Intrathecal haematoma after an epidural blood patch

  1. Yoshimi Ito and
  2. Amit Bhagwat
  1. Anaesthesia and Critical Care, University Hospitals of North Midlands NHS Trust, Stoke-on-Trent, UK
  1. Correspondence to Dr Yoshimi Ito; yoshimi.ito@doctors.org.uk

Publication history

Accepted:06 Sep 2022
First published:29 Sep 2022
Online issue publication:29 Sep 2022

Case reports

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Summary

This case demonstrates a rare but potentially serious complication of an epidural blood patch (EBP). Intrathecal haematoma is a rare complication after an EBP and anaesthetists should be able to promptly identify and manage these patients to prevent long-term damage. This case also highlights the importance of informed consent according to the principles of the Montgomery judgement/principle of consent.

Background

Postdural puncture headache (PDPH) is one of the potential side effects of a neuraxial block. If all conservative management fails, the patient may require an epidural blood patch (EBP). EBP is the gold standard for treating severe PDPH and was first performed in 1960.1 Side effects are often mild and temporary; however, some potentially severe complications include radiculopathy, neuraxial haematoma and infection.1

Intrathecal haematoma after an EBP is extremely rare but can have severe consequences for the patient. This case demonstrates one such rare complication of intrathecal haematoma after an EBP.

Case presentation

A woman in her 20s presented to our delivery suite at 39 weeks of gestation in early labour. She was a primipara and her medical history was unremarkable. At 4 cm of dilatation, she requested an epidural for labour analgesia. Unfortunately, there was an accidental dural tap together with a feeling of a ‘pop’ in her back and an immediate sensation of fullness in the ears. The second attempt at the epidural by a senior anaesthetist was uneventful and worked well. The patient, subsequently, had a normal vaginal delivery. On the next day, her sensation of aural fullness had subsided and there were no other symptoms of PDPH. She was later discharged home on paracetamol and ibuprofen and advised to come back if any symptoms of PDPH appeared. Six days post-delivery, the patient was readmitted to the hospital because of severe headache and tinnitus. The headache was mainly frontal and was described as 8 out of 10 while sitting. The patient was unable to sit up and had to lie down after a few minutes. She was diagnosed as having severe PDPH. As the patient’s symptoms were quite severe, she was offered an EBP, together with analgesics like paracetamol and ibuprofen, according to our protocol. The patient agreed to an EBP and consented accordingly. EBP was done in L4–5 interspace in the left lateral position. A total of 20 mL of autologous blood was given after the loss of resistance to saline. The EBP was uneventful with the patient experiencing immediate relief of symptoms. Her pain, immediately after the EBP, was 1 out of 10. The patient was nursed in the supine position for 4 hours and, after confirming that symptoms had subsided (0 out of 10 on the pain score), she was discharged home on regular paracetamol and ibuprofen. She was followed for the next 2 days by daily telephone calls.

Three days after the EBP, the patient was readmitted due to bilateral shooting pain down to her knees and severe generalised back pain. The pain was described as ‘electric shock’, coming in a burst without any apparent warnings even when the patient was completely still. There was no hyperalgesia or any bruises over the back. Although her symptoms started a day after the EBP, initially, the pain was described as something crawling over the back of her thighs and was mild in nature. The sensation gradually increased in intensity over the next 2 days, developing into bilateral shooting pain on the third day requiring readmission to the hospital. The pain was described as 7 out of 10 with complete remission in between. There were no aggravating or alleviating factors.

Investigations

The patient was reviewed by a senior anaesthetist, and an urgent lumbosacral MRI was performed. A simultaneous neurosurgical consultation was also sought. The MRI showed a subacute intrathecal haematoma extending from L3/4 down to S1 with clumping of the intrathecal nerve roots without any epidural haematoma (figure 1: MRI scan showing intrathecal haematoma). A clumping of the nerve is a situation where adhesion between the nerve roots develops and adheres to the arachnoid lining. This can be a characteristic of arachnoiditis.

Figure 1

MRI scan showing intrathecal haematoma.

