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Anesthesia Technique and Outcomes in Mechanical Thrombectomy for Acute Ischemic Stroke

Comparison of General Anesthesia and Sedoanalgesia on Mortality and Neurological Outcomes in Patients Undergoing Mechanical Thrombectomy for Acute Ischemic Stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07422649
Enrollment
500
Registered
2026-02-20
Start date
2026-04-01
Completion date
2026-04-30
Last updated
2026-04-03

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

Conditions

Acute Ischemic Stroke

Keywords

Acute Ischemic Stroke, Mechanical Thrombectomy, General Anesthesia, Sedoanalgesia

Brief summary

This retrospective cohort study examined clinical outcomes in patients who underwent mechanical thrombectomy for acute ischemic stroke under general anesthesia or sedoanalgesia. Patient data from 2014 to 2018 were obtained from hospital medical records. Mortality and neurological outcomes were compared between anesthesia groups.

Detailed description

This retrospective observational cohort study was conducted at the University of Health Sciences Bakirkoy Dr. Sadi Konuk Training and Research Hospital. Medical records of patients who underwent mechanical thrombectomy for acute ischemic stroke between 2014 and 2018 were reviewed. Patients who received mechanical thrombectomy within 6 hours of symptom onset and achieved a Thrombolysis in Cerebral Infarction (TICI) reperfusion grade of 2a, 2b, or 3 were included. Patients with TICI grades of 0 or 1, those younger than 18 years, patients with an APACHE II score ≥25, a Glasgow Coma Scale score \<10, those requiring endotracheal intubation before the procedure, or patients discharged from the procedure intubated to the intensive care unit were excluded. Based on anesthesia records, patients were classified into two cohorts: those who underwent the procedure under general anesthesia and those managed with sedoanalgesia. No assignment to anesthesia technique was performed as part of the study, and anesthesia management was determined according to routine clinical practice. Demographic characteristics, medical history, radiological findings, procedural details, and perioperative variables were extracted from hospital records. Neurological status was assessed using the National Institutes of Health Stroke Scale (NIHSS) at 4 and 24 hours after the procedure, and functional outcome was evaluated using the modified Rankin Scale during hospitalization and at 3 months after thrombectomy. Intraoperative bispectral index (BIS) values and cerebral oxygenation measured by near-infrared spectroscopy (NIRS) were recorded when available. Safety outcomes including peri-procedural hemodynamic instability, vasopressor or antihypertensive use, need for pacing, and intensive care unit (ICU) length of stay will be evaluated. Neurological outcomes will be assessed longitudinally using NIHSS at baseline, 4 hours, 24 hours, and modified Rankin Scale (mRS/TICI) immediately after the procedure and at 3 months. The primary outcome of the study was all-cause mortality. Secondary outcomes included neurological and functional outcomes, perioperative variables, intensive care unit length of stay, and procedure-related complications. Comparisons between anesthesia cohorts were performed using routinely collected clinical data. Postoperative delirium occurring during the first 7 days after the procedure was evaluated as a secondary safety outcome when documented in the medical records

Interventions

OTHERGeneral Anesthesia

Patients who underwent mechanical thrombectomy under general anesthesia, based on anesthesia records.

Patients who underwent mechanical thrombectomy under sedoanalgesia, based on anesthesia records.

Sponsors

Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
Lead SponsorOTHER
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
CollaboratorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years * Acute ischemic stroke due to large vessel occlusion (MCA M1) * Mechanical thrombectomy performed within 6 hours of symptom onset * Pre-procedural TICI score 0-1

Exclusion criteria

* Age ≥100 years * APACHE II score of 25 or higher * Glasgow Coma Scale score below 10 * Requirement for endotracheal intubation before the procedure * Patients discharged from the procedure to the intensive care unit while intubated * Time from symptom onset to procedure exceeding 6 hours

Design outcomes

Primary

MeasureTime frameDescription
All-Cause MortalityDuring index hospitalization and at 3 months post-procedureComparison of all-cause mortality between patients undergoing mechanical thrombectomy under general anesthesia and sedoanalgesia.

Secondary

MeasureTime frameDescription
NIHSS ScoreBaseline, 4 hours, 24 hours post-procedureThe National Institutes of Health Stroke Scale (NIHSS) is used to quantify stroke severity (score range 0-42; higher scores indicate more severe stroke)
Modified Rankin Scale (mRS)Immediately after completion of the angiographic procedure and at 3 months after the initial thrombectomyThe modified Rankin Scale (mRS) is a global functional outcome measure used after stroke to categorize the level of functional independence.
TICI Reperfusion GradeImmediately after completion of the angiographic procedure and at 3 months after the initial thrombectomy.The Thrombolysis in Cerebral Infarction (TICI) grading system is used after endovascular revascularization to describe angiographic reperfusion (e.g., 0-3; higher grades indicate better reperfusion)
Near-Infrared Spectroscopy (NIRS) ValuesDuring index hospitalization and at 3 months post-procedureRegional cerebral oxygen saturation was monitored using near-infrared spectroscopy (NIRS) during the procedure and throughout the early postoperative period.
Bispectral Index (BIS) ValuesDuring the procedureDepth of anesthesia was monitored using bispectral index (BIS) values recorded during the procedure.
Procedure DurationDuring the procedureTotal duration of the mechanical thrombectomy procedure.
Time From Symptom Onset to ProcedureAt the time of the procedureElapsed time between symptom onset and initiation of mechanical thrombectomy.
ICU Length of StayThrough study completion, an average of 3 monthsDuration of stay in the intensive care unit following the procedure
Hemodynamic ParametersFrom procedure until 3 months post-procedureSystolic and diastolic blood pressure values recorded during the perioperative period
Procedure-Related ComplicationsDuring hospitalizationOccurrence of neurological or procedure-related complications during hospitalization
Postoperative deliriumWithin 30 days after procedureIncidence of postoperative delirium during the first 3 postoperative months
Postoperative demansWithin 30 days after procedureIncidence of postoperative delirium during the first 3 postoperative months

Countries

Turkey (Türkiye)

Contacts

CONTACTFatma Acil, M.D.
acilfatma@gmail.com+905337225225
CONTACTBedih Balkan, Assoc.Prof.
bedihbalkan21@gmail.com+905336195735

Outcome results

None listed

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