Diagnosis of Lyme Disease



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Am Fam Physician. 2005 Jul 15;72(2):297-304.

  Patient information: See related handout about Lyme disease, written by the authors of this article.

The use of serologic testing and its value in the diagnosis of Lyme disease remain confusing and controversial for physicians, especially concerning persons who are at low risk for the disease. The approach to diagnosing Lyme disease varies depending on the probability of disease (based on endemicity and clinical findings) and the stage at which the disease may be. In patients from endemic areas, Lyme disease may be diagnosed on clinical grounds alone in the presence of erythema migrans. These patients do not require serologic testing, although it may be considered according to patient preference. When the pretest probability is moderate (e.g., in a patient from a highly or moderately endemic area who has advanced manifestations of Lyme disease), serologic testing should be performed with the complete two-step approach in which a positive or equivocal serology is followed by a more specific Western blot test. Samples drawn from patients within four weeks of disease onset are tested by Western blot technique for both immunoglobulin M and immunoglobulin G antibodies; samples drawn more than four weeks after disease onset are tested for immunoglobulin G only. Patients who show no objective signs of Lyme disease have a low probability of the disease, and serologic testing in this group should be kept to a minimum because of the high risk of false-positive results. When unexplained non-specific systemic symptoms such as myalgia, fatigue, and paresthesias have persisted for a long time in a person from an endemic area, serologic testing should be performed with the complete two-step approach described above.

Lyme disease is a systemic illness resulting from infection with the spirochete Borrelia burgdorferi.1 According to the Centers for Disease Control and Prevention (CDC) definition for reportable cases of Lyme disease, the annual number of cases increased from 7,943 in 1990 to 17,730 in 2000.2,3 The disease is most prevalent in children two to 15 years of age and in adults 30 to 59 years of age.3 Figure 14 shows the endemicity of Lyme disease in areas of the United States.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendation Evidence rating References

Physicians should assess the pretest probability of a patient with suspected Lyme disease on the basis of clinical signs and symptoms and the likelihood of exposure.

C

9

Lyme disease may be diagnosed without serologic testing in a patient from a highly endemic area with objective clinical findings.

C

79,17,18

When pretest probability is moderate (e.g., a patient from a moderately endemic area with objective clinical findings), laboratory testing should be performed by means of the two- step approach. Samples drawn within four weeks of disease onset should be tested for immunoglobulin M and immunoglobulin G, and samples drawn four weeks or more after disease onset should be tested for immunoglobulin G only.

C

7,9,1719

When objective signs of Lyme disease are absent, but unexplained nonspecific systemic symptoms have persisted for a long time (i.e., several weeks) in an individual from a highly or moderately endemic area for Lyme disease, two-step testing should be considered.

C

19

When objective and nonspecific systemic symptoms of Lyme disease are absent, or when systemic symptoms have not persisted for a sustained period, serologic testing is not recommended.

C

79,17,18


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, see page 209 or http://www.aafp.org/afpsort.xml.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

View Table

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendation Evidence rating References

Physicians should assess the pretest probability of a patient with suspected Lyme disease on the basis of clinical signs and symptoms and the likelihood of exposure.

C

9

Lyme disease may be diagnosed without serologic testing in a patient from a highly endemic area with objective clinical findings.

C

79,17,18

When pretest probability is moderate (e.g., a patient from a moderately endemic area with objective clinical findings), laboratory testing should be performed by means of the two- step approach. Samples drawn within four weeks of disease onset should be tested for immunoglobulin M and immunoglobulin G, and samples drawn four weeks or more after disease onset should be tested for immunoglobulin G only.

C

7,9,1719

When objective signs of Lyme disease are absent, but unexplained nonspecific systemic symptoms have persisted for a long time (i.e., several weeks) in an individual from a highly or moderately endemic area for Lyme disease, two-step testing should be considered.

