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1.
JTCVS Tech ; 8: 211-212, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-34401857
2.
Thorac Surg Clin ; 31(2): 177-188, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-33926671

RESUMEN

Lung volume reduction surgery (LVRS) patient selection guidelines are based on the National Emphysema Treatment Trial. Because of increased mortality and poor improvement in functional outcomes, patients with non-upper lobe emphysema and low baseline exercise capacity are determined as poor candidates for LVRS. In well-selected patients with heterogeneous emphysema, LVRS has a durable long-term outcome at up to 5-years of follow-up. Five-year survival rates in patients range between 63% and 78%. LVRS seems a durable alternative for end-stage heterogeneous emphysema in patients not eligible for lung transplantation. Future studies will help identify eligible patients with homogeneous emphysema for LVRS.


Asunto(s)
Esperanza de Vida , Pulmón/cirugía , Neumonectomía/efectos adversos , Neumonectomía/métodos , Enfisema Pulmonar/cirugía , Anciano , Ensayos Clínicos como Asunto , Femenino , Guías como Asunto , Humanos , Estimación de Kaplan-Meier , Trasplante de Pulmón , Masculino , Persona de Mediana Edad , Selección de Paciente , Enfisema Pulmonar/mortalidad , Enfisema Pulmonar/fisiopatología , Tasa de Supervivencia , Resultado del Tratamiento
3.
Thorac Surg Clin ; 31(2): xv, 2021 05.
Artículo en Inglés | MEDLINE | ID: mdl-33926678
4.
Ann Thorac Surg ; 111(6): 1865-1866, 2021 06.
Artículo en Inglés | MEDLINE | ID: mdl-33144113
5.
JTCVS Tech ; 2: 167, 2020 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-34317792
7.
J Thorac Cardiovasc Surg ; 157(2): 790, 2019 02.
Artículo en Inglés | MEDLINE | ID: mdl-30669238
10.
11.
Ann Thorac Surg ; 103(1): 224-225, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-28007239
12.
J Heart Valve Dis ; 24(6): 736-743, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27997780

RESUMEN

BACKGROUND: The study aim was to examine whether concomitant atrial fibrillation (AF) surgery at the time of mitral valve surgery in the elderly results in increased operative mortality (OM). METHODS: Medicare beneficiaries aged ≥65 years undergoing primary mitral valve repair or replacement between 2004 and 2006 were included. The cohort was divided into three groups: Group 1, AF- (n = 2,705); group 2, AF+AF surgery- (n = 2,119), and group 3, AF+AF surgery+ (n = 1,832). The primary outcomes were OM and long-term survival. A secondary outcome was the association between hospital annual mitral procedure volume and OM. RESULTS: The unadjusted OM was 6.4% for group 1 (AF-), 10.3% for group 2 (AF+AF surgery-), and 7.1% for group 3 (AF+AF surgery+) (p = 0.0001). Adjusted OM for AF+AF surgery+ patients was not significantly different from that of AF- patients (OR 1.16, 95% CI 0.90-1.48), or from AF+AF surgery patients (OR 0.83, 95% CI 0.66-1.06). When comparisons were adjusted for differences in baseline characteristics, AF+AF surgery- patients were more likely to experience long-term mortality than AF- patients (HR 1.30, 95% CI 1.17-1.45), as well as AF+AF surgery+ patients (HR 1.17, 95% CI 1.05-1.31). An annual average mitral procedure volume ≤40 was independently predictive of OM (OR 1.42, 95% CI 1.13-1.78). The effect of institutional volume on mortality was strongest in those who received AF surgery (AF+AF surgery+) (HR 1.75, 95% CI 1.15-2.65), compared to those who did not undergo surgery (AF+AF surgery-) (OR 1.20, 95% CI 0.86-1.67). CONCLUSIONS: Elderly patients undergoing mitral valve surgery do not appear to have an increased mortality when clinical judgment favored the performance of concomitant AF surgery.

13.
Ann Thorac Surg ; 96(5): 1868-70, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-24182480

RESUMEN

Type A intramural hematoma (IMH) is an uncommon entity, the pathophysiology of which is thought to be related to a contained hemorrhage within the medial layer of the aorta as a result of either rupture of the vasa vasorum or an atherosclerotic plaque. We present a case of type A IMH in the setting of acute type B aortic dissection with suspicion for malperfusion syndrome and discuss the treatment algorithm of this uncommon entity.