Treatment

An examination by a neurosurgical consultant showed that the patient did not have a sensorimotor deficit or perianal anaesthesia. The patient had full control of bladder and bowel movement. There were no signs of sepsis. She was later discharged on paracetamol and ibuprofen and an appointment was made for her follow-up with neurosurgeons on an outpatient basis. The diagnosis of intrathecal haematoma was explained to the patient and she was reassured that her symptoms are transient and should get better in due time and do not require any active treatment except for the analgesic to ease the pain.

Outcome and follow-up

She was discharged home with subsequent follow-up to a neurosurgical clinic. She made a full neurological recovery in 6 weeks.

Discussion

The frequency of accidental dural puncture (ADP) ranges from 0.19% to 3.6%.2 The injury to the dura can be due to an obvious puncture of the dura from an epidural needle, or it can be due to an unrecognised dural puncture, either by an epidural needle or from a catheter. If there was a recognised ADP during epidural insertion, then the incidence of PDPH is as high as 16%–86% with a meta-analysis done by Choi et al suggesting an incidence of 50%–55%.3 4

Conservative treatment will not provide complete relief in most patients who have had a large gauge ADP. About two-thirds of them would require an EBP making it not an uncommon procedure in labour wards.5 6 EBP itself has been associated with neurological complications, which, fortunately, are rare. These include paraesthesia, neck ache, facial nerve palsy and lumbovertebral syndrome.7–9 Besides these, seizures, severe headache and transient bradycardia have been reported during and immediately after the procedure.3

Our patient in this case report presented with an intrathecal haematoma after an uneventful blood patch. Intrathecal haematoma is an accumulation of blood around the dura and the vertebrae. Although most patients are asymptomatic, in rare cases, it can cause spinal cord compression, which leads to neurological complications. In such cases, patients can present with neuropathic pain, sensory deficits, bowel or bladder dysfunction, motor weakness, or in severe cases, complete paralysis of the affected limb.10 Kearsley and McCaul reported two cases of subdural haematomas after an uneventful EBP leading to backache and radicular symptoms, both resolved with conservative treatment.11 Intrathecal haematoma can cause meningitis symptoms, epileptic seizures, alterations in consciousness and can be misdiagnosed as cerebral haemorrhage.12 A case report by Seemiller et al describes a serious complication of an EBP causing convulsion, altered mental state, and respiratory distress requiring intubation and critical care stay.13 In their case, the blood had diffusely spread in the cerebrospinal fluid (CSF) with both MRI and CT scans of the brain demonstrating diffuse cortical sulci obscuration due to diluted blood products. Their case demonstrates that if a patient develops any changes in mental state, seizure or respiratory failure, it is vital to consider a diffuse spread of blood rather than just a localised haematoma.

Often patients will present with a severe, constant back pain, with or without a radicular component.10 In our case, there was a localised intrathecal haematoma causing clumping of nerves resulting in generalised back pain and radicular shooting pain down the legs. The patient did not have any sensory deficit, motor weakness or involvement of the bladder or the bowel.

Thorough history taking and clinical examination remain essential in diagnosis of neuropathic pain. If neuropathic pain is suspected, the assessment should include motor, sensory and autonomic system. In cases of sensory deficit, it may be helpful to use a body sensory map to have a visual demonstration of the areas of deficit.14 The Standard Evaluation of Pain (StEP) may be used as a tool to standardise the approach for differentiating the different types of pain. StEP involves 6 interview questions and 10 physical tests.14 In our case, the history and clinical examination directed us towards the suspicion of an intrathecal haematoma, which was subsequently confirmed on MRI.

