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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3597_Библиотеки_им_академика_М_И_Перельмана

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femoral artery (SFA)-profunda bifurcations are below this point and permit access to ipsilateral SFA, profunda, popliteal, and below-the­knee vessels.
2. Retrograde, common femoral: Access of the ipsilateral iliac artery permits a contralateral approach to iliac SFA and below-the-knee lesions.
3. Brachial-axillary (radial with extra long catheters) access requires extra-long catheters and balloons (120 to 145 cm). Access is used when bilateral iliofemoral vessels are occluded.
4. Popliteal: Retrograde access for SFA occlusions avoids the proximal cap and minimizes the likelihood of entering side branches in total occlusions. There is risk of joint space (knee) injury.
5. Tibial: Retrograde access for tibial occlusions avoids the proximal cap.
Interventional Cardiology Procedures
Angiography
1. Cardiac catheterization laboratory equipment (Digital subtraction angiography should be considered for noncoronary imaging.)
Image intensifier, 9-inch mode
Digital imaging subtraction to reduce radiation exposure
Cineframe rates show flow dynamics (helpful in assessing
collaterals)
Speed of 15 frames/sec is adequate
2. Abdominal aortogram
Catheter positioned above or at the level of renal arteries (L1
or L2 disk space)
Contrast medium injection, 15 mL/sec × 3 sec or 20 mL/sec ×
2 sec
Pan to iliofemoral vessels
Lateral plane for celiac, superior mesenteric, or inferior mesen-
teric artery origins
LAO 20 degrees for renal artery origins
3. Selective iliofemoral angiography with runoff to feet
Catheter positioned in proximal common iliac artery
Simmons, SOS Omni Selective Catheter (AngioDynamics,
Latham, NY), VCF, Cobra (Terumo Medical, Somerset, NJ), internal mammary, or pigtail catheters used
Contrast medium injection, 6 to 8 mL/sec × 4 to 6 sec
Lateral angulation of image intensifier at 30 degrees (SFA-
profunda bifurcation)
Pan from common iliac artery to foot vessels
Chapter 5 provides illustrations of common peripheral vascular
interventions and complications
Figure 10-16 shows an example of renal artery stenting.
Structural Heart Disease: Valvuloplasty and Percutaneous Valve Replacement
Percutaneous techniques as alternatives to surgery for the treatment of valvular and congenital heart disease were introduced in the early 1980s and have undergone dramatic advances. Today, we have a large spectrum of therapeutic interventions to address problems once con­fined to the cardiothoracic surgeon (Fig. 10-17).
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Interventional Cardiology Procedures 443
A
B
Figure 10-16 Cineframe of left renal arter y before (A) and after (B) renal
artery stenting.
This section addresses balloon valvuloplasty for aortic and mitral valves in adults, transcatheter aortic valve replacement (TAVR) for adult aortic stenosis, MitraClip (Abbott Vascular, Redwood City, CA) for mitral regurgitation (MR), patent foramen ovale (PFO)/ASD closure devices, left atrial appendage (LAA) closure devices, and alcohol septal ablation for hypertrophic obstructive cardiomyopathy (HOCM). This review is not intended to be comprehensive but merely a source of introductory information regarding some of the available devices and techniques that may be encountered in catheterization laborato­ries across the country.
Percutaneous Balloon Mitral Valvuloplasty
For mitral stenosis, balloon mitral valvuloplasty is as an excellent alternative to surgical commissurotomy or valve replacement and, in selected patients, considered to be the initial mechanical treatment of
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Interventional Cardiology Procedures
Valvular
heart
disease
Hypertrophic
cardiomyopathy
Other
Paravalvular
leak
Patent ductus
artieriosus
Figure 10-17 Spectrum of structural heart disease. (From Steinberg DH,
Staubach S, Franke J, et al: Defining structural heart disease in the adult patient: current scope, inherent challenges and future directions. European Heart Journal Supplements 12(Supplement E), E2–E9, 2010.)
Patent
foramen
ovale
Atrial septal
defect
Ventricular septal
defect
Left atrial
appendage
Left
ventricular
aneurysm
choice. Percutaneous balloon mitral valvuloplasty (PBMV) for the treatment of mitral stenosis has been studied extensively, and when successful, yields marked immediate hemodynamic improvement and sustained clinical benefit. Prospective comparisons of PBMV with sur­gical commissurotomy in selected patients have shown similar hemo­dynamic and clinical results in follow-up. Clinical success is high, and complication rates are low. However, not all patients are optimal can­didates for PBMV. Echocardiography is essential to evaluate mitral valve structure and to exclude LA thrombus before making decisions to proceed with PMBV.
