Article Text
PDF
Abstract
Parkinson’s disease and related disorders (PDRD) are the second most common neurodegenerative disease and a leading cause of death. However, patients with PDRD receive less end-of-life palliative care (hospice) than other illnesses, including other neurologic illnesses. Identification of predictors of PDRD mortality may aid in increasing appropriate and timely referrals. To systematically review the literature for causes of death and predictors of mortality in PDRD to provide guidance regarding hospice/end-of-life palliative care referrals. We searched MEDLINE, PubMed, EMBASE and CINAHL databases (1970–2020) of original quantitative research using patient-level, provider-level or caregiver-level data from medical records, administrative data or survey responses associated with mortality, prognosis or cause of death in PDRD. Findings were reviewed by an International Working Group on PD and Palliative Care supported by the Parkinson’s Foundation. Of 1183 research articles, 42 studies met our inclusion criteria. We found four main domains of factors associated with mortality in PDRD: (1) demographic and clinical markers (age, sex, body mass index and comorbid illnesses), (2) motor dysfunction and global disability, (3) falls and infections and (4) non-motor symptoms. We provide suggestions for consideration of timing of hospice/end-of-life palliative care referrals. Several clinical features of advancing disease may be useful in triggering end-of-life palliative/hospice referral. Prognostic studies focused on identifying when people with PDRD are nearing their final months of life are limited. There is further need for research in this area as well as policies that support need-based palliative care for the duration of PDRD.
- Parkinson's disease
- Lewy body dementia
- multisystem atrophy
- supranuclear palsy
- corticobasal degeneration
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Statistics from Altmetric.com
Introduction
Parkinson’s disease (PD) is the second most common neurodegenerative disorder, affecting more than 1% of adults over the age of 65 years and approximately 10 million people worldwide.1 With increasing access to specialist care coupled with improved diagnostic tools, a growing ageing population and prolonged survival due to better treatment options, the prevalence of PD is increasing and is expected to double by 2030.2 The burden of PD and related disorders (PDRD), such as progressive supranuclear palsy (PSP), dementia with Lewy bodies, corticobasal degeneration and multiple system atrophy (MSA), is substantial and includes physical disability,3–8 dementia,5 7 9–11 mood disorders,12 13 psychosis,14 increased mortality15–17 and financial hardship.15 Hospital admissions, duration of hospital stay and in-hospital mortality are higher among individuals with PDRD compared with patients with other life-limiting conditions.16 18–20
The benefits of palliative care at end of life (hospice) and earlier in the disease course include improved quality of life, reduced healthcare expenditures and caregiver support.21 22 Benefits of earlier palliative care also have been demonstrated by a recent randomised controlled trial, in which patients receiving additional palliative care had better quality of life, symptom control, were more likely to have advanced care plans and better supported caregivers.23 Yet despite repeated calls for improved access,15 24 patients with PDRD spend less time in and are less likely to be referred to end-of-life palliative care/hospice compared with other advanced diseases. Several studies suggest end-of-life palliative care/hospice is underused in PDRD, but estimates of use vary considerably, ranging from 0% (in a UK community sample)25 to 69% (in US nursing homes).16 20 25–27 A multinational review of death certificate data from 2008 revealed that 0% of people with PDRD in New Zealand and 4% in the USA died in hospice.20
In the USA, hospice care is defined as palliative care for persons with a 6-month life expectancy. Other nations differ in their definitions and criteria for receiving palliative care or hospice, with some based on prognosis and others on need. The Medicare hospice benefit in the USA is available to patients certified by two physicians to have a prognosis of 6 months or less and choose to focus medical care on comfort rather than life-extending treatments.28 Although PDRD is among the leading causes of death, there are no specific end-of-life palliative care/hospice eligibility guidelines for PDRD. Current guidelines potentially relevant to patients with PDRDs include those for dementia, amyotrophic lateral sclerosis (ALS; sometimes listed under the heading of generic neurologic disease) and adult failure to thrive (see table 1).29 30 The predictive value of these guidelines in PDRD has not been evaluated but are likely to be limited given: (a) a focus on clinical scenarios unlikely to be relevant in PDRD (eg, respiratory dysfunction); (b) lack of focus on clinical features of advanced PDRD and some common causes of death in this population (eg, falls) and (c) these guidelines are not sensitive even in the populations for which they were designed.31 Moreover, the lack of PDRD-specific guidelines may contribute to the impression that PDRD is not a cause of death or that death in PDRD is not predictable. In the UK, the National Institute for Health and Care Excellence (NICE) guidelines for PD do include recommendations relating to palliative care services based on clinical need rather than estimated prognosis.32 However, referrals to UK specialist palliative care services remain predominantly those with cancer, especially for in-patient services where only 10% had neurological disease (2014–2015), although referrals for those with non-malignant disease, especially cardiorespiratory disease, is increasing.
