An implantable pump Lenus pro® in the treatment of pulmonary arterial hypertension with intravenous treprostinil

被引:20
作者
Kurzyna, Marcin [1 ]
Malaczynska-Rajpold, Katarzyna [2 ]
Koteja, Andrzej [3 ]
Pawlak, Agnieszka [4 ]
Chrzanowski, Lukasz [5 ]
Furdal, Michal [6 ]
Gasior, Zbigniew [7 ]
Jachec, Wojciech [8 ]
Sobkowicz, Bozena [9 ]
Norwa, Justyna [1 ]
Mularek-Kubzdela, Tatiana [2 ]
Torbicki, Adam [1 ]
机构
[1] European Hlth Ctr Otwock, Dept Pulm Circulat Thromboembol Dis & Cardiol, Ctr Postgrad Med Educ, Borowa 14-18, PL-05400 Otwock, Poland
[2] Univ Med Sci, Dept Cardiol 1, Poznan, Poland
[3] European Hlth Ctr Otwock, Dept Anesthesiol & Intens Care, Otwock, Poland
[4] Minist Interior & Adm, Dept Invas Cardiol, Cent Clin Hosp, Warsaw, Poland
[5] Med Univ Lodz, Dept Cardiol, Lodz, Poland
[6] Prov Specialist Hosp Wroclaw, Dept Cardiol, Res & Dev Ctr, Wroclaw, Poland
[7] Med Univ Silesia, Dept Cardiol, SHS, Katowice, Poland
[8] Med Univ Silesia, Sch Med, Dept Cardiol 2, Dent Div, Zabrze, Poland
[9] Med Univ Bialystok, Dept Cardiol, Bialystok, Poland
关键词
Pulmonary arterial hypertension; Treprostinil; Implantable pump; Quality of life; SF-36; form; CONTINUOUS SUBCUTANEOUS INFUSION; RELEASE ORAL TREPROSTINIL; CONTROLLED-TRIAL; EFFICACY; PHARMACOKINETICS; THERAPY; SAFETY; SYSTEM; ANALOG; SF-36;
D O I
10.1186/s12890-017-0474-7
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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 (R) 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 (R) 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 (R) implantable pump results in significant subjective improvement of vitality and physical aspect of the HRQoL with acceptable safety profile.
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页数:8
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