Journal
CRITICAL CARE
Volume 27, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s13054-023-04405-w
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This pilot observational study aimed to explore endothelial-mediated vasoreactivity in immune-mediated thrombotic thrombocytopenic purpura (iTTP) patients at admission and its changes after plasma exchange therapy (PE). The study found that iTTP patients had impaired endothelial-mediated skin microvascular reactivity at admission, but it improved after PE.
Background Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a rare disease characterized by arteriolar and capillary microthrombosis precipitating organ failure. However, the contribution of endothelial dysfunction on impaired microvascular blood flow in iTTP patients has been poorly explored. This pilot observational study aimed to explore endothelial-mediated vasoreactivity in iTTP patients at admission and its changes after plasma exchange therapy (PE). Methods We conducted a prospective observational study in patients (> 18-year old) admitted in ICU for iTTP. Using laser Doppler flowmetry and acetylcholine (Ach) iontophoresis in the forearm, we recorded the skin microvascular blood flow and the endothelium-mediated vasoreactivity at admission and after PE. Demographics, biological, clinical courses, and outcomes were also collected. As a control group, we used a previously published cohort of young diabetic patients after correction of ketoacidosis. Results Eighteen confirmed iTTP patients and 34 controls were included in the study, mainly female (72%) aged 43 +/- 16-year- old. At admission, 55% had neurological abnormalities, 50% cardiac issues and 27.8% an acute kidney injury. Median platelet count was 19 G/mL [10-37]. Baseline microvascular blood flow was decreased in iTTP patients when compared to controls (5.97 +/- 4.5 vs. 10.1 +/- 6.3 PU, P = 0.03), associated with markedly impaired endothelialmediated skin microvascular reactivity (AUC: 9627 +/- 8122 vs. 16,475 +/- 11,738, P = 0.03). Microvascular reactivity improved after the first PE session (AUC: 9627 +/- 8122 vs 16,558 +/- 10,699, P = 0.007, respectively, baseline and postPE1) and much more after the second session (26,431 +/- 23,181, P = 0.04 post-PE1 vs post-PE2). Hemolysis biomarkers (LDH and bilirubin) negatively correlated with skin microvascular flow and vasoreactivity. Conclusion We highlighted a marked yet reversible skin endothelium-mediated microvascular hyporeactivity in iTTP patients that could participate in organ injury pathophysiology.
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