Health-related quality of life among transthyretin amyloid cardiomyopathy patients

被引:10
作者
Eldhagen, Per [1 ]
Lehtonen, Jukka [2 ]
Gude, Einar [3 ]
Gustafsson, Finn [4 ]
Bagger-Bahnsen, Anne [5 ]
Vakevainen, Merja [6 ]
Pilgaard, Trine [5 ]
Wedell-Wedellsborg, Dorte [7 ]
Poulsen, Steen Hvitfeldt [8 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Dept Med, Solna, Sweden
[2] Helsinki Univ Hosp, Heart & Lung Ctr, Helsinki, Finland
[3] Oslo Univ Hosp, Rikshosp, Dept Cardiol, Oslo, Norway
[4] Rigshosp, Dept Cardiol, Copenhagen, Denmark
[5] Pfizer Denmark, Ballerup, Denmark
[6] Pfizer Finland, Helsinki, Finland
[7] WW Projects, Copenhagen, Denmark
[8] Aarhus Univ Hosp, Dept Cardiol, Aarhus, Denmark
来源
ESC HEART FAILURE | 2023年 / 10卷 / 03期
关键词
Amyloidosis; Cardiomyopathy; Transthyretin; ATTR CM; Observational study; Patient-reported outcome measures; Quality of life; MAJOR DEPRESSION INVENTORY; CARDIAC AMYLOIDOSIS; HEART-FAILURE; SEVERITY; VALIDITY; IMPACT;
D O I
10.1002/ehf2.14350
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsTransthyretin 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.
引用
收藏
页码:1871 / 1882
页数:12
相关论文
共 46 条
  • [1] Suspicion, screening, and diagnosis of wild-type transthyretin amyloid cardiomyopathy: a systematic literature review
    Bay, Katrine
    Gustafsson, Finn
    Maiborg, Michael
    Bagger-Bahnsen, Anne
    Strand, Anne Mette
    Pilgaard, Trine
    Poulsen, Steen Hvitfeldt
    [J]. ESC HEART FAILURE, 2022, 9 (03): : 1524 - 1541
  • [2] Applicability and validity of the Major Depression Inventory in patients with Parkinson's disease
    Bech, P
    Wermuth, L
    [J]. NORDIC JOURNAL OF PSYCHIATRY, 1998, 52 (04) : 305 - 309
  • [3] DenHeart: Differences in physical and mental health across cardiac diagnoses at hospital discharge
    Berg, Selina Kikkenborg
    Rasmussen, Trine Bernholdt
    Thrysoee, Lars
    Lauberg, Astrid
    Borregaard, Britt
    Christensen, Anne Vinggaard
    Ekholm, Ola
    Juel, Knud
    Svanholm, Jette Rolf
    [J]. JOURNAL OF PSYCHOSOMATIC RESEARCH, 2017, 94 : 1 - 9
  • [4] Seven factors predict a delayed diagnosis of cardiac amyloidosis
    Bishop, Eve
    Brown, Emily E.
    Fajardo, Johana
    Barouch, Lili A.
    Judge, Daniel P.
    Halushka, Marc K.
    [J]. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2018, 25 (03): : 174 - 179
  • [5] Quality of life status determinants in hypertrophic cardiomyopathy as evaluated by the Kansas City Cardiomyopathy Questionnaire
    Capota, Razvan
    Militaru, Sebastian
    Ionescu, Alin Alexandru
    Rosca, Monica
    Baicus, Cristian
    Popescu, Bogdan Alexandru
    Jurcut, Ruxandra
    [J]. HEALTH AND QUALITY OF LIFE OUTCOMES, 2020, 18 (01)
  • [6] Heart Failure Functional Class Associated with Depression Severity But Not Anxiety Severity
    Celik, Etem
    Cay, Serkan
    Sensoy, Baris
    Murat, Sani
    Oksuz, Fatih
    Cankurt, Tayyar
    Mendi, Mehmet Ali
    [J]. ACTA CARDIOLOGICA SINICA, 2016, 32 (01) : 55 - 61
  • [7] Health-Related Quality of Life in Heart Failure With Preserved Ejection Fraction The PARAGON-HF Trial
    Chandra, Alvin
    Vaduganathan, Muthiah
    Lewis, Eldrin F.
    Claggett, Brian L.
    Rizkala, Adel R.
    Wang, Wenyan
    Lefkowitz, Martin P.
    Shi, Victor C.
    Anand, Inder S.
    Ge, Junbo
    Lam, Carolyn S. P.
    Maggioni, Aldo P.
    Martinez, Felipe
    Packer, Milton
    Pfeffer, Marc A.
    Pieske, Burkert
    Redfield, Margaret M.
    Rouleau, Jean L.
    van Veldhuisen, Dirk J.
    Zannad, Faiez
    Zile, Michael R.
    McMurray, John J. V.
    Solomon, Scott D.
    [J]. JACC-HEART FAILURE, 2019, 7 (10) : 862 - 874
  • [8] THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis
    Coelho, Teresa
    Maurer, Mathew S.
    Suhr, Ole B.
    [J]. CURRENT MEDICAL RESEARCH AND OPINION, 2013, 29 (01) : 63 - 76
  • [9] Criteria Committee of the New York Heart Association, 1994, FUNCT CAP OBJ ASS NO, P253
  • [10] Amyloidosis from the patient perspective: the French daily impact of amyloidosis study
    Damy, Thibaud
    Adams, David
    Bridoux, Frank
    Grateau, Gilles
    Plante-Bordeneuve, Violaine
    Ghiron, Yves
    Farrugia, Agnes
    Pelcot, Francoise
    Taieb, Charles
    Labeyrie, Celine
    Jaccard, Arnaud
    Georgin-Lavialle, Sophie
    [J]. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2022, 29 (03): : 165 - 174