Outcome of pretreatment regimens on hemodynamic parameters and emergence during electroconvulsive therapy-a study on dexmedetomidine and esmolol

Aim: Present study was performed with an aim to observe the effect on hemodynamic parameters and emergence during electroconvulsive therapy using dexmedetomidine and esmolol as pretreatment regimens. Methodology: In this prospective study, we selected all patients undergoing ECT from January 2017 to...

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Veröffentlicht in:Anaesthesia, pain & intensive care pain & intensive care, 2019, Vol.23 (1), p.52
Hauptverfasser: Modh, Dixitkumar B, Parmar, Manthan P, Solanki, Shilpin, Sachidananda, Roopa
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container_start_page 52
container_title Anaesthesia, pain & intensive care
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creator Modh, Dixitkumar B
Parmar, Manthan P
Solanki, Shilpin
Sachidananda, Roopa
description Aim: Present study was performed with an aim to observe the effect on hemodynamic parameters and emergence during electroconvulsive therapy using dexmedetomidine and esmolol as pretreatment regimens. Methodology: In this prospective study, we selected all patients undergoing ECT from January 2017 to February 2018 in our hospital by convenient sampling, and divided them as follows; Group C (Control Group): patients who did not receive any pretreatment. Group D (Dexmedetomidine Group): inj dexmedetomidine 0.5 [micro]g/kg diluted with 10 ml normal saline and administered over 10 min and Group E (Esmolol Group): inj esmolol 1mg/kg diluted in 10 ml normal saline and administered over 2 min during preoxygenation. Pulse rate, systolic, diastolic blood pressure and Sp[O.sub.2] were measured at baseline value and compared after administration of drugs at various intervals. Results: We observed statistically significant reduction in mean heart rate and blood pressure in Group E, followed by Group D after administration of drugs. Highly significant rise in hemodynamic parameters (HR, SBP, DBP) from baseline were observed in Group C at 1, 3 and 5 min after ECT shock and returned to baseline value at 10 min of ECT current. Obeying commands and eye opening were significantly delayed in Group D when compared to Group C and Group E. (p [less than or equal to] 0.05) Conclusion: Attenuation of hemodynamic parameters during ECT are effectively achieved by inj esmolol 1 mg/kg followed by inj dexmedetomidine 0.5 [micro]g/kg, but dexmedetomidine produces delayed recovery and attenuates emergence agitation better than esmolol without affecting seizure duration or any other complications. Key words: Attenuation, Agitation, Dexmedetomidine, Electroconvulsive therapy, Esmolol
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Methodology: In this prospective study, we selected all patients undergoing ECT from January 2017 to February 2018 in our hospital by convenient sampling, and divided them as follows; Group C (Control Group): patients who did not receive any pretreatment. Group D (Dexmedetomidine Group): inj dexmedetomidine 0.5 [micro]g/kg diluted with 10 ml normal saline and administered over 10 min and Group E (Esmolol Group): inj esmolol 1mg/kg diluted in 10 ml normal saline and administered over 2 min during preoxygenation. Pulse rate, systolic, diastolic blood pressure and Sp[O.sub.2] were measured at baseline value and compared after administration of drugs at various intervals. Results: We observed statistically significant reduction in mean heart rate and blood pressure in Group E, followed by Group D after administration of drugs. Highly significant rise in hemodynamic parameters (HR, SBP, DBP) from baseline were observed in Group C at 1, 3 and 5 min after ECT shock and returned to baseline value at 10 min of ECT current. Obeying commands and eye opening were significantly delayed in Group D when compared to Group C and Group E. (p [less than or equal to] 0.05) Conclusion: Attenuation of hemodynamic parameters during ECT are effectively achieved by inj esmolol 1 mg/kg followed by inj dexmedetomidine 0.5 [micro]g/kg, but dexmedetomidine produces delayed recovery and attenuates emergence agitation better than esmolol without affecting seizure duration or any other complications. Key words: Attenuation, Agitation, Dexmedetomidine, Electroconvulsive therapy, Esmolol</description><identifier>ISSN: 1607-8322</identifier><language>eng</language><publisher>Sage Publications Ltd. (UK)</publisher><subject>Alfentanil ; Dexmedetomidine ; Esmolol ; Heart beat ; Medical research ; Medicine, Experimental ; Succinylcholine</subject><ispartof>Anaesthesia, pain &amp; intensive care, 2019, Vol.23 (1), p.52</ispartof><rights>COPYRIGHT 2019 Sage Publications Ltd. 