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1.
Am J Cardiol ; 85(8): 1007-11, 2000 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-10760344

RESUMEN

Shortened head-up tilt testing (HUT) potentiated with sublingual nitroglycerin (60 degrees passive standing for 20 minutes followed, if negative, by 400 microg of sublingual nitroglycerin spray with the test continuing for another 20 minutes) differs from conventional nitroglycerin HUT for a shorter drug-free phase (20 vs 45 minutes). To compare the positivity rate of the 2 protocols, both tests were performed in a randomized sequence in 10 patients with unexplained syncope (study 1), and another 42 patients were randomly assigned either to conventional or to shortened nitroglycerin HUT (study 2). To evaluate the reproducibility of the shortened nitroglycerin HUT, another 38 patients with unexplained syncope underwent 2 consecutive tests within a 7+/-8 day interval (study 3). Finally, to evaluate the specificity of the test, 47 control subjects underwent shortened nitroglycerin HUT (study 4). Seven positive responses were observed during shortened nitroglycerin HUT, and there were 8 positive responses during conventional nitroglycerin HUT (p = NS) in the study 1 group. Fifteen positive (71%) responses, 5 negative responses, and 1 exaggerated response were observed during shortened nitroglycerin HUT; 16 positive (76%, p = NS vs. shortened nitroglycerin HUT), 3 negative, and 2 exaggerated responses were observed during conventional nitroglycerin HUT in the study 2 group. During the first test, 21 patients (55%) had a positive, 15 patients had a negative, and 2 patients had an exaggerated response in study group 3. During the second test, 15 positive (39%), 19 negative, and 4 exaggerated responses were observed. Thus, the reproducibility was 67% for a positive and 94% for a negative test. In control subjects, 2 positive (4%) responses, 38 negative, and 7 exaggerated responses were observed with a specificity of 96% in study group 4. In patients with unexplained syncope, shortened nitroglycerin HUT allowed a positivity rate similar to that of the conventional test. Moreover, the shortened test provided a high specificity and adequate reproducibility for both the positive and the negative responses.


Asunto(s)
Nitroglicerina , Síncope/diagnóstico , Pruebas de Mesa Inclinada/métodos , Vasodilatadores , Administración Sublingual , Adulto , Femenino , Humanos , Masculino , Nitroglicerina/administración & dosificación , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Síncope/etiología , Vasodilatadores/administración & dosificación
2.
Ital Heart J Suppl ; 1(6): 772-6, 2000 Jun.
Artículo en Italiano | MEDLINE | ID: mdl-11204009

RESUMEN

Syncope is a common syndrome that increases in prevalence with the aging of the population. The causes of this common symptom are multiple and the costs for the evaluation and treatment of syncope are enormous, especially with the use of highly technological approaches. Even when syncope is the expression of benign diseases, it may be the cause of significant morbidity for injuries, fractures and subsequent functional impairment, which particularly for elderly patients, matches that of other common chronic diseases. Finally, we cannot ignore the social costs caused by the reduction of working hours for diagnostic and therapeutic procedures and the subsequent loss of productivity.


Asunto(s)
Costo de Enfermedad , Síncope , Humanos , Calidad de Vida , Síncope/complicaciones , Heridas y Lesiones/etiología
4.
Am Heart J ; 135(4): 564-70, 1998 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-9539468

RESUMEN

BACKGROUND: Head-up tilt testing is extensively used to determine the vasovagal origin of syncope in patients with otherwise unexplained loss of consciousness, although issues remain regarding the method of the test. The diagnostic value of a shortened head-up tilt test potentiated with sublingual nitroglycerin was assessed in patients with unexplained syncope. METHODS: Two hundred two patients (mean age 49+/-19 years) with syncope of unknown origin and 34 subjects in a control group (mean age 45+/-17 years) were studied. The patients and the subjects in the control group were tilted upright to 60 degrees for 20 minutes. If syncope did not occur, sublingual nitroglycerin (400 microg) was administered, and observation was continued for 25 more minutes. RESULTS: During the unmedicated phase syncope occurred in 22 (11%) patients and in one member of the control group. After nitroglycerin was administered, syncope occurred in 119 (59%) patients and in 1 (3%) member of the control group. False-positive response (exaggerated response) was observed in eight (4%) patients and in four (12%) subjects in the control group. The total positivity rate of the test was 70% with a specificity rate of 94%. CONCLUSIONS: Short-duration head-up tilt test potentiated with sublingual nitroglycerin provides an adequate specificity and positivity rate in patients with unexplained syncope.


