当社グループは 3,000 以上の世界的なカンファレンスシリーズ 米国、ヨーロッパ、世界中で毎年イベントが開催されます。 1,000 のより科学的な学会からの支援を受けたアジア および 700 以上の オープン アクセスを発行ジャーナルには 50,000 人以上の著名人が掲載されており、科学者が編集委員として名高い
。オープンアクセスジャーナルはより多くの読者と引用を獲得
700 ジャーナル と 15,000,000 人の読者 各ジャーナルは 25,000 人以上の読者を獲得
Richard R Love and Sheikh I Ahamed
The majority of global deaths are characterized by misery and limited palliation and occur in low- and middleincome countries (LMICs). Strategies for addressing the growing challenges of end-of-life palliative care, particularly those concerned with physical aspects of care, have been defined based on high-income country models of health care services and research. In LMICs, access to adequate quality primary care practitioners and oncologists is limited, and calls for training these specialists and palliative care physician specialists, even if heeded, cannot be expected to meet the growing palliative care population needs.
An applicable general framework for addressing this patient-centred abyss however, is now apparent, grounded in emerging favourable data about three components: new kinds of health paraprofessionals; information technology (IT) tools; and innovative health system approaches.
Routinizing palliative care can allow development of paraprofessional palliative care specialists. IT tools of importance include cell phone-based symptom questionnaires; internet facilitated virtual caregiver-patient visits and sharing of personal patient and family educational materials, and automated decision-making algorithms for symptom management. Health system approaches with these foregoing operational efficiencies and improved productivity can allow more and higher-quality care for more patients in need.
New local approaches are needed to address the right questions about public health palliative care.