Characteristics of intracerebral haemorrhage associated with COVID-19: a systematic review and pooled analysis of individual patient and aggregate data


Background and purpose

There are very few studies of the characteristics and causes of ICH in COVID-19, yet such data are essential to guide clinicians in clinical management, including challenging anticoagulation decisions. We aimed to describe the characteristics of spontaneous symptomatic intracerebral haemorrhage (ICH) associated with COVID-19.


We systematically searched PubMed, Embase and the Cochrane Central Database for data from patients with SARS-CoV-2 detected prior to or within 7 days after symptomatic ICH. We did a pooled analysis of individual patient data, then combined data from this pooled analysis with aggregate-level data.


We included data from 139 patients (98 with individual data and 41 with aggregate-level data). In our pooled individual data analysis, the median age (IQR) was 60 (53–67) years and 64% (95% CI 54–73.7%) were male; 79% (95% CI 70.0–86.9%) had critically severe COVID-19. The pooled prevalence of lobar ICH was 67% (95% CI 56.3–76.0%), and of multifocal ICH was 36% (95% CI 26.4–47.0%). 71% (95% CI 61.0–80.4%) of patients were treated with anticoagulation (58% (95% CI 48–67.8%) therapeutic). The median NIHSS was 28 (IQR 15–28); mortality was 54% (95% CI 43.7–64.2%). Our combined analysis of individual and aggregate data showed similar findings. The pooled incidence of ICH across 12 cohort studies of inpatients with COVID-19 (n = 63,390) was 0.38% (95% CI 0.22–0.58%).


Our data suggest that ICH associated with COVID-19 has different characteristics compared to ICH not associated with COVID-19, including frequent lobar location and multifocality, a high rate of anticoagulation, and high mortality. These observations suggest different underlying mechanisms of ICH in COVID-19 with potential implications for clinical treatment and trials.


Coronavirus Disease 2019 (COVID-19) can be complicated by a coagulopathy with a high risk of serious and often life-threatening thromboembolic events including venous thromboembolism [1, 2] and ischaemic stroke [3]. This has led to the widespread use of anticoagulants including heparins, often guided by D-dimer levels as evidence for the degree of hypercoagulability [4]. While anticoagulants appear to improve outcome in severe COVID-19 [5], they also have the potential to increase the risk of serious intracranial bleeding, particularly intracerebral haemorrhage (ICH).

There are a few data available on the clinical features of ICH in people with COVID-19 [6, 7]. Previous reports did not allow for clear conclusions due to small sample sizes. Information about the characteristics and causes of ICH in COVID-19 is essential to guide clinicians in optimising clinical management, including making difficult anticoagulation decisions. We, therefore, undertook a systematic review and pooled analysis of all available studies reporting individual or aggregate-level patient data on ICH in the context of COVID-19.


Search strategy and study selection

We carried out a systematic literature search from PubMed, Embase and Cochrane Central Database, according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [8], with the following search terms ((“stroke” OR “cerebrovascular” OR “intracranial” OR “intracerebral” OR “intraparenchymal”) AND (“haemorrh*” OR “hemorrh*”)) AND (“COVID-19” OR “coronavirus” OR “corona virus” OR “Coronavirus” OR “2019-nCoV” OR “SARS-CoV” OR “Severe Acute Respiratory Syndrome”). We limited the results to 2019–2020 to exclude papers referring to other coronaviruses. We did not limit the search by language. We used EndNote software to run auto de-duplication. After removal of duplicates, two reviewers (RB and JB) performed an initial search and screening for relevant articles through title and abstract; discrepancies were resolved by consensus, and where necessary with a third senior reviewer (DJW). The potential full texts were evaluated by applying the inclusion and exclusion criteria given below. The literature search was finalized on December 12, 2020.

Inclusion and exclusion criteria

We included all studies that reported patients confirmed to have severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection according to the WHO interim guideline [9] (i.e. a nasopharyngeal or oropharyngeal swab positive for SARS-CoV-2 on reverse transcriptase polymerase chain reaction (RT-PCR), or a blood sample positive for SARS-CoV-2 antibodies) with SARS-CoV-2 detected either prior to, at the time of, or up to 7 days post, spontaneous (nontraumatic) symptomatic ICH. We excluded studies reporting other types of intracranial haemorrhage including microhaemorrhages, ischaemic infarcts with haemorrhagic transformation, subdural hematoma, subarachnoid haemorrhage and haemorrhagic leukoencephalopathy. Review articles, editorials, opinion papers and guidelines were excluded. For the pooled individual patient data analysis, we included papers that presented individual-level data on any of our variables of interest. Papers presenting aggregate-level data only were subsequently included in a pooled analysis of both individual patient and aggregate data.

