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1.
Clin Rheumatol ; 38(4): 1117-1124, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30535994

RESUMEN

INTRODUCTION: Our objective was to evaluate the pulmonary hypertension (PH) data for Spanish patients with systemic sclerosis (SSc), define the PH types and determine the associated factors. METHOD: Descriptive study of PH-related data from the multicentre RESCLE registry. Estimated systolic pulmonary artery pressure (esPAP), measured via echocardiogram was considered elevated if ≥ 35 mmHg. Left heart disease (LHD) and interstitial lung disease (ILD) were identified. When performed, data from right heart catheterisation (RHC) were collected. RESULTS: esPAP was elevated in 350 of 808 patients (43.3%). One hundred and forty-four patients (17.8%) were considered to have PH (88 via RHC and the rest due to elevated esPAP along with evidence of significant LHD or ILD): PAH 3.7%, secondary to ILD 8.3%, secondary to LHD 2.8% and unclassified 3%. Prevalence of elevated esPAP was greater in diffuse SSc (dSSc) than in limited scleroderma (lSSc) (50.5 vs. 42.2%, p 0.046). In the group with elevated esPAP, a lower prevalence of anti-centromere antibodies (41.9% vs. 52.3%, p 0.006) and a greater prevalence of anti-topoisomerase-1 antibodies (ATA) (25.1% vs. 18.6%, p 0.04) were observed compared to the group with normal esPAP. Patients with elevated esPAP had a lower rate of digital ulcers (50.6% vs. 60.2%, p 0.007) and esophageal involvement (83.6% vs. 88.7%, p 0.07) and higher rate of renal crisis (4.6% vs. 1.8%, p 0.066). CONCLUSIONS: Prevalence of PAH was lower than expected (3.7%). Probability of having elevated esPAP was higher among patients with dSSc and among those with ATA.


Asunto(s)
Hipertensión Pulmonar/epidemiología , Esclerodermia Sistémica/epidemiología , Adulto , Anciano , Anticuerpos Antinucleares , Centrómero/inmunología , Comorbilidad , Femenino , Humanos , Hipertensión Pulmonar/inmunología , Masculino , Persona de Mediana Edad , Prevalencia , Sistema de Registros , Esclerodermia Sistémica/inmunología , España/epidemiología
2.
Ann Vasc Surg ; 24(5): 690.e1-4, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20579585

RESUMEN

Thromboangiitis obliterans (also known as Buerger's disease) is an inflammatory vascular disorder that affects small and medium-sized arteries and veins in the extremities. There is no specific treatment and the only effective intervention is absolute cessation of tobacco use. Endothelial dysfunction appears to be of relevance to this condition and a report has even found that high serum levels of endothelin correlate with the presence of necrosis. We report two cases of digital necrosis showing a very satisfactory response to treatment with bosentan, a dual endothelin receptor antagonist.


Asunto(s)
Dedos/irrigación sanguínea , Isquemia/tratamiento farmacológico , Úlcera Cutánea/tratamiento farmacológico , Sulfonamidas/uso terapéutico , Tromboangitis Obliterante/tratamiento farmacológico , Vasodilatadores/uso terapéutico , Anciano , Bosentán , Antagonistas de los Receptores de Endotelina , Humanos , Isquemia/diagnóstico , Isquemia/etiología , Angiografía por Resonancia Magnética , Masculino , Angioscopía Microscópica , Persona de Mediana Edad , Pletismografía , Úlcera Cutánea/diagnóstico , Úlcera Cutánea/etiología , Cese del Hábito de Fumar , Tromboangitis Obliterante/complicaciones , Tromboangitis Obliterante/diagnóstico , Resultado del Tratamiento
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