Open Access

Symptomatic hemorrhage after alteplase therapy not due to silent ischemia

  • Michael D Hill1Email author,
  • Philip A Barber,
  • Andrew M Demchuk,
  • Robert J Sevick,
  • Richard Frayne and
  • Alastair M Buchan
BMC Neurology20011:1

https://doi.org/10.1186/1471-2377-1-1

Received: 14 December 2000

Accepted: 19 January 2001

Published: 19 January 2001

Abstract

Background

Stroke thrombolysis-related intracerebral hemorrhage may occur remotely from the anatomical site of ischemia. One postulated mechanism for this is simultaneous multiple embolization with hemorrhage into a "silent" area of ischemia.

Results

A patient suffered a disabling stroke affecting the right cerebral hemisphere. He was treated with intravenous alteplase and underwent extensive early imaging with multimodal MRI. Several hours after treatment he developed a brainstem hemorrhage despite having no evidence of ischemia on DWI MRI in the brainstem.

Conclusion

Not all occurrences of remote ICH after stroke thrombolysis are secondary to multiple emboli with silent ischemia.

Case

A 66-year-old right-handed man awoke from sleep feeling well. At 06:55, while having breakfast, he developed sudden onset of painless weakness of his left arm associated with left facial droop and a subtle change in sensation over the left face and arm. He went directly to his local Emergency room where a diagnosis of stroke was made. He was transferred immediately to our centre for consideration of thrombolytic therapy, arriving at 08:28 (1 h 33 min from onset). He had a past history of a minor stroke with full recovery 3 years previously and longstanding hypertension. He was taking no medication having elected to discontinue his anti-hypertensive therapy two years earlier.

On examination, he was alert with no hemi-neglect or aphasia. He had a left facial droop and slight dysarthria. He was proximally weak but able to hold his left arm up against gravity, but had completely absent left distal hand function. He had reduced left leg power but was able to walk unsteadily. There was a reduction in pinprick sensation over the left arm and face. He was in normal sinus rhythm with a blood pressure of 200/115. A brain CT scan was performed, which demonstrated a small old right anterior parietal infarct which was interpreted as consistent with his previous minor stroke. There were no other acute changes. His National Institutes of Health Stroke Scale Score was 3.

Based on his clinical syndrome of severe distal weakness, it was postulated that his stroke involved the primary motor cortex or underlying fibres. After careful discussion with the patient including explanation of the risks of intracerebral hemorrhage, he was offered intravenous alteplase therapy. His deficits were considered disabling because of his retirement hobby of carpentry. His blood pressure fell to 170/95 with 10 mg of intravenous labetolol, after which an intravenous alteplase infusion was started at 09:28, 2 h 33 min after stroke onset. His blood pressure remained controlled (<185/110) throughout the infusion and subsequently with no change in his neurological status.

Immediately post-infusion (3 h 30 min from onset) he underwent an acute brain magnetic resonance scan (Figure 1), which demonstrated a new stroke in the right primary motor cortex with a parallel perfusion deficit (not shown). There was no perfusion-diffusion mismatch. No additional lesions were observed in the brain (Figure 2). All proximal intracranial arteries were patent on MR angiography.
Figure 1

Post-alteplase infusion (~ 230 min after stroke onset) diffusion weighted brain magnetic resonance image showing cortical infarct in the motor strip

Figure 2

Post-alteplase infusion (~ 230 min after stroke onset) diffusion weighted brain magnetic resonance image showing absence of any acute lesion in the brainstem.

Approximately 3 hours post-alteplase infusion (5 h 30 min from onset), he developed sudden vomiting and hypertension followed by bradycardia. His level of consciousness declined, he developed vertical strabismus and he became hemiplegic on the left. He was intubated and an urgent CT scan was performed (Figure 3) which demonstrated a pontomesencephalic hemorrhage. He died several weeks later from bronchopneumonia. An autopsy was not performed.
Figure 3

6 h CT scan showing new pontomesencephalic hemorrhage.

Discussion

Although most thrombolysis related intracerebral hemorrhages (ICH) occur at the site of stroke, up to 20% occur at sites away from the area of ischemia [1]. Despite this, no brainstem hemorrhages occurred in the NINDS tPA Stroke Trial and only 3% of ICH in the GUSTO-1 trial were in the brainstem [2]. One postulated explanation for the phenomenon of hemorrhage distant from the site of ischemia has been that strokes from proximal embolic sources, may be multiple such that co-existing small silent strokes are the source areas of hemorrhage. Multiple areas of DWI abnormality have been detected in a significant minority of patients with acute stroke [3].

This case concisely demonstrates that other mechanisms are at play. By both clinical examination and early diffusion-weighted imaging, there was no evidence of any area of concomitant brainstem ischemia. It remains possible that he had an initial DWI abnormality in the pons that was reversible with alteplase treatment, or that a small DWI lesion was missed for technical reasons such as slice thickness. DWI lesions associated with a brief duration of ischemia have been clinically shown to be reversible [4]. We consider this possibility to be remote because of his lack of clinical signs suggesting brainstem ischemia. In addition, DWI lesions in both anterior and posterior circulation concurrently are very uncommon [5]. Finally, no perfusion deficit (mean transit time or cerebral blood volume) was demonstrable in the pons.

Hypertensive small vessel disease was likely this patient's major risk factor for ICH. In phase 2 studies of alteplase for ischemic stroke, hypertension (diastolic BP > 100 mmHg immediately pre-treatment) was a clear risk factor for ICH [6]. Although treating patients "off-protocol" has been shown in post-marketing studies to be associated with higher hemorrhage rates and poorer outcomes [7], the NINDS protocol included both the treatment of hypertension prior to administration of thrombolytic therapy and the treatment of patients with low NIHSS scores, but with disabling deficits. Recent experimental evidence suggests that chronically hypertensive rats have higher rates of intracerebral hemorrhage after alteplase therapy for stroke [8]. Nevertheless, the NINDS investigators suggested that the treatment of hypertension (after randomisation) in the alteplase treated group was associated with poorer outcome but could not draw definitive conclusions because of the trial's design [9].

Conclusion

Thrombolysis-related ICH may occur unexpectedly and even DWI MRI may not be predictive. The decision to treat acute stroke patients with alteplase in the setting of hypertension is still one based on clinical judgement rather than solid evidence.

Declarations

Acknowledgements

Drs. Hill and Buchan were funded in part by grants from the Medical Research Council of Canada, the Heart & Stroke Foundation of Canada and the Alberta Heritage Foundation for Medical Research

Dr. Frayne was funded in part by grants from the Heart & Stroke Foundation of Canada and the Alberta Heritage Foundation for Medical Research

Dr. Demchuk was funded in part by a grant from the Medical Research Council of Canada

Authors’ Affiliations

(1)
Department of Clinical Neurosciences, University of Calgary, Stroke Research Office, Foothills Hospital

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  10. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/content/backmatter/1471-2377-1-1-b1.pdf

Copyright

© Hill et al; licensee BioMed Central Ltd. 2001

This article is published under license to BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.

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