Data extraction

The following variables were extracted from the studies: demographics (age, gender); vascular risk factors; ICH characteristics (location, cause); stroke severity (National Institutes of Health Stroke Scale (NIHSS) score); anticoagulant treatment (prophylactic or therapeutic) at the time of ICH; COVID-19 severity and clinical outcome; coagulation and inflammation markers (D-dimers and fibrinogen, APPT, PT, INR, platelets, CRP, ferritin). We classified ICH from reported information according to location as lobar or non-lobar (i.e. deep or infratentorial, defined as ICH in the basal ganglia, thalamus, brainstem or the cerebellum). We then classified ICH aetiology using all information available by predefined criteria as follows: hypertensive arteriopathy (deep or infratentorial haemorrhage with known hypertension before the ICH); cerebral amyloid angiopathy (defined as ≥ 1 lobar, cortical, or cortico-subcortical haemorrhage and age ≥ 55 with no other identified cause); structural macrovascular lesions (aneurysm, pseudoaneurysm, cavernous malformation); coagulopathy (defined as PT ≥ 15 and/or INR ≥ 1.2 and/or APTT ≥ 45 and/or platelets ≤ 100,000); other identified causes (cerebral venous thrombosis, Moya Moya angiopathy); or undetermined.

To estimate the pooled incidence of ICH in patients with COVID-19, we extracted data on the number of hospitalised patients with COVID-19 and the number documented to have ICH in the same time period.

Statistical analysis

A pooled analysis was performed on all of the individual patient data found in the published literature, to estimate means, medians, standard deviations, minimum and maximum values. We then combined the aggregate data from these individual patients with other studies reporting aggregate data according to the two-stage method [10], using a random-effects model. We compared the characteristics of patients who were and were not receiving anticoagulation at the time of their ICH using Fisher’s exact test. Statistical analyses were performed using Microsoft Office Excel version 365 16.0 and Stata 16.


Literature search and screening

The flow diagram (Fig. 1) shows the detailed literature search steps and data selection for our individual patient data pooled analysis. The database searches identified a total of 473 potentially relevant articles. Six further articles were added through a manual search of relevant article references. After the exclusion of duplicate references, 357 articles were considered for the pooled individual data analysis. 297 studies were excluded after screening the title and abstract because they were review articles, editorials, opinion papers and guidelines. A total of 47 studies with individual-level data on our variables of interest qualified for inclusion, identifying 98 reported patients with COVID-19 and ICH. A further 13 studies reported only aggregate-level data on patients with COVID-19-associated intracranial haemorrhage not already included in our individual patient data meta-analysis. These contained 190 cases of intracranial haemorrhage, of which 99 were intracerebral. Five studies including 41 patients with ICH reported ICH-specific data (see Table 1) and were eligible for our two-stage pooled analysis.

Fig. 1

Flow diagram of the literature search and selection process in the pooled individual patient data analysis

Table 1 Aggregate data summary

Pooled individual patient data analysis

Patient demographics and intracerebral haemorrhage characteristics

The characteristics of the patients included in our pooled individual patient data analysis (n = 98) are shown in Table 2; 79% (95% CI 70.0–86.9%) had critically severe COVID-19. Detailed data from all individual patients included are shown in Supplementary Table 2. The median age was 60 years (IQR 53–67); 64% were men. The proportions of patients with vascular risk factors were: hypertension in 53%, diabetes in 29%, dyslipidaemia in 16%, high BMI in 11% and history of smoking in 11% (Table 2); 20% had no history of vascular risk factors.

Table 2 Characteristics of patients included in individual patient data pooled analysis

ICH was frequently lobar (67%), multifocal (36%) and severe, with a median NIHSS score of 28 (IQR 15–28; available in 18 patients). Non-lobar (deep or infratentorial) ICHs were less common (29%), while mixed (lobar and non-lobar) ICHs were reported in only 4% of cases. Coagulopathy was the most common reported cause of ICH (50/98; 51%), nearly always attributed to therapeutic anticoagulation (48/50; 96%).

