- Research article
- Open Access
A research study review of effectiveness of treatments for psychiatric conditions common to end-stage cancer patients: needs assessment for future research and an impassioned plea
BMC Psychiatry volume 18, Article number: 85 (2018)
Rates of psychiatric conditions common to end-stage cancer patients (delirium, depression, anxiety disorders) remain unchanged. However, patient numbers have increased as the population has aged; indeed, cancer is a chief cause of mortality and morbidity in older populations. Effectiveness of psychiatric interventions and research to evaluate, inform, and improve interventions is critical to these patients’ care. This article’s intent is to report results from a recent review study on the effectiveness of interventions for psychiatric conditions common to end-stage cancer patients; the review study assessed the state of research regarding treatment effectiveness. Unlike previous review studies, this one included non-traditional/alternative therapies and spirituality interventions that have undergone scientific inquiry.
A five-phase systematic strategy and a theoretic grounded iterative methodology were used to identify studies for inclusion and to craft an integrated, synthesized, comprehensive, and reasonably current end-product.
Psychiatric medication therapies undoubtedly are the most powerful treatments. Among them, the most effective (i.e., “best practices benchmarks”) are: (1) for delirium, typical antipsychotics—though there is no difference between typical vs. atypical and other antipsychotics, except for different side-effect profiles, (2) for depression, if patient life expectancy is ≥4–6 weeks, then a selective serotonin reuptake inhibitor (SSRI), and if < 3 weeks, then psychostimulants or ketamine, and these generally are useful anytime in the cancer disease course, and (3) for anxiety disorders, bio-diazepams (BDZs) are most used and most effective. A universal consensus suggests that psychosocial (i.e., talk) therapy and spirituality interventions fortify the therapeutic alliance and psychiatric medication protocols. However, trial studies have had mixed results regarding effectiveness in reducing psychiatric symptoms, even for touted psychotherapies.
This study’s findings prompted a testable linear conceptual model of co-factors and their importance for providing effective psychiatric care for end-stage cancer patients. The complicated and tricky part is negotiating patients’ diagnoses while articulating internal intricacies within and between each of the model’s co-factors. There is a relative absence of scientifically derived information and need for more large-scale, diverse scientific inquiry. Thus, this article is an impassioned plea for accelerated study and better care for end-stage cancer patients’ psychiatric conditions.
Not surprisingly, psychiatric symptoms, disorders, and emotional distress are relatively common among cancer patients, in particular those with end-stage cancer (, also see ; see Fig. 1), which is the terminal phase of cancer—including hospice and the latter part of palliative care [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29]).
The psychiatric symptoms and disorders in end-stage cancer patients have remained unchanged over time and include delirium at 20–65%, depression at 21%, and anxiety and adjustment disorder at 14% ([30,31,32,33,34,35,36,37,38,39,40,41,42], also see [4, 5, 7,8,9, 16, 19]). Note that this includes approximately 3% of end-stage cancer patients who also suffer from severe and persistent mental illnesses (e.g., schizophrenia, bi-polar disease, major depressive disorder) (, also see ). Though the rates have been consistent over time, the actual volume has increased due to the growing number of older adults in the general population and cancer within these populations being a chief cause of morbidity and mortality ([44, 45], also see ). Patients 65 years old and older are the fastest growing segment of the population and the incidence and prevalence of cancer and related psychiatric disorders among them is consequently expanding.  This is evidenced by the substantial and statistically significant increments in dispensing all classes of psychotropic medications in recent years among end-stage cancer patients. [46,47,48,49]
Psychiatric symptoms and disorders not only cause extreme suffering in their own right but can also exacerbate physical ailments and substantially degrade the quality of life, which end-stage cancer care aims to ameliorate ([50,51,52], also see ). In response to this growing need, psychiatric therapeutic interventions including psychopharmacology and psychosocial therapy alone or in combination have been used with end-stage cancer patients to treat commonly occurring psychiatric disorders (cf. , see , cf. , see , cf. , see , also see [6, 19, 23]).
Thus, treating psychiatric conditions in end-stage cancer patients is reaching a watershed in terms of both practice and research opportunities to assess treatment effectiveness (cf ). Key to addressing end-stage patients’ psychiatric symptoms and disorders, especially going forward, is the effectiveness of psychiatric interventions and the state of research assessing that effectiveness (cf [4, 18, 19, 23, 29]). Past literature reviews (, also see [7, 19]) on end-stage cancer patients’ psychiatric symptoms and disorders have included particular aspects of psychiatric treatment effectiveness—one of which is an ongoing and expanding internet compilation solely on depression . Few, if any, studies provide a reasonably current comprehensive overview regarding the effectiveness of various psychiatric treatments with an assessment of the state of research and the need for further research. The intent of this article is to report on a recent systematic literature review study regarding the effectiveness of interventions for psychiatric conditions commonly prevalent among end-stage cancer patients; the review study assessed the state of the research into treatment effectiveness. Furthermore, the review study attempted to include non-traditional (i.e., alternative) therapies that have undergone scientific study regarding their effectiveness in treating end-stage cancer patients’ psychiatric symptoms and disorders. This has not been done previously. This article is intended to provide a well-integrated compendium of “pearls” (i.e., a psychiatric pharmacopeia). The goal is to inform oncologists and mental health practitioners regarding how to reduce end-stage cancer patients’ emotional distress and psychiatric discomfort and improve their quality of life—the ultimate goal of end-stage cancer care [1, 2, 11, 49].
A five-phase systematic strategy was used to derive the articles for this literature review, as illustrated in Fig. 2.
An initial PubMed search was undertaken to identify related articles. This also was used to identify and expand the keywords and keyword combinations (i.e., Booleans) in a second and more comprehensive search of the PubMed, Medscape, Cochranes, and Oxford databases. Studies that did not refer to psychiatry, end-stage cancer, or effectiveness of treatment were excluded. All studies, abstracts, reviews, raw reports, observational studies, and (random) controlled clinical trials found relevant have been included. A grounded [59,60,61] qualitative methodology was used to iteratively generate and assign themes to research study articles (i.e., code) until thematic saturation, an exhaustion of themes, was achieved. The inherent risk in this process is that some studies or themes will be missed, but the assumption is that a general and credible assessment will be produced . The ultimate aim of this process was to produce an integrated, synthesized end-product consisting of brief descriptive accounts of the effectiveness of psychiatric interventions and a needs assessment on the state-of-effectiveness research.
Findings are organized in accordance with the prevalence of common psychiatric disorders found among end-stage cancer patients, the most employed treatments (i.e., the “best practices benchmarks”) (cf. [4, 18, 19, 23, 27, 43, 52]) followed by other treatments, and the state of research on their effectiveness, with recommendations for future inquiry.
Delirium is the most prevalent neuropsychiatric disorder in end-stage cancer patients ([62,63,64], also [7, 13, 25, 46, 62]). Antipsychotics (e.g., haloperidol, clorapromazide, methotrimeprazine, olanzapine, risperidone, quentiapine) are the mainstays for effective psychiatric symptom management of delirium ([65,66,67,68,69], also see [7, 13, 18]).
Typical (traditional) antipsychotics
Haloperidol has been and continues to be the psychiatric medication of choice and the best practices benchmark for end-stage cancer delirium symptom relief ([70,71,72], also see [7, 18, 19, 25, 46, 73]) It has low dose tolerance, flexibility in route administration (e.g., by mouth, intravenous, intramuscular, subcutaneous), relative safety, and high efficacy ([74,75,76,77,78], also see [7, 13, 18, 62, 65,66,67, 70]). Haloperidol and other typical antipsychotics (e.g., methotrine, epramazine) have also been reported to have additional analgesic properties. Evidence also suggests they are adjuncts to pain management or have anti-nausea/emetic effects [79,80,81,82,83]—especially for intractable nausea . In addition, they have a controversial and ethically questionable role in terminal sedation, namely, rendering unconscious the end-stage patient who has truly distressing, hyper-aroused, and refractory delirium symptoms ([85, 86], also see ). Note that there are no official guidelines for practitioners and only limited data on the use of antipsychotics for terminal sedation [13, 87]. Antipsychotics may also be used in combination with lorazepam for rapid onset and augmentation of sedative effects in pronounced hyper-aroused delirious patients . Reports have suggested that aripiprazole is effective with hypoactive delirium; however, it is ineffective with hyperactive delirium and may even trigger it. Chlopromazine has calmative effects in agitated or combative delirium patients , also see [19, 73].
Atypical (new-generation) antipsychotics
In studies and case reports, risperidone, clozapine, quetiapine, and levomepromazine have proven effective in low doses compared to traditional/typical antipsychotics but with reduced extra pyramidal symptom side-effects, which is the case in end-stage cancer patients ([89,90,91,92], also see [13, 14, 18, 65, 67, 88]). They also may have hypotensive and cardiac side-effects (e.g., arrhythmias), which must be monitored ([93,94,95,96,97,98], also see [7, 13, 18, 19, 36]). Like haloperidol, new-generation anti-psychotics can be used parenterally, which is advantageous with patients in end-stage cancer where oral medications are not possible [7, 18, 54, 72, 94]. These agents may have other side-effects such as hyperglycemia, hyperlipidemia, and weight gain, which must be reasonably balanced in light of the state of advancement in the end-stage cancer and symptom relief.([99,100,101], also see [7, 18, 19]).
Antipsychotics, whether traditional/typical or atypical/new-generation, are the approved psychiatric medications for patients with severe mental disorders who suffer from schizophrenia and in some cases bi-polar disorders and who also have end-stage cancer [29, 43].
State of antipsychotic scientific research for delirium symptom relief for end-stage cancer patients
To date, except for treating hyper-aroused/distressed delirium and particular medication side-effect profiles, reports in the literature have shown no difference between typical/traditional vs. atypical/new-generation antipsychotics in terms of effectiveness for delirium symptom reduction in end-stage cancer patients (, also see [7, 18, 19, 69, 96]). Thekdi, Trinidad, and Roth  noted that a small study found that advanced prophylactic use of antipsychotic medications in patients at risk for delirium reduced symptom occurrence later on in 50% of the cases. They further argued for early and aggressive use of low-dose antipsychotics with cancer populations with an anticipated trajectory toward end-stage disease. They also noted the absence of and, thus, called for definitive trial studies on the effectiveness of the newer generation of antipsychotic agents for cancer patients experiencing delirium, in particular end-stage cancer patients (e.g., asenapine, iloperidone, lorasidone, paliperidone) and others in the pipeline—about which for end-stage cancer patients almost nothing is known.
Masman ([103,104,105,106], also see ) reported that far more studies have been conducted on the traditional/typical as opposed to the atypical/new generation as the former have been around longer. Nevertheless, most studies are retrospective studies, overviews, or case reports and few have been prospective, large-scale trials, much less randomized controlled trials, regardless of old or new generation . Also there is a tendency to echo shaky previous findings. Thus, critics of the research on antipsychotic treatments for delirium in end-stage cancer patients contend that most of it is the consequence of extrapolation and expert opinion (cf. [74, 103,104,105,106]). Given that one antipsychotic is as effective as any other except for side-effect profiles, there is definitely a need for solid large-scale prospective studies that also take into account patient type and type of delirium (e.g., hypo- vs. hyper-aroused) [18, 102]. Also, more research is needed to support and advance effective therapies for prevention and management of delirium, especially prospective random controlled clinical trials, that account for persistent, refractory symptoms and cumulative antipsychotic use in end-stage cancer patients. In sum, it appears that no large-scale prospective random controlled clinical trials have focused on antipsychotic treatments of delirium in end-stage disease, much less end-stage cancer .
