选择性5 -羟色胺再摄取抑制剂和选择性环氧化酶-2抑制剂对脊髓麻醉后头痛的协同作用

R. F. Iteke, D. Mutombo, Franck Namegabe Zirhumana, O. Mukuku, E. Muyumba, Tinsley Mukakala Kibonge, J. Brichant, A. Kilembe, Y. Brouh, J. Kakoma
{"title":"选择性5 -羟色胺再摄取抑制剂和选择性环氧化酶-2抑制剂对脊髓麻醉后头痛的协同作用","authors":"R. F. Iteke, D. Mutombo, Franck Namegabe Zirhumana, O. Mukuku, E. Muyumba, Tinsley Mukakala Kibonge, J. Brichant, A. Kilembe, Y. Brouh, J. Kakoma","doi":"10.4236/pp.2020.118018","DOIUrl":null,"url":null,"abstract":"Objective: To evaluate the synergistic effect of a Selective \nSerotonin Reuptake Inhibitor (SSRI) and a Selective Cyclooxygenase 2 Inhibitor \n(ISCOx-2) in the management of After Rachianesthesia Headache in Obstetric \nCare. Patients and Methods: This was an experimental double-blind, \nrandomized, multi-center clinical trial of non-inferiority clinical trials over \na 12-month period (May 1, 2018 to April 30, 2019) in six hospitals in \nsoutheastern DR Congo, including all patients undergoing surgery or \nanalgesia on spinal anesthesia for obstetrical indication and with headache \ncharacteristic of a dural breccia, with no known causes, contraindications to \nexperimental products and informed consent to been obtained. The patients were \ndivided into four different groups depending on the protocol used, namely: \nGroup A = Rehydration + Paracetamol, Group B = Rehydration + Celecoxib, Group C \n= Rehydration + Nefopam and Group 4 = Rehydration + Celecoxib + Nefopam (Study \nGroup). Using the Statview II software, the statistical analyzes of data \nobtained from the different tests were made using the ANOVA test for comparing \nthe averages of different samples using the Fisher test. Verification of the \nnormality of the samples was made by the Kurtosis and Skewness flattening and \nasymmetry test. Results: The protocol associating Celecoxib and Nefopam \nsignificantly demonstrates its effectiveness in reducing CPRAOs in the first \ntwo days with a gradual decrease in anxiety and length of stay. In addition, \nthe majority of patients (75.6%) had a high overall level of satisfaction with \nthis protocol. Conclusion: The Nefopam-Celecoxib combination shows its \neffectiveness in the early reduction of these CPRAOs, anxiety and length of \nstay with a high overall level of patient satisfaction. Given the good \ntolerance and accessibility of these products, we strongly suggest the use of \nthis protocol for its validation in our environment and elsewhere, although it \nis desirable to continue research on other non-explored alien pathways.","PeriodicalId":19875,"journal":{"name":"Pharmacology & Pharmacy","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic Effect of a Selective Serotonin Reuptake Inhibitor and a Selective Cyclo-Oxygenase-2 Inhibitor on Post Spinal Anesthesia Headache\",\"authors\":\"R. F. Iteke, D. Mutombo, Franck Namegabe Zirhumana, O. Mukuku, E. Muyumba, Tinsley Mukakala Kibonge, J. Brichant, A. Kilembe, Y. Brouh, J. Kakoma\",\"doi\":\"10.4236/pp.2020.118018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: To evaluate the synergistic effect of a Selective \\nSerotonin Reuptake Inhibitor (SSRI) and a Selective Cyclooxygenase 2 Inhibitor \\n(ISCOx-2) in the management of After Rachianesthesia Headache in Obstetric \\nCare. Patients and Methods: This was an experimental double-blind, \\nrandomized, multi-center clinical trial of non-inferiority clinical trials over \\na 12-month period (May 1, 2018 to April 30, 2019) in six hospitals in \\nsoutheastern DR Congo, including all patients undergoing surgery or \\nanalgesia on spinal anesthesia for obstetrical indication and with headache \\ncharacteristic of a dural breccia, with no known causes, contraindications to \\nexperimental products and informed consent to been obtained. The patients were \\ndivided into four different groups depending on the protocol used, namely: \\nGroup A = Rehydration + Paracetamol, Group B = Rehydration + Celecoxib, Group C \\n= Rehydration + Nefopam and Group 4 = Rehydration + Celecoxib + Nefopam (Study \\nGroup). Using the Statview II software, the statistical analyzes of data \\nobtained from the different tests were made using the ANOVA test for comparing \\nthe averages of different samples using the Fisher test. Verification of the \\nnormality of the samples was made by the Kurtosis and Skewness flattening and \\nasymmetry test. Results: The protocol associating Celecoxib and Nefopam \\nsignificantly demonstrates its effectiveness in reducing CPRAOs in the first \\ntwo days with a gradual decrease in anxiety and length of stay. In addition, \\nthe majority of patients (75.6%) had a high overall level of satisfaction with \\nthis protocol. Conclusion: The Nefopam-Celecoxib combination shows its \\neffectiveness in the early reduction of these CPRAOs, anxiety and length of \\nstay with a high overall level of patient satisfaction. Given the good \\ntolerance and accessibility of these products, we strongly suggest the use of \\nthis protocol for its validation in our environment and elsewhere, although it \\nis desirable to continue research on other non-explored alien pathways.