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Case diagnosis and characterization of suspected paralytic shellfish poisoning in Alaska.
Knaack, Jennifer S; Porter, Kimberly A; Jacob, Justin T; Sullivan, Kate; Forester, Matthew; Wang, Richard Y; Trainer, Vera L; Morton, Steve; Eckert, Ginny; McGahee, Ernest; Thomas, Jerry; McLaughlin, Joseph; Johnson, Rudolph C.
Afiliação
  • Knaack JS; Emergency Response Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, MS F44, Atlanta, GA 30341, USA. Electronic address: Knaack_JS@Mercer.edu.
  • Porter KA; Epidemic Intelligence Service, (Alaska Section of Epidemiology), Centers for Disease Control and Prevention, 1600 Clifton Rd, Atlanta, GA 30333, USA.
  • Jacob JT; Oak Ridge Institute for Science and Education Fellow at the Centers for Disease Control and Prevention, MC-100-44, P.O. Box 117, Oak Ridge, TN, 37831-0117, USA.
  • Sullivan K; Fisheries Technology, University of Alaska Southeast, 2600 7th Ave, Ketchikan, AK 99901, USA.
  • Forester M; Alaska Environmental Health Laboratory, Alaska Department of Environmental Conservation, 5251 Dr. Martin Luther King Jr. Ave., Anchorage, AK 99507, USA.
  • Wang RY; Emergency Response Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, MS F44, Atlanta, GA 30341, USA.
  • Trainer VL; Marine Biotoxins Program, Northwest Fisheries Science Center, National Marine Fisheries Service, National Oceanic and Atmospheric Administration, Seattle, WA 98112 USA.
  • Morton S; National Centers for Coastal Ocean Science, National Oceanic and Atmospheric Administration, Marine Biotoxins Program, 219 Fort Johnson Road, Charleston, SC 29412, USA.
  • Eckert G; School of Fisheries and Ocean Sciences, University of Alaska Fairbanks, 17101 Point Lena Loop Rd., Juneau, AK 99801, USA.
  • McGahee E; Emergency Response Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, MS F44, Atlanta, GA 30341, USA.
  • Thomas J; Emergency Response Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, MS F44, Atlanta, GA 30341, USA.
  • McLaughlin J; Section of Epidemiology, Alaska Department of Health and Social Services, 3601 C Street, Suite 540, Anchorage, AK 99503, USA.
  • Johnson RC; Emergency Response Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, MS F44, Atlanta, GA 30341, USA. Electronic address: RJohnson6@cdc.gov.
Harmful Algae ; 57(Pt B): 45-50, 2016 07.
Article em En | MEDLINE | ID: mdl-28918891
ABSTRACT
Clinical cases of paralytic shellfish poisoning (PSP) are common in Alaska, and result from human consumption of shellfish contaminated with saxitoxin (STX) and its analogues. Diagnosis of PSP is presumptive and based on recent ingestion of shellfish and presence of manifestations consistent with symptoms of PSP; diagnosis is confirmed by detection of paralytic shellfish toxins in a clinical specimen or food sample. A clinical diagnostic analytical method using high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was used to evaluate the diagnosis of saxitoxin-induced PSP (STX-PSP) in 11 Alaskan patients using urine specimens collected between June 2010 and November 2011. Concentrations of urinary STX were corrected for creatinine concentrations to account for dilution or concentration of urine from water intake or restriction, respectively. Of the 11 patients with suspected PSP, four patients were confirmed to have STX-PSP by urine testing (24-364ng STX/g creatinine). Five patients had clinical manifestations of PSP though no STX was detected in their urine. Two patients were ruled out for STX-PSP based on non-detected urinary STX and the absence of clinical findings. Results revealed that dysphagia and dysarthria may be stronger indicators of PSP than paresthesia and nausea, which are commonly used to clinically diagnose patients with PSP. PSP can also occur from exposure to a number of STX congeners, such as gonyautoxins, however their presence in urine was not assessed in this investigation. In addition, meal remnants obtained from six presumptive PSP cases were analyzed using the Association of Official Analytical Chemists' mouse bioassay. All six samples tested positive for PSP toxins. In the future, the clinical diagnostic method can be used in conjunction with the mouse bioassay or HPLC-MS/MS to assess the extent of STX-PSP in Alaska where it has been suggested that PSP is underreported.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Urinálise / Testes Diagnósticos de Rotina / Intoxicação por Frutos do Mar Tipo de estudo: Diagnostic_studies Limite: Animals / Humans País como assunto: America do norte Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Urinálise / Testes Diagnósticos de Rotina / Intoxicação por Frutos do Mar Tipo de estudo: Diagnostic_studies Limite: Animals / Humans País como assunto: America do norte Idioma: En Ano de publicação: 2016 Tipo de documento: Article