Supportive Intervention Challenges for Patients with Breast Cancer: A Systematic Review

Zaker, Mohammad Reza; Safaripour, Amin; Sabegh, Sima Rahdaneh Zade; Barjasteh, Samira

doi:10.31557/apjec.2021.4.1.19-24

Cited by 10 publications

(14 citation statements)

References 12 publications

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“…So that in their research, to investigate the effect of education on the quality of life of breast cancer patients, they concluded that after counseling and education in the field of breast cancer treatment and standard care, the quality of life of patients has increased in all aspects. But the most significant increase was related to the physical element (25). Wang et al (26) and Warzecha et al ( 8) also reached the same conclusion regarding the quality of life of hemodialysis patients and the elderly in their studies, respectively, and it was found that the average scores of people in the dimension of physical health were significantly higher after training.…”

Section: Discussionmentioning

confidence: 65%

Evaluating the effect of nurses' supportive and educational care on GATA2 gene expression and quality of life in patients with endometriosis

Zheng

2022

Cell Mol Biol (Noisy-le-grand)

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Section: Discussionmentioning

confidence: 65%

Evaluating the effect of nurses' supportive and educational care on GATA2 gene expression and quality of life in patients with endometriosis

Zheng

2022

Cell Mol Biol (Noisy-le-grand)

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“…They noted that they received effective emotional support from their husbands and considered it as the main reason for returning to their normal mental state. It is well-documented that family support is crucial for women who underwent mastectomy [ 11 , 23 , 24 ]. On other hand, one participant shared a different opinion that she didn’t receive effective support from her husband.…”

Section: Discussionmentioning

confidence: 99%

The Lived Experience of Ethiopian Women After Mastectomy due to Breast Cancer: A Qualitative Study

Teshome,

Atinafu,

Bekele

et al. 2024

Asian Pac J Cancer Prev

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Background: The impact of breast absence on women’s lived experiences is not well studied in Sub-Saharan Africa particularly in Ethiopia, with implications for service design. This study aimed to explore the lived experiences of Ethiopian women after mastectomy due to breast cancer. Methods: A qualitative study approach was used to explore the experiences of women who underwent a mastectomy at the oncology unit of Tikur Anbessa Specialized Hospital. Before the commencement of the study, consent was obtained from each respondent. An in-depth interview was conducted with twelve post-mastectomy women using a semi-structured interview guide. Audio-recorded data were transcribed verbatim and translated into English. Data were coded, sorted, and themes were developed manually based on the thematic analysis. Results: Five themes illustrating the impact on the women’s life after mastectomy were identified and categorized into (1) Perceived alteration in physical and psychosocial aspects, (2) Perceived social support, and adapting to life after mastectomy. Conclusion: Our finding suggests that women who underwent mastectomy need holistic care including physical, psychosocial, and emotional support from their family, society, and healthcare professionals.

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“…Patients often remember and value the compassionate interactions they have with their caregivers, more than the clinical aspects of their care. This empathetic approach is not only beneficial for emotional well-being but can also positively impact treatment outcomes [62]. The narratives also collectively emphasize the necessity of effective communication and holistic care in cancer treatment.…”

Section: Discussionmentioning

confidence: 99%

Exploring Patient Centered Perspectives on Suicidal Ideation: A Mixed Methods Investigation in Gastrointestinal Cancer Care

Choudhury,

Shahsavar,

Ahmed

et al. 2023

Preprint

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BackgroundGastrointestinal (GI) cancer patients face a 4-fold higher risk of suicide than the general US population. While efforts to reduce suicide risk in cancer patients have been crucial, the issue remains urgent. This study explores the psychosocial aspects of gastrointestinal (GI) cancer patient experiences. It focuses on assessing the prevalence and intensity of suicidal ideation and behavior, evaluating mental distress during different treatment phases, and examining the impact of psychosocial factors on mental health.MethodWe used a two-phase mixed-methods approach. The research began with a web-based survey targeting individuals across the US who were undergoing or had completed GI cancer treatment. Survey respondents were then debriefed and invited to engage in a follow-up interview, which were conducted via video conferencing, recorded, transcribed, and anonymized for analysis. Quantitative data analysis involved confirmatory factor analysis to validate constructs related to mental health and suicidal ideation. Subsequently, significant correlations with mental health and suicidal ideation were extracted and scaled for further bivariate analyses. Qualitatively, an inductive thematic analysis was performed on both survey responses and interview transcripts. The patient journey was charted from diagnosis through the treatment continuum, with sentiment analysis enriching the thematic findings.ResultsTwo hundred-two individuals responded to the survey. Of all the participants, 76 respondents were from the rural Appalachian region, and 78 were undergoing treatment during the study. Quantitative analysis revealed a higher prevalence of passive suicidal ideation compared to active planning. The post-treatment recovery period was reported as the most emotionally challenging. Qualitative data emphasized the crucial role of emotional support, with patients feeling particularly vulnerable to isolation. The quality of care received was another concern, with calls for more individualized treatment plans and better communication. Patients also expressed a need for clear, comprehensive information about their treatment and potential side effects. The in-depth interview with 4 GI cancer patients indicated a healthcare system that prioritizes expedient treatment over comprehensive care, with a noted lack of formal psychological support. The role of artificial intelligence (AI) emerged as a promising avenue for enhancing patient understanding of their condition and treatment options. Patients valued clear, empathetic communication and the provision of comprehensive, understandable information from their healthcare providers. The sentiment analysis associated with their experiences reflected a spectrum of emotional responses, from shock and disbelief at diagnosis to fluctuating emotions during treatment.ConclusionOur research advocates for a more patient-centric model of care, enhanced by the thoughtful integration of technology and consistent, empathetic communication. These findings contribute to a deeper understanding of the GI cancer patient experience and provide a foundation for improving cancer care practices to better address the holistic needs of patients.

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Supportive Intervention Challenges for Patients with Breast Cancer: A Systematic Review

Cited by 10 publications

References 12 publications

Evaluating the effect of nurses' supportive and educational care on GATA2 gene expression and quality of life in patients with endometriosis

Evaluating the effect of nurses' supportive and educational care on GATA2 gene expression and quality of life in patients with endometriosis

The Lived Experience of Ethiopian Women After Mastectomy due to Breast Cancer: A Qualitative Study

Exploring Patient Centered Perspectives on Suicidal Ideation: A Mixed Methods Investigation in Gastrointestinal Cancer Care

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