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The modern-day
cardiac catheterization laboratory (CCL) has truly
become a multimodality interventional suite in which
patients undergo a variety of diagnostic and therapeutic
procedures. The history of human cardiac catheterization
can be traced back to 1929 when Werner Forssmann,
M.D., a surgical resident, inserted a percutaneous
catheter into his right atrium via his antecubital
vein in a small hospital in Eberswald, Germany. In
1964 vascular radiologist Charles T. Dotter, M.D.,
introduced the concept of transluminal angioplasty,
while the first CCL percutaneous transluminal coronary
angioplasty (PTCA) in an awake patient was performed
by Andreas Gruentzig, M.D., a cardiologist in Zurich,
Switzerland, in 1977.8-10
Pediatric cardiac catheterization was first described
in the 1930s by Castellanos4
and was first used purely as a diagnostic tool. Balloon
atrial septostomy, first reported by Rashkind in 1968
in order to palliate neonates with transposition of
the great arteries, was the first widely performed
interventional procedure.14
The scope and practice of pediatric cardiac catheterization
has continued to expand and now includes a multitude
of interventional procedures. Because noninvasive
imaging with echocardiography and/or magnetic resonance
scanning is frequently used for anatomic diagnosis,
cardiac catheterization is reserved for smaller, more
critically ill patients with complex congenital heart
disease who may require interventional procedures
and diagnostic imaging prior to surgical intervention.
At the Texas Heart Institute, approximately 10,000
patients are seen annually in the CCL, and many of
these cases require the consultation of an anesthesiologist.
Procedures performed in the CCL may include diagnostic
angiography, PTCA and stenting, electrophysiology
studies and ablations, exclusion of both thoracic
aortic aneurysms (TAA) and abdominal aortic aneurysms
(AAA), valvuloplasty, transcatheter closure of atrial
septal defects, pacing and defibrillator devices and
even the placement of life-sustaining devices such
as the new TandemHeart™ percutaneous ventricular
assist device (pVAD). At Texas Children’s Hospital,
970 cardiac catheterizations were performed between
September 2002 and August 2003 with anesthesiologists
participating in the care of 74 percent of these patients.
As diagnostic and interventional catheterizations
are performed on smaller and sicker patients with
increasingly complex forms of congenital heart disease,
skillful anesthetic management is critical in maintaining
stable hemodynamics and rapidly managing any complications
that may occur during the procedure.
Performing an anesthetic in the interventional suite
may present quite a challenge for the anesthesiologist,
considering the complexity of the procedures and the
multiple comorbidities of the patients. Preparation
and familiarity with the arrangement of the CCL are
key to the delivery of an uneventful anesthetic. The
interventional laboratories are commonly located in
remote locations separate from the general operating
rooms and usually consist of a large procedural area
and shielded control room. As the CCL is often distant
from the blood bank, packed red blood cells (PRBCs)
are generally held in the CCL during pediatric interventional
procedures. In infants a unit of PRBCs may be split
in the blood bank and a partial unit brought to the
CCL in order to limit the patient’s exposure
to multiple units of blood. The use of fluoroscopy
and X-radiation are prominent in the CCL; therefore,
it is imperative that all anesthesia personnel strictly
adhere to the following three radiation safety principles:
maximize distance from the radiation source, minimize
exposure times and always use proper shielding with
leaded glass, acrylic, gowns, gloves, thyroid collars
and stands. Dosimeters must be worn at all times to
help track cumulative exposure, and practitioners
should keep all radiation doses “as low
as reasonably achievable”
(the ALARA principle), a concept fully supported by
the radiation safety program at the Centers for Disease
Control and Prevention.
The use of radiocontrast media is quite common in
the CCL due to the extensive use of fluoroscopy, and
the anesthesiologist should be aware of the effects
of these agents. Many of the newer low-osmolar, nonionic
agents such as Omnipaque™ (iohexol) have improved
adverse reaction profiles, but caution must be exercised
in patients with pre-existing renal insufficiency
and diabetes mellitus;16
furthermore, these agents continue to be associated
with atrial and ventricular arrhythmias, prolonged
Q-T intervals, vasovagal reactions and thromboembolic
events that may lead to the development of a myocardial
infarction or cerebrovascular accident. Thromboembolic
complications seem to be related to the length of
the procedure, the type of catheter and syringe material
used and the patient’s underlying disease processes.
In infants, hypotension may be seen after contrast
injection. Nephrotoxicity and the development of acute
renal failure also are related to these agents, but
the etiology of the renal failure remains unknown.
