Efficacy and Safety of Percutaneous Dilatation Tracheostomy (PDT) in Critically Ill Patients When Performed Bedside by an Intensivist With Flexible Bronchoscopy Assistance

CHEST Journal ◽  
2011 ◽  
Vol 140 (4) ◽  
pp. 193A
Author(s):  
Kyriaki Tsikritsaki ◽  
Georgios Koukoulitsios ◽  
Agisilaos Dervas ◽  
Maria Kryfti ◽  
Ioannis Dimitroulis
Lung ◽  
2018 ◽  
Vol 196 (6) ◽  
pp. 729-736 ◽  
Author(s):  
Mazen O. Al-Qadi ◽  
Rodrigo Cartin-Ceba ◽  
Rahul Kashyap ◽  
Sumanjit Kaur ◽  
Steve G. Peters

Shock ◽  
2018 ◽  
Vol 50 (4) ◽  
pp. 401-407 ◽  
Author(s):  
Luhao Wang ◽  
Chunfang Qiu ◽  
Xiangdong Guan ◽  
Minying Chen ◽  
Juan Chen ◽  
...  

2013 ◽  
Vol 45 (6) ◽  
pp. 608 ◽  
Author(s):  
Kavita Sekhri ◽  
Ruchika Nandha ◽  
Amit Mandal ◽  
Deepak Bhasin ◽  
Harpal Singh

Critical Care ◽  
2010 ◽  
Vol 14 (Suppl 1) ◽  
pp. P56
Author(s):  
A Skiada ◽  
J Pavleas ◽  
T Topalis ◽  
K Georgiou ◽  
D Siggouna ◽  
...  

Author(s):  
Ming Zhong ◽  
Aijun Sun ◽  
Ting Xiao ◽  
Ge Yao ◽  
Ling Sang ◽  
...  

AbstractObjectTo evaluate the clinical efficacy and safety of α-Lipoic acid (ALA) for critically ill patients with coronavirus disease 2019 (COVID-19).MethodsA randomized, single-blind, group sequential, active-controlled trial was performed at JinYinTan Hospital, Wuhan, China. Between February 2020 and March 2020, 17 patients with critically ill COVID-19 were enrolled in our study. Eligible patients were randomly assigned in a 1:1 ratio to receive either ALA (1200 mg/d, intravenous infusion) once daily plus standard care or standard care plus equal volume saline infusion (placebo) for 7 days. All patients were monitored within the 7 days therapy and followed up to day 30 after therapy. The primary outcome of this study was the Sequential Organ Failure Estimate (SOFA) score, and the secondary outcome was the all-cause mortality within 30 days.ResultNine patients were randomized to placebo group and 8 patients were randomized to ALA group. SOFA score was similar at baseline, increased from 4.3 to 6.0 in the placebo group and increased from 3.8 to 4.0 in the ALA group (P=0.36) after 7 days. The 30-day all-cause mortality tended to be lower in the ALA group (3/8, 37.5%) compared to that in the placebo group (7/9, 77.8%, P=0.09).ConclusionIn our study, ALA use is associated with lower SOFA score increase and lower 30-day all-cause mortality as compared with the placebo group. Although the mortality rate was two-folds higher in placebo group than in ALA group, only borderline statistical difference was evidenced due to the limited patient number. Future studies with larger patient cohort are warranted to validate the role of ALA in critically ill patients with COVID-19.


Nutrition ◽  
2020 ◽  
Vol 78 ◽  
pp. 110960
Author(s):  
Aikaterini Apostolopoulou ◽  
Anna-Bettina Haidich ◽  
Konstantinia Kofina ◽  
William Manzanares ◽  
Emmanouil Bouras ◽  
...  

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