The majority of sources reviewed (n=42, 61.6%) were related to the SARS pandemic, with only two related to the MERS pandemic. Most available evidence originates from regions affected by previous pandemics, with 58.5%% (n=38) contributed by Asian authors and a further 18.5% (n=12) from North American sources. Almost half of the reviewed sources (n=32, 49.2%) investigated the impact of coronavirus pandemics on the general community. Nineteen articles (29.2%) addressed functional impacts on people with coronaviruses (‘patients’) and their families, and a further seventeen (26.1%) focused on healthcare workers (‘HCWs’).
Nineteen (29.2%) sources included in this review were in the form of narrative or commentary, which was particularly prevalent for those addressing the current Covid-19 pandemic. Descriptive quantitative (n=31, 67.4%) methods predominated amongst the research sources, with the majority adopting a cross-sectional approach. The research studies attracted a range of quality ratings, although the majority (n=29, 63.0%) met three of the MMAT criteria or more. A summary of the characteristics of all included sources is displayed in Table 1.
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The review identified coronavirus pandemics as providing both opportunities to promote function, and challenges that may impair, limit or restrict. As shown in Figures 2 and 3, some factors influenced more than one population group.
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Body Function & Structure
Mental Functions
Despite most body functions recovering within 6 to 24 months (32), coronavirus patients may not recover mental health and wellbeing readily or to pre-existing levels (33, 34). Two months after diagnosis, most patients report significant distress (35), poor subjective mental health (33) and psychological wellbeing (36). In the longer term, 64.0% of SARS patients experienced psychiatric morbidity after one year (37), and 42.5% met the criteria for psychiatric diagnoses after three to four years (33). A study by Siu et al (38) eight years post diagnosis also identified widespread self-reported experiences of mental dysfunction. HCWs diagnosed with coronaviruses experience similar levels of mental dysfunction as other patients (39). However, there may be some unique aspects of their experiences, with HCWs found to experience more anxiety symptoms (40, 41), greater distress and poorer quality of life than other patients (35).
Coronavirus pandemics also negatively impact on mental function in the broader community. Current evidence describes variable patterns of recovery, including initially high distress which subsides (42), ongoing fluctuations (41), new symptoms developing over time (43) and differential timelines for cognitive and emotional responses (44). Quarantine restrictions significantly impact on community mental function, with both confinement and boredom identified as particularly negative aspects of this experience (42, 45-50). Many studies (43, 47, 51-55) found community prevalence >25% for depression, anxiety, distress and generally poor mental wellbeing during the acute pandemic phase. However, lower prevalence rates for anxiety (56) and post-traumatic stress symptoms (45) were also recorded at the height of the SARS pandemic. Community members identified family health and wellbeing, social responsibility and economic impacts as their main worries during previous pandemics (53).
Mental dysfunction is also very prevalent in HCWs without coronavirus diagnoses, with to studies (41, 57) finding > 25% prevalence for distress and psychiatric morbidity. Many sources reflected upon the additional psychological burden experienced by HCWs, due to ethical tensions around not being able to meet previously expected levels of service, balancing exposure with social contact, and surge management challenges (58-65). These burdens are described as growing over time (58, 59), with HCWs who are single, female, nurses and doctors, frontline workers and close to outbreaks noted to be at particular risk (41, 57).
Cardiovascular, Haematological, Immunological & Respiratory Systems
Based on experienced with Covid-19, HCWs are advised to suspend patient activity if oxygen saturation is < 95%, or their heart rate exceeds 120 beats per minute (66). A Borg dyspnea score of ≤3 points or signs of cardiovascular or respiratory distress have also been identified as warning signs (67). In the initial months of recovery, tachycardia may be an issue, however a study by Lau et al (36) attributed this to anxiety and deconditioning, rather than cardiac dysfunction. For the general community, maintaining as much physical activity as possible is recommended to sustain good overall health and immune system function (46, 49).