\",\"PeriodicalId\":19875,\"journal\":{\"name\":\"Pharmacology & Pharmacy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmacology & Pharmacy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4236/pp.2020.118018\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology & Pharmacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4236/pp.2020.118018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的:评价选择性5 -羟色胺再摄取抑制剂(SSRI)和选择性环氧化酶2抑制剂(ISCOx-2)在产科护理中治疗腰麻后头痛的协同作用。患者和方法:这是一项为期12个月的实验性双盲、随机、多中心临床试验(2018年5月1日至2019年4月30日),在刚果民主共和国东南部的六家医院进行的非劣效性临床试验,包括所有因产科指征而接受脊髓麻醉手术或镇痛的患者,并伴有硬脑膜角化的头痛特征,无已知原因,实验产品的禁忌症,并获得知情同意。根据治疗方案将患者分为4组,即:A组=补液+扑热息痛,B组=补液+塞来昔布,C组=补液+奈福泮,4组=补液+塞来昔布+奈福泮(研究组)。使用Statview II软件,对不同检验获得的数据进行统计分析,采用方差分析检验,比较不同样本的平均值,采用Fisher检验。通过峰度和偏度的平坦化和不对称检验来验证样品的正态性。结果:将塞来昔布和奈福泮联合使用的方案显着表明其在头两天减少CPRAOs的有效性,并逐渐减少焦虑和住院时间。此外,大多数患者(75.6%)对该方案总体满意度较高。结论:奈福泮-塞来昔布联合用药在早期降低患者CPRAOs、焦虑和住院时间方面具有较好的效果,患者总体满意度较高。鉴于这些产品的良好耐受性和可及性,我们强烈建议在我们的环境和其他地方使用该协议进行验证,尽管希望继续研究其他未探索的外星途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Synergistic Effect of a Selective Serotonin Reuptake Inhibitor and a Selective Cyclo-Oxygenase-2 Inhibitor on Post Spinal Anesthesia Headache
Objective: To evaluate the synergistic effect of a Selective Serotonin Reuptake Inhibitor (SSRI) and a Selective Cyclooxygenase 2 Inhibitor (ISCOx-2) in the management of After Rachianesthesia Headache in Obstetric Care. Patients and Methods: This was an experimental double-blind, randomized, multi-center clinical trial of non-inferiority clinical trials over a 12-month period (May 1, 2018 to April 30, 2019) in six hospitals in southeastern DR Congo, including all patients undergoing surgery or analgesia on spinal anesthesia for obstetrical indication and with headache characteristic of a dural breccia, with no known causes, contraindications to experimental products and informed consent to been obtained. The patients were divided into four different groups depending on the protocol used, namely: Group A = Rehydration + Paracetamol, Group B = Rehydration + Celecoxib, Group C = Rehydration + Nefopam and Group 4 = Rehydration + Celecoxib + Nefopam (Study Group). Using the Statview II software, the statistical analyzes of data obtained from the different tests were made using the ANOVA test for comparing the averages of different samples using the Fisher test. Verification of the normality of the samples was made by the Kurtosis and Skewness flattening and asymmetry test. Results: The protocol associating Celecoxib and Nefopam significantly demonstrates its effectiveness in reducing CPRAOs in the first two days with a gradual decrease in anxiety and length of stay. In addition, the majority of patients (75.6%) had a high overall level of satisfaction with this protocol. Conclusion: The Nefopam-Celecoxib combination shows its effectiveness in the early reduction of these CPRAOs, anxiety and length of stay with a high overall level of patient satisfaction. Given the good tolerance and accessibility of these products, we strongly suggest the use of this protocol for its validation in our environment and elsewhere, although it is desirable to continue research on other non-explored alien pathways.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Safety, Tolerability and Anti-Diarrhoeal Activity of “Diarra”, a Preparation of Medicinal Plants Used in Ivorian Traditional Medicine Design of Traditional Chinese Medicine Extraction Workshop Process and Automation System Nonclinical Study of the Active Components of Doxorubicin Hydrochloride Liposome Injection <i>in Vivo</i> Advancement of Pharmacy Accreditation in the Field of Chinese Higher Education Antinociceptive Effect of Methanol Extract of <i>Diospyros malabarica</i> (Desr.) Kostel Leaves in Mice
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1