Two-Years Comparative Clinical Outcome in the Shunt Treatment of Disproportionately Enlarged Subarachnoid Space Hydrocephalus (DESH) and Non-DESH Idiopathic Normal Pressure Hydrocephalus
Keywords:
idiopathic normal pressure hydrocephalus (iNPH), disproportionately enlargement of subarachnoid space with hydrocephalus (DESH), idiopathic normal pressure hydrocephalus grading scale (iNPHGS), modified Rankin scale (mRS), bulbar symptoms, psychiatric symptomsAbstract
Introduction: Idiopathic normal pressure hydrocephalus (iNPH) is known to be a treatable cause of disability and morbidity in elderly patients such as gait abnormality, cognitive decline, and urinary impairment. There are two types of iNPH, disproportionately enlargement subarachnoid space hydrocephalus (DESH) and non-DESH. This study aimed to compare, two-years outcome of treatment in both DESH and non-DESH.
Methods: We conducted a retrospective cohort study of iNPH patients who received surgical treatment between September 2014 and November 2016. Demographic data and baseline clinical were collected. The patient was classified into DESH and non-DESH iNPH groups. Outcomes after treatment such as idiopathic normal pressure hydrocephalus grading scale (iNPHGS), modified Rankin scale (mRS), bulbar symptoms, psychiatric symptoms, and adverse outcomes were analyzed during immediate post-operation, first visit, 4-6 months, 1 year, and 2 years after surgery. The positive outcome was defined as improvement in iNPHGS or mRS at such time.
Results: Patients with iNPH (n =106) were classified as DESH iNPH (n=72) and non-DESH (n = 34). There was a favorable improvement in both groups during the first visit (73.5% in non-DESH and 88.9% in DESH, p = 0.044), 4-6 months (72.7% in non-DESH and 79.4% in DESH group, p = 0.452), 1 year (65.9% in non-DESH group and 79.7% in DESH, p = 0.141) and 2 years (66.7% in non-DESH and 59.6% in DESH group, p = 0.54). There was no difference in outcome according to the type of surgery either ventriculoperitoneal (VP) or lumboperitoneal (LP) shunt at any time.
Conclusion: All patients with a diagnosis of iNPH should receive surgical treatment with or without DESH findings on radiographic imaging. There was a favorable positive outcome with minor shunt-related complications until at least 2 years after surgery. There were no differences between any shunting surgery at any time (either VP or LP shunt).
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(NESDB), N.E.a.S.D.B. Older statistic. 2019 [cited 2019; Available from: http://social.nesdc.go.th/SocialStat/StatReport_Final.aspx?reportid=697&template=2R1C&yeartype=M&subcatid=116.
Muangpaisan W, Petcharat C, Srinonprasert V. Prevalence of potentially reversible conditions in dementia and mild cognitive impairment in a geriatric clinic. Geriatr Gerontol Int. 2012;12(1):59-64.
Evans Wa. An Encephalographic Ratio For Estimating Ventricular Enlargement And Cerebral Atrophy. Arch NeurPsych. 1942;47(6):931–937.
Relkin N, Marmarou A, Klinge P, Bergsneider M, Black PM. Diagnosing idiopathic normalpressure hydrocephalus. Neurosurgery. 2005;57(3 Suppl):S4-16; discussion ii-v.
Halperin JJ, Kurlan R, Schwalb JM, Cusimano MD, Gronseth G, Gloss D. Practice guideline: Idiopathic normal pressure hydrocephalus: Response to shunting and predictors of response: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology. Neurology. 2015;85(23):2063-71.
Mori E, Ishikawa M, Kato T, Kazui H, Miyake H, Miyajima M, et al. Guidelines for management of idiopathic normal pressure hydrocephalus: second edition. Neurol Med Chir (Tokyo). 2012;52(11):775-809.
Bovonsunthonchai S, Witthiwej T, Ngamsombat C, Sathornsumetee S, Vachalathiti R, Muangpaisan W, et al. Effect of spinal tap test on the performance of sit-to-stand, walking, and turning in patients with idiopathic normal pressure hydrocephalus. Nagoya J Med Sci. 2018;80(1):53-60.
Andersson J, Rosell M, Kockum K, Söderström L, Laurell K. Challenges in diagnosing normal pressure hydrocephalus: Evaluation of the diagnostic guidelines. eNeurologicalSci. 2017;7:27-31.
Bergsneider M, Black PM, Klinge P, Marmarou A, Relkin N. Surgical management of idiopathic normalpressure hydrocephalus. Neurosurgery. 2005;57(3 Suppl):S29-39; discussion ii-v.
