@article{MerkelLindnerGaberetal.2022, author = {Merkel, Helena and Lindner, Dirk and Gaber, Khaled and Ziganshyna, Svitlana and Jentzsch, Jennifer and Mucha, Simone and Gerhards, Thilo and Sari, Sabine and Stock, Annika and Vothel, Felicitas and Falter, Lea and Qu{\"a}schling, Ulf and Hoffmann, Karl-Titus and Meixensberger, J{\"u}rgen and Halama, Dirk and Richter, Cindy}, title = {Standardized classification of cerebral vasospasm after subarachnoid hemorrhage by digital subtraction angiography}, series = {Journal of Clinical Medicine}, volume = {11}, journal = {Journal of Clinical Medicine}, number = {7}, issn = {2077-0383}, doi = {10.3390/jcm11072011}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-270638}, year = {2022}, abstract = {Background: During the last decade, cerebral vasospasm after aneurysmal subarachnoid hemorrhage (SAH) was a current research focus without a standardized classification in digital subtraction angiography (DSA). This study was performed to investigate a device-independent visual cerebral vasospasm classification for endovascular treatment. Methods: The analyses are DSA based rather than multimodal. Ten defined points of intracranial arteries were measured in 45 patients suffering from cerebral vasospasm after SAH at three time points (hospitalization, before spasmolysis, control after six months). Mathematical clustering of vessel diameters was performed to generate four objective grades for comparison. Six interventional neuroradiologists in two groups scored 237 DSAs after a new visual classification (grade 0-3) developed on a segmental pattern of vessel contraction. For the second group, a threshold-based criterion was amended. Results: The raters had a reproducibility of 68.4\% in the first group and 75.2\% in the second group. The complementary threshold-based criterion increased the reproducibility by about 6.8\%, while the rating deviated more from the mathematical clustering in all grades. Conclusions: The proposed visual classification scheme of cerebral vasospasm is suitable as a standard grading procedure for endovascular treatment. There is no advantage of a threshold-based criterion that compensates for the effort involved. Automated vessel analysis is superior to compare inter-group results in research settings.}, language = {en} } @article{ThalSmetakHayashietal.2022, author = {Thal, Serge C. and Smetak, Manuel and Hayashi, Kentaro and F{\"o}rster, Carola Y.}, title = {Hemorrhagic cerebral insults and secondary Takotsubo syndrome: findings in a novel in vitro model using human blood samples}, series = {International Journal of Molecular Sciences}, volume = {23}, journal = {International Journal of Molecular Sciences}, number = {19}, issn = {1422-0067}, doi = {10.3390/ijms231911557}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-288305}, year = {2022}, abstract = {Intracranial hemorrhage results in devastating forms of cerebral damage. Frequently, these results also present with cardiac dysfunction ranging from ECG changes to Takotsubo syndrome (TTS). This suggests that intracranial bleeding due to subarachnoid hemorrhage (SAH) disrupts the neuro-cardiac axis leading to neurogenic stress cardiomyopathy (NSC) of different degrees. Following this notion, SAH and secondary TTS could be directly linked, thus contributing to poor outcomes. We set out to test if blood circulation is the driver of the brain-heart axis by investigating serum samples of TTS patients. We present a novel in vitro model combining SAH and secondary TTS to mimic the effects of blood or serum, respectively, on blood-brain barrier (BBB) integrity using in vitro monolayers of an established murine model. We consistently demonstrated decreased monolayer integrity and confirmed reduced Claudin-5 and Occludin levels by RT-qPCR and Western blot and morphological reorganization of actin filaments in endothelial cells. Both tight junction proteins show a time-dependent reduction. Our findings highlight a faster and more prominent disintegration of BBB in the presence of TTS and support the importance of the bloodstream as a causal link between intracerebral bleeding and cardiac dysfunction. This may represent potential targets for future therapeutic inventions in SAH and TTS.}, language = {en} } @article{VadokasKoehlerWeilandetal.2019, author = {Vadokas, Georg and Koehler, Stefan and Weiland, Judith and Lilla, Nadine and Stetter, Christian and Westermaier, Thomas}, title = {Early antiinflammatory therapy attenuates brain damage after SAH in rats}, series = {Translational Neuroscience}, volume = {10}, journal = {Translational Neuroscience}, number = {1}, doi = {10.1515/tnsci-2019-0018}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-201440}, pages = {104-111}, year = {2019}, abstract = {Background Early inflammatory processes may play an important role in the development of early brain injury (EBI) after subarachnoid hemorrhage (SAH). Experimental studies suggest that anti-inflammatory and membrane-stabilizing drugs might have beneficial effects, although the underlying mechanisms are not fully understood. The aim of this study was to investigate the effect of early treatment with methylprednisolone and minocycline on cerebral perfusion and EBI after experimental SAH. Methods Male Sprague-Dawley rats were subjected to SAH using the endovascular filament model. 