Literature DB >> 22227513

Epoprostenol-induced hypersplenism in portopulmonary hypertension.

Waseem Touma1, Ravi P Nayak, Zulfiqar Hussain, Bruce R Bacon, Ganesh C Kudva.   

Abstract

Portopulmonary hypertension (POPH) is a not infrequent but serious complication of liver cirrhosis. Continuous intravenous epoprostenol infusion is a treatment option for this condition. Progressive splenomegaly with pancytopenia (hypersplenism) is associated with epoprostenol use in POPH. After recognizing a case of epoprostenol-induced hypersplenism that resolved upon stopping the drug, the authors retrospectively reviewed all patients treated with epoprostenol at the center for both POPH and pulmonary hypertension due to other causes. Five of 11 patients with POPH developed hypersplenism secondary to epoprostenol. In 1 patient, and possibly in a second, the hypersplenism resolved upon discontinuation of epoprostenol. None of 9 patients with pulmonary hypertension due to other causes developed splenomegaly. This report confirms hypersplenism as a complication of epoprostenol therapy for POPH. Furthermore, the authors demonstrate for the first time that hypersplenism may be reversed by stopping the medication and propose a mechanism for this phenomenon.

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Year:  2012        PMID: 22227513     DOI: 10.1097/MAJ.0b013e31824184b1

Source DB:  PubMed          Journal:  Am J Med Sci        ISSN: 0002-9629            Impact factor:   2.378


  7 in total

1.  Intra-abdominal bleeding during treprostinil infusion in a patient with pulmonary arterial hypertension.

Authors:  Stephanie Mindus; Jacek Pawlowski; Magnus Nisell; Giovanni Ferrara
Journal:  BMJ Case Rep       Date:  2013-02-27

Review 2.  Pulmonary vascular complications of liver disease.

Authors:  Jason S Fritz; Michael B Fallon; Steven M Kawut
Journal:  Am J Respir Crit Care Med       Date:  2012-11-15       Impact factor: 21.405

Review 3.  Current Approach to the Diagnosis and Management of Portopulmonary Hypertension.

Authors:  Lynn A Fussner; Michael J Krowka
Journal:  Curr Gastroenterol Rep       Date:  2016-06

Review 4.  Effect of PAH specific therapy on pulmonary hemodynamics and six-minute walk distance in portopulmonary hypertension: a systematic review and meta-analysis.

Authors:  Muhammad Faisal; Furqan Siddiqi; Ahmad Alkaddour; Abubakr A Bajwa; Adil Shujaat
Journal:  Pulm Med       Date:  2014-11-16

5.  Portopulmonary hypertension in children: a rare but potentially lethal and under-recognized disease.

Authors:  Jennifer Tingo; Erika B Rosenzweig; Steven Lobritto; Usha S Krishnan
Journal:  Pulm Circ       Date:  2017-07-31       Impact factor: 3.017

Review 6.  Pulmonary manifestations of chronic liver disease: a comprehensive review.

Authors:  Stergios Soulaidopoulos; Ioannis Goulis; Evangelos Cholongitas
Journal:  Ann Gastroenterol       Date:  2020-03-27

7.  The clinical characteristics, treatment, and survival of portopulmonary hypertension in Japan.

Authors:  Yukiko Takahashi; Keiko Yamamoto; Seiichiro Sakao; Takao Takeuchi; Rika Suda; Nobuhiro Tanabe; Koichiro Tatsumi
Journal:  BMC Pulm Med       Date:  2021-03-16       Impact factor: 3.317

  7 in total

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