Feature | Heart Failure | September 01, 2015

Automated Pulmonary Congestion Alert No Benefit In Heart Failure Trial

Patient adherence primary obstacle to improved outcomes

Medtronic, OPTILINK, OptiVol, ICD, pulmonary congestion, ESC 2015

September 1, 2015 — Automated alerts for excess fluid accumulation in the lungs did not improve outcomes for heart failure patients with implantable cardioverter defibrillators (ICDs), according to results of the OPTILINK HF trial.

The findings, presented at the European Society of Cardiology (ESC) Congress 2015, “highlight the challenges and obstacles involved in ICD-based telemonitoring for heart failure (HF),” noted the study’s principal investigator Michael Böhm, M.D., from Saarland University Hospital in Homburg, Germany. 

“Given the considerable, and largely unmitigated burden of HF, the potential for telemonitoring to improve the management of patients with HF is substantial,” said Böhm. “However, in our trial ICD-based telemonitoring did not increase appropriate interventions, despite intensive instruction of patients and physicians in the clinical trial setting,” he suggested.

Because hospital admissions are frequently preceded by increased pulmonary congestion in heart failure patients, the trial used special ICDs that allow for automatic transmission of alerts to a patient’s doctor when this happens. The alert is transmitted from the ICD through a telemedicine monitor that patients have connected to the internet at home.

A total of 1,002 patients received these ICDs, with 505 patients randomly assigned to have the automated transmission turned on, and 497 patients to have it turned off (standard care). 

“If there was an alert, the physician called the patient, provided him with an exact care alert questionnaire, and increased therapies if necessary. Based on a strict algorithm patients were potentially seen or admitted to the hospital and care was initiated,” explained Böhm. 

During the study period there were 1,748 “fluid threshold crossings” which triggered an alert. Three quarters (76 percent) of these alerts were successfully transmitted from the patient’s ICD to the physician, with the remaining 24 percent deemed unsuccessful because the patient was either already in the hospital, on vacation without the monitor or offline.

Medical action was taken by physicians for 30 percent of the successful transmissions – most of these involving medication changes. In the 70 percent of cases where no medical action was taken, the reason was that although the alert indicated a fluid threshold crossing, it was not considered clinically actionable because the patient did not indicate visible signs or symptoms of worsening HF, explained Böhm.

After 18 months of follow-up there was no significant difference between groups in primary endpoint, which was a composite of all-cause death and cardiovascular hospitalization.

The primary outcome occurred in 227 patients (45 percent) in the intervention arm compared with 239 patients (48.1 percent) in the control arm (hazard ratio, 0.87; 95 percent confidence interval [CI], 0.72 to 1.04; p=0.13). There were 59 (11.7 percent) deaths in the intervention arm and 63 (12.7%) in the control arm group (hazard ratio, 0.89; 95 percent CI, 0.62 to 1.28; p=0.52). 

The obstacles to ICD-based HF telemonitoring identified in OPTILINK HF would likely be even more pronounced in a real-life clinical setting, noted Böhm. “Improved outcomes would require better patient adherence in terms of being online all the time,” he said.

For more information: www.escardio.org

Related Content

Tafamidis meglumine (Vyndaqel) is one of two new drugs cleared by the FDA for the treatment of the cardiomyopathy caused by transthyretin mediated amyloidosis (ATTR-CM) in adults. These are the first FDA-approved treatments for ATTR-CM. U.S. Food and Drug Administration (FDA) approved tafamidis meglumine (Vyndaqel) and tafamidis (Vyndamax) capsules for the treatment of the cardiomyopathy.

Tafamidis meglumine (Vyndaqel) is one of two new drugs cleared by the FDA for the treatment of the cardiomyopathy caused by transthyretin mediated amyloidosis (ATTR-CM) in adults. These are the first FDA-approved treatments for ATTR-CM. 

Technology | Heart Failure | May 06, 2019
May 6, 2019 — The U.S.
The Aortic intra-aortic axial flow pump is designed to unload the heart and increase renal perfusion in heart failure patients experiencing cardiorenal syndrome.

The Aortic intra-aortic axial flow pump is designed to unload the heart and increase renal perfusion in heart failure patients experiencing cardiorenal syndrome.

Feature | Heart Failure | April 29, 2019 | Will Clifton, M.D.
The heart and kidneys are inextricably linked through a diverse web of hemodynamic, neural and hormonal mechanisms.
Diabetes Drug May Reverse Heart Failure
News | Heart Failure | April 19, 2019
Researchers at the Icahn School of Medicine at Mount Sinai have demonstrated that the recently developed antidiabetic...
Diabetes Drug Effective Against Heart Failure in Wide Spectrum of Patients
News | Heart Failure | March 29, 2019
The cardiovascular benefits of the diabetes drug dapagliflozin extend across a wide spectrum of patients and are...
New data from a four-week extension of the landmark PIONEER-HF Trial showed the drug sacubitril/valsartan (Entresto) continued to deliver reductions in the heart failure biomarker N-terminal pro–B-type natriuretic peptide (NT-proBNP), an established biomarker for heart failure severity and prognosis.[1] The data was presented as a late-breaker at the American College of Cardiology (ACC) 2019 Annual Scientific Session in March.
News | Heart Failure | March 27, 2019
March 27, 2019 —New data from a four-week extension of the landmark PIONEER-HF Trial showed the drug sacubitril/valsa
Toilet Seat Detects Congestive Heart Failure

Nicholas Conn, a postdoctoral fellow at RIT and founder and CEO of Heart Health Intelligence, is part of the university team that has developed a toilet-seat based cardiovascular monitoring system. Image courtesy of A. Sue Weisler/RIT.

News | Heart Failure | March 26, 2019
March 26, 2019 — A toilet seat-based ...
FDA Approves Optimizer Smart System for Heart Failure Patients offers cardiac contractility modulation.
Technology | Heart Failure | March 21, 2019
The U.S. Food and Drug Administration (FDA) approved Impulse Dynamics’ Optimizer Smart system for treating patients...
William T. Abraham, M.D., Joins V-Wave as Chief Medical Officer

William T. Abraham, M.D., in an interview with DAIC Editor Dave Fornell at TCT 2016.

News | Heart Failure | March 12, 2019
V-Wave Ltd. announced that renowned heart failure cardiologist William T. Abraham, M.D., is joining V-Wave as chief...
Overlay Init