Titration of medications and outcomes in multi‐ethnic heart failure cohorts (with reduced ejection fraction) from Singapore and New Zealand

Author:

Teng Tiew‐Hwa Katherine123,Tay Wan Ting1,Ouwerkerk Wouter14,Tromp Jasper256,Richards A. Mark78,Gamble Greg9,Greene Stephen J.1011,Yiu Kai‐Hang1213,Poppe Katrina9,Ling Lieng Hsi7,Lund Mayanna14,Sim David1,Devlin Gerard915,Loh Seet Yoong16,Troughton Richard8,Ren Qing‐wen1213,Jaufeerally Fazlur17,Lee Shao Guang Sheldon18,Tan Ru San1,Soon Dinna Kar Nee19,Leong Gerald20,Ong Hean Yee21,Yeo Daniel P.S.22,Lam Carolyn S.P.126ORCID,Doughty Rob N.9ORCID

Affiliation:

1. National Heart Centre Singapore Singapore

2. Duke‐NUS Medical School Singapore

3. School of Allied Health University of Western Australia Perth Australia

4. Department of Dermatology Amsterdam Medical Center Amsterdam The Netherlands

5. Saw Swee Hock School of Public Health National University of Singapore Singapore

6. Department of Cardiology University Medical Center Groningen Groningen The Netherlands

7. National University Heart Centre Singapore

8. Department of Medicine University of Otago Dunedin New Zealand

9. School of Medicine University of Auckland Auckland New Zealand

10. Division of Cardiology Duke University School of Medicine Durham NC USA

11. Duke Clinical Research Institute Durham NC USA

12. Cardiology Division, Department of Medicine The University of Hong Kong Shenzhen Hospital Shenzhen China

13. Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong

14. Middlemore Hospital Auckland New Zealand

15. Tairāwhiti District Health Board Gisborne New Zealand

16. Tan Tock Seng Hospital Singapore

17. Singapore General Hospital Singapore

18. Changi General Hospital Singapore

19. Khoo Teck Puat Hospital Singapore

20. Thomson Medical Centre Singapore

21. Cardiac Solutions Medical Centre Singapore

22. Gleneagles Hospital Singapore

Abstract

AbstractAimsWe investigated titration patterns of angiotensin‐converting enzyme inhibitors (ACEis)/angiotensin receptor blockers (ARBs) and beta‐blockers, quality of life (QoL) over 6 months, and associated 1 year outcome [all‐cause mortality/heart failure (HF) hospitalization] in a real‐world population with HF with reduced ejection fraction (HFrEF).Methods and resultsParticipants with HFrEF (left ventricular ejection fraction <40%) from a prospective multi‐centre study were examined for use and dose [relative to guideline‐recommended maintenance dose (GRD)] of ACEis/ARBs and beta‐blockers at baseline and 6 months. ‘Stay low’ was defined as <50% GRD at both time points, ‘stay high’ as ≥50% GRD, and ‘up‐titrate’ and ‘down‐titrate’ as dose trajectories. Among 1110 patients (mean age 63 ± 13 years, 16% women, 26% New York Heart Association Class III/IV), 714 (64%) were multi‐ethnic Asians from Singapore and 396 were from New Zealand (mainly European ethnicity). Baseline use of either ACEis/ARBs or beta‐blockers was high (87%). Loop diuretic was prescribed in >80% of patients, mineralocorticoid receptor antagonist in about half of patients, and statins in >90% of patients. At baseline, only 11% and 9% received 100% GRD for each drug class, respectively, with about half (47%) achieving ≥50% GRD for ACEis/ARBs or beta‐blockers. At 6 months, a large majority remained in the ‘stay low’ category, one third remained in ‘stay high’, whereas 10–16% up‐titrated and 4–6% down‐titrated. Patients with lower (vs. higher) N‐terminal pro‐beta‐type natriuretic peptide levels were more likely to be up‐titrated or be in ‘stay high’ for ACEis/ARBs and beta‐blockers (P = 0.002). Ischaemic aetiology, prior HF hospitalization, and enrolment in Singapore (vs. New Zealand) were independently associated with higher odds of ‘staying low’ (all P < 0.005) for prescribed doses of ACEis/ARBs and beta‐blockers. Adjusted for inverse probability weighting, ≥100% GRD for ACEis/ARBs [hazard ratio (HR) = 0.42; 95% confidence interval (CI) 0.24–0.73] and ≥50% GRD for beta‐blockers (HR = 0.58; 95% CI 0.37–0.90) (vs. Nil) were associated with lower hazards for 1 year composite outcome. Country of enrolment did not modify the associations of dose categories with 1 year composite outcome. Higher medication doses were associated with greater improvements in QoL.ConclusionsAlthough HF medication use at baseline was high, most patients did not have these medications up‐titrated over 6 months. Multiple clinical factors were associated with changes in medication dosages. Further research is urgently needed to investigate the causes of lack of up‐titration of HF therapy (and its frequency), which could inform strategies for timely up‐titration of HF therapy based on clinical and biochemical parameters.

Funder

Health Research Council of New Zealand

Waikato Medical Research Foundation

Auckland Medical Research Foundation

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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