Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/113774
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dc.contributor.authorCamara, Raquel Paulinetti-
dc.contributor.authorCoelho, Francisco das Neves-
dc.contributor.authorCruz-Martins, Natália-
dc.contributor.authorMarques-Alves, Patricia-
dc.contributor.authorCastro, Graça-
dc.contributor.authorBaptista, Rui-
dc.contributor.authorFerreira, Filipa-
dc.date.accessioned2024-03-01T12:01:29Z-
dc.date.available2024-03-01T12:01:29Z-
dc.date.issued2023-03-29-
dc.identifier.issn1422-0067pt
dc.identifier.urihttps://hdl.handle.net/10316/113774-
dc.description.abstractIntravenous 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.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectpulmonary arterial hypertensionpt
dc.subjectbloodstream infectionpt
dc.subjectsurvivalpt
dc.subjectsynthetic prostacyclin analogspt
dc.subject.meshHumanspt
dc.subject.meshEpoprostenolpt
dc.subject.meshIloprostpt
dc.subject.meshRetrospective Studiespt
dc.subject.meshIncidencept
dc.subject.meshAntihypertensive Agentspt
dc.subject.meshFamilial Primary Pulmonary Hypertensionpt
dc.subject.meshHypertension, Pulmonarypt
dc.subject.meshSepsispt
dc.titleIncidence of Bloodstream Infection in Patients with Pulmonary Hypertension under Intravenous Epoprostenol or Iloprost-A Multicentre, Retrospective Studypt
dc.typearticle-
degois.publication.firstPage6434pt
degois.publication.issue7pt
degois.publication.titleInternational Journal of Molecular Sciencespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/ijms24076434pt
degois.publication.volume24pt
dc.date.embargo2023-03-29*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.orcid0000-0002-7411-7039-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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