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Subdural Empyema


Subdural Empyema

Article Author:
Ricardo Fernández-de Thomas
Article Editor:
Orlando De Jesus
Updated:
11/14/2020 10:50:12 AM
For CME on this topic:
Subdural Empyema CME
PubMed Link:
Subdural Empyema

Introduction

Intracranial subdural empyema is a loculated collection of pus in the subdural space between the dura mater and the arachnoid.[1] Prior to 1943, it was referred to as subdural abscess, cortical abscess, purulent pachymeningitis, phlegmonic meningitis, and subdural suppuration.[2] Focal intracranial infections can be classified as brain abscess, epidural abscess, and subdural empyema. If bacterial infections were to be taken into consideration, the spectrum of infections of the central nervous system would also include more generalized or diffuse infections like pyogenic meningitis or ventriculitis.[3] This review will focus on intracranial subdural empyema. Because the subdural space is continuous and has no anatomic barrier, subdural empyemas can spread over the convexity of the brain in between both cerebral hemispheres and, in some cases, to the opposite hemisphere or even the posterior fossa.[4] It is considered a dangerous but treatable entity. Due to the skull being a confined cavity, intracranial subdural empyema can lead to severe symptoms or even death by direct compression and injury of the brain. Prompt diagnosis and adequate treatment can, in most cases, prevent these types of complications resulting in better outcomes. History and physical examination should prompt the clinician to the suspected diagnosis. Imaging techniques will confirm the diagnosis.

Etiology

The etiology of subdural empyema can be multifactorial; however, some of the predisposing factors associated with the development of subdural empyema include prior cranial surgery, head trauma with open skull fractures, or penetrating injury, infected hematoma or subdural effusion, and not properly treated ear and sinus infections. Of the reported literature, up to 40% to 80% of patients with subdural empyema have otorhinologic infections, especially of the paranasal sinuses.[2] Up to 20% of the subdural empyemas occur following head trauma or cranial surgical procedures.[5]

The most common microorganisms are anaerobes, aerobic Streptococci, Staphylococci, Haemophilus influenzae, Streptococcus pneumoniae, and other gram-negative bacilli.[3] However, in cases of subdural empyema secondary to paranasal sinusitis, the most common microorganisms reported have been anaerobic and microaerophilic streptococci (Streptococcus milleri and Streptococcus anginosus).[3][6] In those cases secondary to cranial trauma or surgical procedures, the most common organism is Staphylococcus aureus.[4] Coagulase-negative Staphylococci, anaerobes, Gram-negative organisms can also be found in those cases of trauma or surgical procedures.[1] Many infections are polymicrobial.[6][7][8] Subdural empyema is usually a complication of purulent meningitis in infants, whereas, in older children, it is commonly secondary to direct extension from contiguous foci.[3][6][9][10] The mechanism of the development in infants is through infection of sterile, reactive subdural effusions secondary to meningitis.[10] In adults, subdural empyema secondary to bacterial meningitis is rare.[9]

Epidemiology

Intracranial subdural empyema usually affects children and young adults.[1] Males are more commonly affected, with a male to female ratio of 3:1.[1][6] Subdural empyemas can also develop in the spinal canal but are rarely reported in the literature.[4][1][11] Intracranial subdural empyemas are much less common than brain abscess.[2]

Pathophysiology

Subdural empyema most often occurs due to the direct extension of local infection. The infection can spread to the intracranial compartment due to the valveless diploic veins of Breschet. As a result, blood may flow in either direction, causing the spread of bacterial infection intracranially.[12][2][9] They can also occur after cranial surgical procedures secondary to the inoculation of microorganisms into the subdural space, further developing into a subdural empyema.

History and Physical

Subdural empyema usually presents with signs and symptoms of infection; however, it can also be asymptomatic.[13] Some of the symptoms that can be seen include fever, headache, nausea, vomiting, focal neurological deficits, seizures, and mental status changes. Fever and headache are usually present, and seizures occur in about half of the patients.[6][2][10][9] Signs of meningeal irritation can also be seen.