Neuromusculoskeletal & Movement Related Functions
In the initial weeks after diagnosis, patients commonly experience significant disability with regards to mobility, respiratory function, muscle strength and overall physical function (33, 34, 36). Deconditioning is raised as a particular concern in several studies (36, 68, 69), especially for patients who required prolonged hospitalization or self-isolation. Two studies (69, 70) have also flagged persistent myopathy and neuropathy as an important clinical issue. In the only treatment study within this review, a randomized controlled trial of a six-week exercise training program for SARS patients found significant improvements in mobility, respiratory and neuromuscular function (71).
Other Body Structures & Functions
More generally, maintaining good nutrition and sleep hygiene are both highlighted as important goals during coronavirus recovery (66, 67). One study has found that 27.1% of patients met the criteria for chronic fatigue syndrome, and a further 13.2% reported sub-clinical but functionally disruptive issues, three years after diagnosis (33). Other long term physical symptoms identified by patients included headache, back and hip pain (38), and hip dysfunction secondary to the use of high dose steroids (32). Personal protective equipment (PPE) practices and frequent hand washing may also lead to increased eczema and allergic reactions for HCWs (63).
Bodily Risk & Protective Factors
Several patient groups are reported to experience poorer overall bodily function outcomes from pandemic coronaviruses, including those who are older; immune-compromised; pregnant; indigenous; people with diabetes, cancer and renal failure; and those experiencing severe symptoms, intensive care unit (ICU) admissions and high dose or prolonged steroid treatment (32, 35, 40, 63, 71, 72). Patients admitted to ICU are likely to experience post intensive care unit syndrome (62, 69), including neuromuscular, cardiovascular, sensory and mental function complications from prolonged periods of immobilization and prone positioning (64). In the community, people who are older; have chronic illness; are female; unemployed or with lower educational levels have been identified as being at risk of poorer bodily function during pandemics (73, 74).
A range of individual factors are also particularly associated with poorer mental function for patients, including being a young or older adult; female gender; less education, social capital and sense of control in life; employment as HCWs; using less substances, financial stress, unemployment and experiencing stigma or discrimination (32, 33, 35, 40, 53, 55, 69, 75, 76). Identified mental health risk factors for community members include age, gender, trait anxiety, personal or family history of mental illness, prolonged quarantine, direct contact with coronavirus patients, and inadequate food, clothing and accommodation (40, 43, 48, 49, 52, 54, 77). Community members also highlighted disruptions to expectations and life aspirations as having a particularly negative impact (78).
Some factors that were protective of mental function were also identified in this review. Patients with positive perceptions of their coping and self-care abilities, greater social capital and regular supportive contact with family and friends had generally better outcomes (40, 55, 63, 66, 79). Community members who deployed infection control practices, appropriately used avoidance strategies, and used active coping strategies such as problem solving were also found to have more positive mental function during pandemics (40, 80).
Activities and Participation
Learning & Applying Knowledge
Confusion regarding quarantine requirements, particularly across jurisdictions, may lead to non-compliance with quarantine (47). A lack of available information or discrepant information may also contribute to community distress, and the exercise of unnecessary restrictions on activity participation (50, 78). Sources of information while in quarantine may also influence community mental health and wellbeing, with both exclusive reliance on television (50) and avoiding email, text, and the Internet (77) associated with greater stress.
Access to rapid training for HCWs during coronavirus pandemics is recommended for timely acquisition of required knowledge (63, 65, 68). This training may include exposure to duties outside usual scope, and can be offered regularly to enable currency of skills (63). Negrini et al. (65) also reflect that HCWs need to use different knowledge sources during pandemics, as traditional reviews, guidelines and peer review publications are not sufficiently responsive to rapidly changing circumstances.
General Tasks & Demands
Patients experiencing prolonged hospitalization report struggles with boredom, due to restricted access to their usual activities (63). Zhao et al. (67) recommends patients participate in activities in 15-45 minute sessions, or intermittently depending on their current health status. The upheaval of daily routines and frustration of personal goals takes a significant toll on patient wellbeing (51), but positive aspects of isolation during recovery were also identified such as the adoption of healthier habits, more time for valued activities and greater opportunities to rest. Community quarantine requirements may result in increased sedentary activities, and the avoidance of communal participation (46). However, a study by Yang (81) found that changes to activity and participation during the SARS pandemic depended on both individual circumstances and previous routines and habits.
