Autoimmune Encephalitis in the Intensive Care Unit
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Autoimmune encephalitis is a rapid, progressive encephalopathy due to an autoimmune response directed against the brain parenchyma. It is associated with significant morbidity, often necessitating evaluation and treatment in the intensive care unit (ICU). Patient management centers on rapid diagnosis of the autoimmune encephalitis syndrome with careful assessment for other etiologies of acute encephalopathy, the initiation of immunosuppressive therapy, and the management of associated sequelae including status epilepticus, respiratory failure, elevated intracranial pressure, and dysautonomia.
KeywordsEncephalitis Autoimmune Neurocritical care Intensive care Anti-NMDA receptor encephalitis Anti-LGI1 encephalitis
Autoimmune encephalitis, a rapid, progressive encephalopathy that is secondary to an autoimmune response directed against the brain, is associated with significant morbidity, and often requires evaluation and treatment in the ICU not only for the underlying inflammatory response but also for its medical and neurological sequelae. In this chapter, we will discuss the epidemiology, clinical presentation, diagnostic approaches, and treatment options for autoimmune encephalitis as well as its sequelae, with particular focus on management and triage issues encountered by the intensivist.
Encephalitis is defined as neurologic dysfunction due to inflammation of the brain with the cerebral cortex or deep gray matter nuclei frequently involved. Infectious encephalitides have historically been the most common; however, autoimmune encephalitides have become increasingly recognized and described [1, 2].
Autoimmune encephalitides include not only those syndromes due to a primary autoimmune response but also those that are paraneoplastic. Similar to other paraneoplastic neurological syndromes, paraneoplastic autoimmune encephalitis results when systemic immune responses to peptide antigens of the tumor respond to similar to peptides found in the brain [3, 4]. Paraneoplastic autoimmune encephalitis occurs remotely from a known cancer or metastasis and can precede the detection of an associated cancer or cancer recurrence by years .
Since the original description of paraneoplastic autoimmune encephalitis, and particularly over the past two decades, autoimmune encephalitides have been identified and described in the absence of cancer. These primary autoimmune encephalitis syndromes are typically the result of immune responses directed against cell surface proteins (e.g., neurotransmitter receptors) . For the purposes of this chapter, we will consider both paraneoplastic and non-paraneoplastic autoimmune encephalitis together.
Autoimmune encephalitis is seen in a broad age range but most commonly affects young people. The annual incidence of encephalitis is up to 12.6 per 100,000 individuals [1, 6, 7], 20–30% of whom have an underlying autoimmune etiology [6, 7]. One recent population-based study found the prevalence of autoimmune encephalitis as 13.7 per 1000,000 individuals, comparable to all infectious encephalitides . These observations may still be underestimates if we consider that as many as 50% of encephalitis patients have an unknown etiology [6, 7] and that the paraclinical findings associated with various autoimmune encephalitides included in recent consensus clinical criteria may be transient or of varied sensitivity . Interestingly, new immune activating therapies introduced for oncological purposes are influencing the incidence of autoimmune encephalitis . Although the clinical profile of encephalitic syndromes may suggest autoimmune causes, some clinical presentations may not immediately raise concerns for autoimmune encephalitis. For instance, new onset refractory status epilepticus (which may occur without cognitive or behavioral changes) may appear to be solely epileptic; however, over one third of these cases are found to be due to autoimmune encephalitis . With improved identification of autoantibodies through refined testing practices and assay advances, the development and application of consensus clinical criteria, and the description of novel autoantibody-associated autoimmune encephalitis syndromes over the past decade, the incidence of autoimmune encephalitis is anticipated to continue to rise [1, 2].
Patients with autoimmune encephalitis commonly require care in an ICU [10, 11]. In one retrospective series at a tertiary referral center, 55% of patients meeting consensus clinical criteria for possible autoimmune encephalitis were admitted to the neurocritical care unit . Patients particularly at risk for ICU admission are those who had a longer duration of symptoms before hospitalization and anemia, likely a marker of systemic inflammation . Seizures (including status epilepticus), subacute cognitive decline, and respiratory failure are the most common indications for neurocritical care [10, 11, 12, 13]. Almost 70% of patients with autoimmune encephalitis have critical care needs at some point during their initial hospital stay , with ICU stays greater than 4 days observed in 44% of patients in one series . As discussed below, patients with autoimmune encephalitis are at risk for a variety of neurological and medical complications, with a mortality rate up to 40% in the ICU [11, 13].
In general, the clinical presentation of autoimmune encephalitis is rapid in both onset and progression. Consensus clinical criteria were recently developed to promote the early identification of patients with autoimmune encephalitis and facilitate early initiation of immunosuppressive therapy . These criteria require a subacute and progressive encephalopathy, typically over the course of days to weeks (as opposed to the months or years commonly seen in those with neurodegenerative disorders) . Prodromal symptoms, such as headache and nonspecific respiratory or gastrointestinal illnesses, may precede the development of encephalopathy [15, 16, 17].
