SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Gyllenhammar Eva) "

Sökning: WFRF:(Gyllenhammar Eva)

  • Resultat 1-8 av 8
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Andreassen, Eva, et al. (författare)
  • Kokbok för förändringsledare : Metdoder för att stötta engagerade människor att förverkliga idéer
  • 2020
  • Bok (övrigt vetenskapligt/konstnärligt)abstract
    • Det här är en kokbok för förändringsledare. Du kan använda denna bok om du ska leda  utvecklingsaktiviteter och letar efter bra och beprövade metoder för att leda grupper  och processer. Vi beskriver metoderna som vi har använt inom vårt projekt SMICE, i  vilket sammanhang metoderna använts och när de olika metoderna fungerat bra. Vår förhoppning med att nedteckna dessa metoder är att du ska inspireras och vågar  prova något nytt för att skapa nytta. Vi tror att ett detaljerat sätt att dokumentera  metoderna gör dem mer användbara för dig men också för oss själva.   Metoderna är graderade efter vilket behov av förkunskap och förberedelser du behöver,  från det enklaste, där du kan öppna kokboken och använda metoden på en gång, till  metoder som kräver utbildning eller specialistkompetens innan du sätter igång. Boken är indelad i fyra huvuddelar; Starta, Forma, Utveckla och förankra och Bygga vidare. Till dessa delar har vi identifierat metodstöd som kan användas vid en rad olika tillfällen;  vid idégenerering, vid idéutveckling, vid affärsutveckling, för att inspirera, för att skapa  samsyn och samverkan och för att mobilisera större grupper av människor och  organisationer. Något för alla, alltså. Avslutningsvis finner du tips och stöd för att  driva dessa utvecklingsprocesser på distans med digitala verktyg i digitala möten.  Ska vi sammanfatta någon lärdom av detta arbete så blir det våra nycklar som presenteras på nästa sida. Du kan se dessa nycklar som våra bästa råd för att du ska lyckas med ditt  arbete med att leda processer och att ordna möten. Lycka till! Metoderna har testats och utvecklats inom SMICE - Samskapande Mittnordisk  Innovationsarena för Cirkulär Ekonomi, ett projekt inom Interreg som pågått  2017-2020. 
  •  
2.
  • Fernlund, Eva I., et al. (författare)
  • Serum biomarkers of early stages of hypertrophic cardiomyopathy in a young population
  • 2015
  • Ingår i: Journal of the American College of Cardiology. - 0735-1097. ; 65:10S, s. 787-787
  • Konferensbidrag (refereegranskat)abstract
    • Background: Hypertrophic cardiomyopathy (HCM) is the most common monogenic cardiac disorder and the leading cause of sudden cardiac death in the young. Although in a majority of HCM cases there are gene mutations coding for sarcomere proteins, the onset for the clinical consequences of these mutations are difficult to predict, as these mutations do not show any clear relationship to the degree of myocardial hypertrophy. Hence identification of early markers for this disease is important. The aim of this study was to investigate novel serum biomarkers reflecting myocardial remodeling, microfibrosis and coronary endotheliopathy in young presymtomatic HCM patients and in individuals at risk for developing HCM. Methods: Eighty-nine participants (18 HCM patients, 14 HCM-risk individuals, and 57 healthy controls) with median age of 15 (range 0-30) years underwent assessment with echocardiography and serum analysis for myostatin, cathepsin S, endostatin, type I collagen degradation marker (ICTP), matrix metalloproteinase (MMP) 9, vascular (VCAM) and intercellular adhesion molecules (ICAM). In some individuals, myocardial perfusion was measured both at rest and after adenosine via magnetic resonance. Results: Both cathepsin S and endostatin were increased in the HCM group (p0.3) and diastolic function, expressed as E/e' (p0.3). In the HCM-risk group, myostatin was decreased (p0.1). Conclusion: To the best of our knowledge, this is the first study to suggest early onset changes in biomarkers of myoblast regulation, endothelial function and matrix remodeling in young presymptomatic HCM patients and in HCM-risk individuals.
  •  
3.
  •  
4.
