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Refugees report a diverse array of psychological responses following persecution and displacement. Little is known, however, regarding the mechanisms that underlie differential psychological reactions in refugees. This study investigated the longitudinal impact of negative moral appraisals about one's own actions [i.e. moral injury-self (MI-self) appraisals] and others' actions [i.e. moral injury-other (MI-others) appraisals] on a variety of psychological symptoms over a period of 6 months.
Methods
Participants were 1085 Arabic, Farsi, Tamil, or English-speaking refugees who completed a survey at baseline and 6 months later either on-line or via pen-and-paper. The survey indexed demographic factors, exposure to potentially traumatic events (PTEs), exposure to ongoing stressors, MI-other appraisals, MI-self appraisals, re-experiencing and arousal symptoms, and feelings of sadness, anger and shame.
Results
Findings indicated that, after controlling for demographics, PTE exposure and ongoing stressors, MI-other appraisals predicted increased re-experiencing and hyperarousal symptoms, and feelings of sadness and shame. MI-self appraisals predicted decreased feelings of shame, and decreased re-experiencing symptoms. In contrast, psychological symptoms at baseline did not as strongly influence MI appraisals 6 months later.
Conclusions
These findings highlight the important role that cognitive appraisals of adverse events play in the longitudinal course of psychological symptoms. These results thus have important implications for the development of tailored psychological interventions to alleviate the mental health burden held by refugees.
By
Greg McMahon, Department of Surgery and Cardiovascular Sciences, University of Leicester, Leicester, UK,
Mark McCarthy, Department of Surgery and Cardiovascular Sciences, University of Leicester, Leicester, UK
Currently, treatment options for peripheral vascular disease include angioplasty and reconstructive surgery. An attractive, less invasive alternative could involve the revascularization of ischaemic tissue by the induction of vascular growth. It would be particularly welcome for patients in whom current approaches are difficult or prone to failure, including those with conditions that make surgical intervention unsafe, patients with diffuse occlusive disease and those in whom there is significant downstream microvascular disease. Recent years have witnessed major advances in the understanding of the molecular mechanisms underlying vascular formation and remodelling, as well as the identification of key molecules controlling these processes. Most research has focused on the induction of new vessel formation by stimulating angiogenesis and this has been the goal of the clinical trials directed at peripheral vascular disease. But, whilst the stimulation of angiogenesis may relieve microvascular disease, the bypass of occluded conduit vessels requires the formation of more substantial collateral vessels by the process of arteriogenesis. This chapter will review current understanding of the mechanisms controlling angiogenesis and arteriogenesis; approaches that are, and could be pursued to induce vessel growth in peripheral vascular disease, as well as summarizing the current status of clinical trials.
MECHANISMS OF VASCULAR GROWTH
Strategies currently being developed for the therapeutic induction of vessel growth have evolved, largely, from knowledge of the physiological mechanisms of developmental vascularisation. In development, blood vessels arise initially by the process of vasculogenesis during which precursor cells, known as angioblasts, differentiate into endothelial cells and organize into primitive vessels.
This chapter outlines the hemostatic response to vascular damage in the carotid artery and considers the endogenous hemostatic factors that may determine the likelihood of embolization in patients. It discusses the mechanisms involved in thrombus formation and stabilization. Platelets provide a reinforced loop in the generation of a thrombus, providing a source of thrombin to recruit new platelets and propagate clot formation. The mechanism of stabilization of a thrombus by P-selectin appears to be partly stabilization of platelet-platelet aggregates but mostly through recruitment of leucocytes via interaction of P-selectin with PSGL-1. Many factors are involved in forming a stable thrombus and consequently there are many candidates for regulating the risk of embolization. Antiplatelet and antithrombotic therapies are of benefit in limiting the growth of thrombus within the carotid vessel. In particular, adenosine diphosphate (ADP) seems to have a very specific role in regulating embolization.
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