J Korean Med Sci. 2013 Aug;28(8):1244-1247. English.
Published online Jul 31, 2013.
© 2013 The Korean Academy of Medical Sciences.
Case Report

Effectiveness of Mechanical Embolectomy for Septic Embolus in the Cerebral Artery Complicated with Infective Endocarditis

Gimoon Kang,1 Tae Ki Yang,2 Joon Hyouk Choi,1 and Sang Taek Heo1
    • 1Department of Internal Medicine, Jeju National University School of Medicine, Jeju, Korea.
    • 2Department of Neurosurgery, Jeju National University School of Medicine, Jeju, Korea.
Received November 30, 2012; Accepted April 10, 2013.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

There has been a controversy over data of thrombolytic and endovascular surgical treatment about cerebral infarction secondary to infective endocarditis. We report a woman who received early mechanical embolectomy as a treatment of acute stroke with infective endocarditis. A 35-yr-old woman was hospitalized due to right hemiparesis. Brain image showed cerebral infarction at the middle cerebral artery and echocardiography demonstrated vegetation at the mitral valve. She was successfully treated with embolectomy and parenteral antibiotics without any neurologic sequelae. This report shows that the early retrieve of septic cerebral emboli can be a helpful treatment of acute stroke associated with endocarditis.

Keywords
Mechanical Embolectomy; Acute Ischemic Stroke; Infective Endocarditis

INTRODUCTION

Neurological deficits in the setting of infective endocarditis (IE) are critical conditions. Despite considerable advances in acute stroke therapy, the most promising approach for reducing the burden of stroke and hemorrhage of a patient with ischemic stroke due to IE is not well established. The benefit of anticoagulation has never been demonstrated in patients with native valve diseases (1). Moreover, the safety and efficacy of thrombolysis in an acute ischemic stroke to secondary to IE is not well established (2). Although a few articles have reported about the use of mechanical embolectomy (3-5), the role of embolectomy is unknown. To our knowledge, this is the first reported case of successful mechanical recanalization of middle cerebral artery (MCA) occlusion by secondary to bacterial endocarditis in Korea.

CASE DESCRIPTION

A 39-yr-old woman without any underlying medical conditions including heart problems visited the emergency department with ten minutes of right hemiparesis and aphasia on April 23, 2012. Her National Institutes of Health stroke scale (NIHSS) score was 16.

On presentation, she has been often febrile for 1 month. Her pulse was regular, blood pressure was 124/67 mm Hg and temperature was 37.1℃. Laboratory tests upon admission disclosed mild normocytic anemia (hemoglobin, 11 g/dL), a normal leukocyte count (8,600/mL), and a platelet count of 193,000/µL. The serum C-reactive protein level was 3.48 mg/dL and an erythrocyte sedimentation rate was 53 mm/h. The initial electrocardiogram showed a right bundle branch block. Results of other routine laboratory tests were within normal limits. A chest film was normal.

The brain computed tomography (CT) showed no abnormal findings. The diffusion-weighted magnetic resonance (MR) images and corresponding apparent diffusion coefficient maps revealed hyperacute infarction of left insula cortex, corona radiata, centrum semiovale and posterior inferior cerebellar artery territory of right side cerebellum. The MR angiography showed left MCA proximal segment (M1) occlusion. The diffusion-perfusion mismatch was found in the mean transit time & time to peak perfusion maps. (Fig. 1, 2) She was not given an intravenous tissue plasminogen activator because of the unclear onset time of the neurological deficits. Considering the time window, diffusion-perfusion mismatch and the patient's young age, we decided to perform intra-arterial thrombolysis. The patient received urokinase 150,000 units and tirofiban (Aggrastat; Merck) 100 micrograms intra-arterially. However, there was no flow restoration of the left MCA. After the second trial of mechanical thrombectomy with retrievable stent Solitaire AB 4×15 mm (ev3/Covidien Vascular Therapies, Mansfield, Massachusetts, USA), the MCA was recanalized to the thromobolysis in cerebral infarction (TICI) grade 2b (6). (Fig. 3, 4) After 36-hr procedure, her right side motor power was almost fully recovered. The patient improved greatly and had only right hemifacial palsy and aphasia, which also improved gradually. A postoperative CT scan obtained 24 hr later showed no evidence of infarct or hemorrhage.

