Palmer L S, Zebold K, Firlit C F, Kaplan W E
Division of Urology, Children's Memorial Hospital, Northwestern University Medical School, Chicago, Illinois, USA.
J Urol. 1997 Feb;157(2):638-40.
We report our experience with the intravesical administration of oxybutynin chloride with particular focus on the incidence and characterization of untoward effects and inconvenience of therapy.
From 1990 to 1995, 23 children 5 to 11 years old with myelodysplasia were treated with intravesical oxybutynin chloride. Initial dose was 1.25 mg. in 5 cc sterile water instilled during routine catheterization 3 times daily, which was increased as tolerated and clinically indicated. Oral anticholinergic, antispasmodic and sympathomimetic medications were discontinued during therapy. We reviewed therapeutic indications, doses, frequency duration, reason for discontinuation and untoward effects. Patients/parents were surveyed for convenience of treatment as well as side effects and their timing with respect to drug administration and dose.
In 15 patients (65%) treatment was discontinued and oral formulations were resumed or other therapy was required due to side effects, ineffectiveness or inconvenience. Seven patients had untoward effects, ranging from facial flushing and dizziness to agoraphobia and hyperactivity. Six patients discontinued therapy due to side effects after 1 day to 2 years (mode 1 month) at doses of 1.25 to 5 mg., including 5 who previously had side effects from oral oxybutynin chloride. Inconvenience of therapy was noted irrespective of the degree of independence of the child for performing intravesical therapy.
Untoward effects and inconvenience are the most common reasons for discontinuing intravesical oxybutynin chloride therapy for neurogenic bladder dysfunction. Children who previously had side effects from oral oxybutynin chloride are more likely to have them during intravesical therapy.
我们报告了膀胱内给予氯化奥昔布宁的经验,特别关注治疗的不良反应发生率、特征以及不便之处。
1990年至1995年,对23名5至11岁患有脊髓发育不良的儿童进行膀胱内氯化奥昔布宁治疗。初始剂量为1.25毫克,溶于5毫升无菌水中,在常规导尿时每日灌注3次,根据耐受情况和临床指征增加剂量。治疗期间停用口服抗胆碱能、解痉和拟交感神经药物。我们回顾了治疗指征、剂量、频率、持续时间、停药原因和不良反应。对患者/家长进行了调查,了解治疗的便利性以及副作用及其与给药和剂量的时间关系。
15名患者(65%)因副作用、无效或不便而停药,恢复口服制剂或需要其他治疗。7名患者出现不良反应,从面部潮红、头晕到广场恐惧症和多动。6名患者在剂量为1.25至5毫克的情况下,于1天至2年(中位数1个月)后因副作用停药,其中5名患者之前口服氯化奥昔布宁时曾出现副作用。无论儿童进行膀胱内治疗的独立程度如何,均注意到治疗存在不便之处。
不良反应和不便之处是停止膀胱内氯化奥昔布宁治疗神经源性膀胱功能障碍的最常见原因。之前口服氯化奥昔布宁时出现过副作用的儿童在膀胱内治疗期间更有可能出现副作用。