0
Back To Top Jump Location
Sign In  | Cart
Left Shadow
Right Shadow
Clinical Research |

Stent Gap by 64-Detector Computed Tomographic Angiography: Relationship to In-Stent Restenosis, Fracture, and Overlap Failure FREE

Harvey S. Hecht, MD; Sotir Polena, MD; Vladimir Jelnin, MD; Marcelo Jimenez, MD; Tandeep Bhatti, DO; Manish Parikh, MD; Georgia Panagopoulos, PhD; Gary Roubin, MD, PhD
[+] Author Information

Dr. Hecht is on the Speakers' Bureau of Philips Medical Systems. Dr. Parikh is a consultant for Medtronic, and is on the Speakers' Bureau for Cordis and Abbott Vascular.Address for correspondence: Dr. Harvey S. Hecht, Lenox Hill Heart and Vascular Institute, 130 East 77th Street, New York, New York 10021

American College of Cardiology Foundation

J Am Coll Cardiol. 2009;54(21):1949-1959. doi:10.1016/j.jacc.2009.06.045
Published online

Objectives  The goal of this study was to define the frequency of stent gaps by 64-detector computed tomographic angiography (CTA) and their relation to in-stent restenosis (ISR), stent fracture (SF), and overlap failure (OF).

Background  SF defined by catheter angiography or intravascular ultrasound has been implicated in ISR.

Methods  A total of 292 consecutive patients, with 613 stents, who underwent CTA were evaluated for stent gaps associated with decreased Hounsfield units. Correlations with catheter coronary angiography (CCA) were available in 143 patients with 384 stents.

Results  Stent gaps were noted in 16.9% by CTA and 1.0% by CCA. ISR by CCA was noted in 46.1% of the stent gaps (p < 0.001) as determined by CCA, and stent gaps by CTA accounted for 27.8% of the total ISR (p < 0.001). In univariate analysis, stent diameter ≥3 mm was the only CCA characteristic significantly associated with stent gaps (p = 0.002), but was not a significant predictor by multivariate analysis. Bifurcation stents, underlying calcification, stent type, location, post-dilation, and overlapping stents were not observed to be predisposing factors. Excessive tortuosity and lack of conformability were not associated with stent gaps; however, their frequency was insufficient to permit meaningful analysis.

Conclusions  Stent gap by CTA: 1) is associated with 28% of ISR, and ISR is found in 46% of stent gaps; 2) is associated with ≥3-mm stents by univariate (p = 0.002) but not by multivariate analysis; 3) is infrequently noted on catheter angiography; and 4) most likely represents SF in the setting of a single stent, and may represent SF or OF in overlapping stents.

Figures in this Article
CCA

catheter coronary angiography

CTA

computed tomographic angiography

HU

Hounsfield unit

ISR

in-stent restenosis

IVUS

intravascular ultrasound

OF

overlap failure

SF

stent fracture

Drug-eluting stents have revolutionized percutaneous coronary intervention by dramatically reducing the incidence of in-stent restenosis (ISR). Stent fracture (SF), although a common finding with significant negative clinical implications in the peripheral vasculature (14), has never been reported in multicenter randomized clinical coronary stent trials (514). However, recent data (1532) have suggested that SF, as defined by catheter coronary angiography (CCA) or intravascular ultrasound (IVUS) evidence of a gap, may be a significant contributor to ISR, particularly in sirolimus-eluting stents (1516). ISR has been extensively evaluated by 64-detector computed tomographic angiography (CTA) (33). This study was designed to determine the characteristics and relationship of stent gaps on CTA to ISR, SF, and overlap failure (OF) by CCA, in those selected for invasive angiography.

Population

Two hundred ninety-two consecutive patients, with implantation of 613 stents, undergoing 64-detector CTA were evaluated retrospectively. The patient demographics are shown in (Table 1). All were referred for evaluation of symptoms. Of the 292 patients, CCA data were available in 143, allowing comparison of CTA and CCA findings for 384 stents.

Table Grahic Jump Location
Table 1Demographics
CTA protocol

Metoprolol 50 to 100 mg by mouth and/or 5 mg intravenously ×4 was administered to reduce the heart rate to <60 beats/min. The CTA were acquired on the Philips Brilliance-64 scanner (Philips Medical Systems, Cleveland, Ohio) using the 64 × 0.625-mm detector configuration, 120 kVp, 600 to 1,050 mA, 0.2 pitch, and standard or sharp filters (Philips CC and CD filters). Nonionic contrast (Ioversol 350 mg/ml at 5 to 6 ml/s) was used, followed by 50 ml of saline at the same rate using a double-head injector (Optivantage DH, Mallinkrodt, Cincinnatto, Ohio). Estimated effective radiation dose was 13 mSv for men and 18 mSv for women. The cardiac phase best demonstrating each artery (usually 75% of the R-R interval) was analyzed using a dedicated CT workstation (Philips CT Extended Brilliance Workspace, Philips Medical Systems) and a cardiac adaptive multisegment reconstruction algorithm. Curved and straightened multiplanar reformatted images were constructed and evaluated for stent separation and ISR. All stents were evaluated, irrespective of quality.

MDCT stent analysis
SF

Stent gap was diagnosed when both of the following criteria were fulfilled on the curved multiplanar reformatted images, and on cross-sectional analysis of the straightened multiplanar reformatted images: 1) partial or complete (circumferential) gap or a “crush” pattern on visual inspection (Figure 1); and 2) confirmation of Hounsfield units (HU) <300 (the lowest HU in the normal stent areas) at the site of separation, consistent with the absence of metallic stent material (Figures 2, 3, 4, 5, 6, 7). The length of the separation (i.e., the distance between the normal stent edges surrounding the separation) was measured. All stents were analyzed; none were considered unevaluable because of motion artifact or adjacent very dense calcification capable of producing a gap secondary to shadowing. The CTA analysis was performed by 2 independent observers who did not partake in the CCA analysis. ISR by CTA was evaluated as previously described (33).

Grahic Jump Location
Figure 1

Stent Gap Patterns

Normal (A), partial (B), crush (C), and complete (D, center, preceded [left] and followed [right] by normal areas).