Autoantibodies in autoimmune encephalitis
Syndromes and associated neurological findings
Frequency of cancer
Main cancer type
Response to immunotherapy
AMPA receptor 
Limbic encephalitis, epilepsy, nystagmus
Thymoma, small-cell lung carcinoma
71% with partial (N = 10) or good response (N = 5) after treatment with immunotherapy and oncologic therapy as appropriate (N = 21)
Limbic encephalitis, stiff-person syndrome, more general encephalitis, subacute cerebellar degeneration, myelopathy, subacute sensory neuronopathy, peripheral neuropathy
Small-cell lung carcinoma, breast, thymoma
Among patients with various syndrome who were anti-amphiphysin seropositive, various first-line therapies used with 80% improving who received corticosteroids (N = 5), 50% of those who received IVIG (N = 4), none with plasmapheresis (N = 4). 60% treated with oncologic therapy improved (N = 20)
CASPR2 (contactin-associated protein 2) 
Limbic encephalitis, Morvan syndrome, neuromyotonia
52% with partial and 39% with complete recovery after treatment with various combinations of first-line immunotherapy (N = 23)
Limbic encephalitis, more general encephalitis, chorea, subacute cerebellar degeneration, cranial neuropathies, uveitis, optic neuritis, retinopathy, myelopathy, subacute sensory neuronopathy, autonomic neuropathy, peripheral neuropathy
Small-cell lung carcinoma, thymoma, uterine sarcoma, prostate small cell carcinoma
Limited to case series of various syndromes (mostly movement disorders). Range of response to immunotherapy 13–50%, primarily intravenous methylprednisolone. The primary focus of care is on oncological therapy
GABAB receptor 
Limbic encephalitis, epilepsy, cerebellar ataxia
Small-cell lung carcinoma
33% with a complete response and 40% with partial response to immunotherapy alone; 13% with a complete response and 13% with partial response to immunotherapy and oncological therapy (13%; N = 15)
GAD 65 (65 kDa glutamic acid decarboxylase) 
Limbic encephalitis, stiff-person syndrome, cerebellar ataxia, autoimmune epilepsy, brainstem and more general encephalitis, myelopathy, large fiber peripheral neuropathy, autonomic neuropathy
Small-cell or non-small-cell lung carcinoma, thymoma or thymic carcinoma, testicular seminoma, thyroid neoplasia, breast adenocarcinoma, gastrointestinal carcinomas, renal cancer, lymphoma, myeloma
Across all neurological phenotypes of GAD65 autoimmunity, approximately 50% of patients improve with immunotherapy
Hu (ANNA1) 
Limbic encephalitis, brainstem encephalitis, more general encephalitis, subacute cerebellar degeneration, myelitis, sensory neuronopathy, autonomic neuropathy, peripheral neuropathy
Small-cell or non-small-cell lung carcinoma, prostate cancer, gastrointestinal cancer
Clinical improvement or stabilization in 38% treated with oncological therapy with or without immunotherapy (N = 80) and in 21% treated with immunotherapy alone (N = 34)
LGI1 (leucine-rich glioma-inactivated 1) 
Limbic encephalitis, faciobrachial dystonic seizures, abnormal sleep behavior
50% improve with first-line immunotherapy, and 71% at 24 months had a good outcome (N = 48)
Ma1 or Ma2 
Limbic encephalitis, brainstem encephalitis, hypothalamic encephalitis, mesencephalic encephalitis, subacute cerebellar degeneration
Ma 1: various lung cancers; Ma2: testicular cancer, seminomas
With various immunotherapy regimens, 36% improved and 46% were stable (N = 24)
Acute disseminated encephalomyelitis (ADEM), neuromyelitis optica, optic neuritis, myelitis
Varies by presentation, with brainstem encephalitis and encephalitis least common (14% total). MOG antibodies may be transiently present in postinfectious disorders such as ADEM. Based on data from patients with optic neuritis and those with myelitis (N = 62), complete recovery in 35–52%, partial response in 40–65%
NMDA receptor 
Anti-NMDA receptor encephalitis with anxiety, psychosis, epilepsy, extrapyramidal disorder, hypoventilation, central dysautonomia
Varies with age and sex; 38% across the population
Of those treated with first-line immunotherapy alone or with teratoma resection, 50% improve at 4 weeks. Of those not improved at 4 weeks and then given second-line therapy, 67% with a complete or mild disability at 24 months (N = 472)
Dopamine 2 receptor 
Basal ganglia encephalitis, Sydenham chorea
None or unknown
Limited case series with 7 patients treated with immunotherapy, either corticosteroids or corticosteroids with IVIG, 5 with clinical improvement. Suggestion that more aggressive IV methylprednisolone + IVIG has a better outcome
Aquaporin 4 
Encephalitis, neuromyelitis optica (NMO), optic neuritis, myelitis
