【2h】

Safety and Efficacy of Prehospital Diltiazem

机译:院前地尔硫卓的安全性和有效性

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摘要

>Introduction: Very few studies exist on the use of diltiazem in the prehospital setting. Some practitioners believe this medication is prone to causing hypotension in this setting. Our goals were to determine whether the prehospital administration of diltiazem induced hypotension and to evaluate the efficacy of the drug.>Methods: Our two-tiered system is located in a suburban region of New Jersey with advanced life support (ALS) care provided by fly-car units. The ALS units do not transport patients, and all of them are hospital based. The ALS providers are employed by the hospital system. In New Jersey, all ALS care requires online medical control, including the administration of diltiazem. We retrospectively reviewed patient care records for those who were believed to be in rapid atrial fibrillation and were given diltiazem in a suburban emergeny medical services system over a 22-month period. We examined the differences between heart rate (HR) and blood pressure (BP) on the initial evaluation and on arrival to the emergency department (ED). A hypotensive response was defined as a final systolic BP (SBP) less than 90 mmHg and a drop in SBP of at least 10 mmHg. Diltiazem was considered effective if the ED HR was <100 beats per minute (bpm) or if it decreased ≥20%.>Results: During the study period, 26,979 patients were transported. Of these patients, 2,488 had a documented rhythm of atrial fibrillation or atrial flutter. Of the 320 patients who received diltiazem, 42 patient encounters were excluded for incomplete data, yielding 278 patients for analysis. The average initial SBP was 139 mmHg and the average diastolic BP was 84 mmHg. The average diltiazem dosage was 16.7 mg. Two patients became hypotensive. The average initial HR was 154 bpm. On arrival to the ED, 33% of the patients had an HR < 100 bpm and 69% had a drop in HR ≥ 20%. The overall efficacy of prehospital diltiazem was 73%.>Conclusion: In the prehospital setting, diltiazem is associated with a very low rate of hypotension and appears to be effective in decreasing HR adequately. Prospective studies are needed to confirm these findings.
机译:>简介:院前使用地尔硫卓的研究很少。一些医生认为这种药物在这种情况下容易引起低血压。我们的目标是确定院前服用地尔硫卓是否会引起低血压并评估该药的疗效。>方法:我们的两级系统位于新泽西州郊区,拥有先进的生命支持( ALS)由飞车单位提供的护理。 ALS单位不运送患者,所有患者均在医院工作。 ALS提供者由医院系统雇用。在新泽西州,所有ALS护理都需要在线医疗控制,包括地尔硫卓的管理。我们回顾性地回顾了那些被认为患有快速心房颤动并在郊区紧急医疗服务系统中服地尔硫卓的患者的医疗记录,历时22个月。我们在初步评估和到达急诊室(ED)时检查了心率(HR)和血压(BP)之间的差异。降压反应定义为最终收缩压(SBP)小于90 mmHg,SBP下降至少10 mmHg。如果ED HR≤100次/分(bpm)或下降≥20%,则认为地尔硫卓有效。>结果:在研究期间,运送了26,979例患者。在这些患者中,有2488名患者有房颤或房扑的节律记录。在接受地尔硫卓治疗的320例患者中,由于数据不完整而排除了42例患者,因此有278例患者进行了分析。平均初始SBP为139 mmHg,平均舒张压为84 mmHg。地尔硫卓的平均剂量为16.7 mg。两名患者降压。平均初始HR为154 bpm。到达急诊室时,有33%的患者HR <100 bpm,有69%的患者HR≥20%下降。院前地尔硫卓的总体疗效为73%。>结论:在院前环境中,地尔硫卓与低血压发生率相关,并且似乎可以有效降低HR。需要进行前瞻性研究以证实这些发现。

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