Indications
Symptomatic Mitral Stenosis
Patients with isolated symptomatic mitral stenosis or stenosis com­bined with mixed valvular disease, less than moderate MR, and suitable valvular characteristics can be offered PBMV because of com­parable risk and relative ease of the procedure.
Immobile, severely thickened, and fused or calcified valve leaflets may not respond well to PBMV. However, patients with symptoms of mitral stenosis with these unfavorable characteristics who are not candidates for surgery may still benefit from the procedure. PBMV is contraindicated in the presence of atrial thrombus, which is best detected by transesophageal echocardiography (TEE).
Procedure
Antegrade transseptal access to the mitral valve with use of a single, specially designed balloon catheter (Inoue balloon) (Fig. 10-18) is the easiest and most reliable method for LA access. Because of its
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Interventional Cardiology Procedures 445
A
B
Figure 10-18
mitral valve during mitral valvuloplast y. B, Cineangiogram frame of Inoue balloon catheter in position across the mitral valve during mitral valvulo­plasty. Front and back portions of balloon are inflated, creating a “dogbone” shape that self- positions the balloon in the mitral orifice. The balloon con ­tinues to be inflated until the waist is eliminated. Transmitral pressure gradi­ent must be checked before increasing inflation volume on the next balloon expansion.
A, Diagram of Inoue balloon catheter in position across the
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single-balloon design and relative ease in crossing the mitral valve, use of the Inoue balloon generally requires less fluoroscopic and procedural time than previously used double-balloon techniques.
After baseline hemodynamic measurements are obtained, trans­septal catheterization is performed (see Chapter 7). Experienced operators perform the puncture mid to low on the septal wall to avoid a high puncture, because this location presents great difficulty in crossing the mitral valve and positioning the balloon catheter.
Dilating  the  Interatrial  Septum.  After crossing the atrial septum
with the catheter and placement of the exchange guidewire, a 6- to 8-mm balloon is used to dilate the septum and allow easy passage of the larger dilation catheters. The residual small ASD is not generally clinically important.
Inoue Balloon Technique.  The Inoue balloon catheter has a unique
design that allows inflation of the distal part of the balloon to facilitate crossing the mitral valve. Once across the mitral valve, a step-wise incremental valve dilation can be performed using a calibrated infla­tion syringe. Selection of balloon size is based on patient height. After LA access is obtained, the interatrial septum is dilated, and the Inoue balloon is tracked over the special guidewire into the left atrium. The distal balloon tip is floated across the mitral valve, steered with a stylet. The partially inflated balloon is withdrawn to engage the mitral valve leaflets and then fully inflated to achieve commissural splitting. The transmitral pressure gradient and an echocardiographic assess­ment of commissural splitting and any regurgitation have been recom­mended after each dilating step to assess the need for continued larger balloon dilations to safely obtain the maximum mitral orifice possible without producing MR.
After the last inflation, LA-LV pressure and right-sided oxygen saturation (to detect left-to-right shunting at the atrial septal level) are measured. The average decrease in mitral valve gradient is approxi­mately 50% to 75% of the baseline gradient, and the increase in valve area is usually around 100% (average 2 cm2), leading to a doubling of the cardiac output. Figure 10-19 shows a hemodynamic case example of PBMV.
Interventional Cardiology Procedures
Complications
Procedural and hospital mortality are rare (0% to 2%) and usually the result of ventricular perforation. Complications of transseptal punc­ture, such as hemopericardium or tamponade, are also rare (<2%). Systemic emboli may occur in 1% to 2% of patients. MR increases in 20% to 50% of patients but significantly (by more than one angio­graphic grade) in only 8% to 10% of patients. Significant MR may appear late after PBMV. MR severe enough to require valve replace­ment occurs in 0.9% to 3% of patients after PBMV and is usually the result of noncommissural tearing of the mitral leaflets or chordal rupture. An ASD with left-to-right shunting is detectable in 8% to 87% of patients (depending on the sensitivity of the method used for detec­tion); most of these defects have shunt fractions of <1.4 to 1, are clini­cally unimportant, and decrease or disappear during follow-up.