65/91 (71%) patients were receiving anticoagulation at the time of ICH, which was therapeutic in 53/91 (58%): therapeutic unfractionated heparin (UFH) in 36 (40%); therapeutic low molecular weight heparin (LMWH) in 14 (15%); and warfarin in 3 (3%). Prophylactic LMWH was used in 12/91 (13%). The indication for anticoagulation was extracorporeal membrane oxygenation (ECMO) in 20, concurrent thromboembolic events (pulmonary embolism and deep venous thrombosis) in 5, atrial fibrillation in 3, mechanical cardiac valve replacement in one patient and occlusive femoral artery thrombus in one. 35 patients were started on either therapeutic or prophylactic anticoagulation for suspected COVID-19 hypercoagulability based on local protocols.

The characteristics of patients with known anticoagulation status are shown in Table 3. 26/91 (29%, 95% CI 20–39%) patients were not receiving any anticoagulation at the time of ICH. Of these, 12/26 (46%, 95% CI 27–67%) were lobar, 2/23 (9%, 95% CI 1–28%) were multifocal, 7/26(27%, 95% CI 12–48%) were attributed to hypertensive arteriopathy, and 1/26(4%, 95% CI 0–20%) was associated with coagulopathy. The proportions of patients with lobar ICH and multifocal ICH were lower in those who were not anticoagulated compared to those who were anticoagulated (12/26 (46%, 27–67%) vs 51/63 (81%, 69–90%), p = 0.002; and (2/23 (9%, 1–28%) vs 31/63 (49%, 36–62%), p < 0.001, respectively). The proportion of ICH attributed to coagulopathy was 1/26 (4%, 0–20%) in patients who were not anticoagulated compared to 49/65 (75%, 63–85%) in those who were (p < 0.001). The proportion of ICH attributed to hypertensive arteriopathy was higher in patients who were not anticoagulated compared to those who were (7/26 (27%, 12–48%) vs 0/65 (0%, 0–5%), p < 0.001).

Table 3 ICH characteristics in non-anticoagulated versus anticoagulated patients

Coagulability markers are summarized in Table 2. D-dimers were reported in 64/98 (65%) patients; they were elevated (> 500 μg/L) in 94% of cases with a median of 3387 μg/L (IQR 1745–5670).

Coronavirus disease severity

The time of onset of COVID-19 symptoms (where present) in relation to ICH was reported for 92/98 (94%) patients. Of these, 71 (77%) developed symptoms before ICH with a median interval of 15 days (IQR 5–20), while 21 (23%) had no symptoms at the time of ICH. 77 (79%) were critically ill (developed respiratory failure requiring mechanical ventilation or septic shock or other organ dysfunction or failure that required intensive care [11]) including 20 (21%) who received extracorporeal membrane oxygenation (ECMO) treatment. A further four patients (4%) had severe disease (with one of the following criteria: tachypnoea ≥ 30 breaths per min; or O2 sat ≤ 93% at rest; or PaO2/FiO2 ratio < 300 mmHg [11]), 9 (9%) had moderate disease activity (with fever, respiratory tract symptoms and pneumonia on imaging [11]), 2 (2%) had mild symptoms and no pneumonia on imaging and 5 (5%) were asymptomatic.


The mortality was 53/98 (54%); 18/98 (18%) remained critically ill and 27/98 (28%) were discharged home or to a rehabilitation unit.

Pooled analysis of individual patient and aggregate data

Our two-stage pooled analysis included the pooled individual patient data (Table 2, n = 98) and ICH-specific aggregate-level data (Table 1, n = 41). The results for key variables are shown in Fig. 2. The mean age was 57.9 years (95% CI 55.5–60.4 years). The estimated proportion of patients of the male sex was 73.9% (95% CI 66.0–81.2%). 53.6% (95% CI 43.1–63.9%) were hypertensive, and 74.4% (95% CI 46.6–95.4%) were prescribed therapeutic-dose anticoagulation at the time of ICH. 67.7% (95% CI 46.6–86.0) of ICH were lobar, and 20.1% (95% CI 4.7–40.6%) were multifocal.

Fig. 2

ICH characteristics in our two-stage pooled analysis of individual patient and aggregate data

Incidence of ICH in COVID-19

Twelve cohort studies (n = 63,390 patients) reported data on the incidence of ICH in COVID-19 inpatients, with the incidence ranging from 0.13 to 2.03%. The pooled incidence of ICH across these studies was 0.38% (95% CI 0.22–0.58%) (Fig. 3).

