26 research outputs found

    Changer sa façon de changer – Grandes orientations du CSP Jura pour les décennies à venir

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    In seinem Beitrag « Changer sa façon de changer – Grandes orientations du CSP Jura pour les décennies à venir » ergründet Gabriel de Montmollin die zukünftigen Arbeitsschwerpunkte für die CSP in der Romandie.De Montmollin geht davon aus, dass die Gesellschaft zukünftig mit folgenden sozialen Herausforderungen konfrontiert sein wird: Die ökologischen Entwicklungen, die Digitalisierung der Arbeitswelt, die Migrationsströme sowie die demografische Alterung. Diesen Herausforderungen will de Montmollin begegnen, indem er sie in unterschiedlicher Weise aufeinander bezieht und so neue Stärken und Synergien schafft:Zu den Herausforderungen «Migration» und «demografische Alterung» führt de Montmollin die Leserin / den Leser auf den Wohnungsmarkt der Stadt Genf, der bekanntlich kaum Leerbestände aufweist und in welchem hohe Mieten zu bezahlen sind – junge Menschen sowie Migrantinnen und Migranten finden kaum mehr (bezahlbare) Unterkunft. Zugleich wohnen ältere, alleinstehende Menschen – zuweilen in einsamen Lebenssituationen – alleine in grösseren Wohnungen oder Häusern. Er plädiert dafür, aus mit innovativen Wohnprojekten den beidseitigen Problemlagen (Wohnungsnot einerseits und Einsamkeit andererseits) zu begegnen.Den Herausforderungen «ökologische Entwicklung» und «Digitalisierung der Arbeitswelt» will de Montmollin mit neuen protestantischen Impulsen in der Arbeitswelt begegnen: Wenn mehr und mehr Roboter den Menschen Arbeitsplätze wegnähmen, so müssten diese freiwerdenden Ressourcen eingesetzt werden für Anstrengungen im Bereich des ökologischen Wirtschaftens: die CSP sollten sich zu «grünen» CSP weiterentwickeln.Schliesslich spricht sich de Montmollin – analog den Modellen von Rotem Kreuz und Caritas – dafür aus, dass sich auch die CSP in eine nationale und internationale Struktur integrieren und dem Hilfswerk der evangelischen Kirchen der Schweiz (HEKS) fusionieren

    Prevalence, associated factors and outcomes of pressure injuries in adult intensive care unit patients: the DecubICUs study

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    Funder: European Society of Intensive Care Medicine; doi: http://dx.doi.org/10.13039/501100013347Funder: Flemish Society for Critical Care NursesAbstract: Purpose: Intensive care unit (ICU) patients are particularly susceptible to developing pressure injuries. Epidemiologic data is however unavailable. We aimed to provide an international picture of the extent of pressure injuries and factors associated with ICU-acquired pressure injuries in adult ICU patients. Methods: International 1-day point-prevalence study; follow-up for outcome assessment until hospital discharge (maximum 12 weeks). Factors associated with ICU-acquired pressure injury and hospital mortality were assessed by generalised linear mixed-effects regression analysis. Results: Data from 13,254 patients in 1117 ICUs (90 countries) revealed 6747 pressure injuries; 3997 (59.2%) were ICU-acquired. Overall prevalence was 26.6% (95% confidence interval [CI] 25.9–27.3). ICU-acquired prevalence was 16.2% (95% CI 15.6–16.8). Sacrum (37%) and heels (19.5%) were most affected. Factors independently associated with ICU-acquired pressure injuries were older age, male sex, being underweight, emergency surgery, higher Simplified Acute Physiology Score II, Braden score 3 days, comorbidities (chronic obstructive pulmonary disease, immunodeficiency), organ support (renal replacement, mechanical ventilation on ICU admission), and being in a low or lower-middle income-economy. Gradually increasing associations with mortality were identified for increasing severity of pressure injury: stage I (odds ratio [OR] 1.5; 95% CI 1.2–1.8), stage II (OR 1.6; 95% CI 1.4–1.9), and stage III or worse (OR 2.8; 95% CI 2.3–3.3). Conclusion: Pressure injuries are common in adult ICU patients. ICU-acquired pressure injuries are associated with mainly intrinsic factors and mortality. Optimal care standards, increased awareness, appropriate resource allocation, and further research into optimal prevention are pivotal to tackle this important patient safety threat

    Long-term Quality of Life in Adult Patients Surviving Purpura Fulminans: An Exposed-Unexposed Multicenter Cohort Study

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    International audienceAbstract Background Long-term health-related quality of life (HR-QOL) of patients surviving the acute phase of purpura fulminans (PF) has not been evaluated. Methods This was a French multicenter exposed-unexposed cohort study enrolling patients admitted in 55 intensive care units (ICUs) for PF from 2010 to 2016. Adult patients surviving the acute phase of PF (exposed group) were matched 1:1 for age, sex, and Simplified Acute Physiology Score II with septic shock survivors (unexposed group). HR-QOL was assessed during a phone interview using the 36-Item Short-Form Health Survey (SF-36) questionnaire, the Hospital Anxiety and Depression (HAD) scale, the Impact of Event Scale–Revised (IES-R), and the activity of daily living (ADL) and instrumental ADL (IADL) scales. The primary outcome measure was the physical component summary (PCS) of the SF-36 questionnaire. Results Thirty-seven survivors of PF and 37 of septic shock were phone-interviewed at 55 (interquartile range [IQR], 35–83) months and 44 (IQR, 35–72) months, respectively, of ICU discharge (P = .23). The PCS of the SF-36 was not significantly different between exposed and unexposed patients (median, 47 [IQR, 36–53] vs 54 [IQR, 36–57]; P = .18). There was also no significant difference between groups regarding the mental component summary of the SF-36, and the HAD, IES-R, ADL and IADL scales. Among the 37 exposed patients, those who required limb amputation (n = 12/37 [32%]) exhibited lower PCS (34 [IQR, 24–38] vs 52 [IQR, 42–56]; P = .001) and IADL scores (7 [IQR, 4–8] vs 8 [IQR, 7–8]; P = .021) compared with nonamputated patients. Conclusions Long-term HR-QOL does not differ between patients surviving PF and those surviving septic shock unrelated to PF. Amputated patients have an impaired physical HR-QOL but a preserved mental health. Clinical Trials Registration NCT03216577
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