CRITICAL ILLNESS POLYNEUROPATHY AND FUNCTIONAL OUTCOME IN SUBJECTS WITH COVID-19: REPORT ON FOUR PATIENTS AND A SCOPING REVIEW OF THE LITERATURE

Domenico Intiso, MD1, Antonello Marco Centra, MD1, Antonio Giordano, MD1, Andrea Santamato, MD2, Luigi Amoruso, MD3 and Filomena Di Rienzo, MD1

From the 1Unit of Neuro-rehabilitation and 2Physical Medicine and Rehabilitation Section, “OORR” Hospital, University of Foggia, Unit of Neurology, IRCCS “Casa Sollievo della Sofferenza”, San Giovanni Rotondo (FG), Foggia, Italy

Patients with COVID-19 may develop a range of neurological disorders. We report here 4 COVID-19 subjects with intensive care unit-acquired weakness and their functional outcome. In addition, a scoping review of COVID-19 literature was performed to investigate this issue. Of the post-COVID-19 patients admitted to our Neuro-Rehabilitation Unit, 4 (3 males, 1 female; mean age 59.2 ± 8.62 years) had intensive care unit-acquired weakness, diagnosed with electromyography. Muscle strength and functional evaluation were performed on all patients with Medical Research Council, Disability Rating Scale and Functional Independence Measure, respectively, at admission, discharge and 6-month follow-up after discharge. Electromyography revealed that 3 subjects had critical illness polyneuropathy and 1 had critical illness polyneuropathy/critical illness myopathy. At follow-up, the 3 subjects with critical illness polyneuropathy reached full recovery. The patient with critical illness polyneuropathy/critical illness myopathy showed moderate disability requiring bilateral ankle foot-orthosis and support for ambulation. The scoping review retrieved 11 studies of COVID-19 patients with intensive care unit-acquired weakness, concerning a total of 80 patients: 23 with critical illness myopathy (7 probable), 21 with critical illness polyneuropathy (8 possible), 15 with critical illness polyneuropathy and myopathy (CIPNM) and 21 with intensive care unit-acquired weakness. Of 35 patients who survived, only 3 (8.5%) reached full recovery. All 3 had critical illness myopathy, but 2 of these had a diagnosis of probable critical illness myopathy. Intensive care unit-acquired weakness commonly occurred in subjects with COVID-19. Recovery was variable and a low percentage reached full recovery. However, the heterogeneity of studies did not allow definitive conclusions to be drawn.

Key words: COVID-19; critical illness polyneuropathy; intensive care unit-acquired weakness; outcome; rehabilitation; critical illness myopathy.

Accepted Dec 6, 2021; Epub ahead of print Dec 22, 2021

J Rehabil Med 2022; 54: jrm00257

DOI: 10.2340/jrm.v53.1139

Correspondence address: Domenico Intiso, Unit of Neuro-Rehabilitation and Rehabilitation Medicine, IRCCS “Casa Sollievo della Sofferenza”, Viale dei Cappuccini, IT-71013 San Giovanni Rotondo (FG), Foggia, Italy. E-mail: d.intiso@operapadrepio.it, d.intiso@alice.it

LAY ABSTRACT

Patients with COVID-19 may develop a range of neurological disorders. We report here 4 cases of COVID-19 patients with intensive care unit-acquired weakness and their functional outcome. In addition, a scoping review of the COVID-19 literature was performed to investigate the occurrence of, and recovery from, intensive care unit-acquired weakness and sub-types (critical illness polyneuropathy, critical illness myopathy and critical illness polyneuropathy/critical illness myopathy) in subjects with COVID-19. Of these 4 patients, the 3 patients with critical illness polyneuropathy reached full recovery. The patient with critical illness polyneuropathy/critical illness myopathy showed moderate disability, requiring use of a bilateral device (ankle foot-orthosis). The scoping review of studies of COVID-19 patients with intensive care unit-acquired weakness retrieved a total of 80 patients: 21 with intensive care unit-acquired weakness, 23 with critical illness myopathy, 21 with critical illness polyneuropathy, and 15 with critical illness polyneuropathy/critical illness myopathy. Intensive care unit-acquired weakness commonly occurred in COVID-19 subjects, but the outcome was variable and a low percentage reached full recovery. COVID-19 subjects can develop long-term consequences and limitations, particularly those with intensive care unit-acquired weakness, who need more rehabilitation. New rehabilitative strategies and well-designed studies investigating the benefit of rehabilitation are necessary.

