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SPOT GRADE II: Clinical Validation of a New Method for Reproducibly Quantifying Surgical Wound Bleeding: Prospective, Multicenter, Multispecialty, Single-Arm Study.
Gaizo, Daniel J Del; Spotnitz, William D; Hoffman, Rachel W; Hermann, Mark Christopher; Sher, Linda S; Spotnitz, Russell H; Genyk, Yuri S; Schorn, Ian J; Gillen, Daniel L; White, Bobby L; Miller, Bruce G; Manson, Roberto J.
Afiliação
  • Gaizo DJD; Department of Orthopedics, University of North Carolina, Chapel Hill, NC, USA.
  • Spotnitz WD; Department of Surgery, University of Virginia, Charlottesville, VA, USA.
  • Hoffman RW; Biom'Up France, SAS, Saint-Priest, France.
  • Hermann MC; Biom'Up France, SAS, Saint-Priest, France.
  • Sher LS; NAMSA, Clinical and Consulting, Minneapolis, MN, USA.
  • Spotnitz RH; Spectrum Medical, Danville, VA, USA.
  • Genyk YS; Department of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Schorn IJ; Biom'Up France, SAS, Saint-Priest, France.
  • Gillen DL; Department of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • White BL; Biom'Up France, SAS, Saint-Priest, France.
  • Miller BG; NAMSA, Clinical and Consulting, Minneapolis, MN, USA.
  • Manson RJ; Department of Statistics, University of California, Irvine, CA, USA.
Clin Appl Thromb Hemost ; 26: 1076029620936340, 2020.
Article em En | MEDLINE | ID: mdl-32703005
The SPOT GRADE (SG), a Surface Bleeding Severity Scale, is a unique visual method for assessing bleeding severity based on quantitative determinations of blood flow. This study assessed the reliability of the SG scale in a clinical setting and collected initial data on the safety and efficacy of HEMOBLAST Bellows (HB), a hemostatic agent, in abdominal and orthopedic operations. Twenty-seven patients were enrolled across 3 centers and received the investigational device. Bleeding severity and hemostasis were independently assessed by 2 surgical investigators at baseline and at 3, 6, and 10 minutes after application of HB and compared for agreement. The mean paired κ statistic for assignment of SG scores was .7754. The mean paired κ statistics for determining eligibility for participation in the trial based on bleeding severity and the mean paired κ statistics determining the presence of hemostasis were .9301 and .9301, respectively. The proportion of patients achieving hemostasis within 3, 6, and 10 minutes of HB application were 50.0%, 79.2%, and 91.7%, respectively. There were no unanticipated adverse device effects and one possible serious adverse device effect, as determined by the Independent Data Monitoring Committee (IDMC). The reliability of the SG scale was validated in a clinical setting. Initial data on the safety and efficacy of HB in abdominal and orthopedic operations were collected, and there were no concerns raised by the investigators or the IDMC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Perda Sanguínea Cirúrgica / Ferida Cirúrgica Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Perda Sanguínea Cirúrgica / Ferida Cirúrgica Idioma: En Ano de publicação: 2020 Tipo de documento: Article