5 results on '"Nguyen, B.O."'
Search Results
2. Brady- and tachyarrhythmias detected by continuous rhythm monitoring in paroxysmal atrial fibrillation.
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Frausing, M.H.J.P., Lande, M.E. Van De, Maass, A.H., Nguyen, B.O., Hemels, M.E.W., Tieleman, R.G., Koldenhof, T., Melis, M. De, Linz, D., Schotten, U., Weberndörfer, V., Crijns, H.J.G.M., Gelder, I.C van, Nielsen, J.C., Rienstra, M., Frausing, M.H.J.P., Lande, M.E. Van De, Maass, A.H., Nguyen, B.O., Hemels, M.E.W., Tieleman, R.G., Koldenhof, T., Melis, M. De, Linz, D., Schotten, U., Weberndörfer, V., Crijns, H.J.G.M., Gelder, I.C van, Nielsen, J.C., and Rienstra, M.
- Abstract
Item does not contain fulltext, OBJECTIVE: Atrial fibrillation (AF) is associated with adverse events including conduction disturbances, ventricular arrhythmias and sudden death. The aim of this study was to examine brady- and tachyarrhythmias using continuous rhythm monitoring in patients with paroxysmal self-terminating AF (PAF). METHODS: In this multicentre observational substudy to the Reappraisal of Atrial Fibrillation: interaction between hyperCoagulability, Electrical remodelling and Vascular destabilisation in the progression of AF (RACE V), we included 392 patients with PAF and at least 2 years of continuous rhythm monitoring. All patients received an implantable loop recorder, and all detected episodes of tachycardia ≥182 beats per minute (BPM), bradycardia ≤30 BPM or pauses ≥5 s were adjudicated by three physicians. RESULTS: Over 1272 patient-years of continuous rhythm monitoring, we adjudicated 1940 episodes in 175 patients (45%): 106 (27%) patients experienced rapid AF or atrial flutter (AFL), pauses ≥5 s or bradycardias ≤30 BPM occurred in 47 (12%) patients and in 22 (6%) patients, we observed both episode types. No sustained ventricular tachycardias occurred. In the multivariable analysis, age >70 years (HR 2.3, 95% CI 1.4 to 3.9), longer PR interval (HR 1.9, 1.1-3.1), CHA(2)DS(2)-VASc score ≥2 (HR 2.2, 1.1-4.5) and treatment with verapamil or diltiazem (HR 0.4, 0.2-1.0) were significantly associated with bradyarrhythmia episodes. Age >70 years was associated with lower rates of tachyarrhythmias. CONCLUSIONS: In a cohort exclusive to patients with PAF, almost half experienced severe bradyarrhythmias or AF/AFL with rapid ventricular rates. Our data highlight a higher than anticipated bradyarrhythmia risk in PAF. TRIAL REGISTRATION NUMBER: NCT02726698.
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- 2023
3. Time of onset of atrial fibrillation and atrial fibrillation progression data from the RACE V study
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van de Lande, M.E., Rama, R.S., Koldenhof, T., Arita, V.A., Nguyen, B.O., van Deutekom, C., Weberndorfer, V., Crijns, H.J.G.M., Hemels, M.E.W., Tieleman, R.G., de Melis, M., Schotten, U., Linz, D., Van Gelder, I.C., Rienstra, M., MUMC+: MA Med Staf Spec Cardiologie (9), RS: Carim - H01 Clinical atrial fibrillation, Cardiologie, MUMC+: MA Cardiologie (3), MUMC+: MA Cardiologie (9), Fysiologie, and RS: Carim - H08 Experimental atrial fibrillation
- Subjects
RISK ,Self-terminating atrial fibrillation ,Rhythm monitoring ,Atrial fibrillation progression ,Physiology (medical) ,PATTERNS ,Cardiology and Cardiovascular Medicine ,Time of onset - Abstract
AimsAtrial fibrillation (AF) progression is associated with adverse outcome, but the role of the circadian or diurnal pattern of AF onset remains unclear. We aim to assess the association between the time of onset of AF episodes with the clinical phenotype and AF progression in patients with self-terminating AF.Methods and resultsThe Reappraisal of AF: Interaction Between Hypercoagulability, Electrical Remodelling, and Vascular Destabilization in the Progression of AF study included patients with self-terminating AF who underwent extensive phenotyping at baseline and continuous rhythm monitoring with an implantable loop recorder (ILR). In this subanalysis, ILR data were used to assess the development of AF progression and the diurnal pattern of AF onset: predominant (>80%) nocturnal AF, predominant daytime AF, or mixed AF without a predominant diurnal AF pattern. The median follow-up was 2.2 (1.6–2.8) years. The median age was 66 (59–71) years, and 117 (42%) were women. Predominant nocturnal (n = 40) and daytime (n = 43) AF onset patients had less comorbidities compared to that of mixed (n = 195) AF patients (median 2 vs. 2 vs. 3, respectively, P = 0.012). Diabetes was more common in the mixed group (12% vs. 5% vs. 0%, respectively, P = 0.031), whilst obesity was more frequent in the nocturnal group (38% vs. 12% vs. 27%, respectively, P = 0.028). Progression rates in the nocturnal vs. daytime vs. mixed groups were 5% vs. 5% vs. 24%, respectively (P = 0.013 nocturnal vs. mixed and P = 0.008 daytime vs. mixed group, respectively).ConclusionIn self-terminating AF, patients with either predominant nocturnal or daytime onset of AF episodes had less associated comorbidities and less AF progression compared to that of patients with mixed onset of AF.Clinical trial registrationNCT02726698
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- 2023
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4. Long-term outcome of targeted therapy of underlying conditions in patients with early persistent atrial fibrillation and heart failure: data of the RACE 3 trial
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Nguyen, B.O., Crijns, H., Tijssen, J.G., Geelhoed, B., Hobbelt, A.H., Hemels, M.E.W., Mol, W.J.M., Weijs, B., Alings, M., Smit, M.D., Tieleman, R.G., Tukkie, R., Veldhuisen, D.J. van, Gelder, I.C van, Rienstra, M., Nguyen, B.O., Crijns, H., Tijssen, J.G., Geelhoed, B., Hobbelt, A.H., Hemels, M.E.W., Mol, W.J.M., Weijs, B., Alings, M., Smit, M.D., Tieleman, R.G., Tukkie, R., Veldhuisen, D.J. van, Gelder, I.C van, and Rienstra, M.
