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AJR 2000; 175:443-446
© American Roentgen Ray Society


Original Report

CT-Guided Percutaneous Fibrin Glue Therapy of Cerebrospinal Fluid Leaks in the Spine After Surgery

Mahesh R. Patel1,2, Paul A. Caruso1, Naveed Yousuf1 and Jacob Rachlin3

1 Department of Radiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215.
2 Present address: Santa Clara Valley Medical Center, 3031 Tisch Way, Ste. 02, Plaza South, San Jose, CA 25128.
3 Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215.

Received September 20, 1999; accepted after revision January 4, 2000.

 
Address correspondence to M. R. Patel.


Abstract
Top
Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
OBJECTIVE. The objective of this study is to assess CT-guided percutaneous injection of fibrin glue for the management of cerebrospinal fluid leaks within the spine.

CONCLUSION. Percutaneous CT-guided placement of fibrin glue can provide a treatment option for postoperative cerebrospinal fluid leaks, potentially allowing a major surgical procedure to be avoided. However, the complication of aseptic meningitis may occasionally result from this procedure.


Introduction
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
Cerebrospinal fluid (CSF) leaks involving the spine can occur after surgery as well as accidental trauma. CSF leaks occur most frequently after back surgery or, on rare occasions, after a lumbar puncture. Patients with a CSF leak often present with headaches or a flocculent subcutaneous fluid collection superficial to the leak with drainage. These leaks represent a serious problem because of the secondary complication of meningitis. Typical management consists of surgery with meticulous closure of the dura or closure using a fascial graft.

Prior studies evaluating CT-guided fibrin glue placement for treatment of postoperative dural tears have involved only a small number of patients [1, 2]. We evaluated CT-guided percutaneous fibrin glue placement to seal postoperative CSF leaks in a larger group of patients. This therapy has the potential to allow a major surgical procedure with its associated cost and morbidity to be avoided.


Subjects and Methods
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
Between June 1994 and February 1999, 23 consecutive patients with a CSF leak were treated with percutaneous fibrin glue placement. These patients (12 men and 11 women) ranged in age from 26 to 73 years (average age, 49 years), and they had undergone spinal surgery for either degenerative disk disease (n = 17) or tumor resection (n = 6). They presented with a palpable soft-tissue collection, postural headaches, or persistent CSF wound drainage. Although the first six patients underwent MR imaging within 1 week before fibrin glue placement to accurately assess the relationship of the dura to the CSF leak, preoperative MR imaging was not considered essential beyond this initial experience.

After informed consent was obtained, the patient was placed in the prone position on a 9800 CT scanner (General Electric Medical Systems, Milwaukee, WI), and 5-mm contiguous scans (140 kV, 257 mA, 25-cm field of view) were obtained through the CSF collection. The overlying skin was marked at the site of suspected leak, and with the patient under local lidocaine anesthesia, an 18- to 20-gauge spinal needle was placed into the CSF fluid collection adjacent to the location of the suspected dural tear. The maximal amount of CSF was drained, and repositioning and reaspiration were performed as needed. The fluid was aspirated slowly to avoid aspiration of a nerve root through the dural defect. The patient was continuously monitored for associated neurologic symptoms by the attendant nurse and physician, and the aspiration was titrated accordingly. The needle was repositioned as needed, usually once or twice, to maximally drain the fluid. A subcutaneous fluid collection was not drained unless it was in direct communication with the deeper collection.

The formation of fibrin glue required two components: first, cryoprecipitate was prepared from the patient's blood [3] in the absence of contraindications such as coagulopathy, emergency, or anemia. The preparation of the autologous cryoprecipitate required at least 3 days. Five hundred milliliters of whole blood was collected. The resulting plasma was extracted and frozen at -80°C for 24 hr. The plasma was then thawed gradually over 24 hr at 6°C, at which point a second centrifugation step was performed. The liquid precipitate was harvested again and was frozen for 24 hr. This process yielded 20-25 mL of cryoprecipitate, which must be thawed 30-45 min before use. Once thawed, the cryoprecipitate should be used within 4 hr. The cryoprecipitate served as a concentrated source of fibrinogen. In conjunction with thrombin and factor XIII, it polymerized into fibrin [3]. The second component of fibrin glue was a thrombin and calcium chloride mixture made by mixing 20,000 U of lyophilized thrombin with 10 mL of a 10% calcium chloride solution. This combined solution had a concentration of 2000 U/mL of thrombin.

Before the procedure, approximately 0.25 mL of iopamidol was added to 3 mL of the thrombin-calcium chloride solution to allow improved visualization of the fibrin plug. This mixture and the cryoprecipitate were placed in separate 3-mL syringe assemblies and then connected via a three-way stopcock to an 18- to 20-gauge spinal needle (Fig. 1). The spinal needle was first placed into the suspected site of CSF leak adjacent to the suspected dural rent. Equal volumes of the cryoprecipitate and thrombin-calcium chloride-iopamidol solution were injected simultaneously. During the injection, the patient was monitored for any adverse symptoms including pain and numbness or tingling.



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Fig. 1. —Preparation of two-component fibrin glue assembly shows attachment via two 3-mL syringes to three-way stopcock that is then attached to an 18- to 20-gauge spinal needle. No connecting tubing is used to reduce dead volume.

 

The aggregation of the two solutions resulted in formation of the fibrin plug in vivo at the site of the suspected dural tear. A new syringe assembly was used for repeated deployment of fibrin glue because aggregation of fibrin glue within the stopcock and the syringe may occur as a result of reflux. The total volume instilled ranged from 4 to 24 mL. The aggregation of the fibrin glue mixture is illustrated in Figure 2. The procedure was terminated when one of the following conditions occurred: adequate coverage by the fibrin plug adjacent to the site of suspected dural leak was achieved; appreciable mass effect higher than or equal to that seen on imaging studies before the intervention was seen; or the patient complained of symptoms of radiculopathy or back pain.



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Fig. 2. —In vitro aggregation of fibrin glue within superior portion of tube 5 min after admixture. Note gravity-dependent air—fluid level in container adjacent to tube of fibrin glue (arrows).

 

The position of the fibrin plug was documented on postprocedure CT scans. The success of the procedure was determined by chart review, direct patient interview, and physical examination. In several patients, follow-up MR images were obtained.


Results
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
In 15 (65%) of the 23 patients with a postoperative CSF leak, symptoms either decreased or resolved markedly after the procedure. In five patients (22%), the complication of aseptic meningitis occurred, which we have found to require only analgesic therapy and bed rest.

Of the 23 patients, 20 had undergone surgery in the thoracolumbar spine; one in the sacrum; one in the cervical spine; and one in the skull base. Seventeen patients had undergone surgery for degenerative disk disease, whereas six had undergone surgical resection of tumors. The time between completion of surgery and placement of the fibrin plug ranged from 3 days to 2 years 7 months. Postoperative symptoms of patients presenting for fibrin patch included wound leak, soft-tissue collection, and headache. Follow-up from the time of patch placement for the patients who did not require subsequent definitive repair ranged from 6 months to 3 years 6 months. One of the successful lumbar spine fibrin plug procedures is illustrated in Figure 3A,3B,3C. An image of a patient with a complication of aseptic meningitis from intrathecal placement of fibrin glue is shown in Figure 4. A skull base leak that was successfully treated with fibrin glue is shown in Figure 5A,5B,5C.



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Fig. 3A. —39-year-old man with lumbar cerebrospinal fluid (CSF) leak detected 4 months after L5—S1 disk excision who later underwent successful fibrin glue patch therapy. Axial CT scan shows large posterior CSF collection.

 


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Fig. 3B. —39-year-old man with lumbar cerebrospinal fluid (CSF) leak detected 4 months after L5—S1 disk excision who later underwent successful fibrin glue patch therapy. Axial CT scan after fibrin glue therapy shows placement of plug over suspected site of CSF leak. Note different attenuation of fibrin glue components due to different dilutions of contrast material: fibrin plug (arrows) appears mildly hyperdense to CSF.

