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本文引用的文献

1
Neonatal renal venous thrombosis: clinical outcomes and prevalence of prothrombotic disorders.新生儿肾静脉血栓形成:临床结局与血栓前状态疾病的患病率
J Pediatr. 2005 Jun;146(6):811-6. doi: 10.1016/j.jpeds.2005.02.022.
2
Thrombolytic agents for arterial and venous thromboses in neonates.用于新生儿动脉和静脉血栓形成的溶栓剂。
Cochrane Database Syst Rev. 2005 Jan 25;2005(1):CD004342. doi: 10.1002/14651858.CD004342.pub2.
3
A case series of 72 neonates with renal vein thrombosis. Data from the 1-800-NO-CLOTS Registry.72例新生儿肾静脉血栓形成病例系列。来自1-800-NO-CLOTS注册中心的数据。
Thromb Haemost. 2004 Oct;92(4):729-33. doi: 10.1160/TH04-02-0131.
4
Venous and arterial thrombosis during oral contraceptive use: risks and risk factors.口服避孕药使用期间的静脉和动脉血栓形成:风险及危险因素
Semin Vasc Med. 2003 Feb;3(1):69-84. doi: 10.1055/s-2003-38334.
5
Renal venous thrombosis in neonates: prothrombotic risk factors and long-term follow-up.新生儿肾静脉血栓形成:血栓形成的危险因素及长期随访
Blood. 2004 Sep 1;104(5):1356-60. doi: 10.1182/blood-2004-01-0229. Epub 2004 May 18.
6
Charts of fetal size: kidney and renal pelvis measurements.胎儿大小图表:肾脏及肾盂测量
Prenat Diagn. 2003 Nov;23(11):891-7. doi: 10.1002/pd.693.
7
K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification.《肾脏病生存质量指导(K/DOQI)慢性肾脏病临床实践指南:评估、分类及分层》
Am J Kidney Dis. 2002 Feb;39(2 Suppl 1):S1-266.
8
Factor V Leiden and G20210A prothrombin mutations are risk factors for very early recurrent miscarriage.凝血因子V莱顿突变和凝血酶原G20210A突变是极早期复发性流产的危险因素。
BJOG. 2001 Dec;108(12):1251-4. doi: 10.1111/j.1471-0528.2001.00298.x.
9
Combination thrombolytic and anticoagulant therapy for bilateral renal vein thrombosis in a premature infant.联合溶栓和抗凝治疗早产儿双侧肾静脉血栓形成
Am J Perinatol. 2001 Aug;18(5):293-7. doi: 10.1055/s-2001-16993.
10
Genetic susceptibility to venous thrombosis.静脉血栓形成的遗传易感性。
N Engl J Med. 2001 Apr 19;344(16):1222-31. doi: 10.1056/NEJM200104193441607.

围产期肾静脉血栓形成:患侧肾脏长度可预测预后。

Perinatal renal venous thrombosis: presenting renal length predicts outcome.

作者信息

Winyard P J D, Bharucha T, De Bruyn R, Dillon M J, van't Hoff W, Trompeter R S, Liesner R, Wade A, Rees L

机构信息

Renal Unit, Great Ormond Street Hospital for Children NHS Trust, London, UK.

出版信息

Arch Dis Child Fetal Neonatal Ed. 2006 Jul;91(4):F273-8. doi: 10.1136/adc.2005.083717. Epub 2006 Feb 7.

DOI:10.1136/adc.2005.083717
PMID:16464938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2672730/
Abstract

BACKGROUND

Renal venous thrombosis (RVT) is the most common form of venous thrombosis in neonates, causing both acute and long term kidney dysfunction. Historical predisposing factors include dehydration, maternal diabetes, and umbilical catheters, but recent reports highlight associations with prothrombotic abnormalities.

STUDY

Twenty three patients with neonatal RVT were analysed over 15 years. Predisposing factors, presentation, and procoagulant status were compared with renal outcome using multilevel modelling.

RESULTS

Median presentation was on day 1: 19/23 (83%) had pre/perinatal problems, including fetal distress (14), intrauterine growth retardation (five), and pre-identified renal abnormalities (two); 8/18 (44%) had procoagulant abnormalities, particularly factor V Leiden mutations (4/18). Long term abnormalities were detected in 28/34 (82%) affected kidneys; mean glomerular filtration rate was 93.6 versus 70.2 ml/min/1.73 m2 in unilateral versus bilateral cases (difference 23.4; 95% confidence interval 6.4 to 40.4; p = 0.01). No correlation was observed between procoagulant tendencies and outcome, but presenting renal length had a significant negative correlation: mean fall in estimated single kidney glomerular filtration rate was 3 ml/min/1.73 m2 (95% confidence interval 3.7 to -2.2; p = 0.001) per 1 mm increase, and kidneys larger than 6 cm at presentation never had a normal outcome.

CONCLUSIONS

This subgroup of neonatal RVT would be better termed perinatal RVT to reflect antenatal and birth related antecedents. Prothrombotic defects should be considered in all patients with perinatal RVT. Kidney length at presentation correlated negatively with renal outcome. The latter, novel observation raises the question of whether larger organs should be treated more aggressively in future.

摘要

背景

肾静脉血栓形成(RVT)是新生儿静脉血栓形成最常见的形式,可导致急性和长期肾功能障碍。既往的诱发因素包括脱水、母亲糖尿病和脐导管,但最近的报告强调了与血栓前异常的关联。

研究

对15年间的23例新生儿RVT患者进行了分析。使用多水平模型将诱发因素、临床表现和促凝状态与肾脏预后进行比较。

结果

中位发病时间为第1天:19/23(83%)有产前/围产期问题,包括胎儿窘迫(14例)、宫内生长迟缓(5例)和预先发现的肾脏异常(2例);8/18(44%)有促凝异常,尤其是凝血因子V莱顿突变(4/18)。在34个受影响的肾脏中,有28个(82%)检测到长期异常;单侧与双侧病例的平均肾小球滤过率分别为93.6和70.2 ml/min/1.73 m²(差值23.4;95%置信区间6.4至40.4;p = 0.01)。未观察到促凝倾向与预后之间的相关性,但发病时的肾脏长度有显著负相关:估计的单肾肾小球滤过率每增加1 mm平均下降3 ml/min/1.73 m²(95%置信区间3.7至-2.2;p = 0.001);发病时肾脏大于6 cm者从未有正常预后。

结论

这一新生儿RVT亚组更适合称为围产期RVT,以反映产前和与出生相关的病因。所有围产期RVT患者均应考虑血栓前缺陷。发病时的肾脏长度与肾脏预后呈负相关。这一新颖的观察结果提出了一个问题,即未来对于较大的器官是否应采取更积极的治疗措施。