Asunto(s)
Nitroglicerina , Postura/fisiología , Síncope/diagnóstico , Vasodilatadores , Administración Sublingual , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Presión Sanguínea , Diagnóstico Diferencial , Electrocardiografía , Femenino , Frecuencia Cardíaca , Humanos , Masculino , Persona de Mediana Edad , Nitroglicerina/administración & dosificación , Variaciones Dependientes del Observador , Síncope/etiología , Síncope/fisiopatología , Nervio Vago/efectos de los fármacos , Vasodilatadores/administración & dosificación
6.
Cardiologia ; 41(10): 987-94, 1996 Oct.
Artículo en Italiano | MEDLINE | ID: mdl-8983827

RESUMEN

In coronary care units (CCU) without cardiac catheterization facilities, coronary angiography is rarely carried out when a successful medical treatment in the acute phase of unstable angina has been obtained. However, the unstable angina still has an uncertain prognosis when the remission of pain is obtained with drugs. This study presents a follow-up of 147 consecutive patients (aged 66.8 +/- 10.4 years) admitted to our CCU in 1991 and 1992 for unstable angina; 33 of them (22.4%) were in Braunwald class I. 2 (1.4%) in class II and 112 (76.2%) in class III. The patients were treated according to the usual therapy protocols and class III patients received i.v. heparin. In selected cases we used thrombolysis (10 patients) and intra-aortic balloon pump (5 patients). During hospitalization 1 patient died (0.7%), 5 patients (3.4%) suffered an acute myocardial infarction and 9 patients (6.1%) had angina. Stabilization of unstable angina was achieved in 132 patients (89.9%): in 113 (76.8%) during the first 48 hours, and in 19 (12.9%) later. Coronary angiography was carried out in non-stabilized patients and in 46 (34.8%) of the 132 with successful treatment (Group I). Eighty-six patients, without indication to coronary angiography were discharged in medical therapy (Group II). During the follow-up (mean of 15.0 +/- 9.0 months) Group I 10 patients (18.2%) had cardiac events (death, myocardial infarction, or recurrent angina) vs 26 of Group II (p < 0.05). In Group I coronary angiography together with clinical criteria of high risk allowed the identification of candidates to coronary revascularization (61.8% of Group I patients while). These data show that the initial success of treatment during the acute phase of unstable angina should not be considered as a favourable prognostic index. Coronary angiography appears to be indicated for clinical evaluation and therapeutical decision.


Asunto(s)
Angina Inestable/tratamiento farmacológico , Protocolos Clínicos , Angiografía Coronaria , Unidades de Cuidados Coronarios , Anciano , Angina Inestable/diagnóstico por imagen , Causas de Muerte , Femenino , Estudios de Seguimiento , Humanos , Masculino
7.
Minerva Chir ; 51(10): 765-72, 1996 Oct.
Artículo en Italiano | MEDLINE | ID: mdl-9082203

RESUMEN

Only recently, in our laboratory of experimental surgery, we started with a protocol for orthotopic liver transplantation (OLT) in a pig model. This was felt as mandatory for experimental purposes as well as for future clinical applications at our center. We report herein our own experience with 41 OLTx. Intraoperative "lethal" complications occurred in up to 32% (14/41) whereas postoperative complications occurred in the remainders at different intervals of time with a maximum survival of 30 days. No attention was paid to prevent rejection-infection episodes. The main cause of death was the primary non-function (PNF) or dis-function (PDF) manifested either intra or postoperatively in 16 out the 41 OLTx (39%). Intraoperative technical errors accounted for up to 9% (4/41 OLTx). Acute hemorrhage gastritis and gastric perforations occurred postoperatively in 6 animals (14%) and represent one of the peculiar aspects of OLT in pig model.