Physical examination can show unstable vital signs, including fever, tachycardia, and respiratory compromise, which could all correlate with sepsis. Presentation in most cases is gradually progressive, and if untreated, symptoms may worsen. Some patients can become critically ill quickly, becoming drowsy, stuporous, and eventually comatose or even die.[3] This can be a result of increased intracranial pressure caused by the subdural empyema, which, in turn, can result in Cushing’s triad of hypertension, bradycardia, and bradypnea.

Other physical examination findings related to the neurological exam include meningismus, contralateral hemiplegia, and cranial nerve palsies, anisocoria, and papilledema.[14] A subdural empyema must be considered in a patient diagnosed with sinusitis or otitis who develops a fever, headache, and cranial pain. It should also be considered in a patient who underwent drainage of a subdural hematoma who presents with a fever, seizure, and new neurological deficits. Significant neurological deficits may occur and are caused by localized brain edema and infarction associated with cortical thrombophlebitis.[6][8]

Evaluation

History and physical examination should help tailor case evaluation and diagnosis; however, cranial imaging should be performed in all patients with suspected subdural empyema.[3][14] Subdural empyema appears as a hypodense area over the cerebral hemisphere or along the falx on a computed tomography scan. The collection margins are better delineated with the infusion of intravenous contrast dye.[3] Depending on the extent and size of the subdural empyema, associated mass effect with the shifting of midline structures can also be seen. The diagnostic imaging study of choice for intracranial subdural empyema is a magnetic resonance imaging (MRI) with intravenous gadolinium enhancement. MRI shows better small collections and those that are localized interhemispheric. Imaging findings are usually described as a crescent-shaped or elliptical area of hypointensity on T1-weighted images underneath the skull or adjacent to the falx cerebri.[6] MRI diffusion-weighted imaging sequences have proved to be more sensitive than routine MRI sequences and, therefore, should be performed.[15][16][17]

Laboratory workup can add evidence to the suspected diagnosis. Leukocytosis can be seen, indicating an active process of infection. Immunocompromised or immunosuppressed patients will not always present with elevated white blood cells on complete blood count. Depending on the patient’s immune response, bacterial infections can cause a leftward shift with associated neutrophilia. Further laboratory workup, including serum inflammation markers such as erythrocyte sedimentation rate and C-reactive protein, could add evidence as these are considered acute phase reactants. In cases of infections, some clinicians may recommend blood culture samples to try direct antibiotic therapy early in the disease course; however, in the case of subdural empyema, these rarely identify an organism due to the capsulated nature of the infection.[17][18] 

Spinal puncture is not indicated for the diagnosis and can be dangerous in those patients with increased intracranial pressure and empyemas, causing mass effect.[4][2][6][10]

Treatment / Management

The treatment of cranial subdural empyema is multimodal, including both medical and surgical treatment. Infectious disease service and neurosurgery service are indispensable. The use of antibiotic therapy alone is rare; however, it can be used if the patient is essentially doing well, has no major neurological deficit, the collection is small, and an early response is documented.[8] However, such patients need close monitoring with serial clinical exams and neuroimaging studies. Longer courses of antimicrobial therapy may be required. 

