- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05425147
Correlation Between Perioperative Autonomic Function and Post-induction Hypotension in Elderly Patients
Correlation Between Perioperative Autonomic Function and Adverse Events Such as Post-induction Hypotension in Elderly Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
With the deepening of the aging population, the number of elderly patients undergoing surgery is also increasing. These elderly patients have a declining physiological reserve and face challenges in anesthesia management: studies have shown that elderly patients are at high risk of intraoperative adverse events and postoperative complications. Post-induction hypotension (PIH) refers to the hypotension that occurs between anesthesia induction and skin incision. The current diagnostic criteria have not been fully unified. Patients with intraoperative PIH have a higher risk of postoperative death and damage to vital organs such as the heart and kidneys, and have a poor prognosis. Elderly patients are a high-risk group for PIH. Therefore, it is of great meaning to quantify the risk factors of PIH in elderly patients.
Cardiovascular autonomic function may play an essential role in intraoperative blood pressure regulation. The pressure sensor of the cardiovascular system sends the blood pressure signal to the central nervous system, and regulates the blood pressure to an appropriate level through a compensatory reflex (i.e., baroreflex). Baroreflex function can be quantified by observing the R-R interval response to an arterial blood pressure change and the results are expressed as baroreflex sensitivity (BRS). In addition to BRS, heart rate variability (HRV) can also be used to assess cardiovascular autonomic function. HRV is a promising quantitative marker of autonomic activity, which includes the time domain and frequency domain analysis of R-R interval rhythm.
Some studies have explored the relationship between preoperative cardiovascular autonomic function and PIH. However, these studies did not assess preoperative volume status, and they did not measure BRS, which is probably more connected with baroreflex.
We hypothesized that the decreased baroreflex sensitivity at baseline in elderly patients may contribute to the development of PIH. To explore the effect of preoperative cardiovascular autonomic modulation in PIH in elderly patients, we are going to measure preoperative BRS and HRV in those who were about to undergo general anesthesia surgery.
We are conducting a single-center, prospective cohort study. Elderly patients (over 65 years of age) who are going to have elective surgery under general anesthesia will be recruited and will have BRS and HRV measurements taken for approximately 20 minutes, one day before surgery and on the day of surgery. We use LiDCO rapid to conduct non-invasive pulse and beat-to-beat blood pressure monitoring. In addition to spontaneous BRS and HRV assessment, the patients will be instructed to perform round-lip breathing at 0.1 Hz for 1 minute to gain more information about BRS and HRV through respiratory sinus arrhythmia (RSA).
The primary outcome will be PIH. Secondary outcomes included: early intraoperative hypotension, postoperative complications, and 30-day postoperative mortality. Anesthesia induction medications and intraoperative monitoring data will be recorded. The intraoperative monitoring meets the standards of basic physiologic monitors recommended by American Society of Anesthesiologists (ASA). We will use Clavien-Dindo classification to describe postoperative complications. Patients will be followed up during hospitalization and 30 days after the surgery by telephone.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
-
Beijing, China, 100730
- Recruiting
- Peking Union Medical College Hospital
-
Contact:
- Quexuan Cui, M.D.
- Phone Number: 8610-69156114
- Email: cuiquexuan@pumch.cn
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age ≥ 65 years old;
- Elective non-cardiac surgery;
- ASA Class I-III;
- General anesthesia;
- Use a tracheal tube as an airway management tool;
- Patients and their families can understand the research protocol and are willing to participate in this research
Exclusion Criteria:
- Severe vascular disease;
- Secondary hypertension;
- Parkinson's disease;
- Cannot measure upper extremity blood pressure for various reasons;
- Arrhythmias such as atrial fibrillation cannot perform HRV measurement;
- Mentally abnormal and unable to cooperate
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Post-induction hypotension group
Post-induction hypotension is defined as systolic blood pressure (SBP) <90 mmHg, mean arterial pressure (MAP) <65 mmHg, or a decrease of more than 30% of baseline within 20 minutes after induction or before incision.
|
Patients will have BRS and HRV measurements taken for approximately 20 minutes, one day before surgery and on the day of surgery.
We use LiDCO rapid to conduct non-invasive pulse and beat-to-beat blood pressure monitoring.
|
|
Stable blood pressure group
All enrolled elderly patients will undergo surgery under general anesthesia after preoperative monitoring.
Those patients whose blood pressure is relatively stable after induction and does not meet the PIH criteria is classified as the stable blood pressure group.
|
Patients will have BRS and HRV measurements taken for approximately 20 minutes, one day before surgery and on the day of surgery.
