The impact of long-term warfarin therapy on quality of life. Evidence from a randomized trial. Boston Area Anticoagulation Trial for Atrial Fibrillation Investigators

1991 ◽  
Vol 151 (10) ◽  
pp. 1944-1949 ◽  
Author(s):  
T. R. Lancaster
2006 ◽  
Vol 36 (1) ◽  
pp. 95-97 ◽  
Author(s):  
A. K. Das ◽  
P. D. Willcoxson ◽  
O. J. Corrado ◽  
R. M. West

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 2245-2245 ◽  
Author(s):  
Miranda Murray ◽  
Diane Wild ◽  
Matt Reaney

Abstract Prevention of stroke in patients with atrial fibrillation (AF) requires long-term anticoagulation therapy, and warfarin is currently the only option. Previous studies have indicated that patients are generally satisfied with long-term warfarin therapy; however, this research is mostly limited to simple questions, or modified Likert scales. Psychometric research on measuring satisfaction with medical treatment has indicated that multi-dimensional measures are generally more reliable and sensitive to treatment differences. This qualitative study, conducted in the US, UK, and Spain, was performed to explore the specific treatment satisfaction domains related to warfarin therapy. Interviews were conducted with patients (N=28) who were receiving long-term warfarin therapy for the prevention of stroke in AF, or had discontinued therapy. The interviews, developed from conceptual models, focussed on the patients’ experiences and satisfaction with warfarin therapy. Patients received warfarin for an average of 6 years, with 22% receiving treatment for >5 years. Warfarin therapy was reported to reduce patients’ quality of life, with 28% reporting an impact on their work, 32% an effect on their ability to travel, and 57% experiencing effects on their leisure activities, often because of alcohol restrictions. Domains that were important to patient satisfaction were identified, including monitoring, bruising/bleeding, and the psychological impact of therapy. The requirement for frequent monitoring was a burden in nearly half of the patients (43%); in the majority of these patients (57%), this was due to the amount of time spent attending the clinic. Unsurprisingly, working patients reported monitoring as more of a burden than those who did not work (65% vs 31%). The location and frequency of monitoring affected patients’ perceptions of the burden; patients attending anticoagulation clinics (rather than primary care surgeries), and those attending more than once a month, reported greater inconvenience. However, many patients, particularly those who had been taking warfarin for longer, felt reassured by monitoring. Bruising and/or bleeding was a worry to 17% of patients, with 28% reporting being embarrassed by it, and many patients choosing clothes that covered their bruises. The psychological impact of warfarin therapy was illustrated by the number of patients reporting concern about drug interactions (50%), with one-fifth (21%) worried about the warfarin dose they had been prescribed. Knowledge that their warfarin therapy required alcohol and dietary restrictions was demonstrated by 39% and 28% of patients, respectively; however, some patients thought that dietary restrictions were to encourage weight loss, and 15% of patients reported that the restrictions were a burden. Furthermore, many elderly patients, particularly in the UK and Spain, were unaware that the purpose of their warfarin therapy was for stroke prevention. Patients that had discontinued treatment gave reasons including a feeling of dependence on warfarin, bruising and bleeding, monitoring, and diet and alcohol restrictions. Patients in this study recognized that warfarin is currently the only therapy available to them, and made adjustments to their lifestyles accordingly. However, warfarin adversely affects the quality of life of patients with AF because of the practicalities and psychological impact of therapy. An anticoagulant that does not require frequent monitoring, with limited food and drug interactions would represent a significant advance for patients with AF.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Mads G. Jørgensen ◽  
Navid M. Toyserkani ◽  
Frederik G. Hansen ◽  
Anette Bygum ◽  
Jens A. Sørensen

AbstractThe impact of breast cancer-related lymphedema (BCRL) on long-term quality of life is unknown. The aim of this study was to investigate the impact of BCRL on health-related quality of life (HRQoL) up to 10 years after breast cancer treatment. This regional population-based study enrolled patients treated for breast cancer with axillary lymph node dissection between January 1st 2007 and December 31th 2017. Follow up and assessments of the included patients were conducted between January 2019 and May 2020. The study outcome was HRQoL, evaluated with the Lymphedema Functioning, Disability and Health Questionnaire, the Disabilities of the Arm, Shoulder and Hand Questionnaire and the Short Form (36) Health Survey Questionnaire. Multivariate linear logistic regression models adjusted for confounders provided mean score differences (MDs) with 95% confidence intervals in each HRQoL scale and item. This study enrolled 244 patients with BCRL and 823 patients without BCRL. Patients with BCRL had significantly poorer HRQoL than patients without BCRL in 16 out of 18 HRQoL subscales, for example, in physical function (MDs 27, 95%CI: 24; 30), mental health (MDs 24, 95%CI: 21; 27) and social role functioning (MDs 20, 95%CI: 17; 23). Age, BMI, BCRL severity, hand and dominant arm affection had only minor impact on HRQoL (MDs < 5), suggesting a high degree of inter-individual variation in coping with lymphedema. This study showed that BCRL is associated with long-term impairments in HRQoL, especially affecting the physical and psychosocial domains. Surprisingly, BCRL diagnosis rather than clinical severity drove the largest impairments in HRQoL.