Miyajima M, Kazui H, Mori E, Ishikawa M; , on behalf of the SINPHONI-2 Investigators. One-year outcome in patients with idiopathic normal-pressure hydrocephalus: comparison of lumboperitoneal shunt to ventriculoperitoneal shunt. J Neurosurg. 2016;125(6):1483-92.
Jo KW, Kim Y, Park GY, Park IS, Jang Y, Gyun SD, et al. Oropharyngeal dysphagia in secondary normal pressure hydrocephalus due to corticobulbar tract compression: cases series and review of literature. Acta Neurochir (Wien). 2017;159(6):1005-11.
Chankaew E, Srirabheebhat P, Manochiopinig S, Witthiwej T, Benjamin I. Bulbar dysfunction in normal pressure hydrocephalus: a prospective study. Neurosurg Focus. 2016;41(3):E15.
Peterson KA, Savulich G, Jackson D, Killikelly C, Pickard JD, Sahakian BJ. The effect of shunt surgery on neuropsychological performance in normal pressure hydrocephalus: a systematic review and meta-analysis. J Neurol. 2016;263(8):1669-77.
Jaraj D, Wikkelsø C, Rabiei K, Marlow T, Jensen C, Östling S, et al. Mortality and risk of dementia in normal-pressure hydrocephalus: A population study. Alzheimers Dement. 2017;13(8):850-7.
Radovnicky, T., Adamek, D., Derner, M. Sames M. Disproportionately enlarged subarachnoid space hydrocephalus presence in patients with idiopathic normal pressure hydrocephalus. Fluids Barriers CNS 2015;12 (Suppl 1), P43.
Shinoda N, Hirai O, Hori S, Mikami K, Bando T, Shimo D, Kuroyama T, Kuramoto Y, Matsumoto M, Ueno Y. Utility of MRI-based disproportionately enlarged subarachnoid space hydrocephalus scoring for predicting prognosis after surgery for idiopathic normal pressure hydrocephalus: clinical research. J Neurosurg. 2017;127(6):1436-42.
Ishikawa M, Oowaki H, Takezawa M, Takenaka T, Yamada S, Yamamoto K, et al. Disproportionately Enlarged Subarachnoid Space Hydrocephalus in Idiopathic Normal-Pressure Hydrocephalus and Its Implication in Pathogenesis. Acta Neurochir Suppl. 2016;122:287-90.
Craven CL, Toma AK, Mostafa T, Patel N, Watkins LD. The predictive value of DESH for shunt responsiveness in idiopathic normal pressure hydrocephalus. J Clin Neurosci. 2016;34:294-8.
Kubo Y, Kazui H, Yoshida T, Kito Y, Kimura N, Tokunaga H, et al. Validation of grading scale for evaluating symptoms of idiopathic normal-pressure hydrocephalus. Dement Geriatr Cogn Disord. 2008; 25(1):37-45.
Cabral D, Beach TG, Vedders L, Sue LI, Jacobson S, Myers K, Sabbagh MN. Frequency of Alzheimer’s disease pathology at autopsy in patients with clinical normal pressure hydrocephalus. Alzheimers Dement. 2011;7(5):509-13.
Pomeraniec IJ, Bond AE, Lopes MB, Jane JA Sr. Concurrent Alzheimer’s pathology in patients with clinical normal pressure hydrocephalus: correlation of high-volume lumbar puncture results, cortical brain biopsies, and outcomes. J Neurosurg. 2016;124(2):382-8.
Graff-Radford NR, Jones DT. Normal Pressure Hydrocephalus. Continuum (Minneap Minn). 2019;25(1):165-86.
Espay AJ, Da Prat GA, Dwivedi AK, Rodriguez-Porcel F, Vaughan JE, et al. Deconstructing normal pressure hydrocephalus: Ventriculomegaly as early sign of neurodegeneration. Ann Neurol. 2017;82(4):503- 13.
Lalou AD, Czosnyka M, Donnelly J, Pickard JD; FMedSci; Nabbanja E, Keong NC, Garnett M, Czosnyka ZH. Cerebral autoregulation, cerebrospinal fluid outflow resistance, and outcome following cerebrospinal fluid diversion in normal pressure hydrocephalus. J Neurosurg. 2019;130(1):154-62.
Giordan E, Palandri G, Lanzino G, Murad MH, Elder BD. Outcomes and complications of different surgical treatments for idiopathic normal pressure hydrocephalus: a systematic review and metaanalysis. J Neurosurg. 2018;131(4):1024-36.
Pyykkö OT, Nerg O, Niskasaari HM, Niskasaari T, Koivisto AM, Hiltunen M, et al. Incidence, Comorbidities, and Mortality in Idiopathic Normal Pressure Hydrocephalus. World Neurosurg. 2018;112:e624-e631.
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