Dialogue Volume 11 Issue 3 2015 | Page 35

End-of-life care Helping patients live as well as possible until the end Communications is cornerstone of approved policy photo: istockphoto.com W hen Dr. Carol Leet lost her father after a protracted illness in 2014, she had just become the chair of a working group struck with the responsibility of reviewing and revising a College policy providing guidance and direction to physicians on the issues of end-of-life care. Her own personal experience confirmed that an emphasis on communication needed to ground the policy. “When my father suffered a sudden severe health problem, it was an intense and stressful experience for my family. Fortunately, he had made his wishes clear in advance, which helped us make some very difficult decisions as substitute decision-makers,” said Dr. Leet, who is also the College’s President. “Throughout this experience, we benefited from open and honest communication with physicians on his medical team. Empathy and a full discussion of his options were what helped us make the best decisions, while dealing with our grief,” she said. End-of-life care situations are highly charged and can be difficult for all those involved. That is why communication is of paramount importance. The Planning for and Providing Quality End-of-Life Care policy, which was just approved by Council, makes it clear that physicians must communicate effectively and compassionately with patients and/or substitute decision-makers, in a manner and tone that is suitable to the decisions they may be facing. This includes initiating communication as early as possible and as regularly and as often as is necessary to share information, helping patients and/or substitute decision-makers understand the information shared, and answering questions. When a physician communicates effectively and frequently with a patient or the patient’s substitute decision-maker, it helps build trust and confidence in the relationship. And that, said Dr. Leet, will go a long way to making future difficult conversations easier. The policy also recognizes the contributions of family members or others close to the patient and/or substitute decision-maker, and the role they can play in helping to manage a patient’s ongoing care. Issue 3, 2015 Dialogue 35