| 1. |
- Gooch, Pernille, et al.
(författare)
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Natural resource conflicts in the Capitalocene
- 2019
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Ingår i: Natural Resource Conflicts and Sustainable Development. - London : Routledge. - 9781138576889 - 9781351268646 - 9781138576896 ; , s. 11-23
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Bokkapitel (refereegranskat)
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| 2. |
- Olsson, E. Gunilla Almered, et al.
(författare)
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Preface
- 2019
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Ingår i: Natural Resource Conflicts and Sustainable Development. - 9781138576889 - 9781351268646
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Bokkapitel (övrigt vetenskapligt/konstnärligt)
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| 3. |
- Almered Olsson, Gunilla, 1951, et al.
(författare)
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Matproduktion och urban hållbarhet - Fallstudie från Hisingen och Göteborgs framtida möjligheter. Report 2016:2
- 2016
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Hållbara städer är en frekvent vision i västvärlden och i Sverige som är ett av Europas högst urbaniserade länder. I diskussionen om städers hållbarhet och om system för energiförsörjning, kommunikation och säkerhet tas matförsörjningen ofta för given. I praktiken har svensk matförsörjning följt samma utveckling som i andra västländer med mat- och livsmedelsproduktionssystem som helt integrerade delar i en globaliserad ekonomisk marknad. I detta system ingår att lagerhållning minimeras i strävan för kostnadseffektivitet, att beredskapslager av mat är avskaffat och att det sker en snabb marknadsrespons på efterfrågan. Effektiviteten och funktionen av ett sådant system förutsätter ett antal villkor vars uppfyllande kan ifrågasättas i dagens situation som inte kan frikopplas från en global kontext: tillgång till mark, råvaror och insatsmedel för matproduktion; effektiva och pålitliga transporter och framkomlighet utmed kommunikationsleder i luft, vatten, land och cyberrymd; tillgång till energi som drivmedel för transporter, produktion, förädling och distribution; frånvaro av politiska, militära konflikter eller terrorangrepp. I rapporten diskuteras dels matförsörjning som en försummad och starkt sårbar dimension av urban hållbarhet, dels hur ett alternativ till denna situation skulle kunna se ut och vilka förändringsfaktorer som existerar. Rapporten utgör genom en fallstudie på Hisingen i Göteborg ett exempel på hur stor potential och möjlighet som finns för urban och peri-urban matproduktion. Utöver en beskrivning över de nuvarande förutsättningar som finns i Göteborg innefattar rapporten beräkningar på ytbehov för självförsörjning i Göteborg samt en utvecklad vision med identifierade nyckelfaktorer för framtiden.
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| 4. |
- Holmström, Margareta, et al.
(författare)
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SWEDISH NATIONAL REGISTRY FOR BLEEDING DISORDERS – A SECOND REPORT
- 2019
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Ingår i: EAHAD 2019.
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Konferensbidrag (refereegranskat)abstract
- Introduction: Hemophilia Care in Sweden is centralized to three different and certified European Hemophilia Care Centers (EHCCs) (Stockholm, Gothenburg and Malmö[f1]). A recent web- based National registry has been set up for patients with bleeding disorders in Sweden. The registry is mainly funded by Swedish authorities. Methods: A multi- professional steering committee is running the registry with representatives from all three centers including physicians, nurses, physiotherapist and also a patient representative. A web- based platform, Real- Q, is used for the registry. Results: By the 31st Dec 2017, a total number of 1030 patients with bleeding disorders were included in the registry, mainly patients with hemophilia A, B and Von Willebrand disease. Data regarding bleedings, treatment modality and type of product, inhibitor status, viral infections are collected. Likewise patient reported outcome measurements (PROM)- such as pain and quality of life[.The number of patients with hemophilia A, B and Von Willebrand disease in 2016 resp 2017 were as follows:Hemophilia A; n = 243 in 2016 and n= 691 in 2017.Hemophilia B: n = 49 in 2016 and n = 191 in 2017.Von Willebrand disease: n = 11 in 2016 and n = 152 in 2017.[LMW1] are registered.[LMW2] are registered on a regular basis? Discussion/Conclusion: The number of patients in the Swedish National Registry for bleeding disorders has increased significantly during the last year; from a total of 308 Dec 31st 2016 to 1030 in Dec 31st 2017. Increasing amount of data will enable further evaluation of treatment data and also joint status, quality of life and bleeding reports.