Current Medicare hospice guidelines for neurologic disorders with potential relevance to Parkinson’s disease and related disorders29 30
Identification of events, symptoms and other characteristics of PDRD predicting mortality may aid in triggering timely and appropriate referral to end-of-life palliative care/hospice.21 33 While some mortality-associated factors in this population are known, there is little differentiation between general predictors of overall ‘poor prognosis’ versus specific predictors to suggest that an individual is in the last few weeks or months of life. Further, there has been no examination of whether a focus on predicting poor survival is fit for purpose with regard to increasing access to timely hospice referral.
This manuscript arose from a Parkinson’s Foundation sponsored working group on PDRD and palliative care which identified improved hospice prediction as a high priority area.34 As a first step, we performed a thorough review of predictors of mortality and causes of death in PDRD to assess whether this approach would be of use in developing PDRD-specific guidance to inform timing of end-of-life palliative care/hospice referrals.
Methods
Search strategy
We used the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) checklist to inform our search strategy and reporting of outcomes.35 We conducted a database search using MEDLINE, PubMed, EMBASE and CINAHL in February 2020 and included publications from January 1970 up until that time. We also searched Google Scholar and the bibliographies of retrieved articles. Search terms combined Parkinson’s disease, parkinsonism, progressive supranuclear palsy, dementia with Lewy bodies, corticobasal degeneration and multiple system atrophy with the following terms: Hospice; Palliative; Predictors; Prognosis; Mortality; place of death and cause of death.
Inclusion criteria
We included studies quantifying predictors of mortality and cause of death in patients with PDRD that met the following criteria: original research with quantitative data using patient-level, provider-level or caregiver-level data from medical records, administrative data or survey responses and original research that predicted mortality or cause of death in patients with PDRD.
Data abstraction and risk assessment
Any two of three investigators (UA, JB and RBM) independently screened titles, abstracts and retrieved full papers with eligibility criteria. Differences were resolved by review of the third investigator.
We assessed risk of bias by reviewing study design characteristics, including appropriate temporal relationships between exposures and outcomes, matching populations through individual variables or propensity scores and other adjustment methods. However, given we did not develop a meta-analysis from the findings, we did not exclude reporting any studies that met our inclusion criteria.
Outcomes
The primary outcomes were overall quantitative predictors of mortality and predictors of mortality 6 months prior to death in patients with PDRD. Unadjusted and adjusted measures of association between PDRD predictors and mortality included mean differences with SD, relative risks (RRs), OR and HRs. Cause of death was quantified as percentage of patients by cause of death and standardised mortality ratios (SMRs).
Results
Figure 1 and the online e-supplemental delineate the selection process.
Supplemental material
Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram.