Rheumatology ◽  
2021 ◽  
Vol 60 (Supplement_1) ◽  
Author(s):  
Rosie Barnett ◽  
Anita McGrogan ◽  
Matthew Young ◽  
Charlotte Cavill ◽  
Mandy Freeth ◽  
...  

Abstract Background/Aims  Axial spondyloarthritis (axSpA) is a chronic rheumatic condition, characterised by inflammatory back pain - often associated with impaired function and mobility, sleep disturbance, fatigue, and reduced quality of life. Despite the vast advances in pharmacological treatments for axSpA over the last few decades, physical activity and rehabilitation remain vital for effective disease management. At the Royal National Hospital for Rheumatic Diseases in Bath (RNHRD), the 2-week inpatient axSpA rehabilitation programme has been integral to axSpA care since the 1970’s. Prior research has demonstrated significant short-term improvements in spinal mobility (BASMI), function (BASFI) and disease activity (BASDAI) following course attendance. However, the long-term outcomes are yet to be evaluated in this unique cohort. Methods  Since the early 1990’s, clinical measures of spinal mobility, function and disease activity have been routinely collected at the RNHRD at all clinical appointments through administration of the BASMI, BASFI and BASDAI, respectively. Dates of attending the axSpA course and standard clinical and treatment follow-up data were also collected. Multiple linear regression models were used to investigate the impact of course attendance on final reported BASMI, BASDAI and BASFI scores (final score=most recent). Length of follow-up was defined as time between first and last recorded BASMI. Results  Of the 203 patients within the Bath SPARC200 cohort, 77.8% (158/203) had attended at least one rehabilitation course throughout follow-up. 70.0% (140/203) of patients were male. The mean duration of follow-up was 13.5 years (range 0-35 years); 28.1% (57/203) of individuals with 20+ years of follow-up. Course attendance (yes versus no) significantly reduced final BASMI score by 0.84 (p = 0.001, 95%CI -1.31 to -0.37) and final BASDAI score by 0.74 (p = 0.018, 95%CI -1.34 to -0.13). Although course attendance reduced final BASFI by 0.45 (95%CI -1.17 to 0.28), this relationship did not reach significance (p = 0.225). Whilst minimally clinically important difference (MCID) is, to our knowledge, yet to be defined for BASMI, MCIDs were achieved long-term for both BASDAI and BASFI - defined by van der Heijde and colleagues in 2016 as 0.7 and 0.4 for BASDAI and BASFI, respectively. Conclusion  These results provide novel evidence to support the integral role of education, physical activity and rehabilitation in the management of axSpA. Future work should investigate additional outcomes of critical importance to patients and clinicians, such as fatigue, quality of life and work productivity. Furthermore, a greater understanding of the factors that confound these outcomes may provide insights into those patients who may most benefit from attending a 2-week rehabilitation course. In addition to facilitating identification of those patients who may require additional clinical support. Disclosure  R. Barnett: None. A. McGrogan: None. M. Young: None. C. Cavill: None. M. Freeth: None. R. Sengupta: Honoraria; Biogen, Celgene, AbbVie, Novartis, MSD. Grants/research support; Novartis, UCB.


2017 ◽  
Vol 31 (1) ◽  
pp. 109-138 ◽  
Author(s):  
Mark J. Siedner

Objective: The number of people living with HIV (PLWH) over 50 years old in sub-Saharan Africa is predicted to triple in the coming decades, to 6-10 million. Yet, there is a paucity of data on the determinants of health and quality of life for older PLWH in the region. Methods: A review was undertaken to describe the impact of HIV infection on aging for PLWH in sub-Saharan Africa. Results: We (a) summarize the pathophysiology and epidemiology of aging with HIV in resource-rich settings, and (b) describe how these relationships might differ in sub-Saharan Africa, (c) propose a conceptual framework to describe determinants of quality of life for older PLWH, and (d) suggest priority research areas needed to ensure long-term gains in quality of life for PLWH in the region. Conclusions: Differences in traditional, lifestyle, and envirnomental risk factors, as well as unique features of HIV epidemiology and care delivery appear to substantially alter the contribution of HIV to aging in sub-Saharan Africa. Meanwhile, unique preferences and conceptualizations of quality of life will require novel measurement and intervention tools. An expanded research and public health infrastructure is needed to ensure that gains made in HIV prevention and treamtent are translated into long-term benefits in this region.


2012 ◽  
Vol 10 (7) ◽  
pp. 889-900 ◽  
Author(s):  
Sanghamitra Mohanty ◽  
Luigi Di Biase ◽  
Rong Bai ◽  
Pasquale Santangeli ◽  
Agnes Pump ◽  
...  

2011 ◽  
Vol 23 (2) ◽  
pp. 121-127 ◽  
Author(s):  
STEPHANIE FICHTNER ◽  
ISABEL DEISENHOFER ◽  
SIBYLLE KINDSMÜLLER ◽  
MARIJANA DZIJAN-HORN ◽  
STYLIANOS TZEIS ◽  
...  

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