Ultrasound-Based Assessment of Gastric Fluid Volume in the Pediatric Population Undergoing Elective Surgery: A Prospective, Randomized, Double-Blind Comparison of Carbohydrate-Rich Clear Fluid Versus Water at One- and Two-Hour Fasting Intervals.

Paediatr AnaesthAug 25, 2026 (epub)

Aruna Parameswari, Amrit Kumar Som, Kishore Manivannan et al.

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In 30 seconds

This prospective, randomized, double-blind trial compared gastric fluid volume (GFV) after 3 mL/kg of 10% glucose solution or water, followed by a one- or two-hour fast, in 140 healthy children aged 1–12 years undergoing elective non-gastrointestinal surgery. Ultrasound-measured mean GFV was highest after glucose with a one-hour fast (0.947 ± 0.225 mL/kg) and lowest after water with a two-hour fast (0.268 ± 0.322 mL/kg; overall p < 0.001). No child exceeded 1.5 mL/kg, and no aspiration occurred. Comfort scores were higher with one-hour glucose than with two-hour water fasting.

Key findings

  • Mean GFV was 0.947 ± 0.225 mL/kg after glucose and a one-hour fast, versus 0.340 ± 0.317 mL/kg after glucose and a two-hour fast.
  • No participant in any group had GFV above 1.5 mL/kg; no pulmonary aspiration occurred.
  • Perlas Grade 2 was observed in 31.4% of the one-hour glucose group and 8.6% of the one-hour water group, with none in the two-hour groups.
  • Comfort scores were higher with one-hour glucose fasting than with two-hour water fasting (8.31 ± 0.63 vs 6.66 ± 0.97; p < 0.001).

Why it matters

The trial provides quantitative ultrasound data on gastric contents after abbreviated clear-fluid fasting in children, including carbohydrate-rich fluid. The higher measured volumes after one-hour fasting are relevant to aspiration-risk assessment, while the absence of volumes above the study’s 1.5 mL/kg threshold and the improved comfort scores inform evaluation of shorter fasting intervals.

What to keep in mind

The study involved healthy children undergoing elective non-gastrointestinal surgery at a tertiary referral centre; its findings do not establish safety in other pediatric populations or settings. No aspiration events occurred, so the trial cannot quantify aspiration risk.

Source

Published in Paediatr Anaesth. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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