The main goal of the study is to assess the incidence of respiratory events using the IPI device.
ID
Bron
Verkorte titel
Aandoening
Postoperative condition
Respiration
Monitoring
Postoperatieve conditie
Ademhaling
Monitoring
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The function of the IPI monitor and the number of IPI-events during the first day and night after after anesthesia and the use of opiods (ie. number of IPI events, IPI AUC) are the main end-points.
Achtergrond van het onderzoek
In 40 patients following elective surgery under general anesthesia that require opioid pain relief the IPI will be measured at the PACU (post anesthesia care unit) during the first postoperative night (end of study 8 AM 1st postoperative day). In these 40 patients the IPI will be measured but no action will be undertaken based on the IPI. Local protocol will be followed in which nurses base their decision to intervene (ie. stimulate the patient, call for help) on sedation level and respiratory rate. The study will generate data on the incidence of respiratory events in the study population to be potential used in a next IPI-study where the focus is on interventions as a result of the IPI.
Doel van het onderzoek
The main goal of the study is to assess the incidence of respiratory events using the IPI device.
Onderzoeksopzet
The observation will start from the arrival of the patient on the PACU untill 8 am on the first postoperative day
Onderzoeksproduct en/of interventie
Postoperative respiratoir condition
Publiek
Department of Anesthesiology,
P.O. Box 9600
Albert Dahan
Albinusdreef 2
Leiden 2300 RC
The Netherlands
+31 (0)71 5262301
a.dahan@lumc.nl
Wetenschappelijk
Department of Anesthesiology,
P.O. Box 9600
Albert Dahan
Albinusdreef 2
Leiden 2300 RC
The Netherlands
+31 (0)71 5262301
a.dahan@lumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Adult (> 17 years) ASA 1-3 patients that underwent elective surgery under general anesthesia who require opioid pain relief and are able to wear or retain the IPI device post-operatively.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Patients having ENT, facial or neurological/ brain (head) surgery or are not able to give informed consent.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL5231 |
| NTR-old | NTR5455 |
| Ander register | METC LUMC : P15.170 |