Restenosis and PercutaneousOptions Flashcards

1
Q

What are the clinical and anatomical predictors of restenosis following BMS placement?

A
  • Diabetes mellitus
  • Ostial or SVG lesion location
  • Prior restenosis
  • Smaller reference vessel diameter
  • Smaller postintervention minimum luminal diameter
  • Longer lesions
  • Greater total stent length

These variables also serve as risk factors for restenosis after DES implantation.

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2
Q

What were the findings of the EVOLVE II trial regarding bioabsorbable polymer-coated everolimus-eluting coronary stents versus durable polymer-coated everolimus stents?

A

No significant differences in TVR or stent thrombosis rates between the stents

Kereiakes DJ, et al. Circ Cardiovasc Interv 2015;8(4):e002372.

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3
Q

How does restenosis within BMS compare to restenosis within DES in terms of timing and characteristics?

A
  • Restenosis within BMS presents significantly later after stent implantation
  • Associated with greater volumes of neointimal hyperplasia
  • Shorter lesion lengths compared to restenosis within DES

Goto K, et al. Am J Cardiol 2015;116(9):1351–1357.

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4
Q

What role does inflammation play in the pathogenesis of coronary restenosis?

A

Inflammation promotes proliferation and migration of vascular smooth muscle cells and fibroblasts, leading to neointimal tissue development

Costa MA, et al. Circulation 2005;111(17): 2257–2273.

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5
Q

What are the key differences between restenotic lesions and atherosclerotic plaques?

A
  • Restenotic lesions exhibit more homogenous fibrohyperplastic morphology
  • Atherosclerotic plaques typically show complex features such as lipid pools, necrotic cores, fibrous caps, and focal calcification

Acute plaque rupture with thrombotic vessel occlusion is less common in restenosis.

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6
Q

What factors influence the effectiveness of animal models in studying restenosis?

A
  • Histologic appearance and composition differences
  • Metabolic, physiologic, and hemodynamic differences
  • No single model replicates all features of human restenosis

Various animal models like mice, pigs, and dogs show variability in neointimal formation.

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7
Q

What were the findings of the ISAR DESIRE-3 trial regarding PEB angioplasty and PES placement?

A
  • PEB: 27% angiographic restenosis
  • PES: 24% angiographic restenosis
  • Balloon angioplasty: 57% angiographic restenosis

Byrne RA, et al. Lancet 2013;381(9865):461–467.

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8
Q

Define late loss in the context of percutaneous coronary intervention (PCI).

A

Late loss is the in-stent minimum lumen diameter immediately following stent placement minus the in-stent minimum lumen diameter on late follow-up angiography

Example: Late loss = 3.40 − 2.98 = 0.42 mm.

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9
Q

What is the late loss index and how is it calculated?

A

Late loss index = late loss / acute gain

This normalizes late loss for acute gain achieved during the procedure.

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10
Q

True or False: Stent implantation leads to a reduced frequency of restenosis compared to balloon angioplasty.

A

True

Stent placement eliminates long-term negative remodeling of the vessel wall.

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11
Q

What is neoatherosclerosis and how does it differ from in-stent restenosis?

A
  • Neoatherosclerosis has pathologic features similar to de novo atherosclerosis
  • More prone to plaque rupture and clinical presentation with acute coronary syndrome

Finn AV, et al. Circ Cardiovasc Interv 2012;5(1):6–9.

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12
Q

What is the common timing for in-stent restenosis following BMS implantation?

A

Typically occurs within the first 6 months following stent implantation

After 6 months, spontaneous regression in luminal narrowing may occur (Kimura T, et al. N Engl J Med 1996;334(9):561–566).

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13
Q

What strategies should be considered for symptomatic in-stent restenosis?

A
  • Repeat PCI
  • Medical therapy
  • CABG

Treatment should be based on patient and lesion-specific factors.

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14
Q

What are microtubules and their role in cellular functions?

A

Microtubules are essential for the mitotic spindle apparatus, cellular migration, and growth factor signaling

Paclitaxel stabilizes microtubules, interrupting cellular division.

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15
Q

What were the outcomes of randomized trials comparing PES and EES placement?

A

Higher rates of late loss and/or target vessel failure were observed with PES compared to EES

SPIRIT III, SPIRIT IV, and COMPARE trials.

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16
Q

What is associated with a decreased incidence of major adverse cardiac events (MACE) among patients presenting with ACS?

A

Routine early invasive strategy

A conservative approach is not preferred for treatment in these cases.

17
Q

Which trial indicates that bypass surgery is associated with reduced rates of death and myocardial infarction (MI) in patients with diabetes and multivessel disease?

A

FREEDOM trial

This trial highlights the advantages of bypass surgery over drug-eluting stents (DES) in specific patient populations.

18
Q

What are the patterns of in-stent restenosis identified by Mehran et al.?

A

The patterns are:
* Focal
* Total occlusion
* Diffuse proliferative
* Diffuse intrastent

These classifications are based on the likelihood of late patency following repeat intervention.

19
Q

Which pattern of in-stent restenosis is associated with the lowest need for repeat revascularization?

A

Focal pattern

This is followed by diffuse intrastent, diffuse proliferative, and total occlusion patterns.

20
Q

True or False: Histologically, DES restenosis typically shows more homogenous hypercellular neointima than BMS restenosis.

A

False

DES restenosis is more likely to show organized thrombus and fibrin deposition.

21
Q

What biological factor appears predictive of BMS restenosis but not DES restenosis?

A

Serum markers of inflammation, most notably CRP

Elevated serum CRP levels are associated with a predisposition to restenosis in BMS, but not in DES.

22
Q

Fill in the blank: The tendency toward thrombus deposition within DES reflects the lack of protective _______.

A

neointima

This contrasts with the situation following BMS placement.

23
Q

What is associated with reduced measures of restenosis following both BMS and DES placement?

A

IVUS guidance

A meta-analysis supports the effectiveness of IVUS in optimizing stent sizing.

24
Q

What has randomized trials shown regarding stents with thinner struts?

A

They are associated with a significant reduction of angiographic and clinical restenosis

This finding emphasizes the importance of stent design in preventing restenosis.

25
Q

What is the preferred treatment choice for carotid in-stent restenosis?

A

Uncertain

Although repeat angioplasty or stenting is often performed, clinical outcomes compared to medical therapy are unclear.

26
Q

What clinical risk factors are associated with in-stent restenosis following BMS placement?

A

Risk factors include:
* SVG location
* Ostial lesion location
* Female gender
* Nonsmoking status
* Diabetes mellitus
* ACS
* Lesion length >20 mm
* Smaller vessel diameter
* Prior PCI
* Multiple stents
* ACC/AHA type C lesion classification

These factors can help in assessing the risk for restenosis.

27
Q

What does Sirolimus inhibit in the body?

A

The mechanistic target of rapamycin (mTOR) protein

Sirolimus is known for its role in preventing restenosis through its effects on vascular smooth muscle cell proliferation.

28
Q

What is the incidence of late stent fracture according to recent meta-analysis?

A

Mean incidence is 4.0%

The range among studies is from 0.8% to 8.4%.

29
Q

What are the complications associated with stent fracture?

A

Increased incidences of:
* Angiographic in-stent restenosis
* Target lesion revascularization
* Definite stent thrombosis

Fractures are more common in the RCA than in other arteries.

30
Q

What is the procedure of choice for recoarctation treatment?

A

Catheter-based therapy (angioplasty or stenting)

This approach should be individualized and directed by a heart team.

31
Q

True or False: Balloon valvotomy is contraindicated for the treatment of subvalvular or supervalvular aortic stenosis.

A

True

This procedure is more suitable for children and young adults with severe noncalcific congenital aortic stenosis.

32
Q

When is coarctation repair indicated?

A

Coarctation repair is indicated for symptomatic or asymptomatic individuals when the peak instantaneous pressure gradient is ≥20 mm Hg, or if collateral vessels are detected.

Reference: Warnes CA, et al. Circulation 2008, 118(23):e714–e833.

33
Q

What is the current procedure of choice for recoarctation treatment?

A

Catheter-based therapy (angioplasty or stenting) is the procedure of choice for the treatment of recoarctation.

Treatment should be individualized and directed by a heart team approach.

34
Q

Is recoarctation more common in children or adults?

A

Recoarctation is more common among children than adults following balloon angioplasty.

35
Q

What did a randomized trial compare regarding coarctation lesions?

A

A randomized trial compared covered and bare stents in 120 adolescent and adult patients with discrete coarctation lesions.

36
Q

What were the results of the randomized trial on stents for coarctation lesions?

A

The trial reported no differences in the incidence of recoarctation or pseudoaneurysm at follow-up.