Rarely, NMO patients may present with encephalopathies or encephalitis syndromes. Overall, patients with NMO respond well to immune therapy. 53% who received first-line immunotherapy (IV methylprednisolone alone or followed by plasmapheresis if limited response to corticosteroids) without motor disability (N = 15)
DPPX (dipeptidyl-peptidase-like protein 6) 
Encephalitis, psychiatric symptoms, diarrhea, tremor, nystagmus, hyperekplexia, ataxia, progressive encephalomyelitis with rigidity and myoclonus (PERM)
44% with complete or near complete recovery, 33% with a mild disability after immunotherapy (N = 9)
GABAA receptor 
Encephalitis, epilepsy, cerebellar ataxia
28% complete, 72% partial clinical improvement after immunotherapy and oncologic therapy (N = 21)
Hodgkin’s lymphoma, small-cell lung cancer
55% with complete recovery and 45% with partial recovery following treatment with immunotherapy (N = 4), immunotherapy and oncologic therapy (N = 4), oncological therapy alone (N = 2), or none (N = 1)
Case series of anti-NMDAR encephalitis
Titulaer et al. Late-onset encephalitis. Multicenter multination study. Spain, 2013 
Titulaer et al. Treatment and prognosis for long-term outcomes. Multicenter multination study. Spain, 2013 
Chi et al. Risk factors for mortality in encephalitis. Single center single nation study. China, 2017 
de Montmollin et al. Adults with encephalitis in UCI. Multicenter multination study. France, 2017 
Wang et al. Encephalitis in pediatric population. Single center single nation study. China, 2017 
Gable et al. Encephalitis in pediatric population. Multicenter single nation study. USA, 2017 
de Bruijn et al. Neuropsychological outcome in pediatric population. Multicenter single nation study. Netherlands, 2018 
Ho et al. Encephalitis in pediatric population. Multicenter single nation study. China, 2018 
Granata et al. Movement disorders in Pediatric encephalitis. Single center single nation study. Italy, 2018 
Zhang et al. Late-onset encephalitis. Single center single nation study. China, 2018 
Mueller et al. Genetic predisposition in encephalitis. Multicenter multination study. Germany, 2018 
Case series of anti-LGI encephalitis
Finke et al. Cognitive deficits and structural hippocampal damage in encephalitis. Multicenter single nation study. Germany, 2017 
Gao et al. Clinical characterization of autoimmune LGI1 antibody limbic encephalitis. Single center single nation study. China, 2016 
Celicanin et al. Autoimmune encephalitis associated with LGI1 ab. Denmark, 2017 
Irani et al. Faciobrachial dystonic seizures precede limbic encephalitis. Multicenter multination study. UK, 2011 
Mueller et al. Genetic predisposition in encephalitis. Multicenter multination study. Germany, 2018 
Anti-LGI1 encephalitis accounts for 40% of patients seropositive for antibodies directed against the voltage-gated potassium channel (anti-VGKC) complex. Of the remaining patients, 10% have anti-CASPR2 antibodies and 50% are seronegative for both anti-LGI1 and anti-CASPR. The “double negative” anti-VGKC seropositive population is heterogeneous in terms of syndromes, cancer association, and response to immunosuppression, possibly reflecting immune responses to other proteins associated with the VGKC complex that have yet to be characterized, limiting its value as a specific marker of autoimmune neuroinflammation .
Patients with anti-LGI1 encephalitis most commonly present in their sixth to eighth decade with limbic encephalitis. Anti-LGI1 encephalitis is characterized by short-term memory loss, seizures, and psychiatric symptoms, with evidence of a combination of medial temporal lobe inflammation, temporal lobe epilepsy or dysfunction, or intrathecal inflammation. A large subset of patients (13%) present without evidence of brain inflammation by magnetic resonance imaging (MRI) or cerebrospinal fluid (CSF) analysis . Faciobrachial dystonic seizures (FBDS) have been described preceding the development of short-term memory loss and encephalopathy suggestive of limbic encephalitis by weeks to months in anti-LGI1 encephalitis. These immunotherapy (rather than antiepileptic) responsive seizures are very brief (on the order of seconds), frequent (median of 50 times per day in one series) unilateral or bilateral jerking movements of the arm and ipsilateral face more often than leg [18, 26]. High emotion or auditory or visual stimuli are triggers for FBDS in 28% of patients . In those patients with anti-LGI1 encephalitis presenting with FBDS, earlier treatment with immunotherapy predicted improved outcomes in terms of cognition, disability, and seizure control [18, 19]. As has been observed in patients with antibody responses directed at cell surface proteins, anti-LGI1 is not strongly associated with a particular cancer, with only 7% of patients found to have a malignancy .
