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Anti-Inflammatory Treatment of COVID-19 Pneumonia With Tofacitinib Alone or in Combination With Dexamethasone is Safe and Possibly Superior to Dexamethasone as a Single Agent in a Predominantly African American Cohort.
Hayek, Maroun E; Mansour, Michael; Ndetan, Harrison; Burkes, Quentin; Corkern, Robert; Dulli, Ammar; Hayek, Reya; Parvez, Karim; Singh, Satwinder.
  • Hayek ME; Delta Regional Medical Center, Greenville, MS.
  • Mansour M; Delta Regional Medical Center, Greenville, MS.
  • Ndetan H; Department of Epidemiology and Biostatistics, The University of Texas Health Science Center at Tyler, Tyler, TX.
  • Burkes Q; Delta Regional Medical Center, Greenville, MS.
  • Corkern R; Delta Regional Medical Center, Greenville, MS.
  • Dulli A; Delta Regional Medical Center, Greenville, MS.
  • Hayek R; University of Mississippi Medical School, Jackson, MS.
  • Parvez K; Delta Regional Medical Center, Greenville, MS.
  • Singh S; Delta Regional Medical Center, Greenville, MS.
Mayo Clin Proc Innov Qual Outcomes ; 5(3): 605-613, 2021 Jun.
Article in English | MEDLINE | ID: covidwho-1157600
ABSTRACT

OBJECTIVE:

To explore the survival benefit of tofacitinib in addition to dexamethasone in hospitalized patients treated for coronavirus disease 2019 (COVID-19)-related pneumonia. PATIENTS AND

METHODS:

This is a single-center retrospective observational study. All patients who were hospitalized at Delta Regional Medical Center (a regional hospital in the Mississippi Delta) with a COVID-19 diagnosis and discharged between March 1 and September 30, 2020, are included. The primary outcome was in-hospital mortality in relation to receipt of tofacitinib alone or in addition to dexamethasone (designated as the tofacitinib group), versus dexamethasone alone (designated as the dexamethasone group).

RESULTS:

Of 269 eligible patients, 138 (51.3%) received tofacitinib uniformly and 131 (48.7%) patients received dexamethasone without tofacitinib. A total of 44 patients expired 14 (31.8%) in the tofacitinib group and 30 (68.2%) in the dexamethasone group. The proportions of death among the tofacitinib and dexamethasone groups were, respectively, 10.1% and 22.9%. This represents a 70% reduction in odds of dying among the tofacitinib group compared to the dexamethasone group after adjusting for age and clinical parameters captured at hospitalization (adjusted odds ratio 0.30; 95% CI 0.12 to 0.76; P=.01).

CONCLUSION:

The in-patient treatment of COVID-19 pneumonia has rapidly evolved. The addition of dexamethasone has made a relevant improvement on survival. Other immunomodulators have yet to show an impact. Here we present the potential survival benefit of the Janus kinase-signal transducer and activator of transcription inhibitor tofacitinib on COVID-19 pneumonia. We found that adding tofacitinib-based anti-inflammatory therapy to a treatment regimen including dexamethasone in COVID-19 pneumonia seems to have potential benefit of improving survival when compared to dexamethasone alone.
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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 Language: English Journal: Mayo Clin Proc Innov Qual Outcomes Year: 2021 Document Type: Article

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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 Language: English Journal: Mayo Clin Proc Innov Qual Outcomes Year: 2021 Document Type: Article