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An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil
BACKGROUND: Subcutaneous treprostinil is a prostacyclin analogue used to treat pulmonary arterial hypertension (PAH). Due to local pain it can cause a deterioration of heart related quality of life (HRQoL) or even abandonment of treatment. The aim of this paper was to assess the feasibility of treat...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712081/ https://www.ncbi.nlm.nih.gov/pubmed/29195500 http://dx.doi.org/10.1186/s12890-017-0474-7 |
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author | Kurzyna, Marcin Małaczyńska-Rajpold, Katarzyna Koteja, Andrzej Pawlak, Agnieszka Chrzanowski, Łukasz Furdal, Michał Gąsior, Zbigniew Jacheć, Wojciech Sobkowicz, Bożena Norwa, Justyna Mularek-Kubzdela, Tatiana Torbicki, Adam |
author_facet | Kurzyna, Marcin Małaczyńska-Rajpold, Katarzyna Koteja, Andrzej Pawlak, Agnieszka Chrzanowski, Łukasz Furdal, Michał Gąsior, Zbigniew Jacheć, Wojciech Sobkowicz, Bożena Norwa, Justyna Mularek-Kubzdela, Tatiana Torbicki, Adam |
author_sort | Kurzyna, Marcin |
collection | PubMed |
description | BACKGROUND: Subcutaneous treprostinil is a prostacyclin analogue used to treat pulmonary arterial hypertension (PAH). Due to local pain it can cause a deterioration of heart related quality of life (HRQoL) or even abandonment of treatment. The aim of this paper was to assess the feasibility of treatment with intravenous treprostinil administered by means of the Lenus Pro® implantable pump. METHODS: This was a retrospective, multi-center study involving 12 patients (8 females) with PAH treated with a subcutaneous infusion of treprostinil with intolerable pain at the infusion site. Clinical evaluation, including HRQoL assessment with SF-36 questionnaire was performed, before pump implantation and 2–9 months after. The median time of follow-up time was 14 months (4–29 months). RESULTS: After implantation of the Lenus Pro® pump, no statistically significant changes were observed in the 6-min walking distance and NT-proBNP. After implantation 50% of patients were in II WHO functional class (33% before, p = 0,59). There was a significant improvement in HRQoL within the Physical Component Score (28 ± 7 vs 38 ± 8 pts., p < 0,001) and in specific domains of SF-36 form: physical role (31 ± 7 pts. vs. 41 ± 12 pts., p = 0,03), bodily pain (31 ± 12 vs. 50 ± 14 pts., p = 0,02), and vitality (37 ± 8 pts. vs. 50 ± 14 pts., p = 0,03). During the periprocedural period, one patient developed a recurrent haematoma at the implantation site. During follow-up in one patient, the drug delivering cannula slipped out of the subclavian vein, what required repositioning repeated twice, and in another patient an unexpected increase in the drug administration rate was observed. CONCLUSIONS: In patients with PAH who do not tolerate subcutaneous infusion of treprostinil, the use of the Lenus Pro® implantable pump results in significant subjective improvement of vitality and physical aspect of the HRQoL with acceptable safety profile. |
format | Online Article Text |
id | pubmed-5712081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57120812017-12-06 An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil Kurzyna, Marcin Małaczyńska-Rajpold, Katarzyna Koteja, Andrzej Pawlak, Agnieszka Chrzanowski, Łukasz Furdal, Michał Gąsior, Zbigniew Jacheć, Wojciech Sobkowicz, Bożena Norwa, Justyna Mularek-Kubzdela, Tatiana Torbicki, Adam BMC Pulm Med Research Article BACKGROUND: Subcutaneous treprostinil is a prostacyclin analogue used to treat pulmonary arterial hypertension (PAH). Due to local pain it can cause a deterioration of heart related quality of life (HRQoL) or even abandonment of treatment. The aim of this paper was to assess the feasibility of treatment with intravenous treprostinil administered by means of the Lenus Pro® implantable pump. METHODS: This was a retrospective, multi-center study involving 12 patients (8 females) with PAH treated with a subcutaneous infusion of treprostinil with intolerable pain at the infusion site. Clinical evaluation, including HRQoL assessment with SF-36 questionnaire was performed, before pump implantation and 2–9 months after. The median time of follow-up time was 14 months (4–29 months). RESULTS: After implantation of the Lenus Pro® pump, no statistically significant changes were observed in the 6-min walking distance and NT-proBNP. After implantation 50% of patients were in II WHO functional class (33% before, p = 0,59). There was a significant improvement in HRQoL within the Physical Component Score (28 ± 7 vs 38 ± 8 pts., p < 0,001) and in specific domains of SF-36 form: physical role (31 ± 7 pts. vs. 41 ± 12 pts., p = 0,03), bodily pain (31 ± 12 vs. 50 ± 14 pts., p = 0,02), and vitality (37 ± 8 pts. vs. 50 ± 14 pts., p = 0,03). During the periprocedural period, one patient developed a recurrent haematoma at the implantation site. During follow-up in one patient, the drug delivering cannula slipped out of the subclavian vein, what required repositioning repeated twice, and in another patient an unexpected increase in the drug administration rate was observed. CONCLUSIONS: In patients with PAH who do not tolerate subcutaneous infusion of treprostinil, the use of the Lenus Pro® implantable pump results in significant subjective improvement of vitality and physical aspect of the HRQoL with acceptable safety profile. BioMed Central 2017-12-02 /pmc/articles/PMC5712081/ /pubmed/29195500 http://dx.doi.org/10.1186/s12890-017-0474-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kurzyna, Marcin Małaczyńska-Rajpold, Katarzyna Koteja, Andrzej Pawlak, Agnieszka Chrzanowski, Łukasz Furdal, Michał Gąsior, Zbigniew Jacheć, Wojciech Sobkowicz, Bożena Norwa, Justyna Mularek-Kubzdela, Tatiana Torbicki, Adam An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil |
title | An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil |
title_full | An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil |
title_fullStr | An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil |
title_full_unstemmed | An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil |
title_short | An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil |
title_sort | implantable pump lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712081/ https://www.ncbi.nlm.nih.gov/pubmed/29195500 http://dx.doi.org/10.1186/s12890-017-0474-7 |
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