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膀胱内注射卡前列甲酯治疗环磷酰胺诱导的出血性膀胱炎。

Treatment of cyclophosphamide-induced hemorrhagic cystitis with intravesical carboprost tromethamine.

作者信息

Levine L A, Jarrard D F

机构信息

Section of Urology, University of Chicago, Illinois.

出版信息

J Urol. 1993 Apr;149(4):719-23. doi: 10.1016/s0022-5347(17)36192-x.

Abstract

We review our experience with 18 consecutive patients who received intravesical carboprost tromethamine, an F2-alpha prostaglandin, for severe hemorrhagic cystitis following cyclophosphamide chemotherapy. Of the patients 16 were given cyclophosphamide for conditioning before bone marrow transplantation and 2 received the drug as cytotoxic therapy alone (dose range 3.6 to 15.8 gm.). All patients had severe gross hematuria that was refractory to forced diuresis and to continuous saline bladder irrigation. The intravesical prostaglandin therapy was initiated only after significant transfusion requirements (greater than 1 unit packed red blood cells per day) and/or numerous catheter manipulations for relief of clot retention. Eligible patients underwent complete clot evacuation followed by intravesical instillation of 0.4 to 1.0 mg.% carboprost tromethamine for 2 hours 4 times per day, alternating with continuous saline bladder irrigation for 2 hours. Six patients attempted an alternate protocol of 0.8 to 1.0 mg.% carboprost tromethamine given by continuous saline bladder irrigation. Complete resolution of gross hematuria occurred in 9 patients (50%). Eight patients had a partial response, with decreased transfusion requirements noted. However, complete resolution ultimately required an alternative therapy (for example formalin or urinary diversion). One patient (6%) failed to respond and required formalin therapy on day 4 of carboprost tromethamine therapy. Decreased red blood cell transfusion requirements were noted during and after therapy when compared to pretreatment values. No changes in renal or bladder function were noted during the mean followup of 17 weeks (range 1 to 64 weeks). There were 3 cases of recurrent hematuria. Side effects were limited to bladder spasm in 14 of the 18 patients (78%), with no systemic complications. The results suggest that carboprost tromethamine is a useful bedside therapy for hemorrhagic cystitis due to cyclophosphamide, and treatment appears to have minimal toxicity.

摘要

我们回顾了18例连续接受膀胱内注射卡前列甲酯(一种F2-α前列腺素)治疗环磷酰胺化疗后严重出血性膀胱炎患者的经验。其中16例患者在骨髓移植前接受环磷酰胺预处理,2例患者单独接受该药物作为细胞毒性治疗(剂量范围为3.6至15.8克)。所有患者均有严重肉眼血尿,对强制利尿和持续膀胱冲洗生理盐水均无效。仅在有大量输血需求(每天超过1单位浓缩红细胞)和/或为缓解血凝块潴留进行多次导管操作后才开始膀胱内前列腺素治疗。符合条件的患者先进行完全血凝块清除,然后膀胱内滴注0.4至1.0mg.%卡前列甲酯,每天4次,每次2小时,与持续膀胱冲洗生理盐水2小时交替进行。6例患者尝试了另一种方案,即通过持续膀胱冲洗生理盐水给予0.8至1.0mg.%卡前列甲酯。9例患者(50%)肉眼血尿完全消失。8例患者有部分反应,输血需求减少。然而,最终完全缓解需要替代治疗(例如福尔马林或尿流改道)。1例患者(6%)无反应,在卡前列甲酯治疗第4天需要福尔马林治疗。与治疗前相比,治疗期间和治疗后红细胞输血需求减少。在平均17周(范围1至64周)的随访期间,未发现肾功能或膀胱功能有变化。有3例复发性血尿。18例患者中有14例(78%)的副作用仅限于膀胱痉挛,无全身并发症。结果表明,卡前列甲酯是治疗环磷酰胺所致出血性膀胱炎的一种有用的床边治疗方法,且治疗毒性似乎最小。

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