What Couples Choose to Focus on During Nurse-led Family Health Conversations When Suffering Stroke

2015 ◽  
Vol 19 (2) ◽  
pp. 22-28
Author(s):  
Karin Sundin, ◽  
Susanna Pusa, ◽  
Erika Lundstedt, ◽  
Erika Lundstedt, ◽  
Ulrika Östlund, ◽  
...  

The aim of this study was to illuminate which topics 2 couples, ages younger than 65 years old, where 1 partner has suffered a stroke, choose to focus on when participating in nurse-led family health conversations. Six conversations were audiotaped, transcribed, and analyzed by qualitative content analysis. Three categories emerged illustrating that the couples choose to talk about how they were affected on a personal and family level and, moreover, the importance of support within and outside the family. The altered way of living involved distressed feelings, gratitude, and hopes. This study highlights the importance of nurses viewing the family as a unit.

Psico-USF ◽  
2019 ◽  
Vol 24 (4) ◽  
pp. 661-671
Author(s):  
Meyrielle Belotti ◽  
Alexandra Iglesias ◽  
Luziane Zacché Avellar

Abstract The article aims to analyze the conceptions conferred by the health professionals that compose the Expanded Nuclei of Family Health (NASF) on their work assignments. This is a qualitative research, in which was used, for the data collection, eight focus groups, with a total of 43 participants. The data were submitted to content analysis. The results outlined the following categories: integrating NASF work with the Family Health Teams (ESF); developing specialized care; promoting intersectionality; contributing to the promotion of teamwork in Primary Care (AB) and strengthening AB. The study indicates the importance of a better understanding of the functions of the NASF, so that it does not restrict the opportunity to perform specialized care in AB. It is pointed out, the need for adjustments in the work processes of the ESF, in order to enable the shared work in the AB.


2011 ◽  
Vol 19 (2) ◽  
pp. 396-402 ◽  
Author(s):  
Leticia Silveira Cardoso ◽  
Marta Regina Cezar-Vaz ◽  
Mara Regina Santos da Silva ◽  
Valdecir Zavarese da Costa

This study identified the purposes of the communication process in the group activities of the Family Health strategy from the perspective of nurses. Semi-structured interviews were conducted and recorded with 60 nurses and non-participant observation with 19 group activities, analyzed according to qualitative content analysis. Five categories emerged: Health education, Clinical follow-up, Co-responsibilization of patients, Team-Community Interaction, and Work Organization. These categories revealed that the establishment of reciprocal interactions among professionals, patients and families favor health promotion because it encourages the exchange of knowledge among the participants concerning their health experiences.


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
I. Engqvist ◽  
K. Nilsson

The aim of the study was to describe Swedish psychiatrists’ experiences of involving the family in the treatment of women with postpartum psychosis. A qualitative design was used, and semistructured qualitative research interviews were conducted with nine psychiatrists from the south of Sweden. Data were analysed using qualitative content analysis. Four categories were found:the family as a resource,the family as coworkers,preparing the family for the future, andthe family as a burden. The result showed that the psychiatrists considered the family to be a resource to which they devoted a great deal of care and effort. It was particularly important to involve the partner, informing about the course of the illness and the steps that need to be taken in the event of a relapse and reducing any guilt feelings. The psychiatrists instilled confidence and hope for a future of health and further child bearing. The family members’ limited understanding of the treatment may impede the involvement of the family. Conclusion of the study was that the goal for family involvement was to facilitate the women’s care and treatment. Further studies are needed to provide suggestions on how to develop family involvement in the care of women suffering from postpartum psychosis.


2021 ◽  
pp. 0192513X2110648
Author(s):  
Sonja Anttila ◽  
Päivi Palojoki ◽  
Jaana Vuori ◽  
Hille Janhonen-Abruquah

This study explores the negotiations taking place in LGBTQ families before a child is born or added to the family. It asks who takes part in the negotiations and what issues are negotiated about. An online questionnaire answered by LGBTQ parents (n = 74) was analyzed with qualitative content analysis. The chain of phases leading to having a child can be referred to as a family forming process with various negotiation topics. The four phases are identified as parental desires, consideration of practices, reflecting on the decision, and concrete actions toward having a child. Besides the LGBTQ parents-to-be, significant others such as friends and the family of origin and external others such as donors and fertility clinics took part in the negotiations. Future parents needed to think about their desires in advance to enable fair and equal negotiations.


2013 ◽  
Vol 26 (2) ◽  
pp. 207-228
Author(s):  
Ulrich Riegel

AbstractDaily routine on Sunday is changing. Formerly a day of religious contemplation, Sunday seems to be a day of rest within the family. Does this change in activities done on a typical Sunday imply an end of spiritual quality? To answer this question this paper conceptualizes spirituality as experience of connectedness to some greater reality which is regarded as important and meaningful. Four options are possible concerning this greater reality: a transcendent reality, nature or cosmos, mankind, or the individual’s self. The data has been collected by semi-structured interview and analyzed by qualitative content analysis. 148 individuals did take part in these interviews (57% females, age range: 7 to 59; 64% Catholics and 22% Protestants). The findings point at Sunday spent with family. Further on we could identify activities representing all four types of spirituality. Together these examples point at the conclusion that Sunday still is a special day within the week. Its activities offer spiritual quality, but it is the individual to reassure it.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Fateme Mohammadi ◽  
Khodayar Oshvandi ◽  
Farshid Shamsaei ◽  
Fateme Cheraghi ◽  
Masoud Khodaveisi ◽  
...  

