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1.
Ann Surg ; 274(5): e388-e394, 2021 11 01.
Article de Anglais | MEDLINE | ID: mdl-34617934

RÉSUMÉ

OBJECTIVE: Does extracorporeal membrane oxygenation (ECMO) improve outcomes in ECMO-eligible patients with COVID-19 respiratory failure compared to maximum ventilation alone (MVA)? SUMMARY BACKGROUND DATA: ECMO is beneficial in severe cases of respiratory failure when mechanical ventilation is inadequate. Outcomes for ECMO-eligible COVID-19 patients on MVA have not been reported. Consequently, a direct comparison between COVID-19 patients on ECMO and those on MVA has not been established. METHODS: A total of 3406 COVID-19 patients treated at two major medical centers in Chicago were studied. One hundred ninety-five required maximum ventilatory support, and met ECMO eligibility criteria. Eighty ECMO patients were propensity matched to an equal number of MVA patients using detailed demographic, physiological, and comorbidity data. Primary outcome was survival and disposition at discharge. RESULTS: Seventy-one percent of patients were decannulated from ECMO. Mechanical ventilation was discontinued in 75% ECMO and 16% MVA patients. Twenty-five percent of patients in the ECMO arm expired, 21% while on ECMO, compared with 74% in the MVA cohort. Mortality was significantly lower across all age and BMI groups in the ECMO arm. Sixty-eight percent ECMO and 26% MVA patients were discharged from the hospital. Fewer ECMO patients required long-term rehabilitation. Major complications such as septic shock, ventilator associated pneumonia, inotropic requirements, acute liver and kidney injuries are less frequent among ECMO patients. CONCLUSIONS: ECMO-eligible patients with severe COVID-19 respiratory failure demonstrate a 3-fold improvement in survival with ECMO. They are also in a better physical state at discharge and have lower overall complication rates. As such, strong consideration should be given for ECMO when mechanical ventilatory support alone becomes insufficient in treating COVID-19 respiratory failure.


Sujet(s)
COVID-19/thérapie , Oxygénation extracorporelle sur oxygénateur à membrane/méthodes , Score de propension , Ventilation artificielle/méthodes , Insuffisance respiratoire/thérapie , Adulte , Sujet âgé , COVID-19/complications , COVID-19/épidémiologie , Femelle , Études de suivi , Humains , Mâle , Adulte d'âge moyen , Pandémies , Sortie du patient/tendances , Insuffisance respiratoire/épidémiologie , Insuffisance respiratoire/étiologie , Études rétrospectives , SARS-CoV-2 , Indice de gravité de la maladie , Taux de survie/tendances , États-Unis/épidémiologie , Jeune adulte
3.
J Vasc Surg ; 46(1): 140-3, 2007 Jul.
Article de Anglais | MEDLINE | ID: mdl-17606132

RÉSUMÉ

We present a 56-year-old woman affected by a large leiomyosarcoma originating from the suprarenal inferior vena cava (IVC). A computed tomography (CT) scan revealed near obstruction of the IVC and involvement of the right renal vein. The patient underwent successful en bloc resection of the tumor, right kidney, right adrenal gland, and IVC. Caval reconstruction was performed using a non-type specific allograft, followed by left renal vein re-implantation. The patient tolerated the procedure well without any complications. The use of an IVC allograft allowed for continued graft patency, without the need of immunosuppression or long-term anticoagulation. However, local recurrence did occur.


Sujet(s)
Léiomyosarcome/chirurgie , Tumeurs vasculaires/chirurgie , Procédures de chirurgie vasculaire , Veine cave inférieure/transplantation , Anastomose chirurgicale , Femelle , Humains , Léiomyosarcome/diagnostic , Adulte d'âge moyen , Phlébographie , Veines rénales/chirurgie , Réimplantation , Tomodensitométrie , Transplantation homologue , Résultat thérapeutique , Tumeurs vasculaires/diagnostic , Degré de perméabilité vasculaire , Veine cave inférieure/anatomopathologie , Veine cave inférieure/physiopathologie
4.
J Heart Lung Transplant ; 25(1): 137-9, 2006 Jan.
Article de Anglais | MEDLINE | ID: mdl-16399545

RÉSUMÉ

As the implantation of left ventricular assist devices (LVADs) as destination therapy for patients with heart failure increases in frequency, device durability and malfunction present an increasing concern. Complications such as inflow valve regurgitation, outflow valve distortion, and problems with power cable or pump motors place the LVAD recipient at increased risk for morbidity and mortality. To offset the risk of complications related to the inflow cannula, modifications to the valve conduit were made to the SNAP VE device in November 2002. These modifications were intended to improve durability with cycle performance of up to 6 times longer than the old inflow valve during in vitro testing. We describe here a patient who sustained disruption of the Dacron inlet graft after implantation of the Heart-Mate XVE System as a destination therapy.


Sujet(s)
Panne d'appareillage , Dispositifs d'assistance circulatoire , Sujet âgé , Conception d'appareillage , Femelle , Transplantation cardiaque , Hémorragie/étiologie , Humains , Téréphtalate polyéthylène
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