2011
DOI: 10.1016/j.jaad.2010.03.047
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Lyme disease

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Cited by 30 publications
(5 citation statements)
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“…The Centers for Disease Control and Prevention (CDC) proposed a two-step approach for serological testing in order to identify active disease or past infections. An ELISA or immunofluorescent antibody test (IFA) is recommended as the first-line test, after which western blot (WB) is required as a second-line confirmatory test ( 6 , 7 , 8 ). The IgM and/or IgG antibodies occur in only 20–50% of patients in the early localized stage.…”
mentioning
confidence: 99%
“…The Centers for Disease Control and Prevention (CDC) proposed a two-step approach for serological testing in order to identify active disease or past infections. An ELISA or immunofluorescent antibody test (IFA) is recommended as the first-line test, after which western blot (WB) is required as a second-line confirmatory test ( 6 , 7 , 8 ). The IgM and/or IgG antibodies occur in only 20–50% of patients in the early localized stage.…”
mentioning
confidence: 99%
“…Importantly, about 10-20% of patients (especially those who are diagnosed later), following appropriate antibiotic treatment, may have persistent or recurrent symptoms and are considered to have "post-treatment Lyme disease syndrome" [13]. In some cases, other microorganisms may be cotransmitted through the tick bite [8,12,14]. Patients found to have coinfections should be treated with appropriate therapies.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, for uniformity, a 14-day course of therapy is advised for all of the first-line oral agents [11]. Doxycycline is generally preferred since it has the advantage of being also effective for treatment of human granulocytic anaplasmosis and Borrelia lonestari and Borrelia miyamotoi infections (but not for babesiosis), which may occur simultaneously with early LD; however, it is contraindicated in children <8 years of age and during pregnancy or lactation [11,14,16]. Cefuroxime axetil is usually considered as a second-line treatment because of its cost [14].…”
Section: Introductionmentioning
confidence: 99%
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“…The case definition has become more complex as more knowledge has been gained regarding disease symptom expression and testing specificity and validity [10]. Specificity of testing, complexity of required testing, and the absence of laboratory markers early in LD onset also contribute to inadequate diagnosis of LD, thus affecting LD incidence [11,12]. The deficient knowledge of LD incidence rates may also be attributed to misdiagnosis of symptoms or the lack of recognition of late development of symptoms by providers [13,14].…”
Section: Introductionmentioning
confidence: 99%