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Intraparenchymal intracranial pressure monitoring in patients with acute liver failure

Monitoreo intraparenquimatoso de presión intracraneana en pacientes con falla hepática aguda

Abstracts

BACKGROUND: Elevated intracranial pressure (ICP) is a common cause of death in acute liver failure (ALF) and is determinant for decision-making regarding the timing of liver transplantation. The recommended type ICP monitoring device is controversial in ALF patients. Epidural devices had less risk of hemorrhagic complications, but they are less reliable than intraparenchymal ones. METHOD: Twenty-three patients with ALF were treated, and 19 of them received a liver transplant. Seventeen patients had ICP monitoring because of grade III-IV encephalopathy. All patients received fresh plasma (2-3 units) before and during placing the intraparenchymal device. RESULTS: Eleven cases (64.7%) had elevated ICP, and 6 patients (35.2%) had normal values. One patient (5.9%) had an asymptomatic small intraparenchymal haemorrhage <1cm³ in CTscan, which did not prevent the liver transplantation. CONCLUSION: In our experience, intraparenchymal ICP monitoring in patients with ALF seems to be an accurate method with a low risk of complications.

fulminant hepatic failure; hemorrhagic complications; intracranial pressure monitoring


ANTECEDENTES: La presión intracraneana elevada (PIC) es una causa frecuente de muerte en la falla hepática aguda (FHA) y es determinante para la toma de decisiones respecto del momento del transplante hepático. El tipo de dispositivo para el monitoreo de OIC es controversial em los pacientes em FHA. Los dispositivos epidurales tienen menos riesgo de complicaciones hemorrágicas, pero son menos confiables que los intraparenquimatosos. MÉTODO: Veintitrés pacientes con FHA fueron tratados, y 19 de ellos recibieron un transplante hepático. diecisiete pacientes tuvieron monitoreo de PIC debido a encefalopatía grado III-IV. Todos los pacientes recibieron plasma fresco (2-3 unidades) antes y durante la colocación de la fibra intraparenquimatosa. RESULTADOS: Once casos (64.7%) tuvieron PIC elevada, y 6 pacientes (35.2%) tuvieron valores normales. Un paciente (5.9%) tuvo una pequeña hemorragia intraparenquimatosa asintomática <1cm³ en TAC, la cual no impidió el transplante hepático. CONCLUSIÓN: En nuestra experiencia, el monitoreo intraparenquimatoso de presión intracraneana en pacientes con FHA parece ser un método preciso y con bajo riesgo de complicaciones.

falla hepática fulminante; complicaciones hemorrrágicas; monitoreo de presión intracraneana


ARTICLES

Intraparenchymal intracranial pressure monitoring in patients with acute liver failure

Monitoreo intraparenquimatoso de presión intracraneana en pacientes con falla hepática aguda

Alejandra T. Rabadán; Natalia Spaho; Diego Hernández; Adrián Gadano; Eduardo de Santibañes

Servicio de Neurocirugía y Unidad de Transplante Hepático, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina

ABSTRACT

BACKGROUND: Elevated intracranial pressure (ICP) is a common cause of death in acute liver failure (ALF) and is determinant for decision-making regarding the timing of liver transplantation. The recommended type ICP monitoring device is controversial in ALF patients. Epidural devices had less risk of hemorrhagic complications, but they are less reliable than intraparenchymal ones.

METHOD: Twenty-three patients with ALF were treated, and 19 of them received a liver transplant. Seventeen patients had ICP monitoring because of grade III-IV encephalopathy. All patients received fresh plasma (2-3 units) before and during placing the intraparenchymal device.

RESULTS: Eleven cases (64.7%) had elevated ICP, and 6 patients (35.2%) had normal values. One patient (5.9%) had an asymptomatic small intraparenchymal haemorrhage <1cm3 in CTscan, which did not prevent the liver transplantation.

CONCLUSION: In our experience, intraparenchymal ICP monitoring in patients with ALF seems to be an accurate method with a low risk of complications.

Key words: fulminant hepatic failure, hemorrhagic complications, intracranial pressure monitoring.

RESUMEN

ANTECEDENTES: La presión intracraneana elevada (PIC) es una causa frecuente de muerte en la falla hepática aguda (FHA) y es determinante para la toma de decisiones respecto del momento del transplante hepático. El tipo de dispositivo para el monitoreo de OIC es controversial em los pacientes em FHA. Los dispositivos epidurales tienen menos riesgo de complicaciones hemorrágicas, pero son menos confiables que los intraparenquimatosos.

