Abstract
Abstract
Background:
Palliative care unit (PCU) beds are a limited resource in Canada, so PCU admission is restricted to patients with a short prognosis. Anecdotally, PCUs further restrict admission of patients with noncancer diagnoses out of fear that they will “oversurvive” and reduce bed availability. This raises concerns that noncancer patients have unequal access to PCU resources.
Purpose/Methods:
To clarify survival duration of patients with a noncancer diagnosis, we conducted a retrospective review of all admissions to four PCUs in Toronto, Canada, over a 1-year period. We measured associations between demographic data, prognosis, Palliative Performance Score (PPS), length of stay (LOS), and waiting time.
Results:
We collected data for 1000 patients, of whom 21% had noncancer diagnoses. Noncancer patients were older, with shorter prognoses and lower PPS scores on admission. Noncancer patients had shorter LOS (14 versus 24, p<0.001) than cancer patients and a similar likelihood of being discharged alive to cancer patients. Noncancer patients had a trend to lower LOS across a broad range of demographic, diagnostic, prognostic, and PPS categories. Multivariable analysis showed that LOS was not associated with the diagnosis of cancer (p=0.36).
Discussion/Conclusion:
Noncancer patients have a shorter LOS than cancer patients and a similar likelihood of being discharged alive from a PCU than cancer patients, and the diagnosis of cancer did not correlate with survival in our study population. Our findings demonstrate that noncancer patients are not “oversurviving,” and that referring physicians and PCUs should not reject or restrict noncancer referrals out of concern that these patients are having a detrimental impact on PCU bed availability.
Introduction
In Ontario, Canada, inpatient PCUs generally restrict admission to patients with an anticipated prognosis of less than 3 months. This restriction is understandable but sometimes problematic, as physicians are notoriously inaccurate when it comes to prognostication,2–4 and noncancer diagnoses in particular often defy prognosis.2,5,6 Anecdotally, concerns about noncancer patients “oversurviving” their prognosis has led to a practice of restricting admissions for such patients until very late in the disease course. This raises concerns that patients with noncancer diagnoses may have unequal access to palliative care resources. 7
In the present study, we conducted a retrospective review of admissions to multiple PCUs in Toronto, Canada, over a 1-year period to determine whether noncancer patients are “oversurviving” their prognosis.
Methods
Study design and setting
We conducted a retrospective chart review of all patients admitted to four inpatient PCUs in Toronto, Canada, from April 1, 2009 to March 31, 2010. The four PCUs were located in various settings: Toronto Grace Hospital is a nonacute care hospital specializing in chronic disease management, Toronto East General Hospital is a community academic hospital with a regional PCU on site, Sunnybrook Health Sciences Centre is a tertiary academic hospital with a regional PCU located on its campus, and St. Michael's Hospital is a tertiary academic hospital with a regional PCU in the main hospital building.
Most provincially funded PCUs in Ontario (including the four in our study) limit admission to patients with an anticipated prognosis of less than 3 months. Patient prognosis is determined by the referring physician, either based on the Palliative Performance Score (PPS) or by subjective judgment. Occasionally, PCUs will contact the referring physician to clarify prognosis or care needs before deciding whether or not to admit a patient.
Patients
We included all patients admitted to one of the four participating PCUs during the study period. There were no exclusion criteria. This study was approved by the Research Ethics Board of all participating facilities.
Data collection and analysis
In Toronto, all PCUs require referring physicians to complete a specially designed Palliative Care Common Referral Form (CRF) for prospective admissions. The PCU staff then reviews the CRF and decides whether or not the patient is appropriate for admission, or whether more information is needed. The PCU staff may also need to triage admissions based on urgency if there is a waiting list for admission.
For the present study, we collected admission and discharge/death dates, referral dates, demographic data, admitting diagnosis, PPS, estimated prognosis, comorbidities, source of admission and disposition following discharge from the CRF, the medical record, or from local administrative databases (where available) at each PCU. If more than one CRF was sent, we used the latest one. We excluded the source of referral for 158 patients at one facility because the data could not be interpreted.
Prognostic information is provided in the CRF at the time of referral by the referring physician. Physicians are asked to select one of several categories: <1 month, <3 months, <6 months, <1 year, or indeterminate.
We compared demographic data, length of stay (LOS), prognosis, and PPS between cancer and noncancer patients using Welch's t test. We measured correlations between LOS and patient characteristics using Pearson's test. To perform multivariable regression analyses, we grouped PPS scores into low (10–20), medium (30–40) and high (50+). 8 We constructed a multivariable regression model for LOS that included age and gender, as well as all factors that correlated with LOS on bivariate analysis with a p<0.05 (the PPS and prognostic categories as well as a cancer diagnosis). We also constructed a multivariable regression model for waiting time that included all factors associated with waiting time on bivariate analysis with a p<0.05 (age; gender; prognosis <90 days, <180 days, and <365 days; PPS 30–40; PPS 50+; cancer; and the location of the patient at the time of referral [e.g., inpatient ward versus home, emergency department, or other medical facility]). All statistical tests were performed using SPSS version 15.0 (SPSS Inc., Chicago, IL).
