key: cord-0895190-9mm54re1
authors: Heyns, Arne; Dupont, Jolan; Gielen, Evelien; Flamaing, Johan; Peers, Koen; Gosselink, Rik; Vrijsen, Bart; Lorent, Natalie; Everaerts, Stephanie; Janssens, Wim; Hermans, Greet; Caluwé, Kim; Staes, Blanche; Goeleven, Ann; Meulemans, Ann; Waelkens, Hadi; Beyens, Hilde; Tournoy, Jos
title: Impact of COVID-19: urging a need for multi-domain assessment of COVID-19 inpatients
date: 2021-03-30
journal: Eur Geriatr Med
DOI: 10.1007/s41999-021-00486-4
sha: 77c1e56b2263dcba0bbfce36a16289aaf6feedb9
doc_id: 895190
cord_uid: 9mm54re1

OBJECTIVE: To retrospectively analyse data obtained from the multi-domain assessment of hospitalized COVID-19 patients, to describe their health status at discharge, and to investigate whether subgroups of patients, more specific ICU patients and older adults (> 70 years), had more (or less) risk to experience specific impairments. METHODS: Retrospective case series in the University Hospitals Leuven, Belgium of confirmed COVID-19 patients ‘after surviving an ICU-stay’, ‘aged ≥ 70 years’, or ‘aged < 70 years with a length of hospitalization > 7 days’. Exclusion criteria were ‘unwilling to cooperate’, ‘medically unstable’, or ‘palliative care policy’. Following tests were used: ‘Five Times Sit To Stand Test’, ‘hand grip dynamometry’, ‘Barthel index’, ‘Swallowing screening’, ‘Montreal Cognitive Assessment’, ‘Hospital Anxiety and Depression Scale’, and ‘Nutritional Risk Screening 2002’. RESULTS: One or more tests were obtained in 135/163 patients (83.3%). Physical impairments were present in 43.2–82.8% of the patients. Median BI was 10/20 indicating limited self-dependency. Swallow impairments were present in 3/53 (5.7%) and 24/76 (31.6%) had risk of malnutrition. Impaired memory was seen in 26/43 (60.5%) and 22/47 (46.8%) had elevated anxiety/depression scores. Older adults had more physical, functional, and cognitive impairments. ICU patients had a lower hand grip force. CONCLUSION(S): The high prevalence of physical, cognitive, psychological, and functional impairments in hospitalized COVID-19 patients, both ICU and non-ICU patients, indicates that assessment of impairments is imperative. These results imply that rehabilitation and follow-up is essential for these patients. This paper proposes a short, workable assessment composed with known outcome measures to assess different domains of COVID-19 patients.

created an unforeseen pandemic afflicting a large variety of patients with and without known comorbidities, and led to a high rate of hospitalizations [1] . The peak in Belgium occurred in the beginning of April 2020 (5590 patients hospitalized and 1285 of them admitted to on an intensive care unit (ICU) on the 8th of April). Between 15th of March 2020 and 11th of June 2020, 17.568 COVID-19 patients (= 0.15% of the Belgian population [2] ) were hospitalized in Belgium [3] . This high hospitalization rate, both on ICU and non-ICU, had a great impact on regular hospital care. Furthermore, both epidemiological (rapid spread, regional differences, etc.) and logistic (separate pathways for COVID-19 patients, balance between reducing contacts but providing adequate care, tension between social reinsertion and quarantine, etc.) factors created an additional challenge for health care systems, including rehabilitation services [4] .

The combination of a high hospitalization rate and limitations caused by isolation and logistic factors made the assessment of different health domains of patients in the acute phase more complex. However, an assessment of the functional status is essential for multiple reasons. First, to evaluate which impairments would arise due to this new unknown disease. Indeed, as an unknown disease with unknown consequences, it was difficult to predict which impairments would arise among the infected patients requiring screening of multiple domains. Second, to determine whether or not a patient could be safely discharged. Third, even more important, to identify patients who would benefit from additional care for recovery of the diagnosed impairments. Finally, to evaluate, when additional care was required, which type of care was recommended (e.g. inpatient rehabilitation, outpatient rehabilitation, pulmonary rehabilitation, psychiatric or psychological follow-up, cognitive training, etc.). Specific attention for ICU patients and older adult patients (≥ 70 years) was recommended as both ICU patients and older adults were expected to have a substantial need for rehabilitation [5, 6] . COVID-19 patients hospitalized at the ICU are at risk of developing ICU-acquired muscle weakness (ICU-AW) [7] while older adult patients are more at risk of developing severe symptoms when infected with COVID-19 [6] . When developing this assessment, it was crucial to accept limitations caused by isolation and logistic problems to increase feasibility.