The mechanism of intrathecal haematoma remains undetermined, but few hypotheses have been suggested. The first one is that the blood was deposited in the epidural space as intended, but, due to the resulting increase in the epidural pressure, some blood might have been pushed inadvertently into the intrathecal space through the existing dural puncture hole.15 The second hypothesis by Verduzco et al suggests that the blood was injected into either the subdural space with subsequent leak into the intrathecal compartment or that it was injected directly into the subarachnoid space.16 In the case of a subdural haematoma following an EBP, a subsequent lumbar spine MRI did not show evidence of blood or fluid in the epidural space. The authors hypothesised that the Tuohy needle was placed subdurally during the EBP and that increased pressure from the injection of blood caused dissection of the dura and arachnoid mater. This case by Verduzco et al also demonstrates that the safety and success of EBP depend on the accurate placement of Tuohy needle in the epidural space. While doing an EBP, it is essential to avoid the same interspace as the original dural puncture level. However, in some cases, it might be challenging to identify the dural space accurately, especially in a lateral position in which most of the EBP is performed. Another possible explanation is that the blood in the subarachnoid space may be due to arterial or venous puncture at the initial placement of the epidural catheter before the EBP.15

Narouze, in his editorial, described EBP as an ‘iatrogenic epidural haematoma’. Injection of blood into the epidural space causes a mass effect, reduction in epidural space compliance and results in cephalad CSF shift. This has been demonstrated by MRI, where the haematoma caused thecal sac and nerve root compression.17

In our case, intrathecal haematoma after the EBP resulted in nerve compression leading to shooting pain down the legs. It highlights the importance of urgent MRI in all patients who present with severe back pain or lower leg radicular pain after an EBP. A mass effect demonstrated on MRI, together with radicular symptoms and bladder and bowel problems, might require an urgent laminectomy. If the patient presents with a seizure or altered cognition, we should consider the potential diffuse spread of the blood in the CSF, in which case supportive treatment in critical care may be required.14 A multidisciplinary approach involving neurology and neurosurgery helps to determine the most appropriate treatment options for such patients.

Our case also illustrates that EBP itself is associated with its own complications profile and, as an anaesthetist, it is vital to include these in consent. This is especially true after the ‘Montgomery vs Lanerkshire Health Board’ judgement, where all the material risks need to be discussed with the patient.18–20

Given the possible complications related to EBP, it is also important to consider alternate options to prevent or treat the PDPH. One option could be inserting the intrathecal catheter during the inadvertent dural puncture, which has some evidence of decreasing the need of EBP.16 21 Other options could be a sphenopalatine block or a suboccipital muscle injection. A bilateral transnasal sphenopalatine block has been shown to be effective in management of moderate PDPH.22 Furthermore, if an EBP is essential in the management of the PDPH, it is important to take steps to minimise the risk of developing an intrathecal haematoma. We can ensure that the EBP is performed by senior anaesthetists, and also use appropriate volume and pressure when injecting the autologous blood.16

In addition to the above strategies, it is also important that all patients treated for PDPH should be regularly followed up for worsening of existing or new symptoms. Careful follow-up will allow prompt diagnosis and treatment leading to a better patient outcome.

Learning points

  • An epidural blood patch can have significant complications: severe pain, sensory deficit, bladder or bowel dysfunction, motor deficit, and in very severe cases, paralysis.

  • If suspecting an intrathecal haematoma, urgent clinical steps should be taken:

  • Thorough history taking and examination. It is essential to establish the nature of pain including the site, radiation, precipitating and alleviating factors, and associated symptoms. Furthermore, questions need to be asked about sensory deficit, motor deficit, and any involvement of the bladder or bowel. This should be followed by a neurological examination including motor, sensory and checking for any bladder/bowel involvement.

  • Urgent MRI should be organised.

  • An urgent neurosurgical review is essential to prevent long-term complications. Depending on the patient’s symptoms and MRI scan findings, the patient may require an urgent laminectomy.

  • It is vital to arrange a follow-up with the neurosurgical team after discharge.

  • Importance of informed consent. Although this is a very rare complication of an epidural blood patch, the patient needs to be informed of the material risk.

Ethics statements

Patient consent for publication

Footnotes

  • Contributors This has been written by both YI and AB with both parties contributing equally to the manuscript. The consent has been taken by AB.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Case reports provide a valuable learning resource for the scientific community and can indicate areas of interest for future research. They should not be used in isolation to guide treatment choices or public health policy.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

References

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