Protocol - Blood Pressure (Adult/Primary)
Protocol Name from Source:
The Expert Review Panel has not reviewed this measure yet.
A measure to assess a respondent's systolic and diastolic blood pressure, which is used to determine high blood pressure (hypertension). Assessment must also include measures for personal history of high blood pressure and a history of medication usage.
1. Has a doctor or nurse ever said that you have:
High blood pressure or hypertension?
 1 No
 2 Yes
 8 Not Sure
At what age were you first told this? __ __
FOR WOMEN: Was this during pregnancy only?
 1 No
 2 Yes
2. Have you ever taken medication for hypertension/high blood pressure?
 0 no
 1 yes, now
 2 yes, not now
 9 unknown
If yes, then…
At what age did you begin taking medicine for this? __ __
 99 unknown
3. BLOOD PRESSURE METHODS
This protocol, which was taken from the Coronary Artery Risk Development in Young Adults (CARDIA) Study, is written for use with the Omron® HEM907XL automated BP monitor. Special attention must be placed on assessment and maintenance of the instrument's accuracy as per the manual that accompanies the instrument.
The design and operation of the Omron® HEM907XL are based upon the combined principles of compression of the brachial artery under an elastic, inflatable cuff and estimation of the systolic and diastolic BP levels by oscillimetric methods. The technician should place the correct size cuff on the participant's arm, set the machine to automatic, set the mode button to single, and push the start button on the monitor, then wait for the output. All readings are to be recorded to the nearest digit.
3.1. Measurement Equipment
The following equipment will be required for BP and pulse measurement:
a. One Omron® HEM907XL automated BP monitor.
b. BP cuffs in four sizes: S, M, L, XL
c. One standard clinical mercury sphygmomanometer*
d. One clinical thigh cuff*
e. One Gulick II tape (or Gulick II Plus)
f. A chair with arm support for BP measurement, or a chair and table (table must provide for a comfortable resting posture of the arm with the cubital fossa at the level of the 4th intercostal space at heart level)
g. Form for recording BP and pulse
h. One black pen (marking on skin) and one No. 2 pencil (completing the form)
* used for arms >50 cm in circumference
3.2. Cuff Size Determination
The proper cuff size must be used to avoid under- or over-estimation of BP. Cuff size refers to the cuff's bladder, not the cloth. A copy of the chart below should be attached to the sphygmomanometer for easy reference. In addition, the cuffs must be HEM907 XL-compatible.
a. Cuff Size Indicated by Measured Arm Circumference
[[cardio_003_image002.jpg|Cuff Size Indicated by Measured Arm Circumference]]
b. Measurement of arm circumference. The participant should remove his/her upper garment, or clear the upper arm area so that an unencumbered measurement may be made. The technician should:
i. Have the participant stand, with the right arm hanging and bending the elbow so that the forearm is horizontal (parallel) to the floor.
ii. Measure arm length from the acromion (bony protuberance at the shoulder) to the olecranon (tip of the elbow), using the Gulick II anthropometric tape.
iii. Mark the midpoint on the dorsal surface of the arm.
iv. Have the participant relax arm along side of the body.
v. Draw the tape snugly around the arm at the midpoint mark.
NOTE: Tape should be horizontal and should not indent the skin.
vi. Noting the arm circumference indicated by the tape, use the criteria above for determining cuff size.
3.3. Wrapping the Blood Pressure Cuff Around the Arm
The technician should:
a. Ensure the participant is seated, legs uncrossed, in a quiet room, with the elbow and forearm resting comfortably on the armrest of the BP measurement chair (or table), with the palm of the hand turned upward. The area to which the cuff is to be applied must be bare (free of clothing).
b. Locate the brachial artery by palpation and mark the skin with a small dot, using a black pen. (The brachial artery is usually found just medial and superior to the cubital fossa, posterior to the biceps muscle and slightly toward the body.) For brachial artery palpation, fingertips or thumb may be used (see figure below).
c. Place the appropriate cuff around the upper right arm so that:
i. The midpoint of the length of the bladder lies over the brachial artery.
ii. The cubital fossa is at heart level.
NOTE: The midpoint of the length of the bladder should be confirmed by folding the bladder in two. The marking on the cuff should not be trusted.
d. Place the lower edge of the cuff, with its tubing connections, about 1 inch above the natural crease across the inner aspect of the elbow (the cubital fossa).
e. Wrap the cuff snugly about the arm, with the palm of the participant's hand turned upward, making sure the long edges of the cuff lie on top of each other as the cuff is wrapped around.
f. Secure the wrapped cuff firmly by applying pressure to the locking fabric fastener over the area where it is applied to the cuff.
