Coronavirus disease 2019 (COVID-19) patients present long-lasting physical and neuropsychological impairment, which may require rehabilitation.
The current cross-sectional study characterizes post COVID-19 sequelae and persistent symptoms in patients in an outpatient rehabilitation program.
Thirty patients [16 post-ICU and 14 non-ICU; median age = 54(43.8–62) years; 19 men] presenting sequelae and/or persistent symptoms (>3 months after acute COVID-19) were selected of 41 patients referred for neurorehabilitation. Patients underwent physical, neuropsychological and respiratory evaluation and assessment of impact of fatigue and quality of life.
The main reasons for referral to rehabilitation were: fatigue (86.6%), dyspnea (66.7%), subjective cognitive impairment (46.7%) and neurological sequelae (33.3%). Post-ICU patient presented sequelae of critical illness myopathy and polyneuropathy, stroke and encephalopathy and lower forced vital capacity compared to non-ICU patients. Cognitive impairment was found in 63.3% of patients, with a similar profile in both sub-groups. Increased physical fatigue, anxiety and depression and low quality of life were prevalent irrespective of acute COVID-19 severity.
The variability of post COVID-19 physical and neuropsychological impairment requires a complex screening process both in ICU and non-ICU patients. The high impact of persistent symptoms on daily life activities and quality of life, regardless of acute infection severity, indicate need for rehabilitation.
The coronavirus disease 2019 (COVID-19) is considered primarily a respiratory disease caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The clinical spectrum of acute COVID-19 infection is heterogeneous, with approximately 15% of cases being asymptomatic (Byambasuren et al., 2020), whereas about 73% of patients present symptoms of acute respiratory infection (fever, cough, dyspnea) (Argenziano et al., 2020; Suleyman et al., 2020), with higher risk of severe illness in older adults, males and individuals with baseline comorbidities (hypertension, obesity, diabetes, chronic pulmonary or kidney disease) (Argenziano et al., 2020; Richardson et al., 2020). A relevant proportion of patients develop extrapulmonary manifestations such as musculoskeletal (fatigue and myalgia), cardiovascular (arrhythmias and cardiac injury), gastrointestinal (nausea, vomiting, diarrhea and abdominal pain) and neurological and psychiatric (olfactory and gustatory dysfunctions, headache, cognitive impairment, anxiety and depression) among the most common symptoms (AlSamman, Caggiula, Ganguli, Misak, & Pourmand, 2020; Lechien et al., 2020; Negrini et al., 2020; Zhou et al., 2020). Only a small proportion of COVID-19 positive patients require admission to ICU due to severe hypoxemia and medical complications (acute respiratory distress syndrome, shock, myocardial dysfunction and acute kidney injury) (Phua et al., 2020). However, a significant number of individuals who survived severe COVID-19 may have persistent lung damage and long-term impairment of pulmonary function (Curci et al., 2020; Zhao, Shang, Song, & al., 2020) as well as sequelae associated with critical illness and neurologic complications (cerebrovascular events, altered mental status, peripheral nervous system and muscular alteration) (Varatharaj et al., 2020). Although most patients are expected to recover within weeks after initial symptoms, at 1–1.5 months after discharge, a high proportion of individuals (87.4%) reported persistence of at least 1 symptom, particularly fatigue and dyspnea and worsened quality of life (Carfi, Bernabei, Landi, & Gemelli Against, 2020) and 34.3% referred persistent cognitive complaints (Almeria, Cejudo, Sotoca, Deus, & Krupinski, 2020).
The variability of sequelae and persistent symptoms requires a comprehensive screening and evaluation process by a multidisciplinary expert team and a range of tailored rehabilitation intervention (Wade, 2020). Early detection of persistent symptoms and sequelae in post COVID-19 patients and their inclusion in rehabilitation programs are imperative to reduce disability and to improve patients’ quality of life and community reintegration.
In the current study we characterize persistent symptoms, physical, neurological and respiratory sequelae and their impact on daily life activities and quality of life in post COVID-19 patients included in an outpatient rehabilitation program. In addition, we evaluate the relationship between demographic characteristics, preexisting comorbidities, acute COVID-19 severity (ICU vs non-ICU) and the spectrum of persistent symptoms and sequelae in this cohort. We hypothesize that both ICU and non-ICU patients will present multiple physical, neurological and respiratory persistent symptoms. We also expect that ICU patient will present with more severe symptoms, lower functional independency and quality of life and will initiate rehabilitation earlier after discharge compared to non-ICU patients.