The need for a pre-discharge assessment was prominent, as illustrated by the survey launched by the International Society of Physical and Rehabilitation Medicine to develop a Clinical Functioning Information Tool [8] specifically for COVID-19 [9] and the European Respiratory Society and American Thoracic Society Task force on Interim Guidance on Rehabilitation in the Hospital and Post-Hospital Phase [10] .

At the beginning of the pandemic no pre-existing assessment schedule was available. We developed a short and easy to use, multi-domain assessment in our hospital to evaluate the functional status of the hospitalized COVID-19 patients with a special focus, but not limited to, ICU patients and older adults. The primary goal of this assessment was to screen possible impairments in physical, functional, psychological, nutritional, or cognitive domains. The secondary goal was to identify additional rehabilitation needs based on that information.

The primary objective was to retrospectively analyse the data obtained from the multi-domain assessment of hospitalized COVID-19 patients in the University Hospitals Leuven, Belgium and to describe their health status at hospital discharge. The secondary objective was to investigate whether subgroups of patients, more specific ICU patients and older adults (> 70 years), had more (or less) risk to experience specific impairments. This manuscript also provides information about this multi-domain assessment.

Patients with confirmed COVID-19 infection admitted to the University Hospitals Leuven, Belgium, between the 24th of April, 2020 and the 11th of June, 2020 were eligible for the assessment. Diagnosis of COVID-19 was based on a positive nasopharyngeal or lower respiratory tract sample polymerase chain reaction test or a combination of upper or lower respiratory infection symptoms (cough, fever, dyspnoea, desaturation) with chest CT findings compatible with COVID-19 [11] . The assessment was performed in all patients diagnosed with COVID-19 who were either admitted to the ward after surviving an ICU-stay, aged ≥ 70 years (described in this paper as older adults), or aged < 70 years with a length of hospitalization > 7 days. Exclusion criteria were unwillingness to cooperate, medical instability, or a palliative care policy. Patients were assessed when considered eligible for discharge from the regular (non-ICU) COVID ward unless specified otherwise.

Approval of the Ethical Committee Research UZ/KU Leuven was obtained for this retrospective analysis (S-number 64591). The need for an informed consent of participants was waived by the Ethical Committee.

The assessment battery needed to assess different aspects of the patient's function. A multidisciplinary panel of experts, comprising of physiatrists, geriatricians, pulmonologists, psychiatrists, physiotherapists, occupational therapists, dieticians, psychologists, nurses, speech language pathologists, operational directors, and project coordinators was created in the beginning of April 2020. The assessment battery was based on expert consensus.

The expert panel discussed which outcome measures and test to use. The latter required a minimum of materials, minimal additional workload and patient-caregivers contacts, and was to be performed in the patients' room. The final version of the assessment was completed on the 20th of April, 2020 and testing started on the 24th of April, 2020.

The tests were performed by different members of the regular health care providers of the patients. All of them having pre-existing expertise in performing these tests. The following tests were used for the specific domains:

• Physical domain: Five Times Sit To Stand Test (FTSTST) [12] and the hand grip dynamometry [13] were assessed by the physiotherapists; • Functional domain: Barthel index (BI) [14] as assessed by the occupational therapists and nurses; Swallowing screening according to our own hospital specific protocol, conform international guidelines [15] [16] [17] [20] performed by the nursing staff.

The hand grip strength was assessed using a Jamar Hand Dynamometer (Patterson Medical Ltd, Nottinghamshire, Great Britain) according to a standardized protocol which was already implemented at the ICU [13] . To facilitate clinical interpretation, the measured values of the hand grip force (HGF) were compared to normative values (percentile 50 value) according to age and gender [21] to obtain a percentage. A percentage of < 80% of the predictive value was considered abnormal. This cut-off was based on expert opinion with the knowledge that 80% is often used as a cut-off for abnormality, especially in pulmonary testing [22] . For the FTSTST, patients were instructed to stand up and sit back down five times after each other as quickly as possible with their arms folded across their chest. The time was recorded from the start to the time the patient was seated again for the fifth time. If the patient was not able to perform the test (e.g. need to use the arms, etc.), this was noted as 'unable to perform the test correctly' without registration of the time. A time of > 14 s or the inability of performing the test correctly was considered abnormal [12, 23] .

The BI was assessed by the nurses (feeding, bathing, grooming, dressing, bowel control, bladder control, and toilet use) and the occupational therapist (transfers, mobility, and stairs). The BI ranged from 0 (total dependence) to 20 (total independence). There was no cut-off score for the BI.

