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1.
Int. braz. j. urol ; 37(2): 195-202, Mar.-Apr. 2011. graf, tab
Article in English | LILACS | ID: lil-588992

ABSTRACT

PURPOSE: To evaluate hyoscine N-butyl bromide (HBB) and three different alpha-1 blockers in the treatment of distal ureteral stones. MATERIALS AND METHODS: A total of 140 patients with stones located in the distal tract of the ureter with stone diameters of 5 to 10mm were enrolled in the present study and were randomized into 4 equal groups. Group 1 received HBB, Group 2 received alfuzosin, Group 3 received doxazosin and Group 4 received terazosin. The subjects were prescribed diclofenac injection (75 mg) intramuscularly on demand for pain relief and were followed-up after two weeks with x-rays of the kidneys, ureters, bladder and urinary ultrasonography every week. The number of pain episodes, analgesic dosage and the number of days of spontaneous passage of the calculi through the ureter were also recorded. RESULTS: The average stone size for groups 1, 2, 3 and 4 was comparable (6.13, 5.83, 5.59 and 5.48 mm respectively). Stone expulsion was observed in 11 percent, 52.9 percent, 62 percent, and 46 percent in groups 1, 2, 3 and 4 respectively. The average time to expulsion was 10.55 ± 6.21 days in group 1, 7.38 ± 5.55 days in group 2, 7.85 ± 5.11 days in group 3 and 7.45 ± 5.32 days in group 4. Alpha blockers were found to be superior to HBB (p < 0.05). CONCLUSIONS: Medical treatment of distal ureteral calculi with alfuzosin, doxazosin and terazosin resulted in a signi?cantly increased stone-expulsion rate and decreased expulsion time when compared with HBB. HBB seems to have a negative effect on stone-expulsion rate.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Adrenergic alpha-1 Receptor Antagonists/therapeutic use , Butylscopolammonium Bromide/therapeutic use , Doxazosin/therapeutic use , Prazosin/analogs & derivatives , Quinazolines/therapeutic use , Ureteral Calculi/drug therapy , Prospective Studies , Prazosin/therapeutic use , Treatment Outcome
3.
Rev. bras. odontol ; 60(2): 136-140, mar.-abr. 2003. tab
Article in Portuguese | LILACS, BBO | ID: lil-345069

ABSTRACT

A grande mioria das combinaçöes de fármacos säo irracionais e perigosas. Por outro lado, existem algumas associaçöes medicamentosas que apresentam bases farmacológicas racionais ao lado de uma adequada relaçäo benefício/risco. A associaçäo entre o brometo de N-butilescopolamina com a dipirona é aprovada pelas autoridades sanitárias em vários países apresentando claras indicações terapêuticas, No Brasil particularmente, essa combinaçäo foi aprovada há mais de trinta anos, estando mesmo padronizada em muitos hospitais, principalmente na emergência. A classe médica considera essa combinaçäo fixa como uma associação analgésica de primeira escolha, prática, de baixo custo e muito eficaz


Subject(s)
Butylscopolammonium Bromide/classification , Butylscopolammonium Bromide/pharmacology , Butylscopolammonium Bromide/therapeutic use , Dipyrone , Drug Combinations
5.
Ginecol. obstet. Méx ; 66(1): 35-9, ene. 1998. tab, ilus
Article in Spanish | LILACS | ID: lil-232516

ABSTRACT

Fue realizado un estudio clínico longitudinal abierto, no comparativo, en 30 mujeres con diagnóstico de dismenorrea primaria o secundaria a dispositivo intrauterino. El objetivo del estudio fue evaluar la eficacia y seguridad del compuesto terapéutico, Clonixinato de lisina y Bromuro de butihioscina 125 y 10 mg respectivamente, en cápsulas, durante un periodo de observación de tres ciclos menstruales. El tiempo de evolución de la dismenorrea primaria fue de 4.46 años; para la secundaria fue de 1.77 años. A la dismenorrea le acompañaron síntomas asociados como: náusea 92 por ciento, vómito 92 por ciento, malestar general 82.1 por ciento, pesantez abdominales 85.7 por ciento y cefalea 46.4 por ciento. Respecto a la intensidad del dolor menstrual, al inicio fue muy severo en el 10.7 por ciento, severo en 42.9 por ciento y moderado 46.4 por ciento. Al final del estudio sólo una paciente de las 28, presentó dolor menstrual de intensidad moderada. Encontramos sólo tres menciones de efectos secundarios de intensidad leve y que no requirieron tratamiento; que correspondieron a dos menciones de gastralgía y una de somnolencia. La conclusión del estudio es que la asociación analgésica espasmolítica del Clonixinato de lisina y Bromuro de butilhioscina en el tratamiento de la dismenorrea primaria o secundaria, reduce y previene el dolor menstrual, así como las manifestaciones asociadas con pocos efectos secundarios. Esta asociación analgésica espasmolítica, es eficaz y segura


Subject(s)
Humans , Female , Adolescent , Adult , Administration, Buccal , Analgesics/therapeutic use , Muscarinic Antagonists/administration & dosage , Muscarinic Antagonists/therapeutic use , Butylscopolammonium Bromide/administration & dosage , Butylscopolammonium Bromide/therapeutic use , Clonixin/administration & dosage , Clonixin/analogs & derivatives , Clonixin/therapeutic use , Cyclooxygenase Inhibitors/administration & dosage , Cyclooxygenase Inhibitors/therapeutic use , Dysmenorrhea/drug therapy , Longitudinal Studies , Lysine/administration & dosage , Lysine/analogs & derivatives , Lysine/therapeutic use , Menstrual Cycle , Parasympatholytics/administration & dosage , Parasympatholytics/therapeutic use
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