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A Multicenter Evaluation of the Seraph 100 Microbind Affinity Blood Filter for the Treatment of Severe COVID-19.
Chitty, Stephen A; Mobbs, Sarah; Rifkin, Brian S; Stogner, Steven W; Lewis, Michael S; Betancourt, Jaime; DellaVolpe, Jeffrey; Abouzahr, Fadi; Wilhelm, Andrew M; Szerlip, Harold M; Parikh, Amay; Gaeta, Robert M; Rivera, Ian; Park, Caroline; Levi, Benjamin; Anesi, George L; Alcover, Karl C; Arnold, Thomas B; Howard, Jeffrey T; Sharma, Kumar; Pratt, Kathleen P; Stewart, Ian J; Chung, Kevin K.
  • Chitty SA; Southeast Georgia Health System, Brunswick, GA.
  • Mobbs S; Southeast Georgia Health System, Brunswick, GA.
  • Rifkin BS; Hattiesburg Clinic, Hattiesburg, MS.
  • Stogner SW; Hattiesburg Clinic, Hattiesburg, MS.
  • Lewis MS; Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA.
  • Betancourt J; Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA.
  • DellaVolpe J; Methodist Hospital, San Antonio, TX.
  • Abouzahr F; Methodist Hospital, San Antonio, TX.
  • Wilhelm AM; University of Mississippi Medical Center, Jackson, MS.
  • Szerlip HM; Baylor Scott & White Health, Dallas, TX.
  • Parikh A; Advent Health, Orlando, FL.
  • Gaeta RM; Dwight D. Eisenhower Army Medical Center, Fort Gordon, GA.
  • Rivera I; Dwight D. Eisenhower Army Medical Center, Fort Gordon, GA.
  • Park C; University of Texas Southwestern Medical Center, Dallas, TX.
  • Levi B; University of Texas Southwestern Medical Center, Dallas, TX.
  • Anesi GL; University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
  • Alcover KC; Department of Medicine, Uniformed Services University of the Heath Sciences, Bethesda, MD.
  • Arnold TB; Military Cardiovascular Outcomes Research (MiCOR) Program, Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD.
  • Howard JT; The Metis Foundation, San Antonio, TX.
  • Sharma K; University of Texas San Antonio, San Antonio, TX.
  • Pratt KP; Center of Renal Precision Medicine, Department of Medicine, University of Texas Health San Antonio, San Antonio, TX.
  • Stewart IJ; Department of Medicine, Uniformed Services University of the Heath Sciences, Bethesda, MD.
  • Chung KK; Department of Medicine, Uniformed Services University of the Heath Sciences, Bethesda, MD.
Crit Care Explor ; 4(4): e0662, 2022 Apr.
Article in English | MEDLINE | ID: covidwho-1831398
ABSTRACT
The Seraph100 Microbind Affinity Blood Filter (Seraph 100) (ExThera Medical, Martinez, CA) is an extracorporeal therapy that can remove pathogens from blood, including severe acute respiratory syndrome coronavirus 2. The aim of this study was to evaluate safety and efficacy of Seraph 100 treatment for COVID-19.

DESIGN:

Retrospective cohort study.

SETTING:

Nine participating ICUs. PATIENTS COVID-19 patients treated with Seraph 100 (n = 53) and control patients matched by study site (n = 53). INTERVENTION Treatment with Seraph 100. MEASUREMENTS AND MAIN

RESULTS:

At baseline, there were no differences between the groups in terms of sex, race/ethnicity, body mass index, and need for mechanical ventilation. However, patients in the Seraph 100 group were younger (median age, 54 yr; interquartile range [IQR], 41-65) compared with controls (median age, 64 yr; IQR, 56-69; p = 0.009). Charlson comorbidity index scores were lower in the Seraph 100 group (2; IQR, 0-3) compared with the control group (3; IQR, 2-4; p = 0.006). Acute Physiology and Chronic Health Evaluation II scores were also lower in Seraph 100 subjects (12; IQR, 9-17) compared with controls (16; IQR, 12-21; p = 0.011). The Seraph 100 group had higher vasopressor-free days with an incidence rate ratio of 1.30 on univariate analysis. This difference was not significant after adjustment. Seraph 100-treated subjects were less likely to die compared with controls (32.1% vs 64.2%; p = 0.001), a difference that remained significant after adjustment. However, no difference in mortality was observed in a post hoc analysis utilizing an external control group. In the full cohort of 86 treated patients, there were 177 total treatments, in which only three serious adverse events were recorded.

CONCLUSIONS:

Although this study did not demonstrate consistently significant clinical benefit across all endpoints and comparisons, the findings suggest that broad spectrum, pathogen agnostic, blood purification can be safely deployed to meet new pathogen threats while awaiting targeted therapies and vaccines.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal: Crit Care Explor Year: 2022 Document Type: Article Affiliation country: CCE.0000000000000662

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal: Crit Care Explor Year: 2022 Document Type: Article Affiliation country: CCE.0000000000000662