Bartynski W S, Tan H P, Boardman J F, Shapiro R, Marsh J W
Department of Radiology, Division of Neuroradiology, University of Pittsburgh, Presbyterian University Hospital, Pittsburgh, PA, USA.
AJNR Am J Neuroradiol. 2008 May;29(5):924-30. doi: 10.3174/ajnr.A0960. Epub 2008 Feb 13.
Posterior reversible encephalopathy syndrome (PRES) is known to occur after solid organ transplantation (SOT), potentially associated with cyclosporine and tacrolimus. In this study, we assess the frequency and clinical and imaging characteristics of PRES after SOT.
We identified 27 patients (13 men and 14 women; age range, 22-72 years) who developed PRES after SOT. Features noted included SOT subtype, incidence and timing of PRES, infection and rejection, mean arterial pressure (MAP), and toxicity brain edema.
PRES developed in 21 (0.49%) of 4222 patients who underwent transplantation within the study period (no significant difference among SOT subtypes). Transplantation was performed in 5 patients before the study period, and 1 patient underwent transplantation elsewhere. In consideration of all 27 patients, PRES typically developed in the first 2 months in patients who had SOT of the liver (9 of 10 patients) and was associated with cytomegalovirus (CMV), mild rejection, or systemic bacterial infection. PRES also typically developed after 1 year in patients who had SOT of the kidney (8 of 9 patients) and was associated with moderate rejection or bacterial infection. Toxicity MAP was significantly lower (P < .001) in liver transplants (average MAP, 104.8 +/- 16 mm Hg) compared with that in kidney transplants (average MAP, 143 +/- 20 mm Hg). Toxicity brain edema was significantly greater (P < .001) in patients who had liver transplants and developed PRES compared with patients who had undergone kidney transplants despite severe hypertension in those who had the kidney transplants.
Patients who had undergone SOTs have a similar low incidence of developing PRES. Differences between those who have had liver and kidney transplants included time after transplant, toxicity MAP, and PRES vasogenic edema noted at presentation. In patients who have undergone kidney transplants, severely elevated MAP was associated with reduced, not greater, brain edema.
已知实体器官移植(SOT)后可发生后部可逆性脑病综合征(PRES),可能与环孢素和他克莫司有关。在本研究中,我们评估了SOT后PRES的发生率以及临床和影像学特征。
我们确定了27例在SOT后发生PRES的患者(13例男性和14例女性;年龄范围22 - 72岁)。记录的特征包括SOT亚型、PRES的发生率和发生时间、感染和排斥反应、平均动脉压(MAP)以及中毒性脑水肿。
在研究期间接受移植的4222例患者中,有21例(0.49%)发生了PRES(SOT亚型之间无显著差异)。5例患者在研究期之前接受了移植,1例患者在其他地方接受了移植。考虑所有27例患者,肝移植患者的PRES通常在术后前2个月发生(10例患者中有9例),且与巨细胞病毒(CMV)、轻度排斥反应或全身性细菌感染有关。肾移植患者的PRES通常在术后1年以后发生(9例患者中有8例),且与中度排斥反应或细菌感染有关。与肾移植患者(平均MAP,143±20 mmHg)相比,肝移植患者的中毒性MAP显著更低(P <.001)(平均MAP,104. − 8±16 mmHg)。尽管肾移植患者存在严重高血压,但与肾移植患者相比,发生PRES的肝移植患者的中毒性脑水肿显著更严重(P <.001)。
接受SOT的患者发生PRES的发生率相似。肝移植和肾移植患者之间的差异包括移植后的时间、中毒性MAP以及出现时PRES的血管源性水肿。在肾移植患者中,MAP严重升高与脑水肿减轻而非加重有关。