The Effect of Greater Auricular Nerve Block and Auriculotemporal Nerve Block on The Expression of Inflammatory Factors TNF-α and IL-6 in Mastoidectomy Surgery: A Randomized Controlled Trial
DOI:
https://doi.org/10.63682/jns.v14i8.6527Keywords:
Mastoidectomy, GAN and ATN block, 0.5 % Ropivacaine, Inflammatory, TNF-α, IL-6Abstract
Background: The immune system can be triggered to release different inflammatory mediators like TNF-α and IL-6 in response to trauma and surgical stress. These cytokines in the acute inflammatory reaction take 4 to 6 hours to elicit a response after the initial trigger and can last up to 24 hours. Greater auricular nerve (GAN) and auriculotemporal nerve (ATN) blocks with 0.5% ropivacaine local anaesthetic potentially suppress this inflammatory response. This study evaluates the effectiveness of these blocks on TNF-α and IL-6 expression in mastoidectomy, considering the crucial role of these cytokines in acute inflammatory responses. Methods: The study enrolled 36 patients scheduled for elective mastoidectomy between November 2024 and January 2025. General anesthesia was administered to all participants, while patients in the treatment arm also received greater auricular nerve (GAN) and auriculotemporal nerve (ATN) blocks. Inflammatory markers TNF-α and IL-6 were measured at two timepoints: after general anesthesia induction and following the surgical procedure. Statistical tests will use comparative tests. Results: The research indicated that GAN and ATN blocks utilizing 0.5% ropivacaine significantly mitigated the elevations of TNF-α and IL-6 after mastoidectomy. The block group exhibited no significant elevation in TNF-α (P=0.595) and IL-6 (P=0.420) postoperatively, while the control group demonstrated large elevations (p<0.001) in both markers. Postoperative levels of TNF-α (P<0.001) and IL-6 (P<0.001) exhibited substantial differences between groups, demonstrating the efficacy of GAN and ATN blocks in preventing and reducing the inflammatory response. Conclusion: GAN and ATN blocks with 0.5% ropivacaine in elective mastoidectomy significantly inhibit postoperative increases in TNF-α and IL-6 levels. The use of 0.5% ropivacaine demonstrates an anti-inflammatory effect in elective mastoidectomy surgery.
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S. Vanpatten and Y. Al-Abed, “High Mobility Group Box-1 (HMGb1): Current Wisdom and Advancement as a Potential Drug Target,” J. Med. Chem., vol. 61, no. 12, pp. 5093–5107, 2018, doi: 10.1021/acs.jmedchem.7b01136.
R. G. Kumar, J. A. Boles, and A. K. Wagner, “Chronic inflammation after severe traumatic brain injury: Characterization and associations with outcome at 6 and 12 months postinjury,” J. Head Trauma Rehabil., vol. 30, no. 6, 2015, doi: 10.1097/HTR.0000000000000067.
H. E. Harris, U. Andersson, and D. S. Pisetsky, “HMGB1: A multifunctional alarmin driving autoimmune and inflammatory disease,” 2012. doi: 10.1038/nrrheum.2011.222.
G. S. Papathanasiou, “Local Anesthetics and Covid19 Associated Acute Respiratory Distress Syndrome: A New Therapeutic Indication?,” Clin. Res. Open Access, vol. 6, no. 2, 2020, doi: 10.16966/2469-6714.156.
Y. He, Z. Li, and Y. X. Zuo, “Nerve Blockage Attenuates Postoperative Inflammation in Hippocampus of Young Rat Model with Surgical Trauma,” Mediators Inflamm., vol. 2015, 2015, doi: 10.1155/2015/460125.
N. Rawal, “Analgesia for day-case surgery,” Br. J. Anaesth., vol. 87, no. 1, 2001, doi: 10.1093/bja/87.1.73.
R. M. Mody, “Post-operative analgesia following mastoid surgeries: Comparison between selective nerve blocks (greater auricular and auriculotemporal) v/s parenteral opioid (pentazocine),” MedPulse Int. J. Anesthesiol., vol. 17, no. 1, 2020, doi: 10.26611/10151714.
