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Cancer Research and Treatment > Volume 51(4); 2019 > Article
An, Jeon, Chun, Jung, Ahn, Lee, Kim, Kim, Cheon, Kim, and Koh: Feasibility Study of Physician Orders for Life-Sustaining Treatment for Patients with Terminal Cancer

Abstract

Purpose

Physician Orders for Life-Sustaining Treatment (POLST) form is a legal document for terminally ill patients to make medical decisions with physicians near the end-of-life. A multicenter prospective study was conducted to evaluate the feasibility of POLST administration in actual oncological practice.

Materials and Methods

Patients with terminal cancer, age ≥ 20 years, and capable of communicating were eligible. The primary endpoint was the completion rate of POLST. Data about physicians’ or patients’ barriers were also collected.

Results

From June to December 2017, 336 patients from seven hospitals were eligible. Median patient age was 66 years (range, 20 to 94 years); 52.7% were male; and 60.4% had poor performance status. Primary cancer sites were hepato-pancreato-biliary (26.2%), lung (23.2%), and gastrointestinal (19.9%). Expected survival duration was 10.6±7.3 weeks, with 41.2% receiving hospice care, 37.9% showing progression after cancer treatment, and the remaining patients were under active treatment (15.8%) or initially diagnosed with terminal cancer (5.1%). POLST forms were introduced to 60.1% of patients, and 31.3% signed the form. Physicians’ barriers were reluctance of family (49.7%), lack of rapport (44.8%), patients’ denial of prognosis (34.3%), lack of time (22.7%), guilty feelings (21.5%), and uncertainty about either prognosis (21.0%) or the right time to discuss POLST (16.6%). The patients’ barriers were the lack of knowledge/understanding of POLST (65.1%), emotional discomfort (63.5%), difficulty in decision-making (66.7%), or denial of prognosis (14.3%).

Conclusion

One-third of patients completed POLST forms, and various barriers were identified. To overcome such barriers, social engagement, education, and systematic support might be necessary.

Introduction

In 2009, the Supreme Court of South Korea imposed the withdrawal of a mechanical ventilator used for a female patient, who had been in vegetative status, based on her presumed preferences for end-of-life (EOL) care [1]. This historic judgment aroused public interest regarding discontinuation of futile life-sustaining treatment (LST). An intensive discussion ensued to reach a social consensus for patient autonomy regarding the right to make decisions about EOL treatments. The resulting Life-Sustaining Treatment Decision-Making Act came into full effect in February 2018 [2]. To protect the autonomy and dignity of terminally ill patients, patients can discuss the Physician Orders for Life-Sustaining Treatment (POLST) form with their physicians to decide whether they want to apply or suspend life-prolonging treatment near death. The POLST form is a medical document that mainly pertains to a patient’s future care, including EOL care preferences in case they lose the capacity to make decisions. Decision-making primarily addresses preferences for LST. An advance directive (AD) is a legal document written by anyone regardless of his/her illness, and it includes a future medical care plan, living will, or designation of power of attorney [3]. Both POLST and AD are included in advance care planning (ACP). The ultimate goal of these documents is to respect patient’s autonomy, to facilitate shared goals of care by participating in the decision-making process, including EOL care, and improve patients’ quality of life [4].
In Korea, attitudes toward discussion of EOL care or AD may become more favorable according to previous surveys conducted among patients with cancer, their families, oncologists, and the general public [5,6]. Community-dwelling elderly individuals have positive attitudes toward AD, and most participants completed the Korean-AD model [6]. However, concerns remain regarding the application of an AD or POLST process in actual clinical practice. First, patients are often excluded from the loop of communication of bad news and the decision-making process, which has predominantly occurred between physicians and family members. Furthermore, EOL discussions are delayed until the very EOL when patients rapidly deteriorate and even unaware of their impending death [7-9]. For those reasons, EOL discussion mostly involves family members, and few patients complete an AD or POLST by themselves in hospital-based studies [9,10]. In addition, lack of knowledge, emotional discomfort of talking about death, or systematic complexity of the process could be other potential barriers.
In this study, we aimed to evaluate the feasibility of discussing POLST in actual oncologic practice. Physicians’ and patients’ barriers were also explored, which could be informative in finding systematic solutions that facilitate the process of POLST documentation.