Results
In total, we collected data for 1000 patients at four sites. Demographic data are presented in Table 1. Compared with cancer patients, noncancer patients were older, with a lower PPS and a nonsignificant trend toward a shorter prognosis. Noncancer patients were also less likely to survive until discharge or be discharged home from a PCU, although the difference was nonsignificant. Only 2% of noncancer patients were admitted to a PCU for more than 3 months, compared with 5% of cancer patients (p=0.1; data not shown).
p<0.0001 for comparison between cancer and noncancer patients.
The mean LOS for noncancer and cancer patients is shown in Table 2, and displayed by subgroup according to various characteristics. Overall, noncancer patients had a significantly shorter LOS than cancer patients (14 versus 24 days, p<0.001). A nonsignificant trend to shorter LOS among noncancer patients was evident across all age groups 40 years and older, in both genders, from every admission source, and across all four participating sites (data not shown). Noncancer patients had a significantly shorter LOS than cancer patients with a prognosis <3 months; there was a nonsignificant trend toward shorter LOS among noncancer patients across all PPS scores (Table 3). The mean LOS for cancer and noncancer patients discharged alive was 40 and 53 days, respectively.
p<0.001 for comparison between cancer and noncancer patients.
p<0.005 for comparison between male and female.
p<0.02 for comparison between male and femal
LOS, length of stay.
Table 4 shows the LOS, prognosis, and PPS for patients by disease group. Aside from heart failure, the mean LOS for every noncancer diagnosis was shorter than the mean LOS for every cancer diagnosis (all nonsignificant). Mean PPS scores were lowest for brain injury and stroke; other noncancer diagnoses had broadly similar mean PPS scores. All cancer diagnoses had higher mean PPS scores than all noncancer diagnoses, and cancer PPS scores were broadly similar to one another.
p<0.01 for camparison between cancer and noncancer patients.
PPS, Palliative Performance Score.
Table 5 shows the mean and median waiting time (defined as the time between the date of initial referral to PCU and the date of admission to that PCU). The mean waiting time for noncancer patients was significantly shorter than that of cancer patients.
p<0.0001 for comparison between noncancer and cancer.
SD, standard deviation.
Paired prognosis and PPS scores were not available for all patients. For patients for whom both data were recorded, we used Spearman's test to look for a correlation between LOS, prognosis, and PPS. LOS was weakly correlated with prognosis in both the noncancer and cancer populations (n=158 and n=448; R=0.24 and 0.26, respectively), and with the PPS score for cancer patients (n=318; R=0.24). LOS was more strongly correlated with PPS score in the noncancer population (n=106; R=0.37).
Multivariable regression revealed that LOS correlated with a prognosis of <6 months (p<0.02) and a PPS of 30 to 40 (p<0.02) and 50+(p<0.01), but not the diagnosis of cancer (p=0.36). Waiting time was correlated with gender (p<0.01), a prognosis of <1 year (p<0.01), and the location of the patient (p<0.01) but not with the diagnosis of cancer (p=0.75) on multivariable analysis.
In a post hoc analysis, we looked for differences in waiting time according to the location of the patient at the time of referral. Patients referred from another medical facility waited an average of 4.66 (SE 1.01) days longer than patients referred from an inpatient ward in the same facility (p<0.01). Even in the multivariable model, patients referred from other medical facilities waited 4.6 (standard error [SE] 1.3) days longer than those on an inpatient ward. Furthermore, adding the referral source to the multivariable model eliminated the significant relationship between PPS score and waiting time, as well as the relationship between a prognosis of <6 months and waiting time; the relationship between prognosis of <1 year and waiting time remained significant.
Discussion
In our study, we found that patients admitted to PCU with noncancer diagnoses were older, with lower PPS scores and shorter prognoses. Surprisingly, we also found that the LOS for noncancer patients was shorter than for cancer patients, even within the same demographic, prognostic, and PPS categories, and that noncancer patients were equally likely to be discharged alive from a PCU. Multivariable analysis further demonstrated that a noncancer diagnosis was not associated with either LOS or waiting time.
Similar to other studies, we found that clinician estimates of prognosis generally overestimate survival.2–4 We also found a correlation between PPS and survival.5,9–12 It was not surprising, therefore, to find that noncancer patients had both a lower PPS and a lower survival. However, we did not expect to find a lower survival even when comparing patients with similar prognoses and PPS scores, or that the diagnosis of cancer was not correlated with survival on multivariable analysis. Christakis and Lamont found that noncancer patients referred for hospice care were more likely to outlive their prognosis than cancer patients, 2 whereas Lau and colleagues found that noncancer patients had a lower hazard ratio for mortality than cancer patients once they adjusted for PPS and other significant covariates. 5 Fox and coworkers found that a majority of noncancer patients meeting hospice criteria survived beyond the expected 6-month prognosis. 6 On the other hand, one recent study has found that cancer and noncancer patients referred to a palliative care service were equally likely to defy their prognosis, 13 although this latter study used specialist palliative care physicians to assess prognosis.
The reason for the inconsistency between our findings and previous studies is unclear. The difference would not be explained by PCUs giving higher priority for admission to cancer patients (thus lengthening their stay in the PCU as opposed to their previous location), because noncancer patients actually had a shorter waiting time between referral and admission. If a selection bias was responsible for our results, it would have to be further upstream, either by physicians failing to refer noncancer patients for PCU admission until very late in their illness, or by PCU directors preferentially rejecting many of them. We cannot exclude the possibility that end-stage cancer and noncancer patients have similar prognoses (all other factors being equal), but we cannot confirm this conclusion using data from such a selected population.
Anecdotally, many PCU directors in Ontario are reluctant to accept noncancer patients because they fear that the latter will stabilize and survive beyond their PCU's 3-month “limit.” Such patients may be difficult to transfer because they are often unwilling to be placed in a long-term care facility and too ill to discharge home. As a result, these patients occupy a “short-term” PCU bed for longer than anticipated, denying it to other patients. Our study should reassure such directors and referring physicians, because it shows that noncancer patients have a shorter LOS and are less frequently discharged alive than cancer patients. Directors should also be reassured by the multivariable analysis and the finding that patients who are discharged alive generally leave long before the 3-month “limit,” suggesting that the impact of noncancer patients in general and oversurvival in particular on bed utilization is small. However, our population was highly selected and included a relatively small subset of noncancer patients with a PPS score >30. If PCUs start admitting a larger number of noncancer patients with a PPS of 30+, then their effect on LOS may rise.
Our study showed that the PPS was a better correlate of survival than the clinician's estimated prognosis. This is not surprising, 14 particularly given previous studies of the accuracy of PPS for predicting survival4,5,15 and the fact that the documented prognosis may be strongly influenced by nonclinical, pragmatic considerations (e.g., PCU admission criteria).16,17 However, we did not expect to find that PPS was more strongly correlated with survival in noncancer patients than cancer patients. This has been noted previously, 10 and may be due to the fact that noncancer patients had lower PPS scores overall; lower scores are more closely associated with survival than higher scores.4,5,15 Our findings further support the idea that PPS is a more rational means than prognosis for determining PCU eligibility.
Of course, there are more accurate prognostic tools available for clinicians, including the Palliative Prognostic Score and the Palliative Prognostic Index.18,19 These tools may be particularly accurate when combined with other clinical information. 20 However, even the most precise prognosis would have a limited role in determining when a patient needs admission to a PCU. This decision is complicated, 21 and would ideally be based on symptom and support needs rather than life expectancy alone. PCU directors must therefore find a balance between maximizing bed availability and meeting the needs of the palliative patient population.
We found that patients referred from other medical facilities waited almost 5 days longer than patients from an inpatient ward in the same facility to be admitted to a PCU, and that this difference remained even in a multivariable model. Ideally, PCUs should not prioritize admissions on the basis of location, even though many hospitals face pressure to improve patient “flow” and reduce length of admission on their acute wards. All stakeholders must recognize that this is unfair to dying patients. Many previous authors have suggested that patients face inequitable access to palliative care resources based on age, location, socioeconomic status, gender, ethnicity, education, and diagnosis.7,22–24
The limitations of our study include the fact that the study population was selected both by the referring physician and the accepting PCU, which limits our ability to make broad conclusions about the effects of diagnosis, PPS, and prognosis on survival. We do not have data for dying patients who were rejected by the PCUs, or who were never referred for PCU admission. In addition, the prognostic and PPS data were provided by the referring physician, who was often not a specialist palliative care physician. The data were generally not independently verified prior to admission, so we cannot confirm the accuracy of the information. However, this is often the case when patients are referred to PCUs, so this “limitation” may actually improve the generalizability of our findings. In Canada, we have universal health insurance that covers almost all PCU-related costs for Canadians. Therefore, we could not determine the relationship between health insurance status and LOS and waiting times.
Conclusion
We found that noncancer patients had a shorter LOS and a similar likelihood of being discharged alive to cancer patients, and that a cancer diagnosis was not associated with LOS on multivariable analysis. Referring physicians and PCUs should not reject or restrict end-stage noncancer referrals out of concern that these patients are “oversurviving” and having a detrimental impact on PCU bed utilization.
Footnotes
Acknowledgments
The authors thank Anna Marie Danielson for her help with statistical analysis of the data, as well as Dr. Lawrence Librach, Karina Wulf, Catherine Lacombe, and Ron Lirette for their assistance with this study.
Author Disclosure Statement
No competing financial interests exist.