NOTE: The cuff should not be wrapped too tightly around the arm.
NOTE: If a thigh cuff is needed, the standard mercury sphygmomanometer is used to measure the BP systolic and diastolic pressures at the disappearance of Korotkoff sounds.
3.4. Setting the Mode and P-Set
The technician should:
a. Check that the AC adaptor is attached to the monitor and plug into electrical outlet.
b. Turn the ON/OFF button to ON.
c. Set the MODE selector to SINGLE.
d. Set the P-SET (inflation level) knob to AUTO.
e. Connect the air:
i. For cuff sizes small, medium and large, connect the air tube to the main unit by attaching the air plug to the base of the air connector.
ii. The extra large cuff has an air plug already connected. Attach this to the base of the monitor at the air connector.
3.5. Taking the First Blood Pressure Measurement
The technician should:
a. Have the participant sit quietly for a period of five minutes before the first BP is taken.
b. Push the START button on the monitor and wait for the output.
c. Record the systolic and diastolic BPs.
3.6. Taking the Second and Third Blood Pressure Measurements
The technician should:
a. Hold the participant's arm vertical (without fist-clenching) for a full five seconds between each measurement
b. Wait 25 to 30 seconds between each measurement.
c. Repeat the steps described above to obtain the second and third BPs.
d. Record the systolic and diastolic BP.
Note: Omron® IntelliSense™ Blood Pressure Monitor Model HEM907XL is a registered trademark of OMRON Corporation
Hypertension in adults aged 18 years and older is defined by recorded blood pressures at or above an average of 140 mmHg systolic or 90 mmHg diastolic on two or more seated blood pressures, measured properly with well maintained equipment, at two or more visits to the office or clinic, or the prescription of one or more antihypertensive drugs for the purpose of blood pressure control. A diagnosis of prehypertension may also be used for similarly measured blood pressures with systolic pressures 120-139 mmHg or diastolic pressures of 80-89 mmHg when antihypertensive treatments are not taken.
This chart provides current diagnostic criteria as of August 2009.
Personnel and Training Required
Trained and certified technicians to take blood pressures.
One Omron® HEM907XL automated blood pressure (BP) monitor, BP cuffs in four sizes: S, M, L, XL; one standard clinical mercury sphygmomanometer*; one clinical thigh cuff*; one Gulick II tape (or Gulick II Plus); a chair with arm support for BP measurement, or a chair and table (table must provide for a comfortable resting posture of the arm with the cubital fossa at the level of the 4th intercostal space at heart level).
*Used for arms >50 cm in circumference
Researchers should ensure that the equipment they use has been validated and that they follow the manufacturer's guidelines for administration and calibration. The three most widely used validation protocols are the British Hypertension Society (BHS) Protocol; the Association for the Advancement of Medical Instrumentation (AAMI) Standard; and, more recently, the International Protocol of the European Society of Hypertension (IP).
Note: Manufacturers of blood pressure equipment frequently make improvements and update both their equipment and software with the latest technological advances. The recommended equipment for this protocol in PhenX is current as of July 2009. Please refer to the specifications for your model number to ensure the level of information collected is compatible with the PhenX protocol.
|Average time of greater than 15 minutes in an unaffected individual||No|
|Specialized requirements for biospecimen collection||No|
Mode of Administration
Ask questions "1" and "2," and then proceed to the protocol for obtaining blood pressure. The use of high blood pressure medications must be obtained.
September 9, 2009
DefinitionMeasure to assess respondent's blood pressure.
Blood pressure is used to assess the risk of heart attack, stroke, heart failure, and kidney failure.
The first two protocols were selected because together they obtain a personal history of high blood pressure or hypertension as well as medication usage. These two pieces are a vital component in interpreting the results of a blood pressure measurement. Additionally, both protocols were used on a major U.S. health study. The Coronary Artery Risk Development in Young Adults (CARDIA) Study protocol for measuring blood pressure was selected because of its use of the Omron® machine, which is the latest technology for measuring blood pressure. Conducting a blood pressure measurement provides additional study specificity.
|Common Data Elements (CDE)||Person Hypertension Indicator||2935342||CDE Browser|
|Logical Observation Identifiers Names and Codes (LOINC)||Blood pressure proto||62392-6||LOINC|
Process and Review
The Expert Review Panel has not reviewed this measure yet.
U.S. Department of Health and Human Services. National Institutes of Health. National Heart, Lung and Blood Institute. Coronary Artery Risk Development in Young Adults (CARDIA) Study. Y20 CARDIA VII. Medical History Form. Page 1. Question 1 (source for question 1).