The swallowing screening was performed within 48 h of admission to the ward. In contrast to the other tests that were executed once patients were eligible for discharge from the COVID normal care unit. Additional exclusion criteria specifically for this test were 'nil per os policy' or 'presence of a gastrostomy tube'. The test consisted of two steps. The first step was assessment of eight non-swallow parameters, indicative for potential or premorbid swallowing problems. In the second step, an actual water swallow test (teaspoon and cup drinking) was performed while nurses checked for swallowing activity and aspiration signs. Progression to the next step was only possible if the previous step was normal. If something was aberrant during one of the steps, the screening assessment was stopped, considered 'impaired'.

A specific exclusion criterium for the MOCA was 'known cognitive impairment or dementia' mentioned in the patients' file. This was then noted as 'known cognitive impairment'. The MoCA blind was assessed if a patient suffered from visual impairments. A score of < 26 on the MoCA or < 18 on the MoCA blind was considered abnormal [18] .

The first part of the NRS 2002 was assessed by the nurses within 48 h after admission. Like the swallow screening, this was in contrast to other tests which were performed shortly before discharge. This part comprises of four questions. The test was scored 'risk of malnutrition' if one or more of those questions were answered with 'yes' or if the BMI of the patient was below 18.5 for patients aged < 70-years-old or below 20.5 for patients ≥ 70-years-old.

The HADS was not assessed when patients had known cognitive problems or when the occupational therapists judged that the questionnaire could not be completed in a reliable way. The HADS was considered aberrant when the HADSanxiety (HADS-A) or HADS-depression (HADS-D) subscales had a score > 7, indicating possible anxiety or depression [19] .

We collected the following data from the electronical patient file: date of birth (age), gender, admission to ICU, score on HGF, FTSTST, BI, swallow screening, NRS 2002, HADS, and MoCA. Data were extracted from the patients' records to an Excel database which was pseudonymised. Data were stored on the secure server of the University Hospitals Leuven, Leuven, Belgium.

All patients with one or more results of the assessment test battery available were included. Data were analysed retrospectively. Subgroup analysis was performed between ICU and non-ICU populations as well as between those aged < 70 years and those ≥ 70 years.

Continuous variables were summarized with standard descriptive statistics, normally distributed data were noted as average ± SD while non-normally distributed dated were noted as median with interquartile 25% and 75% ranges [Q1-Q3]. Categorical variables were summarized with frequencies and percentages. Ninety-five percent confidence intervals (CI) were provided for descriptive statistics.

Shapiro-Wilk test was used to check for normality, Levene's test was used to assess equality of variance. Fisher exact test was performed to analyse different subgroups, independent t test was used to compare means, and Mann-Whitney U test to assess distribution between groups. Odds ratio (OR) was calculated using logistic regression. Table 1 shows how many patients were assessed for each specific test. Some patients were eligible for assessment, but were not or incompletely assessed due to limited period of time before discharge, limited supply of protective personal equipment or other logistic problems. The reason for nontesting was not noted in the patient file and, therefore, could not be retrieved. The only exception was that in 29 patients (21.5%) with 'known cognitive problems', or 'not able to complete the questionnaire in a reliable way' the MoCA and HADS were not assessed. 

The results of the assessment show that physical, functional, cognitive, nutritional, and psychological impairments are highly prevalent in the group of COVID-19 patients, both in ICU and non-ICU patients. We found a higher median age in the non-ICU versus our ICU population, likely to be explained by a possible selection bias. The Clinical Frailty Scale [24] was registered for patients with an age ≥ 70 years. Patients with a higher frailty score, which are more likely to be older patients, were less likely to be admitted to the ICU. Also we did not assess patients < 70 years who were not hospitalized for more than 7 days as this group seemed less relevant from a clinical perspective and resources had to be targeted towards groups with the highest risk of developing impairments. This age difference has to be taken into account when comparing the data of ICU vs. non-ICU groups.

Physical impairments are highly prevalent as shown by the FTSTST time and the hand grip dynamometry values. In addition to the physical impairments, the median BI indicates that the level of self-dependency is limited [25] . Both findings are in concordance with the study of Belli et al. [26] and Paneroni et al. [27] .

The HGF was the only test that was significantly lower in ICU patients compared to non-ICU patients with a difference of (95% CI) of 23.9 ± 6.4% predicted value. This could be explained by the fact that the ICU patients had a high risk of developing ICU-acquired weakness [28, 29] . The percentage of aberrant swallowing screenings of COVID-19 patients on ICU was comparable to other non-COVID-19 ICU studies [30] .

Older adults were less able to perform the FTSTST within 14 s. Physical impairment might be explained by disease itself, but quarantine or isolation measures might also lead to diminished physical activity and thus reducing physical strength [31] . The BI was lower in the older adults. On one hand this might be explained by the fact that physical and cognitive functions are also more impaired in this group, on the other hand it is possible that they had a lower premorbid BI because they contained more nursing home residents. These premorbid BI were not available in the patients' files.

