Is automated continuous monitoring of vital signs of patients on the surgical ward more effective than standard practice (= intermittent monitoring)?
ID
Bron
Aandoening
deteriorating patient; monitoring vital signs
vitaal bedreigde patient; monitoring vitale functies
Ondersteuning
-Early Sense Company, Israel
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Number of unplanned ICU admissions per 1000 admissions.
Achtergrond van het onderzoek
Many hospitals introduced rapid response teams (RRT) to provide appropriate care to patients with deteriorating vital functions. Still the number of deteriorating patients, and accompanying healthcare costs, are high and can possibly be reduced by improving the process of early detection. According to care professionals, early detection is crucial to provide timely care. The objective of this single-centre randomised pilot study is to improve early detection of deteriorating patients and investigate the (cost)effectiveness od automated continuous monitoring of patients in hospital wards compared to usual intermittent nurse monitoring. The intervention is the EverOn system. 850 patients in 1 intervention ward and 850 patients in 1 control ward will be monitored. The primary outcome measure is unplanned ICU transfers, secondary outcome measures are cardiac arrests on the ward, patient mortality on the ward, number and intensity of RRT calls and perceived safety culture. An economic evaluation will provide insight into cost effectiveness of continuous automated monitoring compared to usual intermittent nurse monitoring.
Doel van het onderzoek
Is automated continuous monitoring of vital signs of patients on the surgical ward more effective than standard practice (= intermittent monitoring)?
Onderzoeksopzet
T=0 months; start of inclusions;
T=12 months; end of inclusions.
Onderzoeksproduct en/of interventie
1. Automated continuous patientmonitoring;
2. Intermittent patientmonitoring.
Publiek
Albert Schweitzerplaats 25
K.L. So
Dordrecht 3300 AK
The Netherlands
+31 (0)78 6542675
r.so@asz.nl
Wetenschappelijk
Albert Schweitzerplaats 25
K.L. So
Dordrecht 3300 AK
The Netherlands
+31 (0)78 6542675
r.so@asz.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Adult patients (18 years and older);
2. Able to consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Patients younger than 18 years;
2. Unable to consent.
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiƫnten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL3621 |
NTR-old | NTR3787 |
Ander register | METC of Albert Schweitzer Hospital, Dordrecht : 2012.20 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |