Min Sun Kim
Seoul National University · Medicine
About the Lab
Professor Min Sun Kim's research lab focuses on pediatric palliative care, health services research, and health policy, with a strong emphasis on improving end-of-life care for children with life-threatening and complex chronic conditions in South Korea. The lab investigates population-level trends, healthcare utilization, unmet needs, and the implementation of advance care planning in pediatric populations. It also explores health disparities and access to care among vulnerable groups, such as refugee mothers, and examines the impact of policy changes on clinical practices.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15BACKGROUND: Pediatric palliative care (PPC) is the active total care of children suffering from life-threatening illnesses. Palliative care includes symptom management, psychosocial support, and end-of-life care. Despite significant advances in disease diagnosis and treatment, resources for PPC of children with serious illnesses are limited in Korea. This study aimed to investigate the scale, time trends, disease composition, regional distribution, and unmet needs of children dying from complex
To improve the dimensional properties of wool fabric, two kinds of silicone polymers are applied to plasma pretreated wool. With this treatment, hygral expansion increases slightly but still remains smaller than that of silicone treated wool without the plasma pretreatment. The wrinkle recovery angles of wool increase with the treatment, and the values of fabric treated with plasma and silicone polymers are higher than those with no plasma pretreatment. In addition, the harsher handle imparted b
Paediatric palliative care (PPC) is regarded as standard care for children and young people (CYP) with life-limiting conditions (LLCs). There is a lack of knowledge about the rate of CYP with LLCs, hampering the development of PPC. This retrospective study aimed to examine population-based statistics of South Korean CYP with LLCs and the pattern of healthcare use and costs in their last year of life, analysing the National Health Insurance Service claims database for the period 2013-2015. In 201
Background: Pediatric palliative care (PPC) is the active total care of children suffering from life-threatening illnesses. Palliative care includes symptom management, psychosocial support, and end-of-life care. Despite significant advances in disease diagnosis and treatment, resources for PPC of children with serious illnesses are limited in Korea. This study aimed to investigate the scale, time trends, disease composition, regional distribution, and unmet needs of children dying from complex
We identified barriers to maternal and child healthcare and coping strategies among African refugee mothers in Korea. Future research should assess refugees' health status and improve health access and literacy among refugee mothers.
BACKGROUND: The increase in the number of pediatric patients with complex health conditions necessitates the application of advance care planning for children. Earlier, withdrawal of life-sustaining treatment was taboo in the medical society in South Korea due to the history of such practice being punishable by law, and physicians tended to pursue aggressive treatment. With changes in public opinion on end-of-life care, the Korean government enacted a new law that protect human dignity by respec
BACKGROUND: The number of technology-dependent children (TDC) is increasing in South Korea, but available healthcare services after their discharge are poor. This study aimed to examine how TDC and caregivers live at home and identify their difficulties and needs regarding home care with few services to support them. METHODS: This cross-sectional study was conducted in a tertiary hospital for children in South Korea. A self-reported questionnaire was completed by primary caregivers of TDC who we
Our findings indicate that physicians and the general public in Korea differ in their perceptions about informing children of poor prognosis.
Background: Despite advances in medical technology, resources for pediatric palliative care (PPC) for children with serious illnesses are limited in South Korea. Physicians' awareness of and willingness to provide general palliative care and refer to specialized palliative care are key elements for providing PPC. Objective: The aim of this study was to explore physicians' perceptions of PPC and the differences therein between nononcologists and oncologists. Design: A nationwide survey was conduc
연구배경: 렙틴과 갑상선호르몬은 에너지대사 조절 측면에서 유사한 작용을 가진다. 렙틴이 시상하부-뇌하수체-갑상선 축을 활성화시킨다는 사실은 잘 알려져 있으나, 갑상선호르몬이 렙틴에 미치는 영향은 아직 명확히 밝혀져 있지 않다. 본 연구는 단기간의 갑상선 기능 변화에 따른 혈중 렙틴 농도의 변화를 연구하고자 수행되었다. 방법: 6~8주령의 수컷 Wistar 렛트에 갑상선제거술을 시행함으로써 갑상선기능저하증을 유발하였고, 수술 8일째 희생시켰다. 갑상선기능저항진증을 유발하기 위해서 Wistar 렛트에 L-T3(50g/100g body weight/day)을 5일간 피하로 주사하였다. 연구기간 동안 매일 체중과 먹이섭취량을 측정하였고, 연구종료 후 혈액을 채취하여 혈중 갑상선호르몬과 렙틴 농도를 측정하였다. 각 군은 사망 당시의 체중과 연구기간 동안 먹이섭취량을 일치시킨 대조군과 비교하였다. 결과: 갑상선기능항진군의 평균 먹이섭취량은 대조군인 자유식이군과 차이가 없었으나 사망당시 체중은
Background: It is difficult to decide whether to inform the child of the incurable illness. We investigated attitudes of the general population and physicians toward prognosis disclosure to children and associated factors in Korea. Methods: Physicians working in one of 13 university hospitals or the National Cancer Center and members of the general public responded to the questionnaire. The questionnaire consisted of the age appropriate for informing children about the prognosis and the reason w
관광에 대한 학문적 실무적 관심과 소비가 지속적으로 증가하고 있음에 따라 본 연구에서는 최근 약 6년간의 관광분야 주요 등재지에 실린 키워드 데이터를 이용하여 국내 관광연구 동향과 지식구조를 정리해보고자 하였다. 이를 위해 첫 번째, 관광분야의 대표적인 국내 저널들을 선정하고 저널에 게재된 논문 별 키워드를 추출하였다. 두 번째, 동일한 논문에 동시 등장한 키워드들을 링크로 연결하여 키워드 네트워크를 구성하였다. 마지막으로, 여러 논문에서 동시에 키워드로 사용된 키워드들 간의 유사성 분석을 통해 관광 논문들에서 가장 자주 사용된 주요 키워드를 추출하고 전체 네트워크에 대한 컴포넌트 분석을 통해 거시적인 관광연구동향 및 지식구조를 파악하였다. 분석 결과, 국내 관광연구 주제들은 몇몇 주제에 고착되어 있지 않고 빠르고 다양하게 변화하는 양상을 보인다고 할 수 있다. 물론 조직이나 종사원 차원의 주제와 같이 지속적으로 선호되는 연구주제들도 있지만 시간이 지남에 따라 연구대상의 내재적, 외
BACKGROUND: Despite the rising trend of tracheostomies in children, there is a lack of comprehensive resources for families to navigate the challenges of living with a tracheostomy, emphasising the need for evidence-based support in understanding postoperative care and long-term adjustments. This study aimed to examine the pattern of using healthcare services and nationwide medical outcomes in children who underwent a tracheotomy before the age of 2 years. METHODS: This retrospective study used
Research Areas
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