Fig. 1
The change of signal intensity of the left middle cerebral artery in brain magnetic resonance image (MRI). (A) MRI shows hyperintensity in diffusion-weighted image (arrow). (B) The image shows perfusion delay in mean transit time. (C) Time to peak maps of the left middle cerebral artery territory shows diffusion-perfusion mismatch.

Fig. 2
Angiographic findings of cerebral flow. (A) Magnetic resonance angiography shows stopping of left middle cerebral artery (arrow). (B) Left internal cerebral artery angiography reveals abrupt cessation of left proximal middle cerebral flow (arrow).

Fig. 3
Left internal cerebral artery angiography shows recanalization of middle cerebral artery after mechanical intra-arterial embolectomy.

Fig. 4
Retrievable solitaire stent and captured emboli are shown (arrows).

Unfortunately, we had not detected early on, but a cardiac examination revealed a regular heart beat with pansystolic murmur on apex. A transthoracic echocardiogram showed a mass like-lesion on the anterior mitral valve (1.07×0.59 cm) and moderate mitral regurgitation without any functional problems and the evidence of heart failure. Ceftriaxone and gentamicin treatment for IE started immediately. On the third day, Streptococcus gordonii was subsequently grown from the initial blood culture sets. With the patient fulfilled clinical Duke criteria for definite IE (1), she was treated with parenteral penicillin and gentamicin. The patient's NIHSS score was 7 at this time. We underwent a sequential echocardiography once a week during hospitalization. The volume of mitral regurgitation and the size of vegetation on echocardiography did not increase. After two weeks, the size of vegetation on echocardiography was decreased to about 0.7×0.5 cm. During the four weeks of her antibiotics course, the patient's hemiparesis and aphasia improved (NIHSS score of 3). She has had no recurrent infarction and congestive heart failure and has been recovering well at home.

DISCUSSION

Infectious intracranial embolic infarction constitutes a small group of all intracranial infarctions, but is an important cause of neurologic complications in patients with IE. The incidence of stroke in patients with IE is about 10% (7). Many studies have endeavored to detect appropriate strategy to reduce the neurologic complications of IE. However, standard cares are not well established for the treatment or prevention of acute ischemic stroke caused by IE. Despite advances in antimicrobial and surgical therapy, IE remains one of infectious emergency diseases that can lead to rapid severe complications and death.

The most effective strategy for prevention of a stroke is prompt initiation of appropriate antibiotics therapy (8). Typically patients with intracranial hemorrhage were not offered cardiac surgery and anticoagulants would not be initiated for patients with IE with the goal of reducing the risk of stroke. The stroke in IE could be improved by early identification of lesions amenable to an endovascular procedure. Our patient presents several risk factors of mortality from IE, a neurological complication, large vegetation, and a need for surgery. Although some studies have demonstrated a survival benefit with surgery, she was treated only with medical treatment combined with mechanical embolic removal.

Table 1 showed three cases of successful embolectomy for a stroke with IE. Embolectomies in previous two cases were done within one hour after initiation of neurologic symptoms. However, in our case, the procedure was done 4 hr after the onset of neurologic symptoms. We successfully retrieved the septic embolus and the patient experienced functional improvement within hours. Three cases are IE caused by streptococcus. S. gordonii is a member of the viridans group, freshly isolated strains from oral cavities (9), and is among the bacteria most frequently identified as an etiologic agent of subacute endocarditis (10). Staphylococcus aureus is the most common strain which makes neurologic critical complications; infarction and hemorrhage, secondary to IE. We need more data about mechanical embolectomy treatment for acute cerebral stroke with IE due to S. aureus, which results in poor outcome.

Table 1
Successful mechanical embolectomy of acute cerebral infarction due to infective endocarditis

Among cases of IE, up to 65% of embolic events involve the central nervous system, and the distribution of middle cerebral artery is commonly involved (8). When MCA stroke occurred, full neurological recovery was achieved in only 50% after proper valvular heart surgery. This was significantly lower when compared with patients with ischemic events affecting other parts of the brain (11). Three cases were also involved with MCA. However, they were cured with mechanical embolectomy without valvular heart surgery. Some experts recommend delaying surgery for 2 to 3 weeks for IE complicated by stroke (12, 13). Recent studies indicate that early surgery can be accomplished with a similar risk or better outcome in patients with native valve endocartitis (11, 14). Nevertheless, operators in our hospital wanted to delay valvular surgery because early operation will fail mechanical valve to attach the myocardium, during inflammatory reactions. And, cardiologists did not agree early valvular surgery because mitral regurgitation volume was not severe and aggravated. In this situation, mechanical embolectomy will be a useful procedure for prevention from aggravating and early recovery of neurologic symptoms and critical valvular surgery.

