A prospective, multicentre study in acute non-cirrhotic, non-malignant portal vein thrombosis: comparison of medical and interventional treatment.


Journal

Alimentary pharmacology & therapeutics
ISSN: 1365-2036
Titre abrégé: Aliment Pharmacol Ther
Pays: England
ID NLM: 8707234

Informations de publication

Date de publication:
07 2020
Historique:
received: 02 04 2020
revised: 15 04 2020
accepted: 04 05 2020
pubmed: 9 6 2020
medline: 11 11 2020
entrez: 8 6 2020
Statut: ppublish

Résumé

To evaluate medical versus interventional treatment (transjugular thrombus fragmentation, local thrombolysis with or without stent implantation) in patients with acute non-cirrhotic, non-malignant portal vein thrombosis (PVT). This prospective, observational study enrolled 65 patients with acute (<28 days since begin of symptoms, no cavernoma) PVT in nine centres. Thirty patients received medical treatment and 35 patients received interventional treatment. PVT was graded into grade 1: short thrombosis and incomplete occlusion of the vessel lumen and grade 2: extended thrombosis or complete occlusion. Treatment response was classified as partial or complete, if thrombosis was reduced by one grade or to <25% of the vessel diameter respectively. Partial and complete response rates were 7% and 30% in the medical compared to 17% and 54% (P < 0.001) in the interventional treatment group. In the multivariate analysis, interventional treatment showed a strong positive (OR 4.32, P < 0.016) and a myeloproliferative aetiology a negative (OR 0.09, P = 0.006) prediction of complete response. Complications were rare in the medical group and consisted of septicaemia and upper gastrointestinal bleeding of unknown origin in one patient each. Interventional treatment was accompanied by mild and self-limiting bleeding complications in nine patients, moderate intra-abdominal bleeding requiring transfusions (2 units) in one patient and peritoneal bleeding requiring surgical rescue in one patient. Four patients in each group developed intestinal gangrene requiring surgery. One patient died 52 days after unsuccessful interventional treatment. Compared to medical treatment alone, interventional treatment doubled response rates at the cost of increased bleeding complications.

Sections du résumé

BACKGROUND
To evaluate medical versus interventional treatment (transjugular thrombus fragmentation, local thrombolysis with or without stent implantation) in patients with acute non-cirrhotic, non-malignant portal vein thrombosis (PVT).
METHODS
This prospective, observational study enrolled 65 patients with acute (<28 days since begin of symptoms, no cavernoma) PVT in nine centres. Thirty patients received medical treatment and 35 patients received interventional treatment. PVT was graded into grade 1: short thrombosis and incomplete occlusion of the vessel lumen and grade 2: extended thrombosis or complete occlusion. Treatment response was classified as partial or complete, if thrombosis was reduced by one grade or to <25% of the vessel diameter respectively.
RESULTS
Partial and complete response rates were 7% and 30% in the medical compared to 17% and 54% (P < 0.001) in the interventional treatment group. In the multivariate analysis, interventional treatment showed a strong positive (OR 4.32, P < 0.016) and a myeloproliferative aetiology a negative (OR 0.09, P = 0.006) prediction of complete response. Complications were rare in the medical group and consisted of septicaemia and upper gastrointestinal bleeding of unknown origin in one patient each. Interventional treatment was accompanied by mild and self-limiting bleeding complications in nine patients, moderate intra-abdominal bleeding requiring transfusions (2 units) in one patient and peritoneal bleeding requiring surgical rescue in one patient. Four patients in each group developed intestinal gangrene requiring surgery. One patient died 52 days after unsuccessful interventional treatment.
CONCLUSIONS
Compared to medical treatment alone, interventional treatment doubled response rates at the cost of increased bleeding complications.

Identifiants

pubmed: 32506456
doi: 10.1111/apt.15811
doi:

Substances chimiques

Anticoagulants 0
Phenprocoumon Q08SIO485D

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

329-339

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 The Authors. Alimentary Pharmacology & Therapeutics published byJohn Wiley & Sons Ltd.