Abstract Background The bereaved families of COVID-19 victims are among the most vulnerable social groups in the COVID-19 pandemic. This highly infectious and contagious disease has afflicted these families with numerous psychological crises which have not been studied much yet. The present study is an attempt at investigating the psychological challenges and issues which the families of COVID-19 victims are faced with. The present study aims to identify the Mental Health crises which the families of COVID-19 deceased victims are going through. Methods A qualitative research, the present study uses a conventional content analysis design. The participants were 16 members of the families of COVID-19 victims selected from medical centers in Iran from February to May 2020 via purposeful sampling. Sampling continued to the point of data saturation Data were collected via semi-structured individual interviews conducted online. The collected data were analyzed according to the conventional qualitative content analysis approach. Results Analyses of the data yielded two main themes and seven categories. Emotional shock included (feelings of guilt and rumination, bitter farewell, strange burial and concern about unreligious burial), and fear of the future included (instability in the family, lack of job security and difficult financial conditions, Stigmatization and complications in social interactions). Conclusion The families of COVID-19 deceased victims are affected by various psychological crises which have exposed them to a deep sense of loss and emotional shock. Therefore, there is an urgent need for a cultural context which recognizes and supports all the various aspects of the mental health of these families.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Nasim Mousavi ◽  
Marzieh Norozpour ◽  
Zahra Taherifar ◽  
Morteza Naserbakht ◽  
Amir Shabani

Abstract Background Bipolar disorder is a common psychiatric disorder with a massive psychological and social burden. Research indicates that treatment adherence is not good in these patients. The families’ knowledge about the disorder is fundamental for managing their patients’ disorder. The purpose of the present study was to investigate the knowledge of the family members of a sample of Iranian patients with bipolar I disorder (BD-I) and to explore the potential reasons for treatment non-adherence. Methods This study was conducted by qualitative content analysis. In-depth interviews were held and open-coding inductive analysis was performed. A thematic content analysis was used for the qualitative data analysis. Results The viewpoints of the family members of the patients were categorized in five themes, including knowledge about the disorder, information about the medications, information about the treatment and the respective role of the family, reasons for pharmacological treatment non-adherence, and strategies applied by families to enhance treatment adherence in the patients. The research findings showed that the family members did not have enough information about the nature of BD-I, which they attributed to their lack of training on the disorder. The families did not know what caused the recurrence of the disorder and did not have sufficient knowledge about its prescribed medications and treatments. Also, most families did not know about the etiology of the disorder. Conclusion The lack of knowledge among the family members of patients with BD-I can have a significant impact on relapse and treatment non-adherence. These issues need to be further emphasized in the training of patients’ families. The present findings can be used to re-design the guidelines and protocols in a way to improve treatment adherence and avoid the relapse of BD-I symptoms.


Author(s):  
Maryam Solgi ◽  
Zohrehsadat Nabavi ◽  
Maryam Safara

Veil (hijab) is one of the most important elements in the spiritual health of women. This study aimed to investigate the relationship between the veil and spiritual health in women and its impact on the spiritual health of the family, and to explain this issue in the dimension of the health of women and family as well as community by referring to some psychological effects of the veil (hijab). The veil enhances the value of women and above all provides their mental security with protection of human emotions and adherence to moral principles. Veil is responsible for strengthening the family foundation, and guarantees its spiritual health and is as a phenomenon effective in providing family health, which appears as a dynamic and pioneer attribute and saves the family from disintegration. This paper deals with components that consider the veil as a prominent factor in the health of woman and family. The research method used in this study was library method through content analysis.


2021 ◽  
Author(s):  
Aliasghar kheirkhah ◽  
Ehsan Movahed ◽  
Fereshte gheyabi ◽  
Fatemeh kave Farsani ◽  
Fatemeh Rigabadi

Abstract Background: Health providers and patients face many problems in preventing and controlling COVID-19 in the family and the health system.Aim: The aim of the present study was to explore experiences of health providers and patients in COVID‑19.Methods: directional qualitative content analysis was applied and 15 participants, including 10 patients with COVID-19 and 5 health providers. Data were collected using semi-structured interviews and analyzed by Lundman and Graneheim qualitative content analysis methods. The MAXQDA10 software was used to manage qualitative data analysis.Results: During the data analysis, "strengths", "weaknesses", "opportunities", and "threats" were defined in terms of categories. The " Benefits and Barriers " was determined as the main theme.Conclusion: Community members and policymakers should support and reinforce the positive experiences of patients and health providers and the health system and families need to be more prepared for the crisis.


2019 ◽  
Author(s):  
Akram Farhadi ◽  
Farahnaz Mohammadi ◽  
Mahshid Foroughan ◽  
Leila Sadeghmoghadam ◽  
Shima Nazari ◽  
...  

Abstract Background The concept of caring appraisal, which includes positive and negative aspects of care, has been considered as one of the key concepts in caregivers' studies. The aim of the present study was to investigate the self-appraisal concept of caring from the viewpoint of family caregivers in the elderly with dementia in Iran.Methods This study was based on qualitative analysis. Data were collected through in-depth and semi-structured interviews. Twelve participants (family caregivers of elderly people with dementia) were interviewed between January and September 2016. They were selected from visitors to the Alzheimer's Association of Iran and Yadman Memorial Clinic (Tehran- Iran). The interviews were recorded and transcribed. The transcribed texts were analyzed using inductive qualitative content analysis recommended by Graneheim and Lundman (2004).Results The study explored two main categories include "perceived burden", "Losses and Threats," "satisfaction with care", "Personal growth", "caregiving gains", "philosophy of care" and 22 subcategories.Conclusion According to the results of this study, the family caregivers’ appraisal of their care not only does not have negative aspects but also covers a large number of positive aspects, in which the cultural and social conditions prevailing in the Iranian society play a significant role in the formation of these positive aspects.


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