dc.contributor.author
Truckenmueller, Peter
dc.contributor.author
Fritzsching, Jonas
dc.contributor.author
Schulze, Daniel
dc.contributor.author
Früh, Anton
dc.contributor.author
Jacobs, Stephan
dc.contributor.author
Ahlborn, Robert
dc.contributor.author
Vajkoczy, Peter
dc.contributor.author
Prinz, Vincent
dc.contributor.author
Hecht, Nils
dc.date.accessioned
2025-09-11T10:19:01Z
dc.date.available
2025-09-11T10:19:01Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/49228
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-48951
dc.description.abstract
Management of malignant hemispheric stroke (MHS) after cardiothoracic surgery (CTS) remains difficult as decision-making needs to consider severe cardiovascular comorbidities and complex coagulation management. The results of previous randomized controlled trials on decompressive surgery for MHS cannot be generally translated to this patient population and the expected outcome might be substantially worse. Here, we analyzed mortality and functional outcome in patients undergoing decompressive hemicraniectomy (DC) for MHS following CTS and assessed the impact of perioperative coagulation management on postoperative hemorrhagic and cardiovascular complications. All patients that underwent DC for MHS resulting as a complication of CTS between June 2012 and November 2021 were included in this observational cohort study. Outcome was determined according to the modified Rankin Scale (mRS) score at 1 and 3-6 months. Clinical and demographic data, anticoagulation management and postoperative hemorrhagic and thromboembolic complications were assessed. In order to evaluate a predictive association between clinical and radiological parameters and the outcome, we used a multivariate logistic regression analysis. Twenty-nine patients undergoing DC for MHS after CTS with a female-to-male ratio of 1:1.9 and a median age of 60 (IQR 49-64) years were identified out of 123 patients undergoing DC for MHS. Twenty-four patients (83%) received pre- or intraoperative substitution. At 30 days, the in-hospital mortality rate and neurological outcome corresponded to 31% and a median mRS of 5 (5-6), which remained stable at 3-6 months [Mortality: 42%, median mRS: 5 (4-6)]. Postoperatively, 15/29 patients (52%) experienced new hemorrhagic lesions and Bayesian logistic regression predicting mortality (mRS = 6) after imputing missing data demonstrated a significantly increased risk for mortality with longer aPPT (OR = 13.94, p = .038) and new or progressive hemorrhagic lesions after DC (OR = 3.03, p = .19). Notably, all but one hemorrhagic lesion occurred before discontinued anticoagulation and/or platelet inhibition was re-initiated. Despite perioperative discontinuation of anticoagulation and/or platelet inhibition, no coagulation-associated cardiovascular complications were noted. In conclusion, Cardiothoracic surgery patients suffering MHS will likely experience severe neurological disability after DC, which should remain a central aspect during counselling and decision-making. The complex coagulation situation after CTS, however, should not per se rule out the option of performing life-saving surgical decompression.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Anticoagulants / therapeutic use
en
dc.subject
Bayes Theorem
en
dc.subject
Decompressive Craniectomy* / adverse effects
en
dc.subject
Infarction, Middle Cerebral Artery
en
dc.subject
Postoperative Hemorrhage
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Outcome and management of decompressive hemicraniectomy in malignant hemispheric stroke following cardiothoracic surgery
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
12994
dcterms.bibliographicCitation.doi
10.1038/s41598-023-40202-9
dcterms.bibliographicCitation.journaltitle
Scientific Reports
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.volume
13
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
37563196
dcterms.isPartOf.eissn
2045-2322