Approach to Complex Cases in Cardiac Catheterization

A diligent precatheterization work-up can help an operator to suspect the presence of left main disease, and reduce the risk of catastrophic complications of left coronary cannulation (Figure 18.1).1,2



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FIGURE 18.1The diagram shows various types of left main stenosis.


Steps to be performed in the cardiac catheterization laboratory when precatheterization work-up suggests presence of LM coronary stenosis are as follows:



Coronary Anomalies


The most frequent coronary anomaly observed during selective coronary angiography is the absence of a LM coronary artery, with the LCX and LAD either sharing a common origin from the aorta but splitting immediately, or originating separately in the left coronary cusp (LCC).2,3 When approached with a JL coronary catheter, the tip may selectively engage either the LAD or LCX. Most of the time it is difficult to opacify both arteries simultaneously, and each artery should be cannulated separately. Occasionally, it can be accomplished by rotating the JL catheter counterclockwise in order to engage the LAD, and clockwise to get the LCX. Sometimes the catheter needs to be changed according to a simple rule: If the LCX artery is engaged on the initial attempt with the JL4 catheter, the operator should use a JL3.5 catheter to get the LAD, and vice versa (e.g., if the smaller-curve JL catheter engages the LAD, a larger-curve catheter is used to engage the LCX). If the above approach does not yield adequate information, other catheters, including the AL or MP (technique described in Chapter 7), should be considered.


The LM coronary artery occasionally may be difficult to cannulate by a preformed JL coronary catheter, despite originating from the LCC, when the ostium is either deep down or high up in the cusp, or when it is posteriorly or anteriorly oriented. A nonselective “cusp” shot frequently helps the operator to visualize the origin of the LM and choose the appropriate catheter and approach. Usually, an anomalously originating LM coronary artery located in the left coronary sinus can be approached and successfully cannulated by the MP or AL coronary catheters (counterclockwise rotation for posterior location, and clockwise rotation for anterior position). A LM originating from the right sinus of Valsalva is rare (0.15% of patients), and even more rare when originating from the noncoronary sinus.3 Figure 18.2 depicts some of the most common coronary anomalies in adults.



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FIGURE 18.2Coronary anomalies of the LCA (Panel A) and RCA (Panel B) are shown.


WHICH ANOMALIES ARE DANGEROUS?


When the LM or RCA originates from the noncoronary sinus, its course is benign and not associated with major adverse effects. A LM originating from the right sinus of Valsalva is somewhat more problematic. The course of the artery is not necessarily benign, since it can run between the PA and aorta, a course that can be associated with sudden cardiac death. In general, cannulation of the LM originating from the right sinus of Valsalva is accomplished using AR or AL coronary catheters. The origin of the LM anteriorly to the ostium of the RCA, on the other hand, is usually a dangerous course. The same can be said about the anomalous origin of the LAD artery from the right sinus of Valsalva. On the other hand, an anomalous origin of the LCX from the right sinus of Valsalva is always followed by a benign course, although the risk of developing atherosclerosis may be higher. This type of an anomalous origin can be cannulated using modified AR or MP catheters.


Occasionally, the LCX shares a common ostium with the RCA and can be opacified with a JR catheter. When the RCA originates from the left sinus of Valsalva, its course can also frequently be malignant, especially if its ostium is anteriorly located in relation to the LM ostium. To selectively cannulate this artery, the operator may consider using JL5 or JL6, AR, or AL coronary catheters.


Referral to CT angiography in case of a suspected malignant course of an anomalous left or right coronary artery is highly recommended. The RCA origin in the right sinus of Valsalva can also vary: An inferior ectopic origin can be most successfully cannulated with a MP catheter; an anterior ectopic origin in the cusp is best cannulated with AL or AR catheters; a posterior ectopic origin can be cannulated best with an MP catheter; a superior/anterior ectopic origin above the sinotubular junction is best approached with MP (see Chapter 7), AL, or 3D-RCA coronary catheters. When using a 3D-RCA catheter, the operator should slowly withdraw the catheter into the ascending aorta from the cusp with minimal clockwise rotation and frequent test injections to orient the tip of the catheter towards the coronary ostium.


Test injections of contrast are used with attempts to cannulate any anomalous coronary vessel with clockwise or counterclockwise maneuvers of the catheter. For example, if the anomalous coronary artery is located more anteriorly, step-by-step clockwise rotation with test injections will opacify the artery gradually, since the tip of the catheter will be approaching the ostium. On the other hand, step-by-step counterclockwise rotations with nonselective test injections will poorly opacify the same artery, since the tip of the catheter will be pointing away posteriorly from the ostium. Similarly, small, nonselective test injections are helpful when the operator attempts to determine if the ostium of the anomalous coronary artery is located high or low in the cusp. In order to evaluate the course of an anomalous coronary artery arising from another (anomalous) cusp, an operator should take an RAO view. If the initial course of the coronary artery is posteriorly directed, the course is more likely to be “benign”, on the other hand if the initial course of the artery is anteriorly directed the course is more likely to be “malignant”.


