Keyword: Anesthesia
2 results found.
Congress Abstract
Oncology, Nuclear Medicine and Transplantology, 2(3, Suppl. 1), 2026, onmt_A22, https://doi.org/10.63946/onmt/19306
ABSTRACT:
Introduction: Hyperthermic intrapleural chemotherapy combined with cytoreductive surgery is used for malignant pleural neoplasms and tumors with pleural dissemination. Anesthetic management is complicated by prolonged one-lung ventilation, surgical trauma, blood loss, fluid loading, hyperthermia, and the potential nephrotoxicity of cisplatin.
Objective: To evaluate the characteristics of anesthetic management and major perioperative complications associated with cytoreductive thoracic surgeries with hyperthermic intrapleural chemotherapy.
Materials and Methods: A retrospective analysis was conducted on 15 patients who underwent the aforementioned procedures between 2024 and 2025. General anesthesia included intubation with a double-lumen endobronchial tube and one-lung ventilation with a tidal volume of 4–6 mL/kg of ideal body weight and positive end-expiratory pressure of 5–8 cm H₂O. Non-invasive blood pressure, temperature, urine output, acid-base status, and venous blood lactate were monitored; central venous access was used. Perfusion was performed in a closed circuit at 42 °C for up to 60 minutes with cisplatin at 125 mg/m². Descriptive statistics were used.
Results: Patient age ranged from 35 to 68 years, with a mean age of 56.6 years. The median duration of anesthesia was 8 hours and 13 minutes, blood loss – 500 mL, fluid therapy – 5500 mL, and urine output – 900 mL. Respiratory and pleural complications were recorded in 9 (60.0%) patients, acute kidney injury – in 2 (13.3%); one patient required 10 sessions of hemodialysis. One case each (6.7%) of thrombotic complications and atrial fibrillation was observed. The median length of stay in the intensive care unit was 2 days. All patients were discharged from the hospital; two late deaths were recorded during follow-up.
Conclusions: Cytoreductive thoracic surgeries with hyperthermic intrapleural chemotherapy are associated with significant perioperative burden and a risk of respiratory, pleural, and renal complications. Our experience highlights the need for protective one-lung ventilation, adequate fluid and hemodynamic support, monitoring of acid-base status, temperature, and urine output, as well as early detection of renal dysfunction.
Funding: This study was financially supported by the Science Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan, Grant No. BR24992950 "Creation and implementation of innovative methods for the treatment of oncological diseases."
Objective: To evaluate the characteristics of anesthetic management and major perioperative complications associated with cytoreductive thoracic surgeries with hyperthermic intrapleural chemotherapy.
Materials and Methods: A retrospective analysis was conducted on 15 patients who underwent the aforementioned procedures between 2024 and 2025. General anesthesia included intubation with a double-lumen endobronchial tube and one-lung ventilation with a tidal volume of 4–6 mL/kg of ideal body weight and positive end-expiratory pressure of 5–8 cm H₂O. Non-invasive blood pressure, temperature, urine output, acid-base status, and venous blood lactate were monitored; central venous access was used. Perfusion was performed in a closed circuit at 42 °C for up to 60 minutes with cisplatin at 125 mg/m². Descriptive statistics were used.
Results: Patient age ranged from 35 to 68 years, with a mean age of 56.6 years. The median duration of anesthesia was 8 hours and 13 minutes, blood loss – 500 mL, fluid therapy – 5500 mL, and urine output – 900 mL. Respiratory and pleural complications were recorded in 9 (60.0%) patients, acute kidney injury – in 2 (13.3%); one patient required 10 sessions of hemodialysis. One case each (6.7%) of thrombotic complications and atrial fibrillation was observed. The median length of stay in the intensive care unit was 2 days. All patients were discharged from the hospital; two late deaths were recorded during follow-up.
