Thematische Bibliographien / “Women’s quality of life”

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Auswahl der wissenschaftlichen Literatur zum Thema „“Women’s quality of life”“

Autor: Grafiati

Veröffentlicht am 30. Juni 2021

Zuletzt aktualisiert am 10. Februar 2022

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Zeitschriftenartikel zum Thema "“Women’s quality of life”"

Hossain, Irin. „Women’s Quality of Life during Pregnancy“. TEXILA INTERNATIONAL JOURNAL OF PUBLIC HEALTH 8, Nr. 3 (30.09.2020): 204–10. http://dx.doi.org/10.21522/tijph.2013.08.03.art022.

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Gharacheh, M., F. Ranjbar und S. Azadi. „Women’s Quality of Life and Postpartum Depression“. Iran Journal of Nursing 30, Nr. 110 (01.02.2018): 68–77. http://dx.doi.org/10.29252/ijn.30.110.68.

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Korgozha, Maria A. „Women’s quality of life dynamics in postpartum period“. Pediatrician (St. Petersburg) 8, Nr. 6 (28.12.2017): 125–30. http://dx.doi.org/10.17816/ped86125-130.

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The article presents the results of the study of characteristics and dynamics of the women’s quality of life in the third trimester of pregnancy and six weeks after delivery. The study involved 240 women, patients of the Perinatal Center of Saint Petersburg State Pediatric Medical University, during the third trimester of pregnancy and six weeks after the delivery. Research subjects were divided into three study groups, depending on the presence and severity of negative emotional manifestations in women in the third trimester of pregnancy. It was revealed that the indicators of physical, mental and social functioning in women, who underwent negative emotional manifestations of different severity in the third trimester of pregnancy, are below the average population data. It is shown that the intensity of negative emotional manifestations in women in the third trimester of pregnancy does not affect the subjective assessment of the overall health and life status. The appearance of negative emotional manifestations of different severity in women in the third trimester of pregnancy significantly reduces the subjective assessment of pregnant women’s own physical functioning in the context of daily and professional activities. It was revealed that for women underwent mild negative emotional manifestations in the third trimester of pregnancy, the situation of labor is the most stressful and has a significant impact on the quality of life in the late postpartum period. This category of women is at risk and needs more thorough medical support and professional psychological assistance.

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Beckie, Theresa M., Jason W. Beckstead und Mary S. Webb. „Modeling Women’s Quality of Life after Cardiac Events“. Western Journal of Nursing Research 23, Nr. 2 (März 2001): 179–94. http://dx.doi.org/10.1177/019394590102300206.

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Fanslow, Janet. „Partner Violence Screening and Women’s Quality of Life“. JAMA 308, Nr. 22 (12.12.2012): 2334. http://dx.doi.org/10.1001/jama.2012.14870.

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Lazarus, Jeremy, Jacquelyn Campbell und F. David Schneider. „Partner Violence Screening and Women’s Quality of Life“. JAMA 308, Nr. 22 (12.12.2012): 2334. http://dx.doi.org/10.1001/jama.2012.14873.

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Stadnicka, G., C. Łepecka-Klusek und A. B. Pilewska-Kozak. „Pelvic floor muscle disorders and women’s quality of life“. Progress in Health Sciences 6, Nr. 1 (30.06.2016): 95–101. http://dx.doi.org/10.5604/01.3001.0009.5132.

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Purpose: To characterize the symptoms of urinary incontinence of women suffering from pelvic organ disorders (POP) and the effect of these problems on quality of life (QoL). Materials and methods: 215 women from rural regions diagnosed with POP were examined. The research implemented the Life Satisfaction Questionnaire (LISAT-11), used to assess quality of life; the Sexual Quality of Life-Female (SQoL-F) questionnaire, which was employed to assess sexual activity; and the Gaudenz-Incontinence questionnaire, served to assess the occurrence of symptoms of urinary incontinence as well as to define the type of urinary incontinence and its degree of escalation. Results: The average age of the participants was 54.8 years. Most of the participants had urinary incontinence (159; 73.95%). Women with POP and symptoms of urinary incontinence achieved a lower indicator of the sexual function QoL (median - 61.00) when compared to those not suffering from urinary incontinence (median- 78.00). Differences between the groups were statistically significant (p=0.002). The general indicator of QoL for women with symptoms and those without symptoms of stress urinary incontinence (SUI) did not reveal any significant differences between the groups (p=0.643). Conclusions: Urinary incontinence in women with disorders of pelvic floor muscle functions has an insignificant effect on general QoL, whereas it has a decidedly negative impact on sexual function QoL.

