University Hospital Brno
Brno, 625 00, Czechia
Location contact
Adam Koudelka, MD
CONTACT
Adam Koudelka, MD
PRINCIPAL_INVESTIGATOR
Ondrej Ludka, Prof.
CONTACT
NCT Number: NCT06887179
This study aims to determine whether Point-of-Care Ultrasound (POCUS)-guided treatment is non-inferior to standard NT-proBNP-based care in ambulatory patients following hospitalization for heart failure (HF) over a 12-month follow-up period.
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Interventional
Not applicable
Brno, 625 00, Czechia
Adam Koudelka, MD
CONTACT
Adam Koudelka, MD
PRINCIPAL_INVESTIGATOR
Ondrej Ludka, Prof.
CONTACT
Although ultrasound machines are routinely available in ambulatory settings these days, assessing congestion with POCUS during regular visits is not yet established as a standard of care for HF patients. Accurate assessment of congestion is a cornerstone in managing HF since congestion is a major driver of symptoms, hospitalizations, and adverse outcomes. Current standard methods for congestion assessment include clinical examination, laboratory markers such as NT-proBNP, chest X-ray, and sometimes invasive hemodynamic monitoring. However, these approaches have limitations: clinical signs can be subjective, NT-proBNP levels may be influenced by non-cardiac factors, and invasive monitoring is not feasible for routine outpatient use. Chest X-ray bears the risk of irradiation and is more time and money-consuming than bedside tools.
POCUS has emerged as a promising tool for real-time congestion assessment. It allows for direct visualization of pulmonary and systemic congestion, providing rapid bedside insights into the patient's volume status (9). Despite its advantages, POCUS is not yet widely implemented in routine HF ambulatory management, primarily due to the lack of standardized protocols with sufficient evidence.
This study evaluates whether an HF-focused POCUS protocol can enhance congestion assessment in ambulatory HF patients following hospitalization. During a follow-up period of 12 months, they will be regularly examined clinically and with standard laboratory tests. HF-focused POCUS will be performed in the interventional arm instead of standard NT-proBNP testing. For the sake of simplicity and practicality of the examination, a handheld ultrasound device (GE Healthcare Vscan Air SL® or Vscan Extend®) with only a sector probe in B-mode will be employed.
The HF-focused POCUS examination includes several predefined components. Lung assessment to detect pulmonary congestion. Pleural assessment to detect congestion with effusion. The inferior vena cava assessment is used to estimate central venous pressure. The presence of ascites is evaluated by scanning the hepatorenal space and right paracolic gutter for signs of fluid accumulation.
The HF-focused POCUS is performed by treating physicians, allowing immediate diuretic therapy adjustments based on the results. The hypothesis is that HF-focused POCUS can enable more precise diuretic titration, potentially reducing adverse events.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Standard care assessment with NT-proBNP on every scheduled visit.
Time frame: 12 months
The primary outcome is a composite of urgent visits, hospitalization for worsening HF and death from any cause. We defined an urgent visit for worsening HF as an unscheduled visit because of signs and/or symptoms of worsening HF that require IV diuretic treatment or a diuretic increase with a hospital stay of less than 24 hours. Hospitalization for worsening HF is defined as a stay in hospital for more than 24 hours because of signs and/or symptoms of worsening HF.
Time frame: 12 months
The total number of all AHF hospitalizations
Time frame: 12 months
The total number of other unplanned hospitalizations
Time frame: 12 months
The total number of all unscheduled visits for any cause
Time frame: 12 months
The total number of extra visits beyond the protocol schedule for HF treatment
Time frame: 12 months
The change in NT-proBNP (ng/l)
Time frame: 12 months
The change in eGFR (ml/s/1,73m2)
Time frame: 12 months
The change in KCCQ (points). It is scored from 0 to 100 with higher scores indicating better health status.
Time frame: 12 months
The total number of performed chest X-rays
Time frame: 12 months
The total number of drainage procedures for fluidothorax or ascites.
Time frame: 12 months
Diuretics-related decrease in eGFR >50% (with signs of hypovolemia) compared to the 1st-week visit value; the level of hypokalemia <3.5 mmol/L (the number of patients having hypokalemia <3.5 mmol/L).
Time frame: 12 months
The number of patients having hypokalemia <3.5 mmol/L
Contact information is provided by the study sponsor or research team.
Adam Koudelka, MD
CONTACT
Ondrej Ludka, Prof.
CONTACT
Masaryk University
Other
The Role of Point-of-Care Ultrasound in the Management of Chronic Heart Failure
Acronym: POCUS-HF
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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