Materials and Methods

1. Participants

We designed a prospective, multicenter study that included medical oncologists from seven general hospitals. Eligibility criteria were patients aged ≥ 20 years with terminal cancer. Terminal cancer is defined as follows: life expectancy of less than several months due to cancer progression despite anticancer treatment or irreversible deterioration of performance status or organ function due to cancer progression [11]. Patients were excluded if they could not sufficiently communicate due to severe illness or cognitive impairment.

2. Data collection and procedures

First, the physician in charge tried to introduce the concept of the POLST form to eligible patients. If the form was not formally introduced for any reasons, the questionnaire about physicians’ barriers was completed by the physician. Patients who were informed about the form but declined further discussion were asked to complete a questionnaire about patients’ barriers. Patients who agreed to discuss the POLST form received detailed explanations and completed the form with the physicians. If the patient declined to complete the form after discussion with the physician, they were also asked to complete the patients’ barrier questionnaire.
The POLST form included the following themes: information about the current status of the disease and treatment options; decision-making for the use of LST; decisions concerning hospice care; and information on processes for completion, registration, storage, modification, and withdrawal of the form. LST issues included the use of cardiopulmonary resuscitation (CPR), artificial ventilation, hemodialysis, and anticancer treatment at the EOL. The POLST form was completed if the patient signed the form with confirmation from the physician.
The above procedure was repeated if any significant changes occurred in patients’ conditions or personal circumstances. Demographic data, including age, sex, Eastern Cooperative Oncology Group (ECOG) performance status, diagnosis, status of care, follow-up status, and life expectancy were collected.

3. Statistical analysis

The primary endpoint was completion rate of the POLST form defined by the number of patients completed the form divided by the total number of eligible patients. Secondary endpoints were identifying barriers of discussing the POLST. The number of patients was calculated based on the assumption that five patients with terminal cancer are expected to visit each hospital monthly, which estimated that approximately 300 patients would be eligible from the date of institutional review board (IRB) approval until the end of 2017.
Clinical characteristics were presented as counts (percentage) for categorical variables and as median values (range) or mean±standard deviation for continuous variables. Descriptive analysis was used to assess barriers for POLST use.

4. Ethical statement

This study was approved by the Institutional Review Board of Ulsan University Hospital with a waiver of informed consent (UUH IRB No. 2017-05-003) and performed in accordance with the principles of the Declaration of Helsinki.

Results

1. Patient characteristics

From June to December 2017, 336 patients were eligible. The clinical characteristics of the patients are summarized in Table 1. Median age was 66 years (range, 20 to 94 years), 177 (52.7%) were male, and 203 (60.4%) displayed ECOG 3 or 4 performance status. The primary cancer site was hepato-pancreato-biliary (26.2%), followed by lung (23.2%), gastrointestinal (19.9%), and breast (10.1%). The others included brain tumor, leukemia, malignancy with unknown primary, soft tissue sarcoma, neuroendocrine tumor, multiple myeloma, skin cancer, and thyroid cancer. At the time of enrollment, 138 patients (41.2%) were in hospice care, and 127 (37.9%) showed disease progression after anticancer treatment. Remaining patients were still under active treatment (15.8%) or were initially diagnosed as terminal cancer (5.1%). More than half of patients were recently transferred from other departments (27.3%) or hospitals (30.8%), with a median follow-up duration of 90 days (range, 1 to 4,046 days). The mean life expectancy of patients, as estimated by their physicians-in-charge, was 10.6±7.3 weeks.