C

19

When objective and nonspecific systemic symptoms of Lyme disease are absent, or when systemic symptoms have not persisted for a sustained period, serologic testing is not recommended.

C

79,17,18


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, see page 209 or http://www.aafp.org/afpsort.xml.

Figure 1.

Risk map for areas of predicted Lyme disease transmission in the United States. The true relative risk in any given county compared with other counties might differ from that shown here and might change from year to year. Information on risk distribution within states and counties is best obtained from state and local public health authorities. Adapted from http://www.cdc.gov/ncidod/dvbid/lyme/riskmap.htm.

View Large


Figure 1.

Risk map for areas of predicted Lyme disease transmission in the United States. The true relative risk in any given county compared with other counties might differ from that shown here and might change from year to year. Information on risk distribution within states and counties is best obtained from state and local public health authorities. Adapted from http://www.cdc.gov/ncidod/dvbid/lyme/riskmap.htm.


Figure 1.

Risk map for areas of predicted Lyme disease transmission in the United States. The true relative risk in any given county compared with other counties might differ from that shown here and might change from year to year. Information on risk distribution within states and counties is best obtained from state and local public health authorities. Adapted from http://www.cdc.gov/ncidod/dvbid/lyme/riskmap.htm.

Lyme disease is associated with a variety of signs that may present at different stages of the infection. The stages include early localized, early disseminated, and late chronic (Table 1).5 The most common symptoms include skin and musculoskeletal involvement. In endemic areas, about 18 percent of infected persons present with only nonspecific systemic symptoms.6 Early diagnosis is crucial because untreated infection can result in advanced disease involving the heart, nervous system, or joints.7

TABLE 1

Clinical Features of Lyme Disease

System Stage 1 (early localized) Stage 2 (early disseminated) Stage 3 (late chronic)

Cardiac

Atrioventricular block; myopericarditis; pancarditis

Constitutional

Influenza-like symptoms

Malaise; fatigue

Fatigue

Lymphatic

Regional lymphadenopathy

Regional or generalized lymphadenopathy

Musculoskeletal

Myalgia

Migratory pain in joints, bone, muscle; brief arthritis attacks

Prolonged arthritis attacks; chronic arthritis

Neurologic

Headache

Meningitis, Bell’s palsy; cranial neuritis; radiculoneuritis

Encephalopathy; polyneuropathy; leukoencephalitis

Skin

Erythema migrans

Secondary annular lesions

Lymphocytoma; acrodermatitis chronica atrophicans


Adapted with permission from Steere AC. Lyme disease. N Engl J Med 1989;321:589.

TABLE 1   Clinical Features of Lyme Disease

View Table

TABLE 1

Clinical Features of Lyme Disease

System Stage 1 (early localized) Stage 2 (early disseminated) Stage 3 (late chronic)

Cardiac

Atrioventricular block; myopericarditis; pancarditis

Constitutional

Influenza-like symptoms

Malaise; fatigue

Fatigue

Lymphatic

Regional lymphadenopathy

Regional or generalized lymphadenopathy

Musculoskeletal

Myalgia

Migratory pain in joints, bone, muscle; brief arthritis attacks

Prolonged arthritis attacks; chronic arthritis

Neurologic

Headache

Meningitis, Bell’s palsy; cranial neuritis; radiculoneuritis

Encephalopathy; polyneuropathy; leukoencephalitis

Skin

Erythema migrans

Secondary annular lesions

Lymphocytoma; acrodermatitis chronica atrophicans


Adapted with permission from Steere AC. Lyme disease. N Engl J Med 1989;321:589.

Clinical Presentation

The onset of clinical manifestations of Lyme disease typically occurs within seven to 10 days after a tick bite, with a reported range of one to 36 days.8 Most patients (60 to 80 percent) develop the early, localized form of Lyme disease, which is characterized by erythema migrans and influenza-like symptoms.9 Research suggests that erythema migrans most commonly presents as a centrifugally expanding, erythematous annular patch10 (Figure 2). However, a recent observational cohort study11 reported that in highly endemic areas, early erythema migrans mainly presented as homogeneous or central redness rather than a peripheral erythema with partial central clearing.

