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Volumetric effect of shunt adjustments in normal pressure hydrocephalus: a randomized, double-blind trial
Uppsala Univ, Sweden; Ostersund Hosp, Sweden.
Univ Gothenburg, Sweden.
Linköpings universitet, Institutionen för biomedicinska och kliniska vetenskaper, Avdelningen för cell- och neurobiologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Sinnescentrum, Neurologiska kliniken i Linköping. Uppsala Univ, Sweden.ORCID-id: 0000-0002-7504-8354
2024 (Engelska)Ingår i: Journal of Neurosurgery, ISSN 0022-3085, E-ISSN 1933-0693, Vol. 140, nr 5, s. 1493-1500Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

OBJECTIVE MRI volumetry could be used as an alternative to invasive tests of shunt function. In this study, the authors aimed to assess the difference in ventricular volume (VV) before and after surgery and at different performance levels (PLs) of the shunt. METHODS This study was a randomized, double-blind trial with a crossover design. The study sample consisted of 36 patients (25 men, 11 women) with a median age of 76 years. All patients had idiopathic normal pressure hydrocephalus (iNPH) and received a Strata shunt at the regional hospital in & Ouml;stersund, Sweden, with an initial PL of 1.5. Participants underwent MRI with volumetric sequences before surgery and four times postoperatively: at 1 month before randomization to either PL 1.0 (n = 15) or 2.5 (n = 17); at 2 months before crossover to PL 2.5 or 1.0; at 3 months before lowering the PL to 0.5; and finally, at 3 months and 1 day after surgery before resetting the PL to 1.5. VV was measured semiautomatically using quantitative MRI. Both the patient and the examiner of clinical tests and volumetry were blinded to the PL. RESULTS VV changed significantly between the presurgical level (median 129 ml) and the different shunt settings, i.e., PL 1.0 (median 115 ml), 1.5 (median 120 ml), and 2.5 (median 128 ml; p < 0.001). A unidirectional change in VV was observed for all participants between PL 1.0 and PL 2.5 (median 12 ml, range 2.1-40.7 ml, p < 0.001). No significant change was noted in VV after 24 hours at PL 0.5. Eight participants had asymptomatic subdural effusions at PL 1.0. CONCLUSIONS The consistent decrease in VV after shunt surgery and between PL 2.5 and 1.0 supports the idea that MRI volumetry could be a noninvasive method for evaluating shunt function in iNPH, preventing unnecessary shunt revisions. However, further studies on retest variability of VV as well as verification against advanced testing of shunt function are needed before a clinical implementation of this method can be performed.

Ort, förlag, år, upplaga, sidor
AMER ASSOC NEUROLOGICAL SURGEONS , 2024. Vol. 140, nr 5, s. 1493-1500
Nyckelord [en]
cerebral ventricles; cerebrospinal fluid shunt; magnetic resonance imaging; idiopathic normal pressure hydrocephalus; shunt adjustment; performance level; ventricular volume
Nationell ämneskategori
Kirurgi
Identifikatorer
URN: urn:nbn:se:liu:diva-204352DOI: 10.3171/2023.9.JNS23668ISI: 001236719300004PubMedID: 37976516OAI: oai:DiVA.org:liu-204352DiVA, id: diva2:1868711
Anmärkning

Funding Agencies|Uppsala University; Region Jaemtland Haerjedalen

Tillgänglig från: 2024-06-12 Skapad: 2024-06-12 Senast uppdaterad: 2026-04-22
Ingår i avhandling
1. Ventricular volume in normal pressure hydrocephalus: Associations with shunt settings, clinical symptoms, and cerebrospinal fluid biomarkers
Öppna denna publikation i ny flik eller fönster >>Ventricular volume in normal pressure hydrocephalus: Associations with shunt settings, clinical symptoms, and cerebrospinal fluid biomarkers
2026 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Background: Idiopathic Normal Pressure Hydrocephalus (iNPH) is a disease mainly affecting the elderly with the core symptoms of incontinence, gait and cognitive impairment. The standard treatment is cerebrospinal fluid diversion, with ventriculoperitoneal shunts being the most common choice. The main radiological finding in iNPH is the expansion of the cerebral ventricles. Recent radiological and computational advances have made the measurement of ventricular volume increasingly feasible. This thesis, comprising of four papers, focuses on the potential use of ventricular volume as a clinical tool in the postsurgical setting in iNPH. Primarily for assessing suspected shunt malfunction (paper II), but also the individualization of shunt opening pressure settings (paper IV). Additional aims were to investigate associations between ventricular volume and cerebrospinal fluid biomarkers to assess whether there is a dilution effect (paper I), and investigating improvement in excessive daytime sleepiness after surgery (paper III).