Grahic Jump Location
Figure 2

A 63-Year-Old Female With Recurrent Atypical Chest Pain 6 Months After Placement of Overlapping Stents in the LAD

(A) Computed tomographic angiography (CTA) curved multiplanar reconstruction (MPR) reveals clear stent separation (arrow) consistent with fracture as well as luminal hypodensity consistent with neointimal hyperplasia. (B) Catheter angiography demonstrates mild in-stent restenosis (arrow). (C) Stent fracture is evident on a frame without contrast (arrows), but is not seen on a subsequent frame, D. (E) Cross sections obtained from the straightened MPR reveal a low HU of 192 at the separation site, incompatible with the presence of metallic stent material. Densities in the normal area were >400 HU. HU = Hounsfield units; LAD = left anterior descending coronary artery.

Grahic Jump Location
Figure 3

A 58-Year-Old Asymptomatic Male 8 Months After Placement of Overlapping RCA Stents

(A) Two areas of separation are noted on the CTA curved MPR (arrows) as well as luminal hypodensity consistent with neointimal hyperplasia. (B) Catheter angiography reveals significant in-stent restenosis (ISR) (arrow). (C) A single noncontrast frame displays complete separation, which is not visible on any subsequent frames. (D) Cross sections obtained from the straightened MPR reveal partial absence of stent material with HU <300 at both sites (left, middle). The normal area reveals uniformly higher HU (right). Fx = fracture; RCA = right coronary artery; other abbreviations as in (Figure 2).

Grahic Jump Location
Figure 4

A 70-Year-Old Female With Exertional Dyspnea 1 Year After Implantation of a Stent in the Proximal LAD

(A) CTA curved MPR reveals a stent gap (arrow) associated with luminal hypodensity consistent with neointimal hyperplasia. Catheter angiography reveals only moderate ISR (B) and an intact stent in a noncontrast frame (C). (D) Cross sections obtained from the straightened MPR reveal partial absence of stent material and low HU at the gap site (right arrow) and intact stent with HU >400 in the normal area (left arrow). Abbreviations as in (Figures 2, 3).

Grahic Jump Location
Figure 5

A 36-Year-Old Male With Atypical Chest Pain 18 Months After LAD Stent Implantation During an Acute Myocardial Infarction

(A) CTA curved MPR reveals 2 stent gaps (arrows) associated with severe luminal hypodensity consistent with total occlusion. Catheter angiography confirms the total occlusion (B, arrow); an intact stent is noted in a noncontrast frame (C). (D) Cross sections obtained from the straightened MPR reveal partial absence of stent material and low HU at the gap sites (right and left) and intact stent with HU >400 in the normal area (middle). Abbreviations as in (Figure 2).

Grahic Jump Location
Figure 6

A 62-Year-Old Male With Dyspnea 9 Months After Overlapping LAD Stent Implantation

(A) CTA curved MPR reveals obvious separation without ISR (arrow). (B) Catheter angiography revealed only mild ISR (top) and a single noncontrast frame suggested partial fracture (bottom) (arrows). (C and D) Cross-sectional analysis confirmed the gap with decreased HU (D, middle), compared with proximal (D, left) and distal (D, right) stent segments.

Grahic Jump Location
Figure 7

A 59-Year-Old Male With Recurrent Angina 6 Months After Obtuse Marginal Stenting

(A) CTA curved MPR reveals a stent gap (arrow) without clear evidence for contrast, consistent with severe ISR. (B) Catheter angiography reveals critical ISR at a hinge point in systole (top, arrow) and diastole (bottom, arrow), and an intact stent in noncontrast systolic and diastolic frames (C, arrow). (D) Cross sections obtained from the straightened MPR reveal the “crush” pattern with partial absence of stent material and low HU at the gap site (right) and intact stent with high HU in the normal area (left). Abbreviations as in (Figure 1).

CCA

Selective coronary angiography was performed for clinical indications using standard techniques in 143 patients. The reasons for the nonreferral for invasive angiography of the remainder of the patients cannot be accurately ascertained since the patients were referred for CTA by many different community physicians with different thresholds and criteria for proceeding to invasive procedures. Stented areas were reviewed by a separate observer who did not participate in the CTA interpretation. Stents specifically described as single or overlapped were classified accordingly. If specific information was unavailable, stented lengths >40 mm were considered overlapped; the remainder were classified as unknown. Under 3-fold magnification, all stents were evaluated for ISR, defined as >50%, by caliper measurement of percent diameter stenosis, and for separation consistent with SF or OF. Lesions were defined according to the American College of Cardiology/American Heart Association classification (34). SF was classified as partial or complete separation of stent segments. Excessive tortuosity was defined as the presence of 2 or more bends >75° proximal to the target lesion; at least 1 proximal bend >90° (35). Conformability was defined as the degree to which a stent can bend around its longitudinal axis after deployment.

IVUS was acquired in only 5 patients, a number too few to permit meaningful analysis.

Statistical analysis

Descriptive statistics were used to characterize demographic and peri-procedural data. Differences between the 2 groups (gap present vs. gap absent) were examined with the Fisher exact test for categorical variables or the independent-samples t test for continuous variables. Degree of agreement in the stent gap designation between the 2 observers was computed using Cohen's kappa coefficient. In order to minimize the type I error rate, which could result from examining multiple hypotheses, p < 0.01 was considered a priori to indicate statistical significance. Multivariate analysis utilized 2 separate stepwise logistic regression procedures to identify potential predictors of fracture. The first model included the following demographic and patient characteristics as predictors: sex, age, hypertension, hyperlipidemia, smoking, diabetes mellitus, stroke, history of myocardial infarction, and use of statins, aspirin, clopidogrel, and beta-blockers. The second model included all coronary angiography characteristics as presented in (Table 2). A value of p < 0.05 was used to indicate statistical significance in the multivariate analyses. All statistical analyses were performed with SPSS version 16.0.2 (SPSS, Chicago, Illinois). The study was approved by the Institutional Review Board of Lenox Hill Hospital.