The subsequent diagnostic evaluation of a patient with suspected autoimmune encephalitis is directed not only at supporting a diagnosis of autoimmune encephalitis and its sequelae to permit rapid treatment but also at assuring the absence of other etiologies of a subacute and progressive encephalopathy, particularly infectious encephalitides. When evaluating a patient with suspected autoimmune encephalitis, it is crucial to be mindful that the diagnosis of autoimmune encephalitis is clinical, incorporating clinical presentation with paraclinical findings, and is not solely dependent on the detection of an autoantibody.
Diagnostic studies incorporated in the evaluation for possible autoimmune encephalitis include autoantibody testing along with common and widely performed paraclinical diagnostics: CSF studies, electroencephalography, and brain MRI. We will consider each briefly in turn as well as the developing role of brain fluorodeoxyglucose-positron emission tomography (FDG-PET) as a diagnostic modality. In addition, the evaluation includes assessing for occult malignancy in the event that the encephalitis is a paraneoplastic syndrome.
Several autoantibodies have been described in association with autoimmune encephalitis (Table 17.1), each serving as either a marker of an autoimmune response or in a direct pathogenic capacity [4, 27]. Patients with possible autoimmune encephalitis should be tested for the presence of antibodies not only in the serum but also in the CSF . This advisement is made since in some, but not all, autoimmune encephalitis syndromes (e.g., anti-NMDAR encephalitis), CSF antibody assays are more sensitive than those in the serum [5, 20, 25]. CSF antibody testing allows for greater specificity as it is not uncommon for multiple antibodies to be detected in the serum, with only one antibody detected in paired CSF that more likely reflects the underlying immune response . Thus, CSF antibody testing has a lower rate of false-positive and false-negative results than testing in the serum alone .
In addition to antibody testing, CSF testing plays an essential role in the initial management of a patient suspected to have autoimmune encephalitis, both to support the possibility of this diagnosis and to evaluate for other potential diagnoses. Moderate lymphocytic-predominant CSF pleocytosis (>/= 5 white blood cells/milliliter) is a criterion incorporated in the most recent consensus clinical criteria; however, this finding may depend on syndromic timing. Late in the disease course, no abnormalities may be noted in the CSF except for an elevated protein level. Elevated CSF to serum immunoglobulin G index and intrathecal oligoclonal bands are also supportive, though not diagnostic, of an intrathecal autoimmune response. It is, however, important to note that CSF glucose at a depressed level relative to serum would be more suggestive of an infectious etiology than autoimmune encephalitis.
EEG findings are also included in the consensus criteria, namely, temporal lobe slowing (bilateral or unilateral) and electrographic seizures ranging from focal to generalized and including nonconvulsive and convulsive status epilepticus that may be refractory [5, 9, 28]. Otherwise, EEG itself is variable in its sensitivity across the autoimmune encephalitides, with slowing and disorganized activity being the most frequent findings . Some rare electrographic findings have been described in specific syndromes, such as extreme delta brush in anti-NMDAR encephalitis; however, such findings appear to be the exception rather than the rule .
Though included in early descriptions, such as that for anti-NMDAR encephalitis, dedicated brain FDG-PET imaging has recently attracted growing interest as a potential diagnostic and monitoring test in autoimmune encephalitis [33, 34, 35]. Hypermetabolism by FDG-PET of the medial temporal lobes is included in the clinical consensus criteria for definite limbic encephalitis but not those for autoimmune encephalitis in general . Case series reporting a gradient of occipital hypometabolism to frontotemporal hypermetabolism in anti-NMDAR encephalitis, hypermetabolism of the basal ganglia and medial temporal lobes in anti-LGI1 encephalitis, and normalization of these abnormalities with improvement in functional status suggest an expanded utility of FDG-PET in the evaluation and clinical monitoring of patients with autoimmune encephalitis [26, 35]. As the clinical value of brain FDG-PET is evaluated in the future, it will be important for researchers and clinicians to be mindful that abnormal patterns of cerebral metabolism on FDG-PET also have been well-described in neurodegenerative syndromes that can present with subacute cognitive decline, such as posterior cerebral atrophy and Lewy body dementia, which are both associated with occipital hypometabolism . In addition, treatments commonly prescribed to patients in the acute phase of autoimmune encephalitis, such as corticosteroids and antiepileptic medications, have been observed to alter cortical metabolism [37, 38].
Biopsy of Brain Tissue
A biopsy of brain tissue is not generally used to diagnose autoimmune encephalitis for several reasons. Neuropathological findings such as infiltration by lymphocytes or microglia activation are frequently nonspecific and nondiagnostic. Also, one study found that brain biopsy contributed to diagnosis in only 8% of patients with autoimmune encephalitis . Finally, antibody testing as described above yields more specific diagnoses and is noninvasive.