Conclusions: Cytoreductive thoracic surgeries with hyperthermic intrapleural chemotherapy are associated with significant perioperative burden and a risk of respiratory, pleural, and renal complications. Our experience highlights the need for protective one-lung ventilation, adequate fluid and hemodynamic support, monitoring of acid-base status, temperature, and urine output, as well as early detection of renal dysfunction.
Funding: This study was financially supported by the Science Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan, Grant No. BR24992950 "Creation and implementation of innovative methods for the treatment of oncological diseases."
Congress Abstract
Oncology, Nuclear Medicine and Transplantology, 2(3, Suppl. 1), 2026, onmt_A21, https://doi.org/10.63946/onmt/19301
ABSTRACT:
Introduction: The implementation of Enhanced Recovery After Surgery (ERAS) protocols in breast oncology surgery requires optimization of perioperative analgesic management to minimize systemic opioid exposure and enable early mobilization.
Objective: To evaluate the clinical efficacy of the erector spinae plane (ESP) block as a core component of a multimodal ERAS protocol in patients undergoing surgical treatment for breast cancer.
Materials and Methods: This prospective study included 240 patients who underwent breast surgery. Patients were divided into two groups of 120 each:
Main group (n=120): Postoperative analgesia within the ERAS protocol incorporating ultrasound-guided ESP block.
Control group (n=120): Standard systemic postoperative analgesia.
The ESP block was performed under ultrasound guidance at the Th5–Th6 level. A mixture of 15 mL of 0.75% ropivacaine and 15 mL of 0.9% sodium chloride solution was administered (total volume – 30 mL, final ropivacaine concentration – 0.375%, total dose – 112.5 mg).
Pain intensity was assessed using the Visual Analogue Scale (VAS) at 3, 6, 12, and 24 hours. To determine the integrated pain burden, the area under the curve (AUC-VAS) was calculated. Early rehabilitation dynamics and functional activity (deep breathing activation, ability to sit up independently, and upper limb excursion) were assessed at 12 and 24 hours using a 3-point scale (0 – no limitations, 1 – moderate limitations due to discomfort, 2 – severe limitations/inability to perform).
Statistical analysis: Normality of distribution was tested using the Shapiro–Wilk test. VAS dynamics within groups were analyzed using the Friedman test, and intergroup differences using the Mann–Whitney U test. Data are presented as M±SD. Differences were considered statistically significant at p < 0.05.
Results: Incorporation of the ESP block into the ERAS protocol provided stable and pronounced pain control during the first 24 hours. Mean VAS scores in the main group at 3, 6, 12, and 24 hours were 3.96±0.44; 1.87±0.56; 1.15±0.44; and 0.71±0.47, respectively. In the control group, scores were 7.65±0.80; 5.80±1.21; 4.70±1.46; and 3.45±1.36, respectively (p < 0.001 for all time points).
At 3 hours postoperatively, severe pain (VAS ≥ 7) was observed in 95% of patients in the control group, while no such cases were recorded in the ESP block group. At 24 hours, all patients in the main group had pain levels not exceeding 2 on the VAS, whereas in the control group, 65% of patients still had clinically significant pain (VAS ≥ 4).
The total pain burden (AUC-VAS) over the 3–24 hour interval in the main group was 28.94±6.37 score·hours versus 100.58±21.47 score·hours in the control group, corresponding to a 71% reduction in integrated pain burden (p < 0.001).
Effective analgesia contributed to accelerated achievement of ERAS target parameters for early mobilization. At 12 hours, the mean limitation score for attempting to sit up in bed was 0.93 in the main group versus 1.65 in the control; for deep breathing – 0.14 versus 0.95; and for upper limb movement – 0.98 versus 1.75 (p < 0.001). By 24 hours, patients in the ESP block group had virtually no functional limitations.
Conclusions: The erector spinae plane interfascial block (Th5–Th6, 30 mL of 0.375% ropivacaine) provides highly effective pathogenetic protection against acute postoperative pain, reducing the total pain burden by 71% during the first 24 hours after surgical treatment for breast cancer.
