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EDITORIAL
Year : 2020  |  Volume : 15  |  Issue : 1  |  Page : 1-4
 

Postoperative pneumoventricle following posterior fossa tumor surgery in sitting position: Plugging the aqueduct


Department of Neurosurgery, Seth Gordhandas Sunderdas Medical College and King Edward VII Memorial Hospital, Parel, Maharashtra, India

Date of Submission21-Feb-2020
Date of Acceptance24-Feb-2020
Date of Web Publication19-Mar-2020

Correspondence Address:
Dr. Dattatraya Muzumdar
Department of Neurosurgery, Seth Gordhandas Sunderdas Medical College and King Edward VII Memorial Hospital, Parel, Mumbai 400012, Maharashtra.
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jpn.JPN_35_20

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How to cite this article:
Muzumdar D. Postoperative pneumoventricle following posterior fossa tumor surgery in sitting position: Plugging the aqueduct. J Pediatr Neurosci 2020;15:1-4

How to cite this URL:
Muzumdar D. Postoperative pneumoventricle following posterior fossa tumor surgery in sitting position: Plugging the aqueduct. J Pediatr Neurosci [serial online] 2020 [cited 2020 Jun 3];15:1-4. Available from: http://www.pediatricneurosciences.com/text.asp?2020/15/1/1/281005




Kitahata and Katz first described the association of pneumocephalus and posterior fossa surgery in the sitting position in 1976.[1] Pneumoventricle following posterior fossa surgery in sitting position is known. Tension pneumoventricle has been described following resection of a cerebellar medulloblastoma, associated with hydrocephalus and cerebrospinal fluid (CSF) leakage from the suture line.[2] It has also been described following surgical resection of a cerebellar medulloblastoma and insertion of a ventriculoperitoneal shunt due to a petrous bone defect.[3] It is also reported after the removal of an acoustic neurinoma and a CSF shunt procedure due to a concomitant hydrocephalus.[4] It can also occur due to the existence of a craniodural defect without an obvious CSF leak and a massive inflow of air with the patient in the sitting position. The “valve mechanism” does not allow the air to escape, as the brain’s soft tissue blocks the “valve” defect on the exhalation cycle, causing mass effect and increasing intracranial pressure. Other factors include nitrous oxide anesthesia, prolonged surgery, gross hydrocephalus, intraoperative administration of mannitol or frusemide, and head-up position after surgery.[4],[5],[6],[7],[8],[9]

Although known, it is an uncommon condition that may be seen following excessive CSF drainage in the presence of a noncompliant ventricular system. It is usually self-limiting, and the air is absorbed within 2–3 weeks following surgery. However, symptomatic pneumoventricle can occur within few hours of surgery, resulting in acute raised intracranial pressure. It tends to be more pronounced in patients who present with severe hydrocephalus before surgery.

In sitting position, there are circumstances favorable to the development of pneumocephalus and pneumoventricle.[10],[11],[12] It is described as an “inverted pop bottle” mechanism. The combined effects of gravity, moderate hyperventilation (with consequent hypocapnia), and iatrogenic intracranial dehydration (mannitol and/or frusemide) enable the air to enter the ventricle as CSF is drained through the wound. Administration of mannitol can enhance the CSF loss by reducing the brain volume and decreasing the production of CSF. In addition, the presence of blood remnant in the fourth ventricle after surgery can accentuate the obstructive hydrocephalus.

Dilated ventricles pose a problem in surgery for posterior fossa tumor in sitting position[12],[13],[14],[15] [Figure 1]. The breach of the third or fourth ventricle can result in a massive loss of CSF, which possibly leads to accumulation of air within the ventricles. As soon as the tumor is decompressed, rapid egress of CSF from the enlarged lateral and third ventricles creates a vacuum inside the ventricular system. The negative pressure created within the ventricles forces the atmospheric air into the ventricles till equilibrium is attained across the pressure differential. The influx of air into the ventricle is greater in the presence of a noncompliant system because the ventricles do not collapse as the fluid is drained and more air fills it. In addition, inhalational of anesthetic drugs, such as nitrous oxide, can diffuse into air-filled spaces and expand any trapped air loculi. Symptomatic pneumoventricle develops when the volume of sealed intracranial air increases either by expansion of gas on warming to body temperature or by further diffusion of gas into the space based on physical laws discovered by Charles and Gay-Lussac. The temperature of intracranial gas rises from ambient temperature (approximately 20.8°C) to internal body temperature (37.8°C). The resultant volume expansion of the air leads to increased pressure within the ventricular system. It then exerts pressure on adjacent structures with potentially serious consequences. The hydrocephalus might increase manyfold leading to acute raised intracranial pressure.
Figure 1: (A) Sagittal contrast-enhanced magnetic resonance (MR) image showing midline fourth ventricular tumor. The tumor has widened the space between the roof of the fourth ventricle and aqueduct. (B) Axial contrast MR image showing the tumor occupying the fourth ventricle and splaying both the middle cerebellar peduncles

