首页> 外文期刊>The annals of pharmacotherapy >Efficacy, safety, and medication errors associated with the use of inhaled epoprostenol for adults with acute respiratory distress syndrome: A pilot study [Eficacia, seguridad y errores en medicación asociados con el uso de epoprostenol inhalados en adultos con síndrome de dificultad respiratoria aguda: Un estudio piloto]
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Efficacy, safety, and medication errors associated with the use of inhaled epoprostenol for adults with acute respiratory distress syndrome: A pilot study [Eficacia, seguridad y errores en medicación asociados con el uso de epoprostenol inhalados en adultos con síndrome de dificultad respiratoria aguda: Un estudio piloto]

机译:成人急性呼吸窘迫综合征患者使用吸入依普西汀醇的功效,安全性和药物错误:一项试验研究[成人急性呼吸窘迫综合征患者使用吸入依普妥烯醇的功效,安全性和药物错误:A试验研究]

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BACKGROUND: Acute respiratory distress syndrome (ARDS) is a type of hypoxic respiratory failure that results from ventilation and perfusion mismatching. Inhaled epoprostenol induces relaxation of smooth muscle in pulmonary vasculature, leading to improved oxygenation. OBJECTIVE: To determine if the use of inhaled epoprostenol produced a 10% or greater increase in the ratio of arterial partial pressure of oxygen (PaO2) to fraction of inspired oxygen (FiO2) in ARDS patients and to review adverse events and medication errors. METHODS: An observational chart review was performed based on a report generated from the electronic medical record system. Patients who received at least 1 dose of inhaled epoprostenol from January 1, 2008, to December 31, 2010, at any hospital within the Florida Hospital Health System were considered for inclusion. Demographics, dose, duration of therapy, adverse effects, medication errors, and outcomes data were collected. RESULTS: Sixteen patients were included in the study. Oxygenation improved by 10% or more in 62.5% (10/16) of the patients, with an initial (within the first 4 hours) median increase of 44.5% in PaO2/FiO2. The mean (SD) starting dose was 30 (10) ng/kg/min. Medication errors were observed in 25% (4/16) of patients. Hypotension was the most frequently observed adverse event, with a rate of 18.8% (3/16). CONCLUSIONS: Based on study findings, inhaled epoprostenol may improve oxygenation in patients with ARDS, with findings suggesting a 62.5% response to therapy. The significance of these effects on improving survival remains unknown. The frequency of medication errors observed in this study poses a significant concern regarding the administration of epoprostenol. Further controlled prospective studies are needed to determine the role of inhaled epoprostenol in improving survival in patients with ARDS.
机译:背景:急性呼吸窘迫综合征(ARDS)是一种由于通气和灌注不匹配导致的低氧性呼吸衰竭。吸入的依前列烯醇可诱导肺血管中的平滑肌松弛,从而改善氧合。目的:确定ARDS患者使用吸入的依普舒坦醇是否会导致动脉血氧分压(PaO2)与吸入氧分数(FiO2)的比率增加10%或更高,并检查不良事件和用药错误。方法:根据电子病历系统生成的报告进行观察图检查。从2008年1月1日至2010年12月31日在佛罗里达州医院卫生系统内的任何医院接受至少1剂吸入式依普西汀醇吸入的患者被视为包括在内。收集人口统计学,剂量,治疗持续时间,不良反应,用药错误和结果数据。结果:16例患者被纳入研究。在62.5%(10/16)的患者中,氧合作用改善了10%或更多,而PaO2 / FiO2的初始(在最初4小时内)中位数增加了44.5%。平均(SD)起始剂量为30(10)ng / kg / min。在25%(4/16)的患者中观察到用药错误。低血压是最常见的不良事件,比率为18.8%(3/16)。结论:基于研究结果,吸入依普西汀醇可改善ARDS患者的氧合作用,研究结果表明对治疗的反应为62.5%。这些作用对提高存活率的意义仍然未知。在这项研究中观察到的用药错误的频率引起了有关依泊汀的给药的重大关注。需要进一步的对照前瞻性研究来确定吸入依普西汀醇在改善ARDS患者生存中的作用。

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