Fig. 3

Incidence of ICH in inpatients with COVID-19


Spontaneous (non-traumatic) ICH in patients with COVID-19 appears to have distinct characteristics that differ from those previously reported for ICH not associated with COVID-19. Based on our pooled individual patient data analysis, in comparison to non-COVID-19 populations [12, 13], ICH associated with COVID-19 seems to affect a younger (median age 60), more frequently male (64%) and less often hypertensive (53%) population, and appears to be more often lobar, multifocal, and associated with the use of anticoagulant drugs. Our pooled analysis of individual and aggregate data showed similar findings. These results are potentially relevant for understanding underlying mechanisms, and for the management of patients with COVID-19, including the use of anticoagulants to treat or prevent thromboembolic complications. We found a low incidence of ICH in patients with COVID-19 (0.38%), but the high mortality rate (54%) suggests that ICH is among the most severe neurological complications of COVID-19. Furthermore, our data suggest that the majority of ICH occur in the context of critically severe COVID-19.

The high prevalence of lobar ICH (in 67% of patients in our pooled individual patient analysis, and 67.7% in the pooled analysis of individual and aggregate data) is striking, and consistent with the pattern recently described in a systematic review of neuroimaging features of COVID-19 [14]. In non-COVID-19 ICH populations, lobar ICH typically accounts for only 32–38% of cases [15,16,17]. In non-COVID-19 cohorts, lobar ICHs are mainly due to either macrovascular causes (arteriovenous malformations or aneurysms), hyaline arteriolosclerosis or cerebral amyloid angiopathy [18].

Another important finding was that ICH in COVID-19 was multifocal in 36% of patients in our pooled individual patient analysis and 20.6% in our two-stage pooled analysis; this is much more frequent than in typical ICH cohorts in which ICH are multiple in only about 6% of cases [19]. Interestingly this previous study also found that multiple ICHs were more often lobar and associated with systemic coagulopathy [19]. We found hypertension in only 53% of cases, also in keeping with the data in multiple non-COVID-19 ICH [19]. In COVID-19 patients not on anticoagulants, the proportion of multifocal ICH was much lower (9%) than in our full cohort (49%), and similar to the general rate of ICH multifocality in non-COVID-19 ICH populations, suggesting that anticoagulation is an important precipitating factor for multifocal ICH in patients with COVID-19.

The unusual characteristics of ICH associated with COVID-19 raise the possibility that the underlying mechanisms might be different from those of spontaneous ICH in patients without COVID-19. In our pooled individual and aggregate data analysis, 74.4% of ICH were associated with therapeutic anticoagulation, which may have been an important contributory factor. It is also possible that ICH occurs in more severe COVID-19, in which anticoagulation is more likely to be given (including for ECMO). Our findings are consistent with a recent study reporting 33 patients with COVID-19 and intracranial bleeding (primary ICH in 5 patients and haemorrhagic transformation of an infarct in most of the rest) and a high rate of anticoagulation (66.7% therapeutic anticoagulation and 9.1% prophylactic anticoagulation) [20]. In another study, therapeutic anticoagulation use (compared with not using anticoagulation) in COVID-19 patients was associated with a five-fold increased risk of ICH [21]. By contrast, in previous mechanistic classifications of non-COVID-19 ICH, anticoagulation accounted for only 10–15% of cases [22]. Interestingly, only 4% of ICHs were associated with coagulopathy in non-anticoagulated patients, supporting the hypothesis that COVID-19-associated ICH can result from vessel wall pathology rather than requiring the presence of impaired clotting associated with a critical illness, anticoagulation therapy, or both.

D-dimer levels were high in most patients (median (IQR) 3387 μg/L (IQR 1745–5670), surpassing the threshold identified as a predictor of in-hospital mortality [23] and consistent with a recent study in COVID-19 associated acute stroke that found elevated D-Dimers in all patients with haemorrhagic stroke (mean of 3,387 μg/L), which was lower than the levels observed in ischaemic stroke (mean 7148 μg/L) [24]. Arterial and venous thromboembolic events, including ischaemic strokes, have been widely associated with severe coronavirus disease [25], while cerebrovascular disease is associated with increased disease severity in patients with COVID-19 [26]. Similarly, we found that the majority of ICH (79%) occurred in patients with critically severe COVID-19. These findings, together with the findings from the current study, emphasise the challenging combination of thrombotic and haemorrhagic complications, particularly in severe COVID-19 [27].