Figure 2.

Typical erythema migrans rash in a patient with Lyme disease.

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Figure 2.

Typical erythema migrans rash in a patient with Lyme disease.


Figure 2.

Typical erythema migrans rash in a patient with Lyme disease.

Clinical manifestations of Lyme disease in children resemble those in adults. The most common manifestation in children is erythema migrans rash followed by arthritis, facial nerve palsy, aseptic meningitis, and carditis.3 Lyme meningitis has been reported in children with facial nerve palsy.12 As in adults, Lyme meningitis may be subtle and usually occurs without meningismus. When compared with children with viral meningitis, children with Lyme meningitis have presented with much lower rates of fever but with similar rates of headache, neck pain, and malaise.13

[corrected] Ten percent of patients also have another tick-borne illnesses, such as human granulocytic ehrlichiosis (caused by a rickettsial-like pathogen) or babesiosis (caused by Babesia microti).14 Co-infected patients commonly present with a prolonged influenza-like illness that fails to respond to antiborrelial therapy.

The most widely accepted guidelines for the diagnosis of Lyme disease are those from the American College of Physicians (ACP),15  which were based on the 1990 CDC surveillance criteria (Table 2).16 Because of the limitations of laboratory testing for Lyme disease, diagnosis is based primarily on clinical findings.7,9,17,18 An algorithm for the diagnosis of Lyme disease is presented in Figure 3

TABLE 2

CDC Clinical Case Definition for Lyme Disease

Definition

Erythema migrans, or at least one advanced manifestation, as defined below, and laboratory confirmation of infection

Advanced manifestations

Musculoskeletal system

Recurrent, brief attacks (lasting 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 criteria for diagnosis include chronic progressive arthritis, not preceded by brief attacks, and chronic symmetrical polyarthritis; 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 (must be confirmed by showing antibody production against Borrelia burgdorferi in the cerebrospinal fluid, demonstrated by a higher titer of antibody in cerebrospinal fluid than in serum); headache, fatigue, paresthesia, or mild stiff neck alone are not criteria for neurologic involvement

Cardiovascular system

Acute-onset, high-grade (2 or 3) atrioventricular conduction defects that resolve in days to weeks and are sometimes associated with myocarditis; palpitations, bradycardia, bundle branch block, or myocarditis are not criteria for cardiovascular involvement


CDC = Centers for Disease Control and Prevention.

Information from reference 16.

TABLE 2   CDC Clinical Case Definition for Lyme Disease

View Table

TABLE 2

CDC Clinical Case Definition for Lyme Disease

Definition

Erythema migrans, or at least one advanced manifestation, as defined below, and laboratory confirmation of infection

Advanced manifestations

Musculoskeletal system

Recurrent, brief attacks (lasting 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 criteria for diagnosis include chronic progressive arthritis, not preceded by brief attacks, and chronic symmetrical polyarthritis; 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 (must be confirmed by showing antibody production against Borrelia burgdorferi in the cerebrospinal fluid, demonstrated by a higher titer of antibody in cerebrospinal fluid than in serum); headache, fatigue, paresthesia, or mild stiff neck alone are not criteria for neurologic involvement

Cardiovascular system

Acute-onset, high-grade (2 or 3) atrioventricular conduction defects that resolve in days to weeks and are sometimes associated with myocarditis; palpitations, bradycardia, bundle branch block, or myocarditis are not criteria for cardiovascular involvement


CDC = Centers for Disease Control and Prevention.

Information from reference 16.

Diagnosis of Lyme Disease

Figure 3.

Algorithm for the diagnosis of Lyme disease. (IgG = immunoglobulin G; IgM = immunoglobulin M)

View Large

Diagnosis of Lyme Disease


Figure 3.