This is a single center cross-sectional observational study on patients with persistent symptoms and/or sequelae of COVID-19 referred by a primary care physician or a specialist for outpatient rehabilitation at Institute Guttmann (Badalona, Barcelona, Spain).
Inclusion criteria were: adults >18 years with persistent symptoms or sequelae of COVID-19 infection confirmed by either PCR or serology.
Exclusion criteria were: previous neurological, psychiatric or severe medical condition; persistent symptoms of confirmed COVID-19 without indications for rehabilitation interventions (e.g. anosmia, dysgeusia, pain symptoms), clinically diagnosed COVID-19 with non-specific symptoms and negative PCR or serology.
A total of 41 individuals (16 post-ICU and 25 non-ICU) were evaluated in the outpatient department by a multidisciplinary COVID-19 team which included physicians (physical rehabilitation and neurology specialists), neuropsychologists and physical therapists. All recruited patients signed a written informed consent for participation in this research study. The study protocol was approved by the local Research Ethics Committee of and was carried out in accordance with the Declaration of Helsinki.
Before inclusion in the rehabilitation program, a structured medical evaluation gathered: demographic data; preexisting comorbidities; current smoking habits; acute COVID-19 symptoms and current respiratory, neurological and cognitive-affective symptoms from a checklist; duration of hospitalization and duration of ICU stay; required oxygen supplementation and ventilation support; acute COVID-19 treatment and complications.
Participants were asked to answer questionnaires evaluating the impact of the experienced physical, cognitive and social fatigue on daily life activities (Modified Fatigue Impact Scale, MFIS) (Larson, 2013), their sleep habits and perceived sleep quality (The Pittsburgh Sleep Quality Index) (Buysse, Reynolds, Monk, Berman, & Kupfer, 1989) and perceived quality of life (WHOQOL-BREF questionnaire) (WHO, 1996).
2.2Physical and respiratory evaluation
Respiratory function was evaluated using a portable spirometer (Conter® SP10). The following parameters were measured: forced vital capacity (FVC); forced expiratory volume in 1 second (FEV1); FEV1/FVC ratio; and the peek expiratory flow (PEF). Data were expressed as % of the expected value according to their age, gender and height. A FVC and FEV1 >80%, a FEV1/FVC ratio >0.7 and a PEF>80% of the expected value were considered normal (Garcia-Rio et al., 2013).
Maximal handgrip strength (MHS) was measured on the dominant non-affected hand or on the less affected hand using a hand dynamometer (Biometrics). MHS was recorded as the maximum value obtained from three consecutive trials and results were compared to normative values according to individual’s age and gender (Massy-Westropp, Gill, Taylor, Bohannon, & Hill, 2011).
The Short Physical Performance Test (SPPT) assessed lower extremity physical performance status based on gait speed, chair stand and balance tests (Bergland & Strand, 2019).
The Functional Independence Measure (FIM) scale was used to assess measures of independence for self-care, including sphincter control, transfers, locomotion, communication, and social cognition (Mackintosh, 2009).
All patients underwent a baseline neuropsychological evaluation regardless of the presence of subjective cognitive complains. A set of neuropsychological tests was selected to cover the most representative aspects of cognitive functions.
Orientation in person, place and time was measured using the Barcelona Test which is based on the Benton Temporal Orientation Test (Benton, Hamsher, Varney, & Spreen, 1983; Peña-Casanova, 1991). Immediate attention was assessed by means of Digit Span forward subtest of the Wechsler Adult Intelligence Scale III (Wechsler, 1997). Verbal memory was assessed using the Rey Auditory Verbal Learning Test (RAVLT) that include three domains of verbal learning, long-term verbal memory, and verbal recognition (Schmidt, 1996). Working memory was evaluated employing the Digit Span backward subtest of the Wechsler Adult Intelligence Scale III (Wechsler, 1997). Executive control was evaluated using the PMR task (a Spanish version of the FAS letter fluency task) (Benton et al., 1983; Fortuny, 1999). In addition, patients were screened for symptoms of anxiety and depression (Hospital Anxiety and Depression Scale, HADS) (Herrero et al., 2003).