INTRODUCTION

Since the emergence of coronavirus disease COVID-19 (SARS-CoV-2) in China (1), it has spread rapidly to become a severe worldwide pandemic. To date, epidemiological data show more than 277 million people have been infected and more than 5 million have died (2). COVID-19 is a complex disease that predominantly affects the lungs, producing characteristic interstitial pneumonia with respiratory failure and critical conditions, which can require mechanical ventilation (MV) and admission to the intensive care unit (ICU). The large number of people requiring hospital or ICU admission has produced a health “tsunami”, stressing health systems worldwide and resulting in organizational disciplinary changes (3). A severe effect of the pandemic is the saturation of intensive care capacity.

During ICU stay and after discharge critically ill subjects can develop a common neuromuscular complication, defined as ICU-acquired weakness (ICUAW), which includes a spectrum of disorders including critical illness polyneuropathy (CIP), critical illness myopathy (CIM) and overlapping forms (CIP/CIM or CIPNM) (4–6). The occurrence of this neurological complication has been variously detected, with a range of 45–80% (7–8). The types of ICUAW show characteristic histological and electrophysiological features, but are clinically indistinguishable, since all forms produce weakness and bilateral limb paresis with an absence of tendon reflexes. Although several studies have been published about the disorders affecting the central nervous system (CNS) and the peripheral nervous system (PNS) in patients with COVID-19 (9–11), few reports investigating the occurrence of, and recovery from, ICUAW types have been reported.

The aim of this study is to describe the case reports and functional outcomes of 4 COVID-19 patients with ICUAW admitted to our Neuro-Rehabilitation Unit. In addition, a systematic review of the COVID-19 literature was performed to investigate occurrence of, and recovery from, ICUAW in subjects with COVID-19.

CASE REPORTS OF PATIENTS WITH COVID-19 AND ICUAW

After approval from the local Ethics Committee (Sezione Giovanni Paolo II- IRCCS Casa Sollievo della Sofferenza) and informed consent, patients admitted to our Neuro-Rehabilitation Unit between June 2020 and February 2021 with post-COVID-19 were investigated. Ten post-COVID-19 patients (6 males, 4 females) with neuromuscular disorders were found. Of these, 2 subjects had Guillain-Barré syndrome, 4 had bilateral plexus brachial lesion, and 4 (3 males, 1 female; mean age 59.2 years (standard deviation (SD) 8.62) had ICUAW. All post-COVID-19 patients with ICUAW were transferred from the ICU, where they had undergone endotracheal intubation, mechanical ventilation and, subsequently, tracheostomy. During the ICU stay, they had received a pharmacological therapeutic protocol for COVID-19, including antiretroviral drugs and steroids. Furthermore, they had developed infections with multi-drug resistant germs (MDR), including Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and had undergone multiple antibiotic therapy. At admission to our Neuro-Rehabilitation Unit, all subjects were breathing spontaneously, but needed a variable oxygen level treatment. Furthermore, all had a tracheal tube and nasal-gastric tube for nutrition. Clinical characteristics of the post-COVID-19 subjects are reported in Table I. All subjects were evaluated by electromyography (EMG) at admission. ICUAW and sub-types were diagnosed in the neuro-rehabilitation setting, apart from 1 subject who received a diagnosis of ICUAW by EMG during the ICU stay, due to severe weakness involving the upper and lower limbs. Furthermore, quantification of strength was performed for all subjects by means of the Medical Research Council (MRC) scale according to De Jonghe’s method (12). Functional evaluation was performed through the Disability Rating Scale (DRS) and the Functional Independence Measure (FIM). All measurements were performed at admission, at discharge and at 6 months of follow-up. At admission, post-COVID-19 subjects with ICUAW showed variable grades of muscular weakness from paresis to tetraplegia. One of these (patient #3) had severe paralysis of the upper and lower limbs and a global MRC score of 10. No subjects had involvement of cranial nerves.