Algorithm for the diagnosis of Lyme disease. (IgG = immunoglobulin G; IgM = immunoglobulin M)

Diagnosis of Lyme Disease


Figure 3.

Algorithm for the diagnosis of Lyme disease. (IgG = immunoglobulin G; IgM = immunoglobulin M)

Laboratory Tests

The host antibody response to B. burgdorferi infection develops slowly, and only one half of patients with early-stage Lyme disease will have a positive serology. The immunoglobulin M (IgM) and immunoglobulin G (IgG) antibodies appear two to four and four to six weeks, respectively, after the onset of erythema migrans and peak at six to eight weeks. Although IgM usually declines to very low levels after four to six months of illness, IgG remains present at low levels despite successful treatment.18 Therefore, physicians should evaluate the significance of a serologic result in the context of the patient’s epidemiologic history.

Serologic testing may provide valuable information in patients who have endemic exposure and clinical findings that suggest later-stage disseminated Lyme disease, and in patients with prolonged constitutional symptoms that may suggest the early stages of Lyme disease in the absence of erythema migrans. When serologic testing is indicated, physicians should use the two-step approach recommended by the CDC’s Association of State and Territorial Public Health Laboratory Directors (ASTPHLD), in which a positive or indeterminate serology is followed by a more specific Western blot test.19 Samples drawn from patients within four weeks of disease onset undergo Western blot testing for IgM and IgG; samples drawn more than four weeks after disease onset are tested for IgG only, because the risk of false-positive results with IgM at this late stage is high.19

The specificity of this two-step approach is 99 to 100 percent compared with 81 percent for serology alone in late-stage Lyme disease.19,20  This decreases the number of false-positive results. Table 39,19,20 lists the accuracy of individual tests and the combined two-step approach. When ordering laboratory tests for Lyme disease, physicians should report the number of weeks from the onset of disease.

TABLE 3

Accuracy of Diagnostic Tests for Lyme Disease

Diagnostic test (stage of Lyme disease) Sensitivity (%) Specificity (%) LR+ LR− Probability of Lyme disease for positive tests, given different pretest probabilities (%)
2 10 50

Serology (early-stage disease)9

59

93

8.4

0.44

13 to 15

46 to 49

86 to 89

Serology (late-stage disease)9

95

81

5.0

0.06

10

38 to 39

81 to 82

Serology plus Western blot test (early and late stages)19,20*

50 to 75†

99 to 100

50 to 75

0.4 to 0.5

50 to 55

85 to 87

97 to 98


LR = likelihood ratio.

*—Included only studies that followed the complete criteria for two-step testing in the Centers for Disease Control and Prevention’s Association of State and Territorial Public Health Laboratory Directors guidelines in which samples that were positive or equivocal for serology drawn within four weeks of disease onset were followed by immunoglobulin G (IgG) and immunoglobulin M Western blot tests, and samples drawn four weeks after disease onset were followed only by IgG Western blot tests.

†—Decrease in sensitivity is associated with a lack of antibody response or seroconversion in patients with Lyme disease treated with antibiotics.

Information from references 9,19, and 20.

TABLE 3   Accuracy of Diagnostic Tests for Lyme Disease

View Table

TABLE 3

Accuracy of Diagnostic Tests for Lyme Disease

Diagnostic test (stage of Lyme disease) Sensitivity (%) Specificity (%) LR+ LR− Probability of Lyme disease for positive tests, given different pretest probabilities (%)
2 10 50

Serology (early-stage disease)9

59

93

8.4

0.44

13 to 15

46 to 49

86 to 89

Serology (late-stage disease)9

95

81

5.0

0.06

10

38 to 39

81 to 82

Serology plus Western blot test (early and late stages)19,20*

50 to 75†

99 to 100

50 to 75

0.4 to 0.5

50 to 55

85 to 87

97 to 98


LR = likelihood ratio.

