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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3753_Библиотеки_им_академика_М_И_Перельмана
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258 M. Castillo-Sang
with biventricular failure VA-ECMO is a reliable
approach (but does not offload the left ventricle),
while those with isolated left ventricular failure
can be stabilized with either Impella (Abiomed,
Danvers, Massachusetts, USA), IABP or another
temporary percutaneous left ventricular assist
device.
• Mitral valve pathology
The type/etiology of mitral valve pathology is
very relevant in the early stages of evaluation of
the patient in cardiogenic shock. In general,
pathology can be primary (including endocarditis) or secondary mitral valve regurgitation;
mitral regurgitation or stenosis; mitral prosthesis
malfunction (Table 2).
• Different forms of minimally invasive
mitral valve surgery
There are different techniques for minim ally
invasive mitral valve surgery that vary by center
and surgeon. In all, in the United States
approximately 23–25% of all mitral valve operations are performed minimally invasive with 8%
robotic assisted and the rest with other forms of
minimally invasive techniques, predominantly
right minithoracotomy [11, 12]. In Germany 55%
of all mitral valve operations were performed
minimally invasive while in Italy up to 71% of
all mitral operations were performed minimally
invasive based on a multicenter study [13, 14]. In
the United Kingdom, based on study including
three centers 27% of all mitral valve operations
were performed minimally invasive between
2008 and 2016 [15].
• The endoscopic approach to mitral valve
surgery
We perform our operations endoscopically
assisted using a 5 mm 30-degree thoracoscope
positioned in the second intercostal space and
mid clavicular line allowing us to create a small
1.5–2-inches right chest working incision in the
4th intercostal space lateral to the nipple in men
and lateral to the breast in women. We find that
in order to insert mitral prostheses into the chest
without undue deformation the minimal size
incision is 1.5 inches (Fig. 2A and B). We use a
deployable crossclamp (Cygnet clamp, Peters
Surgical, Bobigny France) applied through the
right minithoracotomy. A 5 mm port in the 4th
parasternal space is used for an atrial lift
retractor.
• Contraindications to endoscopic mitral
surgery approach in cardiogenic shock
In the past many have deemed a prior right chest
operation as a contraindication to endoscopic
minimally invasive heart surger y, but we find
that this is relative to the type of previous operation. If the patient had undergone a video
assisted lung resection an endoscopic mitral
valve surgery is possible within the reasonable
time it takes to take down adhesions. We have
routinely performed endoscopic mitral valve
surgery in patients who underwent right thoracotomies, but the time spent carefully taking
down lung adhesions may prove too long in the
setting of cardiogenic shock. Patients who had
empyema and mechanical or chemical pleurodesis on the right side are true contraindications [12].
We perform the endoscopic mitral operation
in patients with systemic or near-systemic pulmonary artery pressures as well as those with a
previous open-heart operation as this has been
proven to be safe in redo sternotomies and in
minimally invasive approaches [16, 17]. One true
anatomical contraindication for endoscopic
mitral surgery in cardiogenic shock is the presence of severe mitral annular calcification unless
there is availability of an off label transcatheter
balloon expandible valve with direct surgical
implantation into mitral annular calcifi
cation
(MAC), but we have not experienced this operation in the setting of cardiogenic shock.
