International Journal of Clinical Pediatrics, ISSN 1927-1255 print, 1927-1263 online, Open Access
Article copyright, the authors; Journal compilation copyright, Int J Clin Pediatr and Elmer Press Inc
Journal website https://www.theijcp.org

Original Article

Volume 12, Number 2, September 2023, pages 29-36


Preliminary Experience With a Continuous Lidocaine Infusion as an Analgesia Adjunct for Acute Pain Management Following Surgery in Pediatric Patients

Tables

Table 1. Patient Characteristics of the Study Cohort (N = 168)
 
VariableN (%)Mean (range)Median (IQR)
IQR: interquartile range; ASA: American society of anesthesiologists.
Age (years)13.8 (1, 21)14 (12, 16)
Gender
  Male65 (38.7%)
  Female103 (61.3%)
Race
  White137 (81.5%)
  Black16 (9.5%)
  Asian5 (3.0%)
  Mixed race10 (6.0%)
Weight (kg)51.1 (6.9, 141.3)48.7 (36.8, 61.4)
Height (cm)152.1 (58.2, 181.4)156.3 (146.4, 163.5)
ASA physical class
  I21 (12.5%)
  II79 (47.0%)
  III63 (37.5%)
  IV5 (3.0%)

 

Table 2. Anesthesia and Surgical Times With Lidocaine Infusion Information
 
VariableN (%)Mean (range)Median (IQR)
IQR: interquartile range.
Surgical procedure
  Posterior spinal fusion142 (84.5%)
  Other26 (15.5%)
Total anesthesia time (min)409.70 (76, 946)400 (345.5, 469.5)
Total surgery time (min)288.54 (13, 800)281.5 (229.0, 343.8)
Lidocaine infusion used intraoperatively148 (88.1%)
Number patients who received lidocaine bolus31 (18.5%)
Amount of lidocaine bolus (mg)53.5 (30, 100)50 (40, 60)
Intraoperative starting dose rate (mg/kg/h)0.97 (0.5, 2)
Total lidocaine infusion time during procedure (min)329 (110, 627)327 (264, 382)
Lidocaine infusion used postoperatively168 (100%)
Infusion rate (mg/kg/h)1 (0, 2)1 (1, 1)
Number of postoperative infusion days
  One5 (2.98%)
  Two43 (25.60%)
  Three97 (57.74%)
  Four14 (8.33%)
  Five2 (1.19%)
  Six3 (1.79%)
  Seven1 (0.60%)
  Eight1 (0.60%)
  Ten1 (0.60%)
  Twelve1 (0.60%)

 

Table 3. Postoperative Pain Scores 0 - 10
 
Postoperative dayNPain score (mean, range)Pain score (median, IQR
IQR: interquartile range.
Day 11642.3 (0, 10)2.0 (0.5, 3.8)
Day 21652.2 (0, 7.5)1.9 (0.9, 3.3)
Day 31552.1 (0, 8)1.9 (0.6, 3.3)
Day 4832.0 (0, 9.5)1.5 (0, 3.20)
Day 5361.4 (0, 4.5)1.1 (0.3, 2.4)
Day 6110.7 (0, 5.3)0 (0, 0.5)
Day 761.2 (0, 5)0.4 (0, 2.5)

 

Table 4. Type of Adverse Eventa
 
Type of adverse eventNPercentageb
aSome patients experienced more than one adverse event. bThe study cohort included 168 patients.
Blurred vision, dizziness, drowsiness/difficult to arouse138.1%
Delirium, hallucinations, agitation, confusion106.2%
Nausea95.6%
Hypotension74.3%
Pruritus74.3%
Headache21.2%
Bradycardia21.2%
Myoclonus/muscle spasms21.2%
Hypertension10.6%
Breathing difficulties10.6%
Circumoral numbness10.6%
Bradypnea10.6%
Edema10.6%
Head bobbing10.6%
Constipation10.6%
High pain scores10.6%
Sore throat10.6%
Total61-