Electrophysiological examination

EMG was performed as described previously (13). Briefly, all patients underwent conventional orthodromic motor and antidromic sensory nerve conduction studies, performed bilaterally on 8 motor nerves (median, ulnar, common peroneal and tibial nerves) and 6 sensory nerves (median, ulnar and sural nerves). Muscular activity at rest and, when possible, during contraction, was assessed with concentric needle electrodes. Sensory nerve action potential (SNAP), distal motor latencies, F wave, compound muscle action potential (CMAP) and nerve conduction velocities were recorded. Abnormal CMAP or SNAP amplitudes were considered significant when found in at least 2 nerves. Spontaneous activity, recruitment and interference patterns were detected bilaterally by needle EMG from deltoid, first dorsal interosseus, tibial anterior and abductor hallucis muscles. CIP was recognized if electrophysiological results revealed very low amplitude or absent sensory responses and low motor amplitudes with normal or mildly reduced conduction velocities. Patients were diagnosed as having myopathy in the setting of low or normal motor amplitudes, with relatively normal sensory responses. Overlapping electrophysiological findings of CIP and CIM were considered as defining the CIP/CIM subtype. Of 4 patients with ICUAW, 3 (patients #1, #2 and #4) had CIP and 1 (patient #3) had CIP/CIM type. A summary of EMG data for the study sample is shown in Table II.

Rehabilitation interventions

All post-COVID patients underwent an individualized and tailored rehabilitation treatment for 3 h per day, 6 days a week. The rehabilitation programme comprised joint mobilization, proprioceptive neuromuscular facilitation according to neuro-developmental techniques, flexibility and strength exercises. The patients underwent 2 h of electrical muscular stimulation daily on the lower limbs, by placing surface electrodes on the quadriceps and anterior tibial muscles, bilaterally. Electrical stimuli involved biphasic rectangular square pulses with a 20-ms duration at a rate of 20 Hz every 25 s. Amplitude of pulses was variable and based on the elicitation of visible muscular contraction (100–100 mA) (14).

Functional outcome

At discharge, only 1 subject (patient #1) had reached full recovery and ability in activities of daily living. Two subjects had incomplete recovery with minor disability (patients #2 and #4). Of these, 1 (patient #2) showed persistent left foot drop that required application of a foot-ankle orthosis, and 1 (patient #4) reported fatigue and mild weakness involving the lower limbs that limited performance and endurance in motor activity. However, she was able to ambulate without support. Patient #2 reached independent ambulation after application of the device. All of these subjects had CIP type according to EMG. Patient #3 showed CIP/CIM according to EMG. At discharge, he had moderate disability and motor limitations due to leg paresis with bilateral foot drop that was reduced with foot-ankle orthosis. However, he was able to stand up and to ambulate with bilateral support. At follow-up, 6 months after discharge, 3 subjects (patients #1, #2 and #4) had full recovery and 1 (patient #3) showed bilateral foot drop still requiring ankle foot-orthosis. Strength evaluation and functional scale scores of admission, discharge and follow-up are reported in Table III.

LITERATURE REVIEW

Methods

To evaluate COVID-19 subjects with ICUAW, a search of the studies was conducted using MEDLINE/PubMed, CINAHL, EMBASE, Web of Science, Scopus databases and Google Scholar. The search was restricted to English language reports published between 1 December 2019 and 31 March 2021. The search terms included “COVID-19”, “critically ill patients”, “intensive care unit acquired weakness”, “ICUAW”, “critical illness polyneuropathy”, “CIP”, “critical illness myopathy”, “CIM”, “critical polyneuropathy and myopathy”, “CIPNM”, “CIP and CIM”; “CIP/CIM”, “acute tetraplegia”, “functional outcome” and “COVID-19”. The search was made either by using MeSH terms, keywords or subject headings. Related terms were combined using the Boolean operators “OR” and “AND”. Search limits included only adults. Abstracts/posters or articles that were not peer-reviewed were excluded. The literature search was conducted by 3 independent authors (AMC, AG, and FDR). Inclusion criteria were: patient age ≥ 18 years; COVID-19 diagnosis; COVID-19 subjects with ICUAW, or the following types: CIP, CIM and CIP/CIM.

The research was conducted according to the Preferred Reporting Items for Systematic Reviews and the Meta-Analyses (PRISMA) diagram, depicting the selection of articles searched for the study (Fig. 1).

Results

The review resulted in 11 studies being included, based on inclusion criteria (15–25) (Table IV). Studies were widely heterogeneous. Of these, 2 were case reports describing single subjects (15–16), 5 were case series with small samples ranging from 3 to 11 patients (17–11), and 4 cohort studies (22–25). Of these, 2 studies investigated neurological manifestations in large cohorts of COVID-19 patients (22–23) and among these, subjects with CIP or CIM were also detected. One was a retrospective study that ascertained COVID-19 subjects with MV who developed ICUAW (24) and 1 study that, with the use of a prospective method design, investigated the incidence of ICUAW in COVID-19 subjects during ICU stay (25).