Follow-Up
The symptomatic status of the patient generally improves immediately and during follow-up. Short-term symptomatic improvement is present in most patients. Long-term results (5 years) remain positive in well­selected patients. In such patients, event-free 5-year survival is >80%. Patients with more deformed valves and higher echocardiographic scores have a higher rate of restenosis. The incidence of restenosis and long-term outcome after PBMV is comparable to closed mitral com­missurotomy in selected patients.
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Interventional Cardiology Procedures 447
A
B
Figure 10-19 A, Directly measured left atrial (LA)-left ventricular (LV) gradi-
ent and transmitral Doppler flow velocity before a percutaneous balloon mitral valvuloplasty (PBMV) shows a gradient of 32 mm Hg. B, After PBMV, the LA-LV gradient is 8, with corresponding reduction in Doppler flow velocity and no mitral regurgitation (MR).
MitraClip for Mitral Regurgitation
The standard of care for treatment of severe degenerative MR is surgi­cal mitral valve repair or replacement. The MitraClip (Fig. 10-20) is the most widely used percutaneous repair system, duplicating a stitched “edge-to-edge” technique to create a smaller double-orifice valve. The MitraClip system has been evaluated in EVEREST I and II studies.
Indications
Patients with a class-I indication for mitral valve surger y (according to the American Heart Association/American College of Cardiology [AHA/ACC] 2014 guidelines for valvular heart disease) are suitable candidates if they are believed to be at high or prohibitive risk for open surgical repair. Symptomatic patients with severe MR in the absence of severe LV dysfunction and/or an LV end systolic dimension > (class-I recommendation, level of evidence [LE] B) are the target population. In asymptomatic patients with severe MR, mitral valve surgery is indicated if LV dysfunction is present (class-I recommenda­tion, LE B). Additionally, patients with severe MR and new-onset atrial fibrillation or pulmonary hypertension are also candidates.
55 mm
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A
Interventional Cardiology Procedures
B
C
Figure 10-20
Vascular). B, Approximation of anterior and posterior mitral valve leaflets as effected by the MitraClip. C, Ventriculogram in systole with MitraClip in place, showing minimal mitral regurgitation (MR). (From Steinberg DH, et al: Eur Heart J Suppl 12:E2–E9, 2010.)
A, MitraClip (Abbott Laboratories, Abbott Park, IL, Abbott
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Interventional Cardiology Procedures 449
MitraClip Procedure
The MitraClip procedure is performed with the patient under gen­eral anesthesia and with the use of fluoroscopy and TEE for device guidance. The right femoral vein is accessed and an 8 -F sheath inserted. Right-heart catheterization is then performed.
Transseptal puncture follows using standard technique via the right femoral vein at a height of 3.5 to 4.0 cm above the mitral valve in a posterior superior orientation. Heparin is then given with a goal ACT of > and 22 F at the atrial septum. The transseptal sheath is exchanged for the guide catheter and tapered dilator. The clip delivery system is advanced through the guide catheter and into the left atrium. Controls on the guiding catheter allow deflection of the distal tip. The clip delivery system has two dials that permit medial-lateral and anteropos­terior steering. Using fluoroscopic and echocardiographic guidance, the MitraClip is steered until axially aligned and centered over the origin of the regurgitant jet. The clip is opened to extend the two arms and then advanced into the LV below the mitral leaflets. The clip is retracted so that each leaflet is grasped by an extended arm and then closed to coapt the mitral leaflets. The inner portion of the clip has two “grippers” adjacent to each arm to secure the leaflets as the clip is closed. Leaflet insertion into the clip and MR reduction are assessed by two-dimensional and Doppler echocardiography. If reduction in MR is not adequate, the clip can be reopened to release the leaflets and the clip repositioned. After adequate reduction of MR has been achieved, the clip is deployed and the delivery system and guide catheter are removed.
cutaneous mitral valve repair system is a safe and effective treat­ment option that reduces MR, has a favorable impact on LV remodeling, improves symptoms, and reduces hospitalizations for heart failure.
tions, and outcomes is provided in the Interventional Cardiac Catheter-
ization Handbook.
300 seconds. The steerable guide catheter is 24 F proximally
In patients who are at high risk for surgery, the MitraClip per-
A full discussion of the indications, contraindications, complica-
Transcatheter Aortic Valve Replacement
The advent of TAVR provided an option for those previously unable to undergo surgical AVR. Indications are limited to those patients with symptomatic critical aortic stenosis if they are deemed by a surgeon to be inoperable or high risk.
