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Physiologic Response to Angiotensin II Treatment for Coronavirus Disease 2019-Induced Vasodilatory Shock: A Retrospective Matched Cohort Study.
Leisman, Daniel E; Mastroianni, Fiore; Fisler, Grace; Shah, Sareen; Hasan, Zubair; Narasimhan, Mangala; Taylor, Matthew D; Deutschman, Clifford S.
  • Leisman DE; Department of Medicine, Massachusetts General Hospital, Boston, MA.
  • Mastroianni F; Sepsis Research Laboratory, Feinstein Institute for Medical Research, Manhasset, NY.
  • Fisler G; Sepsis Research Laboratory, Feinstein Institute for Medical Research, Manhasset, NY.
  • Shah S; Division of Pulmonary and Critical Care Medicine, Northwell Health, New Hyde Park, NY.
  • Hasan Z; Zucker School of Medicine at Hofstra-Northwell, Hempstead, NY.
  • Narasimhan M; Zucker School of Medicine at Hofstra-Northwell, Hempstead, NY.
  • Taylor MD; Division of Critical Care Medicine, Department of Pediatrics, Cohen Children's Medical Center, New Hyde Park, NY.
  • Deutschman CS; Zucker School of Medicine at Hofstra-Northwell, Hempstead, NY.
Crit Care Explor ; 2(10): e0230, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: covidwho-873085
ABSTRACT

OBJECTIVES:

To assess the early physiologic response to angiotensin-II treatment in patients with coronavirus disease 2019-induced respiratory failure and distributive shock.

DESIGN:

Retrospective consecutive-sample cohort study.

SETTING:

Three medical ICUs in New York during the coronavirus disease 2019 outbreak. PATIENTS All patients were admitted to the ICU with respiratory failure and were receiving norepinephrine for distributive shock.

INTERVENTIONS:

The treatment groups were patients who received greater than or equal to 1 hour of angiotensin-II treatment. Time-zero was the time of angiotensin-II initiation. Controls were identified using a 21 hierarchical process that matched for 1) date and unit of admission; 2) specific organ support modalities; 3) age; 4) chronic lung, cardiovascular, and kidney disease; and 5) sex. Time-zero in the control group was 21 hours post vasopressor initiation, the mean duration of vasopressor therapy prior to angiotensin-II initiation in the treated group. MEASUREMENTS AND MAIN

RESULTS:

Main outcomes were trajectories of vasopressor requirements (in norepinephrine-equivalent dose) and mean arterial pressure. Additionally assessed trajectories were respiratory (Pao2/Fio2, Paco2), metabolic (pH, creatinine), and coagulation (d-dimer) dysfunction indices after time-zero. We also recorded adverse events and clinical outcomes. Trajectories were analyzed using mixed-effects models for immediate (first 6 hr), early (48 hr), and sustained (7 d) responses. Twenty-nine patients (n = 10 treated, n = 19 control) were identified. Despite matching, angiotensin-II-treated patients had markedly greater vasopressor requirements (mean 0.489 vs 0.097 µg/kg/min), oxygenation impairment, and acidosis at time-zero. Nonetheless, angiotensin-II treatment was associated with an immediate and sustained reduction in norepinephrine-equivalent dose (6 hr model ß = -0.036 µg/kg/min/hr; 95% CI -0.054 to -0.018 µg/kg/min/hr, p interaction=0.0002) (7 d model ß = -0.04 µg/kg/min/d, 95% CI -0.05 to -0.03 µg/kg/min/d; p interaction = 0.0002). Compared with controls, angiotensin-II-treated patients had significantly faster improvement in mean arterial pressure, hypercapnia, acidosis, baseline-corrected creatinine, and d-dimer. Three thrombotic events occurred, all in control patients.

CONCLUSIONS:

Angiotensin-II treatment for coronavirus disease 2019-induced distributive shock was associated with rapid improvement in multiple physiologic indices. Angiotensin-II in coronavirus disease 2019-induced shock warrants further study.
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Tipo de estudio: Estudio de cohorte / Estudio experimental / Estudio observacional / Estudio pronóstico / Ensayo controlado aleatorizado Idioma: Inglés Revista: Crit Care Explor Año: 2020 Tipo del documento: Artículo País de afiliación: Cce.0000000000000230

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Tipo de estudio: Estudio de cohorte / Estudio experimental / Estudio observacional / Estudio pronóstico / Ensayo controlado aleatorizado Idioma: Inglés Revista: Crit Care Explor Año: 2020 Tipo del documento: Artículo País de afiliación: Cce.0000000000000230