Communication
Technological and telecommunication aids can enable the maintenance of interpersonal relationships for patients throughout recovery (63, 64). Lim et al (63) recommended communication devices be available on request for this purpose, however Griffin et al (59) notes these conversations cannot be private when staff facilitate device use. Increased use of other communication methods (e.g. telephone, email) may also provide a coping strategy for community members during pandemics (44). Regardless of the modality utilized, all communication should be timely, balanced, consistent and clear (50, 60, 68).
The sharing of pandemic specific information may be an important support for HCWs during pandemics (39), and teams may also consider using non-traditional communication to facilitate multidisciplinary work (such as messaging platforms, social media, websites and virtual town halls) (60, 66). Health services should also support patient and family health literacy by providing pandemic information in age appropriate forms, multiple languages and diverse formats (67, 82). The need to increase education and health literacy specifically about Covid-19 in the community is a current priority (83, 84).
Mobility
The only current recommendation for patients is the use of early mobilisation wherever possible (62, 69).
Self-Care
Self-care (including dressing, toileting and bathing) has been identified as a key aspect of recovery from coronaviruses, and should be emphasized during both assessment and treatment (62, 67, 82). Self-care dysfunction is reported at all stages of recovery, usually characterized as direct consequence of bodily dysfunction (64). Lau et al (71) found 67.0% of SARS patients experienced persistent but mild difficulties with activities of daily living two months after diagnosis. Stam et al (69) asserts that at least 25.0% of patients who require ICU admission will experience significant self-care dysfunction during the first year post diagnosis. Patients should be encouraged to actively participate in self-care as much as possible, including the self-monitoring of symptoms (66).
Self-care is also an important coping strategy in the general community (44, 53). Community members (particular older people) should be encouraged to continue with existing exercise and activity programs at home, and access ongoing treatment and support via telehealth as required (49, 68). Self-care related to infection control measures may also significantly impact on food preparation and eating, particularly in cultures which practice communal dining or do not use utensils (56).
Some community members adopt new roles as ‘hygiene monitors’ to ensure compliance by other household members with infection control measures, which may take up significant time and provoke anxiety (78). Fewer than half the community has been found to practice infection control practices during pandemics (45), with younger men, those with less education and people who engage in risk taking behaviors the least likely to comply (56). One study (43) has also reported poorer mental health outcomes for men who practiced infection control measures (43). However, people with empathic responses to pandemics are more likely to comply with infection control measures (85). HCWs must also adopt new and extensive infection control self-care practices in their workplaces, including frequently hand washing, self-isolation if unwell and personal protective equipment (PPE) use (68).
Domestic Life
Shopping is the only domestic activity discussed in the reviewed literature, with tasks such as carrying groceries suggested as a means for maintaining physical function (46). Acquiring adequate supplies is supportive of coping during quarantine (44), however community members are unable to shop as frequently as they would prefer (78). Some groups (such as single people and students living away from home) may also have more difficulties accessing assistance with domestic tasks if required (47).
Interpersonal Interactions & Relationships
Patients and families may suddenly lose valued social roles when diagnosed, and experience a delayed or thwarted return to full participation. For example; Chan et al. (61) described the distress of parents whose children were hospitalized for treatment, including its impact on the broader family. Patients may also be reluctant to utilize established social support networks, for fear of increasing burden or stress for others (61).
Quarantine restrictions also result in forced social isolation for the community, with most social activities stopped or severely restricted (78, 84). Continued access to support from family and friends, dating, and the avoidance of crowded spaces were identified as health promoting (53, 81). For older people, a major factor for enabling wellbeing is maintaining a sense of ‘community connectedness’ (73). However, the avoidance of individuals perceived as ‘at risk’ indicated the use of less effective coping strategies (85). Altered patterns of social participation may persist long after quarantine ceases, with Reynolds et al. (45) finding 25.7% of the community continued to avoid crowded enclosed public spaces, and 20.5% avoided public spaces in general, in the longer term.