Asunto(s)
Enfermedades de la Aorta , Hematoma , Adulto , Enfermedades de la Aorta/clasificación , Enfermedades de la Aorta/complicaciones , Enfermedades de la Aorta/cirugía , Hematoma/clasificación , Hematoma/complicaciones , Hematoma/cirugía , Humanos , Masculino
14.
J Card Surg ; 27(1): 29-33, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-22321110

RESUMEN

BACKGROUND: Cardiovascular disease is the main cause of morbidity and mortality in patients with systemic lupus erythematosus (SLE). SLE as a risk factor for adverse outcomes during mitral surgery has not been studied. The purpose of this investigation was to compare procedure selection and outcomes of patients with and without SLE. METHODS: The 2005-2008 Nationwide Inpatient Sample database was searched to identify patients ≥18 years of age undergoing isolated mitral repair or replacement. Patients with and without SLE were compared on baseline characteristics and hospital outcomes. Within patients with SLE, those undergoing repair and replacement were compared. RESULTS: SLE patients comprised 0.9% (620/70,969) of the isolated mitral valve surgery population. Patients with SLE were significantly younger, more likely to be female, less likely to be white, had higher Charlson comorbidity index, and less often presented electively. Patients with SLE had a higher incidence of prolonged hospitalization (LOS > 10 days; 44.4% vs. 34.7%, p = 0.0392). Mortality was similar for patients with and without SLE undergoing isolated mitral valve surgery (OR = 0.76, 95% CI 0.28-2.05, p = 0.5821). Patients with SLE were less likely to have mitral valve repair (27.1% vs. 45.6%, p = 0.0002). Baseline characteristics were similar between SLE repair and replacement subsets. Median LOS was higher for replacement (10 days vs. 7 days, p = 0.0014). Hospital mortality was 0% for SLE mitral repair patients and <4.0% for SLE replacement patients. CONCLUSIONS: Patients with SLE present for isolated mitral valve surgery at a much younger age and with worse preoperative profiles. Although mitral repair rates were lower in patients with SLE, hospital outcomes were excellent, and comparable to those of patients without SLE.


Asunto(s)
Implantación de Prótesis de Válvulas Cardíacas/métodos , Lupus Eritematoso Sistémico/complicaciones , Insuficiencia de la Válvula Mitral/cirugía , Estenosis de la Válvula Mitral/cirugía , Válvula Mitral/cirugía , Adulto , Factores de Edad , Anciano , Estudios Transversales , Femenino , Implantación de Prótesis de Válvulas Cardíacas/mortalidad , Mortalidad Hospitalaria , Humanos , Tiempo de Internación/estadística & datos numéricos , Lupus Eritematoso Sistémico/mortalidad , Masculino , Persona de Mediana Edad , Válvula Mitral/patología , Insuficiencia de la Válvula Mitral/etiología , Insuficiencia de la Válvula Mitral/mortalidad , Estenosis de la Válvula Mitral/etiología , Estenosis de la Válvula Mitral/mortalidad , Factores de Riesgo , Factores Sexuales , Resultado del Tratamiento
15.
Eur J Cardiothorac Surg ; 41(1): 14-8, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21601469

RESUMEN

OBJECTIVES: Video-assisted thoracoscopic surgery (VATS) and median sternotomy (MS) are two approaches in lung-volume reduction surgery (LVRS). This study focused on the two surgical approaches with regard to postoperative pain. METHODS: In this prospective, non-randomized study, pain was measured preoperatively and postoperatively using the visual analog scale (VAS) and the brief pain inventory (BPI). Incentive spirometry (IS) assessed restriction of the thoracic cage due to pain. Factors associated with treatment complications, medication usage, hospital stay, operating times, and chest-tube duration differences were examined between groups. RESULTS: Of 85 patients undergoing LVRS, 23 patients underwent reduction via MS and 62 patients via bilateral VATS. VAS scores revealed no difference in postoperative pain except for VAS scores on days 6 (PM) and 7 (PM). BPI scores yielded higher scores in the VATS group on postoperative day (POD) 1 in the reactive dimension, but no other overall differences. MS patients receiving tramadol consumed a higher mean amount than VATS patients on POD 5 and POD 6. IS change from baseline to postoperative were similar between groups, and increased pain correlated with decreased IS scores on POD 1. Chest-tube duration, complications, and pain medication were similar between groups. CONCLUSIONS: Bilateral VATS and MS offer similar outcomes with regard to postoperative pain and complications. These results suggest that the choice of LVRS operative approach should be dependent on disease presentation, surgeon expertise, and patient preference, not based upon differences in perceived postoperative pain between MS and bilateral VATS.


