Epinephrine decreases the dose of hyperbaric bupivacaine necessary for tourniquet pain blockade during spinal anesthesia for total knee replacement arthroplasty

Purpose We quantified the dose-sparing effect of epinephrine by comparing the median effective dose (ED 50 ) of intrathecal hyperbaric bupivacaine co-administered with epinephrine with the ED 50 of intrathecal hyperbaric bupivacaine alone. Methods Three groups were randomly generated from 162 patien...

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Veröffentlicht in:Journal of anesthesia 2013-02, Vol.27 (1), p.72-79
Hauptverfasser: Kim, Won Ho, Ko, Justin Sangwook, Ahn, Hyun Joo, Choi, Soo Joo, Shin, Byung Seop, Gwak, Mi Sook, Sim, Woo Seog, Yang, Mikyung
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container_end_page 79
container_issue 1
container_start_page 72
container_title Journal of anesthesia
container_volume 27
creator Kim, Won Ho
Ko, Justin Sangwook
Ahn, Hyun Joo
Choi, Soo Joo
Shin, Byung Seop
Gwak, Mi Sook
Sim, Woo Seog
Yang, Mikyung
description Purpose We quantified the dose-sparing effect of epinephrine by comparing the median effective dose (ED 50 ) of intrathecal hyperbaric bupivacaine co-administered with epinephrine with the ED 50 of intrathecal hyperbaric bupivacaine alone. Methods Three groups were randomly generated from 162 patients undergoing total knee replacement arthroplasty under combined spinal and epidural anesthesia: Group B (bupivacaine), Group BE1 (bupivacaine plus epinephrine 100 μg), and Group BE2 (bupivacaine plus epinephrine 200 μg). Each group was further divided by bupivacaine doses of 6, 7, 8, 9, 10, or 11 mg. The anesthesia was defined as successful if a bilateral T12 sensory block occurred within 15 min, and no intraoperative epidural supplement was required. The ED 50 and ED 95 for successful anesthesia and successful tourniquet pain blockade were determined separately by probit regression analysis. Results The ED 50 and ED 95 of intrathecal hyperbaric bupivacaine for successful anesthesia were not different among the groups: the ED 50 values were 7.1 mg [95 % confidence interval (95 % CI) 6.0–8.0 mg] in Group B, 6.2 mg (95 % CI 4.8–7.2 mg) in Group BE1, and 6.3 mg (95 % CI 4.9–7.2 mg) in Group BE2. However, the ED 50 and ED 95 values for tourniquet pain control were significantly smaller in Groups BE1 and BE2 than in Group B: the ED 50 values were 7.2 mg (95 % CI 6.3–7.9 mg), 5.5 mg (95 % CI 4.1–6.3 mg), and 5.3 mg (95 % CI 3.7–6.2 mg) in Groups B, BE1, and BE2, respectively. The incidence of tourniquet pain was significantly lower in Groups BE1 and BE2 than in Group B. The time to patients’ requests for supplemental analgesia was significantly longer in Groups BE1 and BE2 than in Group B. Conclusions Intrathecal epinephrine did not decrease the dose of intrathecal hyperbaric bupivacaine required for successful anesthesia. However, it reduced the dose required for tourniquet pain blockade.
doi_str_mv 10.1007/s00540-012-1471-x
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Methods Three groups were randomly generated from 162 patients undergoing total knee replacement arthroplasty under combined spinal and epidural anesthesia: Group B (bupivacaine), Group BE1 (bupivacaine plus epinephrine 100 μg), and Group BE2 (bupivacaine plus epinephrine 200 μg). Each group was further divided by bupivacaine doses of 6, 7, 8, 9, 10, or 11 mg. The anesthesia was defined as successful if a bilateral T12 sensory block occurred within 15 min, and no intraoperative epidural supplement was required. The ED 50 and ED 95 for successful anesthesia and successful tourniquet pain blockade were determined separately by probit regression analysis. Results The ED 50 and ED 95 of intrathecal hyperbaric bupivacaine for successful anesthesia were not different among the groups: the ED 50 values were 7.1 mg [95 % confidence interval (95 % CI) 6.0–8.0 mg] in Group B, 6.2 mg (95 % CI 4.8–7.2 mg) in Group BE1, and 6.3 mg (95 % CI 4.9–7.2 mg) in Group BE2. However, the ED 50 and ED 95 values for tourniquet pain control were significantly smaller in Groups BE1 and BE2 than in Group B: the ED 50 values were 7.2 mg (95 % CI 6.3–7.9 mg), 5.5 mg (95 % CI 4.1–6.3 mg), and 5.3 mg (95 % CI 3.7–6.2 mg) in Groups B, BE1, and BE2, respectively. The incidence of tourniquet pain was significantly lower in Groups BE1 and BE2 than in Group B. The time to patients’ requests for supplemental analgesia was significantly longer in Groups BE1 and BE2 than in Group B. Conclusions Intrathecal epinephrine did not decrease the dose of intrathecal hyperbaric bupivacaine required for successful anesthesia. However, it reduced the dose required for tourniquet pain blockade.