1. Introduction
Disasters are massive disruptions to the functioning of a community or society due to hazardous events in conjunction with conditions and exposure that exceed their capacity [1,2,3] (Table 1). Globally, disasters are increasing in both complexity and magnitude due to a variety of mixed natural or human-made causes and increased vulnerabilities [4,5]. The Sendai Framework for Disaster Risk Reduction outlines four priorities for action to prevent and reduce disaster risks: (i) understanding disaster risk; (ii) strengthening disaster risk governance to manage disaster risk; (iii) invention in disaster reduction for resilience; and (iv) enhancing disaster preparedness [6]. With regard to health systems worldwide, the World Health Organization (WHO) recommends investing in a comprehensive all-hazards emergency preparedness framework taking into account the full scope of disasters [7], since the scale and severity of a disaster is strongly impacted by the socio-cultural and geopolitical setting of the affected population and by the type of threat [8].
In disaster contexts, with the surge of deaths and pressure on health services, the importance of hospice and palliative care (HPC) and the ethical obligation to provide comprehensive end-of-life care (EOLC) has been widely recognized, especially since the establishment of a WHO working group in 2016 to develop guidelines for HPC provision in humanitarian emergencies and crises of all types [8]. Although people affected by different types of emergencies in different settings require different kinds of care, according to the WHO, seven palliative care (PC) principles apply to any kind of emergency [8]. These PC principles are widely considered a key component of comprehensive HPC under adverse circumstances [3,8,9,10].
Healthcare systems are overall doubtlessly strained during disasters and providing or maintaining HPC services in the event of a disaster can be particularly challenging. However, a lack of empirical evidence with regard to HPC-specific barriers, challenges, and strategies in times of disasters has been reported, as well as little synthesis of existing evidence [11,12], likely due to limited prioritization and the primacy of lifesaving during disasters, data collection challenges, ethical considerations, and lack of resources and awareness. Systematic analyses of existing literature are essential to identify knowledge gaps and to anticipate the impacts of hazards in order to develop disaster-resilient models of HPC. Accordingly, the present review aims to provide a synthesis of the current literature, addressing the impact of disasters on the provision of HPC by identifying, among others, barriers, care needs, practices, and strategies.
2. Methods
The methodology adopted was a systematic literature review in accordance with the PRISMA-guidelines [13].
2.1. Eligibility Criteria
This systematic review included articles that focused on the impact of disasters on the provision of HPC and the disaster preparedness initiatives in the field. Further eligibility criteria for the selection of studies were: (i) peer-reviewed articles addressing HPC during disasters, (ii) original research papers, (iii) published between 2001 and February 2023, and (iv) in English. The start date was intentionally set to capture the post-9/11 period. All study designs (quantitative, qualitative, mixed- or multi-method) were eligible for inclusion. Studies were excluded if they (i) did not report the impact of disasters on HPC or (ii) were not original and peer-reviewed research papers (e.g., editorials, commentaries, opinions, policy papers).
2.2. Information Sources and Search Strategy
Within this systematic review, a comprehensive database search was performed including quantitative, qualitative, and mixed-method studies. The following databases were searched: (i) MEDLINE, (ii) CINAHL, (iii) APA PsycInfo, (iv) SocINDEX and (v) APA PsycArticles. The literature search was conducted using medical subject headings (MeSH 2022) and an additional keyword strategy. Due to the diffuse nature of this subject and its terminology, diverse MeSH terms and relevant text-words were used.
Although PC, hospice care (HC), and EOLC are often used with little distinction in the literature, they do have relevant conceptual differences: PC refers to specialized symptom-oriented comprehensive care for people with a no longer causally treatable illness to enhance a person’s quality of life throughout the course of the disease. Hospice care (HC) focuses on holistic comfort care and quality of life of a person with a terminal condition, including various social, spiritual, and everyday interventions. EOLC is directed toward the comprehensive care of people who are nearing the end of life, with great emphasis on the dignity of the person, their spirituality, and the maintenance of social relationships. As these concepts are all relevant to the care of patients with serious and/or terminal illnesses and those at the end of life, they were all included in the search (Appendix A). In the analysis of the papers, we use the terms that the authors themselves have used in their work. When we summarize results in which all or several approaches are included, we use the overarching term HPC.
The keywords were linked with the Boolean operator “and“ to increase precision and refine the search, limiting the results to records containing both terms (Appendix A). Additional studies were identified by free-text search and screening reference lists of included studies.
2.3. Selection Process
After duplicates were removed, titles and abstracts were reviewed independently by BP and JB against the inclusion criteria. To improve efficiency, we used Rayyan [14], a web-based systematic review automation software, which allows multiple “blinded” authors to collaborate. The full texts of potentially eligible articles were then retrieved for further review. Full texts were read and analyzed for eligibility by BP and JB and each record identified for inclusion was assessed for quality (see Section 2.5).
2.4. Data Extraction
Data were extracted from the primary source by two members of the research team (BP, JB) and organized in a formal synthesis matrix to facilitate a comprehensive analysis, including the following information: (i) authors, (ii) country where the study was conducted, (iii) study design, (iv) sample, and (v) findings/major themes. Initial pilot testing was performed on a subset of studies to ensure consistency between the two researchers (BP, JB) who met regularly to discuss challenges, refine the extraction process, and address discrepancies.
2.5. Quality Appraisal
Quality was assessed using the Mixed Methods Appraisal Tool 2018 (MMAT) since it provides, within a single tool, methodological quality criteria for different designs, including qualitative research, randomized controlled trials, non-randomized studies, quantitative descriptive studies, and mixed methods [15,16,17,18]. The MMAT includes two initial screening questions assessing the clarity of the research objective/question and the appropriateness of the method. Studies receiving a “no” are not feasible for further appraisal. The tool contains a subset of five questions for each category of study design (e.g., qualitative, quantitative randomized trials, quantitative non-randomized, quantitative descriptive, and mixed methods), the three response options include “yes” (criterion met), “no” (criterion not met), and “can’t tell”.
In contrast to an older version, where an overall score could be calculated by dividing the number of criteria met by four, the current version of the tool (2018) does not provide a score to be calculated, since it is discouraged to use metrics by the current literature in appraisal tools. Also, there is no cut-off value characterizing low- vs. high-quality studies since the categories are arbitrary. Thus, even when studies meet only three out of five categories, they may be included if the overall quality and the content-related added value are verifiable. BP and JB independently analyzed the quality for each article and any disagreements were resolved through discussions between the investigators.
2.6. Data Synthesis
The method of synthesis was based on a combination of textual narrative analysis [19] and content analysis. This hybrid method was chosen because it allows a more comprehensive understanding of the many eligible studies. BP and JB started by conducting a textual narrative analysis to gain a preliminary description of the results of the included studies. As patterns across studies began to emerge, the researchers moved on to thematic synthesis by systematically categorizing and organizing extracted data from the selected studies to identify themes and relationship among the findings.
3. Results
3.1. Study Selection
A total of 57 papers met the inclusion criteria (Figure 1). Most of these papers were published since the outbreak of SARS-CoV-2 in 2020 (n = 51) and dealt with the situation of HPC and EOLC during the pandemic (Table 2). In the pre-pandemic era, there were only a few original research papers about HPC during disasters, with a focus on humanitarian crises and the SARS epidemic in 2003 [20,21,22,23,24]. These studies emphasized the importance of HPC during disasters. The authors agree on the need to include HPC in disaster management plans and to involve all healthcare professionals in the development of these plans. Despite these calls for preparation, our findings presented in the following subchapters indicate that HPC systems worldwide were largely unprepared when the COVID-19 pandemic broke out.
3.2. Study Characteristics
The following table presents an overview of the studies included in the analysis.
Table 2Overview of the included studies (n = 57).