 


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Fig. 3C. —39-year-old man with lumbar cerebrospinal fluid (CSF) leak detected 4 months after L5—S1 disk excision who later underwent successful fibrin glue patch therapy. Sagittal reconstruction shows fibrin glue covering laminectomy defect. Note extension of fibrin glue (arrows) subdurally. Subdural extension of fibrin glue is common after this procedure.

 


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Fig. 4. —63-year-old woman with lumbar cerebrospinal fluid (CSF) leak who later underwent fibrin glue patch therapy with intrathecal extension of fibrin glue, resulting in aseptic meningitis. Axial CT image shows fibrin glue within thecal sac (arrows). Bony fusion material is seen posterior to spine. Dense radiopaque object within left paraspinal soft tissues represents an electrical stimulator device. Because of large size of defect, surgical repair was subsequently performed.

 


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Fig. 5A. —29-year-old man with suboccipital cerebrospinal fluid leak after hemangioblastoma resection who later underwent successful fibrin glue patch therapy. Axial CT image shows collection posterior to C2 level.

 


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Fig. 5B. —29-year-old man with suboccipital cerebrospinal fluid leak after hemangioblastoma resection who later underwent successful fibrin glue patch therapy. Axial CT image shows spinal needle placed into collection with introduction of fibrin glue.

 


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Fig. 5C. —29-year-old man with suboccipital cerebrospinal fluid leak after hemangioblastoma resection who later underwent successful fibrin glue patch therapy. Sagittal reconstruction shows fibrin plug covers site of craniotomy defect.

 


Discussion
Top
Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
A simple fibrin plug procedure for the management of postoperative CSF leaks may help patients avoid a major surgical procedure with its associated costs and morbidity. We have shown its utility in sealing leaks in the lumbosacral spine and in the skull base; this procedure is most frequently used in the setting of a postoperative CSF leak. Our current results, a success rate of 65%, as opposed to the previously reported success rate of 50% [2] suggest that with experience and appropriate patient selection, this technique provides a good alternative to surgical therapy.

The surgical management of postoperative CSF leaks entails providing an adequate seal that is able to withstand CSF pressure during the healing period. Prompt surgery has been advocated to prevent the complication of meningitis, CSF fistulas, and pseudocyst formation with potential resultant neural compression. Surgical methods include meticulous primary closure of the defect and potential interposition of fascia, muscle, or fat graft over the defect.

More recently, direct placement of fibrin glue over the defect has been performed, with or without associated graft placement. Placement of a fibrin plug has been postulated to create adhesion at the site of a dural tear, and this adhesion may also promote healing [3]. The maximal bonding effect is reached within 30-90 min, with 70% of the bonding effect occurring within 2 min of the mixing of the two adhesive components. Subsequent granulation tissue and fibrosis are believed to result in a more definitive repair [4]. It has further been proposed that the fibrin adhesive is completely absorbed so that the process of wound healing remains undisturbed and that wound healing is promoted by the immediate stimulation of fibroblasts [3].

A risk of the procedure is that a small amount of the fibrin glue may be introduced intrathecally and may result in aseptic meningitis. In our experience, aseptic meningitis is a self-limiting complication that may occur in the setting of a CSF leak with or without a fibrin glue patch; this complication resolves in 2-3 days and can be treated with conservative therapy. Bed rest and analgesics are considered appropriate. We believe that antibiotic therapy is not indicated. In rare cases, a large dural tear may be a relative contraindication to this technique because it may result in free introduction of fibrin glue into the subarachnoid space. This contraindication can be determined by injecting myelographic contrast material into the collection to see whether free communication with the thecal sac is present. Although the fibrin glue may serve as a nidus for infection, this finding was not observed in our patients. Also in follow-up to date, neither arachnoiditis nor fibrous adhesions have occurred.

Originally, we performed MR imaging before the procedure to locate the potential site of the CSF leak and to optimally delineate the thecal sac from the extradural CSF collection. This additional imaging may also prevent the inadvertent introduction of fibrin glue into the subarachnoid space. Although CT myelography may also define the dural tear, we did not think it was necessary before performing the fibrin glue procedure. Having gained more experience with the technique, we no longer routinely perform imaging besides CT at the time of fibrin glue placement.

