Embedding metabolic dysfunction-associated steatotic liver disease fibrosis risk stratification within pharmacist-integrated diabetes comanagement in primary care.

IF 3.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Ryan P Wexler, Jeremy Chimene-Weiss, Courtney Cameron, Sandra Schipelliti, Pavan Vuddanda, Aileen Roman, Arpan Mohanty
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引用次数: 0

Abstract

Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) is highly prevalent among patients with type 2 diabetes mellitus (T2DM) but remains underdiagnosed in primary care despite clinical guidelines. We investigated whether a multicomponent workflow that included expanding the role of ambulatory pharmacists, who already manage T2DM under collaborative care agreements to include MASLD risk stratification, is associated with improved detection of liver fibrosis.

Objective: To evaluate the feasibility of a pharmacist-integrated, multicomponent intervention and its association with MASLD fibrosis risk stratification, vibration-controlled transient elastography (VCTE) referral and completion, and detection of clinically significant fibrosis among patients with T2DM in a safety net primary care setting.

Methods: We conducted a 6-month pre-post feasibility and implementation pilot in a safety net family medicine clinic, with the pre-period serving as a baseline of usual care. The multicomponent intervention expanded MASLD risk stratification to pharmacists comanaging T2DM and incorporated targeted education, co-location of VCTE, and internal facilitation. Pharmacists calculated Fibrosis-4 index (FIB-4) scores during T2DM visits and referred patients with FIB-4 greater than or equal to 1.3 for VCTE. Outcomes included VCTE referral among patients with elevated FIB-4 scores, VCTE completion, detection of clinically significant fibrosis (liver stiffness measurement ≥8 kPa) or possible cirrhosis (liver stiffness measurement ≥12 kPa), and hepatology referral.

Results: In the pre-intervention period, 41% (52 of 127) of patients with available laboratory data had FIB-4 greater than or equal to 1.3, and none were referred for VCTE. In the post-intervention period, 45% (61 of 136) of such patients had FIB-4 greater than or equal to 1.3. Of these, 87% (53 of 61) were referred for VCTE, and 85% (45 of 53) completed testing. VCTE identified 8 new cases of clinically significant fibrosis, including 6 with possible cirrhosis, leading to 6 hepatology referrals.

Conclusions: A pharmacist-integrated, multicomponent workflow was associated with increased VCTE referrals and completion, enabled identification of fibrosis, and facilitated specialist referrals among patients with T2DM in a safety net primary care setting. These findings support this pharmacist-integrated workflow as a feasible, patient-centered strategy to enhance MASLD detection, warranting further evaluation of scalability, sustainability, and impact.

将代谢功能障碍相关的脂肪变性肝病纤维化风险分层纳入初级保健中药师综合糖尿病管理。
背景:代谢功能障碍相关脂肪变性肝病(MASLD)在2型糖尿病(T2DM)患者中非常普遍,但尽管有临床指南,但在初级保健中仍未得到充分诊断。我们调查了一个多组件工作流程,包括扩大门诊药剂师的作用,他们已经在合作护理协议下管理T2DM,包括MASLD风险分层,是否与改善肝纤维化的检测有关。目的:评估药师综合多组分干预的可行性及其与MASLD纤维化风险分层、振动控制瞬时弹性成像(VCTE)转诊和完成以及在安全网初级保健环境中T2DM患者临床显著纤维化检测的关系。方法:在某安全网家庭医学门诊开展为期6个月的岗前可行性与实施试点,以岗前期为常规护理基线。多组分干预将MASLD风险分层扩展到管理T2DM的药剂师,并纳入了有针对性的教育、VCTE的同址和内部促进。药师在T2DM就诊时计算纤维化-4指数(FIB-4)评分,并转诊FIB-4大于等于1.3的VCTE患者。结果包括FIB-4评分升高的患者的VCTE转诊、VCTE完成、检测到临床显著的纤维化(肝硬度测量≥8 kPa)或可能的肝硬化(肝硬度测量≥12 kPa),以及肝病转诊。结果:在干预前,有实验室数据的患者中有41% (52 / 127)FIB-4大于或等于1.3,没有人被转诊为VCTE。干预后,45%(136例中的61例)患者FIB-4≥1.3。其中,87%(61人中53人)被转诊为VCTE, 85%(53人中45人)完成了检测。VCTE发现了8例新的临床显著纤维化病例,其中6例可能伴有肝硬化,导致6例肝病转诊。结论:药师集成的多组件工作流程与VCTE转诊和完成度的增加有关,使纤维化的识别成为可能,并促进了在安全网初级保健环境中T2DM患者的专科转诊。这些发现支持这种药剂师集成工作流程作为一种可行的、以患者为中心的策略来增强MASLD检测,保证进一步评估可扩展性、可持续性和影响。
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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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