• Our experience
Our decision-making process in patients presenting with severe mitral stenosis or regurgitation, respiratory failure, on inotropic/pressor

Endoscopic Mitral Surgery in Cardiogenic Shock 259
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Table 2 Etiology and management of severe mitral pathology in cardiogenic shock
Etiology Pulmonary
Primary MR Start if
Infectious
MR
Secondary
MR
Bioprosthetic
valve MR or
MS
(structural
deterioration)
Mechanical
valve MR or
MS
Rheumatic
MS
Rheumatic
MR
Etiological classification of cardiogenic shock accompanying severe mitral valve disease. TMVr = transcatheter mitral
valve repair. TMVR = transcatheter mitral valve replacement. PTMB = percutaneous transcatheter mitral balloon
valvuloplasty. MR = mitral regurgitation. MS = mitral stenosis. RV = right ventricle. SVO2 = mixed venous oxygen
saturation
vasodilator
depressed
RV and/or
PAS 2/3
systemic
Start if
depressed
RV and/or
PAS 2/3
systemic
Start if
depressed
RV and/or
PAS 2/3
systemic
Start if
depressed
RV and/or
PAS 2/3
systemic
Start if
depressed
RV and/or
PAS 2/3
systemic
Start if
depressed
RV and/or
PAS 2/3
systemic
Start if
depressed
RV and/or
PAS 2/3
systemic
Inotropic support Mechanical
Implement early
(SBP >90 mmHg with
elevated lactate, large
base deficit or
SVO2 <60%)
Implement early
(SBP >90 mmHg with
elevated lactate, large
base deficit or
SVO2 <60%)
Implement early
(SBP >90 mmHg with
elevated lactate, large
base deficit or
SVO2 <60%)
Implement early
(SBP >90 mmHg with
elevated lactate, large
base deficit or
SVO2 <60%)
Implement early
(SBP >90 mmHg with
elevated lactate, large
base deficit or
SVO2 <60%)
Implement early
(SBP >90 mmHg with
elevated lactate, large
base deficit or
SVO2 <60%)
Implement early
(SBP >90 mmHg with
elevated lactate, large
base deficit or
SVO2 <60%)
support
When 1 highdose or 2
inotropes with
SVO2 <60%
When 1 highdose or 2
inotropes with
SVO2 <60%
When 1 highdose or 2
inotropes with
SVO2 <60%
When 1 highdose or 2
inotropes with
SVO2 <60%
When 1 highdose or 2
inotropes with
SVO2 <60%
When 1 highdose or 2
inotropes with
SVO2 <60%
When 1 highdose or 2
inotropes with
SVO2 <60%
Transcatheter
(TMVr/R)
TEER option Endoscopic
No TMVr/R
option
TEER option Endoscopic
Valve in
valve option
No TMVr/R
option
Primary
PTMB if
criteria met
No TMVr/R
option
Surgical
therapy
option
Endoscopic
option
option
Endoscopic
option if no
TMVR
Endoscopic
option
Endoscopic
option if no
PTMB
Endoscopic
option
support and/or mechanical circulatory support
hinges on the viability of the patient, expected
quality of life and patient’s wishes. A clear and
candid conversation with the patient and family
about the expected risks and benefits of a mitral
valve operation under the above circumstances is
paramount.
Our experience in managing mitral valve
patients in cardiogenic shock in the last two years
is summarized in Table 3. We have encountered
patients in different levels of shock, some
requiring only an inotrope and/or pressor while
others required advanced mechanical support.
The etiology behind the mitral valve pathology
varied, the most common being ischemic mitral
regurgitation (secondary MR) with an acute on
chronic presentation due to decompensation. The
predominant mechanical support was IABP

260 M. Castillo-Sang
AB
Fig. 2 A and B Surgeon’s view of the operative field using the 5 mm 30-degree angled endoscope
Table 3 Two-year experience of endoscopic mitral valve surgery in cardiogenic shock
Patient Age Etiology Procedure Pharmacologic
1 52 Papillary rupture-ischemic MR MVR Pressor + Inotrope Impella
2 68 Acute on chronic ischemic MR MVR Pressor + Inotrope Impella Yes
3 64 Acute on chronic ischemic MR Redo-
4 70 Acute presentation of chronic
Rheumatic MR
5 69 Acute presentation of chronic
Rheumatic MR
6 65 Acute on chronic ischemic MR MVR/
7 27 Endocarditis acute MR MVR Pressor + Inotrope None Yes
8 31 Endocarditis acute MR MVR Pressor + Inotrope None Yes
9 57 Acute presentation of Rheumatic
MR/MS
