Isolated intracranial hypertension associated with COVID-19.

BACKGROUND: Headache is a frequent complaint in COVID-19 patients. However, no detailed information on headache characteristics is provided in these reports. Our objective is to describe the characteristics of headache and the cerebrospinal fluid (CSF) profile in COVID-19 patients, highlighting the cases of isolated intracranial hypertension.
METHODS: In this cross-sectional study, we selected COVID-19 patients who underwent lumbar puncture due to neurological complaints from April to May 2020. We reviewed clinical, imaging, and laboratory data of patients with refractory headache in the absence of other encephalitic or meningitic features. CSF opening pressures higher than 250 mmH2O were considered elevated, and from 200 to 250 mmH2O equivocal.
RESULTS: Fifty-six COVID-19 patients underwent lumbar puncture for different neurological conditions. A new, persistent headache that prompted a CSF analysis was diagnosed in 13 (23.2%). The pain was throbbing, holocranial or bilateral in the majority of patients. All patients had normal CSF analysis and RT-qPCR for SARS-CoV-2 was negative in all samples. Opening pressure >200 mmH2O was present in 11 patients and, in six of these, > 250 mmH2O. 6/13 patients had complete improvement of the pain, five had partial improvement, and two were left with a daily persistent headache.
CONCLUSIONS: In a significant proportion of COVID-19 patients, headache was associated to intracranial hypertension in the absence of meningitic or encephalitic features. Coagulopathy associated with COVID-19 could be an explanation, but further studies including post-mortem analysis of areas of production and CSF absorption (choroid plexuses and arachnoid granulations) are necessary to clarify this issue.

Several neurological manifestations associated with SARS-CoV-2 infection have been described since the beginning of the pandemic. In a cohort of hospitalized severe COVID-19 patients, neurological complaints occurred in 45.5% of infected individuals, varying from 1–14 days from the onset of SARS-CoV-2 infection (1). The most relevant were acute cerebrovascular disease in 5.7%, impaired consciousness in 14.8%, and skeletal muscle injury in 19.3%. In that clinical series, headache was observed in 28 out of 214 patients (13.1%).

According to the International Classification of Headache Disorders, headache attributed to systemic viral infection is diagnosed when there is an association between the onset of pain and systemic viral infection in the absence of encephalitic or meningitic features (2). The frequency of headaches in COVID-19 patients ranges from 5–34% according to different clinical series (3–8). However, no detailed information on headache characteristics is presented in these reports. Moreover, these clinical series do not describe cerebrospinal fluid (CSF) characteristics in these patients.

Herein, we describe the characteristics of headache and the CSF profile during SARS-CoV-2 infection in a consecutive series of COVID-19 patients, highlighting the cases associated with isolated intracranial hypertension. One of these cases is presented as an illustrative report.

Methods

From April to May 2020, we retrospectively selected all consecutive inpatients with SARS-CoV2 infection from different centers who underwent lumbar puncture due to different neurological symptoms. We analysed those who presented refractory headaches with or without visual symptoms as the predominant neurological complaints and excluded those who presented any clinical or laboratory evidence for meningitis or meningoencephalitis, such as neck stiffness, altered consciousness, focal neurological signs, or inflammatory characteristics in the CSF analysis. For this study, we considered CSF opening pressures less than 200 mmH2O to be normal, higher than 250 mmH2O to be abnormal, and 200 to 250 mmH2O equivocal (9–11). All patients underwent lumbar puncture awake and in lateral decubitus. In all cases, SARS-CoV-2 RNA was detected by RT-qPCR through nasal and oropharyngeal swabs (Biomanguinhos kit (E+P1), FIOCRUZ, Brazil). The Local Ethical Committee at INI/FIOCRUZ approved this study.

Results

Case description

A 26-year old previously healthy, not obese female presented with severe, holocranial throbbing headache with nausea, dizziness, and significant visual blurring on the second day past flu-like symptoms due to SARS-CoV-2 infection. Ophthalmological examination revealed bilateral optic disc oedema. Optical coherence tomography was suggestive of optic disc oedema (Figure 1). No focal deficit, ataxia, or pupil light response abnormalities were found on the neurological examination. Brain and orbital MRI were normal except for discrete white matter lesions in the pons and the cerebral hemispheres suggestive of small vessel disease best observed on T2/FLAIR sequences. Brain venous MRI found no evidence of cerebral venous thrombosis. On the eighth day, she underwent lumbar puncture. CSF analysis revealed an opening pressure of 350 mmH2O, 2 cells/mm3, 15 mg/dL of protein level, and 58 mg/dL of glucose. RT-PCR for SARS-CoV-2 was negative in the CSF. Due to the pontine lesion, extensive laboratory exams were required to exclude demyelinating disease. CSF oligoclonal bands were not present, and serum anti-NMO (CBA method) was negative. No other causes of intracranial hypertension were found. The patient was treated with acetazolamide 500 mg bid and had partial improvement of symptoms to date.

