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Neonatal Portal Vein Thrombosis: Risk Factors, Diagnosis, Treatment Recommendations and Review of the Literature

Overview
Journal Thromb J
Publisher Biomed Central
Date 2023 Jun 4
PMID 37271816
Authors
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Abstract

Background: Neonatal portal vein thrombosis (PVT) is currently more commonly encountered as a result of advances in diagnostic tools and increase in invasive interventions.

Methods: In this study, 11 premature and 12 term infants diagnosed with PVT were retrospectively evaluated for clinical and laboratory characteristics, umbilical catheterization procedure, PVT location, risk factors, treatments, and long-term outcomes.

Results: Median age of the patients at diagnosis was 10 days (range 3-90 days), and 69.6% of patients were girls. Of the 23 patients, 87% had left PVT and, 91.3% had at least one thrombosis risk factor, which was sepsis in 73.9% of patients, and presence of umbilical venous catheter in 87%. Totally, 59.1% of PVTs were completely resolved in a median follow-up of 7 months (1 month to 12 months), and 78.3% of these patients had no anticoagulant therapy (ACT). Partial thrombus resolution was achieved in 9 patients (40.9%). Five patients (%21) received ACT. Overall, 34.8% of patients had long-term complications. neonatal PVT is most commonly reported in the left portal vein and there is no evidence for the impact of ACT on reducing the short- or long-term complications. Well designed and larger studies are necessary to clarify this issue, which can facilitate developing appropriate management algorithms.

Conclusion: Neonatal PVT is most commonly reported in the left portal vein and there is no evidence for the impact of ACT on reducing the short- or long-term complications. Well designed and larger studies are necessary to clarify this issue, which can facilitate developing appropriate management algorithms.

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References
1.
Ferri P, Ferreira A, Fagundes E, Xavier S, Ribeiro D, Fernandes A . Evaluation of the presence of hereditary and acquired thrombophilias in Brazilian children and adolescents with diagnoses of portal vein thrombosis. J Pediatr Gastroenterol Nutr. 2012; 55(5):599-604. DOI: 10.1097/MPG.0b013e318261814d. View

2.
Rios-Mendez R, Gimenez P . [Intracardiac persistence of pericatheter fibrin sheath in a newborn: case report]. Arch Argent Pediatr. 2014; 112(1):e9-e12. DOI: 10.5546/aap.2014.e9. View

3.
Wells P, Owen C, Doucette S, Fergusson D, Tran H . Does this patient have deep vein thrombosis?. JAMA. 2006; 295(2):199-207. DOI: 10.1001/jama.295.2.199. View

4.
Sethi S, Dewan P, Faridi M, Aggarwal A, Upreti L . Liver abscess, portal vein thrombosis and cavernoma formation following umbilical vein catherisation in two neonates. Trop Gastroenterol. 2007; 28(2):79-80. View

5.
Morag I, Shah P, Epelman M, Daneman A, Strauss T, Moore A . Childhood outcomes of neonates diagnosed with portal vein thrombosis. J Paediatr Child Health. 2011; 47(6):356-60. DOI: 10.1111/j.1440-1754.2010.01987.x. View