Evaluation for Occult Malignancy
As autoimmune encephalitis is considered a classic paraneoplastic syndrome, the clinical evaluation of a patient suspected to have this condition entails an assessment for an occult malignancy . Some tumors produce peptides that are similar to those found in the nervous system, leading to immune cross-reactivity and paraneoplastic neurological syndromes. In particular, the immune system reacts against tumors leading to the development of cytotoxic and antibody-mediated responses directed not only at the tumor but also against the nervous system. In 80% of cases, neurological manifestations develop before the cancer diagnosis . Paraneoplastic disorders usually develop during the early stages of cancer, so the tumor may be difficult to find. If detected, an antibody can guide monitoring for strongly associated tumors. A patient should be followed with regular diagnostic imaging to screen for an occult malignancy at regular intervals for 4 years. Studies have shown that after this time, the likelihood of detecting cancer is low .
Differential Diagnostic Considerations
The preceding discussion focused on the diagnostic value of each respective study for autoimmune encephalitis. In parallel, other diagnostic possibilities should be simultaneously evaluated for and eliminated as potential diagnoses. Differential considerations for a subacute, rapidly progressive encephalopathy include infection (e.g., encephalitis or meningoencephalitis due to herpes simplex virus, varicella zoster virus, human immunodeficiency virus (HIV), enterovirus, Cryptococcus, syphilis, and prion disease), encephalopathy due to systemic disease (e.g., sepsis, organ failure, vitamin deficiency, electrolyte abnormalities), rheumatologic and systemic autoimmune disease (e.g., systemic lupus erythematosus), illicit (e.g., ketamine) or prescribed (e.g., anticholinergic, neuroleptic, serotonergic) drug toxicity or withdrawal, metabolic disorder (e.g., mitochondrial and urea cycle disorders), cerebrovascular disease (e.g., recurrent ischemic stroke), cancer (e.g., primary and secondary brain cancers), and seizure (e.g., nonconvulsive status epilepticus) [5, 43, 44]. A detailed clinical history with brain imaging by MRI, CSF analysis, and EEG can be invaluable in the early period of hospitalization to rapidly sift through this broad differential as well as gather information to support the diagnosis of autoimmune encephalitis.
This diagnosis should be made based on the clinical presentation, and diagnostic evaluation should not be reserved for those with a detected commercially testable antibody nor applied to those who respond to systemic immunotherapy. From a practical perspective, antibody testing may not always be readily accessible and, if performed, the results may take weeks to return. In addition, there is a growing catalog of described antibody-associated autoimmune encephalitis syndromes, some of which are not testable at the commercial laboratory level. Thus, failure to detect an antibody in the serum or CSF does not exclude the possibility of autoimmune encephalitis in the appropriate clinical scenario but rather argues for the testing of serum and CSF in a neuroimmunological referral center. With that said, false-positive antibody results can occur. Finally, a variety of conditions respond by varying degrees to systemic immunosuppression, such as corticosteroids in the treatment of primary and secondary cancers of the brain as well as neurosarcoidosis. Together, these points emphasize the importance of the clinical presentation and a careful evaluation to identify those with autoimmune encephalitis.
As early recognition and initiation of immunotherapy appear to be associated with improved clinical outcome in autoimmune encephalitis, the diagnostic evaluation is directed at identifying those patients who may have autoimmune encephalitis, assessing for other encephalitis etiologies (particularly infectious), screening for occult malignancy, initiating immunotherapy with escalation as needed, and managing sequelae of the encephalitis syndrome. We will now turn to immunotherapy and the management of autoimmune encephalitis sequelae commonly encountered in the ICU.
As autoimmune encephalitis is relatively rare, guidelines for immunotherapeutic management are lacking. No controlled prospective clinical trials have been conducted to determine efficacy of treatments in autoimmune encephalitis. At the present, most of the treatments rely on extant understanding of disease mechanisms, expert opinion based on clinical experience and case series, and a few relatively small prospective trials. When considering acute immunotherapy options, it is important to consider the patient’s comorbidities and phase of illness at presentation. Serological status, if known, may guide agent selection and prognostication of recovery. It is essential to mention that delay in therapy initiation could worsen outcomes .
