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Direct intra-abdominal pressure monitoring via piezoresistive pressure measurement: a technical note

BACKGROUND: Piezoresistive pressure measurement technique (PRM) has previously been applied for direct IAP measurement in a porcine model using two different devices. Aim of this clinical study was to assess both devices regarding complications, reliability and agreement with IVP in patients undergo...

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Detalles Bibliográficos
Autores principales: Otto, Jens, Kaemmer, Daniel, Binnebösel, Marcel, Jansen, Marc, Dembinski, Rolf, Schumpelick, Volker, Schachtrupp, Alexander
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2678082/
https://www.ncbi.nlm.nih.gov/pubmed/19383161
http://dx.doi.org/10.1186/1471-2482-9-5
Descripción
Sumario:BACKGROUND: Piezoresistive pressure measurement technique (PRM) has previously been applied for direct IAP measurement in a porcine model using two different devices. Aim of this clinical study was to assess both devices regarding complications, reliability and agreement with IVP in patients undergoing elective abdominal surgery. METHODS: A prospective cohort study was performed in 20 patients randomly scheduled to receive PRM either by a Coach(®)-probe or an Accurate++(®)-probe (both MIPM, Mammendorf, Germany). Probes were placed on the greater omentum and passed through the abdominal wall paralleling routine drainages. PRM was compared with IVP measurement by t-testing and by calculating mean difference as well as limits of agreement (LA). RESULTS: There were no probe related complications. Due to technical limitations, data could be collected in 3/10 patients with Coach(® )and in 7/10 patients with Accurate++(®). Analysis was carried out only for Accurate++(®). Mean values did not differ to mean IVP values. Mean difference to IVP was 0.1 ± 2.8 mmHg (LA: -5.5 to 5.6 mmHg). CONCLUSION: Direct IAP measurement was clinically uneventful. Although results of Accurate++(® )were comparable to IVP, the device might be too fragile for IAP measurements in the clinical setting. Local ethical committee trial registration: EK2024