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Methodology: In this prospective study, we selected all patients undergoing ECT from January 2017 to February 2018 in our hospital by convenient sampling, and divided them as follows; Group C (Control Group): patients who did not receive any pretreatment. Group D (Dexmedetomidine Group): inj dexmedetomidine 0.5 [micro]g/kg diluted with 10 ml normal saline and administered over 10 min and Group E (Esmolol Group): inj esmolol 1mg/kg diluted in 10 ml normal saline and administered over 2 min during preoxygenation. Pulse rate, systolic, diastolic blood pressure and Sp[O.sub.2] were measured at baseline value and compared after administration of drugs at various intervals. Results: We observed statistically significant reduction in mean heart rate and blood pressure in Group E, followed by Group D after administration of drugs. Highly significant rise in hemodynamic parameters (HR, SBP, DBP) from baseline were observed in Group C at 1, 3 and 5 min after ECT shock and returned to baseline value at 10 min of ECT current. Obeying commands and eye opening were significantly delayed in Group D when compared to Group C and Group E. (p [less than or equal to] 0.05) Conclusion: Attenuation of hemodynamic parameters during ECT are effectively achieved by inj esmolol 1 mg/kg followed by inj dexmedetomidine 0.5 [micro]g/kg, but dexmedetomidine produces delayed recovery and attenuates emergence agitation better than esmolol without affecting seizure duration or any other complications. 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(UK)</general><scope/></search><sort><creationdate>2019</creationdate><title>Outcome of pretreatment regimens on hemodynamic parameters and emergence during electroconvulsive therapy-a study on dexmedetomidine and esmolol</title><author>Modh, Dixitkumar B ; Parmar, Manthan P ; Solanki, Shilpin ; Sachidananda, Roopa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g222t-716951129e0bbf539e5ee0050bb9fdaff0e968a7e4e85a2ba45598158baa224f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alfentanil</topic><topic>Dexmedetomidine</topic><topic>Esmolol</topic><topic>Heart beat</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Succinylcholine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Modh, Dixitkumar B</creatorcontrib><creatorcontrib>Parmar, Manthan P</creatorcontrib><creatorcontrib>Solanki, Shilpin</creatorcontrib><creatorcontrib>Sachidananda, Roopa</creatorcontrib><jtitle>Anaesthesia, pain &amp; intensive care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Modh, Dixitkumar B</au><au>Parmar, Manthan P</au><au>Solanki, Shilpin</au><au>Sachidananda, Roopa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcome of pretreatment regimens on hemodynamic parameters and emergence during electroconvulsive therapy-a study on dexmedetomidine and esmolol</atitle><jtitle>Anaesthesia, pain &amp; intensive care</jtitle><date>2019</date><risdate>2019</risdate><volume>23</volume><issue>1</issue><spage>52</spage><pages>52-</pages><issn>1607-8322</issn><abstract>Aim: Present study was performed with an aim to observe the effect on hemodynamic parameters and emergence during electroconvulsive therapy using dexmedetomidine and esmolol as pretreatment regimens. Methodology: In this prospective study, we selected all patients undergoing ECT from January 2017 to February 2018 in our hospital by convenient sampling, and divided them as follows; Group C (Control Group): patients who did not receive any pretreatment. Group D (Dexmedetomidine Group): inj dexmedetomidine 0.5 [micro]g/kg diluted with 10 ml normal saline and administered over 10 min and Group E (Esmolol Group): inj esmolol 1mg/kg diluted in 10 ml normal saline and administered over 2 min during preoxygenation. Pulse rate, systolic, diastolic blood pressure and Sp[O.sub.2] were measured at baseline value and compared after administration of drugs at various intervals. Results: We observed statistically significant reduction in mean heart rate and blood pressure in Group E, followed by Group D after administration of drugs. Highly significant rise in hemodynamic parameters (HR, SBP, DBP) from baseline were observed in Group C at 1, 3 and 5 min after ECT shock and returned to baseline value at 10 min of ECT current. Obeying commands and eye opening were significantly delayed in Group D when compared to Group C and Group E. (p [less than or equal to] 0.05) Conclusion: Attenuation of hemodynamic parameters during ECT are effectively achieved by inj esmolol 1 mg/kg followed by inj dexmedetomidine 0.5 [micro]g/kg, but dexmedetomidine produces delayed recovery and attenuates emergence agitation better than esmolol without affecting seizure duration or any other complications. Key words: Attenuation, Agitation, Dexmedetomidine, Electroconvulsive therapy, Esmolol</abstract><pub>Sage Publications Ltd. (UK)</pub></addata></record>
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subjects Alfentanil
Dexmedetomidine
Esmolol
Heart beat
Medical research
Medicine, Experimental
Succinylcholine
title Outcome of pretreatment regimens on hemodynamic parameters and emergence during electroconvulsive therapy-a study on dexmedetomidine and esmolol
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