scholarly journals LITERATURE REVIEW: PERCEPTION AND QUALITY OF WOMEN'S LIFE WITH INFERTILITY [KAJIAN LITERATUR: PERSEPSI DAN KUALITAS HIDUP PEREMPUAN DENGAN INFERTILITAS]

2020 ◽  
Vol 7 (2) ◽  
pp. 9
Author(s):  
Belet Lydia Ingrit

<p>Infertility is the failure to get a pregnancy after at least one year of sexual intercourse without using contraception. Many efforts that have been made by infertil women to get pregnant but not a few have failed treatment. Perception will affect the adaptation and quality of life of a woman. Therefore the purpose of this literature review is to explore perceptions and quality of life of women with infertility. Research articles were obtained from two databases namely EBSCO and Google Scholar. Literature search uses keywords (Indonesian and English), namely Perception and quality of life of women with infertility with inclusion criteria for research articles from 2009-2019, primary articles, full text and research subjects are infertil women (both primary and secondary). From 464 research articles, six articles were reviewed that met all the inclusion criteria and objectives of this literature review. Six articles obtained were then made critical appraisals which were then analyzed using simplified thematic analysis. The theme that emerged from this literature review was the negative impact, quality of life and handling of infertility. Based on the results of the review of this article, it is necessary to support both social and emotional systems for infertility women to achieve a better quality of life.</p><p><strong>BAHASA INDONESIA ABSTRAK: </strong>Infertilitas adalah kegagalan untuk mendapatkan kehamilan setelah setidaknya satu tahun berhubungan seksual tanpa menggunakan alat kontrasepsi. Banyak upaya yang sudah dilakukan perempuan infertil untuk bisa hamil namun tidak sedikit yang gagal dalam pengobatan. Persepsi akan memengaruhi adaptasi dan kualitas hidup seorang perempuan. Oleh karena itu tujuan kajian literatur ini adalah untuk menggali persepsi dan kualitas hidup peremuan dengan infertil. Artikel penelitian didapatkan dari dua database yaitu EBSCO dan Google Scholar. Pencarian literatur menggunakan kata kunci (bahasa Indonesia dan bahasa Inggris) yaitu persepsi (Perception) dan kualitas hidup perempuan dengan infertilitas (Quality of life women with infertility) dengan kriteria inklusi artikel penelitian dari tahun 2009-2019, artikel primer, fulltext dan subjek penelitian adalah perempuan infertil (baik primer maupun sekunder). Dari 464 artikel penelitian didapatkan enam artikel yang direview yang memenuhi semua kriteria inklusi dan tujuan dari kajian literatur ini. Enam artikel yang didapatkan kemudian dilakukan penilaian kritis (critical appraisal) yang kemudian dianalisis menggunakan simplified thematic analysis. Tema yang muncul dari kajian literatur ini adalah dampak negatif, kualitas hidup dan penanganan infertilitas. Berdasarkan hasil review artikel ini, dibutuhkan support system baik sosial maupun emosional bagi perempuan infertilitas untuk mencapai kualitas hidup yang lebih baik.</p><p> </p>

Author(s):  
Anita Setyawati ◽  
Restuning Widiasih ◽  
Ermiati E ◽  
Ida Maryati

Menarche is the first experience of menstruation would cause anxiety among teenagers, fear, discomfort, and affect the quality of life of teenage. This condition was caused by the taboo assumption to discuss menstruation with family and their environment. Therefore, this study was conducted to identify urban teenagers' readiness toward menarche. This study was conducted with the process of searching, collecting and analyzing articles. The search sources used were Cinahl, Scopus, Cochrane, Pubmed, and Cengage databases. The keywords used were menarche, readiness, and urban teenagers. The inclusion criteria used were 2013 - 2018 research articles, full text, and English articles. The exclusion criteria used was non-urban teenagers. According to the keyword was found 124 articles. After being selected based on the inclusion and exclusion criteria, 7 articles were analyzed. The result showed urban teenagers' readiness consisted of internal and external readiness. Internal readiness consists of age and knowledge. Internal readiness can affect self-acceptance, maturity of mind, and views on the stages of growth and development that are being faced. External readiness consists of social support. Social support for urban teenagers is useful to get information and attention when menarche. External readiness for urban teenagers was already good but lack of internal readiness. Therefore, counseling and health education related to menarche was needed starting from elementary school.Keywords: Menarche, readiness, urban teenager.