Table Grahic Jump Location
Table 2Univariate Comparison of Characteristics on CCA in Stents With and Without Gaps on CTA
Table Footer NoteSingle versus overlap.

The patient demographics are displayed in (Table 1). Stent gap was noted in 14.4%; diabetic patients were more frequently found in the SF/OF group (p = 0.001) but was not a significant predictor in a multivariate analysis. The mean ± SD interval between the CCA and CTA studies was 57.4 ± 130 days.

There were 384 stents in the 143 patients with both CCA and CTA data, Stent gap was noted in 16.9% of the stents by CTA. There were 4 stents with the crush pattern on CTA and 1 with total separation; the remainder had the partial gap pattern. SF was observed in only 1.0% by CCA; 2 had total and 2 had partial separation. There was a highly significant association of stent gap by CTA with ISR on CCA (Tables 2, 3). There were 229 stents in the 159 patients who did not proceed to CCA; stent gap was noted in 6.6% (p < 0.001 compared with those with CCA follow-up).

Table Grahic Jump Location
Table 3Relationship of Stent Gap by CTA to ISR by CCA

ISR on CCA was noted in 46.1% of stent gaps (p < 0.001), and stent gaps accounted for 27.8% of the total ISR (p < 0.001). The HU for the gap area was 196.9 ± 81.1 compared with 481.9 ± 161.8 for the intact portion. The gap length was 2.3 ± 0.9 mm. Stent gap agreement between the 2 observers was very strong (kappa = 0.904). Stent implantation information was available for 124 patients; there were no differences in the interval between implantation and the CCA in stents with (median 618 days, range 1,851 days) and without (median 559 days, range 2,369 days) stent gaps. The only CCA characteristic significantly associated with a stent gap by univariate analysis was stent diameter ≥3 mm; stent gaps were present in 20.0% of ≥3 mm stents compared with 3.4% of <3-mm stents (p = 0.002). By multivariate analysis, stent diameter was not a significant predictor. Stent type, location, length, underlying calcification, post-dilation, and bifurcation stents were not predisposing factors (Table 2). Excessive tortuosity and lack of conformability were not associated with stent gaps; however, their frequency was insufficient to permit meaningful analysis. There were no differences in the frequency of stent gaps noted in single versus overlapped stents (Table 2). However, 26.6% of the stents were in the unknown category and could not be classified as single or overlapped; 46.6% of the gaps were noted in this group. Due to sample-size limitations, it is possible that there was not sufficient power to detect potentially significant predictors in the multivariate analysis. The sensitivity and specificity of the CTA for detection of ISR by CCA were 89.3% and 79.2%, respectively.

(Figures 2, 3, 4, 5, 6, 7) demonstrate the CTA and catheter angiographic characteristics of stent gaps. In (Figure 2)A, there is obvious separation at an overlap site on the CTA. Highlighting the difficulty inherent in the limited sampling of catheter angiographic analysis is the clear gap noted in 1 noncontrast frame (Figure 2C), which is totally unapparent in a second frame (Figure 2D). There was only mild ISR (Figure 2B).

In (Figure 3), there are 2 areas of stent separation by CTA (Figure 3A), with significant ISR at the more proximal site. As in (Figure 2), a single noncontrast frame revealed the stent separation on catheter angiography (Figure 3C); all other frames revealed a normal-appearing stent. In both cases, cross-sectional analyses ((Figure 2)E and Figure 3E) revealed HU at the gap sites that were below the threshold for metallic stent material.

A stent gap is noted on CTA in (Figure 4)A with catheter angiography revealing only moderate ISR (Figure 4B) and an apparently intact stent (Figure 4C). Cross-sectional analysis (Figure 4D) confirmed the more common gap fracture pattern and decreased HU associated with the fracture site.

A totally occluded proximal stent with distal filling of the stent by collaterals, and 2 stent gaps are seen on CTA in (Figure 5)A. Catheter angiography confirmed the total occlusion (Figure 5B), but the stent was intact in noncontrast frames (Figure 5C). Cross-sectional analysis confirmed the gap pattern with clearly decreased HU in the gap areas. In (Figure 6)A, CTA demonstrated obvious separation without ISR. Catheter angiography revealed only mild ISR, and a single noncontrast frame suggested partial fracture (Figure 6B). Cross-sectional analysis ((Figure 6)C and Figure 6D), as in the previous cases, confirmed the gap with decreased HU.

The “crush” pattern is shown in (Figure 7)A and (Figure 7)D in an obtuse marginal branch with severe ISR at a hinge point, a location prone to fracture. Nonetheless, fracture was not visible on catheter angiography ((Figure 7)B and Figure 7C).

This study is the first to systematically evaluate the significance of stent gaps defined by CTA. The strong relationship between stent gaps and ISR has significant implications for the occurrence of SF and OF.

SF and ISR

SF has recently been implicated in ISR. In 530 patients undergoing repeat angiography, Lee et al. (15) noted 10 (1.8%) with SF by angiography. Binary ISR for the SF patients was 70%; all required target lesion revascularization. Predisposing factors were sirolimus stents (100%), excessive tortuosity (40%), and stent overlap (50%) with increased rigidity that may act as a fulcrum for metal deformation. Aoki et al. (16) evaluated 307 sirolimus-eluting stents in 280 patients and noted 8 (2.6%) with SF on catheter angiography within 8 months of implantation, confirmed by IVUS. Binary ISR for the SF patients was 37.5%, and 50% underwent target lesion revascularization. Of the 8 with SF, 7 were at overlapped areas. All were located at hinge points. Predisposing factors were RCA SF location (odds ratio [OR]: 10.00) with greater vessel deformation with cardiac motion, saphenous vein graft location (OR: 35.88), and longer stent length with associated higher radial forces (OR: 1.04). Lee et al. (17) evaluated 366 patients with sirolimus stents; SF was noted in 10 (2.7%). Of the 26 with ISR, 10 (38.5%) were associated with SF (7 by angiography and 3 by IVUS). ISR was present in 44% of the SF; 3 (30%) were in overlapped stents. SF was not found in 30 patients with ISR after bare-metal Bx Velocity (Cordis Corporation, Bridgewater, New Jersey) stent implantation. In addition to the above series, there are 13 case reports evaluating 14 patients with SF: 10 involved sirolimus-eluting stents (1832). Two patients were evaluated by CTA (28,31).

