Parenteral form of ibuprofen for pain relief in the early postoperative period in cancer patients after thoracoscopic and bone-plastic surgery
- Authors: Sуtov A.V.1, Yukhina A.I.1, Vlasenko O.S.1, Matveeva S.O.1, Borzov K.A.1, Kononets P.V.1
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Affiliations:
- N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
- Issue: Vol 3, No 1 (2026)
- Pages: 35-42
- Section: ORIGINAL REPORTS
- Published: 26.06.2026
- URL: https://stio.abvpress.ru/jour/article/view/86
- DOI: https://doi.org/10.17650/3034-2473-2026-3-1-35-42
- ID: 86
Cite item
Abstract
Aim. То compare the safety of use and the analgesic effect of postoperative anesthesia regimens using non-steroidal anti-inflammatory drug (NSAID) – Intrafen-GEN (ibuprofen) with a scheme of postoperative anesthesia based on narcotic analgesics in oncological patients after thoracoscopic and bone-plastic surgery. To evaluate the possibilities of using a postoperative anesthesia regimen using NSAIDs – Intrafen-GEN (ibuprofen) within the framework of the ERAS protocol (Enhanced Recovery After Surgery).
Materials and methods. A single-center prospective comparative study conducted at the N.N. Trapeznikov Research Institute of Clinical Oncology in 2024–2025 included 98 patients who underwent minimally invasive thoracic and bone-plastic surgery.
Results. Based on the area of surgical intervention, all patients (n=98) were divided first into 2 groups, and then into subgroups A and B, according to the schemes of postoperative anesthesia. The first group included 64 patients. It was divided into subgroups A (n = 34) and B (n = 30). The second group included 34 patients and was also divided into subgroups A and B with an equal number of patients in each of the subgroups (n = 17). Patients in subgroup A received a postoperative pain relief regimen using Intrafen-GEN (ibuprofen), and patients in subgroup B received a regimen using trimeperidine. The first intravenous dose of Intrafen-GEN (ibuprofen) – 800 mg was administered 30 minutes before the end of surgery or immediately upon admission to the intensive care unit, then every 8–12 hours for 3 days. In the case of persistent pain, non-opioid and opioid analgesics were added to the treatment until the pain completely disappeared. Patients in subgroup B received anesthesia with trimeperidine 20 mg intramuscularly every 8 hours for 3 postoperative days. The quality of anesthesia in the postoperative period was assessed using the visual analog scale.
Conclusion. In our study, Intrafen-GEN (ibuprofen) was found to be a safe drug, as no complications or side effects were observed during its use. The pain management regimens based on Intrafen-GEN (ibuprofen) demonstrated the complete elimination of opioid analgesics from postoperative pain management in 24 (70.59 %) patients after thoracoscopic surgeries and in 10 (58.85 %) patients after bone-plastic surgeries. When using Intrafen-GEN (ibuprofen), there are no contraindications for the ERAS protocol and early activation of patients in the ICU.
About the authors
Aleksandr V. Sуtov
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Author for correspondence.
Email: drsytov@rambler.ru
ORCID iD: 0000-0002-6426-3200
Russian Federation, 23 Kashirskoe Shosse, Moscow 115522
Anna I. Yukhina
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: drsytov@rambler.ru
ORCID iD: 0009-0007-3112-1429
Russian Federation, 23 Kashirskoe Shosse, Moscow 115522
Olga S. Vlasenko
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: drsytov@rambler.ru
ORCID iD: 0000-0002-9135-0393
Russian Federation, 23 Kashirskoe Shosse, Moscow 115522
Svetlana O. Matveeva
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: drsytov@rambler.ru
ORCID iD: 0009-0009-0154-5233
Russian Federation, 23 Kashirskoe Shosse, Moscow 115522
Kirill A. Borzov
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: drsytov@rambler.ru
ORCID iD: 0000-0002-3512-0390
Russian Federation, 23 Kashirskoe Shosse, Moscow 115522
Pavel V. Kononets
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: drsytov@rambler.ru
ORCID iD: 0000-0003-4744-6141
Russian Federation, 23 Kashirskoe Shosse, Moscow 115522
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