2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Pingkan M. Ruru ◽  
Taufiq F. Pasiak ◽  
Martha M. Kaseke

Abstract: The olfactory nerve is the first cranial nerve. Olfactory disorders can have a negative impact on health and quality of life and affect human psychology. The aim of this study is to determine the basic anatomical, clinical medical and psychological picture of the olfactory nerve. This study was in the form of a literature review. Literature is taken from one database, namely PubMed. The keywords used were olfactory nerve anatomy AND clinical AND psychology. After being selected with inclusion and exclusion criteria, 11 literature will be reviewed. Research from 11 literature reviewed found the basic anatomy of the olfactory nerve. Clinical disorders such as anosmia, hyposmia, phantosmia can occur in several non-neurodegenerative and neurodegenerative events or diseases, namely head injury trauma, Alzheimer's, Parkinson's and COVID-19. Psychological issues related to emotional and psychiatric disorders are also related to smell. In conclusion, the first cranial nerve is the olfactory nerve or the olfactory nerve, which clinically can occur in neurogenerative and non-neurodegenerative diseases. Smell and its disturbances can have a psychological impact.Keywords: olfactory nerve, anatomy, clinical, psychology.  Abstrak: Nervus olfaktorius merupakan saraf kranial pertama. Gangguan olfaktorius dapat berdampak buruk pada kesehatan dan kualitas hidup serta memengaruhi psikologis manusia. Tujuan penelitian untuk mengetahui gambaran dasar anatomi, klinis medis dan psikologis dari nervus olfaktorius. Penelitian ini dalam bentuk literature review. Literatur diambil dari  satu database yaitu PubMed. Kata kunci yang digunakan yaitu olfactory nerve anatomy AND clinical AND psychology. Setelah diseleksi dengan kriteria inklusi dan eksklusi didapatkan 11 literatur yang akan di review. Hasil penelitian dari 11 literatur yang di review didapatkan anatomi dasar nervus olfaktorius. Gangguan klinis seperti anosmia, hiposmia, phantosmia dapat terjadi pada beberapa kejadian atau penyakit non-neurodegeneratif dan neurodegeneratif yaitu Trauma cedera kepala, Alzheimer, Parkinson dan COVID-19. Psikologis yang berkaitan dengan emosional dan gangguan psikiatri juga berhubungan dengan penciuman. Sebagai simpulan, saraf kranial pertama adalah nervus olfaktorius atau disebut saraf penciuman, secara klinis bisa terjadi pada penyakit neurogeneratif dan non-neurodegeneratif. Penciuman dan gangguannya dapat memengaruhi psikologis.Kata kunci: Saraf olfaktori, anatomi, klinis, psikologi.


2012 ◽  
Vol 20 (2) ◽  
pp. 401-410 ◽  
Author(s):  
Fernanda Ribeiro Correia ◽  
Marysia Mara Rodrigues do Prado De Carlo

The use of scales that have been validated and standardized for different cultures is very useful for identifying demands in the field of Palliative Care and implementing the most appropriate care. This integrative literature review focuses on instruments assessing the Quality of Life of patients under Palliative Care through a journal search in electronic databases. The study consisted of 49 papers identified in Medline/PubMed, of which 18 met the inclusion criteria previously defined. Information concerning the selected studies is presented and later categorized, with a greater emphasis on the analysis of the psychometric properties of validations of the Palliative Outcome Scale, conducted in three countries. This review enabled the identification of instruments already developed and validated for different cultures, increasing the possibility of knowledge in the field.


