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首页> 外文期刊>Pain medicine : >Safety of a Novel Parenteral Formulation of Diclofenac after Major Orthopedic or Abdominal/Pelvic Surgery in a Population Including Anticoagulated, Elderly or Renally Insufficient Patients: An Open-Label, Multiday, Repeated Dose Clinical Trial
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Safety of a Novel Parenteral Formulation of Diclofenac after Major Orthopedic or Abdominal/Pelvic Surgery in a Population Including Anticoagulated, Elderly or Renally Insufficient Patients: An Open-Label, Multiday, Repeated Dose Clinical Trial

机译:在患有抗凝,老年或肾脏患者的人群中,Diclofenac新型肠胃外制剂的安全性,包括抗凝,老年或肾不足患者:开放标签,多日期,重复剂量临床试验

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摘要

Objective: Decisions to use or avoid nonsteroidal anti-inflammatory drugs (NSAIDs) for postsurgical pain are often influenced by concerns about bleeding and renal adverse effects. The objective of this study was to evaluate the safety of a novel parenteral NSAID, hydroxypropyl-β-cyclodextrin (HPβCD) diclofenac, in a large postsurgical patient population, with particular focus on bleeding and renal effects. Methods: This was a large open-label study in adult patients with acute moderate-to-severe pain following major surgery. Patients received ≥2 days of continuous treatment with HPβCD diclofenac, administered as a small-volume bolus injection every 6 hours. Few exclusion criteria were applied in order to reflect surgical patient populations commonly managed in clinical practice. Adverse events (AEs) were recorded throughout the study. The incidences of bleeding- and renal-related AEs were examined in patient subpopulations with known risk factors for NSAID-induced complications: advanced age, pre-existing renal insufficiency, concomitant anticoagulant use, prolonged exposure, elevated dosage, and major surgeries. Results: Of the total 971 patients studied, 38% were ≥65 years old (12% >75 years), 62% received concomitant anticoagulants, and 6% had pre-existing renal insufficiency. HPβCD diclofenac was well tolerated by the patient population. AE rates are presented by risk factor to enable clinicians to better describe renal- or bleeding-related AEs. Conclusions: In addition to its previously demonstrated efficacy, this study provides evidence of HPβCD diclofenac's safety in a large postsurgical population including anticoagulated, elderly or renally insufficient patients. Because study exclusion criteria were minimal, these findings may be broadly generalizable to populations commonly treated in clinical practice. Wiley Periodicals, Inc.
机译:目的:使用或避免外科疼痛的非甾体抗炎药物(NSAIDs)的决定通常受到对出血和肾不利影响的担忧的影响。本研究的目的是评估新的肠胃外NSAID,羟丙基-β-环糊精(HPβCD)双氯芬酸在大型后尿的患者群体中的安全性,特别关注出血和肾效应。方法:这是大型手术后成人患者的大型开放式研究。患者接受≥2天的连续处理,用HPβCD双氯芬酸治疗,每6小时每6小时施用小体积烟草注射。少量排除标准应用,以反映临床实践中常规管理的外科患者人群。在整个研究中记录不良事件(AES)。在患者群体中检查出血和肾相关AES的发生率,所述患者群具有已知的NSAID诱导的并发症的危险因素:晚期年龄,预先存在的肾功能不全,伴随的抗凝血剂,延长的暴露,升高剂量和主要手术。结果:总计971例患者,38%≥65岁(12%> 75岁),62%接受综合抗凝剂,6%具有预先存在的肾功能不全。患有患者群体的HPβCD双氯芬酸良好。危险因素提出了AE率,以使临床医生能够更好地描述与肾脏或出血相关的AES。结论:除了以前证明的疗效外,本研究还提供了HPβCDDiclofenac在大型后勤人群中的安全性,包括抗凝,老年人或肾不足患者。因为研究排除标准是最小的,所以这些发现可能是广泛地普遍地普遍地允许在临床实践中常见的群体。 Wiley期刊,Inc。

著录项

  • 来源
    《Pain medicine : 》 |2013年第5期| 共13页
  • 作者单位

    Department of Anesthesiology UPMC Presbyterian-Shadyside Hospital Pittsburgh PA United States;

    Clinical Operations Lotus Clinical Research Inc. Pasadena CA United States;

    Department of Anesthesiology Helen Keller Hospital Sheffield AL United States;

    Pain Management Hospira Inc. Lake Forest IL United States;

    Biostatistics Veristat Inc. Holliston MA United States;

    Department of Anesthesiology Tufts Medical Center Boston MA United States;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 症状诊断学 ;
  • 关键词

    Acute Pain; Analgesia; Bleeding; NSAID; Renal;

    机译:急性疼痛;镇痛;出血;NSAID;肾;

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