Role of high-volume plasmapheresis in the management of paediatric acute liver failure

被引:0
|
作者
Hilberath, Johannes [1 ]
Camelli, Vittoria [1 ,2 ]
Hofer, Christiane [3 ]
Hartleif, Steffen [1 ]
Nadalin, Silvio [4 ]
Peters, Maren [4 ]
Kumpf, Matthias [3 ]
Bevot, Andrea [5 ]
Zirngibl, Matthias [6 ]
Weitz, Marcus [6 ]
Sturm, Ekkehard [1 ]
机构
[1] Univ Childrens Hosp Tubingen, Paediat Gastroenterol & Hepatol, Hoppe Seyler Str 1, D-72076 Tubingen, Germany
[2] Osped Infantile Regina Margherita, SSD Paediat Gastroenterol, Turin, Italy
[3] Univ Childrens Hosp Tubingen, Paediat Cardiol & Intens Care, Tubingen, Germany
[4] Univ Hosp Tubingen, Gen Visceral & Transplant Surg, Tubingen, Germany
[5] Univ Childrens Hosp Tubingen, Paediat Neurol, Tubingen, Germany
[6] Univ Childrens Hosp Tubingen, Paediat Nephrol, Tubingen, Germany
关键词
extracorporeal liver support; hepatic regeneration; HVP; PALF; plasma exchange; PLASMA-EXCHANGE; CHILDREN; OUTCOMES; THERAPY; DISEASE; SYSTEM;
D O I
10.1002/jpn3.12211
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
ObjectivesPaediatric acute liver failure (PALF) is a life-threatening disease. Management aims to support hepatic regeneration or to bridge to liver transplantation. High-volume plasmapheresis (HVP) removes protein-bound substances, alleviates inflammation, and improves survival in adult acute liver failure. However, experience with HVP in PALF is limited. Aim of this study is to report on feasibility, safety, efficacy and outcomes of HVP in PALF. MethodsRetrospective observational study in children with PALF. HVP was performed upon identification of negative prognostic indicators, in toxic aetiology or multiorgan failure (MOF). Exchanged volume with fresh-frozen plasma corresponded to 1.5-2.0 times the patient's estimated plasma volume. One daily cycle was performed until the patient met criteria for discontinuation, that is, liver regeneration, liver transplantation, or death. ResultsTwenty-two children with PALF (body weight 2.5-106 kg) received 1-7 HVP cycles. No bleeding or procedure-related mortality occurred. Alkalosis, hypothermia and reduction in platelets were observed. Haemolysis led to HVP termination in one infant. Seven children (32%) survived with their native livers, 13 patients (59%) underwent liver transplantation. Two infants died due to MOF. Overall survival was 86%. International normalization ratio (INR), alanine aminotransaminases (ALT), bilirubin and inotropic support were reduced significantly (p < 0.05) after the first HVP-cycle (median): INR 2.85 versus 1.5; ALT 1280 versus 434 U/L; bilirubin 12.7 versus 6.7 mg/dL; norepinephrine dosage 0.083 versus 0.009 mu g/kg/min. Median soluble-interleukin-2-receptor dropped significantly following HVP (n = 7): 2407 versus 950 U/mL (p < 0.02). ConclusionsHVP in PALF is feasible, safe, improves markers of liver failure and inflammation and is associated with lowering inotropic support. Prospective and controlled studies are required to confirm efficacy of HVP in PALF.
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页码:1364 / 1373
页数:10
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