Postoperative Complications Clinical Trial
— DECCEPOfficial title:
Delirium in Elderly Undergoing Cardiac Surgery and the Significance of CholinEsterase Activity Measured by Point of Care Method - a Prospective Observational Study
Verified date | April 2018 |
Source | RWTH Aachen University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to assess the association between the "point-of-care" (POC)
measured ChE activity (Acetylcholinesterase (ChE) + Buturylcholinesterase (ChE)) and
postoperative delirium in elderly patients undergoing cardiac surgery.
Furthermore the investigators aim to identify factors, which influence the baseline levels
and the time course of ChE activity.
Status | Completed |
Enrollment | 100 |
Est. completion date | November 2016 |
Est. primary completion date | May 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 65 Years and older |
Eligibility |
Inclusion Criteria: - Written informed consent - = 65 years of age - Scheduled to undergo elective cardiac surgery (coronary artery bypass graft (CABG), valve surgery, combined CABG-valve surgery) with the use of CPB - Both genders Exclusion Criteria: - Planned deep hypothermic arrest - Acute / emergency procedures - Surgery without extracorporeal circulation (ECC) - Patients with a history of pseudocholinesterase deficiency - Employees of the respective study centres - Illiteracy - Severe communication difficulties and severe vision or hearing problems - Patients legally unable to give written informed consent - non-fluency in German language - Severe psychiatric or neuropsychiatric disorders - MMSE < 24 points, short geriatric depression scale (GDS) = 10 points - Recent (<6 months) history of alcohol or drug abuse - The participation in a drug or device trial within the previous 30 days |
Country | Name | City | State |
---|---|---|---|
Germany | Department of Anesthesiology, University Hospital Aachen | Aachen | NRW |
Lead Sponsor | Collaborator |
---|---|
RWTH Aachen University |
Germany,
Arbel Y, Shenhar-Tsarfaty S, Waiskopf N, Finkelstein A, Halkin A, Revivo M, Berliner S, Herz I, Shapira I, Keren G, Soreq H, Banai S. Decline in serum cholinesterase activities predicts 2-year major adverse cardiac events. Mol Med. 2014 Feb 12;20:38-45. doi: 10.2119/molmed.2013.00139. — View Citation
Cerejeira J, Batista P, Nogueira V, Firmino H, Vaz-Serra A, Mukaetova-Ladinska EB. Low preoperative plasma cholinesterase activity as a risk marker of postoperative delirium in elderly patients. Age Ageing. 2011 Sep;40(5):621-6. doi: 10.1093/ageing/afr053. Epub 2011 May 15. — View Citation
Cerejeira J, Lagarto L, Mukaetova-Ladinska EB. The immunology of delirium. Neuroimmunomodulation. 2014;21(2-3):72-8. doi: 10.1159/000356526. Epub 2014 Feb 14. Review. — View Citation
Distelmaier K, Winter MP, Rützler K, Heinz G, Lang IM, Maurer G, Koinig H, Steinlechner B, Niessner A, Goliasch G. Serum butyrylcholinesterase predicts survival after extracorporeal membrane oxygenation after cardiovascular surgery. Crit Care. 2014 Jan 30;18(1):R24. doi: 10.1186/cc13711. — View Citation
Inouye SK, Westendorp RG, Saczynski JS. Delirium in elderly people. Lancet. 2014 Mar 8;383(9920):911-22. doi: 10.1016/S0140-6736(13)60688-1. Epub 2013 Aug 28. Review. — View Citation
Rudolph JL, Inouye SK, Jones RN, Yang FM, Fong TG, Levkoff SE, Marcantonio ER. Delirium: an independent predictor of functional decline after cardiac surgery. J Am Geriatr Soc. 2010 Apr;58(4):643-9. doi: 10.1111/j.1532-5415.2010.02762.x. Epub 2010 Mar 22. — View Citation
Smulter N, Lingehall HC, Gustafson Y, Olofsson B, Engström KG. Delirium after cardiac surgery: incidence and risk factors. Interact Cardiovasc Thorac Surg. 2013 Nov;17(5):790-6. doi: 10.1093/icvts/ivt323. Epub 2013 Jul 25. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Gender effect on delirium assessed by CAM-ICU/CAM | Analysis of the association of postoperative delirium until 5.POD respective discharge day and the gender of the patient | 5-45 days | |
