The primary objective of this observational study is to investigate the risk factors for intraoperative hypotension and identify the underlying pathomechanisms leading to it, both during the period after general anesthesia induction and throughout its course. The main questions it aims to answer are: * how frequent is intraoperative hypotension * what are the underlying pathomechanism causing it The study is including patients who have been identified as having a high risk of perioperative complications (ASA3 or ASA4). Patients included in the study undergo advanced hemodynamic monitoring during the procedure. Anesthesia induction, maintenance, and termination are conducted by an anesthesiologist in accordance with current medical knowledge, and the planned experiment does not in any way influence the course of action. Investigators will analyse medical documentation, including the patient's medical history, anesthesia records, and hemodynamic parameter data obtained from the hemodynamic monitor (an Excel file containing comprehensive data related to specific cardiovascular parameters) to describe the incidence of intraoperative hypotension and answer key questions in accordance with the designed study protocol.
Study Type
OBSERVATIONAL
Enrollment
2,000
Mazovian Regional Hospital
Siedlce, Mazovian, Poland
RECRUITINGIncidence of intraoperative hypotension (IOH)
Incidence of IOH due to the general anesthesia
Time frame: Intraoperative
Risk factors of IOH.
Rate of specific clinical and demographical parameters associated with IOH
Time frame: Perioperative
Development of a risk scale for IOH (MAP < 65mmHg) based on the identified risk factors in the study.
Combination of the most significant risk factors of IOH into risk scale.
Time frame: Perioperative
Determination of indications for intraoperative extended hemodynamic monitoring.
List of pre-operative clinical factors indicating elevated risk of peri-operative complications
Time frame: Perioperative
Assessment of the incidence, duration, and depth of hypotension as a complication of general anesthesia at each stage of anesthesia.
List of specific parameters related to IOH.
Time frame: Perioperative
Evaluation of the relationship between the depth and duration of hypotensive episodes and the occurrence of postoperative complications within 30 days of the surgical procedure.
List of clinical factors associated with IOH impacting clinical adverse events during 30 days follow up.
Time frame: Perioperative to 30 days after surgery
Analysis of the anesthesiologist's management approach in the event of hypotensive episodes or hypotension risks and an attempt to establish an optimal management strategy for its occurrence.
List of routine actions triggered by the IOH in the anesthesiological management.
Time frame: Perioperative
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