Clinical depressive disorder
Selective serotonin reuptake inhibitors (SSRIs)
The approach to treatment of depression depends on the patient’s life expectancy (, also see [110, 111]). If the patient’s life expectancy is 4–6 weeks or longer, then serotonin reuptake inhibitor (SSRI) antidepressants (e.g., escitalopram, citalopram, sertraline, fluoxetine, paroxetine, mirtazapine ([112, 113], also see ) are the medication of choice and the best practices benchmarks for effective treatment (, also see [4, 7, 18, 23, 25, 53, 73]). For end-stage cancer patients, these medications are relatively safe, inexpensive, and useful with co-morbid conditions like anxiety and irritability; they also serve as possible analgesic synergists (, also see [13, 18, 19]). One downside is that they take 4–6 weeks or more to titrate to a normal response dose to achieve a beneficial effect ([117, 118], also see [7, 13, 18, 19, 23, 114]). Reports have suggested that they have some side-effects (e.g., restlessness, agitation, insomnia, sedation, parkinsonianism) that can be problematic with end-stage cancer patients, especially with co-morbid delirium [7, 23]. On the other hand, compared to other classes of antidepressants, they have few interactions with other drugs [7, 13, 18, 19, 23, 119], which is an important consideration with end-stage cancer patients ([117, 118, 120], cf. , also see ). (Note: Kiener, Weixler, Massel, Gartner, et al.  revealed that end-stage cancer patients were taking an average of 4–6 different prescription medications and up to 11 at the point of death.)
Serotonin–norepinephrine reuptake inhibitors (SNRIs)
Serotonin–norepinephrine reuptake inhibitors (SNRIs; e.g., veralfaxine, duloxetine) like SSRIs are well tolerated and have similar side-effects, except that SNRIs lead to hypertension and have been reported to cause bleeding in rare cases . In addition to the side-effects, their downside is that they may take substantially longer than SSRIs to achieve optimal effect (e.g., > 4–6 weeks) and end-stage cancer patients may not have that much time left. [4, 13, 18, 19, 23, 53, 114, 122].
Tricyclic antidepressants (TCAs; e.g., amoxapine, desipramine, imipramine, doxepin, clomipramine, amitriptyline, nortriptyline) are not well tolerated by end-stage cancer patients and have major anti-histaminic and anti-cholonergic side-effects (e.g., delirium, confusion, hallucinations); they also have the potential for serious drug-drug interactions—though some reports suggest they have analgesic effects ([4, 7, 13, 18, 53, 114, 122], cf. [19, 23, 25, 73]).
Bupropione is a well-tolerated antidepressant in end-stage cancer patients, and it triggers mild stimulation as a side-benefit in patients with chronic fatigue (, also see [13, 18, 19, 53]). However, for the same beneficial reasons, it is counter-indicated for patients prone to seizure disorders ([13, 19, 123], also see [53, 114]). Also, it might increase anxiousness, restlessness, and angina .
Mitrazapine was shown to be statistically significantly effective in that it not only improved depression symptoms over other available antidepressants but it also helped with anorexia, anxiety, and insomnia, though it led to constipation ([124, 125] also see [4, 19, 53]). In a small random controlled clinical trial, Cankurtaran, Ozalp, Soygur, Akbiyik, et al.  found that mirtazapine was more effective than imipramine in cancer patients in reducing depressive and adjunct symptoms.
Trazadone is considered too sedating and needs extremely high and potentially risky doses to be effective with end-stage cancer patients .
Monoamine oxidase inhibitors
Monoamine oxidase inhibitors (MAOs) are considered the least effective of antidepression medications for cancer patients in general, much less end-stage cancer patients [7, 23]. Thus, MAOs have been abandoned in favor of SSRIs . MAOs also have a high number of drug-drug interactions and may lead to hypertensive crises with the wrong foods or medications [7, 23].
If the patient’s life expectancy is < 2–3 weeks, then an atypical psychiatric medication option to very effectively treat depression might be ketamine . Ketamine has been studied in limited Phase I trials to treat refractory depression with a statistically significant 93% improvement rate within 0–3 days and an 80% post-dose improvement rate [127,128,129]. A statistically significant number of subjects showed few or no side-effects related to the medication . A meta-analytic study of ketamine use in general palliative care found that it can be extremely effective in patients with refractory depression, especially those with chronic pain ([130,131,132,133,134,135,136,137,138,139], also see [5, 23]). However, it is unclear exactly for which patients ketamine is optimal or what the best modes for administration are.
State of antidepressant scientific research for clinical depression symptoms relief for end-stage cancer patients
Except for the trial for mitrazapine, ketamine, and fluxoetine [23, 140, 122, 126], few large-scale, prospective, systematic, rigorous, scientific randomized controlled clinical trials are reported in the literature on medication effectiveness in end-stage cancer patients ([141,142,143,144,145] also see [58, 140, 122, 126]). Much of what is known or suspected is based heavily on expert opinion extrapolated from case reports and/or small non-end-stage cancer patient studies [58, 114]. What has been clearly established regarding the efficacy of antidepressants in treating cancer patients, including end-stage cancer patients, is that an antidepressant—any antidepressant—is better than none at all—provided the patient has sufficient life expectancy ([146,147,148], also see [5, 7, 13, 18, 19, 23, 25, 53, 58, 73, 135, 141, 145]). That is, any antidepressant is as effective as another, except when considering their different side-effect profiles, potential for overdose, and concomitant drug-drug interactions.
End-stage cancer patient guidelines for antidepressants based on practitioners’ experience, expert opinion, case reports, the few small trials, and extrapolation appear to have been codified as scientific fact through a process of successive repetition and echoing in medical practice journals and then translated into best practices ([146,147,148,149,150,151,152,153,154,155,156,157,158,159, 160], also see [18, 19, 25, 114, 74]). Given that the discipline has recognized a paucity of solid scientific research, researchers have called for closer, more thorough, and more comprehensive examinations of the effectiveness of antidepressants for end-stage cancer patients suffering depressive symptoms ([152, 153], also see ). This is especially the case in the context of ethical considerations surrounding end-stage cancer patients’ refusal of medical care . These calls have included the desperate need for large-scale, prospective, multi-site studies of end-stage histolologically similar cases . Unfortunately, yet ultimately, the use of particular antidepressants with end-stage cancer patients suffering depression depends on practitioners’ preferences and individual preferences (e.g., side-effects, tolerance, poly pharmacy, reactions). As Fitzgerald, Lo, Li, Gagliese, et al.  noted, vital research is desperately needed to better understand treatment effectiveness in terms of the phenomenology of “subthreshold” depression as well as all aspects of depression in end-stage cancer patients to strengthen the evidence-based effectiveness of psychiatric best practice guidelines.
The other treatment option for depressive symptoms in end-stage cancer patients with a short (e.g., 2–3 weeks) life expectancy is low-dose psychostimulants (e.g., methylphenidate, dextro-amphetamine, modofinil) ([156, 157], also see [4, 5, 7, 13, 18, 19, 23, 25, 53, 73]). Low-dose psychostimulants have almost immediate benefit—peaking within 3–8 h ([158,159,160,161,162,163,164,165,166,167,168,169,170,171,172,173,174], also see [7, 13, 19, 23, 53]). Patients experience a marked elevation in mood, self-esteem, alertness, focus, cognitive function, and regulation of appetite [7, 13, 18, 19, 23, 53, 158]. A study of patients taking 10 mg methylphenidate twice a day, limited to 80 mg per day or adequate response, found that 23 out of 30 (77%) end-stage cancer patients treated had moderate to marked improvement in depressive symptoms (, also see ). Only two patients withdrew due to intractable side-effects (, also see ). In a similar study, 30 out of 41 patients (73%) showed improvement in 7 days .
Psychostimulants also are particularly effective in combating opiate sedation and synergizing analgesics . Due to the immediacy of onset, there is no question regarding effectiveness and, thus, they are the treatment of choice and the best practices benchmarks for short-term care of end-stage cancer patients’ depression; they are often combined with SSRIs . Note that there is a black box warning about methylphenidate causing cardiac arrest and mandating consent to use (, also see [13, 114]). Methylphenidate is also associated with side-effects such as headaches, anxiety, hypertension, and cardiac arrhythmias . Additionally, modofinil has sympathomimetic effects and, thus, is a good choice for older end-stage cancer patients [7, 13, 114, 166, 168].
State of psychostimulant scientific research for clinical depression symptom relief for end-stage cancer patients
The effectiveness of psychostimulants in treatment of depression symptoms in cancer patients in general and (in the short term) end-stage cancer patients is fairly well established based on a series of scientifically sound randomized controlled clinical trials, the “gold standard” in research [4, 13, 18, 19, 74]. Nevertheless, and ironically, the use of these medications, though common in this population, may still be off-label (cf. [4, 74]).
Non-traditional/alternative psychiatric therapies
Electroconvulsive treatment (ECT) is extremely effective in ameliorating depression and is remarkably safe in elderly cancer patients except those prone to seizures and cardiac problems (, also see ). ECT is especially effective in depression refractory to antidepressant medications. It does cause short-term memory loss, but cognitive effects are lower with unilateral as opposed to bi-lateral ECT. However, Winnell and Roth  noted ethical questions about the image of electrically shocking terminal cancer patients, especially elderly patients.
In a double-blind, cross-over randomized controlled clinical trial examining the effectiveness of guariana (paullina aipana) on 36 patients with breast cancer, despite guariana’s psychostimulant properties, no difference was detected between those receiving it versus those receiving a placebo [169, 160]. A review of studies on visum album L (European mistletoe) used in cancer patients who also suffered from depression and anxiety found that the treatment was effective for both depression and anxiety; [170, 172] mistletoe treatments were well tolerated with fewer side-effects than conventional treatments.
State of non-standard/alternative psychiatric therapy scientific research for clinical depression symptom relief for end-stage cancer patients
Notably, Breitbart and Dickerman  claimed that of all the psychiatric therapies that treat depression, ECT‘s effectiveness has received the most definitive, extensive, solid, and generalizable scientific examination. Non-standard/alternative herbal studies, though few, seem to be well designed or account for drug-drug interactions well. They are proliferating outside the United States, with the particular herb studied indigenous to the cultural locality and region where found.
Adjustment disorder and anxiety are the third most common psychiatric conditions encountered with end-stage cancer patients. Moivic  reported that “according to the DSM-V (, also see [15, 57]). Adjustment Disorders are emotional/behavioral symptoms in excess of what would be normal response to a given stressor in excess of a mere diagnosis of depression” (, also see ). Since psychiatric medication interventions are similar to those for anxiety, they are included with anxiety, though the symptoms dictate treatment, and these interventions may also have depressive features .
End-stage cancer patients naturally experience anxiety and anxiety-related psychiatric symptoms and disorders, especially at crisis points (, cf. ). This can be considered normal people reacting normally to extremely abnormal circumstances. Determining the point at which anxiety becomes abnormal and pathological is tricky, making exactly when a therapeutic intervention is necessary problematic ([177,178,179], also see [7, 15, 25, 56]), cf. . Also, anxiety can be a component of delirium or depression, as well as a pathological feature of the cancer itself or its treatment . For example, dexamethasone and metoclorapromide can cause anxiety and restlessness along with emotional distress and hyperactivity .
Nevertheless, biodiazepines (BDZs—temazepam, midazolam, alopazalam, lorazepam, oxezapam, diazepam, clonazepam) are the most effective and powerful drugs in treating anxiety and related adjustment disorders, though they do cause sedation, confusion, motor confusion, and un-coordination, build up over time, inordinately affect elderly patients, pose a risk for renal dysfunction, and are associated with drug-drug reactions ([181, 182], also see [4, 7, 13, 18, 19, 74]). Also, there is an exception to their use with lung cancer patients in that the disease is associated with respiratory distress (i.e., air hunger) in patients and BDZs’ depressive effects can exacerbate this condition and increase related anxiety . Similarly, caution must be used with BDZs as they are synergists with opiates, which can lead to deadly pulmonary depression [7, 13, 18, 19, 74]. Nevertheless, several studies have found that BDZs are effective and powerful in relieving anxiety and are adjuncts to relieving the pain, nausea, and emesis that end-stage cancer patients commonly suffer; BDZs can even help with end-stage sedation ([175, 184,185,186,187,188,189,190,191,192], also see [13, 85]) (Note: In lieu of BDZs, other medications that can be employed but are less effective are antidepressants, bupropione, and low-dose antipsychotics ). Whatever the case, Dauchy, Dolbeault, and Reich  cautioned that BDZs should not be prescribed indiscriminately for anxiety or depression because they might further complicate an already complicated clinical picture.