Statistical analyses were conducted with a commercial software package (SPSS, version 13.0; SPSS Inc., Chicago, IL, USA). Descriptive statistics characterized basic demographic and clinical characteristics of the patients enrolled in the study. The Chi-square test for independence was used to assess associations between categorical variables. The Shapiro-Wilk’s test was used to examine the normality of distribution. The Mann-Whitney U test was used to compare differences between subgroups on age, respiratory function variables, MHS and sleep quality parameters. Quade’s test for non-parametric ANCOVAs was conducted on FIM and SPPT as dependent variables and age and gender as covariables. General linear models were conducted to study between group differences in anxiety, depression, impact of fatigue and quality of life measures as dependent variables and age and gender as covariables. A Bonferroni correction was used for multiple comparisons. Spearman’s correlation analyses were run to study relationships between continuous variables. Variables are presented as a median value with interquartile range (25–75%). A two-tailed test with an alpha level of 0.05 was used for all analyses.
Thirty individuals (16 post-ICU and 14 non-ICU) met the inclusion criteria and were recruited for the study. Three patients with clinically diagnosed COVID-19 with non-specific symptoms and negative PCR or serology and 1 patient with persistent symptoms of COVID-19 confirmed by positive PCR and previously known cognitive decline were included in a rehabilitation program but not enrolled in the current study. Other non-enrolled individuals were 4 patients who presented exacerbated symptoms of previously known affective disorders and had a negative PCR and serology for COVID-19; 2 patients with persistent symptoms (e.g. anosmia, dysguesia, pain symptoms) of COVID-19 confirmed by positive PCR and/or serology with no indications for rehabilitation; and 1 patient with symptoms of substance use disorders with negative PCR and serology for COVID-19 (Fig. 1).
3.1Baseline demographic and clinical characteristics
The selected cohort of patients selected for the study consisted of: (I) the ICU subgroup which included 16 patients who developed severe COVID-19 and required admission to ICU and (II) the non-ICU subgroup included 14 patients of which 7 patients required admission to a conventional hospital unit (non-ICU) and 7 patients who were home confined (Table 1).
|Characteristics||Total||ICU sub-group||Non-ICU subgroup||P value|
|Number of patients||30||16||14|
|Age (years)||54 (43.8–262)||61.5 (54–64.75)||43.5 (37.5–53.25)||0.001|
|BMI before COVID-19||27.52 (23.74–31.47)||30.28 (26.9–33.50)||23.80 (22.10–30.32)||0.003|
|BMI after COVID-19||24.30 (21.88–28.05)||25.57 (23.04–29.39)||23.20 (21.09–28.05)||0.15|
|Coronary heart disease||3||2||1||0.63|
|Diabetes Mellitus type 1||0||0||0||NP|
|Diabetes Mellitus type 2||2||2||0||0.17|
|Acute COVID-19 course|
|Required hospital admission||23||16||7||0.01|
|Required admission to ICU||16||16||0||0.001|
|Length of hospital stay (days)||37 (15–69)||57 (36–86)||11 (4–15)||0.001|
|Length of ICU stay (days)||26 (12–44)||26 (12–44)||0||0.001|
|Time from beginning of symptoms||103 (93–116)||98 (95–112)||110.5 (89–124)||0.26|
|to rehabilitation (days)|
|Time from hospital discharge||50 (12–74)||42 (8–64)||79 (64–90)||0.45|
|to rehabilitation (days)|
|Clinical presentation and|
|Cardiac injury or arrhythmia||3||3||0||0.09|
|Acute kidney injury||8||8||0||0.002|
|Weight loss >10 kg||11||11||0||0.001|
|CIP/CIM +Brain stroke||3||3||0||0.04|
|CIP/CIM + Spinal||1||1||0||0.28|
|Brain stroke only||1||1||0||0.28|
|O2 Supplementation and|
|Anti–IL-6 drug (Tocilizumab)||7||7||0||0.005|
Legend: ARDS: Acute Respiratory Distress Syndrome; COPD: Chronic obstructive pulmonary disease; CIP/CIM: Critical illness polyneuropathy/ Critical illness polyneuropathy myopathy; NIV: non-invasive ventilation; IMV: invasive mechanical ventilation. Variables are presented as absolute values and median value with interquartile range (25–75%). The Chi-square test was used for categorical variables and the Mann-Whitney U test for continuous variables, to compare ICU vs non-ICU subgroups.
