Incidence of Bloodstream Infection in Patients with Pulmonary Hypertension under Intravenous Epoprostenol or Iloprost-A Multicentre, Retrospective Study

被引:2
作者
Camara, Raquel Paulinetti [1 ,2 ]
Coelho, Francisco das Neves [1 ,3 ]
Cruz-Martins, Natalia [4 ,5 ,6 ,7 ]
Marques-Alves, Patricia [8 ]
Castro, Graca [8 ]
Baptista, Rui [9 ,10 ,11 ,12 ]
Ferreira, Filipa [1 ]
机构
[1] Hosp Garcia de Orta, Cardiol Dept, P-2805267 Almada, Portugal
[2] Hosp Nossa Senhora Rosario, Ctr Hosp Barreiro Montijo, Pulmonol Dept, P-2830003 Barreiro, Portugal
[3] Hosp Egas Moniz, Ctr Hosp Lisboa Ocidental, Polyvalent Intens Care Unit, P-1349019 Lisbon, Portugal
[4] Univ Porto, Fac Med, P-4099002 Porto, Portugal
[5] Univ Porto, Inst Res & Innovat Hlth i3S, P-4099002 Porto, Portugal
[6] Inst Res & Adv Training Hlth Sci & Technol CESPU, Rua Cent Gandra, P-4585116 Gandra, Portugal
[7] Univ Inst Hlth Sci, TOXRUN Toxicol Res Unit, CESPU, CRL, P-4585116 Gandra, Portugal
[8] Ctr Hosp & Univ Coimbra, Cardiol Dept, Pulm Vasc Dis Unit, P-3004561 Coimbra, Portugal
[9] Ctr Hosp Entre Douro & Vouga, Cardiol Dept, P-4520211 Santa Maria Feira, Portugal
[10] Univ Coimbra, Fac Med, P-3004531 Coimbra, Portugal
[11] Univ Coimbra, ICBR Inst Clin & Biomed Res, Fac Med, P-3004531 Coimbra, Portugal
[12] Clin Acad Ctr Coimbra CACC, P-3004561 Coimbra, Portugal
关键词
pulmonary arterial hypertension; bloodstream infection; survival; synthetic prostacyclin analogs; BURKHOLDERIA-CEPACIA BACTEREMIA; ARTERIAL-HYPERTENSION; PROSTACYCLIN ANALOGS; COMPLEX BACTEREMIA; PEDIATRIC-PATIENTS; OPEN-LABEL; CARE-UNIT; OUTBREAK; THERAPY; PH;
D O I
10.3390/ijms24076434
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intravenous synthetic prostacyclin analogs (iPCAs), such as epoprostenol, treprostinil and iloprost have been widely used for the treatment of pulmonary arterial hypertension (PAH). Despite having good outcomes, continuous infusion of iPCAs has been associated with some adverse effects. Bloodstream infection (BSI) is one of the most severe complications, although poorly recognized, especially under iloprost administration, which few studies have addressed. This study aimed to compare the BSI incidence rates between intravenous iloprost and epoprostenol administration. Patients with pulmonary hypertension (PH) functional class III or IV receiving intravenous iloprost or epoprostenol through Hickman catheter, between 2004 and 2019, were retrospectively selected from two PH treatment centers. From a total of 36 patients (13 for iloprost and 23 for epoprostenol), 75% (n = 27) fulfilled the PAH criteria, mainly belonging to the idiopathic group. Overall BSI rate was 1.5/1000 days of treatment (3.38 and 0.09/1000 days for iloprost and epoprostenol, respectively). Patients receiving iloprost were at a higher risk of developing BSI than those receiving epoprostenol (HR: 12.5; 95% CI: 1.569-99.092). A higher mortality rate from BSI was also identified in the iloprost group (p = 0.04). Twenty-seven patients developed BSI, with 92% of them requiring hospitalization. A total of 29 agents were found, 10 Gram-positive (mainly Staphylococcus aureus; n = 5) and 19 Gram-negative (mainly Pseudomonas aeruginosa; n = 6) bacteria. Iloprost administration was linked to a significantly higher incidence of BSI, worse prognosis, and more BSI-related deaths than epoprostenol. BSI due to Gram-negative, commensal, low-virulence bacteria was also higher in the iloprost group. In short, physicians should be aware when prescribing iPCA to guarantee their patients' safety and best medical care.
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