SwePub
Tyck till om SwePub Sök här!
Sök i SwePub databas

  Extended search

AND is the default operator and can be omitted

Träfflista för sökning "hsv:(MEDICAL AND HEALTH SCIENCES) hsv:(Clinical Medicine) hsv:(Surgery) ;lar1:(hb)"

Search: hsv:(MEDICAL AND HEALTH SCIENCES) hsv:(Clinical Medicine) hsv:(Surgery) > University of Borås

  • Result 1-10 of 17
Sort/group result
   
EnumerationReferenceCoverFind
1.
  • Andersson, Henrik, 1968-, et al. (author)
  • The early chain of care in bacteraemia patients: Early suspicion, treatment and survival in prehospital emergency care
  • 2018
  • In: American Journal of Emergency Medicine. - : Elsevier BV. - 0735-6757 .- 1532-8171. ; 36:12, s. 2211-2218
  • Journal article (peer-reviewed)abstract
    • Introduction: Bacteraemia is a first stage for patients risking conditions such as septic shock. The primary aim of this study is to describe factors in the early chain of care in bacteraemia, factors associated with increased chance of survival during the subsequent 28 days after admission to hospital. Furthermore, the long-term outcome was assessed. Methods: This study has a quantitative design based on data from Emergency Medical Services (EMS) and hospital records. Results: In all, 961 patients were included in the study. Of these patients, 13.5% died during the first 28 days. The EMS was more frequently used by non-survivors. Among patients who used the EMS, the suspicion of sepsis already on scene was more frequent in survivors. Similarly, EMS personnel noted the ESS code "fever, infection" more frequently for survivors upon arriving on scene. The delay time from call to the EMS and admission to hospital until start of antibiotics was similar in survivors and non-survivors. The five-year mortality rate was 50.8%. Five-year mortality was 62.6% among those who used the EMS and 29.5% among those who did not (p < 0.0001). Conclusion: This study shows that among patients with bacteraemia who used the EMS, an early suspicion of sepsis or fever/infection was associated with improved early survival whereas the delay time from call to the EMS and admission to hospital until start of treatment with antibiotics was not. 50.8% of all patients were dead after five years. (C) 2018 Elsevier Inc. All rights reserved.
  •  
2.
  • Weick, Linn, 1991, et al. (author)
  • Patient experience of implant loss after immediate breast reconstruction : An interpretative phenomenological analysis
  • 2023
  • In: Health Care for Women International. - : Taylor & Francis Group. - 0739-9332 .- 1096-4665. ; 44:1, s. 61-79
  • Journal article (peer-reviewed)abstract
    • Immediate breast reconstruction (IBR) is an integral part of modern breast cancer treatment. Our aim was to investigate patient experience with implant loss after IBR by using interpretative phenomenological analysis (IPA). We conducted semi-structured interviews with eight informants. We analyzed data according to the IPA flexible seven-stage process and four main themes were developed: immediate breast reconstruction as the indisputable choice, a difficult experience, an altered body: redefining normality, and trying to cope. The experience of implant loss appears to affect women for many years and might overshadow some of the benefits of IBR.
  •  
3.
  • Bylow, Helene, et al. (author)
  • Supplementary dataset to self-learning training compared with instructor-led training in basic life support.
  • 2019
  • In: Data in Brief. - : Elsevier BV. - 2352-3409. ; 25
  • Journal article (peer-reviewed)abstract
    • In this article, we present supplementary data to the article entitled "Self-learning training versus instructor-led training in basic life support: a cluster randomised trial" [1]. In three supplementary files, we present the informed consent of the included participants, the modified instrument to calculate the total score for practical skills called "the Cardiff Test of basic life support and automated external defibrillation" and the questionnaire to obtain background factors, theoretical knowledge, self-assessed knowledge and confidence and willingness to act, distributed directly after training and six months after training. The results of comparisons between "directly after intervention" and "six months after intervention", for each training group separately, are presented in three tables. We also present two tables showing the reasons why the participants were not prepared to perform compressions and/or ventilations in the event of a sudden out-of-hospital cardiac arrest.
