Abstract
Introduction: Post-intensive care syndrome (PICS) is an emerging problem in critically ill patients and the prevalence and risk factors are unclear in patients with severe coronavirus disease 2019 (COVID-19). This multicenter prospective observational study aimed to investigate the prevalence and risk factors of PICS in ventilated patients with COVID-19 after ICU discharge. Methods: Questionnaires were administered twice in surviving patients with COVID-19 who had required mechanical ventilation, concerning Barthel Index, Short-Memory Questionnaire, and Hospital Anxiety and Depression Scale scores. The risk factors for PICS were examined using a multivariate logistic regression analysis. Results: The first and second PICS surveys were obtained at 5.5 and 13.5 months (mean) after ICU discharge, with 251 and 209 patients completing the questionnaires and with a prevalence of PICS of 58.6% and 60.8%, respectively, along with the highest percentages of cognitive impairment. Delirium (with an odds ratio of (OR) 2.34, 95% CI 1.1–4.9, and p = 0.03) and the duration of mechanical ventilation (with an OR of 1.29, 95% CI 1.05–1.58, and p = 0.02) were independently identified as the risk factors for PICS in the first PICS survey. Conclusion: Approximately 60% of the ventilated patients with COVID-19 experienced persistent PICS, especially delirium, and required longer mechanical ventilation.
Keywords: COVID-19, critically ill patients, delirium, post-intensive care syndrome
1. Introduction
Functional disabilities that occur during an intensive care unit (ICU) stay or after an ICU or hospital discharge include physical, cognitive, and mental impairments, also known as post-intensive care syndrome (PICS), with effects on the long-term prognosis of patients who survive an ICU discharge [1]. It has been reported that 50–70% of patients admitted to ICU develop PICS [2], and that the prevalence of PICS leads to a decrease in the quality of life (QOL) and a disengagement from work, which have a significant effect on society [3,4,5]. For example, the survival rate of patients with sepsis has certainly improved [6]; however, approximately one-third of patients with sepsis continue to have some difficulties in their lives after leaving the ICU, and the long-term prognosis of patients with sepsis has not yet improved [7].
Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) with a reported high mortality rate once mechanical ventilation is required [8,9,10]. Various long-term sequelae of general COVID-19 infection often have been reported, known as long-COVID or post-acute COVID-19, such as pulmonary sequelae, neurologic disorders, difficulty concentrating, fatigue, and muscle weakness [11,12,13]. PICS after a severe COVID-19 infection is likely to differ from other ICU-related diseases in terms of pulmonary sequelae and neurologic disorders, and can possibly disrupt daily life in different ways [14,15,16,17]. While some studies have investigated the prevalence of PICS after COVID-19 [14,15,18,19,20], there have been few studies primarily comprised of ventilated patients and of an adequate sample size in which all the components of PICS in terms of physical, cognitive, and mental impairments were evaluated simultaneously. Thus, it remains necessary to clarify the prevalence and risk factors of PICS in patients with severe COVID-19 to improve their long-term prognoses.
We conducted a large-scale clinical study to investigate and clarify the prevalence and risk factors of PICS in critically ill patients with COVID-19 who required mechanical ventilation during hospitalization.
2. Materials and Methods
2.1. Study Design and Setting
This study forms part of a multicenter observational study, “Post-intensive care outcomes in patients with Coronavirus Disease 2019 study” (PICS-COVID study) that was conducted in collaboration with the Cross ICU Searchable Information System (CRISIS), the national registry in Japan for ICU patients with COVID-19 who require mechanical ventilation or extracorporeal membrane oxygenation (ECMO), covering 80% of the ICU beds throughout Japan [21].
All the patients with COVID-19 admitted to 32 ICUs were considered for this study. A central office was established for the performance of administrative tasks, which included mailing questionnaires to the patients, collecting and tabulating the responses in the questionnaires, and handling inquiries from patients. Details of the participating facilities and central office are outlined in the Supplemental Table S1.
Approval for this study was granted by the Institutional Review Board of the National Hospital Organization Tokyo Medical Center (date: 26 November 2020, approval number: R20-133) and the review boards of each participating hospital. The study protocol was registered in the University Hospital Medical Information Network (UMIN000041276).