Study designs and descriptions of included studies
The 42 studies were published until February 2020. The study designs were: retrospective cohort studies,3 4 6 7 10 14 16 17 21 36–41 prospective cohort and longitudinal studies,5 8 9 11 13 42–49 case–control studies50–54 and cross-sectional studies.12 55–60 Predictors of mortality included demographic and clinical markers, medical events, medication changes, disease-specific symptoms and patient and caregiver’s ratings of health-related quality of life. Eight studies described both predictors of mortality and causes of death.37 38 43–46 53 61
Demographic and general health measures
Baseline demographic and general health predictors of mortality included age at onset or diagnosis, chronological age, male sex, body mass index (BMI) and comorbid illness. For every year increase in age at onset, there was an associated increase in a range of HRs from a minimum 1.05 (95% CI: 1.01 to 1.10) to a maximum 1.11 (95% CI: 1.09 to 1.12), with age ranging from 61 to 77 years of age at baseline for those who died.3 5 9 11 37 42 45 46 52 Multiple analyses estimated the impact of 10-year increases in age at onset on mortality, with increased HRs of 1.4 (p value=0.023) to 2.8 (95% CI: 2.4 to 3.3).39 47 48 61 62 Advanced chronological age or age at onset was estimated using a variety of methods, but in general found that patients with PDRD faced higher risk of death above 78–85 years of age at onset.6 10 43 Male sex was associated with statistically significant increased HRs of 1.36 (95% CI: 1.02 to 1.81) up to 2.9 (95% CI: 1.5 to 5.4) compared with females3 9 11 17 37 39 46 47 62; RR increase of mortality of 1.7 (95% CI: 1.6 to 1.9)10 and fivefold higher odds of death (OR: 5.2; 95% CI: 1.2 to 22.9).13 In a retrospective repeated measures analysis, Goy et al found rapidly declining BMI was significantly associated with progression to death among patients with PDRD.21 A decrease in BMI was seen, from mean of 26 (95% CI: 25.1 to 26.1) at 30–36 months to 24.6 (95% CI: 24.1 to 25.1) at 6–12 months prior to death. Further, an absolute BMI<18 was a predictor of mortality.20
Comorbid illnesses associated with death included congestive heart failure, diabetes mellitus, pressure ulcers and cardiovascular disease. In a retrospective cohort study of 15 237 PDRD nursing home residents over 65 years of age, Fernandez and Lapane found significant decrease in time to death (rate ratios) of 1.49 (95% CI: 1.35 to 1.65), 1.22 (95% CI: 1.11 to 1.35) and 1.24 (1.13–1.37) from comorbid congestive heart failure, diabetes mellitus and pressure ulcers, respectively. Although it was not shown to be a predictor of death, cardiovascular disease was cited as a primary or secondary cause of death among patients with PDRD in multiple studies.37 38 44–46 58 61 Two 20-year follow-up studies of patients with PDRD in Europe found the majority of deaths were caused by cardiovascular disease (30% and 42%).37 44 Other studies found cardiovascular disease was a common cause of death among patients with PDRD, ranging from 12% to 21% of all deaths among patients with PDRD.38 40 45 58 61
Motor symptoms and global disability
Motor symptoms, as measured using the Unified Parkinson’s Disease Rating Scale (UPDRS), Hoehn and Yahr Scale (H&Y) and the Progressive Supranuclear Palsy Rating Scale (PSPRS), were significant predictors of mortality in patients with PDRD.63 64 Beyer et al found higher mean UPDRS scores, 65 (SD: 24) versus 42 (SD: 23), suggesting that greater motor impairment predicted death.43 Studies with median follow-up times ranging from 4 to 8 years estimated the association of 10-unit increases in baseline motor UPDRS Score on mortality and found statistically significant increased HRs for mortality of 1.17 (95% CI: 1.01 to 1.36) up to 1.4 (95% CI: 1.3 to 1.5) for each 10-unit increase in UPDRS Score.39 41 62 Baseline H&Y staging was significantly higher among those who died (mean 3.5 (SD 1)) compared with those who survived (2.5 (0.9)).43 Posada et al went further by splitting H&Y into early and later progression stages at baseline as a predictor for mortality and found that HRs increased by stage, from 1.5 (95% CI: 1.1 to 2.2) for H&Y stages 1 and 2 to 2.3 (95% CI: 1.5 to 3.6) for H&Y stages 3–5, both compared with patients with no PD and after controlling for comorbidities and demographic characteristics.53 Oosterveld et al stratified UPDRS total motor scores by greater than or equal to 30 compared with less than 30 (mean score for cohort 24.4) and found an HR of 1.63 (95% CI: 1.13 to 2.35).11 Chiu et al compared the association of PSPRS scores on mortality and found47 increased HRs of 1.96 (95% CI: 1.07 to 3.58) for 35–48 on the PSPRS, 2.99 (95% CI: 1.65 to 5.43) for 48–62 and 8.55 (95% CI: 4.5 to 16.3) for greater than 62 when compared with scores of 0–34.
