Ultrasound-guided Erector Spinae Muscle Block Versus Ultrasound-guided Caudal Block in Pediatric Patients Undergoing Lower Abdominal Surgeries

BACKGROUND: The erector spinae plane block is a new regional anesthetic technique that is gaining popularity in pediatric medicine. OBJECTIVES: This study aimed to evaluate the safety and efficacy of ultrasound-guided erector spinae block and compare its analgesic effect with that of the ultrasound-...

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Veröffentlicht in:Pain physician 2022-07, Vol.25 (4), p.E571-E580
Hauptverfasser: Abdelrazik, Amr Nady, Ibrahim Talaat Ibrahim, Farghaly, Arwa Essam, h, Shadwa, Rabea Mohamed
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container_issue 4
container_start_page E571
container_title Pain physician
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creator Abdelrazik, Amr Nady
Ibrahim Talaat Ibrahim
Farghaly, Arwa Essam
h
Shadwa, Rabea Mohamed
description BACKGROUND: The erector spinae plane block is a new regional anesthetic technique that is gaining popularity in pediatric medicine. OBJECTIVES: This study aimed to evaluate the safety and efficacy of ultrasound-guided erector spinae block and compare its analgesic effect with that of the ultrasound-guided caudal block in pediatric patients. STUDY DESIGN: Prospective, randomized, double-blind, controlled study. SETTING: Department of Anesthesia and Intensive Care, faculty of medicine, Minia University, Egypt. METHODS: Sixty-three children scheduled for unilateral lower abdominal surgeries, under general anesthesia were randomly allocated into 3 parallel equal groups: Group I (erector spinae block [ESB] group) received ultrasound-guided an erector spinae muscle block in a dose of 0.4 mg/kg of 0.25% bupivacaine between the 10th transverse process and the erector spinae muscles. Group II (caudal block [CB] group) received an ultrasound-guided caudal block in a dose of 2.5 mg/kg of 0.25% bupivacaine. The last group, Group III (control [C] group), did not receive any regional block. Our primary outcome was to evaluate the quality of postoperative analgesia using the Face, Legs, Activity, Cry, Consolability (FLACC) Pain Scale; secondary outcomes were to assess the time to first analgesic request, total analgesic requests during the first 24 hours, and the occurrence of any side effects. RESULTS: The early postoperative FLACC score was less in the ESB group than the CB group; both were lower than the control group. The erector spinae block had a longer duration of analgesia than the caudal block as the median (interquartile range [IQR]) ``of the duration of analgesia in the ESB group was 8 (8-12) hours while it was 6 (6-8) hours in group the CB group; both groups had a longer duration of analgesia compared to the C group 0.25 (0.17-4) hours. The total amount of analgesia was less in the ESB group than the CB group. The number of patients who needed rescue intravenous fentanyl analgesia was 14 patients in the C group while no patient needed intravenous fentanyl in the ESB and CB groups. LIMITATIONS: Sensory evaluation of the patients was not done since the 2 blocks were done under general anesthesia but did not affect the outcome. CONCLUSIONS: Ultrasound-guided erector spinae block was safe and effective in pediatric patients undergoing unilateral lower abdominal surgery as it provided a longer duration of analgesia and less analgesic requirement than caudal block
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OBJECTIVES: This study aimed to evaluate the safety and efficacy of ultrasound-guided erector spinae block and compare its analgesic effect with that of the ultrasound-guided caudal block in pediatric patients. STUDY DESIGN: Prospective, randomized, double-blind, controlled study. SETTING: Department of Anesthesia and Intensive Care, faculty of medicine, Minia University, Egypt. METHODS: Sixty-three children scheduled for unilateral lower abdominal surgeries, under general anesthesia were randomly allocated into 3 parallel equal groups: Group I (erector spinae block [ESB] group) received ultrasound-guided an erector spinae muscle block in a dose of 0.4 mg/kg of 0.25% bupivacaine between the 10th transverse process and the erector spinae muscles. Group II (caudal block [CB] group) received an ultrasound-guided caudal block in a dose of 2.5 mg/kg of 0.25% bupivacaine. The last group, Group III (control [C] group), did not receive any regional block. Our primary outcome was to evaluate the quality of postoperative analgesia using the Face, Legs, Activity, Cry, Consolability (FLACC) Pain Scale; secondary outcomes were to assess the time to first analgesic request, total analgesic requests during the first 24 hours, and the occurrence of any side effects. RESULTS: The early