SF mechanisms

Proposed mechanisms for SF, in addition to those discussed above, are low stent conformability, overexpansion during post-dilation, and bifurcation lesion with high angulation. In the present study, stent diameter ≥3 mm was the only significant predisposing factor for stent gaps by univariate analysis (Table 2); stent gaps were present in 20.0% of ≥3-mm stents compared with 3.4% of <3-mm stents (p = 0.002). However, it was not a significant predictor in multivariate analysis. Stent length, location and type, overlapped stents, post-dilation, underlying calcification, and bifurcation stents were not significantly related. Excessive tortuosity and lack of conformability were rarely noted, and their contribution could not be evaluated.

The high incidence of ISR associated with stent gaps most likely results from the absence of drug-elution protection from neointimal hyperplasia, or a drug-free zone, at the gap site. Other possibilities include broken struts causing local mechanical stimulation of the vessel wall, resulting in inflammation and development of intimal hyperplasia, as well as local uncovered unstable plaque.

CTA diagnosis of SF or OF

The ability of CTA to confidently identify stent gaps is dependent not just on demonstration of a “gap,” which may be more apparent than real, depending on the window settings. Rather, the gap must be associated with HUs below the minimum density of stent material, which is independent of window center and width, and the absence of artifact that may contribute to this finding. The study must be carefully evaluated for shadowing effects of adjacent dense calcification and motion artifacts.

In the absence of artifacts, the most likely explanations for the hypodense gap are fracture- or OF-related absence of strut material. Overinflation, with spreading of struts without true fracture, cannot be excluded. Bifurcation stents, with inflation into a side branch and possible strut damage, were not associated with a higher incidence of stent gaps (Table 2). The absence of strut material for a distance greater than the normal average interstrut distance (1 mm) is convincing evidence for an uncovered portion of the artery. The 46% incidence of ISR in stent gaps and the 28% association of stent gaps with ISR support the pathologic significance of this observation and the likely presence of SF or OF, even though there is no confirmatory gold standard.

The most common gap was a hypodense partial gap suggestive of incomplete SF. The crush pattern, manifested by a flattening of the stent with a hypodense gap, was less frequent. Only 1 case of total separation was noted.

Limitations of catheter angiography and IVUS

The infrequency of catheter angiographic identification of stent separation in the present series (1.0%) is similar to the 1.8% to 2.7% in previously reported studies (1517). The discrepancy between the CTA (16.9%) and catheter angiography frequency in this and previous reports has several possible explanations.

First, successful detection of SF or OF by catheter angiography is directly related to the gap length and inversely related to deviation of image acquisition from the plane perpendicular to the gap; overlap of strut edges on nonperpendicular acquisitions may render the gap invisible. This proof of concept is clearly illustrated in (Figure 2) and (Figure 3), in which the gap was visible only in very few frames and unapparent in all others, in (Figure 4) in which the absence of struts was apparent only by IVUS (not shown), and in (Figure 7) with partial SF suggested on a single catheter angiographic frame yet evident on IVUS (not shown). The problem is magnified by the limited number of acquisitions, typically 5 to 8 for the left coronary artery and 2 to 4 for the right coronary artery. The 3-dimensional quality of CTA renders it immune to the issue of image acquisition; the gap site can be inspected from every conceivable angle.

Second, lesser degrees of separation may have been present in this series compared with prior reports. CTA, as discussed above, is very likely more sensitive in detecting lesser separation if present.

Third, the CTA stent gap findings may not represent true SF or OF. This is highly unlikely since, as discussed in the previous text, there is no other plausible explanation for the decreased HU (<300). Adjacent calcified plaque was not of sufficient density to produce HU reduction by shadowing, and all the studies were of sufficient quality to eliminate other sources of artifacts as contributors. In addition, the high frequency of catheter angiography-proven ISR associated with CTA stent gaps is similar to the previously reported association of ISR with SF diagnosed by catheter angiography and intravascular ultrasound (1517). IVUS would seem to be well suited for SF/OF identification but has not been extensively evaluated. Careful frame-by-frame analysis is essential, and the almost ubiquitous presence of superimposed calcification may render differentiation of stent material from calcified plaque difficult, if not impossible. In addition, the pullback may skip over a fracture site. Nonetheless, expert IVUS evaluation might be expected to yield results similar to CTA. Its highly invasive nature restricts its use to patients already undergoing catheter angiography.

The lower incidence of stent gap in patients not referred for CCA compared with those who underwent invasive evaluation (6.6% vs. 16.9%, p < 0.001) may reflect a lower incidence of ISR-related symptoms requiring further testing.

SF versus OF

In patients with a gap in a single stent, SF is the most likely explanation. In prior reports of fracture at an overlap site, stent separation has always been attributed to fracture rather than to the possibility that the stents were never completely overlapped or migrated over time. The lack of detection by catheter angiography suggests that the stents appeared successfully overlapped at the time of their implantation. However, the intrinsic limited acquisition issue is exaggerated by the even more limited number (1 to 2) of post-stent acquisitions, and inadequate overlap at the time of implantation cannot be excluded. In the present study, stent information was missing for 26.6% of the stents, which could not be classified as single or overlapped; 46.6% of the gaps were noted in this group. Consequently, the true frequencies of possible SF and OF could not be determined. In the 73.4% with implantation data, stent gaps were equally present in single versus overlapped stents.

Study limitations

The patient population represents a retrospective analysis of a consecutive series of stented patients who underwent CTA for clinical indications, with only 49% undergoing CCA, rather than a prospective, consecutive series of patients who underwent stenting with follow-up CCA and CTA. Consequently, there is significant selection bias, and the study very likely overestimates the incidence of SF or OF in the general population of stented patients. Reflecting the problems inherent in tertiary referral centers, in which data regarding stents implanted elsewhere may not be available, is the incomplete stent implantation data in those who underwent CCA. However, sufficient numbers of stents were available for meaningful analysis, and this study is the first to address this topic in a large series of patients. SF and OF cannot be absolutely confirmed in the absence of postmortem examination. However, the absence of other plausible explanations, the 46% incidence of ISR in stent gaps, and the 28% association of stent gaps with ISR support the pathologic significance of this observation.