10 58 Acute presentation of RheumaticMSMVR Pressor IABP Yes
MVR
MVR/
TVR
MVR/
TVR
TVR
MVR Inotrope IABP Yes
support
Pressor + Inotrope Impella Yes
Pressor + Inotrope IABP No
Pressor + Inotrope Impella Yes
Pressor + Inotrope IABP Yes
Mechanical
support
VA-ECMO
Nitric
oxide
Yes
11 50 Papillary rupture non-ischemic MVr Pressor + Inotrope IABP No
12 62 Endocarditis + chronic primary MR MVR/
TVr
13 53 Acute on chronic ischemic MR MVR/
TVr
Unpublished data of endoscopic mitral valve surgeries performed in the setting of cardiogenic shock and mitral valve
disease. MR, mitral regurgitation. IABP, intra-aortic balloon pump. MVR, mitral valve replacement. MVr, mitral valve
repair. TVR, tricuspid valve repair. ABE, acute bacterial endocarditis. VA ECMO, veno-arterial extra-corporeal
membrane oxygenation. MS, mitral stenosis. Impella (Abiomed, Danvers, Massachusetts, USA)
Pressor + Inotrope IABP Yes
Inotrope IABP Yes

Endoscopic Mitral Surgery in Cardiogenic Shock 261
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followed by Impella (Abiomed, Danvers, Massachusetts, USA). There were no operative
mortalities, and all patients were discharged from
the hospital. One patient died at 4 months from
recidivism of IVDA, 12 were alive at follow-up
up to 1 year. There were no operative strokes and
one patient required hemodialysis postoperatively for one month.
2 Operative Considerations
• Anesthesia considerations
There are several considerations for the anesthesia team managing the cardiogenic shock
patient undergoing endoscopic mitral valve surgery. An important one is whether a doublelumen or single-lumen endotracheal tube will be
used. We routinely use single-lumen tubes.
On induction of anesthesia, we focus on right
ventricular protection for those without
mechanical or with only an IABP. We prevent
hypotension and once the patient is orotracheally
intubated, or when connected to the anesthesia
circuit if previously intubated, the inhaled nitric
oxide is started 40 PPM if the systolic pulmonary
artery pressure is greater than 2/3 systemic or at
20 PPM between 50% and 2/3 systemic (Fig. 3A
and B). This dosing is based on the response we
have observed in the operating room in acute
settings with active pulmonary edema complicating right ventricular dysfunction.
• Cannulation strategy
If we have the advantage of a preoperative CT
scan to evaluate the aorto-iliac vasculature we
opt to cannulate via the femoral vessels or
alternatively via the right axillary artery (for
those with prohibitive aorto-iliac disease). Our
axillary cannulation consists of a pursestring on
the artery and direct cannulation with a 15 or 17
Fr cannula with transesophageal echo guidance
to identify the guidewire in the ascending or
descending aorta. In cannulating the axillary
artery, one must have a left arm arterial line, but
we request bilateral arm arterial lines. The
venous cannulation is universally via the common femoral vein with a two-stage 23Fr to 27Fr
cannula (23Fr for BSA 1.6 m2; 25Fr for 1.6–
2.2m2; 2Fr for 2.2m2 or higher) (Fig. 4). We
favor the bicaval cannulas such as the Medtronic
Bio-Medicus NextGen (Medtronic, Minneapolis,
Minnesota, USA). In patients supported with
VA-ECMO we convert the cannulation to the
cardiopulmonary bypass circuit and at the end of
the operation, depending on the myocardial
contractility weaning off bypass we decannulate
or convert again to VA-ECMO.
The mitral valve replacement is performed
with prosthesis selection based on standard
EACTS or AHA guidelines. For those patients
Fig. 3 A intraoperative vital signs at the time of
induction of a patient supported with inotropes showing
systemic pressures preserved, pulmonary artery pressures
(105/50 mmHg) over 2/3 systemic and an elevated CVP
of 27 mmHg. B This patient was supported with an IABP
and inhaled nitric oxide

262 M. Castillo-Sang
Fig. 4 Femoral canulation strategy
on inotropic or IABP support and less than
60 years old we select a mechanical prosthesis if
no contraindications for anticoagulation exist.
