TY - JOUR
T1 - Latent Pulmonary Vascular Disease May Alter the Response to Therapeutic Atrial Shunt Device in Heart Failure
AU - Borlaug, Barry A.
AU - Blair, John
AU - Bergmann, Martin W.
AU - Bugger, Heiko
AU - Burkhoff, Dan
AU - Bruch, Leonhard
AU - Celermajer, David S.
AU - Claggett, Brian
AU - Cleland, John G.F.
AU - Cutlip, Donald E.
AU - Dauber, Ira
AU - Eicher, Jean Christophe
AU - Gao, Qi
AU - Gorter, Thomas M.
AU - Gustafsson, Finn
AU - Hayward, Chris
AU - Van Der Heyden, Jan
AU - Hasenfuß, Gerd
AU - Hummel, Scott L.
AU - Kaye, David M.
AU - Komtebedde, Jan
AU - Massaro, Joseph M.
AU - Mazurek, Jeremy A.
AU - McKenzie, Scott
AU - Mehta, Shamir R.
AU - Petrie, Mark C.
AU - Post, Marco C.
AU - Nair, Ajith
AU - Rieth, Andreas
AU - Silvestry, Frank E.
AU - Solomon, Scott D.
AU - Trochu, Jean Noël
AU - Van Veldhuisen, Dirk J.
AU - Westenfeld, Ralf
AU - Leon, Martin B.
AU - Shah, Sanjiv J.
N1 - Funding Information:
All authors except Dr Celermajer received research grant funding from Corvia to support this study. Drs Massaro, Burkhoff, and Celermajer have received personal consulting fees from Corvia. Dr Celermajer is a shareholder in Corvia and Dr Komtebedde is employed by Corvia. Dr Borlaug has received research grants from AstraZeneca, Medtronic, GlaxoSmithKline, Mesoblast, Novartis, and Tenax Therapeutics, and consulting fees from Actelion, Amgen, Aria, Axon Therapies, Boehringer Ingelheim, Edwards Lifesciences, Eli Lilly, Imbria, Janssen, Merck, Novo Nordisk, and VADovations. Prof Cleland has received research grants from Amgen, Bristol Myers Squibb, Medtronic, Novartis, Pharmacosmos, Servier, and Vifor Pharma; support for travel from Corvia; and consulting fees from Abbott and Boehringer Ingelheim. Dr Petrie has received research funding from Boehringer Ingelheim, Roche, SQ Innovations, Astra Zeneca, Novartis, Novo Nordisk, Medtronic, Boston Scientific, and Pharmacosmos and served on clinical trial committees for Boehringer Ingelheim, Novartis, Astra Zeneca, Novo Nordisk, AbbVie, Bayer, Takeda, Cardiorentis, Pharmacosmos, Siemens, and Vifor. Dr Shah has received research grants from Actelion, AstraZeneca, Corvia, Novartis, and Pfizer and consulting fees from Abbott, Actelion, AstraZeneca, Amgen, Aria CV, Axon Therapies, Bayer, Boehringer Ingelheim, Boston Scientific, Bristol Myers Squibb, Cardiora, Coridea, CVRx, Cyclerion, Cytokinetics, Edwards Lifesciences, Eidos, Eisai, Imara, Impulse Dynamics, Intellia, Ionis, Ironwood, Lilly, Merck, MyoKardia, Novartis, Novo Nordisk, Pfizer, Prothena, Regeneron, Rivus, Sanofi, Shifamed, Tenax, Tenaya, and United Therapeutics. Dr Gustafsson has received consulting fees from Abbott, Pfizer, Pharmacosmos, Ionis, Alnylam, and Bayer and speaker’s fees from Orion Pharma, Novartis, Vifor, and AstraZeneca. Dr Trochu has received research grants from Novartis and Boston Scientific and personal fees from Abbott, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Novartis, and ViforPharma. Dr Mazurek has received research support from Actelion and Tenax Therapeutics and consulting fees from Actelion, United Therapeutics, and Acceleron. Dr Mehta has received research support from Abbott, AstraZeneca, Boston Scientific, Bristol Myers Squibb, and Johnson & Johnson. Dr Nair has received consulting fees from Abiomed. Dr Rieth has received speaker’s fees from AstraZeneca and Bayer and congress fees from Servier. Dr Bugger has received consulting fees from Boehringer Ingelheim.
Funding Information:
REDUCE LAP-HF II (A Study to Evaluate the Corvia Medical, Inc IASD System II to Reduce Elevated Left Atrial Pressure in Patients With Heart Failure) was funded by Corvia Medical, Inc. Dr Borlaug is supported by grants R01 HL128526 and U01 HL160226 from the National Institutes of Health. Dr Shah is supported by grants U54 HL160273, R01 HL107577, R01 HL140731, and R01 HL149423 from the National Institutes of Health. Dr Hummel is supported by grants R01 HL139813, R01 AG062582, and R61 HL155498 from the National Institutes of Health and grant CARA-009-16F9050 from the Veterans Health Administration. Prof Cleland is supported by the British Heart Foundation Center of Research Excellence (grant RE/18/6/34217). Prof Petrie is supported by British Heart Foundation Center of Research Excellence Grant RE/18/6/34217.
Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/5/24
Y1 - 2022/5/24
N2 - Background: In REDUCE LAP-HF II (A Study to Evaluate the Corvia Medical, Inc IASD System II to Reduce Elevated Left Atrial Pressure in Patients With Heart Failure), implantation of an atrial shunt device did not provide overall clinical benefit for patients with heart failure with preserved or mildly reduced ejection fraction. However, prespecified analyses identified differences in response in subgroups defined by pulmonary artery systolic pressure during submaximal exercise, right atrial volume, and sex. Shunt implantation reduces left atrial pressures but increases pulmonary blood flow, which may be poorly tolerated in patients with pulmonary vascular disease (PVD). On the basis of these results, we hypothesized that patients with latent PVD, defined as elevated pulmonary vascular resistance during exercise, might be harmed by shunt implantation, and conversely that patients without PVD might benefit. Methods: REDUCE LAP-HF II enrolled 626 patients with heart failure, ejection fraction ≥40%, exercise pulmonary capillary wedge pressure ≥25 mm Hg, and resting pulmonary vascular resistance <3.5 Wood units who were randomized 1:1 to atrial shunt device or sham control. The primary outcome - a hierarchical composite of cardiovascular death, nonfatal ischemic stroke, recurrent HF events, and change in health status - was analyzed using the win ratio. Latent PVD was defined as pulmonary vascular resistance ≥1.74 Wood units (highest tertile) at peak exercise, measured before randomization. Results: Compared with patients without PVD (n=382), those with latent PVD (n=188) were older, had more atrial fibrillation and right heart dysfunction, and were more likely to have elevated left atrial pressure at rest. Shunt treatment was associated with worse outcomes in patients with PVD (win ratio, 0.60 [95% CI, 0.42, 0.86]; P=0.005) and signal of clinical benefit in patients without PVD (win ratio, 1.31 [95% CI, 1.02, 1.68]; P=0.038). Patients with larger right atrial volumes and men had worse outcomes with the device and both groups were more likely to have pacemakers, heart failure with mildly reduced ejection fraction, and increased left atrial volume. For patients without latent PVD or pacemaker (n=313; 50% of randomized patients), shunt treatment resulted in more robust signal of clinical benefit (win ratio, 1.51 [95% CI, 1.14, 2.00]; P=0.004). Conclusions: In patients with heart failure with preserved or mildly reduced ejection fraction, the presence of latent PVD uncovered by invasive hemodynamic exercise testing identifies patients who may worsen with atrial shunt therapy, whereas those without latent PVD may benefit.
AB - Background: In REDUCE LAP-HF II (A Study to Evaluate the Corvia Medical, Inc IASD System II to Reduce Elevated Left Atrial Pressure in Patients With Heart Failure), implantation of an atrial shunt device did not provide overall clinical benefit for patients with heart failure with preserved or mildly reduced ejection fraction. However, prespecified analyses identified differences in response in subgroups defined by pulmonary artery systolic pressure during submaximal exercise, right atrial volume, and sex. Shunt implantation reduces left atrial pressures but increases pulmonary blood flow, which may be poorly tolerated in patients with pulmonary vascular disease (PVD). On the basis of these results, we hypothesized that patients with latent PVD, defined as elevated pulmonary vascular resistance during exercise, might be harmed by shunt implantation, and conversely that patients without PVD might benefit. Methods: REDUCE LAP-HF II enrolled 626 patients with heart failure, ejection fraction ≥40%, exercise pulmonary capillary wedge pressure ≥25 mm Hg, and resting pulmonary vascular resistance <3.5 Wood units who were randomized 1:1 to atrial shunt device or sham control. The primary outcome - a hierarchical composite of cardiovascular death, nonfatal ischemic stroke, recurrent HF events, and change in health status - was analyzed using the win ratio. Latent PVD was defined as pulmonary vascular resistance ≥1.74 Wood units (highest tertile) at peak exercise, measured before randomization. Results: Compared with patients without PVD (n=382), those with latent PVD (n=188) were older, had more atrial fibrillation and right heart dysfunction, and were more likely to have elevated left atrial pressure at rest. Shunt treatment was associated with worse outcomes in patients with PVD (win ratio, 0.60 [95% CI, 0.42, 0.86]; P=0.005) and signal of clinical benefit in patients without PVD (win ratio, 1.31 [95% CI, 1.02, 1.68]; P=0.038). Patients with larger right atrial volumes and men had worse outcomes with the device and both groups were more likely to have pacemakers, heart failure with mildly reduced ejection fraction, and increased left atrial volume. For patients without latent PVD or pacemaker (n=313; 50% of randomized patients), shunt treatment resulted in more robust signal of clinical benefit (win ratio, 1.51 [95% CI, 1.14, 2.00]; P=0.004). Conclusions: In patients with heart failure with preserved or mildly reduced ejection fraction, the presence of latent PVD uncovered by invasive hemodynamic exercise testing identifies patients who may worsen with atrial shunt therapy, whereas those without latent PVD may benefit.
KW - clinical trial
KW - heart failure
KW - hypertension, pulmonary
KW - lung diseases
KW - therapeutics
KW - vascular diseases
UR - http://www.scopus.com/inward/record.url?scp=85130862805&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85130862805&partnerID=8YFLogxK
U2 - 10.1161/CIRCULATIONAHA.122.059486
DO - 10.1161/CIRCULATIONAHA.122.059486
M3 - Article
C2 - 35354306
AN - SCOPUS:85130862805
SN - 0009-7322
VL - 145
SP - 1592
EP - 1604
JO - Circulation
JF - Circulation
IS - 21
ER -