Intrathecal clonidine decreases propofol sedation requirements during spinal anesthesia in infants

Yatindra K Batra1, Sondekoppam V Rakesh, Nidhi B Panda

  • 1Department of Anaesthesia and Intensive Care, Postgraduate Institute of Medical Education and Research, Chandigarh, India. ykbatra@glide.net.in

Insights

Intrathecal clonidine or clonidine-fentanyl combinations significantly reduce propofol sedation requirements in infants undergoing surgery. Fentanyl alone did not significantly alter propofol needs, highlighting clonidine

Area of Science:

  • Pediatric Anesthesiology
  • Pharmacology
  • Surgical Sedation

Background:

  • Propofol is a common agent for procedural sedation in pediatric patients undergoing lumbar puncture and spinal anesthesia.
  • Intrathecal clonidine and fentanyl are used as adjuvants to prolong spinal anesthesia and provide postoperative analgesia.
  • This study investigated the impact of intrathecal clonidine and fentanyl on propofol requirements in infants undergoing lower abdominal surgery.

Purpose of the Study:

  • To evaluate the effect of intrathecal clonidine and fentanyl on the intraoperative propofol sedation requirement in infants undergoing spinal anesthesia.
  • To compare the propofol infusion rates needed when bupivacaine is combined with clonidine, fentanyl, or both, versus bupivacaine alone.

Main Methods:

  • A prospective, randomized, double-blind study involving 65 ASA I infants undergoing elective lower abdominal surgery.
  • Infants were assigned to four groups receiving bupivacaine alone, or bupivacaine with clonidine, fentanyl, or both.
  • Propofol was administered for sedation, with requirements assessed via infusion rates and sedation/reactivity scores.

Main Results:

  • The mean propofol infusion requirement was significantly reduced in infants who received intrathecal clonidine (16.7 microg kg(-1) min(-1)) or clonidine-fentanyl combination (14.8 microg kg(-1) min(-1)) compared to bupivacaine alone (35.5 microg kg(-1) min(-1)).
  • Intrathecal fentanyl alone (33.4 microg kg(-1) min(-1)) did not significantly alter propofol requirements compared to bupivacaine alone.
  • Higher sedation and reactivity scores were observed in the clonidine-containing groups.

Conclusions:

  • Intrathecal adjuvants, particularly clonidine, significantly decrease the need for propofol sedation during pediatric spinal anesthesia.
  • The combination of clonidine and fentanyl offers a similar reduction in propofol requirements as clonidine alone.
  • Fentanyl alone as an intrathecal adjuvant does not significantly impact propofol sedation needs in this population.
Abstract

Related Concept Videos

Parenteral Anesthetics: Overview01:24

Parenteral Anesthetics: Overview

Intravenous anesthetics are drugs administered parenterally to induce anesthesia or sedation. Propofol is a widely used agent formulated as a 1% emulsion in soybean oil, glycerol, and egg phosphatide. It induces rapid anesthesia primarily due to its rapid distribution from the bloodstream to target tissues and is metabolized in the liver. However, it can cause significant pain on injection and hypertriglyceridemia. Fospropofol, a water-based prodrug of propofol, lacks these adverse effects.
Local Anesthetics: Clinical Application as Epidural Anesthesia01:29

Local Anesthetics: Clinical Application as Epidural Anesthesia

Epidural anesthetics are administered in the fat-filled epidural space, the outermost part of the spinal canal. This technique is commonly employed for pain management and anesthesia during lower abdomen and pelvis surgeries or labor and delivery.
Since epidural anesthetics can be infused through an epidural catheter, all types of drugs, including short-acting ones, can be administered. Chloroprocaine and lidocaine are examples of short and long-duration anesthetics, respectively. Bupivacaine...
Local Anesthetics: Clinical Application as Spinal Anesthesia01:11

Local Anesthetics: Clinical Application as Spinal Anesthesia

Spinal anesthetics are given during lower abdomen and limb surgeries to block sensory and motor neurons. They are administered in the mid to low lumbar regions, primarily acting on the cauda equina's nerve roots. The blockade level depends on the local anesthetic (LA) concentration. Usually, low LA concentrations are sufficient to block sensory fibers, while only high LA concentrations block motor fibers. Other factors like injection volume and speed, the patient's posture, and the drug...
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 as...
Drug Delivery: Parenteral Route01:29

Drug Delivery: Parenteral Route

The parenteral route is a critical method of drug administration. It delivers compounds directly into the systemic circulation and bypasses the gastrointestinal tract. This approach is particularly advantageous for drugs that exhibit poor absorption or instability when administered orally.
There are three primary parenteral routes: intravenous (IV), intramuscular (IM), and subcutaneous (SC). The IV route introduces the drug directly into the bloodstream, ensuring immediate action. The IM route...
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...