External validation of the PROGRESS-CTO complication risk scores: Individual patient data pooled analysis of 3 registries.

Bahadir Simsek, Peter Tajti, Mauro Carlino, Soledad Ojeda, Manuel Pan, Stephane Rinfret, Evangelia Vemmou, Spyridon Kostantinis, Ilias Nikolakopoulos, Judit Karacsonyi, Joseph A Dens, Pierfrancesco Agostoni, Khaldoon Alaswad, Michael Megaly, Alexandre Avran, James W Choi, Farouc A Jaffer, Darshan Doshi, Dimitri Karmpaliotis, Jaikirshan J Khatri, Paul Knaapen, Alessio La Manna, James C Spratt, Masaki Tanabe, Simon Walsh, Olga C Mastrodemos, Salman Allana, Athanasios Rempakos, Bavana V Rangan, Omer Goktekin, Sevket Gorgulu, Paul Poommipanit, Kathleen E Kearney, William L Lombardi, J Aaron Grantham, Kambis Mashayekhi, Emmanouil S Brilakis, Lorenzo Azzalini
Author Information
  1. Bahadir Simsek: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  2. Peter Tajti: The Gottsegen National Cardiovascular Center, Budapest, Hungary.
  3. Mauro Carlino: Interventional Cardiology Division, Cardio-Thoracic-Vascular Department, San Raffaele Scientific Institute, Milan, Italy.
  4. Soledad Ojeda: Division of Interventional Cardiology, Reina Sofia Hospital, University of Cordoba, Maimonides Institute for Research in Biomedicine of Cordoba (IMIBIC), Cordoba, Spain.
  5. Manuel Pan: Division of Interventional Cardiology, Reina Sofia Hospital, University of Cordoba, Maimonides Institute for Research in Biomedicine of Cordoba (IMIBIC), Cordoba, Spain.
  6. Stephane Rinfret: Emory Heart and Vascular Center, Emory University School of Medicine, Atlanta, GA, USA.
  7. Evangelia Vemmou: Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
  8. Spyridon Kostantinis: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  9. Ilias Nikolakopoulos: Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
  10. Judit Karacsonyi: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  11. Joseph A Dens: Department of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium.
  12. Pierfrancesco Agostoni: Hartcentrum, Ziekenhuis Netwerk Antwerpen Middelheim, Antwerp, Belgium.
  13. Khaldoon Alaswad: Henry Ford Health System, Detroit, MI, USA.
  14. Michael Megaly: Division of Cardiology, Willis Knighton Heart Institute, Shreveport, LA, United States of America.
  15. Alexandre Avran: Department of Interventional Cardiology, Clinique Pasteur, Essey-lès-Nancy, France.
  16. James W Choi: Presbyterian Hospital, Dallas, TX, USA.
  17. Farouc A Jaffer: Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  18. Darshan Doshi: Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  19. Dimitri Karmpaliotis: Morristown Medical Center, Morristown, NJ, USA.
  20. Jaikirshan J Khatri: Cleveland Clinic Foundation, Cleveland, OH, USA.
  21. Paul Knaapen: Department of Cardiology, VU University Medical Center, Amsterdam, the Netherlands.
  22. Alessio La Manna: University of Catania, Catania, Italy.
  23. James C Spratt: St. George's University Healthcare NHS Trust, London, United Kingdom.
  24. Masaki Tanabe: Department of Cardiology, Nozaki Tokushukai Hospital, Osaka, Japan.
  25. Simon Walsh: Belfast Health, Belfast, United Kingdom.
  26. Olga C Mastrodemos: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  27. Salman Allana: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  28. Athanasios Rempakos: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  29. Bavana V Rangan: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  30. Omer Goktekin: Division of Cardiology, Memorial Bahcelievler Hospital, Istanbul, Turkey.
  31. Sevket Gorgulu: Division of Cardiology, Biruni University School of Medicine, Istanbul, Turkey.
  32. Paul Poommipanit: University Hospitals, Cleveland, OH, USA.
  33. Kathleen E Kearney: Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA, USA.
  34. William L Lombardi: Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA, USA.
  35. J Aaron Grantham: Saint Luke's Mid America Heart Institute, Kansas City, MO, USA.
  36. Kambis Mashayekhi: Heart Center Lahr, Department for Internal Medicine and Cardiology, Germany.
  37. Emmanouil S Brilakis: Minneapolis Heart Institute, Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.
  38. Lorenzo Azzalini: Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA, USA. Electronic address: azzalini@uw.edu.

Abstract

BACKGROUND: Chronic total occlusion (CTO) percutaneous coronary intervention (PCI) is associated with a considerable risk of complications, and risk stratification is of utmost importance.
AIMS: To assess the clinical usefulness of the recently developed PROGRESS-CTO (NCT02061436) complication risk scores in an independent cohort.
METHODS: Individual patient data pooled analysis of 3 registries was performed.
RESULTS: Of the 4569 patients who underwent CTO PCI, 102 (2.2%) had major adverse cardiovascular events (MACE). patients with MACE were older (69 ± 11 vs. 65 ± 10, p < 0.001), more likely to have a history of prior coronary artery bypass graft surgery, and unfavorable angiographic characteristics J-CTO score (2.4 ± 1.2 vs. 2.1 ± 1.3, p = 0.007), including blunt stump (59% vs. 49%, p = 0.047). Technical success was lower in patients with MACE (59% vs. 86%, p < 0.001). The area under the receiver operating characteristic curve of the PROGRESS-CTO complication risk models were as follows: MACE 0.72 (95% confidence interval [CI], 0.67-0.76), mortality 0.73 (95% CI, 0.61-0.85), and pericardiocentesis 0.69 (95% CI, 0.62-0.77) in the validation dataset. The observed complication rates increased with higher PROGRESS-CTO complication scores. The PROGRESS-CTO MACE score showed good calibration in this external cohort, with MACE rates similar to the original study: 0.7% (score 0-1), 1.5% (score 2), 2.2% (score 3), 3.8% (score 4), 4.9% (score 5), 5.8% (score 6-7).
CONCLUSION: Given the good discriminative performance, calibration, and ease of calculation, the PROGRESS-CTO complication scores could help assess the risk of complications in patients undergoing CTO PCI.

Keywords

MeSH Term

Humans
Treatment Outcome
Percutaneous Coronary Intervention
Coronary Angiography
Risk Factors
Registries
Coronary Occlusion
Chronic Disease

Word Cloud

Created with Highcharts 10.0.0score0riskPROGRESS-CTOcomplication2MACE3vsCTOcoronaryPCIscorespatients95%validationChronictotalocclusioninterventioncomplicationsassesscohortIndividualpatientdatapooledanalysisregistries2%adversecardiovasculareventsp < 0001p = 059%CIratesgoodcalibration8%45ExternalBACKGROUND:percutaneousassociatedconsiderablestratificationutmostimportanceAIMS:clinicalusefulnessrecentlydevelopedNCT02061436independentMETHODS:performedRESULTS:4569underwent102majorPatientsolder69 ± 1165 ± 10likelyhistorypriorarterybypassgraftsurgeryunfavorableangiographiccharacteristicsJ-CTO4 ± 11 ± 1007includingbluntstump49%047Technicalsuccesslower86%areareceiveroperatingcharacteristiccurvemodelsfollows:72confidenceinterval[CI]67-076mortality7361-085pericardiocentesis6962-077datasetobservedincreasedhighershowedexternalsimilaroriginalstudy:7%0-115%9%6-7CONCLUSION:Givendiscriminativeperformanceeasecalculationhelpundergoingscores:MajorMortalityPercutaneousRiskmodel

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