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Tension pneumoventricle may manifest as deterioration of consciousness with or without lateralizing signs, severe restlessness, generalized convulsions, or focal neurologic deficits.[1],[2],[3],[4] Postoperatively, the patients may present with delayed recovery, seizures, arterial hypertension, and reflex bradycardia (Cushing’s reflex) or cardiac arrest due to mass effect. The patient may remain drowsy and show tonic posturing or decerebrating response due to downward pressure on the brain stem. Patients who are asymptomatic or show minor symptoms are administered oxygen supplementation, which helps in the evacuation of the air and anesthetic gases from the ventricular system. If the volume of air is excessive and patient becomes progressively drowsy, an urgent twist drill craniostomy may be needed to stabilize the patient.[2],[8],[9],[14],[15],[16]

During posterior fossa surgery in sitting position, a small amount of pneumoventricle is unavoidable.[14],[15],[16] However, influx of large amount of air in the ventricles should be avoided [Figure 2]A–C. There are certain precautions and maneuvers that need to be taken to minimize pneumoventricle. The resection cavity is carefully and gently irrigated with normal saline, which can reduce the incidence of iatrogenic pneumoventricle and help prevent the entrainment of air. Care must be exercised in the presence of any CSF drainage apparatus as this has been implicated as the major factor in causing pneumoventricle. Intracranial dehydration by mannitol and/or frusemide, which is frequently used to improve operating conditions for the surgeon in the sitting position, should be judiciously used.
Figure 2: (A) Axial plain computed tomography (CT) image showing pneumoventricle involving both frontal horns and suprasellar cisterns. (B) Axial plain CT image showing pneumoventricle involving both frontal horns and third ventricle. (C) Axial plain CT image showing pneumoventricle and hydrocephalus

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An alternative maneuver to prevent large influx of air into the ventricle is to plug the aqueduct by a soft gelatin sponge [Figure 3]A. During resection of the posterior fossa tumor surgery, the initial dissection is always commenced at the superior pole of the tumor. As soon as the tumor is decompressed and the aqueduct is exposed, an adequate-sized soft gelatin sponge is gently placed over the aqueduct covering it completely. The gelatin sponge will swell considerably due to CSF soakage and occlude the aqueduct sufficiently to disallow rapid egress of CSF and influx of air [Figure 3]B. Occasionally, the continuous seepage of CSF from the aqueduct into the fourth ventricle can exert downward force on the swollen gelatin sponge and potentially displace it. An adequate-sized cottonoid is placed over the gelatin sponge to secure it so that it does not descend into the floor of the fourth ventricle. Care is taken to prevent any iatrogenic damage or manipulation of the fourth ventricle. In spite of plugging the aqueduct, a small quantity of CSF does pass from the aqueduct into the fourth ventricle but not sufficient amount of air to cause symptomatic pneumoventricle. Once the inferior and lateral portion of the tumor is removed, the cottonoid and the engorged gelatin sponge are gently removed [Figure 3]C. The roof of the fourth ventricle usually acts a barrier to prevent reflux of CSF [Figure 3]D. Owing to expansion of the fourth ventricular space due to tumor growth, the compliance of the roof of the fourth ventricle is compromised. As a result, the potential space created between the aqueduct and the roof of fourth ventricle following tumor decompression allows large amount of air influx in the aqueduct. The blood remnants in the fourth ventricle are also removed. The aqueduct-plugging technique is relatively safe and simple to perform to prevent large amount of air influx into the aqueduct. The gelatin sponge is time-tested material, relatively cheap, and easily available. It has no untoward reactions. Till now, there are no reports in the literature, which mentions aqueduct-plugging technique to prevent pneumoventricle. Postoperatively, there have been no complications related to use of gelatin sponge for plugging the aqueduct.
Figure 3: (A) Intraoperative photograph showing a soft gelatin sponge placed over the aqueduct occluding it. The tumor adherence to the floor of fourth ventricle is seen vividly. (B) Intraoperative photograph showing the swollen soft gelatin sponge covering the aqueduct. There is still come CSF egress from the aqueduct. (C) Intraoperative photograph showing roof of the fourth ventricle, which prevents excessive influx of air in the aqueduct (D) Intraoperative photograph showing the aqueduct vividly following resection of the fourth ventricular tumor in another patient. The roof of the fourth ventricle is elevated by the suction cannula

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The aqueduct-plugging technique during posterior fossa tumor surgery in sitting position is a sound intraoperative maneuver, which would help to minimize the incidence of pneumoventricle and pneumocephalus.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.



