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Perioperative Early Tiredness (Acute Fatigue) in Patients With Epithelial Ovarian Cancer

Completed
Conditions
Mitochondrial Dysfunction
Electrical Cardiometry
Perioperative Early Tiredness (Acute Fatigue)
Biosignals
Nutrition
Registration Number
NCT03131102
Lead Sponsor
Aarne Feldheiser
Brief Summary

In surgical patients early risk prediction of postoperative complications and organ dysfunctions is still an important clinical challenge whereas appropriate risk predictors are still missing. In this regard, fatigue is a complex phenomenon, is affected by many factors and has been shown to be associated with delayed return to normal activity after surgery. The investigators hypothesize that early tiredness (acute fatigue) assessed shortly after surgery is associated to postoperative complications and organ dysfunctions and might be used for risk stratification. Therefore, in this prospective, observational study the investigators introduce and evaluate a newly developed score to assess early fatigue during the perioperative period ("Acute Fatigue Score", AFS).

The AFS and the Identity-Consequence Fatigue Scala will be used to assess early fatigue and perioperative time courses and inter-rater-variability will be evaluated. The rating of these two fatigue scores will be evaluated regarding the association with hemodynamic, immunologic, endothelial, metabolic, gastrointestinal measures as well as organ dysfunction and complications after surgery.

Furthermore, hemodynamic, immunologic, endothelial, metabolic and gastrointestinal measures are investigated with respect to the intraoperative course and postoperative organ dysfunction and complications. In a subgroup of patients, patients will undergo specialized metabolic measures to investigate mitochondrial dysfunction during the perioperative period.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
30
Inclusion Criteria
  • Patients with epithelial ovarian cancer scheduled for cytoreductive surgery at the Department of Gynecology at Campus Virchow - Klinikum, Charité - University Berlin
  • Offered patient information and written informed consent
Exclusion Criteria
  • Patients aged less than 18 years
  • Persons without the capacity to consent
  • Inability of German language use
  • Lacking willingness to save and hand out data within the study
  • Accommodation in an institution due to an official or judicial order
  • (Unclear) history of alcohol or substances disabuse
  • Coworker of the Charité
  • Known Myopathy
  • Neurological or psychiatric disease at the beginning of hospitalization
  • CHF (congestive heart failure) according to (New York Heart Association) classification - NYHA class IV at the beginning of hospitalization
  • American Society of Anesthesiologists (ASA) classification greater than IV
  • Renal insufficiency (dependency of haemodialysis) at the beginning of hospitalization
  • Pulmonary oedema in thorax x-ray at the beginning of hospitalization
  • History of intracranial hemorrhage within one year before participation in the study
  • Conditions following venous thrombosis within the last three years before study inclusion
  • Known allergies or hypersensitivity on colloidal, starch or gelatine infusion solutions
  • Diabetes mellitus with signs of severe neuropathy
  • Known atrial fibrillation
  • Participation in an interventional clinical trial during the study period; exception: assignment to adjuvant therapy study during this study is allowed.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Acute Fatigue Score (AFS)1 hour after the end of anaesthesia

Rating of the AFS

Secondary Outcome Measures
NameTimeMethod
Hemodynamic variables and catecholamine administrationUp to the fifth postoperative day

Hemodynamic variables are assessed by the anesthesia monitor

Body temperatureUp to the first postoperative day

Body temperature will be assessed continuously and discontinuously

Immunologic, endothelial and hepatic markersUp to the fifth postoperative day

Parameters characterizing the time course of immunological (e.g. Interleukin-6) and endothelial (e.g. Intercellular Adhesion Molecule 1) and hepatic (e.g. cytokeratin-18) response will be determined

Acute Fatigue Score (AFS)Up to the fifth postoperative day, at hospital discharge (an average of two weeks) and before and after the first cycle of chemotherapy (an average of four to six weeks)

Perioperative time course of the ratings of AFS

Identity-Consequence Fatigue Scala (ICFS)Up to the fifth postoperative day, at hospital discharge (an average of two weeks) and before and after the first cycle of chemotherapy (an average of four to six weeks)

Previously published score to measure tiredness

Fluid balancesUp to the fifth postoperative day, at hospital discharge (an average of two weeks) and before, during and after the first cycle of chemotherapy (an average of four to six weeks)

The balances between all orally and intravenously administered fluids and all fluid losses

Organ dysfunctions and complicationsUp to the fifth postoperative day, at hospital discharge (an average of two weeks) and before, during and after the first cycle of chemotherapy (an average of four to six weeks)

Organ complications are classified according to Clavien-Dindo classification

Functional statusAt baseline, hospital discharge (expected average of 14 days) and before and after the first cycle of chemotherapy (an average of four to six weeks)

Measured by the Barthel activities of daily living (ADL) index and activities of daily living (IADL)

Intensive care unit length of stayParticipants will be followed up until intensive care unit discharge (an average of two days)

Time from admission to discharge from the intensive care unit

Inter-Rater Variability of Acute Fatigue Score (AFS)Up to the fifth postoperative day, at hospital discharge (an average of two weeks) and before and after the first cycle of chemotherapy (an average of four to six weeks)

The scores will be assessed by two observers and the variability determined

Hemodynamic shock indices calculated from Electrical Cardiometry (EC)Up to the fifth postoperative day, at hospital discharge (an average of two weeks) and before, during and after the first cycle of chemotherapy (an average of four to six weeks)

EC is a method of bioimpedance

Metabolomics/ProteomicsUp to the first postoperative day

Metabolomic, proteomic, immunological, endothelial and inflammatory markers obtained by intramuscular microdialysis

Mitochondrial respiratory chain activitiesUp to the first postoperative day

Respiratory chain activities are assessed in muscle biopsies using high-resolution respirometry

Blood coagulation markersUp to the fifth postoperative day

Parameters characterizing the humoral and cellular (thrombocytes) coagulation will be determined

Hemodynamic variables obtained by Electrical Cardiometry (EC)Up to the fifth postoperative day, at hospital discharge (an average of two weeks) and before, during and after the first cycle of chemotherapy (an average of four to six weeks)

EC is a method of bioimpedance

Blood lossUp to the fifth postoperative day

Perioperative blood loss characteristics

Hospital length of stayParticipants will be followed up until hospital discharge (expected average of 14 days)

Time from admission to discharge from the hospital

Heart rate variability, cardiorespiratory coupling, pulse wave velocity and new markers calculated from raw biosignalsUp to the fifth postoperative day, at hospital discharge (an average of two weeks) and before, during and after the first cycle of chemotherapy (an average of four to six weeks)

Bioelectrical signals to assess the interaction of the cardiac and pulmonary rhythms

Nutrition associated antibodies and deficiency states of vitamins and trace elementsUp to the fifth postoperative day

Biochemical parameters of nutrition states and immunological marker of alimentary components are determined

Microvascular functionUp to the fifth postoperative day and at hospital discharge (an average of two weeks)

Microvascular function is assessed by near-infrared spectroscopy (NIRS) combined with a vascular occlusion test (VOT)

Trial Locations

Locations (1)

Department of Anesthesiology and Intensive Care Medicine, Campus Charité Mitte and Campus Virchow Klinikum, Charité - University Medicine Berlin

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Berlin, Germany

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