The Influence of Preoperative Cardiopulmonary Capacity on the Perioperative Lactate Level

September 15, 2013 updated by: Armin Zagler, University of Witten/Herdecke

The Influence of Preoperative Cardiopulmonary Capacity Mesured in MET's (Metabolic Equivalents) on the Perioperative Lactate Level

The aim of this study is to identify if there exists a correlation between the preoperative cardiopulmonary capacity - measured in MET's - and the perioperative lactate serum level.

Study Overview

Detailed Description

The determination of the cardiopulmonary (c/p) capacity is very important for the evaluation of every patient undergoing surgery. The ability to climb at least two flight of stairs is seen to be an acceptable c/p capacity for surgery. There are several ways to evaluate the fitness of patients. A common method to estimate the cardiopulmonary capacity is defining patients through the MET's (metabolic equivalents) scale. MET's can be defined relatively easy through a simple questionnaire. Patients with a reduced c/p capacity have less than 4 MET's, patients with a relatively good c/p capacity have 4-10 MET's and patients with a excellent c/p capacity have more than 10 MET's.

The lactate level in blood serum is a common parameter to asses anaerobic metabolism in patients. A high lactate level correlates with higher mortality rates and outcome.

To yet it is not clear if there exists a correlation between the preoperative cardiopulmonary capacity measured in MET's and the perioperative lactate level. We hypothysed that patients with a reduced cardiopulmonary capacity are associated with higher perioperative lactate levels, as these group of patients compensate the stressors operation/anesthesia less than patients with a good c/p capacity.

Study Type

Observational

Enrollment (Actual)

1502

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • NRW
      • Wuppertal, NRW, Germany, 42283
        • Helios Klinikum Wuppertal

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All patients undergoing elective/urgent or emergency surgery

Description

Inclusion Criteria:

  • Age > 18 years

Exclusion Criteria:

  • Cardiac surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
lactate - venous blood gas analysis
Time Frame: venous lactate will be measured at anaesthesia induction and anesthesia termination - the average time frame is 2 hours
mmol/l
venous lactate will be measured at anaesthesia induction and anesthesia termination - the average time frame is 2 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
icu in hospital mortality
Time Frame: icu patients will be followed over their hospital stay over a maximum period of 6 months
icu patients will be followed over their hospital stay over a maximum period of 6 months
hemoglobin - venous blood gas analysis
Time Frame: hemoglobin will be measured at anaesthesia induction and anesthesia termination - the average time frame is 2 hours
g/dl
hemoglobin will be measured at anaesthesia induction and anesthesia termination - the average time frame is 2 hours
icu ventilation time
Time Frame: icu patients will be followed over their hospital stay over a maximum period of 6 months
hours/days
icu patients will be followed over their hospital stay over a maximum period of 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Gerhard Schneider, Prof., Dept. Anaesthesiology

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2013

Primary Completion (Actual)

April 1, 2013

Study Completion (Actual)

August 1, 2013

Study Registration Dates

First Submitted

February 8, 2013

First Submitted That Met QC Criteria

March 26, 2013

First Posted (Estimate)

March 27, 2013

Study Record Updates

Last Update Posted (Estimate)

September 17, 2013

Last Update Submitted That Met QC Criteria

September 15, 2013

Last Verified

September 1, 2013

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Lactate1

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.

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