2.2. Study Population and Eligibility Criteria
The PICS survey was conducted among patients discharged from the ICU between March and December 2020. The inclusion criteria for this study included patients with COVID-19 aged ≥ 20 years who required invasive mechanical ventilation during hospitalization. The indications for invasive mechanical ventilation management were determined at the discretion of the participating institutions. A SARS-CoV-2 infection was confirmed using a polymerase chain reaction test. The exclusion criteria comprised patients from whom written informed consent could not be obtained; and patients who were unable to walk on their own before admission, regardless of the use of assistive devices, because of the possibility of pre-existing PICS. All patients with COVID-19 who require mechanical ventilation are promptly registered in the CRISIS registry in accordance with the national policy when they are admitted to the ICUs of each participating institution. The patients registered in the CRISIS registry were enrolled in our study if they met the inclusion criteria. Written informed consent was obtained from all patients in the analysis.
2.3. Procedures
Two surveys were conducted to evaluate PICS, with questionnaires sent to patients in February and October 2021. We did not send questionnaires to those who could not be contacted post-discharge. The central office made a phone call prior to sending the first PICS survey. Patients who did not respond to the first questionnaire were not sent a second questionnaire. In the second PICS survey, a phone call was also made prior to sending the questionnaire. The questionnaire consisted of simple questions regarding PICS. The Barthel Index (BI) [22,23], Short-Memory Questionnaire (SMQ) [24], Hospital Anxiety and Depression Scale (HADS)-anxiety, HADS-depression [25], and EQ-5D-5L [26] were used for the assessment of physical function, cognitive function, mental health, and QOL, respectively. Responses provided from someone approved by the patient to act in their place were permitted. All the questionnaire items are listed in the Supplemental Table S2. The responses were collected and tabulated at the central office. The patients who responded to the survey were given an incentive worth 1000 yen per survey.
2.4. Variables and Measurements
All the variables and measurements are listed in the Supplemental Table S2.
2.5. Outcomes
The primary outcome was the prevalence of PICS after an ICU discharge as shown in the first PICS survey. The secondary outcomes were the prevalence of PICS after an ICU discharge as shown in the second PICS survey and the prevalence of three elements in the PICS and answers to all the other questions (see the Supplemental Table S2). The risk factors were analyzed for PICS in terms of the presence of three components, namely, a physical impairment, cognitive impairment, or mental disorder [1]. In this study, PICS was defined as any one of the following functional impairments: a physical impairment was defined as a score of ≤90 points on the BI [27], cognitive impairment as a score of <40 points on the SMQ [28], and mental disorder as a score of ≥8 points on the HADS-anxiety or HADS-depression scale [29,30].
2.6. Statistical Analysis
The demographic characteristics and long-term health outcomes of the patients were presented as medians (interquartile ranges) for continuous variables and as absolute values and percentages for categorical variables. The continuous variables of patient characteristics were compared using a Mann–Whitney U test, and the categorical variables were compared using a chi-squared test. The risk factors for PICS (physical and cognitive impairment, and mental disorder) were analyzed using a multiple logistic regression analysis in relation to the following clinically relevant variables: age (per 10 years increase) [31], male sex [31,32], body mass index (BMI) (per 5 kg/m2 increase) [33,34], the Clinical Frailty Scale [35], sequential organ failure assessment (SOFA) [32], delirium [36], duration of mechanical ventilation (per 7 days increase) [32], ECMO [37], continuous neuromuscular blocking drugs [32], maximum daily dose of prednisolone equivalent (per 50 mg/day increase) [38], prone positioning [39], rehabilitation program in the ICU conducted by physical therapists [40], and the time period. The time period refers to the period from ICU survival discharge to February 2021 for the first PICS survey and from ICU survival discharge to October 2021 for the second PICS survey. A univariate regression analysis using a restricted cubic spline model was used to analyze the nonlinear relationship between the three PICS components and age [41,42]/BMI [33,34]. An estimated probability for the three PICS components with 95% confidence intervals (CIs) were calculated and depicted using spline curves. When missing values were noted in a patient’s questionnaire responses, the nominal scale was analyzed as zero, and the continuous variables were excluded from the analysis. A p-value < 0.05 (two-sided) was considered statistically significant. The spline curves were analyzed using R language, version 4.1.1 (R Foundation for Statistical Computing, Vienna, Austria) software; all the other data were analyzed using SPSS software, version 22 (IBM, Chicago, IL, USA).
3. Results
The study outline is shown in Figure 1. During the study period, 562 patients were treated with mechanical ventilation, and 410 eligible patients were registered in the study. Seventy-six patients died in hospital and 334 patients were discharged alive. A total of 251 surviving patients completed the questionnaire in the first PICS survey, and 209 completed the questionnaire in the second PICS survey. The survey response rates were 75.1% and 83.3%, respectively. All those who responded to the second PICS survey had also responded to the first PICS survey. None of the patients had missing clinical information; however, some questionnaire responses had missing data (Supplemental Table S3).
Patient characteristics stratified according to the PICS prevalence in each survey are shown in Table 1 and Table 2. No patient had already been admitted to ICU prior to their enrollment in this study. The first and second surveys were evaluated at a mean of 5.5 and 13.5 months after ICU discharge, respectively. The first PICS survey showed significant differences in the age, BMI, delirium, duration of mechanical ventilation, length of ICU and hospital stay, reintubation, and prednisolone dose with and without PICS, but there were no differences in these patient backgrounds except for the BMI in the second survey. In both the first and second PICS surveys, a lower BMI was associated with a significantly higher prevalence of PICS. The patient backgrounds of those who dropped out of the first and second surveys did not differ from the patient backgrounds of those for whom PICS could be evaluated. The patient background and PICS outcomes for patients who responded to both the first and second questionnaires are shown in the Supplemental Tables S4 and S5. The patient background of the 42 dropout patients before the second questionnaire is shown in the Supplemental Table S6.
Table 1.
First PICS Survey (5.5 ± 3.1 Months after ICU Discharge) |
|||
---|---|---|---|
PICS (n = 147) | Non-PICS (n = 104) | p Value | |
Age, yr, median (IQR) | 68 (60, 75) | 65 (56.3, 72) | 0.010 |
Male, n (%) | 114 (77.6) | 86 (82.7) | 0.32 |
BMI, kg/m2, median (IQR) | 24.7 (22.0, 28.4) |
25.9 (23.3, 29.0) |
0.040 |
SOFA score on the day of ventilation start, median (IQR) | 5 (4, 7) | 5 (4, 7) | 0.73 |
Clinical frailty scale before hospitalization, median (IQR) | 2 (1, 3) | 2 (1, 2) | 0.27 |
Delirium, n (%) | 36 (24.5) | 14 (13.5) | 0.030 |
Duration of delirium within 1 week of ICU admission, day, median (IQR) | 2.5 (1, 5) | 2 (1, 3) | 0.30 |
Duration of invasive mechanical ventilation, day, median (IQR) | 10 (6, 17) | 8 (6, 13) | 0.0030 |
Length of ICU stay, day, median (IQR) | 13 (8, 21) | 10 (8, 17) | 0.010 |
Length of hospital stay, day, median (IQR) | 26 (15, 51) | 20 (10, 32) | 0.0030 |
Comorbidity, n (%) | |||
Hypertension | 62 (42.2) | 52 (50) | 0.22 |
Diabetes | 49 (33.3) | 31 (29.8) | 0.56 |
Cardiac disease | 13 (8.8) | 13 (12.5) | 0.35 |
Chronic kidney disease | 3 (2.0) | 4 (3.9) | 0.32 |
Autoimmune diseases | 7 (4.8) | 2 (1.9) | 0.20 |
Malignant tumors | 7 (4.8) | 7 (6.7) | 0.50 |
COPD | 12 (8.2) | 9 (8.7) | 0.89 |
Immunodeficiency | 5 (3.4) | 3 (2.9) | 0.56 |
Treatment received during hospital stay | |||
Reintubation, n (%) | 9 (6.1) | 1 (1.0) | 0.040 |
ECMO, n (%) | 17 (11.6) | 16 (15.4) | 0.38 |
Duration of ECMO, day, median (IQR) | 14 (9, 18) | 10.5 (9, 17) | 0.79 |
Tracheostomy, n (%) | 35 (23.8) | 16 (15.4) | 0.10 |
Corticosteroid, n (%) | 118 (80.3) | 76 (73.1) | 0.18 |
Maximum prednisolone dose, mg/day, median (IQR) | 44 (30, 100) | 40 (0, 75) | 0.030 |
Continuous neuromuscular blocking agent, n (%) | 63 (42.9) | 49 (47.1) | 0.50 |
Prone position, n (%) | 82 (55.8) | 50 (48.1) | 0.23 |
Continuous renal replacement therapy, n (%) | 12 (8.2) | 7 (6.7) | 0.67 |
Rehabilitation program, n (%) | 83 (56.5) | 57 (54.8) | 0.80 |
Time from ICU admission to rehabilitation program initiation, day, median (IQR) | 5 (2, 20) | 4 (2.5, 12) | 0.37 |
BMI: body mass index, COPD: chronic obstructive pulmonary disease, ECMO: extracorporeal membrane oxygenation, ICU: Intensive Care Unit, IQR: interquartile range, PICS: post-intensive care syndrome, SOFA: Sequential Organ Failure Assessment.
Table 2.
Second PICS Survey (13.5 ± 3.2 Months after ICU Discharge) |
|||
---|---|---|---|
PICS (n = 127) | Non-PICS (n = 82) | p Value | |
Age, yr, median (IQR) | 68 (60, 75) | 66 (56, 73.3) | 0.12 |
Male, n (%) | 98 (77.2) | 69 (84.1) | 0.22 |
BMI, kg/m2, median (IQR) | 24.7 (22, 27.8) |
25.9 (23.1, 29.1) |
0.049 |
SOFA score on the day of ventilation start, median (IQR) | 5 (4, 7) | 4.5 (3, 7) | 0.26 |
Clinical frailty scale before hospitalization, median (IQR) | 2 (1, 3) | 1 (1, 2) | 0.26 |
Delirium, n (%) | 25 (19.7) | 13 (15.9) | 0.48 |
Duration of delirium within 1 week of ICU admission, day, median (IQR) | 2 (1, 4) | 2 (2, 4) | 0.58 |
Duration of invasive mechanical ventilation, day, median (IQR) | 9 (6, 17) | 9 (6, 14) | 0.53 |
Length of ICU stay, day, median (IQR) | 11 (8, 21) | 11 (8, 17) | 0.39 |
Length of hospital stay, day, median (IQR) | 23 (14, 43) | 20 (11, 35) | 0.13 |
Comorbidity, n (%) | |||
Hypertension | 56 (44.1) | 40 (48.8) | 0.51 |
Diabetes | 32 (25.2) | 29 (35.4) | 0.11 |
Cardiac disease | 9 (7.1) | 9 (11) | 0.33 |
Chronic kidney disease | 4 (3.1) | 2 (2.4) | 0.56 |
Autoimmune diseases | 5 (3.9) | 2 (2.4) | 0.44 |
Malignant tumors | 6 (4.7) | 4 (4.9) | 0.60 |
COPD | 10 (7.9) | 7 (8.5) | 0.86 |
Immunodeficiency | 4 (3.1) | 1 (1.2) | 0.35 |
Treatment received during hospital stay | |||
Reintubation, n (%) | 7 (5.5) | 2 (2.4) | 0.24 |
ECMO, n (%) | 12 (9.4) | 13 (15.9) | 0.16 |
Duration of ECMO, day, median (IQR) | 14 (8.3, 23.3) | 10 (9, 14.5) | 0.57 |
Tracheostomy, n (%) | 24 (18.9) | 15 (18.3) | 0.91 |
Corticosteroid, n (%) | 102 (80.3) | 62 (75.6) | 0.42 |
Maximum prednisolone dose, mg/day, median (IQR) | 44 (30, 100) | 42.6 (15, 82.5) | 0.20 |
Continuous neuromuscular blocking agent, n (%) | 54 (42.5) | 39 (47.6) | 0.47 |
Prone position, n (%) | 70 (55.1) | 43 (52.4) | 0.70 |
Continuous renal replacement therapy, n (%) | 13 (10.2) | 5 (6.1) | 0.30 |
Rehabilitation program, n (%) | 72 (56.7) | 42 (51.2) | 0.44 |
Time from ICU admission to rehabilitation program initiation, day, median (IQR) | 6 (2, 16) | 4 (2, 19.3) | 0.60 |
BMI: body mass index, COPD: chronic obstructive pulmonary disease, ECMO: extracorporeal membrane oxygenation, ICU: Intensive Care Unit, IQR: interquartile range, PICS: post-intensive care syndrome, SOFA: Sequential Organ Failure Assessment.
The prevalence of PICS among the patients with COVID-19 who required ventilatory management during hospitalization and the EQ-5D-5L values of each patient in the first and second surveys are shown in Figure 2 and Figure 3. PICS was diagnosed in 147 patients (58.6%) in the first survey and 127 patients (60.8%) in the second survey. There was no difference found in the percentage of those with a functional disability between the first and the second survey, with the most common functional disability being a cognitive impairment in 117 (46.6%) patients in the first survey and 111 (53.1%) patients in the second survey. The second most common functional disability was a mental disorder, identified in 80 (31.9%) patients who responded to the first survey and 60 (28.7%) patients in the second survey, while a physical impairment was identified in 55 (21.9%) patients in the first survey and 39 (18.7%) patients in the second survey. Two or more functional disabilities were present at the same time in 80 (31.9%) patients in the first survey and 66 (31.6%) in the second survey. The EQ-5D-5L values, which indicate the QOL, tended to be lower when two types of functional disability occurred simultaneously, and they were lowest among patients with all three types of functional disability.
Table 3 shows the responses to the questionnaire, categorized according to the survey, of those with and without PICS. Of the 251 patients in the first PICS survey with PICS, the median BI score was 100 (95–100), the median SMQ score was 40 (34.8–44), the median HADS score was 8 (3.8–14), and the median EQ-5D-5L score was 0.831 (0.710–1). The most common subjective symptom was weight loss, followed by anxiety, executive dysfunction, and dyspnea. Of the 209 patients in the second PICS survey with PICS, the median BI score was 100 (95–100), the median SMQ score was 39 (34–43), the median HADS score was 7 (3–14), and the median EQ-5D-5L score was 0.844 (0.759–1). The most common subjective symptom was anxiety, followed by dyspnea, executive dysfunction, and sleep disorder.
Table 3.
First PICS Survey Assessment of PICS (n = 251) |
Second PICS Survey Assessment of PICS (n = 209) |
|
---|---|---|
Dyspnea, n (%) | 118 (47.0) | 96 (45.9) |
Walking difficulty, n (%) | 89 (35.7) | 54 (25.8) |
Weight loss, n (%) | 154 (61.4) | 48 (23.0) |
Memory impairment, n (%) | 74 (29.7) | 66 (31.6) |
Executive dysfunction, n (%) | 120 (47.8) | 93 (44.5) |
Depression, n (%) | 103 (41.0) | 81 (38.8) |
Anxiety, n (%) | 144 (57.4) | 107 (51.2) |
Sleeping disorder, n (%) | 113 (45.0) | 92 (44.0) |
Visual analog scale, median (IQR) | ||
Physical condition (on a scale of 1 to 10) | 7.3 (5.5, 8.5) | 7.4 (6.2, 8.7) |
Cognitive function (on a scale of 1 to 10) | 9 (7.4, 9.9) | 8.6 (7.1, 9.9) |
Mental health (on a scale of 1 to 10) | 8.3 (6.0, 9.5) | 8 (6.5, 9.4) |
Barthel Index, median (IQR) | 100 (95, 100) | 100 (95, 100) |
Short-Memory Questionnaire, median (IQR) | 40 (34.8, 44) | 39 (34, 43) |
HADS score, median (IQR) | 8 (3.8, 14) | 7 (3, 14) |
HADS-Anxiety score | 4 (1, 7) | 3 (1, 7) |
HADS-Depression score | 4 (1, 7) | 4 (1, 7) |
EQ-5D-5L, median (IQR) | 0.831 (0.710, 1) | 0.844 (0.759, 1) |
HADS: Hospital Anxiety and Depression Scale, IQR: interquartile range, PICS: post-intensive care syndrome.
