Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control Trial

Introduction: Various efforts have been made to reduce post tonsillectomy pain in children. The present study was undertaken to evaluate the efficacy and safety of Ropivacaine in post-operative pain management in these children. Materials and Methods: This study is a Randomized control study on 140...

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Main Authors: Arvinder-Singh Sood, Pooja Pal, Gurupreet-Singh Gill
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2020-07-01
Series:Iranian Journal of Otorhinolaryngology
Subjects:
Online Access:https://ijorl.mums.ac.ir/article_16025_6114ec6359a81c77a1c62b277a912892.pdf
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spelling doaj-b75b0db8fabb4a58a948832338c7ab6f2021-01-05T07:12:34ZengMashhad University of Medical SciencesIranian Journal of Otorhinolaryngology2251-72512251-726X2020-07-0132420721210.22038/ijorl.2020.36577.219916025Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control TrialArvinder-Singh Sood0Pooja Pal1Gurupreet-Singh Gill2Department of Otorhinolaryngology, SGRD Institute of Medical Sciences and Research, Amritsar, Punjab, India – 143001.Department of Otorhinolaryngology, SGRD Institute of Medical Sciences and Research, Amritsar, Punjab, India – 143001.Department of Otorhinolaryngology, SGRD Institute of Medical Sciences and Research, Amritsar, Punjab, India – 143001.Introduction: Various efforts have been made to reduce post tonsillectomy pain in children. The present study was undertaken to evaluate the efficacy and safety of Ropivacaine in post-operative pain management in these children. Materials and Methods: This study is a Randomized control study on 140 patients between 4 - 12 years of age, in whom tonsillectomy was performed in a tertiary care centre between January 2017 to November 2018 using standard dissection and snare surgical technique. Postoperatively, patients were randomized into 2 groups of 70 patients each, receiving tonsillar fossa infiltration with 0.2% Ropivacaine or 0.9% normal saline respectively. Patients were assessed as per Wong Baker’s Faces Scoring System at 2 hours, 4 hours, 8 hours, 18 hours, 24 hours, and 48 hours postoperatively.  All the results were analyzed by SPSS software. Chi- square test and Mann-Whitney test were used for assessment of level of significance, with P- value of less than 0.05 taken as significant.    Results: Both the groups were comparable with respect to age and sex. At 48 hours, in study group, maximum number of patients 35 (50%) had Wong Baker score 0, while in control group, maximum number of patients 52 (74.3%) had Wong Baker score 4 (P< 0.01). The difference in the mean Deglutition time between both groups was significant (P< 0.01). Conclusion: Ropivacaine infiltration is a effective modality for post-tonsillectomy pain management in children, with minimal side-effects.https://ijorl.mums.ac.ir/article_16025_6114ec6359a81c77a1c62b277a912892.pdfpost operative analgesiaropivacainetonsillectomy
collection DOAJ
language English
format Article
sources DOAJ
author Arvinder-Singh Sood
Pooja Pal
Gurupreet-Singh Gill
spellingShingle Arvinder-Singh Sood
Pooja Pal
Gurupreet-Singh Gill
Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control Trial
Iranian Journal of Otorhinolaryngology
post operative analgesia
ropivacaine
tonsillectomy
author_facet Arvinder-Singh Sood
Pooja Pal
Gurupreet-Singh Gill
author_sort Arvinder-Singh Sood
title Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control Trial
title_short Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control Trial
title_full Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control Trial
title_fullStr Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control Trial
title_full_unstemmed Peritonsillar Ropivacaine Infiltration in Paediatric Tonsillectomy: A Randomised Control Trial
title_sort peritonsillar ropivacaine infiltration in paediatric tonsillectomy: a randomised control trial
publisher Mashhad University of Medical Sciences
series Iranian Journal of Otorhinolaryngology
issn 2251-7251
2251-726X
publishDate 2020-07-01
description Introduction: Various efforts have been made to reduce post tonsillectomy pain in children. The present study was undertaken to evaluate the efficacy and safety of Ropivacaine in post-operative pain management in these children. Materials and Methods: This study is a Randomized control study on 140 patients between 4 - 12 years of age, in whom tonsillectomy was performed in a tertiary care centre between January 2017 to November 2018 using standard dissection and snare surgical technique. Postoperatively, patients were randomized into 2 groups of 70 patients each, receiving tonsillar fossa infiltration with 0.2% Ropivacaine or 0.9% normal saline respectively. Patients were assessed as per Wong Baker’s Faces Scoring System at 2 hours, 4 hours, 8 hours, 18 hours, 24 hours, and 48 hours postoperatively.  All the results were analyzed by SPSS software. Chi- square test and Mann-Whitney test were used for assessment of level of significance, with P- value of less than 0.05 taken as significant.    Results: Both the groups were comparable with respect to age and sex. At 48 hours, in study group, maximum number of patients 35 (50%) had Wong Baker score 0, while in control group, maximum number of patients 52 (74.3%) had Wong Baker score 4 (P< 0.01). The difference in the mean Deglutition time between both groups was significant (P< 0.01). Conclusion: Ropivacaine infiltration is a effective modality for post-tonsillectomy pain management in children, with minimal side-effects.
topic post operative analgesia
ropivacaine
tonsillectomy
url https://ijorl.mums.ac.ir/article_16025_6114ec6359a81c77a1c62b277a912892.pdf
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