宫颈旁阻滞与双氯芬酸肠外注射对人工真空抽吸镇痛效果的比较研究

IF 0.8 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Iyke F Osinachi, Godwin O Akaba, Nathaniel D Adewole, Kate I Omonua, Bissallah A Ekele
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引用次数: 0

摘要

目的:比较颈旁阻滞与肌注双氯芬酸对早期妊娠流产人工吸吸(MVA)疼痛缓解的效果。方法:这是一项开放标签随机对照试验。参与者使用计算机生成的数字随机分为两个治疗组(A和B)。A组肌注双氯芬酸75mg。B组采用1%利多卡因宫颈旁阻滞。在完成手术后的5分钟内,参与者被要求在连续的10厘米视觉模拟量表(VAS)上对他们的疼痛水平进行评分,从0(无疼痛)到10(有史以来最严重的疼痛)。在完成MVA后30分钟内用李克特量表评估参与者的满意度。数据分析使用统计软件包的社会科学(SPSS),版本20。统计学显著性检验设为95%置信水平(P <0.05)。主要结局是患者在手术过程中感受到的疼痛程度(10cm VAS)。次要结局包括患者满意度和不良事件。 结果:肌注双氯芬酸组患者疼痛水平差异有统计学意义;6.5±1.5(中度)和颈旁阻滞组;2.3±1.5(轻度),p值=0.005。颈旁阻滞组患者满意度也优于肌注双氯芬酸组(p值=0.005)。两组在并发症和药物副作用方面具有可比性。 结论:本研究结果表明,与肌注双氯芬酸相比,使用宫颈旁阻滞缓解不完全流产MVA期间的疼痛可显著减轻疼痛,提高患者满意度,并具有相当的安全性。关键词:颈旁阻滞;双氯芬酸;缓解疼痛;手动真空抽吸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A comparative study on the effectiveness of paracervical block and parenteral diclofenac for pain relief during manual vacuum aspiration
Objective: To compare the effectiveness of paracervical block with intramuscular Diclofenac for pain relief during manual vacuum aspiration (MVA) for early pregnancy losses. Methodology: This was an open label randomized controlled trial. Participants were randomized into two therapeutic groups (A and B) using computer generated numbers. Group A received intramuscular Diclofenac 75 mg. Group B received paracervical block using 1% Lidocaine. Participants were asked to rate their pain level on a continuous 10 cm visual analogue scale (VAS) from 0 (no pain) to 10 (the worst pain ever) within 5 minutes of completing the procedure. Participants’ level of satisfaction was assessed within 30 minutes of completing the MVA using Likert scale. Data was analysed using the Statistical Package for Social Sciences (SPSS), Version 20. Test of statistical significance was set at 95% confidence level (P < 0.05). The primary outcome was the level of pain felt by the patient during the procedure (10 cm VAS). Secondary outcomes included patient’s satisfaction and adverse events. Results: There was significant difference in the mean pain level between the intramuscular diclofenac group; 6.5±1.5 (moderate) and those that received paracervical block; 2.3±1.5 (mild), (p-value=0.005). Patients’ satisfaction was also better in paracervical block group compared to intramuscular diclofenac group, (p-value=0.005). Both groups were comparable in terms of complications and drug side effects. Conclusion: Findings from the study suggest that the use of paracervical block compared to intramuscular Diclofenac for pain relief during MVA for incomplete miscarriage significantly reduced pain, improved patients’ satisfaction and was comparably safe. Keywords: Paracervical block; Diclofenac; Pain relief; Manual vacuum aspiration.
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来源期刊
African Health Sciences
African Health Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
2.30
自引率
0.00%
发文量
179
审稿时长
>12 weeks
期刊介绍: The African Health Sciences is an internationally refereed journal publishing original articles on research, clinical practice, public health, policy, planning, implementation and evaluation, in the health and related sciences relevant to Africa and the tropics. Its objectives are to: Advocate for and promote the growth of reading culture in sub Saharan Africa; Provide a high quality journal in which health and policy and other researchers and practitioners in the region can and world wide, can publish their work; Promote relevant health system research and publication in the region including alternative means of health care financing, the burden of and solution of health problems in marginalized urban and rural communities amongst the displaced and others affected by conflict; Promote research and the systematic collection and collation and publication of data on diseases and conditions of equity and influence; Promote development of evidence-based policies and guidelines for clinical, public health and other practitioners. African Health Sciences acknowledges support provided by the African Health Journals Partnership Project that is funded by the US National Institutes of Health (through the National Library of Medicine and the Fogarty International Center) and facilitated by the Council of Science Editors.
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