Improving Care for Children with Advanced Cancer

改善晚期癌症儿童的护理

• 批准号: 6631458
• 负责人: Joanne Wolfe
• 金额: $ 13.57万
• 依托单位: DANA-FARBER CANCER INST
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-08-01 至 2007-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6631458
• 关键词: adolescence (12-20); behavioral /social science research tag; cancer pain; clinical research; communication; data collection methodology /evaluation; decision making; human subject; longitudinal human study; middle childhood (6-11); neoplasm /cancer palliative treatment; online computer; parent offspring interaction; patient care management; patient oriented research; pediatric neoplasm /cancer; perception; personal computers; physicians; preschool child (1-5); prognosis; psychological aspect of cancer; quality of life; questionnaires; sign /symptom; terminal patient care; adolescence (12-20); behavioral /social science research tag; cancer pain; clinical research; communication; data collection methodology /evaluation; decision making; human subject; longitudinal human study; middle childhood (6-11); neoplasm /cancer palliative treatment; online computer; parent offspring interaction; patient care management; patient oriented research; pediatric neoplasm /cancer; perception; personal computers; physicians; preschool child (1-5); prognosis; psychological aspect of cancer; quality of life; questionnaires; sign /symptom; terminal patient care

DESCRIPTION (provided by applicant): One quarter of children with cancer do not survive and they experience substantial suffering in the last month of life. For example, over fifty percent of children suffer from pain and dyspnea, symptoms known to be amenable to effective palliation. Retrospective studies have suggested that parent and physician communication during this period is poor, with parents lagging behind physicians by over three months in their understanding that the child has no realistic chance of being cured. Yet, earlier recognition of a child's terminal prognosis by both the physician and parents is associated with better integration of palliative care. Using a prospective cohort design we will perform a pilot project in 117 children with advanced cancer to ascertain parent and physician perceptions about the child's prognosis and treatment goals over time (using a paper and pencil survey instrument). In addition, we will use Pediatric Quality of Life Evaluation of Symptoms Technology (PediQUEST), a hand-held, computer-based system to routinely evaluate quality of life and symptoms experienced by children with advanced cancer. In the intervention phase of this project we will introduce immediate feedback of PediQUEST results to providers. In addition, electronic mail messages will be automatically generated if a patient's symptoms surpass a predetermined threshold. We will preliminarily assess the impact of this system on the natural history of symptoms and suffering, satisfaction, and the timing and quality of end-of-life discussions in order to generate data for sample size calculations for a future randomized controlled clinical trial. Mentored research activities during the award period will be complimented by a career development plan including coursework, seminars, teaching, committee work and clinical responsibilities which will ensure that the candidate makes a successful transition into an independent investigator and becomes a leader in pediatric oncology and palliative care.

描述（由申请人提供）：四分之一的癌症儿童无法生存，他们在生命的最后一个月遭受了巨大的痛苦。 例如，超过百分之五十的儿童患有疼痛和呼吸困难，已知症状可受到有效抑制。 回顾性研究表明，在此期间，父母和医师的沟通很差，父母在三个月的时间内落后于医生，因为他们了解孩子没有被治愈的机会。 然而，医生和父母对孩子的最终预后的早期认识与更好地整合姑息治疗有关。 使用前瞻性队列设计，我们将对117名患有晚期癌症儿童进行试点项目，以确定父母和医生对孩子的预后和治疗目标的看法（使用纸和铅笔调查工具）。 此外，我们将使用儿科生活质量评估症状技术（Pediquest），这是一种手持计算机，基于计算机的系统，以常规评估患有晚期癌症儿童经历的生活质量和症状。 在该项目的干预阶段，我们将向提供者介绍Pediquest结果的即时反馈。 此外，如果患者的症状超过预定的阈值，将自动生成电子邮件。 我们将初步评估该系统对症状，痛苦，满意度以及寿命终止讨论的时间和质量的影响，以生成数据计算数据，以进行样本量计算，以进行未来的随机对照临床试验。 奖励期间的指导研究活动将得到一项职业发展计划，包括课程，研讨会，教学，委员会工作和临床责任，这将确保候选人成功过渡到独立的研究者，并成为儿科肿瘤学和姑息治疗的领导者。