Coronary Spasm and Myocardial Bridge


The decision to further investigate a patient with angiographically normal coronary arteries or with physiologically insignificant stenosis is made when the clinical suspicion of coronary vasospasm causing myocardial ischemia is high based on the combination of subjective (history and physical) and objective data (ECG and noninvasive cardiac imaging) (Figure 18.3A).4,5 Occasionally, the simple cannulation of the coronary artery or a simple, forced episode of hyperventilation in patients predisposed to coronary vasospasm may provoke vasospasm that can be directly visualized by selective coronary angiography and resolved by intracoronary administration of nitroglycerin. In patients with symptoms related to cold exposure, a cold pressor test (immersing hands into icy cold water) can be performed in the cardiac catheterization laboratory.



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FIGURE 18.3Panel A is a diagram of coronary vasospasm; Panel B is an example of myocardial bridging.


If these maneuvers do not provoke coronary vasospasm, the operator may proceed with pharmacologic provocative testing. The 2 most frequently used agents for this purpose in the United States are methylergonovine and acetylcholine. In Europe and Japan, ergonovine maleate is used as well. To reverse the effect of these medications, intracoronary nitroglycerin is administered as needed. Bradycardia and hypotension, which may follow acetylcholine infusion, can be treated by intravenous administration of atropine 0.5 mg every 3–5 minutes up to a total dose of 2 mg. Major contraindications to performing pharmacological provocative testing are severe LV dysfunction, severe aortic stenosis, amenorrhea in premenopausal women (possible pregnancy), and significant LM coronary stenosis.


Different protocols for pharmacological provocative testing have been described in the literature. Ergonovine maleate can be given intravenously at doses of 50 mcg every 5 minutes until a total maximal dose of 350 mcg; a positive response or side effects necessitate termination of the test. Ergonovine can also be given by intracoronary injection of 5–10 mcg up to a total cumulative dose of 50 mcg. Methylergonovine can be given every 3 minutes in successive intravenous boluses of 1, 2, 3, and 4 mcg/kg. Again, a positive response or side effects necessitate termination of the test. Acetylcholine can be injected in incremental doses of 20, 50, and 80 mcg every 3 minutes into the RCA, and in incremental doses of 20, 50, and 100 mcg every 3 minutes into the LCA. A positive response or side effects necessitate termination of the test. Intracoronary administration of nitroglycerin reverses vasospasm of the coronary arteries provoked by ergonovine derivatives or acetylcholine.


Epicardial coronary arteries may occasionally take an intramyocardial course, which may lead to the entrapment of various lengths of the artery under the myocardial tissue, described as a “bridge” (Figure 18.3B).6 The mid-LAD followed by the RCA are most commonly involved. In general, myocardial bridging is a benign phenomenon, but in rare cases it can lead to compromised blood flow and myocardial ischemia. The mechanism for this complication includes systolic and more importantly diastolic compression of the vessel lumen, due to an inability or delayed ability of muscle relaxation. Furthermore, vasospasm and the development of atherosclerosis in the proximal or distal segments, just prior to, or right after the “bridge” can be contributing factors. Coronary angiography can reveal the systolic narrowing or “milking effect” of the epicardial coronary artery with or without persistent diastolic reduction in vessel lumen diameter. To assess functional significance of myocardial bridging it may be required to measure fractional flow reserve after dobutamine infusion or evaluate its anatomy by intravascular ultrasound. Detailed description of these methods is beyond the scope of this manual.6


Aortic Stenosis


When dealing with a severely calcified aortic valve, fluoroscopy of the valve in different projections can outline the orifice of the stenotic valve and may help crossing the valve with the guidewire. To cross a severely stenotic aortic valve, a soft, straight-tipped, 0.035-inch guidewire can be used. The optimal view for crossing the aortic valve is RAO; techniques for different catheters have been described in Chapter 9. An intravenous heparin bolus (40 units/kg) should be administered after the arterial access is obtained to keep the ACT ≥ 200 seconds, with frequent (2–3 minutes) removal and cleaning of the guidewire during the procedure. The operator should never apply excessive force in an attempt to push the wire or catheter across the stenotic valve; rather, a patient trial-and-error approach with slight maneuvering of the catheter and guidewire is the way to success. Steps are as follows:





  • Step 6: Remove the catheter and flush both sheaths.


  • Mild AS: mean gradient < 25 mm Hg
  • Moderate AS: mean gradient 25–39 mm Hg
  • Severe AS: ≥ 40 mm Hg


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FIGURE 18.4Simultaneous LV and aortic pressure tracings in aortic stenosis are shown. Panel A: Diagram; Panel B: Patient tracing.

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Oct 31, 2016 | Posted by in CARDIOLOGY | Comments Off on Approach to Complex Cases in Cardiac Catheterization

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