19 research outputs found
The Hubble Catalog of Variables
- Author
- A. Bonanos
- A. Karampelas
- A. Nota
- A. Rest
- B. Whitmore
- Bernard
- Brown
- Budavári
- C. Arviset
- D. Hatzidimitriou
- D. Lennon
- de Diego
- Dolphin
- E. Pouliasis
- Figuera Jaimes
- Fruth
- G. Kakaletris
- Hoffmann
- I. Bellas-Velidis
- I. Georgantopoulos
- Jeffery
- K. Sokolovsky
- K. Tsinganos
- Kim
- Kolesnikova
- L. Strolger
- Lasker
- M. Catelan
- M. Yang
- M.I. Moretti
- Mowlavi
- N. Laskaris
- Nandra
- Nascimbeni
- P. Gavras
- Parks
- R. Downes
- R. White
- Rose
- S. Lubow
- Shin
- Sokolovsky
- Sokolovsky
- Stetson
- T. Budavari
- V. Charmandaris
- Villforth
- W. Gieren
- Welch
- Whitmore
- Wozniak
- Z. Spetsieri
- Zhang
- Publication venue
- 'EDP Sciences'
- Publication date
- 01/01/2017
- Field of study
The gas content of peculiar galaxies: strongly interacting systems
- Author
- Andreani
- Athanassoula
- Bendo
- Bertola
- Bettoni
- Bettoni
- Beuing
- Boselli
- Boselli
- Braine
- Bregman
- Burstein
- Cappellaro
- Casoli
- Casoli
- Ciotti
- Combes
- Corsini
- D. Bettoni
- Davis
- Devereux
- Devereux
- Dressler
- Fabbiano
- Feigelson
- G. Galletta
- Gerin
- Haynes
- Henriksen
- Horellou
- Horellou
- Horellou
- Kim
- Knapp
- Kormendy
- Lavezzi
- Lonsdale
- Maloney
- Nishiyama
- O'Sullivan
- Ochsenbein
- Paturel
- Popescu
- Roberts
- Sage
- Sage
- Sanders
- Schweizer
- Solomon
- Strong
- Thronson
- V. Casasola
- van Driel
- Véron-Cetty
- Welch
- Whitmore
- Wiklind
- Young
- Zhu
- Publication venue
- 'EDP Sciences'
- Publication date
- 01/01/2004
- Field of study
A study of the gas content in 1038 interacting galaxies, essentially selected
from Arp, Arp and Madore, Vorontsov-Velyaminov catalogues and some of the
published literature, is presented here. The data on the interstellar medium
have been extracted from a number of sources in the literature and compared
with a sample of 1916 normal galaxies. The mean values for each of the
different ISM tracers (FIR, 21 cm, CO lines, X-ray) have been estimated by
means of survival analysis techniques, in order to take into account the
presence of upper limits. From the data it appears that interacting galaxies
have a higher gas content than normal ones. Galaxies classified as ellipticals
have both a dust and gas content one order of magnitude higher than normal.
Spirals have in most part a normal dust and HI content but an higher molecular
gas mass. The X-ray luminosity also appears higher than that of normal galaxies
of same morphological type, both including or excluding AGNs. We considered the
alternative possibilities that the molecular gas excess may derive from the
existence of tidal torques which produce gas infall from the surrounding
regions or from a different metallicity which affects the X conversion factor
between the observed CO line luminosity and the H2 calculated mass.
According to our tests, it appears that interacting galaxies possess a higher
molecular mass than normal galaxies but with a similar star formation
efficiency.Comment: 11 pages, 7 figures, accepted for publication in A&
Convalescent plasma in patients admitted to hospital with COVID-19 (RECOVERY): a randomised controlled, open-label, platform trial
- Author
- Abani O.
- Abbas A.
- Abbas F.
- Abbas M.
- Abbasi S.
- Abbass H.
- Abbott A.
- Abdallah N.
- Abdelaziz A.
- Abdelfattah M.
- Abdelqader B.
- Abdo D.
- Abdul Rasheed A.
- Abdul B.
- Abdul-Kadir R.
- Abdul-Raheem R.
