dc.creatorSantamarina, M.
dc.creatorBeddings, I.
dc.creatorLomakin, F.
dc.creatorBoisier Riscal, D.
dc.creatorGutiérrez Claveria, M.
dc.creatorVidal Marambio, J.
dc.creatorRetamal Báez, N.
dc.creatorPavez Novoa, C.
dc.creatorReyes Allende, C.
dc.creatorFerreira Perey, P.
dc.creatorGutiérrez Torres, M.
dc.creatorVillalobos Mazza, C.
dc.creatorVergara Sagredo, C.
dc.creatorAhumada Bermejo, S.
dc.creatorLabarca Mellado, E.
dc.creatorBarthel Munchmeyer, E.
dc.creatorMarchant Ramos, S.
dc.creatorVolpacchio, M.
dc.creatorVega, J.
dc.date.accessioned2022-04-21T17:48:18Z
dc.date.accessioned2024-05-02T15:01:37Z
dc.date.available2022-04-21T17:48:18Z
dc.date.available2024-05-02T15:01:37Z
dc.date.created2022-04-21T17:48:18Z
dc.date.issued2022-01
dc.identifierCritical Care, Volume 26, Issue 1, December 2022, Article number 1
dc.identifier1364-8535
dc.identifierhttps://repositorio.unab.cl/xmlui/handle/ria/22352
dc.identifier10.1186/s13054-021-03885-y
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/9261271
dc.description.abstractBackground: SARS-CoV-2 seems to affect 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 efficacy of oral sildenafil 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-confirmed 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 sildenafil (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 differences 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 sildenafil group); 33 [82.5%] were male; and median age was 57 [IQR 41–68] years. No significant differences 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 sildenafil arm (logrank p = 0.04). Patients in the sildenafil arm showed a significantly 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 significant differences were found in the oxygenation parameters. Sildenafil treatment could have a potential therapeutic role regarding the need for IMV in COVID-19 patients with specific perfusion patterns in sCTA. A large-scale study is needed to confirm these results.
dc.languageen
dc.publisherBioMed Central Ltd
dc.rightshttps://ccforum.biomedcentral.com/articles/10.1186/s13054-021-03885-y#rightslink
dc.rightsAttribution 4.0 International (CC BY 4.0)
dc.subjectBlood gas analysis
dc.subjectCOVID-19
dc.subjectIntensive care unit
dc.subjectLength of stay
dc.subjectMechanical ventilation
dc.subjectSildenafil
dc.subjectSubtraction CT angiography
dc.subjectVentilation–perfusion ratio
dc.subjectHypoxaemia
dc.subjectHappy Hypoxia
dc.titleSildenafil for treating patients with COVID-19 and perfusion mismatch: a pilot randomized trial
dc.typeArtículo


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