Common acute immunotherapies for autoimmune encephalitis
Initial treatment regimen
Time to response
1000 mg daily for 3–5 days
Days to weeks with benefit for weeks
Assess for hypertension, baseline serum glucose and electrolytes, close glucose monitoring and consideration for insulin adjustments in known diabetics
Insomnia, psychiatric symptoms, hyperglycemia (close glucose monitoring with sliding scale insulin advised), electrolyte abnormalities, fluid retention, hypertension, peptic ulcer (gastric ulcer prophylaxis advised), Cushing syndrome, cataracts, infection, osteoporosis, avascular necrosis (patients should be advised of risk and monitored for), addisonian crisis in setting of rapid withdrawal
0.4 g/kg/day for 5 days
Days to weeks with benefit for approximately a month
Consider IgA-level assessment; premedication with acetaminophen and diphenhydramine
Headache, aseptic meningitis, thromboembolic events, acute renal failure, anaphylaxis in those who are IgA deficient
5 exchanges, typically an exchange every other day. Schedules vary by institution
Days to weeks with benefit for months
Plasmapheresis catheter placement of adequate caliber, assessment to assure no active infection
Hypotension, electrolyte imbalance. With central line, infection, hemorrhage, thrombosis, and pneumothorax are risks
1000 mg weekly for 2 weeks, or 375 mg/m2 body surface area weekly for 4 weeks
Screening for hepatitis B and C, screening for tuberculosis
Allergic reaction, opportunistic infection, reactivation of tuberculosis or hepatitis B
500–1000 mg/m2 monthly for 3–6 months
Baseline complete blood cell count, liver function tests, serum creatinine. Assure adequate hydration over 24 h prior to dose (2–3 L), normal saline 500 mL intravenous 1 h prior to a dose, prochlorperazine or ondansetron as nausea and vomiting prophylaxis, mesna for hemorrhagic cystitis prophylaxis
Nausea, vomiting, alopecia, mucositis, hemorrhagic cystitis, infertility, myelosuppression
Corticosteroids are a helpful class of medications in a variety of autoimmune disorders, but their prolonged use is associated with multiple comorbidities including insulin resistance, diabetes mellitus, osteopenia, and increased risk for opportunistic infections. IVIG may be associated with a higher risk for chemical meningitis, hyperviscosity, and thrombotic syndromes. In addition, IVIG occasionally triggers headache, flushing, chest tightness, fever, chills, myalgias, fatigue, dyspnea, back pain, nausea, vomiting, diarrhea, and tachycardia and infrequently acute renal failure, neutropenia, autoimmune hemolytic anemia, skin reactions, and arthritis. PLEX can result in decreased arterial blood pressure, arrhythmias, sensations of cold with temporarily elevated temperature, paresthesias, and rarely life-threatening conditions (e.g., shock, hypotension, persistent arrhythmias, hemolysis) [48, 49, 50].
Immune absorption (IA) is an alternative therapy to PLEX, although this medication is not yet available in many countries, including the United States. Studies have suggested an at least equivalent efficacy of IA compared to PLEX [51, 52]. IA allows rapid and selective elimination of antibodies, making this medication an excellent option. IA produces an immediate intravascular reduction of antibody and immune complex concentration as well as antibody redistribution that causes subsequent immunomodulatory changes. While PLEX is a nonselective medication and associated with a reduction in coagulation factors, IA is selective and has fewer adverse effects. In a retrospective analysis of 30 patients with autoimmune encephalitis treated with PLEX or IA, 65% improved after PLEX and 100% after IA . Furthermore, a retrospective analysis of 13 patients with autoimmune encephalitis treated with IA showed that 85% had improvement of their symptoms; however, this efficacy could not be completely attributed to IA because most patients were treated with concomitant corticosteroids .
When a detected antibody is directed to an intracellular protein, therapies directed at the cell-mediated immune response rather than immunomodulatory therapies are advocated [46, 47]. In the acute setting, therefore, cyclophosphamide plays an important role in suppressing the cytotoxic response with the aim of reducing the extent of neuronal injury due to the cell-mediated immune response [46, 47].
No guidelines exist to otherwise guide the selection of first-line immunotherapy nor subsequent escalation to second-line treatments in the acute phase. Second-line treatments are typically considered once the period of anticipated response (around 2 weeks) to first-line treatment has passed as well as in severe presentations . With that said, there is evidence to suggest a role for rituximab, a monoclonal antibody against CD20, as second-line immunotherapy for both seropositive and seronegative autoimmune encephalitis, with tolerability and improved outcomes observed [54, 55]. Furthermore, studies have shown good efficacy of rituximab in patients with IgG4 subtype antibodies, and IgG4 antibodies predominate in anti-LGI1 and anti-CASPR2 encephalitis.
The most common side effects of rituximab are infusion-related reactions, infections, tiredness, and nausea; however, in general, it is a medication with a good safety profile. On the other hand, cyclophosphamide can potentially cause infertility among other side effects. Therefore, the collection of eggs and sperm and the administration of GnRH agonists in women are recommended .
Complications of Autoimmune Encephalitis in the ICU
As already stated, a large percentage of encephalitis patients require ICU admission. The most common reasons for ICU care in autoimmune encephalitis are altered mental status requiring intubation, status epilepticus/refractory status epilepticus, severe hyperkinetic movements, respiratory failure, autonomic dysfunction, and increased intracranial pressure (Tables 17.2 and 17.3). ICU level care, which is presumably linked to higher costs, is strongly associated with long-term outcome . A recent study in a tertiary referral hospital showed that intensive care charges are around $173,000 vs. $50,000 for autoimmune encephalitis patients who do not require ICU admission . In addition, the mortality rate of ICU-admitted patients ranges between 12% and 40% [13, 39, 57]. The main causes of death are severe pneumonia, multiple organ dysfunction syndromes, and refractory status epilepticus .