Compared to the non-ICU group, patients in the ICU subgroups were older (p = 0.001), predominantly male (p = 0.03) with preexisting obesity (p = 0.003) and hypertension (p = 0.01).
In the acute phase, bilateral pneumonia was the main reason for hospitalization in the ICU subgroup (16 patients) compared to bilateral or unilateral pneumonia (6 patients) and transitory loss of consciousness (1 patient) in the non-ICU subgroup. Acute COVID-19 medical and neurological complications were identified only in the ICU subgroup, which required a longer hospital stay and more aggressive oxygen supplementation and pharmacological treatment.
3.2Reason for referral to rehabilitation
The main reasons for rehabilitation referred by patients during the baseline clinical evaluation, were: fatigue (86.6%), dyspnea (66.7%), cognitive impairment (46.7%) and neurological sequelae (33.3%) (Fig. 2).
On average, patients in the non-ICU subgroup started the rehabilitation 110.5 (89–124) days from the beginning of acute COVID-19 symptoms and 79 (64–90) days after discharge from conventional hospital unit, whereas in the ICU subgroup patients started the rehabilitation at 98 (95–112) days from the beginning of symptoms and 42 (8–64) days after hospital discharge. The time of rehabilitation start after beginning of symptoms and after hospital discharge were not statistically significant sub-groups (p = 0.26 and p = 0.45 respectively).
Prevalence of alterations in spirometry varied among patients in the ICU vs non-ICU subgroup: low FVC (<80%) was found in 31.25% vs 0%; low FEV1 (<80%) in 35.71% vs 37.5%; low FEV1/FVC ratio (<0.7) in 7.1% vs 12.5%; and low PEF (<80%) in 81.25% vs 50% of patients in each subgroup. The FVC was significantly lower in the ICU subgroup compared to the non-ICU subgroup (p = 0.02), but there were no statistically significant differences between subgroups in the FEV1 (p = 0.26), FEV1/FVC (p = 0.20) or PEF (p = 0.80) (Table 2, Fig. 3).
3.4Physical functioning and disability
We did not find significant differences between subgroups for SPPT score [F(1,23) = 0.88; p = 0.36], FIM total score [F(1,25) = 1.41; p = 0.25], FIM motor sub-score [F(1,25) = 1.99; p = 0.17], FIM cognitive sub-score [F(1,25) = 0.57; p = 0.46] or MHS [F(1,25) = 0.99; p = 0.33] (Table 2). Furthermore, MHS correlated with SPPT (R2 = 0.52; p = 0.01) and FIM score (R2 = 0.43; p = 0.025) and PEF (R2 = 0.45, p = 0.02) (Table 3).
Results of the neuropsychological evaluation and answers to questionnaires were missing in one patient in the UCI subgroup due to communication limitations (non-fluent aphasia).
Overall, 12 of 14 patients reporting subjective cognitive complains (e.g. difficulties with focusing attention, concentration and short memory problems) and 13 of 15 patients without cognitive complains scored lower than expected by age and education in at least one cognitive test. However, reporting subjective cognitive complains was unrelated to altered cognitive tests [X2(1) = 0.17, p = 0.68]. Furthermore, there was no significant association between previous admission to ICU and low scores on orientation [X2(1) = 0.97, p = 0.33], attention [X2(1) = 1.01, p = 0.32], verbal learning [X2(1) = 1.77, p = 0.18], long-term verbal memory [X2(1) = 0.28, p = 0.60], verbal recognition [X2(1) = 1.44, p = 0.23], working memory [X2(1) = 1.45, p = 0.50] or executive control [X2(1) = 0.18, p = 0.89] (Table 2, Fig. 4).
At cohort level, 11 patients had high anxiety and depression sub-scores (>8 p) and 4 patients had increased depression score only (Table 2). Furthermore, we found no significant differences in anxiety [F(1,25) = 2.91, p = 0.10] or depression score [F(1, 25) = 3.77, p = 0.06] between subgroups (Table 3).
At cohort level, reporting subjective emotional distress was not associated with altered anxiety [X2(1) = 0.86, p = 0.36] or depression scores [X2(1) = 1.68, p = 0.19]. However, patients presenting depression were more likely to have altered attention [X2(1) = 4.97, p = 0.026] and verbal recognition functions [X2(1) = 5.18, p = 0.023].