  •  
4.
  • Herlitz, Johan, 1949, et al. (author)
  • Quality of life 15 years after coronary artery bypass grafting.
  • 2009
  • In: Coronary artery disease. - : Lippincott Williams & Wilkins. - 1473-5830 .- 0954-6928. ; 20:6, s. 363-9
  • Journal article (peer-reviewed)abstract
    • OBJECTIVES: To describe changes in quality of life (QoL) during 15 years after coronary artery bypass grafting (CABG) and prediction of impaired QoL after 15 years. METHODS: All patients in western Sweden who underwent primary CABG without simultaneous valve surgery between 1988 and 1991 were included. QoL during a period of 15 years after CABG was evaluated with three instruments: the Nottingham Health Profile, the Psychological General Well-Being Index, and the Physical Activity Score. RESULTS: A total of 2000 patients took part in the survey, (none excluded) of whom 808 were still alive after 15 years and 79% answered the inquiry. Despite an ongoing decline in QoL over the years, an improvement in QoL was maintained in most sub-dimensions at the 15-year follow-up compared with that prior to surgery. Seven factors emerged as predictors of impaired QoL 15 years after CABG. They are as follows: (i) high age, (ii) female sex, (iii) history of diabetes, (iv) obesity, (v) prolonged stay in the intensive care unit, (vi) prolonged treatment on a ventilator, (vii) need for inotropic drugs at the time of surgery; of which the latter three might be secondary to left ventricular dysfunction. CONCLUSION: Despite an ongoing decline in QoL over the years, there was still an improvement in most aspects of QoL 15 years after CABG compared with that before surgery. Intensified early treatment of diabetes, obesity, and left ventricular dysfunction in CABG patients might allow an even better long-term QoL.
  •  
5.
  • Herlitz, Johan, 1949, et al. (author)
  • Symptoms of chest pain and dyspnoea during a period of 15 years after coronary artery bypass grafting.
  • 2010
  • In: European journal of cardio-thoracic surgery. - : Elsevier. - 1873-734X .- 1010-7940. ; 37:1, s. 112-118
  • Journal article (peer-reviewed)abstract
    • AIM: To describe changes in chest pain and dyspnoea during a period of 15 years after coronary artery bypass grafting (CABG) and to define factors at the time of operation that were associated with the occurrence of these symptoms after 15 years. DESIGN: Prospective observational study in western Sweden. SUBJECTS: All patients who underwent first-time CABG, without simultaneous valve surgery, between 1 June 1988 and 1 June 1991. There were no exclusion criteria. FOLLOW-UP: All patients were followed up prospectively for 15 years. The evaluation of symptoms took place through postal questionnaires prior to and 5, 10 and 15 years after the operation. RESULTS: Totally, 2000 patients were included in the survey and 904 (45%) of them survived to 15 years. Among these 904 survivors, the percentage of patients with chest pain increased from 44% to 50% between the 5- and 15-year follow-up (p=0.004). The percentage of patients who reported symptoms of dyspnoea increased from 60% after 5 years to 74% after 15 years (p<0.001). Factors at the time of surgery that independently tended to predict chest pain after 15 years were higher age (p=0.04) and prolonged duration of symptoms prior to surgery (p=0.04). Predictors of dyspnoea after 15 years were higher age (p<0.0001), the use of inotropic drugs at the time of surgery (p=0.001), a history of diabetes (p=0.01) and obesity (p=0.01). CONCLUSION: After CABG, relief from chest pain and dyspnoea is generally maintained over a long period of time. Eventually, however, functional-limiting symptoms tend to recur and about half the patients report symptoms of chest pain, while three-quarters report dyspnoea after 15 years. Even if no clear predictor of chest pain was found at the time of surgery, age, the use of inotropic drugs, diabetes and obesity predicted dyspnoea.
  •  
6.
  • Bazzi, May, 1979, et al. (author)
  • Patients' lived experiences of waiting for and undergoing endovascular aortic repair in a hybrid operating room: A qualitative study
  • 2020
  • In: Journal of Clinical Nursing. - : Wiley. - 0962-1067 .- 1365-2702. ; 29:5-6, s. 810-820
  • Journal article (peer-reviewed)abstract
