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1.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 163-170, 2017.
Artigo em Inglês | WPRIM | ID: wpr-111252

RESUMO

BACKGROUND: The absence of atrial contraction (AC) after the maze procedure has been reported to cause subsequent annular dilatation and to increase the risk of embolic stroke. We hypothesized that the lack of AC could increase the risk of permanent pacemaker (PPM) implantation in patients undergoing the maze procedure. METHODS: In 376 consecutive patients who had undergone a cryo-maze procedure and combined valve operation, recovery of AC was assessed at baseline and at immediate (≤2 weeks), early (≤1 year, 4.6±3.8 months), and late (>1 year, 3.5±1.1 years) postoperative stages. RESULTS: With a median follow-up of 53 months, 10 patients underwent PPM implantation. Seven PPM implants were for sinus node dysfunction (pauses of 9.6±2.4 seconds), one was for marked sinus bradycardia, and two were for advanced/complete atrioventricular block. The median (interquartile range) time to PPM implantation was 13.8 (0.5–68.2) months. Our time-varying covariate Cox models showed that the absence of AC was a risk factor for PPM implantation (hazard ratio, 11.92; 95% confidence interval, 2.52 to 56.45; p=0.002). CONCLUSION: The absence of AC may be associated with a subsequent risk of PPM implantation.


Assuntos
Humanos , Fibrilação Atrial , Bloqueio Atrioventricular , Bradicardia , Criocirurgia , Dilatação , Seguimentos , Modelos de Riscos Proporcionais , Fatores de Risco , Síndrome do Nó Sinusal , Acidente Vascular Cerebral
2.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 44-46, 2017.
Artigo em Inglês | WPRIM | ID: wpr-39842

RESUMO

We report the case of a newborn with a rare anatomic variation: a right aortic arch with a retroesophageal left subclavian artery and an anomalous origin of the pulmonary artery from the aorta. This variation was diagnosed using echocardiography and computed tomography, and we treated the condition surgically.


Assuntos
Humanos , Recém-Nascido , Variação Anatômica , Aorta , Aorta Torácica , Síndrome de DiGeorge , Ecocardiografia , Cardiopatias Congênitas , Artéria Pulmonar , Artéria Subclávia
3.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 305-307, 2017.
Artigo em Inglês | WPRIM | ID: wpr-118269

RESUMO

Patients with severe emphysema have a higher risk of developing lung cancer, and their surgical risk increases when emphysema is accompanied by a giant bulla. Here, we describe a patient who had an emphysematous giant bulla in the right upper lobe that was treated with an endobronchial valve placement. Subsequently, a cancerous lesion on the contralateral lung was successfully removed by lobectomy.


Assuntos
Humanos , Enfisema , Neoplasias Pulmonares , Pulmão
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