Abstract
The objective of the study is to introduce the surgical procedure of the lumbosubarachnoid–lumboepidural (L–L) shunting performed as treatment for idiopathic normal-pressure hydrocephalus (iNPH) and its follow-up. The subjects were five patients with probable iNPH (aged 78–85 years; mean age 81 years; four males and one female) who were judged to be at high risk from general or lumbar anesthesia due to their systemic complications and age. The L–L shunt operation was performed for all the patients under local anesthesia using Codman–Hakim Programmable Valve® (Codman & Shurtleff, Inc., Raynham, Massachusetts, USA). The initial pressure for all patients was set at 8 cm H2O. The evaluation of shunt efficacy and the lumbar epidural space cerebrospinal fluid (CSF) absorption test (injection of contrast media into epidural space) were performed both on the operation day and during follow-up period (9–12 months). The shunt operation was judged to be effective in four out of five patients (regarded as shunt responders), whereas no improvement in symptoms was seen in one patient (regarded as shunt nonresponder) where the shunting had no effect after the initial pressure was changed to 4 cm H2O. The lumbar epidural space CSF absorption test both on the operation day and during the follow-up period confirmed absorption in all patients. The L–L shunting is useful for patients with probable iNPH who are at high risk from general or lumbar anesthesia due to their systemic complications and age. CSF was continuously absorbed in the lumbar epidural space during postoperative follow-up period. A longer follow-up is required to establish this surgical procedure.
Keywords: normal-pressure hydrocephalus, idiopathic, lumbosubarachnoid–lumboepidural shunting
Introduction
We have determined the indications for shunting in patients with possible idiopathic normal-pressure hydrocephalus (possible iNPH)5) based on the nature of clinical symptoms, findings on magnetic resonance imaging (MRI), the dynamics of the cerebral circulation as assessed by single-photon emission computed tomography (SPECT), the “lumbar tap test,” and a further supplementary test (the cerebrospinal fluid [CSF] outflow resistance value, Ro).14,17–24) Using this approach we have managed over 500 iNPH patients with long-term follow-up.15,16) Of these patients, many who were diagnosed as having probable iNPH5) could only be managed with intermittent lumbar puncture on an outpatient basis because they were judged to be at high risk from shunting under either general or lumbar anesthesia, due to their advanced age or systemic complications. We here report the satisfactory results achieved with lumbosubarachnoid–lumboepidural (L–L) shunting under local anesthesia, which we developed for use in five patients who were at high risk from conventional shunting.
Materials and Methods
The subjects were five patients (aged 78–85 years; mean age 81 years; four males and one female) with probable iNPH as defined by the guidelines,5) in whom shunting was determined to be appropriate but who were considered to be at high risk from general or lumbar anesthesia due to the presence of serious systemic complications (Table 1). L–L shunting was performed under local anesthesia in all five patients. The shunting system used was the Codman–Hakim Programmable Valve® (Codman & Shurtleff, Inc., Raynham, Massachusetts, USA), with a lumboperitoneal (LP) shunt catheter. An epidural drainage catheter with a diameter of 0.8 mm (Hakko Co., Naniwa, Osaka) was utilized as a guide-wire when inserting the epidural catheter (Fig. 1).
Table 1.
Objective cases (n = 5)
| Case | Age, Sex | Systemic complication | JNPHGS-R | mRS | LTT | Ro (mmHg/ml/min) |
|---|---|---|---|---|---|---|
| 1 | 78, M | Recurrent angina pectoris | G4D3U3 = 10p | 4 | Positive | 16.28 |
| Colon cancer | ||||||
| Prostate cancer | ||||||
| 2 | 79, M | Heart failure DM, HT | G2D3U3 = 8p | 3 | Positive | 10.36 |
| 3 | 80, F | COPD, DM | G3D3U4 = 10p | 4 | Positive | 7.41 |
| 4 | 83, M | Heart failure HT | G3D0U1 = 4p | 2 | Positive | 23.28 |
| 5 | 85, M | Liver dysfunction | G3D2U2 = 7p | 3 | Positive | 15.02 |
| Renal dysfunction |
COPD: chronic obstructive pulmonary disease, DM: diabetes mellitus, HT: hypertension, JNPHGS-R: Japanese Normal Pressure Hydrocephalus Grading Scale—Revised, LTT: lumbar tap test, mRS: modified Rankin scale, Ro: cerebrospinal fluid outflow resistance value.
Fig. 1.

