| Literature DB >> 34865227 |
Saskia Cheyne1,2, Richard I Lindley3,4, Natasha Smallwood5,6, Britta Tendal2, Michael Chapman7, David Fraile Navarro8, Phillip D Good9, Peter Jenkin10, Steve McDonald2, Deidre Morgan11,12, Melissa Murano2, Tanya Millard2, Vasi Naganathan13, Velandai Srikanth6, Penelope Tuffin14,15, Joshua Vogel2,16, Heath White2, Samantha P Chakraborty6, Elizabeth Whiting17, Leeroy William2,18, Patsy M Yates19, Mandy Callary20, Julian Elliott2, Meera R Agar21.
Abstract
INTRODUCTION: Older people living with frailty and/or cognitive impairment who have coronavirus disease 2019 (COVID-19) experience higher rates of critical illness. There are also people who become critically ill with COVID-19 for whom a decision is made to take a palliative approach to their care. The need for clinical guidance in these two populations resulted in the formation of the Care of Older People and Palliative Care Panel of the National COVID-19 Clinical Evidence Taskforce in June 2020. This specialist panel consists of nursing, medical, pharmacy and allied health experts in geriatrics and palliative care from across Australia. MAIN RECOMMENDATIONS: The panel was tasked with developing two clinical flow charts for the management of people with COVID-19 who are i) older and living with frailty and/or cognitive impairment, and ii) receiving palliative care for COVID-19 or other underlying illnesses. The flow charts focus on goals of care, communication, medication management, escalation of care, active disease-directed care, and managing symptoms such as delirium, anxiety, agitation, breathlessness or cough. The Taskforce also developed living guideline recommendations for the care of adults with COVID-19, including a commentary to discuss special considerations when caring for older people and those requiring palliative care. CHANGES IN MANAGEMENT AS RESULT OF THE GUIDELINE: The practice points in the flow charts emphasise quality clinical care, with a focus on addressing the most important challenges when caring for older individuals and people with COVID-19 requiring palliative care. The adult recommendations contain additional considerations for the care of older people and those requiring palliative care.Entities:
Keywords: COVID-19; Geriatrics; Guidelines as topic
Mesh:
Year: 2021 PMID: 34865227 PMCID: PMC9299653 DOI: 10.5694/mja2.51353
Source DB: PubMed Journal: Med J Aust ISSN: 0025-729X Impact factor: 12.776
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Older people with frailty or cognitive impairment and COVID‐19:
This population includes older people (usually aged > 65 years) with impairments of physical, cognitive and/or physiological function, or who have frailty. Frailty is a multifaceted syndrome that includes physical impairments and higher susceptibility to disease. Comorbidities are often present, such as cerebrovascular disease, dementia, heart failure, and chronic lung disease. |
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People with COVID‐19 and who require palliative care:
This population includes people with COVID‐19 whose prognosis due to coexisting advanced progressive disease is limited or uncertain or people with critical COVID‐19 illness where recovery is not expected. |
COVID‐19 = coronavirus disease 2019.
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Do not delay endotracheal intubation and mechanical ventilation in patients with COVID‐19 who are deteriorating despite optimised, less invasive respiratory therapies. For mechanically ventilated adults with COVID‐19 and hypoxaemia despite optimising ventilation, consider prone positioning for more than 12 hours a day. For adults with COVID‐19 and respiratory symptoms who are receiving any form of supplemental oxygen therapy and have not yet been intubated, consider prone positioning for at least 3 hours per day as tolerated. When positioning a patient in prone position, ensure it is used with caution and accompanied by close monitoring of the patient. Use of prone positioning should not delay endotracheal intubation and mechanical ventilation in patients with COVID‐19 who are deteriorating despite optimised less invasive respiratory therapies. Consider early referral to an ECMO centre for patients developing refractory respiratory failure in mechanically ventilated adults with COVID‐19 (despite optimising ventilation, including proning and neuromuscular blockers). |
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For prone positioning and more invasive forms of therapy, including mechanical ventilation and ECMO, the net clinical benefit for each patient should be considered on a case‐by‐case basis, as factors such as frailty, advanced illness or comorbidity may lessen the benefit and increase potential harms. An older person living with frailty may be at particular risk of harm, and the symptom benefits of these therapies in palliative patients remain unclear. It may not be feasible to use prone positioning for patients who are older and living with frailty as they may be at particular risk of harm from being placed in this position. Patients with difficulty communicating before infection may be unable to alert staff when something is wrong while in the prone position. The risk of harm from proning may be compounded when these vulnerable patients are treated outside the intensive care unit, as the feasibility of moving them into prone position and providing adequate ongoing monitoring varies according to the setting. Despite the risks of proning associated with frailty, there may still be benefits for this patient group and the net clinical benefit for each patient should be considered on a case‐by‐case basis. More invasive ventilation options may be very limited in patients with frailty or underlying health issues. Decisions around proceeding to more invasive forms of therapy should consider the preferences and values of the patient, including any advance care directive or plan that may be available, and the patient’s expected short and long term benefits and burdens of treatment. Discussion with the patient, if able, or their substitute medical treatment decision maker should be undertaken to determine their current values and preferences, in association with pre‐existing, documented advance care plans or directives. |
