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Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study

BACKGROUND AND AIMS: The use of propofol as the most common induction agent and the high prevalence of propofol injection pain (PIP) highlight the significance of finding the ideal combination of drug, dosage and mode of administration of premedicants to alleviate PIP. A number of bolus drugs with v...

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Autores principales: Thukral, Seema, Gupta, Priyanka, Lakra, Archana, Gupta, Mayank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551026/
https://www.ncbi.nlm.nih.gov/pubmed/26379292
http://dx.doi.org/10.4103/0019-5049.162987
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author Thukral, Seema
Gupta, Priyanka
Lakra, Archana
Gupta, Mayank
author_facet Thukral, Seema
Gupta, Priyanka
Lakra, Archana
Gupta, Mayank
author_sort Thukral, Seema
collection PubMed
description BACKGROUND AND AIMS: The use of propofol as the most common induction agent and the high prevalence of propofol injection pain (PIP) highlight the significance of finding the ideal combination of drug, dosage and mode of administration of premedicants to alleviate PIP. A number of bolus drugs with variable efficacy have been studied to reduce PIP. The aim of our study was to assess the efficacy of single dose intravenous (IV) infusion of dexmedetomidine 0.5 μg/kg compared with ketamine 0.5 mg/kg to alleviate PIP. METHODS: In this prospective, randomised and double-blind study, 108 patients undergoing elective surgeries under general anaesthesia were randomly allocated to two groups: Group D to receive dexmedetomidine 0.5μg/kg or Group K to receive ketamine 0.5 mg/kg in 20 ml of normal saline over 10 min. Immediately after the infusion, 1% propofol 2 mg/kg IV was injected over 25 s. The patients were assessed for pain every 5 s by asking the question ‘does it hurt?’ until the loss of consciousness. The pain scoring was done using McCririck and Hunter scale. Statistical analysis was done using SPSS 17.0. RESULTS: The incidence of PIP and moderate-severe PIP was higher with Group D (79.6%; 16.7%) compared with Group K (40.7; 1.9%) (P < 0.001; 0.016). No patient in either group had arm withdrawal upon propofol injection. The incidence of hypertension and tachycardia was statistically significant in Group K as compared to Group D (P = 0.027). CONCLUSION: There was no difference in elimination of the arm withdrawal response and in incidence of moderate to severe PIP between the groups.
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spelling pubmed-45510262015-09-14 Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study Thukral, Seema Gupta, Priyanka Lakra, Archana Gupta, Mayank Indian J Anaesth Clinical Investigation BACKGROUND AND AIMS: The use of propofol as the most common induction agent and the high prevalence of propofol injection pain (PIP) highlight the significance of finding the ideal combination of drug, dosage and mode of administration of premedicants to alleviate PIP. A number of bolus drugs with variable efficacy have been studied to reduce PIP. The aim of our study was to assess the efficacy of single dose intravenous (IV) infusion of dexmedetomidine 0.5 μg/kg compared with ketamine 0.5 mg/kg to alleviate PIP. METHODS: In this prospective, randomised and double-blind study, 108 patients undergoing elective surgeries under general anaesthesia were randomly allocated to two groups: Group D to receive dexmedetomidine 0.5μg/kg or Group K to receive ketamine 0.5 mg/kg in 20 ml of normal saline over 10 min. Immediately after the infusion, 1% propofol 2 mg/kg IV was injected over 25 s. The patients were assessed for pain every 5 s by asking the question ‘does it hurt?’ until the loss of consciousness. The pain scoring was done using McCririck and Hunter scale. Statistical analysis was done using SPSS 17.0. RESULTS: The incidence of PIP and moderate-severe PIP was higher with Group D (79.6%; 16.7%) compared with Group K (40.7; 1.9%) (P < 0.001; 0.016). No patient in either group had arm withdrawal upon propofol injection. The incidence of hypertension and tachycardia was statistically significant in Group K as compared to Group D (P = 0.027). CONCLUSION: There was no difference in elimination of the arm withdrawal response and in incidence of moderate to severe PIP between the groups. Medknow Publications & Media Pvt Ltd 2015-08 /pmc/articles/PMC4551026/ /pubmed/26379292 http://dx.doi.org/10.4103/0019-5049.162987 Text en Copyright: © Indian Journal of Anaesthesia http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigation
Thukral, Seema
Gupta, Priyanka
Lakra, Archana
Gupta, Mayank
Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study
title Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study
title_full Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study
title_fullStr Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study
title_full_unstemmed Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study
title_short Dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: A prospective randomized and double-blind study
title_sort dexmedetomidine versus ketamine infusion to alleviate propofol injection pain: a prospective randomized and double-blind study
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551026/
https://www.ncbi.nlm.nih.gov/pubmed/26379292
http://dx.doi.org/10.4103/0019-5049.162987
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