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O’Dell, Kristi. „Book Review: Women’s Work, Health, and Quality of Life“. Affilia 20, Nr. 1 (Februar 2005): 120–21. http://dx.doi.org/10.1177/0886109904272138.

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Klevens, Joanne, und Romina Kee. „Partner Violence Screening and Women’s Quality of Life—Reply“. JAMA 308, Nr. 22 (12.12.2012): 2334. http://dx.doi.org/10.1001/jama.2012.14876.

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Wathen, Nadine, und Harriet MacMillan. „Partner Violence Screening and Women’s Quality of Life—Reply“. JAMA 308, Nr. 22 (12.12.2012): 2334. http://dx.doi.org/10.1001/jama.2012.14879.

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Dissertationen zum Thema "“Women’s quality of life”"

AL, Hasni Alya Ali Abdullah. „URINARY INCONTINENCE AND WOMEN’S QUALITY OF LIFE IN OMAN“. OpenSIUC, 2017. https://opensiuc.lib.siu.edu/dissertations/1481.

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Urinary incontinence (UI) is a common public health concern among women worldwide, with adverse effects on their quality of life (QoL). This study aims to explore the prevalence of UI among Omani women aged 18-49 years old, and to explore the impact of UI on women's daily prayers, physical activities, social life, mental health, and general QoL. The study is of quantitative comparative design, and the researcher used the World Health Organization’s (WHOs) International Classification of Functioning, Disability and Health (ICF), as a conceptual framework. The researcher randomly chose four-hundred and one participants from ten primary health care centres in Muscat. The researcher assessed their UI status and impact on different domains of their life using UDI-6 and IIQ-7 respectively, which are validated self-reported questionnaires. From the results, the researcher highlighted the high prevalence (85%) of UI among young Omani women. Additionally, UI did have a statistically significant impact on Omani women’s ability to perform their daily prayers, physical activities, social life, mental health, as well as, their general QoL. The use of ICF framework allows policymakers and public health officials to see the big picture of UI as public health concern in Oman. It forms the basis for implementing cost-effective health education programs at the Primary Health Care (PHC) institutions in Oman, for the goal of improving women’s health and community health.

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Fischer, Mary A. „Women’s Experiences of Discontinuing Hormone Therapy: A Dissertation“. eScholarship@UMMS, 2011. https://escholarship.umassmed.edu/gsn_diss/23.

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Although many women find relief from menopause through hormone therapy (HT), current guidelines recommend that HT be used only for short-term relief of symptoms. Women who attempt to stop HT often encounter troublesome recurrent symptoms leading to a diminished quality of life (QoL); 25% of women who discontinue eventually resume HT. Unfortunately, there is little information for women and their health care providers as to the best way to discontinue HT or how to prepare and guide women through this process. An in-depth description of women‘s experiences during HT discontinuation and the factors influencing recurrent symptoms, QoL and discontinuation outcome would provide knowledge to develop much needed counseling and support interventions. The purpose of this study was to explore women‘s experiences discontinuing hormone therapy for menopause. This Internet-based mixed-methods study used a dominant Qualitative Descriptive design with embedded quantitative QoL measurements. Participants completed the quantitative questionnaires online while open-ended questions were completed either online or by telephone. Interview data were analyzed through Qualitative Content Analysis; descriptive statistics were used to explore the quantitative measures. Participants were stratified by discontinuation status for comparison of variations in discontinuation experiences, QoL and influencing factors. Thirty-four women (20 stopped, 9 resumed, 4 tapering) were enrolled. One overarching theme--'a solitary journey'--emerged: although all women embarked on this journey, each woman traveled her own path. Two subthemes--'burden and interference' and 'appraising risk'--encompassed the symptom factors (severity, interference and sensitivity) that influenced women's experiences and the manner in which women evaluated their options. Other influencing factors included: readiness viii and reasons for stopping HT, beliefs about menopause and roles. QoL was strongly connected to symptoms for many but not all women. Information from health care providers was inconsistent; women desired more support from providers and other women. The rich description of women's experiences stopping HT highlights the need for providers to assess women's sensitivity to symptoms and readiness to discontinue to determine which women might benefit from more support. Greater health literacy would enhance women's understanding of HT risks. More research is needed on symptom clusters and interference and strategies for minimizing their impact.

