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1.
Circ Heart Fail ; 12(8): e006060, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31525097

RESUMEN

BACKGROUND: A wireless pulmonary artery pressure sensor (CardioMEMS) is approved for implantation via the femoral vein. The internal jugular vein (IJ) is an attractive alternative access route commonly used in pulmonary artery catheterization. METHODS AND RESULTS: Retrospective chart review was performed for all sensor implants from 10 providers at 4 centers from September 2016 to June 2018. To compare procedural outcomes and discharge efficiency between groups, multivariate analyses incorporating potential confounders were performed. Seventy-three (28%) patients had femoral access, and 189 (72%) had IJ access; demographics were similar between the groups. Complications, including one case of hematoma and 4 cases of mild hemoptysis, and 30-day mortality (2%-3%) did not differ between groups. Provider preference for IJ access substantially increased over time, with IJ accounting for 90% of cases in 2018. After risk-adjustment, IJ cases had 20% (5%-33%) shorter fluoroscopy time (P=0.01) and 24% (7%-38%) lower contrast volume (P=0.008). Compared with outpatient femoral cases, outpatient IJ cases had 62% (52%-69%) faster needle-to-door time and were 34 times (6-235) more likely to have same-day discharge (P<0.001 for both). CONCLUSIONS: IJ access for CardioMEMS implant is a safe alternative associated with superior procedural and discharge outcomes. Implanters at 4 high-volume centers adopted IJ access as the preferred implant approach.


Asunto(s)
Cateterismo Venoso Central/métodos , Insuficiencia Cardíaca/diagnóstico , Monitoreo Fisiológico/instrumentación , Arteria Pulmonar/fisiopatología , Presión Esfenoidal Pulmonar/fisiología , Ultrasonografía Intervencional/métodos , Anciano , Diseño de Equipo , Femenino , Insuficiencia Cardíaca/fisiopatología , Humanos , Venas Yugulares , Masculino , Persona de Mediana Edad , Estudios Retrospectivos
4.
Cardiol Rev ; 16(3): 129-41, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18414184

RESUMEN

Fibrates are a class of lipid-lowering medication primarily used as second-line agents behind statins. Acting via the peroxisome proliferators-activated receptor-alpha, their main lipoprotein effects are to lower serum triglyceride levels and to raise high-density lipoprotein-cholesterol, with modest effects on low-density lipoprotein-cholesterol. However, many clinical trials indicate that fibrates may have benefits beyond simply altering one's lipid profile. Several angiographic studies show retardation in the progression of atherosclerotic lesions in coronary vessels. Although clinical trials have failed to show a reduction in mortality with fibrates, several post hoc analyses indicate that there may be a mortality benefit in patients with features of the metabolic syndrome. Given that fibrates are often used as second-line agents, it is essential they are safe to be given in combination with other agents, particularly statins and ezetimibe. Although the side-effect profile of fibrates includes gastrointestinal symptoms, increased liver function tests, a reversible rise in creatinine and myositis, in general, fibrates seem to be safe to use in combination with other lipid lowering medications. Thus far, fibrates have not shown a mortality benefit in randomized clinical trials; as a result, they cannot be considered first-line medication for the primary or secondary prevention of coronary artery disease.


Asunto(s)
Anticolesterolemiantes/uso terapéutico , Ácido Clofíbrico/uso terapéutico , Dislipidemias/tratamiento farmacológico , Anticolesterolemiantes/efectos adversos , Anticolesterolemiantes/farmacología , Aterosclerosis/tratamiento farmacológico , Enfermedades Cardiovasculares/mortalidad , Enfermedades Cardiovasculares/prevención & control , Ácido Clofíbrico/efectos adversos , Ácido Clofíbrico/farmacología , Quimioterapia Combinada , Humanos , Síndrome Metabólico/tratamiento farmacológico , PPAR alfa/agonistas
6.
Am Heart J ; 155(2): 267-73, 2008 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-18215596

RESUMEN

BACKGROUND: Studies suggest that the New York State Cardiac Surgery and Percutaneous Coronary Intervention Reporting System, which makes public the operator-specific mortality for patients undergoing coronary artery bypass graft surgery (CABG) or percutaneous coronary intervention (PCI), may deter operators from providing revascularization to high-risk cardiac patients in New York compared to other states. METHODS: We performed a retrospective analysis of 545 US patients with acute myocardial infarction and cardiogenic shock due to predominant left ventricular failure enrolled in the SHOCK Registry. Adjusting for case mix using a propensity score method, we compared the use of coronary angiography, PCI, CABG, and outcomes between 220 patients in New York and 325 in other states. RESULTS: New York patients were older with similar or less severe baseline characteristics. After propensity score adjustment, New York patients were less likely than non-New York patients to undergo coronary angiography (odds ratio 0.46, 95% CI 0.31-0.68, P < .001) and PCI (odds ratio 0.51, 95% CI 0.33-0.77, P = .002). Coronary artery bypass graft rates were similarly low (14.1% vs 15.1%, P = not significant), but New York patients waited significantly longer after shock onset for surgery (101.2 vs 10.3 hours, P < .001) with only 32.3% of New York patients vs 75.5% of non-New York patients (P < .001) taken for CABG within 3 days of shock onset. CONCLUSIONS: In our propensity-adjusted retrospective analysis, New York patients with acute myocardial infarction and cardiogenic shock were less likely to undergo coronary angiography and PCI and waited significantly longer to receive CABG than their non-New York counterparts. These findings suggest that state-required reporting to the New York State Cardiac Surgery and Percutaneous Coronary Intervention Reporting System may result in the reluctance to revascularize the highest-risk cardiac patients.


Asunto(s)
Angioplastia Coronaria con Balón , Puente de Arteria Coronaria , Infarto del Miocardio/terapia , Sistema de Registros , Gestión de Riesgos , Choque Cardiogénico/etiología , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Notificación Obligatoria , Persona de Mediana Edad , Infarto del Miocardio/complicaciones , New York , Calidad de la Atención de Salud , Estudios Retrospectivos , Choque Cardiogénico/terapia
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