2. Process of POLST

POLST forms were introduced to 202 patients (60.1%), of which 105 (52.0%) signed the form (Fig. 1). Among all eligible patients (n=336), the completion rate of the POLST form was 31.3%. For the 202 patients who started to discuss the POLST, the number of discussions was one (84.7%), two (13.3%), and three (2.0%). The median time required for discussions was 35 minutes (range, 5 to 120 minutes). Most patients who completed the POLST refused LST at EOL: CPR (98.1%), artificial ventilation (99.1%), hemodialysis (98.1%), and anticancer treatment (91.4%). Seventy-four patients (89.2%) agreed to hospice care. There was no difference of POLST completion rate between hospice patients (n=43, 31.2%) and non-hospice patients (n=62, 31.3%, p=0.976).

3. Physicians’ barrier for introducing the POLST

Of the 134 patients that were not introduced to the POLST by the physicians, the questionnaires about the physicians’ barriers were completed for 109 cases. Table 2 shows barriers to introduction of POLST from the physicians’ perspectives. The major barrier was reluctance or conflict within family members (49.7%). Family members were unwilling for patients to engage in EOL discussion or conflicts among family members existed for engaging in such discussions. The second most common barrier was the lack of rapport with patients for discussing sensitive issues, such as EOL care and death (44.8%). Physicians also expressed guilty feelings, such as depriving patients of hope or giving up on patients’ care (21.5%). Patients’ denial or avoidance of their prognosis (34.3%), lack of sufficient time in discussing the POLST (22.7%), uncertainty of cancer prognostication (21.0%), or right time for having such a discussion (16.6%) were also identified as common barriers.

4. Patient’s barrier in completing the POLST

Of the 97 patients who declined to complete the POLST, 63 completed the questionnaire about the patients’ barrier (Table 3). The most frequently reported patient’s barrier was decisional difficulty (66.7%), lack of knowledge/understanding (65.1%) of the POLST, and emotional discomfort (63.5%). Lack of knowledge or understanding of the POLST was the main barrier: 21 patients (41.3%) reported difficulty in understanding the terms or process of the POLST or LST; 21 (41.3%) patients had difficulty in understanding the POLST paradigm. Emotional discomfort was also a common barrier for 40 patients (63.5%). Specifically, 19 patients (29.7%) reported concerns that signing the document considered as giving-up of treatment or being abandoned by their physicians; 28 (43.8%) reported fear of bad things happening after the POLST documentation; 19 (29.7%) felt anxious when talking about death. Forty-two patients (66.7%) did not want to make EOL decision by themselves but want their families or doctors to make the decision for them (44.4% and 34.9%, respectively). Nine patients (14.3%) stated that their disease was not severe enough to discuss the form (not yet, not at this point, or not sick enough). None of the patients answered that they did not trust their physicians.