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Di, Sipio Tracey. „Health-related quality of life among breast cancer survivors : town and country experiences“. Queensland University of Technology, 2009. http://eprints.qut.edu.au/20339/.

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Due to advances in detection and treatment, increasing numbers of women are diagnosed with, and surviving, breast cancer each year, making women with breast cancer one of the largest groups of cancer survivors. Hence, ensuring good healthrelated quality of life (HRQoL) following treatment has become a focal point of cancer research and clinical interest. While our understanding about the impact of breast cancer is improving, little is known about the HRQoL among survivors in non-urban areas. This is important locally, as 45% of breast cancer survivors in Queensland, Australia, live outside major metropolitan areas. Therefore, this study investigated the HRQoL and accompanying correlates among regional and rural breast cancer survivors, and made comparisons with urban breast cancer survivors as well as women from the general population without a history of breast cancer. Three population-based studies comprise this project. Original data were collected by way of self-administered questionnaire from 323 women, diagnosed with a first, primary, invasive, unilateral breast cancer during 2006/2007 and residing in regional or rural areas of Queensland, 12 months following diagnosis. HRQoL was assessed using the Functional Assessment of Cancer Therapy, Breast plus additional concerns (FACT-B+4) questionnaire. Data from two existing data sources were also utilised. Women diagnosed with a first, primary, invasive, unilateral breast cancer in 2002 and residing within 100kms of Brisbane provided information on HRQoL, measured by the FACT-B+4, via self-administered questionnaire at six (n=287), 12 (n=277) and 18 (n=272) months post-diagnosis. Data at 12 months post-diagnosis was utilised for comparison with region and rural women with breast cancer. General population data for HRQoL, collected by self-administered questionnaire in 2004 using the Functional Assessment of Cancer Therapy-General (FACT-G) questionnaire, were derived from a subgroup of female residents without a history of breast cancer from urban (n=675), regional (n=184) and rural (n=281) Queensland. The two studies involving women with breast cancer were recruited sequentially through the Queensland Cancer Registry, whereas the study involving the general population used telephone survey methods initially to identify participants. Women who participated in all studies were aged between 30 and 74 years. Raw scores for overall HRQoL (FACT-B+4, FACT-G) and subscales were computed. According to developers of the instrument, raw score differences of eight points between groups on the FACT-B+4 scale and five points on the FACT-G scale reflect a clinically meaningful differences in HRQoL. Age-adjusted, mean HRQoL was similar between regional and rural women with breast cancer 12 months following diagnosis (e.g., FACT-B+4: 122.9 versus 123.7, respectively, p=0.74). However, younger regional and rural survivors reported lower HRQoL scores compared with their older counterparts (e.g., FACT-B+4: 112.0 and 115.8 versus 129.3 and 126.2, respectively, p<0.05 for all). In addition to age, other important correlates of lower overall HRQoL (FACT-B+4) among regional/rural breast cancer survivors included: receiving chemotherapy, reporting complications post-surgery, poorer upper-body function than most, higher amounts of stress, reduced coping, being socially isolated, not having a confidante for social-emotional support, unmet healthcare needs, and low self-efficacy. Multiple linear regression analysis was used to address the hypothesis regarding similarity of HRQoL following breast cancer among women residing in regional and rural locations. After adjusting for the above factors, there was no statistically significant or clinically important difference in overall HRQoL (FACT-B+4) between regional and rural women with breast cancer 12 months following diagnosis (122.1 versus 125.1, respectively, p=0.07). Data from regional and rural women were pooled, based on the above analyses, and compared with urban women. Multiple linear regression analysis was used to test the hypothesis that HRQoL following breast cancer among women residing in regional/rural locations would be lower than that reported by women residing in urban locations. Potential confounders of the association between overall HRQoL (FACT-B+4) and place of residence included: marital status, upper-body function, amount of stress and perceived handling of stress. After adjusting for factors that differed between urban and regional/rural survivors, overall HRQoL (FACT-B+4) was lower among younger regional/rural survivors than their urban peers, and the findings were both statistically significant and clinically important (115.3 versus 123.7, respectively, p=0.001). Older women reported similar mean HRQoL, regardless of regional/rural or urban residence (128.2 versus 131.6, respectively, p=0.03). Further multiple linear regression analyses were undertaken to investigate whether women with breast cancer would report HRQoL equivalent to that reported by similarly-aged women in the general population. After adjusting for potential confounding factors that are