</description><identifier>ISSN: 0913-8668</identifier><identifier>EISSN: 1438-8359</identifier><identifier>DOI: 10.1007/s00540-012-1471-x</identifier><identifier>PMID: 22911223</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Aged ; Analgesia ; Analysis ; Anesthesia ; Anesthesia, Epidural ; Anesthesia, Spinal - methods ; Anesthesiology ; Anesthetics, Local - administration &amp; dosage ; Arthroplasty, Replacement, Knee - methods ; Blood Pressure - drug effects ; Bupivacaine ; Bupivacaine - administration &amp; dosage ; Critical Care Medicine ; Dosage and administration ; Drug therapy ; Emergency Medicine ; Endpoint Determination ; Epinephrine ; Epinephrine - pharmacology ; Female ; Health aspects ; Humans ; Intensive ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Original Article ; Pain - prevention &amp; control ; Pain Measurement ; Pain Medicine ; Sample Size ; Tourniquets - adverse effects ; Vasoconstrictor Agents - pharmacology</subject><ispartof>Journal of anesthesia, 2013-02, Vol.27 (1), p.72-79</ispartof><rights>Japanese Society of Anesthesiologists 2012</rights><rights>COPYRIGHT 2013 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c502t-befd86334af0e7b6ba11be7f0fb9bae8f8e238d9f652ccf1c9c9e54f4002582b3</citedby><cites>FETCH-LOGICAL-c502t-befd86334af0e7b6ba11be7f0fb9bae8f8e238d9f652ccf1c9c9e54f4002582b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00540-012-1471-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00540-012-1471-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22911223$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Won Ho</creatorcontrib><creatorcontrib>Ko, Justin Sangwook</creatorcontrib><creatorcontrib>Ahn, Hyun Joo</creatorcontrib><creatorcontrib>Choi, Soo Joo</creatorcontrib><creatorcontrib>Shin, Byung Seop</creatorcontrib><creatorcontrib>Gwak, Mi Sook</creatorcontrib><creatorcontrib>Sim, Woo Seog</creatorcontrib><creatorcontrib>Yang, Mikyung</creatorcontrib><title>Epinephrine decreases the dose of hyperbaric bupivacaine necessary for tourniquet pain blockade during spinal anesthesia for total knee replacement arthroplasty</title><title>Journal of anesthesia</title><addtitle>J Anesth</addtitle><addtitle>J Anesth</addtitle><description>Purpose We quantified the dose-sparing effect of epinephrine by comparing the median effective dose (ED 50 ) of intrathecal hyperbaric bupivacaine co-administered with epinephrine with the ED 50 of intrathecal hyperbaric bupivacaine alone. Methods Three groups were randomly generated from 162 patients undergoing total knee replacement arthroplasty under combined spinal and epidural anesthesia: Group B (bupivacaine), Group BE1 (bupivacaine plus epinephrine 100 μg), and Group BE2 (bupivacaine plus epinephrine 200 μg). Each group was further divided by bupivacaine doses of 6, 7, 8, 9, 10, or 11 mg. The anesthesia was defined as successful if a bilateral T12 sensory block occurred within 15 min, and no intraoperative epidural supplement was required. The ED 50 and ED 95 for successful anesthesia and successful tourniquet pain blockade were determined separately by probit regression analysis. Results The ED 50 and ED 95 of intrathecal hyperbaric bupivacaine for successful anesthesia were not different among the groups: the ED 50 values were 7.1 mg [95 % confidence interval (95 % CI) 6.0–8.0 mg] in Group B, 6.2 mg (95 % CI 4.8–7.2 mg) in Group BE1, and 6.3 mg (95 % CI 4.9–7.2 mg) in Group BE2. However, the ED 50 and ED 95 values for tourniquet pain control were significantly smaller in Groups BE1 and BE2 than in Group B: the ED 50 values were 7.2 mg (95 % CI 6.3–7.9 mg), 5.5 mg (95 % CI 4.1–6.3 mg), and 5.3 mg (95 % CI 3.7–6.2 mg) in Groups B, BE1, and BE2, respectively. The incidence of tourniquet pain was significantly lower in Groups BE1 and BE2 than in Group B. The time to patients’ requests for supplemental analgesia was significantly longer in Groups BE1 and BE2 than in Group B. Conclusions Intrathecal epinephrine did not decrease the dose of intrathecal hyperbaric bupivacaine required for successful anesthesia. However, it reduced the dose required for tourniquet pain blockade.