2 research outputs found

    A first search of transients in the Galactic Center from 230 GHz ALMA observations

    Full text link
    The Galactic Center (GC) presents one of the highest stellar densities in our Galaxy, making its surroundings an environment potentially rich in radio transients, such as pulsars and different kinds of flaring activity. In this paper, we present the first study of transient activity in the region of the GC based on Atacama Large Millimeter/submillimeter (mm/submm) Array (ALMA) continuum observations at 230 GHz. This search is based on a new self-calibration algorithm, especially designed for variability detection in the GC field. Using this method, we have performed a search of radio transients in the effective field of view of~∼30 \sim 30\,arcseconds of the GC central supermassive black hole Sagittarius A* (SgrA*) using ALMA 230 GHz observations taken during the 2017 Event Horizon Telescope (EHT) campaign, which span several observing hours (5-10) on 2017 April 6, 7, and 11. This calibration method allows one to disentangle the variability of unresolved SgrA* from any potential transient emission in the wider field of view and residual effects of the imperfect data calibration. Hence, a robust statistical criterion to identify real transients can be established: the event should survive at least three times the correlation time and it must have a peak excursion of at least seven times the instantaneous root-mean-square between consecutive images. Our algorithms are successfully tested against realistic synthetic simulations of transient sources in the GC field. Having checked the validity of the statistical criterion, we provide upper limits for transient activity in the effective field of view of the GC at 230 GHz.Comment: Accepted for publication in Astronomy and Astrophysic

    Prophylactic biological mesh reinforcement versus standard closure of stoma site (ROCSS): a multicentre, randomised controlled trial

    No full text
    Background: Closure of an abdominal stoma, a common elective operation, is associated with frequent complications; one of the commonest and impactful is incisional hernia formation. We aimed to investigate whether biological mesh (collagen tissue matrix) can safely reduce the incidence of incisional hernias at the stoma closure site. Methods: In this randomised controlled trial (ROCSS) done in 37 hospitals across three European countries (35 UK, one Denmark, one Netherlands), patients aged 18 years or older undergoing elective ileostomy or colostomy closure were randomly assigned using a computer-based algorithm in a 1:1 ratio to either biological mesh reinforcement or closure with sutures alone (control). Training in the novel technique was standardised across hospitals. Patients and outcome assessors were masked to treatment allocation. The primary outcome measure was occurrence of clinically detectable hernia 2 years after randomisation (intention to treat). A sample size of 790 patients was required to identify a 40% reduction (25% to 15%), with 90% power (15% drop-out rate). This study is registered with ClinicalTrials.gov, NCT02238964. Findings: Between Nov 28, 2012, and Nov 11, 2015, of 1286 screened patients, 790 were randomly assigned. 394 (50%) patients were randomly assigned to mesh closure and 396 (50%) to standard closure. In the mesh group, 373 (95%) of 394 patients successfully received mesh and in the control group, three patients received mesh. The clinically detectable hernia rate, the primary outcome, at 2 years was 12% (39 of 323) in the mesh group and 20% (64 of 327) in the control group (adjusted relative risk [RR] 0·62, 95% CI 0·43–0·90; p=0·012). In 455 patients for whom 1 year postoperative CT scans were available, there was a lower radiologically defined hernia rate in mesh versus control groups (20 [9%] of 229 vs 47 [21%] of 226, adjusted RR 0·42, 95% CI 0·26–0·69; p<0·001). There was also a reduction in symptomatic hernia (16%, 52 of 329 vs 19%, 64 of 331; adjusted relative risk 0·83, 0·60–1·16; p=0·29) and surgical reintervention (12%, 42 of 344 vs 16%, 54 of 346: adjusted relative risk 0·78, 0·54–1·13; p=0·19) at 2 years, but this result did not reach statistical significance. No significant differences were seen in wound infection rate, seroma rate, quality of life, pain scores, or serious adverse events. Interpretation: Reinforcement of the abdominal wall with a biological mesh at the time of stoma closure reduced clinically detectable incisional hernia within 24 months of surgery and with an acceptable safety profile. The results of this study support the use of biological mesh in stoma closure site reinforcement to reduce the early formation of incisional hernias. Funding: National Institute for Health Research Research for Patient Benefit and Allergan
    corecore