{"title":"一个新的乳腺癌诊断进入共同决策过程的二元经验:定性分析。","authors":"Clizia Cincidda, Serena Oliveri, Valeria Sebri, Gabriella Pravettoni","doi":"10.1002/pon.70277","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>This study explores the dyadic experience of patients newly diagnosed with breast cancer and their caregivers, focusing on emotional responses, informational needs, and shared involvement in clinical decision-making.</p><p><strong>Methods: </strong>Twenty-three patient-caregiver dyads participated in semi-structured interviews conducted by psychologists specializing in clinical and health psychology. The interviews were analyzed using Qualitative Thematic Analysis to identify core themes reflecting the dyadic experience.</p><p><strong>Results: </strong>Findings highlighted the central role of the patient-caregiver relationship in coping with diagnosis and treatment planning. Both patients and caregivers valued sharing medical information, participating together in medical consultation and jointly engaging in treatment decisions, which fostered a sense of unity, reduced anxiety and improved understanding of treatment choice. Trust in healthcare providers, particularly their clarity, empathy, and expertise, emerged as a critical factor in alleviating patients' decisional regret and sustaining caregivers' confidence in supporting the patient. Although both patients and caregivers faced emotional challenges, their fears and concerns often differed, underscoring the need for individualized emotional support. Inclusion of caregivers in clinical discussions was considered essential for promoting a cohesive and supportive care experience.</p><p><strong>Conclusions: </strong>The study underscores the emotional complexity and interdependence of the patient-caregiver dynamic following a breast cancer diagnosis. Being the patient-caregiver relationship central to cancer care, it is important to encourage coordinated involvement of both parties in the clinical process may reduce psychological distress, alleviate decisional conflict, and enhance overall quality of life. These findings support the adoption of a person-centered, relational model of care that recognizes the dyad as a unit of support and decision-making.</p>","PeriodicalId":20779,"journal":{"name":"Psycho‐Oncology","volume":"34 9","pages":"e70277"},"PeriodicalIF":3.5000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12398323/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Dyadic Experience of a New Breast Cancer Diagnosis Into the Shared Decision-Making Process: A Qualitative Analysis.\",\"authors\":\"Clizia Cincidda, Serena Oliveri, Valeria Sebri, Gabriella Pravettoni\",\"doi\":\"10.1002/pon.70277\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>This study explores the dyadic experience of patients newly diagnosed with breast cancer and their caregivers, focusing on emotional responses, informational needs, and shared involvement in clinical decision-making.</p><p><strong>Methods: </strong>Twenty-three patient-caregiver dyads participated in semi-structured interviews conducted by psychologists specializing in clinical and health psychology. The interviews were analyzed using Qualitative Thematic Analysis to identify core themes reflecting the dyadic experience.</p><p><strong>Results: </strong>Findings highlighted the central role of the patient-caregiver relationship in coping with diagnosis and treatment planning. Both patients and caregivers valued sharing medical information, participating together in medical consultation and jointly engaging in treatment decisions, which fostered a sense of unity, reduced anxiety and improved understanding of treatment choice. Trust in healthcare providers, particularly their clarity, empathy, and expertise, emerged as a critical factor in alleviating patients' decisional regret and sustaining caregivers' confidence in supporting the patient. Although both patients and caregivers faced emotional challenges, their fears and concerns often differed, underscoring the need for individualized emotional support. Inclusion of caregivers in clinical discussions was considered essential for promoting a cohesive and supportive care experience.</p><p><strong>Conclusions: </strong>The study underscores the emotional complexity and interdependence of the patient-caregiver dynamic following a breast cancer diagnosis. Being the patient-caregiver relationship central to cancer care, it is important to encourage coordinated involvement of both parties in the clinical process may reduce psychological distress, alleviate decisional conflict, and enhance overall quality of life. These findings support the adoption of a person-centered, relational model of care that recognizes the dyad as a unit of support and decision-making.</p>\",\"PeriodicalId\":20779,\"journal\":{\"name\":\"Psycho‐Oncology\",\"volume\":\"34 9\",\"pages\":\"e70277\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12398323/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Psycho‐Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1002/pon.70277\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Psycho‐Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/pon.70277","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
The Dyadic Experience of a New Breast Cancer Diagnosis Into the Shared Decision-Making Process: A Qualitative Analysis.
Objective: This study explores the dyadic experience of patients newly diagnosed with breast cancer and their caregivers, focusing on emotional responses, informational needs, and shared involvement in clinical decision-making.
Methods: Twenty-three patient-caregiver dyads participated in semi-structured interviews conducted by psychologists specializing in clinical and health psychology. The interviews were analyzed using Qualitative Thematic Analysis to identify core themes reflecting the dyadic experience.
Results: Findings highlighted the central role of the patient-caregiver relationship in coping with diagnosis and treatment planning. Both patients and caregivers valued sharing medical information, participating together in medical consultation and jointly engaging in treatment decisions, which fostered a sense of unity, reduced anxiety and improved understanding of treatment choice. Trust in healthcare providers, particularly their clarity, empathy, and expertise, emerged as a critical factor in alleviating patients' decisional regret and sustaining caregivers' confidence in supporting the patient. Although both patients and caregivers faced emotional challenges, their fears and concerns often differed, underscoring the need for individualized emotional support. Inclusion of caregivers in clinical discussions was considered essential for promoting a cohesive and supportive care experience.
Conclusions: The study underscores the emotional complexity and interdependence of the patient-caregiver dynamic following a breast cancer diagnosis. Being the patient-caregiver relationship central to cancer care, it is important to encourage coordinated involvement of both parties in the clinical process may reduce psychological distress, alleviate decisional conflict, and enhance overall quality of life. These findings support the adoption of a person-centered, relational model of care that recognizes the dyad as a unit of support and decision-making.
期刊介绍:
Psycho-Oncology is concerned with the psychological, social, behavioral, and ethical aspects of cancer. This subspeciality addresses the two major psychological dimensions of cancer: the psychological responses of patients to cancer at all stages of the disease, and that of their families and caretakers; and the psychological, behavioral and social factors that may influence the disease process. Psycho-oncology is an area of multi-disciplinary interest and has boundaries with the major specialities in oncology: the clinical disciplines (surgery, medicine, pediatrics, radiotherapy), epidemiology, immunology, endocrinology, biology, pathology, bioethics, palliative care, rehabilitation medicine, clinical trials research and decision making, as well as psychiatry and psychology.
This international journal is published twelve times a year and will consider contributions to research of clinical and theoretical interest. Topics covered are wide-ranging and relate to the psychosocial aspects of cancer and AIDS-related tumors, including: epidemiology, quality of life, palliative and supportive care, psychiatry, psychology, sociology, social work, nursing and educational issues.
Special reviews are offered from time to time. There is a section reviewing recently published books. A society news section is available for the dissemination of information relating to meetings, conferences and other society-related topics. Summary proceedings of important national and international symposia falling within the aims of the journal are presented.