- Abstract
Contains fulltext : 283517.pdf (Publisher’s version ) (Open Access), AIMS: The Routine vs. Aggressive risk factor driven upstream rhythm Control for prevention of Early persistent atrial fibrillation (AF) in heart failure (HF) (RACE 3) trial demonstrated that targeted therapy of underlying conditions improved sinus rhythm maintenance at 1 year. We now explored the effects of targeted therapy on the additional co-primary endpoints; sinus rhythm maintenance and cardiovascular outcome at 5 years. METHODS AND RESULTS: Patients with early persistent AF and mild-to-moderate stable HF were randomized to targeted or conventional therapy. Both groups received rhythm control therapy according to guidelines. The targeted group additionally received four therapies: angiotensin-converting enzyme inhibitors and/or angiotensin receptor blockers (ARBs), statins, mineralocorticoid receptor antagonists (MRAs), and cardiac rehabilitation. The presence of sinus rhythm and cardiovascular morbidity and mortality at 5-year follow-up were assessed. Two hundred and sixteen patients consented for long-term follow-up, 107 were randomized to targeted and 109 to conventional therapy. At 5 years, MRAs [76 (74%) vs. 10 (9%) patients, P < 0.001] and statins [81 (79%) vs. 59 (55%), P < 0.001] were used more in the targeted than conventional group. Angiotensin-converting enzyme inhibitors/ARBs and physical activity were not different between groups. Sinus rhythm was present in 49 (46%) targeted vs. 43 (39%) conventional group patients at 5 years (odds ratio 1.297, lower limit of 95% confidence interval 0.756, P = 0.346). Cardiovascular mortality and morbidity occurred in 20 (19%) in the targeted and 15 (14%) conventional group patients, P = 0.353. CONCLUSION: In patients with early persistent AF and HF superiority of targeted therapy in sinus rhythm maintenance could not be preserved at 5-year follow-up. Cardiovascular outcome was not different between groups. TRIAL REGISTRATION NUMBER: Clinicaltrials.gov NCT00877643.
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- 2022
5. Temporal patterns and short-term progression of paroxysmal atrial fibrillation: data from RACE V
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With, R.R. De, Erküner, Ö., Rienstra, M., Nguyen, B.O., Körver, F.W.J., Linz, D., Ten, H. Cate, Spronk, H., Kroon, A.A., Maass, A.H., Blaauw, Y., Tieleman, R.G., Hemels, M.E.W., Groot, J.R. de, Elvan, A., Melis, M., Scheerder, C.O.S., Al-Jazairi, M.I.H., Schotten, U., Luermans, J., Crijns, H., Gelder, I.C van, With, R.R. De, Erküner, Ö., Rienstra, M., Nguyen, B.O., Körver, F.W.J., Linz, D., Ten, H. Cate, Spronk, H., Kroon, A.A., Maass, A.H., Blaauw, Y., Tieleman, R.G., Hemels, M.E.W., Groot, J.R. de, Elvan, A., Melis, M., Scheerder, C.O.S., Al-Jazairi, M.I.H., Schotten, U., Luermans, J., Crijns, H., and Gelder, I.C van
- Abstract
Contains fulltext : 225394.pdf (Publisher’s version ) (Open Access), Aims: Atrial fibrillation (AF) often starts as a paroxysmal self-terminating arrhythmia. Limited information is available on AF patterns and episode duration of paroxysmal AF. In paroxysmal AF patients, we longitudinally studied the temporal AF patterns, the association with clinical characteristics, and prevalence of AF progression. Methods and results: In this interim analysis of the Reappraisal of AF: Interaction Between HyperCoagulability, Electrical Remodelling, and Vascular Destabilisation in the Progression of AF (RACE V) registry, 202 patients with paroxysmal AF were followed with continuous rhythm monitoring (implantable loop recorder or pacemaker) for 6 months. Mean age was 64 ± 9 years, 42% were women. Atrial fibrillation history was 2.1 (0.5–4.4) years, CHA2DS2-VASc 1.9 ± 1.3, 101 (50%) had hypertension, 69 (34%) heart failure. One-third had no AF during follow-up. Patients with long episodes (>12 hours) were often men with more comorbidities (heart failure, coronary artery disease, higher left ventricular mass). Patients with higher AF burden (>2.5%) were older with more comorbidities (worse renal function, higher calcium score, thicker intima media thickness). In 179 (89%) patients, 1-year rhythm follow-up was available. On a quarterly basis, average daily AF burden increased from 3.2% to 3.8%, 5.2%, and 6.1%. Compared to the first 6 months, 111 (62%) patients remained stable during the second 6 months, 39 (22%) showed progression to longer AF episodes, 8 (3%) developed persistent AF, and 29 (16%) patients showed AF regression. Conclusions: In paroxysmal AF, temporal patterns differ suggesting that paroxysmal AF is not one entity. Atrial fibrillation burden is low and determined by number of comorbidities. Atrial fibrillation progression occurred in a substantial number. Trial registration number: Clinicaltrials.gov identifier NCT02726698.
- Published
- 2020
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