Asunto(s)
Trasplante de Hígado/métodos , Animales , Complicaciones Intraoperatorias/epidemiología , Complicaciones Intraoperatorias/etiología , Trasplante de Hígado/efectos adversos , Complicaciones Posoperatorias/epidemiología , Complicaciones Posoperatorias/etiología , Tasa de Supervivencia , Porcinos
8.
Bone Marrow Transplant ; 17(4): 527-31, 1996 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8722349

RESUMEN

Previous studies have shown that, unlike in patients submitted to allogeneic BMT, administration of recombinant erythropoietin (Epo) after autologous BMT (ABMT) had no significant effect on erythroid recovery and transfusional requirements. On the other hand, it has also been shown that combining Epo with recombinant granulocyte colony-stimulating factor (G-CSF) in patients with the acquired immunodeficiency syndrome (AIDS) and with myelodysplastic syndromes resulted in additive effects on erythropoiesis. To test the effects of combined G-CSF + Epo therapy on erythroid recovery after autologous bone marrow transplantation a pilot randomized, three-arm trial was designed. Thirty patients suffering from lymphoid malignancies submitted to ABMT were randomly assigned to receive G-CSF alone (5 micrograms/kg, from day + 1 up to reaching an ANC > or = 10(9)/1), G-CSF + Epo (150 U/kg, from day +1 to +21), or neither of these (controls). Patients receiving G-CSF + Epo had significantly more reticulocytes on day +21 and reached 30 x 10(9)/1 reticulocytes earlier when compared to both G-CSF and control patients; however, the number of red blood cell (RBC) transfusions was not modified by the addition of Epo to G-CSF, although both groups had significantly fewer units transfused than controls. No effect on platelet recovery or platelet transfusional requirements was observed. Myeloid recovery was comparable in the G-CSF and G-CSF+Epo groups, and significantly accelerated as compared to controls. We conclude that the addition of Epo to G-CSF causes a slight acceleration of erythroid recovery after ABMT, but is not associated with transfusional benefits. Therefore, the present data do not support the use of Epo in association with G-CSF to hasten erythroid recovery after ABMT.


Asunto(s)
Anemia/prevención & control , Trasplante de Médula Ósea , Eritropoyesis/efectos de los fármacos , Eritropoyetina/uso terapéutico , Factor Estimulante de Colonias de Granulocitos/uso terapéutico , Hematopoyesis/efectos de los fármacos , Linfoma/terapia , Leucemia-Linfoma Linfoblástico de Células Precursoras/terapia , Anemia/etiología , Transfusión Sanguínea/estadística & datos numéricos , Sinergismo Farmacológico , Quimioterapia Combinada , Eritropoyetina/administración & dosificación , Eritropoyetina/farmacología , Factor Estimulante de Colonias de Granulocitos/administración & dosificación , Factor Estimulante de Colonias de Granulocitos/farmacología , Humanos , Linfoma/sangre , Proyectos Piloto , Recuento de Plaquetas/efectos de los fármacos , Leucemia-Linfoma Linfoblástico de Células Precursoras/sangre , Recuento de Reticulocitos/efectos de los fármacos , Seguridad , Acondicionamiento Pretrasplante/efectos adversos , Trasplante Autólogo , Resultado del Tratamiento , Irradiación Corporal Total/efectos adversos
9.
Ann Ital Med Int ; 9(3): 150-2, 1994.
Artículo en Italiano | MEDLINE | ID: mdl-7946891

RESUMEN

We report the case of a young woman suffering from colonic mucinous adenocarcinoma with the unusual clinical presentation as a right atrial metastasis. The tumor was successfully resected, and after histopathological characterization, the primary lesion was searched for and discovered. The tumor had the clinical appearance and echocardiographic pattern of a pedunculated atrial myxoma. The aspects of echo-patterns useful for differential diagnosis are discussed.


Asunto(s)
Adenocarcinoma Mucinoso/secundario , Neoplasias del Colon/diagnóstico , Neoplasias Cardíacas/secundario , Adenocarcinoma Mucinoso/diagnóstico , Adenocarcinoma Mucinoso/patología , Adulto , Biopsia , Neoplasias del Colon/patología , Diagnóstico Diferencial , Ecocardiografía , Femenino , Atrios Cardíacos , Neoplasias Cardíacas/diagnóstico , Neoplasias Cardíacas/cirugía , Humanos
10.
Coron Artery Dis ; 5(2): 137-45, 1994 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-8180744

