Hafez A T, Elsherbiny M T, Ghoneim M A
Urology and Nephrology Center, Mansoura University, Mansoura, Egypt.
J Urol. 2001 Jun;165(6 Pt 2):2428-30. doi: 10.1016/S0022-5347(05)66221-0.
The surgical repair of bladder exstrophy remains challenging for the pediatric urologist. We present our preliminary experience with complete primary repair of exstrophy in neonates and children with failed initial closure.
Between November 1998 and April 1999, 9 boys and 2 girls with bladder exstrophy underwent complete repair. This procedure was performed in the first 72 hours of life in 4 boys and at age 3 months in 1 girl. Complete repair with osteotomy was performed after failed initial closure in 5 boys and 1 girl at a mean age of 28 months (range 15 to 36). The bladder and urethra were closed in continuity and epispadias was repaired by total penile disassembly. All patients were kept in a spica cast for 3 weeks. Ureteral stents and suprapubic tube were removed 10 and 14 days, respectively, after surgery. Ultrasound was performed preoperatively and every 3 months postoperatively, voiding cystourethrography was done 6 to 12 months after surgery.
Mean followup is 14 months (range 12 to 17). All repairs were successful including 1 case of penile scrotal duplication. Concomitant augmentation was done in 2 girls due to a small bladder plate. Complete closure resulted in hypospadias in 3 of the 9 boys. No patient had dehiscence or fistula. Serial followup ultrasound revealed no hydronephrosis and normal renal growth. Febrile urinary tract infection occurred in 1 case 2 months after surgery and was managed conservatively. Bladder capacity was 200 and 270 ml., at 6 months, respectively, in the 2 patients with an augmented bladder and both are dry on intermittent catheterization. The 4 patients in whom the closure was performed at birth are voiding with dry intervals with mean bladder capacity of 75 cc at 1 year (range 60 to 90). The 5 older children had a mean bladder capacity of 120 cc (range 70 to 150) at 6 months, of whom 2 are completely continent and 3 have 1 to 3 hours of dry intervals.
Complete repair of bladder exstrophy is feasible in neonates and children after failed initial closure with minimal morbidity. There is no short-term evidence of worsening reflux or hydronephrosis. Longitudinal followup with adequate recording is required for continence evaluation. This technique may minimize the future need of bladder neck reconstruction and augmentation in patients with exstrophy.
膀胱外翻的手术修复对于小儿泌尿外科医生来说仍然具有挑战性。我们介绍了我们对初次闭合失败的新生儿和儿童进行膀胱外翻完全一期修复的初步经验。
1998年11月至1999年4月,9例男孩和2例女孩接受了膀胱外翻的完全修复。4例男孩在出生后的头72小时内进行了该手术,1例女孩在3个月大时进行了手术。5例男孩和1例女孩在初次闭合失败后平均年龄28个月(范围15至36个月)时进行了截骨术的完全修复。膀胱和尿道连续闭合,阴茎完全离断修复阴茎头型尿道下裂。所有患者均使用髋人字石膏固定3周。输尿管支架和耻骨上管分别在术后10天和14天取出。术前及术后每3个月进行超声检查,术后6至12个月进行排尿性膀胱尿道造影。
平均随访14个月(范围12至17个月)。所有修复均成功,包括1例阴茎阴囊重复畸形。2例女孩因膀胱板小而同时进行了膀胱扩大术。9例男孩中有3例完全闭合后出现尿道下裂。无患者发生裂开或瘘管。系列随访超声显示无肾积水且肾脏生长正常。1例患者术后2个月发生发热性尿路感染,经保守治疗。2例膀胱扩大术患者在6个月时膀胱容量分别为200和270毫升,两者均通过间歇性导尿保持干燥。4例出生时进行闭合手术的患者排尿时有干爽间歇期,1岁时平均膀胱容量为75毫升(范围60至90毫升)。5例年龄较大的儿童在6个月时平均膀胱容量为120毫升(范围70至150毫升),其中2例完全可控,3例有1至3小时的干爽间歇期。
对于初次闭合失败的新生儿和儿童,膀胱外翻的完全修复是可行的,发病率极低。没有短期证据表明反流或肾积水会加重。需要进行长期随访并进行充分记录以评估控尿情况。该技术可能会减少膀胱外翻患者未来膀胱颈重建和膀胱扩大术的需求。