Akbari Ayub, Hladunewich Michelle, Burns Kevin, Moretti Felipe, Arkoub Rima Abou, Brown Pierre, Hiremath Swapnil
Division of Nephrology, Department of Medicine, University of Ottawa, Ottawa, Ontario Canada ; Kidney Research Centre, Ottawa Hospital Research Institute, Ottawa, Ontario Canada ; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario Canada ; The Ottawa Hospital, Riverside Campus, 1967 Riverside Drive, Ottawa, ON K1H 7W9 Canada.
Department of Medicine, Division of Nephrology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario Canada.
Can J Kidney Health Dis. 2016 Feb 23;3:7. doi: 10.1186/s40697-016-0096-7. eCollection 2016.
Pregnancy in patients on chronic hemodialysis therapy, though unlikely, does happen rarely. Intensive hemodialysis is thought to offer a better survival advantage to the unborn child. Circulating angiogenic factors are helpful for prognostication of pregnant patients with chronic kidney disease who are not on dialysis. Data on their utilization in dialysis patients, however, are limited.
We report the case of a patient with a history of interstitial nephritis who had a kidney transplant that failed after 8 years due to membranous nephropathy. She was initiated on hemodialysis three sessions per week and conceived after being on dialysis for 6 weeks. She was switched to intensive hemodialysis at 8 weeks of gestation and had a C-section because of hypertension at 35 weeks, with delivery of a healthy girl weighing 2012 g. Serum angiogenic factors (placental growth factor and soluble fms-like tyrosine kinase) were measured at 32, 33, and 34 weeks of gestation and at 1, 2, and 3 weeks postpartum. Serum angiogenic factors were similar to what has been reported for patients with chronic kidney disease and were not consistent with preeclampsia.
Our case report expands on the literature regarding intensive hemodialysis and angiogenic factor utilization in pregnant dialysis patients. Our case report suggests that starting intensive dialysis early in pregnancy is safe and concentration of angiogenic factors are similar to those reported for patients without kidney disease, except for PIGF levels, which are somewhat higher.
接受慢性血液透析治疗的患者怀孕的情况虽不常见,但确实偶尔会发生。强化血液透析被认为能为未出生的胎儿提供更好的生存优势。循环血管生成因子有助于对未接受透析的慢性肾脏病孕妇进行预后评估。然而,关于其在透析患者中的应用数据有限。
我们报告了一例间质性肾炎病史患者的病例,该患者接受了肾脏移植,8年后因膜性肾病移植失败。她开始每周进行三次血液透析,透析6周后怀孕。妊娠8周时改为强化血液透析,35周时因高血压行剖宫产,产下一名体重2012克的健康女婴。在妊娠32、33和34周以及产后1、2和3周测量血清血管生成因子(胎盘生长因子和可溶性fms样酪氨酸激酶)。血清血管生成因子与慢性肾脏病患者的报告情况相似,与先兆子痫不符。
我们的病例报告扩展了关于妊娠透析患者强化血液透析和血管生成因子应用的文献。我们的病例报告表明,妊娠早期开始强化透析是安全的,血管生成因子浓度与未患肾病患者的报告情况相似,但胎盘生长因子水平略高。