RESUMEN

BACKGROUND: The role of thromboxane A2 (TxA2) in unstable angina has not yet been defined. TxA2 receptor antagonists may be of value in studying this role. METHODS: To investigate whether TxA2 has a pathogenetic effect on the occurrence of myocardial ischemia and from what source TxA2 originates, we studied TxA2 formation by unstimulated monocytes from patients with unstable angina (n = 40), stable effort angina (n = 20), and controls (n = 20). We also compared the effects of picotamide (1200 mg/day), a TxA2-synthase inhibitor and TxA2-receptor antagonist, with those of aspirin (325 mg/day) on myocardial ischemia and TxA2 formation by monocytes and platelets. The double-blind randomized study was performed on patients with unstable angina on continuous Holter monitoring. RESULTS: In the presence of autologous lymphocytes, unstimulated monocytes from patients with unstable angina formed significantly (P < 0.001) more TxA2 than those from controls or from patients with effort angina. Although TxA2 formation by circulating monocytes and platelets was inhibited to a greater degree by aspirin than by picotamide (88 +/- 6 and 98 +/- 2%, respectively, versus 65 +/- 2 and 74 +/- 1%, P < 0.001), aspirin failed to affect the occurrence of myocardial ischemia whereas picotamide significantly (P < 0.001) reduced the number of anginal attacks (84.8%), silent ischemic episodes (64.2%), and overall duration of ischemia (69.8%), in comparison to the run-in period. CONCLUSIONS: These results indicate that TxA2 formed by monocytes contributes to the pathogenesis of myocardial ischemia in unstable angina. TxA2 formation occurs mainly in extravascular spaces, probably within the coronary vascular wall. Picotamide appears to control myocardial ischemia effectively in patients with unstable angina.


Asunto(s)
Angina Inestable/tratamiento farmacológico , Angina Inestable/fisiopatología , Leucocitos Mononucleares/fisiología , Isquemia Miocárdica/prevención & control , Isquemia Miocárdica/fisiopatología , Ácidos Ftálicos/uso terapéutico , Inhibidores de Agregación Plaquetaria/uso terapéutico , Tromboxano A2/fisiología , Anciano , Angina de Pecho/patología , Angina de Pecho/fisiopatología , Angina Inestable/patología , Aspirina/farmacología , Aspirina/uso terapéutico , Método Doble Ciego , Femenino , Estudios de Seguimiento , Humanos , Leucocitos Mononucleares/metabolismo , Linfocitos/metabolismo , Masculino , Persona de Mediana Edad , Isquemia Miocárdica/patología , Ácidos Ftálicos/farmacología , Placebos , Inhibidores de Agregación Plaquetaria/farmacología , Estudios Prospectivos , Tromboxano A2/antagonistas & inhibidores , Tromboxano A2/biosíntesis
11.
G Ital Cardiol ; 23(1): 69-72, 1993 Jan.
Artículo en Italiano | MEDLINE | ID: mdl-8491345

RESUMEN

We report the case of an 82-year-old woman who developed bradyarrhythmia with A-V dissociation and shock, followed by an acute pancreatitis, after ingestion of 2400 mg of verapamil per os for suicidal purposes. Despite her advanced age, the patient promptly improved by a conventional therapy even though started several hours after ingestion of the drug.


Asunto(s)
Intento de Suicidio , Verapamilo/envenenamiento , Anciano , Anciano de 80 o más Años , Sobredosis de Droga/terapia , Femenino , Humanos
13.
G Ital Cardiol ; 21(6): 599-608, 1991 Jun.
Artículo en Italiano | MEDLINE | ID: mdl-1743442

RESUMEN

The use of a single-day protocol for 99mTc MIBI myocardial scintigraphy is particularly well-suited for the nuclear medicine departments that are the referral centres for the cardiology departments of several community hospitals. The aim of the study was to compare, in the same patient population, the diagnostic accuracy of planar and SPECT imaging with 99mTc MIBI using a single-day protocol. Thirty-nine patients (31 males and 8 females, age range 32-69 years) were studied because of effort chest pain. Of them, 7 had a pre-test probability of coronary artery disease less than 2.5%; coronary angiography demonstrated significant coronary obstructions in the remaining 32 subjects and 21 of them also had a history of previous myocardial infarction. All patients underwent 99mTc MIBI myocardial scintigraphy with acquisition of planar and SPECT images after injection of a low dose (370 MBq) at rest and after a second higher dose (1110 MBq), injected approximately four hours later during exercise stress testing. The normalcy rate in the 7 patients with low pre-test probability was 100% using both imaging techniques. For the diagnosis of previous infarction, the sensitivities of planar and SPECT images were 71% and 96% respectively. For the diagnosis of effort ischemia the sensitivity values were 34% and 88%, respectively, using planar and SPECT imaging. With regard to the classification of the diseased coronary arteries, the sensitivities of planar and SPECT studies were 42% and 79% respectively, and the related specificities were 91% and 77%. We may conclude that using a single-day protocol planar imaging seems to allow lower levels of diagnostic accuracy both for the diagnosis of effort ischemia and the classification of the diseased vessels as compared to SPECT, which appears therefore in a similar setting the imaging technique of choice.


