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Unfortunately, BP measurement is often suboptimally performed in clinical practice, which can lead to errors that inappropriately alter management decisions in 20% to 45% of cases. This inaccuracy has persisted despite extensive education and efforts to raise awareness on the adverse consequences of incorrect clinic BP measurement, according to the Lancet Commission on Hypertension Group position statement. That statement was co-written by AMA Vice President of Health Outcomes Michael Rakotz, MD, and Gregory D. Wozniak, PhD, who is vice president of outcomes analytics at the AMA.

“Many measurement errors can be minimized by appropriate patient preparation and standardized techniques. Validated semi-automated or automated upper arm cuff devices should be used instead of auscultation to simplify measurement and prevent observer error,” the consensus document says.

The consensus document cites multiple causes of inaccuracy in measurement. Here are four ways BP measurement goes wrong and how to address them.

There are instances in which the BP-measurement accuracy is affected by patients’ habits or behaviors. Acute meal ingestion, caffeine or nicotine use can all affect BP readings, leading to errors in measurement accuracy. If the patient has a full bladder, that can lead to an error in systolic BP of up to 33 mm Hg, and the white-coat effect can have an error of up to 26 mm Hg.

It is important for the patient to rest comfortably in a quiet environment for five minutes in a chair. The patient should also have an empty bladder and not have eaten, ingested caffeine, smoked or engaged in physical activity at least 30 minutes before the measurement.

Inaccuracies in BP measurement can also occur due to errors related to the procedure. For example, having the patient’s arm lower than heart level can lead to an error of 4 mm Hg up to 23 mm Hg. Procedure related error might also occur if the patient’s legs are crossed at the knees or if talking occurs during BP measurement. A fast cuff deflation rate also can contribute to inaccuracy.

The AMA has developed online tools and resources created using the latest evidence-based information to support physicians to help manage their patients’ high BP. These resources are available to all physicians and health systems as part of Target: BP™, a national initiative co-led by the AMA and American Heart Association.

If a cuff is too small or too large, errors in measurement can occur. Adding to inaccuracy are automated devices that have not been tested for accuracy, which can account for errors in systolic BP.

“An important issue with automated devices is that many have not been clinically validated for measurement accuracy,” says the statement. “Clinical validation involves demonstrating that the device meets the accuracy requirements of international BP measurement standards.”

The process of clinical validation involves performing a protocol-based comparison using multiple measurements against blinded, two-observer auscultatory reference standard. For greater accuracy, only validated devices should be used.

One common error in the clinical setting is failure to include a five-minute rest period. Errors can also include talking during the measurement procedure, using an incorrect cuff size and failure to take multiple measurements.

Time constraints are also quite common for casual measurements. This is because a casual reading takes about two minutes to perform compared with eight minutes for a standardized measurement. Physician readings were also found to be higher than nurse readings, which is the white coat effect in action.

The physician, nurse or other health professional is responsible for performing proper BP measurement while ensuring—to the greatest extent possible—that all potential causes of inaccuracy are avoided.

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In the first instance, he recognized that the accident he had in qualifying left damage to the engine that could affect its performance; However, it was not the only impediment that limited the Guadalajara in Canada, as he explained to ORF, the gearbox was to blame for Serio Pérez abandoning the competition:

The part that failed was not in optimal condition, but that it had a short period of useful life, and that they trusted that it would give for the Canadian Grand Prix, even though it was not in optimal condition. The team's adviser insisted that the accident in Q2 hurt the car, but they didn't bother to adjust the detail.

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