Assessing the Ability of Non-invasive Blood Pressure Measurement in Both Arm for Detecting Hypotension in the Lateral Position

March 17, 2020 updated by: Maha Mostafa Ahmad, MD, Kasr El Aini Hospital

Evaluation of the Ability of Non-invasive Blood Pressure Measurement in the Dependent and Non-dependent Upper Extremities for Detecting Intra-operative Hypotension in the Lateral Position

Intra-operative hypotension is linked to increased postoperative morbidity and mortality. Intra-operative MAP below 60-70 mmHg or SBP below 100 mmHg increase the risk of post operative myocardial injury, acute kidney injury and death. accurate measurement of blood pressure is fundamental in proper mangement of intraperative hypotension.

Measurement of arterial blood pressure through an arterial catheter is restricted to patients with major, rapid changes in blood pressure in the operating room as well as the intensive care units. Among non-invasive blood pressure (NIBP) monitors, oscillometric blood pressure measuring technology is considered the standard and the most widely used method in medical practice. In oscillometric blood pressure monitor, a pressure transducer located in the cuff senses the maximal arterial oscillation, which represents the mean arterial pressure, and according to the device's algorithm the systolic and diastolic blood pressure (SBP and DBP) will be calculated.

The upper arm is the standard location of application of the blood pressure cuff as it is aligned with the heart level regardless the patient position. Many surgical procedures, sometimes major, are conducted in the lateral position; during these operations, the choice of the side for application of the NIBP cuff is a challenging decision with no clear recommendations. The non-dependent upper limb is claimed to be inaccurate measurement site because the cuff position is above the level of the heart. While, the dependent upper limb might be affected by compression of the axilla and the upper arm. No data, to the best of our knowledge are available for the accuracy of NIBP in both upper limbs in the lateral position using the invasive arterial blood pressure (IBP) as a reference for detecting intraoperative hypotension.

Study Overview

Status

Completed

Detailed Description

Preoperatively, the upper limb circumference will be measured at the mid arm, and the NIBP cuff size will be selected according to the recommendations of American Heart Association (cuff length and width will be 80% and 40% of arm circumference respectively) Upon arrival to the operating room, a non-invasive blood pressure (NIBP) reading will be obtained in both upper limbs in supine position. Patients with difference of 10 mmHg or above between both limbs will be excluded from the study.

Induction of general anesthesia will be achieved by administration of 2 mg/kg propofol, 2 mcg/kg fentanyl and 0.5 mg/kg atracurium. A 20 G radial arterial catheter will be inserted in the upper limb which is planned to be dependent. The arterial catheter will be connected to a pressure transducer at the level of the heart. Supine IBP reading will be recorded 5-minutes after intubation of the trachea in the supine position with simultaneous NIBP in both upper limbs at 3-minutes intervals. Five-minutes after settling in the lateral position, NIBP will be obtained alternating between the dependent and non-dependent limbs at 5-minutes intervals till the end of the operation or till reaching a maximum of 10 readings from each side.

The reading of the IBP will be obtained from the contralateral upper limb during inflation of the cuff of the NIBP. Whilst, the reading of the IBP will be obtained from the same upper limb just before the inflation of the cuff of the NIBP

Study Type

Observational

Enrollment (Actual)

42

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

      • Cairo, Egypt, 11562
        • Kasr Alaini hospital

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 to 60 years (Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

adult patients (18-60 years), American Society of Anesthesiologist - Physical Status I-II, scheduled for elective non-cardiac surgery under general anesthesia and invasive blood pressure monitoring is part of their intraoperative management

Description

Inclusion Criteria:

  • adult patients (18-60 years)
  • American Society of Anesthesiologist - Physical Status I-II,
  • scheduled for elective non-cardiac surgery under general anesthesia and invasive blood pressure monitoring is part of their intraoperative management

Exclusion Criteria:

Patients with any of the following morbidities:

  • peripheral vascular diseases,
  • upper limb operations,
  • upper limb scars,
  • upper limb deep venous thrombosis, and
  • arrhythmias

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
accuracy of MAP measurement at dependent arm for detectiong intraoperative hypotension at lateral position
Time Frame: up to 100 minutes
MAP below 70 mmHg
up to 100 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
accuracy of MAP measurement at non-dependent arm for detectiong intraoperative hypotension at lateral position
Time Frame: 5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
MAP below 70 mmHg
5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
accuracy of SBP measurement at dependent arm for detectiong intraoperative hypotension at lateral position
Time Frame: 5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
SBP below 100 mmHg
5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
accuracy of SBP measurement at non-dependent arm for detecting intraoperative at lateral position
Time Frame: 5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
SBP below 100 mmHg
5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
correlation between NIBP measurement at dependent arm in relation to invasive blood at lateral position pressure
Time Frame: 5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
mmHg
5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
mean bias and agreement between NIBP measurement at dependent arm in relation to invasive blood at lateral position pressure
Time Frame: 5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
mmHg
5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
correlation between NIBP measurement at non-dependent arm in relation to invasive blood at lateral position pressure
Time Frame: 5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
mmHg
5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
mean bias and agreement between NIBP measurement at non-dependent arm in relation to invasive blood at lateral position pressure
Time Frame: 5 minutes after settling in the lateral position, every 5 minutes for 100 minutes
mmHg
5 minutes after settling in the lateral position, every 5 minutes for 100 minutes

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (Actual)

January 23, 2020

Primary Completion (Actual)

March 12, 2020

Study Completion (Actual)

March 12, 2020

Study Registration Dates

First Submitted

January 19, 2020

First Submitted That Met QC Criteria

January 22, 2020

First Posted (Actual)

January 23, 2020

Study Record Updates

Last Update Posted (Actual)

March 19, 2020

Last Update Submitted That Met QC Criteria

March 17, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • MS-257-2019

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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