30 minutes after SAH, they were randomly assigned to receive an intravenous injection of methylprednisolone (16mg/kg body weight, n=10), minocycline (45mg/kg body weight, n=10) or saline (n=11). Mean arterial blood pressure (MABP), intracranial pressure (ICP) and local cerebral blood flow (LCBF) over both hemispheres were recorded continuously for three hours following SAH. Neurological assessment was performed after 24 hours. Hippocampal damage was analyzed by immunohistochemical staining (caspase 3). Results Treatment with methylprednisolone or minocycline did not result in a significant improvement of MABP, ICP or LCBF. Animals of both treatment groups showed a non-significant trend to better neurological recovery compared to animals of the control group. Mortality was reduced and hippocampal damage significantly attenuated in both methylprednisolone and minocycline treated animals. Conclusion The results of this study suggest that inflammatory processes may play an important role in the pathophysiology of EBI after SAH. Early treatment with the anti-inflammatory drugs methylprednisolone or minocycline in the acute phase of SAH has the potential to reduce brain damage and exert a neuroprotective effect.}, language = {en} } @article{KunzeLillaStetteretal.2018, author = {Kunze, Ekkehard and Lilla, Nadine and Stetter, Christian and Ernestus, Ralf-Ingo and Westermaier, Thomas}, title = {Magnesium protects in episodes of critical perfusion after aneurysmal SAH}, series = {Translational Neuroscience}, volume = {9}, journal = {Translational Neuroscience}, number = {1}, doi = {10.1515/tnsci-2018-0016}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-177078}, pages = {99-105}, year = {2018}, abstract = {Background: To analyze whether magnesium has a neuroprotective effect during episodes that indicate a critical brain perfusion after aneurysmal subarachnoid hemorrhage (SAH). Methods: 107 patients with aSAH were randomized to continuously receive intravenous magnesium sulfate with target serum levels of 2.0 - 2.5 mmol/l (n = 54) or isotonic saline (n = 53). Neurological examination and transcranial Doppler sonography (TCD) were performed daily, Perfusion-CT (PCT) was acquired in 3-day intervals, angiography in case of suspected vasospasm. The primary endpoint was the development of secondary infarction following episodes of delayed ischemic neurological deficit (DIND), elevated mean flow velocity (MFV) in TCD or pathological findings in PCT. Results: In the magnesium group, 9 episodes of DIND were registered, none was followed by secondary infarction. In the control group, 23 episodes of DIND were registered, 9 were followed by secondary infarction (p < 0.05). In the magnesium group, 114 TCD-measurements showed an elevated MFV(> 140 cm/s). 7 were followed by new infarction. In control patients, 135 measurements showed elevated MFV, 32 were followed by new infarction (p < 0.05). 10 of 117 abnormal PCT-findings were followed by new infarction, compared to 30 of 122 in the control-group (p < 0.05). Conclusion: DIND, elevated MFV in TCD and abnormal PCT are findings which are associated with an increased risk to develop delayed secondary infarction. The results of this analysis suggest that magnesium-treatment may reduce the risk to develop infarction in a state of critical brain perfusion.}, language = {en} } @phdthesis{Johnson2006, author = {Johnson, Alexandra Kirsten}, title = {Perfusions-Computertomographie und transkranielle Dopplersonographie in der Evaluation von Vasospasmen nach aneurysmatischer Subarachnoidalblutung}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-17853}, school = {Universit{\"a}t W{\"u}rzburg}, year = {2006}, abstract = {Die vorliegende Studie vergleicht die beiden diagnostischen Verfahren PCT und TCD zur Erfassung von Vasospasmen bei aneurysmatischer SAB. Durch den Einsatz des PCT gewinnt man bei Patienten mit SAB wichtige zus\&\#1606;tzliche Informationen, die f{\"u}r die weitere Diagnostik und Therapieplanung au\&\#1603;erordentlich hilfreich sind. Im Einzelnen finden sich folgende Ergebnisse: 1. Das Perfusions-CT zeigt eine Sensitivit\&\#1606;t von 0,61, eine Spezifit\&\#1606;t von 0, 71 und einen pr\&\#1606;diktiven Wert des positiven Tests von 0,53. TTP hat eine hohe Sensitivit\&\#1606;t von 0,61; CBV ist h\&\#1616;chst spezifisch (Sp 0, 98). 2. Die TCD zeigt nur eine m\&\#1606;\&\#1603;ige Sensitivit\&\#1606;t (0,48) und Spezifit\&\#1606;t (0,62). 3. Bei zus\&\#1606;tzlicher Durchf{\"u}hrung der TCD zur PCT-Untersuchung steigt die Sensitivit\&\#1606;t auf 0,73 an, was sich jedoch auf Kosten der Spezifit\&\#1606;t (0,48) und des pr\&\#1606;diktiven Werts des positiven Tests (0,42) auswirkt. 4. Die TCD-Untersuchung detektiert trotz t\&\#1606;glicher Durchf{\"u}hrung Vasospasmen nicht fr{\"u}her als die PCT-Untersuchung. Dies wurde mittels des Chiquadrattests (Chiquadrat von 0,46) verdeutlicht. 5. PCT ist ein praktikables Verfahren, das Anhalt f{\"u}r weitere diagnostische und therapeutische Ma\&\#1603;nahmen gibt.}, language = {de} }