For those with deeper hemodynamic compromise
requiring Impella (Abiomed, Danvers, Massachusetts, USA), VA-ECMO or both, we
elect to place a bioprosthesis. The argument for
the latter is that with full unloading of the ventricular preload there will be stasis and poor
washing of the prosthesis which may lead to
thrombosis [18].
• Cardioplegia
We exclusively use Del Nido Cardioplegia for all
minimally invasive mitral valve operations. In
the setting of cardiogenic shock having adequate
cardiac protection to minimize myocardial dysfunction is paramount, but it is also important to
abbreviate the crossclamp time. Our arresting
dose is 1,000 to 1,200 ml and redosing is
performed at 60– 70 min with 300–500 ml extra
if 30 or more minutes of work are required.
Application of the crossclamp can be challenging in cases where there is an indwelling
Impella pump (Abiomed, Danvers, Massachusetts, USA). In our experience applying a
soft insert crossclamp such as the Cygnet clamp
(Peters Surgical, Bobigny France) results in better
occlusion of the aorta. One should turn to bypass
mode the Impella device and advance it as much
as possible into the ventricle so as to crossclamp
only the smaller diameter driveline. Alternatively,
the Impella can be pulled back into the descending
aorta to apply the crossclamp understanding that it
will not be reinserted and that a new one or an
alternative mechanical support will be needed at
the end of the case. In cases where the ascending
aorta cannot be clamped and there is no aortic
insufficiency fibrillatory arrest with hypothermia
is also an acceptable option in the absence of
Impella pump.

Endoscopic Mitral Surgery in Cardiogenic Shock 263
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Fig. 5 Preoperative chest X-ray of a patient presenting in
cardiogenic shock and acute severe mitral regurgitation
secondary to papillary muscle rupture showing pulmonary
• Volume and coagulopathy management on
cardiopulmonary bypass
Patients undergoing emergent mitral valve operations in the setting of acute cardiovascular
decompensation are volume overloaded (Fig. 5).
Managing their volume overload improves pulmonary function, right ventricular recovery as
well as hepatic congestion increasing the probability of renal recovery and weaning off inotropic
and/or mechanical support. Alleviating hepatic
congestion will also improve the coagulation
profile and risk of postoperative bleeding. For
patients with longer standing heart failure and
hepatic congestion with documented coagulopathy and on preoperative anticoagulation we will
prime the cardiopulmonary bypass circuit with
edema. A pulmonary artery catheter, a percutaneous
temporary LVAD and an endotracheal tube are in place
fresh frozen plasma typically 3–4 units. We also
aggressively ultrafiltrate and remove volume
from the patient between 2–5 L depending on the
preoperative condition.
• Conduct of replacement
Mitral valve replacement should be chordal
sparing and the choice of valve prosthesis is a
result of a discussion with the patient/family and
clinical situation. We arrest the heart with antegrade cardioplegia and enter the heart through
the interatrial groove. Once the atrial exposure is
achieved using the USB Medical HV retractor
(USB-Medical, Hatboro, PA, USA) the anterior
leaflet of the mitral valve is resected preserving
the commissural and all posterior chordae. If the

264 M. Castillo-Sang
Fig. 6 Implanted bioprosthesis using an endoscopic technique
replacement is performed for an
ischemic/ruptured papillary muscle it is important to resect all non-viable tissue and if necessary recreate the chords using ePTFE (Fig. 6). It
is important to have appropriate chest and
mediastinal drainage postoperatively as pleural
and pericardial effusions can be common in the
postoperative period. On elective cases we
deploy a 24 Fr soft silastic drain in the pericardium through the oblique sinus and a 19 Fr in
the right pleural cavity. For emergent cases we
use two 24 Fr drains in the pleural cavity and one
hemodynamic stability and recovery. For patients
with biventricular dysfunction and pulmonary
hypertension a combination of epinephrine, milrinone and inhaled nitric oxide are our preferred
combination. Patients will be transported to the
intensive care unit on inhaled nitric oxide for a
wean that will depend on the pulmonary artery
pressures and right sided filling pressures. Once
the patient is capable of taking oral sildenafilwe
start it and continue this treatment if the pulmonary artery pressures and right ventricular
function dictate it.
in the pericardium.
weaned off onto inotropes alone removal of these
devices is important to avoid the need for anti-
3 Postoperative Management
coagulation posto peratively. We universally
perform a groin cutdowns to remove devices
such as Impella, IABP and VA-ECMO cannulas
• Postoperative inotropic support and fate of
the mechanical support
and are prepared to perform a thrombectomy in
all these cases. Our rationale is that attempting a
percutaneous approach for removal may lead to
Once the endoscopic mitral operation is completed, if the patient is not mechanically supported, judicious use of inotropes allows for
complications that can jeopardize a favorable
outcome for the patient. In removing mechanical
support that requires anticoagulation one also
For those on mechanical support that can be

Endoscopic Mitral Surgery in Cardiogenic Shock 265
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decreases the risk for acute blood loss anemia
and transfusions which can perseverate right
ventricular dysfunction.
4 Severe Mitral Valve Stenosis
PULMONARY EDEMA
DIASTOLIC + SYSTOLIC
HEART FAILURE AND
SHOCK
ACUTE ON CHRONIC
SYSTOLIC HEART
FAILURE AND
CARDIOGENIC SHOCK
CHRONIC SECONDARY
MR WITH ACUTE
EXACERBATION (NEW
AMI, WORSENING
LVEF)
CHRONIC RHEUMATIC
MR (VOLUME
DECOMPENSATION)
CHRONIC PRIMARY MR
(ACUTE WORSENING
OF MR)
Patients presenting acutely with decompensated
severe mitral valve stenosis are typically in
diastolic heart failure with pulmonary edema and
a degree of low cardiac output state which
negates afterload reduction but requires support
to improve forward cardiac flow and decrease
pulmonary congestion. This often cannot be
achieved with pharmacological agents alone and
thus needs mechanical support, typically in the
form of an intra-aortic counter pulsation balloon.
In addition, many of these patients will go into
atrial fibrillation which places them in a low
cardiac output state despite of preserved or
ACUTE SYSTOLIC HEART
CARDIOGENIC SHOCK
ACUTE ISCHEMIA WITH
PAPILLARY RUPTURE
slightly depressed LVEF. We have experienced a
systolic function deterioration in these patients
perhaps also secondary to a systemic inflamma-
tory response that compounds the diastolic fail-
ure and ultimately leads to more advanced
hemodynamic support such as Impella
ACUTE PRESENTATION
OF MITRAL VALVE
DISEASE
PULMONARY EDEMA
DIASTOLIC FAILURE
AND LOW CARDIAC
OUTPUT
FAILURE AND
INFECTIOUS ACUTE
DAMAGE (CORONARY
EMBOLIZATION)
CARDIOGENIC AND
SEPTIC SHOCK
RHEUMATIC MITRAL
+
STENOSIS MR WITH
-
NORMAL OR
DEPRESSED LVEF
REGURGITATION OF
ANY NATURE WITH
(Abiomed, Danvers, Massachusetts, USA) and/or
VA-ECMO implantation. Others have reported
the presentation of severe mitral stenosis as car-
diogenic shock with variable outcomes (Fig. 7A–
C) [19]. Atrial fibrillation is poorly tolerated in
mitral stenosis and leads to further decrement of
the cardiac output and use of inotropic drugs
often precipitates this circumstance [20]. For this
reason, it is important to identify the need and
institute mechanical support early to maintain a
better hemodynamic state and preserve end organ
function. In these situations, early operation is
the key to having a favorable outcome.
MITRAL
NORMAL OR
DEPRESSED LVEF
Fig. 7 A Intraoperative transesophageal echo showing smoke in the left atrium and a poorly opening mitral valve.
