Continuous, noninvasive measurement of pulsus paradoxus in patients with acute asthma

To evaluate a continuous, noninvasive measurement technique for pulsus paradoxus (PP) as an objective asthma severity indicator.

Prospective, masked assessment of the relationship between PP, peak expiratory flow rate, oxygen saturation, clinical scoring, and admission decisions.

An urban pediatric emergency department.

Children with acute asthma.

Standardized treatment per National Heart, Lung, and Blood Institute guidelines.

Peak expiratory flow rate, oxygen saturation, pulmonary index score, and masked disposition decision.

Significant positive correlations existed between PP and the pulmonary index score at the initial evaluation (r = 0.44; P < .001) and after 30 minutes (r = 0.51; P < .001) and 60 minutes (r = 0.45; P < .001). Significant negative correlations existed between PP and the percent predicted peak expiratory flow rate (r = -0.31; P = .01) and the oxygen saturation (r = -0.30; P = .02). The mean PP was significantly greater in patients who were admitted for further treatment at all time points (P = .003 or P = .002). At 30 minutes after presentation, a PP greater than 15 mm Hg predicted admission for further treatment or relapse; the sensitivity was 0.42, the specificity was 0.89, and the likelihood ratio was 3.86.

Our measurement technique for PP is a useful objective indicator of the severity of asthma. Pulsus paradoxus correlates with clinical score, peak expiratory flow rate, and oxygen saturation. Furthermore, an elevated PP is associated with the decision to admit a patient for further treatment. These results suggest that this technique may represent a useful research tool for the assessment of acute, severe asthma. Further development of the technology may allow for a clinical application.