Other | Gender effects on the peri-operative AChE and BuChE activity | Measurement of the AChE and BuChE activity until 3.-5.POD. Analysis of the association of the gender of the patient and the peri-operative time-course of the AChE and BuChE activity until the 3. respective 5.POD. | 5-45 days | |
Other | Postoperative bleeding | Measured 12 hours after surgery | 1 day | |
Primary | Acetylcholinesterase (AChE) and buturylcholinesterase (BuChE) activity | The perioperative AChE and BuChE activity will be assessed in the whole blood by a "point-of-care" measuring instrument (ChE check mobile ®) and the association to the incidence and duration of postoperative delirium will be determined. It will be assessed preoperative and maximum until the 5th postoperative day (POD), minimum until the 3.POD. | 5 days | |
Primary | Delirium | Postoperative delirium will be assessed preoperative and daily with the CAM / CAM-ICU test until the 5.POD and on the discharge day from hospital. The incidence of postoperative delirium will be associated with the perioperative AChE and BuChE time course. | 5-45 days | |
Secondary | Pre-existing patient related risk factors | Influence of pre-existing patient related risk factors ( demographic data, medical and surgical history assessed preoperative) on postoperative delirium and the AChE and BuChE activity. | 1 day | |
Secondary | Identification of anticholinergic concomitant medication according to the PRISCUS list | Number of participants with preoperative anticholinergic medication | 1 day | |
Secondary | Survey of treatment associated data | Survey of treatment associated data until discharge (organ dysfunctions, postoperative pain, ICU length of stay, hospital length of stay, duration of mechanical ventilation, readmission rate to ICU, operation time, surgery, anaesthesia, intraoperative and postoperative volume load, postoperative mortality, comorbidities) | 45 days | |
Secondary | Cognitive function | Assessment of the cognitive function preoperative and on 3.POD and at discharge,by mini mental state examination (MMSE) | 45 days | |
Secondary | Routine venous blood parameters | Correlation of AChE and BuChE activity and routine venous blood parameters (Hb, Platelets, Leucocytes, INR, PTT, liver-enzymes (AST, ALT, y-GT, total Bilirubin), Creatinine, BUN, Albumin, sodium and potassium) and the influence on postoperative delirium | 5 days | |
Secondary | Inflammatory markers | Correlation of AChE and BuChE activity to inflammatory markers in serum and the influence on postoperative delirium | 5 days | |
Secondary | Follow up measure of functional decline according to the IADL scale | Patients will be followed up by phone on the 30. and 180.POD. Association of AChE and BuChE activity and the functional decline on the 30. and 180.POD. The preoperative IADL scale will be compared to the data on the 30. and 180.POD to assess the functional decline | 180 days | |
Secondary | Follow up measure of mortality | Patients will be followed up by phone on the 30. and 180.POD. Determination of the association between the peri-operative AChE and BuChE activity and the mortality on the 30. and 180.POD | 180 days | |
Secondary | Follow up measure of the number of MACCE-events | Patients will be followed up by phone on the 30. and 180.POD. Association of AChE and BuChE activity and the postoperative major adverse cardiovascular and cerebral events (MACCE) on the 30. and 180.POD. The number of events will be assessed. | 180 days | |
Secondary | Health related quality of life | Health related quality of life measured by EuroQuol EQ-5D-5L test preoperative, on 30.POD and 180. POD | 180 days | |
Secondary | Instrumental activities of daily living | The Lawton Instrumental Activities of Daily Living (IADL) Scale measured preoperative, on 30.POD and 180. POD | 180 days |
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