known or suspected risk factors for breast cancer (age, marital status, education level, private health insurance, smoking status, physical activity, body mass index, co-morbidities), overall HRQoL (FACT-G) among breast cancer survivors was comparable to the general population 12 months following diagnosis (urban: 88.0 versus 86.9, respectively, p=0.28; regional/rural: 86.2 versus 85.8, respectively, p=0.79). However, 26% of survivors experienced worse overall HRQoL (FACT-G) compared with normative levels. HRQoL subscales contributing most to this deficit were physical well-being, with 29% of breast cancer survivors reporting scores below the norm, and emotional well-being among younger women, with 46% reporting scores below the norm. Logistic regression analysis was used to identify subgroups of breast cancer survivors who reported HRQoL below normative levels; reporting poorer upper-body function than most and not handling stress well increased the odds of reporting overall HRQoL (FACT-G: odds ratios (ORs) = 4.44 and 4.24, respectively, p<0.01 for both), physical well-being (ORs = 5.93 and 2.92, respectively, p<0.01 for both) and emotional well-being (among younger women: ORs = 2.81 and 5.90, respectively, p<0.01 for both) below normative levels. The cross-sectional nature of the study design for regional and rural breast cancer survivors, and the potential selection and response biases in all three studies, represent the main limitations of this work. The cross-sectional design precludes causal inference about observed associations, but even characterising relevant correlates allows for adjustment of potential confounding and provides insight into factors that may be important in contributing to HRQoL among breast cancer survivors. Moreover, the potential impact of the latter limitations is in the conservative direction, whereby differences in HRQoL between groups will be more difficult to identify. Since these biases are expected to be present to a similar degree across all study groups, the absolute difference in HRQoL by residence and cancer status observed are likely to exist. In contrast, the work is supported by a population based, state-wide sample of breast cancer survivors, comparisons with the general population, and use of standardised instruments. Therefore, the conclusions derived from this research are likely to be generalisable to the wider population of women in Queensland with unilateral breast cancer, aged 74 years or younger, and perhaps to similar women in other western countries, depending on variations in healthcare systems and the provision of oncology services. This research supports the initial supposition that while some findings may generalise to all breast cancer survivors, non-urban breast cancer survivors also have distinct experiences that influence their HRQoL. Results from this work highlight the HRQoL domains and characteristics of breast cancer survivors most in need of assistance to facilitate recovery following diagnosis and treatment. Characteristics include some already established and reconfirmed here, namely, emotional wellbeing among younger women, and other novel subgroups, including regional/rural survivors who receive chemotherapy or have a low self-efficacy and all survivors, regardless of residence, with upper-body problems or a low perception of handling stress. These results demonstrate the potential for identifying subgroups of women with breast cancer at risk for low HRQoL who may benefit from additional attention and possible tailored recovery interventions to increase their overall HRQoL. As such, researchers and clinicians need to consider the role of these factors when designing interventions to assist women as they deal with the challenges imposed upon them by their breast cancer. However, it was found here that the FACT-G instrument has ceiling effects. This means that positive changes reflecting improved status, such as those achieved through recovery interventions, will often fail to be measured appropriately if there is no room to indicate improvements. Overall HRQoL results indicated that there is room for improvement past 12 months following treatment, with a significant proportion of breast cancer survivors reporting HRQoL below normative levels. HRQoL concerns 12 months following diagnosis are likely to be distinct from the more acute issues reported earlier on in the literature. Therefore, the development of a cancer survivorship module to accompany the FACT-G would be useful to counteract the ceiling effects observed as well as to capture issues distinct to cancer survivorship. This is the first study to describe in detail the HRQoL of breast cancer survivors across all areas of Queensland and to compare it to the HRQoL reported by the general population of Queensland. Therefore, it represents a unique and substantial contribution to the existing knowledge on survivorship issues following diagnosis and treatment for breast cancer in Australia. Through this research, a number of questions remain that could be addressed by relevant investigations and which are likely to be important in the future to ultimately guide practice. Specifically, implementation of the concept of HRQoL in practice is the next important step forward. Furthermore, the development of a survivorship care plan that incorporates guidelines on HRQoL recovery could provide options for referral and support.