3.6Sleep quality, impact of fatigue and quality of life
Sleep quality was reported as being “fairly bad” or “bad” by 10 individuals in the non-ICU subgroup, and 2 patients were taking daily sleep medication. In the ICU subgroup, 2 patients reported “fairly bad” or “bad” sleep quality and 8 patients were taking sleep medication. Patients in the non-ICU subgroup had lower sleep quality (p = 0.01) and higher daytime dysfunction (p = 0.046) compared to the ICU subgroups but there were no significant differences in PSQI sub-scores for sleep latency, duration, efficacy, disturbance or medication use between subgroups (p > 0.05 for all comparisons) (Table 2).
|Characteristics||Total||ICU sub-group||Non-ICU sub-group||P value|
|FVC||91.5 (81–104.5)||85 (67–96.5)||102 (92.25–105.75)||0.02|
|FEV1||81.0 (76.25–85.75)||81.5 (76.75–87)||80 (74.75–84)||0.26|
|FEV1/FCV||81.4 (76.4–85.75)||82.0 (76.9–87.4)||80.2 (74.9–84.6)||0.20|
|PEF||65.5 (47.75–86.25)||63.5 (44.75–87.5)||67 (48.5–86.25)||0.80|
|FIM total||123 (114–125)||121.5 (104–124.75)||124 (122–125)||0.25|
|FIM motor||89 (81–91)||88.5 (76.76–89.75)||90 (89–91)||0.17|
|FIM cognitive||34 (33–35)||34 (33–35)||34 (32–35)||0.46|
|MHS||24 (18–30)||22.5 (18–29.5)||24 (17–35)||0.33|
|SPPT||10.5 (7.75–12)||10 (5–11)||12 (8–12)||0.36|
|Orientation||35 (35-35)||35 (35-35)||35 (35-35)||0.33|
|Attention||6 (5-6)||5.5 (5-6)||6 (5–7)||0.32|
|Verbal learning||44 (36.5–50.75)||40 (33.75–44.75)||47.5 (40.75–54.5)||0.18|
|Long-term verbal memory||8.5 (6–9.75)||6 (5.75–9)||9 (7.75–12)||0.60|
|Verbal recognition||12.5 (11–14.75)||12 (10–14.25)||13.5 (11–15)||0.23|
|Working memory||4 (4-5)||4 (4-5)||4 (4-5)||0.50|
|Executive control||40.5 (27.5–47)||29.5 (21.75–47)||44.5 (34.5–50)||0.89|
|Anxiety||6 (4–10)||5 (3–7)||8.5 (5.75–11.25)||0.10|
|Depression||8 (3–9)||4 (3–9)||9 (6.5–10)||0.06|
|Quality||1 (0.5–2)||1 (0-1)||2 (1–3)||0.012|
|Latency||1 (0–2)||1 (0–2)||1 (0–3)||0.31|
|Duration||1 (0-1)||1 (0-1)||1 (0–2.25)||0.45|
|Efficacy||1 (0–2)||1 (0–2)||1 (0–2)||0.68|
|Disturbance||1 (1-2)||1 (1-1)||1.5 (1-2)||0.06|
|Medication Use||0 (0–3)||3 (0–3)||0 (0–1.25)||0.25|
|Daytime dysfunction||1 (0.5–2)||1 (0–2)||2 (1–2.25)||0.046|
|Impact of fatigue|
|Physical||80.55 (66.7–94.4)||80.55 (63.9–94.4)||81.9 (68.75–95.1)||0.28|
|Cognitive||72.5 (60–85)||72.5 (57.5–85)||73.75 (61.9–85.6)||0.28|
|Social||30 (38.5–69.5)||20 (10–35)||35 (25–40)||0.40|
|Quality of life|
|Physical||38 (19–50)||38 (31–63)||25 (19–45.5)||0.30|
|Psychological||50 (31–66)||56 (38–69)||44 (23.5–57.75)||0.46|
|Social||56 (44–75)||69 (44–75)||50 (25–70.5)||0.14|
|Environmental||56 (50–63)||56 (50–75)||56 (50–63)||0.48|
Variables are presented as absolute values and median value with interquartile range (25–75%). The Chi-square test was used for categorical variables and the Mann-Whitney U test and the Quade’s test for continuous variables, to compare ICU vs non-ICU subgroups.