Clinical implications

The incidence of stent gaps with possible fracture or OF in a large series of stents evaluated by CTA and CCA was 16.9%, representing 28% of the total ISR population; ISR was present in 46% of SF/OF. This very strong association of stent gaps with ISR suggests that, in patients with drug-eluting stents, it may not be failure of the drug-eluting compound to prevent neointimal hyperplasia that is responsible for all ISR, but rather lack of exposure of the arterial segment to the compound at a gap site in a substantial number. Greater emphasis on those factors that promote SF and on manufacturing techniques that prevent SF appear to be in order. In overlapping stent implantations, IVUS may prove to be a reliable tool for verifying the accuracy of overlap at the time of insertion. The inability of catheter angiography to detect stent gaps and the highly invasive nature of IVUS, and its potential confounding by calcified plaque, suggest that CTA is the diagnostic procedure of choice.

Sacks  B.A., Miller  A., Gottlieb  M.; Fracture of an iliac artery Palmaz stent. J Vasc Interv Radiol. 7 1996:53-55.
CrossRef | PubMed
Scheinert  D., Scheinert  S., Sax  J.; Prevalence and clinical impact of stent fractures after femoropopliteal stenting. J Am Coll Cardiol. 45 2005:312-315.
CrossRef | PubMed
Duda  S.H., Pusich  B., Richter  G.; Sirolimus-eluting stents for the treatment of obstructive superficial femoral artery disease: six-month results. Circulation. 106 2002:1505-1509.
CrossRef | PubMed
Phipp  L.H., Scott  D.J., Kessel  D., Robertson  I.; Subclavian stents and stent-grafts: cause for concern?. J Endovasc Surg. 6 1999:223-226.
CrossRef | PubMed
Morice  M.C., Serruys  P.W., Sousa  J.E.; A randomized comparison of a sirolimus-eluting stent with a standard stent for coronary revascularization. N Engl J Med. 346 2002:1773-1780.
CrossRef | PubMed
Moses  J.W., Leon  M.B., Popma  J.J.; Sirolimus-eluting stents versus standard stents in patients with stenosis in a native coronary artery. N Engl J Med. 349 2003:1315-1323.
CrossRef | PubMed
Stone  G.W., Ellis  S.G., Cox  D.A.; A polymer-based, paclitaxel-eluting stent in patients with coronary artery disease. N Engl J Med. 350 2004:221-231.
CrossRef | PubMed
Schofer  J., Schluter  M., Gershlick  A.H.; Sirolimus-eluting stents for treatment of patients with long atherosclerotic lesions in small coronary arteries: double-blind, randomised controlled trial (E-SIRIUS). Lancet. 362 2003:1093-1099.
CrossRef | PubMed
Schampaert  E., Cohen  E.A., Schluter  M.; The Canadian study of the sirolimus-eluting stent in the treatment of patients with long de novo lesions in small native coronary arteries (C-SIRIUS). J Am Coll Cardiol. 43 2004:1110-1115.
CrossRef | PubMed
Hong  M.K., Mintz  G.S., Lee  C.W.; Paclitaxel coating reduces in-stent intimal hyperplasia in human coronary arteries: a serial volumetric intravascular ultrasound analysis from the Asian Paclitaxel-Eluting Stent Clinical Trial (ASPECT). Circulation. 107 2003:517-520.
CrossRef | PubMed
Gershlick  A., De Scheerder  I., Chevalier  B.; Inhibition of restenosis with a paclitaxel-eluting, polymer-free coronary stent: the European evaLUation of pacliTaxel Eluting Stent (ELUTES) trial. Circulation. 109 2004:487-493.
CrossRef | PubMed
Grube  E., Silber  S., Hauptmann  K.E.; TAXUS I: six- and twelve-month results from a randomized, double-blind trial on a slow-release paclitaxel-eluting stent for de novo coronary lesions. Circulation. 107 2003:38-42.
CrossRef | PubMed
Colombo  A., Drzewiecki  J., Banning  A.;TAXUS II Study Group Randomized study to assess the effectiveness of slow- and moderate-release polymer-based paclitaxel-eluting stents for coronary artery lesions. Circulation. 108 2003:788-794.
CrossRef | PubMed
Lansky  A., Costa  R.A., Mintz  G.S., Tsuchiya  Y.; Non-polymer-based paclitaxel-coated coronary stents for the treatment of patients with de novo coronary lesions. Angiographic follow-up of the DELIVER clinical trial. Circulation. 109 2004:1948-1954.
CrossRef | PubMed
Lee  M.S., Jurewitz  D., Aragon  J.; Stent fracture associated with drug-eluting stents: clinical characteristics and implications. Catheter Cardiovasc Interv. 69 2007:387-394.
CrossRef | PubMed
Aoki  J., Nakazawa  G., Tanabe  K., Hoye  A.; Incidence and clinical impact of coronary stent fracture after sirolimus-eluting stent implantation. Catheter Cardiovasc Interv. 69 2007:380-386.
CrossRef | PubMed
Lee  S., Park  J., Shin  D., Kim  Y.; Frequency of stent fracture as a cause of coronary restenosis after sirolimus-eluting stent implantation. Am J Cardiol. 100 2007:627-630.
CrossRef | PubMed
Chowdhury  P.S., Ramos  R.G.; Images in clinical medicine. Coronary-stent fracture. N Engl J Med. 347 2002:581
CrossRef | PubMed
Brilakis  E.S., Maniu  C., Wahl  M., Barsness  G.; Unstable angina due to stent fracture. J Invasive Cardiol. 16 2004:545
PubMed
Sianos  G., Hofma  S., Ligthart  J.M.; Stent fracture and restenosis in the drug-eluting stent era. Catheter Cardiovasc Interv. 61 2004:111-116.
CrossRef | PubMed
Halkin  A., Carlier  S., Leon  M.B.; Late incomplete lesion coverage following Cypher stent deployment for diffuse right coronary artery stenosis. Heart. 90 2004:e45
CrossRef | PubMed
Hamilos  M.I., Papafaklis  M.I., Ligthart  J.M.; Stent fracture and restenosis of a paclitaxel-eluting stent. Hellenic J Cardiol. 46 2005:439-442.
PubMed
Surmely  J.F., Kinoshita  Y., Dash  D.; Stent strut fracture-induced restenosis in a bifurcation lesion treated with the crush stenting technique. Circ J. 70 2006:936-938.
CrossRef | PubMed
Min  P.K., Yoon  Y.W., Moon Kwon  H.; Delayed strut fracture of sirolimus-eluting stent: a significant problem or an occasional observation?. Int J Cardiol. 106 2006:404-406.
CrossRef | PubMed
Park  J.S., Shin  D.G., Kim  Y.J.; Fractured DES with a patent coronary artery: clinical implications. J Invasive Cardiol. 19 2007:E43-E45.
PubMed
Wilczynska  J., Rdzanek  A., Kochman  J.; Sirolimus eluting stent fracture following angioplasty of diffuse in-stent restenosis in the right coronary artery. Int J Cardiol. 118 2007:126-127.
CrossRef | PubMed
Makaryus  A.N., Lefkowitz  L., Lee  A.D.K.; Coronary artery stent fracture. Int J Cardiovasc Imaging. 23 2007:305-309.
CrossRef | PubMed
Zaizen  H., Tamura  A., Miyamoto  K.; Complete fracture of sirolimus-eluting stent detected by multislice computed tomography. J Int J Cardiol. 118 2007:120-121.
CrossRef
Leong  D.P., Dundon  B.K., Puri  R., Yeend  R.A.S.; Very late stent fracture associated with a sirolimus-eluting stent. Heart Lung Circ. 17 2008:426-428.
CrossRef | PubMed
Jin  X., Zhang  S., Xie  H.; Strut fracture of DES: An increasing problem?. Int J Cardiol. 118 2007:e54-e56.
CrossRef | PubMed
Kuboyama  O., Takei  H., Tokunaga  T.; Strut fracture of a sirolimus-eluting stent at the ostium of the right coronary artery. Heart. 93; 2007:1608
PubMed
Shite  J., Matsumoto  D., Yokoyama  M.; Sirolimus-eluting stent fracture with thrombus, visualization by optical coherence tomography. Eur Heart J. 27 2006:1389
CrossRef | PubMed
Hecht  H.S., Zaric  M., Jelnin  V.; Usefulness of 64-detector computed tomographic angiography for diagnosing in-stent restenosis in native coronary arteries. Am J Cardiol. 101 2008:820-824.
CrossRef | PubMed
Ryan  T.J., Faxon  D.P., Gunnar  R.M.; Guidelines for percutaneous transluminal coronary angioplasty: a report of the American College of Cardiology/American Heart Association Task Force on Assessment of Diagnostic and Therapeutic Cardiovascular Procedures (Subcommittee on Percutaneous Transluminal Coronary Angioplasty). Circulation. 78 1988:486-502.
CrossRef | PubMed
Freed  F.S., Safian  R.D.; Proximal vessel tortuosity and angulated lesions.Safian  R.D., Freed  M.S.; Manual of Interventional Cardiology. 3rd edition 2001 Physician's Press Royal Oak, MI:237-243.