Maida, Ennis, Irani, Corbo, et al. , in a prospective study of nabalone (Casamet)—a cannabinoid—therapy in managing pain found a statistically significant (P = .0284) reduction in anxiety post-nabalone administration; nabalone also lowered or eliminated the use of anti-inflammatories.
In a study on homeopathy and anxiety and anxiety disorders, Pilkington, Kirkwood, Rampes, Fisher, et al.  found that homeopathy was frequently and preferably used by a range of cancer patients suffering anxiety. Homeopathy was shown to be effective without side-effects, but the exact degree of effectiveness was questionable and needs further study.
Su, Wang, Grant, and Liu’s  comprehensive review of Chinese herbal medication trials with a range of cancer patients found that Chinese herbal remedies were ineffective in relieving anxiety. The exact herbal medicines were unclear. Also, though adverse events were related to the medicines, no serious adverse events were reported. A review of studies on visum album L (European mistletoe) found that herbal medicine was effective for both psychiatric disorders (cf. , also see [171, 172, 180]) and the treatments were well tolerated with fewer side-effects than conventional treatments.
State of psychiatric therapy scientific research for adjustment disorder/anxiety relief for end-stage cancer patients
Research studies on BDZ interventions with end-stage cancer patients appear relatively robust and comprehensive. One reason offered for this is the overlap between BDZs and anxiety and the proliferation of post-traumatic stress disorder (PTSD) studies, extensions and extrapolations of those PTSD case and observational studies, meta-analytic reviews, and trials [4, 197,198,199]. Nevertheless, appearances might be deceiving in that Masman, van Dijk, Tibboel, Baar, et al. (, also see [200,201,202]), in their study on midozolam—one of the most prescribed BDZs in hospice settings—found that only case studies and small outdated trials were available to justify this practice in best practices guidelines (cf. ). Whatever the case, at a minimum, more and larger trials are needed on BDZs’ effectiveness to establish best practices guidelines, especially in conforming prescription of these drugs to the particular needs of end-stage cancer patients .
Many reports in the literature address psychosocial (i.e., talk) therapy interventions with communicative and cognizant end-stage cancer patients in terms of relieving psychiatric symptoms and emotional distress, including but not limited to individual counseling, hypnotherapy, group therapy, psychotherapy, cognitive behavioral therapy (e.g., relaxation training, biofeedback), dignity therapy, and existential therapy ([203,204,205,206,207,208,209], also see [4, 5, 17, 23,24,25, 52, 73, 114, 90]). The general consensus in the discipline is that psychosocial interventions can reduce psychiatric disorders in communicative and cognizant end-stage cancer patients. ([210, 211], also see [4, 17, 23, 114]).
Meaning-centered and dignity therapy
Both meaning-centered and dignity therapy have been tested in Phase I, multi-site, randomized controlled clinical trials with promising but mixed results in terms of efficacy with end-stage cancer patients ([210,211,212,213,214,215,216,217,218,219], also see [5, 17, 23, 52, 63, 203, 204]). Dignity therapy (i.e., therapy intended to enhance diminished dignity and achieve a sense of purpose) was related to higher levels of helpfulness, quality of life, and sense of dignity in end-stage cancer patients [52, 215]. However, the patients did not experience a reduction in emotional distress .
Meaning-centered psychotherapy refers to the brief psychotherapeutic intervention predicated in Victor Frankl’s logotherapy (, also see ). It aims to enhance psychosocial well-being in end-stage patients through individual and group applications [52, 203]. In a Phase I randomized controlled clinical trial, end-stage cancer patient study participants received group and individual psychotherapy; in a follow-up trial, individual psychotherapy was compared with a placebo intervention . In both trials, participants receiving individual psychotherapy reported improvements in well-being and quality of life. However, the half-life of the intervention was brief in that differences in treatment outcomes were completely absent 2 months later (also see ).
A small trial examining a hypnotherapy intervention designed to reduce anxiety for patients at an in-patient hospice facility found a statistically significant reduction in anxiety by the fourth treatment session ([221, 222], also see ).
In a random controlled clinical trial, a brief guided self-help intervention was conducted with hospice in-patients targeting their depression symptoms (, also , cf. ). The intervention consisted of a trainer training participants to break cyclic cognitions of worry followed by practice sessions over a four-week period; in contrast, the control group received no intervention but crossed over in 4 weeks to the training intervention to receive treatment (, also see ). Participants experienced statistically significant reductions in anxiety but no reductions in depression (, also see ).
Orientation and cognitive behavioral therapy
Two other trials assessed the effectiveness of psychosocial interventions in cancer patients suffering from major depression. Both trials were enhanced orientation programs with the control group receiving the standard of care and both found reductions in depression symptoms ([224,225,226], also see , cf. ). Two other studies comparing the effectiveness of classic psychotherapy and cognitive behavioral therapy (CBT) found no reductions in depressive symptoms . In a trial with cancer patients, Chen, Chen, and Zhi  found no difference between CBT and busprione and sertraline in terms of reducing depression and anxiety. They inferred that CBT was just as effective as psychiatric medication in treating anxiety and depression.
Between 1999 and 2002, a series of meta-analytic studies was conducted on previous studies (1970–1990) that examined the effectiveness of psychosocial education on emotional distress in cancer patients with respect to reducing depression and anxiety (, also see ). The studies universally found substantial evidence of a positive benefit on depression and anxiety in end-stage adult cancer patients but no difference in treatment effectiveness, especially in advanced disease cancer patients—even when delivered by experienced practitioners ([228,229,230], also see , cf. ). Notably, the investigators concluded that the interventions were beneficially effective in reducing emotional distress (also see ). Put differently, end-stage cancer patients appreciate one-to-one therapeutically delivered management of expectations and this type of intervention may be supportive of other interventions (also see ).
State of psychosocial therapy scientific research for end-stage cancer patients’ psychiatric disorders
Other than the trials previously mentioned, no other reports were found that approximated large-scale, prospective, rigorous scientific inquiry regarding the effectiveness of psychosocial intervention with end-stage cancer patients’ psychiatric disorders. Nevertheless, the fact that psychosocial (i.e., talk) therapy is venturing into clinical trials to scientifically verify interventions’ effectiveness must be commended and encouraged. Dauchy, Dolbeault, and Reich  argued that a specific fit between types of psychosocial therapies that are effective with patients’ expressive capacities, psychosocial situations, and timing in their process of oncological care must be identified.
Despite a seemingly solid universal consensus among experts that psychosocial therapies synergistically augment psychiatric medication interventions’ effectiveness and the two are mutually supportive, the shortage of empirical evidence means that the jury is still out ([232, 233], also see [4, 17, 23, 114, 211, 213, 230], cf. ). Solid, large-scale, prospective trials are needed to investigate whether the therapeutic alliance is supported by psychosocial interventions and augments psychiatric medication interventions with end-stage cancer patients (also see [23, 150, 234], cf. [17, 25, 211]). This research should establish what aspects of psychotherapy are more or less beneficial, such as mutual trust, respect, sensitivity, coping, mechanisms/tools, and decreasing/eliminating maladaptive thinking. The literature contains increasing calls to use less intensive and less invasive data sources, including secondary administrative and medical records . Regarding psychosocial education interventions, after a spate of studies culminating in a series of meta-analytic studies, research on this aspect of psychiatric interventions has dissipated—and this should not be where it ends as there is always more to learn.
Though spirituality and religion (religiosity) were not the province of this study, they may have positive influences on psychiatric interventions and end-stage cancer care that are worthy of informed commentary. Patients in end-stage cancer naturally experience multi-layered and inter-connected physical problems and emotional stressors, such as deterioration in quality of life, pain and increased sensitivity to pain, difficulty communicating, loss of control, physical disfiguration, burdens placed on others, costs of care, self-demoralization, feelings of worthlessness, helplessness, guilt, indifference, loss of interest and pleasure, and pathological pessimism (, also see [25, 114], cf. ). End-stage cancer patients often confront existential questions such as: Why? Why me? What have I done to deserve this? They often need to find meaning in their suffering, death, and the afterlife, and their illness may cause them to draw on or seek refuge in their faith or religion as a way of coping. Recently, small yet promising trials testing the effectiveness of interventions designed to boost spirituality have found that spirituality can positively affect end-stage cancer patients’ mood and quality of life [237,238,239,240,241]. Not surprisingly, these studies found that spirituality interventions increased spirituality among the participants receiving these interventions. The good news is that some of the studies  are in the process of being replicated at several sites worldwide.
In sum, at the risk of over-simplification, this review of the literature revealed a testable linear model of a combination of psychiatric treatments for communicative and cognizant end-stage cancer patients, as shown in Fig. 3.
This model has correlative models that emerged through rigorous scientific retrospective study of the cost-effectiveness of treatments on other psychiatric patient populations  (Note: The weight or importance of co-factors is displayed by their order of precedence, left to right.) First, consistent with best practice guidelines, the goal of psychiatric treatments with end-stage cancer patients is reduction in their psychiatric symptoms and enhancement of their quality of life (, also see, [1, 2, 11, 49, 52, 152, 153]). Second, depending on symptoms, medications are the most powerful tools in the psychiatric arsenal and this armory is expanding and extending with new editions and off-label combinations (cf. ). Third, some form of psychological counseling/intervention appears to support and augment psychiatric medication interventions. Though their effectiveness might be mixed, common sense dictates that the potential harm is relatively minimal, and they can serve as vehicles for fortifying the therapeutic alliance. Fourth, though a connection between psychosocial education and psychiatric therapeutic effectiveness has yet to be established, such education has some beneficial or helpful effects for patients in crisis and research on it should not be abandoned entirely. Fifth, studies on interventions designed to enhance spirituality have shown substantially promising results in terms of quality of life and should be considered for inclusion in the constellation of future psychiatric treatment planning.
Of course, these recommendations take into account that the first priority is always treating physical medical conditions (, also see [7, 17, 27, 58, 74, 183, 211], cf. [22, 53, 114]). In terms of end-stage cancer patients who are cognitively impaired or unable to communicate (e.g., advanced delirium), psychiatric medication is probably the only appropriate therapeutic choice , but counseling, psychosocial education, and spirituality interventions may be appropriate interventions for family members and caregivers (cf. [25, 27, 73, 114]). Nevertheless, “the devil is in the details.” Specifically, the complicated and tricky part of each component in the model is negotiating, balancing, conforming, and/or fitting the right treatment with the right patient, diagnosis (cf. [5, 7, 27, 56, 58]), dose for response, titration and tapering, drug-drug interactions, route of administration, and context and doing so decisively and quickly. Though varying amounts of quality scientific evidence exists in terms of components in the model, the review reported herein noted that some studies lack supporting evidence, or worse offer pseudo-evidence, and that much more rigorous and larger scale scientific studies must be conducted. This is particularly true for research on end-stage cancer patients in general and newly developed treatments and off-label combinations in particular—and of course effectiveness studies that include psychiatric intervention costs (cf. [74, 242]).
As cancer treatments become more aggressive and successful, and as the populations of older adults and, by extension, the populations with end-stage cancer, grow, patients’ quality of life is of paramount importance. Delirium, clinical depression, and anxiety/adjustment disorder are complex and multi-faceted disorders and the psychotherapeutic and psychopharmacological interventions for their treatment require further study to inform more precise and powerful cancer care and best practices, especially in end-stage cancer. Thus, quality of life can be improved for patients dying of cancer. Universally endorsed care principles for end-stage cancer care affirm the importance of psychological health and access to the best mental health care that can be rendered to improve patients’ quality of life at life’s end (, also see [49, 52, 152, 153]). The wide dissemination of findings should alert clinicians and patients and their families as developments emerge. If anything, this article serves as an impassioned plea for further, better, and accelerated study of treatment effectiveness and care improvement for end-stage cancer patients’ psychiatric conditions, if only because these patients cannot wait.
This article reported on a systematic, comprehensive, integrated review that investigated the effectiveness of interventions employed to treat psychiatric conditions common to end-stage cancer patients. The aim of this effort was to provide empirical findings to mental health practitioners so that they can hone their expertise in reducing emotional distress and psychiatric discomfort common to actively dying cancer patients and help these patients cope and improve their overall quality of life. Also, this work attempted to achieve an understanding of the state of the research on which best practices is predicated and to shed light on avenues for further inquiry. Undoubtedly, based on this review, more effective interventions are needed for psychiatric conditions/disorders; also needed are rapid and effective treatments to relieve psychiatric symptoms and disorders as well as strategies and tools to reduce or prevent them in advance .
- > :
Cognitive behavioral therapy
Electroconvulsive shock therapy
Monoamine oxidase inhibitor
Post traumatic stress disorder
Serotonin–norepinephrine reuptake inhibitors
Selective serotonin reuptake inhibitors
Texas medical center
University of Texas MD Anderson cancer center
Roy-Byrne PP. Diagnosis of psychiatric disorders in patients with cancer. https://www.uptodate.com/contents/diagnosis-of-psychiatric-disorders-in-patients-with-cancer?search=diagnosis-of-psychiatricdisorders-in-patients-with-cancerAQ13&source=search_result&selectedTitle=1~150&usage_type=default&display_rank=1
Miovic M, Block S. Psychiatric disorders in advanced cancer. Cancer. 2007;110(8):1665–73. https://doi.org/10.1002/cncr.22980. PMID: 17847017
Marks S, Heinreich T. Assessing and treating depression in palliative care patients. Curr Psychol. 2013;12(8):37–40. https://doi.org/10.1089/jpm.2010.0530. PMID: 21815815
Irwin SA, Rao S, Bower K, Palica J, et al. Psychiatric issues in palliative care recognition of depression in patients enrolled in hospice care. J Palliat Med. 2008;11(2):158–63. https://doi.org/10.1089/jpm.2007.0140. PMID: 18333728
Winell J, Roth AJ. Psychiatric assessment and symptom management in elderly cancer patients. Cancer Network. 2005:1–14. PMID: 16370448
Massie MJ. The prevalence of depression in patients with cancer. J Natl Cancer Inst Monogr. 2004;32:57–71. PMID: 15263042
Fitzgerald P, Miller K, Li M, Rodin G. Depressive disorders: chapter 3. In psycho-oncology. New York: Oxford University Press; 2015. https://doi.org/10.1093/med/9780199363315.003.0037.
Kim S-H, Shin DW, Kim S-Y, Suh BS, et al. Terminal vs. advanced cancer: do the general population and health care professionals share a common language? Cancer Res Treat. 2016;48(2):759–67. https://doi.org/10.4143/crt2015:124
American Cancer Society. Advance directives: why do you need an advance directive? . Mobile: American Cancer Society; 2015. Available from: http://www.cancer.org/treatment/findingandpayingfortreatment/understandingfinancialandlegalmatters/advancedirectives/advance-directives-why-do-we-need-advancedirectives. [Cited 2015 Aug 1].
Levy MH, Back A, Benedetti C, Billings JA, et al. NCCN clinical practice guidelines in oncology: palliative care. J Natl Compr Cancer Netw. 2009;7:436–73. PMID: 19406043
Garcia C, Lynn R, Breitbart W. Psychotropic medications in palliative care. Primary Psychiatry. 2009;16(5):25–32.
Breitbart W, Alici-Evcimen Y, Ruenda-Lara M. Psycho-oncology. In: Sandock BJ, Sandack VA, editors. Kaplan and Sandock’s comprehensive Texbook of psychiatry. 8th ed. New York: Lippicott, Wilkins and Williams; 2008.
Wilson KG, Chochinov HM, Skirko MG, Allard P, et al. Depression and anxiety disorders in palliative Cancer care. J Pain Symptom Mang. 2007;33(2):118–28. https://doi.org/10.1016/j.jpainsymman.2006.07.016. PMID: 17280918
Hotopf M, Chidgey J, Addington-Hall J, Ly KI. Depression in advanced disease: a systematic review, part 1. Prevalence and case finding. Palliat Med. 2002;16:81–97. https://doi.org/10.1191/0269216302pm507oa. PMID: 11969152
Wilson KG, Chochinov HM, de Faye BJ, Breitbart W. Diagnosis management in depression in pailliative care. In: Chochinov HM, Breitbart W, editors. Handbook of psychiatry and palliative medicine. New York: Oxford University Press; 2000. p. 25–49.
Mehta RD, Roth AJ. Psychiatric considerations in the oncology setting. CA Cancer J Clin. 2015;65(4):300–14. https://doi.org/10.3322/Caac.21285. PMID: 26012508
Thekdi SM, Trinidad A, Roth A. Psychopharmacology in cancer. Curr Psyhiatry Rep. 2015;17(529):1–10. https://doi.org/10.1007/s11920-0529-x. PMID: 25417593
Mitchell AJ, Chan M, Bhatti H, Halton M, et al. Prevalence of depression, anxiety, and adjustment disorder in oncological, hematological, and palliative-care settings: a meta-analysis of 94 interview-based studies. Lancet Oncol. 2011;12(2):160–74. https://doi.org/10.1016/S1470-2045(11)70002-X. Epub 2011 Jan 19. PMID: 21251875
Pirl WF, Roth AJ. Diagnosis and treatment of depression in cancer patients. Oncology (Williston Park). 1999;13(9):1293–301. PMID: 10509324
Maixner S, Vitale CA, Stoltz AM, Wisely M, et al. Poster Number: NR 38 Geriatric Psychiatry Consultations in the Hospice Setting: A Case Series. 2012 AAGP Annual Meeting. http://www.ajgponline.org/article/S1064-7481(12)61556-5/pdf.
F W and Dickerman AL. Assessment and management of depression in palliative care. Section Eds Roy-Byrne PR and block AD, deputy Eds Savarese DMF and Solomon D: 2017: https://www.uptodate.com/contents/assessment-and-management-of-depression-in-palliative-care.
Muriel AC, Hwang VS, Kornblith A, Greer J, et al. Management of psychosocial distress by oncologists. Psychiatr Serv. 60(8):1132–4. https://doi.org/10.1176/appi.ps%2060.8.1132.
Dein S. Psychiatric liaison in palliative care. Adv in Psychiatr Treat. 2003;9:241–8. http://apircpsych.org
Blum B, Duane D, Ferris D, Herbst L, et al. Let's talk about hospice and palliative care. San Diego: San Diego Hospice and Palliative Care; 2004. http://www.chpca.net/media/238224/hpc-first-pritnable_booklet-english.pdf.
Irwin SA, Ferris FD. The opportunity for psychiatry in palliative care. Can J Psychiatr. 2008;53 https://doi.org/10.1177/070674370805301103. PMID: 19087465
Ferris FD, Balfour HM, Bowen K, Farley J, et al. A model to guide patient and family care: based on nationally accepted principles and norms of practice. J Pain Symptom Manag. 2002;24(2):106–23. PMID: 1223112
Trachsel M, Irwin SA, Biller-Adorno N, Hoff P, et al. Palliative psychiatry for severe persistent mental illness as a new approach to psychiatry? Definition, scope, benefits, and risks. BMC Psychiatry. 2016;16(260):1-1-6. https://doi.org/10.1186/s12888-016-0970-y. PMID: 27450328 PMCID: PMC4957930
Van der Lee MI, Sware NB, Van der Nom JG, Den Bout V, et al. Positive feelings among terminally ill cancer patients. Eur J Cancer Care (Engl). 2006;15:51–5. https://doi.org/10.1111/j.1365-2354.2005.00619.x. PMID: 16441677
Grabsch B, Clarke DM, Love A, McKenzie DP, et al. Psychological morbidity and quality of life in women with advanced breast cancer: a cross-sectional survey. Palliat Support Care. 2006;4:47–56. PMID: 16889323
Wilson KG, Chocchinov HM, Skirko MG, Allard P, et al. Depression and anxiety disorders in palliative cancer care. J Pain Symptom Manag. 2007;33:118–29. https://doi.org/10.1016/j.jpainsymman.2006.07.016. PMID: 17280918
Kirsh KL, McGrew JH, Dugan M, Passik SD. Difficulties in screening for adjustment disorders, part 1: use of existing screening instruments in cancer patients undergoing bone marrow transplantation. Palliat Support Care. 2004;2:23–31. PMID: 16594232
Kadan-Lottick NS, Vanderwerker LC, Block SD, Zhang B, et al. Psychiatric disorders and mental health service use in patients with advanced cancer: a report from the coping with cancer study. Cancer. 2005;104:2872–81. https://doi.org/10.1002/cncr.21532. PMID: 16284994 PMCID: PMC1459283
Prieto JM, Blanch J, Atala J, Carerreras E, et al. Psychiatric morbidity and impact on hospital length of stay among hematologic cancer patients receiving stem-cell transplantation. J Clin Oncol. 2002;20:1907–17. https://doi.org/10.1200/JCO.2002.07.101. PMID: 11919251
Akechi T, Okamura H, Nishiwaki Y, Uchitomi Y. Psychiatric disorders and associated and predictive factors in patients with unresectable nonsmall cell lung carcinoma: a longitudinal study. Cancer. 2001;92:2609–22.
Roth AJ, Modi R. Psychiatric issues in older cancer patients. Oncol Hematol. 2003;48:185–97. PMID: 14607382
Blazer DG. Epidemiology of late life depression. In: Schneider LS, Reynolds CF, Lebowitz BD, et al., editors. Diagnosis and treatment of depression in late life. Washington, D.C: American Psychiatric Press; 1994. p. 9–19.
Dewey M, de la Camara CJRM, Lobo A, et al. Cross-cultural comparison of depression and depressive symptoms in older people. Acta Psych. 2005;162:184–6. PMID: 8356886
Bergquist H, Ruth M, Hammerlid E. Psychiatric morbidity among patients with cancer of the esophagus or the gastro-esophageal junction: a prospective, longitudinal evaluation. Dis Esophagus. 2007;20(6):523–9. https://doi.org/10.1111/j.1442-2050.2007.00741.x. PMID: 17958729
Teunissen SCCM, Wesker W, Kruiwagen C, de Haes HCJM, et al. Symptom prevalence in patients with incurable cancer: a systematic review. J Pain Symptom Manag. 2007;34:94–104. https://doi.org/10.1016/j.jpainsymman.2006.10.015. PMID: 17509812
Caraceri A, Nanni O, Maltoni M, Piva L, et al. Impact of delirium on the short term prognosis of advanced cancer patients. Italian multicenter study group on palliative care. Cancer. 2000;89(5):1145–9. PMID: 10964345
Ellison N. Mental health and palliative care: a literature review. UK: The Mental Health Foundation; 2008. https://www.mentalhealth.org.uk/publications/mental-health-and-palliative-care-literature-review.
Rao A, Cohen HJ. Symptom management in the elderly cancer patient: fatigue, pain, and depression. J Natl Cancer Inst. 2004;32:150–7. https://doi.org/10.1093/jncimonographs/lgh031. PMID: 15263059
Yanick R, Reis LA. Cancer in older persons: an international issue in an aging world. Semin Oncol. 2004;31:125–296. PMID: 15112144
Farriols C, Ferrandez O, Planas J, Pere O, et al. Changes in the prescription of psychotropic drugs in the palliative care of advanced cancer patients over a 7 year period. J Pain Symptom Manag. 2012;43(5):945–52. https://doi.org/10.1016/j.jpainsymman.2011.05.010. PMID: 22436835
Wilson KG, Chochinov HM, McPherson CJ, LeMay K, et al. Suffering with advanced cancer. J Clin Oncol. 2007;25:1691. https://doi.org/10.1200/JCO.2006.08.6801. PMID: 17470861
Spitzer RI, Kroenke K, Linzar M, Hahn SR, et al. Health-related quality of life in primary care patients with mental disorders: results from the PRIME-MD 1000 study. JAMA. 1995;274:1511–7. PMID: 7474219
Tan WW. Palliative Cancer care guidelines. http://emedicine.medscape.com/article/2500043-overview
Greer JA, Jackson VA, Meier DE, Temel JS. Early integration of palliative care services with standard oncology care for patients with advanced cancer. CA Cancer J Clin. 2013;63(5):349–63. https://doi.org/10.3322/caac.21192. PMID: 23856954
Ferrell BR, Temel JS, Temin S, Alesi ER, et al. Integration of palliative care into standard oncology care: American Cancer Society of clinical oncology clinical practice guideline update. J of Clin Oncol. 2017;35(1):96–112. https://doi.org/10.1200/JCO.2016.70.1474. PMID: 28034065
Fairman N, Irwin SA. Palliative care psychiatry: update on an emerging dimension of psychiatric practice. Curr Psychiatry Rep. 2013;15(7):374. https://doi.org/10.1007/s11920-0374-3.
Ginsburg A. Cancer-related depression and potential pharmacologic therapies. Proc (Bay Univ Med Cent). 2008;21(4):439–41. PMID: 18982092 PMCID: PMC2566922
Franco-Bronson K. The management of treatment-resistant depression in the medically ill. Psychiatr Clin North Am. 1996;19(2):329–50. PMID: 8827193
Check DV, Rosenmstein DL, Dusetzina SB. Early supportive medication use and end-of-life care among Medicare beneficiaries with advanced breast cancer. Support Care Cancer. 2016;24:346–3472. https://doi.org/10.1007/s00520-016-3174-6.
Barnhill JW, Dickerman AL. DSM-5 and psycho-oncology. New York: Oxford University Press; 2015. https://doi.org/10.1093/med/9780199363315.003.0083.
Hoge M, Roth AJ. Training psychiatrists and psychologists in psycho-oncology. New York: Oxford University Press; 2015. https://doi.org/10.1093/med/9780199363315.003.0093.
Rodin G, Katz M, Lloyd N, Green E, et al. Treatment of depression in cancer patients. Curr Onc. 2007;14(5):180–8. PMID: 17938701 PMCID: PMC2002483
Glaser BG and Strauss AL. The Discovery of Grounded Theory: Strategies for Qualitative Research. Aldine Transaction; New Brunswick, 1967 (Reprinted 2006).
Strauss A, Corbin J. Basics of qualitative research – techniques and procedures for developing grounded theory, second edition. London: Sage Publications; 1998.
Ramalho R, Adams P, Huggard P, Hoare K. Literature review and constructivist grounded theory methodology. Forum Qual Soc Res. 2015;16(3):19. http://www.qualitative-research.net/index.php/fqs/article/view/2313/3876
Fang C, Chen H, Liu S, Lin C, et al. Prevalence, detection, and treatment of dellrium in terminal cancer inpatients: a prospective survey. Jpn J Clin Oncol. 2008;38(1):56–63. https://doi.org/10.1093/jjco/hym155. PMID: 18238881
Pereira J, Hanson J, Bruera E. The frequency in clinical course of cognitive impairment in patients with terminal cancer. Cancer. 1997;79:835–41. PMID: 9024722
Lipowski J. Transient cognitive disorders, delirium, acute confusional states in the elderly. AJP. 1983;140:1426–36. https://doi.org/10.1176/ajp.140.11.1426. PMID: 6624987
Gangon PR. Treatment of delirium in supportive and palliative care settings. Curr Opin Support Palliat Care. 2008;2(1):60–6. https://doi.org/10.1097/SPC.0b013e3282f4ce05. PMID: 18685397
Leonard M, Agar M, Mason C, Lawlor P. Delirium issues in palliative care settings. J Psychosom Res. 2008;65(3):289–98. https://doi.org/10.1016/j.jpsychores.2008.05.018. PMID: 18707953
Breitbart W, Freidlander M, Lawlor P. Delirium issues in the terminally ill. In: Chuchinov H, Breitbart W, editors. Handbook of psychiatry and palliative medicine. 2nd ed. New York: Oxford University Press; 2010.
Tune L. The role of anti-psychotics in treating delirium. Curr Psychiatry Rep. 2002;4(3):209–12. PMID: 12003684
Yuppa DP, Braun IM. Psychotropic medications in Cancer care. New York: Oxford University Press; 2015. https://doi.org/10.1093/med/9780199363315.0052.
Breitbart W, Alici Y. Evidence-based treatment of delirium in patients with cancer. J Clin Oncol. 2012;30(11):1206–14. https://doi.org/10.1200/JCO.2011.39.8784. PMID: 22412123 PMCID: PMC3646320
Maldonando JR. Delirium in the acute care setting: characteristics, diagnosis and treatment. Crit Care Clin. 2011;9(4):657–722. https://doi.org/10.1016/j.ccc.2008.05.008. PMID: 18929939
Akechi T, Uchtomi Y, Oamura H, Fukue M, et al. Usage of haloperidol for delirium in cancer patients. Support Care Cancer. 1996;4:390–2. PMID: 8883234
Dein S. Transcultural psychiatry. Br J Psychiatry. 2002;181:535–6. PMID: 12456530
Masman AD, van Dijk M, Tibboel D, Baar FPM, et al. Medication use during end-of-life care in a palliative care Centre. Int J Clin Pharm. 2015;37:767–75. https://doi.org/10.1007/s11096-015-0094-3. PMID: 25854310 PMCID: PMC4594093
Nauck F, Ostgathe C, Klaschick E, Bausewein C, et al. Drugs in palliative care: results from a representative survey in Germany. Palliat Med. 2004;18:100–7. https://doi.org/10.1191/0269216304pm852oa. PMID: 15046406
Lawlor PG, Gangnon B, Mancini IL, Pereira JL, et al. Occurrence, causes, and outcome of delirium in patients with advanced cancer: a prospective study. Arch Intern Med. 2000;160:786–94. PMID: 10737278
Del Fabbro E, Dalal S, Bruera E. Symptom control in palliative care--part III: dyspnea and delirium. J Palliat Med. 2006;9:422–36. https://doi.org/10.1089/jpm.2006.9.409. PMID: 16629571
Michaud L, Burnand B, Stiefel F. Taking care of the terminally ill cancer patient: Delerium as a symptom of terminal disease. Am Oncol. 2004;15(suppl 4):iv 199–203. https://doi.org/10.1093/annonc/mdh927. PMID: 15477308
Seidel S, Aigner M, Ossege M, Pernicka E, et al. Antipsychotics for acute and chronic pain in adults. Cochrane Data Base Sys Rev. 2013;(4):CD004844. https://doi.org/10.1002/14651858.pub3. PMID: 23990266
Langohr HD, Stohr M, Petruch F. An open and double-blind cross-over study on the efficacy of clomipramine (Anafranil) in patients with painful mono- and polyneuropathies. Eur Neurol. 1982;21(5):309–17. PMID: 6126361
Plotkin DA, Plotkin D, Okun R. Halperidol in the treatment of nausea and vomiting due to sytoxic drug administration. Curr Ther Res Clin Exp. 1973;15(9):599–602. PMID: 4201543
Kelly SL, Braun TJ, Meyer TJ, Rempel P, et al. Trial of droperidol as an anti-emetic in cisplatin chemotherapy. Cancer Treat Rep. 1986;70(4):469–72. PMID: 3698040
Mason BA, Dambra J, Grissman B, Catalam RB. Effective control of cisplatin-induced nausea using high-dosed steroids and droperidol. Cancer Ther Rep. 1982;66(2):243–5. PMID: 7198937
Baymaster FP, Falcone JF, Bauzon D, Kennedy S, et al. Patient antagonism of S-HT (3) and 5-HT (6) receptors by olanzapine. Eur J Pharamcil. 2003;430(20–3):341–9. PMID: 11711053
Cowan JD, Palmer TW. Practical guide to palliative sedation. Curr Ocol Rep. 2002;4(3):242–9. PMID: 11937015
Morita T. Palliative sedation to relieve psycho-existential suffering of terminally ill cancer patients. J Pain Sympt Manag. 2004;28(2):445–50. https://doi.org/10.1016/j.jpainsymman.2004.02.017. PMID: 15504621
Sipahinamalani A, Masand PS. Use of risperidone in delirium case reports. Ann Clin Psychiatry. 1997;2:105–7.
Boettger S, Breitbart W. An open trial of aripiprazole for the treatment of delirium in hospitalized cancer patients. Palliat Supp Care. 2011;9(4):351–7. https://doi.org/10.1017/S1478951511000368. PMID: 22104410
Liu CY, Juang YY, Liang HY, Lin NC, et al. Efficacy of risperidone in treating the hyperactive symptoms of delirium. Int Clin Psychopharmcol. 2004;19(3):165–8. PMID: 15107660
Paellada E, Baeza I, de Pablo I, Martinez G. Risperidone in the treatment of patients with delirium. Psychiatry. 2004;65(3):348–53. PMID: 15096074
Han CS, Kim YK. A double-blind trial of risperidone and halperidol in the treatment of delirium. Psychosomatics. 2004;45(4):297–301. https://doi.org/10.1016/S0033-3182(04)70170-X. PMID: 15232043
Dietz I, Schmitz A, Lampey I, Schulz C. Evidence for the use of Levomepromazine for symptom control in the palliative care setting: a systematic review. BMC Palliat Care. 2013;12:2. https://doi.org/10.1186/1472-684X-12-2.
Stiefel F, Rasavi D. Common psychiatric disorders in cancer patients. II. Anxiety and acute confusional states. Supp Care Cancer. 1994;2:223–37. PMID: 8087441
Murray GB. Confusion, delirium, and demetia. In: Hackett TP, Cassem NH, editors. Massachusetts general hospital handbook of general hospital psychiatry, 2nd ed, vol. 84. Littleton: PSG Publishing; 1987.
Stiefel F, Holland J. Int Psychogeriatr. 1991;3:333–6. PMID: 1811785
Yoon HK, Kim YK, Han C, Ko YH, et al. Paliperidone in the treatment of delirium: results of a prospective open-label pilot trial. Acta Neuropsychiatr. 2011;23(4):179–83. https://doi.org/10.1111/j.1601-5215.2011.00568. PMID: 25379796
Pae CU, Lee SJ, Lee CU, Palik IH. A pilot trial of quetiapine. Prim Care Companion J Clin Psychiatry. 2000;2(1):10–2. https://doi.org/10.1002/hup.559. PMID: 14994323
Leso L, Schwartz TL. Ziprazadone treatment of delirium. Psychosomatics. 2002;43(1):61–2. https://doi.org/10.1176/appi.psy.43.1.61. PMID: 11927760
Breitbart W, Tremblay A, Gibson C. An open trial of olanzapine for the treatment of delirium in hospitalized cancer patients. Psychosomatics. 2002;43:175–82.
Wang HR, Woo YS, Bahk WM. Atypical antipsychotics in the treatment of delirium. Psychiatry Clin Neurosci. 2013;67(5):657–722. https://doi.org/10.1111/pcn.12066. PMID: 23859663
Ganzani L, Gross AF. Cancer Care for Patients with schizophrenia. New York: Oxford University Press; 2015. https://doi.org/10.1093/med/9780199363315.003.0044.
Agar MR, Rowett D, McCaffey NM. Efficacy of oral risperidone, haloperidol, or placebo for symptoms of delirium among patients in palliative care: a randomized clinical trial. JAMA Intern Med. 2017;177(1):34–42. https://doi.org/10.1001/jamainternmed.2016.7491. PMID: 27918778
Stiefel F, Fainsinger R, Bruera E. Acute confusional states in patients with advanced cancer. J Pain Symp Manag. 1992;7:94–8. PMID: 157329
Olofsson SM, Weitzner MA, Valentine AD, Baile WF, et al. A retropspective study of the psychiatric management and outcome of delirium in the cancer patient. Supp Care Cancer. 1996;4:351–94. PMID: 8883228
LeGrand SB. Delirium in palliative medicine: a review. J Pain Symp Manag. 2012;44:583–94. https://doi.org/10.1016/j.jpainsymman.2011.10.013. PMID: 22682074
Caraceni A, Simonetti F. Palliating delirium in patients with cancer. Lancet Oncol. 2009;10:164–72. https://doi.org/10.1016/S1470-2045(09)70018-X. PMID: 19185834
McDaniel IS, Musselman DL, Porter MR, Reed DA, et al. Depression in patients with cancer: diagnosis, biology, and treatment. Arch Gen Psychiatry. 1995;52:89–99. PMID: 7848055
Potash M, Breitbart W. Affective disorders in advanced cancer. Hematol Oncol North Am. 2002;16:671–700. PMID: 12170575
Chochinov HM, Tataryn D, Clinch JJ, Dudgeon D. Will to live in the terminally ill. Lancet. 1999;354:816. https://doi.org/10.1016/S0140-6736(99)80011-7. PMID: 10485723
Hinton J. Which patients with terminal cancer are admitted from home care? Palliat Med. 1994;8:197. https://doi.org/10.1177/026921639400800303. PMID: 7952370
Tiernan E, Casey P, O'Boyle C, Birkbeck G, et al. Relations between desire for early death, depressive symptoms and antidepressant prescribing in terminally ill patients with cancer. JRS Med. 2002;95(8):386-390. PMID:12151487 PMCID:PMC1279962
Cipriani A, Furukawa TA, Salanti G, Geddes JR, et al. Comparative efficacy and acceptability of 12 new-generation antidepressants: a multiple-treatments meta-analysis. Lancet. 2009;373(9665):746–58. https://doi.org/10.1016/S0140-6736(09)60046-5.
Theobald DE, Kish KL, Holtsclaw E, Donaghy K, et al. A open label pilot study of citalopram for depression and boredom in ambulatory cancer patients. Palliat Support Care. 2003;1:71–7. PMID: 16594290
Dauchy S, Dolbeault S, Reich M. Depression in cancer patients. EJC Suppl. 2013:205–15. https://doi.org/10.1016/j.ejcsup.2013.07.006
Lyons KS, Bennett JA, Nail LM, Fromme EK, et al. The role of patient pain and physical function on depressive symptoms in couples with lung cancer: a longitudinal dyadic analysis. J Fam Psychol. 2014;28(5):692–700. https://doi.org/10.1037/fam0000017. Epub 2014 Aug 4
Fisch MJ, Loehrer PJ, Kristeller PS, et al. Fluoxetine versus placebo in advanced cancer outpatients: a double-blinded trial of the Hoosier oncology group. J Clin Ocolo. 2003;21(10):1937–43. https://doi.org/10.1200/JCO.2003.08.025. PMID: 12743146
McClean S, Sheehy-Skeffington B, O'Leary N, O'Gorman A. Pharamacological management of co-morbid conditions at the end of life: is less more? Ir J Med Sci. 2013;182:107–12. https://doi.org/10.1007/s11845-012-0841-6. PMID: 22843427
Richelmann RP, Kryzanowski MK, O'Carroll A, Zimmermann C. Symptom and medication profiles among cancer patients attending a palliative care clinic. Support Care Cancer. 2007;15:1407–12. https://doi.org/10.1007/s00520-007-0253-8. PMID: 17429699
Ellershaw J. Care for the dying: what a difference an LCP makes! Palliat Med. 2007;21:365–8. https://doi.org/10.1177/0269216307081117. PMID: 17901095
Currow DC, Stevenson JP, Abernathy AP, Plummer J, et al. Prescribing in palliative care as death approaches. J Am Geriatr Soc. 2007;55:590–5. https://doi.org/10.1111/j.1532-5415.2007.01124.x. PMID: 17397439
Kierner KA, Weixler D, Masel EK, Gartner V, et al. Polypharmacy in the terminal stage of cancer. Supp Care Cancer. 2016;24(5):2067–74. https://doi.org/10.1007/s00520-015-3007-z. Epub 2015 Nov 5. PMID: 26542274 DOI: 10.1007/s00520-015-3007-z
Holland RC, Romano SI, Hollingstein JH, Tepner RG, et al. A controlled trial of fluoxetine and desipramine in depressed women with advanced cancer. Psychopharmacology. 1998;7(4):291–300. https://doi.org/10.1002/(SICI)1099-1611(199807/08)7:4<291::AID-PON361>3.0.CO;2-U. PMID: 9741068
Moss EL, Simpson JS, Pelletier G, Forsyth P. An open-label study of the effects of bupropion SR on fatigue, depression and quality of life of mixed-site cancer patients and their partners. Psycho-Oncology. 2006;15(3):259–67. https://doi.org/10.1002/pon.952. PMID: 16041840
Theobald DE, Ki K, Holtsclaw E, Doughy F, et al. An open-label, cross-over trial of mirtazapine [15 & 230 mg.] in cancer patients with pain and other distressing symptoms. J Pain Sympt Manage. 2002;23:442–7. PMID: 12007762
Kim SW, Shin IS, Kim JM, Kim YC, et al. Effectiveness of mirtazapine for nausea and insomnia in cancer patients with depression. Psychiatry Clin Neurosci. 2008 ;62(1):75–83. doi: https://doi.org/10.1111/j.1440-1819.2007.01778.x. PMID: 18289144 DOI: 10.1111/j.1440-1819.2007.01778.x.
Cankurtaran ES, Ozalp E, Soygur H, Akbiyik DI, et al. Mirtazapine improves sleep and lowers anxiety and depression in cancer patients: superiority over imipramine. Supp Care Cancer. 2008;16(11):1291–8. https://doi.org/10.1007/s00520-008-0425-1. Epub 2008 Feb 26. PMID: 18299900 DOI: 10.1007/s00520-008-0425-
Inglewicz A, Morrison K, Nelesen RA, Tingting Z, et al. Ketamine for the treatment of depression in patients receiving hospice care: a retrospective chart review of thirty-one cases. Psychosomatics. 2015;56(4):329–37. https://doi.org/10.1016/j.psym.2014.05.005. PMID: 25616995 PMCID: PMC4308579
Murrough JW, Iosifescu DV, Chang LC, Al Jurdi RK, et al. Antidepressant efficacy of ketamine in treatment-resistant major depression: a two-site randomized controlled trial. Am J Psychiatry. 2013;170(10):1134–42. https://doi.org/10.1176/appi.ajp.2013.13030392. PMID: 23982301 PMCID: PMC3992936
Murrough JW, Perez AM, Pillemer S, Stern J, et al. Rapid and longer-term anti-depressant effects of repeated ketamine infusions in treatment-resistant major depression. Biol Psychiatry. 2013;74(4):250–6. https://doi.org/10.1016/j.biopsych.2012.06.022. PMID: 22840761 PMCID: PMC3725185
Zanicotti CG, Perez D, Glue P. Mood and pain response to repeat dose intramuscular ketamine in a depressed patient with advanced cancer. J Palliat Med. 2012;15:400. https://doi.org/10.1089/jpm.2011.0314. PMID: 22468772
Stefanczyk-sapieha L, Oneschuk D, Demas M. Intravenous ketamine “burst” for refractory deression in a patient with advanced cancer. J Palliat Med. 2008;11:1268. https://doi.org/10.1089/jpm.2008.9828. PMID: 19021495
Yang C, Zhou ZQ, Yang JJ. Be prudent of ketamine in treating resistent depression in patients with cancer. J Palliat Med. 2011;14:537. https://doi.org/10.1089/jpm.2010.0525. PMID: 21592028
Thangathural D, Roby J, Roffey P. Treatment of resistent depression in patients with cancer with low doses of ketamine and desiprimine. J Palliat Med. 2010;13:235. https://doi.org/10.1089/jpm.2009.0312. PMID: 20178430
Kollmar R, Markovic K, Thurauf SH, et al. Ketamine followed by memantine for the treatment of major depression. Aust N Psychiatry. 2008;42:170. https://doi.org/10.1080/00048670701787628. PMID: 18197514
Irwin SA, Inglewicz A, Nelesen RA, Lo JY, et al.. Daily oral ketamine for the treatment of depression and anxiety in patients receiving hospice care: a 28-day open-label proof-of-concept trial. J Palliat Med. 2013;16(8):958–65. doi: https://doi.org/10.1089/jpm.2012.0617. Epub 2013 Jun 27. PMID: 23805864 PMCID: PMC3717203 DOI: 10.1089/jpm.2012.0617.
Jafarinia M, Afarideh M, Tafakhori A, Arbabi M, et al. Efficacy and safety of oral ketamine versus diciofenac to alleviate mild to moderate depression in chronic pain patients: a double-blind, randomized, controlled trial. J Affect Disord. 2016;204:1. https://doi.org/10.1016/j.jad.2016.05.076. PMID: 27317968
Singh JB, Fedgchin M, Daly EJ, DeBoer P, et al. A double-blind, randomized, placebo-controlled, dose-frequency study of intravenous ketamine in patients with treatment-resistant depression. Am J Psychiatry. 2016;173:816. https://doi.org/10.1176/appi.ajp.2016.16010037. PMID: 27056608
Berman RM, Pereira J, Cappiello A, Anand A, et al. Anti-depressant effects of ketamine and anxiety in patients needing hospice care. Biol Psychiatry. 2000;47(4):351–4. PMID: 10686270
Irwin SA, Inglewicz A. Oral ketamine for the rapid treatment of depression and anxiety patients receiving hospice care. J Palliat Med. 2010;24(4):903–8. https://doi.org/10.1089/jpm.2010.9808. PMID: 20636166 PMCID: PMC3120058
Miller AH, Maletic V, Raison CL. Inflammation and its discontents: the role of cytokins in the pathophysiology of major depression. Biol Psychiatry. 2008;65(9):732–41. https://doi.org/10.1016/j.biopsych.2008.11.029. PMID: 19150053 PMCID: PMC2680424
Costa D, Magos I, Toma T. Efficacy and safety of mianserin in the treatment of depression in women with cancer. Acta Psychiatr Scand Suppl. 1985;320:85–92. PMID: 3901675
Holland RC, Morrow GR, Schmale A, et al. A randomized clinical trial of alprazolam versus progressive muscle realization in cancer patients with anxiety and drepressive symptoms. J Clin Oncol. 1991;9:1004–11. https://doi.org/10.1200/JCO.1918.104.22.1684. PMID: 2033413
Pezella G, Moslinger-Gehmayr R, Contu A. Treatment of depression in patients with breast cancer: a comparison between paroxetine and amitriptyline. Breast Cancer Res Treat. 2001;701:1–10. PMID: 11766999
Razavi D, Allilaire JF, Smith M, et al. The effect of fluoxetine on anxiety and depressive symptoms in cancer patients. Acta Psychiatr Scand. 1996;94:205–10. PMID: 8891089
van Heeringen K, Zivkov M. Pharmacological treatment of depression in cancer patients. A placebo-controlled study of mianserin. Br J Psychiatry. 1996;169:440–3. PMID: 8894194
Murlow CD, William JW Jr, Chiquette E, Aquilar C, et al. Efficacy of newer medications for treating depression in primary care patients. Am J Med. 2000;108:54. PMID: 11059441
Hansen RA, Gartlehner G, Lohr KN, Gaynes BN, et al. Efficacy and safety of second-generation antidepressants in the treatment of major depressive disorder. Ann Intern Med. 2005;143:415. PMID: 16172440
Attard A, Ranjith G, Taylor D. Alternative route to oral antidepressant therapy: case vignettes and literature review. Psychopharmacol. 2010;24(4):449–54. https://doi.org/10.1177/0269881109102545. PMID: 19264816
Callari A, Mauri M, Miniati M, Mancino M, et al. Treatment of depression in patients with breast cancer: a critical review. Tumori. 2013;99(5):623–33. https://doi.org/10.1700/1377.15313.
Jacobsen PB, Donovan KA, Swaine ZN, Watson IS. Management of Anxiety and Depression in adult Cancer patients: toward an evidenced-based approach #89. Oncology:1561–88. https://link.springer.com/chapter/10.1007%2F0-387-31056-8_89.
Carr D, Goudas L, Lawrence D, et al. Management of cancer symptoms, pain, depression, and fatigue. Evidenced report/technology assessment no. 61. AHRQ publication no 02-E032. Rockville: Agency for Health Care Research and Quality; 2002. PMID: 12187571 PMCID: PMC4781249
Kissane DW. The contribution of demoralization to end of life decision making. Hast Cent Rep. 2004;34(4):21–31. PMID: 15379099
Schuman-Olivier Z, Bendel DH, Forstein M, Price BH. The use of palliative sedation for existential distress: a psychiatric perspective. Harv Rev Psychiatry. 2008;16(6):339–51. https://doi.org/10.1080/10673220802576917. PMID: 19085388
Fitzgerald P, Lo C, Li M, Gagliese L, et al. The relationship between depression and physical symptom burden in advanced cancer. BMJ Supp Palliat Care. 2015;5(4):381–8. https://doi.org/10.1136/bmjspcare-2012-000380. Epub 2013 Aug 6. PMID: 24644172 DOI: 10.1136/bmjspcare-2012-000380
Jackson V, Block S. Use of psycho-stimulants in palliative care. 2nd ed: End of Life/Palliative Education Resource Center. Medical College of Wisconcin. https://www.capc.org/fast-facts/.
Rozans M, Dreisbach A, Lertora JJ, Kahn MJ. Palliative uses of methylphenidate in patients with cancer: a review. J Clin Oncol. 2002;20(1):335–99. https://doi.org/10.1200/JCO.2002.20.1.335. PMID: 11773187
Dean S, George R. A place for psychostimulants in palliative care. J Palliat Care. 2002;18:196–9. PMID: 12418371
Mansand PS, Tesar GE. Use of stimulants in the medically ill. Psychitr Clin North Am. 1996;19(3):515–47. PMID: 8856815
Macleod AD. Methylphenidate in terminal depression. J Pain Symptom Manag. 1998;16(3):193–8. PMID: 9769622
de Oliveira Campos MP, Riechelmann R, Martins LC, Hassan BJ, et al. Guarana (Paullinia cupana) improves fatigue in breast cancer patients undergoing systemic chemotherapy. J Altern Complement Med. 2011;17(6):505–12. https://doi.org/10.1089/acm.2010.0571. Epub 2011 May 25. PMID: 21612429
Olin J, Masand P. Psychostimulants for depression in hospitalized cancer patients. Psychossomatics. 1996;37(1):57–62. https://doi.org/10.1016/S0033-3182(96)71599-2. PMID: 1381072 PMID: 8600496
Bruera E, Fainsinger R, MacEachern T, Hanson J. The use of methylphenidate in patients with incident cancer pain receiving regular opiates. A preliminary report. Pain. 1992;50(1):75–7. PMID: 1381072
Gagnon B, Low G, Schreier G. Methylphenidate hydrochloride improves cognitive function in patients with advanced cancer and hypoactive delirium: a prospective clinical study. J Psychiatry Neurosci. 2005;30(2):100–7. PMID: 15798785 PMCID: PMC551162
Prommer E. Methylphenidate: established and expanding roles in symptom management. Am J Hosp Palliat Care. 2012;29(6):483–90. https://doi.org/10.1177/1049909111427029. Epub 2011 Dec 4. PMID: 22144657 DOI: 10.1177/1049909111427029
Rifkin A, Reardon G, Siris S, Karagji B, et al. Trimipramine in physical illness with depression. J Clin Psychiatry. 1985;46(2 Pt 2):4–8. PMID: 3881418
Centeno C, Sanz A, Cuervo MA, Ramos D, et al. Multicentre, double-blind, randomized placebo-controlled clinical trial on the efficacy of methylphenidate on depressive symptoms in advanced cancer patients. BMJ Support Palliat Care. 2012;2(4):328–33. https://doi.org/10.1136/bmjspcare-2011-000093. Epub 2012 Jun 1. PMID: 24654216 DOI: 10.1136/bmjspcare-2011-000093
Homsi J, Walsh D, Nelson KA, LeGrand S, et al. Methylphenidate for depression in hospice practice: a case series. Am J Hosp Palliat Care. 2000;17(6):393–8. https://doi.org/10.1177/104990910001700610. PMID: 11886041
Breitbart W, Alici Y. Pharmacologic treatment options for cancer-related fatigue: current state of clinical research. Clin J Oncol Nursing. 2008;1215(Suppl 1):27–36. https://doi.org/10.1188/08.CJON.S2.27-36. PMID: 18842522
deCosta MV, Trufelli DC, Santos J, Campos MP, et al. Effectiveness of guaraná (Paullinia cupana) for postradiation fatigue and depression: results of a pilot double-blind randomized study. J Altern Complement Med. 2009;15(4):431–3. https://doi.org/10.1089/acm.2008.0324. PMID: 19388866
Kienle GS, Kiene H. Complementary cancer therapy: a systematic review of prospective clinical trials on anthroposophic mistletoe extracts. Eur J Med Res. 2007;12(3):103–19. PMID: 17507307
Kienle GS, Kiene H. Review article: influence of Viscum album L (European mistletoe) extracts on quality of life in cancer patients: a systematic review of controlled clinical studies. Integr Cancer Ther. 2010;9(2):142–57. https://doi.org/10.1177/1534735410369673. Epub 2010 May 18. PMID: 20483874
Kienle GS, Glockmann A, Schink M, Kiene H. Viscum album L. extracts in breast and gynaecological cancers: a systematic review of clinical and preclinical research. J Exp Clin Cancer Res. 2009;28:79. https://doi.org/10.1186/1756-9966-28-79. PMID: 19519890 PMCID: PMC2711058
American Psychiatric Association. Diagnostic and statistical manual of mental disorders. Fifth ed. Lake St. Louis: APA Publishing; 2013. http://dsm.psychiatryonline.org/doi/book/10.1176/appi.books.9780890425596
Clarke DM, Kissane DW. Demoralization its phenomenology and importance. Aust N Z Psychiatry. 2002;36:733–42. https://doi.org/10.1046/j.1440-1614.2002.01086.x. PMID: 12406115
Coda BA, Mackie A, Jill HF. Influence of alprazolam on opiod analgesics and steady state during morphione infusion. Pain. 1992;50(3):309–16.
Mangelli L, Fava GA, Grandi GL, et al. Assessing demoralization and depression in the setting of medical disease. J Clin Psychiatry. 2005;66:391–4. PMID: 15766307
Maguire P, Lee E, Bevington D, et al. Psychiatric problems in the first year after mastectomy. BMJ. 1978;1:963–5. PMID: 565239 PMCID: PMC1603831
Peck A, Bowland J. Emotional reactions to radiation treatment. Cancer. 1977;40:180–4. PMID: 880549
Alter C, Pelovitz D, Axelrod A, Goldenberg B, et al. The identification of PTSD in cancer survivors. Psychosomatics. 1996;37:137–43. https://doi.org/10.1016/S0033-3182(96)71580-3. PMID: 8742542
Sykes N, Thorns A. Sedative use in the last week of life and the implications for end-of-life decision making. Arch Intern Med. 2003;163(3):341–4. PMID: 12578515
Good PD, Ravenscroft PJ, Cavenagh J. Effects of opioids and sedatives on survival in an Australian inpatient palliative care population. Intern Med J. 2005;35(9):512–7. https://doi.org/10.1111/j.1445-5994.2005.00888.x. PMID: 16105151
Good PD, Cavenagh JD, Currow DC, Woods DA, et al. What are the essential medications in pallative care? - a survey of Australian palliative care doctors. Aust Fam Physician. 2006;35(4):261–4. PMID: 16642246
Key RG. Psychiatric care of lung cancer patients. Oncology (Williston Park). 2015;29(3):195–7. PMID: 25772455
Fernandez F, Adams F, Holmes VF. Analgesic effect of alprozolam in patients with chronic, organic pain of malignant origin. J Clin Psychopharmacol. 1987;7(3):167–9. PMID: 3597802
National Cancer Institute. Nausea and vomiting PDQ. Health professional. www.cancer.gov/cancertopics/pdq/supportivecare/nausea/HealthProfessional.
Greenberg DB, Surman OS, Clarke J, Baer L. Alprazolam for phobic nausea and vomiting related to cancer chemotherapy. Cancer Treat Rep. 1987;71(3):549–50. PMID: 3567983
Mori K, Saito Y, Tominaga K. Antiemetic efficacy of alprazolam in the combination of metoclopramide plus methylprednisone. Double-blind randomized crossover study with patinets with cisplatic-induced emisis. Am J Clin Oncol. 1993;16(4):338–41. PMID: 8392288
Potanovich LM, Pisters KM, Kris MG, Tyson LB, et al. Midazolam in patients receiving anticancer chemotherapy and anti-emetics. J Pain Symptom Manag. 1993;8(8):519–24. PMID: 7963777
Bishop JF, Oliver IN, Wolf MM, Matthews JP, et al. Lorazepam: a randomized double-blind crossover study of a new antiemetic in patients receiving cytoxin chemotherapy and prochlorpersine. J Clin Oncol. 1984;2(6):691–5. https://doi.org/10.1200/JCO.1922.214.171.1241. PMID: 6374058
Hasselaar JG, Reuzel RP, Verhagen SC, de Graff A, et al. Improving prescription in palliative sedation: compliance with Dutch guidelines. Arch Intern Med. 2007;167(11):1166–71. https://doi.org/10.1001/archinte.167.11.1166. PMID: 17563025
Reuzel RP, Hasselaar GJ, Vissers KC, der Wilt V, et al. Inappropriateness of using opiods for end-stage palliative sedation: a Dutch study. Palliat Med. 2008;22(5):641–6. https://doi.org/10.1177/0269216308091867. PMID: 18612030
Cowan JD, Palmer TW. Terminal sedation in palliative medicine--definition and review of the literature. Am J Hosp Palliat Care. 2008;22(5):403–7. PMID: 11585266
Maida V, Ennis M, Irani S, Corbo M, et al. Adjunctive nabilone in cancer pain and symptom management: a prospective observational study using propensity scoring. J Support Oncol. 2008;6(3):119–24.
Pilkington K, Kirkwood G, Rampes H, Fisher P, et al. Homeopathy for anxiety and anxiety disorders: a systematic review of the research. Homeopathy. 2006;95(3):151–62.
Su CX, Wang LQ, Grant SJ, Liu JP. Chinese herbal medicine for cancer-related fatigue: a systematic review of randomized clinical trials. Complement Ther Med. 2014;22(3):567–79. https://doi.org/10.1016/j.ctim.2014.04.007. Epub 2014 May 5
Kienle GS, Glockmann A, Schink M, Kiene H. Viscum album L. extracts in breast and gynaecological cancers: a systematic review of clinical and preclinical research. J Exp Clin Cancer Res. 2009;28:79. PMID: 17507307
Gurevich M, Devins GM, Rodin GM. Stress response syndromes and cancer: conceptual and assessment issues. Psychosomatics. 2002;43:259–81. https://doi.org/10.1176/appi.psy.43.4.259. PMID: 12189252
Pitman RK, Lanes DM, Williams SK, Guillaume JL, et al. Psychophysiologic assessment of post-traumatic stress disorder in breast cancer patients. Psychosomatics. 2001;42:133–40. https://doi.org/10.1176/appi.psy.42.2.133. PMID: 11239126
Stark D, Kiely M, Smith A, Morley S, et al. Reassurance and the anxious cancer patient. Br J Cancer. 2004;91:893–9. https://doi.org/10.1038/sj.bjc.6602077. PMID: 15292934 PMCID: PMC2409992
Bottomley DM, Hanks GW. Subsuctaneous, idazolam infusion in palliative care. J Pain Symptom Manag. 1990;5:259–61. PMID: 2384705
de Souza E, Jepson BA. Midazolam in terminal care. Lancet. 1988;1:67–8. PMID: 2891939
Bleasel MD, Peterson GM, Dunne PF. Plasma concentrations of midazolam during continuous subcutaneous administration in palliative care. Palliat Med. 1994;8:231–6. https://doi.org/10.1177/026921639400800307. PMID: 7952373
Breitbart W, Rosenfeld B, Gibson C, Pessin H, et al. Meaning centered group psychotherapy for patients with advanced cancer: a pilot randomized controlled trial. Psyhco-Oncology. 2010;19:21–8. https://doi.org/10.1002/pon.1556. PMID: 19274623 PMCID: PMC3648880
Breitbart W, Popito S, Rosenfeld B, Vickers AJ, et al. Pilot randomized controlled trial of individual meaning-centered psychotherapy for patients with advanced cancer. J Clin Oncol. 2012;30(12):1304–9. https://doi.org/10.1200/JCO.2011.36.2517. PMID: 22370330 PMCID: PMC3646315
Spiegel D, Bloom JR, Yalom I. Group support for patients with metastic cancer: a randomized outcome study. Arch Gen Psychiatry. 1981;38:527. PMID: 7235853
Spiegel D, Bloom JR. Group therapy and hypnosis to reduce breast cancer carcinoma pain. Psyhcosom Med. 1983;45:333. PMID: 6622622
Massie MJ, Holland JC, Straker N. Psychotherapuetic interventions. In: Holland JC, Rowland JH, editors. Handbook of psycho-oncology: psychological Care of the Patient with Cancer. New York: Oxford University Press; 1989. p. 455.