Discussion

In this study, we assessed the feasibility of the POLST documentation for patients with terminal cancer in actual oncologic practice. Approximately one-third of patients completed the POLST form, and various barriers were identified from both physicians’ and patients’ perspectives.
Numerous studies have assessed the use of ACP or AD, but POLST use has been less commonly studied. Particularly, reports about the preferences for LST including ‘do not resuscitate’ were found in few studies that examined ACP or AD [12-14], and even fewer were documented by physicians [12,15]. To date, the POLST form is widely accepted in some states in the United States, where completion rate for the POLST form is much higher than that reported in current and previous studies [16,17]. In line with the growing interest in patient’s autonomy in Korea, recent studies have shown that patients are becoming more involved in EOL discussions (35.5%-55.6%) [18,19]. However, most studies have been retrospective or cross-sectional studies without intervention, or they included too limited or broad populations.
To the best of our knowledge, this study is the first prospective, multicenter study that assesses the feasibility of completing the POLST form for patients with terminal cancer in Korea. The strength of our study is that a wide range of patients with terminal cancer was included: patients with various cancer types; treatment status ranging from patients recently diagnosed with cancer to patients receiving hospice cares; and follow-up status from new patients to patients with long-term follow-up. Seven hospitals from various regions participated, and a consistent process for POLST administration was followed. Considering that our study reflected the real oncologic situation in encountering patients with terminal cancer, a completion rate of 31.3% suggests that the POLST process may be applicable to patients with terminal cancer.
A variety of barriers of discussing the POLST form emerged from the perspectives of both physicians and patients in this study. The POLST was not even introduced in 39.9% of patients. From the physician’s perspectives, reluctance of family members was the most common barrier to introduce the form. This reluctance was more frequent in this study than in previous studies conducted in Western countries [20-22]. Family-centered culture in Eastern countries including Korea, in which family makes important decisions about a patient’s care, could be possible reason [8]. Consistent with previous reports [20,22,23], emotional discomfort for discussing the POLST was also a common barrier for physicians. In the Korean society where talking about death or dying is considered taboo, physicians have difficulty in delivering bad news or having POLST discussions directly with their patients. The belief that patients are not willing to participate in EOL discussion, fear of destroying patients’ hope, fear of losing their patients, or lack of longstanding relationships with the patients were primary emotional barriers. Patient’s denial of their disease prognosis, uncertainty about prognostication, or right time for POLST discussion was also important barriers [13,20,23]. Despite the fact that the prognosis of cancer is relatively predictable compared with other non-cancerous disease [23] and that hematooncology specialists participated in the study, it is still challenging to determine the exact prognosis and right time discussing the POLST.
From the patients’ perspectives, lack of knowledge or poor understanding of the POLST was the major barrier for its completion, consistent with previous studies [13,19,20,24]. Patients had difficulty in understanding the POLST, such as concept, the process, and advantages and disadvantages. Emotional discomfort for discussing the POLST was also an important barrier, which was also consistent with previous reports [19,21,23]. Patients showed fear of being abandoned by their physicians and fear of losing hope or experiencing unfavorable events if they sign the POLST form. In addition, some patients preferred letting their family or doctors make decisions for their future medical care. These barriers might reflect emotional discomfort related to EOL discussions or lack of capacity to make decisions for EOL medical care. In Eastern countries, people favor making EOL decisions with their family members [25].
Systematic barriers, including lack of infrastructure (time, space, trained human resources, or systemic support), were also important in previous studies [20,21,26,27]. Our study also revealed lack of time as a barrier. The median time required for the POLST discussion was 35 minutes, which is significantly longer than the average outpatient consultation time of 5 minutes in Korea [28].
These barriers are interrelated and should not be interpreted in isolation. Means of overcoming barriers might be also interconnected. First, public engagement in an open discussion about death or dying should become more natural in Korean society to relieve the emotional barrier. Evidence shows that patients expect their physicians to initiate an honest and open conversation about their disease and prognosis [7,21,25]. Simply being asked to discuss AD or POLST facilitates such a process [12,15]. In fact, half of the patients in this study completed the POLST document after being asked. Unfortunately, health-care providers, including physicians, are not adequately trained for delivery of bad news and EOL communication. Therefore, education regarding communication skills among health-care providers who engage in EOL discussion is extremely important [29]. Professional training may ease emotional and technical difficulties associated with EOL discussions.
Further, patients want to know what ensues after completing the POLST form. Detailed explanations about palliative care to relieve suffering might be helpful in decreasing emotional barriers of patients [21]. Since lack of knowledge was the main barrier, public awareness or educational campaigns using decision support tools are needed to increase knowledge in the general public about EOL discussions [30].
Third, designation of surrogates who can make EOL decisions for patients could enhance the completion rate of the POLST document. Designation of surrogates is a major component of ACP, AD, and POLST, and surrogates participate in POLST documentation in other countries, though not in Korea. Our study shows that major barriers included reluctance of family members, physicians, and patients to directly discuss this sensitive issue with patients. In addition, some terminal cancer patients could not initiate the POLST discussion because of physical or mental insufficiency. Although patients’ autonomy is an important aspect of the POLST form, designation of surrogates can indirectly reflect the best interests of patients.
The limited time of physicians is also a challenging barrier. Systemic support, such as simplifying the process, involving trained non-physician facilitators, and being compensated for health-care costs, might help overcome this barrier [27].
This study had limitations. First, some selection bias existed for overestimating results. Hemato-oncology specialists who might be more familiar and experienced with EOL discussions participated in this study. Few large tertiary hospitals focusing on active anticancer treatment participated. In addition, we included patients who were capable of communicating, which excluded the majority of patients with terminal cancer because of poor performance status and inability to communicate. A considerable number of patients had already chosen hospice care. Although the completion rate of POLST was not different between hospice and non-hospice patients in our study, caution should be taken when generalizing our results. Second, some physicians and patients did not complete the questionnaire, and the barriers from the family members’ perspectives were not investigated. Third, we focused on the completion of the POLST but not evaluated the qualities or outcomes of the documents.
In conclusions, one-third of patients with terminal cancer completed the POLST, and a wide range of barriers from physicians, families, patients, and systematic aspects were identified. These were interconnected, and there are rooms for the improvement of the POLST discussion. Further studies need to be conducted to investigate the quality or outcomes of the POLST decision in the future.