postoperative FLACC score was less in the ESB group than the CB group; both were lower than the control group. The erector spinae block had a longer duration of analgesia than the caudal block as the median (interquartile range [IQR]) ``of the duration of analgesia in the ESB group was 8 (8-12) hours while it was 6 (6-8) hours in group the CB group; both groups had a longer duration of analgesia compared to the C group 0.25 (0.17-4) hours. The total amount of analgesia was less in the ESB group than the CB group. The number of patients who needed rescue intravenous fentanyl analgesia was 14 patients in the C group while no patient needed intravenous fentanyl in the ESB and CB groups. LIMITATIONS: Sensory evaluation of the patients was not done since the 2 blocks were done under general anesthesia but did not affect the outcome. CONCLUSIONS: Ultrasound-guided erector spinae block was safe and effective in pediatric patients undergoing unilateral lower abdominal surgery as it provided a longer duration of analgesia and less analgesic requirement than caudal block and fewer side effects.</description><identifier>ISSN: 1533-3159</identifier><identifier>EISSN: 2150-1149</identifier><language>eng</language><publisher>Paducah: American Society of Interventional Pain Physician</publisher><subject>Abdomen ; Abdominal surgery ; Analgesics ; Drug dosages ; Fentanyl ; General anesthesia ; Pain ; Pediatrics ; Ultrasonic imaging</subject><ispartof>Pain physician, 2022-07, Vol.25 (4), p.E571-E580</ispartof><rights>2022. This work is published under https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Abdelrazik, Amr Nady</creatorcontrib><creatorcontrib>Ibrahim Talaat Ibrahim</creatorcontrib><creatorcontrib>Farghaly, Arwa Essam</creatorcontrib><creatorcontrib>h</creatorcontrib><creatorcontrib>Shadwa, Rabea Mohamed</creatorcontrib><title>Ultrasound-guided Erector Spinae Muscle Block Versus Ultrasound-guided Caudal Block in Pediatric Patients Undergoing Lower Abdominal Surgeries</title><title>Pain physician</title><description>BACKGROUND: The erector spinae plane block is a new regional anesthetic technique that is gaining popularity in pediatric medicine. OBJECTIVES: This study aimed to evaluate the safety and efficacy of ultrasound-guided erector spinae block and compare its analgesic effect with that of the ultrasound-guided caudal block in pediatric patients. STUDY DESIGN: Prospective, randomized, double-blind, controlled study. SETTING: Department of Anesthesia and Intensive Care, faculty of medicine, Minia University, Egypt. METHODS: Sixty-three children scheduled for unilateral lower abdominal surgeries, under general anesthesia were randomly allocated into 3 parallel equal groups: Group I (erector spinae block [ESB] group) received ultrasound-guided an erector spinae muscle block in a dose of 0.4 mg/kg of 0.25% bupivacaine between the 10th transverse process and the erector spinae muscles. Group II (caudal block [CB] group) received an ultrasound-guided caudal block in a dose of 2.5 mg/kg of 0.25% bupivacaine. The last group, Group III (control [C] group), did not receive any regional block. Our primary outcome was to evaluate the quality of postoperative analgesia using the Face, Legs, Activity, Cry, Consolability (FLACC) Pain Scale; secondary outcomes were to assess the time to first analgesic request, total analgesic requests during the first 24 hours, and the occurrence of any side effects. RESULTS: The early postoperative FLACC score was less in the ESB group than the CB group; both were lower than the control group. The erector spinae block had a longer duration of analgesia than the caudal block as the median (interquartile range [IQR]) ``of the duration of analgesia in the ESB group was 8 (8-12) hours while it was 6 (6-8) hours in group the CB group; both groups had a longer duration of analgesia compared to the C group 0.25 (0.17-4) hours. The total amount of analgesia was less in the ESB group than the CB group. The number of patients who needed rescue intravenous fentanyl analgesia was 14 patients in the C group while no patient needed intravenous fentanyl in the ESB and CB groups. LIMITATIONS: Sensory evaluation of the patients was not done since the 2 blocks were done under general anesthesia but did not affect the outcome. CONCLUSIONS: Ultrasound-guided erector spinae block was safe and effective in pediatric patients undergoing unilateral lower abdominal surgery as it provided a longer duration of analgesia and less analgesic requirement than caudal block and fewer side effects.