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红细胞同种免疫性溶血病新生儿胆汁淤积症:发生率、危险因素和结局。

Cholestasis in neonates with red cell alloimmune hemolytic disease: incidence, risk factors and outcome.

机构信息

Division of Neonatology, Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Neonatology. 2012;101(4):306-10. doi: 10.1159/000335333. Epub 2012 Feb 18.

Abstract

BACKGROUND

Etiology of cholestatic liver disease in neonates with hemolytic disease of the newborn (HDN) has been associated with iron overload due to intrauterine red cell transfusions (IUTs). Data on the incidence and severity of cholestasis in neonates with HDN are scarce, and little is known about pathogenesis, risk factors, neonatal management and outcome.

OBJECTIVE

To evaluate incidence, risk factors, management and outcome of cholestasis in neonates with red cell alloimmune hemolytic disease.

METHODS

All (near-) term neonates with HDN due to red cell alloimmunization admitted to our center between January 2000 and July 2010 were included in this observational study. Liver function tests (including conjugated bilirubin) were routinely performed in the neonatal period. We recorded the presence of cholestasis, investigated several potential risk factors and evaluated the management and outcome in affected neonates.

RESULTS

A total of 313 infants with red cell alloimmune hemolytic disease treated with or without IUTs were included. The incidence of cholestasis was 13% (41/313). Two risk factors were independently associated with cholestasis: treatment with at least one IUT (OR 5.81, 95% CI 1.70-19.80, p = 0.005) and rhesus D type of alloimmunization (OR 4.66, 95% CI 1.05-20.57, p = 0.042). Additional diagnostic tests to investigate possible causes of cholestasis were all negative. In 5 infants (12%), supportive medical and nutritional therapy was started, and one neonate required iron chelation therapy.

CONCLUSION

Cholestasis occurs in 13% of neonates with HDN due to red cell alloimmunization, and it is independently associated with IUT treatment and rhesus D type of alloimmunization.

摘要

背景

新生儿溶血病(HDN)导致的胆汁淤积性肝病的病因与宫内红细胞输注(IUT)引起的铁过载有关。关于新生儿溶血病患儿胆汁淤积的发生率和严重程度的数据很少,对其发病机制、危险因素、新生儿管理和结局知之甚少。

目的

评估红细胞同种免疫性溶血病新生儿胆汁淤积的发生率、危险因素、处理方法和结局。

方法

本观察性研究纳入了 2000 年 1 月至 2010 年 7 月期间因红细胞同种免疫而入住我院的所有(近)足月 HDN 患儿。新生儿期常规进行肝功能检查(包括结合胆红素)。我们记录了胆汁淤积的存在,调查了一些潜在的危险因素,并评估了受累新生儿的处理方法和结局。

结果

共纳入 313 例接受或未接受 IUT 治疗的红细胞同种免疫性溶血病患儿。胆汁淤积的发生率为 13%(41/313)。两个危险因素与胆汁淤积独立相关:至少接受一次 IUT 治疗(OR 5.81,95%CI 1.70-19.80,p = 0.005)和 RhD 型同种免疫(OR 4.66,95%CI 1.05-20.57,p = 0.042)。进行了额外的诊断性检查以调查胆汁淤积的可能原因,但均为阴性。5 例患儿(12%)接受了支持性的医疗和营养治疗,1 例患儿需要铁螯合治疗。

结论

红细胞同种免疫性溶血病导致的新生儿胆汁淤积发生率为 13%,与 IUT 治疗和 RhD 型同种免疫独立相关。

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