Notes

Conflict of interest relevant to this article was not reported.

Acknowledgments

The research was supported by the Korean Cancer Study Group (KCSG PC17-01).

Fig. 1.
Patients’ diagram. POLST, Physician’s Order for Life-sustaining Treatment.
crt-2019-009f1.jpg
Table 1.
Baseline characteristics of the eligible patients
Characteristic No. of patients (n=336)
Age, median (range, yr) 66 (20-94)
Sex
 Male 177 (52.7)
 Female 159 (47.3)
ECOG
 1/2 133 (39.6)
 3/4 203 (60.4)
Diagnosis
 Hepato-pancreato-biliary cancer 88 (26.2)
 Lung cancer 78 (23.2)
 Gastrointestinal cancer 67 (19.9)
 Breast cancer 34 (10.1)
 Genitourinary tract cancer 26 (7.7)
 Head and neck cancer 19 (5.7)
 Others 24 (7.1)
Treatment status
 Initially diagnosed with terminal cancer 17 (5.1)
 Under anticancer treatment 53 (15.8)
 After disease progression 127 (37.8)
 Hospice care 138 (41.1)
Follow-up status
 During follow-up 140 (41.9)
 Transferred from other departments 91 (27.3)
 Transferred from other hospitals 103 (30.8)
Life expectancy (wk) 10.6±7.3

ECOG, Eastern Cooperative Oncology Group.

Table 2.
Physicians’ barriers
Type of barrier No. (%) (n=181)
Families’ reluctance and/or conflict 90 (49.7)
Lack of rapport with patients 81 (44.8)
Patients’ denial or avoidance of the prognosis 62 (34.3)
Lack of time for discussing the POLST 41 (22.7)
Fear of depriving patients’ hope or of abandonment 39 (21.5)
Uncertainty of cancer prognostication 38 (21.0)
Uncertainty of the right time for POLST discussion 30 (16.6)

POLST, Physician’s Order for Life-sustaining Treatment.

Table 3.
Patients’ barriers
Type of barrier No. (%) (n=63)
Lack of knowledge/Understanding 41 (65.1)
 Lack of knowledge about POLST 26 (41.3)
 Lack of understanding of the POLST paradigm 26 (41.3)
Emotional discomfort 40 (63.5)
 Fear of giving-up or being abandoned by their physicians 19 (30.2)
 Fear of bad things happening after a POLST documentation 28 (44.4)
 Discomfort in talking about death 19 (30.2)
Refusal or difficulty in decision-making 42 (66.7)
 Trust for family as a surrogate decision-maker 28 (44.4)
 Trust for a physician as a surrogate decision-maker 22 (34.9)
Denial of prognosis 9 (14.3)

POLST, Physician’s Order for Life-sustaining Treatment.

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