Author | Country & Year | Design | Sample |
---|---|---|---|
Aaronson et al. [25] | USA |
Interview study/ |
ED and PC clinicians (n = 31) |
Baker Rogers et al. [26] | USA |
Online survey | Members of the AAHPM |
Becqué et al. [27] | Netherlands |
Interview study/in-depth narrative interviews | Purposively sampled bereaved relatives of patients who died during the COVID-19 |
Beltran-Aroca et al. [28] | Spain |
Retrospective observational cohort study | PC internal management database including all cancer patients treated in the period 2018–2021 |
Bradshaw et al. [29] | United Kingdom |
Qualitative multiple case study using semi-structured interviews | PC professionals (n = 24) |
Bradshaw et al. [30] | United Kingdom |
Online survey | Palliative/hospice services |
Chen et al. [20] | Taiwan |
Descriptive study | Comparison of in-patient admissions during 2002 and 2003 from the National Health Insurance Research Database with before-and-after comparisons |
Chisbert-Alapont et al. [31] | Spain |
Cross-sectional |
Nursing professionals |
Chou et al. [32] | Taiwan |
Cohort study | All patients cared for at Taipei Hospital from 2019 to 2020 |
Costantini et al. [33] | Italy |
Cross-sectional telephone survey | Purposively sampled hospices (n = 16) |
Doherty et al. [24] | Bangladesh |
Cross-sectional study with closed-ended interview questioning | Convenience sampling of individuals with serious health problems (n = 156) and caregivers (n = 155) |
Dunleavy et al. [34] | United Kingdom |
Online multinational cross-sectional survey | Hospice and specialist PC providers |
Finuf et al. [35] | USA |
Online survey | Members of palliative medical teams among 14 hospitals |
Fish and Lloyd [36] | Scotland |
Interview study/in-depth narrative interviews | PC doctors (n = 8) |
Franchini et al. [37] | Italy |
Survey/semi-structured telephone interviews | Home palliative care professionals; physicians (n = 15) |
Garcia et al. [38] | Brazil |
Descriptive, cross-sectional survey with an online questionnaire | Healthcare professionals |
Garner et al. [39] | United Kingdom |
Mixed-method |
Online survey with UK hospices (n = 143); qualitative interviews with hospice professionals (n = 24) |
Gerlach et al. [40] | Germany |
Interview study/ |
Patients (n = 15) and family caregivers (n = 16) |
Gonella et al. [41] | Italy |
Descriptive interview-study/inductive thematic analysis | Healthcare professionals |
Hanna et al. [42] | United Kingdom |
Interview study/ |
Health and social care professionals supporting dying patients |
Hanna et al. [43] | United Kingdom |
Interview study/ |
Bereaved family members |
Hanna et al. [44] | United Kingdom |
Interview study/semi-structured interviews | Family carers (n = 26) and |
Hasson et al. [45] | United Kingdom |
Online census survey | Managers of hospices |
Haydar et al. [46] | USA |
Retrospective single-center study | Patients with COVID-19 |
Hunt et al. [21] | Canada |
Interview study/ |
Humanitarian policy-makers |
Jansky et al. [47] | Germany |
Interview study/focus groups/guided interviews | Representatives of SPHC teams (n = 18) and stakeholders |
Kates et al. [48] | USA |
Cross-sectional survey | Hospice and PC workforce |
Klinger et al. [49] | Germany |
Interview study/semi-structured expert interviews | People involved in pandemic management as a staff member attached to a healthcare facility or public institution (n = 41) |
Lalani et al. [50] | USA |
Interview study/ |
PC professionals in rural areas |
Leong et al. [22] | Singapore |
Interview study/semi-structured interviews | PC professionals |
Lin et al. [51] | Taiwan |
Online cross-sectional survey | Subscribers (n = 1551) and organizational members |
Macchi et al. [52] | Italy |
Qualitative study | Patients (n = 108) |
Mitchell et al. [53] | United Kingdom |
Cross-sectional online survey | Community nurses (n = 387); general practitioners (n = 156) |
Mitchinson et al. [54] | United Kingdom |
Semi-structured telephone interviews | Healthcare workers (n = 22/100 interviews mentioning death) |
Nestor et al. [55] | Ireland |
Cross-sectional study using standardized questionnaires | Healthcare professionals |
Nyblom et al. [56] | Sweden |
Interview study/semi-structured interviews | Patients (n = 22) |
Obata et al. [57] | USA |
Descriptive study | Clinical characteristics and comparisons between patients (n = 225) with COVID 19 with and without PC team consults |
Oluyase et al. [58] | Multinational |
Online survey | Palliative care services (n = 458; UK n = 277; rest of Europe n = 85; rest of world n = 95) |
Onwuteaka-Philipsen et al. [59] | Netherlands |
Observational online questionnaire survey | Healthcare professionals (n = 747) |
Pastrana et al. [60] | Multinational |
Semi-structured online survey | PC professionals (n = 77) |
Prokopová et al. [61] | Czech Republic |
Cross-sectional study | Healthcare professionals working in intensive care units (n = 313) |
Rowe et al. [62] | USA |
Interview study/semi-structured interviews | PC clinicians (n = 25) |
Sabolish et al. [63] | USA |
Retrospective exploratory study | Patients with PC consult (n = 174) and patients without PC |
Samala et al. [64] | USA |
Cross-sectional study | Healthcare professionals |
Schallenburger et al. [65] | Germany |
Interview study/ |
Healthcare workers (n = 31) |
Schloesser et al. [66] | Germany |
Post-bereavement online survey with free text options | Bereaved relatives (n = 81) from people who died during the pandemic with and without SARS-CoV2 |
Schneider et al. [23] | Switzerland |
Interview study/in-depth interviews | Expatriate health workers |
Schoenherr et al. [67] | USA |
Evaluation of a pilot program for proactive identification of PC needs | Patients with COVID-19 (n = 29) |
Seibel et al. [68] | Germany |
Interview study/qualitative interviews | Manager and health |
Selman et al. [69] | United Kingdom |
Open-web survey | Bereaved people |
Sleeman et al. [70] | United Kingdom |
Cross-sectional online survey | PC services (n = 277) |
Strang et al. [71] | Sweden |
Descriptive national registry data study | All registered patients who died |
Tanzi et al. [72] | Italy |
Single holistic case study design | Physicians (n = 9) and |
Varani et al. [73] | Italy |
Online survey | PC physicians and nurses (n = 145) working in home assistance compared to data collected in 2016 in the same setting (n = 179) |
Wind et al. [74] | Denmark |
Semi-structured telephone interviews | Family carers |
Yildiz et al. [75] | Netherlands |
Open observational online survey | Bereaved family members and friends (n = 393); relatives who lost a family member or friend at home (n = 68); in a hospital (n = 114), nursing home (n = 176) or hospice (n = 35) |
Zheng et al. [76] | China |
Cross-sectional study | Healthcare professionals |
3.3. Results of Syntheses
During the pandemic, single-center studies prevailed, while multi-center and mixed method surveys with larger sample sizes were rarer (Table 2). Most of the included articles were from Europe (n = 35), followed by the USA (n = 11), Asia (n = 6), Canada (n = 1), and South America (n = 1), and two multinational surveys were included. The content analysis identified four main themes (Table 3): (i) disruption of the system, (ii) setting-specific differences, (iii) emotional challenges, and (iv) system adaptation.
3.3.1. Disruption of the System
Underutilization and Shift from Hospitals to Home Services
While there has been an increase in deaths during crises, a seemingly paradoxically underutilization of HPC services in hospitals has been reported [20,21,42,46]. During the pandemic, this was mainly due to a shift towards services providing care where requests increased [34,37,45,70]. The reasons for this shift appear manifold: Foremost, PC patients themselves did not want to be admitted because they were afraid of catching the infection. Furthermore, they wanted to stay close to the people who were important to them [56,58]. An overall reduction in referrals to hospitals from primary care was observed, as they appear to have been carried out only in particularly complex clinical cases [28,58]. Additionally, reallocation of resources toward lifesaving patient care and the perception of peoples’ EOLC and HPC needs as secondary to other challenges further led to HPC underapplication [49].
Compared to other pathologies, COVID-19 patients had lower utilization of PC. The possibility of having an EOLC discussion and dying with someone present was negatively affected by hospitalization [46,71]. Where HPC teams were involved, their outreach into the hospital and the community was reported to be helpful regarding patient care and family support. Furthermore, the HPC teams could ease the health workers’ psychological distress by helping to clarify advance directives and minimize unwanted resuscitative efforts [25,34,57,61,62,63,64,72]. Altogether, the underutilization of PC services during the pandemic was negatively perceived by experts and contrasted with the WHO’s “seven principles”.
Disruption of Social Connectedness
As different as disasters are, so are the associated challenges. However, during a public health emergency due to an infectious disease outbreak, the loss of social connectedness is a key theme, as described back in 2003 during the SARS-CoV outbreak and repeated on a large scale during the COVID-19 pandemic [22,45,60]. The implementation of strict infection prevention and control measures (IPC) lead to a disruption of social connectedness at multiple levels: between patients, families, healthcare workers, and communities [22]. As a result of restricted visiting to hospitals and nursing homes, relatives relied on connecting virtually with their family, which could, however, only happen when facilitated by creative and equipped health and social care professionals—which was not always the case [43]. However, the use of digital tools in health care increased rapidly during the COVID-19 pandemic. Despite this development, a discrepancy was described between the level of information desired by the relatives and what was provided in practice. This discrepancy may have been due to a lack of time and communication skills of the professionals in the field [43]. In general, both health professionals and family caregivers preferred in-person communication over technology-based communication because of its many shortcomings (e.g., frequent misunderstandings, “missing pieces”, lack of body language, etc.). ICT-based communication was at best perceived as a complementary option [61].
Dehumanization of Care
While measures in reaction to the COVID-19 pandemic varied amongst countries (see Section 3.3.4), strict visitor restrictions were negatively associated with healthcare staff’s appreciation of EOLC and the dying process [59]. Where family members were unable to plan for death, say farewell, or engage in traditional bereavement and death rituals, the risk for complicated and extended grief, anxiety, and depression, as well as for aggressive behaviors, distrust, and uncertainty increased [27,41]. Overall, IPC measures diluted health worker’s ability to provide care in accordance with their core values, resulting in experiences of moral distress, internal conflicts, and potential burnout [29,36,61]. Indeed, a major task for HPC providers during the pandemic was to continually manage the IPC-associated constraints on an organizational and individual level.
Lack of Resources
Several studies have reported that HPC services, in particular, lacked staff during disasters. On top of the already scarce professionals due to pre-existing staff shortages, absence due to illness and quarantine became a problem and volunteer support declined sharply. From the responding services within the CovPall study [58] who had volunteers, 79% used them much less during the pandemic. Material shortages included lack of medications, PPE, and other equipment, with charity-managed PC services being especially badly equipped [33,51,58]. A lack of opioids was reported by Médecins sans Frontières during various humanitarian emergencies [23,24]. In the CovPall study, however, a shortage of anaesthetic drugs was noted during the pandemic [58]. Overall, due to resource constraints, HPC services during the crisis had to rely on “quick fixes” and improvisation to provide fast low-cost solutions for their patients [34].
Lack of Information and Expertise
The lack of disaster-related protocols and setting-specific guidelines for HPC services in different settings, already described before the pandemic [22], became a major challenge during the COVID-19 outbreak [33,35]. It was notable that the pandemic response lacked consideration of HPC issues, including pre-determined responsibilities and trained specialist expertise in disaster mitigation strategies, as well as clarity in communication structures between macro, meso, and micro levels [49]. Without formal systems or guidelines to identify patients in need, HPC is often underused, especially in in-patient settings [25].
The definition of HPC expertise during the pandemic, especially in quickly formed COVID-19 PC units, was sometimes rather broad, as not all staff were trained PC experts [31,49,76]. Overall, with PC being only scarcely considered in disaster response, it was left to individuals with or without PC expertise at the micro level to balance ICP measures and care needs, while coordination from macro levels was lacking or only slowly developed [49].
3.3.2. Setting-Specific Differences
HPC operates within numerous different contexts. In some studies, the specific setting was not explicitly indicated (e.g., studies that involved bereaved family members, irrespective of whether the patients passed away at home, in a hospital, or within a hospice facility, and surveys involving HPC providers working across different settings).
Preferred Place of Death
In general, hospitals and care homes are the least favoured place to die, especially during the pandemic [40,69]. Overall, dying at a place other than home, with medical and psychosocial care and visits being restricted, was associated with a lower likelihood to evaluate the place of death as appropriate by family members and healthcare staff, and was associated with challenges in the bereavement process [50,59,69,71].
Home Palliative Care during Disasters: Between Benefit and Burden
Due to an overall shift away from hospital care to home and community care, there was an increased demand for HPC outside of institutionalized care settings. As a response to this demand, home HPC flexibly reconfigured services, redeployed staff, and introduced new policies to minimize virus transmission [45]. Overall, post-bereavement analysis indicated that relatives of patients who died at home felt less burdened by the pandemic situation than relatives of patients who died in institutions, such as nursing homes or hospitals [66].
Cultural, Organizational, and Funding Differences in Disaster Response
Disaster reactions and mitigation strategies vary based on socio-political dimensions, healthcare system structure, and the extent of the disaster. Pandemic strategies thus ranged from countries with repeated lockdowns, loss of services, and social interactions, leading to negative emotional responses in the HPC sector [52], to countries with minor restrictions, where HPC workers found the impact of the disaster noticeable, but bearable [56]. Also, some health systems were widely unprepared to implement telehealth interventions, while others reported positive experiences [47]. Even crisis-experienced Asian countries lacked preparation, as the HPC sector was not equipped with advanced disaster management plans [20]. As well as country-specific differences, organizational and funding differences had an impact on disaster management: charitably managed HPC appeared especially fragile as their services were less integrated with national health services [39] and had a greater likelihood of material shortages [58].
3.3.3. Emotional Challenges
Emotional challenges were a common theme in the available post-pandemic literature and many studies reported a wide spectrum of emotions while balancing HPC between disaster pressure and core values of care [42]. Overall, emotional challenges were framed by the availability of human, material, and knowledge resources, the patient’s vulnerability, visitation policies, and self-efficacy. There were concerns about contracting the virus and passing it on to vulnerable family members, challenges in supporting patients isolated from their relatives, the need to adapt to ever-changing protocols, difficulties in communication associated with the wearing of PPE, and reduced direct peer support [37,43,55,60,65]. Redeployed professionals felt less equipped and confident, even after “fast-tracked training” about PC [42].
Many studies reported that the practical and emotional challenges caused distress by destabilizing professional identity, which, in turn, may have impacted on the provision of patient care. However, the literature also highlighted that HPC workers adjusted their goals, developed staff resilience, showed commitment to their role, and were empowered by engaging in new forms of care and human connection [50,54]. Some studies reported high work satisfaction, professional self-confidence, and feeling supported by the (initial) national outpouring of goodwill towards front-line workers [36,37,55,73]. Interestingly, an Italian study reported that the frequency of burnout decreased during the peak of the pandemic, while psychological distress was significantly worse [73]. Another study found a possible explanation for this phenomenon: PC workers were observed to use avoidance techniques to reduce burnout perceptions; however, these maladaptive coping behaviors could have future negative effects, such as increased depression or post-traumatic symptoms [35].
For family caregivers, the pandemic situation led to emotional challenges as they struggled between worrying that a COVID-19 infection would lead to the patients’ untimely death, and living the limited time left to the fullest possible [40,56,74]. Relational aspects were of utmost importance for the relatives, and, where social connectedness was disrupted, care was considered “inhuman” [27]. Only a few studies examined the patient’s perspective: They expressed fears of infection risk, wasting precious time, insufficient healthcare resources, and abnormal death, while the patients’ already existing HPC needs remained unchanged during the pandemic [40,56].
3.3.4. System Adaptation
Health systems were largely unprepared for the COVID-19 outbreak and plans and protocols were mostly lacking. However, HPC services in hospitals, communities and home care settings adapted dynamically to the various new challenges and restrictions; they tried to balance IPC measures and HPC needs, and adopted low-cost solutions [30,33,34,58,60]. In response to staff shortages, the improvisational and adaptive efforts of the system included new forms of collaboration, such as ad hoc establishment of COVID-19 PC units, increased involvement of specialized PC consult services for educating clinical staff, symptom management communication, and care guidance [51,58,68]. Additionally, staff worked longer hours, took greater responsibility, day-care services were closed, hospice beds were reduced, new staff were rapidly trained, and nonclinical staff were used [53,58]. Primary healthcare providers, which had previously experienced tensions with specialist PC teams, had the opportunity during the pandemic to strengthen mutual relationships through interprofessional training and collaborative practice approaches [53]. In response to shortages of equipment, PC services contacted various stakeholders, made their own supplies, and deployed staff to gather PPE as their main task, as they explored ways to use less material [58]. On a systemic level, services explored new strategies to proactively identify and meet the PC needs of all patients with COVID-19 at the intensive care unit or in the emergency department [25,67]. Against the loss of social connectedness, PC staff made efforts to re-humanize interactions and communication with patients and family by personal acts of care [36,54].
4. Discussion
HPC service provision, which is already resource-limited under conventional capacity, is inevitably further strained and under-resourced in crises and disasters [8,12]. During the COVID-19 pandemic, multiple dynamics were observed, such as a shift from the inpatient setting to home and community care services, a general lack of resources and/or its reallocation, a dehumanization of care, and the neglect of HPC services, both for those who were directly affected by the disasters (e.g., patients with COVID-19) and those who had pre-existing HPC needs. The vacuum of anticipating protocols led to “quick” fixes and improvisational strategies at the micro level of both inpatient and home care settings neglecting the holistic pretensions of standard HPC in adverse circumstances [8]. While the available literature highlights the dedication of healthcare professionals in providing the best possible service, our findings reveal that ad hoc disaster management strategies were often carried out by professionals who were lacking HPC expertise as well as lacking disaster education and training, and, often, the delivery of HPC could not be carried out in accordance with the very definition of HCP. In sum, under disaster pressure, HPC services worldwide adapted to a significantly lower level of care. Patient’s EOL and palliative needs were frequently treated as secondary to other challenges, resulting in these important resources being underutilized during disasters. The improvisational and altered ways of delivering HPC (if at all) led to multiple challenges amongst professionals, family caregivers, and patients since they often contrasted fundamental beliefs and values of HPC care.
The numerous studies included in the present review reveal that HPC has been given too little consideration in disaster management plans and/or providers were lacking education and training in disaster preparedness and/or palliative education. The Sendai Framework’s priorities, which specify that people with HPC needs should be included in disaster management policies and plans, remain mostly unmet [6]. However, with the pandemic, the utility and urgency of incorporating HPC into disaster preparedness plans has become evident and, thus, many, if not almost all, the included papers propose manifold strategies for strengthening crisis resilience and effective disaster planning. Indeed, our review clearly indicates that more efforts are needed in order to meet the goals set by the Sendai Framework for Disaster Risk Reduction 2015–2030 [6,77].
While hospitals may have disaster plans that encompass all wards, including PC units, they usually do not differentiate in terms of different patient groups or specialized care needs. Indeed, these plans seem to lack the specificity required for HPC approaches, while hospices and community-based services often lack any form of disaster preparedness. This is even more of a problem, as there was a shift from hospital-based services to primary care and community-based services during the pandemic. Indeed, the observed shift prompts a crucial reflection on healthcare organization and indicates that investing in home- and community-based HPC not only enhances the quality of EOL, HC and PC, but also contributes to the overall resilience and adaptability of healthcare systems, particularly, but not only, in times of crises. Strengthening community-based care may thereby help to alleviate the strain on hospitals and healthcare systems during disasters and may also enable a more distributed and flexible HPC delivery during disasters. Hence, the call for an intensive debate about healthcare organization, and extending this debate beyond hospitals to encompass, strengthen, and support hospices and home- and community-based settings, can play a pivotal role in fostering a comprehensive approach to disaster preparedness and building resilient HPC systems.
To develop crisis-resilient healthcare systems, hospice and palliative support needs must be included in systematic all-hazards disaster preparation efforts including a variety of disasters [10,11]. Planning should not only take micro levels into account, but should also consider, meso and macro levels and the respective organizational and federal structures. Since ethically, makeshift solutions appear mostly unsatisfactory and burdensome for all parties involved, potential conflicts of values (e.g., life-saving efforts vs. social connectedness) should be anticipated and addressed in concepts and guidelines. Staff training is an essential element in ensuring that an HPC team can provide care to patients and their families, particularly in the event of a disaster, as the team must be able to respond effectively and efficiently to ensure that patient care is not compromised. Regular training can help maintain their emotional resilience and ability to cope with the stress in challenging circumstances [78]. Additionally, strengthening outpatient and community- and home-based care services is necessary to tackle EOLC and HPC care needs under disaster pressure. Providing HPC services with adequate supplies and resources, and investing in tele-health, psychosocial, and practical support for patients, professionals and informal caregivers, is central to guarantee the continuity of HPC during disasters. However, not only in delivering direct patient care, but also in addressing public health needs, HPC providers are central in disaster mitigation, for instance, by providing training to other sectors of the healthcare system, by educating patients and family caregivers, by supporting community bereavement needs, and by providing public health surveillance [79].
The explosive increase in publications due to COVID-19 has had both positive and negative effects. On the one hand, it has generated new concepts and expanded our knowledge. On the other hand, hyper-prolific productivity and quick study set-ups may have resulted in research suffering from low validity and overall quality as evidenced by the exclusion of many papers. Nevertheless, even after sorting out weaker papers, robust evidence remains and existing models, policies, and strategies are now more than ever supported by evidence-based data. However, due to the very specific nature of COVID-19, the new body of literature may only be partially applicable to an all-hazards approach, making future all-hazards analysis necessary.
5. Limitations
This systematic review has several limitations: Since the identified empirical work relates to infectious health threads, with over 90% of all included papers being COVID-related, the results cannot be interpreted in terms of the all-hazards approach. It, therefore, remains largely unclear to what extent strategies exist to maintain HPC in the event of non-infectious disasters, such as heat waves, floods, or warfare, for example. Additionally, the included studies rarely assessed the patient’s perspective. Another limitation of the available literature is that authors framed the concepts of HC, PC, and EOLC differently and did not always provide a clear definition of their approaches, contributing to a lack of clarity. Moreover, papers were mostly from high-income countries and very few papers from low- and middle-income countries (LMICs) were included [8]. Since PC needs vary depending on sociopolitical and geopolitical backgrounds, and values regarding dying and death are culturally situated, the present evidence may not apply to health systems in LMICs. Additionally, due to reasons of space, we excluded literature focusing on telehealth solutions, non-original research (e.g., policy papers, letters, opinions), as well as the grey literature, and papers in languages other than English.
6. Conclusions
HPC occurs across various settings (e.g., hospitals, hospices, emergency care, nursing homes, and community care settings) and is an essential component of disaster response. However, while multiple barriers and challenges inevitably hamper the delivery of HPC during disasters, strategies to tackle EOLC and HPC needs have been poorly integrated in disaster preparedness planning. Strengthening the HPC sector is not a trivial matter, but a key disaster management strategy. With its special position in the medical care continuum, a well-prepared and equipped HPC system is able to tackle important public healthcare needs during disasters by supporting both healthcare systems and communities. Since, thus far, the resources and strengths of HPC are under-recognized and under-utilized, as, especially under crisis pressure, the primacy of lifesaving makes HPC needs less visible, they urgently need to be incorporated into disaster preparedness planning. Further emergency preparedness efforts, including all-hazards approaches and best practice analyses, and continued evaluation of HPC disaster planning, is needed to understand whether and how the transferral of the newly generated knowledge due to COVID-19 can be implemented into practical planning.
Conceptualization, B.P. and M.E.; methodology: B.P. and M.E.; software, J.B.; data curation, B.P. and J.B.; analysis, B.P. and J.B.; writing—original draft preparation, B.P.; writing—review and editing, B.P., J.B. and M.E. All authors have read and agreed to the published version of the manuscript.
Not applicable.
Not applicable.
The data presented in this study are available on request from the corresponding author.
We thank Steve Allen for proofreading the manuscript.
The authors declare no conflict of interest.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Classification of disasters.
Disasters | Group | Type (Examples) |
---|---|---|
Disasters triggered by natural hazards * | Biological | Pandemic, epidemic, insect infestation, animal stampede |
Geophysical | Earthquake, volcano, mass movement | |
Meteorological | Storm | |
Hydrological | Flood, mass movement | |
Climatological | Extreme temperature, drought, wildfire | |
Man-made disasters | Warfare | National conflicts, international conflicts |
Socio-technical disaster | Technological disasters (e.g., leakage, toxic release, structure collapse), transportations disasters, production failure, public places failures |
* The term “natural disaster” is misleading as it ignores the role humans play in this type of environmental disaster.
Main themes and sub-themes related to disaster preparedness in HPC.
