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1 Bureau of Communicable Diseases, Wisconsin Division of Public Health, Madison, Wis
2 Epidemic Intelligence Service, Division of Applied Public Health Training, Epidemiology Program Office, Centers for Disease Control and Prevention, Atlanta, Ga
3 Marshfield Clinic Research Foundation, Marshfield Clinic, Marshfield, Wis
CORRESPONDING AUTHOR: Edward A. Belongia, MD, Epidemiology Research Center, Marshfield Clinic Research Foundation, 1000 N. Oak Ave., Marshfield, WI 54449, belongia.edward{at}mmrf.mfldclin.edu
| ABSTRACT |
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METHODS LDSTs performed at 2 large Wisconsin reference laboratories were systematically sampled for 12 consecutive months. A standardized questionnaire was used to gather data about the submitting clinician and the patient tested. Tests were categorized as appropriate, inappropriate, or discretionary, and associations were assessed using logistic regression analysis. A test was defined as inappropriate if the patient was asymptomatic, had erythema migrans, or was treated empirically, or if the test was ordered as a test of cure.
RESULTS We surveyed 303 clinicians regarding 356 LDSTs: 72 tests (20%) were appropriate, 95 (27%) were inappropriate, and 189 (53%) were discretionary. Tests were more likely to be inappropriate if they were ordered by an emergency or urgent care physician compared with other specialists (adjusted odds ratio [AOR] 5.2, 95% confidence interval [CI], 1.320.6), or if preceded by a known tick bite (AOR 6.8, 95% CI, 2.617.6). The patient rather than the clinician requested 26% of tests, which were more likely to be inappropriate than clinician-requested tests (crude odds ratio [COR] 5.8, 95% CI, 2.513.6). Tests were more likely to be patient-requested if they were ordered by an internist (AOR 2.6, 95% CI, 1.44.8) or if the patient was
40 years old (AOR 2.2, 95% CI, 1.33.9).
CONCLUSIONS Many LDSTs are ordered inappropriately, often influenced by patient demand. Education of clinicians and patients about testing indications and contraindications is needed to reduce the number of inappropriate LDSTs.
Key Words: Lyme disease serologic tests/utilization Borrelia burgdorferi
| INTRODUCTION |
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There is persisting concern that LDSTs are used inappropriately by clinicians.57 Early serologic testing based only on tick bite or potential exposure to ticks has low sensitivity and specificity and is not recommended.8 For patients who live in areas where Lyme disease is endemic, and who have erythema migrans, serologic testing is not routinely recommended. The likelihood that these patients have Lyme disease exceeds the positive predictive value of serologic testing, and the negative predictive value of serologic testing of these patients is exceedingly low.9,10
To assess factors contributing to appropriate and inappropriate use of LDSTs, we conducted a prospective, cross-sectional survey of clinicians ordering LDSTs.
| METHODS |
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Consenting clinicians or other providers with access to the medical record completed a standardized survey questionnaire by telephone. Data gathered pertained to clinician characteristics and clinical circumstances related to each test.
Tests were classified as appropriate, inappropriate, or discretionary (indeterminate appropriateness) using clinical criteria based on published recommendations.3,4,810 A test was defined as appropriate if the patient had any objective findings consistent with disseminated Lyme disease, including joint, neurologic, or cardiac symptoms, such as arthritis, lymphocytic meningitis, cranial neuritis, or atrioventricular conduction defects. A test was defined as inappropriate if the patient was asymptomatic, had clinician-diagnosed erythema migrans, or was treated empirically with antibiotics, or the test was ordered as a test of cure (Table 1
). Because evidence-based practice guidelines do not address Lyme disease testing for other clinical symptoms (eg, arthralgias, myalgias, malaise, or fatigue), the test was defined as discretionary if it met none of these criteria.
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.10) were entered into a multivariate unconditional logistic regression model using forward stepwise selection, followed by backward elimination. Discretionary tests were excluded from this analysis. All reported P values are 2-sided and P
.05 was considered statistically significant. Statistical analyses were done with SAS version 6.12 (SAS Institute, Cary, NC). | RESULTS |
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Of the 356 LDST requests, 20% were classified as appropriate, 27% inappropriate, and 53% discretionary. Reasons for classifying tests as inappropriate were not mutually exclusive and included absence of symptoms (55%), empiric antibiotic treatment (27%), test of cure (27%), and diagnosis of erythema migrans (24%). Stratified by specialty, family physicians, internists, and emergency and urgent care physicians ordered 70% of all tests and 75% of inappropriate tests (Table 2
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Patient-initiated tests were more likely to be inappropriate than tests initiated by clinicians (Table 3
). Other characteristics significantly associated with inappropriate tests by univariate analysis included known or suspected tick bite within 30 days of illness onset, test ordered by an emergency or urgent care physician, and test done during the summer. Patient referral from another clinician and patient hospitalization were associated with a reduced likelihood of inappropriate testing.
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| DISCUSSION |
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In this study, more than one half of the inappropriate tests were for asymptomatic patients. Compared with family physicians and internists, physicians in emergency or urgent care were significantly more likely to order inappropriate tests. The reason for this finding is unclear, but we speculate that physicians in these settings may use testing as a temporizing measure, delaying final treatment decisions until the patient can follow up with his or her primary care physician. A known or suspected preceding tick bite was also strongly associated with inappropriate testing, suggesting a need for more clinician education on the risk of Lyme disease after a tick bite. A controlled study has shown that single-dose doxycycline given prophylactically can reduce the risk of Lyme disease after tick attachment in an endemic region,16 but there is no benefit to serologic testing regardless of the treatment decision. Interventions should be focused on educating providers about indications for Lyme disease testing, particularly that the absence of symptoms with or without a known or suspected recent tick bite obviates the need for testing.
We found 53% of all tests could not be classified as either appropriate or inappropriate based on published recommendations. The existing diagnostic guidelines base testing decisions on the pretest probability of Lyme disease as calculated by an expert panel.4 From a practical standpoint, clinicians and others might have difficulty calculating the pretest probability of Lyme disease; hence, the high proportion of discretionary tests.
We also found that patients requested a large number of tests, which is consistent with previous findings.6 Nearly 40% of these tests were inappropriate, although most inappropriate tests were initiated by physicians.
A limitation of this study is that clinical information was provided by clinicians without validation by medical record review, although respondents often used the medical record to complete the interview. In addition, sampling from 2 laboratories in Wisconsin might not be representative of all clinicians ordering LDSTs.
We conclude that inappropriate Lyme disease serologic testing is common in Wisconsin, and patients initiate many of these tests. Expanded education for clinicians and patients about testing indications and contraindications may reduce the number of inappropriate LDST requests. Clarification of existing testing guidelines is needed to promote optimal use of LDSTs.
| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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Funding support: Centers for Disease Control and Prevention (Atlanta, GA) cooperative agreement on applied research in emerging infections-tick-borne diseases (#UR8/CCU513366-01).
Received for publication July 28, 2003. Revision received October 7, 2003. Accepted for publication October 17, 2003.
| REFERENCES |
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