Login
Search
Search
0 Dates
2024
2023
2022
2021
2020
2019
2018
0 Events
CPC 2018
CPC 2019
Curso de Atualização em Medicina Cardiovascular 2019
Reunião Anual Conjunta dos Grupos de Estudo de Cirurgia Cardíaca, Doenças Valvulares e Ecocardiografia da SPC
CPC 2020
CPC 2021
CPC 2022
CPC 2023
CPC 2024
0 Topics
A. Basics
B. Imaging
C. Arrhythmias and Device Therapy
D. Heart Failure
E. Coronary Artery Disease, Acute Coronary Syndromes, Acute Cardiac Care
F. Valvular, Myocardial, Pericardial, Pulmonary, Congenital Heart Disease
G. Aortic Disease, Peripheral Vascular Disease, Stroke
H. Interventional Cardiology and Cardiovascular Surgery
I. Hypertension
J. Preventive Cardiology
K. Cardiovascular Disease In Special Populations
L. Cardiovascular Pharmacology
M. Cardiovascular Nursing
N. E-Cardiology / Digital Health, Public Health, Health Economics, Research Methodology
O. Basic Science
P. Other
0 Themes
01. History of Cardiology
02. Clinical Skills
03. Imaging
04. Arrhythmias, General
05. Atrial Fibrillation
06. Supraventricular Tachycardia (non-AF)
07. Syncope and Bradycardia
08. Ventricular Arrhythmias and Sudden Cardiac Death (SCD)
09. Device Therapy
10. Chronic Heart Failure
11. Acute Heart Failure
12. Coronary Artery Disease (Chronic)
13. Acute Coronary Syndromes
14. Acute Cardiac Care
15. Valvular Heart Disease
16. Infective Endocarditis
17. Myocardial Disease
18. Pericardial Disease
19. Tumors of the Heart
20. Congenital Heart Disease and Pediatric Cardiology
21. Pulmonary Circulation, Pulmonary Embolism, Right Heart Failure
22. Aortic Disease
23. Peripheral Vascular and Cerebrovascular Disease
24. Stroke
25. Interventional Cardiology
26. Cardiovascular Surgery
27. Hypertension
28. Risk Factors and Prevention
29. Rehabilitation and Sports Cardiology
30. Cardiovascular Disease in Special Populations
31. Pharmacology and Pharmacotherapy
32. Cardiovascular Nursing
33. e-Cardiology / Digital Health
34. Public Health and Health Economics
35. Research Methodology
36. Basic Science
37. Miscellanea
0 Resources
Abstract
Slides
Vídeo
Report
CLEAR FILTERS
20 year-follow up of mitral stenosis patients after percutaneous valve commissurotomy: invasive transmitral pressure gradient diferential as a predictor of events
Session:
Comunicações Orais - Sessão 02 - Intervenção não coronária
Speaker:
Ana Amador
Congress:
CPC 2023
Topic:
H. Interventional Cardiology and Cardiovascular Surgery
Theme:
25. Interventional Cardiology
Subtheme:
25.3 Non-coronary Cardiac Intervention
Session Type:
Comunicações Orais
FP Number:
---
Authors:
Ana Amador; Catarina Costa; João Calvão; André Cabrita; Catarina Marques; Ana Pinho; Cátia Oliveira; Luís Santos; Helena Moreira; Miguel Rocha; Pedro Palma; Mariana Paiva; João Carlos Silva; Filipe Macedo
Abstract
<p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-family:"Calibri Light",sans-serif"><span style="color:#333333">Background: </span></span></strong><span style="font-family:"Calibri Light",sans-serif"><span style="color:#333333">Percutaneous valve commissurotomy (PMC) is a viable alternative to mitral valve (MV) surgery in the treatment of patients (pts) with clinically significant mitral stenosis (MS). About 40% of pts treated with PMC will require at least one reintervention (either PMC or MV surgery) along time. The aim of our study was to evalute the long-term results of PMC in pts with rheumatic MS and to seek for an immediate intra operative predictor of events.</span></span></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-family:"Calibri Light",sans-serif">Methods: </span></strong><span style="font-family:"Calibri Light",sans-serif">We retrospectively analysed all consecutive patients between 1991 and 2008 with <span style="color:#333333">clinically significant rheumatic MS undergoing PMC. Clinical and echocardiographic data were collected at baseline and during early and long-term follow-up. MACE was a composite of adverse events defined as all-cause mortality, MV re-intervention or cardiovascular hospitalization.</span></span></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-family:"Calibri Light",sans-serif">Results: </span></strong><span style="font-family:"Calibri Light",sans-serif">A total of 124 pts were enrolled: 108 (87%) female, mean age at the time of PMC of 46 ± 11 years. </span></span></span><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-family:"Calibri Light",sans-serif">At baseline, 34% pts were in NYHA class ≥III and 81% had a Wilkins score ≤ 8; all patients had preserved biventricular systolic function and 83% presented pulmonary hypertension. In 20 cases, there was concomitant moderate disease of other valve (3/4 tricuspid regurgitation).</span></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-family:"Calibri Light",sans-serif">Most of the procedures were successful (91%) and without complications (94%), with a median reduction in pulmonary artery systolic pressure PASP of 8 mmHg (IQR 10) and a mean reduction in mitral valve gradient of 8±7 mmHg. </span></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-family:"Calibri Light",sans-serif">During the mean follow-up of 20 ± 6 years, 51 (42%) of patients had MV re-intervention (86% surgery and 14% re-PMC), 37 (30%) were hospitalized and 30 (24%) died. Concerning time-to-event analysis, approximately 80% of patients kept MACE-free after 10 years; after 30 years, more than 20% continued MACE-uneventful, approximately 50% were alive and about 45% were free from re-intervention.</span></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-family:"Calibri Light",sans-serif">Using Cox regression, we found that a reduction <5 mmHg in transmitral pressure gradient at PMC time (before and immediately after PMC) was associated with a 2,1-fold greater rate of MACE compared to pts with a reduction ≥ 5 mmHg (HR<sub>crude</sub>=2,2; 95%CI 1,319-3,813 p=0,003). After adjusting for the presence of mitral regurgitation after PMC (HR<sub>crude</sub>=1,7; 95%CI 1,020-2,950, p=0,042) and for moderate disease of other valves (HR<sub>crude</sub> 1,9; 95%CI 1,070-3,267, p=0,028) the observed effect remained significant and was even greater (HR<sub>adjusted</sub> = 2,7; 95% CI 1,395-5,298, p=0,003). </span></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-family:"Calibri Light",sans-serif">Of note, diferential in PSAP or in left atrium pressure intra-operatorive did not show an association with occurrence of events (p=0,285 and p=0,769).</span></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-family:"Calibri Light",sans-serif">Conclusion:</span></strong><span style="font-family:"Calibri Light",sans-serif"> PMC was safe and effective in <span style="font-family:"Calibri Light",sans-serif"><span style="color:#333333">clinically significant rheumatic MS</span></span>. Most of the patients were free from adverse events after 10 years and half were alive after 30 years; still, about 40% required re-intervention. A reduction <5 mmHg in transmitral gradient at PMC time was associated with events during follow up; more studies are needed to validate this pratical independent predictor.</span></span></span></p>
Slides
Our mission: To reduce the burden of cardiovascular disease
Visit our site