Higginson et al conducted a 1-year longitudinal study analysing changes in symptoms in 82 patients with PDRD including MSA and PSP. All patients at study entry were stages 3–5 H&Y with over 60% of patients having a severe disability (indicated by H&Y) and 30% being wheelchair bound or bedridden. Compared with PD, patients with PSP and MSA had more disability and were more likely to die in 1 year (6% vs 47%). Baseline mean (range) Palliative Outcomes Scale scores for PD were 13.7 (14.5–5.7), 11.9 (10.0–6.1) for patients with PSP and 14.3 (16.0–4.5) for patients with MSA.13
Motor disability and functional impairment were significantly associated with increased risk of mortality. Compared with mild impairment, a more severe score on Activities of Daily Living (ADL) Scale was associated with an increased mortality RR of 1.8 (95% CI: 1.5 to 2.1).10 Symmetry of motor signs at baseline was associated with an increased HR of 2.0 (95% CI: 1.1 to 3.7).5 Presence of akinesia plus rigidity at onset was associated with an increased HR of 2.2 (95% CI: 1.06 to 4.88).44
We found only one study examining shift in prescribing of dopaminergic medication as an association with mortality. Goy et al found a shift in prescribing occurred during the last 6–12 months of life, with the proportion of patients with ≤2 dopaminergic medications increasing from 0.5 in 18–24 months to 0.6 in 6–12 months prior to death.21
Falls and infections
In two studies, location of bone fractures from falls were associated with increased mortality with PDRD after controlling for comorbidities and other demographic and clinical factors: upper limb fracture OR: 1.7 (95% CI: 1.4 to 2.2); lower limb fracture OR: 1.2 (95% CI: 1.1 to 1.3) and hip fracture OR: 1.13 (95% CI: 1.03 to 1.24).4 Kempster et al found frequent falls antemortem were present in 35% of PDRD decedents, with falls preceding death by 4.1 years on average. Frequency and timing of falls preceding death varied by age at death, but majority of falls occurred in older patients (>70 years) and were reported 3.2–5.2 years before death.59
Two studies found the same increase in hazards for one point increase in postural instability gait disorder (PIGD) scores using different scales: the Short Parkinson’s Evaluation Scale/Scales for Outcomes in Parkinson’s disease (SPES/SCOPA) (HR: 1.3; 95% CI: 1.1 to 1.5)9 and the Tinetti balance and gait assessment65 (HR: 1.3; 95% CI: 1.1 to 1.5).3 Four other studies did not specify diagnostic tools for PIGD but found a range of HRs from a minimum 1.48 (95% CI: 1.01 to 2.18)37 to a maximum 2.1 (95% CI: 1.2 to 3.7)42 compared with no PIGD.5 37 42 46
Pneumonia is a common cause of death among patients with PDRD and occurs at a higher frequency than in patients without PDRD.38 43 45 46 51 61 A study of 237 patients with PDRD with a mean of 32.5-year follow-up found pneumonia had a higher SMR (3.5; 95% CI: 1.4 to 7.3) than cerebrovascular disease (1.8; 95% CI: 1.2 to 2.7) and cardiovascular disease (1.6; 95% CI: 1.2 to 2.0).46 Other studies found an 11%–23% likelihood of death from pneumonia among patients with PDRD compared with 8%–9% in control patients.40 43 51 Lethbridge et al found that patients with PDRD were 1.83 (95% CI: 1.58 to 2.08) times more likely to have pneumonia at the time of death, compared with controls.56 Fernandez and Lapane found the mortality rate ratio of 1.58 (95% CI: 0.97 to 2.56) from aspiration pneumonia was highest among all other comorbidities among a sample of PDRD nursing home residents.
Non-motor symptoms
The most frequent significant non-motor disability predictors of mortality were dementia and psychotic symptoms. Dementia was largely diagnosed using the Diagnostic and Statistical Manual of Mental Disorders versions 4 and earlier.66 Dementia was associated with increased HRs ranging from 1.7 (95% CI: 1.7 to 1.8) up to 5 (95% CI: 2.1 to 3.7).16 42 52 53 62 Dementia was listed as the most58 or second-most common59 clinical feature at death for postmortem patients with PDRD, with symptoms preceding death by 3.3 years on average.59 Lethbridge et al found that patients with PDRD were 2.5 (95% CI: 2.2 to 2.9) times more likely on average to have dementia when dying with PDRD compared with age–sex-matched controls without PDRD.56 In a study analysing contributing causes of death among patients with PDRD in Italy and France, SMRs for dementia were 49 per 1 000 000 people in both countries, compared with death from pneumonia (34 in Italy and 39 in France).55 A long-term follow-up study found the percentage of surviving patients with dementia increased dramatically from 24% at baseline to over 80% at 20-year follow-up.67 Multiple studies using various scales have reported HR of 2.7–3 with severe cognitive impairment.5 9 68 Garcia-Ptacek et al found that compared with Mini-Mental Status Exam scores above 25, there were increased HRs for scores between 20–24, 10–19 and 0–9 of 1.45 (95% CI: 1.32 to 1.58), 2.14 (95% CI: 1.96 to 2.34) and 2.91 (95% CI: 2.47 to 3.44), respectively.17 Another study found severe cognitive impairment, defined using the Cognitive Performance Scale, increased risk of mortality compared with mild cognitive impairment of 1.5 (95% CI 1.4 to 1.7).10
