The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Clinical Progression of Incidental, Asymptomatic Lesions Discovered During Culprit Vessel Coronary Intervention
Open accessAbstract
Background— With the reduction in restenosis rates by drug-eluting stents, there is new controversy concerning the optimal management of incidental, nontarget lesions identified during percutaneous coronary intervention (PCI). Such lesions have been treated conservatively because of risk of restenosis but now are being considered for PCI to prevent plaque instability. However, the impact of incidental stenoses on future cardiac events remains unknown. Methods and Results— We performed a retrospective cohort study to determine the rate and features of clinical plaque progression using the National Heart, Lung, and Blood Institute Dynamic Registry of consecutive patients undergoing PCI at multiple centers in 1997 to 1998 and 1999. Of 3747 PCI patients, 216 (5.8%) required additional nontarget lesion PCI for clinical plaque progression at 1 year. Fifty-nine percent presented with new unstable angina, and 9.3% presented with nonfatal myocardial infarction. Patients with multivessel coronary artery disease during original PCI were more likely to require nontarget lesion PCI during follow-up (adjusted odds ratio, 1.72 [95% CI, 1.18 to 2.52] for 2 vessels; adjusted odds ratio, 3.37 [95% CI, 2.32 to 4.89] for 3 vessels). Angiographic review showed that the majority (86.9%) of lesions requiring subsequent PCI were ≤60% in severity during original PCI, with the mean lesion stenosis 41.8±20.8% at the time of the initial PCI and 83.9±13.9% during the recurrent event. Conclusions— Approximately 6% of PCI patients will have clinical plaque progression requiring nontarget lesion PCI by 1 year. Greater coronary artery disease burden confers a significantly higher risk for clinical plaque progression.
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1 retracted
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The Prognostic Value of C-Reactive Protein and Serum Amyloid A Protein in Severe Unstable Angina
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Cited by
A Prospective Natural-History Study of Coronary Atherosclerosis
Stone, G. W., Maehara, A., Lansky, A. J., de Bruyne, B., Cristea, E., Mintz, G. S., Mehran, R., McPherson, J., Farhat, N., Marso, S. P., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1002358 · Cited by 3,276
Randomized Trial of Preventive Angioplasty in Myocardial Infarction
Wald, D. S., Morris, J. K., Wald, N. J., Chase, A. J., Edwards, R. J., Hughes, L. O., Berry, C., & Oldroyd, K. G. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1305520 · Cited by 1,048
Cheng, J. M., Garcia-Garcia, H. M., de Boer, S. P. M., Kardys, I., Heo, J. H., Akkerhuis, K. M., Oemrawsingh, R. M., van Domburg, R. T., Ligthart, J., Witberg, K. T., et al. (2014) · European Heart Journal · doi:10.1093/eurheartj/eht484 · Cited by 379
Kubo, T., Maehara, A., Mintz, G. S., Doi, H., Tsujita, K., Choi, S.-Y., Katoh, O., Nasu, K., Koenig, A., Pieper, M., et al. (2010) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2009.07.078 · Cited by 351
Metadata
- Authors
- Glaser, R., Selzer, F., Faxon, D. P., Laskey, W. K., Cohen, H. A., Slater, J., Detre, K. M., & Wilensky, R. L.
- Venue
- Circulation
- Published
- 2005-01-18
- Volume
- 111
- Issue
- 2
- Pages
- 143-149
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- OpenAlex
- W2064753214
- Cited by
- 269
- References
- 33
- FWCI
- 9.39
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Clinical Progression of Incidental, Asymptomatic Lesions Discovered During Culprit Vessel Coronary Intervention. https://app.cochat.ai/papers/10.1161/01.cir.0000150335.01285.12
- The paper
- Glaser, R., Selzer, F., Faxon, D. P., Laskey, W. K., Cohen, H. A., Slater, J., Detre, K. M., & Wilensky, R. L. (2005). Clinical Progression of Incidental, Asymptomatic Lesions Discovered During Culprit Vessel Coronary Intervention. Circulation. https://doi.org/10.1161/01.cir.0000150335.01285.12
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
