Physician preferences and knowledge regarding the care of childhood cancer survivors in Japan: A mailed survey of the Japanese Society of Pediatric Oncology.

Abstract

Objective: Japanese physicians' attitudes regarding the health-care needs of young adult childhood cancer survivors (CCSs) are not well described. Thus, we examined the self-reported preferences and knowledge of pediatric oncologists and surgeons. Methods: A mailed survey was sent to 858 physician members of the Japanese Society of Pediatric Oncology. We compared the responses of pediatric oncologists and pediatric surgeons. Results: The pediatric oncologists' response rate was 56% (300 out of 533) and that of pediatric surgeons 32% (105 out of 325). The median age of respondents was 46 and 48 years, respectively; 79 and 84% were men. When comfort levels in caring for CCSs were described (i.e. 1 ¼ very uncomfortable; 7 ¼ very comfortable), the mean levels were 4.4 and 3.8 with CCSs 21 years, 3.6 and 3.6 with 21 years , CCSs 30 years, and 2.8 and 3.3 with CCSs . 30 years, respectively. In clinical vignette questions, 62% of the pediatric oncologists and 43% of the surgeons answered three or more questions appropriately. Pediatric surgeons reported significantly lower familiarity with long-term follow-up guidelines than pediatric oncologists. Most pediatric oncologists and many surgeons conducted truth-telling of cancer diagnosis to adult CCSs now. They thought that the most important issues are an original long-term follow-up guideline suitable for the Japanese situation and collaborations with adult-based general physicians. Conclusions: Many Japanese pediatric oncologists are uncomfortable with caring for survivors as they age and have suboptimal knowledge regarding late effects. The change in truth-telling situation and preference for collaboration with adult-based physicians was demonstrated also in Japan.

Japanese childhood cancer survivors' readiness for care as adults: a cross-sectional survey using the Transition Scales

“…The first step is to define the concept of care transition for CCSs based on existing evidence. Many Japanese pediatric oncologists are uncomfortable with caring for survivors as they age and have suboptimal knowledge regarding late effects . The change in truth‐telling situation and preference for collaboration with physicians who treat adults was also demonstrated in Japan .…”

“…Many Japanese pediatric oncologists are uncomfortable with caring for survivors as they age and have suboptimal knowledge regarding late effects . The change in truth‐telling situation and preference for collaboration with physicians who treat adults was also demonstrated in Japan . We must overcome the same doctor barrier to allow conceptualization of the transition to adult care in Japan …”

Childhood cancer survivors: Anxieties felt after treatment and the need for continued support

“…In the present survey, some of the CCS who sought health care at departments or hospitals besides the pediatric department where they underwent childhood cancer treatment stated that it was hard to know who to talk to and that the physicians knew little about childhood cancer. In past surveys, childhood cancer specialists and pediatric surgeons considered the creation of original long‐term follow‐up guidelines, suited to Japan, for general practitioners who treat adult CCS, as the most important issue in the care of CCS . Cooperation with hospitals and general practitioners other than those involved in the CCS childhood cancer treatment is considered necessary, as is the introduction of specific health‐care sites for CCS and CCS parents.…”

“…In past surveys, childhood cancer specialists and pediatric surgeons considered the creation of original long-term follow-up guidelines, suited to Japan, for general practitioners who treat adult CCS, as the most important issue in the care of CCS. 16 Cooperation with hospitals and general practitioners other than those involved in the CCS childhood cancer treatment is considered necessary, as is the introduction of specific health-care sites for CCS and CCS parents.…”