医学
血管活性
病危
观察研究
血压
血流动力学
平均动脉压
麻醉
感染性休克
内科学
重症监护
心脏病学
前瞻性队列研究
入射(几何)
败血症
危重病
疾病严重程度
脉冲压力
重症监护室
复苏
毛细管再灌注
作者
Zbigniew Putowski,Ryszard Gawda,Tomasz Czarnik,Tomasz Królicki,Julia Trzebicka,Mateusz Zawadka,Karol P. Steckiewicz,Radosław Owczuk,Anna J. Szczepańska,Piotr Liberski,Anna Kluzik,Bartosz Kudliński,Pawel Nowak,Szymon Białka,Krzysztof Węgrzyn,Paweł Zatorski,Anna Janowska-Rodak,Dariusz Onichimowski,Mirosław Ziętkiewicz,Łukasz Sadowski
标识
DOI:10.1097/ccm.0000000000007391
摘要
Objectives: To determine the incidence of a significant noninvasive brachial-to-radial arterial pressure gradient (NIBR-APG) and its clinical associations in critically ill patients receiving vasoactive agents. Design: Prospective, multicenter, observational study. Setting: Thirteen ICUs in Poland. Patients: Adult ICU patients with radial arterial catheters receiving vasoactive agents hospitalized between April 2025 and July 2025. Interventions: None. Measurements and Main Results: Invasive radial mean arterial pressure (MAP) and noninvasive brachial MAP were measured twice and averaged. A NIBR-APG greater than 11 mm Hg was predefined as clinically significant. Baseline characteristics, hemodynamic variables, and outcomes were recorded. Among 303 patients, 49.5% were surgical admissions and 33.3% had septic shock. The median NIBR-APG was 4.5 mm Hg (interquartile range, 0.0–10.0 mm Hg). Fifty-six patients (18.4%) exhibited a NIBR-APG greater than 11 mm Hg. Compared with patients without a significant gradient, these patients received higher norepinephrine-equivalent doses (0.23 vs. 0.10 µg/kg/min), had higher Sequential Organ Failure Assessment scores (11 vs. 10), prolonged capillary refill time (3.0 vs. 2.5 s), and higher lactate concentrations (2.7 vs. 1.3 mmol/L). In multivariable analysis, only vasoactive drug dose was independently associated with NIBR-APG greater than 11 mm Hg (odds ratio, 1.68; 95% CI, 1.12–2.52). ICU mortality was higher in patients with significant gradients (48.0% vs. 30.1%). Conclusions: Nearly one in five critically ill patients receiving vasoactive agents demonstrated a clinically significant NIBR-APG. The presence of this gradient was independently associated with higher vasoactive drug requirements and was accompanied by greater illness severity and higher ICU mortality.
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