Abstract
Abstract
Background:
Patients with treatment-resistant advanced cancer rarely benefit from cardiopulmonary resuscitation (CPR) but infrequently discuss end-of-life care with physicians until hospitalized. Admitting resident physicians may conduct initial code status discussions, but may elicit patients' preferences without providing necessary guidance.
Objective:
We surveyed residents' approach to code status discussions to identify barriers hindering informed decision making.
Methods:
We developed an online case-based survey and enrolled subjects via e-mail requests to program directors. U.S. internal medicine residents (n=358; response rate 22.0%) from 19 programs participated. We measured respondents' likelihood of discussing prognosis and benefit of CPR, likelihood of offering code status recommendations, preference for discussing code status independent of attending physicians, and satisfaction with end-of-life discussions.
Results:
Nearly all residents felt CPR would be unhelpful. Yet fewer than half (46.7%) were likely to discuss an estimate of prognosis and the value of CPR with the patient. Only 30% were likely to offer a recommendation on CPR. A majority (69%) of residents who were unwilling to offer a recommendation stated that deference to patient autonomy prevented them from providing guidance. Residents preferred to discuss code status independent of attendings, primarily due to a sense of responsibility. Ultimately, only a minority was satisfied with end-of-life discussions.
Conclusion:
U.S. internal medicine resident physicians are unlikely to discuss prognosis or offer recommendations on CPR in treatment-refractory cancer principally because of a conflict with their concept of patient autonomy. Given the futility associated with CPR in this setting, these data define an unmet need in training and practice.
Introduction
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Despite recommendations, 9 a minority of outpatients with advanced cancer has a documented code status. 10 Therefore, the first code status discussion may occur upon hospitalization for complications. Limited data address whether resident physicians, frequently responsible for such discussions at teaching hospitals, advise seriously ill patients on end-of-life decision making.11,12 To address this question we surveyed U.S. internal medicine residents to assess willingness to share prognostic information and recommendations on code status, given a hypothetical patient hospitalized for complications of treatment-resistant advanced cancer.
Methods
The Tufts Medical Center institutional review board reviewed this project. All participants gave informed consent. We developed an online survey using Qualtrics (Provo, UT). Table 2 details the hypothetical case and survey questions. In Part 1 of the survey we asked respondents about their likelihood of sharing prognostic information and providing a recommendation on code status in the hypothetical case. Next we asked whether respondents felt that attendings should be primarily responsible for conducting code status discussions. In Part 2 we asked general questions about code status discussions, including frequency of conducting them and satisfaction with both one's own discussions and with attendings' discussions.
The target population was the approximately 25,000 internal medicine residents at all 387 U.S. programs accredited by the Accrediation Council for Graduate Medical Education (ACGME). 13 Using contact information obtained from ACGME and program websites, we e-mailed every program director with a request to participate by forwarding the online survey to their residents. We followed up with nonresponders and called programs with unlisted or nonfunctional addresses. We analyzed data with Stata statistical software version 12.1 (StataCorp; College Station, TX) and tested hypothesized correlations between variables. Because our dependent variables were ordered categorical variables and dichotomous variables, we used appropriate linear regression models, the ordered logit and logit models, respectively. 14
Results
Of the 387 programs we contacted, 22 program directors responded: 19 agreed to participate and 3 declined (see Fig. 1). The participating programs represented 1627 residents and varied widely in size (median size 96, mean 85.6, standard deviation 49) and geographic region. A total of 375 respondents began the survey and 358 completed it. We present all recorded responses, including 17 incomplete surveys. Based on completed surveys, the response rate was 22.0%. Table 1 displays demographic information.

Study enrollment.
Table 2 presents survey responses and distributions. Following the hypothetical case presentation, less than half (46.7%) of respondents reported they were likely or very likely to share prognostic information. Over two-thirds (69.6%) reported they were neither likely or very likely to offer a recommendation on code status.
We explored respondents' reasoning in follow-up questions, allowing for multiple answers and free-text answers. Of the 155 respondents who declined to recommend a code status, many (69%) thought the patient should make the decision without the resident's influence. One-quarter (26.5%) felt the attending might not want the resident to make a recommendation. Free-text answers included endorsements of patient autonomy:
“Code status is supposed to be a decision a patient makes for him/herself.”
Others were hesitant about giving advice without being asked or making a recommendation during an initial meeting:
“If asked I would offer my opinion but not unprompted.” “I may not have that rapport to make such a recommendation [during the first meeting] but would consider it if I already had a [prior] relationship.”
Importantly, very few (1.3%) felt that CPR offered a reasonable chance of resuscitation. Likewise, the 187 respondents who reported they would recommend a code status overwhelmingly recommended “do not resuscitate/do not intubate” (DNR/DNI).
