J Knee Surg 2023; 36(04): 389-396
DOI: 10.1055/s-0041-1735312
Original Article

Gonyautoxins 2/3 Local Periarticular Injection for Pain Management after Total Knee Arthroplasty: A Double-Blind, Randomized Study

Jaime Hinzpeter
1   Department of Orthopedics, Hospital Clinico Universidad de Chile, Santiago, Chile
,
1   Department of Orthopedics, Hospital Clinico Universidad de Chile, Santiago, Chile
,
Julián Aliste
2   Department of Anesthesiology and Perioperative Medicine, Hospital Clínico Universidad de Chile, Santiago, Chile
,
Cristian Barrientos
1   Department of Orthopedics, Hospital Clinico Universidad de Chile, Santiago, Chile
3   Department of Orthopedics, Clínica Santa María, Santiago, Chile
,
Alvaro Zamorano
1   Department of Orthopedics, Hospital Clinico Universidad de Chile, Santiago, Chile
,
Miguel Palet
1   Department of Orthopedics, Hospital Clinico Universidad de Chile, Santiago, Chile
,
Jaime Catalan
1   Department of Orthopedics, Hospital Clinico Universidad de Chile, Santiago, Chile
,
Miguel del Campo
4   Membrane Biochemistry Laboratory, Department of Physiology and Biophysics, Faculty of Medicine Universidad de Chile, Santiago, Chile
,
Néstor Lagos
4   Membrane Biochemistry Laboratory, Department of Physiology and Biophysics, Faculty of Medicine Universidad de Chile, Santiago, Chile
› Author Affiliations
Funding None.

Abstract

The purpose of this study was to compare the efficacy of periarticular infiltration of gonyautoxin 2/3 (GTX 2/3) and a mixture of levobupivacaine, ketorolac, and epinephrine for pain management after total knee arthroplasty (TKA). Forty-eight patients were randomly allocated to receive periarticular infiltration of 40 µg GTX 2/3 (n = 24) diluted in 30 mL of sodium chloride 0.9% (study group) or a combination of 300 mg of levobupivacaine, 1 mg of epinephrine, and 60 mg ketorolac (n = 24) diluted in 150 mL of sodium chloride 0.9% (control group). Intraoperative anesthetic and surgical techniques were identical for both groups. Postoperatively, all patients received patient-controlled analgesia (morphine bolus of 1 mg; lockout interval of 8 minutes), acetaminophen, and ketoprofen for 72 hours. A blinded investigator recorded morphine consumption, which was the primary outcome. Also, the range of motion (ROM) and static and dynamic pain were assessed at 6, 12, 36, and 60 hours after surgery. The incidence of adverse events, time to readiness for discharge, and length of hospital stay were also recorded. The median of total cumulative morphine consumption was 16 mg (range, 0–62 mg) in the GTX 2/3 group and 9 mg (range, 0–54 mg) in control group, which did not reach statistical difference (median test, p = 0.40). Furthermore, static and dynamic pain scores were similar at all time intervals. GTX 2/3 was inferior in range of motion at 6 and 12 hours; nevertheless, we noted no difference after 36 hours. No differences between groups were found in terms of complications, side effects, or length of hospital stay. No significant differences were found between groups in terms of breakthrough morphine requirement. However, local anesthetic use resulted in an increased ROM in the first 12 hours. This prospective randomized clinical trial shows that GTX 2/3 is a safe and efficient drug for pain control after TKA; nevertheless, more studies using GTX 2/3 with larger populations are needed to confirm the safety profile and efficiency. This is level 1 therapeutic study, randomized, double-blind clinical trial.

Note

The datasets used or analyzed during the current study are available from the corresponding author on reasonable request


Authors' Contributions

J.H.C contributed the original idea, conceived the study, was senior surgeon, and performed a critical review of the final paper. M.B. supervised the study, performed surgery, performed the statistical analysis, and drafted the manuscript. J.A. was senior anesthesiologist, designed, and supervised the anesthetic protocol. C.B. was senior surgeon, conceived the study, and performed a critical review of the manuscript. A.Z. performed surgery, presented the investigation to the ethical committee. MP recollected data, performed surgery, and drafted the manuscript. J.C. recollected data and drafted the manuscript. M.C. was laboratory coordinator, administered the drug, and executed a critical review of the document. N.L. was gonyautoxin developer and performed a final essential analysis to the manuscript.