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Consider using HFNO therapy for patients with hypoxaemia associated with COVID‐19, ensuring it is used with caution and strict attention is paid to staff safety, including the use of appropriate PPE. If HFNO is being used, ideally, this should be in a negative pressure room. If none is available, other alternatives are single rooms or shared ward spaces with cohorting of confirmed COVID‐19 patients only. Do not use HFNO therapy for patients with hypoxaemia associated with COVID‐19 in shared wards, emergency department cubicles or during interhospital patient transfer or retrieval. Consider using NIV therapy for patients with hypoxaemia associated with COVID‐19, ensuring it is used with caution and strict attention is paid to staff safety including the use of appropriate PPE. If NIV is being used, ideally this should be in a negative pressure room. If none is available, other alternatives are single rooms, or shared ward spaces with cohorting of confirmed COVID‐19 patients only. Do not use NIV therapy for patients with hypoxaemia associated with COVID‐19 in shared wards, emergency department cubicles or during interhospital patient transfer or retrieval. In patients with COVID‐19 for whom NIV is appropriate for an alternate clinical presentation (eg, concomitant COPD with type 2 respiratory failure and hypercapnia, acute pulmonary oedema), ensure airborne and other infection control precautions are optimised. In adults with COVID‐19 undergoing endotracheal intubation, consider using videolaryngoscopy over direct laryngoscopy if available and the operator is trained in its use. For mechanically ventilated adults with COVID‐19 and moderate to severe ARDS, do not routinely use continuous infusions of neuromuscular blocking agents. For mechanically ventilated adults with COVID‐19 and hypoxaemia despite optimising ventilation, consider using recruitment manoeuvres. If recruitment manoeuvres are used, do not use staircase or stepwise (incremental PEEP) recruitment manoeuvres. |
ARDS = acute respiratory distress syndrome; COPD = chronic obstructive pulmonary disease; COVID‐19 = coronavirus disease 2019; ECMO = extracorporeal membrane oxygenation; HFNO = high flow nasal oxygen; NIV = non‐invasive ventilation; PEEP = positive end‐expiratory pressure; PPE = personal protective equipment.
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Dexamethasone |
Use dexamethasone 6 mg daily intravenously or orally for up to 10 days (or acceptable alternative regimen) in adults with COVID‐19 who are receiving oxygen (including mechanically ventilated patients). Do not routinely use dexamethasone (or other corticosteroids) to treat COVID‐19 in adults who do not require oxygen. |
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Remdesivir |
Consider using remdesivir for adults admitted to hospital with moderate to severe COVID‐19 who do not require ventilation. Do not start remdesivir in adults admitted to hospital with COVID‐19 who require ventilation. |
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Special considerations for older people living with frailty and those receiving palliative care |
It is unclear whether older people or those requiring palliative care were included in the studies on which these recommendations are based. Until further evidence in these populations is available, the Taskforce does not believe a different recommendation should apply, unless contraindicated. Additional variability may be expected in these populations given the potentially different preferences and values placed on outcomes and goals for care, such as symptom relief. Because the benefit to harm ratio is uncertain, the acceptability may vary in these populations due to individual decision making around goals of care. |
The primary panel for the recommendations is the Disease‐Modifying Treatment and Chemoprophylaxis Panel. Recommendations are reviewed by the Guidelines Leadership Group and approved by the Steering Committee before being published. In addition, all recommendations are reviewed by the Consumer Panel.
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Azithromycin Hydroxychloroquine |
Subcutaneous or intravenous interferon‐β‐1a |
Lopinavir–ritonavir |
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Aprepitant Baloxavir marboxil Bamlanivimab Baricitinib Bromhexine hydrochloride Chloroquine Colchicine Combined metabolic cofactor supplementation (CMCS) Convalescent plasma Darunavir–cobicistat Dutesteride |
Favipiravir Fluvoxamine Human umbilical cord mesenchymal stem cells Hydroxychloroquine plus azithromycin Immunoglobulin plus methylprednisolone Inhaled interferon‐β‐1a Interferon‐β‐1b Interferon‐Ɣ Interferon‐κ plus TFF2 Ivermectin Intravenous immunoglobulin |
N‐acetylcysteine Peginterferon‐λ Recombinant human granulocyte colony‐stimulating factor REGN COV2 Ruxolitinib Sarilumab Sofosbuvir–daclatasvir Telmisartan Tocilizumab Triazavirin Umifenovir Vitamin D (calcifediol– cholecalciferol) Other disease‐modifying treatments |
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Trials are needed in special populations, including older people living with frailty and those receiving palliative care, for treatments currently recommended only in the context of randomised controlled trials with appropriate ethics approval. Until further evidence is available, do not use these disease‐modifying treatments to treat COVID‐19 in these populations unless they are eligible to be enrolled in trials. As older people living with frailty or cognitive impairment are particularly at risk from COVID‐19, we encourage trials that include this population (with appropriate baseline measurement of frailty and cognitive impairment). In people requiring palliative care, trials should consider symptom management and quality of life outcomes. Because the benefit to harm ratio is uncertain, acceptability may vary due to individual decision making around goals of care. Given the absence of trials and uncertain benefit to harm ratio, this recommendation protects these more vulnerable populations. | ||
The primary panel for the recommendations is the Disease‐Modifying Treatment and Chemoprophylaxis Panel. Recommendations are reviewed by the Guidelines Leadership Group and approved by the Steering Committee before being published. In addition, all are reviewed by the Consumer Panel.