July 3rd, 2012
07:39 PM ET
Shingles is a painful but common condition, affecting half of Americans by age 85. All adults aged 60 and older should receive a vaccine against it, according to the CDC's Advisory Committee on Immunization Practices.
But not everyone is eligible for this preventive measure. The vaccine is not recommended for people being treated with immune-suppressing drugs called “biologics,” which control how the body reacts to inflammation in a variety of conditions such as rheumatoid arthritis and psoriasis.
Contrary to that advice, a new study found no increased risk for shingles among people with rheumatoid arthritis, psoriasis, psoriatic arthritis, ankylosing spondylitis, or inflammatory bowel disease who have been treated with biologic medicines and receive the shingles vaccine. The study is published in the Journal of the American Medical Association.
He says researchers worried that exposing people with weakened immunity to a live virus could result in actually infecting them rather than preventing them from getting sick. But Curtis says that really was a "theoretical concern."
Imagine a skin disease that begins with burning, itching, or tingling and progresses to a blotchy rash that erupts with blisters and can produce a sensation where anything that brushes against your skin produces unbearable, intense pain. That’s how the pain of having shingles has been described.
Shingles is caused by varicella zoster virus - the same virus that causes chickenpox. Anybody who has had chickenpox is susceptible to developing shingles because the virus remains in the nerve cells of the body after the chickenpox clears, and can later reactivate as shingles.
Curtis and his team analyzed data for 463,541 Medicare beneficiaries age 60 and older who had rheumatoid arthritis, psoriasis, psoriatic arthritis, ankylosing spondylitis or inflammatory bowel disease. Of them, 18,683 patients received the shingles vaccine during the study period, which was from January 2006 through December 2009. Out of that population, 633 patients had been treated with biologics.
However none of those 633 patients developed shingles within the 42-day period after the vaccination, which is when shingles would be expected to develop. One hundred thirty-eight of these patients did gone to develop shingles, but only after the 42-day period.
Curtis says that is due to the overall effectiveness of the vaccine, which has been shown to be about 40 to 50% effective. He also says this study's findings on effectiveness are comparable to what larger studies have revealed about the shingles vaccine.
How is that people who were exposed to biologics, got the shingles vaccine, despite the warning about contraindications? Probably because many people can get vaccines at large chain pharmacies without a prescription, Curtis said.
It's possible that pharmacies didn't carefully screen some customers, or patients didn't reveal all the drugs they were being treated with. Either way, this offered researchers a window of opportunity to study the effect of the shingles vaccine on people who had been treated with these immune-suppressing drugs.
Curtis doesn’t expect these trial results to be practice-changing or change the current recommendations for the shingles vaccine. But he does hope these findings will prompt future clinical trials that can include prospective, randomized, placebo controlled study of the vaccine among this particular population and perhaps reveal practice-changing results.
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