(Circulation. 1997;96:3928-3933.)
© 1997 American Heart Association, Inc.
Articles |
From the Department of Pediatrics, Kurume (Japan) University School of Medicine, and the Department of Cardiology, Kokura (Japan) Memorial Hospital.
Correspondence to Hirohisa Kato, MD, Department of Pediatrics, Kurume University School of Medicine, 67 Asahi-machi, Kurume 830, Japan. E-mail hkato{at}kurume.ktarn.or.jp
| Abstract |
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Methods and Results Four children (three boys and one girl; age, 12 to 13 years) with coronary artery stenosis underwent percutaneous transluminal coronary angioplasty (PTCA) and PTCRA 11.8±0.9 years after the onset of KD. Morphology of the coronary artery wall was evaluated by intravascular ultrasound imaging. In one patient, the targeted lesion for intervention was in the left anterior descending artery (90% stenosis); in the other three patients, it was in the middle of the right coronary artery (75% to 90% stenosis). PTCA failed in three patients because of severe stenosis with calcification. However, PTCRA proved effective, with stenosis rates reduced from 90% to 25%. Follow-up coronary angiography performed 4 months after the procedure demonstrated no restenosis, but mild aneurysms occurred in two patients.
Conclusions This study suggests that PTCRA is useful for revascularizing coronary arteries with severe stenosis and calcification as long-term sequelae of KD. Intravascular ultrasound imaging is useful in assessing the coronary artery wall pathology and in selecting the best treatment intervention.
Key Words: Kawasaki disease coronary disease aneurysm angioplasty ultrasonics
| Introduction |
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| Methods |
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The study protocol was approved by the Kurume University School of Medicine Ethics Committee. Informed consent was obtained from the parents of all patients.
Coronary Angiography
A 9F sheath was inserted percutaneously into the
femoral artery. Through it, a 5F or 6F Judkins-Kato catheter for
pediatric coronary angiography (Cook Comp) was advanced to the
ostium of the RCA or LCA by use of the Judkins technique. We measured
the systemic arterial pressure through the sheath and
checked the heart rate by ECG monitoring. Cineangiography of the LCA
and RCA was performed by manual injection of Iohexol through an
angiographic catheter under ECG monitoring. The right anterior oblique
30° projection, the posterior anterior projection, or the
left anterior oblique 60° projection was used. After the
coronary artery lesions were ascertained, IVUS and PTCRA or
PTCA were performed. Heparin administration was carried out, and the
activated clotting time was maintained at >300 seconds.
Interventional Procedure (PTCA or PTCRA)
Oral premedication included aspirin and calcium channel
antagonists. A 6F pacing catheter was inserted into the
right ventricle, and intracoronary injection of isosorbide
dinitrate (1 mg) was performed before PTCA or PTCRA.
Initially, PTCA was tried in all patients. However, the catheter failed to advance into the target lesions because of severe stenosis in three patients. The PTCA balloon catheter (ASUKA) was advanced over a 0.014-in angioplasty guide wire and positioned at the target coronary lesion. Two or three 30-second balloon inflations were performed at pressures ranging from 5 to 10 atm. The balloon was changed, and the diameter was sequentially increased from 2.5 to 4.0 mm.
Rotational ablation was performed in the three patients in whom PTCA was not successful. Then a 9F high-flow coronary guiding catheter was used to cannulate the target vessel, and the Rotablator was advanced to the coronary lesion while spinning at 160 000 to 180 000 rpm over a 0.009-in (0.023-cm) Rotablator guide wire. The Rotablator (Heart Technology Inc) consists of a football-shaped, stainless steel burr impregnated with diamond microchips (diameter, 30 to 50 µm) and is powered by a compressed airdriven turbine. The burr was changed, and the diameter was sequentially increased 1.25 to 2.25 mm.
Patients were discharged 3 days after the interventional procedure on a maintenance dose of aspirin (5 mg · kg-1 · d-1). A follow-up coronary angiography and IVUS were performed 4 months later.
Intravascular Ultrasound Imaging
Insertion of the imaging catheter was difficult before the
interventional procedures (PTCA and PTCRA) in three patients; in two of
these patients, the imaging catheter placement was successful after the
intervention. The sheath was placed in the femoral artery, and then a
7F or 8F right or left Judkins large-lumen guiding catheter with a
0.14-in angioplasty guide wire was advanced into the coronary
ostium. After this guide wire was withdrawn, an ultrasound imaging
catheter with a 30-MHz transducer (CVIS Inc) at the tip was advanced
over a another finer guide wire (0.014-in) through the guiding catheter
to record the coronary artery lesion. The size of the
ultrasound imaging catheter was 4.3F. The intracoronary
ultrasound image was displayed on a fluoroscope. The location of the
tip of the IVUS catheter was determined by angiography. The IVUS was
recorded on videotape. The images of the important coronary
lesions also were recorded on Polaroid photographic paper.