Incorporation of the ESP block as a multimodal component of the ERAS protocol significantly accelerates the postoperative rehabilitation process, restoring full respiratory excursion and shoulder girdle mobility by the end of the first postoperative day, supporting the recommendation of this technique for widespread use in breast oncology surgery.
Funding: This research was funded by the Science Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan under Grant No. BR24992950 ("Creation and implementation of innovative methods for the treatment of oncological diseases").
Objective: To evaluate the clinical efficacy of the erector spinae plane (ESP) block as a core component of a multimodal ERAS protocol in patients undergoing surgical treatment for breast cancer.
Materials and Methods: This prospective study included 240 patients who underwent breast surgery. Patients were divided into two groups of 120 each:
Main group (n=120): Postoperative analgesia within the ERAS protocol incorporating ultrasound-guided ESP block.
Control group (n=120): Standard systemic postoperative analgesia.
The ESP block was performed under ultrasound guidance at the Th5–Th6 level. A mixture of 15 mL of 0.75% ropivacaine and 15 mL of 0.9% sodium chloride solution was administered (total volume – 30 mL, final ropivacaine concentration – 0.375%, total dose – 112.5 mg).
Pain intensity was assessed using the Visual Analogue Scale (VAS) at 3, 6, 12, and 24 hours. To determine the integrated pain burden, the area under the curve (AUC-VAS) was calculated. Early rehabilitation dynamics and functional activity (deep breathing activation, ability to sit up independently, and upper limb excursion) were assessed at 12 and 24 hours using a 3-point scale (0 – no limitations, 1 – moderate limitations due to discomfort, 2 – severe limitations/inability to perform).
Statistical analysis: Normality of distribution was tested using the Shapiro–Wilk test. VAS dynamics within groups were analyzed using the Friedman test, and intergroup differences using the Mann–Whitney U test. Data are presented as M±SD. Differences were considered statistically significant at p < 0.05.
Results: Incorporation of the ESP block into the ERAS protocol provided stable and pronounced pain control during the first 24 hours. Mean VAS scores in the main group at 3, 6, 12, and 24 hours were 3.96±0.44; 1.87±0.56; 1.15±0.44; and 0.71±0.47, respectively. In the control group, scores were 7.65±0.80; 5.80±1.21; 4.70±1.46; and 3.45±1.36, respectively (p < 0.001 for all time points).
At 3 hours postoperatively, severe pain (VAS ≥ 7) was observed in 95% of patients in the control group, while no such cases were recorded in the ESP block group. At 24 hours, all patients in the main group had pain levels not exceeding 2 on the VAS, whereas in the control group, 65% of patients still had clinically significant pain (VAS ≥ 4).
The total pain burden (AUC-VAS) over the 3–24 hour interval in the main group was 28.94±6.37 score·hours versus 100.58±21.47 score·hours in the control group, corresponding to a 71% reduction in integrated pain burden (p < 0.001).
Effective analgesia contributed to accelerated achievement of ERAS target parameters for early mobilization. At 12 hours, the mean limitation score for attempting to sit up in bed was 0.93 in the main group versus 1.65 in the control; for deep breathing – 0.14 versus 0.95; and for upper limb movement – 0.98 versus 1.75 (p < 0.001). By 24 hours, patients in the ESP block group had virtually no functional limitations.
Conclusions: The erector spinae plane interfascial block (Th5–Th6, 30 mL of 0.375% ropivacaine) provides highly effective pathogenetic protection against acute postoperative pain, reducing the total pain burden by 71% during the first 24 hours after surgical treatment for breast cancer.
Incorporation of the ESP block as a multimodal component of the ERAS protocol significantly accelerates the postoperative rehabilitation process, restoring full respiratory excursion and shoulder girdle mobility by the end of the first postoperative day, supporting the recommendation of this technique for widespread use in breast oncology surgery.
Funding: This research was funded by the Science Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan under Grant No. BR24992950 ("Creation and implementation of innovative methods for the treatment of oncological diseases").