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A Novel Combination of Blood Biomarkers and Clinical Stroke Scales Facilitates Detection of Large Vessel Occlusion Ischemic Strokes.
Gaude, Edoardo; Nogueira, Barbara; Ladreda Mochales, Marcos; Graham, Sheila; Smith, Sarah; Shaw, Lisa; Graziadio, Sara; Ladreda Mochales, Gonzalo; Sloan, Philip; Bernstock, Joshua D; Shekhar, Shashank; Gropen, Toby I; Price, Christopher I.
  • Gaude E; Pockit Diagnostics Ltd., Cambridge CB4 2HY, UK.
  • Nogueira B; Pockit Diagnostics Ltd., Cambridge CB4 2HY, UK.
  • Ladreda Mochales M; Pockit Diagnostics Ltd., Cambridge CB4 2HY, UK.
  • Graham S; CEPA Biobank, The Newcastle NHS Foundation Trust, Newcastle upon Tyne NE3 3HD, UK.
  • Smith S; NovoPath Biobank, Newcastle MRC Node, Newcastle NHS Foundation Trust, Newcastle upon Tyne NE1 4LP, UK.
  • Shaw L; Stroke Research Group, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
  • Graziadio S; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne NE2 4HH, UK.
  • Ladreda Mochales G; Pockit Diagnostics Ltd., Cambridge CB4 2HY, UK.
  • Sloan P; CEPA Biobank, The Newcastle NHS Foundation Trust, Newcastle upon Tyne NE3 3HD, UK.
  • Bernstock JD; Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
  • Shekhar S; University of Mississippi Medical Center, Jackson, MS 39216, USA.
  • Gropen TI; University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Price CI; Stroke Research Group, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Diagnostics (Basel) ; 11(7)2021 Jun 22.
Article in English | MEDLINE | ID: covidwho-1323140
ABSTRACT
Acute ischemic stroke caused by large vessel occlusions (LVOs) is a major contributor to stroke deaths and disabilities; however, identification for emergency treatment is challenging. We recruited two separate cohorts of suspected stroke patients and screened a panel of blood-derived protein biomarkers for LVO detection. Diagnostic performance was estimated by using blood biomarkers in combination with NIHSS-derived stroke severity scales. Multivariable analysis demonstrated that D-dimer (OR 16, 95% CI 5-60; p-value < 0.001) and GFAP (OR 0.002, 95% CI 0-0.68; p-value < 0.05) comprised the optimal panel for LVO detection. Combinations of D-dimer and GFAP with a number of stroke severity scales increased the number of true positives, while reducing false positives due to hemorrhage, as compared to stroke scales alone (p-value < 0.001). A combination of the biomarkers with FAST-ED resulted in the highest accuracy at 95% (95% CI 87-99%), with sensitivity of 91% (95% CI 72-99%), and specificity of 96% (95% CI 90-99%). Diagnostic accuracy was confirmed in an independent cohort, in which accuracy was again shown to be 95% (95% CI 87-99%), with a sensitivity of 82% (95% CI 57-96%), and specificity of 98% (95% CI 92-100%). Accordingly, the combination of D-dimer and GFAP with stroke scales may provide a simple and highly accurate tool for identifying LVO patients, with a potential impact on time to treatment.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Language: English Year: 2021 Document Type: Article Affiliation country: Diagnostics11071137

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Language: English Year: 2021 Document Type: Article Affiliation country: Diagnostics11071137