| Literature DB >> 32904497 |
Demelza Emmerton1, Ahmed Abdelhafiz1.
Abstract
Delirium is a potentially fatal acute brain dysfunction that is characterised by inattention and fluctuating mental changes. It is indicative of an acute serious organ failure or acute infection. Delirium is also associated with undesirable health outcomes that include prolonged hospital stay, long-term cognitive decline and increased mortality. The new SARS-CoV-2 shows, not only pulmonary tropism but also, neurotropism which results in delirium in the acute phase illness particularly in the older age groups. The current assessment for COVID-19 in older people does not routinely include screening for delirium. Implementation of a rapid delirium screening tool is necessary because, without screening, up to 75% of cases can be missed. Delirium can also be exaggerated by health care policies that recommend social isolation and wearing personal protective equipment in addition to less interaction with patients. Non-pharmacological intervention for delirium prevention and management may be helpful if implemented as early and as often as possible in hospitalised older people with COVID-19. A holistic approach that includes psychological support in addition to medical care is needed for older people admitted to hospital with COVID-19. © Springer Nature Switzerland AG 2020.Entities:
Keywords: COVID-19; Delirium; Hospitalised; Management; Older people
Year: 2020 PMID: 32904497 PMCID: PMC7455775 DOI: 10.1007/s42399-020-00474-y
Source DB: PubMed Journal: SN Compr Clin Med ISSN: 2523-8973
Comparison of patients with COVID-19 presenting with delirium and those without delirium
| Parameter (%) | Delirium symptoms (%) | Non-delirium symptoms (%) | Difference (95% CI) |
|---|---|---|---|
| Number of patients | 12 (17) | 59 (83) | |
| Age (years) | |||
| • Range | 70–90 | 26–97 | |
| • ≥ 75 | 10 (83) | 24 (41) | 42% (17.3 to 66.7) |
| Gender, male | 7 (58.3) | 34 (57.6) | 0.7% (− 29.9 to 31.3) |
| Comorbidities (%) | |||
| • Any comorbidity | 12 (100) | 48 (78) | 22% (15.4 to 36.6) |
| • Hypertension | 9 (75) | 23 (39) | 36% (8.8 to 53.2) |
| • DM | 4 (33) | 12 (17) | 16% (− 11.7 to 44.3) |
| • COPD | 6 (50) | 18 (31) | 19% (− 10.3 to 49.7) |
| • CVD | 6 (50) | 18 (31) | 19% (− 10.3 to 49.7) |
| • CKD | 3 (25) | 6 (10) | 15% (− 9.3 to 40.7) |
| • CLD | 1 (8) | 4 (7) | 1% (− 8.7 to 11.3) |
| • Dementia | 4 (33) | 6 (10) | 23% (− 3.3 to 50.7) |
| • CFS | |||
| ▪ Range | 2–7 | 1–7 | |
| ▪ ≥ 5 | 8 (67) | 21 (36) | 31% (1.7 to 60.3) |
| Presentation (%) | |||
| • Fever | 5 (42) | 37 (63) | − 21% (− 51.5 to 9.5) |
| • Hypoxia | 10 (83) | 37 (63) | 20% (− 11.4 to 51.4) |
| • Tachypnoea | 8 (67) | 45 (76) | − 9% (− 38.0 to 20.0) |
| • Tachycardia | 6 (50) | 17 (30) | 20% (− 9.4 to 50.6) |
| • AKI | 6 (50) | 16 (27) | 23% (− 6.2 to 53.8) |
| • Acute hepatic impairment | 5 (42) | 21 (36) | 6% (− 23.5 to 36.5) |
| • High CRP | 10 (83) | 47 (80) | 3% (− 20.6 to 26.6) |
| • Leucocytosis | 4 (33) | 11 (19) | 14% (− 14.4 to 42.4) |
| • Lymphopenia | 10 (83) | 42 (71) | 12% (− 11.8 to 36.2) |
| • CXR opacification | 6 (50) | 28 (47) | 3% (− 28.0 to 34.0) |
| Outcomes | |||
| • Discharged home | 5 (42) | 43 (73) | − 31% (− 1.0% to − 61.0) |
| • ICU admission | 0 | 9 (15) | − 9% (− 18.0 to 0.0) |
| • Died | 7 (58) | 16 (27) | 31% (1.0 to 61.0) |
CI confidence interval, DM diabetes mellitus, COPD chronic obstructive pulmonary disease, CVD cardiovascular disease, CKD chronic kidney disease, CLD chronic liver disease, CFS clinical frailty score, AKI acute kidney injury, CRP C-reactive protein, CXR chest X-ray, ICU intensive care unit
Factors associated with delirium in older people with COVID-19
| Patient-related | |
| • Old age | |
| • Comorbidity | |
| • Frailty | |
| Direct neurological | |
| • Direct CNS invasion by the virus. | |
| ▪Intra-nasal access | |
| ▪Crossing blood-brain barrier | |
| • Viral encephalitis | |
| • Acute haemorrhagic necrotising encephalitis | |
| Indirect neurological | |
| • CNS inflammation | |
| • Cerebral hypoxia | |
| • Cerebrovascular involvement | |
| • Multiple organ failure | |
| • Persistent pyrexia | |
| • Neurotransmitter imbalance | |
| • Metabolic dysregulation | |
| • Autoimmune encephalopathy | |
| Environmental | |
| • Isolation | |
| • Limited interaction with family and hospital staff | |
| • Use of personal protective equipment | |
| • Prolonged mechanical ventilation | |
| • Long hospital stay | |
| • Sleep deprivation | |
| • Immobility | |
| Iatrogenic | |
| • Use of sedatives | |
| • Constipation | |
| • Dehydration | |
| • Urinary retention |
4AT delirium screening tool
| Parameter | Score |
|---|---|
| 1. Alertness | |
| Normal = fully alert | 0 |
| Mild sleepiness for < 10 s after waking then normal | 0 |
| Clearly abnormal | 4 |
| 2. AMT4* | |
| No mistakes | 0 |
| 1 mistake | 1 |
| ≥ 2 mistakes | 2 |
| 3. Attention** | |
| States 7 months correctly | 0 |
| Less than 7 months or refuses to start | 1 |
| Cannot start, drowsy or inattentive | 2 |
| 4. Acute change*** | |
| No | 0 |
| Yes | 4 |
| Score: | |
| ≥ 4: possible delirium ± cognitive impairment. | |
| 1–3: possible cognitive impairment. | |
| 0: unlikely delirium or severe cognitive impairment. | |
| Features | |
| • Takes <2 min to do | |
| • No special training required | |
| • Easy and simple | |
| • Suitable for use in different settings of clinical practice | |
| • Suitable for all patients including those unable to communicate (drowsy or agitated) | |
| • Includes brief cognitive testing | |
AMT abbreviated mental test; *Ask about: age, date of birth, place and current year. **Ask about months of the year backwards. ***Significant change in alertness, cognition or mental function over last 2 weeks and still ongoing
Fig. 1Delirium in older people—risk factors, detection and management