Status Epilepticus (SE) and Refractory Status Epilepticus (RSE)
SE is a frequent, and sometimes the only, manifestation of autoimmune encephalitis. SE represents the principal cause for ICU admission and may evolve into RSE [58, 59]. Studies have reported generalized, nonconvulsive, partial, and complex seizures. In a cohort of patients with autoimmune encephalitis, 28% of patients suffered from SE for 7 or more days and required on average 5 antiepileptic medications .
SE treatment in autoimmune encephalitis centers on the use of antiepileptic medications for seizure control as well as immunosuppression . There are validated protocols for seizure control in SE that include IV lorazepam, diazepam, and phenytoin or intramuscular midazolam or rectal diazepam as first-line therapy (Class I). Valproate and levetiracetam are second-line options (Class I–III), and IV sedative medications such as pentobarbital, propofol, or midazolam are used in case of failure of first- and second-line therapies. If seizures are uncontrolled, topiramate and phenobarbital can also be considered. Of note, phenobarbital is associated with more adverse effects such as hypotension and a high mortality rate. In addition, once infectious etiologies have been eliminated, first-line immunotherapy as per the discussion above should be rapidly initiated. In case of severe seizures, a vagus nerve stimulator or surgical resection of the seizure focus may be necessary . Early diagnosis and treatment of SE/RSE are associated with better neurological outcomes and fewer relapses .
Another alternative for uncontrolled seizures with poor response to antiepileptic medications is the ketogenic diet (KD). This is a high-fat and low-carbohydrate diet that induces ketone bodies and has been effective in drug-resistant epilepsy in children and adults. The KD has been used in patients with anti-NMDAR encephalitis with success, and it is thus a potential therapy option . A recent study in a tertiary referral center showed seizure control in 73% of patients with super-refractory SE after 2 days of the diet. At discharge, 67% were alive and the majority recovered to their baseline .
Elevated Intracranial Pressure
Intracranial hypertension is a well-known indication for ICU admission in patients with autoimmune encephalitis. Elevated intracranial pressure has been reported (in 34.4% and 21.5% of patients) in only two cohorts of patients with anti-NMDAR encephalitis [58, 65]. Given these reported frequencies, it is interesting that this condition has not been more widely reported, perhaps because it has not been previously identified as a predictor of poor prognosis or mortality. Given the potential for additional brain injury in the setting of persistent intracranial hypertension, further studies are necessary for evaluating the impact of this finding in patients’ outcomes as well as its possible correlation with a specific syndrome. Acute management of elevated intracranial pressure may include interventions such as head of bed elevation, hyperventilation with normal oxygenation, careful blood pressure management, hyperosmolar or hypertonic saline therapy, IV corticosteroids, or neurosurgical interventions depending on etiology and clinical status.
Autonomic dysregulation has been reported in 25–45% of patients with autoimmune encephalitis. Children are frequently less affected than adults. Common dysautonomic manifestations include fever without infection, hypoventilation or hyperventilation, tachycardia or bradycardia, blood pressure crises, diarrhea, hypersalivation, and erectile dysfunction. The presence of autonomic instability is a predictor of poor response to first-line immunotherapy. In addition, autonomic dysfunction appears to be associated with disease progression, particularly in anti-NMDAR encephalitis.
The underlying mechanism of autonomic instability is not clearly understood. Cardiac function is the result of a careful balance between the bradycardiogenic parasympathetic and the positive chronotropic sympathetic system . An experimental study showed several brain regions that could potentially affect cardiac autonomic outflow such as the insula, anterior cingulate cortices, and amygdala, areas commonly involved in limbic encephalitis. Also, cardiac autonomic discharges can synchronize with epileptogenic activity triggering a lethal bradyarrhythmia or asystole .
Therefore, careful monitoring is necessary in all cases of autoimmune encephalitis. Dantrolene, external and internal cooling, pacemakers, mechanical ventilation, and hypertensive medications have been used in the management of dysautonomia in autoimmune encephalitis. In addition, temporary pacemakers have a Class I recommendation in cases of asystole, symptomatic bradycardia with hypotension that is not responsive to atropine, and bifascicular block. Certainly some patients require a permanent pacemaker as autonomic instability can last for several weeks or months [20, 66].
Need for Mechanical Ventilation
Mechanical ventilation is a common complication in patients with autoimmune encephalitis. In a recent study, 57% of patients were intubated for approximately 1 month on average . Some required tracheostomy (68%) and others developed ventilator-associated pneumonia (57%) . Reasons for mechanical ventilation include depressed level of consciousness, respiratory insufficiency, absent airway protection reflexes, hypoventilation, pneumonia, and sedation in psychosis or SE. Reported complications of mechanical ventilation are pneumonia, need for pleural drainage, and acute respiratory distress syndrome (ARDS).