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| 5. |
- Holmström, Margareta, et al.
(författare)
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Swedish national registry for bleeding disorders - first report
- 2018
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Ingår i: 11th Annual Congress of the European Association for Haemophilia and Allied Disorders 2018, 7–9 February 2018, Madrid, Spain. Haemophilia, 24 (S1). - : Wiley. - 1365-2516.
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Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
- Introduction : Hemophilia care in Sweden is centralized to 3 centers localized in Gothenburg, Malmö and Stockholm. All centers are certi-fied as European Hemophilia Comprehensive Care Centers (EHCCs). Recently a web- based Swedish national registry has been established with funding from Swedish authorities. Methods : One of the conclusions from the earlier reports from the Swedish agency for health technology assessment and assessment of social services (SBU) and the Dental and Pharmaceutical benefits agency (TLV) was that a national registry for hemophilia and other bleeding disorders was needed to be able to follow the long- term effects of the disease and treatment strategies. An application was submitted in 2012 to apply for funding from Swedenʹs municipali-ties and count councils (SKL). The registry was validated as an official national registry. A multi- professional steering committee is running the registry with representatives from all 3 hemophilia centers includ-ing physicians, nurses, physiotherapist and a patient representative. Support regarding legal aspects, IT- solutions, statistics and economy is provided by QRC Stockholm. Results : By now, 780 patients with bleeding disorders are included in the Swedish national Registry and data regarding bleedings, treat-ment with factor concentrate, inhibitor status, mutations, viral infections such as hepatitis C and HIV are collected. Patient reported outcome measurements (PROM)- such as pain and quality of life - HJHS and target joints are followed continuously. Discussion/Conclusion : The establishment of a Swedish National Registry enables us to perform national annual reports, have a close follow- up of our patients and perform clinical research. Currently are working on an on- line patient treatment application recording directly into the registry. Data from the registry will be an important tool for further evaluation of the treatment of hemophilia and how it affects the long- term consequences of the disease.
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| 6. |
- Kehoe, Laura, et al.
(författare)
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Make EU trade with Brazil sustainable
- 2019
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Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 364:6438, s. 341-
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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| 7. |
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| 8. |
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| 9. |
- Alaie, Iman, et al.
(författare)
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Uppsala Longitudinal Adolescent Depression Study (ULADS)
- 2019
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Ingår i: BMJ Open. - : BMJ Publishing Group Ltd. - 2044-6055. ; 9:3
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Tidskriftsartikel (refereegranskat)abstract
- Purpose: To present the Uppsala Longitudinal Adolescent Depression Study, initiated in Uppsala, Sweden, in the early 1990s. The initial aim of this epidemiological investigation was to study the prevalence, characteristics and correlates of adolescent depression, and has subsequently expanded to include a broad range of social, economic and health-related long-term outcomes and cost-of-illness analyses.Participants: The source population was first-year students (aged 16-17) in upper-secondary schools in Uppsala during 1991-1992, of which 2300 (93%) were screened for depression. Adolescents with positive screening and sex/age-matched peers were invited to a comprehensive assessment. A total of 631 adolescents (78% females) completed this assessment, and 409 subsequently completed a 15year follow-up assessment. At both occasions, extensive information was collected on mental disorders, personality and psychosocial situation. Detailed social, economic and health-related data from 1993 onwards have recently been obtained from the Swedish national registries for 576 of the original participants and an age-matched reference population (N=200 000).Findings to date: The adolescent lifetime prevalence of a major depressive episode was estimated to be 11.4%. Recurrence in young adulthood was reported by the majority, with a particularly poor prognosis for those with a persistent depressive disorder or multiple somatic symptoms. Adolescent depression was also associated with an increased risk of other adversities in adulthood, including additional mental health conditions, low educational attainment and problems related to intimate relationships.Future plans: Longitudinal studies of adolescent depression are rare and must be responsibly managed and utilised. We therefore intend to follow the cohort continuously by means of registries. Currently, the participants are approaching mid-adulthood. At this stage, we are focusing on the overall long-term burden of adolescent depression. For this purpose, the research group has incorporated expertise in health economics. We would also welcome extended collaboration with researchers managing similar datasets.
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