-testing."

Women younger than age 21: You do not need a Pap test.

Women 21-29: Have a Pap test every 3 years. Your doctor should check cytology only and should not do HPV testing as long as the cells are normal. Women up to age 26 should receive the HPV vaccine series for added protection.

Women 30-65: Have a Pap test every 5 years. Your doctor should do "co-testing." If your most recent test was done without HPV testing, have a Pap test in 3 years.

Women older than 65: Stop having Pap tests if you have had either 3 normal Pap tests or 2 normal Paps with "co-testing" between age 55 and your current age.

Here are some special situations:

- If you have HIV or take medicine that suppresses the immune system, have yearly Pap tests.

- If you have had a recent abnormal Pap test, your doctor will need to recommend a specific follow-up plan for the timing of your next Pap test. After treatment for your abnormal Pap test, it's likely that you can return to a typical screening schedule.

- If you are over 65 and have not had an abnormal pap test in the last 20 years that was rated as "CIN-2" or higher (cells that are capable of changing to cervical cancer), you can stop having Pap tests.

- If you have received the HPV vaccine, you still need to have Pap tests.

Transplant Technique Ends Need For Anti-Rejection Drugs

The initial findings from a study about organ transplants were released March 7, before the study was fully completed. The journal Science Translational Medicine1 published this research early because the study might end the need for anti-rejection drugs in the years after transplant surgery.

These strong medicines suppress the immune system. But you need a healthy immune system to fight infection and cancer. It would be ideal if immune-suppressant drugs weren't needed after transplants. People who have received their donated organ from a twin or very close relative don't need the drugs. The immune system does not see the organ as foreign.

An exciting technique called "chimerism" might prevent the need for taking immune-suppressant drugs forever after a transplant. Cells from the kidney donor's immune system are transplanted along with the organ. Before the transplant, doctors give the patient mild doses of radiation and chemotherapy. This makes the patient's immune system less active. The new immune cells along with the transplanted organ must be introduced while the immune system is not at its most active.

Because the donor's immune cells are mixed with the patient's own immune cells, the body seems to accept the transplanted tissue as if it had always been there.

People in the study received organs donated by strangers. There was a high chance the organs would be rejected without use of this new technique.

Five of the eight kidney transplant patients from the study now do not need any immune system drugs. Two more patients are able to take only one drug. These are extraordinarily successful results for such a new technique.

More than 25,000 transplants are done each year. Transplants with chimerism may be a way to provide what doctors are calling "transplant tolerance." If this technique seems safe and successful after more experience, it is likely to become the standard of care for transplant surgery.

More News in Brief

Statins are Linked to Forgetfulness and Diabetes. Millions of Americans take statin drugs, such as atorvastatin (Lipitor) and simvastatin (Zocor), to help lower cholesterol. In a news release from February 28, the U.S. Food and Drug Administration (FDA) advised that statin drugs can cause forgetfulness and confusion, or can trigger new diabetes in some people.

Although the FDA has requested new labels for cholesterol drugs to warn of these possible side effects. But it did not recommend to doctors that the drugs should be used any less often than they are now. The effects on memory and thinking went away when people stopped taking the medicine. The effect on blood sugar levels was minor. Although this news has made some people with diabetes wonder if stopping the drug might make their diabetes disappear, this is not realistic. Most people with diabetes could not make their diabetes go away by stopping a statin drug. Stopping the drug is not recommended for diabetics. Statins help to prevent heart attack in people who are at increased risk.

In the same news release, the FDA announced that after years of close monitoring, liver inflammation has been shown to be a very uncommon side effect of statin drugs. As a result, the FDA says that regular blood tests to check the liver are no longer necessary for people who take statins.

Drug Speeds Recovery of Brain Function After Head Trauma. People who have severe brain damage or coma after a head injury have an uncertain recovery. Doctors often prescribe the drug amantadine to patients who are newly hospitalized with traumatic brain injury. This drug can change the mix of neurotransmitters (brain hormones) in a way that might help recovery. Previously, doctors weren't sure whether this drug had a true benefit. Other studies of amantadine were small and were not rigorously designed. But on March 1 the New England Journal of Medicine published a randomized study of 184 patients2. This study showed a clear benefit. Patients who received amantadine improved faster. Amantadine was originally designed to fight viral infections. Now it will become standard treatment for the initial recovery weeks after traumatic brain injury.

Deaths Due to Infection Doubled in a Decade. According to a report by the U.S. Centers for Disease Control on March 20, deaths from infections more than doubled in the 10 years from 1997 and 2007. This increase is primarily due to two infections that have become increasingly common: Clostridium difficile colitis ("C Diff") and norovirus. Most of the deaths that accounted for the increase occurred in people who were older than 65.

"C Diff" is an infection caused by a bacterial spore. There are several risk factors that make it more likely you might have a C. difficile infection. Having a hospital stay increases your chance of being exposed to C. difficile spores. Regular use of antacid medicines make it easier for these spores to survive. Antibiotics change your normal flora in the intestines. This allows the spore to become a form of bacteria that causes severe inflammation in the colon. To reduce C. difficile infections, doctors must isolate patients who have this infection from others in the hospital. And doctors have to minimize unnecessary use of antibiotics. It is common for C. difficile to be resistant to antibiotics, so some cases are difficult to treat.

Norovirus has caused several outbreaks in the last decade, including diarrhea illnesses on a cruise ship and in hospitals.

Mary Pickett, M.D. is an Associate professor at Oregon Health & Science University where she is a primary care doctor for adults. She supervises and educates residents in the field of Internal Medicine, for outpatient and hospital care. She is a Lecturer for Harvard Medical School and a Senior Medical Editor for Harvard Health Publications.

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1. J. Leventhal, et al. "Chimerism and tolerance without GVHD or engraftment syndrome in HLA-mismatched combined kidney and hematopoietic stem cell transplantation." Science Translational Medicine. 2012; Vol 4: 124-128.
2. J. Giacino, et al. "Placebo-controlled trial of amantadine for severe traumatic brain injury." New England Journal of Medicine. 2012; 366(9): 819-826.

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