    • Aims and objectives The overall aim of the study was to illuminate the patients' lived experiences of waiting for and undergoing an endovascular aortic repair (EVAR) in a hybrid operating room (OR). Background The hybrid OR is an example of the technological advancements within hospitals. The environmental impact on humans is well recognised but is rarely taken into account when hospitals are designed or rebuilt. The patient's experience of a hybrid OR is not earlier described. Design A qualitative design based on hermeneutic phenomenology was implemented. Methods Interviews were conducted with 18 patients. A thematic interpretation based on van Manen's approach was then used to analyse the findings. The consolidated criteria for reporting qualitative studies (COREQ) were used (Data S1). Results The following three themes emerged from the interviews: (a) being scheduled for surgery induced both anxiety and hopefulness; (b) feeling watched over and surrendering to others in the technology intense environment and (c) feeling relief but unexpected exhaustion after surgery. In the discussion, the results were additionally reflected upon out from the four lifeworld existentials: lived body, lived space, lived time and lived others. Conclusions The hybrid OR technology did not frighten the patients, but it was also not an environment that promoted or was conductive to having a dialogue with the staff. The disease and surgery brought feelings of anxiety, which was largely associated with the uncertainty of the situation. We suggest that continuity in contact with staff and patient-centred information could be solutions to further calm the patients. Relevance to clinical practice The hybrid OR environment itself did not seem to frighten the patient, but the way the high-tech environment increased the distance between the patient and the multiple staff members needs further investigation.
  •  
7.
  • Berndtsson, Ina, 1953-, et al. (author)
  • Long-term adjustment to living with an ileal pouch-anal anastomosis.
  • 2011
  • In: Diseases of the colon and rectum. - : Lippincott Williams & Wilkins. - 1530-0358 .- 0012-3706. ; 54:2, s. 193-9
  • Journal article (peer-reviewed)abstract
    • The aim of this study was to describe long-term adjustment to life with an ileal pouch-anal anastomosis after surgery for ulcerative colitis, to investigate the relationship of pouch function to adjustment, and to explore factors affecting quality of life.
  •  
8.
  •  
9.
  • Caesar, Ulla, 1964, et al. (author)
  • Incidence and root causes of delays in emergency orthopaedic procedures: a single-centre experience of 36,017 consecutive cases over seven years
  • 2018
  • In: Patient Safety in Surgery. - : Springer Science and Business Media LLC. - 1754-9493. ; 12:2
  • Journal article (peer-reviewed)abstract
    • Background Emergency surgery is unplanned by definition and patients are scheduled for surgery with minimal preparation. Some patients who have sustained emergency orthopaedic trauma or other conditions must be operated on immediately or within a few hours, while others can wait until the hospital’s resources permit and/or the patients’ health status has been optimised as needed. This may affect the prioritisation procedures for both emergency and elective surgery and might result in waiting lists, not only for planned procedures but also for emergencies. Method The main purpose of this retrospective, observational, single-centre study was to evaluate and describe for the number and reasons of delays, as well as waiting times in emergency orthopaedic surgery using data derived from the hospital’s records and registers. All the emergency patients scheduled for emergency surgery whose procedures were rescheduled and delayed between 1 January 2007 and 31 December 2013 were studied. Result We found that 24% (8474) of the 36,017 patients scheduled for emergency surgeries were delayed and rescheduled at least once, some several times. Eighty per cent of these delays were due to organisational causes. Twenty-one per cent of all the delayed patients had surgery within 24 h, whilst 41% waited for more than 24 h, up to 3 days. Conclusion A large number of the clinic’s emergency orthopaedic procedures were rescheduled and delayed and the majority of the delays were related to organisational reasons. The results can be interpreted in two ways; first, organisational reasons are avoidable and the potential for improvement is great and, secondly and most importantly, the delays might negatively affect patient outcomes.