Figures

Grahic Jump Location
Figure 1

Stent Gap Patterns

Normal (A), partial (B), crush (C), and complete (D, center, preceded [left] and followed [right] by normal areas).

Grahic Jump Location
Figure 2

A 63-Year-Old Female With Recurrent Atypical Chest Pain 6 Months After Placement of Overlapping Stents in the LAD

(A) Computed tomographic angiography (CTA) curved multiplanar reconstruction (MPR) reveals clear stent separation (arrow) consistent with fracture as well as luminal hypodensity consistent with neointimal hyperplasia. (B) Catheter angiography demonstrates mild in-stent restenosis (arrow). (C) Stent fracture is evident on a frame without contrast (arrows), but is not seen on a subsequent frame, D. (E) Cross sections obtained from the straightened MPR reveal a low HU of 192 at the separation site, incompatible with the presence of metallic stent material. Densities in the normal area were >400 HU. HU = Hounsfield units; LAD = left anterior descending coronary artery.

Grahic Jump Location
Figure 3

A 58-Year-Old Asymptomatic Male 8 Months After Placement of Overlapping RCA Stents

(A) Two areas of separation are noted on the CTA curved MPR (arrows) as well as luminal hypodensity consistent with neointimal hyperplasia. (B) Catheter angiography reveals significant in-stent restenosis (ISR) (arrow). (C) A single noncontrast frame displays complete separation, which is not visible on any subsequent frames. (D) Cross sections obtained from the straightened MPR reveal partial absence of stent material with HU <300 at both sites (left, middle). The normal area reveals uniformly higher HU (right). Fx = fracture; RCA = right coronary artery; other abbreviations as in (Figure 2).

Grahic Jump Location
Figure 4

A 70-Year-Old Female With Exertional Dyspnea 1 Year After Implantation of a Stent in the Proximal LAD

(A) CTA curved MPR reveals a stent gap (arrow) associated with luminal hypodensity consistent with neointimal hyperplasia. Catheter angiography reveals only moderate ISR (B) and an intact stent in a noncontrast frame (C). (D) Cross sections obtained from the straightened MPR reveal partial absence of stent material and low HU at the gap site (right arrow) and intact stent with HU >400 in the normal area (left arrow). Abbreviations as in (Figures 2, 3).