A total of 80 patients, age range 51–81 years, was reported. Of these, 23 were diagnosed with CIM (7 probable), 21 with CIP (8 possible), 15 with CIP/CIM, and 21 with ICUAW. Twelve (15%) patients died. ICUAW was diagnosed by EMG in all studies except the study by Van Aerde et al. (24), in which ICUAW was diagnosed on MRC scale, and the study by Nersesian et al. (22), in which ICUAW diagnosis was performed clinically. In this study, the authors detected 8 subjects with possible CIP and only 1 was diagnosed by EMG. Biopsy was performed in 1 study (20) involving, globally, 3 subjects. Of these, 1 subject revealed scattered necrotic and regenerative fibres in the absence of inflammatory infiltrates and 2 subjects showed non-specific findings, consisting of very occasional atrophic and regenerative fibres (20).

Five studies did not report the outcome of COVID-19 subjects with ICUAW because they addressed different issues, such as occurrence (25), electrophysiological parameters (20, 25), neurological manifestations of COVID-19 patients (23), or described the clinical phenomenon (15, 16). Recovery was reported in 6 studies (15, 17, 19, 21, 22, 24). Of these, 1 was a case report, by Bagnato et al. (15), who described a 62-year-old woman with COVID-19 diagnosed with CIM. After discharge, she had a mild weakness in the lower limb proximal muscles and was able to walk without assistance. Of the remaining studies, 4 were case series (17, 19, 21, 22), with samples ranging from 3 to 8 subjects, and 1 was a cohort study that investigated COVID-19 patients with ICUAW compared with no ICUAW subjects (24). Globally, the outcome was reported for 42 (52.5%) subjects: 10 with CIM (6 had probable CIM), 8 with probable CIP, 4 with CIP/CIM, and 20 with ICUAW. Seven (16.6%) patients died. In detail, Madia et al. reported 6 subjects with probable CIM. Of these, 2 patients reached full recovery and 3 (51.2%) showed disability due to CNS lesions (17). Yildiz et al. described 3 women with COVID-19 with severe weakness and tetraparesis due to CIM. Of these, 2 subjects died after 60 and 200 days, respectively, during ICU stay and only 1, who had MV weaning after 57 days from ICU admission, recovered slowly with intensive physiotherapy. However, the level of functional outcome was not specified (21). Nasuelli et al. described 4 subjects with CIP/CIM. Of these, 3 subjects died after 3 weeks and only 1 had a positive outcome, but showed slow recovery of motor skills, in particular due to foot flexion deficit that improved after intensive rehabilitation (19). Nersesjan et al. described 8 subjects with definite or possible CIP. At discharge, all patients were tetraparetic and had muscle atrophy and hyporeflexia (22). Finally, Van Aerde et al. performed a retrospective, observational study to detect COVID-19 patients with MV who developed ICUAW. At discharge, COVID-19 subjects with ICUAW had significantly poorer functional outcome than those without ICUAW: Barthel 8 (2.5–11.5) vs 10.5 (8–18), (p = 0.040) for COVID subjects with and without ICUAW, respectively.

Of 35 COVID-19 patients with ICUAW who survived, and for whom it was possible to detect the outcome, only 3 (8.5%) subjects reached full recovery. All 3 of these had CIM, although 2 of the 3 subjects had a diagnosis of probable CIM. On the other hand, the majority of COVID-19 patients with ICUAW reported a variable disability. No measure was employed to evaluate functional outcome, except in the study by Nersesjan et al. (22), which used mRS, and that by Van Aerde et al. (24), which used the mobility score and the Barthel scale. Muscle weakness was quantified by the MRC scale in only 2 studies (16, 18). It was not possible to compare our post-COVID-19 subjects with a matched group of post-COVID-19 patients published in the literature, due to the heterogeneity of enrolled samples, including sitting, timing of neuro-muscular disorder ascertainment, functional measures, demographics (mean age 73.6 ± 8.7 vs 59.2 ± 8.62 years, respectively, in subjects reported in the literature and our sample) and rehabilitative treatment.