A majority of respondents (66.8%) felt they should discuss code status themselves while a minority (20.6%) preferred to defer to an attending. The 75 respondents who preferred an attending discussion most commonly believed that the primary oncologist would have known the patient for longer and would be better able to estimate prognosis. Free-text answers included statements of support for the primary oncologist's preexisting relationship with the patient:
“The primary oncologist will know the patient and have a trusting relationship, which is the ideal setup for a difficult yet crucial conversation.”
Of the 243 respondents who preferred to discuss code status, the vast majority (93.4%) felt that this discussion was part of their responsibility as a physician, and a majority (65.8%) felt that they had enough training and knowledge to do so.
Overall, only 34.2% were satisfied or very satisfied with their discussions. But a very small minority (5.4%) was dissatisfied or very dissatisfied, while the dissatisfied proportion was significantly higher when it came to attendings' discussions (18.1%, p<0.01).
We tested for hypothesized correlations between responses, as shown in Table 3. Unsurprisingly, more-senior residents were more likely to share prognostic information and offer recommendations. Interestingly, those planning on pursuing hematology/oncology or palliative care training were more likely to share prognostic information, but were not more likely to provide recommendations. This is an important test of response bias, since these respondents are presumably above-average in interest in end-of-life discussions.
Discussion
By discussing end-of-life planning with patients with limited life expectancy, physicians uphold several bioethical principles: respect for patient autonomy through documentation of wishes, beneficence by decreasing end-of-life distress, and nonmaleficence in avoiding futile care. By focusing on documentation of wishes alone, residents may not fulfill the professional responsibility of physicians to guide their patients through difficult medical decisions. 15 Incomplete discussions can cause, at minimum, improper documentation of patients' wishes and, at most, psychological harm, damage to the physician-patient relationship, and the potential for unwanted and futile attempts at resuscitation. 16
In this survey, U.S. internal medicine residents knew the limitations of CPR in patients with advanced treatment-refractory cancer, yet were frequently reluctant to provide the information on prognosis and treatment outcome necessary to make informed decisions on code status. Less than one-third of respondents reported that they were likely to provide a recommendation on code status, largely attributable to an emphasis on the concept of patient autonomy. Nonetheless, residents did prefer to retain responsibility for code status discussions, primarily due to a sense of physician responsibility, as seen previously. 17 Whether justified or not, they did not feel underprepared to conduct such discussions, contrasting with prior reports. 18
Only one third of residents were substantially satisfied with the code status discussions that they or their attendings conduct in this common scenario. This discontent may result from tension between residents' strong sense of the futility of CPR in advanced cancer and their inability to communicate this opinion because of a priority given to patient autonomy instead of informed decision making. Residents' dissatisfaction may also communicate to medical students. 19 Given an anticipated rise in cancer incidence 20 and deaths 21 as well as the associated increase in end-of-life care costs, 22 end-of-life communication is of increasing importance, 23 and these findings suggest an unmet need in training and practice.
There are several strengths of this study. This is the first nationwide survey that illuminates residents' self-assessed attitudes, skills, and practice in treatment-refractory cancer, the major emerging cause of worldwide mortality. The survey sample included participants from across the United States and from programs of varying size, allowing good external validity. Although most of the program directors we contacted did not respond, the response rate among residents we did reach allowed for generalizability and was comparable to other resident surveys.19,24
Our study is limited by problems of self-report and response bias. Response bias is of particular concern with a low response rate, although our within-sample test of response bias was negative. Both self-report and response bias may cause us to overestimate the actual likelihood of providing prognostic information or recommendations. However, this bolsters our conclusion that residents provide insufficient guidance. Our findings also cannot be generalized to residents outside the United States, who may receive different training and experience different attitudes on end-of-life decision making.
Ideally, attending physicians should discuss advance planning early in the disease course, but in practice, residents are often the first to document code status while admitting patients who have developed complications. Previous authors have argued that prognostication and making recommendations should be taught as medical competencies but acknowledge that attendings often fail to model such skills. 25 Indeed, in a study of attending hospitalists discussing code status, none shared an estimate of the benefit of CPR or provided a recommendation about code status. 26 Furthermore, 41 of our respondents felt that attendings would discourage them from offering recommendations. Physicians, residents, and attendings alike should be expected to provide guidance on the utility of medical interventions, including CPR. If unsure of what to recommend, they should seek guidance from expert resources, which may in turn encourage oncologists to discuss end-of-life planning early.
Footnotes
Acknowledgments
We wish to thank the Tufts Medical Center residents who provided feedback on a pilot survey and Dr. Michael Fisch for comments on this manuscript.
Author Disclosure Statement
No competing financial interests exist.
