Comparing the Effects of Combined General/Epidural Anaesthesia and General Anaesthesia on Serum Cytokine Levels in Radical Cystectomy

Surgical stress combined with general anaesthesia (GA) suppresses the immune system and leads to cancer cell growth and premature metastasis in major oncological interventions. Epidural analgesia decreases the need for inhalation agents and opioids during surgery by suppressing sympathetic and neuro...

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Veröffentlicht in:Turkish Journal of Anaesthesiology and Reanimation 2017-08, Vol.45 (4), p.203-209
Hauptverfasser: Karadeniz, Meltem Savran, Mammadov, Orkhan, Çiftci, Hayriye Şentürk, Usta, Sebahat Akgül, Pembeci, Kamil
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Sprache:eng
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Zusammenfassung:Surgical stress combined with general anaesthesia (GA) suppresses the immune system and leads to cancer cell growth and premature metastasis in major oncological interventions. Epidural analgesia decreases the need for inhalation agents and opioids during surgery by suppressing sympathetic and neuroendocrine responses in the postoperative period. This study aimed to compare the effects of combined general/epidural anaesthesia (GEA)+patient-controlled epidural analgesia (PCEA) and GA+IV patient-controlled analgesia (PCA) on serum tumour necrosis factor-alpha TNF-α), interleukin-1 beta (IL-1β) and interferon-gamma (IFN-γ) levels in patients undergoing radical cystectomy. Sixty-five patients were enrolled in this prospective study. Patients were randomly enrolled to the GEA group, i.e., combined GEA+ PCEA (0.1% bupivacaine+1 μg mL fentanyl), and the GA group, namely combined GA+IV PCA (0.03 mg mL morphine). To evaluate the cytokine response, blood samples were collected at preoperative, postoperative 1 and 24 hours. There was no statistically significant difference in serum TNF-α, IL-1β and IFN-γ levels between groups GA and GEA at preoperative and postoperative 1 hour and 24 hour. Total remifentanil consumption was significantly lower and length of hospital stay was significantly shorter in the GEA group than in the GA group (p
ISSN:2149-0937
2667-677X
2149-276X
2667-6370
DOI:10.5152/TJAR.2017.13285