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Using Information on Patient Adherence to Antipsychotic Medication to Understand Their Adherence to Other Medications. 使用患者抗精神病药物依从性的信息来了解他们对其他药物的依从性。
Q1 Medicine Pub Date : 2019-06-01
Jason Shafrin, Alison R Silverstein, Joanna P MacEwan, Darius N Lakdawalla, Ainslie Hatch, Felicia M Forma

Purpose: To assess how patient adherence to atypical antipsychotic medications is associated with adherence to concurrently used medications that treat other serious mental illnesses (SMIs), type-2 diabetes, or hypertension.

Methods: Among patients who had been diagnosed with an SMI (i.e., bipolar disorder, major depressive disorder, or schizophrenia) in the previous year, we used health-insurance claims data to measure adherence based on medication fills. Patients diagnosed with an SMI were required to have 1) a prescription for an atypical oral antipsychotic, and 2) another SMI therapy or oral anti-diabetic or antihypertensive agent in the same year. The patient's concurrent adherence to an antipsychotic and one of 23 other medications was measured by the proportion of days covered (PDC) over a one-year period. Patients were considered adherent when the PDC was ≥ 80%. The strength of the association between their atypical antipsychotic adherence and their concurrent medication adherence was evaluated using the following metrics: accuracy, positive predictive value (PPV), and negative predictive value (NPV).

Results: The average (standard deviation) age of patients (N = 129,614) was 44.8 (14.8) years and 62.2% of patients were female. The median accuracy based on atypical antipsychotic adherence to the other 23 medications was 67% (range, 55-71%; statistically different from 50% accuracy in all cases, P < 0.001). Accuracy was higher than physician predictions of adherence from previous studies (53%). The negative predictive value of antipsychotic adherence (75%; range, 62-88%) was generally higher than the PPV (62%; range, 43-67%; all, P < 0.001).

Conclusion: Information on patient adherence to antipsychotics provides significant insight into adherence to other medications often used by patients with SMI. Because NPV is higher than PPV, adherence to antipsychotics is likely to be a necessary but not sufficient condition for patients with SMI regarding adherence to non-SMI medications.

目的:评估患者对非典型抗精神病药物的依从性与同时使用治疗其他严重精神疾病(SMIs)、2型糖尿病或高血压药物的依从性之间的关系。方法:在前一年被诊断为重度精神障碍(即双相情感障碍、重度抑郁症或精神分裂症)的患者中,我们使用健康保险索赔数据来衡量基于药物填充的依从性。被诊断为重度精神障碍的患者需要1)非典型口服抗精神病药物处方,2)同年另一次重度精神障碍治疗或口服抗糖尿病或抗高血压药物。患者同时对抗精神病药物和23种其他药物中的一种的依从性通过覆盖天数的比例(PDC)来测量。当PDC≥80%时,认为患者粘附。使用以下指标评估非典型抗精神病药物依从性与同时服药依从性之间的关联强度:准确性、阳性预测值(PPV)和阴性预测值(NPV)。结果:患者平均(标准差)年龄(N = 129614)为44.8(14.8)岁,女性占62.2%。基于非典型抗精神病药物对其他23种药物依从性的中位准确率为67%(范围55-71%;所有病例的准确率均低于50%,P < 0.001)。准确性高于先前研究中医生对依从性的预测(53%)。抗精神病药物依从性的阴性预测值(75%;范围,62-88%)普遍高于PPV (62%;范围,43 - 67%;均P < 0.001)。结论:患者对抗精神病药物的依从性信息为重度精神分裂症患者对其他药物的依从性提供了重要的见解。由于NPV高于PPV,对于重度精神分裂症患者,抗精神病药物的依从性可能是对非重度精神分裂症药物依从性的必要条件,但不是充分条件。
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引用次数: 0
Article on Hospital Consolidation Misleads. 医院合并误导文章。
Q1 Medicine Pub Date : 2019-06-01
Melinda Hatton
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引用次数: 0
A Drug Pricing "Transparency" Bill With Strong Bipartisan Support But Would It Accomplish Much? 两党大力支持的药品定价“透明度”法案,但它能取得多大成效吗?
Q1 Medicine Pub Date : 2019-06-01
Stephen Barlas

Several drug-price "remedy" bills are floating around Congress, with most being described as a "first step." So why is no one referring to that step as significant?

几项药品价格“补救”法案正在国会讨论,其中大多数被描述为“第一步”。那么,为什么没有人认为这一步意义重大呢?
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引用次数: 0
Drug and Device News. 药品和器械新闻。
Q1 Medicine Pub Date : 2019-06-01

Approvals, new indications and formulations, and safety issues.

批准,新的适应症和配方,以及安全问题。
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引用次数: 0
Intravenous Versus Oral Acetaminophen in Ambulatory Surgical Center Laparoscopic Cholecystectomies: A Retrospective Analysis. 门诊外科中心腹腔镜胆囊切除术中静脉与口服对乙酰氨基酚的对比:回顾性分析。
Q1 Medicine Pub Date : 2019-06-01
Ryan J Johnson, Danny K Nguyen, Jose M Acosta, Alice L O'Brien, Peter D Doyle, Glorimar Medina-Rivera

Study objective: The primary aim was to compare postoperative pain scores in patients undergoing laparoscopic cholecystectomy and receiving intravenous (IV) or oral (PO) acetaminophen (APAP) as part of a multimodal analgesic regimen to examine whether PO APAP is non-inferior to IV APAP.

Design: Retrospective analysis.

Setting: Ambulatory surgical center (ASC) in an academic setting.

Patients: 579 patients (18-70 years old), American Society of Anesthesiologists physical status I-III, undergoing laparoscopic cholecystectomy.