Références

Ögren M, Bergqvist D, Björck M, et al. Portal vein thrombosis: prevalence, patient characteristics and lifetime risk: a population study based on 23796 consecutive autopsies. World J Gastroenterol. 2006;12:2115-2119
Rajani R, Björnsson E, Bergquist A, et al. The epidemiology and clinical features of portal vein thrombosis: a mulicentre study. Aliment Pharmacol Ther. 2010;32:1154-1162
Deleve LD, Valla DC, Garcia-Tsao G. Vascular disorders of the liver. Hepatology. 2009;49:1729-1764
European Association for the Study of the Liver. Clinical practice guidelines: vascular diseases of the liver. J Hepatol. 2016;64:179-202
Tait C, Baglin T, Watson H, et al. Guidelines on the investigation and management of venous thrombosis at unusual sites. Br J Haematol. 2012;159:28-38
Martín-Llahí M, Albillos A, Bañares R, et al. Vascular diseases of the liver. Clinical Guidelines from the Catalan Society of Digestology and the Spanish Association for the Study of the Liver. Gastroenterol Hepatol. 2017;40:538-580
De Gaetano AM, Lafortune M, Patriquin H, et al. Cavernous transformation of the portal vein: patterns of intrahepatic and splanchnic collateral circulation detected with Doppler sonography. Am J Roentgenol. 1995;165:1151-1155
Noronha Ferreira C, Seijo S, Plessier A, et al. Natural history and management of esophagogastric varices in chronic noncirrhotic, nontumoral portal vein thrombosis. Hepatology. 2016;63:1640-1650
Chen H, He C, Lv Y, et al. Long-term results of variceal bleeding management in 302 patients with extrahepatic portal vein obstruction. J Gastroenterol Hepatol. 2019. https://doi.org/10.1111/jgh.14902 [Epub ahead of print].
Fanelli F, Angeloni S, Salvatori FM, et al. Transjugular intrahepatic portosystemic shunt with expanded-polyteratfluoroethylene-covered stents in non-cirrhotic patients with portal cavernoma. Dig Liver Dis. 2011;43:78-84
Klinger C, Riecken B, Schmidt A, et al. Transjugular portal vein recanalization with creation of intrahepatic portosystemic shunt (PVR-TIPSS) in patients with chronic non-cirrhotic, non-malignant portal vein thrombosis. Z Gastroenterol. 2018;56:221-237
Qi X, Han G, Yin Z, et al. Transjigular intrahepatic portosystemic shunt for portal cavernoma with symptomatic portal hypertension in non-cirrhotic patients. Dig Dis Sci. 2012;57:1072-1082
Senzolo M, Patch D, Cholongitas E, et al. Transjugular intrahepatic portosystemic shunt for portal vein thrombosis with and without underlying cirrhosis. Cardiovasc Intervent Radiol. 2007;30:545
Luo X, Nie L, Zhou B, et al. Transjugular intrahepatic portosystemic shunt for the treatment of portal hypertension in noncirrhotic patients with portal cavernoma. Gastroenterol Res Pract. 2014;2014:659726
Bilbao JI, Elorz M, Viva I, et al. Transjugular intrahepatic portosystemic shunt (TIPSS) in the treatment of venous symptomatic chronic portal thrombosis in non-cirrhotic patients. Cardiovasc Intervent Radiol. 2004;27:474-480
Rössle M. TIPSS: 25 years later. J Hepatol. 2013;59:1081-1093
Dindo D, Demartines N, Clavien PA. Classification of surgical complications. A new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240:205-213
Hollingshead M, Burke CT, Mauro MA, et al. Transcatheter thrombolytic therapy for acute mesenteric and portal vein thrombosis. J Vasc Interv Radiol. 2005;16:651-661
Malkowski P, Pawlak J, Michalowicz B, et al. Thrombolytic treatment of portal thrombosis. Hepatogastroenterology. 2003;50:2098-2100
Grisham A, Lohr J, Guenther JM, et al. Deciphering mesenteric venous thrombosis: imaging and treatment. Vasc Endovascular Surg. 2005;39:473-479
Smalberg JH, Spaander MVMCW, Jie K-S, et al. Risks and benefits of transcatheter thrombolytic therapy in patients with splanchnic venous thrombosis. Thromb Haemost. 2008;100:1084-1088
Ferro C, Rossi UG, Bovio G, et al. Transjugular intrahepatic portosystemic shunt, mechanical aspiration thrombectomy, and direct thrombolysis in the treatment of acute portal and superior mesenteric vein thrombosis. Cardiovasc Intervent Radiol. 2007;30:1070-1074
Wang C-Y, Wei L-Q, Niu H-Z, et al. Agitation thrombolysis combined with catheter-directed thrombolysis for the treatment of non-cirrhotic acute portal vein thrombosis. World J Gastroenterol. 2018;24:4482-4488
Rosenqvist K, Ebeling Barbier C, Rorsman F, Sangfelt P, Nyman R. Treatment of acute portomesenteric venous thrombosis with thrombectomy through a transjugular intrahepatic portosystemic shunt: a single-centre experience. Acta Radiol. 2018;59:953-958
Wang MQ, Liu FY, Duan F, et al. Acute symptomatic mesenteric venous thrombosis: treatment by catheter-directed thrombolysis with transjugular intrahepatic route. Abdom Imaging. 2011;36:390-398
