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New chronic disease medication prescribing by nurse practitioners, physician assistants, and primary care physicians: a cohort study

机译:护士执业医师,助理医师和初级保健医师开出的新的慢性病药物处方:一项队列研究

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Background Medications to treat and prevent chronic disease have substantially reduced morbidity and mortality; however, their diffusion has been uneven. Little is known about prescribing of chronic disease medications by nurse practitioners (NPs) and physician assistants (PAs), despite their increasingly important role as primary care providers. Thus, we sought to conduct an exploratory analysis to examine prescribing of new chronic disease medications by NPs and PAs compared to primary care physicians (PCPs). Methods We obtained prescribing data from IMS Health’s Xponent? on all NPs, PAs, and PCPs in Pennsylvania regularly prescribing anticoagulants, antihypertensives, oral hypoglycemics, and/or HMG-Co-A reductase inhibitors pre- and post-introduction of five new drugs in these classes that varied in novelty (i.e., dabigatran, aliskiren, sitagliptin or saxagliptin, and pitavastatin). We constructed three measures of prescriber adoption during the 15-month post-FDA approval period: 1) any prescription of the medication, 2) proportion of prescriptions in the class for the medication, and 3) time to adoption (first prescription) of the medication. Results From 2007 to 2011, the proportion of antihypertensive prescriptions prescribed by NPs and PAs approximately doubled from 2.0 to 4.2?% and 2.2 to 4.9?%, respectively. Similar trends were found for anticoagulants, oral hypoglycemics, and HMG-Co-A reductase inhibitors. By 2011, more PCPs had prescribed each of the newly approved medications than NPs and PAs (e.g., 44.3?% vs. 18.5?% vs. 20?% for dabigatran among PCPs, NPs, and PAs). Across all medication classes, the newly approved drugs accounted for a larger share of prescriptions in the class for PCPs followed by PAs, followed by NPs (e.g., dabigatran: 4.9?% vs. 3.2?% vs. 2.8?%, respectively). Mean time-to-adoption for the newly approved medications was shorter for PCPs compared to NPs and PAs (e.g., dabigatran, 7.3 vs. 8.2 vs. 8.5?months; P all medications Conclusions PCPs were more likely to prescribe each of the newly approved medications per each measure of drug adoption, regardless of drug novelty. Differences in the rate and speed of drug adoption between PCPs, NPs, and PAs may have important implications for care and overall costs at the population level as NPs and PAs continue taking on a larger role in prescribing.
机译:背景用于治疗和预防慢性疾病的药物大大降低了发病率和死亡率。但是,它们的扩散并不均匀。尽管护士作为初级保健提供者的作用日益重要,但对于执业护士(NPs)和医师助理(PAs)处方慢性疾病药物的了解却很少。因此,我们寻求进行探索性分析,以检查与初级保健医师(PCP)相比,NP和PA处方新的慢性病药物。方法我们从IMS Health的Xponent获得处方数据?在宾夕法尼亚州的所有NP,PA和PCP上定期开具抗凝剂,降压药,口服降糖药和/或HMG-Co-A还原酶抑制剂处方,在这些类别的五种新药上市前后均采用新颖性(例如,达比加群) ,阿利吉仑,西他列汀或沙格列汀和匹伐他汀)。在FDA批准后的15个月内,我们构建了三种采用处方者的方法:1)药物的任何处方; 2)药物类别中处方的比例,以及3)药物采用的时间(第一个处方)药物。结果从2007年到2011年,NP和PA处方的降压处方所占比例分别从2.0%增至4.2%和2.2%增至4.9%。抗凝剂,口服降糖药和HMG-Co-A还原酶抑制剂的趋势相似。到2011年,与NP和PA相比,每种新批准的药物处方的PCP数量都更多(例如,PCP,NP和PA中达比加群的44.3%比18.5%对20%)。在所有药物类别中,新批准的药物在PCP类别中占较大比例,其次是PA,接着是NP(例如达比加群:分别为4.9%,3.2%和2.8%)。与NPs和PAs相比,PCPs新批准药物的平均采用时间要短(例如达比加群,7.3 vs. 8.2 vs. 8.5?months;所有药物结论结论PCPs更有可能开出每种新批准的药物每种药物采用量度的药物,无论药物是否新颖,PCP,NP和PA之间药物采用率和速度的差异都可能对人群水平的护理和总体费用产生重要影响,因为NP和PA继续承担着在处方中扮演更大的角色。

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