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

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Capital Medical University

Status

Not yet enrolling

Conditions

Cardiac Surgery Intensive Care Treatment
Hemodynamics

Treatments

Other: Blood Pressure Variability and Perfusion Index

Study type

Observational

Funder types

Other

Identifiers

NCT07316634
KS2025145

Details and patient eligibility

About

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.

Enrollment

1,200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

1,200 participants in 1 patient group

Adult Patients After Cardiac Surgery
Treatment:
Other: Blood Pressure Variability and Perfusion Index

Trial contacts and locations

0

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Central trial contact

Nan Liu Director of the Center for Cardiac Intensive Care, MD, PhD

Data sourced from clinicaltrials.gov

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