Figure 1.

A 26-year-old female presenting bilateral papilledema related to post COVID-19 infection. The optic nerve head OCT B scans show elevation of the optic disc in both eyes ((a) and (b)). The peripapillary OCT circle scans show increased retinal nerve fiber layer thickness in all sectors ((c) and (d)). Retinography ((e) and (f)) showing papilledema and haemorrhage (arrow) in the right eye and papilledema in the left eye. In both eyes, oedema of the optic disc with high elevation is observed.

The clinical and laboratory characteristics of this clinical series are presented in Table 1. In this study, 56 consecutive COVID-19 patients underwent lumbar puncture for different neurological conditions during the SARS-CoV-2 infection, and 13 of these (23.2%) had a new, persistent headache that prompted a CSF analysis. The most frequent complaint in these patients was a throbbing, holocranial, or bilateral intense daily headache. In four patients, there was a previous history of migraine without aura. However, the current headache was different, with more intense and more persistent pain than usual for them. Other relevant neurological complaints in these patients were peripheral facial palsy in one and blurred vision in three, with documented papilledema in two; all other patients had normal fundoscopy.

Table 1

. Clinical and laboratorial characteristics of headache associated with SARS-CoV-2 infection.

Age/gender	Main COVID symptoms/sigs	Headache onset1	Headache characteristics and Nx symptoms/signs	CSF analysis2	Follow-up
42/M	Anosmia, fever, myalgia	12 days	Intense, daily, throbbing, holocranialLasted 4 days	200/120/2/59/39	Recovered
47/F	Myalgia, anosmia, cough	2 days	Intense, throbbing, frontotemporal bilateral Lasted 15 days	220/100/1/58/25	Recovered
42/M	Myalgia, fever, diarrhea	2 days	Intense, pressing or tightening, bilateral. Lasted 8 days	600/300/1/59/26	Recovered
27/F	Sore throat, cough, anosmia, fever	1 day	Orbital, intense, throbbing, blurred vision3, bilateral papilledema	210/120/2/51/31	Partial recovery. Acetazolamide 1.5g/day
26/F*	Cough, myalgia, fever	2 days	Intense, throbbing, pulsatile tinnitus, vertigo, blurred vision3, papilledema, and attention deficit	350/180/2/51/15	Partial recovery. Acetazolamide 3 g/day + Furosemide 20 mg/day
34/F	Fever, myalgia	0 day	Intense, daily, throbbing, bilateral frontotemporal, insomnia	150/90/1/56/30	Partial recoveryDaily, mild headache
34/F	Headache, myalgia	0 day	Intense, throbbing, frontotemporal, insomnia	210/120/2/71/22	Partial recovery
39/F	Headache, low backpain, D-dimer 10.000 ng/ml	0 day	Intense, throbbing, holocranial, left facial palsy (3rd day), attention deficit; lasted 3 days	300/100/1/38/31	Recovered
47/F	Headache, anosmia, cough, fatigue, fever; thorax CT w/50% of ground glass involvement	0 day	Intense, occipital, throbbing	250/150/1/61/25	Recovered
45/F	Fever, headache, diarrhea, sweating, anosmia	0 day	Intense, fluctuating, bilateral, non-throbbing headache	200/120/2/59/31	Not recovered; daily fluctuating headache, although less severe
35/F	Low fever, tiredness, dry cough, anosmia, confusional state, drowsiness	0 day	Moderate, daily, non-throbbing headache, without other features.4 Lasted 7 days	400/300/2/54/39	Recovered
68/M	Runny nose, asthenia, fever, cough	10 days	Progressively intense, daily, non-throbbing, occipital slowly spreading to the whole skull; dizziness and nausea	200/110/4/43/45	Refractory, intense, daily for 50 days. Slowly improved and to date is recovered
44/F	Myalgia, fever, cough, mild dyspnea	12 days	Intense, daily, holocranial pressure, sometimes throbbing, blurred vision associated with nausea	280/180/1/63/27	Recovered

*This patient appears in case description in the section Results of this manuscript.