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Huang, Qinghai. „The Nature of Women’s Career Development : Determinants and Consequences of Career Patterns“. Doctoral thesis, Stockholm University, Department of Psychology, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-1216.

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Existing career theories are largely based on a stable working environment and have focused excessively on men and single work roles. In the postindustrial era, however, women’s careers, characterized by the constant negotiation of multiple roles and more frequent job changes, have had implications on the changing nature of careers. The general purpose of this thesis is to increase knowledge about the process of career development of women. The focus is on two aspects: Life Career (characterized by multiple role constellations over the life course) and Occupational Career (characterized by different shapes of occupational movement over the life course). Three sets of questions addressed these two aspects of career: trajectory patterns, interrelationships, and antecedents and consequences. Career biographies covered ages 16 to 43. Antecedents reflecting individual agency (e.g., life role value, aspiration, and early experiences) were investigated. The impact of family context on occupational choice was also examined. Among the consequences examined were midlife work wellness and stress, health, and wellbeing.

Results showed that (1) Career patterns were highly diverse, including nine distinct life career patterns and ten occupational career patterns. (2) Occupational and life careers were significantly related, indicating that the paid work career is embedded in the overall life role structure throughout the life course. (3) Individual agency factors predicted life career. Occupational career was related to life career more than family context. (4) Occupational career did matter in work wellbeing. In terms of stress, health, and wellbeing at midlife, there was little difference among life career patterns, but more significant differences among occupational career patterns. The thesis indicates career theory can benefit from taking multiple roles and career development into account. Implications for career counseling, social policy, and organizations are discussed.

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Tang, Wai-ha Sherman. „Quality of life of gynaecological cancer patients“. Hong Kong : University of Hong Kong, 1994. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13990949.

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Schwendeman, Elizabeth. „Quality of life in women with heart failure“. Muncie, Ind. : Ball State University, 2009. http://cardinalscholar.bsu.edu/711.

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Payne, Sheila. „Quality of life in women with advanced cancer“. Thesis, University of Exeter, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328512.

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Tang, Wai-ha Sherman, und 鄧惠霞. „Quality of life of gynaecological cancer patients“. Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1994. http://hub.hku.hk/bib/B43893521.

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Jakobsson, Emma, und Märtha Jansson. „Kvinnors upplevelse av att leva med urininkontinens : En litteraturbaserad studie“. Thesis, Högskolan Väst, Avdelningen för omvårdnad - grundnivå, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-12599.

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Background: The definition of urinary incontinence is involuntary loss of urine that is objectively detectable and results in a social and hygienic inconvenience for the individual. There are different types and causes of urinary incontinence and the symptoms often occur more frequently with higher age. Women are affected to a greater extent than men. Urinary incontinence may affect everyday life and lead to changes in quality of life. Aim: To illuminate women's experiences of living with urinary incontinence. Method: A literature study was conducted using qualitative analysis through five steps. An analysis of ten qualitative articles was carried out. Results: Four main themes emerged, a suffering in everyday life, perceived body perception, feelings about sexuality and hope and despair. The results showed that living with urinary incontinence affected everyday life activities. The women felt limited and learned to cope through different strategies. Urinary incontinence affected the women's body image and could result in less confidence and the feeling of powerlessness. The complex situation sometimes leads to negative sexual effects. Women lived with the hope to recover but at the same time there were feelings of despair for what the future would hold for them. Conclusion: Women suffering from urinary incontinence experience restrictions in their everyday life, in physical, mental and social aspects. It creates a feeling of loss of control. And many women suffer in silence without seeking help. Urinary incontinence has a negative effect on their quality of life.

