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1.
Oncology ; 49(6): 489-91, 1992.
Artículo en Inglés | MEDLINE | ID: mdl-1465290

RESUMEN

We started a treatment trial for malignant pericardial tamponade with intracavitary oxytetracycline, 500-1,000 mg/day, administered via an indwelling pericardial cannula after extraction of as much pericardial fluid as possible. This procedure was repeated every 24 h for 6 consecutive days or until no more fluid could be drained. Eleven consecutive patients were entered in the study. The responses were obtained by clinical examination, chest roentgenogram and echocardiogram, prior to and after treatment. The primary cancer was located in the breast in 7 patients, in the stomach in 2 patients, and in the lung in 2 patients. In all cases, systemic chemotherapy or hormonal therapy was started after the pericardial tamponade was cured. The mean tetracycline dose per patient was 3,000 mg (range 1,500-6,000). All patients responded to the treatment with rapidly improving symptoms. Response persisted during a median of 9 months coinciding roughly with the median survival because all patients died because of progression of the neoplasm at sites other than the pericardium with no evidence of pericardial relapse. The main concomitant effects were mild local pain during tetracycline instillation in 4 patients, and transient fever (less than 39 degrees C) in 3. These data suggest that intracavitary oxytetracycline is perhaps less toxic and similar by successful as tetracycline hydrochloride in malignant pericardial tamponade.


Asunto(s)
Taponamiento Cardíaco/tratamiento farmacológico , Oxitetraciclina/uso terapéutico , Adulto , Anciano , Taponamiento Cardíaco/etiología , Femenino , Neoplasias Cardíacas/complicaciones , Neoplasias Cardíacas/secundario , Humanos , Masculino , Persona de Mediana Edad , Oxitetraciclina/administración & dosificación , Derrame Pericárdico/etiología , Pericardio
2.
J Int Med Res ; 18(4): 298-304, 1990.
Artículo en Inglés | MEDLINE | ID: mdl-2227077

RESUMEN

A randomized double-blind trial was performed to evaluate the efficacy of a new non-steroidal anti-inflammatory analgesic drug, ketorolac, in the treatment of cancer pain compared with the opioid pentazocine. A total of 40 patients with moderate to severe cancer pain were studied, 20 patients being treated with 10 mg ketorolac given orally every 6 h and 20 receiving 50 mg pentazocine given orally every 6 h for up to 7 days. A reduction in the severity of the pain was recorded in both treatment groups with no significant difference in efficacy being found between the two therapies, although withdrawals due to adverse reactions were significantly less in the ketorolac-treated group (p less than 0.005). It is concluded that ketorolac may be a useful and more acceptable alternative to opioids in the treatment of cancer pain.


Asunto(s)
Antiinflamatorios no Esteroideos/uso terapéutico , Neoplasias/fisiopatología , Dolor Intratable/tratamiento farmacológico , Pentazocina/uso terapéutico , Tolmetina/análogos & derivados , Adolescente , Adulto , Anciano , Método Doble Ciego , Femenino , Humanos , Ketorolaco , Masculino , Persona de Mediana Edad , Tolmetina/uso terapéutico
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