U.S. Department of Health and Human Services. National Institutes of Health. National Heart, Lung and Blood Institute and Boston University. Framingham Heart Study (FHS). Generation 3. Exam 1. Medical History—Medications. Page 23. No question number provided (source for question 2).
U.S. Department of Health and Human Services. National Institutes of Health. National Heart, Lung and Blood Institute. Coronary Artery Risk Development in Young Adults (CARDIA) Study. Year 20 (2005–2006) Manual of Operations. Section 3—Blood Pressure and Pulse (source for question 3).
Chobanian, A. V., Bakris, G. L., Black, H. R., Cushman, W. C., Green, L. A., Izzo, J. L., Jr., Jones, D. W., Materson, B. J., Oparil, S., Wright, J. T., Jr., & Roccella, E. J.; National Heart, Lung and Blood Institute Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure; National High Blood Pressure Education Program Coordinating Committee. (2003). The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure: The JNC 7 report. Journal of the American Medical Association, 289, 2560–2572. Retrieved July 16, 2009, from http://www.nhlbi.nih.gov/guidelines/hypertension/jnc7full.pdf (source for Diagnostic Criteria).
O'Brien, E., Petrie, J., Littler, W. A., de Swiet, M., Padfield, P. L., Altman, D., Bland, M., Coats, A., & Atkins, N. (1993). The British Hypertension Society protocol for the evaluation of blood pressure measuring devices. Journal of Hypertension, 11(2), S43–S62.
Association for the Advancement of Medical Instrumentation. American National Standard. Manual, electronic or automated sphygmomanometers ANSI/AAMI SP10-2002/A1. 3330 Washington Boulevard, Suite 400, Arlington, VA 22201-4598, USA: AAMI; 2003.
O'Brien, E., Pickering, T., Asmar, R., Myers, M., Parati, G., Staessen, J., Mengden, T., Imai, Y., Waeber, B., Palatini, P., Atkins, N., & Gerin, W.; the Working Group on Blood Pressure Monitoring of the European Society of Hypertension. (2002). International protocol for validation of blood pressure measuring devices in adults. Blood Pressure Monitoring, 7, 3–17. Retrieved on July 21, 2009, from http://www.dableducational.org/pdfs/International%20Protocol%202002.pdf
|Variable Name||Variable ID||Variable Description||Version||dbGaP Mapping|
|PX040301_Ever_Have_High_Blood_Pressure||PX040301010100||Has a doctor or nurse ever said that you have high blood pressure or hypertension?||4||Variable Mapping|
|PX040301_Age_Have_High_Blood_Pressure||PX040301010200||At what age were you first told this?||4||N/A|
|PX040301_HBP_During_Pregnancy_Only||PX040301010300||Was this during pregnancy only?||4||N/A|
|PX040301_Ever_Take_HBP_Medication||PX040301020100||Have you ever taken medication for hypertension/high blood pressure?||4||N/A|
|PX040301_Age_Take_HBP_Medication||PX040301020200||At what age did you begin taking medicine for this?||4||N/A|
|PX040301_Age_Take_HBP_Medication_Coded||PX040301020201||At what age did you begin taking medicine for this?||4||N/A|
|PX040301_Sphygmomanometer||PX040301030100||Blood pressure measurement, sphygmomanometer name and model.||4||N/A|
|PX040301_Cuff_Size||PX040301030200||Blood pressure measurement, cuff size.||4||N/A|
|PX040301_Systolic_Blood_Pressure_1||PX040301030300||Systolic Pressure measurement 1 (mm Hg).||4||Variable Mapping|
|PX040301_Diastolic_Blood_Pressure_1||PX040301030400||Diastolic Pressure measurement 1 (mm Hg).||4||Variable Mapping|
|PX040301_Systolic_Blood_Pressure_2||PX040301030500||Systolic Pressure measurement 2 (mm Hg).||4||Variable Mapping|
|PX040301_Diastolic_Blood_Pressure_2||PX040301030600||Diastolic Pressure measurement 2 (mm Hg).||4||Variable Mapping|
|PX040301_Systolic_Blood_Pressure_3||PX040301030700||Systolic Pressure measurement 3 (mm Hg).||4||Variable Mapping|
|PX040301_Diastolic_Blood_Pressure_3||PX040301030800||Diastolic Pressure measurement 3 (mm Hg).||4||Variable Mapping|
|PX040301_Blood_Pressure_Measurement_Date||PX040301030900||Date of measurement of blood pressure.||4||N/A|