We hypothesize that a reduction of the current radiographic follow-up protocol for patients with ankle and wrist fractures will lead to significant cost savings without compromising quality of care
ID
Bron
Verkorte titel
Aandoening
distal radius fractures, ankle fractures
pols fracturen, enkel fracturen
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary outcome is area-specific functional status, which for both types of fracture will be measured using Dutch versions of the following questionnaires:
<br><br>
For ankle fractures the Olerud and Molander ankle score (OMAS).<br>
For wrist fractures the Disabilities of the Arm, Shoulder and Hand Score (DASH).
Achtergrond van het onderzoek
Background: Extremity fractures such as ankle and wrist fractures are a common and costly health care problem affecting all age groups. The management of patients with these fractures depends on fracture type and loss of congruity of the involved joint; resulting in cast immobilization or operative treatment. Loss of congruity or displacement leading to uneven joint loading, osteoarthritis and a increased probability of a poor functional outcome, should be identified within the first 2 weeks following trauma, based upon conventional radiographic imaging to determine optimal treatment. After this period, routine radiographs and clinical assessments are often scheduled for monitoring the bone-healing process and clinical outcomes, respectively. Many currently used protocols for timing of radiographic assessment describe standard imaging at 1, 2, 6 and 12 weeks following baseline. However, it is questionable whether routine radiography following the initial follow-up (i.e. 2-weeks post trauma) is cost-effective.
The aim of this study is to investigate whether a reduction of the current radiographic follow-up protocol in patients with uncomplicated wrist or ankle fractures leads to significant cost savings without compromising quality of care.
Methods/design: In a multicentre randomized controlled non-inferiority trial, 418 patients aged 18 years or older will be included, of whom 279 ankle fracture patients and 139 wrist fracture patients. Patients will be randomized in 2 groups. Group 1 is to receive usual care, consisting of routine radiographs at baseline and after 1, 2, 6 and 12 weeks of follow-up. Group 2 is to receive radiographs beyond the initial 2-week follow-up only when clinically indicated. Primary outcome is the extremity-specific functional status, measured using web-based questionnaires. For the ankle fractures the Olerud and Molander ankle score will be used. For the wrist fractures, the Disabilities of the Arm, Shoulder and Hand Score will be used. Secondary outcomes include: Extremity function measured with the American Academy of Orthopaedic Surgeons Foot and Ankle questionnaire (ankle fractures) and the Patient Rated Wrist and Hand Evaluation (wrist fractures), pain intensity, health-related quality of life, self-perceived recovery, and complications such as bone infections, nonunion, malunion, implant failure and costs. Both groups will be monitored clinically at 1,2,6, and 12 weeks and at 6 and 12 months.
Discussion: This study will provide data on (cost-)effectiveness of routine radiography in the follow-up of uncomplicated ankle and wrist fractures, without compromising the quality of care and could pave the way for a change in (inter)national protocols.
Doel van het onderzoek
We hypothesize that a reduction of the current radiographic follow-up protocol for patients with ankle and wrist fractures will lead to significant cost savings without compromising quality of care
Onderzoeksopzet
Follow-up at 1,2,6 and 12 weeks, 6 months and 1 year
Onderzoeksproduct en/of interventie
Group 1 is to receive usual care according to the current national protocol, indicating clinical follow-up as well as radiographic evaluations, which shall take place in the outpatient clinics at 1, 2, 6, and 12 weeks.
Group 2 is to receive the same clinical evaluations as the usual care group (see above); however, no routine radiographs will be performed beyond the initial 2 weeks. Radiography during follow-up will be allowed (10% estimated), if any of the following are present: 1) new trauma to the wrist or ankle; 2) pain > 6 based upon the visual analogue scale (11-point VAS); 3) loss of range of motion (ROM) > 20 degrees; 4) neurovascular symptoms; or 5) at the discretion of the clinician
Algemeen / deelnemers
Datacenter Heelkunde, K6-R<br>
P.O. Box 9600
P. van Gerven
Leiden 2300 RC
The Netherlands
+31715297981
p.van_gerven@lumc.nl
Wetenschappers
Datacenter Heelkunde, K6-R<br>
P.O. Box 9600
P. van Gerven
Leiden 2300 RC
The Netherlands
+31715297981
p.van_gerven@lumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Adult (> 18 years);
- Fracture of the ankle (uni-or bimalleolar fractures /Lauge-Hansen classification SA II, SE II-IV, PA I-IV) or fracture of the distal radius (AO classification type A-C);
- Sufficient understanding of the Dutch language
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Psychiatric conditions;
- Pathological fractures;
- Complicated fractures (Gustilo grade 2 & 3);
- Multi-extremity fractures;
- Unable to complete follow-up
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiƫnten Data (IPD)
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