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Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy

BACKGROUND: This randomized controlled study evaluated the efficacy of intravenous patient-controlled analgesia (IV-PCA) with fentanyl and ketorolac for neurosurgical patients, and compared the effectiveness of IV-PCA with intermittent analgesics injection. METHODS: The patients undergoing craniotom...

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Autores principales: Na, Hyo-Seok, An, Sang-Bum, Park, Hee-Pyoung, Lim, Young-Jin, Hwang, Jung-Won, Jeon, Young-Tae, Min, Seong-Won
Formato: Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040429/
https://www.ncbi.nlm.nih.gov/pubmed/21359078
http://dx.doi.org/10.4097/kjae.2011.60.1.30
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author Na, Hyo-Seok
An, Sang-Bum
Park, Hee-Pyoung
Lim, Young-Jin
Hwang, Jung-Won
Jeon, Young-Tae
Min, Seong-Won
author_facet Na, Hyo-Seok
An, Sang-Bum
Park, Hee-Pyoung
Lim, Young-Jin
Hwang, Jung-Won
Jeon, Young-Tae
Min, Seong-Won
author_sort Na, Hyo-Seok
collection PubMed
description BACKGROUND: This randomized controlled study evaluated the efficacy of intravenous patient-controlled analgesia (IV-PCA) with fentanyl and ketorolac for neurosurgical patients, and compared the effectiveness of IV-PCA with intermittent analgesics injection. METHODS: The patients undergoing craniotomy were randomly assigned to two groups. Patients of group P (n = 53) received fentanyl (0.2 µg/kg/hr) and ketorolac (0.3 mg/kg/hr) via IV-PCA, and those of group N (n = 53) received intermittent fentanyl or ketorolac injection as needed. Pain was evaluated using a 0-10 visual analogue scale (VAS) at postoperative 1, 4, and 24 hr. The amount of infused analgesic drugs, Glasgow Coma Scale (GCS) score, systolic arterial pressure, heart rate, respiratory rate, and the incidence of nausea and miosis were measured at the same time points. RESULTS: Although VAS of pain (VASp) was comparable at postoperative 1 hr (P = 0.168) between the two groups, the group P had significantly lower VASp at postoperative 4 hr (P = 0.007) and 24 hr (P = 0.017). In group P, less analgesic drugs were administered at postoperative 1 hr, and more analgesic drugs were administered at postoperative 24 hr. There were no differences between two groups with respect to nausea, GCS, systolic arterial pressure, and heart rate. IV-PCA did not further incur respiratory depression or miosis. CONCLUSIONS: IV-PCA with fentanyl and ketorolac after craniotomy is more effective analgesic technique, without adverse events, than the intermittent administration of analgesics.
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spelling pubmed-30404292011-02-25 Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy Na, Hyo-Seok An, Sang-Bum Park, Hee-Pyoung Lim, Young-Jin Hwang, Jung-Won Jeon, Young-Tae Min, Seong-Won Korean J Anesthesiol Clinical Research Article BACKGROUND: This randomized controlled study evaluated the efficacy of intravenous patient-controlled analgesia (IV-PCA) with fentanyl and ketorolac for neurosurgical patients, and compared the effectiveness of IV-PCA with intermittent analgesics injection. METHODS: The patients undergoing craniotomy were randomly assigned to two groups. Patients of group P (n = 53) received fentanyl (0.2 µg/kg/hr) and ketorolac (0.3 mg/kg/hr) via IV-PCA, and those of group N (n = 53) received intermittent fentanyl or ketorolac injection as needed. Pain was evaluated using a 0-10 visual analogue scale (VAS) at postoperative 1, 4, and 24 hr. The amount of infused analgesic drugs, Glasgow Coma Scale (GCS) score, systolic arterial pressure, heart rate, respiratory rate, and the incidence of nausea and miosis were measured at the same time points. RESULTS: Although VAS of pain (VASp) was comparable at postoperative 1 hr (P = 0.168) between the two groups, the group P had significantly lower VASp at postoperative 4 hr (P = 0.007) and 24 hr (P = 0.017). In group P, less analgesic drugs were administered at postoperative 1 hr, and more analgesic drugs were administered at postoperative 24 hr. There were no differences between two groups with respect to nausea, GCS, systolic arterial pressure, and heart rate. IV-PCA did not further incur respiratory depression or miosis. CONCLUSIONS: IV-PCA with fentanyl and ketorolac after craniotomy is more effective analgesic technique, without adverse events, than the intermittent administration of analgesics. The Korean Society of Anesthesiologists 2011-01 2011-01-28 /pmc/articles/PMC3040429/ /pubmed/21359078 http://dx.doi.org/10.4097/kjae.2011.60.1.30 Text en Copyright © the Korean Society of Anesthesiologists, 2011 http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research Article
Na, Hyo-Seok
An, Sang-Bum
Park, Hee-Pyoung
Lim, Young-Jin
Hwang, Jung-Won
Jeon, Young-Tae
Min, Seong-Won
Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy
title Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy
title_full Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy
title_fullStr Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy
title_full_unstemmed Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy
title_short Intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy
title_sort intravenous patient-controlled analgesia to manage the postoperative pain in patients undergoing craniotomy
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040429/
https://www.ncbi.nlm.nih.gov/pubmed/21359078
http://dx.doi.org/10.4097/kjae.2011.60.1.30
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