*—Included only studies that followed the complete criteria for two-step testing in the Centers for Disease Control and Prevention’s Association of State and Territorial Public Health Laboratory Directors guidelines in which samples that were positive or equivocal for serology drawn within four weeks of disease onset were followed by immunoglobulin G (IgG) and immunoglobulin M Western blot tests, and samples drawn four weeks after disease onset were followed only by IgG Western blot tests.

†—Decrease in sensitivity is associated with a lack of antibody response or seroconversion in patients with Lyme disease treated with antibiotics.

Information from references 9,19, and 20.

Diagnostic Strategy

A critical factor in the interpretation of laboratory tests for Lyme disease is the pretest probability of disease. This is an estimate of the likelihood of Lyme disease based on the geographic location and the patient’s signs and symptoms. Figure 14 and Table 4 provide guidance on estimating the pretest probability of Lyme disease. If the pretest probability is high, a negative test is more likely to be falsely negative. Conversely, if the pretest probability is low, a positive test is more likely to be falsely positive.

TABLE 4

Pretest Probability of Lyme Disease and Interpretation of Serologic Testing

Endemicity of Lyme disease* Objective clinical signs and symptoms Pretest probability Laboratory testing

None or low

Absent

Very low (< 5 percent)

Not recommended (high false-positive rate)

Present

Moderately low

Recommended

Absent, but has prolonged, unexplained, nonspecific symptoms (duration of at least two weeks)

Relatively low

Consider

Moderate

Present

Moderate (20 to 80 percent)

Recommended

Moderate to high

Absent

Low

Not recommended

Absent, but has prolonged, unexplained, nonspecific symptoms (duration of at least two weeks)

Moderately low (≤ 5 to 20 percent)

Recommended

High

Present

High (≥ 80 percent)

Not recommended (high false-negative rate); diagnose Lyme disease on the basis of clinical grounds alone.


*—See Figure 14 to determine endemicity of Lyme disease in patient’s area.

†—Objective signs and symptoms are only those considered “advanced manifestations” for Lyme disease as defined by the Centers for Disease Control and Prevention (see Table 216). Therefore, a patient may present with a pretest probability of less than 2 percent with subjective signs and symptoms such as headache, malaise, or fatigue. When these symptoms persist for more than two weeks and cannot be explained, testing is recommended.

TABLE 4   Pretest Probability of Lyme Disease and Interpretation of Serologic Testing

View Table

TABLE 4

Pretest Probability of Lyme Disease and Interpretation of Serologic Testing

Endemicity of Lyme disease* Objective clinical signs and symptoms Pretest probability Laboratory testing

None or low

Absent

Very low (< 5 percent)

Not recommended (high false-positive rate)

Present

Moderately low

Recommended

Absent, but has prolonged, unexplained, nonspecific symptoms (duration of at least two weeks)

Relatively low

Consider

Moderate

Present

Moderate (20 to 80 percent)

Recommended

Moderate to high

Absent

Low

Not recommended

Absent, but has prolonged, unexplained, nonspecific symptoms (duration of at least two weeks)

Moderately low (≤ 5 to 20 percent)

Recommended

High

Present

High (≥ 80 percent)

Not recommended (high false-negative rate); diagnose Lyme disease on the basis of clinical grounds alone.


*—See Figure 14 to determine endemicity of Lyme disease in patient’s area.

†—Objective signs and symptoms are only those considered “advanced manifestations” for Lyme disease as defined by the Centers for Disease Control and Prevention (see Table 216). Therefore, a patient may present with a pretest probability of less than 2 percent with subjective signs and symptoms such as headache, malaise, or fatigue. When these symptoms persist for more than two weeks and cannot be explained, testing is recommended.

The ACP recommendations15  suggest that the diagnosis of early Lyme disease can be made on clinical grounds alone in patients who have a high pretest probability (i.e., more than 80 percent). This includes persons who reside in areas of high endemicity and have objective signs and symptoms of Lyme disease (Table 2).16 These patients should be diagnosed and treated without testing. Empiric antibiotic prophylaxis is not recommended for patients who seek care after a tick bite but who are asymptomatic. Physicians should ask these patients to return immediately if they develop any signs or symptoms such as rash, fever, or arthralgias.

