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
Esther W. Nafula
Advance care planning (ACP) is a term that was first used in the literature in the early 1990s to describe interventions that involved discussions about healthcare between a patient, their family and health care professionals. It has been considered as a way of having on record specific treatment choices that represent an individual’s values and would be acceptable to the individual in the event of a serious illness or mental incapacitation (Seymour 2011). In the past the emphasis was on documentation of the individual’s wishes in an advance directive or living will. Current focus is on having discussions to understand the wishes of the patient for their healthcare. The discussion is between the patient, their family or significant others and a healthcare professional (Shimada et al 2016). The aim of this discussion is to either document the patient’s wishes in an advance directive or to have an oral statement of the wishes and have the patient appoint a proxy decision maker (Thomas 2011). Advance directives may include the patient’s preferences on resuscitation and life-sustaining therapies. ACP should be done by adults of sound mind who are able to make decisions about their healthcare before the diagnosis of a debilitating illness or mental incapacitation (Thomas 2011).