 
   References Top

1.
Kitahata LM, Katz JD. Tension pneumocephalus after posterior-fossa craniotomy, a complication of the sitting position. Anesthesiology 1976;44:448-50.  Back to cited text no. 1
    
2.
Daszkiewicz P, Dziedzic D. Tension pneumocephalus following suboccipital sitting craniotomy in the pediatric population. Neurol Neurochir Pol 2017;51:286-9.  Back to cited text no. 2
    
3.
Ram Z, Knoller N, Findler G, Sahar A. Delayed intraventricular tension pneumocephalus complicating posterior fossa surgery for cerebellar medulloblastoma. Childs Nerv Syst 1992;8:351-3.  Back to cited text no. 3
    
4.
Mineo JF, Phong DH, Seizeur R, Mériot P, Besson G. Delayed isolated tension intraventricular pneumocephalus after ventriculoperitoneal shunt. Neurochirurgie 2004;50:96-100.  Back to cited text no. 4
    
5.
Ruelle A, Severi P, Andrioli G. Intraventricular pneumocephalus after posterior fossa and CSF shunting surgery. Case report. J Neurosurg Sci 1994;38:167-70.  Back to cited text no. 5
    
6.
Perrin RG, Bernstein M. Tension pneumoventricle after placement of a ventriculoperitoneal shunt: a novel treatment strategy. Case report. J Neurosurg 2005;102:386-8.  Back to cited text no. 6
    
7.
Garg N, Devi I, Dua R, Arivazhagan A. Tension pneumoventricle following exposure of shunt chamber. Br J Neurosurg 2008;22:121-2.  Back to cited text no. 7
    
8.
Gupta N, Rath GP, Mahajan C, Dube SK, Sharma S. Tension pneumoventricle after excision of third ventricular tumor in sitting position. J Anaesthesiol Clin Pharmacol 2011;27:409-11.  Back to cited text no. 8
[PUBMED]  [Full text]  
9.
Gonçalves MB, Nunes CF, Melo JO Jr, Guimarães RD, Klescoski J Jr, Landeiro JA. Tension pneumoventricle after resection of a fourth ventricle choroid plexus papilloma: an unusual postoperative complication. Surg Neurol Int 2012;3:116.  Back to cited text no. 9
    
10.
Salem-Memou S, Vallee B, Jacquesson T, Jouanneau E, Berhouma M. Pathogenesis of delayed tension intraventricular pneumocephalus in shunted patient: possible role of nocturnal positive pressure ventilation. World Neurosurg 2016;85:365.e17-20.  Back to cited text no. 10
    
11.
Krishnan SS, Manuel A, Vasudevan MC. Delayed pneumoventricle following endonasal cerebrospinal fluid rhinorrhea repair with thecoperitoneal shunt. Asian J Neurosurg 2019;14:325-8.  Back to cited text no. 11
[PUBMED]  [Full text]  
12.
Lin YH, Lin HL, Cho DY. Tension pneumoventricle after endoscopic transsphenoidal surgery for Rathke cleft cyst. World Neurosurg 2019;135:228-32.  Back to cited text no. 12
    
13.
Gupta T, Sarkar C, Rajshekhar V, Chatterjee S, Shirsat N, Muzumdar D, et al. Indian Society of Neuro-oncology consensus guidelines for the contemporary management of medulloblastoma. Neurol India 2017;65:315-32.  Back to cited text no. 13
[PUBMED]  [Full text]  
14.
Muzumdar D, Deshpande A, Kumar R, Sharma A, Goel N, Dange N, et al. Medulloblastoma in childhood—King Edward Memorial hospital surgical experience and review: comparative analysis of the case series of 365 patients. J Pediatr Neurosci 2011;6:S78-85.  Back to cited text no. 14
    
15.
Muzumdar D, Ventureyra EC. Treatment of posterior fossa tumors in children. Expert Rev Neurother 2010;10:525-46.  Back to cited text no. 15
    
16.
Muzumdar DP. Ventricular CSF drainage and medulloblastoma. Pediatr Neurosurg 2007;43:74-5; author reply 75.  Back to cited text no. 16
    


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