We hypothesize (based on literature) that the incidence of chronic pain in The Netherlands is around 15-20% in patients presenting to the emergency department with (acute) pain related complaints. We have no further hypothesis, because of the…
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Verkorte titel
Aandoening
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Aandoening
Chronic pain Acute pain Emergency deparment Prediction model Factors of influence Predictors Netherlands Acute pijn Chronische pijn Spoedeisende Hulp Predictie model Voorspellend model Factoren van invloed Predictoren Nederland
Betreft onderzoek met
Ondersteuning
Onderzoeksproduct en/of interventie
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Uitkomstmaten
Primaire uitkomstmaten
The primary objective is to develop and internally validate a prediction model for the transition to chronic pain (ongoing pain after 90 days) in patients with acute pain based on pre-defined predictors and patient characteristics.
For this the 90 days cumulative incidence of chronic pain has to be observed.
Achtergrond van het onderzoek
Pain is one of the most common presenting complaints in an Emergency Department (ED). Nevertheless, undertreatment of this pain remains a problem. The consequence of undertreatment of patients with acute pain could be the transitioning into chronic pain. Chronic pain, defined as pain lasting for more than 3 months, is an important cause of healthcare (over)utilization. The incidence of chronic pain is still unknown, yet the prevalence is estimated to be 18% in The Netherlands. Until now, studies have focused on the treatment of acute pain on an emergency department and on identifying the risk factors for developing chronic pain. Differentiating patients at risk of developing chronic pain in an early stage can help prevent chronification as these patients can receive efficient and adapted treatment at an earlier stage. To our knowledge there were a few initiatives towards the development of a prediction model to distinguish patients in an early stage whom have an increased risk of developing chronic pain. However, those studies only determined the risk factors for the development of chronic pain in specific groups of patients.
Objective: To develop a prediction model to distinguish patients with an increased risk of developing chronic pain in an early – acute pain- stage and target them to efficient and adapted treatment to prevent the development of chronic pain.
Study design: Prospective multicenter longitudinal study
Study population: Patients 18 years and older who presented to the ED for a pain related cause and are not hospitalized.
During the first 7 consecutive days after visiting the ED, after 90 and 180 days patients will be asked to complete a short questionnaire using a specifically developed electronic application. The questionnaires will concern questions about general health, quality of life and pain. The first period of the trial, for the duration of 1 month, traditional paper questionnaires will be used to compare response rate between the web-based electronic survey and paper questionnaires.
Doel van het onderzoek
We hypothesize (based on literature) that the incidence of chronic pain in The Netherlands is around 15-20% in patients presenting to the emergency department with (acute) pain related complaints.
We have no further hypothesis, because of the observational aspect of our study. The list of candidate predictors for the development of chronic pain is based on a literature search in 2018.
Onderzoeksopzet
1st August
Start period 1 ( Start with paper questionnaires in Franciscus Gasthuis & Vlietland)
1st September
Continuation of period 1 (Start with electronical questionaires in Franciscus Gasthuis & Vlietland)
End of paper questionnaires
1st October
Stop with period 1
Start with period 2 (inclusion in all hospitals with electronic questionnaires)
January 2019 Introduction first article
February 2019 Methods first article
March 2019 Interim analysis & start syntax
April 2019
1st May 2019 END of inclusion period in all hospitals
June 2019 Statistical analysis
July 2019 Statistical analysis
August 2019 Finalize article
September 2019 Finalize article
October 2019 Finalize article
Onderzoeksproduct en/of interventie
No interventions
Publiek
Wetenschappelijk
Leeftijd
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
* Acute pijn (pijn < 48 uur bestaand) als voornaamste klacht voor SEH bezoek
* Ontslag naar huis na behandeling op de SEH
* Gegeven informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
* Indien ten tijden van SEH bezoek ook al chronische pijn op de locatie van de ingangsklacht
(N.B. chronische pijn op zichzelf is geen exclusie criterium)
* Acute pijn binnen 7 dagen na een chirurgische ingreep Acute
* Indien patiënt direct na het SEH bezoek wordt opgenomen in het ziekenhuis
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten 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 | NL7079 |
NTR-old | NTR7277 |
Ander register | : 2018-39 |
Samenvatting resultaten
borderline statistically significant with an odds ratio of 1.45 (95% confidence interval: 0.99–2.13, P 5 0.054). Various sensitivity analyses using a different (V)NRS at discharge and different definitions of chronic pain at 90 days showed a significant difference in the chronification of pain.
Conclusion: This study suggests that pain intensity at discharge from the ED, regardless of the localization or cause of pain,
increased the risk of developing chronic pain. By distinguishing patients at risk and providing an effective treatment, chronic pain
and the associated burden of disease might be preventable. "