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Camino icp monitor

Manufactured by Integra LifeSciences
Sourced in United States

The Camino ICP Monitor is a medical device designed to measure and monitor intracranial pressure (ICP) in patients. It provides continuous, real-time data on ICP levels, allowing healthcare professionals to track changes and make informed clinical decisions.

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9 protocols using camino icp monitor

1

Invasive Intracranial Pressure Monitoring

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Arterial blood pressure (ABP) was obtained through either radial or femoral arterial lines connected to pressure transducers (Baxter Healthcare Corp. CardioVascular Group, Irvine, CA, or similar devices). ICP was acquired via an intra-parenchymal strain gauge probe (Codman ICP MicroSensor; Codman & Shurtleff Inc., Raynham, MA), parenchymal fiber optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ, United States; https://www.integralife.com/) or external ventricular drain (in 3 patients). All signals were recorded using digital data transfer or digitized via an A/D converter (DT9801; Data Translation, Marlboro, MA), where appropriate, sampled at frequency of 100 Hertz (Hz) or higher, using the ICM + software (Cambridge Enterprise Ltd, Cambridge, UK, http://icmplus.neurosurg.cam.ac.uk) or Moberg CNS Monitor (Moberg Research Inc, Ambler, PA, USA) or a combination of both. Signal artifacts were removed using both manual and automated methods prior to further processing or analysis.
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2

Multimodal Intracranial Pressure Monitoring

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Arterial blood pressure (ABP) was obtained through either radial or femoral arterial lines connected to pressure transducers. ICP was acquired via an intra-parenchymal strain gauge probe (Codman ICP MicroSensor; Codman & Shurtleff Inc., Raynham, MA), parenchymal fiber optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ, USA; https://www.integralife.com/) or external ventricular drain. All signals were recorded using digital data transfer or digitized via an A/D converter (DT9801; Data Translation, Marlboro, MA), where appropriate, sampled at frequency of 100 Hz (Hz) or higher, using the ICM+ software (Cambridge Enterprise Ltd., Cambridge, UK; http://icmplus.neurosurg.cam.ac.uk) or Moberg CNS Monitor (Moberg Research Inc., Ambler, PA, USA) or a combination of both. Signal artifacts were removed using automated methods prior to further processing or analysis.
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3

Comprehensive Traumatic Brain Injury Database

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For this ongoing prospective TBI database, all patient demographics, injury and treatment information were either manually collected by a medical professional or automatically recorded using Clinisoft (Centricity Critical Care, CCC, General Electric Company, Boston). The drug infusion rates and physiological variables were recorded with Clinisoft, which included the timestamped pharmacological and physiological data. In this study, continuous infusions as well as bolus doses of the sedatives propofol, midazolam, morphine, fentanyl and alfentanil and the vasopressor agents dobutamine, noradrenaline, vasopressin, and ephedrine, and the physiological variables (ABP and ICP) were analyzed.
Arterial blood pressure (ABP) was obtained through either radial or femoral arterial lines connected to pressure transducers (Baxter Healthcare Corp. CardioVascular Group, Irvine, CA, or similar devices). ICP was acquired via an intra-parenchymal strain gauge probe (Codman ICP MicroSensor; Codman & Shurtleff Inc., Raynham, MA), raumedic catheter Neurovent-P (Raumedic AG, Münchberg, Germany), parenchymal fiber optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ, United States; https://www.integralife.com/) or using external ventricular drains (Medtronic, Minneapolis, MN). Again, both ABP and ICP data were directly linked to a Clinisoft database.
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4

Invasive Neuromonitoring for Intracranial Pressure

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Arterial blood pressure (ABP) was obtained through arterial lines connected to pressure transducers. ICP was acquired from an intra-parenchymal strain gauge probe (Codman ICP MicroSensor; Codman & Shurtleff Inc., Raynham, MA) and parenchymal fiber optic pressure sensor (Camino ICP Monitor; Integra Life Sciences, Plainsboro, NJ, United States; https://www.integralife.com/). PbtO2 monitoring occurred via invasive parenchymal monitoring (Licox probe; Integra, Licox Brain Oxygen Monitoring System, Plainboro, NJ), typically placed in the frontal lobe. All signals were recorded using digital data transfer or digitized via an A/D converter (DT9803; Data Translation, Marlboro, MA), where appropriate; sampled at frequency of 100 Hz (Hz) or higher, using the ICM+ software (Cambridge Enterprise Ltd., Cambridge, UK, http://icmplus.neurosurg.cam.ac.uk) or Moberg CNS Monitor (Moberg Research Inc., Ambler, PA, USA, https://www.moberg.com) or a combination of both. Signal artifacts were removed using both manual and automated methods prior to further processing or analysis.
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5

