首页> 美国卫生研究院文献>Morbidity and Mortality Weekly Report >Hydroxychloroquine and Chloroquine Prescribing Patterns by Provider Specialty Following Initial Reports of Potential Benefit for COVID-19 Treatment — United States January–June 2020
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Hydroxychloroquine and Chloroquine Prescribing Patterns by Provider Specialty Following Initial Reports of Potential Benefit for COVID-19 Treatment — United States January–June 2020

机译:提供者特色羟基氯喹和氯喹订明图案在Covid-19治疗的潜在利益初步报告之后 - 美国1月6月20日

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摘要

Hydroxychloroquine and chloroquine, primarily used to treat autoimmune diseases and to prevent and treat malaria, received national attention in early March 2020, as potential treatment and prophylaxis for coronavirus disease 2019 (COVID-19) ( ). On March 20, the Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for chloroquine phosphate and hydroxychloroquine sulfate in the Strategic National Stockpile to be used by licensed health care providers to treat patients hospitalized with COVID-19 when the providers determine the potential benefit outweighs the potential risk to the patient. Following reports of cardiac and other adverse events in patients receiving hydroxychloroquine for COVID-19 ( ), on April 24, 2020, FDA issued a caution against its use and on June 15, rescinded its EUA for hydroxychloroquine from the Strategic National Stockpile. Following the FDA’s issuance of caution and EUA rescindment, on May 12 and June 16, the federal COVID-19 Treatment Guidelines Panel issued recommendations against the use of hydroxychloroquine or chloroquine to treat COVID-19; the panel also noted that at that time no medication could be recommended for COVID-19 pre- or postexposure prophylaxis outside the setting of a clinical trial ( ). However, public discussion concerning the effectiveness of these drugs on outcomes of COVID-19 ( , ), and clinical trials of hydroxychloroquine for prophylaxis of COVID-19 continue. In response to recent reports of notable increases in prescriptions for hydroxychloroquine or chloroquine ( ), CDC analyzed outpatient retail pharmacy transaction data to identify potential differences in prescriptions dispensed by provider type during January–June 2020 compared with the same period in 2019. Before 2020, primary care providers and specialists who routinely prescribed hydroxychloroquine, such as rheumatologists and dermatologists, accounted for approximately 97% of new prescriptions. New prescriptions by specialists who did not typically prescribe these medications (defined as specialties accounting for ≤2% of new prescriptions before 2020) increased from 1,143 prescriptions in February 2020 to 75,569 in March 2020, an 80-fold increase from March 2019. Although dispensing trends are returning to prepandemic levels, continued adherence to current clinical guidelines for the indicated use of these medications will ensure their availability and benefit to patients for whom their use is indicated ( , ), because current data on treatment and pre- or postexposure prophylaxis for COVID-19 indicate that the potential benefits of these drugs do not appear to outweigh their risks.
机译:羟基氯喹和氯喹,主要用于治疗自身免疫性疾病并预防和治疗疟疾,在2020年初获得国家关注,作为冠状病毒疾病2019(Covid-19)()潜在治疗和预防。 3月20日,食品和药物管理局(FDA)发出了氯喹磷酸盐和羟基氯喹硫酸盐的紧急使用授权(Eua),以便由许可的医疗保健提供者使用许可的医疗保健提供者治疗住院的患者,当供应商时确定潜在的益处超过了患者的潜在风险。在2020年4月24日接受羟氯喹的心脏和其他不良事件的报告,2020年4月24日,FDA宣布谨慎宣布其使用和6月15日,从战略国民储存中撤销其Eua羟基氯喹。在FDA发布谨慎和欧盟撤回之后,于5月12日和6月16日,联邦Covid-19治疗指南小组发布了针对使用羟基氯喹或氯喹的建议,以治疗Covid-19;小组还注意到,当时没有药物可以在临床试验()的设置外的Covid-19预曝光或后曝光预防。然而,关于这些药物对Covid-19(,)和羟氯喹的临床试验的有效性的公众讨论,用于Covid-19的预防。为了回应羟基氯喹或氯喹()处方的最新报告,CDC分析了门诊零售药房交易数据,以确定由提供者类型在2020年1月至2019年1月 - 6月在2019年的同一期间销售所处方的潜在差异。在2020年之前,常规规定羟基氯喹的初级护理提供者和专家,如风湿病学家和皮肤病学家,占新处方的约97%。通常不规定这些药物的专家的新处方(定义为2020年之前的新处方的专业人数)从2020年2月2020年2月的1,143处处方增加到75,569日,从2019年3月的80倍。虽然分配趋势正在恢复到预处理水平,继续遵守目前用于表明使用这些药物的临床指南,将确保其可用性和利益对其使用的患者(),因为当前关于治疗和预先或后期预防的数据Covid-19表明这些药物的潜在益处似乎不会超过其风险。

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