</description><subject>Aged</subject><subject>Analgesia</subject><subject>Analysis</subject><subject>Anesthesia</subject><subject>Anesthesia, Epidural</subject><subject>Anesthesia, Spinal - methods</subject><subject>Anesthesiology</subject><subject>Anesthetics, Local - administration &amp; dosage</subject><subject>Arthroplasty, Replacement, Knee - methods</subject><subject>Blood Pressure - drug effects</subject><subject>Bupivacaine</subject><subject>Bupivacaine - administration &amp; dosage</subject><subject>Critical Care Medicine</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Emergency Medicine</subject><subject>Endpoint Determination</subject><subject>Epinephrine</subject><subject>Epinephrine - pharmacology</subject><subject>Female</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Intensive</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Original Article</subject><subject>Pain - prevention &amp; control</subject><subject>Pain Measurement</subject><subject>Pain Medicine</subject><subject>Sample Size</subject><subject>Tourniquets - adverse effects</subject><subject>Vasoconstrictor Agents - pharmacology</subject><issn>0913-8668</issn><issn>1438-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9ks2KFDEUhQtRnHb0AdxIwI2bGpPUX7IchhkVBtzoOiSpm-7MVFXKJCXTb-OjeotqBaGRQEKS75z83FMUbxm9YpR2HxOlTU1LynjJ6o6VT8-KHasrUYqqkc-LHZWsKkXbioviVUoPlNKWseplccG5ZIzzalf8up39BPMhYk96sBF0gkTyAWchAQmOHI4zRKOjt8Qss_-prV7hCSykpOORuBBJDkuc_I8FMplxm5gh2Efdo8uC1nuS8Bg9ED1BQu_k9UmVcfFxAiAR5kFbGGHKRMd8iAHnKR9fFy-cHhK8OY2Xxfe72283n8v7r5--3Fzfl7ahPJcGXC_aqqq1o9CZ1mjGDHSOOiONBuEE8Er00rUNt9YxK62EpnY1pbwR3FSXxYfNd44Bn5GyGn2yMAx45bAkxbgQUjLRMUTfb-heD6D85EKO2q64usYb0JrKiiJVnqH2MEHUQ5jAeVz-h786w2PrYfT2rIBtAhtDShGcmqMfsSCKUbXmQ235UJgPteZDPaHm3emVixmh_6v4EwgE-Aakea0bRPWwVhZ__j-uvwHSvcnc</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Kim, Won Ho</creator><creator>Ko, Justin Sangwook</creator><creator>Ahn, Hyun Joo</creator><creator>Choi, Soo Joo</creator><creator>Shin, Byung Seop</creator><creator>Gwak, Mi Sook</creator><creator>Sim, Woo Seog</creator><creator>Yang, Mikyung</creator><general>Springer Japan</general><general>Springer</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130201</creationdate><title>Epinephrine decreases the dose of hyperbaric bupivacaine necessary for tourniquet pain blockade during spinal anesthesia for total knee replacement arthroplasty</title><author>Kim, Won Ho ; Ko, Justin Sangwook ; Ahn, Hyun Joo ; Choi, Soo Joo ; Shin, Byung Seop ; Gwak, Mi Sook ; Sim, Woo Seog ; Yang, Mikyung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c502t-befd86334af0e7b6ba11be7f0fb9bae8f8e238d9f652ccf1c9c9e54f4002582b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Analgesia</topic><topic>Analysis</topic><topic>Anesthesia</topic><topic>Anesthesia, Epidural</topic><topic>Anesthesia, Spinal - methods</topic><topic>Anesthesiology</topic><topic>Anesthetics, Local - administration &amp; dosage</topic><topic>Arthroplasty, Replacement, Knee - methods</topic><topic>Blood Pressure - drug effects</topic><topic>Bupivacaine</topic><topic>Bupivacaine - administration &amp; dosage</topic><topic>Critical Care Medicine</topic><topic>Dosage and administration</topic><topic>Drug therapy</topic><topic>Emergency Medicine</topic><topic>Endpoint Determination</topic><topic>Epinephrine</topic><topic>Epinephrine - pharmacology</topic><topic>Female</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Intensive</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Original Article</topic><topic>Pain - prevention &amp; control</topic><topic>Pain Measurement</topic><topic>Pain Medicine</topic><topic>Sample