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早期开始治疗可保留脊柱裂患者的肾功能。

Early start to therapy preserves kidney function in spina bifida patients.

作者信息

Dik Pieter, Klijn Aart J, van Gool Jan D, de Jong-de Vos van Steenwijk Catherine C E, de Jong Tom P V M

机构信息

Paediatric Renal Centre, Wilhelmina Children's Hospital, University Medical Centre, Utrecht, The Netherlands.

出版信息

Eur Urol. 2006 May;49(5):908-13. doi: 10.1016/j.eururo.2005.12.056. Epub 2006 Jan 19.

Abstract

OBJECTIVE

Renal scarring and renal failure remain life-threatening for children born with spinal dysraphism. We reviewed our data of spina bifida patients to evaluate whether optimal treatment of the neurogenic bladder from birth onwards can preserve kidney function.

METHODS

We reviewed data on all newborns with spinal dysraphism who were referred to our hospital between January 1988 and June 2001. We looked at their situations at referral and at follow-up: the type of treatment, antimuscarinic agents, clean intermittent catheterisation (CIC), antibiotic prophylaxis, and operations (sling procedures, bladder augmentations, antireflux procedures). Renal function (ultrasound, DMSA scan, serum creatinin, creatinin clearance) and bladder function (urodynamic studies) were evaluated over time.

RESULTS

Data of 144 children of 176 could be evaluated by the end of the study: 5 patients had pre-existing renal abnormalities, 69 had an overactive sphincter, 27 had reflux, and six had renal scarring. None are currently developing end-stage renal disease. All patients with spina bifida aperta started CIC and antimuscarinic therapy shortly after birth. Five of the six patients with renal scarring were started on therapy with intermittent catheterisation and antimuscarinic therapy several months after birth. Sixty-three of 82 children with spina bifida were dry at school age (age six), although 37 of these had not had an operation.

CONCLUSION

We show that an early start to therapy helps to safeguard renal function for children born with spina bifida. Our data support other recent reports that children born with spina bifida can probably use their own kidneys for a lifetime, if they are given adequate urological treatment. To protect the upper urinary tract, we need to ensure low intravesical pressure by starting children early on CIC (the preferred treatment); antimuscarinic agents to counteract detrusor instability are indispensable in most cases. Proactive treatment of risks for upper tract deterioration results in a negligible loss of renal function, even when early urinary continence is included in the treatment protocol.

摘要

目的

肾瘢痕形成和肾衰竭对患有脊柱裂的儿童来说仍然危及生命。我们回顾了脊柱裂患者的数据,以评估从出生起对神经源性膀胱进行最佳治疗是否能保留肾功能。

方法

我们回顾了1988年1月至2001年6月期间转诊至我院的所有患有脊柱裂的新生儿的数据。我们观察了他们转诊时和随访时的情况:治疗类型、抗毒蕈碱药物、清洁间歇性导尿(CIC)、抗生素预防以及手术(吊带手术、膀胱扩大术、抗反流手术)。随着时间的推移评估肾功能(超声、二巯基丁二酸扫描、血清肌酐、肌酐清除率)和膀胱功能(尿动力学研究)。

结果

到研究结束时,176名儿童中的144名儿童的数据可进行评估:5名患者有既往肾脏异常,69名患者有括约肌过度活跃,27名患者有反流,6名患者有肾瘢痕形成。目前尚无患者发展为终末期肾病。所有开放性脊柱裂患者在出生后不久即开始CIC和抗毒蕈碱治疗。6名有肾瘢痕形成的患者中有5名在出生后几个月开始接受间歇性导尿和抗毒蕈碱治疗。82名脊柱裂儿童中有63名在学龄期(6岁)实现了干爽,尽管其中37名未接受手术。

结论

我们表明,早期开始治疗有助于保护患有脊柱裂的儿童的肾功能。我们的数据支持最近的其他报告,即患有脊柱裂的儿童如果得到充分的泌尿外科治疗,可能一生都能使用自己的肾脏。为了保护上尿路,我们需要通过尽早让儿童开始CIC(首选治疗方法)来确保膀胱内压力较低;在大多数情况下,使用抗毒蕈碱药物来对抗逼尿肌不稳定是必不可少的。对上尿路恶化风险进行积极治疗,即使治疗方案中包括早期尿失禁,肾功能的损失也可忽略不计。

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