Chest
Volume 118, Issue 2, August 2000, Pages 348-352
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Clinical Investigations: Cardiology
Analysis of Physician Ability in the Measurement of Pulsus Paradoxus by Sphygmomanometry

https://doi.org/10.1378/chest.118.2.348Get rights and content

Context

Measurement of pulsus paradoxus (PP) is one of several measures previously advocated in the National Heart, Lung, and Blood Institute asthma management guidelines: a pulsus of > 12 mm Hg warranted hospital admission. It is one of only a few measures that is not effort dependent and therefore important in the evaluation of patients with asthma.

Objective

Determination of physician accuracy in measuring PP.

Design

A model of induced PP in a trained healthy subject without respiratory disease was constructed with a fixed inspiratory resistance with measurement of inspiratory air pressure and beat-to-beat BP noninvasively.

Setting

Laboratory.

Participants

Attending physicians from emergency medicine and critical care disciplines who served as consecutive examiners of the trained reference subject generating known PP.

Interventions

A total of 19 attending physicians were assessed for ability in measuring PP by sphygmomanometry and by palpation. The reference subject generated 4° of PP sequentially, with each examiner blinded to the value of negative inspiratory pressure and PP. Examiners first assessed PP qualitatively by palpation, followed by its measurement within 2 min.

Main outcome measure

Proximity of physician-measured PP (PPm) to true PP (PPt).

Results

At inspiratory pressures of − 10, − 15,− 20, and − 25 mm Hg, PPt was 13.7, 16.2, 19.1, and 20.7 mm Hg, respectively (F = 14.8, p < 0.0001; analysis of variance[ANOVA]). At the same pressures, PPm was 13.1, 17.5, 17.7, and 18.0 mm Hg (p > 0.10; ANOVA). Linear regression of PPm against PPt for each examiner revealed a slope (SE) of 0.53 (0.23), and not a 1:1 relationship.

Conclusions

Past and present guidelines do not account for the challenges in measuring PP, especially in tachypneic patients. Sphygmomanometric determination of PP should be augmented by new aids developed through technological innovation.

Section snippets

Study Design

Physicians’ ability to accurately measure experimentally induced PP was assessed in a single reference subject. Attending-level physicians from emergency and critical care disciplines served as examiners who were self-selected based on subjective ability to measure PP. The study was conducted in a quiet laboratory setting, and the examiners were blinded to degree of PP. The reference subject (R.D.) was trained to generate incremental and predetermined degrees of PP by self-measured inspiratory

Results

A total of 19 examiners were used in this study; all were board certified in their respective disciplines of emergency medicine (n = 12), pediatric emergency medicine (n = 5), and pulmonary medicine/intensivists (n = 2). The combined level of experience for examiners was 9.2 ± 7.4 SD years since the end of postgraduate medical training, with two of the authors (D.S. and A.M.) serving as examiners. Across all examiners, the test subject generated values (mean ± SD) of PPt as follows: 13.7 ± 2.2,

Discussion

A limitation of our study is that the examining physicians did not practice their skill in determining PP prior to measurement. However, asking emergency physicians and critical care specialists who feel comfortable measuring PP to do so in an ad hoc manner is in keeping with clinical reality. Physicians are unable to “practice” this element of physical examination unless provided with some objective criterion that presently does not exist. There were no attempted measurements of physiologic PP

ACKNOWLEDGMENTS

We wish to thank Constantine Gatsonis, PhD, for his input.

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