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The physician–patient relationship in treatment decision making at the end of life: A pilot study of cancer patients in a Southeast Asian society

Published online by Cambridge University Press:  18 July 2012

Zheng Jie Marc Ho*
Affiliation:
Singapore General Hospital, National Cancer Centre, Singapore Department of Palliative Medicine, National Cancer Centre, Singapore
Lalit Kumar Radha Krishna
Affiliation:
Department of Palliative Medicine, National Cancer Centre, Singapore
Cynthia Goh
Affiliation:
Department of Palliative Medicine, National Cancer Centre, Singapore
Chung Pheng Alethea Yee
Affiliation:
Department of Palliative Medicine, National Cancer Centre, Singapore
*
Address correspondence and reprint requests to: Zheng Jie Marc Ho, Department of Palliative Medicine, National Cancer Centre, 11 Hospital Drive, Singapore 169610. E-mail:[email protected]

Abstract

Background:

The traditional relationship between patient and physician in East Asian society has often been described as “paternalistic.” However, in an increasingly Westernized world, our knowledge of how patients perceive the role of the physician in their decision making regarding treatment is lacking.

Objective:

This article is part of a larger pilot study exploring the patient–physician dynamic on decision making among Southeast Asian palliative cancer patients. We explore: (1) influence of physicians, (2) the effect of symptom control and quality of life, and (3) dynamics and communication of physicians.

Design:

An interviewer-administered questionnaire was distributed, with 18 questions related to physician–patient interactions asked. Most questions followed a three point scale: “agree,” “neutral,” and “disagree,” and spontaneous answers beyond this framework were recorded.

Setting/Participants:

Thirty patients from the palliative care service were interviewed, including inpatients at Singapore General Hospital and those attending outpatient clinics at the National Cancer Centre.

Results:

Patients said that they themselves and their physicians were the main influences (80% each), over family members (48.3%). Some patients (26.7%) felt that symptoms were not well controlled, and 42.9% identified low mood or anxiety. Some patients (44.8%) felt that their condition had an effect on decision making. Most patients (89.3%) had a good relationship with the staff, with >80% being comfortable with discussions held. However, 20.7% of patients felt dissatisfied with the information provided, and 62.1% of patients wanted full disclosure of information.

Significance of results:

Patients appeared to place highest regard in both autonomy and physician input in making decisions, accompanied by an increased desire for more information. These reflect deviation away from traditional thinking of paternalistic doctoring in East Asia.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2012

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