Tafamidis medication adherence and persistence in patients with transthyretin amyloid cardiomyopathy in Japan

被引:0
作者
Kato, Takao [1 ]
Ines, Monica [2 ]
Minamisawa, Masatoshi [3 ]
Benjumea, Darrin [4 ]
Keohane, Denis [5 ]
Alvir, Jose [5 ]
Kim, Ruth [5 ]
Chen, Yong [6 ]
Peixoto, Telma [2 ]
Kent, Matthew [4 ]
Wogen, Jenifer [4 ]
Ishii, Tomonori [7 ]
Crowley, Aaron [4 ]
Sugino, Toshiya [7 ]
Izumiya, Yasuhiro [8 ]
机构
[1] Kyoto Univ Hosp, Inst Advancement Clin & Translat Sci, Dept Cardiovasc Med, Kyoto, Japan
[2] Pfizer Portugal, Porto Salvo, Portugal
[3] Shinshu Univ, Sch Med, Dept Cardiovasc Med, Matsumoto, Japan
[4] Genesis Res Grp, Hoboken, NJ USA
[5] Pfizer Inc, New York, NY 10017 USA
[6] Pfizer Inc, Collegeville, PA USA
[7] Pfizer Japan Inc, Tokyo, Japan
[8] Osaka Metropolitan Univ, Grad Sch Med, Dept Cardiovasc Med, Osaka, Japan
来源
ESC HEART FAILURE | 2024年 / 11卷 / 05期
关键词
ATTR-CM; Cardiomyopathy; Tafamidis; Adherence; Persistence; Japan; BASE-LINE CHARACTERISTICS; RETROSPECTIVE ANALYSIS; PRESCRIPTIONS; BENEFICIARIES;
D O I
10.1002/ehf2.14736
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsThis study aimed to describe baseline characteristics and adherence among patients with transthyretin amyloid cardiomyopathy (ATTR-CM) treated with tafamidis (VYNDAQEL (R)) in Japan using the Japanese Medical Data Vision (MDV) database.Methods and resultsThis study was a non-interventional, retrospective cohort study of adult (>= 18 years old) patients in the Japanese MDV claims database diagnosed with ATTR-CM and with at least two tafamidis prescriptions of dose strength 4 x 20 mg/day between 1 March 2019 and 31 August 2021. The date of the first prescription was defined as the index date, with follow-up time defined as the time between the first and last prescription plus the days' supply from the last refill. Baseline characteristics were assessed during a 12 month pre-index period. Adherence was measured using two metrics: (i) the modified medication possession ratio (mMPR), calculated by taking the sum of days supplied for all fills within the follow-up period, divided by the number of days of follow-up, and reported as a percentage, with patients classified as adherent with an mMPR of >= 80%, and (ii) the proportion of days covered (PDC), calculated by taking the total number of days' supply dispensed during the follow-up period divided by the number of days of follow-up, adjusting for any days' supply overlap. A total of 210 patients were identified; the mean (standard deviation) age of the cohort was 77 (5.9) years, and the majority (89%) were male. The most common baseline cardiovascular comorbidities were heart failure (85%), ischaemic heart disease (66%), hypertensive diseases (49%), and diabetes (35%); 75% of patients received heart failure medications in the 12 months prior to index, with the most common being beta-blockers (49%), diuretics (48%), angiotensin receptor blockers (30%), angiotensin-converting enzyme inhibitors (22%), and sodium-glucose cotransporter-2 inhibitors (8.1%). Over an average 14 month follow-up, mean mMPR was 96% with a median of 100% [inter-quartile range (IQR): 97-101%]; 93% of patients were adherent (defined as an mMPR >= 80%). In the same follow-up period, mean PDC was 93.6% with a median of 99% (IQR: 93-100%). Persistence was high with 78% of patients having a 0 day gap between prescription refills.ConclusionsThis study found high adherence rates to tafamidis in this real-world Japanese patient population. Adherence rates in this study were similar to those reported by the tafamidis clinical trial and a previously published US commercial claims adherence analysis. Further studies should be conducted to assess the impact of real-world adherence on real-world outcomes.
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页码:2481 / +
页数:977
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