Two studies defined hallucinations using the UPDRS I question 2 with a score≥2 and found increased HRs of 1.45 (95% CI: 1.02 to 2.07)62 and 2.1 (95% CI: 1.3 to 3.2)5 compared with no hallucinations. The SCOPA-Psychiatric Complications69 was used as an assessment tool for hallucinations in one study (ie, presence of hallucinations, illusions, paranoid ideation or altered dream phenomena over the past month) and found an increased HR of 2.6 (95% CI: 1.1 to 5.9).9 Psychotic symptoms in PD have been shown to increase the risk of nursing home placement (RR 3.4, CI 2.9 to 3.9) and death (1.3, CI 1.2 to 1.5)14 and were found to be the most frequent clinical feature at death (61%), preceding death by 5.1 years on average.59
Studies differ about the prognostic value of inspiratory stridor in patients with MSA. An international consensus conference was convened in Bologna in 2017 to discuss definition, diagnosis, prognosis and treatment of stridor.70 The experts concluded that the effect of stridor on survival is uncertain, but early stridor presenting within 3 years of diagnosis of MSA may shorten survival, and that daytime stridor (during wakefulness) portends a worse prognosis than purely nocturnal stridor. Continuous positive airway pressure can improve stridor but its effect on survival is uncertain. Tracheostomy can improve stridor and may improve survival as well.70
Other non-motor complications significantly predictive of mortality included dysphagia, cognitive impairment without a formal dementia diagnosis, sleep disorders, autonomic symptoms and neurologic bladder disturbances. Dysphagia, defined as a score of >1 on UPDRS II question 3, was associated with an increased HR of 1.4 (95% CI: 1.08 to 1.86).5 In a study by dell'Aquila et al, early signs of dysphagia and cognitive decline (<3 years from onset) among patients with PSP were associated with increased HRs of 2.3 (95% CI: 1 to 5.3) and 3.6 (95% CI: 1.6 to 8.2), respectively.48 Sleep disorders were associated with a RR increase of 1.3 (95% CI: 1.2 to 1.6)10 and an increased HR of 2.7 (95% CI: 1.1 to 6.7) associated with rapid eye movement sleep behaviour disorder54 Finally, two studies found associations between urinary incontinence and mortality (statistics not reported)38 and incomplete bladder emptying (HR 2.10 (95% CI 1.02 to 4.30)).8 Early development of stridor in MSA, especially while awake, portends decreased survival.70 71
Discussion
Patients with PDRD suffer from severe disease burden in advanced disease and may be less likely to be referred for hospice and/or palliative care services than other similarly burdensome disorders. Important findings from this systemic review include: (1) mortality is heightened in PDRD and complications of PDRD contribute to death; (2) general markers of health decline may predict mortality in PDRD; (3) disease-specific markers of advanced disease may predict mortality in PDRD and (4) predictors of death are linked to common causes of excess mortality in PDRD (eg, dysphagia and aspiration pneumonia). We found four main domains of mortality predictors or causes of death for PDRD (table 2).
Summary of predictors of mortality for Parkinson’s and related disorders
Demographic and general health measures: Older age at disease onset, male sex, rapidly decreasing BMI and higher number—and especially cardiovascular—comorbidities are associated with higher mortality. Medication changes can occur at any stage of the disease, but decreasing medication when control of motor symptoms is outweighed by the disability caused by the cumulative burden of disease has been associated with death within 6–12 months.
Motor dysfunction and global disability: More severe motor symptoms and worse performance on ADL scales is associated with global disability and mortality. Motor signs presenting symmetrically, presence of akinesia/rigidity and the PIGD subtype were all associated with increased mortality.
Falls and infections: Bone fractures and their locations are associated with increased mortality, but may precede death by months to years. Aspiration pneumonia is a common occurrence in advanced disease, and recurrent pneumonia portends poor short-term prognosis (months).
Non-motor symptoms: Cognitive dysfunction, specifically dementia and psychotic symptoms are the most common non-motor features present prior to death in PDRD. Other reported non-motor features associated with mortality include dysphagia, sleep disorders, autonomic symptoms, stridor and neurologic bladder disturbances.
