Surgical management for venous leg ulcers: The role of hope, investment and agency

2016 ◽  
Vol 23 (8) ◽  
pp. 1075-1084
Author(s):  
Philippa Tollow ◽  
Jane Ogden

A recent systematic review suggests that minimally invasive venous surgery for the treatment of leg ulcers may have a greater impact on quality of life than traditional approaches. A total of 11 participants who had previously undergone surgical management for leg ulcers took part in semi-structured interviews regarding their experiences. Using thematic analysis, three themes were identified: ‘Living in Flux’, ‘Perceptions of Chronicity’ and ‘Expectations’. Surgical treatment may not only improve patients’ quality of life due to treatment of the condition but also by opening up a sense of hope, investment and agency not associated with traditional treatment approaches.

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 5020-5020
Author(s):  
Anisha Patel ◽  
Karina Raimundo ◽  
Corey Stepule ◽  
Jennifer Whiteley ◽  
Richard H Ko

Abstract Introduction: Emicizumab, a bispecific antibody to factors IXa/X, was approved by the Food and Drug Administration in 2017 for prophylactic treatment of persons with hemophilia A (PwHA) with inhibitors. Compared with other treatments for PwHA, emicizumab has a novel mechanism of action. It is the first hemophilia A (HA) treatment administered subcutaneously and has a much longer half-life than previous treatments; hence, disease management with emicizumab can be different. This study aimed to evaluate how physicians manage HA in patients treated with emicizumab. Methods: This qualitative analysis is the first phase of a planned mixed-methods approach study and comprised 1-hour, blinded telephone interviews with 5 hematologists in all 4 geographic regions of the US. Physicians were included if they met the following criteria: 1) MD or DO degree; 2) board-certified hematologist; 3) practice in the US; 4) ≥2 years of experience post-residency; and 5) currently treat PwHA. To evaluate experience with emicizumab, physicians were also required to have treated a minimum number of patients receiving emicizumab (5 for physicians in hemophilia treatment centers [HTCs] and 3 for physicians in non-HTCs). A total of 5 qualitative interviews were conducted in May and June 2018 to understand the physicians' perspectives on treating PwHA with emicizumab. Interview topics included general management of PwHA, inhibitor screening and testing, management of PwHA with inhibitors, and physicians' experiences treating patients with emicizumab. We report common themes that descriptively emerged from the qualitative interviews, which will inform survey development for the quantitative phase of the study. Results: Of the 5 physicians, 3 were adult hematologists and 4 physicians reported seeing patients in an HTC. All physicians reported having at least 10 years of experience in practice post-residency. Regarding management of PwHA, physicians indicated disease severity, inhibitor status and annual bleed rate as critical factors in guiding treatment decision making. Patients who develop inhibitors require more medical engagement and frequent monitoring. Physicians reported that, from their experience, emicizumab results in a reduction in bleeds, leading to fewer office visits and less monitoring in PwHA with inhibitors. In addition, physicians reported that the need for disease management, even among patients with a phenotype with more bleeding, is lower as a result of emicizumab treatment due to decreased bleed rate and a reduction in need for additional treatments. Physicians reported that emicizumab's subcutaneous, once-weekly dosing leads to improved patients' quality of life and confidence in performing activities without bleeds. Acute bleed management with emicizumab was reported to be slightly different than before, given the boxed warning around concomitant treatment with activated prothrombin complex concentrate; however, the physicians indicated that they still recommend to treat bleeds as soon as one is suspected. Physicians articulated that some questions remain, including the role of immune therapy induction (ITI), use in low-titer inhibitors, and surgical management in patients treated with emicizumab. Physicians reported that there have been no significant access challenges and none of their patients have discontinued therapy; however, long-term monitoring and safety data are needed. Conclusions: This qualitative study suggests that management of PwHA with inhibitors receiving emicizumab is evolving. The interviewed physicians reported that their patients receiving emicizumab experience fewer bleeds and have an improved quality of life. However, questions regarding the role of ITI, surgical management, and long-term safety of emicizumab remain. Future research will provide additional insights into the current management of PwHA with inhibitors treated with emicizumab among US physicians. Disclosures Patel: Genentech Inc: Employment. Raimundo:Genentech Inc: Employment, Other: Ownership interests PLC. Stepule:MedPanel, Inc.: Employment. Whiteley:Genentech, Inc.: Employment, Other: Ownership interests none PLC. Ko:Genentech Inc: Employment; F. Hoffmann-La Roche Ltd: Other: Ownership interests non-PLC.


2020 ◽  
Vol 30 (Supplement_5) ◽  
Author(s):  
S Marini ◽  
A Masini ◽  
P Maietta Latessa ◽  
T Sanna ◽  
A Raggi ◽  
...  

Abstract Background Osteoporosis is a major health burden worldwide and require a multi-modal approach including exercise. Fractures have a substantial impact on quality of life (QoL) so exercise programs may to be conducted by trainers able to deal with this condition, because exercise alone, even if in the right dosage, seems to be not enough to improve QoL. A quasi-experimental pilot study performed to determine the feasibility and safety of an Adapted Physical Activity (APA) protocol specifically designed for osteoporotic women with vertebral fractures and its effect on QoL, with a specific focus on trainer's role. Methods The Experimental Group (EG) performed APA protocol 1hour twice a week for 6 months, while the Control Group (CG) received standard care. QoL was assessed at baseline and follow-up with ECOS-16 questionnaire and semi structured interviews to understand women perceptions regarding trainer's role. Using mixed-methods quantitative and qualitative data were analyzed using SPSS 5 and NVivo 12, respectively. Results 40 post-menopausal women (mean age: 67.6±4.6) divided in 2 groups EG = 22 and CG = 18, completed the study. At follow-up, EG improved significantly QoL (EG: -0.5±0.5 vs CG: 0.0±0.3 p = 0.02). The APA intervention had a significant effect on all the components of QoL, as measured by the disease-specific ECOS-16 questionnaire: Physical Component Summary (PCS) (EG: -0.4±0.5 vs CG: 0.0±0.4 p = 0.06) and Mental Component Summary (MCS) (EG: -0.5±0.6 vs CG: 0.1±0.5 p = 0.02). The interviews confirmed this result, emphasizing the key role of the trainer in improving their QoL. The adherence calculated as number of sessions performed compared to the sessions proposed was 75.8%. No injuries were observed. Conclusions The feasibility, the safety, and the positive effect of the proposed exercise protocol on QoL confirmed also by the interviews, show that principles of exercise education applied by trainers should be extended also to patients with other chronic condition. Key messages Trainers specifically educated, could be a means of achieving the goal improving people’s QoL, as they occupy the role of exercise experts and also an educational, relational and support role. The management of osteoporosis is multi-modal and includes exercise, often recommended as a beneficial non-pharmacological treatment to slow the rate of bone loss and improve quality of life.


2020 ◽  
Author(s):  
Tayah M. Liska ◽  
Angie Kolen

Abstract Purpose As a result of a cancer diagnosis and treatment, many cancer survivors experience persistent physical, mental, and emotional symptoms that affect their quality of life. Physical activity has been identified as an intervention that may help to manage the side effects of a cancer diagnosis and its treatment. The purpose of this study was to investigate the role of physical activity on overall quality of life in adult cancer survivors.Methods One-on-one semi structured interviews were conducted in person or via telephone with 13 adult (≥18 yrs) cancer survivors who had completed cancer treatment.Results These cancer survivors described their physical activity as improving their physical functioning and mental health, as a means of positive social engagement, and adding positivity to their daily life.Conclusion These results support the role of physical activity to enhance cancer survivors’ quality of life regardless of the treatment(s) type, duration, or time since the end of active cancer treatment. Further research is warranted to (a) expand this research with a larger sample, (b) examine healthcare providers’ knowledge and application of exercise guidelines to cancer survivors in cancer care, and (c) explore implementation strategies for greater advocacy for healthcare providers to share the exercise recommendations with cancer survivors.


2011 ◽  
Vol 6 (3) ◽  
pp. 208 ◽  
Author(s):  
Marco Riva ◽  
Giuseppe Casacel i ◽  
Antonel la Castellano ◽  
Enrica Fava ◽  
Andrea Falini ◽  
...  

The aims of the surgical management of cerebral gliomas are to achieve the widest feasible resection and preserve the patient’s functional integrity. This results in an improved survival rate and a favourable quality of life. When treating this disease, current neuroradiological techniques are important for preoperative depiction and planning, and intraoperative image-guided resection, especially when the tumour involves eloquent cortical and subcortical structures. Knowledge of these techniques and their limitations, and appropriate expertise are therefore necessary to gain the complete benefit of their diagnostic and therapeutic power.