The pathogenesis of intracerebral haemorrhage in COVID-19 patients is likely to be complex. One report describing 41 cases of COVID-19 indicated that prolonged prothrombin time, elevated D-dimer, and severe platelet reduction occur in critical COVID-19 patients [28], all of which are associated with increased propensity for haemorrhagic complications. Although anticoagulation was common in our study, it is not considered to be a sufficient or necessary cause for ICH but is hypothesised to aggravate haemorrhage from vessels prone to bleeding due to other pathologies. SARS-CoV-2 has both direct and indirect effects on the cerebral vasculature that could increase the risk of haemorrhage through various potential mechanisms [29]. First, it has been widely reported that SARS-CoV-2 binds to the angiotensin-converting enzyme 2 (ACE2) receptors largely present in the brain vessels [30] which could cause endothelial injury and blood–brain barrier (BBB) disruption [31]. Endothelial cell infection and endotheliitis have been demonstrated in COVID-19 via histological identification of viral elements within endothelial cells and an accumulation of inflammatory cells and apoptosis [32]. A diffuse bleeding-prone endotheliitis, perhaps aggravated by the use of therapeutic anticoagulation, could thus be a contributory factor in explaining our findings. Other studies in COVID-19 have found evidence of a haemorrhagic leukoencephalopathy with multiple cerebral microbleeds, in keeping with the presence of a diffuse haemorrhage-prone vasculopathy [33]. Other accumulating evidence suggests that SARS-CoV-2 may be associated with a cytokine storm syndrome and excessive oxidative stress [34], which could disrupt endothelial function, causing blood–brain-barrier breakdown and ICH [35]. Finally, disruption of the renin-angiotensin system (RAS) may also play a role in COVID-19-mediated ICH; down-regulation of endothelial ACE2 receptors can cause dys-autoregulation of cerebral blood flow [36].

The majority of patients with COVID-19-associated ICH (77%) presented with COVID-19 symptoms prior to haemorrhagic stroke onset, with a median delay of 15 days in keeping with previous studies [37, 38], also suggesting that a delayed haemorrhagic vasculopathy could be a contributory factor.

In our review, 79% of reported patients were critically ill requiring ICU admission or mechanical ventilation, with very high mortality (54%), consistent with previous studies reporting that ICH was more likely in patients with severe pulmonary COVID-19 (81.8%) with an extremely poor overall prognosis and a mortality rate of 63.6% [39]. Furthermore, 21% of patients received ECMO in our study, which may increase the risk of thrombotic and bleeding complications as indicated by a recent case series that reported 4 out of 10 patients with COVID-19 placed on ECMO developed intracranial haemorrhage, 3 of whom died [40]. By contrast, in non-COVID-19 cohorts, the incidence of ECMO-associated ICH varied between 1.8 and 21% [41].

The incidence of ICH in COVID-19 patients in our study was 0.38% which is lower than the reported incidence of acute ischemic stroke in COVID-19 patients which ranges from 0.9 to 2.7% [42].

The main strength of our study is the inclusion of all available individual patient and aggregate data regarding ICH in patients with COVID-19, allowing us to describe distinct characteristics that are not clearly apparent in small case series. In addition, our review highlights that COVID-19 can be associated with both prothrombotic and haemorrhage-prone states, which might be relevant for anticoagulation strategies.

We acknowledge several limitations of our study. First, we included hospital case series which are likely to be affected by selection and publication bias. Second, we did not have access to data from a contemporaneous control group of patients with non-COVID-19 associated ICH; comparison to historical ICH controls is not likely to be helpful because of the change in the spectrum of stroke presenting to hospital associated with the COVID-19 pandemic [50]. Third, we did not have access to detailed investigations including neuroimaging markers of small vessel disease or vascular imaging to exclude macrovascular causes and assign causes in a systematic and standardised way across cohorts; moreover, limited MRI access during the pandemic might have led to misclassification of haemorrhagic transformation of infarcts as ICHs. Finally, due to the limitations in published data, we were not able to report on the causes of death (for example the proportions attributed to respiratory or neurological disease).

Nevertheless, despite limitations related to the small patient numbers described in most studies, our findings suggest that ICH in COVID-19 has distinct characteristics with potential implications for understanding mechanisms, management of anticoagulation, and clinical trials. Ongoing randomised controlled trials to clarify the risk, benefit, and optimal dose of anticoagulation in patients with COVID-19 should include ICH as a key safety outcome.


  1. 1.

    Tang N, Li D, Wang X, Sun Z (2020) Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost 18(4):844–847

    CAS  Article  Google Scholar 

  2. 2.

    Han H, Yang L, Liu R, Liu F, Wu KL, Li J et al (2020) Prominent changes in blood coagulation of patients with SARS-CoV-2 infection. Clin Chem Lab Med.

    Article  PubMed  Google Scholar 

  3. 3.

    Beyrouti R, Adams ME, Benjamin L et al (2020) Characteristics of ischaemic stroke associated with COVID-19. J Neurol Neurosurg Psychiatry 91:889–891

    Article  Google Scholar 

  4. 4.

    Moores LK, Tritschler T, Brosnahan S et al (2020) Prevention, diagnosis, and treatment of vte in patients with coronavirus disease 2019: CHEST guideline and expert panel report. Chest 158(3):1143–1163.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Tang N, Bai H, Chen X, Gong J, Li D, Sun Z (2020) Anticoagulant treatment is associated with decreased mortality in severe coronavirus disease 2019 patients with coagulopathy. J Thromb Haemost.

    Article  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Trifan G, Goldenberg FD, Caprio FZ et al (2020) Characteristics of a diverse cohort of stroke patients with SARS-CoV-2 and outcome by sex. J Stroke Cerebrovasc Dis 29(11):105314.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  7. 7.

    Ellul MA, Benjamin L, Singh B et al (2020) Neurological associations of COVID-19. Lancet Neurol 19(9):767–783.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  8. 8.

    Moher D, Shamseer L, Clarke M et al (2015) Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev 4(1):1

    Article  Google Scholar 

  9. 9.

    WHO Clinical management of severe acute respiratory infection when novel coronavirus (nCoV) infection is suspected 2020. Accessed 27 Oct 2020

  10. 10.

    Riley RD, Simmonds MC, Look MP (2007) Evidence synthesis combining individual patient data and aggregate data: a systematic review identified current practice and possible methods. J Clin Epidemiol 60(5):431–439. (PMID: 17419953)

    Article  PubMed  Google Scholar 

  11. 11.

    Chinese clinical guidance for COVID-19 pneumonia diagnosis and treatment (7th edition) Accessed 27 Oct 2020

  12. 12.

    An SJ, Kim TJ, Yoon BW (2017) Epidemiology, risk factors, and clinical features of intracerebral hemorrhage: an update. J Stroke 19:3–10.

    Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Javalkar V, Kuybu O, Davis D, Kelley RE (2020) Factors associated with inpatient mortality after intracerebral hemorrhage: updated information from the United States nationwide inpatient sample. J Stroke Cerebrovasc Dis 29:104583.

    Article  PubMed  Google Scholar 

  14. 14.

    Ladopoulos T, Zand R, Shahjouei S, Chang JJ, Motte J, Charles James J, Katsanos AH, Kerro A, Farahmand G, Vaghefi Far A, Rahimian N, Ebrahimzadeh SA, Abedi V, Papathanasiou M, Labedi A, Schneider R, Lukas C, Tsiodras S, Tsivgoulis G, Krogias C (2021) COVID-19: neuroimaging features of a pandemic. J Neuroimaging. (PMID: 33421032)

    Article  PubMed  Google Scholar 

  15. 15.

    Safatli DA, Günther A, Schlattmann P, Schwarz F, Kalff R, Ewald C (2016) Predictors of 30-day mortality in patients with spontaneous primary intracerebral hemorrhage. Surg Neurol Int 7(Suppl 18):S510–S517. (PMID: 27583176; PMCID: PMC4982350)

    Article  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Rannikmäe K, Woodfield R, Anderson CS et al (2016) Reliability of intracerebral hemorrhage classification systems: a systematic review. Int J Stroke 11(6):626–636.

    Article  PubMed  Google Scholar 

  17. 17.

    Seiffge DJ, Curtze S, Dequatre-Ponchelle N, Pezzini A, Tatlisumak T, Cordonnier C, Werring D (2019) Hematoma location and morphology of anticoagulation-associated intracerebral hemorrhage. Neurology 92(8):e782–e791. (PMID: 30674603)

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Wilson D, Charidimou A, Werring DJ (2014) Advances in understanding spontaneous intracerebral hemorrhage: insights from neuroimaging. Expert Rev Neurother 14(6):661–678

    CAS  Article  Google Scholar 

  19. 19.

    Wu TY, Yassi N, Shah DG, Ma M, Sharma G, Putaala J et al (2017) Simultaneous multiple intracerebral hemorrhages (SMICH). Stroke 48(3):581–586.

