Tuesday, November 5, 2024
Subscribe American Journal of Medicine Free Newsletter
CardiologyGrowing Mismatch Between Evidence Generation and Implementation in Heart Failure

Growing Mismatch Between Evidence Generation and Implementation in Heart Failure

Heart failure is a leading cause of morbidity and mortality globally. The natural history of heart failure with reduced ejection fraction (HFrEF) has been altered with the development of multiple therapeutic agents targeting maladaptive biologic pathways, including angiotensin-converting enzyme inhibitors (ACEI) and angiotensin receptor blockers, beta-blockers, and mineralocorticoid receptor antagonists. Although mechanistic studies overlapped, the landmark trials and their publications that led to the acceptance of these therapies as standards of care generally occurred sequentially. Such evolution allowed for each therapy to be viewed as incremental to a patient population on the optimal background therapy.
This traditional path of drug development has become more complex in the recent past. The Prospective Comparison of ARNI with ACEI to Determine Impact on Global Mortality and Morbidity in Heart Failure (PARADIGM-HF) trial showed superiority of sacubitril/valsartan, an angiotensin receptor–neprilysin inhibitor, over enalapril. While the use of this therapy continues to slowly evolve, the Dapagliflozin And Prevention of Adverse-outcomes in Heart Failure (DAPA-HF) trial (NCT03036124), the first large, outcomes trial to report the effects of sodium-glucose co-transporter-2 inhibitor in heart failure, showed that dapagliflozin reduced its primary composite endpoint (cardiovascular mortality, heart failure hospitalization, or urgent heart failure visit), and all-cause mortality (at nominal significance) in patients with HFrEF. Additionally, multiple ongoing trials are planning to report full results in the near future, evaluating myosin activators (omecamtiv mecarbil), soluble guanylate cyclase stimulators (vericiguat), and other SGLT2 inhibitors in HFrEF. This recent accelerated drug development and near-simultaneous evaluation of multiple novel agents have created a rich and exciting landscape poised to redefine modern treatment of HFrEF.
Despite these advances in therapeutic options, clinical practice data continues to show that guideline-directed medical therapy (GDMT) for HFrEF remains at disappointingly low levels, and few patients, for multiple reasons, are actually on optimal therapy. From an evidence generation perspective, this issue has another dimension of concern. If a therapy is evaluated when patients, at baseline, are not on ‘optimal ‘medical therapy, how do we assess its incremental value? At least for ACEI, beta-blockers, and mineralocorticoid receptor antagonists, patients were by design on as tolerated GDMT as background therapy. However, for patients enrolled in recent trials, because evidence generation is occurring in parallel and not in sequence, the majority of patients may not be on “optimal GDMT at baseline,” the definition of which itself is evolving. For instance, in the DAPA-HF trial, only ~1 in 10 patients were on baseline angiotensin receptor–neprilysin inhibitor therapy. This issue with low baseline therapy will compound in ongoing trials as well. Is it time for traditional stepped regimens to give way to more nuanced care with a menu of options, with investment in an implementation framework to meet the pace of evidence generation and help us choose wisely?
Current efforts in evidence generation will not live up to their promise if they do not translate into clinical use. It is imperative that we develop an implementation framework dedicated to the understanding of strategies to best accelerate the adoption of disease-modifying therapies among eligible patients. This framework will require collaboration across academia, industry, payers, and health systems, and will need to be evaluated with similar rigor and high quality evidence that we hold to the study of new therapeutic modalities. Implementation avenues must be safe, effective, scalable, and generalizable. Implementation trials should be conceived at the time of planning the efficacy trials, allowing for staged implementation science to be completed and therapeutic uptake to be optimized. Though the methods and mechanisms of action of this implementation framework may be complex, its integration into healthcare systems must be both simple and nimble. Successful strategies will have to rely on design and funding of implementation trials and utilization of the emergence of health data science. These efforts must aim to simplify prescribing, relieve provider therapeutic inertia, allow less onerous monitoring, and improve patient compliance.
The initial step in an implementation framework should include implementation trials that may borrow methodologically from traditional clinical trials. Specific early aims should include evaluation of strategies for early initiation and faster titration of any given therapy and determining optimal and tailored combinations of HFrEF therapies. Potential trials should include considerations surrounding the optimal setting for drug initiation (in hospital vs outpatient), the effect of direct patient-facing interventions, and the use of non-physician partners for protocol-based care provision. Dedicated multidisciplinary teams may be needed to optimize GDMT, both in inpatient and ambulatory settings.

To read this article in its entirety please visit our website.

-Ankeet S. Bhatt, MD MBA, Muthiah Vaduganathan, MD MPH, Javed Butler, MD MPH MBA

This article originally appeared in the January 2020 issue of The American Journal of Medicine

Latest Posts

lupus

Sarcoidosis with Lupus Pernio in an Afro-Caribbean Man

A 54-year-old man of Afro-Caribbean ancestry presented with a 2-month history of nonproductive cough, 10-day history of constant subjective fevers, and a 1-day history...
Flue Vaccine

Flu Vaccination to Prevent Cardiovascular Mortality (video)

0
"Influenza can cause a significant burden on patients with coronary artery disease," write Barbetta et al in The American Journal of Medicine. For this...
varicella zoster

Varicella Zoster Virus-Induced Complete Heart Block

0
Complete heart block is usually caused by chronic myocardial ischemia and fibrosis but can also be induced by bacterial and viral infections. The varicella...
Racial justice in healthcare

Teaching Anti-Racism in the Clinical Environment

0
"Teaching Anti-Racism in the Clinical Environment: The Five-Minute Moment for Racial Justice in Healthcare" was originally published in the April 2023 issue of The...
Invisible hand of the market

The ‘Invisible Hand’ Doesn’t Work for Prescription Drugs

0
Pharmaceutical innovation has been responsible for many “miracles of modern medicine.” Reliance on the “invisible hand” of Adam Smith to allocate resources in the...
Joseph S. Alpert, MD

New Coronary Heart Disease Risk Factors

0
"New Coronary Heart Disease Risk Factors" by AJM Editor-in Chief Joseph S. Alpert, MD was originally published in the April 2023 issue of The...
Cardiovascular risk from noncardiac activities

Cardiac Risk Related to Noncardiac & Nonsurgical Activities

0
"Assessment of Cardiovascular Risk for Noncardiac and Nonsurgical Activities" was originally published in the April 2023 issue of The American Journal of Medicine. Cardiovascular risk...