We use LiDCO rapid to conduct non-invasive pulse and beat-to-beat blood pressure monitoring.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Post-induction hypotension
Time Frame: within 20 minutes after induction or before incision
|
Systolic blood pressure (SBP) <90 mmHg, mean arterial pressure (MAP) <65 mmHg, or a decrease of more than 30% of baseline
|
within 20 minutes after induction or before incision
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Early intraoperative hypotension
Time Frame: within 30 minutes after incision
|
Systolic blood pressure (SBP) <90 mmHg, mean arterial pressure (MAP) <65 mmHg, or a decrease of more than 30% of baseline
|
within 30 minutes after incision
|
|
postoperative complications
Time Frame: 30 days after the surgery
|
postoperative complications (Clavien-Dindo classification)
|
30 days after the surgery
|
|
mortality
Time Frame: 30 days after the surgery
|
death
|
30 days after the surgery
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Heart rate variability. Standards of measurement, physiological interpretation, and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Eur Heart J. 1996 Mar;17(3):354-81. No abstract available.
- Ziemssen T, Siepmann T. The Investigation of the Cardiovascular and Sudomotor Autonomic Nervous System-A Review. Front Neurol. 2019 Feb 12;10:53. doi: 10.3389/fneur.2019.00053. eCollection 2019.
- Padley JR, Ben-Menachem E. Low pre-operative heart rate variability and complexity are associated with hypotension after anesthesia induction in major abdominal surgery. J Clin Monit Comput. 2018 Apr;32(2):245-252. doi: 10.1007/s10877-017-0012-4. Epub 2017 Mar 14.
- La Rovere MT, Pinna GD, Raczak G. Baroreflex sensitivity: measurement and clinical implications. Ann Noninvasive Electrocardiol. 2008 Apr;13(2):191-207. doi: 10.1111/j.1542-474X.2008.00219.x.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PUMCHanesthesia-elderly
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Intraoperative Hypotension
-
University of Hamburg-EppendorfRecruitingIntraoperative HypotensionGermany
-
National and Kapodistrian University of AthensAttikon HospitalRecruiting
-
Tampere University Hospitalgeneral electric healthcare FinlandCompletedIntraoperative Complications | Intraoperative Hypotension | Intraoperative HypertensionFinland
-
Beijing Tsinghua Chang Gung HospitalPeking University People's HospitalNot yet recruitingHemodynamic Instability | Intraoperative HypotensionChina
-
Lanyue ZhuNot yet recruitingIntraoperative Hypotension | Postoperative Acute Kidney InjuryChina
-
Academisch Medisch Centrum - Universiteit van Amsterdam...Edwards LifesciencesCompletedHypotension | Intraoperative Hypotension | Postoperative HypotensionNetherlands
-
Fondazione IRCCS Policlinico San Matteo di PaviaActive, not recruiting
-
National Taiwan University HospitalNot yet recruitingthe Severity and Duration of Intraoperative Hypotension
-
John Paul II Hospital, KrakowRecruiting
-
Seoul National University HospitalRecruiting
Clinical Trials on Perioperative autonomic function assessment
-
Vanderbilt University Medical CenterTerminatedComplex Regional Pain SyndromeUnited States
-
Wuerzburg University HospitalCompletedPneumothorax | Respiratory Insufficiency | Pleural Effusion | Atelectasis | Pulmonary Infection | Bronchospasm | Aspiration PneumonitisGermany
-
Wuerzburg University HospitalCompletedRespiratory Insufficiency | Atelectasis | Pulmonary Infection | Bronchospasm | Aspiration PneumonitisGermany
-
Ankara UniversityCompletedPostoperative Cognitive Dysfunction | Delirium, PostoperativeTurkey (Türkiye)
-
Aydin Adnan Menderes UniversityDr. Behcet Uz Children's HospitalCompletedPostoperative Pain | Preoperative Anxiety | Urogenital Diseases | Emergence Delirium in Pediatric AnesthesiaTurkey (Türkiye)
-
Hospital Universitario La FeUnknown
-
Aarhus University HospitalOdense University Hospital; University of Aarhus; Aalborg University HospitalRecruitingBladder CancerDenmark
-
University Hospital OlomoucRecruitingHeart Failure | Chronic Obstructive Pulmonary DiseaseCzechia
-
University of New MexicoNational Cancer Institute (NCI)Completed
-
National Taiwan University HospitalNot yet recruitingLocally Advanced or Metastatic Urothelial CarcinomaTaiwan