DISCUSSION

ICUAW is a common neurological complication in COVID-19 subjects during ICU stay and after discharge, which requires intensive rehabilitation. Recovery was found to be variable, but, unlike the general ICUAW population, a low percentage of COVID-19 patients reached full functional recovery. COVID-19 infection can result in characteristic interstitial pneumonia with severe respiratory failure, which may involve multi-organ systems. An increasing number of studies are being published on the role and pathophysiological mechanisms of COVID-19 (9) in producing and favouring neurological manifestations that affect the central (CNS) and peripheral nervous system (PNS). Among the disorders of PNS, variable conditions and neuropathies have been described, including Guillain-Barré syndrome and its variants (26, 27), cranial multifocal neuropathy, dysautonomia (28) and brachial plexus lesion (29). Likewise, neuromuscular disorders, such as myalgia, myositis and, in particular, myasthenia gravis, have also been described (30). Our experience and the current review show that ICUAW is also a common neurological disorder in critically ill COVID-19 subjects who require ICU stay.

Among COVID-19 patients admitted to neuro-rehabilitation in our department, we detected 4 subjects with ICUAW. A scoping review of the COVID-19 literature showed that a total of 80 COVID-19 patients with ICUAW were reported in the literature between 1 December 2019 and 31 March 2021. ICUAW can cause variable disabling conditions and, consequently, an important aspect to consider concerns rehabilitation interventions in order to obtain full recovery and a good quality of life (31, 32). In this respect, despite the lack of treatments and the limitations of rehabilitative strategies (33), subjects with ICUAW can achieve recovery with variable functional outcomes. An extensive literature review of the neuromuscular sequelae of ICU subjects with critical illness revealed that 68.8% made a complete recovery and regained the ability to walk independently (31). It was reported that the outcome depended on the type of ICUAW, as confirmed by the fact that CIM had an earlier and better functional outcome than CIP (34, 35). However, the current review shows that the outcome was described in a low number of COVID-19 subjects, consisting of 35 (43.7%) survivals, of whom only 3 (8.5%) reached full recovery. This finding is much lower than that of general critically ill subjects with ICUAW. On the other hand, the functional outcome in our COVID-19 subjects with ICUAW was in line with the findings reported in the literature. Indeed, after rehabilitation, 2 (50%) subjects reached full recovery and, after 6 months, only 1 showed mild disability and limitation of gait. This contrasting finding has several possible reasons. Almost all studies did not use proper functional scales to quantify disability, and the evaluation of functional outcome was based on the neurological examination or on the improvement in muscle strength on the MCR scale. Furthermore, the studies were performed by ICU specialists, who might have preferentially described this neurological complication in COVID-19 subjects during the ICU stay or at discharge and overlooked reporting the recovery. Furthermore, our patients underwent intensive rehabilitative treatment, which might have produced some benefit and improved the outcome. All 3 subjects in the current review who reached full recovery had CIM, but 2 of these had a diagnosis of probable CIM. However, in considering only COVID-19 patients with CIM who survived, full recovery was detected in 22.3% of subjects. Conversely, it was observed that 3 COVID-19 patients with CIP reached full recovery, whereas 1 subject with overlapping CIP/CIM had disability at 6 months after discharge. Although some of the studies analysed in the current review differentiated the ICUAW types, no conclusion can be drawn regarding recovery from different forms of ICUAW, due to the lack of data addressing this issue. Nevertheless, the outcome of COVID-19 subjects with ICUAW, regardless of type, appeared poorer than that of subjects with general ICUAW, although on the basis of the number and quality of published studies, the level of recovery remains unclear.

Likewise, whether occurrence of ICUAW in ICU COVID-19 subjects is higher than in the ICU general population also remains unclear. The occurrence of this disorder has been variously detected, and a systematic review reported a median prevalence of 43% (36). Frithiof et al. investigated the occurrence of ICUAW in adult subjects with COVID-19 admitted to ICU between 13 March and 8 June 2020. The ICUAW incidence was higher in COVID-19 patients compared with a general ICU population treated during 2019 (9.9% vs 3.4%). In particular, CIP was more frequent in the COVID-19 ICU cohort (50%) than in the non-COVID-19 ICU cohort (0%, p = 0.008) (25). On the other hand, Cabañes-Martínez et al. described, out of a total of 225 patients treated in the ICU, 11 patients with a clinical and neurophysiological diagnosis of CIM or CIP, but they stated that it was not possible to calculate the exact incidence of the presence of neuropathy or myopathy (20). It is well known that several risk factors can result in ICUAW in critically ill patients, including sepsis, ICU length of stay, and multiple organ failure (7, 8), as well as the use of neuromuscular blocking and several drugs. In this respect, Neresian et al. (22) compared COVID-19 ICU patients with ICUAW to COVID-19 ICU patients without neuromuscular complications. Interestingly, those with ICUAW had a significantly longer stay (median 49.5 vs 23 days, p< 0.001), had been admitted to ICU more frequently (100% vs 40%, p = 0.002), were more often treated with renal replacement therapy (62% vs 14%, p = 0.008), and were more often delirious (75% vs 30%, p = 0.02) (22). Likewise, Van Aerde et al. noticed that COVID-19 subjects with ICUAW had significantly longer ICU stays (days) (p = 0.008), lower mobility scores at ICU discharge (p < 0.001), compared with those without ICUAW (24). Therefore, the same risk factors and the severity of systemic disease itself might favour the occurrence of ICUAW in COVID-19 subjects. In this respect, Bax et al. suggested a possible association with the duration of intubation and with increased IL-6 levels at admission (18).

Another factor to take into account when considering ICUAW in COVID-19 is the possible direct damage to nerves and muscles caused by the virus. It has been reported that some neurological disorders are caused by the direct action of COVID-19 on the brain tissue, such as encephalitis and myelitis (37). Even without evidence of viral invasion of the nervous system, immune-mediated events, through the cytokine or chemokine pathways, may lead to vascular leakage, demyelination, activation of complement and organ damage. Indeed, the dominant characteristics of COVID-19 infection are the excessive immune response of the host to virus invasion of the organs, through the production of inflammation factors, in particular cytokines (38, 39). Therefore, it is possible that the same underlying pathological conditions in critically ill subjects characterize COVID-19 patients and may represent an environment that favours neuromuscular disorders (20).

The current study has some limitations. We report here 4 post-COVID-19 patients with ICUAW among those with neuromuscular disorders admitted to a neuro-rehabilitation setting. Therefore, the results concern a single centre and are not generalizable. The review of the COVID-19 literature aimed to determine the occurrence and recovery of ICUAW subjects with COVID-19, but the cohort studies and case series were highly heterogeneous. A further limitation concerns the recovery of subjects with ICUAW types due to the lack of functional measurements and of trials focusing on rehabilitative interventions.

Suggestions and implications for future research

After discharge COVID-19 subjects may have long-term consequences and limitations. A recent study showed that, 6 months after acute infection, COVID-19 survivors were mainly affected by fatigue or muscle weakness, sleep difficulties, and anxiety or depression (40). Therefore, multi-component rehabilitative interventions and new approach strategies are being applied to address the respiratory, muscular, psychological and affective disorders that can persist in these patients. In this respect, COVID-19 subjects with ICUAW need more intensive rehabilitation, but, at present, rehabilitative interventions and proper investigations concerning ICUAW recovery are scant. Therefore, there is a strong need to find new rehabilitative strategies and plan well-designed studies investigating the efficacy and the benefit of rehabilitation. Further research is needed into the following aspects of neurological manifestations occurring in COVID-19 patients:

CONCLUSION

This review found that ICUAW is common in COVID-19 patients, producing disabling conditions for which rehabilitation is required. Recovery is variable, but a low percentage of COVID-19 patients with ICUAW gain a full functional outcome. However, the small size of samples and the heterogeneity of studies in this review do not permit definitive conclusions to be drawn. Rehabilitation interventions and further detailed studies should be carried out to improve functional outcome and to answer unsolved questions.

Funding. The authors received no financial support for the research, authorship, and/or publication of this article.

The authors have no conflicts of interest to declare.