At cohort level, most patients reported high impact of fatigue on physical and cognitive activities (Fig. 5), but we found no significant differences between subgroups on measures of impact of fatigue on physical [F (1, 26) = 1.22, p = 0.28], cognitive [F (1, 26) = 1.22, p = 0.28] or psychosocial activities [F (1, 26) = 0.75, p = 0.40] (Table 2).
Overall, patients reported low quality of physical: 38 (19–50)%; psychological: 50 (31–66) %; social: 56 (44–75)%; and environmental health: 56 (50–63)%. However, the reported quality of physical health [F (1, 25) = 1.12, p = 0.30], psychological health [F (1, 25) = 0.56, p = 0.46], social relationship [F (1, 25) = 2.31, p = 0.14] or environmental [F (1, 25) = 0.53, p = 0.48] did not differ between the ICU and non-ICU subgroups (Table 2). Measures of impact of fatigue correlated with aspects of affective impairment, sleep quality and quality of live (Table 3).
|Impact of fatigue||HADS||Quality of life||Sleep Quality|
|Impact of fatigue||Physical||1||1.00 **||0.68 **||0.27||0.49 **||–0.55 **||–0.33||–0.38 *||–0.01||0.64 **|
|Cognitive||1.0 **||1||0.68 **||0.27||0.49 **||–0.55 **||–0.33||–0.38 *||–0.01||0.64 **|
|Social||0.68 **||0.68 **||1||0.34||0.54 **||–0.65 **||–0.51 **||–0.62 **||–0.30||0.62 **|
|HADS||Anxiety||0.27||0.27||0.34||1||0.73 **||–0.62 **||–0.60 **||–0.50 **||–0.28||0.61 **|
|Depression||0.49 **||0.49 **||0.54 **||0.73 **||1||–0.70 **||–0.45 *||–0.63 **||–0.31||0.63 **|
|Quality of life||Physical||–0.55 **||–0.55 **||–0.65 **||–0.62 **||–0.70 **||1||0.67 **||0.75 **||0.54 **||–0.70 **|
|Psychological||–0.33||–0.33||–0.51 **||–0.60 **||–0.45 *||0.67 **||1||0.71 **||0.53 **||–0.53 **|
|Social||–0.38 *||–0.38 *||–0.62 **||–0.50 **||–0.63 **||0.75 **||0.71 **||1||0.46 *||–0.60 **|
|Environmental||–0.01||–0.01||–0.30||–0.28||–0.313||0.54 **||0.53 **||0.46 *||1||–0.16|
|Sleep Quality||Total score||0.64 **||0.64 **||0.62 **||0.61 **||0.63 **||–0.70 **||–0.53 **||–0.60 **||–0.16||1|
*p < 0.05; **p < 0.001; Spearman Correlation coefficient.
The current cross-sectional study describes sequelae and persistent symptoms at more than 3 months after acute COVID-19 and their impact on activities of daily living, sleep and quality of life in patients in an outpatient rehabilitation program. Our main findings reveal that multiple persistent symptoms of COVID-19, such as fatigue, dyspnea and cognitive impairment, were main reasons for inclusion in the outpatient rehabilitation program irrespective the acute COVID-19 severity. Patients in the ICU subgroup were older, mostly male, and with obesity and arterial hypertension. Similarly, they more often presented with restrictive ventilatory impairment, single or multiple neurological sequelae of severe acute COVID-19 and were also more likely to be on treatment for sleep alterations. However, in contradiction to our hypothesis post-ICU patients did not start rehabilitation earlier than non-ICU patients and their functional independence measures, cognitive-affective state and quality of life were similar to the non-ICU sub-group.
