European Journal of Echocardiography Advance Access originally published online on March 30, 2008
European Journal of Echocardiography 2008 9(3):412-413; doi:10.1093/ejechocard/jen029
Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2008. For permissions please email: journals.permissions@oxfordjournals.org
Functional mitral stenosis: a rare complication of the Impella assist device
Stefan Toggweiler,
Peiman Jamshidi and
Paul Erne*
Division of Cardiology, Kantonsspital Luzern, CH-6000 Luzern 16, Switzerland
Received 18 May 2007; accepted after revision 18 November 2007; online publish-ahead-of-print 30 March 2008.
* Corresponding author. Tel: +41 41 205 52 08; fax: +41 41 205 22 34. E-mail address: paul.erne{at}ksl.ch
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Abstract
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In patients with left ventricular output failure, the Impella
left ventricular assist device increases total cardiac output
despite a drop in output provided by the left ventricle itself.
We present a patient with cardiogenic shock after myocardial
infarction in whom an Impella recover 2.5 was implanted. Correct
placement was ensured by fluoroscopy, pressure and current signals
displayed on the console of the system, and transthoracic echocardiography.
On follow-up, the Impella device was dislocated with the shaft
of the device lying on the anterior mitral leaflet causing a
functional mitral stenosis evident by an increased transmitral
diastolic flow gradient. After removing the device, the patients'
haemodynamics improved within minutes. Other than a mild regurgitation,
mitral valve was without pathological findings. Although infrequent,
this case shows a possible complication of the Impella ventricular
assist device and highlights the importance of periodical echocardiographic
surveillance, especially in patients who show a poor response
to therapy.
Keywords: Impella; Functional mitral stenosis; Cardiogenic shock; Left ventricular assist device; Echocardiography
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Case report
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A 70-year-old woman with diabetes and hypertension presented
in emergency room with decompensated heart failure as a result
of myocardial infarction. ECG showed a new complete left bundle
brunch block. Acute coronary angiography revealed significant
stenoses of the left anterior descending (LAD) and the right
coronary arteries (RCAs). The RCA was stented with drug-eluting
stents. During stenting of the LAD, the left main artery was
dissected with the tip of the guiding catheter and immediately
stented with a drug-eluting stent. The patient became unstable
and was intubated and put on inotropes. In order to stabilize
the patient after left main stenting, an Impella left ventricular
assist device (Abiomed Europe, Aachen, Germany) and an intra-aortic
balloon pump were inserted. Correct placement of the Impella
device was ensured by fluoroscopy, the pressure and current
signals displayed on the console of the system, and transthoracic
echocardiography showing the plastic pig tail tip placed nearby
the left ventricular apex without evidence of movement limitation
of the anterior mitral leaflet or an increased mitral valve
gradient. Left ventricular ejection fraction was 43% with the
two devices installed. Mitral valve of the patient was structurally
normal despite a mild pre-existing regurgitation. Over the next
2 days, the patient remained stable but catecholamines could
not be reduced. Chest X-ray showed pulmonary congestion and
follow-up echocardiography revealed a dislocation of the Impella
device with the shaft lying nearby the anterior mitral leaflet
compromising diastolic excursion (see Supplementary material
online, videos 1 and 2). This caused a mild functional mitral
stenosis (
Figure 1) with a mean transvalvular gradient
of 4.72 mmHg (
Figure 2). After removing the Impella, transmitral
gradient declined to a mean of 2.97 mmHg (
Figure 3). The
patient improved clinically, blood pressure rose from 110/80
to 130/80 mmHg and heart rate decreased from 118 to 102 bpm
(sinus tachycardia) within minutes. The next days, the patient
was extubated and intra-aortic balloon pump was removed.
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Discussion
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The Impella left ventricular assist device has been used in
the setting of cardiogenic shock alone or in combination with
other assist devices like intra-aortic balloon pump counterpulsation.
1–3 The Impella was associated with good results in unstable patients
undergoing coronary revascularization including stenting of
the left main coronary artery.
4–6 In a case study by Valgimigli
et al., an increase of 1.43 L/min in cardiac output was noticed
when running the pump at maximal speed (50 000 rpm). This increase
consisted of a 2.41 L/min gain provided by the Impella device
and a 0.98 L/min drop in output provided by the left ventricle.
6 The left ventricular coaxial pump seems to make complete revascularization
in patients with off pump coronary artery bypass graft surgery
possible.
7 Common device-related complications are sensor failure,
pump displacement, and haemolysis.
8 Echocardiography is the
most frequently used non-invasive modality to evaluate placement
and function of the Impella device.
9 Before device implantation,
echocardiography is useful to rule out anatomic contraindications.
During and after implantation, correct positioning and left
ventricular filling necessary to optimize pump performance can
be evaluated with echocardiography. During assistance, echocardiography
helps assessing left and right ventricular function and patient-device
interaction.
In this case, an Impella Recover LP 2.5 assist device was used in an unstable patient undergoing coronary revascularization including left main artery stenting. Two days after the procedure, transthoracic echocardiography showed that the formerly correctly placed Impella device dislocated. The shaft of the Impella was lying nearby the anterior mitral valve leaflet causing a mild functional mitral stenosis by compromising complete diastolic excursion of the anterior leaflet (see Supplementary material online, Videos 1 and 2). After removing the device, haemodynamics improved immediately.
Although this complication is rare, this case highlights the importance of regular echocardiographic evaluation for correct position in patients treated with this assist device despite normal function of the device based on the pressure and current signals displayed on the console of the system. Among others, myxoid degeneration of the mitral valve is a known contraindication for use, but this patient had a normal mitral valve apart from mild regurgitation.
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Supplementary material
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Supplementary material is available at EJECHO online.
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References
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- Meyns B, Dens J, Sergeant P, Herijgers P, Daenen W, Flameng W. Initial experiences with the Impella device in patients with cardiogenic shock. Thorac Cardiov Surg (2003) 51:312–7.[CrossRef]
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- Isgro F, Kiessling AH, Rehn E, Lang J, Saggau W. Intracardiac left ventricular support in beating heart, multi-vessel revascularization. J Card Surg (2003) 18:240–4.[CrossRef][Medline]
- Meyns B, Dens J, Sergeant P, Herijgers P, Daenen W, Flameng W. Initial experiences with the Impella device in patients with cardiogenic shock—Impella support for cardiogenic shock. Thorac Cardiovasc Surg (2003) 51:312–317.[CrossRef][Web of Science][Medline]
- Catena E, Milazzo F, Merli M, Paino R, Garatti A, Colombo T, Vitali E. Echocardiographic evaluation of patients receiving a new left ventricular assist device: the Impella revocer 100. Eur J Echocardiogr (2004) 5:430–7.[Abstract/Free Full Text]

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