The implementation of a bundel of pharamcological interventions aimed at stress reduction leads to lower pain scores and lower use of opioids in the PACU
ID
Bron
Verkorte titel
Aandoening
Surgical population
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Our co-primary endpoints will be the proportion of patients with moderate or severe pain during their PACU stay and the proportion of patients requiring any opioid during their PACU stay.
Achtergrond van het onderzoek
Surgical stress, pain and anxiety activate a stress response that can negatively influence post-operative outcomes. This stress response can be influenced by pharmacological and non-pharmacological interventions. Opioids are the cornerstone for the treatment of moderate to severe postoperative pain. However, opioids are associated with adverse respiratory events and opioid addiction. In the U.S, 10% of opioid-naïve patients with cancer undergoing curative-intent surgery develop new persistent opioid use. Non-pharmacological interventions that are aimed at reducing stress have been shown to be cheap, low-risk interventions that affect pain perception and patient outcomes positively.
For this study, a bundle of non-pharmacological interventions will be implemented in the post-anesthesia care unit. The bundle consists of:
a) acces to natural elements in the PACU
b) positive distraction through music
c) aromatherapy
d) introduction of communication techniques that enhance placebo effects and reduce nocebo effects of communication
The effect of the bundle on pain, use of opioids, lenght-of-stay, opioid-related side-effects and adverse events, patient satisfaction and staff satisfaction will be compared to the 6 months prior to implementation of the bundle.
Doel van het onderzoek
The implementation of a bundel of pharamcological interventions aimed at stress reduction leads to lower pain scores and lower use of opioids in the PACU
Onderzoeksopzet
Before arm: 6 months data gathering
Implementation of the bundle
After arm: 6 months data gathering
Onderzoeksproduct en/of interventie
1. Acces to nature (full lenght wall coverings and leighted ceiling pannels with nature images)
2. Positive distraction through music
3. Aromatherapy
4. Comfort Talk communication course for nurses
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Patients from all surgical disciplines undergoing surgery with a minimum duration of 2 hours and a minimal hospital length of stay of 1 postoperative night will be eligible for inclusion.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Use of neuraxial anesthesia or analgesia, a history of psychiatric illness, chronic pain conditions or chronic use of opioids.
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
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In overige registers
Register | ID |
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NTR-new | NL9835 |
Ander register | METC AVL : METC 031 |