Pulmonary artery pressure monitoring useful even in chronic HF patients who did not require recent hospitalization: Study

USA: An analyis of the GUIDE-HF study revealed that wireless pulmonary artery pressure monitoring with CardioMEMS (Abbott) could be an option in patients with chronic heart failure (HF) who have increased natriuretic peptides and presymptomatic congestion but have not had a recent hospitalization. 

CardioMEMS is an implantable censor that was approved by the US Food and Drug Administration as a preventive strategy to reduce hospitalization risk in those who have had a hospital stay for HF within the prior year in patients with class III HF. In the GUIDE-HF trial since slightly less than half of all patients were enrolled on the basis of elevated natriuretic peptides alone, the researchers compared their outcomes with patients in the trial with a recent hospitalization by treatment assignment. 

The GUIDE-HF trial, findings of which were resented and published in 2021 was aimed at examining 12-month outcomes in two types of stable outpatients: those with mild or severe HF symptoms (NYHA class II or IV) and those with elevated natriuretic peptides without a recent HF hospitalization. The patients were implanted with the sensor. They were then randomised to pulmonary artery pressure monitoring or usual care with no access to the sensor data. 

The findings of the analysis were presented by Akshay S. Desai, Brigham and Women's Hospital, Boston, MA, in a late-breaking presentation at the inaugural Technology and Heart Failure Therapeutics (THT) 2022 meeting in New York.

"Our conclusions from this analysis are that despite lower event rates in those with elevated natriuretic peptides but no recent heart failure hospitalizations, the effects of hemodynamic-guided heart failure management were similar across enrollment strata," Desai told tctMD.

Findings showed no statistically significant differences in the primary endpoint between those managed hemodynamically or with usual care. The study at that time was however was impacted by the COVID-19 pandemic resulting in a marked reduction in hospitalizations for HF. Recently, the researchers from the GUIDE-HF trial presented a subgroup analysis of clinical events that occurred before March 2020, which showed a statistical advantage in hemodynamically managed patients, regardless of ejection fraction status, driven by fewer HF hospitalizations. The latest analysis focused on presymptomatic patients. The outcomes were analyzed by Dr. Desai and colleagues by treatment enrollment for the full study duration, as well as for the pre-COVID period only.