A prompt and accurate diagnosis will result in a more favorable clinical outcome, and this directly depends on the level of suspicion the clinician has as a result of the patient’s history, physical examination, laboratory workup, and imaging findings. Treatment options, including multiple burr holes or a craniotomy for drainage and debridement, have been previously described in the literature. A craniotomy usually offers better results and fewer recurrences.[7] Infants are treated with a burr hole, multiple subdural taps through the anterior fontanelle, or a craniotomy.[9][10] Preoperative imaging will help in accurately localizing the site of pus collection, which will direct where the surgery is to be performed.[3] Once the surgical area is chosen, multiple burr holes can be performed over the collection, and after the dura mater is incised, the pus is drained, and the cavity irrigated with saline solution. When a craniotomy is chosen, a large skin incision followed by a wide craniotomy is performed. A wide craniotomy is usually recommended as it allows for adequate exposure, exploration, and possibly more complete evacuation of the subdural purulent collection.[3] The dura is opened carefully, and the subdural empyema will be encountered as a collection of frank pus. A sample should be sent to the laboratory for both aerobic and anaerobic culture.[3] The patient is started on antibiotics based on the results of the Gram staining and the pathogenesis of the infection until cultures are reported. If Gram staining is negative or unavailable, the patient should be started in broad-spectrum antibiotics. Cultured microorganisms will help adjust the desired antibiotic therapy. Unfortunately, operative culture results can be negative without any reported microorganisms in up to 7% to 53% of patients.[6] This can be accounted for due to the frequent use of preculture/preoperative antimicrobial therapy.[6]

Intravenous antibiotic therapy, coordinated by the infectious disease team, for a period of 3 to 6 weeks, is required. Longer periods of therapy are required for those patients with osteomyelitis. In infants, subdural empyema is often secondary to meningitis, and antibiotic therapy is required for 6 to 8 weeks.[19]

Further monitoring and follow up can be done with laboratory workup. Imaging can be done with a repeat head computed tomography scan or brain MRI. Antiepileptic drugs should be given in view of the high incidence of preoperative and postoperative seizures.[7]

Differential Diagnosis

  • Epidural abscess
  • Brain abscess
  • Brain tumor
  • Leptomeningeal disease
  • Subdural hematoma
  • Meningitis
  • Cerebritis
  • Subdural hygroma

Prognosis

The outcome is dependent on the preoperative level of consciousness, the timing of intervention, and the aggressiveness of the treatment. Awake and alert patients have a good prognosis in the majority of the cases. Stuporous and comatose patients have high mortality. Older age patients have the worst prognosis.[8] Up to half of the patients have permanent residual neurological deficits.[7] Late seizures may occur despite the use of antiepileptic medications.[1][7] An unfavorable prognosis can be seen in cases of brain herniation.

Complications

Complications of subdural empyema include seizures, cerebritis, cerebral abscess, cerebral edema, cortical venous thrombosis with cerebral venous infarction, cavernous sinus thrombosis, sepsis, septic shock, electrolyte imbalances, hydrocephalus, cranial osteomyelitis in adjacent cranial bones, osteomyelitis of the craniotomy bone flap, and residual neurological deficits.[3][14][6]

Deterrence and Patient Education

Patients who are being treated for sinusitis or otitis should be warned that if they develop headaches, nausea, seizure, or disorientation, they should immediately return to their primary physician for reevaluation. Those patients who are using antiepileptic medication should not discontinue them without medical recommendations as they may experience the return of the seizures.

Pearls and Other Issues

  1. Subdural empyema is a medical and surgical emergency; time is of utmost importance in this type of pathology, and early recognition and management are required.
  2. During the evaluation and treatment process, attempts to identify the causative agent and tailor further therapy accordingly should be prioritized. 
  3. The choice of antibiotics should be guided by the patient’s age, likely pathogen, predisposing conditions, and local resistance patterns.

Enhancing Healthcare Team Outcomes

The management of intracranial subdural empyema is complex. Most cases need emergent management and treatment to avoid complications and unfavorable prognosis. It requires an interprofessional team that includes a neurosurgeon, infectious disease specialist, critical care intensivist, neurologist, and physiatrist. Pharmacists review antibiotic and antiseizure medications to check for interactions and contraindications. Emergency, critical care, and neuroscience nurses provide care and update the interprofessional team on changes in patient status. A good level of suspicion is needed to avoid delaying treatment. Once the patient resolves the infection, many require long term antiepileptic medications and physical therapy for further recovery. Inpatient or outpatient rehabilitation may be needed for physical, occupational, or speech therapy.


References

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