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Implementation of a new CSF dynamic device: a multicenter feasibility study in 562 patients

Malm, Jan (author)
Umeå universitet,Klinisk neurovetenskap
Sundström, Nina (author)
Umeå universitet,Radiofysik
Cesarini, Kristina G. (author)
Uppsala universitet,Neurokirurgi,Department of Neuroscience, Uppsala University, Uppsala, Sweden
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Edsbagge, Mikael (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology,Institute of Neuroscience and Physiology, University of Gothenburg, Göteborg, Sweden
Kristensen, B (author)
Department of Neurology, Aalborg University, Aalborg, Denmark
Leijon, Göran (author)
Östergötlands Läns Landsting,Linköpings universitet,Neurologi,Hälsouniversitetet,Neurologiska kliniken,Division of Neurology, Faculty of Health Sciences, University Hospital, Linköping, Sweden
Eklund, Anders (author)
Umeå universitet,Radiofysik
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 (creator_code:org_t)
2011-06-09
2012
English.
In: Acta Neurologica Scandinavica. - : John Wiley and Sons. - 0001-6314 .- 1600-0404. ; 125:3, s. 199-205
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objectives - The cerebrospinal fluid (CSF) infusion test is frequently used when selecting hydrocephalus patients for shunt surgery. Very little has been reported regarding adverse events. We present a prospective feasibility study. Methods -Standardized devices for measuring CSF dynamics were built and 562 patients investigated: Needles were placed by lumbar puncture (LP). An automatic CSF infusion protocol was performed. Course of events during the investigation as well as adverse events were registered. Results Preoperative evaluation of normal-pressure hydrocephalus was the most common indication (63%), followed by evaluation of shunt function (23%) and intracranial pressure recordings (14%). The LP was successfully performed in all but nine cases with 24 patients (4.3%) reporting major discomfort. Ringer infusion was performed in 474 investigations, and a valid measurement of the outflow resistance was received in 439 (93%). During the infusion phase, 17 (4%) patients reported severe headache. Infusion volume was significantly higher in patients having subjective symptoms during the infusion phase compared with those without adverse events. During 269 preoperative CSF tap tests, six (2%) patients had severe headache. Postinvestigational headache was reported by 83 (15%) patients at the 24-h follow-up. No serious adverse events were observed. Conclusion Infusion testing was safe and without serious adverse events with a high rate of successful procedures. The investigation was associated with expected mild to moderate discomfort.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

hydrocephalus
normal pressure
intracranial pressure
cerebrospinal fluid
physiology
cerebrospinal fluid dynamics
cerebrospinal fluid pressure
cerebrospinal fluid outflow resistance
infusion test
predictive test
cerebrospinal fluid shunts
MEDICINE
MEDICIN
Cerebrospinal fluid dynamics
Cerebrospinal fluid outflow resistance
Cerebrospinal fluid pressure
Cerebrospinal fluid shunts
Cerebrospinal fluid/physiology
Hydrocephalus
Infusion test
Intracranial pressure
Normal pressure
Predictive test

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