In conclusion, mechanical embolectomy in cases of stroke due to infective endocarditis manifesting with major neurologic deficits is a subject of controversy and needs additional clinical experience and evaluation in a randomized trials. Nevertheless, the benefit of this intervention introduced in these cases, can be one of the options for patients to whom thrombolysis or anticoagulation is unsuccessful or is contraindicated.

References

    1. Baddour LM, Wilson WR, Bayer AS, Fowler VG Jr, Bolger AF, Levison ME, Ferrieri P, Gerber MA, Tani LY, Gewitz MH, et al. Infective endocarditis: diagnosis, antimicrobial therapy, and management of complications: a statement for healthcare professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, and the Councils on Clinical Cardiology, Stroke, and Cardiovascular Surgery and Anesthesia, American Heart Association: endorsed by the Infectious Diseases Society of America. Circulation 2005;111:e394–e434.
    1. Walker KA, Sampson JB, Skalabrin EJ, Majersik JJ. Clinical Characteristics and Thrombolytic Outcomes of Infective Endocarditis-Associated Stroke. Neurohospitalist 2012;2:87–91.
    1. Kan P, Webb S, Siddiqui AH, Levy EI. First reported use of retrievable stent technology for removal of a large septic embolus in the middle cerebral artery. World Neurosurg 2012;77:591.e1–591.e5.
    1. Sukumaran S, Jayadevan ER, Mandilya A, Sreedharan SE, Harikrishnan S, Radhakrishnan N, Sylaja PN. Successful mechanical thrombectomy of acute middle cerebral artery occlusion due to vegetation from infective endocarditis. Neurol India 2012;60:239–240.
    1. Dababneh H, Hedna VS, Ford J, Taimeh Z, Peters K, Mocco J, Waters MF. Endovascular intervention for acute stroke due to infective endocarditis: case report. Neurosurg Focus 2012;32:E1.
    1. Higashida RT, Furlan AJ, Roberts H, Tomsick T, Connors B, Barr J, Dillon W, Warach S, Broderick J, Tilley B, et al. Trial design and reporting standards for intra-arterial cerebral thrombolysis for acute ischemic stroke. Stroke 2003;34:e109–e137.
    1. Bhuva P, Kuo SH, Claude Hemphill J, Lopez GA. Intracranial hemorrhage following thrombolytic use for stroke caused by infective endocarditis. Neurocrit Care 2010;12:79–82.
    1. Heiro M, Nikoskelainen J, Engblom E, Kotilainen E, Marttila R, Kotilainen P. Neurologic manifestations of infective endocarditis: a 17-year experience in a teaching hospital in Finland. Arch Intern Med 2000;160:2781–2787.
    1. Jenkinson HF, Lamont RJ. Oral microbial communities in sickness and in health. Trends Microbiol 2005;13:589–595.
    1. Douglas CW, Heath J, Hampton KK, Preston FE. Identity of viridans streptococci isolated from cases of infective endocarditis. J Med Microbiol 1993;39:179–182.
    1. Ruttmann E, Willeit J, Ulmer H, Chevtchik O, Höfer D, Poewe W, Laufer G, Müller LC. Neurological outcome of septic cardioembolic stroke after infective endocarditis. Stroke 2006;37:2094–2099.
    1. Sila C. Anticoagulation should not be used in most patients with stroke with infective endocarditis. Stroke 2011;42:1797–1798.
    1. Gillinov AM, Shah RV, Curtis WE, Stuart RS, Cameron DE, Baumgartner WA, Greene PS. Valve replacement in patients with endocarditis and acute neurologic deficit. Ann Thorac Surg 1996;61:1125–1129.
    1. Kang DH, Kim YJ, Kim SH, Sun BJ, Kim DH, Yun SC, Song JM, Choo SJ, Chung CH, Song JK, et al. Early surgery versus conventional treatment for infective endocarditis. N Engl J Med 2012;366:2466–2473.

Metrics
Share
Figures

1 / 4

Tables

1 / 1

PERMALINK