Intracranial hemorrhage complicating anticoagulant prophylactic therapy in three hospitalized COVID-19 patients.

SARS-CoV2 has led to a global pandemic affecting almost 3 million people in almost over 3 months. Various clinical presentations have been reported so far and no definite therapy is established. Anticoagulation is recommended by several experts to address the potential prothrombotic complications from COVID-19, but its safety and regimen need further clinical trials and safety and efficacy profile. Here, we present three cases of intracranial hemorrhage in three critically ill patients with COVID-19 and discuss their course in relation to various regimens of anticoagulation used.

Introduction

SARS-CoV2, like other respiratory viruses, may invade the central nervous system (Desforges et al. 2020). As data on COVID-19 is emerging, various neurological manifestations have been observed (Mao et al. 2020). To our knowledge, one case of intraparenchymal hemorrhage has been reported in a patient with COVID-19 in the USA (Vu et al. 2020). Given the reports of thrombotic complications in this disease, anticoagulation protocols have been implemented by many institutions. Here, we present three cases of fatal intracranial hemorrhage in patients with severe SARS-CoV2 infection on therapeutic anticoagulation.

Case presentations

Patient 1

A 59-year-old man with well-controlled hypertension presented with acute hypoxic respiratory failure from COVID-19 pneumonia and required intubation. The patient was found to have an elevated d-dimer to > 3 and received therapeutic anticoagulation with unfractionated heparin (UFH). His aPTT remained therapeutic (45–60 s) and systolic blood pressure ranged from 120 to 130 mmHg without medications. On day 18, he was found to have absent brainstem reflexes. A computed tomography (CT) scan of the head revealed acute subarachnoid and intraparenchymal hemorrhages within the posterior fossa. He had severe cerebral edema and transtentorial, uncal, and tonsillar herniation (Fig. 1). aPTT on the day of CT scan was 57 s. A subsequent apnea test revealed no respiratory effort after 12 min which is consistent with brain death.

Fig. 1

Acute hypoxic brain injury with severe global cerebral swelling resulting in transtentorial, uncal, and tonsillar herniation. Acute subarachnoid and intraparenchymal hemorrhage within the posterior fossa involving the brainstem

Patient 2

A 61-year-old woman with type 2 diabetes mellitus presented with COVID-19 pneumonia and was intubated. She was found to have acute respiratory distress syndrome (ARDS). Initially, she received prophylactic anticoagulation with apixaban, but was then switched to therapeutic UFH on day 10, as her d-dimer levels were up-trending. Physical examination on day 10 of hospitalization revealed fixed dilated pupils with no brainstem reflexes. CT head showed diffuse brain anoxia with scattered subarachnoid hemorrhages, a subdural hematoma with left to right midline shift and tonsillar herniation (Fig. 2). aPTT at the time of detection of intracranial hemorrhage was 63 s. She was subsequently declared brain-dead.

Fig. 2

Diffuse bilateral loss of gray-white matter differentiation consistent with brain anoxia. Diffuse bilateral effacement of the cerebral sulci and cerebellar folia secondary to cerebral edema and scattered bilateral acute subarachnoid hemorrhage

Patient 3

A 59-year-old woman with hypertension was admitted with COVID-19 pneumonia and intubated for hypoxic respiratory failure. Prophylactic anticoagulation with apixaban was started and then switched on day 6 to therapeutic enoxaparin due to rising d-dimer levels. She remained comatose despite being off intravenous sedation for 1 week. CT scan of the head on day 15 revealed a large intraparenchymal hemorrhage and cerebral edema, with transtentorial-herniation causing brainstem compression (Fig. 3). Neurological exam and apnea test were consistent with brain death. Throughout the hospital stay, systolic blood pressure ranged between 125 and 140 mmHg.

Fig. 3

A large left-sided intraparenchymal hemorrhage with intraventricular extension, superficial subarachnoid blood, and left-sided cerebral swelling

Discussion

Here, we report three patients with severe COVID-19 who developed intracranial hemorrhage visualized on CT imaging while on therapeutic anticoagulation. They all had normal baseline neurological status on admission and had no known predisposition to life-threatening bleeding. During their admission, these patients all received steroids, hydroxychloroquine, and anticoagulation per our institutional guidelines at the time of the COVID-19 pandemic.

All patients were found to have cerebral anoxia with variable degrees of intracranial hemorrhage. While patient 3 had the largest area of intracranial hemorrhage, patient 2 suffered from subdural and subarachnoid hemorrhage with midline shift. Cerebral edema and tentorial and transtentorial herniation were common findings in these three patients.

Previous reports during the MERS-CoV epidemic documented similar cases of intracranial hemorrhage (Al-Hameed 2017; Algahtani et al. 2016). In our patients with SARS-CoV2, it is difficult to ascertain whether these neurologic complications were the result of their severe COVID-19 or due to the therapeutic anticoagulation they received. Emerging evidence suggests that coagulopathy is associated with COVID-19 and elevated d-dimer and fibrinogen levels are indicative of a prothrombotic state. The current hematology expert opinion approach toward thromboprophylaxis in hospitalized COVID-19 patients is to avoid therapeutic dosing of anticoagulant therapy unless there is a documented thrombotic event (Thachil et al. 2020). There is some data suggesting a mortality benefit with the use of anticoagulation in COVID-19 patients (Tang et al. 2020). A prospective multicenter study reported at least 40% thrombotic complications in patients with COVID-19 (Helms et al. 2020). Further, a recent study reporting neurological manifestations in COVID-19 patients observed cerebrovascular complications including ischemic and hemorrhagic strokes (Mao et al. 2020). At this time, it is unclear which patients will have greater benefit than harm from therapeutic anticoagulation.

All of our patients had intracranial bleeding and it is uncertain if this is a complication from COVID-19 or anticoagulation. Clinicians should remain cautious while starting therapeutic anticoagulation in patients with severe COVID-19 and impaired consciousness. Routine neurological examination and maintaining a low threshold for brain imaging in critically ill patients are imperative to detect life-threatening intracranial hemorrhagic complications in these patients. More studies are needed to fully elucidate the neurologic complications of COVID-19 and the benefits and risks of therapeutic anticoagulation in patients with COVID-19.