Operative instruments of lumbosubarachnoid–lumboepidural (L–L) shunting.
The patients were assessed as follows. (1) Symptom evaluation: changes in presurgical symptoms during the follow-up period (9–12 months; mean 10.4 months), assessed using the Japan Normal Pressure Hydrocephalus Grading Scale—Revised (JNPHGS-R)5); (2) evaluation of the lumbar epidural space CSF absorption capacity: CSF absorption capacity was assessed by lumbar epidural space CSF absorption tests performed immediately after surgery and during the follow-up period (axial and sagittal computed tomographic [CT] images performed immediately after and 48 hours after injection of 2–5 ml of Omnipaque® [iohexol] into the valve pump); and (3) postoperative complications. On evaluation of symptoms, patients with an improvement in symptoms of ≥ 1 point based on the JNPHGS-R in the follow-up period were defined as shunt responders, and patients without improvement were defined as shunt nonresponders. In the evaluation of lumbar epidural space CSF absorption capacity, patients in whom the contrast medium disappeared in the CT images acquired 48 hours after injection were defined as CSF absorption positive (+) (Fig. 2) and patients in whom this did not occur were defined as CSF absorption negative (−).
Fig. 2.

A three-dimensional computed tomography (3D-CT) image of the lumbar epidural space CSF absorption test on the operation day (Case 1, block arrow: contrast media).
Operative Technique
The following steps were performed as part of the operative technique:
Insert the shunt catheter and guidewire into the lumbar epidural space between the fourth and fifth lumbar vertebrae to a depth of approximately 5 cm using the loss-of-resistance method with saline.
Insert the catheters ≥ 5 cm into the lumbar subarachnoid space between the second and third lumbar vertebrae (or between the first and second lumbar vertebrae, depending on the case) using the same procedure as that used for LP shunting.
Make an approximately 5 cm longitudinal skin incision along the spine in the midline between the fascia insertion sites of the two catheters.
Connect the epidural space and subarachnoid space catheters to the shunt valve using a stainless steel straight connector. The catheters should not be connected too firmly so as to avoid kinking at the connector site of the catheter and the shunt value.
Loop both the catheters, close the fascia insertion sites of the two catheters, and fix the catheter loop and valve to the paravertebral fascia.
Suture the skin (Fig. 3). The surgical position is as specified for LP shunting1,12,13,25) (i.e., lying on the left side, with the neck bent slightly forward, and the legs flexed). The initial pressure was set at 8 cm H2O in all patients. The surgery took between 80 and 120 minutes (mean duration 105 minutes). The postoperative catheter and valve positions were confirmed on lumbar three-dimensional CT (3D-CT) images (Fig. 4).
Fig. 3.

Surgical procedures of lumbosubarachnoid–lumboepidural (L–L) shunting. A: Insertion of the lumboepidural catheter. B: Insertion of the lumbosubarachnoid catheter. C: Cutting out of the skin. D: Coupling between valve and catheter. E: Setting the catheter with loop formation and fixation of the valve on paravertebral fascia. F: Suturing of the skin.
Fig. 4.

A three-dimensional computed tomography (3D-CT) image of lumbosubarachnoid–lumboepidural (L–L) shunting after operation.
Results
I. Symptom evaluation
During the follow-up period, an improvement in symptoms of ≥ 1 point, based on the JNPHGS-R, was noted in four of the five patients who were considered to be responders. Symptoms did not improve after the surgery in one patient (Case 3), the sole nonresponder, in whom symptoms did not change even with modification of the initial pressure from 8- to 4-cm H2O (Table 2).
Table 2.
Postoperative follow-up (n = 5)
| Case | Age, Sex | Follow-up period | Preope. and Postope. JNPHGS-R | Preope. and Postope. mRS | Epidural space absorption test | Shunt efficacy |
|---|---|---|---|---|---|---|
| 1 | 78, M | 12 mos | G4D3U3 = 10p | 4 | Absorption (+) | R |
| G3D3U0 = 6p | 3 | |||||
| 2 | 79, M | 11 mos | G2D3U3 = 8p | 3 | Absorption (+) | R |
| G1D2U1 = 5p | 2 | |||||
| 3 | 80, F | 10 mos | G3D3U4 = 10p | 4 | Absorption (+) | NR |
| G3D3U4 = 10p | 4 | |||||
| ↓ | ||||||
| Pressure reset (8- → 4-cm H2O) | ||||||
| ↓ | ||||||
| G3D3U4 = 10p | 4 | |||||
| 4 | 83, M | 10 mos | G3D0U1 = 4p | 2 | Absorption (+) | R |
| G2D0U0 = 2p | 2 | |||||
| 5 | 85, M | 9 mos | G3D2U2 = 7p | 3 | Absorption (+) | R |
| G1D2U0 = 3p | 2 |
JNPHGS-R: Japanese Normal Pressure Hydrocephalus Grading Scale—Revised, mos: months, mRS: modified Rankin scale, NR: shunt nonresponder, R: shunt responder.