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Devine, Debbie T. „Levels of Distress Among Women Veterans Attending a Women’s Health Specialty Clinic in the VA Healthcare System“. Scholar Commons, 2016. http://scholarcommons.usf.edu/etd/6490.

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Currently, between 21.9 and 23 million veterans have served in the United States armed forces. Of those, 2 million are women, and of those, only 6.5% use the Veterans Health Administration system. These females often suffer from physical and mental health disorders, and overall impaired quality of life (QOL), rendering their healthcare needs complex. Seeking, and providing care in this specialty area may become overwhelming not only for the women seeking the care, but also for healthcare systems that are unfamiliar with the specific needs of this population. A retrospective medical records review was completed of 51 female veterans between the ages of 40 and 60 years, and who attended a women’s health specialty clinic in a women’s health center in the VA healthcare system. This center provides comprehensive women’s health services to female veterans. By attending this center, female veterans are having most if not all of their healthcare needs met in one location. Some of the services provided at the center include: primary care; gynecology; other gender specific health care needs; mental health care; and social assistance among other issues that may be associated with the overall QOL and depression. Despite this study having a small sample size (n = 51), the participants were ethnically diverse: White (52.9%); African American (29.4%); Hispanic/Latino (15.7%); and Asian/Pacific Islander (2%). The overall results of this study reveal that female veterans who attend this clinic, have significantly lower baseline scores for QOL when compared to a North American population reference value. Means and standard deviation for total Menopause Rating Scale (MRS) score were; (n = 51, M = 21.2, SD = 9.2) compared to the North American women population reference values (n = 1,376, M = 9.1, SD = 7.6), z = 9.41, p < .0001, cohens d = 1.31. These results were significantly lower for all MRS subsets. The higher the means and standard deviation, the lower the QOL. A paired sample t-test indicated significant improvement in QOL after treatment in QOL (t = 7.80, p < .0001), and depression levels (t = 3.74, p < .0001) among female veterans attending the women’s health specialty clinic. Forward stepwise multiple linear regression models were fit to explore the association between the following variables and the outcomes of QOL and depression levels: low socioeconomic status (SES); number of deliveries; years of service; and military sexual trauma (MST). The only predictor that appeared to be significantly associated with higher MRS scores at baseline was a history of MST (β = .363; t = 2.44; p = 0.02). Higher MRS scores can be interpreted as lower QOL among female veterans. Despite the complexities and unique needs of female veterans, the findings of this study suggest that timely, comprehensive and gender specific healthcare can significantly improve overall QOL and depression levels. In addition, further studies are need to assess what other variables may have a direct association with QOL, depression levels, and overall health of female veterans.

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Bücher zum Thema "“Women’s quality of life”"

Rural women and their quality of life. Jaipur: Point Publishers, 2007.

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Stevenson, Judi. The quality of education and school life. Ottawa, ON: Canadian Teachers' Federation, 1993.

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N, Mathur R. Quality of working life of women construction workers. New Delhi, India: Commnonwealth Publishers, 1989.

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A, Lobo Rogerio, Hrsg. Women's health and menopause: New strategies--improved quality of life. Dordrecht: Kluwer Academic Publishers, 2002.

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Robertson, Heather-Jane. Progress revisited: The quality of (work)life of women teachers. Canada: Canadian Teachers' Federation, 1993.

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Great Britain. Work Research Unit. Women and quality of working life: A selection from the literature. London: Work Research Unit, 1985.

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Roybal, Edward Ross. The quality of life for older women: Older women living alone : a report. Washington: U.S. G.P.O., 1989.

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Roybal, Edward Ross. The quality of life for older women: Older women living alone : a report. Washington: U.S. G.P.O., 1989.

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Roybal, Edward Ross. The quality of life for older women: Older women living alone : a report. Washington: U.S. G.P.O., 1989.

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Lem, Ellyn A. The work-family debate in popular culture: Can women and men "have it all?". Lewiston, New York: The Edwin Mellen Press, 2014.

