59 research outputs found

    Polarised attitudes within Switzerland mean a pragmatic solution to the issue of EU free movement might no longer be possible

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    A proposal to reintroduce immigration quotas was approved by the Swiss electorate in a vote on 9 February. The vote has raised questions about Switzerland and the EU’s relationship as immigration quotas are incompatible with the principle of free movement which is contained within the bilateral treaties underpinning the Swiss-EU relationship. Clive H Church writes on the reaction both in Europe and within Switzerland over the last six months. He notes that opinion has become polarised over the issue in the country and that it may now be difficult for a pragmatic solution to emerge which is acceptable to both the EU and the supporters of the proposal

    Switzerland is facing a dual crisis over its relations with the EU

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    On 26 May, Switzerland pulled out of negotiations over a new partnership with the European Union. Clive H. Church writes the country is now facing both a crisis in its relations with the EU and a democratic crisis over how the decision was made

    Switzerland's 'green tsunami' slows to a trickle

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    Green parties were the main winners from the 2019 Swiss federal elections held on 20 October. However, as Clive H. Church writes, developments since the vote have illustrated the extent to which Swiss politics remains resistant to change. While the election generated some momentum behind efforts to strengthen the country’s climate policies, it remains unclear how far the process of ‘greening’ Swiss politics might go

    The UK could be in line for years of Swiss-style negotiations with the EU

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    Prior to the Brexit referendum, it was common to cite Switzerland as a model for the UK to follow after leaving the European Union. Clive H. Church writes that while Brexiteers’ enthusiasm for this approach largely evaporated following the referendum, the UK has ultimately ended up on a path that has many potential similarities with the Swiss-EU relationship

    Dark sectors 2016 Workshop: community report

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    This report, based on the Dark Sectors workshop at SLAC in April 2016, summarizes the scientific importance of searches for dark sector dark matter and forces at masses beneath the weak-scale, the status of this broad international field, the important milestones motivating future exploration, and promising experimental opportunities to reach these milestones over the next 5-10 years

    Convalescent plasma in patients admitted to hospital with COVID-19 (RECOVERY): a randomised controlled, open-label, platform trial

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    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

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    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

    Switzerland's Approach to EU Engagement: a Financial Services Perspective

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    This report examines Switzerland’s past and present political engagement with the EU, and how this operates for one of its key industries, the financial services sector. The report will help to inform debate around how the UK engages with the EU, by considering the experiences of Switzerland as a European country outside the EU, with a significant financial services industry. Key points to note are: 1) A complex approach to engagement The Swiss approach is complex, consisting of a set of disparate sector-specific bilateral agreements developed over time, including on Schengen but excluding financial services, together with much informal Europeanisation, including autonomous adoption of EU law. 2) Reliance on London for access to European capital markets Despite there being no comprehensive services accord, the Swiss financial sector has, so far, benefitted from largely unfettered access to the EU market, often through its presence in London. New EU regulations could change this. Tighter regulations would mean third countries constantly having to amend their parallel legislation, in line with any changes in Single Market legislation, in order to maintain equivalence over the course of time. 3) A means of moving closer to the EU Switzerland’s bilateral approach has been a means of moving closer to the EU rather than maintaining distance – and around 40% of Swiss legislation derives from EU rules. 4) Access to EU markets Maintaining Switzerland’s level of access to the Single Market requires continual closeness to the EU. A Free Trade agreement is not sufficient, especially for the financial sector. Maintaining access to European capital markets necessitates formal agreements and parallel legislation to that of the EU. 5) Overall The Swiss approach is an exception, developed over time, rather than a formal model, and is a means of closer engagement with the EU. Forgoing complete access to the Single Market has had implications for the Swiss financial services sector, namely through the associated necessity of establishing operations in London, and has reduced Switzerland’s ability to engage in EU policy making

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