    Article  PubMed  Google Scholar 

  20. 20.

    Dogra S, Jain R, Cao M et al (2020) Hemorrhagic stroke and anticoagulation in COVID-19. J Stroke Cerebrovasc Dis 29(8):104984.

    Article  PubMed  PubMed Central  Google Scholar 

  21. 21.

    Melmed KR, Cao M, Dogra S et al (2020) Risk factors for intracerebral hemorrhage in patients with COVID-19. J Thromb Thrombolysis.

    Article  PubMed  PubMed Central  Google Scholar 

  22. 22.

    Flaherty ML, Kissela B, Woo D, Kleindorfer D, Alwell K, Sekar P, Moomaw CJ, Haverbusch M, Broderick JP (2007) The increasing incidence of anticoagulant-associated intracerebral hemorrhage. Neurology 68(2):116–121. (PMID: 17210891)

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Zhang L, Yan X, Fan Q, Liu H, Liu X, Liu Z et al (2020) D-dimer levels on admission to predict in-hospital mortality in patients with Covid-19. J Thromb Haemost.

    Article  PubMed  PubMed Central  Google Scholar 

  24. 24.

    Hernández-Fernández F, Valencia HS, Barbella-Aponte RA et al (2020) Cerebrovascular disease in patients with COVID-19: neuroimaging, histological and clinical description. Brain.

    Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Klok FA, Kruip MJHA, van der Meer NJM, Arbous MS, Gommers D, Kant KM, Kaptein FHJ, van Paassen J, Stals MAM, Huisman MV, Endeman H (2020) Confirmation of the high cumulative incidence of thrombotic complications in critically ill ICU patients with COVID-19: an updated analysis. Thromb Res 191:148–150.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Aggarwal G, Lippi G, Michael Henry B (2020) Cerebrovascular disease is associated with an increased disease severity in patients with coronavirus disease 2019 (COVID-19): a pooled analysis of published literature. Int J Stroke 15:385–389

    Article  Google Scholar 

  27. 27.

    Connors JM, Levy JH (2020) Covid-19 and its implications for thrombosis and anticoagulation. Blood 135:2033

    CAS  Article  Google Scholar 

  28. 28.

    Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, Zhang L, Fan G, Xu J, Gu X, Cheng Z, Yu T, Xia J et al (2020) Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 395:497–506. (PMID: 31986264)

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  29. 29.

    Dong S, Liu P, Luo Y, Cui Y, Song L, Chen Y (2020) Pathophysiology of SARS-CoV-2 infection in patients with intracerebral hemorrhage. Aging 12(13):13791–13802.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Xia H, Lazartigues E (2008) Angiotensin-converting enzyme 2 in the brain: properties and future directions. J Neurochem 107(6):1482–1494

    CAS  Article  Google Scholar 

  31. 31.

    Hoffmann M, Kleine-Weber H, Schroeder S et al (2020) SARS-CoV-2 entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 181(271–80):e8

    Google Scholar 

  32. 32.

    Varga Z, Flammer AJ, Steiger P, Haberecker M, Andermatt R, Zinkernagel AS et al (2020) Endothelial cell infection and endotheliitis in COVID-19. Lancet 395(10234):1417–1418

    CAS  Article  Google Scholar 

  33. 33.

    Radmanesh A, Derman A, Lui YW et al (2020) COVID-19-associated diffuse leukoencephalopathy and microhemorrhages. Radiology 297(1):E223–E227.

    Article  PubMed  PubMed Central  Google Scholar 

  34. 34.

    Chen G, Wu D, Guo W, Cao Y, Huang D, Wang H et al (2020) Clinical and immunological features of severe and moderate coronavirus disease 2019. J Clin Invest 130:2620–2629.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Wilkinson DA, Pandey AS, Thompson BG, Keep RF, Hua Y, Xi G (2018) Injury mechanisms in acute intracerebral hemorrhage. Neuropharmacology 134:240–248

    CAS  Article  Google Scholar 

  36. 36.

    Zhang H, Penninger JM, Li Y, Zhong N, Slutsky AS (2020) Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV-2 receptor: molecular mechanisms and potential therapeutic target. Intensive Care Med 46(4):586–590

    CAS  Article  Google Scholar 

  37. 37.

    Nawabi J, Morotti A, Wildgruber M et al (2020) Clinical and imaging characteristics in patients with SARS-CoV-2 infection and acute intracranial hemorrhage. J Clin Med 9(8):2543.

