Introduction
In 2011 approximately 136,000 persons died in the Netherlands, almost one-third of them from the consequences of cancer [
1]. A systematic review on symptom prevalence in patients with incurable cancer found that the most reported symptoms were: fatigue (88 %), appetite loss (56 %), pain (45 %), dyspnea (39 %), drowsiness (38 %), dry mouth (34 %), constipation (29 %), confusion (24 %), nausea (17 %), and insomnia (14 %) [
2].
The goal of palliative care is symptom control by a combination of non-pharmacological measures and drugs. Palliative experts have reached consensus on the essential drugs to treat specific symptoms. These have been compiled in two different but largely overlapping lists: one published by the International Association for Hospice and Palliative Care (IAHPC) [
3] and one based on a survey of Australian palliative care physicians [
4]. Regrettably, both lack recommendations on optimal dose or route of administration.
Existing recommendations [
5,
6] on dose and route of administration are mainly based on level 3 and 4 evidence from case studies or from expert panels. Level 1 evidence from a systematic review or randomized controlled trials is available only for NSAIDs administered to relieve nociceptive pain [
7] and morphine to alleviate dyspnea [
8]. Level 3 evidence is available for the treatment of cancer pain with oral morphine [
9]. Haloperidol treatment of a delirium in hospitalised patients is based on level 2 evidence from well designed, non-randomized trials [
10]. Recent updates of systematic reviews for morphine and haloperidol found no new significant information [
11,
12].
The choice of drug and dose tailored to the individual patient is thus hardly supported by evidence from prospective clinical trials. Likewise, there is little evidence for the optimal route of administration, although the subcutaneous route is often preferred in palliative care. Dose adjustment may be needed because liver and kidney function undergo changes at the end of life [
13,
14]. It follows that a number of drugs used in palliative care are unlicensed or off-label [
15,
16].
Only a few studies in palliative care units [
17‐
19] and services for mainly outpatients groups [
20‐
23] have described medication use in palliative care. To our knowledge, there are no published studies describing the most used drugs with their doses and administration routes, on admission and at the day of death in a large group of patients receiving palliative care.
Methods
Design and setting
This retrospective cohort study was performed in Laurens Cadenza in Rotterdam, the Netherlands. This is the largest palliative care centre in the Netherlands, with 20 beds for terminal care and symptom management; from 200 to 250 patients are admitted annually. A multidisciplinary team of health care professionals is available 24 h per day.
Measurements and technical information
Age, gender, primary diagnosis, comorbidities, and duration of admission were extracted from the electronic medical records. The primary diagnosis was assigned according to the WHO’s International Classification of Diseases (ICD-10 classification) coding for the patient’s terminal illness.
Medication data of all deceased patients in 2010 were extracted: name, dose, frequency, and route of administration, and dates of start and discontinuation of the prescription. Only the regular prescriptions for maintenance therapy were included, because the electronic prescription system does not detail how much as needed medication was given.
Drugs were prescribed according to the symptom-specific Dutch national palliative guidelines [
5]. The presence of symptoms was daily checked by the nurses and reported to the physicians, but validated assessment instruments were not standard of care.
Two top-10 s of individual drugs prescribed were constructed: One covering the day of admission (Ta), the other the day of death (Td).
Medication was categorized by the anatomical therapeutic chemical (ATC) classification system [
24]. The ATC system groups the drugs into 5 different levels according to the organ or system on which they act and according to their chemical, pharmacological and therapeutic properties. For this study we used the main therapeutic-group level. Furthermore, the WHO classification of analgesic drugs was applied: non-opioids, NSAIDs and opioids.
Morphine and haloperidol doses per 24 h were calculated taking into account route of administration. Oral bioavailability of morphine and haloperidol is 30 and 50 %, respectively, versus almost 100 % after subcutaneous, intravenous and intramuscular administration. Equivalent subcutaneous doses of oral drugs were calculated by dividing oral morphine doses by 3 and oral haloperidol doses by 2 [
5,
25,
26]. An oral morphine dose of <300 mg/24 h is considered a low-to-moderate dose [
27‐
29]. Consequently, a daily subcutaneous morphine dose of <100 mg/24 h was considered a low-to-moderate dose.