Methods: For Paper I, participants with iNPH were examined (n=136). Lumbar CSF was sampled as a part of routine care and concentrations of Amyloid β 1-42, total tau and phosphorylated tau results extracted from medical charts. Ventricular volume for the lateral and third ventricles was manually segmented on presurgical MRI using ITK-SNAP. Papers II-IV were based on one study population of participants with iNPH (n=36). All participants received Strata II shunts with adjustable performance levels (PL) corresponding to different opening pressures. Clinical evaluation and MRI were performed repeatedly: before surgery and at one, two, three months as well as three months plus one day after surgery. At surgery, all shunts were set at PL 1.5. After the first follow-up, participants were randomly assigned to either PL 1.0 or 2.5. After the two months follow-up, the assignments were crossed over. At the third follow-up, all shunts were set to PL 0.5 for the final 24 hours. Clinical assessment included the Timed Up and Go test, 10-meter walking test, Mini-Mental State Examination, continence scale, gait scale, balance scale, modified Rankin scale, and Epworth Sleepiness Scale. Ventricular volume was manually segmented using SyMRI.

Results: Ventricular volume and Amyloid β 1-42 were weakly associated (β=-0.20 p=0.027). Ventricular volume was not significantly associated with the tau forms, though the estimates were positive. Ventricular volume decreased gradually according to lower opening pressures of the shunts: the median change from presurgical to PL 2.5 was 6.9 mL (p<0.001), from PL 2.5 was PL 1.5 of 3.5 mL (p=0.01), from PL 1.5 was PL 1.0 of 9.6 mL (p<0.001). Daytime sleepiness significantly improved following surgery with a median change of -1.5 points, p=0.026, though it did not change further at subsequent follow-ups. Clinical outcomes did not change following randomization to PL 1.0 versus PL 2.5, despite an overall significant clinical improvement following surgery. Clinical outcomes were not consistently associated with change in ventricular volume. There was an increased incidence of subdural effusion after randomization to PL 1.0, occurring in eight participants (p=0.005).

Conclusions: In this thesis, ventricular volume shows substantial and predictable change with shunt adjustments, supporting its usefulness as a marker of shunt patency. In contrast, the pattern of associations between ventricular volume and CSF biomarkers does not support dilution as a primary cause of lower biomarker concentrations in iNPH, and ventricular volume does not meaningfully relate to clinical outcomes within a one-month time frame. Lower shunt opening pressures increase risk without providing clinical benefit. Another key finding was that excessive daytime sleepiness appears to be a symptom of iNPH that is amenable to treatment.

Ort, förlag, år, upplaga, sidor
Linköping: Linköping University Electronic Press, 2026. s. 95
Serie
Linköping University Medical Dissertations, ISSN 0345-0082 ; 2031
Nyckelord
Normal Pressure Hydrocephalus, Ventricular Volume, Randomized Trial, Ventriculoperitoneal Shunt, Excessive Daytime Sleepiness
Nationell ämneskategori
Neurologi
Identifikatorer
urn:nbn:se:liu:diva-223187 (URN)10.3384/9789181184662 (DOI)9789181184655 (ISBN)9789181184662 (ISBN)
Disputation
2026-05-22, Granitsalen, building 440, Campus US, Linköping, 09:00
Opponent
Handledare
Tillgänglig från: 2026-04-22 Skapad: 2026-04-22 Senast uppdaterad: 2026-04-29Bibliografiskt granskad

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Avdelningen för cell- och neurobiologiMedicinska fakultetenNeurologiska kliniken i Linköping
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