dc.creatorSantamarina, Mario G.
dc.creatorBeddings, Ignacio
dc.creatorMartínez Lomakin, Felipe
dc.creatorBoisier Riscal, Dominique
dc.creatorGutiérrez Claveria, Mónica
dc.creatorVidal Marambio, Jaime
dc.creatorRetamal Báez, Nicole
dc.creatorPávez Novoa, Cristian
dc.creatorReyes Allende, Cesar
dc.creatorFerreira Perey, Paulina
dc.creatorGutiérrez Torres, Miguel
dc.creatorVillalobos Mazza, Camila
dc.creatorVergara Sagredo, Constanza
dc.creatorAhumada Bermejo, Sebastián
dc.creatorLabarca Mellado, Eduardo
dc.creatorBarthel Munchmeyer, Elizabeth
dc.creatorMarchant Ramos, Solange
dc.creatorVolpacchio, Mariano
dc.creatorVega, Jorge
dc.date.accessioned2022-09-30T13:26:05Z
dc.date.available2022-09-30T13:26:05Z
dc.date.created2022-09-30T13:26:05Z
dc.date.issued2022
dc.identifierCritical Care (2022) 26:1
dc.identifier10.1186/s13054-021-03885-y
dc.identifierhttps://repositorio.uchile.cl/handle/2250/188277
dc.description.abstractBackground: SARS-CoV-2 seems to afect the regulation of pulmonary perfusion. Hypoperfusion in areas of well-aerated lung parenchyma results in a ventilation–perfusion mismatch that can be characterized using subtraction computed tomography angiography (sCTA). This study aims to evaluate the efcacy of oral sildenafl in treating COVID-19 inpatients showing perfusion abnormalities in sCTA. Methods: Triple-blinded, randomized, placebo-controlled trial was conducted in Chile in a tertiary-care hospital able to provide on-site sCTA scans and ventilatory support when needed between August 2020 and March 2021. In total, 82 eligible adults were admitted to the ED with RT-PCR-confrmed or highly probable SARS-COV-2 infection and sCTA performed within 24 h of admission showing perfusion abnormalities in areas of well-aerated lung parenchyma; 42 were excluded and 40 participants were enrolled and randomized (1:1 ratio) once hospitalized. The active intervention group received sildenafl (25 mg orally three times a day for seven days), and the control group received identical placebo capsules in the same way. Primary outcomes were diferences in oxygenation parameters measured daily during follow-up (PaO2/FiO2 ratio and A-a gradient). Secondary outcomes included admission to the ICU, requirement of non-invasive ventilation, invasive mechanical ventilation (IMV), and mortality rates. Analysis was performed on an intention-to-treat basis. Results: Totally, 40 participants were enrolled (20 in the placebo group and 20 in the sildenafl group); 33 [82.5%] were male; and median age was 57 [IQR 41–68] years. No signifcant diferences in mean PaO2/FiO2 ratios and A-a gradients were found between groups (repeated-measures ANOVA p=0.67 and p=0.69). IMV was required in 4 patients who received placebo and none in the sildenafl arm (logrank p=0.04). Patients in the sildenafl arm showed a signifcantly shorter median length of hospital stay than the placebo group (9 IQR 7–12 days vs. 12 IQR 9–21 days, p=0.04). Conclusions: No statistically signifcant diferences were found in the oxygenation parameters. Sildenafl treatment could have a potential therapeutic role regarding the need for IMV in COVID-19 patients with specifc perfusion patterns in sCTA. A large-scale study is needed to confrm these results.
dc.languageen
dc.publisherBMC
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/us/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States
dc.sourceSantamarina et al. Critical Care
dc.subjectSildenafl
dc.subjectSubtraction CT angiography
dc.subjectVentilation–perfusion ratio
dc.subjectBlood gas analysis
dc.subjectMechanical ventilation
dc.subjectIntensive care unit
dc.subjectLength of stay
dc.subjectCOVID-19 (Enfermedad)
dc.titleSildenafil for treating patients with COVID-19 and perfusion mismatch: a pilot randomized trial
dc.typeArtículo de revista


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