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Clinical effects of oxybutynin hydrochloride in the treatment of unstable bladder and overactive neurogenic bladder: a long-term clinical trial

机译:盐酸奥昔布宁治疗不稳定型膀胱和活动性神经源性膀胱的临床疗效:一项长期临床试验

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摘要

Clinical effects and therapeutic usefulness of oxybutynin hydrochloride were evaluated in a long-term clinical trial on patients with unstable bladders and neurogenic bladders. Of the 46 patients entered into the trial, 37 were those diagnosed with an unstable bladder and 9 with a neurogenic bladder with overactive detrusor. In 37 of the cases (80%), the period of drug administration reached up to 12 weeks and in 16 cases (34%) the drugs were administered for more than 24 weeks. The average administration period was 165.9 days. The average total given dose was 1776.9 mg and average dose per day was 10.7 mg. Excellent and good responses were obtained in 76.3, 88.9 and 69.6% at 12 and 24 weeks after start of administration and at the time of discontinuing the drug, respectively. The cystometric changes at pre- and post-administration were evaluated on 23 cases and revealed a significant increase in volume at first sensation and maximum desire to void. Maximum resting intravesical pressure was significantly declined and uninhibited detrusor contractions were significantly suppressed. Side effects were noted in 11 of the 46 cases (23.9%), most of which were well tolerated by the patients. In 4 cases the drug had to be discontinued because of the side effects. Dry mouth was the most common side effect, occupying almost half of the incidents. No significant abnormality was noted on blood laboratory data, blood pressure or heart rate, following the drug administration. In one case slight increase in serum glutamic-oxalacetic transaminase and glutamic-pyruvic transaminase was encountered, but its relationship with the drug was obscure. The clinical usefulness of this drug (excellent and good) was 78.9, 88.9 and 69.6% at 12 and 24 weeks after start of administration, and at the time of drug discontinuation, respectively. The present long-term trial proved that oxybutynin hydrochloride is an exceedingly effective and safe agent for clinical management of unstable bladder and overactive neurogenic bladder.
机译:在一项长期的临床试验中,评估了盐酸奥昔布宁在不稳定膀胱和神经源性膀胱患者中的临床效果和治疗效果。在参加该试验的46位患者中,有37位被诊断为膀胱不稳定,而9位为逼尿肌过度活动的神经源性膀胱。其中37例(80%)的药物使用期限长达12周,而16例(34%)的药物使用时间超过24周。平均给药期为165.9天。给定的平均总剂量为1776.9 mg,每天平均剂量为10.7 mg。在开始给药后12周和24周以及停药时,分别有76.3%,88.9%和69.6%的患者获得了优异和良好的反应。评估了23例患者在给药前和给药后的膀胱测量变化,发现初次感觉时体积明显增加,并且最大程度地希望排尿。最大静息膀胱内压显着下降,未抑制的逼尿肌收缩被显着抑制。在46例病例中有11例(23.9%)出现了副作用,大多数患者对此耐受良好。在4种情况下,由于副作用,必须停药。口干是最常见的副作用,几乎占了一半。给药后,血液实验室数据,血压或心率均未发现明显异常。在一种情况下,血清谷氨酸-草酰乙酸转氨酶和谷氨酸-丙酮酸转氨酶略有增加,但与药物的关系不清楚。该药物在开始给药后第12周和第24周以及停药时的临床效用(优异和良好)分别为78.9、88.9和69.6%。本项长期试验证明,盐酸奥昔布宁对不稳定的膀胱和活动过度的神经源性膀胱的临床管理是一种极其有效和安全的药物。

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