Fentanyl is mainly given via transdermal patches, which are replaced every 2–3 days. The daily dose was calculated as the dose of the prescribed patch divided by the number of days the patch was in place. Midazolam for continuous palliative sedation was administered either by subcutaneous boluses six times every 24 h or by constant subcutaneous infusion. Insomnia was mainly treated by a single subcutaneous bolus of midazolam or by intermittent boluses.
Statistics
Data were analysed using descriptive statistics. Data are presented as mean (standard deviation; SD) in case of normally distributed variables and as median (interquartile range = IQR or minimum–maximum range = range) in case of non-normally distributed variables. IBM SPSS Statistics 20 was used for data analysis.
McNemar test served to detect differences in numbers of patients receiving the 3 most frequently used drugs both at Ta and Td. We limited ourselves to these three drugs to prevent repeated testing with too small samples. Differences in the daily doses of these drugs for patients receiving these both at Ta and Td were evaluated with the Wilcoxon signed rank test. A p value of <0.05 (two-sided) was deemed statistically significant.
Discussion
This study found that morphine, midazolam and haloperidol were the most frequently prescribed drugs at the day of death for patients in the largest palliative care centre in the Netherlands. Doses of these drugs were statistically significantly higher than those at the day of admission. Upon admission almost 90 % of patients received oral medication but over the admission period a shift occurred to the effect that at the day of death more than 90 % of patients received subcutaneous medication.
Other studies, too, found that morphine, midazolam and haloperidol were the most prescribed drugs in the palliative setting [
30‐
33]. These drugs are given to relieve symptoms such as pain, restlessness and agitation, which are frequently seen in advanced cancer [
2]. Nauck and co-workers [
17] in a similar study found that 26 % of patients received morphine at admission (versus 21 % in the present study), but corresponding figures at the end of treatment were 42 versus 87 %. The latter difference is probably explained by the fact that Nauck and co-workers also included patients who were discharged from the centre, whereas we solely considered patients who died in the palliative centre. Nevertheless, other studies reported opioid use in 82–97 % [
28,
30,
32], and morphine use in 66–93 % [
27,
28,
30,
32] of patients at the end of life, which percentages correspond well with our results.
We found that midazolam was prescribed for 58 % of patients at the day of death, while in other studies this was the case for 23 % of patients in the last 48 h of life [
30] or 82 % of patients in their last week [
31]. An explanation for this wide range could be the studied time frame. Midazolam is often stopped in the last days before death, to avoid that patients become comatose. On the other hand, midazolam may be started for palliative sedation, notably in the last 24 h before death.
Many more patients in the present study were prescribed haloperidol than in the study by Nauck et al. [
17]; at admission 23 versus 3 %, respectively, and at end of treatment 50 versus 13 %, respectively. Our higher figures may be explained by the difference in the studied patient population; we only included patients who died in the palliative centre. Other studies, however, found percentages (21–43 %) comparable to the present study [
30‐
33]. Haloperidol is the drug of first choice to treat delirium. In other studies, delirium was suspected in approximately 50 % of cancer patients admitted to a palliative care centre and in up to almost 90 % of all cancer patients in the last day or hours before death [
34,
35]. We suspect, however, that haloperidol is also prescribed in agitated or restless patients who have not been clearly diagnosed with a delirium. Therefore, assessing delirium with a validated scale, such as the Confusion Assessment Method, should become standard of care. [
36,
37].
In the present study the median number of drugs decreased from 6 to 4 as death approached, probably because in our centre oral drugs are stopped when a patient enters a recognizable dying phase [
38]. Other studies, however, have reported increasing numbers of drugs towards death [
20,
22,
23], possibly to control a new or advancing symptom.
The doses of the top-10 drugs compared well to the titration schemes given in the national symptom specific guidelines [
5]. Eighty-three percent of patients in the present study received a subcutaneous morphine dose of <100 mg/24 h at the day of death, which is considered a low-to-moderate dose [
27‐
29]. In two other studies more than 90 % of the patients received low-to-moderate morphine doses either upon admission [
27] or in the last 24 h before death [
28] .
The median subcutaneous midazolam dose (60 mg/24 h) at the day of death in the present study fits within the range found in other studies; mean midazolam doses of 26–70 mg/24 h during the last days of life [
30,
31,
39]. Moreover, these doses (IQR 30-65 mg/24 h, in present study) are recommended in the Dutch national guideline for palliative sedation [
5]. However, midazolam dose titration should be guided by regular assessment of level of sedation.
The median haloperidol dose was 2 mg/day, both at admission and the day of death. Other studies found median haloperidol doses of 2.5–3.8 mg/day during the last days of life [
30,
32]. The Dutch national guideline for delirium treatment, however, recommends a maximum parenteral maintenance dose of 10 mg/day [
5]. In practice the recommended starting dose of 0.5–2 mg/day seems sufficient to treat delirium in most patients. Moreover, in elderly patients a low starting dose is recommended to prevent neurological and cardiovascular effects [
25].
Over the admission period a shift occurred from the oral route to mainly the subcutaneous route, in line with recommendations from both the guidelines [
5,
6] and the Liverpool Care Pathway for the dying [
38]. The subcutaneous route is preferred in palliative care because most patients are unable to take oral medication at the end of life and the intravenous route is often complicated by infection or discomfort. Absorption via the subcutaneous route may be suboptimal, however, especially in cachectic cancer patients with very little or no subcutaneous fat.
Although the subcutaneous route is preferred in palliative care, this route has not been fully studied. In addition, midazolam and haloperidol are unlicensed or off-label in this patient group [
15,
16,
40,
41]. Regarding opioids, only small and mostly non-randomized controlled clinical trials have compared the subcutaneous route with another route of administration [
12,
42]. In those studies similar feasibility, efficacy and opioid doses were found for the subcutaneous route and the intravenous route. Moreover, in some studies the subcutaneous route was preferred because of lower complication risks. Only small and outdated prospective studies are available for midazolam, which all found subcutaneous administration of midazolam to be feasible and effective [
39,
43,
44]. Regarding haloperidol, only retrospective descriptive studies or overview articles are available, even without addressing the administration route [
45‐
48]. In conclusion, strict monitoring of the efficacy of subcutaneous morphine, midazolam and haloperidol is essential and more pharmacokinetic and pharmacodynamics studies are needed.
Strengths and limitations
A strength of the present study is that actually administered regular medication in the palliative care setting was evaluated at two significant time points, detailing drug doses and routes of administration. In addition, electronically recorded prescriptions were available, preventing the errors of written medication orders when extracting data.
Several limitations should be addressed however. First, this was a single-centre study of which the results cannot be extrapolated to other palliative care settings or other countries as prescription practices may differ. Second, as needed prescriptions were excluded from analysis, since our electronic prescription system did not detail how much as needed medication was actually given. In our centre, ‘as needed’ prescriptions mainly serve to increase the already prescribed doses of the medications, for example when worsening of symptoms is expected. When a patient is given the ‘as needed’ medication on a regular basis, the maintenance prescription dose is adapted accordingly. Unfortunately, also indications for drugs could not be analysed, since this information was not electronically recorded. In future research, both the as needed medication and the indications should be included, so as to provide a complete overview of administered symptom-specific drugs. Lastly, outcomes of validated assessment instruments for pain, sedation and delirium were not available. In future research these assessments should be included to add information on the efficacy of drugs.
Recommendation
From the above it follows that pharmacotherapy in palliative care offers room for improvement. Therefore, we would recommend to strictly monitor the efficacy of the subcutaneously administered drugs with the use of validated pain, sedation and delirium assessment instruments. This will help recognize worsening of symptoms and enable to taper treatment to a patient’s needs.