Department of Social Sciences and Health Policy, Wake Forest School of Medicine & the Wake Forest Baptist Comprehensive Cancer Center, Medical Center Boulevard, Winston-Salem, NC, 27157, USA.
Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Support Care Cancer. 2021 Oct;29(10):5945-5955. doi: 10.1007/s00520-021-06158-0. Epub 2021 Mar 25.
Young adults (YAs, ages 18-39) diagnosed with cancer face multiple challenges that affect their health-related quality of life, including the potential for cancer-related infertility. Providing information about the risk of infertility and options to maintain fertility is critical for YAs who are newly diagnosed. However, barriers to effective communication exist for oncologists and their patients. The purpose of this study was to interview medical oncologists and YAs from the same cancer center to examine attitudes and practices about fertility preservation.
Semi-structured interviews were conducted with medical oncologists (N=12) and YAs within 2 years post-treatment (N=24), representing the most common cancers affecting YAs. Interviews were audio-recorded, transcribed, and coded using qualitative methodologies with the analysis software NVivo 10.
Twelve oncologists (50% female, 67% <50 years) and 24 YAs (67% female, M=29 years) completed interviews. Common themes across oncologist and YA interviews were the roles of cancer type or stage and patient interest or parity in influencing the decision. The most important factor for YAs was to receive accurate, in-depth information. Unique themes for oncologists focused on clinical aspects of their patient's disease. For YAs, they shared about the emotional impact of cancer-related infertility and desire for support from trusted others.
Results provide a better understanding of the attitudes and practices about fertility preservation discussions among YAs. Given the common factors affecting fertility preservation decisions, models of shared decision-making may be ideal for YAs and oncologists. Future interventions should explore tailored applications of this approach for YAs newly diagnosed with cancer.
被诊断患有癌症的年轻人(18-39 岁)面临着许多影响其健康相关生活质量的挑战,包括癌症相关不育的风险。为刚被诊断出患有癌症的年轻人提供有关不育风险和保持生育能力的选择信息至关重要。然而,肿瘤学家及其患者之间存在有效沟通的障碍。本研究的目的是采访来自同一癌症中心的肿瘤内科医生和年轻人,以检查他们对生育力保存的态度和实践。
对 12 名肿瘤内科医生(50%为女性,67%年龄<50 岁)和 24 名在治疗后 2 年内的年轻人(67%为女性,平均年龄 29 岁)进行了半结构化访谈,他们代表了最常见的影响年轻人的癌症类型。访谈使用 NVivo 10 分析软件以定性方法进行录音、转录和编码。
共有 12 名肿瘤内科医生(50%为女性,67%年龄<50 岁)和 24 名在治疗后 2 年内的年轻人(67%为女性,平均年龄 29 岁)完成了访谈。在肿瘤内科医生和年轻人的访谈中,常见的主题是癌症类型或阶段以及患者的兴趣或生育史在影响决策方面的作用。年轻人最重要的因素是获得准确、深入的信息。肿瘤内科医生的独特主题侧重于患者疾病的临床方面。对于年轻人来说,他们分享了癌症相关不育的情绪影响以及希望从信任的人那里获得支持的愿望。
结果提供了对年轻人中有关生育力保存讨论的态度和实践的更好理解。鉴于影响生育力保存决策的常见因素,共同决策模式可能是年轻人和肿瘤内科医生的理想选择。未来的干预措施应探索针对新诊断为癌症的年轻人的这种方法的定制应用。