Ethical Approval

This study was approved by Hospital Clínico Universidad de Chile Ethics Research Board.




Publication History

Received: 17 November 2020

Accepted: 22 July 2021

Article published online:
10 September 2021

© 2021. Thieme. All rights reserved.

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

 
  • References

  • 1 Price AJ, Alvand A, Troelsen A. et al. Knee replacement. Lancet 2018; 392 (10158): 1672-1682
  • 2 Huang T, Wang W, George D, Mao X, Graves S. What can we learn from Australian Orthopaedic Association National Joint Replacement Registry 2016 annual report?. Ann Joint 2017; 2 (04) DOI: 10.21037/aoj.2017.02.01.
  • 3 Hughes RE, Batra A, Hallstrom BR. Arthroplasty registries around the world: valuable sources of hip implant revision risk data. Curr Rev Musculoskelet Med 2017; 10 (02) 240-252
  • 4 Kim TK, Chang CB, Kang YG, Kim SJ, Seong SC. Causes and predictors of patient's dissatisfaction after uncomplicated total knee arthroplasty. J Arthroplasty 2009; 24 (02) 263-271
  • 5 Cusick KD, Sayler GS. An overview on the marine neurotoxin, saxitoxin: genetics, molecular targets, methods of detection and ecological functions. Mar Drugs 2013; 11 (04) 991-1018
  • 6 Llewellyn LE. Saxitoxin, a toxic marine natural product that targets a multitude of receptors. Nat Prod Rep 2006; 23 (02) 200-222
  • 7 Alonso E, Alfonso A, Vieytes MR, Botana LM. Evaluation of toxicity equivalent factors of paralytic shellfish poisoning toxins in seven human sodium channels types by an automated high throughput electrophysiology system. Arch Toxicol 2016; 90 (02) 479-488
  • 8 Andrinolo D, Iglesias V, García C, Lagos N. Toxicokinetics and toxicodynamics of gonyautoxins after an oral toxin dose in cats. Toxicon 2002; 40 (06) 699-709
  • 9 Lattes K, Venegas P, Lagos N. et al. Local infiltration of gonyautoxin is safe and effective in treatment of chronic tension-type headache. Neurol Res 2009; 31 (03) 228-233
  • 10 Lagos N. Clinical applications of paralytic shellfish poisoning toxins. Toxins Biol Active Compound Microalgae 2014; 2: 309-329
  • 11 Garrido R, Lagos N, Lagos M. et al. Treatment of chronic anal fissure by gonyautoxin. Colorectal Dis 2007; 9 (07) 619-624
  • 12 Rodriguez-Navarro AJ, Lagos M, Figueroa C. et al. Potentiation of local anesthetic activity of neosaxitoxin with bupivacaine or epinephrine: development of a long-acting pain blocker. Neurotox Res 2009; 16 (04) 408-415
  • 13 Lobo K, Donado C, Cornelissen L. et al. A phase 1, dose-escalation, double-blind, block-randomized, controlled trial of safety and efficacy of neosaxitoxin alone and in combination with 0.2% bupivacaine, with and without epinephrine, for cutaneous anesthesia. Anesthesiology 2015; 123 (04) 873-885
  • 14 Hinzpeter J, Barrientos C, Barahona M. et al. New pain management procedure after total knee arthroplasty: gonyautoxins are safe and effective after a single intra-articular infiltration. Int Physiol J 2018; 1 (01) 15
  • 15 Hinzpeter J, Barrientos C, Zamorano Á. et al. Gonyautoxins: first evidence in pain management in total knee arthroplasty. Toxicon 2016; 119: 180-185
  • 16 Jakobsen TL, Christensen M, Christensen SS, Olsen M, Bandholm T. Reliability of knee joint range of motion and circumference measurements after total knee arthroplasty: does tester experience matter?. Physiother Res Int 2010; 15 (03) 126-134
  • 17 Escobar A, Quintana JM, Bilbao A, Azkárate J, Güenaga JI. Validation of the Spanish version of the WOMAC questionnaire for patients with hip or knee osteoarthritis. Western Ontario and McMaster Universities Osteoarthritis Index. Clin Rheumatol 2002; 21 (06) 466-471