  • I. Fernlund, Eva, et al. (författare)
  • Serum Biomarkers of Myocardial Remodeling and Coronary Dysfunction in Early Stages of Hypertrophic Cardiomyopathy in the Young
  • 2017
  • Ingår i: Pediatric Cardiology. - : Springer Science and Business Media LLC. - 0172-0643 .- 1432-1971. ; 38:4, s. 853-863
  • Tidskriftsartikel (refereegranskat)abstract
    • Hypertrophic cardiomyopathy (HCM) remains the leading cause of sudden cardiac death in the young. Early markers for HCM are important to identify individuals at risk. The aim of this study was to investigate novel serum biomarkers reflecting myocardial remodeling, microfibrosis, and vascular endotheliopathy in the early stages of familial HCM in young patients. Twenty-three HCM patients, 16 HCM-risk individuals, and 66 controls (median 15 years) underwent echocardiography and serum analysis for cathepsin S, endostatin, myostatin, type I collagen degradation marker (ICTP), matrix metalloproteinase (MMP)-9, vascular endothelial growth factor receptor (VEGFR)-1, and vascular and intercellular adhesion molecules (VCAM, ICAM). In a subset of the population, global myocardial perfusion was performed by magnetic resonance imaging. Cathepsin S (p = 0.0009), endostatin (p < 0.0001), MMP-9 (p = 0.008), and VCAM (p = 0.04) were increased in the HCM group and correlated to left ventricular mass index and mitral E/e′ (p < 0.01). In the HCM-risk group, myostatin was decreased (p = 0.004), whereas ICAM was increased (p = 0.002). Global perfusion was decreased in the HCM group (p < 0.05) versus controls. Endostatin and mitral E/e′ correlated inversely to myocardial perfusion (p ≤ 0.05). This is the first study demonstrating adverse changes in biomarkers reflecting myocardial matrix remodeling, microfibrosis, and vascular endotheliopathy in early stage of hypertrophic cardiomyopathy in the young.
  •  
5.
  • Lundin, Magnus, et al. (författare)
  • Left ventricular global wall thickness is easily calculated, detects and characterizes hypertrophy, and has prognostic utility
  • 2019
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
    • BACKGROUND: Cardiovascular magnetic resonance (CMR) can be used to measure left ventricular end-diastolic volume (LVEDV) and left ventricular mass (LVM). However, there is currently no good way to measure the normality of LVM in relation to a given LVEDV. We hypothesized that a simple measure of left ventricular global wall thickness (GWT) would be accurate, beneficial for detecting and characterizing hypertrophy, and have prognostic significance.METHODS: Subjects underwent CMR at 1.5T, including healthy volunteers (n=99) and patients assessed for heart disease (n=2828).RESULTS: GWT calculated from LVEDV and LVM had excellent agreement with measured mean end-diastolic wall thickness of the entire left ventricle (bias 0.01±0.23mm). GWT was most predictive of death or hospitalization for heart failure in patients with normal findings by CMR (n=326, log-rank 26.8, p<0.001, median [interquartile range] follow-up 5.8 [5.0–6.7] years). GWT indexed to body surface area (GWTi) was most predictive of outcomes in patients with normal LVEDV index (n=1352, log-rank 36.4, p<0.001, follow-up 5.5 [4.1–6.5] years). Patients with concentric remodeling had worse prognosis than the normal patients (p=0.02), and the patients with hypertrophy had worse prognosis than both normal patients (p<0.001) and patients with concentric remodeling (p=0.045), see Figure 1. Of patients with suspected heart disease but normal CMR findings regarding left ventricular volumes, function, mass, and scar, 22% were found to have increased mean GWTi corresponding to concentric remodeling, see Figure 2.CONCLUSIONS: Left ventricular GWT is an intuitive measure that can be easily calculated from mass and volume with high accuracy, and has prognostic utility in patients with normal CMR findings. Also, GWTi classifies hypertrophy as concentric or eccentric, and detects concentric remodeling in a substantial portion of patients with otherwise normal findings.
  •  
6.
  •  
7.
  • Lundin, Magnus, et al. (författare)
  • Prognostic utility and characterization of left ventricular hypertrophy using global thickness
  • 2023
  • Ingår i: Scientific Reports. - 2045-2322. ; 13:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Cardiovascular magnetic resonance (CMR) can accurately measure left ventricular (LV) mass, and several measures related to LV wall thickness exist. We hypothesized that prognosis can be used to select an optimal measure of wall thickness for characterizing LV hypertrophy. Subjects having undergone CMR were studied (cardiac patients, n = 2543; healthy volunteers, n = 100). A new measure, global wall thickness (GT, GTI if indexed to body surface area) was accurately calculated from LV mass and end-diastolic volume. Among patients with follow-up (n = 1575, median follow-up 5.4 years), the most predictive measure of death or hospitalization for heart failure was LV mass index (LVMI) (hazard ratio (HR)[95% confidence interval] 1.16[1.12-1.20], p < 0.001), followed by GTI (HR 1.14[1.09-1.19], p < 0.001). Among patients with normal findings (n = 326, median follow-up 5.8 years), the most predictive measure was GT (HR 1.62[1.35-1.94], p < 0.001). GT and LVMI could characterize patients as having a normal LV mass and wall thickness, concentric remodeling, concentric hypertrophy, or eccentric hypertrophy, and the three abnormal groups had worse prognosis than the normal group (p < 0.05 for all). LV mass is highly prognostic when mass is elevated, but GT is easily and accurately calculated, and adds value and discrimination amongst those with normal LV mass (early disease).