Chuckinov HM. Dignity-conserving care-a new model for palliative care: helping the patient feel valued. JAMA. 2002;287(17):2253–60. PMID: 11980525
Bausewein C, Booth S, Gyseis M, Higginson I. Non-pharmacological interventions for breathlessness in advanced stages of malignant and non-malignant diseases. Conchrane Database Syst Rev. 2008;2:CD005623. https://doi.org/10.1002/14651858.CD005623.pub2. PMID: 18425927
Block SD. Assessing and managing depression in the terminally ill patient. ACP-ASIM end-of-life consensus panel. American College of Physicians - American Society of Internal Medicine. Ann Intern Med. 2000:132–209. PMID: 10651602
Solomon BK, Wilson KG, Henderson PR, Poulin PA, et al. Loss of dignity in severe chronic obstructive pulmonary disease. J Pain Symptom Manag. 2016;51(3):529–37. https://doi.org/10.1016/j.jpainsymman.2015.11.007. Epub 2015 Nov 24. PMID: 26620235
Chochinov HM. Dignity-conserving care: a new model for palliative care. JAMA. 2002;287:22253–60. PMID: 11980525
Chuckinov HM, Hack T, Hassard T, et al. Dignity therapy: a novel psychotherapeutic intervention for patients nearing death. J Clin Oncol. 2005;23:5520–5. https://doi.org/10.1016/j.jpainsymman.2007.12.018. PMID: 18579340
Montross L, Winters KD, Irwin SA. Dignity therapy implementation in a community-based hospice setting. J Palliat Med. 2011;14:729. https://doi.org/10.1089/jpm.2010.0449. PMID: 21548823 PMCID: PMC3120093
Chochinov HM, Kristainson LJ, Breitbart W, McClements S, et al. Effect of dignity therapy on distress and end-of-life experience in terminally ill patients: a randomized controlled trial. Lancet Oncol. 2011;12:753. https://doi.org/10.1016/S1470-2045(11)70153-X. PMID: 21741309 PMCID: PMC3185066
Vuksanovic D, Green HJ, Duck M, Morrissey SA. Dignity therapy and life review for palliative care patients: a randomized controlled trial. J Pain Symptom Manag. 2017;53:162. https://doi.org/10.1016/j.jpainsymman.2016.09.005. PMID: 27810568
Martinez M, Arantzamedi M, Belar A, et al. ‘Dignity therapy,’ a promising intervention in palliative care: a comprehensive literature review. Palliat Med. 2017;31:492. https://doi.org/10.1177/0269216316665562. PMID: 27566756 PMCID: PMC5405836
Greenstein M, Breitbart W. Cancer and the experience of meaning: a group psychotherapy program for people with cancer. Am J Psychother. 2000;54:486. PMID: 11109133
Keall RM, Clayton JM, Butlow PN. Therapeutic life review in palliative care: a systematic review of qualitative evaluations. J Pain Symptom Manag. 2015;49:747. https://doi.org/10.1016/j.jpainsymman.2014.08.015. PMID: 25261637
Breitbart W, Gibson C, Poppito S, Berg A. Psychotherapeutic interventions at the end of life: a focus on meaning and spirituality. Can J Psychiatr. 2004;49:366–72. https://doi.org/10.1177/070674370404900605. PMID: 15283531
Fonzo-Christie C, Vukasovic C, Wasilewski-Rsaca AF, Bonnabry P. Subcutaneous administration of drugs in the elderly: survey of practice and systematic literature review. Palliat Med. 2005;19:208–19. https://doi.org/10.1191/0269216304pm1006oa. PMID: 15920935
Plaskota M, Lucas C, Evans R, Cook K, Pizzoferro K, et al. A hypnotherapy intervention for the treatment of anxiety in patients with cancer receiving palliative care. Int J Palliat Nurs. 2012;18(2):69–75. https://doi.org/10.12968/ijpn.2012.18.2.69. PMID: 22399044
Galfin JM, Watkins ER, Harlow T. A brief guided self-help intervention for psychological distress in palliative care patients: a randomized controlled trial. Palliat Med. 2012;26(3):197–205. https://doi.org/10.1177/0269216311414757. PMID: 21807750
Sharpe M, Strong V, Allen K, Rush R, et al. Management of major depression in outpatients attending a cancer center: a preliminary evaluation. Br J Cancer. 2004;90(2):310–3.
Greer S, Moorery S, Baruch JD, Watson M, et al. Adjuvant psychological therapy for patients with cancer: a prospective randomized trial. BMJ. 1992;304:675–80. PMID: 1472184 PMCID: PMC1881503
McQuellon RP, Wells M, Hoffman S, Craven B, et al. Reducing distress in cancer patients with an orientation program. Psycho-Oncology. 1998;7:207–17. https://doi.org/10.1002/(SICI)1099-1611(199805/06)7:3<207::AID-PON304>3.0.CO;2-T. PMID: 9638782
Chen J, Chen C, Zhi S. Retrospective comparison of cognitive behavioral therapy and symptom-specific medication to treat anxiety and depression in throat cancer patients after laryngectomy. Shanghai Arch Psychiatry. 2014;26(2):95–100. https://doi.org/10.3969/j.issn.1002-0829.2014.02.006.
Barseveck AM, Sweeney C, Haney E, Chung E. A systematic qualitative analysis of psychoeducational interventions for depression patients with cancer. Oncol Nurs Forum. 2002;29:73–84. https://doi.org/10.1188/02.ONF.73-87. PMID: 11817494
Devine EC, Westlake SK. The effects of psychoeducational care provided to adults with cancer: meta-analysis of 116 studies. Oncol Nursing Forum. 1995;22:1369–81. PMID: 8539178
Sheard T, McGuire P. The effect of psychological interventions on axiety and depression in cancer patients: results of two meta-analyses. Br J Cancer. 1999;80:1770–80. https://doi.org/10.1038/sj.bjc.6690596. PMID: 10468295 PMCID: PMC2363129
Ell K, Xie B, Quon B, Quinn DI, et al. Randomized controlled trial of collaborative care management of depression among low-income patients with cancer. J Clin Oncol. 2008;26(27):4488–96. https://doi.org/10.1200/JCO.2008.16.6371.
Osborn RI, Demoncada AC, Feurestein M. Psychosocial interventions for depression and quality of life in cancer survivors: meta-analysis. Int J Psychiatry Med. 2006;36:13–34. https://doi.org/10.2190/EUFN-RV1K-Y3TR-FK0L. PMID: 16927576
Krebber AM, Jansen F, Witte BI, Cuijpers P, et al. Stepped care targeting psychological distress in head and neck cancer and lung cancer patients: a randomized, controlled trial. Ann Oncol. 2016;27(9):1754–60. https://doi.org/10.1093/annonc/mdw230. Epub 2016 Jun 10. DOI: 10.1093/annonc/mdw230, PMID: 27287209
Kwiatkowski F, Bignon YJ. To test the impact of hypnotherapy upon immunity and circadian rhythms among palliative cancer patients: a promising goal? Pathol Biol. 2007;55(3–4):186–93. https://doi.org/10.1016/j.patbio.2006.12.006. Epub 2007 Mar 27 PMID: 17391864
Check DK, Samuel CA, Rosenstein DL, Dusetzina SB. Investigation of racial disparities in early supportive medication use and end-of-life care among Medicare beneficiaries with stage IV breast cancer. J Clin Oncol. 2016;34(19):2265–70. https://doi.org/10.1200/JCO.2015.64.8162. Epub 2016 May 9. PMID: 27161968 PMCID: PMC4962709
Balyn RE, Rubin JE. Psychiatric treatment challenges at the end of life. Clinical View. 2003;1(2):3–5. http://www.aagponline.org/clientuploads/Clinical%20View/clinicalView_v2n1.pdf
de Souza BF, Pires FH, Dewulf Nde L, Inocenti A, et al. Patients on chemotherapy: depression and adherence to treatment. Rev Esc Enferm USP. 2013;47(1):61–8. PMID: 23515804
Wang CW, Chow AY, Chan CL. The effects of life review interventions on spiritual well-being, psychological distress, and quality of life in patients with terminal or advanced cancer: a systematic review and metaanalysis of randomized controlled trials. Palliat Med. 2017;31(10):883–94. https://doi.org/10.1177/0269216317705101. PMID: 28488923
Scheffold K, Schulz-Kinderman F, Rosenberger C, Wollbrueck D, et al. Pilot results of the German managing concern and living meaningfully (CALM) RCT: a brief individual psychotherapy for advanced cancer patients. Psycho-Oncology. 2014;23(28) Doi:10111/j.1099-1611.2014.3693
Miller DK, Chibnall JT, Videen SD, Duckro PN. Supportive-affective group experience for persons with life-threatening illness: reducing spirtual, psychological, and death-related distress in dying patients. J Palliat Med. 2005;2(8):333–43. https://doi.org/10.1089/jpm.2005.8.333. PMID: 15890044
Steinhauser KE, Alexander SC, Byock IR, George LK, et al. Do preparation and life completion discussions improve functioning and quality of life in seriously ill patients? Pilot randomized control trial. J Palliat Med. 2008;9(11):1234–40. https://doi.org/10.1089/jpm.2008.0078. PMID: 19021487
Johnson RJ. Cost-effectiveness of mental health services for persons with a dual diagnosis: a literature review and the CCMHCP. The cost-effectiveness of community mental health Care for Single and Dually Diagnosed Project. J Subst Abus Treat. 2000;18(2):119–27. PMID: 10716095
Kvale E, Balentine A, Walker E. Depression and fatigue. New York: Oxford University Press; 2015.
NCCN. Clinical Practice Guidelines in Oncology. Distress management. Version 3. 2015. National Comprehensive Cancer Network. Htpp://https://www.nccn.org/professionals/physician_gls/pdf/distress.pdf.
The Author wishes to acknowledge Ms. Lore Lagrone for materials and encouragement. The Author also gratefully recognizes Ms. Carla Miller research study nurse and Ms. Liliana Vallejo research coordinator for the review of the diagrams and proof of concept. The Author also thanks Ms. Jacqueline Ramey freelance copy-editor for proofing and copyediting.
Support has been provided by the U.S. Army and University of Texas-MD Anderson Cancer Center. The funding bodies had no involvement with the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
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The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
RJJ is the sole author and accepts sole responsibility for content. The author read and approved the final manuscript.
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Johnson, R.J. A research study review of effectiveness of treatments for psychiatric conditions common to end-stage cancer patients: needs assessment for future research and an impassioned plea. BMC Psychiatry 18, 85 (2018). https://doi.org/10.1186/s12888-018-1651-9
- End stage cancer care
- Adjustment disorder
- Literature review
- Research needs assessment