Cognitive impairment was frequent in our cohort as reflected in the high proportion of patients with impaired MoCA scores. More studies are investigating the possible impact of COVID-19 on cognitive function. Zhou et al. [32] investigated 29 recovered COVID-19 patients and found that even after recovery, they performed less on online neuropsychological tests compared to healthy controls. The inflammatory response, hypercoagulability, neurotropic characteristics of the virus, or post-infectious immune mediated processes are all possible threats of COVID-19 to the central nervous system which could lead to several problems (e.g. stroke, hypoxia, delirium, etc.) that can diminish cognitive function [33] [34] [35] . There was no significant difference in the number of impaired MoCA scores between ICU and non-ICU patients. Literature concerning post-intensive care syndrome (PICS) shows that patients with prolonged ICU stay have high risk of impairments on neuropsychological test. Specifically for ARDS survivors, some studies show up to 71% of the patients having impairments on the neuropsychological tests [36] , mainly problems with memory, executive function, language, attention, and visuospatial abilities [37] . The fact that the MoCA scores are comparable with non-ICU population might be explained by the fact that the non-ICU population was older. Our data already showed that older adults had a significantly higher number of impaired MoCA scores. This older non-ICU population is more likely to experience delirium [38] and/or have other causes of pre-existing cognitive impairments present which are more prevalent in the older adult population (e.g. delirium, vascular dementia, etc.) which might have been previously unknown/undiagnosed.

The HADS was aberrant in almost half of the tested patients. These results are in line with results of a systematic review concerning mental health consequences caused by COVID-19 [39] and reinforce the need for further psychological evaluation and follow-up if deemed necessary. There was no significant difference between ICU or non-ICU patients concerning HADS scores. This is not completely unexpected as studies have shown that the levels of anxiety and depression were higher in the general population (non-infected people) compared to before the COVID-19 epidemic [39] .

The risk of malnutrition according to the NRS 2002 was present in almost 1/3 of the tested population. It was more pronounced in ICU patients compared to non-ICU patients but this difference did not reach statistical significance.

There are some limitations to this retrospective study. The number of patients for some specific tests was low and these numbers diminish even further with subgroup analyses. The low number of participants for some tests might impair the statistical power of the observations. However, this paper primarily contributes with an important descriptive component concerning the assessment of the functional status of COVID-19 patients. The reason why some patients were not tested could not be retrieved from the patients' files. It is possible that patients who performed better were tested less because this would have less impact on clinical decision making and resources might have been needed elsewhere. There was no information concerning the premorbid function of these patients. This could have impacted the results as patients with a lower premorbid function which was known might have been tested less because they were already care-dependent and the assessment would have changed less in the organization of their discharge care.

Despite its limitations, this paper offers an important basis for the assessment COVID-19 patients. Others have indicated the need for a broad evaluation of the COVID-19 patient. For example, Klok et al. [40] already suggested a simple post-COVID tool assessment to measure the functional status over time using ordinal patient reported outcome measures. In contrast to proposed tool of Klok et al., we used a combination of patient reported outcome measures (e.g. HADS, etc.) and objective outcome measures (e.g. FTSTST, HGF, etc.) which might provide more detailed information. The British Society of Rehabilitation Medicine developed a framework for the assessment of post-ICU (COVID-19) patients [41] . However, based on our findings we would recommend to assess both ICU and non-ICU patients since both have high prevalence of physical, cognitive, psychological, and functional impairments. We, therefore, believe that this paper provides a base for future studies to optimise an assessment to evaluate the needs of (COVID-19) patients and install adequate follow-up trajectories. Future (prospective) studies should focus on an assessment of the patients functioning, ideally comparing this with premorbid functioning, which should lead to the optimal care/rehabilitation.

The high prevalence of physical, cognitive, psychological, nutritional, and functional impairments in hospitalized COVID-19 patients, both ICU as non-ICU patients, indicates that a pre-discharge assessment of impairments is imperative. Based on our data, we would recommend a minimal screening of physical, functional, cognitive, psychological and nutritional impairments. The high prevalence of impairments in multiple domains implies that adequate care and/ or multidisciplinary rehabilitation and follow-up after discharge seem to be essential for these patients.

Screening for possible impairments in different domains allows us to evaluate which type of rehabilitation is most adequate for each patient. This paper gives a short, workable assessment composed with known outcome measures to assess different domains of COVID-19 patients. The results of this assessment can be used to plan further care of the patient within the possibility of the hospital/home environment.

Availability of data and material Data are available on reasonable request to the corresponding author.

Conflict of interest None of the authors has a conflict of interest.

Ethics approval Approval of the Ethical Committee Research UZ/KU Leuven was obtained for this retrospective analysis (S-number 64591). The need for an informed consent of participants was waived by the Ethical Committee.

Informed consent All authors consent for publication.

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