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A comparison of Pharmaceutical Regiments Following First Stage Root Canal Treatment.

机译:第一阶段根管治疗后的药物治疗方案比较。

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AIM: The purpose of this clinical trial was to investigate the analgesic efficacy of four oral medication groups on postoperative endodontic pain after first stage root canal treatment. The four groups will be.;Methodology: Patients presenting to the University of Minnesota emergency graduate endodontic clinic experiencing pain greater than or equal to 3/10 were considered potential condidiates. 22 patients were included based on an established inclusion criteria. Following administration of local anaestheisa, a pulpectomy was performed. The patients were administered the following at 4 hour time intervals: (1) 2 doses of Placebo; (2) 2 800mg doses of Ibuprofen; (3) 2 800mg Ibuprofen with Vicodin 325/7.5mg; (4) 1 dose of 550mg Anaprox DS (Naproxen) and 1 dose of Placebo. Patients recorded pain intensity following treatment on a visual analogue scale, Heft parker scale and a baseline four-point category pain scale before and immediately after treatment, then one hour after the initial dose of medication, and one hour after the second dose of medication. The following day, pain was recorded at breakfast, lunch, dinner and bedtime.;Results: At about 24 hours, 27% had moderate to severe pain. All patients showed significant pain reduction after initial root canal therapy. The ibuprofen group showed a rebound in pain the following day. Males had more rebound pain compared to females. Anaprox DS and the combination of Ibuprofen and Vicodin showed the most pain reduction at all time periods. In our study, the results suggested that pulp vitality had little effect on post operative pain.;Conclusion: Primary endodontic treatment will greatly decrease the pain felt by the patient. High doses of Ibuprofen followed by an abrupt stop might lead to a rebound in pain. Tooth vitality did not seem to affect post operative discomfort, nor did patient gender. More research using this model and analgesic combination is necessary to ensure statistically significant results.
机译:目的:该临床试验的目的是研究四个口服药物组在第一阶段根管治疗后对术后牙髓痛的镇痛效果。这四组患者将是:方法:在明尼苏达大学紧急研究生牙髓诊所就诊且疼痛大于或等于3/10的患者被视为潜在的条件。根据确定的纳入标准,纳入22例患者。局部麻醉后,进行牙髓切除术。在4小时的时间间隔内对患者进行以下给药:(1)2剂安慰剂; (2)2 800毫克布洛芬剂量; (3)2800毫克布洛芬和维考丁325 / 7.5毫克; (4)1剂550mg Anaprox DS(萘普生)和1剂安慰剂。在治疗之前和之后,然后在初始剂量的药物治疗后一小时和第二剂药物的治疗后一小时,患者在治疗后分别以视觉模拟量表,Heft Parker量表和基线四点类别疼痛量表记录疼痛强度。第二天,早餐,午餐,晚餐和就寝时间记录了疼痛。结果:大约24小时,有27%的患者出现中度至重度疼痛。最初的根管治疗后,所有患者均显示疼痛明显减轻。第二天,布洛芬组显示疼痛反弹。男性比女性有更多的反弹疼痛。 Anaprox DS以及布洛芬和维考丁的组合在所有时间段均显示出最大程度的疼痛减轻。在我们的研究中,结果表明牙髓活力对术后疼痛影响不大。结论:根管治疗可以大大减轻患者的疼痛感。大剂量布洛芬后突然停药可能导致疼痛反弹。牙齿的活力似乎并没有影响术后不适,患者的性别也没有影响。为了确保统计学上有意义的结果,有必要使用该模型和止痛药进行更多的研究。

著录项

  • 作者

    Lewis, Riley J. H.;

  • 作者单位

    University of Minnesota.;

  • 授予单位 University of Minnesota.;
  • 学科 Dentistry.;Pharmaceutical sciences.
  • 学位 M.S.
  • 年度 2015
  • 页码 104 p.
  • 总页数 104
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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