High-Resolution Neuromonitoring in Neurocritical Care

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High-resolution signals were collected using either ICM+ software (Cambridge Enterprise Ltd, Cambridge, U.K.; http://icmplus.neurosurg.cam.ac.uk), Moberg CNS monitor (Moberg Research Inc, Ambler, PA, USA; https://www.moberg.com), or both. Blood pressure was obtained through arterial lines connected to pressure transducers. High-resolution ICP (ICPHR) was acquired from either an intraparenchymal strain gauge probe (Codman ICP MicroSensor, Codman and Shurtleff Inc., Raynham, MA, USA), a parenchymal fiber optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ, USA; https://www.integralife.com/), or an external ventricular drain. Detailed data collection and pre-processing methods (i.e., artefact cleaning and down-sampling to ten-second averaged time series) applied to high resolution signals in our study have been described previously.21 (link) Ten-second averaged ICP (ICPHR_10sec) and CPP (CPPHR_10sec) time-series were retrieved for this analysis, and, from ICPHR_10sec and CPPHR_10s, we calculated ICP24/CPP24, ICPmax/CPPmin, and ICPmedian/CPPmedian as described above.
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6

Comprehensive Multimodal Monitoring in TBI

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Data were collected using ICM + software (Cambridge Enterprise Ltd., Cambridge, UK, http://icmplus.neurosurg.cam.ac.uk) or the Moberg CNS monitor (Moberg Research Inc, Ambler, PA, USA, https://www.moberg.com), or both. MAP was obtained through arterial lines connected to pressure transducers. ICP was acquired from an intraparenchymal strain gauge probe (Codman ICP MicroSensor; Codman & Shurtleff Inc., Raynham, MA) or a parenchymal fiber optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ; https://www.integralife.com/). CPP was calculated as specified above. The whole process of HR CENTER-TBI signal acquisition and data processing is described in previous publications [9 (link)].
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7

Invasive Hemodynamic Monitoring Protocol

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Arterial blood pressure (ABP) was obtained through either radial or femoral arterial lines connected to pressure transducers (Baxter Healthcare Corp. CardioVascular Group, Irvine, CA). ICP was acquired via an intra-parenchymal strain gauge probe (Codman ICP MicroSensor; Codman & Shurtleff Inc., Raynham, MA), parenchymal fiber optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ, USA; https://www.integralife.com/) or external ventricular drain. All signals were recorded using digital data transfer or digitized via an A/D converter (DT9801; Data Translation, Marlboro, MA), where appropriate, sampled at frequency of 100 Hz or higher, using the ICM+ software (Cambridge Enterprise Ltd., Cambridge, UK, http://icmplus.neurosurg.cam.ac.uk) or Moberg CNS Monitor (Moberg Research Inc., Ambler, PA, USA) or a combination of both. Signal artifacts were removed using both manual and automated methods prior to further processing or analysis.
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8

Continuous Monitoring of Arterial and Intracranial Pressure

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Arterial blood pressure (ABP) was obtained through arterial lines connected to pressure transducers. ICP was acquired from an intra-parenchymal strain gauge probe (Codman ICP MicroSensor; Codman & Shurtleff Inc., Raynham, MA), parenchymal fibre optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ, United States; https://www.integralife.com/). All signals were recorded using digital data transfer or digitized via an A/D converter (DT9803; Data Translation, Marlboro, MA), where appropriate; sampled at frequency of 100 Hertz (Hz) or higher, using the ICM+ software (Cambridge Enterprise Ltd, Cambridge, UK, http://icmplus.neurosurg.cam.ac.uk) or Moberg CNS Monitor (Moberg Research Inc, Ambler, PA, USA, https://www.moberg.com) or a combination of both. Signal artefacts were removed using both manual and automated methods prior to further processing or analysis.
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9

Monitoring Arterial Blood Pressure and ICP

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Arterial blood pressure (ABP) was obtained through either radial or femoral arterial lines connected to pressure transducers (Baxter Healthcare Corp. CardioVascular Group, Irvine, CA). ICP was acquired via an intra-parenchymal strain gauge probe (Codman ICP MicroSensor; Codman and Shurtleff Inc., Raynham, MA), parenchymal fiber optic pressure sensor (Camino ICP Monitor, Integra Life Sciences, Plainsboro, NJ; https://www.integralife.com) or external ventricular drain. All signals were recorded using digital data transfer or digitized via an A/D converter (DT9801; Data Translation, Marlboro, MA), where appropriate, sampled at frequency of 100 Hz or higher, using the ICM+ software (Cambridge Enterprise Ltd, Cambridge, UK; http://icmplus.neurosurg.cam.ac.uk) or Moberg CNS Monitor (Moberg Research Inc, Ambler, PA) or a combination of both. Signal artifacts were removed using both manual and automated methods prior to further processing or analysis.
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