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1.
Braz. j. med. biol. res ; 28(8): 875-9, Aug. 1995. ilus, tab
Artículo en Inglés | LILACS | ID: lil-156282

RESUMEN

Most controlled studies in humans indicate that ranitidine does not alter theophylline metabolism, even at high doses. However, there have been several case reports published recently which demostrate the development of theophylline toxicity mostly in older patients receiving stable oral doses of this drug when ranitidine was administered simultaneously. We studied eleven elderly (mean age, 69,0 + or - 6.2 years) patients with chronic obstructive pulmonary disease (COPD). During one week the patients took slow-release theophylline, 200 mg every 12 h, followed by one week intake of the same dose of theophylline plus ranitidine tables, 150 mg every 12h. At the end of each period, blood samples were obtained 0,1,2,3,4,6,7,8 and 12h after the morning dose for the determination of serum theophylline levels. the peak theophylline concentration was achieved after 4.1 + or - 0.9 h while the patients were taking theophylline, and after 2.9 + or - 1.4 h with the combined regimen. This difference was statistically significant. These results suggest that the reported increases in serum theophylline levels in older patients receiving theophylline and ranitidine cannot be ascribed to slower theophylline metabolism in the geriatric patient with COPD who is also given ranitidine.


Asunto(s)
Humanos , Persona de Mediana Edad , Antagonistas de los Receptores H2 de la Histamina/administración & dosificación , Enfermedades Pulmonares Obstructivas/metabolismo , Ranitidina/administración & dosificación , Teofilina/administración & dosificación , Factores de Edad , Cromatografía Líquida de Alta Presión , Interacciones Farmacológicas , Quimioterapia Combinada , Ranitidina/sangre , Ranitidina/metabolismo , Teofilina/sangre , Teofilina/metabolismo
2.
Braz. j. med. biol. res ; 27(12): 2869-77, Dec. 1994. tab
Artículo en Inglés | LILACS | ID: lil-153286

RESUMEN

1. Studies in asthmatic subjects have reported conflicting results about the arrhythmogenic effects of beta agonist and theophylline. The purpose of the present study was to evaluate the effects of the combination of these drugs in patients with chronic obstructive pulmonary disease (COPD). 2. Twelve COPD patients (FEV1 = 1.2 + or - 0.3 L; PaO2 = 65.7 + or - 9.0 mmHg) we evaluated by 24-h Holter monitoring on three different days. The first evaluation was done after the patient had been without any treatment for at least 24 h, the second after sustained-release theophylline for one week and the third after oral beta agonist (albuterol) and theophylline for one week. 3. Mean serum level of theophylline was 1.9, 15.6 an 17.7 µg/ml, and mean heart rate was 78.3, 82.0 and 84.5 beats/min for the first, second and third period, respectively. Four patients showed more than 10 premature atrial contractions/h in the baseline Holter, and this rate did not increase after either treatment. Three patients had more than 10 premature ventricular contractions/h (PVC) at baseline, with no increase while receiving theophylline or the combination of theophylline and albuterol. However, one patient did have worsening of the arrhythmia while taking both drugs. There were 5 single PVCs/h at baseline and 150 single and 9 coupled PVCs/h plus 1 episode of non-sustained ventricular tachycardia during combined therapy. 4. We conclude that the combination of theophylline and a beta agonist (albuterol) may increase the premature ventricular contraction rate and the complexity of ectopic activity in COPD patients


Asunto(s)
Humanos , Masculino , Femenino , Persona de Mediana Edad , Albuterol/administración & dosificación , Arritmias Cardíacas/inducido químicamente , Quimioterapia Combinada , Enfermedades Pulmonares Obstructivas/tratamiento farmacológico , Teofilina/sangre , Administración Oral , Albuterol/sangre , Arritmias Cardíacas/fisiopatología
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