Comparison of analgesic activity of the addition to neostigmine and fentanyl to bupivacaine in postoperative epidural analgesia
dc.contributor.author | Tekin S. | |
dc.contributor.author | Topcu I. | |
dc.contributor.author | Ekici N.Z. | |
dc.contributor.author | Caglar H. | |
dc.contributor.author | Erincler T. | |
dc.date.accessioned | 2024-07-22T08:23:21Z | |
dc.date.available | 2024-07-22T08:23:21Z | |
dc.date.issued | 2006 | |
dc.description.abstract | Objectives: To compare the analgesic and side effects of bupivacaine in combinations with neostigmine and fentanyl using patient-controlled-epidural analgesia (PCEA) methods in the postoperative period after abdominal hysterectomy. Methods: Seventy-five adult American Society of Anesthesiologists physical status I-II patients, aged 18-65 years were included in the study. The study took place in Celal Bayar University Hospital, Turkey between 2003-2004 years. After preoperative epidural catheterization, the patients were operated under general anesthesia. After surgery, the patients were randomly allocated in a double-blinded manner to receive PCEA and divided into 3 groups: Group B: 0.125% bupivacaine, Group N: 0.125% bupivacaine plus neostigmine 4 μg kg-1 and Group F: 0.125% bupivacaine plus 1 μg kg-1 fentanyl solutions (10 mL loading dose, 5 mL bolus dose, 10 min lockout time, 30 mL in 4 hour limit). During the following 24 hours, hemodynamic parameters, pain score using visual analog scale, total analgesic consumption, additional analgesic requirements, sedation, satisfaction, nausea scores and probable side-effects were evaluated. Results: Total analgesic consumption was 143.7 ± 7.2 mL in Group B, 123.4 ± 6.2 mL in Group N and 106 ± 8.3 mL in Groups F. The mean value in Group F was significantly lower than Group N and Group B (p<0.05), and was lower in Group N than Group B. Visual analog scale scores were lower in Group F than other groups (p<0.05). There were no differences in side effects between all groups. Conclusions: Fentanyl and neostigmine by the PCEA method can be used safely for postoperative analgesia after gynecologic surgery. They increase analgesia quality and satisfaction without an increase in side effects. | |
dc.identifier.issn | 03795284 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/19490 | |
dc.language.iso | English | |
dc.subject | Adolescent | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Analgesia, Epidural | |
dc.subject | Analgesics | |
dc.subject | Anesthetics, Local | |
dc.subject | Bupivacaine | |
dc.subject | Cholinesterase Inhibitors | |
dc.subject | Double-Blind Method | |
dc.subject | Female | |
dc.subject | Fentanyl | |
dc.subject | Humans | |
dc.subject | Hysterectomy | |
dc.subject | Middle Aged | |
dc.subject | Narcotics | |
dc.subject | Neostigmine | |
dc.subject | Pain, Postoperative | |
dc.subject | bupivacaine | |
dc.subject | diclofenac | |
dc.subject | fentanyl | |
dc.subject | neostigmine | |
dc.subject | nitrous oxide | |
dc.subject | oxygen | |
dc.subject | sevoflurane | |
dc.subject | thiopental | |
dc.subject | vecuronium | |
dc.subject | analgesic agent | |
dc.subject | bupivacaine | |
dc.subject | cholinesterase inhibitor | |
dc.subject | fentanyl | |
dc.subject | local anesthetic agent | |
dc.subject | narcotic agent | |
dc.subject | neostigmine | |
dc.subject | abdominal hysterectomy | |
dc.subject | adult | |
dc.subject | aged | |
dc.subject | analgesic activity | |
dc.subject | anesthesist | |
dc.subject | article | |
dc.subject | bolus injection | |
dc.subject | clinical trial | |
dc.subject | controlled clinical trial | |
dc.subject | controlled study | |
dc.subject | double blind procedure | |
dc.subject | drug efficacy | |
dc.subject | drug safety | |
dc.subject | epidural anesthesia | |
dc.subject | general anesthesia | |
dc.subject | hallucination | |
dc.subject | hemodynamic parameters | |
dc.subject | human | |
dc.subject | hypotension | |
dc.subject | loading drug dose | |
dc.subject | major clinical study | |
dc.subject | nausea | |
dc.subject | pain assessment | |
dc.subject | patient controlled analgesia | |
dc.subject | patient satisfaction | |
dc.subject | postoperative analgesia | |
dc.subject | postoperative pain | |
dc.subject | postoperative period | |
dc.subject | practice guideline | |
dc.subject | pruritus | |
dc.subject | randomized controlled trial | |
dc.subject | sedation | |
dc.subject | Turkey (republic) | |
dc.subject | university hospital | |
dc.subject | uterus disease | |
dc.subject | visual analog scale | |
dc.subject | vomiting | |
dc.subject | adolescent | |
dc.subject | female | |
dc.subject | hysterectomy | |
dc.subject | middle aged | |
dc.subject | postoperative pain | |
dc.title | Comparison of analgesic activity of the addition to neostigmine and fentanyl to bupivacaine in postoperative epidural analgesia | |
dc.type | Article |