Critical Care
Showing 17 of 17 topics
  A
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            Use KDIGO criteria for staging, correct reversible causes, and choose CRRT for hemodynamic instability or cerebral edema while intermittent hemodialysis suits stable patients.
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            Use 6 mL per kg predicted body weight tidal volume, limit plateau and driving pressures, and titrate PEEP with oxygenation tables.
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            Use low tidal volume ventilation (4–8 mL/kg PBW) and limit plateau pressure ≤30 cm H2O; apply appropriate PEEP and early prolonged prone positioning in moderate–severe ARDS. Consider neuromuscular blockade and conservative fluid strategy; ECMO in refractory hypoxemia.
I
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            Use analgesia first, target light sedation with validated scales, employ daily sedation interruption or titration, and avoid prolonged benzodiazepines when possible.
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            Screen regularly, correct modifiable risks, prefer nonpharmacologic bundles, and reserve antipsychotics for severe distress or safety.
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            Start early enteral nutrition in hemodynamically stable patients, assess protein-calorie targets, and avoid overfeeding; use post-pyloric access when aspiration risk is high.
M
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            Set low tidal volume based on predicted body weight, choose appropriate PEEP and FiO2, and adjust respiratory rate to pH and PaCO2 while ensuring patient safety.
P
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            Critically ill patient on high‑dose or prolonged propofol sedation develops unexplained metabolic acidosis, rhabdomyolysis, acute kidney injury, and cardiac dysfunction—concerning for propofol‑related infusion syndrome (PRIS).
R
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            For severe hypoxemia despite optimized ventilation, use prone positioning, short-course neuromuscular blockade in select cases, recruitment and PEEP strategies, inhaled vasodilators as a bridge, and early ECMO consultation.
S
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            Screen early, obtain cultures, start broad-spectrum antibiotics, give fluids and vasopressors to maintain MAP, and monitor lactate and perfusion.
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            Apply Surviving Sepsis bundles: obtain cultures, start broad antibiotics, and give 30 mL/kg balanced crystalloids for hypotension or lactate ≥4. Use norepinephrine as first‑line vasopressor to target MAP ≥65; add vasopressin or epinephrine as needed. Achieve early source control.
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            Identify sepsis early; obtain cultures and start broad-spectrum antibiotics promptly; give 30 mL/kg crystalloid for shock or hypoperfusion; use norepinephrine as first-line vasopressor; reassess frequently.
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            Early recognition and treatment with cultures, broad-spectrum antibiotics, 30 mL/kg crystalloid for hypotension or lactate ≥4, and norepinephrine as first-line vasopressor to MAP ≥65; add vasopressin and corticosteroids for refractory shock.
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            Recognize suspected infection plus organ dysfunction; start antibiotics within 1 hour; 30 mL/kg balanced crystalloids for hypotension or lactate ≥4; norepinephrine is first-line vasopressor; reassess lactate and perfusion.
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            Suspected infection with hypotension requiring vasopressors to maintain MAP ≥65 mmHg or lactate ≥2 mmol/L despite fluids. Begin antibiotics within 1 hour, give initial 30 mL/kg crystalloid, use norepinephrine as first-line vasopressor (add vasopressin), target MAP and perfusion, and ensure early source control.
V
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            Norepinephrine is first line; add vasopressin to reduce norepinephrine dose, consider epinephrine for refractory shock, and titrate to perfusion targets.
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            Pair daily spontaneous awakening trials with spontaneous breathing trials and use standardized weaning criteria to reduce time on the ventilator.
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