II. Evaluation of the lumbar epidural space CSF absorption capacity
Lumbar epidural space CSF absorption tests performed immediately after surgery and during the follow-up period revealed absorption of contrast medium 48 hours after injection in all patients; the patients were determined to be lumbar epidural space CSF absorption positive (+) (Table 2 , Fig. 5).
Fig. 5.

A three-dimensional computed tomography (3D-CT) image of the lumbar epidural space cerebrospinal fluid (CSF) absorption test on the operation day and during the follow-up period (Case 3, block arrow: contrast media).
III. Relationship between shunt responder and CT image
The typical disproportionately enlarged subarach-noid-space hydrocephalus sign was revealed only in one case (Case 5) out of four shunt responders on preoperative CT image. In this case, decreased ventricular size and appearance of high convexity cerebral sulcus were appreciated on postoperative follow-up period on CT image (Fig. 6).
Fig. 6.

Preoperative (left) and postoperative follow-up period (right) coronal computed tomography (CT) image on Case 5.
IV. Postoperative complications
Subcutaneous leakage of CSF due to “side-leakage” of CSF was noted in one patient (Case 5) on postoperative Day 5; this resolved after the initial pressure was changed (from 8 to 12 cm H2O).
Discussion
Unlike the intracranial dura mater, the spinal dura mater is divided into outer and inner layers. The outer layer is attached to the periosteal tissue that lines the spinal canal, whereas the inner layer alone covers the spinal cord. Therefore, the commonly used term “spinal epidural space” refers to the space between the inner and outer layers of the spinal dura mater. The spinal epidural space is under negative pressure relative to atmospheric pressure and contains connective tissue, venous plexuses, and fat tissue. This space is used for various tests and therapeutic maneuvers such as epidural nerve blocks with injection of local anesthetic for sciatica. This usage shows that the spinal epidural space is capable of absorbing drugs and contrast media.10) Furthermore, Kaijima et al.6) recently reported two cases of overdrainage induced by CSF side-leakage into the lumbar epidural space after LP shunting. This report clearly indicates that the lumbar epidural space can absorb CSF.
Based on this evidence, we developed L–L shunting under local anesthesia. This procedure can be performed in patients with high risk for ventriculoperitoneal shunting2–4,7–9,11,26) or LP shunting1,12,13,25) under general or lumbar anesthesia because of their advanced age or systemic complications, including the cases where it is not possible to insert the catheter into abdominal cavity because of the existence of severe abdominal disease. The follow-up results in our five patients who underwent L–L shunting demonstrated that four of them were shunt responders during the follow-up period (mean duration 10.4 months), and CSF was absorbed from the lumbar epidural space during the follow-up period in all patients, including the single nonresponder. The postoperative complication of subcutaneous leakage of CSF was noted in one patient. Because this problem resolved after an increase in the initial pressure, it was assumed to be due to the CSF outflow volume exceeding the absorptive capacity of the epidural space.
Future investigation should establish the initial pressure setting for L–L shunting and the duration of the shunt effect because no treatise on lumbar epidural space absorption capacity or relationship between lumbar CSF pressure and lumbar epidural pressure are reported till now. Further long-term follow-up is essential in order to establish the indications for this procedure.
Acknowledgments
The authors greatly thank the members of “Study of Idiopathic Normal Pressure Hydrocephalus on Neurological Improvement” (SINPHONI) in Japan who gave advice on and assistance with the L–L shunting procedure that they subsequently developed. The authors obtained the approval of the ethics committee of the hospital for the enforcement of this new surgical procedure, and written informed consent was obtained from the patient and/or their family.