B Severe mitral stenosis with color flow. C Intraoperative picture of the severely stenotic rheumatic mitral valve

266 M. Castillo-Sang
Patient with decompensated presentation of
mitral stenosis require management in the
intensive care unit with invasive monitoring in
the form of pulmonary artery catheter, arterial
line and foley catheter. Goal directed therapies
need to be instituted to maintain adequate cardiac
output, minimize pulmonary edema and to preserve the right ventricular function [21, 22]. In
doing this end-organ function is preserved in the
kidneys and liver. Maintaining mean arterial
pressure of at least 65 mmHg, a cardiac index of
2 L/min/m
2
and a central venous pressure below
15 mmHg are important goals. Often times these
patients have significant pulmonary hypertension
and elevated pulmonary vascular resistance
which taxes the right ventricular function and can
lead to cardio-renal syndrome. We are relatively
liberal in the use of inhaled pulmonary
vasodilators such as inhaled iloprost or nitric
oxide (for non-intubated patients) or nitric oxide
(in intubated patients) to support the right ventricle [23, 24]. We also favor the use of milrinone
for pulmonary vasodi lation if tolerated by the
hemodynamics and cardiac rhythm without
inducing vasoplegia or atrial fibrillation. For
those with a uremic syndrome and vo lume
overload it is important to institute renal
replacement therapy and improve the overall
metabolic state of the patient as well as to
improve platelet function.
The first-line management of mitral stenosis is
percutaneous transcatheter mitral balloon valvuloplasty (PTMB) and this has been used even in
the setting of cardiogenic shock [25]. Patients
with rheumatic stenosis and accompanying
regurgitation or valve calcification are not candidates to PTMB and in these patients our
approach for isolated mitral or mitral and tricuspid valve surgery is universally through the
right chest endoscopically with a 1.5– 2-inch
incision at the 4th intercostal space and with a
5 mm 30-degree angled scope in the 2nd intercostal space mid-clavicular line (Fig. 8) with a
femoral vessel cutdown of 1–2-inch incision
which has been proven to be safe and effective in
rheumatic mitral stenosis [26]. This is the case
even in emergency operations and reoperations
with no sternotomy conversions and an average
of 5–7 such operations per year.
We would be remiss not to emphasize that it is
paramount that not only the surgeon be comfortable with elective complex endoscopic mitral
valve surgery, but also the anesthesia, perfusion
and nursing members of the team as many of
these operations take place outside of regular
work hours and are performed perhaps with less
familiarized members of the team. To this end we
recommend that everyone in the cardiac team
gets experience performing endoscopic valve
surgery.
5 Ruptured Papillary Muscle
CHRONIC SECONDARY MR
WITH ACUTE
EXACERBATION (NEW
AMI, WORSENING LVEF)
ACUTE ON CHRONIC
SYSTOLIC HEART FAILURE
AND
CARDIOGENIC SHOCK
CHRONIC RHEUMATIC MR
(VOLUME
DECOMPENSATION)
CHRONIC PRIMARY MR
(ACUTE WORSENING OF
MR)
PULMONARY EDEMA
DIASTOLIC + SYSTOLIC
HEART FAILURE AND
SHOCK
ACUTE SYSTOLIC HEART
FAILURE AND
CARDIOGENIC SHOCK
ACUTE ISCHEMIA WITH
PAPILLARY RUPTURE
ACUTE PRESENTATION OF
MITRAL VALVE DISEASE
INFECTIOUS ACUTE
DAMAGE
(EMBOLIZATION)
CARDIOGENIC AND SEPTIC
SHOCK
DIASTOLIC FAILURE AND
RHEUMATIC MITRAL
+
STENOSIS MR WITH
-
NORMAL OR DEPRESSED
LVEF
PULMONARY EDEMA
LOW CARDIAC OUTPUT
MITRAL REGURGITATION
OF ANY NATURE WITH
NORMAL OR DEPRESSED
LVEF

Endoscopic Mitral Surgery in Cardiogenic Shock 267
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Fig. 8 Postoperative picture 10 days after surgery showing the endoscopic approach. A =5 mm 30-degree endoscope.
B =Atrial lift retractor port. C =Chest drain
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