C. Liu and J. Tang, “Expression levels of tumor necrosis factor‑α and the corresponding receptors are correlated with trauma severity,” Oncol. Lett., vol. 8, no. 6, 2014, doi: 10.3892/ol.2014.2575.
L. Koelman, O. Pivovarova-Ramich, A. F. H. Pfeiffer, T. Grune, and K. Aleksandrova, “Cytokines for evaluation of chronic inflammatory status in ageing research: Reliability and phenotypic characterisation,” Immun. Ageing, vol. 16, no. 1, 2019, doi: 10.1186/s12979-019-0151-1.
S. D. Nash et al., “Long-term variability of inflammatory markers and associated factors in a population-based cohort,” J. Am. Geriatr. Soc., vol. 61, no. 8, 2013, doi: 10.1111/jgs.12382.
R. Elosua, B. Bartali, J. M. Ordovas, A. M. Corsi, F. Lauretani, and L. Ferrucci, “Association between physical activity, physical performance, and inflammatory biomarkers in an elderly population: the InCHIANTI study,” Journals Gerontol. Ser. A Biol. Sci. Med. Sci., vol. 60, no. 6, pp. 760–767, 2005.
M. R. Dewi, D. Pratiwi, and P. W. Kandhi, “High TNF-α Levels in Active Phase Chronic Suppurative Otitis Media Caused by Gram-positive Bacteria,” Mol. Cell. Biomed. Sci., vol. 7, no. 2, 2023, doi: 10.21705/mcbs.v7i2.321.
D. Pratiwi et al., “TNF-α and TGF-β Contributes in Recurrent Otorrhea of Active Mucosal Chronic Otitis Media,” Indones. Biomed. J., vol. 14, no. 1, 2022, doi: 10.18585/inabj.v14i1.1759.
Y. Edward, J. Munilson, R. Rosalinda, H. Ali, D. Irfandy, and D. Swanda, “Expression of tumor necrosis factor-α and interleukin-6 in chronic suppurative otitis media,” Turkish J. Immunol., vol. 7, no. 1, 2019, doi: 10.25002/tji.2019.782.
M. H. Liu, J. Tian, Y. P. Su, T. Wang, Q. Xiang, and L. Wen, “Cervical sympathetic block regulates early systemic inflammatory response in severe trauma patients,” Med. Sci. Monit., vol. 19, no. 1, 2013, doi: 10.12659/MSM.883833.
L. Wu, L. Li, F. Wang, X. Wu, X. Zhao, and N. Xue, “Anti-Inflammatory Effect of Local Anaesthetic Ropivacaine in Lipopolysaccharide-Stimulated RAW264.7 Macrophages,” Pharmacology, vol. 103, no. 5–6, 2019, doi: 10.1159/000496425.
J. S. Jang et al., “Changes in the tumor necrosis factor‐α level after an ultrasound‐guided femoral nerve block in elderly patients with a hip fracture,” Brazilian J. Anesthesiol., vol. 68, no. 6, 2018, doi: 10.1016/j.bjan.2018.03.004.
F. Behnaz, P. Soltanpoor, H. Teymourian, N. Tadayon, G. R. Mohseni, and M. Ghasemi, “Sympatholytic and anti-inflammatory effects of ropivacaine and bupivacaine after infraclavicular block in arterio venous fistula surgery,” Anesthesiol. Pain Med., vol. 9, no. 1, 2019, doi: 10.5812/aapm.85704.
S. Weinschenk, C. Weiss, J. Benrath, V. von Baehr, T. Strowitzki, and M. Feißt, “Anti-Inflammatory Characteristics of Local Anesthetics: Inhibition of TNF-α Secretion of Lipopolysaccharide-Stimulated Leucocytes in Human Blood Samples,” Int. J. Mol. Sci., vol. 23, no. 6, 2022, doi: 10.3390/ijms23063283.
