Publications by authors named "L Van Pelt"

Article Synopsis
  • The study aimed to evaluate plasma procalcitonin and urine biomarkers (IL-8, NGAL, calprotectin) for diagnosing urinary tract infections (UTIs) in the emergency department.
  • While 46.4% of patients were clinically diagnosed with UTIs, procalcitonin was ineffective as a diagnostic tool, and the urine biomarkers showed elevated levels but had low specificity and only moderate accuracy compared to routine tests.
  • The urine biomarkers mainly indicated the presence of white blood cells in urine (leukocyturia) rather than providing significant additional diagnostic value, except for a slight advantage in patients with low white blood cell counts.
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Background: Diagnosis of urinary tract infections (UTIs) is a frequent challenge at the emergency department (ED). The clinical usefulness of the urine Gram stain (GS) is uncertain.

Objective: We studied the GS performance to clarify its clinical utility at the ED.

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Susceptibility of free-ranging US wildlife to SARS-CoV-2 infection has been documented. Nasal or oral swabs and blood from 337 wild mammals (31 species) in Arizona USA, tested for antibodies and by reverse-transcription PCR, did not reveal evidence of SARS-CoV-2. Broader surveillance efforts are necessary to understand the role of wildlife.

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Throughout the Americas, Lyssavirus rabies (RV) perpetuates as multiple variants among bat and mesocarnivore species. Interspecific RV spillover occurs on occasion, but clusters and viral host shifts are rare. The spillover and host shift of a big brown bat (Eptesicus fuscus) RV variant Ef-W1 into mesocarnivores was reported previously on several occasions during 2001-2009 in Flagstaff, Arizona, USA, and controlled through rabies vaccination of target wildlife.

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It is not possible to systematically screen the environment for rabies virus (RABV) using current approaches. We sought to determine under what conditions RABV is detectable from feces and other accessible samples from infected wildlife to broaden the number of biological samples that could be used to test for RABV. We employed a recently-developed quantitative RT-PCR assay called the "LN34 panlyssavirus real-time RT-PCR assay", which is highly sensitive and specific for all variants of RABV.

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