Grahic Jump Location
Figure 5

A 36-Year-Old Male With Atypical Chest Pain 18 Months After LAD Stent Implantation During an Acute Myocardial Infarction

(A) CTA curved MPR reveals 2 stent gaps (arrows) associated with severe luminal hypodensity consistent with total occlusion. Catheter angiography confirms the total occlusion (B, arrow); an intact stent is noted in a noncontrast frame (C). (D) Cross sections obtained from the straightened MPR reveal partial absence of stent material and low HU at the gap sites (right and left) and intact stent with HU >400 in the normal area (middle). Abbreviations as in (Figure 2).

Grahic Jump Location
Figure 6

A 62-Year-Old Male With Dyspnea 9 Months After Overlapping LAD Stent Implantation

(A) CTA curved MPR reveals obvious separation without ISR (arrow). (B) Catheter angiography revealed only mild ISR (top) and a single noncontrast frame suggested partial fracture (bottom) (arrows). (C and D) Cross-sectional analysis confirmed the gap with decreased HU (D, middle), compared with proximal (D, left) and distal (D, right) stent segments.

Grahic Jump Location
Figure 7

A 59-Year-Old Male With Recurrent Angina 6 Months After Obtuse Marginal Stenting

(A) CTA curved MPR reveals a stent gap (arrow) without clear evidence for contrast, consistent with severe ISR. (B) Catheter angiography reveals critical ISR at a hinge point in systole (top, arrow) and diastole (bottom, arrow), and an intact stent in noncontrast systolic and diastolic frames (C, arrow). (D) Cross sections obtained from the straightened MPR reveal the “crush” pattern with partial absence of stent material and low HU at the gap site (right) and intact stent with high HU in the normal area (left). Abbreviations as in (Figure 1).

Tables

Table Grahic Jump Location
Table 1Demographics
Table Grahic Jump Location
Table 2Univariate Comparison of Characteristics on CCA in Stents With and Without Gaps on CTA
Table Footer NoteSingle versus overlap.
Table Grahic Jump Location
Table 3Relationship of Stent Gap by CTA to ISR by CCA

Interactive Graphics

Video

References

Sacks  B.A., Miller  A., Gottlieb  M.; Fracture of an iliac artery Palmaz stent. J Vasc Interv Radiol. 7 1996:53-55.
CrossRef | PubMed
Scheinert  D., Scheinert  S., Sax  J.; Prevalence and clinical impact of stent fractures after femoropopliteal stenting. J Am Coll Cardiol. 45 2005:312-315.
CrossRef | PubMed
Duda  S.H., Pusich  B., Richter  G.; Sirolimus-eluting stents for the treatment of obstructive superficial femoral artery disease: six-month results. Circulation. 106 2002:1505-1509.
CrossRef | PubMed
Phipp  L.H., Scott  D.J., Kessel  D., Robertson  I.; Subclavian stents and stent-grafts: cause for concern?. J Endovasc Surg. 6 1999:223-226.
CrossRef | PubMed
Morice  M.C., Serruys  P.W., Sousa  J.E.; A randomized comparison of a sirolimus-eluting stent with a standard stent for coronary revascularization. N Engl J Med. 346 2002:1773-1780.
CrossRef | PubMed
Moses  J.W., Leon  M.B., Popma  J.J.; Sirolimus-eluting stents versus standard stents in patients with stenosis in a native coronary artery. N Engl J Med. 349 2003:1315-1323.
CrossRef | PubMed
Stone  G.W., Ellis  S.G., Cox  D.A.; A polymer-based, paclitaxel-eluting stent in patients with coronary artery disease. N Engl J Med. 350 2004:221-231.
CrossRef | PubMed
Schofer  J., Schluter  M., Gershlick  A.H.; Sirolimus-eluting stents for treatment of patients with long atherosclerotic lesions in small coronary arteries: double-blind, randomised controlled trial (E-SIRIUS). Lancet. 362 2003:1093-1099.
CrossRef | PubMed
Schampaert  E., Cohen  E.A., Schluter  M.; The Canadian study of the sirolimus-eluting stent in the treatment of patients with long de novo lesions in small native coronary arteries (C-SIRIUS). J Am Coll Cardiol. 43 2004:1110-1115.
CrossRef | PubMed
Hong  M.K., Mintz  G.S., Lee  C.W.; Paclitaxel coating reduces in-stent intimal hyperplasia in human coronary arteries: a serial volumetric intravascular ultrasound analysis from the Asian Paclitaxel-Eluting Stent Clinical Trial (ASPECT). Circulation. 107 2003:517-520.
CrossRef | PubMed
Gershlick  A., De Scheerder  I., Chevalier  B.; Inhibition of restenosis with a paclitaxel-eluting, polymer-free coronary stent: the European evaLUation of pacliTaxel Eluting Stent (ELUTES) trial. Circulation. 109 2004:487-493.
CrossRef | PubMed
Grube  E., Silber  S., Hauptmann  K.E.; TAXUS I: six- and twelve-month results from a randomized, double-blind trial on a slow-release paclitaxel-eluting stent for de novo coronary lesions. Circulation. 107 2003:38-42.
CrossRef | PubMed
Colombo  A., Drzewiecki  J., Banning  A.;TAXUS II Study Group Randomized study to assess the effectiveness of slow- and moderate-release polymer-based paclitaxel-eluting stents for coronary artery lesions. Circulation. 108 2003:788-794.
CrossRef | PubMed
Lansky  A., Costa  R.A., Mintz  G.S., Tsuchiya  Y.; Non-polymer-based paclitaxel-coated coronary stents for the treatment of patients with de novo coronary lesions. Angiographic follow-up of the DELIVER clinical trial. Circulation. 109 2004:1948-1954.
CrossRef | PubMed
Lee  M.S., Jurewitz  D., Aragon  J.; Stent fracture associated with drug-eluting stents: clinical characteristics and implications. Catheter Cardiovasc Interv. 69 2007:387-394.
CrossRef | PubMed
Aoki  J., Nakazawa  G., Tanabe  K., Hoye  A.; Incidence and clinical impact of coronary stent fracture after sirolimus-eluting stent implantation. Catheter Cardiovasc Interv. 69 2007:380-386.
CrossRef | PubMed
Lee  S., Park  J., Shin  D., Kim  Y.; Frequency of stent fracture as a cause of coronary restenosis after sirolimus-eluting stent implantation. Am J Cardiol. 100 2007:627-630.
CrossRef | PubMed
Chowdhury  P.S., Ramos  R.G.; Images in clinical medicine. Coronary-stent fracture. N Engl J Med. 347 2002:581
CrossRef | PubMed
Brilakis  E.S., Maniu  C., Wahl  M., Barsness  G.; Unstable angina due to stent fracture. J Invasive Cardiol. 16 2004:545
PubMed
Sianos  G., Hofma  S., Ligthart  J.M.; Stent fracture and restenosis in the drug-eluting stent era. Catheter Cardiovasc Interv. 61 2004:111-116.
CrossRef | PubMed
Halkin  A., Carlier  S., Leon  M.B.; Late incomplete lesion coverage following Cypher stent deployment for diffuse right coronary artery stenosis. Heart. 90 2004:e45
CrossRef | PubMed
Hamilos  M.I., Papafaklis  M.I., Ligthart  J.M.; Stent fracture and restenosis of a paclitaxel-eluting stent. Hellenic J Cardiol. 46 2005:439-442.
PubMed
Surmely  J.F., Kinoshita  Y., Dash  D.; Stent strut fracture-induced restenosis in a bifurcation lesion treated with the crush stenting technique. Circ J. 70 2006:936-938.
CrossRef | PubMed
Min  P.K., Yoon  Y.W., Moon Kwon  H.; Delayed strut fracture of sirolimus-eluting stent: a significant problem or an occasional observation?. Int J Cardiol. 106 2006:404-406.
CrossRef | PubMed
Park  J.S., Shin  D.G., Kim  Y.J.; Fractured DES with a patent coronary artery: clinical implications. J Invasive Cardiol. 19 2007:E43-E45.
PubMed
Wilczynska  J., Rdzanek  A., Kochman  J.; Sirolimus eluting stent fracture following angioplasty of diffuse in-stent restenosis in the right coronary artery. Int J Cardiol. 118 2007:126-127.
CrossRef | PubMed
Makaryus  A.N., Lefkowitz  L., Lee  A.D.K.; Coronary artery stent fracture. Int J Cardiovasc Imaging. 23 2007:305-309.
CrossRef | PubMed
Zaizen  H., Tamura  A., Miyamoto  K.; Complete fracture of sirolimus-eluting stent detected by multislice computed tomography. J Int J Cardiol. 118 2007:120-121.
CrossRef
Leong  D.P., Dundon  B.K., Puri  R., Yeend  R.A.S.; Very late stent fracture associated with a sirolimus-eluting stent. Heart Lung Circ. 17 2008:426-428.
CrossRef | PubMed
Jin  X., Zhang  S., Xie  H.; Strut fracture of DES: An increasing problem?. Int J Cardiol. 118 2007:e54-e56.
CrossRef | PubMed
Kuboyama  O., Takei  H., Tokunaga  T.; Strut fracture of a sirolimus-eluting stent at the ostium of the right coronary artery. Heart. 93; 2007:1608
PubMed
Shite  J., Matsumoto  D., Yokoyama  M.; Sirolimus-eluting stent fracture with thrombus, visualization by optical coherence tomography. Eur Heart J. 27 2006:1389
CrossRef | PubMed
Hecht  H.S., Zaric  M., Jelnin  V.; Usefulness of 64-detector computed tomographic angiography for diagnosing in-stent restenosis in native coronary arteries. Am J Cardiol. 101 2008:820-824.
CrossRef | PubMed
Ryan  T.J., Faxon  D.P., Gunnar  R.M.; Guidelines for percutaneous transluminal coronary angioplasty: a report of the American College of Cardiology/American Heart Association Task Force on Assessment of Diagnostic and Therapeutic Cardiovascular Procedures (Subcommittee on Percutaneous Transluminal Coronary Angioplasty). Circulation. 78 1988:486-502.
CrossRef | PubMed
Freed  F.S., Safian  R.D.; Proximal vessel tortuosity and angulated lesions.Safian  R.D., Freed  M.S.; Manual of Interventional Cardiology. 3rd edition 2001 Physician's Press Royal Oak, MI:237-243.

