直接口服抗凝剂剂量不当:来自临床研究和医师调查的结果。

Q2 Medicine Journal of market access & health policy Pub Date : 2023-10-29 eCollection Date: 2023-01-01 DOI:10.1080/20016689.2023.2267327
Ahmet Fuat, Emmanuel Ako, David Hargroves, Douglas Holden, Amrit Caleyachetty, Matthew Carter, James Harris, Carol Roberts, Nnanyelu Nzeakor, Burcu Vardar, Helen Williams
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引用次数: 0

摘要

目的:直接口服抗凝剂(DOACs)是英国140万房颤(AF)患者预防脑卒中的一线治疗方法。然而,DOAC剂量低于循证建议的比率估计在9%至22%之间。本研究探讨了与处方不当DOAC剂量不足相关的特定患者和医生因素。方法:英国的DOAC处方医生完成了一项临床小调查,其中包含12个假想的患者资料,旨在复制DOAC处方场景,以及一项医生调查,以获取社会人口统计学,临床经验,处方者与DOAC处方相关的信念和动机。基于文献检索和专家咨询过程的八个患者因素在小插曲中有所不同。通过多水平逻辑回归探讨处方者的剂量选择与患者因素之间的关系。分析的重点是最常选择的doac,阿哌沙班和利伐沙班,两者都有不同的剂量指南。结果:共有336名开处方者(69%为男性;233/336)完成了调查,主要是全科医生(45%)或心脏病专家(36%),平均工作经验17.9年。大多数开处方者(73%;(244/336)至少一次用药不当;全科医生和专科医生之间的比率几乎相同。与阿哌沙班不适当剂量不足最密切相关的患者因素包括大出血和跌倒史。对于利伐沙班,这些是大出血和严重虚弱。只有32%(106/335)的开处方者报告DOAC给药指南是影响其开处方行为的唯一因素。在没有不适当剂量不足的开处方者中,更大的处方信心与不适当剂量不足风险的感知增加一致。结论:总体而言,患者因素如大出血和严重虚弱被发现与阿哌沙班和利伐沙班剂量不足有关。此外,对DOAC处方更有信心,更担心中风风险的开处方者,不适当的剂量不足的可能性显著降低。这些发现表明,所有开处方者,无论其专业如何,都可以从教育和培训中获益,以提高对不当DOAC剂量不足相关风险的认识。
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Inappropriate dosing of direct oral anticoagulants: findings from a clinical vignette study and physician survey.

Objective: Direct oral anticoagulants (DOACs) are first-line therapy for stroke prevention for 1.4 million atrial fibrillation (AF) patients in the UK. However, the rates of DOAC dosing below evidence-based recommendations are estimated between 9% and 22%. This study explores specific patient and physician factors associated with prescribing inappropriate DOAC underdoses.

Methods: DOAC-prescribing physicians within the UK completed both a clinical vignette survey, which contained 12 hypothetical patient profiles designed to replicate DOAC prescribing scenarios, and a physician survey to capture sociodemographic, clinical experience, and prescriber-related beliefs and motivations related to DOAC prescribing. Eight patient factors based on a literature search and an expert consultation process were varied within the vignettes. Associations between the prescribers' dosing choices and patient factors were explored via multilevel logistic regression. The analysis is focused on the most frequently selected DOACs, apixaban and rivaroxaban, both of which have different dosing guidelines.

Results: In all, 336 prescribers (69% male; 233/336) completed the survey, mostly general physicians (GPs) (45%) or cardiology specialists (36%) with a mean of 17.9 years' experience. Most prescribers (73%; 244/336) inappropriately underdosed at least once; rates between GPs and specialists were nearly identical. Patient factors most strongly associated with apixaban inappropriate underdosing included a history of major bleeding and falls. For rivaroxaban, these were major bleeding and severe frailty. Only 32% (106/335) of prescribers reported DOAC dosing guidelines as the sole influence on their prescribing behaviour. Among prescribers who did not inappropriately underdose, greater prescribing confidence was aligned to increased perception of inappropriate underdose risk.

Conclusions: Overall, patient factors such as major bleeding and severe frailty were found to be associated with inappropriate underdosing of apixaban and rivaroxaban. Furthermore, prescribers who were more confident in DOAC prescribing, and were more worried about the risk of stroke, were significantly less likely to inappropriately underdose. These findings suggest that all prescribers, regardless of speciality, may benefit from education and training to raise awareness of the risks associated with inappropriate DOAC underdosing.

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CiteScore
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