- Abdulakeem A.
- Abdulle A.
- Abdulmumeen A.
- Abdulshukkoor N.
- Abdusamad K.
- Abed El Khaleq Y.
- Abedalla M.
- Abeer Ul Amna A.U.A.
- Abernethy K.
- Abo-Leyah H.
- Aboaba A.
- Abou-Haggar A.
- Abouibrahim M.
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- Abraheem A.
- Abrams J.
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- Abubacker S.M.
- Abung A.
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- Achara A.
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- Zullo C.
- Zuriaga-Alvaro A.
- Zuurbier W.
- Zyengi S.
- Publication venue
- 'Elsevier BV'
- Publication date
- 29/05/2021
- Field of study
Background:
Many patients with COVID-19 have been treated with plasma containing anti-SARS-CoV-2 antibodies. We aimed to evaluate the safety and efficacy of convalescent plasma therapy in patients admitted to hospital with COVID-19.
Methods:
This randomised, controlled, open-label, platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]) is assessing several possible treatments in patients hospitalised with COVID-19 in the UK. The trial is underway at 177 NHS hospitals from across the UK. Eligible and consenting patients were randomly assigned (1:1) to receive either usual care alone (usual care group) or usual care plus high-titre convalescent plasma (convalescent plasma group). The primary outcome was 28-day mortality, analysed on an intention-to-treat basis. The trial is registered with ISRCTN, 50189673, and ClinicalTrials.gov, NCT04381936.
Findings:
Between May 28, 2020, and Jan 15, 2021, 11558 (71%) of 16287 patients enrolled in RECOVERY were eligible to receive convalescent plasma and were assigned to either the convalescent plasma group or the usual care group. There was no significant difference in 28-day mortality between the two groups: 1399 (24%) of 5795 patients in the convalescent plasma group and 1408 (24%) of 5763 patients in the usual care group died within 28 days (rate ratio 1·00, 95% CI 0·93–1·07; p=0·95). The 28-day mortality rate ratio was similar in all prespecified subgroups of patients, including in those patients without detectable SARS-CoV-2 antibodies at randomisation. Allocation to convalescent plasma had no significant effect on the proportion of patients discharged from hospital within 28 days (3832 [66%] patients in the convalescent plasma group vs 3822 [66%] patients in the usual care group; rate ratio 0·99, 95% CI 0·94–1·03; p=0·57). Among those not on invasive mechanical ventilation at randomisation, there was no significant difference in the proportion of patients meeting the composite endpoint of progression to invasive mechanical ventilation or death (1568 [29%] of 5493 patients in the convalescent plasma group vs 1568 [29%] of 5448 patients in the usual care group; rate ratio 0·99, 95% CI 0·93–1·05; p=0·79).
Interpretation:
In patients hospitalised with COVID-19, high-titre convalescent plasma did not improve survival or other prespecified clinical outcomes.
Funding:
UK Research and Innovation (Medical Research Council) and National Institute of Health Research
Tocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
- Author
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/05/2021
- Field of study
Background:
In this study, we aimed to evaluate the effects of tocilizumab in adult patients admitted to hospital with COVID-19 with both hypoxia and systemic inflammation.
Methods:
This randomised, controlled, open-label, platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing several possible treatments in patients hospitalised with COVID-19 in the UK. Those trial participants with hypoxia (oxygen saturation <92% on air or requiring oxygen therapy) and evidence of systemic inflammation (C-reactive protein ≥75 mg/L) were eligible for random assignment in a 1:1 ratio to usual standard of care alone versus usual standard of care plus tocilizumab at a dose of 400 mg–800 mg (depending on weight) given intravenously. A second dose could be given 12–24 h later if the patient's condition had not improved. The primary outcome was 28-day mortality, assessed in the intention-to-treat population. The trial is registered with ISRCTN (50189673) and ClinicalTrials.gov (NCT04381936).