Persons who reside in areas of moderate endemicity and who present with objective signs and symptoms of Lyme disease in the absence of erythema migrans rash have an intermediate probability of Lyme disease (20 to 80 percent). An example of this would be a resident of a moderately endemic area who develops joint pain. This patient should have two-step testing (serology followed by confirmatory Western blot test), with treatment guided by the results.

When the pretest probability of Lyme disease is low (less than 20 percent), serologic testing is controversial. This applies to persons who present with only nonspecific, systemic symptoms of Lyme disease (e.g., arthralgia, myalgia, or paresthesia), and asymptomatic patients who request screening. Symptoms can include all conditions that cannot be classified as advanced manifestations of Lyme disease (Table 2).16 The ACP guidelines15 recommend that physicians minimize laboratory testing in these individuals. However, experts have noted the value of the two-step approach in otherwise low-risk persons who have experienced nonspecific symptoms for at least two weeks.7,9,17,18 In one study,6 researchers found that these patients constitute 18 percent of Lyme disease cases in endemic areas during the summer months.

Patients at Low Risk

The following three clinical scenarios have been devised to help physicians determine whether the two-step approach should be used for persons who have a low pretest probability for Lyme disease.

HIGH ENDEMICITY, CONSTITUTIONAL SYMPTOMS, NO ERYTHEMA MIGRANS RASH

A patient from an area of high endemicity of Lyme disease presents with fever, headache, and arthralgias that had lasted several weeks, but no erythema migrans rash. After a thorough clinical evaluation, the cause of the symptoms remains unresolved.

The physician should consider serologic testing with the complete two-step approach. For this patient, the pretest probability is moderately low, taking into account the endemicity of the disease and the presence of prolonged (at least two weeks), unexplained nonspecific symptoms. In this scenario, if the two-step approach is positive, the probability of Lyme disease is about 90 percent. Although testing probably is beneficial in this type of patient, this has not been proven. There is no clear evidence that treatment is beneficial in patients with Lyme disease who exhibit only nonspecific symptoms.

MODERATE ENDEMICITY, SHORT-TERM NONSPECIFIC SYMPTOMS, NO ERYTHEMA MIGRANS RASH

A patient from an area of moderate endemicity of Lyme disease presents with headache and fatigue that have lasted for three days, but no erythema migrans or arthralgias.

Serologic testing should not be ordered for this patient because of the high risk (more than 50 percent) of a false-positive test result at this early stage of nonspecific disease. The patient should be advised to return for follow-up if symptoms persist. In this scenario, the pretest probability is estimated to be very low.

HIGH ENDEMICITY, SCREENING OF A CHILD

A healthy child from an area of high endemicity receives an annual physical. The mother notes that the child enjoys playing in the backyard, which is adjacent to a heavily wooded area.

Serologic testing should not be ordered because the child is asymptomatic. A false-positive test result would expose the child unnecessarily to the risks of treatment. In this scenario, the probability that a positive test represents true infection is less than 25 percent.

False-Positive and False-Negative Test Results

Among healthy persons living in a region of low endemicity, the false-positive rate with serology is about 2 to 5 percent.9,17,18 The most common reason for a positive serology test in the absence of Lyme disease is the presence of another spirochetal infection such as syphilis, spirochete periodontal infection, or relapsing fever.17 Patients with rheumatoid diseases or infectious mononucleosis also may have false-positive reactions, especially IgM.7,9,17,18

A high rate of false-positive test results is associated with the first vaccine against Lyme disease (Lymerix), which has been withdrawn from the market. This vaccine was a recombinant form of the OspA lipoprotein of B. burgdorferi. Because standard whole-cell kits use in vitro cultivated spirochetes, OspA is one of the antigens present. Therefore, a patient receiving the vaccine most likely will exhibit a positive result in any of the standard whole-cell enzyme-linked immunosorbent assay kits. To alleviate this problem, physicians should consider ordering only a Western blot test and disregarding the OspA band when determining whether the test is positive or negative in vaccinated persons.

