Critical Illness: SMART MED and SMART Surg (Isotonic Solutions and Major Adverse Renal Events Trial in Medicine)2018 Flashcards

1
Q

SMART-MED/SURG Clinical Q

A

Among medical and surgical ICU patients, does the choice of fluid (normal saline versus a balanced crystalloid such as LR or Plasma-Lyte) impact rates of death, need for renal-replacement therapy, or persistent renal dysfunction?

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2
Q

SMART-MED/SURG Bottom Line

A

Among medical and surgical ICU patients, balanced crystalloids such as LR or Plasma-Lyte reduce the rate of death, need for renal-replacement therapy, or persistent renal dysfunction, when compared to normal saline.

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3
Q

SMART-MED/SURG Primary outcome

A

Composite of death, new renal-replacement therapy, or persistent renal dysfunction

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4
Q

SMART-MED/SURG Inclusion Criteria

A

Admission to a participating adult ICU at Vanderbilt University Medical Center Eligible again if discharged and later readmitted to ICU

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5
Q

SMART-MED/SURG Intervention

A
  • ICUs were randomized to use either normal saline on even-numbered months and balanced crystalloids (LR or Plasma-Lyte A) on odd-numbered months, or vice versa.
  • Group assignments were non-blinded. The choice of LR or Plasma-Lyte A in the balanced crystalloids group was at the discretion of the treating physician.
    • For patients with a relative contraindication to balanced crystalloid (eg, hyperkalemia or brain injury) or in whom clinicians felt saline was most appropriate, the treating physician was permitted to use saline.
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6
Q

SMART-MED/SURG Criticism

A
  • Concern about application to traumatic brain injury, where balanced crystalloid hypotonicity could adversely increase intracranial pressure
  • Single-center study limits generalizability
  • Non-blinded study
  • No separate analysis of LR vs. Plasma-Lyte
  • A Patients populations determined by hospital location, composite outcomes inherently not patient-centered and susceptible to confounding
    • However, the authors state that the NIDDK recommends the adverse renal event outcome used this trial as a patient-centered outcome.
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