Benedetti E, Najarian J S, Gruessner A C, Nakhleh R E, Troppmann C, Hakim N S, Pirenne J, Sutherland D E, Gruessner R W
Department of Surgery, University of Minnesota, USA.
Surgery. 1995 Nov;118(5):864-72. doi: 10.1016/s0039-6060(05)80277-6.
Urinary amylase (UA) remains the most common biochemical parameter to detect rejection in bladder-drained pancreas allografts. With the development of the cystoscopic transduodenal pancreas transplant biopsy technique, tissue samples of the pancreas graft are now frequently obtained. A definitive correlative analysis between UA activity and biopsy results has not been done in the three different pancreas transplant categories (simultaneous pancreas-kidney, pancreas transplant alone, and pancreas after kidney).
We studied 66 pancreaticoduodenal biopsy specimens obtained for hypoamylasuria. Rejection was defined as a greater than 25% decrease from stable posttransplantation baseline on two consecutive measurements at least 12 hours apart. To perform biopsies we used our newly developed 14- and 16-gauge core-cut needles (50 cm long). Biopsy specimens were considered positive if either pancreatic or duodenal rejection was found. To assess the quality of UA activity we studied 13 biopsy specimens from patients with stable UA levels; these 13 specimens were negative for rejection.
Acute rejection was diagnosed in 36 biopsy specimens (55%). The mean decrease in UA levels was 67% +/- 8% (range, 28% to 99%) for the positive biopsy results, and 57% +/- 16% (range, 22% to 92%) for the negative biopsy results (p = 0.147). Within 1 month, UA levels returned to baseline in 19% of our patients with positive biopsy results versus 97% with negative results; postbiopsy 1-year graft survival was 64% versus 97% (p < or = 0.05). In assessing the test quality of our biopsy specimens (including 13 obtained for reasons other than hypoamylasuria), we found a sensitivity of 100% (stable UA levels mean no rejection) and a specificity of 30%. The predictive value of a positive test was 53%; of a negative test it was 100%. By performing biopsies we avoided antirejection treatment in 47% of the patients studied. We found no biopsy-related complications.
Stable UA levels reliably rule out rejection; a decrease is a marker for acute rejection but is unspecific. Performing biopsy is currently the only way to reliably diagnose rejection in solitary pancreas recipients (pancreas transplant alone and pancreas after kidney) and in simultaneous pancreas-kidney recipients with isolated hypoamylasuria. The procedure is safe and should always be attempted to avoid unnecessary rejection treatment.
尿淀粉酶(UA)仍然是检测膀胱引流式胰腺移植排斥反应最常用的生化指标。随着膀胱镜经十二指肠胰腺移植活检技术的发展,现在可以频繁获取胰腺移植物的组织样本。在三种不同类型的胰腺移植(胰肾联合移植、单纯胰腺移植、肾移植后胰腺移植)中,尚未对UA活性与活检结果进行明确的相关性分析。
我们研究了66例因低淀粉酶尿症而获取的胰十二指肠活检标本。排斥反应定义为在至少间隔12小时的两次连续测量中,较移植后稳定基线水平下降超过25%。为了进行活检,我们使用了新开发的14号和16号芯针(长50厘米)。如果发现胰腺或十二指肠排斥反应,则活检标本被视为阳性。为了评估UA活性的质量,我们研究了13例UA水平稳定的患者的活检标本;这13个标本排斥反应为阴性。
36例活检标本(55%)诊断为急性排斥反应。活检结果阳性者UA水平平均下降67%±8%(范围28%至99%),活检结果阴性者UA水平平均下降57%±16%(范围22%至92%)(p = 0.147)。在1个月内,活检结果阳性的患者中有19%的UA水平恢复到基线,而活检结果阴性的患者中有97%恢复到基线;活检后1年移植物存活率分别为64%和97%(p≤0.05)。在评估我们活检标本的检测质量时(包括13例因低淀粉酶尿症以外原因获取的标本),我们发现敏感性为100%(UA水平稳定意味着无排斥反应),特异性为30%。阳性检测的预测价值为53%;阴性检测的预测价值为100%。通过进行活检,我们在47%的研究患者中避免了抗排斥治疗。我们未发现与活检相关的并发症。
UA水平稳定可可靠地排除排斥反应;UA水平下降是急性排斥反应的一个指标,但不具有特异性。目前,对于单纯胰腺移植受者(单纯胰腺移植和肾移植后胰腺移植)以及胰肾联合移植且伴有孤立性低淀粉酶尿症的受者,进行活检是可靠诊断排斥反应的唯一方法。该操作是安全的,应始终尝试进行以避免不必要的抗排斥治疗。