  •  
8.
  • Lundstrom, Staffan, et al. (författare)
  • Together we can : experiences from 7 years of cross-sectional studies in a Swedish palliative care clinical research network
  • 2010
  • Ingår i: Palliative Medicine. - : SAGE Publications. - 0269-2163 .- 1477-030X. ; 24:3, s. 261-266
  • Tidskriftsartikel (refereegranskat)abstract
    • During recent years, research networks and collaboratives focusing on palliative care research have been established both nationally and internationally resulting in several ongoing projects. In 2002, a clinician-based research network, the Palliative Care Research Network in Sweden (PANIS), was established to stimulate research and development of palliative care in Sweden. The growing network, which today includes 60 specialized palliative care units, has used a web-based survey generator to collect data on symptom prevalence, treatment traditions and important issues in palliative care. Eleven different studies involving almost 11,000 patients have been performed within the network including studies on prevalence of antitumoral treatment, the use of opioids, corticosteroids, blood transfusions, parenteral nutrition and prevalence of palliative sedation therapy in specialized palliative care. The working method of the research network is described, and demographic data from 9,298 patients in six cross-sectional studies are presented. Using a relatively simple research methodology, the network has succeeded in addressing key clinical questions and in this article we share experiences and challenges met during the journey.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-8 av 8
Typ av publikation
tidskriftsartikel (4)
konferensbidrag (3)
bok (1)
Typ av innehåll
refereegranskat (5)
övrigt vetenskapligt/konstnärligt (3)
Författare/redaktör
Carlsson, Marcus (5)
Gyllenhammar, Tom (5)
Arheden, Håkan (4)
Engblom, Henrik (4)
Atar, Dan (3)
Lundin, Magnus (3)
visa fler...
Erlinge, David (3)
Maret, Eva (3)
Borgquist, Rasmus (3)
Heiberg, Einar (3)
Nordlund, David (3)
Khoshnood, Ardavan (3)
Ekelund, Ulf (3)
Steding-Ehrenborg, K ... (3)
Schelbert, Erik B. (3)
Sörensson, Peder (3)
Sigfridsson, Andreas (3)
Ugander, Martin (3)
Themudo, Raquel (3)
Nickander, Jannike (3)
Kozor, Rebecca (3)
Larsson, Anders (2)
Liuba, Petru (2)
Caidahl, Kenneth (2)
Jablonowski, Robert (2)
vanderPals, Jesper (2)
Moon, James (2)
Johansson, Karin (1)
Strang, Peter (1)
Hedlund, Christer, 1 ... (1)
Fernlund, Eva (1)
Lilja, Johan (1)
Carlsson, M (1)
Ahlin, Karin, 1963- (1)
Persson Slumpi, Thom ... (1)
Caidahl, Kenneth, 19 ... (1)
Liuba, P. (1)
Lundstrom, Staffan (1)
Jögi, Jonas (1)
Ärnlöv, Johan (1)
Andreassen, Eva (1)
Solveig, Gyllenhamma ... (1)
Stenmark, Petter (1)
Blomqvist, Maja (1)
Nätterlund, Karolina (1)
Jablonowski, R (1)
Van Der Pals, Jesper (1)
Arnlov, Johan (1)
Martinsson, Ulla (1)
Fernlund, Eva I. (1)
visa färre...
Lärosäte
Lunds universitet (6)
Karolinska Institutet (3)
Uppsala universitet (2)
Göteborgs universitet (1)
Linköpings universitet (1)
Mittuniversitetet (1)
visa fler...
Karlstads universitet (1)
visa färre...
Språk
Engelska (8)
Forskningsämne (UKÄ/SCB)
Medicin och hälsovetenskap (6)
Teknik (1)
Samhällsvetenskap (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy