Effect of intravenous paracetamol for post-operative pain relief after tonsillectomy - A study of 70 cases

M. KawinKumar
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Effective preventive analgesic technique may not only be useful in reducing the acute pain, but also chronic post surgical pain and disabilities. Paracetamol is an effective analgesic and an antipyretic agent. The efficiency and tolerability for intravenous Paracetamol are well established. It has a favourable safety profile and it is the most commonly prescribed drug for the treatment of mild to moderate pain. The objective of the present study is to evaluate the post operative analgesia, the haemodynamic profile and the side effects of IV Paracetamol. AIM OF THE STUDY: 1. To evaluate the efficacy of Intravenous Paracetamol as a pre-emptive analgesic in relieving the post operative pain. 2. To study the hemodynamic variables during the post-operative period. 3. To establish the safety of Intravenous paracetamol in patients. MATERIALS AND METHODS: Study Design: Prospective, randomized, double blinded, comparative study. Double blinding was done by taking appropriate dose of intravenous paracetamol calculated in mg/kg and was added to a solution of normal saline to make a volume of 100 ml. This was labelled as drug A. Plain 100 ml of normal saline was labelled as drug B. Neither the person administering the drug nor the person observing the patient in the post operative period did not know the drug. Study Population: After obtaining the institutional ethical committee approval and written informed consent from the parent/guardian, 70 ASA I physical status patients undergoing tonsillectomy were selected between the age group of 6-16 years and weighing between 10-30 kg. Sample Size: 35 patients in the paracetamol group (P group) and 35 in the control group (N group). Probability sampling: All the70 patients were randomised in two groups and the entire patients stood an equal chance of getting into any group. Data collection: 1. Age, Sex, Weight, 2. Pre operative and intra operative pulse rate and blood pressure, Spo2, 3. Duration of surgery, 4. Sedation score using Ramsays Sedation Scale, 5. Visual analogue pain scale at the end of surgery, 1h 2h, 3h, 4h, 5h, 6h. 6. Post operative complications such as: • Drug intolerance, • Nausea and vomiting, • Epigastric pain, • Bleeding, Exclusion Criteria: 1. Upper and lower respiratory tract infections, 2. Cardiac valvular abnormalities, 3. Abnormal bleeding and clotting time, 4. Obstructive sleep apnea, 5. Known history of allergy to paracetamol, 6. Past history of jaundice, 7. Patients on aspirin, 8. Any other concurrent antipyretic, analgesic or anti inflammatory Medications. OBSERVATION AND RESULTS: Data were analysed using SPSS version 13.0 computer software at level of significance p = 0.05. Numerical variables were presented as mean and standard deviation (SD) and categorical variables were presented as frequency (%). Unpaired Student ‘t’ test was used for between-group comparisons between categorical variables. Time to first analgesic administration was analysed by the Kaplan–Meier survival analysis. SUMMARY: 1. Intravenous Paracetamol achieved significant post operative pain relief up to 6 hours. 2. Intravenous Paracetamol delayed the requirement of first dose of rescue analgesic for a mean duration of 6 hours in the post-operative period. 3. Intravenous Paracetamol had a better haemodynamic profile in the post-operative period. 4. Intraveous Paracetamol had a smooth and better post-operative recovery profile rendering a calm, co-operative and tranquil patient. 5. Intravenous Paracetamol did not exhibit any adverse effects in the patients. CONCLUSION: 1. Intravenous Paracetamol can be used as an effective analgesic for providing pre-emptive analgesia. 2. Intravenous Paracetamol provides excellent post operative pain relief. 3. Intraveous Paracetamol has a better hemodynamic profile. 4. Intraveous Paracetamol is safe for use in patients.","PeriodicalId":18595,"journal":{"name":"MedPulse International Journal of Anesthesiology","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MedPulse International Journal of Anesthesiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26611/10151411","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

INTRODUCTION: Tonsillectomy is one of the commonest surgical procedures performed in the field of otorhinolaryngology. The most common and distressing symptoms, which follow anaesthesia and surgery, are pain and emesis. The provision of adequate analgesia after tonsillectomy presents the anaesthesiologist with difficulties, as this is a painful procedure and may be associated with significant bleeding into the airway. As evidence continues to accumulate concerning the role of central sensitisation in post operative pain, many researchers have followed methods to prevent central neuropathic changes from occurring, through the utilization of pre-emptive analgesic techniques. Effective preventive analgesic technique may not only be useful in reducing the acute pain, but also chronic post surgical pain and disabilities. Paracetamol is an effective analgesic and an antipyretic agent. The efficiency and tolerability for intravenous Paracetamol are well established. It has a favourable safety profile and it is the most commonly prescribed drug for the treatment of mild to moderate pain. The objective of the present study is to evaluate the post operative analgesia, the haemodynamic profile and the side effects of IV Paracetamol. AIM OF THE STUDY: 1. To evaluate the efficacy of Intravenous Paracetamol as a pre-emptive analgesic in relieving the post operative pain. 2. To study the hemodynamic variables during the post-operative period. 3. To establish the safety of Intravenous paracetamol in patients. MATERIALS AND METHODS: Study Design: Prospective, randomized, double blinded, comparative study. Double blinding was done by taking appropriate dose of intravenous paracetamol calculated in mg/kg and was added to a solution of normal saline to make a volume of 100 ml. This was labelled as drug A. Plain 100 ml of normal saline was labelled as drug B. Neither the person administering the drug nor the person observing the patient in the post operative period did not know the drug. Study Population: After obtaining the institutional ethical committee approval and written informed consent from the parent/guardian, 70 ASA I physical status patients undergoing tonsillectomy were selected between the age group of 6-16 years and weighing between 10-30 kg. Sample Size: 35 patients in the paracetamol group (P group) and 35 in the control group (N group). Probability sampling: All the70 patients were randomised in two groups and the entire patients stood an equal chance of getting into any group. Data collection: 1. Age, Sex, Weight, 2. Pre operative and intra operative pulse rate and blood pressure, Spo2, 3. Duration of surgery, 4. Sedation score using Ramsays Sedation Scale, 5. Visual analogue pain scale at the end of surgery, 1h 2h, 3h, 4h, 5h, 6h. 6. Post operative complications such as: • Drug intolerance, • Nausea and vomiting, • Epigastric pain, • Bleeding, Exclusion Criteria: 1. Upper and lower respiratory tract infections, 2. Cardiac valvular abnormalities, 3. Abnormal bleeding and clotting time, 4. Obstructive sleep apnea, 5. Known history of allergy to paracetamol, 6. Past history of jaundice, 7. Patients on aspirin, 8. Any other concurrent antipyretic, analgesic or anti inflammatory Medications. OBSERVATION AND RESULTS: Data were analysed using SPSS version 13.0 computer software at level of significance p = 0.05. Numerical variables were presented as mean and standard deviation (SD) and categorical variables were presented as frequency (%). Unpaired Student ‘t’ test was used for between-group comparisons between categorical variables. Time to first analgesic administration was analysed by the Kaplan–Meier survival analysis. SUMMARY: 1. Intravenous Paracetamol achieved significant post operative pain relief up to 6 hours. 2. Intravenous Paracetamol delayed the requirement of first dose of rescue analgesic for a mean duration of 6 hours in the post-operative period. 3. Intravenous Paracetamol had a better haemodynamic profile in the post-operative period. 4. Intraveous Paracetamol had a smooth and better post-operative recovery profile rendering a calm, co-operative and tranquil patient. 5. Intravenous Paracetamol did not exhibit any adverse effects in the patients. CONCLUSION: 1. Intravenous Paracetamol can be used as an effective analgesic for providing pre-emptive analgesia. 2. Intravenous Paracetamol provides excellent post operative pain relief. 3. Intraveous Paracetamol has a better hemodynamic profile. 4. Intraveous Paracetamol is safe for use in patients.
70例扁桃体切除术后静脉注射扑热息痛缓解疼痛的疗效分析
扁桃体切除术是耳鼻喉科最常见的外科手术之一。麻醉和手术后最常见和最痛苦的症状是疼痛和呕吐。扁桃体切除术后提供足够的镇痛给麻醉师带来了困难,因为这是一个痛苦的过程,可能与气道大量出血有关。随着关于中枢致敏在术后疼痛中的作用的证据不断积累,许多研究人员通过使用先发制人的镇痛技术来防止中枢神经性改变的发生。有效的预防性镇痛技术不仅可用于减轻急性疼痛,也可用于减轻术后慢性疼痛和残疾。扑热息痛是一种有效的止痛剂和解热剂。静脉注射扑热息痛的有效性和耐受性已得到证实。它具有良好的安全性,是治疗轻度至中度疼痛的最常用处方药。本研究的目的是评价静脉注射扑热息痛的术后镇痛、血流动力学特征和副作用。研究目的:目的评价静脉注射扑热息痛作为先发制人镇痛药对术后疼痛的缓解效果。2. 目的:探讨术后血流动力学指标。3.目的:探讨患者静脉注射扑热息痛的安全性。材料和方法:研究设计:前瞻性、随机、双盲、比较研究。采用双盲法,取适当剂量的静脉注射扑热息痛,单位为mg/kg,加入生理盐水溶液,体积为100 ml,标记为药物a。将100 ml生理盐水标记为药物b。给药者和术后观察患者的人都不知道这种药物。研究人群:在获得机构伦理委员会批准和父母/监护人的书面知情同意后,选择年龄在6-16岁,体重在10-30 kg之间的ASA I身体状态的扁桃体切除术患者70例。样本量:扑热息痛组35例(P组),对照组35例(N组)。概率抽样:所有70名患者被随机分为两组,所有患者都有均等的机会进入任何一组。数据收集:1;年龄,性别,体重,2。术前、术中脉搏率、血压、Spo2、3。4.手术时间;使用ramsay镇静量表进行镇静评分,5。手术结束时、1h、2h、3h、4h、5h、6h的视觉模拟疼痛评分。6. 术后并发症如:•药物不耐受、•恶心呕吐、•胃脘痛、•出血。2.上、下呼吸道感染;3.心脏瓣膜异常;4、异常出血凝血时间;5.阻塞性睡眠呼吸暂停。已知对扑热息痛过敏史,6岁。7.黄疸病史;服用阿司匹林的患者,8人。任何其他同时使用的解热、镇痛或抗炎药物。观察与结果:采用SPSS 13.0计算机软件进行数据分析,p = 0.05。数值变量以均值和标准差(SD)表示,分类变量以频率(%)表示。分类变量间的组间比较采用Unpaired Student ' t检验。通过Kaplan-Meier生存分析分析首次给药时间。总结:1。静脉注射扑热息痛可显著缓解术后疼痛长达6小时。2. 静脉注射扑热息痛延迟了术后第一次抢救镇痛药的需要,平均持续时间为6小时。3.静脉注射扑热息痛在术后有较好的血流动力学特征。4. 静脉注射扑热息痛具有平稳和较好的术后恢复概况,使患者平静,合作和平静。5. 静脉注射扑热息痛在患者中未出现任何不良反应。结论:1。静脉注射扑热息痛可作为一种有效的镇痛药提供先发制人的镇痛。2. 静脉注射扑热息痛可以很好地缓解术后疼痛。3.静脉注射扑热息痛具有更好的血流动力学特征。4. 静脉注射扑热息痛对病人是安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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