Diagnostic pathways, cardiac manifestations and outcomes in light chain amyloidosis: analysis of a US claims database.

IF 2.8 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Open Heart Pub Date : 2025-04-04 DOI:10.1136/openhrt-2024-003124
Genevieve Lyons, Jeffrey Thompson, Isabelle Lousada, Julia Catini, Richa Manwani, Mathew S Maurer
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Abstract

Background: Patients with light chain (AL) amyloidosis, a rare life-threatening disease, often go through a lengthy diagnostic journey. We qualitatively and quantitatively characterised the diagnostic pathway and the impact of delayed diagnosis on health outcomes among patients with AL amyloidosis.

Methods: We conducted a retrospective cohort analysis of adults (age ≥18 years) with ≥2 AL amyloidosis diagnoses (index date: first diagnosis date) using the IQVIA PharMetrics Plus US claims data from 1 January 2016 to 31 December 2022. We stratified patients based on time from first cardiovascular (CV) manifestation onset to diagnosis. Patients were categorised as having a delayed diagnosis if the first CV manifestation occurred >1 year prior to diagnosis, and patients were categorised as without a delayed diagnosis if the first CV manifestation occurred <1 year prior to diagnosis.

Results: Our study included 470 patients (mean age 61.8 years, 60% males). In the 24 months before diagnosis, CV manifestations occurred in 86% of patients and renal manifestations in 74%. Patients most frequently visited on average four different cardiologists. Patients were most frequently diagnosed by haematologists/oncologists (49.8%). Patients with a delayed diagnosis (179/470, 38.1%) were twice as likely as those without a delayed diagnosis to have CV-related emergency room visits (adjusted OR: 1.98; 95% CI: 1.21 to 3.24; p<0.010). Patients with a delayed diagnosis were one and a half times more likely than those without a delayed diagnosis to have CV-related inpatient hospitalisations (adjusted OR: 1.65; 95% CI: 1.1 to 2.46; p=0.020).

Conclusions: This claims database study suggests that patients with delayed diagnosis experienced more CV-related emergency room visits and inpatient hospitalisations, underscoring the need for timely diagnosis of AL amyloidosis and the role of cardiologists in the diagnostic pathway.

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轻链淀粉样变性的诊断途径、心脏表现和结果:美国索赔数据库分析。
背景:轻链(AL)淀粉样变性是一种罕见的危及生命的疾病,患者往往经历漫长的诊断过程。我们定性和定量地描述了AL淀粉样变性患者的诊断途径和延迟诊断对健康结果的影响。方法:我们使用IQVIA PharMetrics Plus美国索赔数据,对2016年1月1日至2022年12月31日期间诊断≥2例AL淀粉样变性(索引日期:首次诊断日期)的成人(年龄≥18岁)进行回顾性队列分析。我们根据从首次心血管(CV)表现开始到诊断的时间对患者进行分层。如果首次CV表现在诊断前1年出现,则将患者归类为延迟诊断,如果首次CV表现出现,则将患者归类为无延迟诊断。结果:我们的研究包括470例患者(平均年龄61.8岁,60%为男性)。在诊断前24个月,86%的患者出现CV表现,74%的患者出现肾脏表现。病人最常去的地方平均有4个不同的心脏病专家。患者最常由血液科医生/肿瘤科医生诊断(49.8%)。延迟诊断的患者(179/470,38.1%)有cv相关急诊室就诊的可能性是没有延迟诊断的患者的两倍(调整OR: 1.98;95% CI: 1.21 ~ 3.24;结论:这项索赔数据库研究表明,延迟诊断的患者经历了更多与cv相关的急诊室就诊和住院治疗,强调了及时诊断AL淀粉样变的必要性以及心脏病专家在诊断途径中的作用。
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来源期刊
Open Heart
Open Heart CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
4.60
自引率
3.70%
发文量
145
审稿时长
20 weeks
期刊介绍: Open Heart is an online-only, open access cardiology journal that aims to be “open” in many ways: open access (free access for all readers), open peer review (unblinded peer review) and open data (data sharing is encouraged). The goal is to ensure maximum transparency and maximum impact on research progress and patient care. The journal is dedicated to publishing high quality, peer reviewed medical research in all disciplines and therapeutic areas of cardiovascular medicine. Research is published across all study phases and designs, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Opinionated discussions on controversial topics are welcomed. Open Heart aims to operate a fast submission and review process with continuous publication online, to ensure timely, up-to-date research is available worldwide. The journal adheres to a rigorous and transparent peer review process, and all articles go through a statistical assessment to ensure robustness of the analyses. Open Heart is an official journal of the British Cardiovascular Society.
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