Analysis of Wall Morphology and Lumen Size
The coronary artery wall morphology was evaluated for
the echogenicity of the wall structures, intimal thickening, presence
of calcification, and lumen size. We chose the better interventional
method for each patient. PTCA was performed in patients who had
coronary artery stenosis with hard plaque or
calcification of <50% around the surface of the lumen, whereas PTCRA
was performed in those with stenosis and calcification of
>50% or in whom severe stenosis prevented insertion of the
PTCA catheter. The smallest axis of the site in the coronary
artery was identified by visual inspection, and the diameter was
measured by placing an electronic cursor at the acoustic interface
between the lumen and the intimal leading edge at opposite sides of the
coronary artery on the IVUS image.
All patients underwent heparinization during the PTCA or PTCRA procedure and received aspirin postoperatively. Preoperative and postoperative analyses included creatine kinase measurement every 8 hours for 24 hours and daily ECGs during hospitalization for 3 days.
| Results |
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Case 2: 13-Year-Old Boy
On angiography, the LCA was intact without aneurysms,
stenosis, or irregular lesions. The RCA demonstrated 75%
localized stenosis at the site of the proximal segment (Fig 2A
). At this site, intimal thickening and
calcification were observed on IVUS before PTCA (Fig 2D
). The
calcification was located on the surface of lumen side of the intima.
The other side of the intima demonstrated only low echogenicity,
indicating that it was composed of soft tissue. After PTCA was
performed (3 mm at 5 atm and 3.5 mm at 5 atm for 30 seconds),
the degree of right coronary stenosis improved from
75% to 25% (Fig 2B
). The IVUS demonstrated a dilated lumen without
dissection of the intima at the site of the procedure just after the
PTCA procedure (Fig 2E
).
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Case 3: 13-Year-Old Boy
The LCA was intact on angiography, without aneurysms,
stenosis, or irregular lesions. The RCA demonstrated 90%
localized stenosis at the site of the proximal segment (Fig 3A
). Calcification was detected at the
site by fluoroscopy. Because it was difficult to insert the catheter
through the severely narrowed segment, PTCA could not be performed.
After coronary angiography, PTCRA was performed with maximum
diameter of the rotational ablation catheter burr (2.25 mm). The
stenosis decreased from 90% to less than 25% after PTCRA (Fig 3B
). When IVUS was performed after the ablation, calcification was
demonstrated on all surfaces of the lumen side of the intima, with an
acoustic shadow at the target site. The wall had no dissection or
rupture at the site (Fig 3D
).
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Case 4: 12-Year-Old Boy
The LCA showed mild dilatation without stenosis or
irregular lesions in the main tract on angiography. The RCA
demonstrated 90% localized stenosis at the site of the
proximal segment (Fig 4A
). Calcification
was detected at the site by fluoroscopy. We could not perform PTCA
because it was difficult to insert the balloon catheter through the
severely narrowed segment of the site. After coronary
angiography, PTCRA was performed. Ablation of the site was achieved by
the maximum diameter of the rotational ablation catheter burr
(2.25 mm). The stenosis decreased from 90% to 50% after
PTCRA (Fig 4B
). On IVUS, performed after the procedure, calcification
was located on the surface of the lumen side of the intima, and the
other side of the intima seemed to be soft tissue (Fig 4E
). After
PTCRA, PTCA was performed at the site of the procedure (3 mm at 5
to 10 atm and 3.5 mm at 5 to 10 atm For 60 seconds), which further
decreased the stenosis from 50% to <25% (Fig 4C
). Localized
dissection at the intima with calcification was demonstrated by IVUS
after PTCA (Fig 4F
).
|
Follow-up
Follow-up coronary angiography and IVUS were performed 4
months after the PTCA or PTCRA treatment. No patient developed
restenosis at the coronary artery where the procedure
had been done (Figs 2C
, 3C
, and 4D
). New aneurysms appeared at
the site of PTCA in cases 2 (Fig 2C
) and 4 (Fig 4D
). Progression of
intimal thickening or presence of thrombus was not
demon-strated in any patient by IVUS. No patient had
ischemic findings in a follow-up exercise stress test,
echocardiography, or ECG at rest. These patients
were released from restriction on exercise. The patients remained on
aspirin (5 mg · kg-1 ·
d-1). They were followed up 12 to 18 months
after the procedure. They have had no symptoms or events that suggest
the presence of ischemic heart disease.