Author(s):  
Kimberlee Flike ◽  
Teri Aronowitz

Background: An emerging category of morbidity in research among people experiencing homelessness (PEH) is quality of life (QoL). Conceptual Framework: The Commission on Social Determinants of Health (CSDH) framework was used to explain the relationship between the resulting factors and their impact on QoL among PEH. Purpose: The purpose of this systematic mixed studies review was to explore the factors that are associated with QoL among homeless individuals. Method: A systematic mixed studies review was conducted using CINAHL, Medline, PubMed, and SocIndex databases. Quantitative, qualitative, and mixed methods studies were included and synthesized employing results-based convergent synthesis design. Results: The initial search resulted in 757 studies with 55 studies meeting the inclusion criteria. Thematic analysis revealed themes influencing QoL among PEH categorized by the CSDH determinants of structural, social cohesion and social capital, and intermediary determinants. Among these themes, higher social status, strong relationships, better reported physical and mental health, and a positive life outlook were associated with increased QoL. Social isolation, substance use, poorer life outlook, increased years spent homeless, and perceived quality of housing were associated with decreased QoL. Age, sex, and housing programs revealed inconsistent results on QoL. Implications: While the factors presented in this review indicate some consistent relationships with QoL in PEH, this review has shown QoL among this population is complex and multifactorial. Future research should focus on relationships between the CSDH determinants, particularly the psychosocial factors and the QoL priorities defined by PEH, and how they may influence QoL among PEH.


JKEP ◽  
2021 ◽  
Vol 6 (2) ◽  
pp. 146-158
Author(s):  
Nanda Agustia ◽  
Gamya Tri Utami ◽  
Fathra Annis Nauli

Head injury is a type of trauma that is commonly found in emergency departements, this is evidence by the large number of deaths resulting from the incidence of head injuries. if the patient survives and they will have physiological or anatomical disorders that affect to the quality of life. The purpose of this literature study is to find out the quality of life of patients after suffering a head injury. The method used is a literature study obtained from scientific reseach article that searches in accordance with the inclusion criteria, start from 2015 up to 2019 using Google Scholar,Science Direct, and Pubmed. The keyword used are Quality of life, Head Injury. Based on 7 research articles, it was found that 6 out 7 articles stated that there was a decrease in quality of life in post-injury patients with duration of 3, 6, and 12 months, evaluation quality of life the domain of assessment of quality of life that experienced the most decrease was in the physical, psychological, social and cognitive domains, 1 research article stated that there was increase in quality of life after head injury. Based on result there was a decrease in quality of life in post-injury patients


2020 ◽  
Vol 3 (2) ◽  
pp. 143-152
Author(s):  
Akbar U Saun ◽  
Erna Rochmawati

Background: Cancer patients choose to understand at home. Families have an important role in the care of clients specifically at home. Readiness is needed in order to provide optimal care and will be able to improve the quality of life of patients. This literature review aims to see how families are prepared to care for patients with cancer at home. Method: Writing this journal literature uses study literature originating from the database, namely EBSCO, PROQUEST, PubMed, and Google Scholar using the keywords Family Preparedness, Family Caregiver, Symptom Management, Palliative Care, family quality of life, Care Parenting. Using inclusion criteria that contain literature sources taken from 2009 to 2019, inclusion criteria, using English, conformity of approval keywords, linkages between the results of literature research and the discussion raised.Results: There are 4 themes found in this literature review, namely family care in patient care, instruments in measuring family readiness, self-affection for families who care for patients at home, and psycho-education in increasing family readiness to care for patients at home. Conclusion: Family readiness to treat patients at home needs to be considered. Nurses play an important role in providing education to the family in providing patient care at home so that the patient's welfare is fulfilled.


2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Stefano Brunelli ◽  
Cinzia Bonanni ◽  
Calogero Foti ◽  
Marco Traballesi