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Buchteile zum Thema "“Women’s quality of life”"

Glasser, Brandy. „Quality of Life“. In Encyclopedia of Women’s Health, 1111–13. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48113-0_371.

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Sadik, Nafis. „Longevity and Women’s Health“. In Longevity and Quality of Life, 7–11. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4249-0_3.

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Lavack, Anne M. „Case 14: Qimaavik Women’s Shelter“. In Applying Quality of Life Research:, 231–40. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5878-0_15.

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Gemelli, Marcella. „Women’s Employment“. In Encyclopedia of Quality of Life and Well-Being Research, 7150–54. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-0753-5_3251.

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Chen, Yin-Zu, und Hiromi Tanaka. „Women’s Empowerment“. In Encyclopedia of Quality of Life and Well-Being Research, 7154–56. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-0753-5_3252.

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Johnson, Joy L. „Women’s Health“. In Encyclopedia of Quality of Life and Well-Being Research, 7156–59. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-0753-5_3253.

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Gemelli, Marcella. „Women’s Employment“. In Encyclopedia of Quality of Life and Well-Being Research, 1–5. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-319-69909-7_3251-2.

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Lips, Hilary, und Alynn Gordon. „Women’s Well-Being“. In Encyclopedia of Quality of Life and Well-Being Research, 7168–72. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-0753-5_3257.

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Lips, Hilary, und Alynn Gordon. „Women’s Well-Being“. In Encyclopedia of Quality of Life and Well-Being Research, 1–7. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-319-69909-7_3257-2.

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Fahs, Breanne, und Eric Swank. „Women’s Sexual Satisfaction Predictors“. In Encyclopedia of Quality of Life and Well-Being Research, 7166–68. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-0753-5_4020.

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Konferenzberichte zum Thema "“Women’s quality of life”"

Hesti Ermawati, Dwi, Uki Retno Budihastuti und Bhisma Murti. „Biopsychosocial Factors and Menopause Affecting Women’s Quality of Life in Surakarta, Central Java“. In Mid International Conference on Public Health 2018. Masters Programme in Public Health, Universitas Sebelas Maret, 2018. http://dx.doi.org/10.26911/mid.icph.2018.03.17.

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Tarigan, Imarina, und Sri Rahayu Sanusi. „Dominant Factors Affecting In Quality Of Life Menopause Women“. In 2nd Public Health International Conference (PHICo 2017). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/phico-17.2018.16.

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LS Winnie, Cheng, und Wong MF Florence. „Menopausal-Specific Quality of Life among Women in Hong Kong“. In 6th Annual Global Healthcare Conference (GHC 2017). Global Science & Technology Forum (GSTF), 2017. http://dx.doi.org/10.5176/2251-3833_ghc17.04.

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Ganieva, E. A., Z. A. Garifullina und R. A. Garifullin. „Health Influence on Life Quality and Social Acitivities of Women“. In International Session on Factors of Regional Extensive Development (FRED 2019). Paris, France: Atlantis Press, 2020. http://dx.doi.org/10.2991/fred-19.2020.63.

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Hartanti, Retno, Satiyem Satiyem, I. Wayan Arsana Wiyasa, Nurdiana Nurdiana, Umi Kalsum, Maya Devi Arifiandi und Bagus Putu Putra Suryana. „The correlation between estradiol, 25 hidroxyvitamin D and quality of life among postmenopausal women“. In INTERNATIONAL CONFERENCE ON LIFE SCIENCES AND TECHNOLOGY (ICoLiST 2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0052864.

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Ozturk, Nur Selin, Rengin Demir, Nihal Sakalli und Sansin Tuzun. „Relationship between sleep quality and quality of life in women with low bone mineral density“. In ERS/ESRS Sleep and Breathing Conference 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/23120541.sleepandbreathing-2017.p88.

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Patnaik, Sourav S., Benjamin Weed, Ali Borazjani, Robbin Bertucci, Mark Begonia, Bo Wang, Lakiesha Williams und Jun Liao. „Biomechanical Characterization of Sheep Vaginal Wall Tissue: A Potential Application in Human Pelvic Floor Disorders“. In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80886.

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Annotation:

Pelvic Organ Prolapse (POP) is a leading women’s health issue affecting a significant portion of the population and has been recently coined as a “silent epidemic”. POP leads to a considerable reduction in women’s quality of life and can cause chronic pelvic pain, sexual dysfunction, and social/psychological issues. The lifetime risk for having surgery for POP is approximately 11% with 200,000 POP procedures performed each year in USA, with an annual direct cost of over $1000 million. Exact etiology of POP is unclear, but it is understood that POP is multi-factorial in nature. Risk factors for POP include increasing age, obesity, multiple vaginal births, gravidity, history of hysterectomy, smoking, chronic cough conditions, frequent heavy lifting, and some genetic factors. POP results due to loss or damage of structural supports that support the pelvic organs (i.e. rectum, bowel, bladder, etc). Vaginal wall prolapse (anterior and posterior) is the most common presentation. This can result from weakening of the levator ani muscle and other connective tissue structures which not only control the mechanical function, but also help support neurological and anatomical function[1].

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FERNANDES, DARCI RAMOS, SUELI CARNEIRO und ROSELINE OLIVEIRA CALISTO LIMA. „QUALITY OF LIFE IN WOMEN WITH LUPUS NEPHRITIS UNDERGOING RENAL TRANSPLANTATION“. In 36º Congresso Brasileiro de Reumatologia. São Paulo: Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-565.

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Park, Eunok, und Kyungja Kang. „Incontinence-Quality of Life (I-QOL) Among Women with Urinary Incontinence“. In Healthcare and Nursing 2014. Science & Engineering Research Support soCiety, 2014. http://dx.doi.org/10.14257/astl.2014.72.19.

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Song, Mi Ryeong, und Li Ra Song. „Factors Influencing Quality of Life among Women Participating in Health Dance“. In Healthcare and Nursing 2013. Science & Engineering Research Support soCiety, 2013. http://dx.doi.org/10.14257/astl.2013.40.27.

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Berichte der Organisationen zum Thema "“Women’s quality of life”"

Research Institute (IFPRI), International Food Policy. Women’s empowerment in agriculture and dietary quality across the life course: Evidence from Bangladesh. Washington, DC: International Food Policy Research Institute, 2018. http://dx.doi.org/10.2499/1024320686.

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Avis, Nancy E., und Brigitte Miller. A Treatment Stage Specific Approach to Improving Quality of Life for Women with Ovarian Cancer. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2002. http://dx.doi.org/10.21236/ada413317.

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Avis, Nancy E., und Brigitte Miller. A Treatment Stage Specific Approach to Improving Quality of Life for Women With Ovarian Cancer. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2006. http://dx.doi.org/10.21236/ada462076.

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Arslantas, Didem, Mustafa Tozun, Alaettin Unsal, Gokce Dagtekin, Sevil Aydogan und Aziz Soysal. Relationships between Depression, Quality of Life and Other Possible Factors among Postmenopausal Women in Western Turkey. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, Mai 2020. http://dx.doi.org/10.7546/crabs.2020.05.16.

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Klemp, Jennifer R. The Use of a Cognitive Protectant to Help Maintain Quality of Life and Cognition in Premenopausal Women with Breast Cancer Undergoing Adjuvant Chemotherapy. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2006. http://dx.doi.org/10.21236/ada468521.

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Poleshuck, Ellen, Iwona Juskiewicz, Marsha Wittink, Hugh Crean und Catherine Cerulli. Is a Patient Navigation Program More Helpful than a Referral Program for Reducing Depression and Improving Quality of Life among Women Living in Neighborhoods with Few Resources? Patient-Centered Outcomes Research Institute (PCORI), Mai 2019. http://dx.doi.org/10.25302/5.2019.ad.12114261.

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Benson, Vivienne, und Kelly Shephard. ESRC-DFID Research for Policy and Practice: Women’s life choices. Institute of Development Studies and The Impact Initiative, März 2018. http://dx.doi.org/10.35648/20.500.12413/11781/ii308.

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Naughton, Michelle J. Quality of Life and Functional Status Across the Life Course. Fort Belvoir, VA: Defense Technical Information Center, Mai 2006. http://dx.doi.org/10.21236/ada457557.

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