Complications
No ischemic events such as acute myocardial infarction,
angina pectoris, or coronary artery rupture occurred during
PTCA or PTCRA treatment. However, the RCA lesion progressed to a new
aneurysm in cases 2 and 4, as demonstrated by the follow-up
coronary angiography 4 months after PTCA. Localized intimal
dissection was demonstrated by IVUS just after the PTCA in case 4.
| Discussion |
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The mechanism of coronary artery stenosis in KD is uncertain. One possibility is acute occlusion by massive thrombus formation in the coronary aneurysms, which occur mostly in acute or subacute stages of illness. Another mechanism of coronary artery stenosis after KD may be the progression of marked thickening of the intima often associated with calcification, which is similar to an arteriosclerotic lesion.12,13 In our only patient in whom a PTCA catheter could be inserted through a stenotic coronary lesion, the wall structure at the site of coronary stenosis had a localized area of high echogenicity on the inner surface of the lumen and in other areas had intimal thickening without calcification, as assessed by IVUS. Ino et al7 reported that PTCA should be attempted within 6 to 8 years after KD, which means that the stenotic lesions may develop arteriosclerotic changes over the long term. We conclude that PTCA may successfully dilate stenotic coronary arteries that have relatively soft intima with only localized mild calcification. However, PTCRA may be the most useful method for intervention in cases of long-term coronary stenosis after KD. Interventional devices (PTCRA or PTCA) must be selected based on assessment of wall morphology and tissue characteristics by IVUS.
Complications
Myocardial infarction, arrhythmias, and death during PTCRA
have been reported in the coronary artery
disease.8,9 Death in a child after KD was
attributed to acute LAD occlusion from balloon rupture during a PTCA
procedure.10 No such serious cardiac events
occurred in our study. Creatine kinase was not elevated in our four
patients, and their ECGs demonstrated no abnormal Q waves or ST-T
changes.
The RCA lesion progressed to a new aneurysm in case 2 and in case 4 four months after the interventional procedures. These patients underwent PTCA (in case 4, PTCA was performed after PTCRA) with a relatively high pressure in the balloon. The new aneurysm may have occurred because of PTCA. It is necessary to study how much pressure in the balloon is adequate for PTCA after KD. We speculated that the Rotablator procedure did not result in aneurysms because the procedure can shatter the calcification at the coronary stenotic lesion without high tension to the coronary vessel wall.
Restenosis and Follow-up
Restenosis occurred in 17% to 52% of adult patients with
coronary artery disease after PTCA or
PTCRA.1416 Teirstein et
al17 reported that restenosis occurred
less frequently in patients with localized stenotic lesions
after PTCRA. Nobuyoshi et al15 reported that
restenosis is most prevalent between 1 and 3 months and rarely
occurs beyond 3 months after PTCA in adults. We performed follow-up
angiography 4 months after PTCA or PTCRA in children who had KD. None
developed restenosis at the site of the coronary
lesions on follow-up coronary angiography or IVUS. The outcome
in KD patients with localized, short-term stenosis of the
coronary artery after PTCA or PTCRA may be favorable, but
further follow-up is necessary to evaluate the possibility of
coronary aneurysm.
Indications and Limitations
The method of coronary intervention for children after KD
is not established at the present time. American College of
Cardiology/American Heart Association
guidelines18 have been used for PTCA in adult
patients with symptomatic ischemic status without
major complications. In this study, we chose patients with >75%
localized stenosis in the coronary artery who had no
history of myocardial infarction and no ischemic symptoms. The
coronary stenotic lesions of KD had rich calcification
and intimal thickening with coronary
aneurysm.12 The site of coronary
stenosis in KD was hard and stiff, indicating that the lesions
had developed over a long time. As a result, the procedure of PTCA or
PTCRA became increasingly difficult because the cath-eter could
not be inserted into the severe coronary stenosis. PTCA
or PTCRA should be performed to prevent myocardial infarction or sudden
death in patients with 75% coronary stenosis after KD
and unrelated symptomatic ischemic status. Stent
implantation is another important strategy for adults with
coronary artery disease. However it may be difficult to insert
a catheter or stent into the severe stenotic and stiff lesions
with calcification after KD. For PTCA or stent implantation in KD
patients, we should select patients with moderate stenotic
lesions, probably within 6 to 8 years from the onset of
KD.7 One of the great limitations of
coronary intervention is that the PTCA or PTCRA catheter is too
big for infants and young children. In the future, we need a smaller
interventional catheter that may contribute greatly to the increased
indications for and use of these methods in young children.
Conclusions
This study suggests that PTCRA is a safe, effective treatment for
revascularization of severe stenosis with
calcification as long-term coronary artery sequelae after KD.
The procedure can postpone aortocoronary bypass surgery.
Furthermore, IVUS is useful in the assessment of wall morphology and
tissue characterization of the pathological coronary artery as
well as in the selection of the best device for interventional
treatment. We hope that our study leads to progressive interventional
trials using this procedure for the treatment of children with
coronary stenosis.
| Selected Abbreviations and Acronyms |
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Received April 29, 1997; revision received August 18, 1997; accepted August 28, 1997.
| References |
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