Correspondence

Latest JACC CME

Continuing Medical Education through JACC is a convenient way to fulfill your CME requirements while learning important information about the latest advances in cardiovascular medicine.

April 2013- JACC CME Activity
Repeat Revascularization and Outcome

March 2013- JACC CME Activity
Extreme Lipoprotein(a) Levels and Improved Cardiovascular Risk Prediction

Feb 2013- JACC CME Activity
Results from the BARI 2D Trial

Jan 2013- JACC CME Activity
Prognosis Among Healthy Individuals Discharged With a Primary Diagnosis of Syncope

Dec 2012- JACC CME Activity
Incidence of Heart Failure or Cardiomyopathy After Adjuvant Trastuzumab Therapy for Breast Cancer

Nov 2012- JACC CME Activity
A Collaborative Analysis of Individual Patient Data From 10 Randomized Trials

Oct 2012- JACC CME Activity
Radiofrequency Ablation of Premature Ventricular Ectopy Improves the Efficacy of Cardiac Resynchronization Therapy in Nonresponders

Sept 2012- JACC CME Activity
Exercise and Pharmacological Treatment of Depressive Symptoms in Patients With Coronary Heart Disease

Aug 2012- JACC CME Activity
Reduction in Life-Threatening Ventricular Tachyarrhythmias in Statin-Treated Patients With Nonischemic Cardiomyopathy Enrolled in the MADIT-CRT (Multicenter Automatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy)

July 2012- JACC CME Activity
Relationship of Beta-Blocker Dose With Outcomes in Ambulatory Heart Failure Patients With Systolic Dysfunction

For previous CME quizzes, please follow this link to CardioSource Lifelong Learning and MOC.

 

NOTE:
Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s “Cited By” API will populate this tab (http://www.crossref.org/citedby.html).
Submit a Comment
Submit a Comment

Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging & repositioning the boxes below.

Articles Related By Topic
Related Topics