REFERENCES

  1. Kahn N. New virus discovered by Chinese scientists investigating pneumonia outbreak. Wall Street J. (2020). Available from: https://www.wsj.com/articles/new-virus-discovered-by-chinese-scientists-investigatingpneumonia-outbreak-11578485668.
  2. Center for Systems Science and Engineering (CSSE) at Johns Hopkins University (JHU). Available from: https://coronavirus.jhu.edu/map.html.
  3. Bartolo M, Intiso D, Lentino C, Sandrini G, Paolucci S, Zampolini M; Board of the Italian Society of Neurological Rehabilitation (SIRN). Urgent measures for the containment of the coronavirus (Covid-19) epidemic in the neurorehabilitation/rehabilitation departments in the phase of maximum expansion of the epidemic. Front Neurol 2020; 11: 423.
  4. Kress JP, Jesse BA. ICU-acquired weakness and recovery from critical illness. N Engl J Med 2014; 371: 287–288.
  5. Latronico N, Bolton CF. Critical illness polyneuropathy and myopathy: a major cause of muscle weakness and paralysis. Lancet Neurol 2011; 10: 931–941.
  6. Piva S, Fagoni N, Latronico N. Intensive care unit-acquired weakness: unanswered questions and targets for future research. F1000Res. 2019; 17; 8: F1000 Faculty Rev-508.
  7. Bednarík J, Vondracek P, Dusek L, Moravcova E, Cundrle I. Risk factors for critical illness polyneuromyopathy. J Neurol 2005; 252: 343–351.
  8. Nanas S, Kritikos K, Angelopoulos E, Siafaka A, Tsikriki S, Poriazi M, et al. Predisposing factors for critical illness polyneuromyopathy in a multidisciplinary intensive care unit. Acta Neurol Scand 2008; 118: 175–181.
  9. Zubair AS, McAlpine LS, Gardin T, Farhadian S, Kuruvilla DE, Spudich S. Neuropathogenesis and neurologic manifestations of the coronaviruses in the age of coronavirus disease 2019: a review. JAMA Neurol 2020; 77: 1018–1027.
  10. Helms J, Kremer S, Merdji H, Clere-Jehl R, Schenck M, Kummerlen C, et al. Neurologic features in severe SARS-CoV-2 infection. N Engl J Med 2020; 382: 2268–2270.
  11. Khatoon F, Prasad K, Kumar V. Neurological manifestations of COVID-19: available evidences and a new paradigm. J Neurovirol 2020; 26: 619–630.
  12. De Jonghe B, Sharshar T, Lefaucheur JP, Authier FJ, Durand-Zaleski I, Boussarsar M, et al. Groupe de Réflexion et d’Etude des Neuromyopathies en Réanimation Paresis acquired in the intensive care unit: a prospective multicenter study JAMA 2002; 288: 2859–2867.
  13. Kerbaul F, Brousse M, Collart F, Pellissier JF, Planche D, Fernandez C, et al. Combination of histopathological and electromyographic patterns can help to evaluate functional outcome of critical ill patients with neuromuscular weakness syndromes. Crit Care 2004; 8: R358–366.
  14. Salmons S, Ashley Z, Sutherland H, Russold MF, Li F, Jarvis JC. Functional electrical stimulation of denervated muscles: basic issues. Artif Organs 2005; 29: 199–202.
  15. Bagnato S, Boccagni C, Marino G, Prestandrea C, D’Agostino T, Rubino F. Critical illness myopathy after COVID-19. Int J Infect Dis 2020; 99: 276–278.
  16. Tankisi H, Tankisi A, Harbo T, Markvardsen LK, Andersen H, Pedersen TH. Critical illness myopathy as a consequence of Covid-19 infection. Clin Neurophysiol 2020; 131: 1931–1932.
  17. Madia F, Merico B, Primiano G, Cutuli SL, De Pascale G, Servidei S. Acute myopathic quadriplegia in patients with COVID-19 in the intensive care unit. Neurology 2020; 95: 492–494.
  18. Bax F, Lettieri C, Marini A, Pellitteri G, Surcinelli A, Valente M, et al. Clinical and neurophysiological characterization of muscular weakness in severe COVID-19. Neurol Sci 2021; 23: 1–6
  19. Nasuelli NA, Pettinaroli R, Godi L, Savoini C, De Marchi F, Mazzini L, et. Critical illness neuro-myopathy (CINM) and focal amyotrophy in intensive care unit (ICU) patients with SARS-CoV-2: a case series. Neurol Sci 2021; 42: 1119–1121.
  20. Cabañes-Martínez L, Villadóniga M, González-Rodríguez L, Araque L, Díaz-Cid A, Ruz-Caracuel I, et al. Neuromuscular involvement in COVID-19 critically ill patients. Clin Neurophysiol 2020; 131: 2809–1816.
  21. Yildiz OK, Yildiz B, Avci O, Hasbek M, Kanat S. Clinical, neurophysiological and neuroimaging findings of critical illness myopathy after COVID-19. Cureus 2021; 13: e13807.
  22. Nersesjan V, Amiri M, Lebech AM, Roed C, Mens H, Russell L, et al. Central and peripheral nervous system complications of COVID-19: a prospective tertiary center cohort with 3-month follow-up. J Neurol 2021; 13; 1–19.
  23. Rifino N, Censori B, Agazzi E, Alimonti D, Bonito V, Camera G, et al. Neurologic manifestations in 1760 COVID-19 patients admitted to Papa Giovanni XXIII Hospital, Bergamo, Italy. J Neurol 2020; 7: 1–8.
  24. Van Aerde N, Van den Berghe G, Wilmer A, Gosselink R, Hermans G; COVID-19 Consortium. Intensive care unit acquired muscle weakness in COVID-19 patients. Intensive Care Med 2020; 46: 2083–1085.
  25. Frithiof R, Rostami E, Kumlien E, Virhammar J, Fällmar D, Hultström M, et al. Critical illness polyneuropathy, myopathy and neuronal biomarkers in COVID-19 patients: a prospective study. Clin Neurophysiol 2021; 132: 1733–1740.
  26. Manganotti P, Bellavita G, D’Acunto L, Tommasini V, Fabris M, Sartori A, et al. Clinical neurophysiology and cerebrospinal liquor analysis to detect Guillain-Barré syndrome and polyneuritis cranialis in COVID-19 patients: a case series. J Med Virol 2021; 93: 766–774.
  27. Sriwastava S, Kataria S, Tandon M, Patel J, Patel R, Jowkar A, et al. Guillain Barré Syndrome and its variants as a manifestation of COVID-19: a systematic review of case reports and case series. J Neurol Sci 2021; 420: 117263.
  28. Andalib S, Biller J, Di Napoli M, Moghimi N, McCullough LD, Rubinos CA, et al. Peripheral nervous system manifestations associated with COVID-19. Curr Neurol Neurosci Rep 2021; 21: 9.
  29. Miller C, O’Sullivan J, Jeffrey J, Power D. Brachial plexus neuropathies during the COVID-19 pandemic: a retrospective case series of 15 patients in critical care. Phys Ther 2021; 101: pzaa191.
  30. Restivo DA, Centonze D, Alesina A, Marchese-Ragona R. Myasthenia gravis associated with SARS-CoV-2 infection. Ann Intern Med 2020; 173: 1027–1028.
  31. Latronico N, Shehu I, Seghelini E. Neuromuscular sequelae of critical illness. Curr Opin Crit Care 2005; 11: 381–390.
  32. Intiso D. ICU-acquired weakness: should medical sovereignty belong to any specialist? Crit Care 2018; 22: 1.
  33. Mehrholz J, Pohl M, Kugler J, Burridge J, Mückel S, Elsner B. Physical rehabilitation for critical illness myopathy and neuropathy. Cochrane Database Syst Rev 2015; 3: CD010942.
  34. Guarneri B, Bertolini G, Latronico N. Long-term outcome in patients with critical illness myopathy or neuropathy: the Italian multicentre CRIMYNE study. J Neurol Neurosurg Psychiatry 2008; 79: 838–841.
  35. Koch S, Wollersheim T, Bierbrauer J, Haas K, Mörgeli R, Deja M, et al. Long-term recovery in critical illness myopathy is complete, contrary to polyneuropathy. Muscle Nerve 2014; 50: 431–436.
  36. Fan E, Cheek F, Chlan L, Gosselink R, Hart N, Herridge MS, et al. An official American Thoracic Society Clinical Practice guideline: the diagnosis of intensive care unit-acquired weakness in adults. Am J Respir Crit Care Med 2014; 190: 1437–1446.
  37. Gasmi A, Tippairote T, Mujawdiya PK, Gasmi Benahmed A, Menzel A, Dadar M, et al. Neurological involvements of SARS-CoV2 infection. Mol Neurobiol 2021; 58: 944–949.
  38. Mehta P, McAuley DF, Brown M, Sanchez E, Tattersall RS, Manson JJ. COVID-19: consider cytokine storm syndromes and immunosuppression. Lancet 2020; 395: 1033–1034.
  39. Espíndola OM, Gomes YCP, Brandão CO, Torres RC, Siqueira M, Soares CN, et al. Inflammatory cytokine patterns associated with neurological diseases in coronavirus disease 2019. Ann Neurol 2021; 89: 1041–1045.
  40. Huang C, Huang L, Wang Y, Li X, Ren L, Gu X et al. 6-month consequences of COVID-19 in patients discharged from hospital: a cohort study. Lancet 2021; 397: 220–132.