2015 ◽  
Vol 31 (2) ◽  
pp. 82-93 ◽  
Author(s):  
Philippa Tollow ◽  
Jane Ogden ◽  
Mark S Whiteley

Objectives Leg ulcers are known to have a profound effect on patients’ quality of life; however, the influence of different treatment approaches is unclear. This review aims to evaluate the comparative impact of conservative treatments and superficial venous surgery, for venous leg ulcers, on patients’ Quality of Life. Data sources Three electronic databases (PsycInfo, Medline and CINAHL), and reference lists of relevant articles, were searched. A total of 209 articles were initially identified, and 16 articles were included in the review. Results The results lend cautious support to the suggestion that all treatments have a positive effect on quality of life, regardless of type, whilst wound status also appears to be an important factor. Conclusions Some evidence suggests that surgical treatment methods may lead to greater improvements in patients’ quality of life than compression bandaging alone; however, future research may focus on the psychological mechanisms underlying such changes.


2016 ◽  
Vol 23 (7) ◽  
pp. 893-904 ◽  
Author(s):  
Narelle Warren ◽  
Deirdre M Melrose ◽  
Joanne E Brooker ◽  
Sue Burney

Many women with gynecological cancer report psychosocial distress, and clarification of the risks, vulnerabilities, and protective factors is required. The aim of this study was to investigate the lived experience of gynecological cancer patients and to understand the factors that underlie psychosocial distress. Semi-structured interviews with seven women diagnosed with gynecological cancer revealed the role of social support, or its absence, selective withholding of information, and existential loneliness in women’s experience of distress. Social support provided a buffer against distress, while feelings of alienation and being alone exacerbated distress. Interventions to address these concerns may lead to improved quality of life for this patient group.


1970 ◽  
Vol 3 (3) ◽  
pp. 25-34 ◽  
Author(s):  
Katrine de Freitas Valeriano ◽  
Thais de Paiva Guimarães Barreiro ◽  
José Vitor Da Silva ◽  
Jorge Leonardo Narcy ◽  
Maria Tereza de Jesus Pereira

Objetivos: conhecer os significados e os sentimentos emergentes dos médicos em relação aos cuidados paliativos, bem como identificar a atuação desses profissionais frente aos pacientes com necessidades de cuidados paliativos numa instituição hospitalar da cidade de Pouso Alegre-MG. Materiais e métodos: o presente trabalho foi de abordagem qualitativa, do tipo exploratório e transversal.  A amostra foi de 25 médicos atuantes no Hospital Universitário Samuel Libânio, Pouso Alegre, MG. A amostragem foi do tipo intencional ou teórica. A coleta de dados ocorreu por meio de entrevista semiestruturada e usaram-se as estratégias metodológicas do Discurso do Sujeito Coletivo (DSC) para a análise e tratamento dos dados. Resultados e discussão: do tema “significado de cuidados paliativos”, emergiram-se as ideias de cuidados diversificados, aliviar a dor e o sofrimento e proporcionar conforto. Do tema “sentimento ao prestar assistência”, as representações sociais dos médicos foram diversos sentimentos negativos, diversos sentimentos positivos e sentimentos ambivalentes. Sobre o “atendimento aos pacientes”, os médicos mencionaram as ideias de oferecer conforto e qualidade de vida, atendendo o paciente normalmente e dando atenção. Conclusão: A atuação profissional dos médicos abordados, em paliação, visa a oferecer conforto e qualidade de vida, mas se verifica que há uma diversidade de significados e sentimentos em relação aos cuidados paliativos na percepção destes profissionais.  Palavras chave: Cuidados paliativos; Medicina; Terminalidade.   ABSTRACT Objectives: To know the meanings and feelings emerging of physicians in relation to palliative care, and to identify the role of these professionals against patients in need of palliative care in a hospital in the city of Pouso Alegre-MG. Materials and methods: This study was a qualitative, exploratory and cross. The sample consisted of 25 doctors working at the University Hospital Samuel Libânio, Pouso Alegre, MG. Sampling was the intentional or theoretical. The data were collected through semi-structured interviews and used up the methodological strategies of the Collective Subject Discourse (CSD) for the analysis and processing of data. Results and discussion: theme "meaning of palliative care," sprang up ideas diversified care, relieve pain and suffering and provide comfort. Theme "feeling to assist" the social representations of the doctors were many negative feelings, many positive feelings and ambivalent feelings. On the "patient care" physicians mentioned the ideas of comfort and quality of life, given the patient normally and paying attention. Conclusion: The role of physicians addressed in palliation, aims to offer comfort and quality of life, but it turns out that there is a diversity of meanings and feelings in relation to the perception of palliative care professionals.  Keywords: Palliative care; Medicine; Terminality.


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