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   <subfield code="a">10.1007/s12630-013-9912-z</subfield>
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   <subfield code="a">Cerebrovascular autoregulation in critically ill patients during continuous hemodialysis</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Patrick Schramm, Dorothea Closhen, Janosch Wojciechowski, Manfred Berres, Klaus Klein, Marc Bodenstein, Christian Werner, Kristin Engelhard]</subfield>
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   <subfield code="a">L'autorégulation vasculaire cérébrale chez les patients gravement malades pendant l'hémodialyse continue</subfield>
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   <subfield code="a">Purpose: In chronic renal failure, intermittent hemodialysis decreases cerebral blood flow velocity (CBFV); however, in critically ill patients with acute renal failure, the effect of continuous venovenous hemodialysis (CVVHD) on CBFV and cerebrovascular autoregulation (AR) is unknown. Therefore, a study was undertaken to investigate the potential effect of CVVHD on CBFV and AR in patients with acute renal failure. Methods: This cohort study investigated 20 patients with acute renal failure who required CVVHD. In these patients, the CBFV and index of AR (Mx) were measured using transcranial Doppler before and during CVVHD. Results: The median Mx values at baseline were 0.33 [interquartile range (IQR): 0.02-0.55], and during CVVHD, they were 0.20 [0.07-0.40]. The differences in Mx (CVVHD - baseline) was (median [IQR]) −0.015 [−0.19-0.05], 95% confidence interval (CI) −0.16 to 0.05. The Mx was&gt;0.3 in 11/20 patients at baseline measurement. Six of these patients recovered to Mx&lt;0.3 during CVVHD. The CBFV was (median [IQR]) 47 [36-59] cm·sec−1 at baseline and 49 [36-66] cm·sec−1 during CVVHD. The difference of CBFV was 0.0 [−4 - 2.7], 95% CI −2.5 to 4.2. Conclusion: Compared with patients with intermittent hemodialysis, CVVHD did not influence CBFV and AR in critically ill patients with acute renal failure, possibly due to lower extracorporeal blood flow, slower change of plasma osmolarity, and a lower fluid extraction rate. In a subgroup of patients with sepsis, the AR was impaired at baseline in more than half of the patients, and this was reversed during CVVHD. The trial was registered at ClinicalTrials.gov ID: NCT01376531.</subfield>
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   <subfield code="a">Canadian Anesthesiologists' Society, 2013</subfield>
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   <subfield code="a">Schramm</subfield>
   <subfield code="D">Patrick</subfield>
   <subfield code="u">Department of Anesthesiology, University Medical Centre of the Johannes Gutenberg-University Mainz, Langenbeckstr.1, 55131, Mainz, Germany</subfield>
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   <subfield code="a">Closhen</subfield>
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   <subfield code="u">Department of Anesthesiology, University Medical Centre of the Johannes Gutenberg-University Mainz, Langenbeckstr.1, 55131, Mainz, Germany</subfield>
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   <subfield code="a">Wojciechowski</subfield>
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   <subfield code="u">Department of Anesthesiology, University Medical Centre of the Johannes Gutenberg-University Mainz, Langenbeckstr.1, 55131, Mainz, Germany</subfield>
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   <subfield code="u">Institute of Medical Biometry, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany</subfield>
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   <subfield code="a">Klein</subfield>
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   <subfield code="u">Department of Anesthesiology, University Medical Centre of the Johannes Gutenberg-University Mainz, Langenbeckstr.1, 55131, Mainz, Germany</subfield>
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   <subfield code="u">Department of Anesthesiology, University Medical Centre of the Johannes Gutenberg-University Mainz, Langenbeckstr.1, 55131, Mainz, Germany</subfield>
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   <subfield code="u">Department of Anesthesiology, University Medical Centre of the Johannes Gutenberg-University Mainz, Langenbeckstr.1, 55131, Mainz, Germany</subfield>
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   <subfield code="u">Department of Anesthesiology, University Medical Centre of the Johannes Gutenberg-University Mainz, Langenbeckstr.1, 55131, Mainz, Germany</subfield>
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   <subfield code="t">Canadian Journal of Anesthesia/Journal canadien d'anesthésie</subfield>
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