Liu FY, Wang MQ, Duan F, Wang ZJ, Song P. Interventional therapy for symptomatic-benign portal vein occlusion. Hepatogastroenterology. 2010;57:1367-1374
Gerwing M, Wilms C, Heinzow H, et al. Escalating interventional recanalization therapy in non-cirrhotic, non-malignant acute portal vein thrombosis. Eur J Gastroenterol Hepatol. 2019;31:1584-1591
Klinger C, Riecken B, Schmidt A, et al. Transjugular local thrombolysis with/without TIPSS in patients with acute non-cirrhotic, non-malignant portal vein thrombosis. Dig Liver Dis. 2017;49:1345-1352
Rodrigues SG, Sixt S, Abraldes JG, et al. Systematic review with meta-analysis: portal vein recanalization and transjugular intrahepatic portosystemic shunt for portal vein thrombosis. Aliment Pharmacol Ther. 2019;49:20-30
Turnes J, García-Pagán JC, González M, et al. Portal hypertension-related complications after acute portal vein thrombosis: impact of early anticoagulation. Clin Gastroenterol Hepatol. 2008;6:1412-1417
Plessier A, Darwish-Murad S, Hernandez-Guerra M, et al. Acute portal vein thrombosis unrelated to cirrhosis: a prospective multicentre follow-up study. Hepatology. 2010;51:210-218
Hall TC, Garcea G, Metcalfe M, et al. Management of acute non-cirrhotic and non-malignant portal vein thrombosis: a systematic review. World J Surg. 2011;35:2510-2520
De Gottardi A, Trebicka J, Klinger C, et al. Antithrombotic treatment with direct-acting oral anticoagulants in patients with splanchnic vein thrombosis and cirrhosis. Liver Int. 2017;37:694-699
Priyanka P, Kupec JT, Krafft M, et al. Newer oral anticoagulants in the treatment of acute portal vein thrombosis in patients with and without cirrhosis. Int J Hepatol. 2018;2018:8432781
Hanafy AS, Abd-Elsalam S, Dawoud MM. Randomized controlled trial of rivaroxaban versus warfarin in the management of acute non-neoplastic portal vein thrombosis. Vascul Pharmacol. 2019;113:86-91
Qi X, Guo X. An early decision of transjugular intrahepatic portosystemic shunt may be considered for non-malignant and non-cirrhotic portal vein thrombosis with ascites: a concise review of the theoretical possibility and practical difficulty. Arch Med Sci. 2016;12:1381-1383
Webb IJ, Sherlock S. The aetiology, presentation and natural history of extra-hepatic portal venous obstruction. Q J Med. 1979;48:627-639
Orr DW, Harrison PM, Devlin J, et al. Chronic mesenteric venous thrombosis: evaluation and determinants of survival during long-term follow-up. Clin Gastroenterol Hepatol. 2007;5:80-86
Borgel D, Bianchini E, Lasne D, Pascreau T, Saller F. Inflammation in deep vein thrombosis: a therapeutic target? Hematology. 2019;24:742-750
Mosevoll KA, Lindås R, Tvedt TA, Bruserud Ø, Reikvam H. Altered plasma levels of cytokines, soluble adhesion molecules and matrix metalloproteases in venous thrombosis. Thromb Res. 2015;136:30-39
Gremmel T, Ay C, Seidinger D, et al. Soluble p-selectin, D-dimer, and high-sensitivity C-reactive protein after acute deep vein thrombosis of the lower limb. J Vasc Surg. 2011;54:48S-55S
Rabinovich A, Cohen JM, Cushman M, et al. Inflammation markers and their trajectories after deep vein thrombosis in relation to risk of post-thrombotic syndrome. J Thromb Haemost. 2015;13:398-408
Sarin SK, Philips CA, Kamath PS, et al. Toward a comprehensive new classification of portal vein thrombosis in patients with cirrhosis. Gastroenterology. 2016;151:574-577
Stieber AC, Zetti G, Todo S, et al. The spectrum of portal vein thrombosis in liver transplantation. Ann Surg. 1991;213:199-206
Nonami T, Yokoyama I, Iwatsuki S, et al. The incidence of portal vein thrombosis at liver transplantation. Hepatology. 1992;16:1195-1198
Yerdel MA, Gunson B, Mirza D, et al. Portal vein thrombosis in adults undergoing liver transplantation: risk factors, screening, management, and outcome. Transplantation. 2000;69:1873-1881
Ma J, Yan Z, Luo J, et al. Rational classification of portal vein thrombosis and its clinical significance. PLoS ONE. 2014;9:e112501
Jamieson NV. Changing perspectives in portal vein thrombosis and liver transplantation. Transplantation. 2000;69:1772-1774
Bauer J, Johnson S, Durham J, et al. The role of TIPSS for portal vein patency in liver transplant patients with portal vein thrombosis. Liver Transpl. 2006;12:1544-1551
De Franchis R. Revising consensus in portal hypertension: report of the Baveno V consensus workshop on methodology of diagnosis and therapy in portal hypertension. J Hepatol. 2010;53:762-768
Qi X, Han G, Wang J, Wu K, Fan D. Degree of portal vein thrombosis. Hepatology. 2010;51:1089-1090