4.1COVID-19-related alterations in respiratory function
COVID-19 is considered primarily a respiratory disease with increased risk of residual lung damage and long-term alteration of pulmonary function. Although longitudinal studies are needed, recent research reveals abnormal lung function characterized by impairment of diffusion capacity and restrictive ventilatory defects at the moment of discharge in patients with non-critical COVID-19 (Mo et al., 2020). This may still be detected in more than 50% of patients at 1 month after COVID-19 infection (Frija-Masson et al., 2020). Furthermore, respiratory impairment were found in 25.45% of COVID-19 survivors who were free of respiratory symptoms at 3 months after discharge (Zhao et al., 2020). In our study, dyspnea was the second most prevalent reason of referral to rehabilitation in both subgroups. However, only patients in the ICU subgroup (31.25%) showed altered spirometry with low FVC, suggesting restrictive pulmonary function. Data from SARS survivors indicate that severe pneumonia may determine long-term restrictive ventilatory dysfunction and impaired diffusion capacity for carbon monoxide in 28% of patients at 1 year (Hui et al., 2005) and 23.7% of patients at 2-year follow-up (Ngai et al., 2010). However, although fibrotic irreversible interstitial lung disease is central to severe ARDS, with higher risk in people of advanced age, more severe illness, longer ICU stay with need of mechanical ventilation (Gentile et al., 2020; Ojo, Balogun, Williams, & Ojo, 2020), irreversible fibrotic interstitial lung disease in COVID-19 survivors remains speculative. Restrictive chest wall mobility in people with obesity and neuromuscular disorders such as critical illness myopathy and deconditioning may also contribute to ventilatory dysfunction (Melo, Silva, & Calles, 2014; Nusair, 2020).
4.2COVID-19-related physical and neurological impairment
Persistent fatigue was the most prevalent symptom of COVID-19 affecting 53.1% of patients discharged from the hospital after recovery from acute COVID-19 (Carfi et al., 2020). Persistent fatigue is commonly reported by ARDS survivors at 1-year (Neufeld et al., 2020) and 4-year follow up (Lam et al., 2009). Main determinants of persistent fatigue may include ARDS severity, cytokine storm in the acute phase and the use of cortisol (Lam et al., 2009). Other studies suggest that ARDS severity and the length of ICU stay had little association with persistent fatigue, which seems to be conditioned by worse physical, cognitive, and mental health symptoms (Neufeld et al., 2020), in line with our findings. In our study, 81.25% patients in the ICU subgroup ad 92.86% in the non-ICU subgroup reported persistent fatigue at more than 3 months after acute COVID-19, and its prevalence and impact on daily life activities were independent of acute COVID-19 severity. Furthermore, the impact of physical fatigue correlated with higher depression score and low quality of physical and social life.
Severe COVID-19 patients referred for rehabilitation are characterized by older age, high prevalence of sequelae of multiple medical and neurological complications, preexisting comorbidities, long ICU stay and prolonged mechanical ventilation, consistent with studies (Argenziano et al., 2020; Jurado et al., 2020; Petrilli et al., 2020; Richardson et al., 2020; Suleyman et al., 2020; Varatharaj et al., 2020; Wendel Garcia et al., 2020). In our study, 62.5% of patients who required admission to ICU presented single or multiple neurological complications. The diffuse and symmetrical muscle weakness due to CIP/CIM was the most prevalent neurological complication affecting 43.75% of patients in the ICU subgroup. Potential mechanisms of CIP/CIM include microcirculatory changes associated with systemic inflammation, increased vascular permeability, metabolic alterations, denervated muscles exposed to high-dose corticosteroids (Shepherd, Batra, & Lerner, 2017), low-grade myotoxicity in patients with prolonged periods of mechanical ventilation and use of sedative drugs (Lonnqvist et al., 2020). Surprisingly, although CIP/CIM is the most common cause of neuromuscular weakness in the intensive care settings, affecting approximately 25% to 45% of patients admitted to the ICU (Lacomis, 2011), there are a few case reports of CIP/CIM in patients with COVID-19 (Bagnato et al., 2020; Tankisi et al., 2020). Furthermore, 25% of patients in the ICU subgroup presented sequelae of cerebral or spinal stroke in addition to CIP/CIM, probably due to preexisting vascular risk factors and complications of the critically ill settings (e.g., hypercoagulable state, shock, heart failure, arrhythmogenic cardiomyopathy, etc.), which increase the risk of stroke (Fifi & Mocco, 2020; Montalvan, Toledo, & Nugent, 2020). Although the presence of multiple neurological and medical complications determines longer hospital stays and increases the disability rates in the subacute COVID-19 phase, we found no differences in functional independence measures and lower extremity functioning between the ICU and non-ICU subgroups at >3 months after acute COVID-19.
4.3Neuropsychological functioning, sleep quality and quality of life
During the acute COVID-19, patients may present alteration in personality, behavior, cognition and consciousness resulting from cerebrovascular events, encephalopathy and other complications such as sepsis and hypoxia and the use of sedative drugs (Helms et al., 2020; Rogers et al., 2020; Troyer, Kohn, & Hong, 2020; Varatharaj et al., 2020). Zhou et al. (Zhou et al., 2020) report cognitive dysfunction in sustained attention in recovered COVID-19 patients as compared to healthy controls, which correlated with the level of inflammatory markers. Another study reported specific decline in attention, memory, language and praxis abilities in severe COVID-19 patients entering in the post-acute phase, which seemed to be associated with the length of ICU stay (Negrini et al., 2020). During the first months after hospital discharge and 34.3% of patients referred persistent cognitive complaints and neuropsychological evaluation revealed alterations in memory domains, attention and semantic fluency, working memory and mental and phonetic fluency as well as high anxiety and depression scores (Almeria et al., 2020). In our study, patients in the ICU and non-ICU subgroup reported persistent subjective cognitive and affective symptoms (difficulties focusing attention, altered concentration, short term memory impairment and anxiety) beyond the considered recovery, constituting the third most prevalent reason for rehabilitation referral. However, their perception was not related with altered cognitive performance or clinically relevant anxiety or depression symptoms in clinical evaluation. Furthermore, whereas patients with more severe COVID-19 and longer ICU stay would be expected to have more severe cognitive impairment (Rogers et al., 2020) we did not observe any significant differences in the cognitive domains and affective measures between subgroups.
The COVID-19 pandemic can impact the mental health of people in the general population with higher rates of depression, anxiety and sleep disorders (Stanton et al., 2020). In our study, patients in the non-ICU subgroup more frequently reported untreated sleep alterations with lower sleep quality and higher daytime dysfunction compared to ICU patients, whereas higher anxiety and depression score correlated significantly with low physical, psychological and social quality of life at cohort level. Furthermore, at the cohort level, patients presenting with depression were more likely to have altered attention and verbal recognition functions. Subjective cognitive impairment is commonly seen in patients with sleep alterations (Bubbico et al., 2019) and affective symptoms (Hill et al., 2016; Zlatar et al., 2018), supporting the relevance of screening for sleep alterations and affective symptoms in post COVID-19 patients with subjective cognitive impairment.
4.4Implication for rehabilitation
Our study showed that post COVID-19 patients may present multiple physical, neuropsychological and respiratory sequelae and persistent symptoms months after acute infection. The prevalence and severity of fatigue, cognitive-affective impairment and low quality of life, irrespective of the acute infection severity (ICU vs non-ICU patients) advocate complex evaluation and design of multidisciplinary rehabilitation. The European Respiratory Society and American Thoracic Society-coordinated International Task Force recommend the screening for treatable traits and more comprehensive assessment of rehabilitation needs, including physical as well as mental aspects, at 6–8|weeks after discharge (Spruit et al., 2020). The high prevalence of dyspnea, physical and cognitive fatigue could be important limiting factors for rehabilitation therefore should be considered when designing rehabilitation interventions to improve patients’ tolerance and adherence to treatment.
Our study has several limitations. We describe the profile of a specific subgroup of patients with post COVID-19 sequelae and persistent symptoms in individuals included in an outpatient rehabilitation program >3 months after acute phase therefore their clinical characteristic cannot be generalized to the broad population of COVID-19 patients. The study was conducted in a small population of post ICU and non-ICU COVID-19 patients therefore there is a possibility that comparisons between sub-groups were underpowered. We did not include patients with clinically diagnosed COVID-19 with criteria for physical and cognitive rehabilitation as we could not rule out other infective/non-infective etiology of symptoms. The study has a cross-sectional design therefore we do not have baseline (before COVID-19 infection) clinical measures and we cannot discard potential for preexisting respiratory, physical and cognitive-affective alterations. In addition, despite the high prevalence of dyspnea among post COVID-19 patients, we did not evaluate its severity and impact on daily life activities.
Following acute COVID-19 infection, patients may present multiple physical, cognitive-affective and respiratory impairments. The high impact of persistent symptoms on daily life activities and quality of life advocate for a multidisciplinary evaluation and clinical profiling of post COVID-19 patients before rehabilitation interventions, regardless of the severity of acute infection.
We would like to thank our colleagues from Institute Guttmann: María Sainz Pelayo, Rocio Sanchez Carrión-Abascal, Antonia Enseñat Cantallos, Cristina Silvestre, Ivan Castro, Elisabeth Blanco, María Mateo and Mónica Salvador, for their clinical work in the post COVID-19 rehabilitation program.
Conflict of interest
The authors declare no conflicts of interest.
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