Potential barriers to hospice and palliative care referral
Although palliative and end-of-life care for PDRD is attracting increased attention, there remain many barriers to improving care including clinician discomfort, poor integration and coordination of palliative care within neurology, misperception of the potential for death from PDRD and patient misperception of palliative and hospice care.72 Notably, caregivers of PDRD decedents indicated that physicians rarely discussed end-of-life expectations and that the caregiver usually initiated such discussions.60 The unpredictability of the disease trajectory, especially at end of life, and how to address this uncertainty with patients may hinder these discussion. In addition, patients with PDRD may have clinical plateaus at very low levels of function which may lead to inappropriate discharges from palliative care or hospice, particularly in medical systems where end-of-life palliative care services are tied to prognosis and disease progression. Where the system operates as mutually exclusive, admission to hospice care, due to the waxing-waning course the patient may be discharged from hospice ‘comfort’ care to seek ‘curative’ care, a practice that is driven by three main factors: physician perception, patient/family preference and stability/improvement of medical condition.73 A study of national live discharges from hospice74 found that one in four discharged patients were hospitalised within the following 30 days, 75% were admitted within 1 day of discharge and 34% of them died within 30 days of hospice discharge.74 Other system issues, such as restrictions on care for persons receiving hospice, such as exclusion of physical therapy services that may still be beneficial to patients with PDRD with advanced illness, may lead to inappropriate underutilisation of these services and could contribute to misperceptions that all palliative care is incompatible with disease-targeted treatments. In addition, in healthcare systems such as in the UK, many hospice services are charity, rather than state, funded and arose out of oncology palliative care and some still may not accept patients with neurological illness.
Mortality assessment tools
In the USA, hospice referral is predicated on the risk of mortality and estimation of time to death, which differs from other nations that base hospice/end-of-life palliative care on need rather than prognosis. Currently, there are no PDRD-specific hospice/end-of-life palliative care referral guidelines in the USA, and the closest potentially relevant Medicare guidelines to PDRD are for dementia, failure to thrive or ‘other neurological diseases’ which include ALS, myasthenia gravis and multiple sclerosis. These guidelines have poor predictive power of mortality and more sensitive and specific tools have been developed. For example, the Minimum Data Set-Changes in Health, End-stage disease and Symptoms and Signs (MDS-CHESS) Score75 76 (range 0–5) was developed to predict mortality in the frail, elderly nursing home population. Of the nursing home residents with CHESS Score of 5, 95% died within 2 years, compared with 24% of those admitted with a baseline score of 0.76 The CHESS Score was found to be a valid predictor of 6-month mortality among Canadians with 1 of 11 neurological diagnoses, including PDRD.77 Mitchell et al used the MDS to develop the Advanced Dementia Prognostic Tool (ADEPT)78 which was designed to predict 6-month mortality in nursing home dementia patients. The 6-month mortality rate increased across risk scores (possible range, 0–19): 0 points, 8.9% mortality; 1–2, 10.8% mortality; 3–5, 23.2% mortality; 6–8, 40.4% mortality; 9–11, 57.0% mortality and at least 12, 70.0% mortality in the validation cohort. The area under the receiver operating curve for predicting 6-month mortality was 0.74 and 0.70 in the derivation and validation cohorts, respectively.78
Although these and other prognostic tools have improved predictive power, still they share the disadvantage of lacking specificity for the PDRD population. Given that PDRD are notoriously variable in presentation, progression and symptom burden in the last months of life, guidelines for other neurological diseases may be unsuitable for people with PDRD. Nonetheless, in the absence of more specific prognostic tools for PDRD, we suggest that clinicians should consider current Medicare hospice eligibility criteria, the MDS-CHESS tool or the ADEPT to consider whether an individual may benefit from hospice and/or palliative care referrals. Of note, the NICE guidance in the UK has opted to place the emphasis on the needs of the patient rather than the likely proximity to death.