</description><subject>Abdomen</subject><subject>Abdominal surgery</subject><subject>Analgesics</subject><subject>Drug dosages</subject><subject>Fentanyl</subject><subject>General anesthesia</subject><subject>Pain</subject><subject>Pediatrics</subject><subject>Ultrasonic imaging</subject><issn>1533-3159</issn><issn>2150-1149</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNplzs9KAzEQBvBFFKzVdwh48bKQv5vdYy1VCxULtV5LdjNZUtOkJht8C5_ZRXtSGJjL7_tmzooJJQKXhPDmvJgQwVjJiGgui6uU9hizqmnYpPjauiGqFLLXZZ-tBo0WEbohRLQ5Wq8APefUOUD3LnTv6A1iygn9D81V1sqdlPVoDdqqIdoOrdVgwQ9jyGuIfbC-R6vwCRHNWh0O4w2HNjn2EC2k6-LCKJfg5rSnxfZh8Tp_Klcvj8v5bFUeKamGsgKsZEtrw0EQ2TJDm8qA0VTUBBvA3FBjWGN019a6BSYpo1UtWYOx4JJLNi3ufnuPMXxkSMPuYFMHzikPIafdqAXn41Qjvf1D9yHH8esfJSXhlNbsG_5McPo</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Abdelrazik, Amr Nady</creator><creator>Ibrahim Talaat Ibrahim</creator><creator>Farghaly, Arwa Essam</creator><creator>h</creator><creator>Shadwa, Rabea Mohamed</creator><general>American Society of Interventional Pain Physician</general><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20220701</creationdate><title>Ultrasound-guided Erector Spinae Muscle Block Versus Ultrasound-guided Caudal Block in Pediatric Patients Undergoing Lower Abdominal Surgeries</title><author>Abdelrazik, Amr Nady ; Ibrahim Talaat Ibrahim ; Farghaly, Arwa Essam ; h ; Shadwa, Rabea Mohamed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p216t-6e0a7b28f4e517b3f296fefd25810fe04f2ff39fdcb8dbe372326873900547473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abdomen</topic><topic>Abdominal surgery</topic><topic>Analgesics</topic><topic>Drug dosages</topic><topic>Fentanyl</topic><topic>General anesthesia</topic><topic>Pain</topic><topic>Pediatrics</topic><topic>Ultrasonic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abdelrazik, Amr Nady</creatorcontrib><creatorcontrib>Ibrahim Talaat Ibrahim</creatorcontrib><creatorcontrib>Farghaly, Arwa Essam</creatorcontrib><creatorcontrib>h</creatorcontrib><creatorcontrib>Shadwa, Rabea Mohamed</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; 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OBJECTIVES: This study aimed to evaluate the safety and efficacy of ultrasound-guided erector spinae block and compare its analgesic effect with that of the ultrasound-guided caudal block in pediatric patients. STUDY DESIGN: Prospective, randomized, double-blind, controlled study. SETTING: Department of Anesthesia and Intensive Care, faculty of medicine, Minia University, Egypt. METHODS: Sixty-three children scheduled for unilateral lower abdominal surgeries, under general anesthesia were randomly allocated into 3 parallel equal groups: Group I (erector spinae block [ESB] group) received ultrasound-guided an erector spinae muscle block in a dose of 0.4 mg/kg of 0.25% bupivacaine between the 10th transverse process and the erector spinae muscles. Group II (caudal block [CB] group) received an ultrasound-guided caudal block in a dose of 2.5 mg/kg of 0.25% bupivacaine. The last group, Group III (control [C] group), did not receive any regional block. Our primary outcome was to evaluate the quality of postoperative analgesia using the Face, Legs, Activity, Cry, Consolability (FLACC) Pain Scale; secondary outcomes were to assess the time to first analgesic request, total analgesic requests during the first 24 hours, and the occurrence of any side effects. RESULTS: The early postoperative FLACC score was less in the ESB group than the CB group; both were lower than the control group. The erector spinae block had a longer duration of analgesia than the caudal block as the median (interquartile range [IQR]) ``of the duration of analgesia in the ESB group was 8 (8-12) hours while it was 6 (6-8) hours in group the CB group; both groups had a longer duration of analgesia compared to the C group 0.25 (0.17-4) hours. The total amount of analgesia was less in the ESB group than the CB group. The number of patients who needed rescue intravenous fentanyl analgesia was 14 patients in the C group while no patient needed intravenous fentanyl in the ESB and CB groups. LIMITATIONS: Sensory evaluation of the patients was not done since the 2 blocks were done under general anesthesia but did not affect the outcome. CONCLUSIONS: Ultrasound-guided erector spinae block was safe and effective in pediatric patients undergoing unilateral lower abdominal surgery as it provided a longer duration of analgesia and less analgesic requirement than caudal block and fewer side effects.</abstract><cop>Paducah</cop><pub>American Society of Interventional Pain Physician</pub><oa>free_for_read</oa></addata></record>
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Abdomen
Abdominal surgery
Analgesics
Drug dosages
Fentanyl
General anesthesia
Pain
Pediatrics
Ultrasonic imaging
title Ultrasound-guided Erector Spinae Muscle Block Versus Ultrasound-guided Caudal Block in Pediatric Patients Undergoing Lower Abdominal Surgeries
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