The results of the multiple logistic regression analysis are shown in a forest plot. In terms of PICS, delirium (with an odds ratio [OR] of 2.34, 95% CI 1.1–4.9, and p = 0.03) and the duration of mechanical ventilation per 7 days increase (with an OR of 1.29, 95% CI 1.05–1.58, and p = 0.02) were independent risk factors for PICS in the first PICS survey; however, in the second PICS survey, none of these factors were found to be associated with the prevalence of PICS (Figure 4). In the first PICS survey, the details concerning the three components of PICS were as follows (Figure 5): for cognitive impairment, a duration of mechanical ventilation increase was an independent risk factor; for mental disorder, delirium and a duration of mechanical ventilation increase were independent risk factors; and for physical impairment, an age increase, being female, delirium, and the duration of mechanical ventilation were independent risk factors. This trend was similar in the second PICS survey, with the exception of cognitive impairment (Figure 5).
To analyze the nonlinear risk for the prevalence of each component of PICS, univariate spline curves were used to examine the association between age/BMI and the three PICS components. An older age tended to be more likely to cause a cognitive and physical impairment, but was less likely to be associated with mental disorder. A low BMI was more likely to be related to a functional impairment in all three PICS factors, whereas obesity was less likely to be related to functional impairment. The first and second surveys showed similar spline curves (Figure 6).
4. Discussion
In patients with COVID-19 requiring mechanical ventilation, the prevalence of PICS after a mean ICU discharge of 5.5 and 13.5 months was 58.6% and 60.8%, respectively, with cognitive impairment being the most common type of functional impairment. Delirium and the duration of mechanical ventilation were independent risk factors for the prevalence of PICS.
In terms of the prevalence of PICS in general ICU patients, the prevalence has been reported as 64% and 56% at three and twelve months after ICU discharge; at three months, the cognitive impairment was 37.6%, mental impairment was 33%, and physical impairment was 23.6%; at twelve months, the cognitive impairment was 32.6%, mental impairment was 30.9%, physical impairment was 17.5%, while the prevalence of multiple functional impairments was 25% at three months and 21% at twelve months [43]. In an epidemiological study of PICS in ventilated patients in Japan, the prevalence of PICS after six months from ICU discharge was found to be 63.5%, with 37.5% having cognitive impairment, 14.6% having mental impairment, 32.3% having physical impairment, and 17.8% having multiple functional impairments [44]. Compared to previous studies, the present study showed no difference in the prevalence of PICS; however, a novel finding of this study was that patients with COVID-19 requiring mechanical ventilation had an unusually high prevalence of cognitive impairment. SARS-CoV-2 directly invades the lung tissue, causing a systemic inflammatory response and microvascular damage, leading to cerebral neuropathy [45,46] and affecting cognitive functions [47]. Moreover, the administration of corticosteroids during the acute phase of COVID-19 may cause adverse effects in the central nervous system, such as cognitive impairment, sleep disorders, and delirium [48]. Thus, PICS, in terms of cognitive dysfunction, may be more common after a severe COVID-19 infection.
Furthermore, delirium was found to be strongly associated with the prevalence of PICS in this study. Delirium is generally considered to be a risk factor for cognitive dysfunction [36]. Delirium in critically ill patients with COVID-19 is likely due to microvascular disease and inflammatory mechanisms [49]. Another key mechanism of delirium in patients with COVID-19 is the development of secondary encephalopathy, possibly related to the cytokine storm phenomenon. Immune-mediated injury is mainly due to cytokines and the activation of T lymphocytes, macrophages, and endothelial cells [50]. Furthermore, these cytokines may damage the blood–brain barrier and induce encephalopathy [50]. The development of delirium in patients with COVID-19 might be influenced by patient factors such as age, sex, severity of illness, and comorbidities, as well as environmental factors such as a poor compliance with the ABCDEF bundle in relation to patients being managed for COVID-19 [51], medications such as midazolam and steroids, and visitation restrictions that may also contribute to the prevalence of delirium [49,52]. It is unclear whether bundling responses improve the incidence and outcome of delirium in patients with COVID-19, but if delirium is a strong risk factor for PICS, as shown in this study, it may be necessary to make efforts to minimize delirium through providing standard ICU care to patients with COVID-19 [53].