The presumed mechanism is related to direct chemical
toxicity and the effects of hypertonicity on red blood
cells leading to altered deformability and thus compromised
flow characteristics resulting in hypoperfusion of
end organs. Adjuncts such as furosemide, mannitol,
dopamine, fenoldapam and acetylcysteine have been
used in an attempt to prevent renal impairment; however,
adequate hydration and stable hemodynamics remain
as the most reliable defenses against contrast-induced
nephrotoxicity.1,2,3,5,12,17
Anesthetic requirements in the CCL may range from
monitored anesthesia care (MAC) to full general anesthesia
with invasive monitoring and other modalities such
as transesophageal echocardiography. As interventional
procedures may be lengthy, and the potential exists
for hemodynamic instability and significant blood
loss, general anesthesia with endotracheal intubation
is commonly performed in infants and children undergoing
procedures such as balloon valvuloplasty, coiling
of aortopulmonary collaterals, dilation or stenting
of pulmonary arteries, balloon dilatation of coarctation
of the aorta and device closure of a ventricular septal
defect. With the advent of intracardiac echocardiography,
however, device closure of an atrial septal defect
may now be accomplished with deep sedation and spontaneous
ventilation, even in children. Even regional techniques
such as spinals and epidurals may be performed depending
on the procedure at hand. Due to the prevalent use
of antihemostatic and antithrombotic drugs, however,
such as clopidogrel, low molecular weight heparin
and warfarin, the risk of hemorrhage and the formation
of an epidural hematoma should always be considered,
even though the incidence of neurologic compromise
has been estimated at <1/200,000 cases with spinal
anesthesia and <1/150,000 cases with epidural anesthesia.6,7,11,13,15,18
Caution also should be exercised when dealing with
medications such as abciximab and eptifibatide, which
significantly affect platelet function and hemostasis.
Ready access to skilled anesthesia personnel, the
pharmacy and the stat laboratory are also important
when working in the CCL. For example there is always
the potential for acute blood loss during the stenting
of a tortuous AAA due to perforation or rupture of
the aneurysm. The CCL is then rapidly converted into
an operating suite, and the need for frequent blood
sampling and rapid transfusion is immediate. The presence
of a transfusion device such as the Belmont FMS 2000™
and experienced colleagues and assistants are invaluable
in helping to manage such an unfortunate situation.
The care of critically ill patients in the interventional
laboratory does not cease upon completion of the posted
procedure, and arranging for an intensive care bed
may be necessary to help continue an acute level of
care.
Regarding electrophysiology mapping studies and ablations,
the use of inotropic drugs and vasopressors should
be held to a minimum due to their proarrhythmogenic
effects. This will help the electrophysiologist to
determine an accurate mapping baseline for the patient,
leading to more effective ablation of ectopic foci
and tracts. Patients with pacing devices and automatic
implantable cardioverter-defibrillator devices (AICDs)
also should receive special attention in the CCL.
When using electrocautery, exit pads should be placed
in positions that direct electrical current away from
pacing and AICD leads; otherwise suppression of pacing
and inappropriate triggering of AICDs may occur. Due
to the negative effects of electromagnetic interference,
a transdermal magnet should be available at all times
to convert pacemakers into asynchronous mode and also
to suppress antitachycardic therapies on AICDs. When
specifically working on a pacing device, the anesthesiologist
must be aware of the presence of unipolar leads; if
the generator loses physical contact with the patient
on a unipolar lead setup, the device will be unable
to pace due to an open circuit, and immediate means
for backup pacing must be readily available to avoid
hemodynamic compromise.
Electrophysiologic studies and radiofrequency ablations
of arrhythmogenic foci are frequently performed on
children with supraventricular tachycardia and Wolff-Parkinson-White
syndrome. Increasingly, however, patients undergoing
pediatric electrophysiologic studies and ablations
may have significant underlying congenital heart disease
and arrhythmias resulting from surgical treatment
of these lesions. Implantation of an AICD may be necessary
for children with ventricular arrhythmias after Tetralogy
of Fallot repair while supraventricular arrhythmias
are often seen in patients who have undergone a Mustard
or Senning repair of transposition of the great arteries
or a Fontan procedure. It is essential that inotropes,
resuscitative medications and, if necessary, alternative
methods of pacing be available for these patients
during their catheterization.