References
- 1). Aoki N: Lumboperitoneal shunt; clinical applications, complications and comparison with ventriculoperitoneal shunt. Neurosurgery 26: 998– 1003; discussion 1003–1004, 1990. [PubMed] [Google Scholar]
- 2). Black PM: Idiopathic normal-pressure hydrocephalus. Results of shunting in 62 patients. J Neurosurg 52: 371– 377, 1980. [DOI] [PubMed] [Google Scholar]
- 3). Boon AJ, Tans JT, Delwel EJ, Egeler-Peerdeman SM, Hanlo PW, Wurzer HA, Avezaat CJ, de Jong DA, Gooskens RH, Hermans J: Dutch normal-pressure hydrocephalus study; randomized comparison of low- and medium-pressure shunts. J Neurosurg 88: 490– 495, 1998. [DOI] [PubMed] [Google Scholar]
- 4). Hashimoto M, Ishikawa M, Mori E, Kuwana N, Study of INPH on neurological improvement (SINPHONI) : Diagnosis of idiopathic normal pressure hydrocephalus is supported by MRI-based scheme: a prospective cohort study. Cerebrospinal Fluid Res 7: 18, 2010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5). Ishikawa M, Hashimoto M, Kuwana N, Mori E, Miyake H, Wachi A, Takeuchi T, Kazui H, Koyama H: Guidelines for management of idiopathic normal pressure hydrocephalus. Neurol Med Chir (Tokyo) 48 Suppl: S1– S23, 2008. [DOI] [PubMed] [Google Scholar]
- 6). Kaijima M, Fukuda H, Yamamoto K: [Post-operative complications peculiar to lumboperitoneal shunt; possible consequences due to side leakage of CSF from around the inserted spinal tube into the lumbar epidural space]. No Shinkei Geka 39: 497– 504, 2011. (Japanese with English abstract) [PubMed] [Google Scholar]
- 7). Krauss JK, Droste DW, Vach W, Regel JP, Orszagh M, Borremans JJ, Tietz A, Seeger W: Cerebrospinal fluid shunting in idiopathic normal-pressure hydrocephalus of the elderly: effect of periventricular and deep white matter lesions. Neurosurgery 39: 292– 299; discussion 299–300, 1996. [DOI] [PubMed] [Google Scholar]
- 8). Malm J, Kristensen B, Karlsson T, Fagerlund M, Elfverson J, Ekstedt J: The predictive value of cerebrospinal fluid dynamic tests in patients with the idiopathic adult hydrocephalus syndrome. Arch Neurol 52: 783– 789, 1995. [DOI] [PubMed] [Google Scholar]
- 9). Mori K: Management of idiopathic normal-pressure hydrocephalus: a multiinstitutional study conducted in Japan. J Neurosurg 95: 970– 973, 2001. [DOI] [PubMed] [Google Scholar]
- 10). Ohta T, Matsutani M: [Neurosurgery, ed 10]. Kyoto, Kinpodo, 2008. (Japanese with English abstract) [Google Scholar]
- 11). Petersen RC, Mokri B, Laws ER: Surgical treatment of idiopathic hydrocephalus in elderly patients. Neurology 35: 307– 311, 1985. [DOI] [PubMed] [Google Scholar]
- 12). Philippon J, Duplessis E, Dorwling-Carter D, Horn YE, Cornu P: [Lumboperitoneal shunt and normal pressure hydrocephalus in elderly subjects]. Rev Neurol (Paris) 145: 776– 780, 1989. (French) [PubMed] [Google Scholar]
- 13). Selman WR, Spetzler RF, Wilson CB, Grollmus JW: Percutaneous lumboperitoneal shunt: review of 130 cases. Neurosurgery 6: 255– 257, 1980. [DOI] [PubMed] [Google Scholar]
- 14). Takeuchi T, Goto H, Izaki K, Kokubu K, Oda M, Sasanuma J, Maeno K, Kikuchi Y, Koizumi J, Watanabe Z, Ito Y, Ohara H, Kowada M, Watanabe K: [Reinvestigation of CSF outflow resistance value in idiopathic normal pressure hydrocephalus—comparing epidural pressure monitoring with lumbar subarachnoid cerebrospinal fluid pressure monitoring]. No Shinkei Geka 33: 579– 584, 2005. (Japanese with English abstract) [PubMed] [Google Scholar]
- 15). Takeuchi T, Goto H, Izaki K, Oda M, Watanabe Z, Kikuchi Y, Meano K, Koizumi J, Kokubun K, Sasanuma J, Ito Y, Ohara H, Kowada M, Watanabe K: Long-term follow-up study in patients with operated idiopathic normal pressure hydrocephalus. Nihon Univ J Med 47: 1– 15, 2005. [Google Scholar]
