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Avoidance of Delirium in Older Patients After Major Non-cardiac Surgery (ADOM)

Primary Purpose

Delirium

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
PulsioflexTM Monitoring
Sponsored by
Technical University of Munich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Delirium focused on measuring postoperative delirium, hemodynamic management, goal directed therapy

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 70 years
  • Risk of perioperative delirium (Marcantonio) ≥6

Exclusion Criteria:

  • Emergency surgery
  • Valvular disorders grad II or higher
  • History of major aortic surgery
  • Major aortic surgery
  • Repeated surgery (within 30 days before)
  • Neurosurgery

Sites / Locations

  • Klinik für Anästhesiologie Klinikum Rechts der Isar

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Group GDT

Group Co

Arm Description

Goal-directed Management according to pulse contour analysis (PulsioflexTM Monitoring)

Conventional fluid management

Outcomes

Primary Outcome Measures

Incidence of delirium until day 7 (CAM-Score and clinical diagnosis)
Delirium according to CAM-Score and clinical diagnosis

Secondary Outcome Measures

Factors defining delirium
Duration of delirium, total amount of haloperidol administered
Short-term cognitive impairment
Mini Mental State on day 7
Mortality
in-hospital mortality, mortality after one year
Influence on brain oxygen saturation
Influence of GDT on the frontal oxygen saturation of the brain assessed with Near-InfraRed-Spectroscopy (NIRS)-Monitoring
Intra- and postoperative Measurements
Time until discharge, total fluids and amount of catecholamines administered, incidence of overall postoperative complications

Full Information

First Posted
April 4, 2013
Last Updated
April 6, 2021
Sponsor
Technical University of Munich
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1. Study Identification

Unique Protocol Identification Number
NCT01827501
Brief Title
Avoidance of Delirium in Older Patients After Major Non-cardiac Surgery
Acronym
ADOM
Official Title
Can Perioperative Goal Directed Hemodynamic Management Reduce the Incidence of Delirium in Older Patients After Major Non-cardiac Surgery?
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
February 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Technical University of Munich

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is designed to compare the incidence of postoperative delirium in older patients after major non-cardiac surgery with different perioperative hemodynamic managements: a goal directed hemodynamic management group and a control group
Detailed Description
Delirium is a common postoperative complication in the elderly. The incidence depends on several factors like the comorbidities of the patient and the type of surgery. Mortality is almost twofold increased after two years for patients suffering from delirium after surgery. Different studies showed that with a multimodal strategy it was possible to reduce the risk of delirium. As several different organ systems are involved in the development of delirium the patient's hemodynamic state seems to be important and is a target point of intervention. Also sufficient perfusion and oxygen delivery is essential in order to avoid impairment of the brain. Recent studies showed that goal directed hemodynamic management can reduce all kind of postoperative complications and improve outcome. However, whether the use of goal-directed hemodynamic management also improves the neurological outcome and reduces the rates of postoperative delirium has not been studied yet. Aim of this study is to investigate the impact of goal directed hemodynamic management using pulse contour analysis on the incidence of delirium in older patients undergoing non-cardiac surgery, presenting with an intermediate to high risk for delirium. This risk will be assessed preoperatively using a score suggested by Marcantonio. Patients will be randomized in one of two groups, the goal-directed therapy group and the control group. In the goal-directed therapy (GDT) group hemodynamic management is performed according to an established algorithm obtained by pulse contour analysis. To prove our theory that goal-directed therapy influences the brain by increasing oxygen supply we will use near infrared spectroscopy, which is safe and non-invasive, in our patients. The hemodynamic management is continued in the recovery room or at the intensive care unit according to the mentioned algorithm. The intervention will be terminated as soon as patients fulfil the standard criteria for discharge from recovery room or intensive care. In the control group hemodynamic management is performed according to heart rate and blood pressure without using extended monitoring. As the actual incidence has a significant impact on the number needed per group, we are going to perform an interims analysis after 100 included patients according to the O'Brian-Fleming technique. Is the difference of delirium between the two groups significant with an α < 0,002 the study will be finished. Otherwise, the sample size needed per group will be determined assuming an α = 0,048, a two-tailed test and a power of 80%. UPDATE 19-10-2016: The interims-analysis of incidences after 100 patients revealed, that 86 patients per group will be needed (α = 0,048, power 80%).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium
Keywords
postoperative delirium, hemodynamic management, goal directed therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
172 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group GDT
Arm Type
Experimental
Arm Description
Goal-directed Management according to pulse contour analysis (PulsioflexTM Monitoring)
Arm Title
Group Co
Arm Type
No Intervention
Arm Description
Conventional fluid management
Intervention Type
Device
Intervention Name(s)
PulsioflexTM Monitoring
Intervention Description
Fluid and catecholamine management according to PulsioflexTM measurements
Primary Outcome Measure Information:
Title
Incidence of delirium until day 7 (CAM-Score and clinical diagnosis)
Description
Delirium according to CAM-Score and clinical diagnosis
Time Frame
Before induction of anesthesia until 7 days after surgery
Secondary Outcome Measure Information:
Title
Factors defining delirium
Description
Duration of delirium, total amount of haloperidol administered
Time Frame
7 days
Title
Short-term cognitive impairment
Description
Mini Mental State on day 7
Time Frame
7 days
Title
Mortality
Description
in-hospital mortality, mortality after one year
Time Frame
1 year
Title
Influence on brain oxygen saturation
Description
Influence of GDT on the frontal oxygen saturation of the brain assessed with Near-InfraRed-Spectroscopy (NIRS)-Monitoring
Time Frame
until discharge from recovery room/ICU
Title
Intra- and postoperative Measurements
Description
Time until discharge, total fluids and amount of catecholamines administered, incidence of overall postoperative complications
Time Frame
Until discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 70 years Risk of perioperative delirium (Marcantonio) ≥6 Exclusion Criteria: Emergency surgery Valvular disorders grad II or higher History of major aortic surgery Major aortic surgery Repeated surgery (within 30 days before) Neurosurgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bettina Jungwirth, MD
Organizational Affiliation
Klinik für Anaesthesiologie Technische Universität München
Official's Role
Principal Investigator
Facility Information:
Facility Name
Klinik für Anästhesiologie Klinikum Rechts der Isar
City
Munich
ZIP/Postal Code
81675
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22669559
Citation
Marcantonio ER. Postoperative delirium: a 76-year-old woman with delirium following surgery. JAMA. 2012 Jul 4;308(1):73-81. doi: 10.1001/jama.2012.6857.
Results Reference
background
PubMed Identifier
35935775
Citation
Fuest KE, Servatius A, Ulm B, Schaller SJ, Jungwirth B, Blobner M, Schmid S. Perioperative Hemodynamic Optimization in Patients at Risk for Delirium - A Randomized-Controlled Trial. Front Med (Lausanne). 2022 Jul 13;9:893459. doi: 10.3389/fmed.2022.893459. eCollection 2022.
Results Reference
derived

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Avoidance of Delirium in Older Patients After Major Non-cardiac Surgery

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