N. S. Komarulloh, W. Hamzah, C. S. Walojo, P. S. Airlangga, D. A. Santosa, and P. Kriswidyatomo, “Effect of Scalp Nerve Block on Fentanyl Consumption and Levels of TNF-α, Cortisol, and Blood Glucose in Elective Craniotomy,” Pak Hear. J., vol. 56, no. 4, 2023, [Online]. Available: https://doi.org/10.48047/PHJ.56.4.2023
X. Yang et al., “A comparison of effects of scalp nerve block and local anesthetic infiltration on inflammatory response, hemodynamic response, and postoperative pain in patients undergoing craniotomy for cerebral aneurysms: A randomized controlled trial,” BMC Anesthesiol., vol. 19, no. 1, 2019, doi: 10.1186/s12871-019-0760-4.
L. Ning, L. Jiang, Q. Zhang, M. Luo, D. Xu, and Y. Peng, “Effect of scalp nerve block with ropivacaine on postoperative pain in pediatric patients undergoing craniotomy: A randomized controlled trial,” Front. Med., vol. 9, 2022, doi: 10.3389/fmed.2022.952064.
M. Nicoletti et al., “Impact of neuropeptide substance P, an inflammatory compound on arachidonic acid compound generation,” 2012. doi: 10.1177/039463201202500403.
D. Fletcher et al., “Antiinflammatory effect of peripheral nerve blocks after knee surgery: Clinical and biologic evaluation,” Anesthesiology, vol. 109, no. 3, 2008, doi: 10.1097/ALN.0b013e318182c2a1.
T. Christin, Z. Ali, L. Legiran, and F. Ferawaty, “Overview Of Peripheral Neuropathy In Chronic Kidney Disease Patients Undergoing Hemodialysis At Dr. Mohammad Hoesin Hospital Palembang,” Pharmacol. Med. Reports, Orthop. Illn. Details, vol. 2, no. 3, pp. 1–18, 2023, doi: 10.55047/comorbid.v2i3.890.
M. Klimek et al., “Inflammatory profile of awake function-controlled craniotomy and craniotomy under general anesthesia,” Mediators Inflamm., vol. 2009, 2009, doi: 10.1155/2009/670480.
T. Tanaka, M. Narazaki, and T. Kishimoto, “Il-6 in inflammation, Immunity, And disease,” Cold Spring Harb. Perspect. Biol., vol. 6, no. 10, 2014, doi: 10.1101/cshperspect.a016295.
G. Szabo, K. Kodys, and C. L. Miller-Graziano, “Elevated monocyte interleukin-6 (IL-6) production in immunosuppressed trauma patients. I. Role of FcγRI cross-linking stimulation,” J. Clin. Immunol., vol. 11, no. 6, 1991, doi: 10.1007/BF00918798.
W. L. Biffl, E. E. Moore, F. A. Moore, and V. M. Peterson, “Interleukin-6 in the injured patient: Marker of injury or mediator of inflammation?,” Ann. Surg., vol. 224, no. 5, 1996, doi: 10.1097/00000658-199611000-00009.
R. Serban et al., “IL‑1α, IL‑6 and IL‑8 serum values in patients with chronic suppurative otitis media,” Exp. Ther. Med., vol. 22, no. 5, 2021, doi: 10.3892/etm.2021.10660.
A. A. Kirana, P. Setiawan, H. S. Putri, C. Soemartono, P. Kriswidyatomo, and P. Lestari, “Effect of Serratus Anterior Plane Block Combined with Dexmedetomidine as an Adjuvant to Ropivacaine on Inflammatory Response and Opioid Doses in Patients Undergoing Video Assisted Thoracoscopic Surgery,” African J. Biol. Sci., vol. 6, no. 9, pp. 5256–5267, 2024, doi: 10.48047/AFJBS.6.9.2024.5256-5267.
P. Desiree et al., “Effect of scalp block with 0.5% ropivacaine on interleukin-6 and neutrophil lymphocyte ratio in elective craniotomy,” Bali Med. J., vol. 13, no. 1, pp. 668–674, 2024, doi: 10.15562/bmj.v13i1.5194.
Y. Shaik et al., “Role of cytokines in the pathogenesis of bone resorption,” J. Orthop., vol. 1, no. 1, pp. 25–28, 2009.
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