MÉTODO: Veintitrés pacientes con FHA fueron tratados, y 19 de ellos recibieron un transplante hepático. diecisiete pacientes tuvieron monitoreo de PIC debido a encefalopatía grado III-IV. Todos los pacientes recibieron plasma fresco (2-3 unidades) antes y durante la colocación de la fibra intraparenquimatosa.

RESULTADOS: Once casos (64.7%) tuvieron PIC elevada, y 6 pacientes (35.2%) tuvieron valores normales. Un paciente (5.9%) tuvo una pequeña hemorragia intraparenquimatosa asintomática <1cm3 en TAC, la cual no impidió el transplante hepático.

CONCLUSIÓN: En nuestra experiencia, el monitoreo intraparenquimatoso de presión intracraneana en pacientes con FHA parece ser un método preciso y con bajo riesgo de complicaciones.

Palabras clave: falla hepática fulminante; complicaciones hemorrrágicas; monitoreo de presión intracraneana.

Being intracranial hypertension the most common, immediate cause of death in acute liver failure, intracranial pressure (ICP) monitoring has become a procedure of paramount importance1,2.

In acute liver failure (ALF), whether fulminant or subfulminant, epidural transducers -although less accurate- are currently recommended for ICP monitoring based on their lower rate of hemorrhagic complications as compared with subdural, intraparenchymal, or intraventricular transducers3,4.

On the other hand, since the precise knowledge of ICP is determinant for the management of patients with ALF and for decision-making regarding the opportunity of a liver transplantation, we used a highly reliable method for ICP monitoring, such as the intraparenchymal transducer.

The objective of this presentation was to analyse the hemorrhagic complications of ICP monitoring with this type of device in patients with ALF who were candidates for liver transplantation.

METHOD

We present a consecutive series of 23 adult patients with ALF and encephalopathy. Nineteen of them received a liver transplant (period 1990-2004). Of this series, 17 patients had ICP monitoring because of grade III-IV encephalopathy grade. Thirteen patients had fulminant liver failure, while 4 had subfulminant liver failure. Causes of liver failure were: hepatitis A virus, 3 patients; hepatitis B virus, 3 patients; autoimmune hepatitis, 11 patients; Budd-Chiari syndrome, 1 patient; cryptogenic, 4; and toxic hepatitis, 1 patient (Table 1).

ICP monitoring was carried out with an intraparenchymal-monitoring device, placed by neurosurgeons. Fresh plasma (median, 2 units) was administered before and during the procedure. A twist drill hole was performed, and bone wax, bipolar coagulation of duramater, and generous irrigation were used to provide hemostasis. ICP was considered high when >20 mmHg. Following the insertion of the intraparenchymal device, and due to the severe clinical condition of the patients, computed tomography scan (CT) was only performed if patients present neurological deterioration or new neurological deficit.

RESULTS

The median age for patients was 40 years (range, 20-60 years). There were 15 women and 8 men. ICP monitoring was carried out in 17 patients, while intracranial hypertension was registered in 11 cases (64.7%). In 6 patients (35.2%), ICP was within normal range. The median ICP for the 11 patients with intracranial hypertension was 38 mmHg (range, 21-100 mmHg.). The median time of ICP monitoring was 5 days, ranging from 1 to 8 days (Table 1).

Of this series, 4 patients were not transplanted (one of them with an autoimmune hepatitis who improved at 48 h), 2 patients died on waitlist, and 1 patient was not eligible due a persistent intracranial hypertension (100 mmHg). In the group of non-transplanted patients, 3 presented intracranial hypertension (Table 2).

All patients had severe coagulopathy. Median prothrombin time (PT) was 50 seconds (sec) (range, 21- >70 sec). PT normal range was considered between 13-17 sec.

As a complication associated with intraparenchymal transducer placement, a symptomatic intraparenchymal bleeding was observed in one patient, clinically manifested by a seizure (1/17cases, 5.88%, CI95% 0.14-28%). CT confirmed the small hematoma. It was localized in the right frontal lobe directly related with the placement site and the volume was approximately 1 cc. The small volume of bleeding did not impede the liver transplant, which was carried out uneventfully. The cerebral hematoma resolved spontaneously without neurological consequences.

CT will be doing if the patient is on transplant list or if he had encephalopathy I-II with a new focal deficit or if ICP is elevated.