BACKGROUND: Several reviews have been published regarding quality of life (QoL) and Health Status (HS) in persons with lower limb amputation (LLA). However, little has been discussed in the literature with respect to older populations (i.e. age>60 years) with trans-tibial amputation. Furthermore, the perceived satisfaction with prosthesis is another important aspect for consideration in the amputees’ life. OBJECTIVE: The purpose of this review was to evaluate the impact of trans-tibial amputation on the QoL, HS and prosthesis satisfaction, in order to determine the appropriate intervention to improve these aspects in older population of trans-tibial amputees (TTA). METHODS: Research articles, published between January 2000 to March 2019, were found using Scopus, PubMed and Google Scholar databases. The methodological quality of the selected articles was assessed using the Critical Review Form-Quantitative Studies checklist. RESULTS: Ten articles that met the inclusion criteria were selected. In these papers, we can summarize that people with trans-tibial amputation have a better QoL compared to those with above knee amputation. Moreover, physical functioning and mobility are the most influencing factors for QoL and HS in older people with lower limb amputation. Finally, the prosthesis weight reduction may improve satisfaction with the prosthetic limb. CONCLUSION: Efforts have to be made in order to improve mobility in older population with transtibial amputation for better QoL and HS. This can be accomplished by means of adequate rehabilitation, pain management and an accurate choice of appropriate prosthetic components. We observed that the quality of evidence in the literature available is inadequate and future research would benefit from more prospective observational cohort studies with appropriate inclusion criteria and larger sample sizes to better understand the QoL and HS in this population. Layman’s Abstract: Few studies have deeply investigated the effect of aging on Quality of Life, perceived Health Status and satisfaction with the prosthesis on older trans-tibial amputees. This review focuses on these aspects, which can guide professionals on how to improve prosthetic and rehabilitative intervention in this particular amputees’ population. The results of this review indicate that the Quality of Life and Health Status seem to be influenced by adequate rehabilitation, pain management and an accurate choice of appropriate prosthetic components. Article PDF Link: https://jps.library.utoronto.ca/index.php/cpoj/article/view/33640/26354 How To Cite: Brunelli S., Bonanni C., Foti C., Traballesi M. A literature review of the quality of life, health status and prosthesis satisfaction in older patients with a trans-tibial amputation. Canadian Prosthetics & Orthotics Journal. 2020;Volume3, Issue1, No.3. https://doi.org/10.33137/cpoj.v3i1.33640 Corresponding Author: Stefano Brunelli, MDSanta Lucia Foundation, Scientific Institute for Research, Hospitalization and Health Care, Rome, Italy.E-Mail: [email protected]: https://orcid.org/0000-0002-5986-1564


2020 ◽  
Vol 5 (2) ◽  
pp. 1-17
Author(s):  
Suharta

MengasuhindividudenganSindrom Down (SD) denganbanyaknyaketerlambatan dan kecacatanbaiksecara mental maupunfisikmenjadikan orang tua ataupengasuh(caregivers) cenderung mengalami beban yang lebihtinggi, dimanasecaralangsung bepengaruh pada kualitas hidup mereka sebagai caregivers. Tujuan: mengetahui faktor yang berpengaruh pada kualitashidupcaregiversindividudengan SD. Desain: literature review. Metode: Pencarianartikelpada database jurnal yang relevan termasuk Scopus (n=27), Science Direct (n=141), dan Google Scholar (n=170) dengan menggunakan kombinasi pencarian:“quality of life“and “cargivers”or “kualitashidup” and“pengasuh “ or”orang tua” or“pendamping“ and“sindrom down”. Peneliti meninjau (n=10)  artikel dari (n=338) artikel yang diidentifikasi. Hasil: lima jurnal menyebutkan faktor dukungan keluarga, dukungan sosial, status ekonomi, kondisifisik-kesehatan dan penerimaankepadaindividu SD adalahfaktor yang berpengaruh pada kualtiashidupcaregiverKesimpulan: Secara garis besar peneliti menemukan lima faktor yang berpengaruh pada kualitas hidup caregivers anak-remaja dengan SD. Pentinguntukdilakukanpenelitianlebihlanjutterkaitkualitashidupindividu SDdengancakupanyang lebihluas dan beragamgunamendapatkanlandasanteoritissebagaidasaruntukperumusanasuhankeperawatankeluarga dan komunitas.   Kata Kunci:KualitasHidupPengasuh, Sindrom Down, Kualitas Hidup, Caregivers.


2010 ◽  
Vol 4 (4) ◽  
pp. 1929
Author(s):  
Isabelle Katherinne Fernandes Costa ◽  
Gabriela de Sousa Martins Melo ◽  
Walkíria G Nóbrega ◽  
Daniele Vieira Dantas ◽  
Eurides Araújo Bezerra de Macêdo ◽  
...  

