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1.
Transplant Direct ; 6(10): e604, 2020 Oct.
Article in English | MEDLINE | ID: mdl-33134484

ABSTRACT

Our aim was to determine whether hyponatremia is associated with waiting list or posttransplantation mortality in children having liver transplantation (LT). METHODS: A retrospective analysis of the united network for organ sharing/organ procurement transplantation network database on pediatric LT performed between 1988 and 2016 was conducted. Hyponatremia was defined as a serum sodium of 130 mEq/L or below. Subjects were divided into 2 age groups: I (0-6 y old) and II (7-18 y old). Patient survival before and after LT, as well as graft survival, were compared in patients with and without hyponatremia. Multivariable Cox proportional hazards models were constructed for perioperative mortality. RESULTS: Data from 6606 children were available for analysis of waiting list mortality, and 4478 for postoperative mortality. The prevalence of hyponatremia at the time of registration was 2.8% and 3.7% at the time of LT. Waiting list mortality in patients with hyponatremia was significantly higher in group I (P < 0.001) but not in group II (P = 0.09). In group I, the relative risk of mortality adjusted to pediatric end-stage liver disease score was significantly associated with hyponatremia (P < 0.001). A sodium level below 130 mEq/L (hazard ration [HR] = 1.7), younger age (group I) (HR = 2.01), and need for dialysis (HR = 2.3) were independent predictors for increased waiting list mortality. There was no difference in overall postoperative patient or graft survival related to hyponatremia. CONCLUSIONS: Hyponatremia is associated with increased waiting list mortality for pediatric LT candidates, particularly in younger children. Future studies examining incorporation of age-specific serum sodium levels into organ allocation policies in children seems warranted based on our findings.

2.
Transplant Direct ; 4(11): e403, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30534594

ABSTRACT

In this review, we analyze the epidemiology of thromboses related to end-stage liver disease (ESLD), discuss causes of hypercoagulability, describe susceptible populations, and critically evaluate proposed prophylaxis and treatment of thromboses. Classically, ESLD has been regarded as a model for coagulopathy, and patients were deemed to be at high risk for bleeding complications. Patients with ESLD are not auto-anticoagulated, and they do not have a lower risk of portal vein thrombosis, intracardiac thrombus formation, pulmonary embolism or hepatic artery thrombosis. Though the cause of hypercoagulability is multifactorial, endothelial dysfunction likely plays a central role for all patients with ESLD. Some subpopulations, such as patients with nonalcoholic steatohepatitis and autoimmune conditions, are at increased risk of thrombotic events as are patients of Hispanic ethnicity. The science behind prophylaxis of different types of clotting and treatment of thromboses is developing rapidly. A number of medications, including low molecular weight heparin, unfractionated heparin, aspirin, vitamin K antagonists, and direct oral anticoagulants can be used, but clear guidelines are lacking. Acute intraoperative clotting can be associated with high mortality. Routine use of transesophageal echocardiography can be helpful in early recognition and treatment of intraoperative thrombosis. Heparin should be reserved for cases of intracardiac thrombus/pulmonary embolism without hemodynamic instability. In unstable patients, low dose of recombinant tissue plasminogen activator can be used. In this new era of heightened awareness of thrombotic events in ESLD patients, prospective randomized trials are urgently needed to best guide clinical practice.

3.
Transplantation ; 102(4): 578-592, 2018 04.
Article in English | MEDLINE | ID: mdl-29337842

ABSTRACT

We review contemporary coagulation management for patients undergoing liver transplantation. A better understanding of the complex physiologic changes that occur in patients with end-stage liver disease has resulted in significant advances in anesthetic and coagulation management. A group of internationally recognized experts have critically evaluated current approaches for coagulopathy detection and management. Strategies for blood component and factor replacement have been evaluated and recommended therapies proposed. Pharmacologic treatment and prevention of coagulopathy, management of patients receiving antiplatelet medications, and the role of transesophageal echocardiography for early detection and management of thromboses are presented.


Subject(s)
Anticoagulants/administration & dosage , Blood Coagulation/drug effects , Blood Loss, Surgical/prevention & control , Blood Transfusion/methods , End Stage Liver Disease/surgery , Liver Transplantation , Perioperative Care/methods , Postoperative Hemorrhage/prevention & control , Thrombosis/prevention & control , Animals , Anticoagulants/adverse effects , Blood Coagulation Tests , Drug Monitoring/methods , End Stage Liver Disease/blood , End Stage Liver Disease/diagnosis , Hemorrhage/chemically induced , Humans , Liver Transplantation/adverse effects , Postoperative Hemorrhage/blood , Postoperative Hemorrhage/etiology , Risk Factors , Thrombosis/blood , Thrombosis/diagnosis , Thrombosis/etiology , Treatment Outcome
4.
Ann Hepatol ; 12(1): 92-9, 2013.
Article in English | MEDLINE | ID: mdl-23293199

ABSTRACT

BACKGROUND: Combination therapy with terlipressin and albumin substitution is considered a widely accepted treatment regimen for patients with hepatorenal syndrome (HRS). However, only half of the patients respond to treatment and to date albumin substitution and terlipressin therapy are among the most expensive medical treatments available for patients with liver diseases. Thus, we aimed to identify clinical and etiological parameters to predict treatment response and overall mortality in patients with HRS. MATERIAL AND METHODS: We retrospectively evaluated 21 patients, 13 male/8 female, aged 43-72 years with HRS. Four patients were transplanted after following combination treatment. Terlipressin was administered by continuous intravenous perfusion (2-6 mg/d) and albumin drips (50 mg) were given daily. Treatment response was defined by a decrease in serum creatinine level to ≤ 1.5 mg/dL or by a ≥ 50% reduction of the baseline concentration. RESULTS: 57% of the patients responded to treatment, which was associated with improved survival at day 60, compared to non-responders. However, the overall mortality was not different between the two groups. Median age of 63 years was a significant negative predictor for therapy response. High baseline urinary sodium levels were of prognostic value for survival. The Model of End stage Liver Disease score (MELD score) did not correlate with therapy response. CONCLUSION: In conclusion high age is a predictor of non-response. Low urinary sodium before treatment is associated with poor survival. Terlipressin and albumin co-treatment is associated with increased two-months survival rate. This seemingly moderate extension in survival rate can, however, be decisive for obtaining liver transplantation.


Subject(s)
Albumins/therapeutic use , Hepatorenal Syndrome , Liver Cirrhosis , Lypressin/analogs & derivatives , Sodium/urine , Vasoconstrictor Agents/therapeutic use , Adult , Age Factors , Aged , Creatinine/blood , Drug Therapy, Combination , Female , Hepatorenal Syndrome/drug therapy , Hepatorenal Syndrome/mortality , Hepatorenal Syndrome/urine , Humans , Liver Cirrhosis/mortality , Liver Cirrhosis/urine , Lypressin/therapeutic use , Male , Middle Aged , Prognosis , Retrospective Studies , Severity of Illness Index , Terlipressin , Treatment Outcome
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