DISCUSSION

The advent of liver transplantation as a treatment option for ALF requires also the management of associated hepatic encephalopathy. diagnosis and monitoring of intracranial hypertension contributes to the care of candidates for liver transplantation, both before and during the surgical procedure. Nevertheless, in the case of patients with ALF, it is important to consider the disadvantages related with the use of an invasive method, not only because of the severe disorders of the coagulation, but also because of the immunological compromise associated with this type of pathology1-3.

In the common neurosurgical practice, ICP monitoring can be performed using intraventricular, intraparenchymal, subdural, or epidural devices. The intraventricular transducer is widely accepted as the "gold standard system" for ICP monitoring, being its main complication the bacterial colonization with an incidence of up to 40%. In patients without coagulopathy, the reported incidence of hemorrhagic complications was 1.1%, and the incidence of the device malfunction was 6.3%. Intraparenchymal transducers are currently most used because the procedure of placement is very easy and it is associated with a low rate of complications. The main disadvantage is the dysfunction of the optical fiber (9-40%). The hemorrhagic complication is observed in 2.8% of the cases, and the incidence of bacterial colonization has been brought down to 0-14% of the cases5-7 . In a prospective study of intraparenchymal monitoring, haemorrhage was observed in 2.1% of patients without alteration of the coagulation, and in 15.3% of their counterparts with coagulopathy8. In another study, 118 patients with intracranial pathology but without coagulopathy were evaluated, and the incidence of observed complications was: infection (0.7%), intraparenchymal haematoma (5.1%) and complications related with technical aspects (23.5%)9. Subdural devices present an infection incidence of 4-5%, whereas the risk of haemorrhage is extremely low6,7 .

In ALF, the election of the type of ICP monitoring is very important owed to the high risk of bleeding attributable to the basal coagulopathy. The majority of authors recommend the epidural monitoring as a safer procedure, in spite of its lower accuracy3,10. Blei et al. reported a series of patients with ALF, with a lesser index of complications (3.8%) with the use of epidural transducers, compared with complications observed with subdural and intraparenchymal devices, which presented a procedure-related bleeding incidence of 20% and 22% respectively. Fatal haemorrhage occurred in 1%, 5%, and 4% of patients with epidural, subdural, and intraparenchymal monitors, respectively1. In a study of 36 patients with intracranial hypertension and encephalopathy grade IV, Keays et al. reported few complications, including bleeding at the placement site of epidural ICP transducers3. The Mayo Clinic group published an analysis of 11 patients with ALF and ICP monitoring using subdural devices, showing only one patient presenting a complication, a focal haemorrhage secondary to the transducer placement11.

Since the first report in 1993, the majority of the centers use epidural transducers in patients with acute liver failure in order to avoid hemorrhagic complications3. The first patient of our present series was treated in 1990 with intraparenchymal device, and following this case, the procedure continued in the same way. We are reporting a retrospective study, and we would like to emphasize that the present communication is focused on the technical aspects and not on the management and effectiveness of the treatment of intracranial hypertension. In our series, we used intraparenchymal transducers to privilege the accuracy of ICP monitoring for patients with ALF. The monitor used was Camino Inc, and no malfunctions of ICP devices occurred in this group of patients. Prevention of complications was performed by prophylactic administration of periprocedural fresh plasma, and by the placement of devices done by neurosurgeons in all cases. The procedure was a blind insertion via a twist drill hole. It was carried out by neurosurgeons in the Intensive Care Unit. Coagulation was used to control bleeding.

In our series, the incidence of complications was similar to that obtained by other authors who utilized subdural or epidural transducers. No infectious complications were observed, and the median ICP-monitoring time was 5 days (range, 1-8 days).

In conclusion, based on our experience we can suggest that intraparenchymal ICP monitoring in patients with ALF is a precise method, with a low risk of complications. The possibility of hemorrhagic complications at the placement site is similar to patients without coagulopathy with the appropriate prophylactic treatment.

Received 29 January 2008, received in final form 12 April 2008. Accepted 22 April 2008.

Dra. Alejandra T. Rabadán - Av. La Plata 393 / 8º C - 1235 Buenos Aires - Argentina.

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  • 2. Jalan R. Intracranial hypertension in acute liver failure: pathophysiological basis of rational management. Semin Liver Dis 2003;23:271-282.
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Publication Dates

  • Publication in this collection
    29 Sept 2008
  • Date of issue
    June 2008

History

  • Received
    29 Jan 2008
  • Accepted
    22 Apr 2008
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