Kolettis Peter N, Bugg Charles E, Lockhart Mark E, Bynon Steven J, Burns John R
Department of Surgery, Division of Urology, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama 35294-3411, USA.
Urology. 2004 Apr;63(4):656-9. doi: 10.1016/j.urology.2003.11.026.
To review the outcomes for live donor renal transplantation using kidneys with fibromuscular dysplasia.
We performed a retrospective review and searched a departmental database to identify all renal donors with fibromuscular dysplasia from 1995 through 2001. These donors were then paired with the recipient using the institution's renal transplant database. A single radiologist reviewed the original arteriographic studies. Mild disease was defined as mild irregularity of the artery without significant stenosis. Moderate disease was defined as arterial irregularity with less than 50% stenosis. Severe disease was defined as irregularity with greater than 50% stenosis or with aneurysms.
Thirty-six donor/recipient pairs were identified. Twenty-six donors had unilateral and 10 bilateral disease. Twenty-eight had mild and eight moderate disease. Four grafts were lost during the follow-up period (three acute rejection and one chronic rejection) for an overall graft survival rate of 89%. The median graft survival/follow-up was 37.1 months (range 0.5 to 82). The median serum creatinine was 1.6 mg/dL. The median systolic and diastolic blood pressure was 155 and 82 mm Hg, respectively. Six recipients required no antihypertensive agents. All but 9 of the remaining patients required two or fewer antihypertensive agents.
Selected patients with medial fibroplasia can be used as renal donors, and satisfactory functional outcomes can be achieved. Renal donors with mild anatomic abnormalities such as medial fibroplasia could be used to increase the potential donor pool and decrease the waiting time for renal transplantation.
回顾使用患有纤维肌性发育异常的肾脏进行活体供肾肾移植的结果。
我们进行了一项回顾性研究,并检索了科室数据库,以确定1995年至2001年间所有患有纤维肌性发育异常的肾供体。然后使用该机构的肾移植数据库将这些供体与受者进行配对。由一名放射科医生复查原始血管造影研究。轻度疾病定义为动脉轻度不规则但无明显狭窄。中度疾病定义为动脉不规则且狭窄小于50%。重度疾病定义为不规则且狭窄大于50%或伴有动脉瘤。
共确定了36对供体/受者。26名供体为单侧疾病,10名供体为双侧疾病。28名供体患有轻度疾病,8名供体患有中度疾病。在随访期间有4个移植物丢失(3个急性排斥反应和1个慢性排斥反应),总体移植物存活率为89%。移植物存活/随访的中位数为37.1个月(范围为0.5至82个月)。血清肌酐中位数为1.6mg/dL。收缩压和舒张压中位数分别为155mmHg和82mmHg。6名受者不需要使用抗高血压药物。其余患者中除9名外,均需要两种或更少的抗高血压药物。
选定的患有中膜纤维增生的患者可作为肾供体,并可取得满意的功能结果。患有轻度解剖学异常(如中膜纤维增生)的肾供体可用于增加潜在供体库并减少肾移植的等待时间。