Evaluation for TAVR is very detailed and includes determination of any coronar y artery disease, LV dysfunction, presence of concomi­tant medical comorbidities (chronic obstructive pulmonary disease [COPD], renal insufficiency, carotid disease), assessment of the pati­ent’s frailty, and determination of the degree of peripheral vascular disease. The workup requires transthoracic echocardiography (TTE) and/or, cardiac catheterization with coronary angiography and pulmo­nary function testing, carotid duplex imaging, and body computed to­mography (CT) angiography. CT is the imaging modality of choice for the preprocedural workup of the TAVR patient and assists in device size selection and route of placement. Preprocedural evaluation of vas­cular access with CT angiography is an important step to determine suit­ability for a transfemoral (TF) or transapical (TA) approach for TAVR.
Standard for TAVR is a hybrid operating room/catheterization laboratory for simultaneous fluoroscopy guided catheter manipu­lation and conversion to open surgery, if needed. The room should be large enough to accommodate a team consisting of cardiac anes­thesiologists, echocardiographers, cardiac surgeons, and interven­tional cardiologists.
Two valves for TAVR are currently available: the balloon­expandable Edwards SAPIEN system and the self-expanding Medtronic CoreValve system (Fig. 10-21).
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Interventional Cardiology Procedures
A
CoreValve PHV
Edwards SAPIEN PHV
1
2
3
Valve loaded
1 2
3 4
B
Figure 10-21
Edwards SAPIEN (Edwards Lifesciences Corp., Irvine, CA) percutaneous heart valve (PHV). Bovine pericardium leaflets 1, (blue arrowhead) sutured (expanded polytetrafluoroethylene) 3, (black arrow) onto a stainless-steel stent frame 2, (blue arrow). Bottom right, Delivery catheter (RetroFlex II, Edwards Lifesciences Corp., Irvine, CA) with valve loaded (red arrow). B, Percutaneous aortic valves: 1, Edwards SAPIEN. 2, Fluoroscopic image of Edwards SAPIEN device in place. 3, CoreValve. 4, Aortogram with CoreValve in place. (A, From Chiam PTL, et al: J Am Coll Cardiol Intv 1:341–350, 2008. B, From Steinberg DH, et al: Eur Heart J Suppl 12:E2–E9, 2010.)
A, Left, CoreValve (Medtronic, Inc., Minneapolis, MN). Right,
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Interventional Cardiology Procedures 451
Procedural Details
Large-bore vascular access (or TA access) is obtained followed by guidewire crossing of the aortic valve with balloon valvuloplasty (Fig.
10-22). Delivery of the valve catheter is performed under fluoroscopic
guidance and positioned across the aortic valve. An aortogram identi­fies calcific aortic and valvular landmarks and overall valve position before deployment (Fig. 10-23). Once position is confirmed, usually using fluoroscopy and TEE guidance, rapid pacing is initiated to halt ventricular ejection. Once achieved, the valve can be deployed using fluoroscopic and echocardiographic guidance. TEE before and during the procedure is important for defining valvular anatomy, annular sizing, valvular regurgitation, and ventricular function. Postdeploy­ment, TEE is necessary to accurately assess for either valvular or paravalvular (PVL) aortic regurgitation, ventricular function, mitral valve function, coronary ostial blood flow, and complications, such as annular rupture, pericardial effusion, or tamponade. An immediate assessment can be helpful in identifying a potential complication of the valve deployment (Fig. 10-24). Procedural risks of TAVR are sum­marized in Box 10-3.
Structural Heart Disease: Atrial Septal Defects and Patent Foramen Ovale Closure
Most full service catheterization laboratories treat ASDs and PFO with specific closure devices used by experienced operators. In brief, the technique involves placing an 8-F or 9-F sheath across the defect (Fig.
10-25). An appropriately sized closure device (Fig. 10-26) is delivered
to the left atrium. The device is partially deployed, pulled back into the septal defect, and the right-sided disk is deployed, capturing the
Figure 10-22 Diagram of two techniques of aortic balloon valvuloplast y.
A, Retrograde approach; B, antegrade, transseptal approach.
Box 10 -3 Transcatheter Aortic Valve Replacement
Procedural Risks
Stroke Vascular complications Conduction system abnormalities Valvular insuf ficiency Coronary ostial compromise
BA