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Métodos Terapéuticos y Terapias MTCI
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1.
Ann Cardiol Angeiol (Paris) ; 58(1): 57-60, 2009 Feb.
Artículo en Francés | MEDLINE | ID: mdl-18614152

RESUMEN

We describe a case of a young patient admitted for recurrent ischemic stroke caused by a papillary fibroelastoma of the mitral valve and a hyperhomocysteinemia. A papillary fibroelastoma is a benign cardiac tumor which can be associated with serious embolic complications. A moderate plasma level of hyperhomocysteinemia is considered as a risk factor of ischemic stroke. The authors suggest that this association increases the risk of ischemic stroke in their patient. The tumor was surgically removed to avoid new embolic events associated with a vitamin B supplementation. After surgery and acid folic supplementation, no recurrence was observed.


Asunto(s)
Fibroelastosis Endocárdica/complicaciones , Neoplasias Cardíacas/complicaciones , Hiperhomocisteinemia/complicaciones , Ataque Isquémico Transitorio/etiología , Válvula Mitral , Músculos Papilares , Procedimientos Quirúrgicos Cardíacos , Ecocardiografía Transesofágica , Fibroelastosis Endocárdica/diagnóstico por imagen , Fibroelastosis Endocárdica/cirugía , Femenino , Neoplasias Cardíacas/diagnóstico por imagen , Neoplasias Cardíacas/cirugía , Humanos , Hiperhomocisteinemia/diagnóstico por imagen , Hiperhomocisteinemia/cirugía , Ataque Isquémico Transitorio/diagnóstico por imagen , Ataque Isquémico Transitorio/cirugía , Persona de Mediana Edad , Válvula Mitral/diagnóstico por imagen , Válvula Mitral/cirugía , Músculos Papilares/diagnóstico por imagen , Músculos Papilares/cirugía , Recurrencia , Resultado del Tratamiento
2.
Ann Cardiol Angeiol (Paris) ; 39(5): 305-9, 1990 May.
Artículo en Francés | MEDLINE | ID: mdl-2195978

RESUMEN

This randomized multicentre study in elderly hypertensives with two unbalanced groups (2 patients under labetalol for 1 patient under nifedipine) compared the efficacy and safety of labetalol, whose dosage could be adjusted (1, 2, then 3 tablets/day) according to blood pressure level (BP greater than or equal to 160/95 mmHg), to that of nifedipine given at its recommended dosage (2 tablets/day). The treatment period lasted 6 weeks (D42). The main judgment criteria was the rate of patients with normalized BP under treatment (SBP less than 160 and DBP less than 95 mmHg). The analysis was carried out on 170 patients, 112 labetalol and 58 nifedipine. Both groups were homogeneous when entering into the study. The only difference was a higher rate of smokers in the nifedipine group compared with labetalol's (29% vs 13%). The rate of patients with normalized BP (SBP less than 160 and DBP less than 95 mmHg) were 66% in the labetalol group and 48% in the nifedipine's (p less than 0.05). Treatment withdrawals for all causes during the study were more frequent in the nifedipine group (19%) than in the labetalol's (6%). Treatment withdrawals for adverse events occurred in 3.5% of patients in the labetalol group and in 12% of the nifedipine's. The overall adverse events rate was 9% with labetalol and 29% with nifedipine (p less than 0.001). In this comparative study in elderly hypertensives, labetalol given in a dose titration schedule proved significantly superior to nifedipine, given at recommended maximal dosage, in terms of both BP control and side effects profile.(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Hipertensión/tratamiento farmacológico , Labetalol/uso terapéutico , Nifedipino/uso terapéutico , Anciano , Anciano de 80 o más Años , Humanos , Estudios Multicéntricos como Asunto , Ensayos Clínicos Controlados Aleatorios como Asunto , Método Simple Ciego
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