Asunto(s)
Dolor Postoperatorio/etiología , Neumonectomía/efectos adversos , Esternotomía/efectos adversos , Cirugía Torácica Asistida por Video/efectos adversos , Anciano , Femenino , Volumen Espiratorio Forzado , Humanos , Masculino , Persona de Mediana Edad , Dimensión del Dolor/métodos , Neumonectomía/métodos , Complicaciones Posoperatorias , Estudios Prospectivos , Espirometría/métodos , Esternotomía/métodos , Cirugía Torácica Asistida por Video/métodos , Resultado del Tratamiento
16.
Eur J Cardiothorac Surg ; 40(6): 1285-90, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21497509

RESUMEN

OBJECTIVE: The literature is inconsistent regarding the role of chronic obstructive pulmonary disease (COPD) as a risk factor for blood product transfusion during coronary artery bypass graft (CABG). One reason may be lack of objective criteria to define COPD in previously published reports. We examined the role of COPD as a risk factor for transfusion using a strict definition based on objective pulmonary function test (PFT) data. METHODS: We identified 180 patients, who underwent primary isolated non-emergent CABG and had PFTs performed preoperatively. COPD was defined as forced expiratory volume in 1s/forced vital capacity (FEV1/FVC) <70% and further stratified into mild/moderate/severe/very severe based on the Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines. Patients with and without COPD were compared with respect to preoperative and postoperative characteristics and transfusion requirements. RESULTS: The overall transfusion rate was 59.4% (107/180). COPD patients (31.1%, 56/180) were older (66.6 ± 11.4 vs 62.3 ± 10.3 years, p = 0.01), had lower body mass index (BMI) (28.5 ± 5.8 vs 31.7 ± 6.0 kg/m(2), p=0.001), and were more often smokers (51.8% vs 36.3%, p = 0.05). COPD patients had shorter cardiopulmonary bypass (CPB) times (99.4 ± 27.9 vs 110.9 ± 32.4 min, p = 0.02), but left internal mammary artery (LIMA) use, number of bypass grafts, mortality, and postoperative complications were similar (p > 0.05). Transfusion rates were similar for patients with and without COPD. Further stratification into mild/moderate/severe/very severe COPD failed to identify COPD as a predictor of blood transfusion. CONCLUSIONS: Using objective PFT data, our study clarifies the disagreement in the literature with respect to the role of COPD as a risk factor for transfusion in CABG. Decreased pulmonary function does not appear to increase risk of transfusion during CABG, even for patients with severe COPD.


Asunto(s)
Transfusión Sanguínea , Puente de Arteria Coronaria/efectos adversos , Enfermedad Pulmonar Obstructiva Crónica/complicaciones , Factores de Edad , Anciano , Índice de Masa Corporal , Femenino , Volumen Espiratorio Forzado/fisiología , Humanos , Masculino , Persona de Mediana Edad , Atención Perioperativa/métodos , Enfermedad Pulmonar Obstructiva Crónica/fisiopatología , Factores de Riesgo , Fumar/efectos adversos , Capacidad Vital/fisiología
17.
Ann Thorac Surg ; 90(1): 270-1, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20609791
18.
Thorac Surg Clin ; 18(2): 217-22, 2008 May.
Artículo en Inglés | MEDLINE | ID: mdl-18557594

RESUMEN

Primary focal hyperhidrosis has a significant, negative impact on quality of life, causing impairments in social, physical, leisure, and occupational activities. The outcome of different surgical and medical treatment modalities is best assessed by using a combination of tools. Quantitative tools include gravimetry, evaporimetry, and Minor's starch and iodine test. Qualitative assessment tools include general health surveys and hyperhidrosis-specific surveys. Of these, the HDSS has been found to have a good correlation to other assessment tools and to be practical in the clinical setting. The surgical literature has primarily used qualitative tools to assess outcomes and many of these tools are investigator-developed, rather than standardized surveys, which may be partly because of the largely retrospective nature of these studies. A surgical investigator's goal tends to be focused on obtaining specific postoperative information regarding symptom improvement and potential surgical complications. The VATS can have a major positive impact on the quality of life of patients who have hyperhidrosis. The impairment that this disorder causes is often underappreciated by the medical community.


Asunto(s)
Hiperhidrosis/terapia , Simpatectomía , Humanos , Hiperhidrosis/psicología , Calidad de Vida , Toracoscopía , Factores de Tiempo , Resultado del Tratamiento
20.
Thorac Surg Clin ; 17(1): 73-9, 2007 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-17650699

RESUMEN

VATS is a valuable and safe way to manage many problems in thoracic trauma. It may allow earlier diagnosis and treatment of posttraumatic complications of chest injuries with less morbidity. This approach has already demonstrated advantages in such entities as retained hemothorax. The reduced pain and morbidity are attractive features compared with open thoracotomy. VATS continues to evolve in thoracic trauma, but unquestionably has proved value.


Asunto(s)
Enfermedades Pleurales/cirugía , Traumatismos Torácicos/cirugía , Cirugía Torácica Asistida por Video , Diafragma/lesiones , Humanos , Enfermedades Pleurales/etiología , Traumatismos Torácicos/complicaciones
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