Risk factors for administration of additional reversal following neuromuscular blockade with rocuronium in children:

Susan R Vishneski1, Amit K Saha1, Madeline R Fram2

  • 1Department of Anesthesiology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.

Paediatric Anaesthesia
|April 19, 2022
PubMed

Insights

Residual neuromuscular blockade in children is often treated with additional reversal agents. Key risk factors include short time to reversal, high rocuronium dose, low initial neostigmine dose, and African American race.

Area of Science:

  • Anesthesiology
  • Pediatric Anesthesia
  • Pharmacology

Background:

  • Residual neuromuscular blockade (RNB) in pediatric patients is not well understood.
  • Risk factors for requiring additional reversal after initial rocuronium reversal are unclear.

Purpose of the Study:

  • To identify patient and anesthetic factors associated with the need for additional reversal in children.
  • To investigate risk factors for residual neuromuscular blockade after neostigmine reversal of rocuronium.

Main Methods:

  • Retrospective electronic health record review of pediatric patients (<18 years) receiving rocuronium and neostigmine reversal (2017-2020).
  • Defined outcome as administration of additional neostigmine or sugammadex post-initial reversal.
  • Analyzed covariates including time to reversal, rocuronium dose, initial neostigmine dose, race, and monitoring use.

Main Results:

  • 1.58% (101/6373) of patients required additional reversal.
  • Significant risk factors included time <28 minutes from rocuronium to neostigmine (OR 1.52), cumulative rocuronium dose >0.45 mg/kg/hr (OR 1.71), initial neostigmine dose <0.05 mg/kg (OR 4.98), and African American race (OR 1.78).

Conclusions:

  • Time to reversal, cumulative rocuronium dose, initial neostigmine dose, and African American race are associated with increased need for additional reversal.
  • These findings highlight key factors contributing to residual neuromuscular blockade in pediatric patients.
  • Optimizing reversal strategies may reduce the incidence of residual neuromuscular blockade.
Abstract

Related Concept Videos

Depolarizing Blockers: Pharmocokinetics01:19

Depolarizing Blockers: Pharmocokinetics

Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
394
Nondepolarizing (Competitive) Neuromuscular Blockers: Pharmacological Actions01:27

Nondepolarizing (Competitive) Neuromuscular Blockers: Pharmacological Actions

Nondepolarizing neuromuscular blockers prevent the membrane depolarization of muscle cells and inhibit muscle contraction. These are usually administered with anesthetics to achieve complete muscle relaxation. Upon administration, these drugs first block the small, rapidly contracting muscles of the face and hands, followed by the larger muscles of the trunk and the intercostal muscles. The diaphragm is the last muscle to be affected.
Although all competitive neuromuscular blockers are designed...
578
Skeletal Muscle Relaxants: Therapeutic Uses01:31

Skeletal Muscle Relaxants: Therapeutic Uses

Skeletal muscle relaxants are used to relax muscle tone and alleviate painful muscle contractions. However, the choice of skeletal muscle relaxants depends on the duration of the surgical procedure in order to minimize potential side effects. Skeletal muscle relaxants like neuromuscular blocking agents [NMBAs] are commonly employed as adjuvants alongside general anesthetics in clinical settings. NMBAs are also used to maintain controlled ventilation during surgery of the larynx or pharynx...
654
Nondepolarizing (Competitive) Neuromuscular Blockers: Mechanism of Action01:17

Nondepolarizing (Competitive) Neuromuscular Blockers: Mechanism of Action

Nondepolarizing neuromuscular blockers induce paralysis by competitively blocking nicotinic acetylcholine receptors at the muscle end plate. Examples include pancuronium, mivacurium, vecuronium, and rocuronium. These quaternary ammonium derivatives are administered intravenously, are poorly absorbed, and are excreted via the kidneys.
Competitive antagonists prevent acetylcholine from binding to its receptor, inhibiting membrane depolarization. Without conformational changes or intrinsic...
2.2K
Skeletal Muscle Relaxants: Adverse Effects01:21

Skeletal Muscle Relaxants: Adverse Effects

Skeletal muscle relaxants are widely used for muscle paralysis and relieving pain following any muscle injury or stiffness. However, depending on the drug type, they can have adverse effects that range from mild to severe. Usually, nondepolarizing neuromuscular blockers have minimal side effects. For example, drugs like d-tubocurarine, cisatracurium, and rocuronium cause hypotension, whereas drugs like baclofen, when stopped abruptly, can lead to the recurrence of spastic conditions.
Unlike...
502
Nondepolarizing (Competitive) Neuromuscular Blockers: Pharmacokinetics01:11

Nondepolarizing (Competitive) Neuromuscular Blockers: Pharmacokinetics

All neuromuscular blocking agents are injected intravenously because they are poorly absorbed from the GI tract. Rapid onset is achieved with intravenous administration, although absorption is also adequate from an intramuscular injection. Since these agents are highly ionized, they do not readily penetrate cell membranes or cross the blood-brain barrier.
Instead, they are transported by the blood to different tissues. Muscles with a greater blood supply (arteries) and blood flow receive more...
548