Amyloid Screening and Treatment Drop Off in Patients with Left Ventricular Hypertrophy: Associations with Patient Socio-demographic Characteristics

Author:

Walenczyk Kristie M.,Singh Avinainder,Tong Kimhouy,Burg Matthew M.ORCID,Miller Edward J.ORCID

Abstract

AbstractBackgroundCompared to estimated population prevalence rates, relatively few patients at risk are ultimately diagnosed with and treated for transthyretin cardiac amyloidosis (ATTR-CA). Where along the clinical imaging and treatment pathway patient drop off occurs, and the association of drop off at each step with patient socio-demographic characteristics remains unknown.MethodsUsing data from a healthcare system-wide cardiovascular imaging repository and specialty pharmacy we characterized the multi-level clinical pathway from screening for left ventricular hypertrophy (LVH) with transthoracic echocardiograms (TTE), diagnosis with technetium-99m pyrophosphate scintigraphy (PYP), and tafamidis prescription, initiation, and adherence. Standardized differences (d≥0.20 indicating a small effect size or larger) were used to compare socio-demographics (age, sex, race, national and state Area Deprivation Index) among patients with TTE-identified LVH by PYP referral status, patients with PYP-identified ATTR-CA by tafamidis prescription status, and patients prescribed tafamidis by initiation status.ResultsA total of 8575 patients had LVH on TTE, with 1.6% referred for PYP. Of 97 patients with PYP-identified ATTR-CA, 58.8% were prescribed tafamidis, with 80.7% of those initiating therapy. Referral from LVH on TTE to PYP was higher among men, older patients, and those of Black/African American or American Indian/Alaskan Native race (alld’s≥0.20). Patients with PYP-identified ATTR-CA prescribed tafamidis were younger than those not prescribed tafamidis (d=-0.30). Utilization of a specialty pharmacy resulted in enrichment of treatment in subgroups traditionally undertreated in cardiovascular medicine, with higher rates of tafamidis initiation among women (100% initiation), patients of Black/African American race (d=0.40), and those living in more economically disadvantaged areas (d’s≥0.30).ConclusionThese findings highlight the tremendous opportunity for more robust imaging and clinical ATTR-CA screening programs, including potential patient subgroups that should be targeted to reduce disparities. Among patients diagnosed with ATTR-CA, utilization of a specialty pharmacy process appears to ensure the equitable provision of tafamidis therapy.

Publisher

Cold Spring Harbor Laboratory

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