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Correlation Between Postoperative Blood Pressure Variability, Perfusion Index and Perioperative Adverse Events in Cardiac Surgery

Correlation Between Postoperative Blood Pressure Variability, Perfusion Index and Perioperative Adverse Events in Cardiac Surgery: A Single-Center Prospective Observational Cohort Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07316634
Enrollment
1200
Registered
2026-01-05
Start date
2026-01-01
Completion date
2026-08-01
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgery Intensive Care Treatment, Hemodynamics

Keywords

Blood Pressure Variability, Perfusion Index, Cardiac Surgery

Brief summary

In patients after cardiac surgery, disturbances in macrocirculatory fluctuations and tissue perfusion commonly coexist. The stress state induced by factors such as surgical manipulation, cardiopulmonary bypass, anesthetic agents, pain, and ischemia-reperfusion injury, along with the use of vasoactive drugs postoperatively, often leads to increased blood pressure fluctuations in the early postoperative period. Additionally, dysregulation of organ blood flow autoregulation post-surgery contributes to peripheral circulatory impairment, rendering perfusion pressure an unreliable indicator of actual organ perfusion. We aim to assess postoperative blood pressure fluctuation using blood pressure variability and evaluate peripheral circulatory status via the perfusion index. In this prospective cohort study, we will examine the correlation between these two parameters and perioperative adverse events.

Interventions

OTHERBlood Pressure Variability and Perfusion Index

All patients in this cohort will undergo invasive hemodynamic monitoring and noninvasive pulse oximetry, postoperative 24-hour blood pressure variability (from minute-to-minute invasive arterial pressure data) and perfusion index (from half-hourly recordings) were obtained through these monitoring modalities.

Sponsors

Beijing Anzhen Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age at surgery ≥ 18 years * Patients admitted to the ICU for the first time after undergoing their first cardiac surgical procedure during the current hospitalization ③ Expected to receive continuous invasive blood pressure monitoring and noninvasive pulse oximetry monitoring for at least 12 hours postoperatively in the ICU ④ Written or verbal informed consent obtained from the patient or their family members

Exclusion criteria

* Patients with severe peripheral vascular disease in the arm used for noninvasive pulse oximetry monitoring * Patients not undergoing invasive hemodynamic monitoring ③ Patients requiring preoperative or intraoperative support with IABP or ECMO * Patients expected to have incomplete postoperative monitoring data or a monitoring duration of less than 12 hours * Postoperative patients who are not admitted to the ICU for the first time during the current hospitalization ⑥ Patients admitted to the ICU prior to undergoing cardiac surgery ⑦ Patients with critically insufficient baseline preoperative data

Design outcomes

Primary

MeasureTime frameDescription
Incidence of the composite endpoint of adverse events within 30 days postoperativelyWithin 30 days after surgeryTotal incidence of death, stroke, perioperative myocardial infarction, infection, reoperation, and continuous renal replacement therapy. Diagnostic criteria: Stroke was characterized by a new focal deficit associated with a compatible image on computed tomography. Perioperative myocardial infarction was diagnosed when cardiac troponin I shows an acute change with at least one value exceeding the 99th percentile upper reference limit, along with one of the following: new pathologic Q waves, imaging evidence of coronary artery occlusion, or imaging evidence of new loss of viable myocardium. Infection was considered if one of the following diagnoses was made by an Infectious Disease specialist who followed specific protocols: 1) Pneumonia; 2) Catheter related blood stream infection; 3) Sternal wound infection or osteomyelitis.

Secondary

MeasureTime frameDescription
Incidence of acute kidney injury within 30 days postoperatively.Within 30 days after surgeryDiagnostic criteria are based on the KDIGO guidelines.
Incidence of acute respiratory distress syndrome within 30 days postoperativelyWithin 30 days after surgeryDiagnostic criteria are based on the 2012 Berlin definition of ARDS.
Incidence of low cardiac output syndrome within 30 days postoperatively.Within 30 days after surgeryDiagnostic criteria: Cardiac index \< 2.0 L/min/m².
Incidence of prolonged ventilation (>24 hours) within 30 days postoperatively.Within 30 days after surgery
Length of intensive care unit stayWithin 30 days after surgery
Incidence of new-onset atrial arrhythmias within 30 days postoperatively.Within 30 days after surgeryDiagnostic criteria: atrial fibrillation or atrial flutter lasting more than 1 hour on continuous electrocardiographic monitoring, requiring pharmacological or electrical cardioversion.

Contacts

Primary ContactNan Liu Director of the Center for Cardiac Intensive Care, MD, PhD
ln9102@126.com+8613370103573

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026