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Peripheral ischemic reserve in sepsis and septic shock as a new bedside prognostic enrichment tool: A Brazilian
Ana Carolina de Miranda1, Fernanda do Carmo De Stefani1, Bruna Cassia Dal Vesco2
1Department of Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, Paraná, Brazil.
Abstract:
Microvascular dysfunctions are associated with poor prognosis in sepsis. However, the potential role of clinical assessment of peripheral ischemic microvascular reserve (PIMR), a parameter that characterizes the variation of peripheral perfusion index (PPI) after brief ischemia of the upper arm, as a tool to detect sepsis-induced microvascular dysfunction and for prognostic enrichment has not been established. To address this gap, this study investigated the association of high PIMR with mortality over time in patients with sepsis and its subgroups (with and without shock) and peripheral perfusion (capillary-refill time). This observational cohort study enrolled consecutive septic patients in four Intensive-care units. After fluid resuscitation, PIMR was evaluated using the oximetry-derived PPI and post-occlusive reactive hyperemia for two consecutive days in septic patients. Two hundred and twenty-six patients were included-117 (52%) in the low PIMR group and 109 (48%) in the high PIMR group. The study revealed differences in mortality between groups on the first day, which was higher in the high PIMR group (RR 1.25; 95% CI 1.00-1.55; p = 0.04) and maintained its prognostic significance after multivariate adjustment. Subsequently, this analysis was made for sepsis subgroups and showed significant differences in mortality only for the septic-shock subgroup, with was higher in the high PIMR group (RR 2.14; 95% CI 1.49-3.08; p = 0.01). The temporal ΔPPI peak values (%) analyses did not demonstrate maintenance of the predictive value over the first 48 h in either group (p > 0.05). A moderate positive correlation (r = 0.41) between ΔPPI peak (%) and capillary-refill time (s) was found within the first 24 hours of diagnosis (p < 0.001). In conclusion, detecting a high PIMR within 24 h appears to be a prognostic marker for mortality in sepsis. Furthermore, its potential as a prognostic enrichment tool seems to occur mainly in septic shock.
Insights
High peripheral ischemic microvascular reserve (PIMR) indicates increased mortality risk in sepsis patients. This finding is particularly significant for those with septic shock, suggesting PIMR
Area of Science:
- Critical Care Medicine
- Cardiovascular Physiology
- Sepsis Pathophysiology
Background:
- Sepsis-associated microvascular dysfunction is linked to poor patient outcomes.
- Peripheral ischemic microvascular reserve (PIMR) and its clinical utility in sepsis remain unestablished.
- Assessing PIMR may offer prognostic insights into sepsis-induced microvascular dysfunction.
Purpose of the Study:
- To investigate the association between high PIMR and mortality in sepsis patients.
- To evaluate PIMR's prognostic value in sepsis subgroups, including septic shock.
- To explore the relationship between PIMR and peripheral perfusion parameters like capillary refill time.
Main Methods:
- An observational cohort study involving 226 consecutive septic patients across four ICUs.
- PIMR was assessed using oximetry-derived peripheral perfusion index (PPI) and post-occlusive reactive hyperemia over two days.
- Statistical analyses included risk ratios, multivariate adjustment, and correlation coefficients.
Main Results:
- Higher mortality was observed in patients with high PIMR on day one (RR 1.25, p=0.04), a finding sustained after adjustment.
- The association between high PIMR and mortality was significant in the septic shock subgroup (RR 2.14, p=0.01).
- A moderate positive correlation (r=0.41) was found between PIMR (ΔPPI peak) and capillary refill time within 24 hours.
Conclusions:
- High PIMR detected within 24 hours of sepsis diagnosis is a prognostic marker for mortality.
- PIMR shows potential as a prognostic enrichment tool, especially in patients with septic shock.
- Further research may elucidate PIMR's role in guiding sepsis management and improving outcomes.
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