HCWs may experience additional restrictions on social interactions than the general community due to their roles (58), including curtailment of team meetings, face to face collaboration with peers and cessation of group treatments or therapy (63). Sin et al (39) found the availability of a specific person to talk to, especially about their workplace experiences, was a significant support for rehabilitation HCWs during the SARS pandemic.
Major Life Areas
Leisure and recreation activities provide positive experiences for patients, and may include both active and passive pursuits such as communal meals, watching television, dancing, reading, tai chi, square dancing and celebrating birthdays (67, 86). The availability of play and distraction materials is recommended for younger patients (50). These activities can enable both health and social outcomes for patients, and encourage their active participation in longer term recovery (38).
Community members are more able to actively seek and schedule pleasurable activities as a stress relieving strategy (61), as they have less stringent restrictions on participation. Activities that address both physical and mental function, such as yoga, dancing, Tai Ji Quan and Tai Chi, were prevalent in the reviewed literature (46, 49, 87). Spiritual activities related to religious or faith practices have also been identified as supportive (53). Studies of ongoing participation in leisure and recreation during pandemics have identified benefits for health and wellbeing, agency, participation and social inclusion for both younger and older adults (81, 87). Outdoor recreation was also sought by the community following the SARS pandemic (88), as a means for meeting their need for contact with nature, healthy environments and social companionship.
Community, Social & Civic Life
Six weeks after diagnosis, Lau et al (71) found 39.8% of SARS patients had returned to employment, which rose to 87.0% after twelve weeks. However, nearly a third of patients with post ICU syndrome never return to work, and a further third do not resume their previous position (69). After fifteen years, Zhang et al (32) reported 12.7% of SARS patients remained on long term sick leave. Regardless of employment status, patients report disruptions to their working life have a significant impact on their health and wellbeing (35).
Disruption to economic participation and decreased financial resources was also frequently discussed as a major negative influence on community wellbeing (42, 43, 47, 77, 78, 82). However, maintaining access to cultural, recreational, leisure, political, economic and social groups and the use of a community-based perspective may mitigate the negative impact of coronavirus pandemics (55, 84). The provision of teleworking for education and employment is also a way to enhance community coping, as are the collective approaches support by the introduction and availability of government guidelines (82).
Assessing and Measuring Activity and Participation
A recent Delphi study (89) to identify a core outcome set for Covid-19 clinical trials did not recommend any specific measures of activity or participation. Data from the Functional Impairment Checklist from SARS patients correlated closely with standardized measures of mobility, muscle strength and quality of life, with the checklist combining both body and activity / participation items (90). Zhao et al (67) recommend the Barthel Index in Covid-19 rehabilitation, which is limited to mobility and self-care activities only. More broadly, Jalali et al. (82) asserts accurate data collection for all community members will be important to understanding the functional impact of the Covid-19 pandemic.
Activity and Participation Risks and Protective Factors
O’Sullivan (72) discussed the important distinction between being ‘medically’ at risk (which focuses on bodily function) and ‘functionally’ at risk (which focuses on activity and participation). People experiencing disability, older age, low health literacy, language barriers, homelessness, unemployment, poverty, substance abuse, frailty, and migration or asylum seekers are all identified in the reviewed literature as being at significant functional risk during pandemics (72, 82, 84).
Environmental Factors
Natural & Built Environment
Geographical location was highlighted as an important variable in several studies, with people located closer to outbreaks and clusters consistently reporting worse health and wellbeing (42, 44, 52, 57, 73, 74). Overcrowded community environments which offer poor housing conditions and limited access to clean water have a particularly negative impact on their residents ability to manage the impacts of pandemics (72). People living in rural and remote areas may also experience additional disadvantage, due to both travel and service restrictions (82). Both home and hospital environments are recognized as providing potentially limited space and resources for activity and participation (67, 78). The environmental persistence of the Covid-19 virus is also relevant to the use of resources (including healthcare equipment), particularly in shared health and community environments (68).