    CAS  Article  PubMed Central  Google Scholar 

  38. 38.

    Rothstein A, Oldridge O, Schwennesen H, Do D, Cucchiara BL (2020) Acute cerebrovascular events in hospitalized COVID-19 patients. Stroke 51(9):e219–e222. (PMID: 32684145; PMCID: PMC7386677)

    CAS  Article  PubMed  Google Scholar 

  39. 39.

    Altschul DJ, Unda SR, de La Garza RR, Zampolin R, Benton J, Holland R, Fortunel A, Haranhalli N (2020) Hemorrhagic presentations of COVID-19: risk factors for mortality. Clin Neurol Neurosurg 198:106112. (PMID: 32738585; PMCID: PMC7382923)

    Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Usman AA, Han J, Acker A et al (2020) A Case Series of Devastating intracranial hemorrhage during venovenous extracorporeal membrane oxygenation for COVID-19. J Cardiothorac Vasc Anesth 34(11):3006–3012.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  41. 41.

    Fletcher-Sandersjöö A, Thelin EP, Bartek J Jr, Broman M, Sallisalmi M, Elmi-Terander A, Bellander BM (2018) Incidence, outcome, and predictors of intracranial hemorrhage in adult patients on extracorporeal membrane oxygenation: a systematic and narrative review. Front Neurol 6(9):548. (PMID: 30034364; PMCID: PMC6043665)

    Article  Google Scholar 

  42. 42.

    Tan YK, Goh C, Leow AST et al (2020) COVID-19 and ischemic stroke: a systematic review and meta-summary of the literature. J Thromb Thrombolysis 50(3):587–595.

    CAS  Article  PubMed  Google Scholar 

  43. 43.

    Jain R, Young M, Dogra S et al (2020) COVID-19 related neuroimaging findings: a signal of thromboembolic complications and a strong prognostic marker of poor patient outcome. J Neurol Sci 414:116923.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  44. 44.

    John S, Hussain SI, Piechowski-Jozwiak B et al (2020) Clinical characteristics and admission patterns of stroke patients during the COVID 19 pandemic: a single center retrospective, observational study from the Abu Dhabi, United Arab Emirates. Clin Neurol Neurosurg 199:106227.

    Article  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Katz JM, Libman RB, Wang JJ, Sanelli P, Filippi CG, Gribko M, Pacia SV, Kuzniecky RI, Najjar S, Azhar S (2020) Cerebrovascular complications of COVID-19. Stroke 51(9):e227–e231. (PMID: 32757751; PMCID: PMC7467046)

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  46. 46.

    Shahjouei S, Naderi S, Li J, Khan A, Chaudhary D et al (2020) Risk of stroke in hospitalized SARS-CoV-2 infected patients: a multinational study. EBioMedicine. 59:102939. (PMID: 32818804; PMCID: PMC7429203)

    Article  PubMed  PubMed Central  Google Scholar 

  47. 47.

    Siegler JE, Cardona P, Arenillas JF et al (2020) Cerebrovascular events and outcomes in hospitalized patients with COVID-19: the SVIN COVID-19 multinational registry. Int J Stroke.

    Article  PubMed  PubMed Central  Google Scholar 

  48. 48.

    Yoon BC, Buch K, Lang M, Applewhite BP, Li MD, Mehan WA Jr, Leslie-Mazwi TM, Rincon SP (2020) Clinical and neuroimaging correlation in patients with COVID-19. Am J Neuroradiol 41(10):1791–1796. (PMID: 32912875; PMCID: PMC7661080)

    CAS  Article  PubMed  Google Scholar 

  49. 49.

    Pavlov V, Beylerli O, Gareev I, Torres Solis LF, Solís Herrera A, Aliev G (2020) COVID-19-related intracerebral hemorrhage. Front Aging Neurosci 12:600172.

    Article  PubMed  PubMed Central  Google Scholar 

  50. 50.

    Perry R, Banaras A, Werring DJ et al (2020) What has caused the fall in stroke admissions during the COVID-19 pandemic? J Neurol 267:3457–3458.

    CAS  Article  PubMed  Google Scholar 

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Beyrouti, R., Best, J.G., Chandratheva, A. et al. Characteristics of intracerebral haemorrhage associated with COVID-19: a systematic review and pooled analysis of individual patient and aggregate data. J Neurol (2021).

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  • COVID-19
  • Intracerebral haemorrhage
  • Stroke
  • Anticoagulation