ABSTRACTObjective: identify in the Brazilian scientific literature, the utilization of the SF-36 in assessing the quality of life related to chronic diseases. Method: this is a literature systematic review study, conducted in October 2009, in the databases of BIREME using the descriptors quality of life (QL) and chronic diseases, being selected one study in BDENF and three in LILACS. In the database Google Scholar were selected 20, using as descriptors quality of life, chronic diseases and SF-36. Inclusion criteria were: studies published from 2004 to 2009, held in Brazil, available in full text and free access. The results will be presented in table form. Results: of the 24 items surveyed, 83.3% were located in Scholar Google, 12.5% in LILACS and 4.2% in BDENF. Articles predominated (79.2%) in the year 2008 (29.2%), the journal of Arquivos de Neuropsiquiatria was the most raised the issue (16.7%), chronic illness was the most discussed renal chronic disease. Conclusion: the SF-36, despite being a tool to evaluate changes in QL in the last 4 weeks has been applied to diseases with chronic obtaining satisfactory results. Descriptors: quality of life; chronic diseases; a literature review.RESUMOObjetivo: Identificar na literatura cientifica nacional a utilização do SF-36 na avaliação da qualidade de vida relacionada a doenças crônicas. Método: revisão de literatura realizada em outubro de 2009, nas bases de dados da BIREME utilizando os descritores qualidade de vida (QV) e doenças crônicas, sendo selecionado um estudo na BDENF e três na LILACS. Na base de dados Google Acadêmico foram selecionados 20 estudos, usando como descritores qualidade de vida, doenças crônicas e SF-36. Os critérios de inclusão foram: estudos publicados no período de 2004 a 2009, realizados no Brasil, disponível em texto completo e de acesso livre. Os resultados serão apresentados em forma de tabela. Resultados: dos 24 artigos pesquisados, 83,3% estava localizado no Google acadêmico, 12,5% no LILACS e 4,2% na BDENF. Predominaram artigos (79,2%), no ano de 2008 (29,2%); o periódico Arquivos de Neuropsiquiatria foi o que mais abordou o tema (16,7%), a doença crônica mais abordada foi a insuficiência renal crônica (29,2%) e quanto a aplicabilidade, a maioria (58,3%) não relatou dificuldades. Conclusão: o SF-36, apesar de ser um instrumento que avalie as alterações na QV nas últimas 4 semanas tem sido aplicado para doenças com caráter crônico obtendo resultados satisfatórios. Descritores: qualidade de vida; doenças crônicas; revisão de literatura.RESUMENObjetivo: identificar en la literatura científica brasileña, el uso del SF-36 para evaluar la calidad de vida relacionada con las enfermedades crónicas. Método: revisión de la literatura realizada en octubre de 2009, las bases de datos indexados usando palabras clave de la calidad de vida (CV) y enfermedades crónicas, siendo seleccionada 1 estudio en la BDENF y 3 en el LILACS. En la base de datos Google Scholar, fueron seleccionados 20 estudios, con los descriptores calidad de vida, enfermedades crónicas y SF-36. Los criterios de inclusión fueron: estudios publicados desde 2004 hasta 2009, realizada en Brasil, disponible en texto completo y acceso libre. Los resultados se presentan en forma tabular. Resultados: de los 24 artículos de la encuesta, 83,3% estaban localizados en Google Académico, un 12,5% en LILACS y 4,2% en BDENF. Predominaron artículos (79,2%) en el año 2008 (29,2%), en la revista Arquivos de Neuropsiquiatria (16,7%), la enfermedad crónica más abordada fue la insuficiencia renal crónica (29, 2%) y cuanto la aplicabilidad, la mayoría (58,3%) no informaron dificultades. Conclusión: el SF-36, a pesar de ser una herramienta para evaluar los cambios en la calidad de vida en las últimas 4 semanas ha sido aplicado a las enfermedades crónicas con la obtención de resultados satisfactorios. Descriptores: calidad de vida; enfermedad crónica; revisión de la literatura. 


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