Appropriateness of Hemostatic Agent Use in Cardiovascular Surgery (HAEMOVAX)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Milan

About this trial

Hemostatic agents are widely used in cardiac and vascular surgery to support intraoperative bleeding control. Despite their clinical relevance and substantial economic impact, little is known about real-world patterns of use, adherence to evidence-based recommendations, and the alignment between clinicians' perceived knowledge and actual decision-making.

HAEMOVAX is a single-center mixed-methods observational study conducted at IRCCS Galeazzi-Sant'Ambrogio Hospital, Milan, Italy. The study combines an anonymous survey of cardiovascular surgeons with a retrospective audit of institutional hemostatic agent consumption. The primary objective is to evaluate the appropriateness of hemostatic agent selection using a Knowledge-Practice Alignment Score (KPA-Score) derived from standardized clinical vignettes based on current EACTS and ESA recommendations. Secondary objectives include assessment of usage patterns, barriers to appropriate use, concordance between declared practice and real-world consumption, and opportunities for evidence-based standardization.

Eligibility criteria

Qualifiers

Physicians with a surgical role in the Departments of Cardiac Surgery or Vascular Surgery at IRCCS Galeazzi-Sant'Ambrogio, Milan Including attending surgeons, consultant surgeons, and surgical residents

Active participation in cardiovascular operative procedures during the study period (or within the preceding 12 months)

Employment at the study institution at the time of survey administration Willingness to participate and complete the anonymous structured questionnaire

Disqualifiers

Non-surgical healthcare personnel (e.g., nurses, anesthesiologists, administrative staff, or allied health professionals)

Surgeons not involved in operative cardiovascular practice during the study period

External collaborators or visiting surgeons without regular clinical activity at the institution

Individuals who do not provide informed consent for participation in the anonymous survey

Trial design

Treatments tested in this trial

  • observational study

Treatment groups

15 Participants
are divided into 1 treatment group

Sponsors and collaborators