The cardiac catheterization laboratory is an evolving
entity, and as cardiologists, surgeons and interventional
radiologists continue to develop protocols for procedures
performed in the CCL, the anesthesiologist must be
able to formulate and fully adapt a care plan to this
remote environment. Patient needs are ever-changing
due to the increased complexity of procedures, and
it is readily apparent that the well-prepared and
experienced anesthesiologist is an integral part of
the CCL team responsible for maintaining a high level
of care with minimal complications and improved outcome.
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| References: |
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| 1. Brezis M, Epstein FH. A closer look at
radiovontrast-induced nephropathy. N Engl
J Med. 1989; 320:179-181. |
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| 2. Briguori C, Manganelli F, Scarpato P, et
al. Acetylcysteine and contrast agent-associated
nephrotoxicity. J Am Coll Cardiol.
2002; 40(2):298-303. |
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| 3. Briguori C, Tavano D, Colombo A. Contrast
agent-associated nephrotoxicity. Prog Cardiovasc
Dis. 2003; 45(6):493-503. |
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| 4. Castellanos AR, Pereiras R, Varcia A. Angiocardiography
in the child. Proceedings of the 7th Congress
of the Pan-American Medical Association, Havana.
1939; 75-82,109-113. |
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| 5. Gerlach AT, Pickworth KK. Contrast medium-induced
nephrotoxicity: Pathophysiology and prevention.
Pharmacotherapy. 2000; 20(5):540-548. |
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| 6. Horlocker TT, Wedel DJ, Benzon H, et al.
Regional anesthesia in the anticoagulated patient:
Defining the risks (the second ASRA consensus
conference on neuraxial anesthesia and anticoagulation).
Reg Anesth Pain Med. 2003; 28(3):172-97. |
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| 7. Horlocker TT. Complications of spinal and
epidural anesthesia. Anesthesiol Clin North
America. 2000; 18(2):461-85. |
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| 8. King, SB. Angioplasty from bench to bedside
to bench, Circulation. 1996; 93:1621-1629
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| 9. Mueller R, Sanborn T. The history of interventional
cardiology. Am Heart J. 1995; 129:146-172
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| 10. Myler R, Stertzer S. Coronary and Peripheral
Angioplasty: Historic Perspective, Textbook
of Interventional Cardiology, 2nd ed.,
Vol. 1. Topol E, ed. Philadelphia: WB Saunders
Co;1993. |
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| 11. Onishchuk JL, Carlsson C. Epidural hematoma
associated with epidural anesthesia: Complications
of anticoagulant therapy. Anesthesiology.
1992; 77:1221-1223. |
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| 12. Parfrey PS, Griffiths SM, Barrett BJ,
et al: Contrast-induced renal failure. N
Engl J Med. 1989; 320:143-149. |
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| 13. Rao TLK, El-Etr AA. Anticoagulation following
placement of epidural and subarachnoid catheters:
An evaluation of neurologic sequelae. Anesthesiology.
1981; 55:618-620. |
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| 14. Rashkind WJ, Miller WW. Transposition
of the great arteries. Results of palliation
by balloon atrioseptostomy in thirty-one infants.
Circulation. 1968; 38:453-462. |
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| 15. Rosenquist RW, Brown DL. Neuraxial bleeding:
Fibrinolytics/thrombolytics. Reg Anes Pain
Med. 1998; 23:152-156. |
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| 16. Rudnick MR, Goldfarb S, Wexler L, et.
al. Nephrotoxicity of ionic and nonionic contrast
media in 1,196 patients: A randomized
trial. The Iohexol Cooperative Study.
Kidney Int. 1995; 47(1):254-261. |
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| 17. Schwab M, Healthy MA, et al. Contrast
nephrotoxicity: A randomized controlled
trial of a nonionic and ionic radiographic contrast
agent. N Engl J Med. 1989; 320:149-153. |
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| 18. Vandermeulen EP, Van Aken H, Vermylen
J. Anticoagulants and spinal-epidural
anesthesia. Anesth Analg. 1994; 79:1165-1177. |
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Randall R. Joe, M.D., is a cardiovascular anesthesiologist
at the Texas Heart Institute, St. Luke’s
Episcopal Hospital and Assistant Professor of
Anesthesiology, University of Texas Health Science
Center at Houston, Houston, Texas. |
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Laura K. Diaz, M.D., is Assistant Professor
of Anesthesiology, Baylor College of Medicine
and is a pediatric cardiovascular anesthesiologist
at Texas Children’s Hospital, Houston,
Texas. |
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