  •  
10.
  • Carlsson, Eva, 1959, et al. (author)
  • Concerns and quality of life before surgery and during the recovery period in patients with rectal cancer and an ostomy
  • 2010
  • In: Journal of Wound, Ostomy and Continence Nursing (WOCN). - : Lippincott, Williams & Wilkins. - 1071-5754 .- 1528-3976. ; 37:6, s. 654-661
  • Journal article (peer-reviewed)abstract
    • PURPOSE: Rectal cancer is the most common reason for a person to undergo ostomy surgery. The aim of this study was to assess concerns and health-related quality of life (HRQOL) before surgery and during the first 6 months following ostomy surgery in the presence of rectal cancer. SUBJECTS AND SETTINGS: The sample comprised 57 patients at a university hospital in Gothenburg, Sweden. Their median age was 66 years (range, 30-87); 35 men and 22 women participated in the study. METHODS: Participants prospectively answered questionnaires preoperatively, and at 1, 3, and 6 months postoperatively.Concerns were assessed using the rating form of the Inflammatory Bowel Disease Patient Concerns, and HRQOL was evaluated using the 36-Item Short Form Health Survey. Results were compared with population norms. RESULTS: Participants expressed concerns associated with developing cancer, being a burden on others, and related to the uncertain nature of disease. Health-related quality of life scores dropped significantly in 6 of 8 domains when preoperative scores were compared to those obtained 1 month postoperatively, but scores improved at 6 months. There were significant differences between preoperative study group scores and population norms on physical and emotional role function, social function, and for mental health domains. Significant differences persisted when population norms were compared to study group scores 6 months following surgery on all these domains except mental health. Participants identified good relations with significant others, social and leisure activities, psychological issues, and health as important for maintaining QOL. Obstacles to maintaining QOL included fatigue, pain, illness-induced limitations in life, and worries over what their new life would entail. CONCLUSION: Surgical management of rectal cancer raises concerns and profoundly impairs QOL during the first several postoperative months. © 2010 Wound, Ostomy and Continence Nurses Society.
  •  
Skapa referenser, mejla, bekava och länka
  • Result 1-10 of 17
Type of publication
journal article (14)
editorial collection (1)
conference paper (1)
doctoral thesis (1)
Type of content
peer-reviewed (14)
other academic/artistic (3)
Author/Editor
Herlitz, Johan, 1949 (4)
Berndtsson, Ina, 195 ... (4)
Carlsson, Eva, 1959 (4)
Lundberg, Lars (3)
Persson, Eva (3)
Hansson, Emma, 1981 (3)
show more...
Lindholm, Elisabet, ... (3)
Karlson, Björn W., 1 ... (2)
Karlsson, Thomas, 19 ... (2)
Karason, Kristjan, 1 ... (2)
Caidahl, Kenneth, 19 ... (2)
Fridh, Isabell, 1954 ... (2)
Sandman, Lars, 1965- (2)
Brandrup-Wognsen, Gu ... (2)
Hartford, Marianne, ... (2)
Haglid Evander, Mari ... (2)
Hallén, A. M. (2)
Bergbom, Ingegerd, 1 ... (1)
Axelsson, Christer (1)
Karlsson, Jón, 1953 (1)
Bremer, Anders, Doce ... (1)
Ahlberg, Karin, 1965 (1)
Larsson, A (1)
Ericson, A (1)
Davidson, Thomas (1)
Thomas, Karlsson, 19 ... (1)
Claesson, Andreas (1)
Hellström, Mikael, 1 ... (1)
Lennerling, Annette, ... (1)
Lepp, Margret, 1954 (1)
Lundén, Maud, 1959 (1)
Lundgren, Solveig M, ... (1)
Andersson, Henrik, 1 ... (1)
Gellerstedt, Martin, ... (1)
Bång, Angela, 1964 (1)
Ljungstrom, L. (1)
Hansson-Olofsson, El ... (1)
Rizell, Magnus, 1963 (1)
Forsberg, Anna, 1969 (1)
Sandman, Lars (1)
Bazzi, May, 1979 (1)
Persson, Eva, 1953- (1)
Blimark, M (1)
Örtenwall, P (1)
Boström, Petra, 1972 (1)
Sjöland, Helen, 1959 (1)
Bylow, Helene (1)
Lindqvist, Jonny (1)
Caesar, Ulla, 1964 (1)
Fingren, J (1)
show less...
University
University of Gothenburg (14)
University West (5)
Linköping University (3)
Karolinska Institutet (3)
Uppsala University (1)
show more...
University of Skövde (1)
Linnaeus University (1)
show less...
Language
English (17)
Research subject (UKÄ/SCB)
Medical and Health Sciences (17)
Social Sciences (4)
Humanities (1)

Year

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 Close

Copy and save the link in order to return to this view