Support & Relationships
The negative impact on health and wellbeing of isolation from social supports (beyond family and friends) is widely recognized (40, 63). In response, ‘Fangcang’ shelter hospitals were recently deployed in China, as communal quarantine facilities for patients with mild to moderate symptoms that provide social engagement and daily living essentials to aid recovery (86). Fung and Hung (84) found practical demonstrations of care and concern, including thank you cards, banners and compliments, had a positive community impact during the SARS pandemic. Peer support groups for home-quarantined university students were also found to make a positive contribution to their quality of life (91). For community members with other illnesses or disability, the availability and continuity of carers, barriers to transport for healthcare appointments and restrictions on obtaining other health supports are all identified as significant concerns (82, 83).
Attitudes
SARS patients and community members reported experiences of stigma and discrimination in regards to education, employment, relationships, and service access, which diminished over time but never completely ceased (84, 92). Lim et al (63) also identified experiences of stigma from community members towards HCWs, which were attributed to fear of infection.
Services, Systems & Policies
The majority of existing evidence focuses on healthcare services and systems, although other sectors are also mentioned briefly in some sources. Coronavirus pandemics have profound and rapid impacts on the function of healthcare systems, and changes implemented should be based on well-developed knowledge of the healthcare and welfare needs, awareness, communication, engagement, leadership and resources of the local community (72, 84, 87). Health system responses are also dependent on existing pathways and service structures (61), which may contribute to significant variability and adaptation. Fung and Huang (84) advocate for strengths based approaches implemented at the community level, rather than a focus on problems or victimhood.
The pervasive changes required of healthcare systems during pandemics include alterations to workplace practices (e.g. longer shifts, expanded scopes of practice, split teams, working from home, movement restrictions) and workforce management (e.g. absences due to school closures, staff illness) (62-64, 68, 93). Healthcare systems may need to mobilize the provision of material assistance to quarantined patients, such as supplying cleaning and infection control materials and domestic supports (84). Health service planning must therefore be comprehensive, including non-clinical areas such as food services, laundry services, and facilities management (93).
Boldrini et al. (58) advises it is not been feasible to keep Covid-19 patients isolated within designated service areas, while leaving other areas to function as normal. The management of surges and in-facility outbreaks may impact upon discharge planning for all patients, creating workload and resource consequences across multiple services or locations (58, 62, 63). Some HCWs may also experience a significant decrease in workload as resources are shifted to other services, leading to underutilization or stand downs (93).
The impact of such wholesale change on HCW health and wellbeing is extensive, and healthcare systems may need to offer additional welfare support for their workforces (59). Fatigue and distress can compound over time, leading to lapses in vigilance which could precipitate errors (63). Donning and doffing PPE takes additional time that decreases workplace efficiency, and it use may also contribute to fatigue due to increased heat and respiration effort (63)
The rapid uptake of eHealth (e.g. e-commerce and appointment platforms, video conferencing, telehealth) has also emerged during coronavirus pandemics (58, 63, 68). Telehealth may be unsuitable for some healthcare settings and practices, or limited by device availability, technical malfunctions, privacy and security concerns, the need for physical examination and variable digital literacy (62) Telehealth provision is also dependent on the availability of reliable internet infrastructure, smartphones or other connected devices (82). Koh et al. (68) cautions the evidence available for effective telehealth is relatively sparse, except for the field of stroke rehabilitation. However, some self-care rehabilitation activities and telephone based emotional support are reported to be feasible (84, 94). Electronic medical records are also supportive, allowing for rapid information access and mitigating infection risks associated with paper records (64, 93).
Restricted interpersonal activities also impact upon the community’s relationship with healthcare services and systems, which some reporting a lack of consistency and personal connection with their treating team during pandemics (50, 78). Infection control procedures and communication about pandemics from health services may be perceived as both comforting and anxiety provoking by patients (50, 56, 61). While changes to healthcare services during pandemics are often described as reactive, community engagement in planning processes and participatory governance is recommended in both the short and long term (72, 84).
Adaptations to the healthcare environment in response to coronavirus pandemics are also reported in the reviewed literature. Larger departments and therapy areas may not be available, leading to the development of smaller ‘mini’ treatment spaces closer to wards (62, 93), and rehabilitation and treatment equipment may also need to be redistributed to these areas (63). Detailed, locally produced guidelines to support consistency in new practices is recommended, provided they are responsive to user feedback (59, 60).