Asunto(s)
Medios de Contraste/administración & dosificación , Corazón/diagnóstico por imagen , Nitrilos , Compuestos de Organotecnecio , Tomografía Computarizada por Rayos X , Adulto , Anciano , Dolor en el Pecho/diagnóstico por imagen , Dolor en el Pecho/epidemiología , Distribución de Chi-Cuadrado , Enfermedad Coronaria/diagnóstico por imagen , Enfermedad Coronaria/epidemiología , Estudios de Evaluación como Asunto , Prueba de Esfuerzo , Femenino , Humanos , Masculino , Persona de Mediana Edad , Cintigrafía , Tecnecio Tc 99m Sestamibi , Tomografía Computarizada por Rayos X/estadística & datos numéricos
14.
Angiology ; 41(10): 877-83, 1990 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-2221466

RESUMEN

Doppler flow velocity waveform analysis (FVWFA), recorded from the dorsalis pedis artery (DPA) and the radial artery (RA), was performed on 36 women in attempting to detect an initial diabetic microangiopathy (DM). The study comprised two groups of women affected by non-insulin-dependent diabetes mellitus, 6 patients (pts) of reproductive age (1), 12 pts in menopause (II), and two groups of age-matched healthy controls (C) (III and IV). Clinical signs of initial DM were present in group I. All the examined pts were nonsmokers and normotensive and without cardiopathy, signs of diabetic macroangiopathy, collagen vascular disease and/or Raynaud's phenomenon, and renal failure. Four waveform dimensions capable of separating different degrees of peripheral obstructive arteriolar disease were determined on velocity tracing and the results used in a single best discriminant equation. The resultant discriminant score (DS), derived by FVWFA on DPA, showed a highly accurate rate of separating the young pts with DM from both C and the pts in menopause without DM. Furthermore, the resultant DS was statistically not different in groups II, III, and IV. In conclusion, FVWFA on DPA, in this experience, has proved to be an accurate and sensitive method in the detection of initial DM.


Asunto(s)
Diabetes Mellitus Tipo 2/complicaciones , Angiopatías Diabéticas/diagnóstico por imagen , Adulto , Anciano , Velocidad del Flujo Sanguíneo , Angiopatías Diabéticas/fisiopatología , Análisis Discriminante , Femenino , Humanos , Persona de Mediana Edad , Ultrasonografía
15.
Lancet ; 335(8690): 615-8, 1990 Mar 17.
Artículo en Inglés | MEDLINE | ID: mdl-1969013

RESUMEN

399 out of 474 inpatients with unstable angina were monitored for 48 h and 97 of these were found to be refractory to conventional antianginal treatments and entered a randomised double-blind study. With the initial protocol heparin infusion or bolus were compared with aspirin; with a modified protocol, heparin infusion, the best of these three treatments, was compared with alteplase. Patients were monitored for 3 days after starting treatment and then observed clinically for 4 more days. On the first days of treatment heparin infusion significantly decreased the frequency of angina (by 84-94%), episodes of silent ischaemia (by 71-77%), and the overall duration of ischaemia (by 81-86%). Heparin bolus and aspirin were not effective. Alteplase caused small (non-significant) reductions on the first day only. Only minor bleeding complications occurred.


Asunto(s)
Angina de Pecho/tratamiento farmacológico , Angina Inestable/tratamiento farmacológico , Aspirina/uso terapéutico , Heparina/uso terapéutico , Infarto del Miocardio/prevención & control , Terapia Trombolítica , Activador de Tejido Plasminógeno/uso terapéutico , Administración Oral , Anciano , Análisis de Varianza , Angina Inestable/complicaciones , Aspirina/administración & dosificación , Método Doble Ciego , Femenino , Estudios de Seguimiento , Heparina/administración & dosificación , Humanos , Infusiones Intravenosas , Masculino , Persona de Mediana Edad , Infarto del Miocardio/complicaciones , Ensayos Clínicos Controlados Aleatorios como Asunto , Recurrencia , Activador de Tejido Plasminógeno/administración & dosificación , Activador de Tejido Plasminógeno/efectos adversos
16.
G Ital Cardiol ; 20(3): 202-6, 1990 Mar.
Artículo en Italiano | MEDLINE | ID: mdl-2344897