False-negative results often are attributable to tests taken too early in the course of infection. Because the antibody response develops slowly, tests taken within the first two weeks of infection have low sensitivities (less than 50 percent). Antibiotics also can influence the results of serologic tests when given early in the course of infection, and have been shown to abort seroconversion, even if inadequate therapy is provided.7 True seronegativity in the later stages of Lyme disease is uncommon.7,17

Overdiagnosis and Underdiagnosis

Overdiagnosis most commonly is attributable to incorrect interpretation of Western blot test results, misidentification of rashes as erythema migrans, or ascribing nonspecific symptoms to Lyme disease.2123 Physicians must keep in mind that Western blot test results cannot be intermediate and should only be classified as negative or positive according to the CDC’s ASTPHLD guidelines.

Underdiagnosis may occur if physicians apply the CDC surveillance criteria too strictly (Table 2).16 A recent study24 showed that patients with prolonged nonspecific symptoms but no erythema migrans rash or advanced manifestations constitute almost 20 percent of Lyme disease cases in endemic areas during the summer months. Antibiotic therapy in these patients is useful in preventing progression to late-stage disseminated disease where response to treatment is less favorable.6,24

The Authors

DANIEL L. DEPIETROPAOLO, M.D., is medical director of Heartland Hospice, a division of HCR-Manor Care, Newark, Del., and on staff at Nemour’s-Dupont Hospital for Children, Wilmington, Del. In additon, he is clinical assistant professor of family medicine at Jefferson Medical College of Thomas Jefferson University School of Medicine in Philadelphia, and is also adjunct associate professor at the University of Delaware School of Nursing, Newark, Del., and the Wilmington College School of Nursing, Wilmington, Del. Dr. DePietropaolo was director of the Family Practice Residency Program at Christiana Care Health Services, Wilmington, Del., from 1992 to 2004. Dr. DePietropaolo received his medical degree from the University of Pittsburgh and completed his family practice residency at the Wilmington Medical Center (now Christiana Care Health Services), Wilmington, Del.

JOHN H. POWERS, M.D., F.A.C.P., is an infectious disease attending physician at the National Institute of Allergy and Infectious Diseases, National Institutes of Health, in Bethesda, Md. He is also clinical assistant professor of medicine at George Washington University School of Medicine, Washington, D.C., and the University of Maryland School of Medicine, Baltimore. Dr. Powers received his medical degree from Temple University School of Medicine, Philadelphia, and was chief resident at Temple University Hospital.

JAMES M. GILL, M.D., M.P.H., is director of the Health Services Research Group and associate program director of the family practice residency program at Christiana Care Health Services. He is also associate professor in the Department of Family Medicine at Thomas Jefferson University School of Medicine. Dr. Gill received his medical degree from the University of Medicine and Dentistry of New Jersey’s Robert Wood Johnson Medical School, Piscataway, N.J., and a master of public health degree from Johns Hopkins University, Baltimore.

ANDREW J. FOY is a first-year medical student at Jefferson Medical College of Thomas Jefferson University School of Medicine.

Address correspondence to Daniel L. DePietropaolo, M.D., 11 Lindsey Pl., Wilmington, DE 19809–2254 (e-mail: drdan1954@aol.com). Reprints are not available from the authors.

Author disclosure: Nothing to disclose.

The authors thank Anna Quisel, M.D., for her assistance with the preliminary stages of the manuscript, which was funded in part by a grant from the State of Delaware Division of Public Health.

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17. Bunikis J, Barbour AG. Laboratory testing for suspected Lyme disease. Med Clin North Am. 2002;86:311–40.

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