Health‐related quality of life among transthyretin amyloid cardiomyopathy patients

Author:

Eldhagen Per1,Lehtonen Jukka2,Gude Einar3,Gustafsson Finn4,Bagger‐Bahnsen Anne5,Vakevainen Merja6,Pilgaard Trine5,Wedell‐Wedellsborg Dorte7,Poulsen Steen Hvitfeldt8,

Affiliation:

1. Department of Medicine, Karolinska Institute Karolinska University Hospital Solna Sweden

2. Heart and Lung Center Helsinki University Hospital Helsinki Finland

3. Department of Cardiology Oslo University Hospital Rikshospitalet Oslo Norway

4. Department of Cardiology Rigshospitalet Copenhagen Denmark

5. Pfizer Denmark Ballerup Denmark

6. Pfizer Finland Helsinki Finland

7. WW Projects Copenhagen Denmark

8. Department of Cardiology Aarhus University Hospital Aarhus Denmark

Abstract

AbstractAimsTransthyretin amyloid cardiomyopathy (ATTR CM) is a progressive and severe heart disease with physical and psychological implications. The Nordic PROACT study was conducted to investigate the health‐related quality of life (HRQoL) in ATTR CM patients.Methods and resultsThe Nordic PROACT study was a cross‐sectional non‐interventional study conducted in 12 cardiology hospital clinics across Norway, Sweden, Finland and Denmark. Men and women aged ≥18 years diagnosed with symptomatic ATTR CM were included. The investigator provided information on medical history, biomarkers, current treatment, co‐morbidities and disease severity according to the New York Heart Association (NYHA) class and the National Amyloidosis Centre (NAC) staging. Patients completed the HRQoL questionnaires in the form of the Kansas City Cardiomyopathy Questionnaire (KCCQ), the EQ‐5D‐5L index with Visual Analog Scale (VAS), and the Major Depression Inventory (MDI). A total of 169 patients (mean ± SD age 77.7 ± 6.2 years) were included. Ninety‐two per cent were men. Seventy‐six per cent had wildtype ATTR CM (ATTRwt CM) and 15% had a hereditary form of ATTR CM (ATTRv CM) while 9% were genetically unclassified. Most patients were in NYHA class II (54%) and NAC stage 1 (53%). Participation in randomized clinical trials (RCT) was noted in 58% of the patients. The 169 ATTR CM patients had a mean ± SD KCCQ score of 64.3 ± 23.1 for total symptom score, 64.8 ± 20.9 for overall summary score (OSS) and 65.1 ± 21.5 for clinical summary score. The EQ‐5D‐5L total utility score was 0.8 ± 0.2 and the EQ‐5D‐5L VAS score was 62.9 ± 20.6. The vast majority (89%) did not report any signs of depression. Patients with ATTRv CM had a higher KCCQ OSS as compared with ATTRwt CM, while EQ‐5D‐5L utility score, EQ‐5D‐5L VAS and MDI were similar. Non‐RCT participants had a poorer HRQoL as compared with RCT participants as reflected in lower KCCQ OSS and EQ‐5D‐5L VAS scores and a higher MDI score. Patients with higher NYHA classes and NAC disease stages had a poorer HRQoL as demonstrated by lower KCCQ and EQ‐5D‐5L scores and higher MDI scores. Correlation between KCCQ, EQ‐5D‐5L and MDI and the covariate NYHA class remained significant (P < 0.05) after adjusting for multiple testing.ConclusionsKCCQ scores were lower than previously reported for patients with other heart diseases of non‐ATTR CM origin. The HRQoL measures correlated well to NYHA class and NAC disease stage. The prevalence of depression appeared to be low.

Funder

Pfizer

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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