RESUMEN

In order to compare the efficacy of oral lidoflazine (240 mg/die) and oral quinidine (1200 mg/die) in re-establishing sinus rhythm, we studied 115 patients (mean age 63.8 years; range 32-91) with atrial fibrillation of recent onset (less than 3 months). Patients with cardiac failure, acute myocardial infarction, severe intraventricular conduction disturbances, kaliemia less than 3.8 mEq/L or digoxinemia greater than 2 ng/ml were not included. Patients were randomly given one of the 2 drugs, until conversion to sinus rhythm was achieved, severe side effects occurred or for a maximum therapy of 5 days. No significant differences were present between the 2 groups in terms of age, male/female ratio, duration of atrial fibrillation, presence of an enlarged left atrium, presence of organic heart disease (or arterial hypertension) or digitalis therapy. Sinus rhythm resumption was obtained in 41/58 (71%) patients treated with quinidine and in 47/57 (82%) patients treated with lidoflazine (p = ns). In successful cases, the mean treatment time was 79 +/- 33 (SD) hours for quinidine and 66 +/- 36 hours for lidoflazine (p = ns). Both drugs showed the same efficacy in 3 subgroups of patients in whom the arrhythmia had different duration (less than 24 hours; between 24 hours and 3 days; more than 3 days). Treatment was stopped in 5 patients receiving quinidine (gastrointestinal side effects) and in 3 patients receiving lidoflazine (frequent premature ventricular beats in 2 and polymorphic ventricular tachycardia of the "torsade de pointes" type in 1).(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Fibrilación Atrial/tratamiento farmacológico , Lidoflazina/uso terapéutico , Piperazinas/uso terapéutico , Quinidina/uso terapéutico , Adulto , Anciano , Anciano de 80 o más Años , Fibrilación Atrial/fisiopatología , Evaluación de Medicamentos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Factores de Tiempo
17.
Int J Clin Pharmacol Res ; 9(4): 269-75, 1989.
Artículo en Inglés | MEDLINE | ID: mdl-2476406

RESUMEN

In a multicentre double-blind, inpatient, placebo-controlled trial the effects on premature ventricular beats (PVBs) of mexiletine in a standard, submaximal dose were studied by Holter monitoring in 144 outpatients. After wash-out, mexiletine was administered for 14 days. The effects were re-tested, after one week of a placebo, in a second 14-day period of mexiletine administration. Of the patients 73% in the first period and 82.5% in the second period responded to mexiletine (a reduction of 75% or more of PVBs/24 h--p less than 0.001 compared with the placebo for both periods). Mexiletine also significantly reduced the Lown class of PVBs and the frequence of paired PBVs, ventricular tachycardia, multiform beats and R on T wave phenomenon. Mexiletine showed an equivalent effectiveness in the four main aetiological groups of arrhythmias. Fifty nine patients complained of adverse effects (gastrointestinal or neurological) the intensity of which led to the stopping of the treatment in 16 of them. These results show that mexiletine is highly effective, even in submaximal doses, in preventing ventricular arrhythmias of whatever origin.


Asunto(s)
Arritmias Cardíacas/tratamiento farmacológico , Mexiletine/uso terapéutico , Adulto , Anciano , Anciano de 80 o más Años , Complejos Cardíacos Prematuros/tratamiento farmacológico , Enfermedad Crónica , Ensayos Clínicos como Asunto , Método Doble Ciego , Femenino , Humanos , Masculino , Mexiletine/efectos adversos , Persona de Mediana Edad , Estudios Multicéntricos como Asunto
18.
Angiology ; 39(11): 942-52, 1988 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-3052183