- 16). Takeuchi T, Goto H, Izaki K, Tamura S, Sasanuma Z, Maeno K, Kikuchi Y, Tomii M, Koizumi Z, Watanabe Z, Numazawa S, Ito Y, Ohara H, Kowada M, Watanabe K: [Postoperative patterns of improvement of symptoms and degrees of satisfaction in families of patients after operations for definite idiopathic normal pressure hydrocephalus: a long term follow-up study]. No Shinkei Geka 35: 773– 779, 2007. (Japanese with English abstract) [PubMed] [Google Scholar]
- 17). Takeuchi T, Goto H, Izaki K, Tamura S, Tomii M, Sasanuma J, Maeno K, Kikuchi Y, Koizumi J, Watanabe Z, Numazawa S, Itoh Y, Watanabe K, Kojima M, Mishima M, Onishi Y, Okada T, Arai T: Pathophysiology of cerebral circulatory disorders in idiopathic normal pressure hydrocephalus. Neurol Med Chir (Tokyo) 47: 299– 306; discussion 306, 2007. [DOI] [PubMed] [Google Scholar]
- 18). Takeuchi T, Iwasaki M, Shirata K, Yokota K, Kojima S, Yamazaki M, Ninomiya K, Iwai Y, Aso F, Sasaki Y: [Evaluation of lumbar tap test combined with mean cerebral blood flow measurement and electroencephalographic topography on idiopathic normal pressure hydrocephalus patients]. No Shinkei Geka 32: 247– 255, 2004. (Japanese with English abstract) [PubMed] [Google Scholar]
- 19). Takeuchi T, Kasahara E, Iwasaki M: Clinical characteristics and serum-alpha-1-antichymotrypsin levels in atypical idiopathic normal pressure hydrocephalus. Current Tr Hyd (Tokyo) 7: 69– 73, 1997. [Google Scholar]
- 20). Takeuchi T, Kasahara E, Iwasaki M: Idiopathic normal pressure hydrocephalus accompanied by cerebral atrophy (atypical idiopathic normal pressure hydrocephalus: AINPH)—comparison lumbar tap test with alpha-1-antichymotrypsin, cerebral arterio venous difference of oxygen content, cerebrospinal fluid outflow resistance. Current Tr Hyd (Tokyo) 9: 84– 89, 1999. [Google Scholar]
- 21). Takeuchi T, Kasahara E, Iwasaki M: [Clinical characteristics and indications for shunting in patients with idiopathic normal pressure hydrocephalus with brain atrophy (atypical normal pressure hydrocephalus)]. No Shinkei Geka 28: 505– 515, 2000. (Japanese with English abstract) [PubMed] [Google Scholar]
- 22). Takeuchi T, Kasahara E, Iwasaki M, Mima T, Mori K: Indications for shunting in patients with idiopathic normal pressure hydrocephalus presenting with dementia and brain atrophy (atypical idiopathic normal pressure hydrocephalus). Neurol Med Chir (Tokyo) 40: 38– 46; discussion 46–47, 2000. [DOI] [PubMed] [Google Scholar]
- 23). Takeuchi T, Uki J, Yagi S, Inoue H, Kawataki T, Yagi T, Shimizu Y, Hurui K, Hujita T, Igarashi M, Kanzawa N, Shimizu T: [Evaluation of dynamic susceptibility contrast-enhanced (DSC)-MR imaging in patients with idiopathic normal pressure hydrocephalus]. Geriatr Neurosurg 23: 131– 137, 2012. (Japanese with English abstract) [Google Scholar]
- 24). Takeuchi T, Watanabe K, Shimizu T: [Relevances between cerebral circulatory disorder and symptom in idiopathic normal pressure hydrocephalus]. Jpn J Neurosurg (Tokyo) 19: 478– 483, 2010. (Japanese with English abstract) [Google Scholar]
- 25). Wang VY, Barbaro NM, Lawton MT, Pitts L, Kunwar S, Parsa AT, Gupta N, McDermott MW: Complications of lumboperitoneal shunts. Neurosurgery 60: 1045– 1048; discussion 1049, 2007. [DOI] [PubMed] [Google Scholar]
- 26). Weiner HL, Constantini S, Cohen H, Wisoff JH: Current treatment of normal-pressure hydrocephalus: comparison of flow-regulated and differential pressure shunt valves. Neurosurgery 37: 877– 884, 1995. [DOI] [PubMed] [Google Scholar]