Triage and Administrative Considerations for Patients with Autoimmune Encephalitis
With these complications in mind, the triage of a patient with autoimmune encephalitis is dependent not only on their neurological status but also on their overall medical status. In the emergency department setting, management begins with the clinical survey of airway, breathing, circulation, and glucose status. With the identification and treatment of potential vital sign-related issues, management progresses to the initial diagnostic evaluation including diagnosing autoimmune encephalitis and considering alternative diagnoses discussed earlier in this chapter. Patients may be treated empirically for some of these etiologies while awaiting diagnostic results (e.g. IV acyclovir for herpes simplex encephalitis while awaiting CSF test results). In addition, emergency room providers must assess for decreased or altered level of consciousness as well as their potential etiologies (e.g., seizure, elevated intracranial pressure due to cerebral edema). The management of each of these will likely continue through to triage to the ICU .
Intra- and inter-facility transfer discussions are founded on an understanding of a patient’s cardiovascular, pulmonary, and neurological status, with emergent management (e.g., mechanical ventilation, treatment of SE) initiated before transfer.
Disposition from the emergency room or ICU varies by institution; however, it primarily depends on independence from mechanical ventilation, cardiovascular stability, normalization of intracranial pressure, and resolution of SE. Subsequent discharge from the hospital is most commonly to an acute or subacute rehabilitation center for recovery, particularly for those who required prolonged ICU care.
Discussions regarding posthospital care should be held beginning at the time of admission, with plans made to address clinical issues as they arise, resolve, or persist throughout the course of hospitalization. The decision to transition from the acute care setting to rehabilitation or home is made upon completion of the diagnostic evaluation and treatment, which requires inpatient care. One should be mindful that the period of recovery following an episode of autoimmune encephalitis is on the order of weeks to months and is facilitated by directed physical, occupational, speech and language, and cognitive therapy. Psychiatric co-management may also be required for those patients with psychiatric symptoms (e.g., psychosis), which will require longitudinal care. A critical factor in disposition planning is close hospital follow-up of not only diagnostic results and clinical recovery but also the identification and management of potential sequelae such as epilepsy.
Given the complexities entailed in managing patients with autoimmune encephalitis, their clinical care is collaborative and multidisciplinary. Intensivists, neurologists and neurological subspecialists, medical specialists, psychiatrists, and physiatrists have essential roles to play in collaboration with nursing staff, therapists, and pharmacists. The epoch of inpatient care can last weeks to months, with understandable strain on not only patients but also on their families and other loved ones. Social work, palliative care, and spiritual/chaplaincy services also play important roles in the care of patients with autoimmune encephalitis and their families throughout the hospitalization and during the transition to the outpatient setting.
Factors associated with poor neurologic outcomes are delay in administering immunotherapy, longer ICU stay, need for mechanical ventilation, intrathecal inflammation, severe sepsis, medical comorbidities, need for tracheostomy, and malignancy . Furthermore, prognosis depends on the antibody subtype, with better prognosis for cases involving cell surface antigens and worse prognosis for those associated with paraneoplastic disorders and intracellular antigens.
Our understanding of the long-term neurobehavioral outcomes in autoimmune encephalitis is limited; some preliminary observations are hopeful, while others are sobering. In one large study of long-term outcomes of 77 patients with autoimmune encephalitis treated at a single tertiary center, 53% had a “good” functional outcome (modified Rankin Score ≤2). However, in detailed interviews, while 85% of patients were employed prior to developing autoimmune encephalitis, only 42% were employed afterward; in addition, only 50% reported independence in traveling within their community, and 46% were responsible for their own finances . In addition to these functional and practical aspects of recovery, patients commonly reported symptoms of fatigue, emotional lability, short-term memory loss, and difficulty with concentration years after the initial episode of autoimmune encephalitis . Much work remains to characterize the outcomes and sequelae of autoimmune encephalitis in order to guide refinements to initial and longitudinal management of patients with this disorder.
There are still aspects of autoimmune encephalitis that remain unresolved, including the correlation of time to diagnosis and administration of immunotherapy versus outcomes and the elucidation of new serum, CSF, and radiological biomarkers that predict outcomes or measure disease activity. In addition, the role of brain FDG-PET in the diagnosis and prediction of outcomes needs to be clarified. Further studies are needed to determine a correlation between antibody titers and outcomes as well as the role of autonomic dysfunction and underlying malignancy in specific antibody subtypes. Work to thoroughly evaluate and clarify management strategies such as first-line versus second-line therapies, individual therapies, and new immunotherapies is also needed. Additionally, a detailed knowledge of postencephalitis sequelae is crucial to understand and attempt to ameliorate the impact on quality of life after the acute period.
Autoimmune encephalitis is a diverse category of primary autoimmune and secondary paraneoplastic syndromes that have gained increased attention over the past two decades. The diagnosis of autoimmune encephalitis is clinical, with outcomes dependent on early initiation of immunotherapy. Intensivists play a central role in the management of these patients, particularly in light of frequently associated complications such as SE, cardiovascular instability, and need for mechanical ventilation. ICU-level management is also critical given the high rate of mortality among patients with autoimmune encephalitis and to help optimize their outcomes.
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