RESUMEN

The effects of two potent vasodilating drugs, captopril (C) (25 mg tid), nicardipine (N) (20 mg tid), and placebo (P) were evaluated and compared, in 10 men (mean age of sixty-five years) with intermittent claudication from moderate to severe multilevel chronic occlusive arterial disease (COAD) of the lower extremity, by use of the Doppler ultrasonic method, at rest and after Carter's exercise test. All the examined subjects were normotensive, without diabetes or cardiopathy; all have been smokers. The eight-week total protocol consisted of an initial two-week placebo run-in period followed by two active drug phases and a two-week placebo phase, according to a double-blind, randomized, crossover design. At the end of each two-week period, ankle-arm index (AAI) and, following exercise, onset of lower extremity discomfort time (ODT), duration of exercise (ET), decrease of ankle systolic pressure after test (APD), and recovery time (RT) were determined. Moreover, at rest, just after exercise, and after recovery, simultaneous common femoral artery velocity waves were recorded and analyzed by a quantitative approach to detect the peripheral vasomotor adjustments. None of the patients required the withdrawal of the active treatments. Compared with P, C significantly reduced APD and RT, and N reduced RT and AAI; furthermore N caused a significant decrease in ODT, whereas C showed a trend, although not statistically significant, to increase ODT. Neither active therapy modified ET. These results suggest that C and N have different short-term effects on peripheral circulation in COAD. During exercise, C induces hemodynamic improvement in the ischemic lower extremity probably by inhibition of the sympathetic system and consequent reduction in collateral vessel vasoconstriction.


Asunto(s)
Arteriopatías Oclusivas/tratamiento farmacológico , Captopril/uso terapéutico , Claudicación Intermitente/tratamiento farmacológico , Pierna/irrigación sanguínea , Nicardipino/uso terapéutico , Ultrasonografía , Velocidad del Flujo Sanguíneo , Ensayos Clínicos como Asunto , Método Doble Ciego , Prueba de Esfuerzo , Humanos , Masculino , Persona de Mediana Edad , Distribución Aleatoria
19.
G Ital Cardiol ; 17(10): 889-92, 1987 Oct.
Artículo en Italiano | MEDLINE | ID: mdl-3436502

RESUMEN

The case presented concerns a patient of whom the double mitral valve diagnosis was made by means of both the M-mode and two dimensional echocardiography. Diagnosis was not pronounced after the first cineangiocardiography test, but it was confirmed by the following test. The double mitral valve was associated with an aneurysm of the interventricular septum, bicuspid aortic valve, and isthmic coarctation of the aorta.


Asunto(s)
Coartación Aórtica/complicaciones , Válvula Aórtica/anomalías , Aneurisma Cardíaco/complicaciones , Tabiques Cardíacos , Válvula Mitral/anomalías , Adulto , Coartación Aórtica/diagnóstico , Cineangiografía , Ecocardiografía/métodos , Aneurisma Cardíaco/diagnóstico , Atrios Cardíacos , Humanos , Masculino
20.
J Int Med Res ; 12(2): 73-80, 1984.
Artículo en Inglés | MEDLINE | ID: mdl-6202571

RESUMEN

A double-blind, crossover study was designed to compare the safety and efficacy of mexiletine with that of placebo in reducing premature ventricular complexes (PVC) in ambulatory patients and to find out the dose which gives a good therapeutic response with a minimal incidence of side-effects. Twenty-six patients, who had on average 427.9 PVCs/hour, were admitted to the study. The doses given were designed to reduce the frequency of PVCs by 50% or more from the baseline value. Two out of the twenty-six patients stopped treatment because of major side-effects. In the remaining twenty-four patients the 3 weeks of treatment with mexiletine significantly reduced the rate of PVCs by comparison with placebo (-63.8% versus +7.5%). In the nineteen responders (per cent reduction of PVCs over 50%) the dose of mexiletine was 600 mg daily (200 mg every 8 hours). In the non-responders plasma levels of mexiletine proved to be in the therapeutic range, not in any way different from responders. The most frequent side-effects were digestive difficulties (fifteen patients taking mexiletine and six taking placebo). These results show that mexiletine is an effective anti-arrhythmic drug in the management of ventricular arrhythmias occurring in ambulatory patients. In the majority of patients mexiletine was found to be effective even at the lowest dose studied of 600 mg/day.


Asunto(s)
Atención Ambulatoria , Complejos Cardíacos Prematuros/tratamiento farmacológico , Mexiletine/uso terapéutico , Propilaminas/uso terapéutico , Adulto , Anciano , Presión Sanguínea/efectos de los fármacos , Ensayos Clínicos como Asunto , Método Doble Ciego , Dispepsia/inducido químicamente , Electrocardiografía , Femenino , Frecuencia Cardíaca/efectos de los fármacos , Pirosis/inducido químicamente , Humanos , Masculino , Mexiletine/administración & dosificación , Mexiletine/efectos adversos , Persona de Mediana Edad , Monitoreo Fisiológico , Náusea/inducido químicamente , Distribución Aleatoria
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