Key result
Acute community-acquired pneumonia was associated with a significantly delayed hemodynamic adaptation to cortical activation compared to healthy controls (rate time 1.6 vs 3.6 seconds, p<0.0005), indicating early neurovascular uncoupling.
Observational (n=80)
No
Community-acquired pneumonia is associated with early, reversible microcirculatory dysfunction and neurovascular uncoupling in the brain that correlates with disease severity.
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Neurovascular uncoupling in acute pneumonia may flag deterioration risk; leaves open whether it drives encephalopathy or merits targeted intervention.
INTRODUCTION: Sepsis leads to microcirculatory dysfunction and therefore a disturbed neurovascular coupling in the brain. To investigate if the dysfunction is also present in less severe inflammatory diseases we studied the neurovascular coupling in patients suffering from community acquired pneumonia. METHODS: Patients were investigated in the acute phase of pneumonia and after recovery. The neurovascular coupling was investigated with a simultaneous electroencephalogram (EEG)-Doppler technique applying a visual stimulation paradigm. Resting EEG frequencies, visual evoked potentials as well as resting and stimulated hemodynamic responses were obtained. Disease severity was characterized by laboratory and cognitive parameters as well as related scoring systems. Data were compared to a control group. RESULTS: Whereas visually evoked potentials (VEP) remained stable a significant slowing and therefore uncoupling of the hemodynamic responses were found in the acute phase of pneumonia (Rate time: control group: 3.6 ± 2.5 vs. acute pneumonia: 1.6 ± 2.4 s; P < 0.0005). In the initial investigation, patients who deteriorated showed a decreased hemodynamic response as compared with those who recovered (gain: recovered: 15% ± 4% vs. deteriorated: 9% ± 3%, P < 0.05; control: 14% ± 5%). After recovery the coupling normalized. CONCLUSIONS: Our study underlines the role of an early microcirculatory dysfunction in inflammatory syndromes that become evident in pre-septic conditions with a gradual decline according to disease severity.
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Rosengarten et al. (2012) conducted an observational in Community-acquired pneumonia (n=80). Acute community-acquired pneumonia vs. Healthy controls was evaluated on Hemodynamic response rate time (initial speed of flow velocity adaptation) (p=<0.0005). Acute community-acquired pneumonia was associated with a significantly delayed hemodynamic adaptation to cortical activation compared to healthy controls (rate time 1.6 vs 3.6 seconds, p<0.0005), indicating early neurovascular uncoupling.
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