优化家族性高胆固醇血症管理:来自大西洋降脂治疗优化项目的早期发现

IF 5.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Jeffrey N. Feldman MD , Robert D. Fishberg MD, FACC , Deatrah Dubose APN , Lise Cooper DMH , Anjali Kakwani PharmD , Cassidy Maggio PharmD
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引用次数: 0

摘要

治疗领域预防心脏病学最佳实践-临床操作,团队方法,结果研究背景尽管建立了指南,但高危ASCVD患者的脂质管理仍然不够理想。这项前瞻性、多中心研究,经irb批准,评估支持治疗对高危ASCVD患者LDL-C管理的影响,为期两年,最终将招募250例患者。这些早期发现代表了第一批19名达到随访LDL-C水平第一个6个月里程碑的患者。通过电子病历、专业执业护士(NP)、临床药剂师和初级保健合作伙伴,我们确定了高风险患者,并在六个月内将LDL-C控制在100mg /dL。我们根据2022 ACC指南评估24-96周内LDL-C目标实现情况,患者作为自己的对照。我们的目标是开发一种一级和二级预防模式,将实践层面的治疗指南整合起来,从而有可能改善结果。例如,pci术后较高的LDL-C增加了不良事件,强调有针对性的控制。脂质诊所使用电子病历识别未确诊的FH病例并改进治疗。EHR警告仅适度提高了降脂疗法(LLT),需要进一步的依从性策略。多学科护理模型显示出较好的LDL-C降低效果。方法通过EHR和其他数据库(如FeelBetter、临床医生推荐和ClinicalTrials.gov)确定参与者,并且必须具有LDL-C≥160。支持性护理包括一个专门的NP,每周提供面对面或虚拟的教育和随访。临床药师审查药物治疗问题(MTPs),包括药物获取和依从性的障碍。其他支持包括基因检测、社会服务和专家转诊。结果在随访6个月的19名参与者中,14人(74%)的LDL-C水平平均降低了48点。14人中有7人(50%)达到LDL-C <;100, 3人(21%)达到LDL-C <;70。临床药师审查确定了20个MTPs,包括药物依从性障碍、剂量调整和需要额外的llt。16名参与者完成了基因检测,其中一人被确定患有杂合子家族性高胆固醇血症(HeFH)相关基因变异,需要进行随访和级联检测,并改变生活方式。结论ALLTOP研究的初步证据支持结构化、多学科模型在优化高胆固醇血症和HeFH管理方面的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
OPTIMIZING FAMILIAL HYPERCHOLESTEROLEMIA MANAGEMENT: EARLY FINDINGS FROM THE ATLANTIC LIPID LOWERING TREATMENT OPTIMIZATION PROGRAM (ALLTOP)

Therapeutic Area

Preventive Cardiology Best Practices – clinic operations, team approaches, outcomes research

Background

Despite established guidelines, lipid management in high-risk ASCVD patients remains suboptimal. This prospective, multicenter study, IRB-approved study evaluates the impact of supportive care focused on LDL-C management in high-risk ASCVD patients over two years and will eventually enroll 250 patients. These early findings represent the first 19 patients who have reached their first 6-month milestone for follow-up LDL-C levels. Using the EHR, a dedicated nurse practitioner (NP), clinical pharmacists, and primary care partnerships, we identify high-risk patients and target an LDL-C <100 mg/dL in six months. We assess LDL-C goal achievement based on 2022 ACC guidelines over 24–96 weeks, with patients as their own controls. Our goal is to develop a model for primary and secondary prevention that integrates guidelines for treatment at the practice level that has the potential to improve outcomes. For instance, higher LDL-C post-PCI increases adverse events, emphasizing targeted control. Lipid clinics using EHRs identified undiagnosed FH cases and improved therapy. EHR alerts only modestly boosted lipid-lowering therapies (LLT), requiring further adherence strategies. A multidisciplinary care model showed superior LDL-C reductions.

Methods

Participants were identified via the EHR and other databases, such FeelBetter, clinician referrals, and ClinicalTrials.gov and must have an LDL-C ≥160. Supportive care includes a dedicated NP providing weekly education and follow-up, in-person or virtually. Clinical pharmacists review medication therapy problems (MTPs), including barriers to medication access and adherence. Additional support includes genetic testing, social services, and specialist referrals.

Results

Among the 19 participants with six-month follow-up lab values, 14 (74%) reduced their LDL-C levels an average of 48 points. Seven of the 14 (50%) achieved LDL-C <100, with three (21%) achieving an LDL-C <70. Clinical pharmacist reviews identified 20 MTPs, including barriers to medication adherence, dose adjustments, and the need for additional LLTs. Sixteen participants completed genetic testing, with one identified as having a heterozygous familial hypercholesterolemia (HeFH)-related gene variant, necessitating follow-up and cascade testing, and lifestyle modifications.

Conclusions

Preliminary evidence from the ALLTOP study supports the effectiveness of a structured, multidisciplinary model for optimizing hypercholesterolemia and HeFH management.
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来源期刊
American journal of preventive cardiology
American journal of preventive cardiology Cardiology and Cardiovascular Medicine
CiteScore
6.60
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76 days
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