1) Epidemiology of postoperative pain What is the correlation between pain intensity scores and type of surgical procedure in relation to patient characteristics and analgesia? Is it possible to specify surgical procedures indicating its pain…
ID
Bron
Aandoening
Postoperative Pain
Pain Management
Anaesthesia
Surgery
Ondersteuning
Oosterpark 9
1091 AC Amsterdam
The Netherlands
Attention: prof. dr. M.A.A.J. van den Bosch
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1) Epidemiology of postoperative pain<br>
To establish the epidemiology of postoperative pain versus surgical procedures and type of analgesia; pain scores vs. different procedures, location surgery, patient characteristics and combinations of aforementioned. To be able to identify procedures and patients with a high risk of severe postoperative pain and to be able tot identify surgical indicator procedures that can be used as a correction model for differences in surgical case mix between hospitals.<br><br>
2) Risk and prediction<br>
To Identify patient- and surgical procedure characteristics correlating with severe postoperative pain
<br><br>
3) Best practice advice<br>
Drafting a best practice advise for procedure specific postoperative pain treatment.
Achtergrond van het onderzoek
Introduction:
Pain intensity registration after surgery remains a major challenge due to poor compliance and outdated unidimensional assessment using VAS or NRS. No study has yet explored the epidemiology and quality of pain registration following many types of surgery in everyday day clinical practice amongst different Dutch general and academic hospitals. We want to conduct a retrospective observational study using patient data from 5 different hospitals with OLVG as primairy centre. The goal is to improve postoperative pain management, predict severe postoperative pain and develop procedure specific, optimized pain-treatment protocols with automated reminders and decision support build in PDMS. Futhermore to identify standardized surgical indicator procedures that can be used as a correction model for differences in surgical case mix between hospitals.
Objectives:
1) Epidemiology of postoperative pain
Primary Objective: To establish the epidemiology of postoperative pain versus surgical procedures and type of analgesia; pain scores vs. different procedures, location surgery, patient characteristics and combinations of aforementioned. To be able to identify procedures and patients with a high risk of severe postoperative pain and to be able to identify surgical indicator procedures that can be used as a correction model for differences in surgical case mix between hospitals.
Secondary Objective: To provide a ranking of surgical procedures in relationship to severe postoperative pain, administered analgesics and locoregional techniques.
Secondary objective: To identify indicator surgical procedures with high risk of postoperative pain
Secondary objective: To determine the quality and quantity of VAS and NRS registration for post operative pain intensity measurement
2) Risk and prediction
Primary Objective: To Identify patient- and surgical procedure characteristics correlating with severe postoperative pain
Secondary Objective: To design a model predicting postoperative and form the basis of a decision support application customizing pain treatment for specific groups of patients and to the individual patient’s needs.
3) Best practice advice
Primary Objective: Drafting a best practice advise for procedure specific postoperative pain treatment.
Secondary Objective: build an algorithm advising for the best (procedure specific) post operative pain treatment build in the PDMS or an independent application to tailor pain treatment to the patients needs and facilitate early intervention.
Study Population:
All adult non-cardiac non-day care surgical patients who had surgery between October 1st 2015 and April 1st 2017 in OLVG, AMC, UMCU, WFG and LUMC. We estimate that between 80,000 and 120,000 patient files will be eligible for data analysis.
Inclusion: patients aged 18y or older, elective non day care surgery and surgical emergency procedures with an admission of at least 24hr
Exclusion: Day care surgery, palliative surgery, re-do surgical procedures, repeated surgery within the same hospital stay or 72 hours after the first surgery. Sequential surgeries during the same stay, rare surgical procedures performed less than 5 times a year.
Methods:
Research data will be collected by querying the patient data management system of each hospital for the period between October 1st 2015 and April 1st 2017– by an information specialist. Information on pain management protocols will be obtained by checking site specific protocol data warehouse.
Data analysis will be carried out in 3 phases. Phase 1: evaluating the epidemiology of postoperative pain. Phase 2: identifying risk factors for severe postoperative pain and building a prediction model. Phase 3: comparing pain intensity scores in relation tot administered analgesic and pain protocols amongst the participating hospitals for a best practice recommendation.
Doel van het onderzoek
1) Epidemiology of postoperative pain
What is the correlation between pain intensity scores and type of surgical procedure in relation to patient characteristics and analgesia? Is it possible to specify surgical procedures indicating its pain intensity ranking from severe to no pain using pain intensity data from PDMS up to 72 hr in relationship with the type of postoperative analgesia technique and variation in surgical case mix amongst the cooperating hospitals?
2) Risk and prediction
Which patient characteristics and surgical procedures are predictors for severe postoperative pain? Is it possible to develop a postoperative pain prediction rule?
3) Best practice advice
Is it possible to compose a best practice advice for (procedure specific) treatment of post operative pain based on the epidemiology of postoperative pain in relation to postoperative analgesia technique using data from different hospitals?
Onderzoeksopzet
Start study: October 1st 2017
End study: March 1st 2018
Onderzoeksproduct en/of interventie
not applicable
Publiek
B. Thiel
Oosterparkstraat 9
Amsterdam 1091 AC
The Netherlands
+31 (0)20 59992512 (dect: 4773)
b.thiel@olvg.nl
Wetenschappelijk
B. Thiel
Oosterparkstraat 9
Amsterdam 1091 AC
The Netherlands
+31 (0)20 59992512 (dect: 4773)
b.thiel@olvg.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Patients aged 18y or older, elective non day care surgery and surgical emergency procedures with an admission of at least 24hr
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Day care surgery, palliative surgery, , repeated surgery within the same hospital stay or 72 hours after the first surgery. rare surgical procedures performed less than 5 times a year.
Opzet
Deelname
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 | NL7030 |
NTR-old | NTR7235 |
Ander register | OLVG : WO17.051 |