Expert guidance and recommendations for end-of-life palliative care/hospice referrals
Based on this review, we provide recommendations for providers on identifying patients with PDRD—who may be nearing end of life—for hospice (end-of-life palliative care) referral in table 3. These recommendations include patients exhibiting (1) evidence of advanced disease, or (2) rapid or accelerated disease progression, or (3) advanced dementia. These guidelines differ from current Medicare guidelines in that they are specifically targeted for PDRD and have expanded hospice/end-of-life palliative care triggers to include falls with fractures, loss of efficacy of medications and cover both motor and non-motor symptoms. We have also added that rapid or accelerated decline should trigger consideration for hospice/end-of-life palliative care in that our collective experience suggests that decline rarely follows a straight line and often accelerates as patients are nearing the end of life. Even when patients may not be appropriate for services which are limited by prognosis (eg, hospice in the USA), these guidelines may be used as event triggers for goals of care discussions, anticipatory guidance for patients and families and suggest areas for clinical monitoring (eg, nutrition) that are often not emphasised with current standards of care.79 It is worthy of note that atypical parkinsonian conditions may merit earlier palliative care. However, there is currently no sufficient evidence to suggest that triggers for hospice would be different, and it is our experience that patients with advanced PDRD have similar predictors of the terminal phase.
Suggested hospice guidance for Parkinson’s disease and related disorders, one of the following three criteria are required
These guidelines are perhaps better placed in terms of being used to identify the patient who is likely to have needs which could be benefited by referral to hospice/palliative care, rather than who is likely to die within a certain timeframe. This obviates the need to have robust predictors of mortality, instead, it re-frames the issue in terms of the need to have robust predictors of clinical need. This frees the referrer from having to be sure that the patient should now stop disease management and change to palliation alone. It also frees the clinician and patient from the anomaly of needing to choose between the two approaches, when ongoing optimisation of PDRD disease management is a cornerstone of excellent palliation.
For clinicians caring for this population, we recommend that this guidance be used and specifically cited when making hospice/palliative care referrals and framed in terms of need. Other data reviewed in this paper can also be used in one’s clinical documentation to further support hospice referral where the healthcare system requires an estimation of prognosis. This could include mentioning that a patient’s age, gender or comorbid illnesses place him/her at higher risk for death in the ensuing 6 months. We would like to emphasise that the determination of mortality risk estimates ultimately rests on the referring and hospice clinicians and that our recommendations and Medicare guidelines are not requisite criteria. We also suggest that discussions regarding hospice/end-of-life palliative care begin with goals of care and how the services provided by hospice may support those goals rather than focusing on prognosis which, even with the best of guidelines, is an inexact science. Access to hospice services based on a problem-based approach informed, but not dictated, by prognostic information would allow intermittent, as necessary, access to services skilled in supporting complex and persistent symptoms and other concerns in a timely manner.
Limitations
While we performed a rigorous search and followed PRISMA guidelines, there are limitations to our systematic review. We did not include every database in our search and excluded non-English papers. Additionally, in order to present the full extent of the knowledge available in this area, quality assessment was not conducted because: (1) only limited data are available in this field, (2) restricting inclusion criteria would further decrease the quantity of publications and (3) strict exclusion may have led to inclusion only of certain papers with significant bias. Further attempts are needed to both assess quality and conduct a meta-analysis to combine these quantitative predictors. We also recognise that end-of-life hospice care may also be defined as palliative care depending on country-specific definitions. Majority of the studies evaluated in this review included patients with PD, while only a few studies included patients with other parkinsonian disorders. Lastly, we acknowledge that the proposed recommendations presented here are likely to evolve as more, high-quality research becomes available, but this, we believe, is a good starting point.
Conclusions and future directions
The strength of this review is the systematic approach we followed including involvement of an international working group with expertise in palliative care and movement disorders. Further research is needed to determine the effectiveness of these recommendations in terms of maximising remaining quality of life by allowing patients with PDRD access to timely palliative care and hospice services based on clinical need and not estimated survival alone. An integrated approach to palliation and disease-directed management would remove the eligibility requirement of a short prognosis allowing both aspects of care to contribute to the patient living as well as they can for as long as they can.
References
Supplementary materials
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Footnotes
UA and RBM are joint first authors.
UA and RBM contributed equally.
Contributors Planning/idea: ERG, JK, MJJ, JMM and BK. Conducting review/manuscript preparation: UA, RBM, JB and BK. Critical review of the manuscript: UA, RBM, JC, ERG, JK, MJJ, JMM and BK. Guarantors: UA and BK (accept full responsibility for the work).
Funding Support for this study includes 2015 Parkinson’s Foundation Conference grant for International Working Group on Palliative Care and Parkinson’s Disease.
Competing interests None declared.
Provenance and peer review Commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.