  • 18 Roos MK, Lohmander LS. EM. WOMAC Osteoarthritis Index: Reliability, validity, and responsiveness in patients with arthroscopically assessed osteoarthritis. Scand J Rheumatol 1999; 28 (04) 210-215
  • 19 Affas F, Nygårds EB, Stiller CO, Wretenberg P, Olofsson C. Pain control after total knee arthroplasty: a randomized trial comparing local infiltration anesthesia and continuous femoral block. Acta Orthop 2011; 82 (04) 441-447
  • 20 Caldwell JH, Schaller KL, Lasher RS, Peles E, Levinson SR. Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses. Proc Natl Acad Sci U S A 2000; 97 (10) 5616-5620
  • 21 Luo TD, Ashraf A, Dahm DL, Stuart MJ, McIntosh AL. Femoral nerve block is associated with persistent strength deficits at 6 months after anterior cruciate ligament reconstruction in pediatric and adolescent patients. Am J Sports Med 2015; 43 (02) 331-336
  • 22 Sharma S, Iorio R, Specht LM, Davies-Lepie S, Healy WL. Complications of femoral nerve block for total knee arthroplasty. Clin Orthop Relat Res 2010; 468 (01) 135-140
  • 23 Krause A, Sayeed Z, El-Othmani M, Pallekonda V, Mihalko W, Saleh KJ. Outpatient total knee arthroplasty: are we there yet? (Part 1). Orthop Clin North Am 2018; 49 (01) 1-6
  • 24 Pujol O, García B, Faura T, Nuevo M, Maculé F. Results of a fast-track knee arthroplasty according to the experience of a multidisciplinary team. J Orthop 2019; 16 (03) 201-205
  • 25 Fan L, Yu X, Zan P, Liu J, Ji T, Li G. Comparison of local infiltration analgesia with femoral nerve block for total knee arthroplasty: a prospective, randomized clinical trial. J Arthroplasty 2016; 31 (06) 1361-1365
  • 26 Moghtadaei M, Farahini H, Faiz SH, Mokarami F, Safari S. Pain management for total knee arthroplasty: single-injection femoral nerve block versus local infiltration analgesia. Iran Red Crescent Med J 2014; 16 (01) e13247
  • 27 Leone S, Di Cianni S, Casati A, Fanelli G. Pharmacology, toxicology, and clinical use of new long acting local anesthetics, ropivacaine and levobupivacaine. Acta Biomed 2008; 79 (02) 92-105
  • 28 Toftdahl K, Nikolajsen L, Haraldsted V, Madsen F, Tønnesen EK, Søballe K. Comparison of peri- and intraarticular analgesia with femoral nerve block after total knee arthroplasty: a randomized clinical trial. Acta Orthop 2007; 78 (02) 172-179
  • 29 Affas F, Stiller CO, Nygårds EB, Stephanson N, Wretenberg P, Olofsson C. A randomized study comparing plasma concentration of ropivacaine after local infiltration analgesia and femoral block in primary total knee arthroplasty. Scand J Pain 2012; 3 (01) 46-51
  • 30 Bajwa SJ, Kaur J. Clinical profile of levobupivacaine in regional anesthesia: A systematic review. J Anaesthesiol Clin Pharmacol 2013; 29 (04) 530-539
  • 31 Zhang X, Zhang L, Zhang Y. Side effects of long-acting local anaesthetics in patients with preexisting cardiovascular condition. Cell Biochem Biophys 2014; 69 (03) 405-409
  • 32 Albrecht E, Guyen O, Jacot-Guillarmod A, Kirkham KR. The analgesic efficacy of local infiltration analgesia vs femoral nerve block after total knee arthroplasty: a systematic review and meta-analysis. Br J Anaesth 2016; 116 (05) 597-609
  • 33 Wall PDH, Parsons NR, Parsons H. et al; P. D. H. Wall on behalf of A. P. Sprowson,† M. L. Costa, PAKA Study Group. A pragmatic randomised controlled trial comparing the efficacy of a femoral nerve block and periarticular infiltration for early pain relief following total knee arthroplasty. Bone Joint J 2017; 99-B (07) 904-911