A systemic, tickborne disease with protean manifestations, including
dermatologic, rheumatologic, neurologic, and cardiac abnormalities. The best
clinical marker for the disease is the initial skin lesion (i.e., erythema migrans
[EM]) that occurs in 60%-80% of patients.
Laboratory criteria for diagnosis
Isolation of Borrelia burgdorferi from a clinical
specimen or
Demonstration of diagnostic immunoglobulin M or immunoglobulin
G antibodies to B. burgdorferi in serum or cerebrospinal fluid (CSF).
A two-test approach using a sensitive enzyme immunoassay or immunofluorescence
antibody followed by Western blot is recommended (7).
Case classification
Confirmed: a) a case with EM or
b) a case with at least one late manifestation (as defined below) that is laboratory
confirmed.
Comment
This surveillance case definition was developed for national
reporting of Lyme disease; it is not intended to be used in clinical diagnosis.
Definition of terms used in the clinical description and case
definition:
Erythema migrans. For purposes of surveillance, EM
is defined as a skin lesion that typically begins as a red macule or papule
and expands over a period of days to weeks to form a large round lesion, often
with partial central clearing. A single primary lesion must reach greater
than or equal to 5 cm in size. Secondary lesions also may occur. Annular erythematous
lesions occurring within several hours of a tick bite represent hypersensitivity
reactions and do not qualify as EM. For most patients, the expanding EM lesion
is accompanied by other acute symptoms, particularly fatigue, fever, headache,
mildly stiff neck, arthralgia, or myalgia. These symptoms are typically intermittent.
The diagnosis of EM must be made by a physician. Laboratory confirmation is
recommended for persons with no known exposure.
Late manifestations. Late manifestations include
any of the following when an alternate explanation is not found:
Musculoskeletal system. Recurrent, brief attacks
(weeks or months) of objective joint swelling in one or a few joints,
sometimes followed by chronic arthritis in one or a few joints. Manifestations
not considered as criteria for diagnosis include chronic progressive arthritis
not preceded by brief attacks and chronic symmetrical polyarthritis. Additionally,
arthralgia, myalgia, or fibromyalgia syndromes alone are not criteria
for musculoskeletal involvement.
Nervous system. Any of the following, alone or
in combination: lymphocytic meningitis; cranial neuritis, particularly
facial palsy (may be bilateral); radiculoneuropathy; or, rarely, encephalomyelitis.
Encephalomyelitis must be confirmed by demonstration of antibody production
against B. burgdorferi in the CSF, evidenced by a higher titer
of antibody in CSF than in serum. Headache, fatigue, paresthesia, or mildly
stiff neck alone are not criteria for neurologic involvement.
Cardiovascular system. Acute onset of high-grade
(2nd-degree or 3rd-degree) atrioventricular conduction defects that
resolve in days to weeks and are sometimes associated with myocarditis.
Palpitations, bradycardia, bundle branch block, or myocarditis alone
are not criteria for cardiovascular involvement.
Exposure. Exposure is defined as having been (less
than or equal to 30 days before onset of EM) in wooded, brushy, or grassy
areas (i.e., potential tick habitats) in a county in which Lyme disease is
endemic. A history of tick bite is not required.
Disease endemic to county. A county in which Lyme
disease is endemic is one in which at least two confirmed cases have been
previously acquired or in which established populations of a known tick vector
are infected with B. burgdorferi.
References
7. CDC. Recommendations for test performance and interpretation from the Second National
Conference on Serologic Diagnosis of Lyme Disease. MMWR 1995;44:590-1.