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常染色体显性多囊肾病的疼痛管理与肾神经支配解剖学

Management of pain in autosomal dominant polycystic kidney disease and anatomy of renal innervation.

作者信息

Tellman Matthew W, Bahler Clinton D, Shumate Ashley M, Bacallao Robert L, Sundaram Chandru P

机构信息

Department of Urology, Indiana University School of Medicine, Indianapolis, Indiana.

Department of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana.

出版信息

J Urol. 2015 May;193(5):1470-8. doi: 10.1016/j.juro.2014.10.124. Epub 2014 Dec 19.

Abstract

PURPOSE

Chronic pain is a prominent feature of autosomal dominant polycystic kidney disease that is difficult to treat and manage, often resulting in a decrease in quality of life. Understanding the underlying anatomy of renal innervation and the various etiologies of pain that occur in autosomal dominant polycystic kidney disease can help guide proper treatments to manage pain. Reviewing previously studied treatments for pain in autosomal dominant polycystic kidney disease can help characterize treatment in a stepwise fashion.

MATERIALS AND METHODS

We performed a literature search of the etiology and management of pain in autosomal dominant polycystic kidney disease and the anatomy of renal innervation using PubMed® and Embase® from January 1985 to April 2014 with limitations to human studies and English language.

RESULTS

Pain occurs in the majority of patients with autosomal dominant polycystic kidney disease due to renal, hepatic and mechanical origins. Patients may experience different types of pain which can make it difficult to clinically confirm its etiology. An anatomical and histological evaluation of the complex renal innervation helps in understanding the mechanisms that can lead to renal pain. Understanding the complex nature of renal innervation is essential for surgeons to perform renal denervation. The management of pain in autosomal dominant polycystic kidney disease should be approached in a stepwise fashion. Acute causes of renal pain must first be ruled out due to the high incidence in autosomal dominant polycystic kidney disease. For chronic pain, nonopioid analgesics and conservative interventions can be used first, before opioid analgesics are considered. If pain continues there are surgical interventions such as renal cyst decortication, renal denervation and nephrectomy that can target pain produced by renal or hepatic cysts.

CONCLUSIONS

Chronic pain in patients with autosomal dominant polycystic kidney disease is often refractory to conservative, medical and other noninvasive treatments. There are effective surgical procedures that can be performed when more conservative treatments fail. Laparoscopic cyst decortication has been well studied and results in the relief of chronic renal pain in the majority of patients. In addition, renal denervation has been used successfully and could be performed concurrently with cyst decortication. Nephrectomy should be reserved for patients with intractable pain and renal failure when other modalities have failed.

摘要

目的

慢性疼痛是常染色体显性多囊肾病的一个显著特征,难以治疗和管理,常导致生活质量下降。了解肾神经支配的基础解剖结构以及常染色体显性多囊肾病中出现疼痛的各种病因,有助于指导疼痛管理的恰当治疗。回顾先前研究的常染色体显性多囊肾病疼痛治疗方法,有助于逐步明确治疗特征。

材料与方法

我们使用PubMed®和Embase®对1985年1月至2014年4月期间常染色体显性多囊肾病疼痛的病因及管理以及肾神经支配的解剖结构进行了文献检索,检索局限于人体研究和英文文献。

结果

大多数常染色体显性多囊肾病患者会出现疼痛,其源于肾脏、肝脏及机械性因素。患者可能经历不同类型的疼痛,这使得临床上难以确认其病因。对复杂的肾神经支配进行解剖学和组织学评估,有助于理解可能导致肾痛的机制。了解肾神经支配的复杂性对于外科医生进行肾去神经支配至关重要。常染色体显性多囊肾病疼痛的管理应采取逐步推进的方式。由于常染色体显性多囊肾病中肾痛急性病因的发生率较高,必须首先排除。对于慢性疼痛,可首先使用非阿片类镇痛药和保守干预措施,再考虑使用阿片类镇痛药。如果疼痛持续存在,有一些手术干预措施,如肾囊肿去顶减压术、肾去神经支配术和肾切除术,可针对由肾囊肿或肝囊肿产生的疼痛。

结论

常染色体显性多囊肾病患者的慢性疼痛通常对保守、药物及其他非侵入性治疗无效。当更保守的治疗失败时,有一些有效的手术方法可以实施。腹腔镜囊肿去顶减压术已得到充分研究,大多数患者的慢性肾痛可得到缓解。此外,肾去神经支配术已成功应用,可与囊肿去顶减压术同时进行。肾切除术应保留给其他治疗方法均无效且伴有顽固性疼痛和肾衰竭的患者。

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