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

Sponsor
Kasr El Aini Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04238052
Collaborator
(none)
42
1
1.6
26.1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase

    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 Design

    Study Type:
    Observational
    Actual Enrollment :
    42 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    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
    Actual Study Start Date :
    Jan 23, 2020
    Actual Primary Completion Date :
    Mar 12, 2020
    Actual Study Completion Date :
    Mar 12, 2020

    Outcome Measures

    Primary Outcome Measures

    1. accuracy of MAP measurement at dependent arm for detectiong intraoperative hypotension at lateral position [up to 100 minutes]

      MAP below 70 mmHg

    Secondary Outcome Measures

    1. accuracy of MAP measurement at non-dependent arm for detectiong intraoperative hypotension at lateral position [5 minutes after settling in the lateral position, every 5 minutes for 100 minutes]

      MAP below 70 mmHg

    2. accuracy of SBP measurement at dependent arm for detectiong intraoperative hypotension at lateral position [5 minutes after settling in the lateral position, every 5 minutes for 100 minutes]

      SBP below 100 mmHg

    3. accuracy of SBP measurement at non-dependent arm for detecting intraoperative at lateral position [5 minutes after settling in the lateral position, every 5 minutes for 100 minutes]

      SBP below 100 mmHg

    4. correlation between NIBP measurement at dependent arm in relation to invasive blood at lateral position pressure [5 minutes after settling in the lateral position, every 5 minutes for 100 minutes]

      mmHg

    5. mean bias and agreement between NIBP measurement at dependent arm in relation to invasive blood at lateral position pressure [5 minutes after settling in the lateral position, every 5 minutes for 100 minutes]

      mmHg

    6. correlation between NIBP measurement at non-dependent arm in relation to invasive blood at lateral position pressure [5 minutes after settling in the lateral position, every 5 minutes for 100 minutes]

      mmHg

    7. mean bias and agreement between NIBP measurement at non-dependent arm in relation to invasive blood at lateral position pressure [5 minutes after settling in the lateral position, every 5 minutes for 100 minutes]

      mmHg

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 60 Years
    Sexes Eligible for Study:
    All
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Kasr Alaini Hospital Cairo Egypt 11562

    Sponsors and Collaborators

    • Kasr El Aini Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Maha Mostafa Ahmad, MD, Principal Investigator, Kasr El Aini Hospital
    ClinicalTrials.gov Identifier:
    NCT04238052
    Other Study ID Numbers:
    • MS-257-2019
    First Posted:
    Jan 23, 2020
    Last Update Posted:
    Mar 19, 2020
    Last Verified:
    Mar 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 19, 2020