Size</topic><topic>Tourniquets - adverse effects</topic><topic>Vasoconstrictor Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Won Ho</creatorcontrib><creatorcontrib>Ko, Justin Sangwook</creatorcontrib><creatorcontrib>Ahn, Hyun Joo</creatorcontrib><creatorcontrib>Choi, Soo Joo</creatorcontrib><creatorcontrib>Shin, Byung Seop</creatorcontrib><creatorcontrib>Gwak, Mi Sook</creatorcontrib><creatorcontrib>Sim, Woo Seog</creatorcontrib><creatorcontrib>Yang, Mikyung</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Won Ho</au><au>Ko, Justin Sangwook</au><au>Ahn, Hyun Joo</au><au>Choi, Soo Joo</au><au>Shin, Byung Seop</au><au>Gwak, Mi Sook</au><au>Sim, Woo Seog</au><au>Yang, Mikyung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epinephrine decreases the dose of hyperbaric bupivacaine necessary for tourniquet pain blockade during spinal anesthesia for total knee replacement arthroplasty</atitle><jtitle>Journal of anesthesia</jtitle><stitle>J Anesth</stitle><addtitle>J Anesth</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>27</volume><issue>1</issue><spage>72</spage><epage>79</epage><pages>72-79</pages><issn>0913-8668</issn><eissn>1438-8359</eissn><abstract>Purpose We quantified the dose-sparing effect of epinephrine by comparing the median effective dose (ED 50 ) of intrathecal hyperbaric bupivacaine co-administered with epinephrine with the ED 50 of intrathecal hyperbaric bupivacaine alone. Methods Three groups were randomly generated from 162 patients undergoing total knee replacement arthroplasty under combined spinal and epidural anesthesia: Group B (bupivacaine), Group BE1 (bupivacaine plus epinephrine 100 μg), and Group BE2 (bupivacaine plus epinephrine 200 μg). Each group was further divided by bupivacaine doses of 6, 7, 8, 9, 10, or 11 mg. The anesthesia was defined as successful if a bilateral T12 sensory block occurred within 15 min, and no intraoperative epidural supplement was required. The ED 50 and ED 95 for successful anesthesia and successful tourniquet pain blockade were determined separately by probit regression analysis. Results The ED 50 and ED 95 of intrathecal hyperbaric bupivacaine for successful anesthesia were not different among the groups: the ED 50 values were 7.1 mg [95 % confidence interval (95 % CI) 6.0–8.0 mg] in Group B, 6.2 mg (95 % CI 4.8–7.2 mg) in Group BE1, and 6.3 mg (95 % CI 4.9–7.2 mg) in Group BE2. However, the ED 50 and ED 95 values for tourniquet pain control were significantly smaller in Groups BE1 and BE2 than in Group B: the ED 50 values were 7.2 mg (95 % CI 6.3–7.9 mg), 5.5 mg (95 % CI 4.1–6.3 mg), and 5.3 mg (95 % CI 3.7–6.2 mg) in Groups B, BE1, and BE2, respectively. The incidence of tourniquet pain was significantly lower in Groups BE1 and BE2 than in Group B. The time to patients’ requests for supplemental analgesia was significantly longer in Groups BE1 and BE2 than in Group B. Conclusions Intrathecal epinephrine did not decrease the dose of intrathecal hyperbaric bupivacaine required for successful anesthesia. However, it reduced the dose required for tourniquet pain blockade.</abstract><cop>Japan</cop><pub>Springer Japan</pub><pmid>22911223</pmid><doi>10.1007/s00540-012-1471-x</doi><tpages>8</tpages></addata></record>
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subjects Aged
Analgesia
Analysis
Anesthesia
Anesthesia, Epidural
Anesthesia, Spinal - methods
Anesthesiology
Anesthetics, Local - administration & dosage
Arthroplasty, Replacement, Knee - methods
Blood Pressure - drug effects
Bupivacaine
Bupivacaine - administration & dosage
Critical Care Medicine
Dosage and administration
Drug therapy
Emergency Medicine
Endpoint Determination
Epinephrine
Epinephrine - pharmacology
Female
Health aspects
Humans
Intensive
Male
Medicine
Medicine & Public Health
Middle Aged
Original Article
Pain - prevention & control
Pain Measurement
Pain Medicine
Sample Size
Tourniquets - adverse effects
Vasoconstrictor Agents - pharmacology
title Epinephrine decreases the dose of hyperbaric bupivacaine necessary for tourniquet pain blockade during spinal anesthesia for total knee replacement arthroplasty
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