Lyme disease, transmitted by a bite from a tick infected by the Borrelia burgdorferi bacteria, had long been considered easy to treat, usually requiring a single doctor’s visit and a few weeks of antibiotics for most people.
But new research from the Johns Hopkins Bloomberg School of Public Health suggests that a prolonged illness associated with the disease in some patients is more widespread and serious than previously understood.
With an estimated 240,000 to 440,000 new cases of the tick-borne illness diagnosed every year, the researchers found that Lyme disease costs the U.S. health care system between $712 million and $1.3 billion a year — or nearly $3,000 per patient on average — in return doctor visits and testing, likely to investigate the cause of some patients’ lingering symptoms of fatigue, musculoskeletal pain and memory problems. These visits come after patients have finished their original course of antibiotics.
Some doctors call those persistent symptoms post-treatment Lyme disease syndrome (PTLDS); others call it chronic Lyme disease. Still others attribute the complaints of fatigue, headaches and memory problems to the hum of daily life, the aches and pains that come with aging. At the core of the controversy is whether PTLDS can be a severe and chronic condition that requires more than reassurance and symptomatic therapy. While a blood test can confirm Lyme disease, there is no definitive test for PTLDS and there are no approved or proven treatments. It’s a controversial topic in medicine, the Johns Hopkins researchers say.
A report on the findings was published online Feb. 4 by the journal PLOS ONE.
“Our study looks at the actual costs of treating patients in the year following their Lyme diagnosis,” says study author Emily Adrion, MSc, a PhD candidate in the Department of Health Policy and Management at the Johns Hopkins Bloomberg School of Public Health.
“Regardless of what you call it, our data show that many people who have been diagnosed with Lyme disease are in fact going back to the doctor complaining of persistent symptoms, getting multiple tests and being retreated. They cost the health care system about $1 billion a year and it is clear that we need effective, cost-effective and compassionate management of these patients to improve their outcomes even if we don’t know what to call the disease.”
Read more at outbreaknewstoday.com
Pat Brown
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I had all of the symptoms that are mentioned. The treatment that was effective for me was doxycycline and metronidazole given together in relatively high doses. I recovered in a short time after receiving this treatment. Adding stevia to that regimen might add an extra measure of safety to the treatment.
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Martina Jolicoeur
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I was diagnosed in July 2012. I did not have any rash that I know of. I was bit by a tick when I was on vacation in Gettysburg, PA. I became very lethargic and my joints, especially my neck was hurting, some flu-like symptoms. My doctor checked EBV, Mono and Lymes. Lymes was positive. Tried 21-days of Doxy. Felt a little better, but then the bottom dropped out. Retested by PCR and positive. I was on 30-days of IV Rocephin. I felt better, but still had bad days, so I decided to start on a Natural Lyme Formula treatment protocol from Organic Herbal Clinic (ww w. organicherbalclinic. com), the treatment effectively treated my Lyme disease condition. The stiffness, fatigue and joint/muscle/body pains has subsided, I feel better overall than i have felt in years. 3 months after the treatment, I made an appointment with a rheumatologist in Houston, after examining me, she looked at me and told me I did not have Lyme disease because all the usual Lyme symptoms had stopped. Its almost like a miracle!
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