Lyme disease: recommendations for diagnosis and treatment
Abstract
The incidence and the endemic range of Lyme disease in the United States have increased steadily since the disease was originally recognized in Lyme, Connecticut, in 1975. Because of the varied clinical manifestations of this illness and the use of unstandardized serologic testing methods, diagnosis is often uncertain and treatment outcomes are often difficult to evaluate. The antibiotic regimens that are commonly used in clinical practice have changed rapidly. They show much regional variation with little critical comparison of treatment results. The clinical diagnosis and the literature on the treatment of the various stages of Lyme disease are reviewed. The reported data are supplemented with recommendations based on 15 years of clinical experience with this illness.
Cited By (13)
- Persistence of borrelia burgdorferi in ligamentous tissue from a patient with chronic lyme borreliosisArthritis & Rheumatism · 1993
- Invasion of Human Skin Fibroblasts by the Lyme Disease Spirochete, Borrelia burgdorferiThe Journal of Infectious Diseases · 1993
- Reversible cerebral hypoperfusion in Lyme encephalopathyNeurology · 1997
- Detection of Borrelia burgdorferi DNA by polymerase chain reaction in synovial fluid from patients with Lyme arthritisNew England Journal of Medicine · 1994
- Persistence of serum antibodies to Borrelia burgdorferi in patients treated for Lyme diseaseClinical Infectious Diseases · 1992
- Borrelia burgdorferi–Specific Immune Complexes in Acute Lyme DiseaseJAMA · 1999
- Antibodies against whole sonicated Borrelia burgdorferi spirochetes, 41-kilodalton flagellin, and P39 protein in patients with PCR- or culture-proven late Lyme borreliosis
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