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Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery
BACKGROUND: Postpartum hemorrhage is the leading cause of maternal mortality. Oxytocin being the most popular uterotonic agent, has been routinely administered after both vaginal delivery and cesarean section. Carbetocin is a newer uterotonic agent and provides the benefit of a longer duration of ac...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Anesthesiologists
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713823/ https://www.ncbi.nlm.nih.gov/pubmed/33329809 http://dx.doi.org/10.17085/apm.2020.15.2.167 |
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author | Kwon, Kihyug Kim, Dohyung Jo, Hyunmin Park, Ji Eun Kim, Kyung Ok |
author_facet | Kwon, Kihyug Kim, Dohyung Jo, Hyunmin Park, Ji Eun Kim, Kyung Ok |
author_sort | Kwon, Kihyug |
collection | PubMed |
description | BACKGROUND: Postpartum hemorrhage is the leading cause of maternal mortality. Oxytocin being the most popular uterotonic agent, has been routinely administered after both vaginal delivery and cesarean section. Carbetocin is a newer uterotonic agent and provides the benefit of a longer duration of action without additional administration post-delivery. METHODS: We recruited 34 women undergoing elective cesarean section under spinal anesthesia. All patient was received spinal anesthesia using 0.5% hyperbaric Marcaine 8–10 mg in conjugation with fentanyl 20 μg in the left lateral decubitus position. Hartmann’s solution 10–15 ml/kg was administered before carbetocin. The operation started as soon as sensory block at level T4–T6 was confirmed. A non-invasive hemodynamic monitoring cuff (Finometer(®)) was attached to the patient’s finger soon after the induction of spinal anesthesia. Using the Finometer, we recorded the heart rate and mean arterial pressure at every 15 s, starting from 15 s before the administration of carbetocin to 5 min after. After the removal of the placenta, the bolus group was administered intravenous bolus injection of carbetocin 100 μg and the infusion group was administered carbetocin 100 μg diluted in 50 ml normal saline, over 5 min using an infusion pump. RESULTS: The demographic data showed no significant difference between the two groups. Furthermore, there were no significant hemodynamic differences between the two groups. CONCLUSIONS: The method of administration of carbetocin does not influence its hemodynamic effects. |
format | Online Article Text |
id | pubmed-7713823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korean Society of Anesthesiologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-77138232020-12-15 Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery Kwon, Kihyug Kim, Dohyung Jo, Hyunmin Park, Ji Eun Kim, Kyung Ok Anesth Pain Med (Seoul) Obstetric Anesthesia BACKGROUND: Postpartum hemorrhage is the leading cause of maternal mortality. Oxytocin being the most popular uterotonic agent, has been routinely administered after both vaginal delivery and cesarean section. Carbetocin is a newer uterotonic agent and provides the benefit of a longer duration of action without additional administration post-delivery. METHODS: We recruited 34 women undergoing elective cesarean section under spinal anesthesia. All patient was received spinal anesthesia using 0.5% hyperbaric Marcaine 8–10 mg in conjugation with fentanyl 20 μg in the left lateral decubitus position. Hartmann’s solution 10–15 ml/kg was administered before carbetocin. The operation started as soon as sensory block at level T4–T6 was confirmed. A non-invasive hemodynamic monitoring cuff (Finometer(®)) was attached to the patient’s finger soon after the induction of spinal anesthesia. Using the Finometer, we recorded the heart rate and mean arterial pressure at every 15 s, starting from 15 s before the administration of carbetocin to 5 min after. After the removal of the placenta, the bolus group was administered intravenous bolus injection of carbetocin 100 μg and the infusion group was administered carbetocin 100 μg diluted in 50 ml normal saline, over 5 min using an infusion pump. RESULTS: The demographic data showed no significant difference between the two groups. Furthermore, there were no significant hemodynamic differences between the two groups. CONCLUSIONS: The method of administration of carbetocin does not influence its hemodynamic effects. Korean Society of Anesthesiologists 2020-04-30 2020-04-29 /pmc/articles/PMC7713823/ /pubmed/33329809 http://dx.doi.org/10.17085/apm.2020.15.2.167 Text en Copyright © the Korean Society of Anesthesiologists, 2020 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Obstetric Anesthesia Kwon, Kihyug Kim, Dohyung Jo, Hyunmin Park, Ji Eun Kim, Kyung Ok Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery |
title | Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery |
title_full | Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery |
title_fullStr | Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery |
title_full_unstemmed | Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery |
title_short | Hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery |
title_sort | hemodynamic effects of carbetocin administered as an intravenous bolus or infusion during cesarean delivery |
topic | Obstetric Anesthesia |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713823/ https://www.ncbi.nlm.nih.gov/pubmed/33329809 http://dx.doi.org/10.17085/apm.2020.15.2.167 |
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