Auteurs

Jonel Trebicka (J)

Bonn, Germany.
Frankfurt am Main, Germany.

Christoph Klinger (C)

Ludwigsburg, Germany.

Lukas Sturm (L)

Freiburg, Germany.

Karel Caca (K)

Ludwigsburg, Germany.

Victoria Therese Mücke (VT)

Frankfurt am Main, Germany.

Klaus Radecke (K)

Saarbrücken, Germany.

Cornelius Engelmann (C)

Leipzig, Germany.

Alexander Zipprich (A)

Halle (Saale), Germany.

Hauke Heinzow (H)

Münster, Germany.

Carsten Meyer (C)

Bonn, Germany.

Ulrich Tappe (U)

Hamm, Germany.

Beate Appenrodt (B)

Homburg, Germany.

Arthur Schmidt (A)

Freiburg, Germany.

Christian Lange (C)

Frankfurt am Main, Germany.
Essen, Germany.

Stefan Zeuzem (S)

Frankfurt am Main, Germany.

Daniel Grandt (D)

Saarbrücken, Germany.

Hartmut Schmidt (H)

Münster, Germany.

Joachim Moessner (J)

Leipzig, Germany.

Thomas Berg (T)

Leipzig, Germany.

Frank Lammert (F)

Homburg, Germany.

Robert Thimme (R)

Freiburg, Germany.

Michael Schultheiß (M)

Freiburg, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH