Volume 30, Number 3—March 2024
Dispatch
Delayed Diagnosis of Locally Acquired Lyme Disease, Central North Carolina, USA
Table
Select clinical and laboratory information for a patient with Lyme disease, central North Carolina, USA*
Characteristic | Range | Day of illness (provider) |
||||
---|---|---|---|---|---|---|
Day 10 (PCP) | Day 28 (PCP) |
Day 43 (PCP) | Day 83 (ID clinic) | |||
Signs/symptoms | ||||||
Fever >38.0°C | X | |||||
Rash | X | |||||
Fatigue | X | |||||
Headache | X | |||||
Itching | X | |||||
Left-sided ear pain | X | X | ||||
Left sided asymmetric smile | X | |||||
Inability to close left eye | X | |||||
Cognitive impairment | X | X | ||||
Other |
||||||
Laboratory testing | ||||||
Complete blood count | ||||||
Leukocytes, cells/mm3 | 4.0–11.0 | 6.1 | ||||
Hemoglobin, mg/dL | 12.9–16.0 | 13.3 | ||||
Platelets, × 109/L | 150–400 | 193 | ||||
Metabolic panel | ||||||
Sodium, mmol/L | 136–145 | 138 | ||||
Potassium, mmol/L | 3.5–5.5 | 4.0 | ||||
Creatinine, mg/dL | 0.6–1.30 | 0.70 | ||||
Liver function, U/L | ||||||
Alkaline phosphatase | 38–126 | |||||
Aspartate aminotransferase | 0–39 | |||||
Alanine aminotransferase | 0–52 | |||||
C-reactive protein, mg/L | <10 | 10.2 | <4.0 | |||
Sedimentation rate, mm/h | 0–30 | 42 | 16 | |||
Tick-borne disease testing | ||||||
Lyme EIA | <0.91 | Positive | ||||
Lyme Western blot | ||||||
IgM | 0 of 3 bands | p41, p39, p23 | ||||
IgG | 0 of 10 bands | p66, p45, p41, p39, p23, p18 | ||||
SFGR IgG | <1:64 | <1:64 | ||||
Ehrlichia IgG | <1:64 | <1:64 | ||||
α-gal IgE, kUA/L | <0.35† | 0.43 | ||||
Other infectious diseases | ||||||
HIV antigen/antibody | Nonreactive | Nonreactive | ||||
Syphilis antibody RPR |
Nonreactive |
Nonreactive |
||||
Diagnosis |
Cellulitis |
Bell’s palsy |
Lyme disease |
|||
Treatment | Cephalexin, bactrim |
Erythromycin | Valacyclovir, prednisone | Doxycycline |
*EIA, enzyme immunoassay; ID, infectious disease; PCP, primary care provider; RPR, rapid plasma reagin; SFGR, spotted fever group Rickettsia; X, present. †Reference range <0.1 kUA/L (kUA/L level of allergy): <0.35 absent, 0.35–0.69 low, 0.70–3.49 moderate, 3.50–17.5 high, >17.5 very high.
Page created: January 31, 2024
Page updated: February 22, 2024
Page reviewed: February 22, 2024
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