Wrist NIBP During Elective Cesarean Delivery

Comparison of Arm and Forearm Blood Pressure During Elective Cesarean Delivery

Blood pressure is typically measured with a non-invasive cuff placed on the upper arm. This cuff cannot take accurate measurements when the patient's arm is moving. Anesthesia for a cesarean delivery frequently causes the patient to shiver and their arm to shake, and sometimes to the extent that blood pressure cannot be measured. A cuff placed on the wrist may be more effective when a patient is shivering because their lower arm moves less and can be more easily stabilized. We will be taking simultaneous blood pressure measurements both just before and during cesarean deliveries in order to compare blood pressure at the upper arm versus the wrist.

Study Overview

• Status: Completed
• Conditions: Wrist Blood Pressure Measurements; Anesthesia Resulting in Shivering

Detailed Description

Upper arm non-invasive blood pressure (NIBP) measurement is the most commonly accepted method of blood pressure (BP) monitoring. During a cesarean delivery it may be challenging to obtain an accurate measurement from the automated devices in over 50% of the attempts due to arm movement.1 Patients may voluntarily move their arm, but more often neuraxial (spinal, epidural, combined spinal-epidural) anesthesia is known to induce shivering that causes the patient's arm to shake.2 To eliminate the effect of movement of the upper arm, NIBP has been tested on the leg because it is immobilized during neuraxial anesthesia. However, studies monitoring NIBP on an ankle or a calf were unable to accurately detect changes (increase or decrease) in blood pressure in patients undergoing a cesarean delivery.3,4 It seems clinically reasonable that in the case of a shivering patient, the forearm, with less muscle mass, would shake less and could be stabilized more easily than the upper arm (stabilizing the forearm is easily done by holding the patient's hand with a light pressure on the arm rest). Therefore, positioning an NIBP cuff on the forearm (near the wrist) may be useful to obtain an accurate blood pressure measurement in shivering patients.

Previous studies have found that forearm BP overestimates blood pressure measured at the upper arm in a variety of clinical settings and patient populations under static (patient at rest, not submitted to an intervention that might alter BP) circumstances.5-8 It is unknown whether this overestimation is clinically relevant when blood pressure change occurs rapidly, such as during a cesarean delivery. During neuraxial anesthesia for cesarean delivery, it is important for the anesthesiologist to know both absolute values and clinically significant changes in blood pressure to determine their treatment. The detection of dynamic changes in blood pressure (as when the patient is submitted to an intervention that might alter BP per se, e.g. neuraxial anesthesia) has been studied in obstetric patients. Nevertheless, either due to the location where the BP cuff was placed4 (as on the lower limb with interference of the aorto-caval compression) or to the technology used to measure blood pressure,9 (the penaz technology was not consistent with oscillometric technology in a previous study) the forearm blood pressure was not comparable to upper arm blood pressure when measured using an oscillometric monitor.

This study will compare the upper arm (the current gold-standard) and the forearm NIBP measurements in patients undergoing an elective cesarean delivery under subarachnoid anesthesia. We hypothesize that the forearm systolic BP measurement values will be within 10% (lower or higher) of the systolic BP values measured in the upper arm at the same time-points

• Study Type: Observational
• Enrollment (Actual): 71

Contacts and Locations

Study Locations

• Canada
  • British Columbia
    • Vancouver, British Columbia, Canada, V6H 3N1
      • British Columbia's Women's Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 19 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

• Sampling Method: Non-Probability Sample

Study Population

Women having an elective cesarean delivery at BC Women's Hospital in Vancouver, British Columbia.

Description

Inclusion Criteria:

• Healthy (American Society of Anesthesiologist's (ASA) physical status I or II) patients
• Having an elective cesarean delivery under spinal or combined spinal epidural anesthesia
• ≥19 years old

Exclusion Criteria:

• Contra-indication to neuraxial anesthesia
• General anesthesia for any reason prior to delivery of the baby
• Use of the epidural component (epidural top-up) of combined spinal epidural anesthesia (prior to delivery of the baby)
• History of cardiovascular disease, e.g. hypertension (either essential or pregnancy-induced)
• A difference of more than 10% between both upper arms and forearms in mean blood pressure measurement prior to surgery (see below)
• BMI >35kg/m2 (it is more difficult to ensure the cuff size is correct in these obese patients)
• Inability to read and understand English for the purpose of informed consent

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort
Pregnant women; Pregnant women undergoing a cesarean section

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Compare trends in NIBP measurements between the upper arm and forearm	Measure NIBP at the upper arm and forearm simultaneously during surgery. NIBP cuffs will be on opposite arms.	30 minutes

Secondary Outcome Measures

Outcome Measure	Time Frame
To estimate the accuracy of blood pressure measured on the forearm	30 minutes

Collaborators and Investigators

• Sponsor: University of British Columbia
• Investigators: Principal Investigator: Simon Massey, MD, University of British Columbia, BC Women's Hospital

Study record dates

Study Major Dates

• Study Start: August 1, 2012
• Primary Completion (Actual): May 1, 2013
• Study Completion (Actual): May 1, 2013

Study Registration Dates

• First Submitted: August 29, 2012
• First Submitted That Met QC Criteria: August 29, 2012
• First Posted (Estimate): August 31, 2012

Study Record Updates

• Last Update Posted (Estimate): July 3, 2013
• Last Update Submitted That Met QC Criteria: July 2, 2013
• Last Verified: July 1, 2013

More Information

Terms related to this study

• Keywords: Blood pressure
• Other Study ID Numbers: H12-01797