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Bedside Snapshot
  • Core dose: Resuscitation: 500–1000 mL IV bolus as needed; Maintenance: 1–2 mL/kg/hr; Large volume resuscitation preferred over NS
  • Onset/duration: Volume effect immediate; similar intravascular persistence to NS (~25% at 1 hr); most redistributes to interstitium
  • Key danger: Volume overload in heart/renal failure; mild hyperkalemia risk (contains K⁺ 5 mEq/L); avoid in hyperkalemia
  • Special: Balanced crystalloid with acetate/gluconate buffers; near-physiologic pH; less hyperchloremic acidosis vs NS; preferred for large-volume resuscitation per SMART/SALT-ED trials
Brand & Generic Names
  • Generic/Official: Plasma-Lyte A Injection, pH 7.4 (Multiple Electrolytes Injection, Type 1, USP)
  • Brand Names: Plasma-Lyte A
Medication Class

Balanced isotonic crystalloid (acetate/gluconate buffered)

Pharmacology

Mechanism of Action (Pharmacodynamics):

  • Expands extracellular fluid (intravascular + interstitial)
  • Compared with 0.9% saline, lower chloride load and buffer anions reduce risk of hyperchloremic metabolic acidosis and help maintain acid–base neutrality

Disposition (Pharmacokinetics/Physiology):

  • Distribution: Rapid distribution from plasma to interstitium; ~25–30% of a bolus persists intravascularly after equilibration
  • Metabolism: Acetate/gluconate are quickly metabolized (liver, muscle, kidney) to bicarbonate and CO₂/H₂O
  • Elimination: Electrolytes are renally excreted under hormonal control
Dosing & Administration

Adults (Sepsis/Shock):

  • Initial crystalloid: 30 mL/kg within 3 hours (guideline suggestion)
  • Reassess after each bolus and titrate to perfusion endpoints (MAP ≥65 mmHg, mental status, UOP)
  • General bolus examples: 500–1,000 mL with frequent reassessment
  • Maintenance rates per institutional protocol and clinical status

Pediatrics:

  • Shock/Dehydration bolus: 10–20 mL/kg over 5–20 minutes
  • Repeat to 40–60 mL/kg in first hour for septic shock with ICU capability
  • Special populations: Adjust aliquots in neonates/cardiac disease
Contraindications

Contraindications:

  • Hyperkalemia or risk of hyperkalemia — contains 5 mEq/L K⁺
  • Hypermagnesemia or severe renal impairment — contains 3 mEq/L Mg²⁺; avoid if predisposed
  • Metabolic alkalosis or hypocalcemia — alkalinizing effect can lower ionized Ca²⁺; contains no calcium

Cautions:

  • Fluid overload states (HF, cirrhosis, renal failure)
  • Conditions with non-osmotic vasopressin release (SIADH) — risk of hyponatremia/edema with large volumes
⚠️ Hyperkalemia Risk: Contains 5 mEq/L potassium. Use with extreme caution in patients with hyperkalemia or renal failure.
Adverse Effects

Common:

  • Fluid overload (peripheral/pulmonary edema)
  • Electrolyte shifts (K⁺/Mg²⁺)

Less Common:

  • Hypernatremia (less common than with normal saline)
  • Metabolic alkalosis with excessive volumes

Local Reactions:

  • Phlebitis
  • Infiltration
Compatibility

Lithium:

  • Sodium-containing solutions may increase renal clearance — monitor levels if co-administered

Drugs that Increase Vasopressin Effect:

  • Some antidepressants/antiepileptics: higher hyponatremia risk with large-volume infusions — monitor sodium

Blood Products:

  • Institutional policies vary; many centers prefer 0.9% saline for co-infusion/line priming
  • Check local policy before Y-site with PRBCs
Monitoring

Perfusion:

  • MAP, heart rate, mental status, capillary refill
  • Urine output (≥0.5 mL/kg/h adults; ≥1 mL/kg/h children)

Electrolytes/Acid-Base:

  • Na⁺, K⁺, Mg²⁺, Cl⁻
  • Bicarbonate/base excess; lactate
  • ABG/VBG if needed

Renal Function:

  • SCr/BUN
  • Monitor MAKE30 endpoints in ICU populations during large-volume resuscitation

Cumulative Balance:

  • Signs of overload (weights, edema, oxygenation, exam)
Composition & Physicochemical Properties (per 1,000 mL)
Component Concentration
Sodium (Na⁺) 140 mEq/L
Potassium (K⁺) 5 mEq/L
Magnesium (Mg²⁺) 3 mEq/L
Chloride (Cl⁻) 98 mEq/L
Acetate 27 mEq/L
Gluconate 23 mEq/L
Osmolarity ≈294 mOsm/L (calculated)
pH ~7.4

Properties:

  • Near-physiologic osmolality
  • Buffer anions (acetate, gluconate) are metabolized to bicarbonate, producing an alkalinizing effect
  • Strong ion difference (SID) ≈ 50 mEq/L
Clinical Uses & Indications (IV)
  • Initial resuscitation of hypovolemia, sepsis, peri-operative and trauma fluid therapy when a balanced crystalloid is preferred
  • Medication carrier and maintenance fluid (institution-specific)
  • Acid–base sensitive scenarios to limit hyperchloremic acidosis (e.g., large-volume resuscitation)
ℹ️ Note: Balanced crystalloids (Plasma-Lyte A or LR) reduced kidney event composites compared with saline in pragmatic ED/ICU trials.
Clinical Pearls
Evidence-Based Choice: Balanced crystalloids (Plasma-Lyte A or LR) reduced kidney event composites compared with saline in pragmatic ED/ICU trials.
No Calcium Content: Plasma-Lyte A contains no calcium, avoiding ceftriaxone–calcium precipitation concerns seen with LR in neonates. Still follow line-flush guidance and policy.
When to Choose Plasma-Lyte A: Consider when chloride load is a concern (metabolic acidosis, AKI risk signal with saline) and when near-physiologic pH is desired.
ℹ️ Crystalloid Comparison (At-a-Glance):
Property Plasma-Lyte A Lactated Ringer's 0.9% Saline
Na⁺ / Cl⁻ (mEq/L) 140 / 98 130 / 109 154 / 154
K⁺ / Mg²⁺ (mEq/L) 5 / 3 4 / 0 0 / 0
Buffer Acetate 27 / Gluconate 23 Lactate 28 None
Osmolarity / pH ≈294 mOsm; ~7.4 ≈273 mOsm; ~6.5 ≈308 mOsm; ~5.5
Acid–base tendency Balanced/alkalinizing Balanced/alkalinizing Hyperchloremic acidosis risk
References
  • Baxter Healthcare Corporation. (2024). PLASMA-LYTE A Injection pH 7.4 (Multiple Electrolytes Injection, Type 1, USP) — Prescribing Information. DailyMed.
  • DailyMed. (2024). PLASMA-LYTE A Injection pH 7.4 — Drug Label.
  • Semler, M. W., Self, W. H., Wanderer, J. P., et al. (2018). Balanced crystalloids versus saline in critically ill adults (SMART). New England Journal of Medicine, 378, 829–839.
  • Self, W. H., Semler, M. W., Wanderer, J. P., et al. (2018). Balanced crystalloids versus saline in noncritically ill adults (SALT-ED). New England Journal of Medicine, 378, 819–828.
  • Evans, L., Rhodes, A., Alhazzani, W., et al. (2021). Surviving Sepsis Campaign: International guidelines for management of sepsis and septic shock 2021. Intensive Care Medicine, 47, 1181–1247.