Another risk factor for the prevalence of PICS found in this study was the duration of mechanical ventilation. In patients with COVID-19, a prolonged duration of mechanical ventilation, along with prolonged immobilization, can lead to prolonged inflammation followed by immunodeficiency and hypercatabolism. These conditions are referred to as persistent inflammation, immune suppression, and catabolism syndrome (PIICS) [54]. A PIICS prevalence can lead to persistent mild inflammation, the coexistence of anti-inflammation and immunosuppression to counteract or further counteract inflammation and cause infection, and a prolonged wasting of the body, especially the muscles, which can lead to the development of PICS [54,55,56]. Appropriate nutrition therapy and rehabilitation have been promoted as possible PIICS treatment interventions [57], and PIICS may also be controlled by providing appropriate ICU care and interventions intended to prevent PICS [56].
This study identified specific trends in relation to age/BMI and the three PICS components in patients with COVID-19. The prevalence of physical and cognitive impairment tended to be higher in older as well as in general critically ill patients [58,59]. The prevalence of mental disorder in general critically ill patients has been shown to exhibit a bimodal pattern between younger and older patients [60,61]. However, there was no age-related trend in the prevalence of mental disorders found in this study. This may be related to the relatively high prevalence of anxiety and depression among working-age adults [62]. Obesity is known to be associated with increased mortality in patients with COVID-19 [63,64], but was not found to be associated with the prevalence of functional disability in this study; rather, a low BMI was associated with worse trends for functional disability. The mechanism by which being underweight confers health risks has been suggested to be due to hypoleptinemic disorders characterized as fat loss, severe insulin resistance, hypertriglyceridemia, and ectopic fat accumulation [65,66]. In older adults with frailty, not only physical frailty but also cognitive impairment and mental disorder have been associated with frailty, and frailty is an independent risk factor for delirium, moderate cognitive impairment, and dementia [67,68].
This study had some limitations. First, since patients requiring ventilatory management were included in this study, it was difficult to assess the cognitive function and mental health in the acute phase. Only patients who could walk unassisted were selected; therefore, their physical and cognitive functions were stabilized to some extent before hospitalization. However, some patients might have had certain organic mental disorder characteristics or mild cognitive dysfunction prior to the onset of COVID-19. Second, the time taken to assess PICS and QOL differs between patients, which might have affected the internal validity of the results. Third, this study only involved the assessment of outcomes obtained using self-reported measures, which might have caused data bias. Fourth, PICS studies conducted using different assessment tools may not be comparable, and a minor physical impairment may have been missed using the BI. Fifth, we could not compare the prevalence and risk factor of PICS between ventilated- and non-ventilated patients with COVID-19 as non-ventilated patients with COVD-19 were not included in this study. Further research is needed in which these limitations are addressed.
5. Conclusions
Approximately 60% of the ventilated patients with COVID-19 were found to have experienced persistent PICS after 5.5 and 13.5 months of ICU discharge, with a higher prevalence of cognitive impairment than physical impairment and mental disorder. Delirium and a longer mechanical ventilation were identified as independent risk factors for PICS after 5.5 months of ICU discharge.
