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Invasive intracranial pressure monitoring takes on essential importance in patients with traumatic brain injury and in all cerebral pathologies in which intracranial hypertension is the main cause of death. Prolonged Intracranial Hypertension has been related to poor outcome and its occurrence has therefore to be assessed as soon as possible. Invasive intracranial pressure monitoring performed by placing an intracerebral catheter is currently the gold standard technique for continuous ICP invasive monitoring. This maneuver has usually been performed by neurosurgeons, but recently this procedure has more often been carried out by intensivists, at the bedside. Management of intracranial pressure handling and treatment is currently achieved by joint decisions between neurosurgeons and intensive care physicians, but differences in logistic matters and in the executive availability could impact on the dose of intracranial pressure to which patient is exposed. The aim of this study is to compare timing of invasive intracranial pressure monitoring placement performed by intensive care physicians and neurosurgeons and to detect possible differences in the incidence of complications between the two groups.
This perspective, multicentric and observational study will enroll patients at risk for developing intracranial hypertension, for whom it is thought invasive ICP monitoring is crucial for achieving the most appropriate treatment. Indication to invasive ICP monitoring and its modalities will be set through a joint decision between neurosurgeons and intensive care physician, which will be led by clinical and instrumental data. This study will be carried out in Intensive Care Unit and in Neurosurgery department. Sample size assessment: Sample size assessment has been performed by Monte Carlo simulation (B=500). Assuming a timing decrease (T2-T1) of 20 minutes in the procedure carried out by an intensivist compared to a neurosurgeon, with a mean time of 100 minutes, a standard deviation between center and intra-center of 10 minutes, 16 centers, each one with the same number of patients and a balance 1:1 between the two groups (intensivist:neurosurgeon), a total number of 64 patients (32 treated by intensivists and 32 by neurosurgeons), it allows us to evaluate the interest effect with a power of at least 95%, and a significance level of 5%. This elevated power has been decided according to the simplicity of the assumed design (same number of entities and conditions for center) and not evaluable in his real configuration. Statistical analysis plan: Delta time in the placement of invasive ICP monitoring is assumed as T2-T1, declared in minutes. Typology operator (neurosurgeon vs intensivist) impact on delta time will be evaluated through a multilevel model elaborated with a linear mixed model. The model will assume the center in which the maneuver is carried out as clustering factor. The place where the maneuver is carried out (intensive care unit vs operating room) and the confidence in performing the procedure (routine vs sporadic, defined as less than 5 times a year) will be assumed as covariates. The incidence of complications, valued as a binary variable, will be evaluated through logistic model GLMM (generalized linear mixed model) with the organization exposed in the dedicated data element. Timings are defined as: * T0: suspect of pathology at risk for developing intracranial hypertension * T1: neurointensive and neurosurgical indication to invasive ICP monitoring (it can be the time when brain CT is performed or, in the absence of a brain CT, the time at which indication to invasive ICP monitoring is stated) * T2: skin incision at skull for BOLT/EVD placement Place of positioning: The place (intensive care unit or operating room) where the procedure is carried out must be declared.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Ospedale "M. Bufalini", Intensive Care Unit (U.O. Anestesia e Rianimazione), Neurosurgery Unit (U.O. Neurochirurgia)
Cesena, Forlì-Cesena, Italy
Azienda Socio Sanitaria Territoriale Ovest Milanese (Neurosurgery Unit)
Legnano, Milano, Italy
Ospedale Papa Giovanni XXIII, Intensive Care Unit (U.O. Anestesia e rianimazione 2), Neurosurgery Unit (U.O. Neurochirurgia)
Bergamo, Italy
Spedali Civili di Brescia, Neurosurgery Unit (U.O. Neurochirugia)
Brescia, Italy
Spedali Civili, Neuro Critical Care Unit (U.O. Anestesia e Rianimazione 2)
Brescia, Italy
Azienda Ospedaliera Sant'Anna e San Sebastiano di Caserta (Neurosurgery Unit)
Caserta, Italy
Ospedale Sant'Anna di Como, Intensive Care Unit (U.O. Anestesia e Rianimazione 2), Neurosurgery Unit (U.O. Neurochirurgia)
Como, Italy
Ospedale Policlinico San Martino (Neurosurgery Unit)
Genova, Italy
Ospedale Santa Maria Goretti (Neurosurgery Unit)
Latina, Italy
Ospedale A. Manzoni (Intensive Care Unit and Neurosurgery Unit)
Lecco, Italy
Start Date
April 27, 2021
Primary Completion Date
May 3, 2022
Completion Date
May 3, 2022
Last Updated
September 16, 2021
64
ESTIMATED participants
Time necessary for ICP catheter placement by Intensive Care Physician vs Neurosurgeon following indication
OTHER
Lead Sponsor
Università degli Studi di Brescia
NCT07440277
NCT06254534
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT03556085