Main Themes | Sub-Themes |
---|---|
Disruption |
Underutilization and shift from hospitals to home services
|
Disruption of social connectedness
|
|
Dehumanization of care
|
|
Lack of resources
|
|
Lack of information and expertise
|
|
Setting-specific differences | Hospitals and nursing homes
|
Home and community care
|
|
Cultural, organizational, and funding differences in disaster response
|
|
Emotional challenges | Increased emotional demands under disaster pressure for
|
System adaption | Implementation of low-cost and ad hoc solutions especially at micro and meso levels
|
System preparedness | Lack of PC-specific disaster management
|
Appendix A
MeSH-search-combinations (each combined with ‘AND’) | |
Palliative care; Palliative medicine; Terminal care; End of life care; Hospices; Hospice care; Hospice and palliative care nursing | Disasters; Eruption, volcanic; Earthquakes; Floods; Hurricane; Drought; Droughts; Typhoon; Avalanche; Cyclonic storms; Pandemics; Epidemics; Warfare and armed conflicts; Terrorism; Weapons; Radioactive hazard release |
Additional textword search in databases and alert
|
|
(palliative care or palliative medicine or end of life care or terminal care or terminal care or hospice care or hospices or hospice and palliative care nursing) AND (disaster or crisis) AND (eruption* or earthquake* or flood* or hurricane* or drought* or cyclonic storm* or typhoon* or avalanche* or cyclone* or pandemic* or epidemic* or war* or armed conflict* or terrorism or weapon* or accident* or power failure or famine or civil war or war) |
References
1. WHO & EHA. Disasters & Emergencies Definitions. Training Package; 2002; Available online: https://lms.must.ac.ug/claroline/backends/download.php?url=Lzc2NTZfd2hhdF9pc19kaXNhc3Rlci5wZGY%3D&cidReset=true&cidReq=BALFP3209_001 (accessed on 20 August 2023).
2. United Nations Office for Disaster Risk Reduction (UNDRR). Terminology Disaster. Available online: https://www.undrr.org/terminology/disaster (accessed on 22 February 2023).
3. Lancet, T. Palliative care and the COVID-19 pandemic. Lancet; 2020; 395, 1168. [DOI: https://dx.doi.org/10.1016/S0140-6736(20)30822-9] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32278369]
4. Shaluf, I. An Overview on Disasters. Disaster Prev. Manag.; 2007; 16, pp. 687-703. [DOI: https://dx.doi.org/10.1108/09653560710837000]
5. CRED. Human Cost of Natural Disasters 2015. A Global Perspective. 2015; Available online: https://climate-adapt.eea.europa.eu/en/metadata/publications/the-human-cost-of-natural-disasters-2015-a-global-perspective/11258275 (accessed on 23 February 2023).
6. UN. Sendai Framework for Disaster Risk Reduction 2015–2030; The United Nations Office for Disaster Risk Reduction: Geneva, Switzerland, 2015; Available online: https://www.preventionweb.net/files/43291_sendaiframeworkfordrren.pdf?_gl=1*1451gp*_ga*NDQ5MjIxMzAxLjE2NzcxNjI2OTk.*_ga_D8G5WXP6YM*MTY3NzE2OTI4NC4yLjEuMTY3NzE2OTUwMy4wLjAuMA (accessed on 22 February 2023).
7. WHO. Building Health Systems Resilience for Universal Health Coverage and Health Security during the COVID-19 Pandemic and Beyond. 2021; Available online: https://www.who.int/publications/i/item/WHO-UHL-PHC-SP-2021.01 (accessed on 23 February 2023).
8. WHO. Integrating Palliative Care and Symptom Relief into the Response to Humanitarian Emergencies and Crises: A WHO guide. 2018; Available online: https://www.who.int/publications/i/item/9789241514460 (accessed on 23 February 2023).
9. Ciottone, G.R. Chapter 1—Introduction to Disaster Medicine. Ciottone’s Disaster Medicine; 2nd ed. Elsevier: Amsterdam, The Netherlands, 2016; pp. 2-5.
10. Powell, R.A.; Schwartz, L.; Nouvet, E.; Sutton, B.; Petrova, M.; Marston, J.; Munday, D.; Radbruch, L. Palliative care in humanitarian crises: Always something to offer. Lancet; 2017; 389, pp. 1498-1499. [DOI: https://dx.doi.org/10.1016/S0140-6736(17)30978-9] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28422014]
11. Kelly, M.; Mitchell, I.; Walker, I.; Mears, J.; Scholz, B. End-of-life care in natural disasters including epidemics and pandemics: A systematic review. BMJ Support. Palliat. Care; 2021; 13, 1. [DOI: https://dx.doi.org/10.1136/bmjspcare-2021-002973] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33731463]
12. Nouvet, E.; Sivaram, M.; Bezanson, K.; Krishnaraj, G.; Hunt, M.; de Laat, S.; Sanger, S.; Banfield, L.; Rodriguez, P.F.E.; Schwartz, L.J. Palliative care in humanitarian crises: A review of the literature. J. Int. Humanit. Action; 2018; 3, 5. [DOI: https://dx.doi.org/10.1186/s41018-018-0033-8]
13. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E. et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ; 2021; 372, n71. [DOI: https://dx.doi.org/10.1136/bmj.n71]
14. Ouzzani, M.; Hammady, H.; Fedorowicz, Z.; Elmagarmid, A. Rayyan—A web and mobile app for systematic reviews. Syst. Rev.; 2016; 5, 210. [DOI: https://dx.doi.org/10.1186/s13643-016-0384-4]
15. Hong, Q.N.; Pluye, P.; Fàbregues, S.; Bartlett, G.; Boardman, F.; Cargo, M.; Dagenais, P.; Gagnon, M.-P.; Griffiths, F.; Nicolau, B. et al. Improving the content validity of the mixed methods appraisal tool: A modified e-Delphi study. J. Clin. Epidemiol.; 2019; 111, pp. 49-59.e1. [DOI: https://dx.doi.org/10.1016/j.jclinepi.2019.03.008]
16. Hong, Q.N.; Pluye, P.; Fàbregues, S.; Bartlett, G.; Cargo, M.; Boardman, F.; Dagenais, P.; Gagnon, M.-P.; Griffiths, F.; Nicolau, B. et al. Mixed Methods Appraisal Tool (MMAT), Version 2018. User Guide; McGill University: Montreal, AC, Canada, 2018.
17. Harden, A.; Gough, D. Quality and relevance appraisal. An Introduction to Systematic Reviews; Gough, D.; Oliver, S.; Thomas, J. Sage Publications Ltd.: Thousand Oaks, CA, USA, 2012; pp. 153-179.
18. Petticrew, M.; Roberts, H. How to Appraise the Studies: An Introduction to Assessing Study Quality. Systematic Reviews in the Social Sciences; Wiley: Hoboken, NJ, USA, 2006; pp. 125-163.
19. Popay, J.; Roberts, H.; Sowden, A.; Petticrew, M.; Arai, L.; Rodgers, M.; Britten, N.; Roen, K.; Duffy, S. Guidance on the Conduct of Narrative Synthesis in Systematic Reviews. A Product from the ESRC Methods Programme; Lancaster University: Lancaster, UK, 2006; Available online: https://www.lancaster.ac.uk/media/lancaster-university/content-assets/documents/fhm/dhr/chir/NSsynthesisguidanceVersion1-April2006.pdf (accessed on 29 March 2023).
20. Chen, T.-J.; Lin, M.-H.; Chou, L.-F.; Hwang, S.-J. Hospice utilization during the SARS outbreak in Taiwan. BMC Health Serv. Res.; 2006; 6, 94. [DOI: https://dx.doi.org/10.1186/1472-6963-6-94]
21. Hunt, M.; Nouvet, E.; Chénier, A.; Krishnaraj, G.; Bernard, C.; Bezanson, K.; de Laat, S.; Schwartz, L. Addressing obstacles to the inclusion of palliative care in humanitarian health projects: A qualitative study of humanitarian health professionals’ and policy makers’ perceptions. Confl. Health; 2020; 14, 70. [DOI: https://dx.doi.org/10.1186/s13031-020-00314-9]
22. Leong, I.Y.; Lee, A.O.; Ng, T.W.; Lee, L.B.; Koh, N.Y.; Yap, E.; Guay, S.; Ng, L.M. The challenge of providing holistic care in a viral epidemic: Opportunities for palliative care. Palliat. Med.; 2004; 18, pp. 12-18. [DOI: https://dx.doi.org/10.1191/0269216304pm859oa]
23. Schneider, M.; Chappuis, F.; Pautex, S. How do expatriate health workers cope with needs to provide palliative care in humanitarian emergency assistance? A qualitative study with in-depth interviews. Palliat. Med.; 2018; 32, pp. 1567-1574. [DOI: https://dx.doi.org/10.1177/0269216318794091]
24. Doherty, M.; Power, L.; Petrova, M.; Gunn, S.; Powell, R.; Coghlan, R.; Grant, L.; Sutton, B.; Khan, F. Illness-related suffering and need for palliative care in Rohingya refugees and caregivers in Bangladesh: A cross-sectional study. PLoS Med.; 2020; 17, e1003011. [DOI: https://dx.doi.org/10.1371/journal.pmed.1003011] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32126076]
25. Aaronson, E.L.; Daubman, B.R.; Petrillo, L.; Bowman, J.; Ouchi, K.; Gips, A.; Traeger, L.; Jackson, V.; Grudzen, C.; Ritchie, C.S. Emerging Palliative Care Innovations in the ED: A Qualitative Analysis of Programmatic Elements During the COVID-19 Pandemic. J. Pain Symptom Manag.; 2021; 62, pp. 117-124. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2020.10.035]
26. Baker Rogers, J.E.; Thompson, J.M.; Mupamombe, C.T.; Vanin, J.M.; Navia, R.O. Hospice Emergency Planning and COVID-19. J. Palliat. Care; 2022; 37, pp. 34-40. [DOI: https://dx.doi.org/10.1177/08258597211037428]
27. Becqué, Y.N.; van der Geugten, W.; van der Heide, A.; Korfage, I.J.; Pasman, H.R.W.; Onwuteaka-Philipsen, B.D.; Zee, M.; Witkamp, E.; Goossensen, A. Dignity reflections based on experiences of end-of-life care during the first wave of the COVID-19 pandemic: A qualitative inquiry among bereaved relatives in the Netherlands (the CO-LIVE study). Scand. J. Caring Sci.; 2022; 36, pp. 769-781. [DOI: https://dx.doi.org/10.1111/scs.13038]
28. Beltran-Aroca, C.M.; Ruiz-Montero, R.; Llergo-Muñoz, A.; Rubio, L.; Girela-López, E. Impact of the COVID-19 Pandemic on Palliative Care in Cancer Patients in Spain. Int. J. Environ. Res. Public Health; 2021; 18, 11992. [DOI: https://dx.doi.org/10.3390/ijerph182211992]
29. Bradshaw, A.; Dunleavy, L.; Garner, I.; Preston, N.; Bajwah, S.; Cripps, R.; Fraser, L.K.; Maddocks, M.; Hocaoglu, M.; Murtagh, F.E.M. et al. Experiences of staff providing specialist palliative care during COVID-19: A multiple qualitative case study. J. R. Soc. Med.; 2022; 115, pp. 220-230. [DOI: https://dx.doi.org/10.1177/01410768221077366]
30. Bradshaw, A.; Dunleavy, L.; Walshe, C.; Preston, N.; Cripps, R.L.; Hocaoglu, M.; Bajwah, S.; Maddocks, M.; Oluyase, A.O.; Sleeman, K. et al. Understanding and addressing challenges for advance care planning in the COVID-19 pandemic: An analysis of the UK CovPall survey data from specialist palliative care services. Palliat. Med.; 2021; 35, pp. 1225-1237. [DOI: https://dx.doi.org/10.1177/02692163211017387]
31. Chisbert-Alapont, E.; García-Salvador, I.; De La Ossa-Sendra, M.J.; García-Navarro, E.B.; De La Rica-Escuín, M. Influence of Palliative Care Training on Nurses’ Attitudes towards End-of-Life Care during the COVID-19 Pandemic in Spain. Int. J. Environ. Res. Public Health; 2021; 18, 11249. [DOI: https://dx.doi.org/10.3390/ijerph182111249] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34769767]
32. Chou, Y.C.; Yen, Y.F.; Feng, R.C.; Wu, M.P.; Lee, Y.L.; Chu, D.; Huang, S.J.; Curtis, J.R.; Hu, H.Y. Impact of the COVID-19 Pandemic on the Utilization of Hospice Care Services: A Cohort Study in Taiwan. J. Pain Symptom Manag.; 2020; 60, pp. e1-e6. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2020.07.005] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32663615]
33. Costantini, M.; Sleeman, K.E.; Peruselli, C.; Higginson, I.J. Response and role of palliative care during the COVID-19 pandemic: A national telephone survey of hospices in Italy. Palliat. Med.; 2020; 34, pp. 889-895. [DOI: https://dx.doi.org/10.1177/0269216320920780] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32348711]
34. Dunleavy, L.; Preston, N.; Bajwah, S.; Bradshaw, A.; Cripps, R.; Fraser, L.K.; Maddocks, M.; Hocaoglu, M.; Murtagh, F.E.M.; Oluyase, A.O. et al. ‘Necessity is the mother of invention’: Specialist palliative care service innovation and practice change in response to COVID-19. Results from a multinational survey (CovPall). Palliat. Med.; 2021; 35, pp. 814-829. [DOI: https://dx.doi.org/10.1177/02692163211000660]
35. Finuf, K.D.; Lopez, S.; Carney, M.T. Coping Through COVID-19: A Mixed Method Approach to Understand How Palliative Care Teams Managed the COVID-19 Pandemic. Am. J. Hosp. Palliat. Med.; 2022; 39, pp. 874-880. [DOI: https://dx.doi.org/10.1177/10499091211045612] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34496668]
36. Fish, E.C.; Lloyd, A. Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study. Palliat. Med.; 2022; 36, pp. 955-963. [DOI: https://dx.doi.org/10.1177/02692163221088930]
37. Franchini, L.; Varani, S.; Ostan, R.; Bocchi, I.; Pannuti, R.; Biasco, G.; Bruera, E. Home palliative care professionals perception of challenges during the COVID-19 outbreak: A qualitative study. Palliat. Med.; 2021; 35, pp. 862-874. [DOI: https://dx.doi.org/10.1177/02692163211008732]
38. Garcia, A.C.M.; Ferreira, A.C.G.; Silva, L.S.R.; da Conceição, V.M.; Nogueira, D.A.; Mills, J. Mindful Self-Care, Self-Compassion, and Resilience Among Palliative Care Providers During the COVID-19 Pandemic. J. Pain Symptom Manag.; 2022; 64, pp. 49-57. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2022.03.003]
39. Garner, I.W.; Walshe, C.; Dunleavy, L.; Bradshaw, A.; Preston, N.; Fraser, L.K.; Murtagh, F.E.M.; Oluyase, A.O.; Sleeman, K.E.; Hocaoglu, M. et al. Charitably funded hospices and the challenges associated with the COVID-19 pandemic: A mixed-methods study (CovPall). BMC Palliat. Care; 2022; 21, 176. [DOI: https://dx.doi.org/10.1186/s12904-022-01070-8]
40. Gerlach, C.; Ullrich, A.; Berges, N.; Bausewein, C.; Oechsle, K.; Hodiamont, F. The Impact of the SARS-CoV-2 Pandemic on the Needs of Non-Infected Patients and Their Families in Palliative Care-Interviews with Those Concerned. J. Clin. Med.; 2022; 11, 3863. [DOI: https://dx.doi.org/10.3390/jcm11133863]
41. Gonella, S.; Di Giulio, P.; Antal, A.; Cornally, N.; Martin, P.; Campagna, S.; Dimonte, V. Challenges Experienced by Italian Nursing Home Staff in End-of-Life Conversations with Family Caregivers during COVID-19 Pandemic: A Qualitative Descriptive Study. Int. J. Environ. Res. Public Health; 2022; 19, 2504. [DOI: https://dx.doi.org/10.3390/ijerph19052504]
42. Hanna, J.R.; Rapa, E.; Dalton, L.J.; Hughes, R.; Quarmby, L.M.; McGlinchey, T.; Donnellan, W.J.; Bennett, W.J.; Mayland, C.R.; Mason, S.R. Health and social care professionals’ experiences of providing end of life care during the COVID-19 pandemic: A qualitative study. Palliat. Med.; 2021; 35, pp. 1249-1257. [DOI: https://dx.doi.org/10.1177/02692163211017808] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34006159]
43. Hanna, J.R.; Rapa, E.; Dalton, L.J.; Hughes, R.; McGlinchey, T.; Bennett, K.M.; Donnellan, W.J.; Mason, S.R.; Mayland, C.R. A qualitative study of bereaved relatives’ end of life experiences during the COVID-19 pandemic. Palliat. Med.; 2021; 35, pp. 843-851. [DOI: https://dx.doi.org/10.1177/02692163211004210] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33784908]
44. Hanna, K.; Cannon, J.; Gabbay, M.; Marlow, P.; Mason, S.; Rajagopal, M.; Shenton, J.; Tetlow, H.; Giebel, C. End of life care in UK care homes during the COVID-19 pandemic: A qualitative study. BMC Palliat. Care; 2022; 21, 91. [DOI: https://dx.doi.org/10.1186/s12904-022-00979-4] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35641946]
45. Hasson, F.; Slater, P.; Fee, A.; McConnell, T.; Payne, S.; Finlay, D.A.; McIlfatrick, S. The impact of COVID-19 on out-of-hours adult hospice care: An online survey. BMC Palliat. Care; 2022; 21, 94. [DOI: https://dx.doi.org/10.1186/s12904-022-00985-6] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35642052]
46. Haydar, A.; Lo, K.B.; Goyal, A.; Gul, F.; Peterson, E.; Bhargav, R.; DeJoy, R., III; Salacup, G.; Pelayo, J.; Albano, J. et al. Palliative Care Utilization among Patients with COVID-19 in an Underserved Population: A Single-Center Retrospective Study. J. Pain Symptom Manag.; 2020; 60, pp. e18-e21. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2020.05.022]
47. Jansky, M.; Schade, F.; Rieder, N.; Lohrmann, D.; Gebel, C.; Kloppenburg, L.; Wedding, U.; Simon, S.T.; Bausewein, C.; Nauck, F. ‘It felt like a black hole, great uncertainty, but we have to take care for our patients’-Qualitative findings on the effects of the COVID-19 pandemic on specialist palliative home care. PLoS ONE; 2021; 16, e0260767. [DOI: https://dx.doi.org/10.1371/journal.pone.0260767]
48. Kates, J.; Gerolamo, A.; Pogorzelska-Maziarz, M. The impact of COVID-19 on the hospice and palliative care workforce. Public Health Nurs.; 2021; 38, pp. 459-463. [DOI: https://dx.doi.org/10.1111/phn.12827]
49. Klinger, I.; Heckel, M.; Shahda, S.; Kriesen, U.; Schneider, C.; Kurkowski, S.; Junghanss, C.; Ostgathe, C. COVID-19: Challenges and solutions for the provision of care to seriously ill and dying people and their relatives during SARS-CoV-2 pandemic—Perspectives of pandemic response team members: A qualitative study on the basis of expert interviews (part of PallPan). Palliat. Med.; 2022; 36, pp. 1092-1103. [DOI: https://dx.doi.org/10.1177/02692163221099114]
50. Lalani, N.; Cai, Y.; Wang, Y. “Hard to Say Goodbye Over iPad”: Experiences of Palliative Care Providers and Lessons Learned During the COVID-19 Pandemic in Rural Communities of Indiana, United States. J. Hosp. Palliat. Nurs.; 2022; 24, pp. E94-E100. [DOI: https://dx.doi.org/10.1097/NJH.0000000000000856]
51. Lin, C.P.; Boufkhed, S.; Kizawa, Y.; Mori, M.; Hamzah, E.; Aggarwal, G.; Namisango, E.; Higgingson, I.J.; Goh, C.; Harding, R. Preparedness to Face the COVID-19 Pandemic in Hospice and Palliative Care Services in the Asia-Pacific Region: A Rapid Online Survey. Am. J. Hosp. Palliat. Care; 2021; 38, pp. 861-868. [DOI: https://dx.doi.org/10.1177/10499091211002797]
52. Macchi, Z.A.; Ayele, R.; Dini, M.; Lamira, J.; Katz, M.; Pantilat, S.Z.; Jones, J.; Kluger, B.M. Lessons from the COVID-19 pandemic for improving outpatient neuropalliative care: A qualitative study of patient and caregiver perspectives. Palliat. Med.; 2021; 35, pp. 1258-1266. [DOI: https://dx.doi.org/10.1177/02692163211017383] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34006157]
53. Mitchell, S.; Harrison, M.; Oliver, P.; Gardiner, C.; Chapman, H.; Khan, D.; Boyd, K.; Dale, J.; Barclay, S.; Mayland, C.R. Service change and innovation in community end-of-life care during the COVID-19 pandemic: Qualitative analysis of a nationwide primary care survey. Palliat. Med.; 2022; 36, pp. 161-170. [DOI: https://dx.doi.org/10.1177/02692163211049311] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34915759]
54. Mitchinson, L.; Dowrick, A.; Buck, C.; Hoernke, K.; Martin, S.; Vanderslott, S.; Robinson, H.; Rankl, F.; Manby, L.; Lewis-Jackson, S. et al. Missing the human connection: A rapid appraisal of healthcare workers’ perceptions and experiences of providing palliative care during the COVID-19 pandemic. Palliat. Med.; 2021; 35, pp. 852-861. [DOI: https://dx.doi.org/10.1177/02692163211004228] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33775169]
55. Nestor, S.; O’Tuathaigh, C.; O’Brien, T. Assessing the impact of COVID-19 on healthcare staff at a combined elderly care and specialist palliative care facility: A cross-sectional study. Palliat. Med.; 2021; 35, pp. 1492-1501. [DOI: https://dx.doi.org/10.1177/02692163211028065] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34296637]
56. Nyblom, S.; Benkel, I.; Carling, L.; Löfdahl, E.; Molander, U.; Öhlén, J. Pandemic impact on patients with advanced non-COVID-19 illness and their family carers receiving specialised palliative home care: A qualitative study. BMJ Open; 2022; 12, e059577. [DOI: https://dx.doi.org/10.1136/bmjopen-2021-059577]
57. Obata, R.; Maeda, T.; Rizk, D.; Kuno, T. Palliative Care Team Involvement in Patients With COVID-19 in New York City. Am. J. Hosp. Palliat. Care; 2020; 37, pp. 869-872. [DOI: https://dx.doi.org/10.1177/1049909120940986]
58. Oluyase, A.O.; Hocaoglu, M.; Cripps, R.L.; Maddocks, M.; Walshe, C.; Fraser, L.K.; Preston, N.; Dunleavy, L.; Bradshaw, A.; Murtagh, F.E.M. et al. The Challenges of Caring for People Dying From COVID-19: A Multinational, Observational Study (CovPall). J. Pain Symptom Manag.; 2021; 62, pp. 460-470. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2021.01.138]
59. Onwuteaka-Philipsen, B.D.; Pasman, H.R.W.; Korfage, I.J.; Witkamp, E.; Zee, M.; van Lent, L.G.G.; Goossensen, A.; van der Heide, A. Dying in times of the coronavirus: An online survey among healthcare professionals about end-of-life care for patients dying with and without COVID-19 (the CO-LIVE study). Palliat. Med.; 2021; 35, pp. 830-842. [DOI: https://dx.doi.org/10.1177/02692163211003778]
60. Pastrana, T.; De Lima, L.; Pettus, K.; Ramsey, A.; Napier, G.; Wenk, R.; Radbruch, L. The impact of COVID-19 on palliative care workers across the world: A qualitative analysis of responses to open-ended questions. Palliat. Support. Care; 2021; 19, pp. 187-192. [DOI: https://dx.doi.org/10.1017/S1478951521000298]
61. Prokopová, T.; Hudec, J.; Vrbica, K.; Staŝek, J.; Pokorná, A.; Štourač, P.; Rusinová, K.; Kerpnerová, P.; Štěpánová, R.; Svobodník, A. et al. Palliative care practice and moral distress during COVID-19 pandemic (PEOpLE-C19 study): A national, cross-sectional study in intensive care units in the Czech Republic. Crit. Care; 2022; 26, 221. [DOI: https://dx.doi.org/10.1186/s13054-022-04066-1]
62. Rowe, J.G.; Potts, M.; McGhie, R.; Dinh, A.; Engel, I.; England, K.; Sinclair, C.T. Palliative Care Practice During the COVID-19 Pandemic: A Descriptive Qualitative Study of Palliative Care Clinicians. J. Pain Symptom Manag.; 2021; 62, pp. 1111-1116. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2021.06.013] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34147579]
63. Sabolish, R.M.; Wilson, J.M.; Caldwell, H.K. Palliative Care in a Pandemic: A Retrospective Review of the Impact of Early Palliative Care Consultation During the Coronavirus Disease 2019 Pandemic. J. Hosp. Palliat. Nurs; 2022; 24, pp. 50-56. [DOI: https://dx.doi.org/10.1097/NJH.0000000000000807] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34550916]
64. Samala, R.V.; Range, P.; Hoeksema, L.J.; Fong, K.; Shoemaker, L. Health Professionals’ Perceptions of the Contributions of Palliative Care Consultation for Patients with COVID-19. J. Palliat. Med.; 2021; 24, pp. 1872-1876. [DOI: https://dx.doi.org/10.1089/jpm.2021.0253]
65. Schallenburger, M.; Reuters, M.C.; Schwartz, J.; Fischer, M.; Roch, C.; Werner, L.; Bausewein, C.; Simon, S.T.; van Oorschot, B.; Neukirchen, M. Inpatient generalist palliative care during the SARS-CoV-2 pandemic—Experiences, challenges and potential solutions from the perspective of health care workers. BMC Palliat. Care; 2022; 21, 63. [DOI: https://dx.doi.org/10.1186/s12904-022-00958-9] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35501750]
66. Schloesser, K.; Simon, S.T.; Pauli, B.; Voltz, R.; Jung, N.; Leisse, C.; van der Heide, A.; Korfage, I.J.; Pralong, A.; Bausewein, C. et al. “Saying goodbye all alone with no close support was difficult”—Dying during the COVID-19 pandemic: An online survey among bereaved relatives about end-of-life care for patients with or without SARS-CoV2 infection. BMC Health Serv. Res.; 2021; 21, 998. [DOI: https://dx.doi.org/10.1186/s12913-021-06987-z] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34551766]
67. Schoenherr, L.A.; Cook, A.; Peck, S.; Humphreys, J.; Goto, Y.; Saks, N.T.; Huddleston, L.; Elia, G.; Pantilat, S.Z. Proactive Identification of Palliative Care Needs Among Patients With COVID-19 in the ICU. J. Pain Symptom Manag.; 2020; 60, pp. e17-e21. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2020.06.008]
68. Seibel, K.; Couné, B.; Mueller, M.; Boehlke, C.; Simon, S.T.; Bausewein, C.; Becker, G. Implementation of an acute palliative care unit for COVID-19 patients in a tertiary hospital: Qualitative data on clinician perspectives. Palliat. Med.; 2022; 36, pp. 332-341. [DOI: https://dx.doi.org/10.1177/02692163211059690]
69. Selman, L.E.; Farnell, D.; Longo, M.; Goss, S.; Seddon, K.; Torrens-Burton, A.; Mayland, C.R.; Wakefield, D.; Johnston, B.; Byrne, A. et al. Risk factors associated with poorer experiences of end-of-life care and challenges in early bereavement: Results of a national online survey of people bereaved during the COVID-19 pandemic. Palliat. Med.; 2022; 36, pp. 717-729. [DOI: https://dx.doi.org/10.1177/02692163221074876]
70. Sleeman, K.E.; Cripps, R.L.; Murtagh, F.E.M.; Oluyase, A.O.; Hocaoglu, M.B.; Maddocks, M.; Walshe, C.; Preston, N.; Dunleavy, L.; Bradshaw, A. et al. Change in Activity of Palliative Care Services during the COVID-19 Pandemic: A Multinational Survey (CovPall). J. Palliat. Med.; 2022; 25, pp. 465-471. [DOI: https://dx.doi.org/10.1089/jpm.2021.0315]
71. Strang, P.; Bergström, J.; Martinsson, L.; Lundström, S. Dying From COVID-19: Loneliness, End-of-Life Discussions, and Support for Patients and Their Families in Nursing Homes and Hospitals. A National Register Study. J. Pain Symptom Manag.; 2020; 60, pp. e2-e13. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2020.07.020]
72. Tanzi, S.; Alquati, S.; Martucci, G.; De Panfilis, L. Learning a palliative care approach during the COVID-19 pandemic: A case study in an Infectious Diseases Unit. Palliat. Med.; 2020; 34, pp. 1220-1227. [DOI: https://dx.doi.org/10.1177/0269216320947289]
73. Varani, S.; Ostan, R.; Franchini, L.; Ercolani, G.; Pannuti, R.; Biasco, G.; Bruera, E. Caring Advanced Cancer Patients at Home During COVID-19 Outbreak: Burnout and Psychological Morbidity Among Palliative Care Professionals in Italy. J. Pain Symptom Manag.; 2021; 61, pp. e4-e12. [DOI: https://dx.doi.org/10.1016/j.jpainsymman.2020.11.026] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33249082]
74. Wind, G.; Vedsegaard, H.W.; Marsaa, K.; True, T.S.; Konradsen, H. The significance of the COVID-19 pandemic for family caregivers of non-COVID-19 patients in need of specialized palliative care at home: A qualitative study. Int. J. Qual. Stud. Health Well-Being; 2022; 17, 2113021. [DOI: https://dx.doi.org/10.1080/17482631.2022.2113021] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35979626]
75. Yildiz, B.; Korfage, I.J.; Witkamp, E.F.; Goossensen, A.; van Lent, L.G.G.; Pasman, H.R.; Onwuteaka-Philipsen, B.D.; Zee, M.; van der Heide, A. Dying in times of COVID-19: Experiences in different care settings—An online questionnaire study among bereaved relatives (the CO-LIVE study). Palliat. Med.; 2022; 36, pp. 751-761. [DOI: https://dx.doi.org/10.1177/02692163221079698] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35264024]
76. Zheng, Z.H.; Luo, Z.C.; Zhang, Y.; Chan, W.C.H.; Li, J.Q.; Pang, J.; Jia, Y.L.; Tang, J. Hospice care self-efficacy among clinical medical staff working in the coronavirus disease 2019 (COVID-19) isolation wards of designated hospitals: A cross-sectional study. BMC Palliat Care; 2020; 19, 188. [DOI: https://dx.doi.org/10.1186/s12904-020-00692-0]
77. WHO. Health Systems Resilience Toolkit: A WHO Global Public Health Good to Support Building and Strengthening of Sustainable Health Systems Resilience in Countries with Various Contexts; WHO: Geneva, Switzerland, 2022.
78. Khorram-Manesh, A.; Ashkenazi, M.; Djalali, A.; Ingrassia, P.L.; Friedl, T.; von Armin, G.; Lupesco, O.; Kaptan, K.; Arculeo, C.; Hreckovski, B. et al. Education in Disaster Management and Emergencies: Defining a New European Course. Disaster Med. Public Health Prep.; 2015; 9, pp. 245-255. [DOI: https://dx.doi.org/10.1017/dmp.2015.9]
79. Baker Rogers, J.E. Hospices and Emergency Preparedness Planning: A Scoping Review of the Literature. J. Palliat. Care; 2023; [DOI: https://dx.doi.org/10.1177/08258597231176410]
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
Providing and maintaining hospice and palliative care during disasters poses significant challenges. To understand the impact of disasters on the provision of hospice and palliative care and the disaster preparedness initiatives in the field, a systematic review was undertaken. Eligibility criteria for the selection of studies were: peer-reviewed original research papers addressing HPC during disasters published between January 2001 and February 2023 in English. The databases CINAHL, MEDLINE, APA PsycInfo, APA PsycArticles, and SocINDEX were searched with textword and MeSh-terms between October 2022 and February 2023. The Mixed Methods Appraisal Tool (MMAT) was used to assess the quality of the studies. Content analysis was performed. The results are presented in the form of a narrative synthesis. Of 2581 studies identified, 57 met the inclusion criteria. Most studies were published recently on the impact of the COVID-19 pandemic. Four main themes were identified in the literature: disruption of the system, setting-specific differences, emotional challenges, and system adaptation. Overall, strategies to tackle hospice and palliative care needs have been poorly integrated in disaster preparedness planning. Our findings highlight the need to strengthen the resilience of hospice and palliative care providers to all types of disasters to maintain care standards.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details



1 Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Institute of Health and Nursing Science, 13353 Berlin, Germany
2 Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Institute of Health and Nursing Science, 13353 Berlin, Germany