Acknowledgments
Yasushi Nakamori (Kansai Medical University Medical Center), Masanari Hamaguchi (Department of Critical Care Medicine, Yao Tokushukai General Hospital), Kentaro Motoda (Clinical Research Center, Yao Tokushukai General Hospital), Asase Yamaguchi (Department of Emergency and Critical Care Medicine, Osaka Medical and Pharmaceutical University), Jiro Ito (Department of Anesthesiology and Critical Care, Kobe City Medical Center General Hospital), Kazuya Kiyota (Department of Emergency and Critical Care Medicine, Saitama Red Cross Hospital), Akinori Uchiyama (Department of Anesthesiology and Intensive Care Medicine, Osaka University Graduate School of Medicine), Haruhiko Hirata (Department of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine), Yuji Fujino (Department of Anesthesiology and Intensive Care Medicine, Osaka University Graduate School of Medicine), Jiro Fujita (Department of Infectious, Respiratory, and Digestive Medicine, Control and Prevention of Infectious Diseases, Graduate School of Medicine, University of the Ryukyus), Masaki Yamasaki (Department of Anesthesiology and Intensive Care Medicine, Kyoto Prefectural University of Medicine), Masahito Horiguchi (Department of Emergency and Critical Care Medicine, Japanese Red Cross Kyoto Daiichi Hospital), Mitsunobu Nakamura (Japanese Red Cross Maebashi Hospital, Advanced Medical Emergency and Critical Care Center, Intensive Care Unit and Department of Emergency & Critical Care Medicine), Hayato Taniguchi (Advanced Critical Care and Emergency Center, Yokohama City University Medical Center), Takahiro Inagawa (Department of Emergency and Critical Care Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University), Hiroshi Ono (Department of Infectious Diseases, National Hospital Organization Kumamoto Medical Center), Toshihiro Sakurai (Department of Emergency and Critical Care, National Hospital Organization Kumamoto Medical Center), Isao Nagata (Department of Intensive Care Medicine, Yokohama City Minato Red Cross Hospital), Kosuke Yoshida (Department of Emergency & Critical Care Medicine, National Hospital Organization Kyoto Medical Center), Masayoshi Nishijima (Department of Respiratory Medicine, Yodogawa Christian Hospital), Kuraishi Hiroshi (Nagano Red Cross Hospital, Department of Respiratory Medicine), Kengo Hiwatashi (Department of Emergency and Critical Care Medicine, Hitachi General Hospital), Takuya Shiga (Department of Intensive Care, Tohoku University Hospital), Yoshiaki Iwashita (Department of Emergency and Critical Care Medicine, Faculty of Medicine, Shimane University), Hiroaki Watanabe (Department of Acute Care Surgery, Shimane University Faculty of Medicine).
List of Abbreviations
BI | Barthel Index |
BMI | Body mass index |
CRISIS | Cross ICU Searchable Information System |
HADS | Hospital Anxiety and Depression Scale |
ICU | Intensive care unit |
PICS | Post-intensive care syndrome |
QOL | Quality of life |
SMQ | Short-Memory Questionnaire |
SOFA | Sequential organ failure assessment |
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcm11195758/s1, Table S1: Details of the central office and participating facilities; Table S2: All data extraction items; Table S3: Number of missing values from patient survey results; Table S4: Patient background with both responses to the first and second questionnaires; Table S5: PICS outcomes for 209 patients who responded to both of the first and second questionnaires; Table S6: Patient background of 42 dropout patients before the second PICS survey
Author Contributions
J.H., K.N. and K.L. contributed to the concept and the design of the study. J.H., S.I, K.L., K.Y., T.N. (Takeshi Nishida), S.O., S.H., N.K. (Naoki Kanda), S.M., Y.O., D.K., H.S., K.H., A.T., T.O., T.F., H.Y. (Hironori Yawata), K.O., A.K., H.Y. (Hidehiro Yamagata), M.H., Y.S., T. N. (Tomoyuki Nakamura), K.S., T.H., S.B., M.A., N.K. (Noboru Kato), T.I., H.K., Y.K., M.N., H.N., K.T., O.N., and K.N. par-ticipated in the data collection. J.H. and K.N. analyzed the data. N.K. (Naoki Kanda) performed the restricted cubic spline analysis. J.H. and K.N. wrote the first draft with input from K.Y., K.L., T.N. (Takeshi Nishida), S.I., S.O., S.H., N.K. (Naoki Kanda) and O.N. All the authors contributed to and approved the final manuscript. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
This study was performed in line with the principles of the Declaration of Helsinki. Approval was granted by the Institutional Review Board of National Hospital Organization Tokyo Medical Center (Date: 26 November 2020, Approval number: R20-133).
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
Individual participant data that underlie the results reported in this article are available from the corresponding author upon reasonable request.
Conflicts of Interest
All authors have disclosed that they do not have any potential conflict of interest.
Funding Statement
This research was funded by the Nestlé Health Science Company of Nestlé Japan. The funder of this study had no role in the study design, data collection, data analysis, data interpretation, or writing of the report. The funds were used to conduct the electronic data capture for the study, operate the central office, pay for questionnaire postage, and provide honoraria to patients.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Supplementary Materials
Data Availability Statement
Individual participant data that underlie the results reported in this article are available from the corresponding author upon reasonable request.