Polyethylene glycol 3350

Polyethylene glycol 3350

Generic Name

Polyethylene glycol 3350

Mechanism

Polyethylene glycol 3350 (PEG‑3350) is a non‑absorbable, high‑molecular‑weight polymer that functions as an osmotic laxative.
• PEG draws water from the intestinal lumen by *osmotic gradient*, increasing the water content and bulk of the stool.
• The increased stool mass activates mechanoreceptors along the colon, stimulating peristaltic reflexes and accelerating transit time.
• No systemic absorption occurs; the drug remains within the GI tract, minimizing systemic drug interactions.

Pharmacokinetics

  • Absorption: Negligible; <1% of a dose is absorbed, primarily via the large intestine.
  • Distribution: Minimal; drug stays in the GI lumen.
  • Metabolism: None; PEG is chemically inert.
  • Elimination: Primarily by fecal routes; unchanged PEG passes from ingestion to excretion.
  • Half‑life: Not applicable to systemic circulation; effectiveness is driven by continuous luminal presence.

Indications

  • Chronic constipation (primary or secondary).
  • Analgesic‑induced constipation (e.g., opioid therapy).
  • Pre‑operative bowel preparation for colonoscopy or abdominal surgery.
  • Short‑term treatment of functional bloating and mild fecal impaction.
  • Adjunctive therapy in irritable bowel syndrome with constipation (IBS‑C) when no other laxatives are effective.

Contraindications

  • Absolute Contraindications:
  • Mechanical bowel obstruction, paralytic ileus, or gross intestinal obstruction.
  • Severe gastroparesis at the time of dosing.
  • Warnings:
  • Use cautiously in patients with chronic kidney disease (CKD) stages 4–5 or on dialysis: monitor serum electrolytes.
  • Risk of dehydration; advise adequate oral fluid intake, especially in elderly or debilitated patients.
  • Caution in patients on ACE inhibitors or ARBs; potential for hyperkalemia.
  • Drug Interactions: No clinically significant interactions because of minimal absorption, but concomitant intestinal motility agents (like prokinetics) may alter response times.

Dosing

ConditionTypical DoseAdministrationNotes
Adult chronic constipation670–1,840 g per day (1–3 sachets)Oral sachet, 1 g water, taken once daily0.35 g/kg body weight may guide starting dose; titrate up to 1.5 g/kg.
Pediatric constipation (≥5 y)0.35 g/kg/day (up to 2 g)Oral powder mixed with water or formulaDo not exceed 2 g for children <5 y.
Bowel prep for colonoscopy1 g/kg (up to 50 g)Oral, 4–6 h prior to procedureStepwise dilution recommended; often split into two doses.
Short‑term use (analgesic‑induced)1 sachet dailyOral with waterUsually 3–7 days, but may extend to 4–6 weeks depending on symptom severity.

*Take doses with a full glass (200–300 ml) of water; patients should also increase total daily fluid intake (≥2 L).*

Adverse Effects

  • Common:
  • Abdominal cramping or discomfort
  • Flatulence
  • Bloating or mild nausea
  • Diarrhea or loose stools
  • Serious (Rare):
  • Electrolyte disturbances: hyponatremia, hyperkalemia, hypomagnesemia (esp. in CKD).
  • Dehydration, especially in geriatric or critically ill patients.
  • Aspiration risk in patients with impaired swallowing.

Management:
• Monitor electrolytes in high‑risk patients.
• Re‑hydrate with oral or intravenous fluids as needed.
• For electrolyte imbalance, discontinue or adjust dose and treat underlying imbalance.

Monitoring

  • Fluid Balance: Assess intake/output; ensure adequate hydration.
  • Serum Electrolytes: Sodium, potassium, magnesium, especially in CKD, heart failure, or those on diuretics/ACEi/ARB.
  • Renal Function: Serum creatinine/BUN in at-risk populations.
  • Stool Frequency/Consistency: Use Bristol Stool Scale; documentation of improvement aids titration.
  • Adverse Events: Document any severe abdominal pain, persistent diarrhea, or signs of obstruction.

Clinical Pearls

  • Use the “PEGA‑FITS” mnemonic to remember patient selection: Patients with constipation, Elevated risk of iatrogenic dehydration, Geriatric, Aligned with Fluids, In patients on Treated with Supplemental electrolytes.
  • Double‑sook dosing strategy: Some patients benefit from splitting the total daily dose into 2–3 administrations, especially in elderly or hypotensive patients, to reduce cramping and allow gradual colonic retention.
  • Co‑administer electrolytes: In CKD or dialysis patients, regular oral potassium or magnesium supplementation can offset PEG‑induced losses.
  • PEG in the ICU: Offers a non‑systemic laxative; can be administered via nasogastric tube when oral intake is limited.
  • Avoid sodium‑loaded preparations (PEG‑3350 + sodium chloride) in patients at risk of hypernatremia; opt for potassium‑containing or isotonic formulations if needed.

*By adhering to these principles, healthcare professionals can effectively harness PEG‑3350 to alleviate constipation while minimizing potential complications.*

Medical & AI Content Disclaimers
Medical Disclaimer: Medical definitions are provided for educational purposes and should not replace professional medical advice, diagnosis, or treatment.

AI Content Disclaimer: Some definitions may be AI-generated and may contain inaccuracies. Always verify with authoritative medical references.

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