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移植后红细胞增多症:一种正在消失的现象?

Post-transplant erythrocytosis: a disappearing phenomenon?

机构信息

Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Clin Transplant. 2009 Nov-Dec;23(6):800-6. doi: 10.1111/j.1399-0012.2008.00947.x. Epub 2008 Dec 19.

DOI:10.1111/j.1399-0012.2008.00947.x
PMID:19191802
Abstract

BACKGROUND

Erythrocytosis is relatively common post-kidney transplantation and may have adverse consequences. This study examined whether the incidence of erythrocytosis has remained stable over time and explored the impact of this condition on patient outcomes.

METHODS

This was a retrospective single center review of an incidence cohort (transplanted between 1993 and 2005). Predictors of erythrocytosis and hemoglobin levels and subsequent patient and allograft survival were examined.

RESULTS

Erythrocytosis (hemoglobin >170 g/L for >1 month) was observed in 59 of 511 recipients. Erythrocytosis developed in only 8.1% of those transplanted from 1997 to 2005, compared with 18.7% in those transplanted from 1993 to 1996 (p = 0.0005). Independent predictive factors were use of angiotensin converting enzyme inhibitors/angiotensin receptor blockers (ACEi/ARBs) (HR 0.176, 95% CI 0.040-0.71, p = 0.016), male gender (HR 3.72, 95% CI 1.54-9.0, p = 0.003), and mycophenolic acid agents (HR 0.49, 95% CI 0.237-0.99, p = 0.049). Patients with erythrocytosis had superior overall survival (HR for death 0.105, 95% CI 0.014-0.760, p = 0.026) but a trend for worse death censored graft loss (univariate HR 2.06, 95% CI 0.91-4.65, p = 0.084).

CONCLUSIONS

The incidence of erythrocytosis is falling and is likely related to greater ACEi/ARB use and possibly more antiproliferative immunosuppression. Patient survival is excellent in those with erythrocytosis, but long-term graft survival may be compromised.

摘要

背景

肾移植后红细胞增多症较为常见,可能会产生不良后果。本研究旨在探讨红细胞增多症的发生率是否随时间推移而保持稳定,并分析该病症对患者预后的影响。

方法

这是一项回顾性单中心队列研究(1993 年至 2005 年期间移植)。分析了红细胞增多症(血红蛋白>170g/L 持续>1 个月)的发生率、血红蛋白水平以及患者和移植物存活率的预测因素。

结果

511 例受者中共有 59 例发生红细胞增多症。1997 年至 2005 年期间移植的患者中仅 8.1%发生红细胞增多症,而 1993 年至 1996 年期间移植的患者中这一比例为 18.7%(p=0.0005)。独立预测因素为使用血管紧张素转换酶抑制剂/血管紧张素受体阻滞剂(ACEi/ARBs)(HR 0.176,95%CI 0.040-0.71,p=0.016)、男性(HR 3.72,95%CI 1.54-9.0,p=0.003)和霉酚酸制剂(HR 0.49,95%CI 0.237-0.99,p=0.049)。红细胞增多症患者的总生存率更高(死亡风险 HR 0.105,95%CI 0.014-0.760,p=0.026),但死亡相关移植物丢失风险有增高趋势(单因素 HR 2.06,95%CI 0.91-4.65,p=0.084)。

结论

红细胞增多症的发生率正在下降,可能与 ACEi/ARBs 使用增加和更具增殖抑制作用的免疫抑制治疗有关。红细胞增多症患者的生存率较高,但长期移植物存活率可能会降低。

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