We also recommend that autologous cryoprecipitate be used to avoid the risks of blood-born pathogens, including hepatitis C. The blood needs to be harvested several days before the procedure to allow preparation of the cryoprecipitate as described. After the procedure, we generally recommend a period of overnight absolute bed rest.

Other alternative procedures to surgical closure have been proposed as therapy for CSF leaks, including epidural blood patches [5,6,7] and persistent lumbosacral drainage [8]. These alternative therapies can also have complications. Epidural blood patches can result in persistent headache, neurologic deterioration, and subdural hematoma [9, 10]. The intrathecal administration of RBCs can cause severe headaches. According to one large series, the success rate of lumbar subarachnoid catheterization and drainage was 94%; however, complications can occur such as infections (5%), including meningitis (2%); overdrainage with temporary neurologic decline (3%); occlusion of the drain requiring replacement (9%); and transient nerve root irritation (14%) [11]. Persistent CSF leak, coma, and injury to the soft tissues as well as to the nerve roots have also been reported [12]. The only complication of the fibrin patch has been self-limiting aseptic meningitis. Furthermore, the lumbar catheter technique requires a 14- to 16-gauge tear in the dura above the site of the leak, and this additional rent may not heal spontaneously. Also, the subsequent continuous bed rest for at least 3 days necessitates a prolonged hospital stay and results in a predisposition to infection.

In summary, CT-guided fibrin glue therapy has significant potential to lower the morbidity and cost of treating patients with postoperative CSF fistulas. Given our experience to date, we advocate percutaneous CT-guided fibrin glue therapy as an initial treatment for a CSF leak.


References
Top
Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 

  1. Fraioli B, Pastore FS, Floris R, et al. Computed tomography-guided transsphenoidal closure of post-surgical cerebrospinal fluid fistula: a transmucosal needle technique. Surg Neurol 1997;48:409 -413[Medline]
  2. Patel MR, Louie W, Rachlin J. Postoperative cerebrospinal fluid leaks of the lumbosacral spine: management with percutaneous fibrin glue. AJNR 1996;17:495 -500[Abstract]
  3. Sidentop KH, Harris DM, Ham K, Sanchez B. Extended experimental and preliminary surgical findings with autologous fibrin tissue adhesive made from the patient's own blood. Laryngoscope 1986;96:1062 -1064[Medline]
  4. Bundschuh CV. Imaging of the postoperative lumbar spine. Neuroimaging Clin N Am 1993;3:499 -516
  5. Chauchan C, Frances GA, Kemeny AA. The avoidance of surgery in the treatment of subarachnoid cutaneous fistula by the use of an epidural patch: technical case report. Neurosurgery 1995;36:612 -613[Medline]
  6. Di Giovani AJ, Galbert MW, Wahle WM. Epidural injection of autologous blood for post-lumbar headache. Anesth Analg 1972;51:226 -232[Free Full Text]
  7. Maycock NF, van Essen J, Pfitzner J. Post-laminectomy cerebrospinal fluid fistula treated with an epidural blood patch. Spine 1994;19:2223 -2225[Medline]
  8. Findler G, Sahar A, Beller AJ. Continuous lumbar drainage of cerebrospinal fluid in neurosurgical patients. Surg Neurol 1977;8:455 -457[Medline]
  9. Seeberger MD, Urwyler A. Lumbosacral syndrome after extradural blood patch. Br J Anaesth 1992;69:414 -416[Abstract/Free Full Text]
  10. Woodward WM, Levy DM, Dixon AM. Exacerbation of post-dural puncture headache after epidural blood patch. Can J Anaesth 1994;41:628 -631[Abstract/Free Full Text]
  11. Shapiro SA, Scully T. Closed continuous drainage of cerebrospinal fluid via a lumbar subarachnoid catheter for treatment or prevention of cranial/spinal cerebrospinal fluid fistula. Neurosurgery 1992;30:241 -245[Medline]
  12. Francel PC, Persing JA, Cantrell RW, Levine PA, Newman SA. Neurological deterioration after cerebrospinal fluid drainage. J Craniofac Surg 1992;3:145 -148[Medline]

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