1Headache onset after COVID symptoms/signs.

2Cerebrospinal fluid analysis: Opening pressure mmH2O/closing pressure mmH2O/cell count/mm3/glucose level mg/dl/protein level mg/dl.

3Transitory symptom, normal visual acuity test.

4Brain MRI unremarkable except for signs of intracranial hypertension (distension of perioptic subarachnoid space and empty sella).

The opening CSF pressure of one of these patients with papilledema was 210 mmH2O, below the level required for the diagnosis of pseudotumor cerebri syndrome (PTCS), according to a revised diagnostic criteria (12). All patients had normal cell counts and glucose and protein levels on the CSF analysis. Besides, RT-qPCR for SARS-CoV-2 in CSF was negative in all patients. Median values for cell counts, glucose, and protein were of 1.6/mm3 (1-4/mm3), 55.6 mg/dL (38–71mg/dL), and 29.6 mg/dL (15–45mg/dL), respectively. CSF opening pressure ranged from 150 to 600 mmH2O (median of 270 mmH2O). In 12 patients, the opening pressure was ≥200 mmH2O (median of 251 mmH2O) and in six of these ≥250 mmH2O (median of 355 mmH2O). No other causes for intracranial hypertension, such as obesity, venous thrombosis, or drugs, were identified in these patients. All patients were submitted to brain MRI and only in one patient were abnormalities typically seen in intracranial hypertension detected (see Table 1).

To date, nine out of 13 patients were pain-free 8 days after the headache onset on average (3–15 days), and five had a partial recovery, with mild headache (follow-up of 66 days to date).

Other neurological conditions that prompted lumbar puncture were meningoencephalitis/encephalopathy in 35 patients, Guillain-Barré syndrome in four, Miller-Fisher syndrome in two, and acute myelitis in two individuals. Median CSF opening pressure in this group was of 200 mmH2O (150–400).

Discussion

In this clinical series, 13 patients had severe and persistent headache in the course of SARS-CoV-2 infection, which justified an analysis of the CSF. Of note, intracranial hypertension in the absence of meningitis/encephalitis was seen in 84.6% of patients (11 out of 13) assuming a normal CSF opening pressure of up to 200 mmH2O. If we consider the cut-off of 250 mmH2O, as proposed by the revised criteria for PTCS (12), 46.1% of our patients (six out of 13) still fulfil the criteria for intracranial hypertension.

Interesting, in our series, 10 out of 13 patients were women (Table 1). The prevalence of idiopathic intracranial hypertension is characteristically higher among women, at a rate of 3.3 per 100,000 per year in females aged 15–44 years, corresponding to a female: male ratio of 8:1 (13). We could consider that the same would be expected in cases of intracranial hypertension associated with COVID-19.

Recently, one case of benign intracranial hypertension was published (14). In this case report, a 35-year-old female patient presented headache 2 days before COVID-19 symptoms and signs, rapidly evolving to mental confusion. CSF analysis was normal except for a high opening pressure (400 mmH2O) and brain MRI disclosed prominent subarachnoid space around optic nerves, vertical tortuosity of the optic nerves, and superior compression of the hypophysis.

The normal value of CSF pressure in an appropriate clinical setting could be a matter of debate, with some arguing that pressures between 200 to 250 mmH2O are equivocal (15). Because the CSF pressure naturally fluctuates, intracranial pressure monitoring at another time may be necessary to establish the diagnosis with certainty. Patients with a transient or intermittent elevation of the CSF pressure below the threshold required to produce oedema at the optic nerve head are described. This could justify the absence of ophthalmological symptoms and signs (16). Furthermore, a classic example of acute neurological disease with elevated intracranial hypertension and the absence of papilledema in a significant proportion of cases is subarachnoid haemorrhage. In addition, patients with headache and elevated opening pressure on lumbar puncture but no papilledema have been described (17–21).

Only two of our patients had a documented papilledema. Although fundus was examined as part of neurological examination in all patients, not all enrolled patients were formally evaluated by an ophthalmologist, which is a limitation of our study. Optic fundi examination is part of neurological examination and of utmost importance in recognition of raised intracranial pressure. However, the protective additional measures such as face shield and close contact with patients during the exam impose additional difficulties to physicians evaluating COVID-19 patients with headache.

Importantly, patients without papilledema are at lower risk of vision loss compared to typical patients with intracranial hypertension with papilledema (12,17,22). Ophthalmologic evaluation is advised to confirm the presence of papilledema and to evaluate those patients with questionable or subtle papilledema (23).

Intracranial hypertension has been associated with diverse conditions such as obesity, autoimmune diseases, use of certain medications, vitamin deficiencies, vitamin excesses, bacterial infections, and viral infections such as HIV, measles, varicella, herpes virus, and hepatitis A virus (24–26).

The real pathogenesis of intracranial hypertension in the absence of an occupying mass lesion is a matter of debate. The main hypotheses indicate that it can be caused by increased abdominal and/or intracranial venous pressure, venous outflow abnormalities, alterations in absorption or production of CSF, low-grade inflammation, intracranial vascular clotting, or cerebral edema (15).

Recently, it has been described that SARS-CoV-2 infection can be associated with coagulation dysfunction, predisposing infected individuals to venous thromboembolism in several ways (27). Pathogenic mechanisms, including endothelial dysfunction with increased levels of von Willebrand factor, systemic inflammation with Toll-like receptor activation, and a procoagulatory state via tissue factor pathway activation, are involved (28). Intracranial venous thrombosis has been implicated as a cause for intracranial hypertension secondary to CSF outflow obstruction (29). Thus, we could speculate that venous congestion could be precipitated during a hypercoagulable state caused by SARS-CoV-2 infection.

Although our cases presented normal brain MRI, with magnetic resonance venography indicating normal venous sinuses, a possible hyperviscosity mechanism caused by SARS-CoV-2 would increase the venous pressure without actual venous sinus thrombosis. Thus, a low-grade inflammation determined by SARS-CoV-2 infection in conjunction with this hyperviscosity and hypercoagulable state could result in intracranial hypertension in some infected individuals. Indeed, in a recent study by Duarte-Neto et al., evidence of brain small vessel disease was observed in 30% of autopsies from COVID-19 patients (30). Further pathological studies are necessary to confirm this hypothesis.

A practical issue is that headaches secondary to intracranial hypertension occurred in a significant proportion of our patients, highlighting the importance of prompt recognition. Optic fundi examination is part of the neurological examination and of utmost importance in recognition of raised intracranial pressure. However, the additional protective measures such as the use of a face shield and the close contact with patients during this exam impose additional difficulties to physicians evaluating COVID-19 patients with headache. Additionally, an optic disc photo is an option as a diagnostic tool, but is only available in eye departments.

In our series, neurological complaints other than headache were peripheral facial palsy in one and cognition symptoms in two individuals, who reported poor concentration and inattention affecting some activities of daily living. Patients with intracranial hypertension do not usually have cognitive deficits. However, one study showed deficits in reaction time and processing speed that persisted on retesting at 3 months despite improvement in measured ICP and headache (31). Regarding peripheral facial palsy, it is infrequently reported in idiopathic intracranial hypertension (32,33). In addition, the involvement of the facial nerve has been associated with SARS-CoV-2 infection, but generally in the context of Guillain-Barré syndrome (34,35).

Conclusion

Headache is one of the frequent neurological symptoms associated with COVID-19. According to the present study, in the absence of evidence of meningitis or cerebrovascular disease, headache can be severe, persistent, and associated to intracranial hypertension in a significant proportion of cases. The recently described coagulopathy associated with COVID-19 could be an explanation for such cases that could be due to the induction of a hyperviscosity state, leading to less absorption of CSF. Necropsy studies examining areas of production and CSF absorption; that is, choroid plexuses and arachnoid granulations, may help to clarify this issue.

Clinical implications

What are the characteristics of headache in COVID-19 patients? What is the cerebrospinal fluid (CSF) profile of these individuals? In this cross-sectional study, 13 out of 56 COVID-19 patients submitted to CSF analysis had severe, persistent headache. In 11 patients, the opening pressure was above 200 mmH2O and in 6 of these, above 250 mmH2O. RT-qPCR for SARS-CoV-2 was negative in all samples. Headache can be attributed to isolated intracranial hypertension in the absence of meningitic or encephalitic features in a significant number of COVID-19 patients.