Volume 80, Issue 4 pp. 593-599
Research Article

Cerebral white matter lesions and post-thrombolytic remote parenchymal hemorrhage

Sami Curtze MD, PhD

Corresponding Author

Sami Curtze MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

Address correspondence to Dr Curtze, Department of Neurology, Helsinki University Hospital, PO Box 340, FI-00029 HUS, Helsinki, Finland. E-mail: [email protected]Search for more papers by this author
Jukka Putaala MD, PhD

Jukka Putaala MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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Gerli Sibolt MD

Gerli Sibolt MD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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Susanna Melkas MD, PhD

Susanna Melkas MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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Satu Mustanoja MD, PhD

Satu Mustanoja MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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Elena Haapaniemi MD, PhD

Elena Haapaniemi MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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Tiina Sairanen MD, PhD

Tiina Sairanen MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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Marjaana Tiainen MD, PhD

Marjaana Tiainen MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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Turgut Tatlisumak MD, PhD

Turgut Tatlisumak MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden

Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden

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Daniel Strbian MD, PhD

Daniel Strbian MD, PhD

Division of Neurology, Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland

Department of Neurology, Helsinki University Hospital, Helsinki, Finland

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First published: 17 August 2016
Citations: 17

Abstract

Objective

Parenchymal hematoma (PH) following intravenous thrombolysis (IVT) in ischemic stroke can occur either within the ischemic area (iPH) or as a remote PH (rPH). The latter could be, at least partly, related to cerebral amyloid angiopathy, which belongs to the continuum of cerebral small vessel disease. We hypothesized that cerebral white matter lesions (WMLs)—an imaging surrogate of small vessel disease—are associated with a higher rate of rPH.

Methods

We analyzed 2,485 consecutive patients treated with IVT at the Helsinki University Hospital. Blennow rating scale of 5 to 6 points on baseline computed tomographic head scans was considered as severe WMLs. An rPH was defined as hemorrhage that—contrary to iPH—appears in brain regions without visible ischemic damage and is clinically not related to the symptomatic acute lesion site. The associations between severe WMLs and pure rPH versus no PH, pure iPH versus no PH, and pure rPH versus pure iPH were studied in multivariate logistic regression models.

Results

rPHs were mostly (74%) located in lobar regions. After adjustments, the presence of severe WMLs was associated with pure rPH (odds ratio [OR] = 6.79, 95% confidence interval [CI] = 2.57–17.94) but not with pure iPH (OR = 1.45, 95% CI = 0.83–2.53) when compared to patients with no PH. In direct comparison of pure rPH with pure iPH, severe cerebral WMLs were further associated with higher iPH rates (OR = 3.60, 95% CI = 1.06–12.19).

Interpretation

Severe cerebral WMLs were associated with post-thrombolytic rPH but not with iPH within the ischemic area. Ann Neurol 2016;80:593–599

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