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Clinical and Radiological Evolution of Idiopathic Normal Pressure Hydrocephalus: A Critical Review
David Campo-Caballero1,2,3, Elissa Ash4,5, Alfonso Fasano6,7
1Department of Neurology, Movement Disorders Unit, Hospital Universitario Donostia, San Sebastián, Spain.
Movement Disorders Clinical Practice
|November 3, 2025
Summary
Idiopathic normal pressure hydrocephalus (iNPH) evolves heterogeneously, with gait disturbance appearing earliest. Identifying preclinical iNPH stages is crucial for effective treatment outcome assessment.
Area of Science:
- Neurology
- Neurosurgery
- Geriatrics
Background:
- The pathophysiology of idiopathic normal pressure hydrocephalus (iNPH) is not fully understood.
- Preclinical and early stages of iNPH development are largely unknown.
- Understanding iNPH evolution is critical for patient management.
Purpose of the Study:
- To investigate the clinical and radiological manifestation of iNPH.
- To understand the evolution of major clinical symptoms in non-shunted iNPH patients.
- To gain insights into the natural history of iNPH.
Main Methods:
- Critical literature review on the evolution of iNPH.
- Search for manuscripts detailing early clinical features and symptom progression.
- Categorization of literature based on clinical and radiological findings.
Main Results:
- Gait disturbance is the earliest clinical symptom of iNPH.
- Cognitive impairment varies, influenced by comorbidities; urinary dysfunction progresses from urgency to incontinence.
- Radiological features like ventricular enlargement are present preclinically, but their sequence and impact of white matter lesions are unclear.
Conclusions:
- iNPH evolution exhibits significant heterogeneity.
- Defining distinct clinical stages and identifying preclinical iNPH are essential.
- Treatment outcome assessment must account for disease stage at intervention.