Interventions: Patients received 1,000 mg IV APAP intraoperatively (n = 319) or 1,000 mg PO APAP preoperatively (n = 260).

Measurements: The primary outcome was the median difference in post-anesthesia care unit (PACU) end-pain scores between the groups. Median pain scores were also compared on PACU admission, and at 15, 30, 45, and 60 minutes. Additional measures include PACU rescue-analgesia consumption, time to first PACU rescue analgesia, intraoperative use of opioid and nonopioid analgesics, PACU length of stay, and PACU rescue nausea and vomiting therapy.

Main results: In both groups, the PACU median end-pain score was 2. The 90% confidence interval (CI) for difference in median pain scores between groups was [0, 0]; the CI upper limit was below the non-inferior margin of 1 pain-score point, indicating PO APAP's non-inferiority to IV APAP. There were no statistically significant differences in the percentages of patients receiving PACU hydromorphone equivalents between the IV and PO groups (75% vs. 77%, P = 0.72) or in the mean dose received (0.5 mg vs. 0.5 mg, P = 0.66).

Conclusion: Single-dose PO APAP is non-inferior to IV APAP for postoperative analgesia in ASC laparoscopic cholecystectomy patients. The value of single-dose IV APAP in this population should be further explored.

研究目的:主要目的是比较腹腔镜胆囊切除术患者接受静脉(IV)或口服(PO)对乙酰氨基酚(APAP)作为多模式镇痛方案的一部分的术后疼痛评分,以检查PO APAP是否优于IV APAP。设计:回顾性分析。设置:门诊外科中心(ASC)在学术设置。患者:579例患者(18-70岁),美国麻醉医师协会身体状况I-III级,行腹腔镜胆囊切除术。干预措施:患者术中接受1000mg IV APAP (n = 319)或术前接受1000mg PO APAP (n = 260)。测量:主要结果是两组麻醉后护理单元(PACU)终末疼痛评分的中位数差异。还比较了PACU入院时、15分钟、30分钟、45分钟和60分钟的中位疼痛评分。其他措施包括PACU抢救镇痛消耗、首次PACU抢救镇痛时间、术中阿片类和非阿片类镇痛药物的使用、PACU住院时间、PACU抢救恶心呕吐治疗。主要结果:两组患者PACU中位末痛评分均为2分。组间中位疼痛评分差异的90%置信区间(CI)为[0,0];CI上限低于1个疼痛评分点的非劣效性,说明PO APAP对IV APAP的非劣效性。静脉注射组和静脉注射组接受PACU氢吗啡酮等效物的患者百分比(75%对77%,P = 0.72)或平均接受剂量(0.5 mg对0.5 mg, P = 0.66)无统计学差异。结论:单剂量PO APAP在ASC腹腔镜胆囊切除术患者术后镇痛效果不逊于静脉注射APAP。单剂量静脉注射APAP在该人群中的应用价值有待进一步探讨。
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引用次数: 0
Pharmaceutical Approval Update. 药品审批更新。
Q1 Medicine Pub Date : 2019-06-01
Michele B Kaufman

Sunosi (solriamfetol) tablets for excessive daytime sleepiness with narcolepsy or obstructive sleep apnea; Zulresso (brexanolone) injection for postpartum depression in adults; Mayzent (siponimod) tablets for adults with relapsing forms of MS.

Sunosi (soliamfetol)片用于日间过度嗜睡伴发作性睡病或阻塞性睡眠呼吸暂停;布雷沙诺酮佐剂治疗成人产后抑郁症用于复发型多发性硬化症成人的梅赞特(西泊尼莫德)片。
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引用次数: 0
Intranasal Esketamine (SpravatoTM) for Use in Treatment-Resistant Depression In Conjunction With an Oral Antidepressant. 鼻用艾氯胺酮(SpravatoTM)联合口服抗抑郁药治疗难治性抑郁症。
Q1 Medicine Pub Date : 2019-06-01
Rebecca Bahr, Alicia Lopez, Jose A Rey

Intranasal esketamine for treatment-resistant depression.

鼻用艾氯胺酮治疗难治性抑郁症。
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引用次数: 0
European Association for the Study of the Liver The International Liver Congress 2019. 欧洲肝脏研究协会2019年国际肝脏大会。
Q1 Medicine Pub Date : 2019-06-01
Walter Alexander

We cover key sessions on hepatitis B, C, and D virus infections, hepatocellular carcinoma, nonalcoholic steatohepatitis, acute hepatic porphyria, and liver growth in polycystic kidney disease.

我们涵盖了乙型肝炎、丙型肝炎和丁型肝炎病毒感染、肝细胞癌、非酒精性脂肪性肝炎、急性肝卟啉症和多囊肾病的肝脏生长等关键会议。
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引用次数: 0
Evaluation of Warfarin Patients with Low Time in Therapeutic Range (TTR) for Transition to Non-Vitamin-K Oral Anticoagulant (NOAC) Therapy. 华法林患者转入非维生素k口服抗凝剂治疗时间较短(TTR)的评价
Q1 Medicine Pub Date : 2019-06-01
Lindsey M Fovel, Christopher D Miller, Robert W Seabury, Luke A Probst, Lara Horvath
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引用次数: 0
FTC Gives Generics Victory On "Pay for Delay": Reverse Payments Crimped, Patent Thickets Untouched. 美国联邦贸易委员会在“延迟支付”上给予仿制药胜利:反向支付受阻,专利丛林未受影响。
Q1 Medicine Pub Date : 2019-05-01
Stephen Barlas

How easy is it for generics to enter the market? It could be easier with legislation that opens up the field for generic competitors, but it is unlikely that such a bill will ever be introduced.

仿制药进入市场有多容易?通过立法为仿制药竞争者打开市场可能会更容易,但这样的法案不太可能被引入。
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引用次数: 0
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