Department of Gastroenterology, Hepatology and Liver Transplant, Queensland Children's Hospital, 501, Stanley Street, South Brisbane, Queensland, 4101, Australia.
Department of Pediatric Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Raebareli Road, Lucknow, 226014, India.
Indian J Pediatr. 2024 Mar;91(3):270-279. doi: 10.1007/s12098-023-04596-8. Epub 2023 Jun 13.
Development of ascites in children with chronic liver disease is the most common form of decompensation. It is associated with a poor prognosis and increased risk of mortality. A diagnostic paracentesis should be performed in liver disease patients with- new-onset ascites, at the beginning of each hospital admission and when ascitic fluid infection (AFI) is suspected. The routine analysis includes cell count with differential, bacterial culture, ascitic fluid total protein and albumin. A serum albumin-ascitic fluid albumin gradient of ≥1.1 g/dL confirms the diagnosis of portal hypertension. Ascites has been reported in children with non-cirrhotic liver disease like acute viral hepatitis, acute liver failure and extrahepatic portal venous obstruction. The main steps in management of cirrhotic ascites include dietary sodium restriction, diuretics and large-volume paracentesis. Sodium should be restricted to maximum of 2 mEq/kg/d (max 90 mEq/d) of sodium/day. Oral diuretic therapy comprises of aldosterone antagonists (e.g., spironolactone) with or without loop-diuretics (e.g., furosemide). Once the ascites is mobilized, the diuretics should be gradually tapered to the minimum effective dosage. Tense ascites should be managed with a large-volume paracentesis (LVP) preferably with albumin infusion. Therapeutic options for refractory ascites include recurrent LVP, transjugular intrahepatic porto-systemic shunt and liver transplantation. AFI (fluid neutrophil count ≥250/mm) is an important complication, and requires prompt antibiotic therapy. Hyponatremia, acute kidney injury, hepatic hydrothorax and hernias are the other complications.
儿童慢性肝病并发腹水是最常见的失代偿形式。它与预后不良和死亡率增加有关。对于新发腹水、每次住院开始时以及怀疑腹水感染(AFI)时,应在肝病患者中进行诊断性腹腔穿刺。常规分析包括细胞计数和分类、细菌培养、腹水总蛋白和白蛋白。血清白蛋白-腹水白蛋白梯度≥1.1 g/dL 可确诊门静脉高压。非肝硬化性肝病患儿也会发生腹水,如急性病毒性肝炎、急性肝衰竭和肝外门静脉高压。肝硬化腹水管理的主要步骤包括限制饮食中的钠摄入、使用利尿剂和大量腹腔穿刺术。钠摄入量应限制在每天最大 2 mEq/kg/d(最大 90 mEq/d)。口服利尿剂治疗包括醛固酮拮抗剂(如螺内酯)联合或不联合袢利尿剂(如呋塞米)。一旦腹水被动员,利尿剂应逐渐减少至最低有效剂量。张力性腹水应通过大量腹腔穿刺术(LVP)进行管理,最好同时输注白蛋白。难治性腹水的治疗选择包括反复 LVP、经颈静脉肝内门体分流术和肝移植。腹水感染(液体中性粒细胞计数≥250/mm)是一种重要的并发症,需要及时进行抗生素治疗。低钠血症、急性肾损伤、肝性胸水和疝是其他并发症。