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Critical Closing and Tissue Perfusion Pressures in Sepsis: Implications for Risk Stratification-A Retrospective
Jing-Yi Wang1, Shi-Tong Diao2, Tian-Yuan Zhu3
1Jing-Yi Wang, M.D.: Emergency Department, Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, and National Infrastructures for Translational Medicine, Institute of Clinical Medicine, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
Background:
The optimal target of mean arterial pressure (MAP) remains controversial in sepsis management. Critical closing pressure (Pcc), the arterial pressure at which blood flow ceases, is the key determinant of vascular waterfall phenomenon. Tissue perfusion pressure (TPP), the difference between MAP and Pcc, represents the driving pressure for arterial blood flow. This study evaluated the prognostic value of Pcc and TPP for improving risk stratification in sepsis.
Methods:
This retrospective cohort study included adult patients with sepsis in 18 hospitals between August 2013 to October 2022 from two independent data sets (the Study on the Epidemiology, Diagnosis and Treatment of Sepsis [SEPSIS-EDT] registry and the critical care database of Peking Union Medical College Hospital, Beijing, China). Pcc was estimated via linear regression of hourly MAP against product of heart rate and pulse pressure, while TPP was calculated as MAP minus Pcc. Patients were categorized into four groups based on the optimal thresholds for mean Pcc and TPP within 24 h of sepsis diagnosis: low TPP-low Pcc, low TPP-high Pcc, high TPP-low Pcc, and high TPP-high Pcc. Clinical outcomes included mortality rates and development of acute kidney injury within 2 and 7 days of sepsis diagnosis. External validation was performed using the Medical Information Mart for Intensive Care IV (MIMIC-IV) cohort.
Results:
A total of 6,769 patients (mean age, 61 yr; 61.0% men) were included. Intensive care unit mortality was highest in the low TPP-low Pcc group and lowest in the high TPP-high Pcc group (35.1% vs . 20.1%; risk difference, 15.0%; 95% CI, 10.2 to 19.8%). Similar patterns were observed for other outcomes. After adjustment for MAP, increased Pcc with concomitant reduced TPP showed a significant U-shaped association with both mortality and acute kidney injury development ( P < 0.001). The findings were consistent in the MIMIC-IV cohort.
Conclusions:
While MAP remains central to sepsis management, Pcc and TPP provide complementary prognostic information. Incorporating these parameters into clinical assessment may improve risk stratification and optimize blood pressure management.
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