Findings:
Between April 23, 2020, and Jan 24, 2021, 4116 adults of 21 550 patients enrolled into the RECOVERY trial were included in the assessment of tocilizumab, including 3385 (82%) patients receiving systemic corticosteroids. Overall, 621 (31%) of the 2022 patients allocated tocilizumab and 729 (35%) of the 2094 patients allocated to usual care died within 28 days (rate ratio 0·85; 95% CI 0·76–0·94; p=0·0028). Consistent results were seen in all prespecified subgroups of patients, including those receiving systemic corticosteroids. Patients allocated to tocilizumab were more likely to be discharged from hospital within 28 days (57% vs 50%; rate ratio 1·22; 1·12–1·33; p<0·0001). Among those not receiving invasive mechanical ventilation at baseline, patients allocated tocilizumab were less likely to reach the composite endpoint of invasive mechanical ventilation or death (35% vs 42%; risk ratio 0·84; 95% CI 0·77–0·92; p<0·0001).
Interpretation:
In hospitalised COVID-19 patients with hypoxia and systemic inflammation, tocilizumab improved survival and other clinical outcomes. These benefits were seen regardless of the amount of respiratory support and were additional to the benefits of systemic corticosteroids.
Funding:
UK Research and Innovation (Medical Research Council) and National Institute of Health Research
Effects of fluoxetine on functional outcomes after acute stroke (FOCUS): a pragmatic, double-blind, randomised, controlled trial
- Author
- Abano N
- Abbott L
- Abbott W
- Abdul-Hamid A
- Abdul-Saheb M
- Abousleiman Y
- Abubakar S
- Adedoyin T
- Adie K
- Affley B
- Ahlquist K
- Ahmad N
- Ahmed A
- Ahmed S
- Ahmed Z
- Al Hussayni S
- Al-Samarrai N
- Alam I
- Alam S
- Ali A
- Ali K
- Allen C
- Allen J
- Allison J
- Allsop H
- Allsop L
- Almadenboyle C
- Alvares W
- Alwis L
- Alwis L
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- Zhang L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2019
- Field of study
Background
Results of small trials indicate that fluoxetine might improve functional outcomes after stroke. The FOCUS trial aimed to provide a precise estimate of these effects.
Methods
FOCUS was a pragmatic, multicentre, parallel group, double-blind, randomised, placebo-controlled trial done at 103 hospitals in the UK. Patients were eligible if they were aged 18 years or older, had a clinical stroke diagnosis, were enrolled and randomly assigned between 2 days and 15 days after onset, and had focal neurological deficits. Patients were randomly allocated fluoxetine 20 mg or matching placebo orally once daily for 6 months via a web-based system by use of a minimisation algorithm. The primary outcome was functional status, measured with the modified Rankin Scale (mRS), at 6 months. Patients, carers, health-care staff, and the trial team were masked to treatment allocation. Functional status was assessed at 6 months and 12 months after randomisation. Patients were analysed according to their treatment allocation. This trial is registered with the ISRCTN registry, number ISRCTN83290762.
Findings
Between Sept 10, 2012, and March 31, 2017, 3127 patients were recruited. 1564 patients were allocated fluoxetine and 1563 allocated placebo. mRS data at 6 months were available for 1553 (99·3%) patients in each treatment group. The distribution across mRS categories at 6 months was similar in the fluoxetine and placebo groups (common odds ratio adjusted for minimisation variables 0·951 [95% CI 0·839–1·079]; p=0·439). Patients allocated fluoxetine were less likely than those allocated placebo to develop new depression by 6 months (210 [13·43%] patients vs 269 [17·21%]; difference 3·78% [95% CI 1·26–6·30]; p=0·0033), but they had more bone fractures (45 [2·88%] vs 23 [1·47%]; difference 1·41% [95% CI 0·38–2·43]; p=0·0070). There were no significant differences in any other event at 6 or 12 months.
Interpretation
Fluoxetine 20 mg given daily for 6 months after acute stroke does not seem to improve functional outcomes. Although the treatment reduced the occurrence of depression, it increased the frequency of bone fractures. These results do not support the routine use of fluoxetine either for the prevention of post-stroke depression or to promote recovery of function.
Funding
UK Stroke Association and NIHR Health Technology Assessment Programme
Complexity and Emergence as Design Principles for Engineering Decentralized Nanoscale Systems
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